PASS MED Flashcards

1
Q

A 27-year-old female presents with weakness of both hands. On examination you note wasting and weakness of the small muscles of the hands and loss of pain and temperature sensation over the trunk and arms. Vibration sense is intact.

What is the most likely diagnosis?

A

Syringomyelia - yringomyelia is a condition whereby fluid filled cavities develop within the spinal cord. Pressure can increase resulting in compression of the spinal cord tracts. The syrinx can extend to and damage the anterior horn cells, thereby resulting in lower motor neurone features. The spinothalamic tract axons decussate to the other side of the spinal cord via the anterior white commissure, and they are particularly susceptible to damage from the syrinx. Pain and temperature sensation are lost due to spinothalamic tract damage, and one side may be affected more than the other. Classically, the sensation loss is experienced in a shawl-like distribution over the arms, shoulders and upper body. Light touch, vibration and proprioception may also be affected as the syrinx enlarges into the dorsal columns.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Complications of aneurysmal SAH:

A

Re-bleeding
happens in around 10% of cases and most common in the first 12 hours
if rebleeding is suspected (e.g. sudden worsening of neurological symptoms) then a repeat CT should be arranged
associated with a high mortality (up to 70%)
Vasospasm (also termed delayed cerebral ischaemia), typically 7-14 days after onset
Hyponatraemia (most typically due to syndrome inappropriate anti-diuretic hormone (SIADH))
Seizures
Hydrocephalus
Death

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

window for thrombolysis stroke

A

A combination of thrombolysis AND thrombectomy is recommend for patients with an acute ischaemic stroke who present within 4.5 hours

NICE have also made recommendations to use a modified Rankin score of less than 3 and a National Institutes of Health Stroke Scale (NIHSS) score of more than 5 when considering the selection of patients for mechanical thrombectomy.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Contraindications to thrombolysis:

A

Absolute

  • Previous intracranial haemorrhage
  • Seizure at onset of stroke
  • Intracranial neoplasm
  • Suspected subarachnoid haemorrhage
  • Stroke or traumatic brain injury in preceding 3 months
  • Lumbar puncture in preceding 7 days
  • Gastrointestinal haemorrhage in preceding 3 weeks
  • Active bleeding
  • Pregnancy
  • Oesophageal varices
  • Uncontrolled hypertension >200/120mmHg

relative
Concurrent anticoagulation (INR >1.7)
- Haemorrhagic diathesis
- Active diabetic haemorrhagic retinopathy
- Suspected intracardiac thrombus
- Major surgery / trauma in the preceding 2 weeks

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

A 68-year-old gentleman was diagnosed with glaucoma and commenced on treatment. He returned in one month for review, his eye pressures had improved but he complains his eyelashes have increased in length. What medicine is likely to have caused his eyelashes to grow in length?

A

Lantanprost - treatment for glaucoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

preferred antiplatelet for secondary prevention following stroke

A

Clopidogrel is the preferred antiplatelet for secondary prevention following stroke

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q
In baby (neonate) feeding intolerance, abdominal distension and bloody stools, which can quickly progress to abdominal discolouration, perforation and peritonitis.  
Xray - pneumatosis intestinalis (intramural gas)
A

Necrotising enterocolitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Bone protection for patients who are going to take long-term steroids

A

should start immediately= start vitamin D and calcium supplements

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

tetanus vaccination - unsure history - management?

A

Patients with an uncertain tetanus vaccination history should be given a booster vaccine + immunoglobulin, unless the wound is very minor and < 6 hours old

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Infective exacerbation of COPD antibiotics

A

Infective exacerbation of COPD: first-line antibiotics are amoxicillin or clarithromycin or doxycycline

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Laryngomalacia

A

Congenital abnormality of the larynx.

Infants typical present at 4 weeks of age with:
stridor

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Bacterial endocarditis - causative organism

A

he vast majority of cases of bacterial endocarditis are caused by gram positive cocci.

Common causes:
Streptococcus viridans
Staphylococcus aureus (in intravenous drugs uses or prosthetic valves)
Staphylococcus epidermidis (in prosthetic valves)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

HBA1c diagnostic of diabetes.

A

A HbA1c of 48mmol/mol is diagnostic of diabetes.

Over 58 = 2nd medication

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

A 17-year-old male presents to the Ear Nose and Throat clinic to discuss the results from the fine needle aspirate taken from a smooth, fluctuant, non-tender, non-translucent mass located anterior to his left sternocleidomastoid muscle. It does not move on tongue protrusion. The aspirate reveals an acellular fluid with cholesterol crystals.

