AIP Flashcards

1
Q

What is alveolar-arterial O2 gradient used for

A

In type 2 resp failure

  • if A-a gradient normal = not due to lung disease
  • if A-a gradient is raised = intrinsic lung disease
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2
Q

causes of a complete white out on CXR

A

Trachea deviated towards = total lung collapse, pneumonectomy

Trachea central = consolidation (pneumonia), ARDS

Tracheal away = large pleural effusion

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3
Q

Electrolyte daily requirements

A

Na - 1-2 mmol/kg/24hr
Cl - 1 mmol/kg/24hr
K - 0.5-1 mmol/kg/24hr (max safe dose is 10mmol/hr)
(1 of each)

Glucose - 50-100g
Water - 25-30 ml/kg/24hr (20-25 if elderly, HF or CKD)

When doing maintenance fluids for obese patients - use ideal bodyweight based on BMI and use lower end of range e.g. 25 ml/kg/24hr

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4
Q

Signs of dehydration on U&E

A

Hypernatraemia, high haematocrit, raised Hb

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5
Q

Transfusion threshold - normally and with ACS

A

70g/L normally

80g/L with ACS

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6
Q

G&S vs crossmatch

A

G&S - just looks at patients blood - identifies Rhesus status, ABO blood group and antibodies present

  • no blood is issued
  • used if no current blood loss, anticipate might be needed in future

Crossmatch - assesses transfusion by mixing small amount of patient and donor blood to look for a reaction

  • following testing blood is issued
  • need a G&S before hand
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7
Q

Blood product thresholds

A

Platelets - bleeding and <30x10^9
Plasma - if bleeding and abnormal coag (APPT ratio >1.5)
Cryoprecipitate - DIC with fibrinogen < 1g/L, von willebrand

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8
Q

Immediate immune reactions to transfusion, how they present and management

A

ABO incompatibility - fever, tachycardia, hypotension, anxiety, may have red urine. Treat by stopping transfusion, starting IV fluids and giving platelets/ other blood products as needed to prevent DIC.

TRALI - transfusion related acute lung injury - present with fever, SOB, hypoxaemia, hypotension. Diffuse infiltrates on CXR. Stop transfusion, give O2, IV fluids and ionotropes (dobutamine or adrenaline)

Anaphylaxis - itchy rash, angioedema, SOB, vomiting, light headed, hypotension. Stop transfusion, IM adrenaline 0.5mg every 10 mins, salbutamol nebs, O2. Steroids, chloramphenamine 2nd line/ post initial stabilisation.

Not a reaction but can get fluid overload causing SOB, bibasal creps, hypoxia, tachycardia, raised JVP. Treat with IV furosemide and O2.

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9
Q

Indications for arterial line + what the trace tells us + complications

A

Continuous real time monitoring of BP, need for repeat ABG’s

Tells us:

  • blood pressure
  • myocardial contractility - gradient of upwards curve
  • volume status - narrow waveform = hypovolaemia

Complications:

  • bleed - apply 3-5 mins of pressure post removal
  • thrombus
  • emboli
  • infection
  • accidental drug injection
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10
Q

Causes of raised and low CVP - how it is measured?

A

High - fluid overload, RHF, pulmonary hypertension, tricuspid disease, SVC obstruction

Low - hypovolaemia, distributive shock

Measured using central venous catheter e.g. central line, Hickmann, picc line

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11
Q

Catecholamine drugs used in ICU - what are their target receptor and action

A

Noradrenaline - Acts on alpha 1 - cause peripheral vasoconstriction increasing SVR and CO

Adrenaline - Acts on alpha 1 (high doses) doing same as above and acts on Beta 1 (low doses) causing increased SV, HR, CO

Dopamine - same as adrenaline

Dobutamine - Acts on Beta 1 and Beta 2 - causes increased HR, SV, CO but causes vasodilation

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12
Q

Classes of anti-arrhythmics

A

Class I - sodium channel blocker e.g. lidocaine, phenytoin, quinidine, flecainide
Class II - Beta blocker e.g. propanalol
Class III - K+ channel blocker e.g. amiodarone
Class IV - calcium channel blocker e.g. verapamil, diltiazem

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13
Q

Indications for NG tube + when to do a PEG tube

A

Feeding

  • dysphagia or unsafe swallow due to neuro issue
  • reduced consciousness
  • protect stomach after surgery
  • insufficient oral intake

Removal of gastric contents

  • bowel obstruction for immediate decompression
  • For resting of the bowel in bowel obstruction

Do a PEG tube when need long term feeding e.g.

  • burns
  • oesophageal carcinoma
  • coma, stroke
  • Crohn’s
  • fistulae
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14
Q

How is TPN given

A

Via a central line

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15
Q

Refeeding syndrome

A

Malnutritioned patients get energy by breaking down existing tissues, hence have low vitamin, electrolyte levels

Occurs when high amount of carbohydrates are given to a malnourished patient. Causes for high insulin secretion,

Insulin leads to K+, PO4, Mg movement into cells, causing a significant drop in levels and an increased extracellular fluid volume

Get an increase in O2 demand leading to increased cardio and respiratory effort

Can cause rhabdomyolysis, cardiac/resp failure, seizure, coma

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16
Q

what to give patients in a coma

A

glucose, thiamine IV if cause unclear

may also trial naloxone or flumazenil

raised ICP consider mannitol

fluids + ventilation, nutrition, pressure sores

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17
Q

How to confirm brainstem death

A

First need to meet two criteria

  • evidence that condition due to irreversible structural brain damage
  • all reversible causes of coma excluded

Then:

  • Pupils fixed and unresponsive to bright light
  • Absent corneal reflexes
  • Absent vestibulo-ocular reflexes (irrigation of the ear with ice-cold water, dolls eye reflex)
  • No motor response to trigeminal pain response. An example of this would be no facial grimace to nail bed pressure
  • No gag or cough reflex
  • Apnoea
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18
Q

What number to call if no signs of life in suspected cardiac arrest

A

2222

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19
Q

When to give adrenaline/amiodarone during CPR

A

Give 1mg IV adrenaline and amiodarone 300mg IV after 3rd shock. Then give adrenaline every 3-5 minutes after

Give an additional 150mg amiodarone after 5 shocks

If not shockable give 1mg IV adrenaline as soon as IV access

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20
Q

Reversible causes of cardiac arrest to treat during CPR

A

4 H’s

  • Hypoxia
  • Hypovolaemia
  • Hypothermia
  • Hyper or hypokalaemia

4 T’s

  • Tension pneumothorax
  • Tamponade
  • Toxins
  • Thromboembolism
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21
Q

Cardiogenic shock - definition, causes, presentation, ix, mx

A

Caused by failure of heart to achieve required cardiac output

Causes include: HF, MI, acute dysrhythmia, acute mitral regurg, cardiomyopathy, thyrotoxicosis, severe valvular disease

Defined as SBP <90 for >30 mins or poor peripheral/ end organ perfusion (<0.5ml/kg/hr urine output)

Present as pale, mottled, cold skin. Prolonged CRT. Cold peripheries. Tachycardia, hypotension. Often pulmonary oedema, raised JVP (signs of HF)

Ix: bloods (U&E for renal failure, FBC for anaemia, LFT), ABG, BNP (low can help rule out), ECG, Echo, cardiac enzymes (trops)

Another cause is obstructive e.g. PE, tension pneumothorax, tamponade - do CXR, CTPA

Mx:
O2 to maintain sats >94% (check vs 96%)
250ml fluid boluses if intravascular volume depletion
Monitor with - cardiac monitoring, BP via central line, CVP via central line, catheter for urine output

Treat cause e.g. thrombolysis, percutaneous intervention for MI
vasopressors - dobutamine
Intra-aortic balloon pump - increases cardiac output and improves coronary artery blood flow

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22
Q

Hypovolaemic shock

A

Presents with dizziness, fainting, cold/clammy/confused. Skin pale, sweaty. Prolonged CRT, hypotension, tachycardia.

Causes include blood loss, burns, excessive exercise, diarrhoea and vomiting

Ix:
AtoE
Bloods - Hb, U&E, FBC, LFT, Coag, crossmatch, G&S
ABG 
Urine output 
US can differentiate from cardiogenic 
CVP monitoring 
Mx:
AtoE
Look for cause - try to stop bleeding 
Oxygen - keep sats 94
Fluid boluses - 500ml over 15 mins
Blood as needed 
IV pain relief 
Tranexamic acid 
If non responsive to fluids may consider vasopressors 

If needed:
Resuscitative endovascular balloon occlusion of the aorta
Surgery to stop bleeding

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23
Q

anaphylactic shock

A

Present with SOB, angioedema, urticaria, itching

serum mast cell tryptase - use to confirm diagnosis

Mx:
2222
Lie flat with legs raised, secure airway, give O2
0.5mg IM adrenaline - repeat after 5 mins if no improvement
Fluid challenge - 500ml over 5-20 mins
Chlorphenamine 10mg, hydrocortisone 200mg after initial resus
further deterioration treat as acute asthma

observe for 6-12 hours

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24
Q

Neurogenic shock - cause, triad of signs and mx

A

Cause is cervical and upper thoracic injury (above T6)
Loss of sympathetic tone that causes vasodilation and bradycardia

Can also be caused by iatrogenic spinal anaesthesia placement

Develop triad of bradycardia, hypotension and hypothermia

Mx:
IV fluids
Treat cause
Atropine if haemodynamically significant bradycardia
Vasopressors e.g. dopamine, dobutamine may be needed if fluid resus not effective

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25
*Asthma - cough, breathlessness, wheeze, chest tightness
Hyper-inflated chest, wheeze, tachypnoea on exam Worse at night or in early morning, diurnal variation Worse in cold air, dust, allergens, when exercising Hx of atopy Ix: FeNO - eosinophil inflammation (>40) Spirometry w. bronchodilator - FVC increase by 200ml, FEV1 by 12% Peak flow - >50-75% mod, 33-50% severe, <33% life threatening 20% diurnal variation Bronchial challenge test Tx: Educate - lifestyle ``` ABCDE + ABG Oxygen (>94%) Salbutamol neb 5mg Hydrocortisone 100mg IV or pred 40mg PO Ipratropium bromide neb 500mcg Magnesium sulfate 1.2-2g IV IV Aminophylline Escalate if pH <7.3, Intubate ``` Be stable on discharge meds for 12-24hrs before discharge ``` Long term: SABA SABA+ICS (if using >3x a week, waking once at night) SABA+ICS+LTRA SABA+ICS+LABA +/- LTRA MART Intermediate dose ICS Thophylline ```
26
Definition and causes of type 1 resp failure | - polycythemia can indicate long term hypoxia
PO2 < 8kpa Causes = problems with diffusion at alveoli level Hypoxia present with - Signs of respiratory distress - Cyanosis - Restlessness, agitation - Confusion - Tachycardia and cardiac arrhythmias Causes: - pneumothorax - pneumonia - pleural effusion - pulmonary oedema - R-L shunt - PE - Lung fibrosis
27
Definition and causes of type 2 resp failure | - symptoms of hypercapnia
PO2 < 8kpa PCO2 > 6kpa Causes = issues with ventilation High CO2 present with: - headache due to cerebral vasodilation - flushing - warm peripheries - bounding pulse - CO2 retention flap - Drowsiness, confusion, coma - Acute asthma attack (exhaustion) - Severe COPD - Foreign body inhalation, CF or bronchiectasis secretions - Chest wall deformity - Kyphoscoliosis - Neuromuscular disease - GB - Opioid overdose, stroke - brainstem resp depression Start on 24% Venturi due to risk of hypoxic drive, repeat ABG at 20 mins, if PaCO2 has risen by >1.2 consider invasive ventilation
28
What imaging sign is needed to diagnose idiopathic pulmonary fibrosis + how to treat Can lead to pulmonary HTN and heart failure
Honeycombing without any clear cause On CT see ground glass/ honeycombing Restrictive pattern on spirometry Can confirm with lung biopsy Tx - acutely - high dose steroids - Long term - Pulmonary rehab, exercise, stop smoking, PPI, pirfenidone/ nintedanib, opiates for cough, LTOT, lung transplant Only use drugs if FVC 50-80% predicted, stop if drop in FVC >10% in a year
29
Cause of fine vs coarse crackles
Fine crackles - commonly pulmonary fibrosis (>45yo) - associated with dry cough, SOB, chest discomfort, end inspiratory crackles, clubbing, weight loss, restrictive pattern on spirometry Coarse crackles = fluid due to oedema, pneumonia, chronic bronchitis, bronchiectasis, aspiration
30
30 yr old black female presents with SOB, cough, painful red nodules on shin. CXR reveals bilateral hilar lymphadenopathy, pulmonary infiltrates - What are the two top differentials? What findings on blood tests would point towards diagnosis How is diagnosis confirmed How treated
Sarcoidosis - serum ACE, calcium level raised - long term Diagnosis confirmed by biopsy - non-caseating granulomata with epithelioid cells Majority get better on own - may need corticosteroids. High dose for 4-6w then taper over course of a year. Give bisphosphonate. If needed give IV Methylpred or immunosuppressants e.g. methotrexate Lofgrens syndrome - acute form of sarcoidosis - triad of bilateral hilar lymphadenopathy, erythema nodosum and polyarthralgia - NSAID, steroid, colchicine
31
Pleural effusion Cough, SOB, pleuritic chest pain Empyema presents with above + fever, rigors, productive cough
On exam looking for stony dullness, reduced breath sounds, reduced chest expansion, reduced vocal resonance Take detailed history to elucidate cause Do CXR, bloods to differentiate causes (D-dimer, LDH, protein, amylase, WCC), ABG, CT if suspect malignancy, ECG/echo for HF Important take a sample of pleural fluid using US to differentiate cause - look at protein, LDH. Not needed if bilateral effusion typical of transudate if asymptomatic - 50ml, if symptomatic aspirate till sx improve Send for biochem (pH, protein, LDH, glucose), cytology (blood), microbiology (gram stain and culture) If protein >35 = exudate (unilateral) - cancer, infection, PE, AI, pancreatitis If <25 = transudate (bilateral) - HF, LF, RF, hypo-albumin, peritoneal dialysis Can also be haemothorax, chylothorax, empyema (pH <7.2) If blood do haematocrit, if >1/2 of level in peripheral blood = haemothorax If between the two use lights criteria - is exudate if Protein pleural: blood >0.5 LDH pleural:blood >0.6 LDH pleural >2/3 upper limit of normal for serum pH<7.2 = empyema until proven otherwise Treatment If transudate - treat underlying failure - diuretics etc If exudate - small - observe - infection - Abx, antipyretics - Large - therapeutic aspiration (no >1.5L), chest drain - If recurrent - long term chest drain or pleurodesis using talc or pleurectomy
32
Chronic bronchitis definition = part of COPD
chronic productive cough for at least 3m in each of the last 2 years
33
COPD
``` Ix: Respiratory exam Peak flow Spirometry with bronchodilator - restrictive picture (FEV1 <80%, FEV1/FVC <0.7) CXR for cor pulmonale If acute exacerbation do sputum culture, ABG Sputum culture if purulent MRC dyspnoea score - activity limitation BODE index - prognosis GOLD staging ``` Tx Lifestyle modification and patient education, stop smoking Acute: O2 (start on 15L, reduce to 24% venturi if hypoxic drive), salbutamol, ipratropium, prednisolone, Abx, physio, NIV (if academia/ rising CO2, pulmonary oedema, tiring T1 failure), Theophylline Start on SAMA or SABA Add either LABA + LAMA or LABA +ICS LAMA + LABA + ICS COPD rescue pack - prednisolone - if increasing breathlessness - Amoxicillin/ doxy/ clarithro - if change in sputum colour - Salbutamol - extra incase needed Long term oxygen therapy if PO2 <7.3 or between 7.3-8 and have secondary polycythaemia, peripheral oedema or pulmonary HTN Long term abx prophylaxis = azithromycin Consider mucolytic if bronchiectasis
34
Pneumonia
Criteria: Symptoms of acute LRTI (cough and at least one other LRT symptom) New focal chest sign on exam At least one systemic feature (sweating, temp of >38, shivers, aches, pains) No other explanation for the illness Most common CAP = s pneumoniae, H influenzea in COPD HAP - 48hrs post admission, within 5d most likely s pneumoniae, after 5 most likely H influenzea, MRSA, pseudomonas ``` Ix: Respiratory exam O2 sats CXR FBC, U+E, LFT, CRP, ABG Lung function test Blood + sputum culture Sepsis 6 is suspect systemic infection, dropping vitals Procalcitonin to monitor ``` Do CURB 65 - who needs admission Confusion, Urea >7, RR >30, BP <90/60, >65 home: 0-1, hosp >2, ITU assessment >3 ``` Tx: Educate, stop smoking Fluids Oxygen if hypoxic Analgesics for pleuritic pain Start on antibiotics - low severity: amoxicillin 5-7d - Mod: amoxicillin + clarithro 5-7d - severe: co-amox + clarithro 7-10d ``` If suspect aspiration -> metronidazole For hospital acquired - co-amox for mild, tazocin for severe Do repeat CXR 6w after symptom resolution - look for malignancy hid by consolidation/ effusion
35
Causes of pleuritic chest pain
PE, pleural effusion, pneumonia
36
Pneumothorax mx - sudden onset pain, SOB, reduced breath sounds, hyper-resonance on percussion, tachycardia
If >50 and smoke or evidence of lung disease on exam/ CXR -> secondary Tension - haemodynamically unstable, compromised CO, mediastinal shift Ix: - CXR - erect - US if supine - CT if diagnostic uncertainty, not clear from CXR/US - ABG Pleural surface to Lung edge at hilum - measure Primary <2cm AND no breathlessness = discharge with outpatient x-ray Primary, >2cm OR breathless = percutaneous aspiration and oxygen then 2nd x ray to confirm gone Secondary <1cm = oxygen and admit for 24 hours Secondary 1-2cm = aspiration (if fails then chest drain) Secondary >2cm OR breathless = chest drain (if fails then discuss with thoracic surgeon) Do chest drain for any ventilated, tension, bilateral or if haemo unstable Tension = needle decompression in 2nd IC space MC line, oxygen then chest drain in triangle of safety Refer for pleurodesis if recurrence or surgery for open thoracotomy and pleurectomy or video-assisted thoracoscopic surgery with pleurectomy and pleural abrasion (better tolerated than open surgery) Catamenial pneumothorax is around time of menstruation due to endometriosis forming necrotic holes in the diaphragm
37
*Bowel obstruction - causes and management
Can be mechanical - e.g. due to volvulus, intussusception, hernia, cancer, adhesions, strictures, diverticular disease. Or can be paralytic - e.g. post op, due to drugs such as opioids, gastroparesis, hypokalaemia, bowel ischaemia Sx - Diffuse abdominal pain, worse on movement - third spacing causes diarrhoea and water loss - vomiting (contains bile, faeces), dehydration - abdominal distension - no stool passage - if perforation - guarding, tenderness - tympanic percussion, high pitch bowel sounds Ix - Assess for dehydration - ABG if suspect sepsis, abnormal electrolytes - FBC, U&E, LFT, G&S, crossmatch for surgery - Abdo xray - bowel dilation, air-fluid levels, no distal gas - CT - CXR if suspect perforation (air under diaphragm) - MRI/ US can be helpful Mx - NBM - Drip and suck - NG tube for aspiration and drainage of stomach, IV infusion for rehydration - Analgesia, antiemetic - Monitor urine output as marker of dehydration - catheter Laparotomy may be essential if diagnosis unclear, signs of ischaemia, closed loop obstruction or perforation For volvulus may be reducible with sigmoidoscopy/ flatus tube insertion For malignant obstruction - endoscopic stenting in palliative care For adhesions do gastrografin imaging and either treat conservatively or with adhesiolysis. Neostigmine for acute colonic pseudo-obstruction
38
Mesenteric ischaemia triad - presentation, ix, mx Often due to thrombus
CVD, high lactate, abdomen soft but tender Pain disproportionate to clinical findings, limited abdo tenderness with lots of pain Presents with mild to moderate colicky pain or constant poorly localised pain, loose bloody stools, N+V. Later stage get sepsis, peritonism, ileus. Ix - ABG showing metabolic acidosis and FBC showing raised WCC can raise suspicion - AXR to rule out other causes - CT angiography is gold standard to identify occlusive event - normal CT may show pneumatosis intestinal, Mesenteric oedema, bowel dilation - ECG/ Echo to identify cardiac RF/ cause Mx - NBM, IV fluids, oxygen, broad spectrum Abx, NG for decompression, analgesia - Start IV unfractionated heparin - May use local thrombolytics if angiography performed - Surgery to remove necrotic bowel or revascularise bowel
39
Chronic mesenteric ischaemia Due to atherosclerosis
Presents with weight loss, abdominal pain after eating, fear of eating on background of CV risk factors Ix: Angiography Mesenteric duplex US to assess blood flow Tx - asymptomatic - smoking cessation and antiplatelets - symptomatic - endo-vascular or open revascularisation
40
Ischaemic colitis - often due to hypovolaemia
Mild, colicky abdominal pain typically in LIF, N+V, prominent bloody diarrhoea -> dehydration, shock, metabolic acidosis Ix: - ABG show metabolic acidosis - Colonoscopy show blue mucosa, limited bleeding - AXR shows gas surrounding bowel - Barium enema shows thumb printing sign Mx - correct cause of hypovolaemia - often resolves - broad spectrum abx - If ileus NG tube - surgery if guarding and rebound tenderness, fever, uncontrollable bleeding or paralytic ileus indicating possible infarction of the colon
41
Treatment in GI perforation
Resus - IV fluids, O2 IV abx NG tube for decompression Surgery to repair + washout
42
What classifies as AAA, indications for surgery - all men over 65 in uk are offered abdo US to look for AAA
>3cm = AAA, >5.5cm = surgery If 3cm-5.4cm refer to vascular to be seen within 12w, monitor via US - 3-4.4 - yearly US - 4.5-5.4 - 3 monthly US BP control with beta blocker, control CV risk factors e.g. stop smoking, exercise If 5.5 or greater refer to vascular to be seen within 2w Surgery if >5.5 or >4 and expanding at rate of >1cm per year Can do open or endovascular repair
43
AAA rupture - Ix/ Mx | what is triad of abdominal rupture presentation
Thoracic - retrosternal/ central back pain, haemoptysis, collapse - often causes rapid cardiac tamponade Abdominal - flank or back pain, hypotension and a pulsatile, expansile abdominal mass - signs of shock - hypotension, tachycardia, collapse, weak thready pulse Ix: - Bloods - FBC, U&E, LFT, clotting - G&S, Crossmatch 6U - Portable US if unsure - If not yet ruptured: CT/ CT angiogram - ECG if thoracic to identify MI Mx: - AtoE - High flow O2 - IV access - O-ve blood - Aim SBP <100 - Prophylactic Abx - Cefuroxime and metronidazole - If stable do CT angio - If unstable emergency theatre <70 - open >70 or women or Comorbs consider end-vascular repair
44
Acute cholecystitis/ cholangitis management - how present, Ix and Mx Biliary colic - RUQ pain after eating fatty food
Acute cholecystitis - fever + RUQ pain, N+V Ascending cholangitis - fever + RUQ pain + jaundice (+ shock + mental confusion) If swinging pyrexia = gallbladder empyema Ix: Do a GI exam - look for jaundice, Murphy's sign +ve FBC, U+E, CRP, LFT (ALP/GGT/billirubin), amylase/lipase (pancreatitis) ABG, culture if suspect sepsis US gallbladder ECRP, MRCP or HIDA cholescintigraphy if US -ve Contrast CT for cholangitis or if suspect complication e.g. perforation Mx: Acute cholecystitis: Monitor BP, pulse, urine output NBM, IV fluids Analgesics - diclofenac or opioid IV abx - trust guideline (cefuroxime and metro) Laparoscopic cholecystectomy - Nil by mouth, IV fluid, analgesia, ondasteron Cholangitis - Ecoli Monitor BP, pulse urine output NBM, IV fluids Analgesics - diclofenac or opioid IV abx - trust guideline (cefuroxime and metro) ERCP to remove stone or can stent/lithotripsy Cholecystectomy
45
Ureteric stone - present with sudden onset severe loin to groin pain - lasts mins to hours - may be haematuria
Ix: Bedside - urinalysis and Mc&S (look for haematuria) Bloods - urate and calcium levels, FBC, U+E, LFT, CRP, bone profile, Ca, PTH (exclude high ca as cause), uric acid Imaging - US for hydronephrosis, CT KUB within 24hr Stone analysis Struvite stones - stag horn calculi Mx: Advice to increase fluids, loose weight, reduce salt/urate/oxalate/protein in diet At home if <5mm - fluids, pain relief (Paracetamol/ tramadol), antiemetic - Watchful waiting - most pass on own within 3w - Refer to stone clinic Can help passage with CCB (nifedipine) or alpha blocker (tamsulosin) if 5-10mm ``` In hosp if >10mm AtoE, give IV fluids IM diclofenac, antiemetic If hydronephrosis - stent, nephrostomy, catheterise Treat infection Shock wave lithotripsy Percutaneous removal Uretero-renoscopy ``` Prevention - potassium citrate, thiazide diuretics for calcium stones
46
Diverticular disease - LLQ pain worse on eating, better after stool - Change in bowel habit, bloating, intermittent signif bleeding - rectal mucus Diverticulitis: - N+V - may have fever/ tachycardia - may have urgency of urination as can irritate bladder
Ix: Routine obs + bloods CXR - look for air under diaphragm (perforation) CT of abdomen Barium enema Sigmoid/colonoscopy - not do in diverticulitis due to risk of perforation Mx: If asymptomatic diverticulosis - reassure, suggest lifestyle changes and increase fibre in diet (aim 30g a day) Diverticular disease - 30g fibre a day, bulk forming laxatives 2nd line, give paracetamol and antispasmodics. Avoid NSAIDS and opioids (increase risk of perforation) Diverticulitis - Co-amoxiclav, if complications admit for IV fluids, Abx, analgesia. Consider surgery if peritonitis or sepsis, percutaneous drainage if abscess.
47
Appendicitis
Umbilical pain that worsens and migrates to RIF over 24-48 hours. Worse on movement, low grade fever, N+V, change in bowel habit On exam: - Rovsing's sign - pain in RIF when push in Left - Psoas sign - lie on left side, extend right hip, causes RIF pain - often walk slowly, bent over, holding RIF Ix - Bloods - FBC, U&E, LFT, CRP - Urine dipstick + mc&s to exclude renal cause - US to exclude suspected gynae differentials e.g. ovarian cyst - Pregnancy test to exclude ectopic - CT to confirm prior to surgery Mx - NBM - IV fluids - IV abx - laparoscopic appendicectomy
48
Pancreatitis Acute abdominal pain in epigastric/ LUQ. Radiates to back, better when in foetal position, N+V, fever, peritonitis, flank and periumbilical bruising
Main causes are gallstones, alcohol, steroids Ix: Serum lipase/amylase (also high) Obs Blood sugar, ECG, pregnancy test FBC, U&E, LFT (cholestasis), CRP + bone profile + LDH Do blood gas for grading Do US, if negative consider MRCP for gallstones AXR/ CXR can rule out bowel obstruction/ perforation CT only if diagnostic uncertainty or nor improving after 10-14days ``` Do Glasgow score in first 48hrs to assess severity - greater or equal to 3 = severe - refer to ITU PaO2 <8 Age >55 Neutrophils >15 Calcium <2 Renal function, Urea >16 Enzymes - LDH >600, AST >200 Albumin <32 Sugar >10 ``` Mx: Cut down on alcohol, review meds IV fluids (Hartmans) - 1L stat then 1L over 2, 4, 6, 8 hrs Analgesia - paracetamol, codeine, oramorph Nutritional support Antiemetics (ondansetron) Catheterise to monitor urine output Manage gallstones, Abx if infected/ necrosis - ERCP |+/- lap cholecystectomy If suspect pancreatic necrosis - aspirate and culture - may need surgery Other complication is retroperitoneal bleed ARDS is complication if become breathless - may need CPAP
49
Chronic pancreatitis
Presents as chronic epigastric/ RUQ pain, N+V, reduced appetite and progressive endo/exocrine insufficiency e.g. steatorrhoea, weight loss, malnutrition, DM Ix: Bloods, obs (FBC, U&E, creatinine, LFTs, calcium, amylase (usually normal)) Blood glucose, HbA1c If suspect malnutrition do serum trypsinogen and faecal elastase Secretin stimulation test - if impaired exocrine function CT first line investigation Endoscopic US or secretin enhanced MRI alternatives Mx Lifestyle - weight loss, stop smoking/ alcohol, dietician Pain relief - pain ladder + ERCP stents Pancreatic enzyme replacement - Lipase e.g. creon Steroids if AI DM management + screening Surgery for complications e.g. pseudo-cyst
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Coeliac ``` In kids - failure to thrive and below: Weight loss Fatigue Weakness Abdominal pain Bloating Flatulence Loose stools Steatorrhoea ``` Associated with dermatitis herpetiformis
Ix confirm individual eaten gluten twice a day over last 6 weeks - IgA Ttg and Total IgA, (2nd line IgG Ttg/ IgA EMA) - If +ve send to GI for endoscopy and duodenal biopsy - villous atrophy and crypt hyperplasia - stool culture, MC+S - FBC (anaemia), U+E, LFT, CRP, ESR, Vit b12/ folate - Skin biopsy if rash Mx Avoid gluten - dietary counselling, referral to dietician No wheat, barley, rye Vit D, Ca supplements if insufficient in diet Assess and manage osteoporosis risk Yearly follow up, assess sx, BMI, diet adherence, blood tests If refractory - refer to dietician, specialist and consider short term prednisolone Complications are dermatitis herpetiformis and Enteropathy-associated T-cell lymphoma (EATCL)
51
Dyspepsia CBD - differentials and mx GORD: Heartburn - worse post meal when lying flat or leaning forwards, acid regurg, bloating, early satiety Peptic ulcer: Present with Abdominal fullness, heartburn, nausea, belching, epigastric pain, heartburn, malaena, coffee ground vomit Eating worsens gastric, improved duodenal
``` GORD Peptic ulcer Hiatus hernia Gastroparesis - DM Malignancy Drugs lactose intolerance Coeliac ``` Lifestyle - smaller more regular meals, lift head in bed, eat meals earlier, weight loss, avoid trigger foods, smoking, reduce alcohol, stress/anxiety GORD: Ix - 4w PPI trial, OGD if any alarm symptoms (anorexia, anaemia, loss of weight, IDA, melaena) Mx Consider a month trial of PPI to help the oesophagus heal, if severe 2months. If recurrent put on lowest effective dose long term stop any exacerbating drugs If persistent, oesophagitis - consider doubling PPI dose or adding ranitidine If ineffective consider laparoscopic fundoplication Peptic ulcer: Ix - Hpylori breath test or stool antigen test (not have taken PPI for 2w or Abx for 4), OGD with biopsy (urease testing), FBC for anaemia due to blood loss, Mx Review meds (aspirin, bisphosphonates, corticosteroids, potassium supplements, SSRIs, cocaine) Ask about prev Abx that could affect H pylori tx 7d - Omeprazole, clarithro/metro and amoxicillin Retest endoscopy and breath or stool test as TOC at 6-8w If due to NSAID give 2month PPI If NSAID + H pylori - 2month PPI then eradication If bleeding consider clipping, thermal coag, adrenaline Interventional radiology if not improve with endoscopic management, surgery if not available Hiatus hernia/ malignancy - Barium swallow or endoscopy
52
Crohns management - mouth ulcers - Diarrhoea (nocturnal) - abdo pain - Blood in stool - B12 deficiency (malabsorption in terminal ileum), tingling in fingers Skip lesions, transmural, entire GI tract
``` Ix: GI exam, PR and Oral examination FBC (anaemia), U+E, LFT, CRP, ESR, ferritin, B12, folate Stool sample - culture and calprotectin ASCA +ve, pANCA -ve Colonoscopy + biopsy from terminal ileum OGD to differentiate from peptic ulcer Bowel CT/ MRI to look for fistula ``` Mx: Induce remission with corticosteroid e.g. prednisolone/ budesonide (modified release steroid) or 5-ASA if steroids CI/ not tolerated If >2 acute episodes in last 12 months add azathioprine or mercaptopurine If severe induce with IV hydrocortisone, consider parental nutrition, Abx and blood transfusion Maintain remission with azathioprine/mercaptopurine, second line methotrexate To treat diarrhoea - loperamide - antispasmodic e.g mebeverine - bulk forming laxative - bile acid sequestrant e.g. cholestyramine Surgery if obstruction, stricture, perforation, abscesses, enterocutaneous fistula - colectomy, segmental repair, widen stricture, stoma Strictures, fistuae, obstruction are complications
53
Management of UC Bloody diarrhoea, tenesmus, LLQ pain often improved on defecation, urgency/ incontinence, Only LI, superficial, crypt abscesses Ask if eye, skin, MSK, hepatobilliary
``` Admit if systemically unwell Ix: FBC (blood loss, anaemia), U+E (dehydration), ESR, CRP Stool sample to exclude infection, do calprotectin Colonoscopy + Biopsy pANCA +ve, ASCA -ve CT to stage, look for complications Abdo xray- lead pipe ``` Assess severity with true love and Witts Tx: Induce remission with 5ASA either topical or oral, if resistant can add corticosteroids, if still not improving over 2w start biologic e.g. adalimumab If severe episode consider IV steroids + PPI supplemented with IV ciclosporin if no improvement over 72 hours, also IV fluids, Abx, VTE prophylaxis Maintenance use ASA topical or oral, if >2 relapses in last 12mo that required steroid treatment add azathioprine or mercaptopurine Protocolectomy - 1st line surgery Subtotal colectomy with end ileostomy, preservation of rectum - if malignancy, toxic megacolon, failure of medical mx Don't give loperamide - risk of toxic megacolon Avoid NSAIDs UC associated with increased risk of colorectal cancer and PSC
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Causes of cardiovascular syncope Pale before, become flushed after collapse, lasts seconds Physical exertion is often a trigger, often no prodrome (unlike vasovagal, have lightheadedness, sweating, nausea) sudden uncontrolled fall to ground (slow and controlled in vasovagal)