A

A branchial cyst is typically a benign, lateral, unilateral neck mass

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

VTE post warfarin length

A

Venous thromoboembolism - length of warfarin treatment
provoked (e.g. recent surgery): 3 months
unprovoked: 6 months

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Pyloric stenosis

A

Pyloric stenosis typically presents in the second to fourth weeks of life with vomiting, although rarely may present later at up to four months. It is caused by hypertrophy of the circular muscles of the pylorus.

Epidemiology
incidence of 4 per 1,000 live births
4 times more common in males
10-15% of infants have a positive family history
first-borns are more commonly affected

Features
‘projectile’ vomiting, typically 30 minutes after a feed
constipation and dehydration may also be present
a palpable mass may be present in the upper abdomen
hypochloraemic, hypokalaemic alkalosis due to persistent vomiting

Diagnosis is most commonly made by ultrasound.

Management is with Ramstedt pyloromyotomy.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Myocardial infarction: secondary prevention

A

NICE produced guidelines on the management of patients following a myocardial infarction (MI) in 2013. Some key points are listed below

All patients should be offered the following drugs:
dual antiplatelet therapy (aspirin plus a second antiplatelet agent)
ACE inhibitor
beta-blocker
statin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Parotid gland mass - Benign pleomorphic adenoma or benign mixed tumor

A

Most common parotid neoplasm (80%)
Proliferation of epithelial and myoepithelial cells of the ducts and an increase in stromal components
Slow growing, lobular, and not well encapsulated
Recurrence rate of 1-5% with appropriate excision (parotidectomy)
Recurrence possibly secondary to capsular disruption during surgery
Malignant degeneration occurring in 2-10% of adenomas observed for long periods, with carcinoma ex-pleomorphic adenoma occurring most frequently as adenocarcinoma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Paranoid gland mass

A

Second most common benign parotid tumor (5%)
Most common bilateral benign neoplasm of the parotid
Marked male as compared to female predominance
Occurs later in life (sixth and seventh decades)
Presents as a lymphocytic infiltrate and cystic epithelial proliferation
May represent heterotopic salivary gland epithelial tissue trapped within intraparotid lymph nodes
Incidence of bilaterality and multicentricity of 10%
Malignant transformation rare (almost unheard of)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

COPD management

A

General management
>smoking cessation advice: including offering nicotine replacement therapy, varenicline or bupropion
annual influenza vaccination
one-off pneumococcal vaccination
pulmonary rehabilitation to all people who view themselves as functionally disabled by COPD (usually Medical Research Council [MRC] grade 3 and above)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

synchronised DC cardioversion indications

A

Unstable atrial fibrillation, atrial flutter, atrial tachycardia, and supraventricular tachycardias

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Klebsiella pneumonia

A
Features of Klebsiella pneumonia
more common in alcoholic and diabetics
may occur following aspiration
'red-currant jelly' sputum
often affects upper lobes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Progressive multifocal leukoencephalopathy

A

Caused by JC or BK virus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

superior vena cava obstruction presentation?