Structural heard disease: CAD, valve disease, tamponade, cardiomyopathy, dissection Pulmonary disease e.g PE Sudden onset headache and collapse - SAH If complete heart block - stokes Addams attacks
55
Collapse when working with arms above head - cause?
Subclavian steel syndrome
56
Epilepsy Hx and management >2 unprovoked seizures occurring more than 24 hours apart – within a year of each other
``` Ix: CV, neuro, MSE - identify injuries Routine obs FBC, U+E, LFT, CRP, BM (hypoglycaemia), toxicology screen, blood cultures if think infection, lactate, Raised prolactin and CK ECG MRI - look for structural cause EEG ``` Mx: Advise on water safety (shower not bath, buddy system), leave bathroom door unlocked, fire safety and cooking, environment and work safety. Care with heights, high risk activities and consider contraception for certain meds. Advise family and carers. 1st seizure - 6months for car 5 years for HGV epileptic seizure 1 year for car >1 seizure - 10 years for HGV Focal - carbamazepine Tonic-clonic seizures: sodium valproate or lamotrigine. Absence seizures: ethosuximide or sodium valproate Myoclonic seizures: sodium valproate or topiramate. Status epilepticus = seizure >30 mins or recurrent without regaining consciousness (treat at >5mins) AtoE Lorazepam 4 mg IV, if unavailable; Diazepam 10 mg PR, if unavailable; Midazolam 10 mg buccal if 2 doses of above 10 mins apart, if not work give phenytoin If phenytoin not work transfer to ITU for GA
57
Loss of consciousness hx + Ix
Triggers, what happening before - exercising? flashing lights? arms above head? lying/standing? Prodrome - light headed, dizzy, nausea, sweating if vasovagal, none if cardiac, deja vu, hallucination, feeling of doom if seizure Look pale before, sudden, without warning, on exertion = cardiac Remember hitting floor - if so is a fall not collapse How collapse - sudden and uncontrolled = cardiac, slow and controlled = vasovagal Motor symptoms? Duration - seconds = cardiac, 30 seconds = vasovagal, mins = seizure Tongue biting, incontinence Time till recovery - seconds = cardiac/ syncope, seizures can be longer, can have post-ictal drowsiness, amnesia, transient focal paralysis (Todd’s paralysis) Relieving factors - better when sat down? Any injuries/ any pain/ vomiting Then look for cause - any resent sx (fever (meningitis), chest pain (PE), headache, rashes, weight loss (SOL), DM) PMH, drug Hx, FHX, Social hx Investigations: - BP, HR, tilt table test - Echo/ ECG for cardiac issues - ABG - lactate raised in seizure - EEG for seizure - Bloods - U&E, FBC, LFT, blood glucose, AED levels
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TIA management Definition = Transient neurological dysfunction caused by focal brain, spinal cord, or retinal ischaemia, without evidence of acute infarction or tissue injury usually last 10-15 mins
Ix: Do neurological examination Do routine obs (BP often rise), perform a GCS, listen to carotids for bruit Can use FAST screening tool in primary care Refer to specialist centre for appointment within a day FBC, ESR, U+E, LFTs (including PT, INR), TFT, cholesterol, ECG/ echo if cardiac cause MRI preferable for identifying small infarcts, do CT head if suspect haemorrhage Carotid doppler to look for stenosis Assess risk of stroke using ABCD2 score - no longer recommended by nice Mx: 300mg aspirin loading dose immediately (unless risk of bleed) Cont. for 2w After 2w give 300mg clopidogrel loading dose then continue on 75mg a day long term Discuss lifestyle: diet, exercise, smoking, alcohol, no driving for 1 month Treat CV risk factors e.g. BP, cholesterol, AF (anticoagulant) If >70% stenosis - carotid endarterectomy
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Ischaemic stroke Difference between total anterior circulation stroke and partial: ``` Total = 3/3 Partial = 2/3 - hemiparesis/hemiplegia - problem with higher mental function (aphasia, apraxia, inattention) - hemianopia ``` Lacunar stroke - motor/sensory impairment but no change in higher cerebral function
A-E CV exam, ECG (24hr for AF) Always do BMs FBC, U&E, LFT, Coag, Cholesterol, antiphospholipid syndrome Toxicology Imaging - CT head within 24 hrs to exclude haemorrhage, CT angiography or magnetic resonance angiography if considering thrombectomy, CT perfusion scan can show salvageable tissue Carotid US doppler general - oxygen (sats>95%), blood glucose, swallow assessment, nutrition screen, mobilise, consider for carotid endartectomy - >50% on US <4.5 hours - alteplase infusion, 300mg aspirin after 24 hrs for 2 weeks then clopidogrel long term + thrombectomy if <6hrs and confirmed prom anterior circulation occlusion on CTA or MRA, or 6-34hrs if above + salvageable tissue on CT perfusion scan >4.5 hours - aspirin 300mg for 2 weeks then clopidogrel long term If cant tolerate clopidogrel - Aspirin 75 mg daily with modified-release dipyridamole 200 mg twice daily manage comorbidites such as lipids etc Confirm size of infarct, check for any complications of thrombolysis with CT at 24hrs If haemorrhage = poor prognosis, supportive care, manage BP, contact neurosurgery Rehab, physio
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How does carotid dissection present
Unilateral head/face/neck pain, horners syndrome, anterior circulation stroke/TIA
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Haemorrhagic stroke
``` A-E, CV exam Always do BMs FBC, U&E, LFT, Coag, Cholesterol Toxicology FAST rapid assessment CT - haemorrhage = white If suspect SAH do a lumbar puncture (do after 12 hours, look for xanthochromia) ``` Mx Oxygen (sats>95%), blood glucose, swallow assessment, nutrition screen, mobilise BP control - aim for 130 to 140 mmHg with IV labetalol swallow assessment Stop any anticoagulants Early mobilisation Falls risk assessment Decompressive hemicraniectomy (do within 48hrs if meet NIHSS based criteria) Rehab, physio
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What is pyramidal weakness, when is it seen
= UMN damage, seen commonly in CVA, have fixed flexion of upper limbs and extension of lower limbs
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PE management Massive PE = >50% obstruction and SBP <90 Provoked: flight, immobility, surgery, trauma, pregnancy, COCP, HRT, malignancy SOB, pleuritic chest pain, tachypnoea, cough up blood
Ix: Calculate the wells score - >4 -> CTPA - <4 -> Ddimer, if +ve do CTPA Start apixaban/ rivaroxaban while await result If allergic to contrast, GFR <30 or pregnant do V/Q SPECT Do FBC, U+E, CRP, LFT, Coag, thrombophilia ABG Do ECG to identify AF, PE changes (S1,Q3, T3) CXR to exclude other causes Screen for cancer if >40, unprovoked Mx: AtoE Give O2, analgesia, iv access, assess circulation (BP) If low risk, outpatient anticoagulant If high risk, admit to hosp 1st line: rivaroxaban or apixaban Or LWMH for 5 days then dabigatran or edoxaban Or LMWH for 5 days with warfarin until INR normal then warfarin alone If renal failure - LMWH or warfarin 3 months for provoked, 3-6 months provoked with cancer, 6 months for unprovoked Massive PE (SBP <90 or drop by 40) - continuous UFH infusion and consider thrombolytic with alteplase If repeated: IVC filter or pulmonary embolectomy
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Meningitis most common bacterial cause is strep pneumoniae, N meningitidis causes meningococcal septicaemia
Ix: Assess GCS If suspect raised intracranial pressure do CT before LP LP within an hour - WCC, gram stain, glucose, protein, lactate, culture, PCR, Ziehl-Neelson If cant LP do: FBC, CRP, coag, culture, PCR, BM, ABG non blanching rash, headache, photophobia, neck stiffness, fever, hypotension/shock, bulging fontanelle, Kernigs and brudzinski signs differential if altered mental status - encephalitis, usually herpes, treat with acyclovir Mx: Raised ICP -> ITU -> fluids, analgesics, antiemetics, antipyretic Viral - often self limiting, may give acyclovir Bacterial - IM or IV benzylpenicillin immediately (only if meningococcal rash). When in hosp start ceftriaxone if >3mo old, add ampicillin or amoxicillin if >60 yo. Give dexamethasone asap, continue for 4 days if pneumococcal Length of treatment depends on cause Cryptococcal - fluconazole, amphoteracin B Consider prophylaxis of contacts - ciprofloxacin If TB - RIPE for 2m then I+R for 10m (4 normally) + IV dexamethasone
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Uraemic complications
Pericarditis and encephalopathy
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Adrenal insufficiency (Addisons) management + adrenal crisis presentation/ management
Hypotension (postural), fatigue, weight loss, GI/MSK sx, hyperpigmentation, pubic/ axillary hair loss, salt craving, low libido Ix: Early morning serum cortisol - <100 Synacthen test < 550 Test ACTH level to differentiate primary and secondary - high in primary Electrolytes - low sodium, high potassium test glucose lvl Mx: Educate that it is a chronic condition, will need to take medication for the rest of their life. Is important they take the medication every day, not suddenly stop. Ensure they know how to recognise an adrenal crisis (hypotension, hypovolaemic shock, low blood glucose, N+V, abdo pain, low grade fever) Treatment involves a combination of hydrocortisone taken 3x daily 10mg on waking, 5mg at noon and 5mg in the evening and fludrocortisone Can get all their medications for free Wear a medic alert bracelet Educate on sick rules - mild to mod (fever, Abx) - 2x dose for 2 days - severe - 2x dose, cont until better - vomit - if vomit within 30 mins, double dose again immediately, if again then 100mg hydrocortisone inject - minor surgery - double dose on day - maj surgery - cont infusion If go abroad take enough for double doses + injection kit Addisonian crisis - hypotension resistant to fluids, high K, low Na, vomiting, weight loss - do ACTH, cortisol level, ABG (metabolic acidosis), BMs ``` AtoE Identify cause, screen for infection, cardiac monitoring Iv hydrocortisone 100mg-200mg IV fluid rehydration Monitor BMs ```
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Hypothyroid + when to treat subclinical Causes: - Congenital - Hashimoto - thyroidectomy, radiotherapy - iodine deficiency - carbimazole/ptu - subacute (de quervains) thyroiditis - viral - hyperthyroid first then hypo 2ndry - pituitary tumours, surgery, radio, infarct (Sheehan)
Ix: TFTs - TSH high, T3/T4 low Anti thyroid peroxidase, antithyroglobulin antibodies, US if goitre MRI if suspect secondary cause Also check cholesterol (raised), FBC (pernicious anaemia), HbA1c (T1DM), CK (myopathy) Tx: Levothyroxine - titrate until TSH normalises For secondary - transphenoidal surgery Myxoedema - IV levo, IV steroids, IV fluids, warming Treat subclinical if TSH > 10
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Hyperthyroid Causes - graves - eye signs + pretibial myxoedema - toxic multi nodular goitre - subacute (painful thyroid) - viral Secondary - HCG - multiple pregnancy, molar pregnancy, gestational thyrotoxicosis - Pituitary adenoma
``` Ix: TFT: TSH low, T3/T4 high TSH receptor antibodies US of goitre, radio-iodine scan (diffuse vs hot nodules) Biopsy if suspect neoplasm ECG for AF CRP/ ESR - subacute ``` Tx: Carbimazone, propylthiouracil - titration block or block replace Beta blocker for tremor Radioactive iodine treatment - not recommended in orbitopathy, 3w radio protection after tx, contraception for 6m (4m for men) Surgical removal Eyes - steroids, prism glasses, covers, artificial tears, decompressive surgery ``` Thyrotoxic storm Cool, fluids, resp support Hydrocortisone Carbimazole or propylthiouracil Beta blocker Iodine after 4 days ``` Treat subclinical if <0.1
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CO poisoning - what to ask in Hx and how to treat Low dose - dizziness, headache, N+V Higher - confusion, LOC, resp failure, MI
C - anyone else in house affected O - better when outdoors M - maintenance of heating/ cooking equipment A - Alarm (do they have a CO alarm) Ix - exhaled CO using breath test on site - carbon monoxide pulse oximeter (bedside) or a HbCO blood analysis - ABG Mx - Give 100% O2 until HbCO levels are < 3% in non-smokers or <10% in smokers - if cerebral oedema give mannitol 1g/kg IV - Monitor ECG
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Alcohol - questionnaires? - ix? - managing withdrawal - drugs to help maintain abstinence + how does wernicke's (triad)/ Korsacoff/ DT present?
CAGE or AUDIT questionnaire Ix - FBC (MCV often raised) - LFT (GGT raised), clotting, U&E - Amylase if suspect pancreatitis - Blood glucose - Breath/ blood levels Withdrawal - CIWA-Ar score - IV fluids - glucose only after thiamine - IV or oral thiamine - prevent wernicke's - Tapering dose of chlordiazepoxide over 5-7 days, confirm abstinence with breath test - MgSO4 can reduce seizure/ arrhythmia risk Abstinence - Disulfram/ Antabuse - headache, N+V, flushing when drink - Acamprosate - reduces cravings - Naltrexone - reduces high associated with drinking Delirium tremens = most severe form of withdrawal - after 72hrs- delirium (clouding of consciousness, delusions), tremor and hallucinations + haemodynamic instability Wernicke's triad = mental confusion, ataxia, ophthalmoplegia Korsakoff - longstanding confusion after withdrawal - anterograde amnesia (no new memories), confabulation (says something not true but with conviction), telescoping (says something in past happened recently), personality change, no clouding of consciousness.
71
Delirium - causes + DSM-V criteria + Ix Do 4AT or AMT
``` Causes: Pain Infection Nutrition Constipation Head injury, hypoxia Endocrine + electrolyte - altered pH, hypo/hyper Na+ Ca++, acute liver or renal failure, hypoglycaemia Stroke Medication and alcohol Environment ``` Ix: Take a Hx from person and third party Baseline Cognitive assessment based on DSM-V (inattention, cognitive change, acute/fluctuation, physiological cause) criteria or a 4AT or CAM, AMT10 Admit for investigations for above causes - assess for fractures - FBC, CRP, CXR, urinalysis, blood culture, sputum sample, examine for skin infections - B12, Folate - Rectal exam, AXR, GI exam - Assess for dehydration, U&E - U&E, glucose, LFT (encephalopathy), TFT, ECG, calcium, bone profile - Neuro exam, ABG - Medication hx, Drug lvls - home hazard review confusion screen: FBC, LFT, CRP, U+E, ABG, Coag, TFT, Bone profile, Mg, b12, folate, ferritin Mx: Treat cause Optimise treatment of Comorbs, medications Reorientation strategies Quiet side room, normalise sleep/wake cycle Home comforts PT/OT assessment, safe mobility Home hazard assessment Give haloperidol or benzodiazepines as sedation may be used if very agitated Explain diagnosis to carers
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AKI
Prerenal - hypo perfusion due to haemorrhage, low blood pressure, sepsis, renal artery occlusion (embolus, infarct, stenosis), reduced cardiac output (HF, MI, PE Intrinsic - rhabdomyolysis (+ve blood on dipstick), myeloma, ATN (drugs), glomerulonephritis, haemolytic uraemic syndrome (anaemia) tubular interstitial nerphritis - abx (penicillin), ppi, chemo, nasi Post renal - bilateral renal stone, lymphoma, bladder outflow obstruction (tumour, stricture, stone), tumours, BPH, neurogenic bladder Stage 1 - Creatinine >26.5, 1.5-1.9x baseline, urine <0.5 ml/kg/hr for 6-12 hrs Stage 2 - Creatinine 2.0-2.9x baseline <0.5ml/kg/h for >12 hours Stage 3 - Creatinine >3x baseline <0.3ml/kg/h for >24 hours OR anuria for >12 hours hospital acquired AKI - after 48 hours post admission Ix: Observe urine output Do lying/standing BP urine dip + urinalysis (looking for raised protein, blood, casts), MSU, PCR, PSA U+E, bicarb, inflam markers, nephritic/MM screen ABG (pH - metabolic acidosis) USS KUB Admit if stage 3, urgent treatment for cause e.g. obstruction, hypovolaemic, complications e.g. pulmonary oedema, sepsis, unknown cause ``` Tx Catheter + daily U&Es Correct high K+ If hypovolaemic - fluid challenge and maintenance, stop BP meds - aim SBP > 100mmHg If hypervolaemic - furosemide, diamorphine and nitrate plus fluid restrict - or dialysis If acidosis - sodium bicarbonate Relieve obstruction, remove stones etc If sepsis - sepsis 6 ``` Stop DAAAMN- Aminoglycosides, NSAID, ACEi, Metformin, Amphoteracin, Diuretics, Lithium, Digoxin Insulin renally cleared - if develop AKI reduce dose by 10-20% ATN - prerenal or post renal cause to an extreme TIN - sensitivity reaction to Abx, NSAID - give steroids
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When to initiate dialysis
Hyperkalaemia unresponsive to medical treatment or in an oliguric patient Pulmonary oedema unresponsive to medical treatment Uraemic complications such as pericarditis, encephalopathy Severe metabolic acidosis (pH <7.2 or base excess below –10) Fluid overload
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Causes of hypernatraemia (>145) | + management (incl diabetes insipidus)
Hypovolaemic - diarrhoea, vomiting, dehydration, burns, loop diuretics, osmotic diuresis (DKA, mannitol), ATN Euvolaemic - Diabetes insipidus (low ADH due to reduce production in pituitary or effect in kidneys e.g. CKD) - polyuria + polydipsia - water deprivation/ desmopressin test Hypervolaemic - too much saline, abx containing sodium, conn's (primary aldosteronism, high Na, low K), cushings Urine osmolality - high = burns or vomiting as water los via other means - isotonic = diuretic use or osmotic diuresis - low = diabetes insipidus, conns, cushings Tx - Hypovolaemic - IV NaCl - Hypervolaemic (primary hyperaldosteronism) - Spironolactone, IV dextrose and diuretics - Isovolaemic (DI) - Increase fluid intake, IV dextrose 5% slowly IV (not too quick as risk of cerebral oedema), desmopressin if cranial, desmopressin/ thiazide/ NSAID if nephrogenic - if very high consider dialysis
75
Hyponatraemia/ SIADH - to do
= Na <135 Hypovolaemic (dehydrated) - low urine osmolality = diarrhoea/ vomiting/ burns - high urine osmolality = diuretics Euvolaemic - urine osmolality/ Na low = acute water load, anorexia, hypothyroidism - urine osmolality/ Na high = SIADH or Addisons/ CAH Hypervolaemic - low urine Na - cardiac failure, low albumin (cirrhosis) - high urine Na - renal failure Tx - hypovolaemic - give NaCl 0.9% slowly to avoid central pontine myelinosis - SIADH - fluid restrict to 500ml-1L per day + demeclocycline or vaptans - hypervolaemic - treat cause, loop diuretics If acute/ severe sx - 3% hypertonic saline SIADH can be caused by meningitis,GBS, MS, small cell lung cancer, SSRI, carbamazepine Present with fluid overload, sx of hyponatraemia (N+V, headache, muscle cramp, confusion, seizure) Differential if K+ raised = Addisons Ix: U+E Confirm true hyponatraemia with finding of low serum osmolality Plasma and urine osmolality (high in urine, low in blood) Urine sodium TFT, synatchen test or early morning cortisol ``` Mx of SIADH: Treat cause Fluid restrict Demeclocycline Vaptans ```
76
Hyperkalaemia - causes, presentation and ECG = >5.5
Increased intake: dietary, IV fluids, blood transfusion, Decreased excretion: K+ sparing diuretic, ACEi, spironolactone, Addisons, AKI/ CKD Extracellular shift: Acidosis (DKA), TLS, Rhabdo, burns ``` Presents with Fatigue Generalised weakness Chest pain Palpitations SOB ``` Ix: Full set of bloods - U&E for K+ level/ AKI, CK for rhabdo, cortisol for Addisons ABG - see electrolyte levels, metabolic acidosis Urinalysis ECG - tented T wave, prolonged PR/ flattening of P waves, wide QRS, VF Mx: ABCDE Cardiac monitoring Protect myocardium - calcium gluconate - 10ml 10% over 10 mins Reduce K+ with insulin/dextrose solution - 10U act rapid in 50ml 50% dextrose Nebulised salbutamol - back to back 5mg nebs to 10-20mg max dose Dialysis if needed Chronically - calcium resonium and lactulose
77
Hypercalcaemia Causes = hyperparathyroidism, cancer (bone mets, myeloma, squamous cell lung cancer)
Myeloma, Squamous cell carcinoma (PTHrP) Bone metastasis in lung, breast, renal, prostate (increase osteoclast action and bone resorption Hodgkins lymphoma (active vit D - increase gut absorption) ``` Present with Ca >2.6 Stones Thrones - constipation, polyuria Groans - abdo pain, N+V Bones - Bone pain Psychic moans - depression, anxiety, cognitive dysfunction Cardiac - HTN, Bradycardia, arrhythmia ``` Want to rule out hyperparathyroid hormone as a cause Ix: Rapid onset - malignancy PTH - high = hyperparathyroidism, low due malignancy Do relevant exams and CT to look for malignancy Plasma electrophoresis - raised plasma protein in MM ECG, bloods including Bone profile, LFTs Can confirm with: Then test PTHrP and Vitamin D/Calcitriol lvl Phosphate - low in hyper, high in malignancy Raised ALP - bone mets ECG - short QT interval US of parathyroids Renal, breast, PR, Resp exams Mx: Admit if Ca >3 or symptoms Rehydration - IV saline to increase renal excretion Bisphosphonate e.g. Zoledronic acid used to reduce bone turnover. Alternative is calcitonin If concurrent kidney disease consider dialysis For hyperparathyroidism - surgery can be considered if symptomatic For cancer - chemo/radio therapy
78
Hypocalcaemia - causes
Most common causes - vit d deficiency - hypoparathyroidism - surgery, radiotherapy, AI - CKD - hypomagnesia - pancreatitis - bisphosphonate - rhabdo/ TLS Ix - Do PTH, Vit D, Ca lvls - High PTH, low Ca = Vit D deficiency, vit D receptor issues or CKD - Low PTH, low Ca = primary hypoparathyroidism, congenital, hypomagnesia - Also do U&E for CKD, ECG for long QT, amylase, CK, phosphate Tx - 10ml 10% calcium gluconate slow IV - correct low Mg - Oral vit D - If persistent give oral calcium supplements
79
Acute angle closure glaucoma
Sudden onset red painful eye with associated headache. Blurred vision, haloes around light, N+V, fixed mid-dilated pupil with hazy cornea Precipitated by watching TV in dark room, reading at night Ix - gonioscopy - trabecular meshwork not visible - slit lamp - Tenometry - Humphrey's visual fields Tx - lie patient on back, face up with no pillows - one drop of pilocarpine (2% if blue eyes, 4% if brown) - 500mg oral acetazolamide - analgesia/ antiemetic as needed - laser irridotomy in both eyes once acute event resolved
80
POAG
Can present with gradual onset of fluctuating pain, headaches, blurred vision and halos appearing around lights, particularly at nighttime Ix: Fundoscopy - cupping of optic disc (>0.4), notching, retinal haemorrhage Vision assessment - scotoma, loss of peripheral vision (Humphrey visual field) Tonometry (>21mmhg) Goniometry - exclude AACG Slit lamp MRI scan of orbit if suspect graves or orbital cellulitis Tx: 1st line - latanoprost (prostaglandin analogue) or timolol (beta blocker) 2nd line - switch, combine or add pilocarpine, acetazolamide, bimonidine Laser trabeculoplasty, trabeculotomy, aqueous shunt Monitor yearly for rest of life -
81
Raised ICP
Sx - headache worse on bending over, vomiting, visual changes Signs - Cushing triad - hypertension/ wide pulse pressure, bradycardia, irregular breathing - unilateral ptosis Ix - Bloods - U&E, coag, FBC, LFT, glucose, osmolality - fundoscopy - blurring of disc margins - CT/MRI - LP for opening pressure/ diagnosis - ICP monitoring Tx - General - fluid restrict, raise head of bed, analgesics (morphine reduces coughing), sedation (propofol) - treat cause e.g. bleed, tumour - manage seizures - CSF drainage - IV Mannitol, Hypertonic NaCl 2nd line - hyperventilation - avoid pyrexia/ active cooling - decompressive craniectomy
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Angina Stable/Unstable Unstable if - new onset - deteriorating - occurs at rest
Ix: Take history and perform cardiac examination Do an ECG to look for ST elevation, Q wave or LBBB Take serial troponins Do routine bloods: FBC, U+E, LFT, CRP, CK, myoglobin, lipids, TSH, blood glucose CXR, echo Consider exercise stress test (Echo), CT angiogram or Coronary angiogram to investigate angina Sx and degree of CAD ``` Mx: (acute) O2 if sats less than 94% Morphine, metoclopramide 10mg of each Nitrates Aspirin 300mg Ticagrelor according to Chadvas/hasbled Fondaparinux - if going for PCI within 24hrs give unfractionated heparin instead Glycoprotein inhibs if high risk of CV events ``` Use grace score to decide the risk of MI and need for PCI Discuss lifestyle risk factors e.g. diet, exercise, smoking, alcohol Evaluate CV risk factors and start on BARDS = acei, BB, aspirin/clopidogril, rehab, statin For stable angina: Stop smoking, activity, weight loss, diet, alcohol Provoking factors e.g. stress, exercise, cold, large meal 1st line - rest +GTN (up to every 1/2 hour) - take second dose at 5 mins if not improved, if second not help call 999 2nd line - Beta blocker or CCB (verapamil/diltiazem) 3rd line - Beta blocker + CCB (bisoprolol and nifedipine) 4th line - Add in long acting nitrate (isosorbide mononitrate), nicorandil, ivabradine, ranolazine + Secondary prevention: 3A’s: aspirin (75mg OD), atorvastatin (80mg OD), ACEi (e.g. ramipril, titrated up to max dose) + statin if cholesterol >4mm/l
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Stemi
Ix: Hx, Exam O2 sats Serial troponin, CK-MB, myoglobin if recent MI ECG - look for ST elevation, new LBBB, Q wave ECHO/ CXR Bloods - FBC look for anaemia, U+E to check renal function for contrast, BNP O2 sats ``` Mx Morphine +metoclopramide 10mg each IV O2 if sats <94% Nitrates - GTN sublingual, IV if not enough Aspirin 300 Relocate to cardiac intensive unit Ticagrelor 180 Unfractionated heparin - give for max of 5 days, stop post PCI - if possible within 90 mins ``` PCI with stent (or CABG if multi vessel disease) within 90 mins, if not possible within 120 give thrombolysis w. alteplase or streptokinase If low CO consider ionotrope e.g. dobutamine Post MI discuss lifestyle - smoking, alcohol (<14), exercise (150 mins a week, weight training at least 2days), cardio protective diet (reduced salt and fat, more fruit, seeds and nuts, more fish). ``` Start on ACEi Beta blocker Antiplatelet - aspirin + ticagrelor - 12m, after this cont aspirin, stop ticagrelor Rehab Statin ``` Antianginals - give ranolazine if low BP
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Migraine Unilateral, throbbing 4-72hrs have to lie down in dark room Associated N+V, aura, photophobia and photophobia Ask about prodrome and postdrome Cant carry out normal daily life For diagnosis - without aura need 5 characteristic headaches - with aura need 2 headaches with associated visual, sensory or speech/language aura
Ix: Comprehensive history Visual assessment, fundoscopy if eye signs Neuro exam/CN exam if neurological symptoms Take drug history to identify if medication overuse Mx: Educate, do headache diary to understand triggers and avoid them. Limit standard analgesics Optimise Comorbs e.g. OSA, insomnia, depression Take off oral contraceptive pill 1st - Ibuprofen, aspirin, paracetamol + metoclopramide + sumatriptan - take at start of headache not aura Prevention: Propanalol (1st line in women of childbearing age), Topiramate, amytriptalline - start if 2 or more attacks a month that last 3 or more days, or significant effect on quality of life In pregnancy - 1st line = paracetamol If linked to menstruation consider mefanamic acid or a combination of aspirin, paracetamol and caffeine Consider mindfulness, acupuncture, riboflavin
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GCA
Ask about joints (polymyalgia rheumatica), tender scalp, vision, jaw, resp tract/ ENT sx Ix: Exam, bloods: FBC (normochromic normocytic anaemia and an elevated platelet count) , U+E, LFT (raised ALP), ESR, CRP Fundoscopy (CRAO - painless sudden loss of vision with RAPD) Biopsy Duplex US PET PMR - >50, bilateral shoulder/ pelvic girdle ache, last >2w, raised ESR/CRP, morning stiffness >45 mins Mx: If strong clinical suspicion start high dose corticosteroids immediately prior to confirmation with biopsy - IV Methylpred if eye - 60mg pred if jaw, 40mg if no jaw - Assess response after 48 hrs - Taper and continue for 1-2 years Start aspirin 75mg daily unless contraindications + PPI If recurrent/ contraindications to steroids - tocilizumab, methotrexate
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cluster headache
Tx: Avoid triggers such as alcohol and smoking Acute: 100% O2 via non rebreathe and sumatriptan subcut, metoclopramide if nausea Prevention: verapamil 1st line, lithium alternative. prednisolone can help break cluster
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IIH
``` Ix: MRI/CT - look at size of ventricles (normal, large in hydrocephalus) LP - assess pressure Visual field mapping FBC, CRP, ESR, COAG ``` ``` Mx: Loose weight, lifestyle Acetazolamide, serial LP can drop ICP Prednisolone acutely for papilloedema Surgery - bariatric, CSF shunt, optic nerve fenestration ```
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Rhino-sinusitis
Diagnosed if have facial discomfort/pain, nasal obstruction or purulent discharge, loss of sense of smell May consider nasal endoscopy to look for polyps, inflammation, oedema, purulent discharge CT if atypical or severe disease Mx Reassure, most resolve within 3 weeks Anti-pyretic, nasal decongestant max a week, nasal irrigation with saline, fluid + rest, warm face mask If >10 days consider 14 days of high dose intranasal corticosteroid If prolonged beyond this or very severe, or rapid decline may consider Abx, first line = phenoxymethylpenicillin If recurrent consider endoscopic sinus surgery
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Trigeminal neuralgia management | - vascular compression of trigeminal nerve, also: MS, tumours, abnormalities of the skull base, AVM
Ix: CN exam Examine face and dental cavity MRI if diagnostic uncertainty, young, suspect malignancy or MS, not improve with treatment Tx: Educate patient, get to understand their triggers e.g. shaving, cold air to face etc Carbamazepine 1st line - titrate up to effective dose, explain not work immediately alternatives - baclofen, lamotrigine Can give botulinum, perform decompression
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SAH management berry aneurysm in the Circle of Willis - sudden onset severe headache, loss of consciousness N+V, signs of raised ICP, meningism look at subdural vs epidural
``` Ix: Assess consciousness Baseline bloods + coag Do fundoscopy and neuro exam Do Ct without contrast - if -ve do LP after 12 hrs for xanthochromia angiography to identify bleed origin ECG ``` Mx: Analgesics, antiemetics, supportive care - analgesia, antiemetic, ng tube, intubation nimodipine 60mg every 4 hours for 21 days - prevent vasospasm and ischaemia Nitropuriside, labetalol used to maintain bp, keep < 180 CT angiogram to locate aneurysm Neurosurgical clipping or coiling Treat hydrocephalus with drain
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Extradural/ subdural mx
Ix: CT head - extradural lemon, subdural banana If small, no sx watch and wait If large, causing symptoms then consider surgical decompression with burr hole Manage fall holistically
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How to differentiate costochondritis from MI or Pleuritic chest pain
Tender on palpation - not in other causes Costochondritis presents with aching/pressure/sharp pain over ribs/sternum, worse when active/ coughing Simple analgesia, steroid injection if bad
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Aortic dissection - Type A vs B (stanford classification) RF are male, age, HTN, atherosclerosis, smoking, high cholesterol, marfans/ Ehlers danlos, aortic valve disease, FHx
Present with sudden onset central tearing chest pain radiating to the back - may also have signs of other vessel occlusion e.g. focal neuro signs, anuria, angina On exam - tachycardia, hypotension, aortic regurg murmur, different pulse, BP and CRT between two limbs Ix - Bloods - FBC, U&E, LFT, coag, CRP, troponin, D-dimer - ABG - ECG to exclude/ identify MI - CT aortogram = first line - Echo can also be used - CXR may show widened mediastinum Type A - involves ascending aorta Type B - not involve ascending aorta Mx - O2 as needed - Analgesia - morphine 2-5mg - Cross match at least 4 units of blood - Monitor urine output - end organ perfusion - IV labetalol to maintain SBP 100-120 and reduce cardiac contractions to prevent further aortic injury - IV fluids/ noradrenaline if low BP Type A - emergency open surgery w. graft Type B - Can manage conservatively with BB - surgery (Thoracic endovascular aortic repair) if leaking, expanding, compressing vital organs or ruptured Lifelong antihypertensives and monitoring with CT
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Becks triad in cardiac tamponade
Muffled heart sounds Raised JVP Hypotension
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Pericarditis Common causes: - viral - coxsackie/ echovirus - Post MI - Acute or dresslers (AI - weeks- years) - Malignant - Uraemic - Post surgery/radiotherapy
Ix: Look for triad of pleuritic chest pain, pericardial rub, serial ECG changes Do cardiovascular exam, ECG looking for widespread saddle shaped ST elevation Do FBC, LFT, U+E (creatinine, uraemia), CRP, Troponin (high if myocardium involvement), INR Do CXR, echo to look for fluid - usually normal Do blood culture, pericardial fluid culture if unclear cause and suspect bacterial infection Tx: restrict physical activity until symptoms resolve or CRP, ECG resolve NSAID for 4 weeks + PPI (aspirin over nsaid if recent MI due to risk of rupture) Colchicine for 3 months steroids if refractory pain majority as an outpatient unless fever, large effusion, cardiac tamponade, immunosuppressed, due to trauma, on anticoagulation, poor response to treatment and treat cause - anti-tb for tb, antibiotics if bacterial pericardiocentesis for symptomatic effusion
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Presentation, Ix and treatment of cardiac tamponade/effusion What is presenting triad? Get light-headedness, SOB, syncope in tamponade due to reduced CO
Tamponade = where pericardial effusion fluid limits filling of the heart Raised JVP, low BP, muffled heart sounds Also get cough, pulsus paradoxus = drop in SBP >10mmHg with inspiration - SOB, tachycardia, tachypnoea Ix: - Bloods/ culture - uraemia, WCC, CK - CXR - large pear shaped heart - Echo - Bouncing of heart in pericardium, fluid - ECG - small QRS, PR depression, electrical alternans - CT if located effusions, pericardiocentesis if suspect malignancy or purulent effusion (high CEA = malignancy) - Pericardial biopsy Mx: ICU Lie with feet up Treat cause (infection, malignancy, aortic dissection, AI), most resolve on own IV fluids, O2 Ionotropes e.g. dobutamine Pericardiocentesis, pericardial fenestration, surgical drainage if malignant/ purulent/ blood Constrictive pericarditis - raised JVP that doesn't fall with inspiration (kussmauls sign)
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Boerhaave - presentation and management
Present with retrosternal chest pain, resp distress, subcutaneous emphysema, hx of vomiting Often septic and haemodynamically unstable Ix - bloods + G&S - CXR may show pneumomediastinum - CT TAP with contrast is gold standard - May also do urgent OGD if high level of suspicion Mx - Resus with O2 and fluids - NBM - Broad spectrum Abx - Analgesia - Emergency surgery to repair perforation with insertion of feeding jejunostomy - If mild/ iatrogenic/ old may be able to treat conservatively with ITU, Abx/ anti fungal, NBM, TPN/ feeding jejunostomy, NG tube and chest drain for drainage
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Anaphylaxis
Airway swelling, hoarse voice, stridor, SOB, urticaria, signs of shock (tachycardia, hypotension, pale, clammy) Ix - Do mast cell tryptase to confirm diagnosis - immediately and after 1-2 hours - O2 sats, ECG, BP Mx - 2222 - ABCDE - Remove trigger - lie flat with legs raised - Ensure patent airway, give O2 aim 94-98% - IM adrenaline 0.5mg 1in1000 (anterolateral middle 1/3 thigh), repeat after 5 mins if little improvement - IV fluid challenge - 500ml NaCl over 15 mins - After stabilisation give IV hydrocortisone and chlorphenamine Observe for 6-12 hours due to risk of biphasic reaction Allergy clinic + give adrenaline injector
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Pleural thickening/ plaques - suspected cause
Asbestosis/ mesothelioma
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HF - common causes, Ix, Mx RHF - raised jvp, peripheral oedema, ascites LHF - pulm oedema, SOB, exercise intolerance, cough (pink sputum), orthopnea, multiple pillows, paroxysmal nocturnal dyspnoea, wheeze
HTN, CAD, Valvular, Myopathies, pericardial, arrhythmia, high output states (anaemia, hypothyroid) Ix: Routine obs, cardiovascular examination Bloods - FBC (anaemia), LFT, U+E, CRP, TFT, Lipids BNP - >400 do ECHO (look for dilated CM, valve issues) CXR - batwing (alveolar oedema), kerley B line (interstitial oedema), Bilat effusion, increased heart size, prominent upper lobe vessels ECG - LVH, HF, Bipid P wave (atrial enlargement) NYHA score - I no limitation, II some fatigue/SOB with exercise, III gentle activity, not at rest, IV at rest Tx: Manage Comorbs, lifestyle - salt, exercise, smoking Ejection fraction maintained - observe, furosemide as needed Ejection fraction reduced give ACEi, BB, spironolactone if fluid overloaded/ sx. Further specialist treatment = digoxin/ ivabradine/ valsartan/ isosorbide dinitrate+hydralazine Consider statin/ antiplatelet ICD to prevent sudden cardiac death if prev VT/MI or cardiac resynchronisation therapy if LVEF <35%
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Lung Ca - types, sx
Small cell, NSC (adenocarcinoma, squamous cell, large cell) Present with SOB, Cough, worse at night, haemoptysis, Weight loss, Chest pain, finger clubbing, facial engorgement if SVC obstruction Pan-coast tumour can present with horners syndrome: ptosis, miosis, anhidrosis. Also get pain, weakness, atrophy, oedema in upper limb, hoarse voice Differential = lung abscess, cervical disc prolapse with concurrent TB, Lung mets 2ww if evidence of cancer on CXR or >40 with haemoptysis Ix: Obs, FBC (anaemia), LFT (ALP high in bone mets), U+E, bone profile (Ca may be raised due to PTH or bony mets, Na may be low if SIADH) CXR, CT TAP, Bronchoscopy with biopsy or CT guided percutaneous biopsy Paraneoplastic Squamous - PTH Small cell - ACTH, SIADH, Lambert eaton (antibodies to voltage-gated calcium channels, prox and ocular weakness better with exercise) Mx: Stage fitness with ECOG Early disease consider surgery (lobectomy) Consider adjuvant or neoadjuvant chemotherapy (platinum based), especially stage III/ IV Radiotherapy often used in palliative cases or as alternative to surgery in early disease Radiotherapy for bronchial obstruction, SVC obstruction, bone pain and cerebral mets
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Anaemia - how can severe anaemia present, ix, mx <130 in men <120 in women <110 in pregnant
Severe anaemia can present with - SOB - Angina - Peripheral oedema - Ejection systolic murmur - Tachycardia - HF Ix - FBC - look at Hb level - Blood film - Ferritin - low in IDA, high in ACD - Transferrin - Opposite to above - B12/ Folate lvls - CRP/ESR - chronic disease - LFT - alcohol/ bilirubin for haemolytic - Coombs/ haptoglobin - haemolytic IDA - ferrous sulphate - check lvl 2-4w late, cont for 3m B12 - Hydroxocobalamin and folic acid Folate - Folic acid Severe - transfusion
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What is the cause of megaloblastic and non-megaloblastic macrocytic anaemia
Megaloblastic - B12, folate | Non-megaloblastic - alcohol, liver disease, hypothyroid
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What is pernicious anaemia
= AI condition where patient has antibodies to intrinsic factor preventing the absorption of Vit B12 In B12 deficiency get glossitis and peripheral neuropathy
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Sudden onset watery diarrhoea with accompanying blood and abdo discomfort. Started 5 days after dose of abx - cause, Ix, mx
Cdiff Ix - Bloods - Stool sample - look for enterotoxins, also MC&S, virology, ova/cyst/parasite - ABG if suspect sepsis - CT if complications, endoscopy + biopsy if diagnosis uncertain - AXR if abdominal distension, suspected perforation/ megacolon Mx - report to public health - Side room - stop laxatives/ abx/ PPI - do not give anti-motility agents - Start abx - 1st line oral vanc, 2nd line oral fidaxomicin, if severe oral vanc and IV Metro - IV fluids - Surgery for severe colitis, Faecal tranplant
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Acute diarrhoea ix
- Abdo/ PR exam/ look for clubbing/ ulcers/ masses - assess hydration status - temperature - Bloods - Stool sample ``` Oral rehydration solution/ IV fluids Racecadotril Loperamide Antispasmodics Abx if bacterial ```
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IBS - diagnosis, ix, mx Differential for chronic watery, non bloody diarrhoea is bile acid malabsorption - bile acid draws fluid and electrolytes into the bowel - treat with low fat diet and cholestyramine
Abdo pain, related to defacation/ altered stool frequency/ altered stool appearance At least 2 of: altered stool passage, bloating, worsened by eating, rectal mucus, exclusion of alternative conditions Ix - FBC, ESR, CRP - Coeliac serology - stool sample, faecal calprotectin - H breath test - Sigmoidoscopy - CA125 in women Mx - Fluids, exercise, dietician - Fibre - insoluble for constipation - OTC probiotics for diarrhoea - Antispasmodic, TCA for refractory pain - constipation: bulk forming laxative e.g. fybogel, linaclotide if refractory - diarrhoea: loperamide
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NOF #
Intracapsular vs extra capsular vs subtrochanteric Use garden classification - intracapsular # - I - incomplete #, minimal displacement - II - Complete #, undisplaced - III - Complete #, partially displaced - IV - complete #, completely displaced RF - smoking, steroids, age, osteoporosis, alcohol Inability to weight bear, pain, reduced ROM - Shortened and externally rotated leg Ix - Obs - Try to identify cause of trauma/ fall - Bloods, ECG, urine dip - Bone profile - Ca, vit D, phosphate, ALP - Pelvic Xray from multiple planes - AP and lateral - MRI/ CT if needed Mx - Catheter for urine output - Fluids due to internal bleeding - Analgesia - Iliac fascial block - LA - Med review - AKI risk, hold anticoags if need op - NBM - Immobilise Surgery - gardens I or II - dynamic hip screw - gardens III or IV - total hip replacement - Extra-capsular - DHS or intramedullary nail Post op - VTE prophylaxis - LMWH - delirium assessment, screen for infection - mobility assessment - physio/ OT, pain relief - Bisphosphonate if osteoporosis
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Pelvic # Ix + Mx
Ix - 3 plane Xray or CT - Serial Hb for blood loss - Assess pelvic stability - Check peripheral pulses - iliac vessel dmg - LL neuro exam - Look for blood in urine, dipstick - Angiography, cystography, urethrogram Mx - AtoE - IV fluids + O2 - Pelvic binder - If stable/ avulsion treat conservatively with bed rest, VTE and gradual physio - If unstable, haemorrhage, open or urological injury - surgery
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Spinal cord injury - types/ consequences + Mx
Ant - loose motor, pain and temp Post - loose vibration and proprioception Complete - loss of sensory and motor Brown-sequard - loss of ipsilateral vibration + proprioception + motor and contralateral pain + temp Neurogenic shock - injury above T6 can affect sympathetics leading to vasodilation, hypotension, bradycardia and hypothermia Mx - Immobilise C spine - Canadian C spine rules to determine risk - adults do CT (then MRI if see lesion), children do MRI. Do radiology if >66, dangerous mechanism, parasthesia. If none of these and spinous processes not tender, able to rotate head right and left 45 degrees then can clear spine - T/ L spine - Xray if no neuro signs, CT if neuro signs - Modified A-E = Catastrophic haemorrhage, A + C spine stabilisation, BCDE - GCS - Head blocks, strap to backboard - IV morphine - IV fluids - O2 - Atropine if bradycardia - catheterisation - Surgery if progressive neuro sx or unstable + displaced fracture - Physio
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TBI
Hx including - mechanism, LOC, amnesia, vomiting, headache, neck pain, anticoags, alcohol intake Ix - GCS - Neuro/ CN exam - balance, motor/ sensory, speech - Check for base of skull fracture (battle sign behind ear, CSF leak, periorbital haematoma) - CT - within 1 hour if GCS <13 at initial assessment or <15 after 2 hours, basal skull or open skull fracture, focal neuro signs, seizure, repeated vomiting - CT - within 8hr if >65, clotting disorder, dangerous mechanism, >30mins amnesia Mx: - AtoE - airway support, fluids, O2 as needed - Immobilise C spine if suspected injury - Neurosurgical input - Anti emetics, analgesics - Nutritional support - Mannitol if risk of haematoma, oedema - in emergency with significant swelling consider craniectomy
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What test is done to identify CSF
Beta transferrin
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Extradural bleed - what is key about their presentation? Ix, Mx?
Fractured temporal/ parietal bone at pterion damaging middle meningeal artery/vein Present with initial LOC followed by a lucid interval then further deterioration - headache of increasing severity, vomiting, seizure, dropping GCS See brisk reflexes, upgoing plantars, limb weakness, aphasia, visual defects, raised ICP (cushings triad) Ix - AtoE + obs (GCS, pupils) - Baseline bloods, coag, G+S/ crossmatch, glucose, bone profile - CT head - biconcave (lens shaped) haematoma, not cross suture lines - Angiography if spontaneous - look for AVM Management - AtoE - O2/ fluids - resus - maintain SBP >90 - Reverse or pause anticoags - IV mannitol or hypertonic saline 2.7% to reduce ICP - Abx if open fracture - Levetiracetam for seizure prophylaxis - for large bleeds > 30cm3, midline shift, focal neuro or GCS< 8 - Burr hole craniotomy - Alternative is open craniotomy with cauterisation/ ligation
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Subdural haematoma Due to bridging veins, blunt trauma
Elderly, alcoholics, HTN, anticoags at increased risk Slower sx onset than extradural - drowsiness, personality changes, LOC, fluctuating headache Can have chronic presentation 2-3w post fall Ix - AtoE + obs (GCS, pupils, HTN) - Neuro exam - Baseline bloods, coag, G+S/ crossmatch, glucose, bone profile - CT head - crescent shaped haematoma, not limited by suture lines - Angiography if spontaneous - look for AVM Mx - AtoE - O2/ fluids - resus - maintain SBP >90 - Reverse or pause anticoags - IV mannitol or hypertonic saline 2.7% to reduce ICP - If small - monitoring and repeat CT - for large bleeds > 30cm3, midline shift, focal neuro or GCS< 8 - Burr hole craniotomy - Alternative is open craniotomy with clot evacuation, cauterisation/ ligation - For recurrent bleeds - subdural drain - For chronic bleed that doesn't need surgery - dexamethasone
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Burns - classification and management Causes: thermal, chemical, electrical, friction or radiation
Non complex - Not affect face, perineum, genitalia, hands, feet, crossing joints, circumferential. <15% total body surface area. Deep burn < 1% Complex - opposite to above, any chemical/ electrical Superficial - Epidermis - red/ painful, no blister, blanches and returns - Superficial dermal - pale to dark pink, painful, blistered, weeping/ wet, slow to regain colour after blanching - Deep dermal - Blotchy red, reduced sensation, blistering, non-blanching - Full thickness - white/ brown/ black, no blisters, dry, painless, non-blanching - Fourth degree - subcut fat, muscle or bone Get systemic hypotension due to evaporation and third spacing Inhalational injury - Hoarse voice, black mucus, stridor, SOB, burns to face and neck, raised HbCO Ix - Rule of nines or Lund and brower chart - Assess burn depth - Assess for inhalational injuries - Establish time of burn - Bloods - FBC,U&E, CK, LFT, G&S, Crossmatch, HbCO, BM, ABG - BP (art line), cardiac monitoring, UO - Trauma CT if needed - Temp for hypothermia Mx: Acute severe - AtoE - Intubation if inhalational injuries - High flow O2 - 100% if CO, elevate head - Escharotomy if circumferential chest burns/ ischaemic limbs - Fluids if >15% tbsa or >10% in kids - parkland formula - 3-4ml x % tbsa x kg - 1/2 over 8hr then 1/2 over 16 - prevent hypothermia - IV abx if >10-15% burns - trust guidelines - IV morphine, sedatives - NG tube and catheter - Tetanus Excise and graft full thickness, other depths: wound care Fluclox if secondary infection First aid mx - rinse under cold tap for 20 mins - layer cling film over wound - elevate Electrical - remove source, check myoglobin/ CK, ECG for arrhythmia, compartment syndrome Chemical - Remove clothing, brush off and irrigate for 1hr, TOXBASE, poison centre
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Splenic rupture
LUQ pain following blunt trauma (EBV, haem malignancy place at higher risk), Get hypovolaemic shock, Kehr's sign (shoulder pain due to blood in peritoneum irritating diaphragm) Ix - If haemo unstable - laparotomy - If stable - CT TAP Mx If stable - bed rest, fluids, monitor with US If unstable - laparotomy - splenectomy or splenic salvage - Pen V and prophylactic vaccinations
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Anal fisure management - Anal pain on defecation, severe and sharp, bright red blood on paper, tearing sensation
Primary (no cause) or secondary (constipation, IBD, STI, malignancy) Mx Primary care - Soften stool – fluid, fibre, laxative - Analgesia (paracetamol/NSAID), warm bath If not improved within a week: - GTN ointment BD - topical lignocaine if extreme pain (max 14d) - Refer if not resolved within 6-8w Secondary care - Topical diltiazem or nifedipine - Botulinum toxin - Sphincterotomy
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Colorectal cancer
L side: bleeding, altered bowel habit R side: anaemia, weight loss, abdo pain Ix: Abdominal and PR exam looking specifically form mass Routine observations FBC (anaemia), U+E, LFT (mets), CRP, CEA, CA19-9, BRAF 2ww: 1st line: Colonoscopy with biopsy 2nd line: Barium enema (apple core) or CT colonography CT TAP - staging and metastatic identification Liver Ultrasound PET scan Trans rectal US Screening: Faecal immunochemical testing - every 2 years from age of 60-74. If +ve have colonoscopy - remove adenoma, if intermediate risk colonic surveillance 2ww: >40 with unexplained weight loss and abdominal pain >50 with unexplained rectal bleeding >60 with IDA or changes in their bowel habit Mx: Remove polyp on colonoscopy and send for histology Segmental resections with anastomosis or stoma Radiotherapy Chemo: FOLFOX, anti-VEGF Stenting if palliative
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Oesophageal cancer
Presents with dysphagia, haematemesis, vomiting, weight loss, odynophagia, anaemia, feel lump in throat, virchows LN RF are alcohol, smoking, barrett's (GORD, achalasia), coeliac 2ww if issues swallowing, or >55 with weight loss and any of: dyspepsia, reflux, upper abdo pain Ix - Baseline bloods, Glucose - Endoscopy + biopsy - Barium swallow if endoscopy not tolerated - Look for mets with CXR, liver US - CT/ PET for staging Mx - Endoscopic resection or oesophagectomy - For palliative consider radiation/ chemo/ stenting, PEG feeding and analgesia
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Variceal bleed - dilated veins due to liver disease
Haematemesis/ coffee ground vomit, abdo pain, haematochezia, tachycardia, hypotension Ix: - Obs for shock - BP, UO, CRT, HR - FBC, U&E (raised urea due to bleed), LFT, G&S, crossmatch, coag - OGD - CXR if risk of perforation - CT for liver disease Assess risk with Glasgow blatchford score >1 - inpatient Assess risk of rebreeding post procedure with rockall score Mx - AtoE - Assess airway, O2, Look for shock - IV fluid bolus/ transfusion if needed - Catheterise - UO as proxy for organ perfusion - Stop any anticoags/ NSAIDS - IV terlipressin - Prophylactic cipro or cef - Omeprazole - Band ligation, balloon tamponade if continued bleeding - Beta blocker for long term prevention If not controlled with band ligation or recurrent - TIPS Call on call gastroenterologist for immediate endoscopy post stabilisation if acute shock
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Causes of increased portal pressure
Pre-hepatic - portal vein thrombosis Intra-hepatic - hepatitis, cirrhosis idiopathic Post-hepatic - budd chiari, compression from tumour
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Hypoglycaemia = BM < 3.5 Causes -Insulin/SU, Addisons, Insulinoma, Factitious (C-peptide low), post prandial Presents with dizziness, light headedness, sweating, palpitations, hunger, weakness, vision changes, irritability, anxiety, drowsiness, LOC, seizure Whipple's triad - low plasma glucose, sx of low glucose, resolution with correction of hypoglycaemia
Ix: Do BMs = fasting glucose <3 Do neurological assessment and calculate GCS Do serum insulin - see if due to insulin C-peptide - high if endogenous cause (insulinoma, SU) ECG SU level Cortisol level to look for adrenal insufficiency Management: Get the hypo box If conscious and able to swallow - 10-20g carbs, retest in 15 mins - jelly babies, glucose tablets If confused give 2 tubes of buccal glucogel, IM glucagon Repeat up to 3x times before escalating to below If cant swallow, low GCS give IM glucagon or IV dextrose- 200ml 10% over 15mins (IM glucagon not effective if malnutrition) Cant give glucagon if alcoholic, SU, liver disease, malnourished If due to SU give ocreotide Important to alert DVLA, refrain from driving until BMs under control - test BM before driving and then 2hrly throughout the journey After stable assess hypo awareness with GOLD score If repeated hypos: Blood Glucose Awareness Training (BGAT) programme
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DKA management Present with dehydration, vomiting, abdo pain, polyuria, confusion, hyperventilation Commonly caused by inadequate insulin therapy or infection Differentials for ketosis are alcoholics and starvation Can have normal glucose DKA if taking SGLT-2 inhibitors - treat same, switch from SGLT2 inhib to other drug
Ix: AtoE assessment Urine ketones 2+ (dipstick) or blood ketones >3 Blood glucose >11 ABG: Bicarb <15 or pH <7.3 FBC - look for raised WCC, U&E - raised K in acidosis CXR to exclude pneumonia as cause Anion Gap >13 (Na – Cl + HCO3) Beta-HCG if abdo pain - pregnancy can precipitate, are at high risk Plasma osmolality >320, normal ketones - think HHS Routine bloods, TFT, CK, amylase, cultures, trops Mx: AtoE Obs - Sats, BP, ECG monitoring, cannula, catheterise to assess urine output If BP<90 - fluid challenge (500ml over 15 mins), repeat if still low Following this give 1L over 1st hour then over 2,2,4,4,6hrs Give fixed rate 0.1 unit/kg/hr act rapid insulin - 50U actrapid in 49.5ml Nacl - aim for ketone drop of 0.5 per hour, glucose 3/hr, HCO3 increase >3/hr, keep K+ between 4-5.5 - if not enough increase rate by 1U/hr - when glucose <14 start 10% dextrose IV (1L over 8hrs) alongside normal fluids Continue long acting insulin K+ replacement if < 5.5 - 40mmol KCL in second bag of fluid onwards Treat underlying cause (infection, MI etc), monitor BM, Ketones, K+, urine output hourly (resolved when ketones <0.6 and pH >7.3) If eating/drinking can stop and go back to normal regime, if not eating and drinking then switch to variable rate Aim to get patient eating and drinking on normal insulin regimen and biochemically resolved within 24hrs
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HHS
Hyperglycaemia (>30), raised blood osmolality (>320), no evidence of ketosis (< 3 in blood) Present with weakness, exhaustion, dehydration, leg cramps, vision changes, focal neuro signs Mx - AtoE - First line is IV fluid replacement with 0.9% NaCl - not too quick due to risk of cerebral oedema/ central pontine myelinosis (2-3L positive balance + urine output in first 6 hours) - If glucose not falling by >5mmol/L/hr or ketones rising - start IV insulin 0.05U/kg/hr + start dextrose when glucose <14 - Replace potassium - monitor U&E, BM, urea, pH, creatinine Aim drop in osmolality 8/hr Resolved when glucose <12.2, osmolality <315 mmol/kg
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Cause of metabolic ketoacidosis with low or normal ketones
Alcohol
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Metabolic acidosis - causes if high and low anion gap
High anion gap = organic acids e.g. lactic acidosis, ketoacidosis Normal anion gap = loss of bicarbonate either via diarrhoea, renal tubular acidosis, Addisons, drug causes. Have a high chloride.
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Insulinoma mx
Immediate potassium and dextrose Surgery to remove pancreatic endocrine islet cell tumour Avoid exercise, eat small frequent, high starch meals + diazoxide.
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Critical illness polyneuropathy
Critical illness leads to diffuse, symmetrical, placid paralysis of limbs and diaphragm - reduced reflexes ``` MRC score Serum CK CSF normal Normal conduction velocity on N studies muscle biopsy ``` General care, exercises, passive stretching Can cause difficulty weaning, increased risk of VTE
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MSCC
``` Ix: MRI whole spine PR for anal tone Bloods - Ca 15-3 for breast cancer, PSA for prostate Neuro exam ``` ``` Tx Lie flat Dexamethasone Catheterise if urinary incontinence Bisphosphonates DVT Analgesics Laminectomy/ radiotherapy ```
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Spinal cord compression - presentation + causes
Radicular pain at level of injury, altered sensation, spastic paraparesis below, may be autonomic sx e.g. urinary retention, paralytic ileus, priapism, constipation Causes - Trauma - Malignant spinal cord compression - Disc herniation - Epidural/ subdural haematoma - OA - cervical spondylitis myelopathy
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Guillain Barre Hx of viral illness followed by progressive symmetrical ascending weakness, neuropathic pain, peripheral loss of sensation and reduced reflexes
``` Ix Clinical diagnosis of ascending weakness, parasthesia and hyporeflexia occurring post infection Do NCS, EMG Look for antibodies Do LP - protein in CSF Spirometry if suspect resp involvement Routine bloods Check Ig levels as if IgA deficient might get anaphylaxis when given IV-Ig ``` Mx: Immunoglobulins (0.4g/kg/24hrs) and/or plasma exchange Supportive care - treat resp failure, monitor heart, give analgesics and DVT prophylaxis Physio, rehab Splinting to prevent join contracture Improves over time
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MG management Lamber eaton - better with exercise MS, MND, hypothyroidis, horners sx are other differentials
Often first sign is drooping of eyelid (ptosis) and diplopia, then get muscle weakness that is worse with exertion. Worse at end of day. Can also get fatiguable chew, dysarthria/ dysphagia, weak breathing, dropped head. No change in tone, reflexes, sensation, no wasting. Weakness more marked in proximal than distal, arms than legs Myopathy, eye trauma, third nerve palsy, cyst or swelling - differentials for MG eye symptoms Ix: Do a full neuro exam, assess vision and muscle weakness Crushed ice on eye for 3 mins, improves ptosis Ask to count to 50 and see if fatigue Anti-Acetylcholine receptor antibodies Repetitive nerve stimulation test or EMG CT/MRI of thymus to look for thymoma Tensilon test - rarely done as can cause bradycardia General bloods, TFTs Mx: Myasthenic crisis - intubation, mechanical ventilation + immunoglobulins, plasma exchange and steroids Treat with acetylcholinesterase inhibitor e.g. pyridostigmine, add steroids +/- azathioprine if not sufficient. Is also rituximab, biologics TPMT before start azathioprine, not combine with allopurinol Oral atropine for muscarinic SE of pyridostigmine (diarrhoea, colic, sweats, salivation, lacrimation) If thymoma present - thymectomy
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MND - most common = ALS (degen of anterior horn cells and cranial motor nuclei) - No sensory loss, no sphincter deficits (MS) - No eye sx (MG)
Limb onset - asymmetrical distal weakness, UMN and LMS signs, no sensory issues - spasticity, wasting, upgoing plantars, reduced reflexes Bulbar onset - slurring of speech, wasting + fasciculation of tongue, dysphagia Resp onset - dyspnoea, orthopnea Ix - hx and exam show UMN/LMN and no sensory signs - Neuroimaging and electrophysiological tests exclude other causes - Bloods to exclude thyroid, b12/folate deficiency, Antibody testing, CK can be raised in MND - Muscle biopsy to exclude myopathy - LP to exclude GB Mx - patient education - MDT - physical, occupational and speech therapy - exercise regimes to maximise mobility - Riluzole - glutamate release inhib - only prolong life by 2-4m - Hyoscine for drooling - Quinine (1st line) then Baclofen for cramps - Baclofen for spasticity - Analgesics - Feeding/ speech support (may need NG, gastrostomy when cant feed by mouth) - Opioids or benzodiazepines for breathlessness - NIV (BIPAP) may be used overnight - Hospice care and respite
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Aortic stenosis Caused by calcification, bicuspid aortic valve, rheumatic heart disease
Presents with ejection systolic murmur, dyspnoea, angina and syncope If radiates to carotids, narrow pulse pressure, slow rising, symptoms = stenosis not sclerosis Displaced apex = LVH Differential for aortic stenosis - hypertrophic cardiomyopathy (also presents with syncope, dyspnoea, angina) Ix: Cardio exam, obs, ECG, transthoracic ECHO, CXR Tx: Conservative HF: Diuretic, ACEi Angina: BB or CCB TAVI or AVR, or balloon valvuloplasty - if severe sx, LVEF <50, already undergoing cardiac surgery, pressure gradient >40 on echo Assess QRISK - Statins, BP etc
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Polymyositis/ dermatomyositis
Fever, malaise, weight loss - Proximal weakness (shoulder + pelvis) with distal sparing - Difficulty combing hair, climbing stairs - NOT tender Dermato - heliotrope rash, gottrons sign, shawl sign, mechanics hands ix - raised ck - ESR/CRP raised - antibody testing - ANA, anti-jo - EMG - short, low amplitude movements - Diagnose with muscle biopsy - regular spirometry to monitor for resp muscle failure mx - Rest + exercise programme - Prednisolone is mainstay – topical in mild up to IV in v.severe - 2nd line – azathioprine, cyclophosphamide - IV IG therapy
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Tests indicative of haemolytic anaemia
Raised LDH Reduced haptoglobin Intravascular - haemosiderin urine (brown) - not present in extravascular causes Intravascular causes include mechanical heart valve, haemolytic uraemic syndrome, DIC, HELPP, acute transfusion reaction, Extravascular causes - sickle cell, thalassaemia, G6PD deficiency spherocytosis, warm or cold AI haemolytic anaemia, hypersplenism, malaria
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AI hepatitis
ANA/ anti-sma/ anti-lkm1 +ve, raised IgG, raised ALT/AST, raised PT and low albumin, raised bilirubin, liver biopsy diagnostic Treat with prednisolone initially and then in combination with azathioprine Treat for 2 years or until LFTs better for 12m May require liver transplant
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PBC management Dark urine, pale stool and raised liver markers with background of AI conditions Fatigue common Vs PSC
Ix: IgM, AMA +ve, ALP/GGT raised and no other explanation In late stage disease may see raised PT, low albumin Do liver biopsy to confirm Fibroscan can be used to evaluate degree of liver fibrosis ``` Mx UDCA (obeticholic acid is 2nd option) Sedating antihistamine or cholestryamine for itching Rituximab for fatigue Avoid the pill, HRT Supportive treatment - fat soluble vitamins, osteoporosis prophylaxis Steroids and azathioprine liver transplant if above fail ``` PSC more common in men, younger - ve AMA, confirm with MRCP or ERCP - Treat with stent/ balloon insertion, cholestyramine, rifampicin, fat soluble vitamins, avoid alcohol, transplant,
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NAFLD - alcohol cutoff, presentation, Ix, Mx - after diagnosis screen for cirrhosis every 2yrs
<2.5 (F), <3.75 (M) units per day progresses from steatosis to non-alcoholic steatohepatitis to fibrosis then cirrhosis RF: Obesity, HTN, Type 2 diabetes, Hyperlipidaemia, Smoking Ix - LFTs, coagulation screen, albumin - Lipids/ HbA1c/ FBC - AMA, ANA, SMA etc - Caeruloplasmin for Wilson, ferritin for haemochromatosis, alpha 1 antitrypsin - viral studies - US to confirm fatty liver - Enhanced liver fibrosis (ELF) blood test -> fibroscan if signs of fibrosis - CT/ MRI - Liver biopsy to confirm diagnosis Mx - Patient education - Diet, exercise, gradual weight loss, alcohol abstinence - Manage HTN, T2DM, High lipids - Pioglitazone, metformin, statins may help - Bariatric surgery, Liver transplant, TIPS
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Acute liver failure management Fulminant if no known prev liver disease and altered clotting - onset within 8w of disease onset Present with jaundice and encephalopathy
Causes - toxins e.g. alcohol, paracetamol - viral hepatitis - Metabolic - Wilsons, alpha 1, haemochromatosis - NAFLD - HCC or metastasis - pregnancy - HELLP, acute fatty liver disease of pregnancy - Budd chiari or portal vein thrombosis - AI liver disease Ix: Hx - ask about onset of jaundice and encephalitis, ask about toxins and fhx of wilsons etc Asses consciousness/ mental state and do abdo exam for asterixis/ ascites Raised PT, low Albumin Do routine bloods (FBC, LFT, U+E, glucose, INR (>1.5), ammonia) and liver screen (hep b/c, AI, toxicology, ferritin, caeruloplasmin etc) High ammonia -> encephalopathy Do G+S, blood culture if suspect infection ABG for lactate Liver US + doppler for Budd chiari/ cancer CT - Assess for cerebral oedema, raised ICP, other causes of altered mental state EEG to define level of encephalopathy Investigate for cause - caeruloplasmin (low), alpha 1 antitrypsin, ferritin (haemochomatosis), ANCA, AI screen, Alcohol, viral Mx: Treat cause Treat in ITU/ HDU due to need for intubation Fluid resus - fix distributive shock with: CVC line, Fluids/ ionotropes, monitoring urine output, BP Ascites- restrict fluid, low salt diet. spironolactone +/- furosemide - if large: paracentesis + human albumin solution Encephalopathy - Lactulose with neomycin, raise head of bed, repeated enemas. Mannitol can reduce ICP, rifaximin can help in prevention IV 10% glucose Coagulopathy - clotting factors, plasma, platelets, PPI to stop bleeding AKI - Correct electrolytes, for hepatorenal type 1 may need terlipressin + albumin, dialysis/ TIPS if needed Abx prophylaxis Consider transplant based on kings college criteria if high INR/ PT, quick onset encephalopathy, high bilirubin
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ALD - alcoholic liver disease
>12.5 units per day for 15-20 years Do CAGE - cut down, annoyed, guilty, eye opener Ix - AST:ALT ratio >2 - Raised GGT/ MCV - indicate alcohol abuse - Coag screen, albumin levels - Bloods - FBC, U&E, CRP - US, fibroscan - biopsy Mx - Alcohol abstinence - Antabuse, acamprosate, naltrexone - Chlordiazepoxide + pabrinex for acute withdrawal - counselling, brief intervention psychotherapy, alcoholics anonymous - Lifestyle - Steroids can help in acute hepatitis - important - Transplant Can commonly revert to normal liver once alcohol stopped
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Cirrhosis
Causes are - alcoholic, NAFLD, hepatitis B/C, Wilsons, hereditary haemochromatosis, alpha-1-antitrypsin, CF, Budd-chiari sx - lethargy, weight loss, nausea on exam - hepatomegaly, asterixis, dupuytrens, gynaecomastia, caput medusae, palmar erythema, leukonychia, easy bruising, clubbing, xanthelasma In decompensation - jaundice, variceal haemorrhage, encephalopathy (asterixis due to ammonia), ascites, abnormal clotting ix - LFT, coag, albumin - Baseline bloods - Caeruloplasmin, ferritin, alpha fetoprotein, alpha-1-antitrypsin - Hepatitis serology - fibroscan - transient elastography - CT - Biopsy - Ascitic tap - neutrophil >250= SBP Use child-pugh score to grade cirrhosis, MELD score for prognosis Mx - Lifestyle - high protein, low sodium/ fat diet - Alcohol abstinence - Colestyramine for pruritis - treat cause - penicillamine (Wilsons), UDCA (PBC), etc - Ascites- spironolactone +/- furosemide - if large: paracentesis + human albumin solution - if persistent TIPS - continued screening for varices - every 3 years, HCC, decompensation, do MELLD score 6 monthly - Liver transplant based on UKELD score
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Ascites - how to determine cause, ix, mx
SAAG - serum ascites albumin gradient - >1.1 = transudate - raised portal pressure - <1.1 = exudate - normal portal pressure - e.g. due to cancer, infection, pancreatitis, nephrotic syndrome Ix: Regular bloods, Clotting, albumin, ascitic tap, liver screen, US, MRI/CT Perform ascitic tap if suspect SBP - raised WCC and neutrophils (> 250). Treat with abx (cefotaxime/ ceftriaxone) and human albumin solution Put on a low salt diet - in some this will be enough to resolve 1st line fluid restrict and spironolactone 2nd line furosemide Aim for no more than 1kg loss a day If large, refractory or causing resp compromise paracentesis followed by plasma expansion If persistent - TIPS Cholestyramine for pruritis
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Liver cancer - HCC
Mainly caused by cirrhosis or hepatitis B/C infection Presents with weight loss, fatigue, fever, night sweats, pruritus, jaundice, ascites, encephalopathy, RUQ pain If hep B/C carrier or have cirrhosis should have 6&12 monthly screening via AFP and US - lesions>2cm should be biopsied and CT scanned Ix - Bloods - LFT, FBC, U&E, coag - AFP - Ca 19-9 - cholangiocarcinoma/ pancreatic cancer - US - CT - bone scan, look for mets - biopsy rarely done Mx - conservative if elderly - if singular <3cm, small, confined can consider resection - Can transplant liver if fit Milan criteria (1 x <5cm, 3 x <3cm, no metastasis and no vessel invasion on CT/ MRI) - Ablative therapy - Systemic chemo/ radiotherapy rarely used (transarterial chemoembolization)
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Pancreatic cancer
Adenocarcinoma Presents with weight loss, fever, epigastric discomfort/ back ache and progressive painless jaundice Ix - routine bloods - Ca 19-9 - faecal elastase - glucose levels - US - CT - Biopsy via ERCP or endoscopic US Mx - Surgical resection - pancreaticoduodenectomy with antrectomy (Whipple's procedure) - chemotherapy - analgesia, creon, stenting
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How can gastric tumour affecting pylorus present?
Reflux, early satiety, fullness, vomiting, weight loss, anaemia, melaena
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Hypertension
<55 or diabetes - ACEi or ARB >55 or black - CCB 2nd line ACEi + CCB or Thiazide / CCB+ ACEi or thiazide 3rd line - All 3 4th - K < 4.5 - spironolactone, K > 4.5 - alpha or beta blocker
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Psoriasis - hyper proliferation of keratinocytes
Symmetrical erythematous patches, papules and plaques with overlying silver scale Differentials - dermatitis, lichen planus, cutaneous lymphoma Recent alcohol binge -> rash = psoriasis Ix: Clinical diagnosis, skin biopsy only if doubt Auspitz sign - removal of scales causes capillary bleeding IBD, assess CV risk Ask about nails (pitting and onycholysis), joints, dactylics (swelling of digit) Dermatology quality of life index score Use psoriasis area and severity index (PASI) to assess severity, also assess body surface area affected Tx: Educate, is chronic condition, help sx not cure Identify + avoid precipitants, stop smoking, alcohol, healthy lifestyle diet and exercise Emollient, salicylic acid for scale/itch 1st line - vit D analogue OD + topical corticosteroid OD If after 4-8 weeks not gone stop steroid and try vit d analogue BD for 12 w. If still not better consider corticosteroid BD or coal tar If ongoing treatment resistant consider referral and dithranol Dermatology - topical calcineurin inhib, ciclosporin, acitretin, narrow band UVB. If UVB ineffective consider methotrexate, ciclosporin or TNF alpha inhibitors e.g. adalimumab For joint - do xray (central erosions), bloods, joint aspiration. Treat with NSAID first line, 2nd line corticosteroid injection and if active disease methotrexate, if dactylitis or entheses - adalimumab, NSAID Guttate psoriasis - rain drop lesions, commonly post strep throat, treat with phototherapy Pustular psoriasis - acute withdrawal of psoriasis meds - treat with supportive care and systemic management
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Sepsis
AtoE Septic shock (distributive) = need for vasopressors to maintain MAP > 65 or hypovolaemia unresponsive to fluids - present as flushed, dry, warm, tachycardia, hypotension Ix - FBC - WCC, low platelets (DIC) - U&E - LFT - CRP, ESR, procalcitonin - Clotting - ABG (lactate) + cultures - ECG - Glucose - GCS/ neuro obs Mx - AtoE - Sepsis 6 (fluids, abx, O2 (>94%), lactate (+ glucose on A BG), UO (>0.5ml/kg/hr), blood culture - If not improving, shock consider critical care outreach, central line and admin of noradrenaline 1st line or vasopressin 2nd line. - Dobutamine, hydrocortisone can be used as ionotropes - Paracetamol as antipyretic - NIV, cardiac, renal, liver monitoring - VTE prophylaxis - can develop stress ulcer so give omeprazole or ranitidine
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Peritonitis
Presents often initially with generalised abdominal pain, becomes focal and well localised, fever, tachycardia, tenderness, rebound tenderness and guarding on palpation Lie with knees flexed Caused by SBP, perforation, trauma/surgery, AI, leakage of bodily fluids into peritoneum Ix - FBC, U&E, LFT, CRP - AXR/ CXR to look for perf - urinalysis - Blood culture - Peritoneal fluid sample (neutrophil > 250 = SBP) Mx - IV fluids - IV abx - Exploratory laparotomy if perforation - For SBP give cefotaxime/ ceftriaxone + human albumin solution and await culture sensitivities
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PID symptoms and treatment = Endometritis, Salpingitis, Oophoritis, Tubo-ovarian abscess, Pelvic peritonitis
Uterine, cervical motion tenderness Lower abdo pain, pain on urination and sex Uterine bleeding (inter-menstual, post coital or breakthrough) Abnormal cervical or vaginal discharge Fever, nausea and vomiting Ask about recent termination of pregnancy or IUD Ix: Bimanual + obs - adnexal tenderness, cervical motion tenderness Vulvovaginal or high vaginal swab for chlamydia/ gonorrhoea Urinalysis + culture Bloods - CRP, ESR, WCC Pregnancy test - exclude ectopic Transvaginal US Tx: Pain relief Empirical antibiotics: Ceftriaxone 1mg IM, doxy 100mg BD and metro 400 mg BD for 14 days Consider removing IUD If mycobacterium genitalia - moxifloxacin TOC if chlamydia, gonorrhoea, mycoplasma genitalium Contract trace all partners in last 6 months, give 7 days doxycycline to all partners
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Management of chlamydia and gonorrhoea gonorrhoea - yellow/green discharge
First catch urine/ vulvovaginal swab NAAT test - 2w window period Gonorrhoea can also be examined by microscopy and culture - gram-negative diplococci Transvaginal US, cervical motion tenderness - can be used to identify endometritis and salpingitis of PID Chlamydia - 7d 100mg doxycycline or 1g azithromycin oral - also treat partner - avoid sex until completed course - partner notification - 1 month or last partner for symptomatic males, 6 months for others - if under 25 retest in 3-6 months Gonorrhoea - 1g Ceftriaxone IM - also treat partner - abstain from sex until completed treatment - partner notification - 2w or last partner if symptomatic male, 3m for all else - Follow up after 1 week to ensure treatment successful, test of cure 2w after
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Infective endocarditis Most commonly affected valve = mitral, in IVDU is tricuspid Due to bacteraemia and abnormal cardiac endothelium - Get infective vegetation formation - Causes regurg murmurs and HF - embolus formation
Normal valve - staph A Abnormal valve - strep viridens Prosthetic valve - early: within 2m epidermis, later staph a Presentation - May have new heart murmur - pan systolic mitral regurg, early diastolic murmur of aortic regurg - Fever, chills, weight loss - Splinter haemorrhages, Roth spots, Janeway lesions (painless, red, on palm) and oslers nodes (red tender nodules on fingers) - clubbing if longstanding - CVA, splenic/ renal/ pulmonary abscess Investigate with DUKE criteria 2 major (2x +ve blood cultures, evidence of endocardial involvement - new murmur, vegetation, abscess) 1 major, 3 minor 5 minor Minor = IVDU, fever >38, predisposing heart condition, vascular phenomenon, immunological phenomenon (oslers, Janeway, glomerulonephritis, Roth spot), +ve cultures of uncommon pathogen Ix - examine for signs + murmur - FBC, CRP, ABG for infection markers - Urinalysis - microscopic haematuria - glomerulonephritis - CXR - ECG, Echo within 4 hours - Blood cultures (3 sets, 3 sites, 3 different times) - Cardiac CT if diagnostic uncertainty Mx - native or late prosthetic valve: ampicillin, flucloxacillin and gentamicin - early prosthetic valve: vancomycin and gentamicin and rifampicin - Then treat based on organism (staph a = fluclox, MRSA = vancomycin, strep = amoxicillin or ceftriaxone) - surgery to remove vegetation, repair/ replace valve
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What model is used for treating schizophrenia?
Biopsychosocial model - Antipsychotic, general medical care - CBT, family therapy - Alcohol, drug management, social skills training, employment opportunities
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Anxiety ASK ABOUT SUICIDAL THOUGHTS GAD 7, GAD2
Persistent worry most days for last 6m, inability to control worrying and associated with at least 3 of: restlessness, fatigue, lack of concentration, irritability, muscle tension, poor sleep. Ask about how impacting work, school, relationships, social life Ask about mental and physical symptoms - any panic attacks? Ask about self harm, risk of suicide Assess with GAD2, GAD7 Screen for organic causes e.g. hyperthyroid, SVT, anaemia, hypoglycaemia etc. Step 1 - educate, sleep hygiene, exercise, Beta blocker Step 2 - Low intensity psychological interventions based on CBT (individual self help) Step 3 - CBT or drug therapy with SSRI (2nd line SNRI, 3rd pregabalin) Step 4 - Refer for specialist care, medication
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Depression hx PHQ2, PHQ9 - can be used for screening and understanding severity respectively Organic - steroid use, DM, hypothyroid, adrenal issues
Open consultation - Acknowledge difficult topic say if want to stop and have a break at any time please say ``` How long been going on for, any triggers? How much been affecting life - appetite, sleep, exercise, social life, hobbies, mood, libido How changed over time Anything your worrying about Anything pre-occupying your mind When is it at its worst What do you feel is getting you through What is your view of yourself ``` Hows your concentration, how feel about self, how feel about future Have you ever thought about harming yourself or others Have you ever felt the opposite to how you are now, particularly high? What do you think is causing this, anything you're worried about? Have you ever felt like this before? Have you ever suffered with mental health conditions before or been on any medication How are you otherwise, fit and healthy Any family history of mental health conditions? ``` Do you drink, smoke, take drugs? Live alone, with family? Able to look after self? Relationships? Support network? ``` If high risk of suicide contact crisis resolution and home treatment team
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Depression mx
Last at least 2w, no hypo or mania Core symptoms are low mood, fatigue and reduced energy, loss of interest in activities that are normally pleasurable Can do routine bloods to screen for organic causes ``` Mx: Assess suicide risk PHQ-9 >5 – mild >10 – moderate >15 – moderately severe >20 – severe ``` Sleep hygiene, exercise Crisis team if suicidal If mild Discuss concerns, sleep hygiene, regular sleep/wake times Exercise programmes Provide information Active monitoring Follow up in 2 weeks, make contact if not attend Mild - mod low intensity self guided or computerised CBT, second line is group CBT Mod to severe High intensity individualised CBT SSRI first line - continue for 6m post remission ECT can be considered for fast short term improvement
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Suicide risk assessment
Before - Events leading up to incident - any precipitant? - Was the attempt planned? - Suicide note/tell anyone? - Attempts not to be found? - Affairs put in order? During - Exactly what happened including number of tablets, timings - How they were discovered - Concurrent use of alcohol or other drugs - What did they think would happen? After - What happened straight after? - How do they feel now? Any feelings of regret? - Current mood/current plans of ending their life or self harm - What would happen if they went home?
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Eating disorder Hx + Mx
Defined as BMI below 17.5 kg/m2 Ask about binge eating, purging, vomiting, perceptions towards appearance, typical food consumption in a day, how often weigh self or look in mirror, make excuses not to eat. Ask about excessive exercise, any tablets used to loose weight. Lack of insight into own weight loss. Ask about menstrual irregularities, sexual dysfunction, weakness, fainting, fatigue, constipation, changes in skin or hair, seizures? SCOFF questionnaire do you make yourself Sick have you lost Control over how much you eat lost > One stone in last 3m Do you believe you are Fat when others say you are thin would you say Food dominates your life Routine obs + blood glucose Sit-up, Squat–stand test - rank difficulty BMI, FBC, U+E, LFT, CRP, ESR, TFT, Bone profile, Mg ECG Pregnancy test Consider DEXA if <18, >1year Assess risk with marsipan document Immediate referral to CAHMs, community mental health team or eating disorder specialist If high risk, risk of referring syndrome admit <18 - anorexia focussed family therapy or individual CBT/ psychotherapy second line >18 - eating disorder based CBT, group therapy If refuse to eat - NG tube and TPN, consider sedation if refusing, emergency crash team General monitor food consumption + U+Es Avoid QT prolonging drugs e.g. citalopram If vomiting - dental checkup, rinse mouth with mouthwash after rather than cleaning Stop excessive exercise/laxatives Dexa scan, refer to diabetes if insulin misuse Advise against conception until weight improves, give contraception even if amenorrhoea
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Peripheral arterial disease - chronic, critical and acute limb ischaemia Usually affects both sides to some degree Can get haemosiderin deposits in PAD, chronic venous insufficiency due to DVT, thrombophlebitis (superficial veins) or pregnancy
Most common cause = atherosclerosis Chronic limb ischaemia - present with intermittent claudication, weak pulses and hairless/ impaired healing Can develop into critical limb ischaemia if pain at rest, particularly at night and improved by hanging leg out of bed, cold and pale limb, ischaemic lesions or gangrene Ix - CV exam + BP + pulses + CRT - FBC, Glucose (diabetes), lipids - Thrombophilia test if <50 - ECG - ABPI - claudication 0.6-0.9, rest pain 0.3-0.6, critical ischaemia/ gangrene = <0.3 - Treadmill test - walk until claudication - Duplex US especially if considering revascularisation - CT angiography - gold standard - MR angiogram or catheter angiogram Mx - Stop smoking, exercise, weight loss - statins, antihypertensives, ACEi, manage diabetes - Exercise regime + Antiplatelets (aspirin and clopidogrel) - If exercise regime not improved 2nd line = balloon angioplasty +/- stent, 3rd line = bypass. - Non surgical alternative is Naftidrofuryl oxalate (vasodilator). In critical limb ischaemia - always treat as can cause ulcers, necrosis and amputations - discuss in MDT - revascularisation without delay - analgesics +/- laxatives/ antiemetics as needed - amputation last resort
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Acute limb ischaemia Most commonly due to an embolus/ thrombotic plaque - can be caused by trauma, popliteal aneurysm thrombosis, aortic dissection, compartment syndrome, iatrogenic Tends to only affect one side
6 P's - acute limb ischaemia - pain - pallor - perishingly cold - pulselessness - parasthesia - paralysis Often other leg is normal - or can develop on back of chronic limb ischaemia Use Rutherford classification to grade acute limb ischaemia Ix - Assess arterial disease RF - FBC, lipids, glucose, ESR (temporal arteritis) - thrombophilia screen - Doppler US to assess arterial flow - CT angiogram 1st line - MR angiography or Catheter angiography can be considered - ECG, echo, aortic US, popliteal and femoral US - ABG for lactate - ABPI after initial management to assess for chronic ischaemia Mx - AtoE - 15L O2, IV access, immediate heparin bolus followed by infusion, morphine + antiemetic, NBM - If Rutherford I or IIa can manage conservatively with prolonged course of heparin, monitoring - Compartment syndrome - fasciotomy - If embolic: surgical embolectomy, bypass graft, local intra-arterial thrombolysis (streptokinase) - If thrombotic: intra-arterial thrombolysis, angioplasty or bypass graft - If irreversible - leg mottled and muscle hard and woody - urgent amputation - Treat any MI/ AF - consider antiplatelets/ anticoagulant Post surgery - ischaemic reperfusion syndrome - can cause compartment syndrome, high K+, acidosis, high myoglobin causing AKI
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Differentials for swollen foot and mx of charcots
Localised: DVT, cellulitis, rheumatoid arthritis, lymphedema, malignancy Systemic: Heart failure, liver failure, nephrotic syndrome calcium antagonists, NSAIDS, hypothyroid Have neuropathy, greater than 2 degrees difference in temp between two feet Charcot foot = red, warm, swollen and deformed Charcot Mx: Xray/ MRI and screen for infection and ulcers: involves MDT, nurses, podiatry, diabetes drs, orthopaedics Immobilisation of the joint in a cast (or with orthopaedic stabilisation), which will usually remain in place for 3 – 6 months (monthly X-Rays are used to assess progress) - takes weight off of foot to allow healing Surgery is required if foot deformity puts the patient at risk of ulcers or protective footwear (custom braces and orthotic footwear) is not effective. Also if is unstable fractures or dislocations. Longer term management is with optimisation of diabetic control, including BP and lipids, as well as specialised footwear and education Important to regularly check the feet for ulcers May require amputation if not healing and infection The total process of healing usually takes 1 – 2 years Give antibiotics as needed,
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Diabetes management and Annual review
Diabetes is diagnosed as a HbA1c > 48, Fasting >7 or random glucose >11.1 1 +ve result with sx, 2x if no symptoms First line management is lifestyle, education (DESMOND, X-pert programmes) - exercise, reduce intake of sugar, low GI foods, reduce alcohol, stop smoking, weight loss, screening If HbA1c > 48 start metformin 500mg OD, each week increase by 500 to max of 2g If HbA1c >53 then start then add DPP4, SGLT2, pioglitazone, SU If still >53 - triple therapy SU - hypo, gain weight SGLT2 - (gliclazide) Improve weight, cardio and renal protective (not work if eGFR <60 TZT - contraindicated with haematuria DPP4 - (-gliptin) not improve weight, use in liver or renal failure GLP-1 - (-tide) third line, only use if already on triple therapy If insulin/ SU - aim 53 If others aim 48 Consequences Microvascular - neuro, nephropathy (peripheral, autonomic e.g. gastroparesis, erectile dysfunction), retinopathy Microvascular - ischaemic heart disease, stroke, PVD Annual review Take a hx, ask about how managing, sx, SE of tablets Depression and anxiety Qrisk to look for CV disease - cholesterol, BP, BMI Do a blood glucose measurement - HbA1c Diabetic retinopathy screen Foot exam - check sensation (glove and stocking, pain, tingling), for ulcers, do ABPI, pulses, CRT, inspect footwear Ask about autonomic SE including erectile dysfunction, gastroparesis Nephropathy - early morning first pass urine specimen for ACR, also do creatinine level for eGFR
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Diabetic foot mx
Educate - appropriate footwear, check feet daily, report any injuries that dont heal, no barefoot walking Charcot - immobilisation, realignment arthrodesis/ surgery Ulcers - off-loading/ bed rest - therapeutic shoes, wound management, diabetic control Infection- swab, blood culture, xray for osteomyelitis, IV abx Painful neuropathy - bed foot cradles, analgesia (TCA first line) alternatives = gabapentin, carbamazepine PAD - exercise, antiplatelets, revascularisation Last resort = amputation
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Foot ulcers - appearance,
Venous - granulated, shallow, irregular - medial malleolus - painful, worse at end of day + when standing - Age, obesity, prev VTE, pregnancy - thrombophlebitis, haemosiderin, atrophie blanche, lipodermatosclerosis, oedema - Duplex US for venous insufficiency, ABPI to rule out arterial, swab if infection - Raise leg, exercise, weight loss, compression bandaging (only if ABPI >0.6), emollients, endovascular treatment of varicose veins, abx if infection Arterial - punched out, well defined, deep, necrotic base, little granulation, at pressure points - foot cold, reduced pulse, painful (better if hang out of bed at night) - Obese, smoker, DM, HTN, hyperlipidaemia - Hx of intermittent claudication, PAD: hair loss, necrotic toes, cold, reduced pulses - Do ABPI, duplex US, angiography, swab for infection, xray for osteomyelitis - debridement, wound care, graft, - Treat PAD - exercise, antiplatelets, endovascular surgery e.g. balloon angioplasty/ stent Neuropathic - Punched out, painless, loss of sensation in glove and stocking, warm foot, good pulses - burning/ tingling neuropathic pain in legs - DM, B12, Charcot marie tooth - Do BM's, bloods, assess sensation, ABPI for accompanying PAD, swab/ xray if infection - Optimise diabetes, diet, exercise, podiatrist, foot hygiene, manage CV risk factors, may need debridement/ surgery.
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Pressure sores Management
Ix: Assess cause, location, grade, size, infection, odor, exudate Waterlow risk assessment Grade based on appearance and depth Tx: Pressure redistribution, nutrition, analgesia, dressing (-ve pressure) Rotate position, address incontinence, malnutrition, regular skin assessment Debridement 6w fluclox if osteomyelitis Plastic surgery
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DVT
Unilateral throbbing pain worse when standing or walking, swollen, red calf/ leg, warm and tender to touch Cellulitis, thrombophlebitis, PAD/ Acute ischaemia, ruptured baker cyst are differentials Measure calf circumference 10cm below tibial tuberosity, if >3cm difference suspect DVT Ix - Bloods - FBC, U&E, LFT, CRP, coag - Wells score - If wells >1 - Doppler US within 4hrs (if cant be done do D dimer and give interim apixaban) - If wells <1 - D dimer (if cant be done within 4hrs start apixaban) - If positive do US, negative stop anticoagulant Mx - 1st line apixaban/ rivaroxaban - Alternative LMWH then warfarin - 3m if provoked (transient risk factor e.g. surgery, immobility, pregnancy), 6m if unprovoked - if unprovoked offer thrombophilia, cancer testing Consider thrombolytic treatment if illiofemoral DVT IVC filter if repeated DVT/ PE or non responsive to anticoagulant Can develop post thrombotic syndrome: chronic venous hypertension and varicose veins causing: limb pain, swelling, hyperpigmentation, dermatitis, ulcers, venous gangrene, and lipodermatosclerosis - exercise, leg elevation, compression
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Virchows triad - DVT
venous stasis, hypercoagulable state, endothelial injury
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Cardiac arrest: Pulseless VT/ VF - Causes, management and investigations post management
4h's and 4t's Hypoxia, hypothermia, hypo/hyperkalaemia, hypovolaemia Thrombus, tamponade, Tension pneumothorax, Toxins Pulseless: CPR + non-synchronised DC defibrillation - High flow O2 - 15L, secure airway - IV fluid resus - Adrenaline 1mg 1in10000 and amiodarone 300mg after 3rd shock - Repeat adrenaline dose every 3-5 mins - Further 150mg amiodarone after 5th shock - If PE - Thrombolytic therapy, continue CPR for 60-90 mins - once resolved amiodarone 900mg over 24 hours - Post arrest care in ITU Ix - Trops - Temperature - ABG, U&E for electrolytes/ hypoxia - CXR for pneumothorax/ tamponade, HF - Toxin screen - Drug levels e.g. digoxin - ECG for MI, long QT etc - TFTs - Coronary angiography
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VT with pulse monomorphic and polymorphic management | VF is always pulseless
Monomorphic, Unstable: synchronised defib up to 3 attempts, followed by 300mg amiodarone over 10-20mins - then can re-shock or consider procainamide or sotalol as needed - once resolved amiodarone 900mg over 24 hours Monomorphic, Stable: amiodarone 300mg IV over 10-20 mins - once resolved amiodarone 900mg over 24 hours - Alternative = flecainide or synchronised cardioversion/ pacing Polymorphic - torsades de pointes - Stop any drugs prolonging QT - citalopram, erythromycin, ondansetron, ciprofloxacin etc - Correct any electrolyte imbalances e.g. hypokalaemia - IV MgSO4 2g over 10-15mins - If refractory - increase HR to reduce QTc using adrenaline if hypotension or dobutamine if normotensive - Can consider transcutaneous/ transvenous pacing - If congenital - long term treatment with BB Following VT consider ICD fitting to prevent further events, beta blocker + amiodarone can be given in addition or as alternative ICD acts like a pacemaker but can also shock to reset heart rhythm if needed
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PEA/ Asystole - cardiac arrest Causes = 4H's 4T's
Non shockable - Give adrenaline immediately and continue chest compressions - repeat adrenaline every 3-5 mins - recheck rhythm every 2 mins - Secure airway, IV fluids
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Sinus bradycardia - when and how to treat
Can be normal in sleep, athletes Can be caused by hypothermia, cushings triad (raised ICP), MI, anorexia Treat if any adverse features (MI, shock, syncope, HF) or if risk of asystole (recent asystole, mobitz type II or complete heart block, ventricular pauses >3s) 1st give 500mcg IV Atropine In not improved - repeat above to max of 3g - isoprenaline 5mcg/min IV - Adrenaline 2-10mcg/min IV - Or transcutaneous pacing
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SVT - presentation, Ix, Mx AVNRT, AVRT e.g. WPW (short PR, wide QRS, delta wave)
Palpitations, Fatigue, Pre-syncope/syncope , Chest pain Ix - Thorough clinical history - ECG, echo - response to adenosine/ vagal manoeuvres Mx - Haemo unstable: defibrillate - Haemo stable: 1st vagal manœuvres (Valsalva, carotid massage - not if recent stroke), 2nd 6mg adenosine via wide bore cannula (verapamil if asthma), 12mg if no improvement after 2 mins, repeat once more. 3rd line is DC cardioversion Long term: Depends on cause - BB or CCB's - Flecainide, sotalol or amiodarone may also be effective - Catheter ablation - AVRT (WPW - remove accessory pathway), AVNRT - stop smoking, alcohol, caffeine, drugs that might be precipitating
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Atrial flutter
Due to re-entry circuit around tricuspid valve in most cases Atrial rate of 250-350, 2:1 conduction ratio with ventricular rate around 150 On ECG: - multiple p (f waves) waves per QRS - regular QRS intervals - Loss of flat isoelectric line - Flutter waves have saw tooth appearance - Regular rhythm tachycardia Suspect if vagal manoeuvres/ adenosine for treatment of SVT haven't worked Mx - 3 options - If haemo unstable - cardioversion, can also do if stable and within 48hrs of presentation (if not need to anticoagulant for 3w) - Best treatment - catheter ablation - If not suitable for above - pharmacological cardioversion with amiodarone, sotalol, digoxin, verapamil, flecainide Important to also treat underlying cause e.g. alcoholism, obesity, hyperthyroid Long term anticoagulation often needed - apixaban or warfarin - risk of thromboembolism
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AF management Absent P waves, Admit to hosp if: HR >150bpm and/or BP <90 Loss of consciousness, severe dizziness, chest pain, or breathlessness Complications: stroke, TIA or acute HF Onset within 48h? Options to refer CDU for immediate cardioversion without need for anticoagulation or manage in primary care if stable Doac - better stroke risk reduction, but shorter half life so need better adherence, less monitoring Aim for pulse rate of 60-80 on rate control
Paroxysmal - >30s <7d Persistent - >7d or <7d but need pharm/ elect cardioversion Permanent - longstanding (>1yr), failed to cardiovert, cardiovert but revert within 24hrs Most common causes = IHD, HTN, Valvular heart disease, Hyperthyroidism Ix: Pulse, ECG, holter monitor or event recorder if paroxysmal, Bloods, ECHO, TFT Tx: If present with collapse or are haemodynamically unstable - O2, fluid, airway adjunct, emergency cardioversion If new, young, reversible, HF - Cardiovert with DC if within 48hrs or after 3w of anticoagulation. Alternative = pharmacologically with rhythm control Treat cause e.g. hyperthyroid If paroxysmal - pill in pocket (sotalol or flecainide) or catheter ablation Long term: Rate - BB (propanolol), CCB (diltiazem) or digoxin (if pt sedentary). If monotherapy fails combine BB and CCB Rhythm - BB, flecainide (if no structural heart disease), amiodarone Left atrial catheter ablation, AVN ablation or pacing can be considered ``` CHADVAS vs HASBLED - Offer anticoagulant if chadvas >2 - Consider Anticoagulant in men with Chadvas >1 Hasbled >3 - at risk of bleeding - DOAC or warfarin ```
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Heart block types and mx Commonly caused by MI, drugs e.g. CCB/ BB/ digoxin/ flecainide, endocrine e.g. hyperkalaemia, Addisons, hyper magnesia
1st degree - prolonged PR >0.2s or 3-5 small squares 2nd degree - Mobitz type 1 - prolonging PR until QRS dropped - Mobitz type 2 - QRS dropped every 2/3 P waves, constant PR 3rd degree - no relation between P wave and QRS Present with fatigue, dyspnoea, syncope, chest pain/ nausea/ palpitations - Type 2/3 can present with stokes Adams attacks causing syncope - last seconds Mx Look for + treat reversible causes Type 1 - If young, no sx - no need to treat - Avoid disopyramide, flecainide, propafenone, beta-blockers, calcium-channel blockers, digoxin and magnesium - Annual ECG Type 2 - Ix with 24hr ECG, echo, cardiac catheterisation - Avoid above drugs - If low HR - 1st atropine or 2nd pacing - Permanent pacemaker for mobitz type 2 Type 3 - If low HR/ haemo unstable - 1st atropine, noradrenaline, dopamine, if refractory - transcutaneous pacing may be needed - Avoid above drugs - Permanent dual chamber pacemaker
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When need a pacemaker + when is a biventricular pacemaker used Use temporary if only expect arrhythmia to be temporary or as temporary treatment until permanent pacemaker is put in place
Complete or mobitz type 2 heart block Symptomatic bradycardia - non respondent to atropine Sick sinus syndrome HF (cardiac resynchronisation therapy) - use biventricular (RA, RV, LV) - can also add defib (CRT-D) if NYHA class III or IV Drug resistant SVT/ arrhythmias Post MI
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HEADSS - suicide/ general teenage assessment - what stand for
``` Home and environment Education Activities Drugs and alcohol Sexuality Suicide ```
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Paracetamol overdose - what to ask in hx, specific Ix and Mx Presents with N+V followed by signs of hepatic necrosis after 24 hours - encephalopathy, RUQ pain, change in consciousness, hypoglycaemia, haemorrhage, jaundice.
Hx - Why taken - Accidental, deliberate or therapeutic - How much, other drugs/ alcohol - When - Staggered or all at once - Risk will happen again? - Suicide hx if deliberate - What happened, sx ``` Ix: Take plasma paracetamol lvl 4 hours post ingestion or immediately if ingestion unknown/ staggered U+E, LFT as baseline Regular BM for hypoglycaemia Clotting screen, INR ABG for Acidosis ``` Mx: AtoE Charcoal 1g/kg if within 1 hour of ingestion If lvl above treatment line, no vomiting, occurred <24hrs before start IV N-acetylcysteine If unclear about when taken/ staggered start immediately Also start immediately if 8-24 hours ago and taken >150mg/kg - not want to delay tx Regime - Bag 1 over 1 hour: 150mg/kg in 200ml 5% glucose - Bag 2 over 4 hours: 50mg/kg in 500ml 5% glucose - Bag 3 over 16 hour: 100mg/kg in 1000ml 5% glucose Stop when level <10, bloods normalise If pH <7.3, Lactate, creatinine or INR high, high grade encephalopathy consider transplant
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Epilepsy causes, ix and management = >2 unprovoked seizures occurring more than 24 hours apart within a year of each other Can be triggered by alcohol, sleep deprivation, drugs, flashing lights, infections, medication Frontal lobe seizures - motor sx, jacksonium march Temporal lobe seizures - deja vu, motor sx, hallucinations, vertigo Tonic clonic - stiff then rhythmic jerking Myoclonic - Brief, 'shock-like' involuntary single OR multiple jerks Atonic - loss of all tone causing a fall Absence - loss of awareness and a vacant expression for 10s before returning abruptly and continuing as though nothing has happened
Causes: - Idiopathic - Trauma - Mass effect lesions - surgery - vascular e.g. stroke - Genetics - Infection - electrolytes - glucose Ask about before, during and after ``` Ix: CV, neuro, MSE - identify injuries Routine obs FBC, U+E, LFT, CRP, BM (hypoglycaemia), urea, Ca (bone profile), thiamine (alcohol withdrawal) AED levels Raised prolactin and CK ECG - long QTc can precipitate epilepsy MRI - look for structural cause EEG ``` Mx: Advise on water safety (shower not bath, buddy system), not swim alone, no machinery, leave bathroom door unlocked, fire safety and cooking, environment and work safety. Care with heights, high risk activities and consider contraception for certain meds. Advise family and carers, record seizure - support head, remove dangerous objects. Once stop seizing check airway and put in recovery position. 1st seizure - 6months for car 5 years for HGV After diagnosis of epilepsy (second seizure) - 1 year for car, 10 years for HGV Start after diagnosis (2nd seizure) Focal - carbamazepine, lamotrigine Tonic-clonic seizures: sodium valproate or lamotrigine. Absence seizures: ethosuximide or sodium valproate Tonic, atonic and myoclonic seizures: sodium valproate or topiramate vagal n stimulation can also help Status epilepticus = seizure >30 mins or recurrent without regaining consciousness (treat at >5mins) AtoE - O2 sats, ABG, bloods, cultures, AED levels, BMs - secure airway and high flow O2 - IV access, start fluids to help lower lactate - D: Check GCS, pupils, BM temp - E: check for injuries, rash, infection, liver signs of alcohol abuse Cont existing AED Lorazepam 4 mg IV, if unavailable; Diazepam 10 mg PR, if unavailable; Midazolam 10 mg buccal If after 10 mins (5 mins later) no improvement give 2nd dose, if not work give phenytoin 15mg/kg loading dose then 50mg/min (give in ITU as need ECG monitoring) If phenytoin not work transfer to ITU for GA Last choice - RSI, propofol, midazolam Repeat AtoE once seizure stopped Afterwards - CT head, EEG, LP, Neuro review, MRI, Discharge after 48hrs
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Facial nerve palsy - CBD
UMN - forehead sparing LMN - non forehead sparing Assess facial movements against resistance, ask about changes in taste (ant 2/3) and intolerance to load noises Can grade degree of paralysis by House-Brackmann LMN causes - Idiopathic bells palsy, parotid tumour, base of skull fracture, cholesteatoma, acoustic neuroma, herpes (Ramsey hunt), GB UMN causes - brainstem stroke, MS, tumour, HIV, syphilis Refer if suspected cause or red flag features (cancer, UMN, ENT sx etc) Mx: Eye care - Refer to ophthalmology: lubricating eye drops, patches, taping, eye weights, botulinum, surgery Give steroids if present within 72 hours, cont for 10 days. Most resolve spontaneously. If refractory consider facial nerve decompression surgery or reanimation surger
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Hyperaldosteronism - how presents and what investigation is first line
Presents with hypertension and hypokalaemia | - First line investigation is aldosterone/renin ratio
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Palliative prescribing, presentation in dying
Secretions, Agitation, Pain, N/V, Constipation, Abdo cramps, SOB, Drowsiness Meds: Give subcut - Haloperidol, midazolam for agitation/ confusion - Levomepromazine, metoclopramide - Hyoscine butylbromide - cramps and secretions - Morphine
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TB
Ix: CXR - apical opacification, effusion, millet seed Early morning sputum sample for AFB, culture NAAT Antibiotic sensitivity HIV test ``` Tx Notify infection control body, place in ventilated side room Isoniazid (pyridoxine) Ethambutol Rifampicin Pyrazinamide ``` All for 2m then I+R for 4m (10m if CNS) Contact trace, screen others with Mantoux and IGRA
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Ear discharge CBD
Otitis media Sx: Earache, fullness, hearing loss, fever Ix: Otoscopy to look for bulging, redness of TM, fluid level or perforation, impedance audiometry to measure pressure in middle ear, do nasal endoscopy to check the openings of eustachian tubes, audiometry if hearing loss Mx: Analgesics, warm compress, most self limiting. If severe, <2yo, bilateral: oral amoxicillin Consequences include mastoiditis, facial nerve palsy, meningitis, cerebral abscess. If mastoiditis - IV abx, consider CT (if consider surgery or abscess, have headache, lethargy etc) and mastoid air cell clearance. Otitis media with effusion - due to closure of Eustachian tube. Get negative pressure in middle ear, draws fluid in from middle ear. hearing loss, poor speech development, ear popping, imbalance If effusion - fullness, hearing loss persists after infection treated. Observe for 6-12 weeks for spont resolution, if ongoing, limiting development, bilateral consider grommets, adenoidectomy If perforation persists (Chronic otitis media) - antibiotics and surgery to fix eardrum Otitis externa Sx: Ear pain, itch, discharge often post water based activity. If unrelenting pain that interferes with sleep, hearing loss, FN involvement, fever think necrotising otitis externa (do CT, CRP, ESR) Ix: otoscopy - red swollen external auditory canal, ear swab if recurrent, if necrotising do CT/ MRI Mx: Clean ear, analgesic, often self limiting - if severe: ear wick, topical antibiotic (aminoglycoside e.g. gent or ciprofloxacin) +/- hydrocortisone drops, keep ears dry. Acetic acid for prevention. For necrotising, same day referral to ENT, 6w oral ciprofloxacin Cholesteatoma Sx: Non resolving unilateral offensive discharge thats unresponsive to antibiotics Ix: Retraction of pars flaccida on otoscopy, if facial nerve involvement or planned surgery do an MRI Tx: Surgical removal often required - canal wall up mastoidectomy Also want to rule out CSF if base of skull fracture - test for glucose and beta 2 - transferrin
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Osteoarthritis management
Ix Assess level of pain and limitations of activity - on exam see stiffness and limitation of ROM Assess psychological impact Do examination of joint and one above/below Calculate BMI Bloods: FBC (WCC), U+E (before starting on NSAID), LFT as baseline, CRP/ESR (identify inflammation) Do Xray of the joint - Loss of joint space - Osteophytes - Subchondral sclerosis - Subchondral cysts Consider joint aspiration to rule out gout, septic arthritis Hand signs: - Sparing of the metacarpophalangeal joints - Bony enlargement of the proximal interphalangeal joints known as Bouchard’s nodes - Bony enlargement of the distal interphalangeal joints known as Heberden’s nodes - Squaring of base of thumb - Reduced functional movement (e.g. reduced grip strength) Diagnostic criteria - >45yo - activity related joint pain - no morning stiffness or stiffness lasting <30 mins Mx Educate, weight loss, exercise, physio, hot/cold compress, stop smoking, foot wear, psych, TENS WHO pain ladder - topical NSAID - Topical NSAID + paracetamol - NSAID, paracetamol and topical capsaicin - Above + opioid Joint replacement or arthrodesis (fusion)
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Rheumatoid arthritis management
Sx - weight loss, night sweats, fever, malaise, low appetite, weakness, joint swelling/ red/ hot/ painful, joint stiffness worse in morning, better with exercise, lasts >30mins - 1hr. Affects >5 joints, is symmetrical - affect metacarpo-phalangeal joints Refer if: Small joints of hands/feet are affected >1 joint affected Been delay of more than 3 months between symptom onset and seeking advice look for rheumatoid nodules on skin, ask about previous eye conditions e.g. anterior uveitis Can cause baker cysts increased risk of atherosclerosis Can also cause pleural effusion, lung fibrosis Ix Examination and history - systems review FBC, U+E, LFT, CRP/ESR, RF, Anti-CCP, ANA Xray - bony erosions, joint space narrowing, soft tissue swelling, juxta-articular osteoporosis US - look for effusion and thickening/blood flow in synovial membrane Joint aspiration if suspect septic Assess disease activity with DAS28 Hand signs - boutonnieres - Swann necking - Z thumb - ulnar deviation Mx Educate, lifestyle, psych Assess psych wellbeing NSAID for pain relief Corticosteroid if flare - up to 3x a year 1st Line: cDMARD e.g. methotrexate, if palindromic hydroxychloroquine. Bridge with glucocorticoid. 2nd Line: bDMARD (if 2x above ineffective) e.g. TNF inhibit adalimumab, Anti CD20 rituximab 3rd line: surgery Drug SE Steroids - Infection, osteoporosis, DM, cushings Methotrexate – liver toxicity, pneumonitis, oral ulcers
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Gout Common causes are hereditary, alcohol, renal impairment, NSAID, Diuretic (thiazide), purine rich foods, Fever, collapse, Recent infections, trauma, rashes, weight loss
History of acute attack of pain, swelling, redness and warmth. Commonly 1st metatarsophalangeal joint May have tophi on extensor surfaces of limbs, ears and achilles tendon Ix: Hx - ask about prev attacks, diet, alcohol Often clinical diagnosis Do joint aspiration to confirm (urate crystals) Do uric acid lvl 4-6w post attack Xray to exclude other causes Screen for CV and renal disease Mx: Discuss lifestyle changes - loose weight, reduce purine in diet (red meat, seafood), reduce alcohol consumption Rest, ice, elevate 1st line: NSAID (naproxen + PPI) or colchicine 2nd line: oral or corticosteroid injections Prevention - once acute attack resolved - Weight loss, reduce alcohol, reduce purine in diet - allopurinol - titrate dose to reduce uric acid <300. Give colchicine alongside for first 6 months. Can cause rash/fever, if renal impairment monitor U+E - 2nd line febuxostat
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BPH - present with LUTS Storage - frequency - nocturia - incontinence - urgency Voiding - Poor flow - Hesitancy - Dribbling - incomplete emptying ``` Hx ask about these things + - fever - Pain/ backache - Weight loss - problems passing stool - Any burning when go to the toilet - Any pain - ```
Ix: IPSS - int. prostate symptom score DRE Dipstick - Diabetes, UTI Blood tests including PSA, U&E, FBC Urodynamics - flow rate <10mls = obstruction (or neuro/DM) Bladder, kidney US to look for chronic retention (recurrent UTI, CKD, hydronephrosis, stones, overflow incontinence) May do MRI, CT KUB, flexible cystoscopy in secondary care Mx: If mild - reassure and reduce alcohol/caffeine, incontinence pads, bladder training, follow up If moderate - Alpha blockers (tamsulosin - relax neck of bladder and prostate - dizziness and issues with ejaculation), 5-alpha reductase inhibs (finasteride - reduce size of prostate), catheters If severe (recurrent UTI, haematuria, acute retention) - surgery -Transurethral resection of prostate Complications Acute urinary retention - catheterise Bladder diverticular Chronic urinary retention and hydronephrosis
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Domestic abuse Signs include - withdrawn - downplaying symptoms - large bruises in shape of hand/ fist - repeated attendance - delayed attendance - multiple bruises of different ages Safeguarding, social services
Ask about home life, ask directly if there has been any physical abuse or threats, ask if they are scared of their partner Reassure about patient privacy, safety and confidentiality Ask about - physical - ever hurt you - sexual - ever made you do sexual things you don't want to do - emotional - try to belittle or control you Who is it - do they drink/take drugs, psych health conditions? convictions? How often happen, how long been going on for, is it getting worse How have you been coping, have you tried anything to get away, tried to get help before Anyone else in the house Who live with Any weapons in the house Do they have a safety plan Do they work Assess risk - currently in danger? what happen if went home? - thoughts of hurting self or others? Offer advice and support acknowledge was difficult to disclose and next part is probably hardest step, prepared to support the person to take it in their own time Say not their fault ``` Family/ friends for support? counselling, support, helplines - give leaflet Refuge if cant go home Refer to - police - local domestic abuse services - counselling/ support - social services if child involved ```
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BCC, SCC
Refer on 2ww for SCC Routine referral for BCC Ix: Biopsy, dematoscopy, CT if suspect spread, FNA of local nodes RF - UV exposure, fair skin, weakened immune system, personal or family history SCC looks wet, sloughy, ulcer, from keratinocytes. Comes on more quickly, tender, more common on back of hand, may be nearby actinic keratitis BCC from hair follicles - pearly, nodular, depression in middle, telengectasia, non tender Superficial BCC - patch/plaque, pale ping, Clear rolled edge High risk Diameter >2 cm Location on the ear, vermilion of the lip, central face, hands, feet, genitalia Elderly or immune suppressed patient Histological thickness greater than 2 mm, poorly differentiated histology, or with the invasion of the subcutaneous tissue, nerves and blood vessels Tx: Excision with 4mm margins If complex, deep or unclear boarders do MOHs Radiotherapy alternative if not want surgery (increased scarring), For superficial BCC or actinic keratitis or Bowens disease - cryotherapy, photo-dynamic therapy , curettage, 5-FU, immiquimod Actinic Keratosis - Diclofenac
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Types of dementia - key features How to investigate, treatment of AD
AD: early impairment of memory. Manifests as short-term memory loss and difficulty learning new information. VD: typically a ‘stepwise’ decline in function. Predominant gait, attention and personality changes. May have focal neurological signs (e.g. previous stroke) DLB: parkinsonism (tremor, rigidity, bradykinesia, postural instability). Fall, syncope and hallucinations predominant feature FTD: marked personality change and behavioural disturbances. Memory and perception relatively preserved. What to ask in hx - when start - gradual or step wise - any triggers - associated depression, psych sx, behavioural change, sleeping pattern, cognitive changes, parkinsons like features, sensory changes, fluctuating awareness - head injury, psych hx, vascular disease, diabetes, parkinsons - focal neuro, vision etc (vascular) - medication - fhx - shx - who live with, who looks after, work, can they perform AODL, work/drive, smoking/ alcohol/ drugs - assess risk to self - ever done anything that put themselves at risk - ICE ``` Investigate with cognitive tests - Abbreviated mental test score - Mini mental state exam Refer to memory clinic then: - MOCA (26/30) - Addenbrookes ``` DSM-V Diagnosis - functional impairment, affect >2 cognitive domains, no other cause (depression, delirium) Do Brain MRI Mx: Advanced planning, capacity, care plan, end of life care Supportive care Physical and mental health Inform DVLA Exercise, group cognitive stimulation programmes Mild to moderate - acetylcholinesterase inhibitors e.g. rivastigmine or donepezil Moderate to severe - NMDA antagonist e.g. memantine
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Vertigo CBD
Ask: how long for? Tinnitus, hearing loss, what makes better, what makes worse, headaches, visual changes? If seconds to minutes, comes on when turning head, no tinnitus or hearing loss: BPPV - diagnose with dicks hall pike manoeuvre (rotary nystagmus) - treat with epley manoeuvre - educate, advise against sudden head movements and sit/lie down in stages - no driving until condition under control If >20 mins to hours, fullness in ear, sensorineural hearing loss, tinnitus, N+V = Menieres - do audiology to confirm sensorineural deafness - inform DVLA - not drive until under control - limit salt, alcohol, caffeine, chocolate, smoking as can trigger - avoid dangerous activities like driving - prochlorperazine for vertigo and nausea - beta-histone as prophylaxis, diuretics in 2dry care - hearing aid for hearing loss If spont vertigo lasting days = acute labyrinthitis (hearing loss) or vestibular neuritis (no hearing loss). Often post viral infection. - resolves on own in few weeks - start moving as soon as possible - not drive when dizzy - if severe consider antihistamine/ antiemetic e.g. prochlorperazine - give antiemetics, hydration, vestibular rehab If central (also sx of dysphagia, dysarthria, diplopia, dysmetria) - brainstem lesion or acoustic neuroma
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Atypical antipsychotic counselling
Schizophrenia is caused by problems with dopamine receptors in the brain Onlanzapine works by blocking receptors in the brain that are involved in transmitting these messages between cells Comes in a daily tablet form or in a depot injection every 2-4w - depot often used if issues with compliance Start at a low dose and built up over a week or two depending on individual response Once started is likely will return on the medication long term unless it isn't helping in which case switch to another drug Will need to measure LFTs, lipids, weight, HbA1c levels prior to starting. Lipids, weight, HbA1c, prolactin, U&E, LFT, FBC, ECG will be monitored regularly throughout treatment Important to inform doctor if want to become pregnant Some side effects include - weight gain - high prolactin causing - low libido, menstrual issues, gynaecomastia, sexual dysfunction - sedation - HTN - Glucose intolerance - Anticholinergic se e.g. dry mouth, constipation, dry eyes, urinary retention - orthostatic hypertension - less risk of extrapyramidal SE Is a risk of neuroleptic malignant syndrome in overdose so if think have taken too many tablets or develop fever, muscle rigidity, tremor, altered mental status visit GP/ A&E Is also a risk of agranulocytosis and increased rate of infections Can have withdrawal symptoms so let dr know if want to stop
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Schizophrenia explanation/ counselling
ICE, ask patient what already know Info - schizophrenia is a long term condition that affects peoples ability to distinguish between abnormal thoughts and reality. This can mean experiencing hallucinations, paranoia, loss of interest in doing things. Does this resonate with you? Cause - the cause of schizophrenia isn't clear, each person is different. However it commonly affects young people like yourself. Some things can trigger or worsen schizophrenia, these include significant stress or drugs. Does this apply to you? Effect on life - Schizophrenia will always be there however with medication most people can make a recovery. There may be times when the symptoms come back and this is called a relapse. Having schizophrenia puts you at increased risk of other mental health disorders like depression and suicide. If you feel like this or your symptoms are getting worse and you think you might be having a relapse please tell someone. We hope however that with continued treatment this won't happen. Do you understand all this? Treatment - long term medication that you will need to continue even if your symptoms stop. Are things you can do and things I can do however: You - healthy lifestyle, exercise, avoid drugs and alcohol as they can make your condition worse. Is important you attend your appointments Us: Antipsychotics, manage in combination with GP, can also use talking therapies . Put in touch with other services for employment, finances etc. Summarise
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Lithium counselling - check photo on phone
ICE Do you have any questions about your condition or what's happened so far Alters signals in the brain to help stabilise your mood Comes in tablet and liquid form. If taking the tablet form is important to swallow with lots of water Take the tablet once a day - usually recommend to take in the evening so that monitoring is easier - need to assess levels 12 hours after taking dose - not strict - but must take at same time every day Can take 1-2w to work - if miss a dose and <6hrs since normal time then take, if after this skip dose and return to normal the next day - do not double dose Important not to stop suddenly and not to change dose without speaking to DR first Will receive a lithium monitoring book - this can be used to keep track of blood tests, appointments and can be used in emergencies Can take several weeks to months for lithium to start working - will need to take a blood sample every week to get appropriate level - once stable this can then go to monthly and then 3 monthly Will also need to monitor some blood levels including thyroid function tests, urea and electrolytes and calcium Lithium can have some side effects including - increased thirst, nausea, increased urination, diarrhoea, tiredness, weight gain, tremor, metallic taste - usually resolve with time It is also important you are aware of symptoms of lithium toxicity - these can be life threatening so need to seek urgent medical help - confusion - drowsiness - vision changes - difficulty speaking - seizures - vomiting, tremor Can affect kidneys leading to renal toxicity, neophrogenic diabetes insipidus, hypothyroidism, hyperparathyroidism, hypercalcaemia Should not take NSAIDs as increase lithium level Are risks of birth defects associated with pregnancy when taking lithium so important on a reliable form of contraception, speak to psychiatrist if want to start a family
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Peripheral venous exam Varicose veins present with itching, discomfort and heaviness of the legs, night cramps, oedema, burning sensations, paraesthesiae, exercise intolerance, or restless legs - may have a dull ache worse when standing Tx - weight loss, exercise, avoid prolonged standing, keep legs elevated when possible - consider compression stockings if intervention not appropriate - do ABPI first - Endothermal ablation - Sclerotherapy - Excision
General inspect - body habitus, oedema, scars, ulcers, medical equipment, mobility aids Inspection of legs - scars, venous eczema (red, blotchy), haemosiderin (brown/red), atrophy blanche (white, lack of pigment), lipodermatosclerosis - Look for venous ulcers over medial malleolus - saphena varies - dilation of saphenous vein at its junction with femoral vein in the groin - put hand over and ask to cough assess for arterial disease - temp - pulse - femoral, popliteal, ant tibial, dorsalis pedis - pallor - cyanosis - cap refil - hair loss, ulcers Great saphenous - medial leg Lesser saphenous - lateral to posterior leg Assess varicosities - temp - increased temp = phlebitis - palpate - tender = phlebitis, hard and tender = thrombophlebitis Assess for pitting oedema - go up leg to find level stops (HF) tap test - finger on SFJ (4cm inferolateral to pubic tubercle), tap varicose vein and feel for thrill - if felt shows valve insufficiency Listen with Steph for bruit Venous duplex scan Tourniquet test - lie flat, life leg, milk veins, place tourniquet at level of SFJ then get to stand up, look for filling of veins. Go lower by 3cm each time, when filling stops are at level of incompetent valve perthe's test - apply tourniquet to mid thigh whilst standing, get patient to walk around for 5 mins. If veins less distended is no deep venous issues, if veins more distended or same is superficial and deep venous issues Do doppler, duplux US, ABPR, arterial vascular exam, abdo exam
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Discharge planning - what to include
Patient details - name, DOB, hosp number, address, GP details - Hospital stay - ward, consultant name, admission and discharge date, discharge destination - Date written and personal signature Clinical details - Admission details - PC - hx and exam - Investigations - results and any awaited tests/ results - Diagnosis and Comorbs - Management - how managed/ treated, any complications Plan - Plan for post discharge - Follow up - Actions for GP Medication - Changes to regular medication - Medication to continue post discharge - drug, dose, form, frequency, length (qqt) - PRN meds - write meds in handwriting, include pt name and address, dose written as 5 (five) mg, total amount as 10 (ten)
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BCC/SCC management
Refer on 2ww for SCC Routine referral for BCC Ix: Biopsy, dematoscopy, CT if suspect spread, FNA of local nodes RF - UV exposure, fair skin, weakened immune system, personal or family history SCC looks wet, sloughy, ulcer, from keratinocytes. Comes on more quickly, tender, more common on back of hand, may be nearby actinic keratitis BCC from hair follicles - pearly, nodular, depression in middle, telengectasia, non tender Superficial BCC - patch/plaque, pale ping, Clear rolled edge High risk Diameter >2 cm Location on the ear, vermilion of the lip, central face, hands, feet, genitalia Elderly or immune suppressed patient Histological thickness greater than 2 mm, poorly differentiated histology, or with the invasion of the subcutaneous tissue, nerves and blood vessels Tx: Excision with 4mm margins If complex, deep or unclear boarders do MOHs Radiotherapy alternative if not want surgery (increased scarring), For superficial BCC or actinic keratitis or Bowens disease - cryotherapy, photo-dynamic therapy , curettage/ cautery, 5-FU, immiquimod Actinic Keratosis - Diclofenac
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Melanoma Mx
Ix: Do a dermatological exam - ABCDE, determine classification (superficial, nodular) Use Glasgow 7 point checklist = ABCDE + looking for inflammation, itch, oozing Dematoscopy Biopsy - excisional with 2mm margins Breslow (depth in mm), Clarkes (layer of skin descends to, not part of staging), ulceration, mitotic index give indicator of prognosis Do CT if suspect metastatic spread, assess for BRAF mutation ``` Mx: Wide local excision with margin based on breslow thickness insitu - 5mm <1mm - 10mm 1-2 - 10-20 2-4 - 20-30 >4 - 30mm +/- lymphadenectomy/ sentinel LN biopsy Can also do electrochemotherapy ``` If metastatic - BRAF inhib, immunotherapy e.g. ipilimumab, chemo, interferon alpha
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Warfarin counselling
Warfarin is a blood thinner that helps stop clots from blocking blood vessels within the body. It does this by blocking the function of vitamin K It can be taken to treat people who have had a previous blood clot or those at high risk due to AF or prosthetic heart valve The action of warfarin can be rapidly reversed with an antidote of activated vit k called phytomenadione It is taken once a day in the tablet form - at same time each day to keep level steady - different colour tablets indicate the dose If you miss a dose for any reason take as soon as you remember, if the next day then just take a single tablet, do not double dose Takes 2-3 days to begin working, on these days re given a higher loading dose INR is a measure of how long it takes the blood to clot in health people it is 1 - as we want to reduce your risk of clots we aim for 2-3 - to get your medication dose to the right level we need to monitor your INR every 3-4days at first until we reach the correct dose with 2 consecutive readings in range, then every 1-2 weeks until same then can measure 3 monthly - will record results in a yellow book 2. 5 +/- 0.5 for PE/DVT 3. 5 +/- 0.5 for recurrent PE/DVT and already on anticoag or if prosthetic heart valve take 3m for DVT take 6m for PE Lifelong AF Wear warfarin alert bracelet It is common for you to bleed a little more than normal e.g. heavier periods, gum bleeding when brush teeth, nose bleeds, easy bruising, prolonged bleeding if cut self However if experience blood in urine/ stool/ vomit, large bruises without cause, nose bleeds lasting >10 mins, sever headaches or fits, changes to eye sight or ams. legs need to seek medical help Some side effects include - mild rash, hair loss, nausea, diarrhoea Can interact with medications including over the counter like St johns wart - read information leaflet and inform pharmacist when purchasing medication, same when starting medication at the drs Avoid foods high in Vit K including liver, spinach, cranberry. Avoid alcohol binges. Avoid contact sports. Carry alert card, take yellow book to any appointments Contraindicated in pregnancy - need to be on a reliable contraceptive
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ECG interpretation
Name and DOB Date and time Look at rate - number x6 or 300/ large squares Look at rhythm - irregularly irregular/regularly irregular Look at axis - highest in II = norm, III right, I left Look at p wave - present, absent, followed by QRS, shape, duration Look at PR interval (3-5 small squares or 0.2s - longer = heart block) Look at QRS (<3 squares), look for wide (BBB, abnormal depolarisation), Q wave (>20% height of R wave), hypertrophy, RSR in V1 = RBBB, RSR in V6 = LBBB Look for ST elevation (>1mm in >2 contiguous limb Leeds or >2mm in >2 chest leads) Look for T wave tenting (>5mm in limb leads, >10mm in chest), inversion (ischaemia, PE, LVH, HOCM), biphasic in hypokalaemia Look for U wave
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ABG
WIPE Check contraindications - infection, peripheral vascular disease, AV fistula (relative = impaired coag) Allergies - Chlorhexadine Allens test - get to clench fist, occlude both arteries, check blanched, release ulnar a colour should return within 5-15s Palpate and clean for 30s insert at 45 degrees until flashback remove, remove needle and dispose, expel air and invert add cap and patient label Apply pressure over site for 3-5mins
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Prescribing
Identify the therapeutic indication Identify the patient’s perspective of medication use Document the name, date of birth and address of the patient, hosp number Document the name of the medication Document the appropriate dose of the medication (how many mg etc per dose) Document the strength and formulation of the medication Document the quantity of the medication - total amount of tablets for entire course Sign the prescription and include your GMC number Document your address and contact details Document the date of the prescription Advise the patient how to use the medication Explain how the medication with be monitored if relevant
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BM
WIPE - explain: Today I need to measure your blood glucose level, which involves taking a very small blood sample from your fingertip. You will experience a sharp scratch when I take the sample, but this should be very brief Ask if any pain, allergy, consent ``` Clean if dirty Turn on machine Check strips are in date Place in machine take cap off lancet, draw blood and place strip to blood Apply gauze and tape ```
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Cannulation
Indications - drug therapy - fluids - blood products - emergency drugs Is a risk of infection if not wear gloves, not wash hands, touch key parts WIPE - allergies - indication Clean tray and gather equipment - cannula, flush, syringe, blunt needle, octopus, tourniquet, bandaging, gauze Do not cannulate if prev cannulation site, bruising, haematoma or infection Clean for 30s Insert cannula Clean port on octopus before and after flushing Assess 8hrly and VIP score calculated - pain, erythema, swelling, induration, palpable venous cord, pyrexia Tell patient to speak to member of the team if becomes painful or start bleeding/ discharging
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Inhaler technique
Explain what been started on and why Show inhaler and its components Explain why that type of inhaler is used and when (rinse mouth out if steroid) Happy with everything I have said so far, any questions? Before use if not used in last 5 days take lid off shake and do one test spray Look at dose counter and ensure not empty Check expiry date Hold upright, check nothing in mouthpiece, shake sit up straight put chin up, breath out till lungs empty, form a tight seal. Breath in slow and steady while push canister, continue to breath in till lungs full. Remove inhaler from mouth and hold breath for 10s, breath out If second puff do after 30 seconds, put back on cap after Assess their technique Spacer - increase drug to lungs and reduce SE Prep, attach, breath out away from inhaler, form seal, puff once then breath in and out 2-3 times Wash with detergent once a month, air dry. Do not wipe as causes static If in asthma attack not improve after 10 puffs then call 999 leaflet, follow up
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Blood cultures
Gel hands, confirm patient ID, ensure indication, gain consent and check allergies. Clean equipment tray as per guidelines Collect equipment Ensure packaging intact and within expiry date Prepare bottles: Mark 10mls above fluid line, remove caps off bottles, disinfect tops with a sepa-rate 2% CHG in 70% IPA wipe for a minimum of 30 secs, allow to air dry. Re-apply tourniquet and palpate and select appropriate vein Loosen tourniquet Decontaminate site with 2% CHG in 70% IPA cleansing for 30 seconds, allow to air dry Do not re-palpate site ``` Puncture vein with winged collection system Take cultures prior to other samples. Aerobic First Fill each bottle with 10mls Keep bottles vertical ``` Release tourniquet On removal of needle apply pressure. Dispose of sharps immediately into sharps bin, apply gauze, remove gloves and apron Gel hands Label appropriately and according to trust/local policy Dispose and clean equipment as policy Wash hands Document procedure, indication and treatment plan in patient’s notes
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Suicidal hx
If no immediate risk of harm to patient - refer to community mental health team If immediate risk of harm refer to crisis
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Bisphosphonate
Introduce Ask if know why starting Brief Hx - Prev fractures - Menopause - Reflux, any other meds - Alcohol, smoking Explain osteoporosis = bone thinning and function of bisphosphonates Taken 1xweekly on same day each week Take 2 hours before food in morning, plenty of water, sit upright for 30 mins after Can take 6m to have affect Work in background - important to continue Can cause heartburn, nausea, GI upset and some muscle pain - tends to resolve. More serious SE include gastric ulcers - blood in vomit or stool, osteonecrosis of jaw - pain on chewing and facial swelling - problems swallowing Important not to take alongside NSAIDS e.g. ibuprofen Important to remain active, eat leave green veg, nuts, fish, stop alcohol and smoking May give calcium supplements alongside Conclude
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GP tired station
In hx ask to identify any causes - low mood/ depression - hypothyroid - anaemia - CO - sleep Council on exercise, diet, wellbeing/ lifestyle Consider testing for organic causes above Review in 4w
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CKD
``` 1 - >90 2 - 60-89 3a - 45-59 3b - 30-44 4 - 15-29 5 <15 ``` Counselling - CKD is a lifelong condition where the kidneys don't work as well as they should - it is commonly associated in getting older. Sometimes there is a clear cause like high blood pressure, diabetes, infections, or autoimmune conditions but in others there isn't one. - People with CKD can experience symptoms such as tiredness, shortness of breath, swelling of their feet and ankles, blood in their urine, nausea, have you experienced any of these - We diagnose CKD via blood tests like the ones you had, - CKD can get worse over time to the point where the kidneys stop working (kidney failure), this is uncommon (1in50 cases) and many people live healthy long lives. Its important to be aware however that having CKD increases your risk of strokes, heart attacks - It is treated by a combination of lifestyle changes and some medication including drugs to lower your blood pressure and cholesterol levels. In later stages some people need treatment with dialysis or transplants. - Lifestyle changes include: stop smoking, healthy balanced diet, restrict salt intake to <6g/day, do regular exercise 150min a week, reduce alcohol to <14, loose weight, avoid NSAIDS. - Medication include: ACEi to keep BP < 140/90, statins, water tablets for swelling, erythropoietin for anaemia - We will review you after starting the medication and then follow up long term with 6-12 monthly appointments - Can have pneumococcal vaccine and yearly influenza vaccines - Support is available in the form of CKD groups, counselling services and leaflets ACEi: U+E and BP check in 2 w Statin: LFT check at 12w, 12m
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HTN Aim for a 40% drop in non-HDL cholesterol over 3 months
>140/90 in clinic do ABPM or home BP measurement >180/120 - consider immediate treatment for malignant hypertension Based on ABPM - <135/85 - no need to treat - >135/85 = stage 1 - start if >80, <60 or between two with end organ damage, raised Qrisk >10%, diabetes - >150/95 = stage 2 - start treatment - >180/120 = stage 3 - start treatment End organ dmg - Eyes, heart, kidneys - LVH on ECG - S wave in V1 + R wave in V5/6 >35mm - Fundoscopy - arteriolar narrowing, retinal haemorrhages, papilloedema - Raised ACR, abnormal U&E, protein/albuminuria Discuss what is hypertension Risks - Renal damage, stroke, CVD <55 or diabetes - acei >55 or black - CCB e.g. amlodipine If still high - ACEi + CCB/ thiazide like or CCB + Acei/ thiazide like If still - All 3 If still - confirm resistant hypertension, check for postural, discuss adherence - low-dose spironolactone4 if blood potassium level is ≤4.5 mmol/l - alpha-blocker or beta-blocker if blood potassium level is >4.5 mmol/l In <80 - BP <140/90 In >80 - BP <150/90
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Back pain management ``` Fit note - patient can self certify for 7 days Write - Cause of symptoms - Date of assessment - Timeframe ``` ``` Can decide if not fit for work or if fit with: Phased return to work Altered hours Amended duties Workplace adaptations ```
Self help is very important – PIL or video back exercises, avoid bed rest Explain that movement helps improve the back, and pain doesn’t equal harm Best to pace – frequent short bouts rather than overdoing things Going to need pain relief and possible diazepam initially if spasms (although NICE doesn’t recommend this CKS does) or Acute analgesia; Paracetamol PLUS ibuprofen, codeine, diazepam 2mg tds Add amitriptyline or duloxetine only if neuropathic pain (sciatica) Applying heat pads may help No evidence for paracetamol alone, or opioids, or SSRIs, or gabapentin Acupuncture may help some people (but evidence is poor and may not be available) is not recommended (although some patients may find it he
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Clozapine
Liquid or tablet SE: sedation, weight gain, hypersalivation, tachycardia, constipation Serious SE: reduce seizure threshold, cause neutropenia and increase risk of infections, cardiomyopathy Monitoring - BM, ECG, BP - FBC, U&Es, LFTs, prolactin, HbA1c and lipids. For clozapine, a baseline troponin is also requested. First 18w - test FBC weekly then every 2w until 1year then monthly Not smoke! or change smoking habit
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Look at rheumatoid
On NHS