A
Features
dyspnoea is the most common symptom
swelling of the face, neck and arms - conjunctival and periorbital oedema may be seen
headache: often worse in the mornings
visual disturbance
pulseless jugular venous distension
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
superior vena Cava obstruction causes and management
Causes common malignancies: small cell lung cancer, lymphoma other malignancies: metastatic seminoma, Kaposi's sarcoma, breast cancer aortic aneurysm mediastinal fibrosis goitre SVC thrombosis Management general: dexamethasone, balloon venoplasty, stenting small cell: chemotherapy + radiotherapy non-small cell: radiotherapy
26
ECG: hypokalaemia
``` ECG features of hypokalaemia U waves small or absent T waves (occasionally inversion) prolong PR interval ST depression long QT ```
27
Palliative care prescribing: pain
when starting treatment, offer patients with advanced and progressive disease regular oral modified-release (MR) or oral immediate-release morphine (depending on patient preference), with oral immediate-release morphine for breakthrough pain oral modified-release morphine should be used in preference to transdermal patches laxatives should be prescribed for all patients initiating strong opioids patients should be advised that nausea is often transient. If it persists then an antiemetic should be offered drowsiness is usually transient - if it does not settle then adjustment of the dose should be considered
28
Palliative care prescribing: pain SIGN
the breakthrough dose of morphine is one-sixth the daily dose of morphine all patients who receive opioids should be prescribed a laxative opioids should be used with caution in patients with chronic kidney disease oxycodone is preferred to morphine in palliative patients with mild-moderate renal impairment if renal impairment is more severe, alfentanil, buprenorphine and fentanyl are preferred
29
Palliative care prescribing: pain - increasing dose
When increasing the dose of opioids the next dose should be increased by 30-50%.
30
``` Conversion between opioids Codine -> morphine = tramadol -> morphine Morphine -> oxy Oral morphine -> Subcutaneous morphine Oral morphine -> Subcutaneous dimorphine Oral oxycodone ->Subcutaneous dimorphine ```
Codine -> morphine = Divide by 10 tramadol -> morphne = Divide by 10 Morphine -> oxy = Divide by 1.5-2 Oral morphine -> Subcutaneous morphine = divide by 2 Oral morphine -> Subcutaneous dimorphine = divide by 3 Oral oxycodone ->Subcutaneous dimorphine = divide by 1.5
31
Small bowel bacterial overgrowth syndrome Diagnosis Management
Diagnosis hydrogen breath test small bowel aspiration and culture: this is used less often as invasive and results are often difficult to reproduce clinicians may sometimes give a course of antibiotics as a diagnostic trial Management correction of underlying disorder antibiotic therapy: rifaximin is now the treatment of choice due to relatively low resistance. Co-amoxiclav or metronidazole are also effective in the majority of patients.
32
Undescended testes
A congenital undescended testis is one that has failed to reach the bottom of the scrotum by 3 months of age consider age - may watch and wait Treatment Orchidopexy at 6- 18 months of age. The operation usually consists of inguinal exploration, mobilisation of the testis and implantation into a dartos pouch. Intra-abdominal testis should be evaluated laparoscopically and mobilised. Whether this is a single stage or two stage procedure depends upon the exact location. After the age of 2 years in untreated individuals the Sertoli cells will degrade and those presenting late in teenage years may be better served by orchidectomy than to try and salvage a non functioning testis with an increased risk of malignancy.
33
epigastric ulcers
Features epigastric pain nausea duodenal ulcers -more common than gastric ulcers epigastric pain when hungry, relieved by eating gastric ulcers- epigastric pain worsened by eating
34
non-invasive ventilation indications
Non-invasive ventilation - key indications COPD with respiratory acidosis pH 7.25-7.35* type II respiratory failure secondary to chest wall deformity, neuromuscular disease or obstructive sleep apnoea cardiogenic pulmonary oedema unresponsive to CPAP weaning from tracheal intubation
35
Keratoacanthoma
Features - said to look like a volcano or crater initially a smooth dome-shaped papule rapidly grows to become a crater centrally-filled with keratin Spontaneous regression of keratoacanthoma within 3 months is common, often resulting in a scar. Such lesions should however be urgently excised as it is difficult clinically to exclude squamous cell carcinoma. Removal also may prevent scarring.
36
Osteoporosis: assessing risk
They advise that all women aged >= 65 years and all men aged >= 75 years should be assessed. Younger patients should be assessed in the presence of risk factors, such as: previous fragility fracture current use or frequent recent use of oral or systemic glucocorticoid history of falls family history of hip fracture other causes of secondary osteoporosis low body mass index (BMI) (less than 18.5 kg/m²) smoking alcohol intake of more than 14 units per week for women and more than 14 units per week for men. Use FRAX
37
neuroleptic malignant syndrome management
Management stop antipsychotic patients should be transferred to a medical ward if they are on a psychiatric ward and often they are nursed in intensive care units IV fluids to prevent renal failure dantrolene may be useful in selected cases thought to work by decreasing excitation-contraction coupling in skeletal muscle by binding to the ryanodine receptor, and decreasing the release of calcium from the sarcoplasmic reticulum bromocriptine, dopamine agonist, may also be used
38
Gastro-oesophageal reflux disease presentation
oesophagitis secondary to refluxed gastric contents
39
Gastro-oesophageal reflux disease: management
Endoscopically proven oesophagitis full dose proton pump inhibitor (PPI) for 1-2 months if response then low dose treatment as required if no response then double-dose PPI for 1 month Endoscopically negative reflux disease full dose PPI for 1 month if response then offer low dose treatment, possibly on an as-required basis, with a limited number of repeat prescriptions if no response then H2RA or prokinetic for one month
40
otitis externa Features and management
Features ear pain, itch, discharge otoscopy: red, swollen, or eczematous canal Give Topical combination steroid and antibiotic drops s Swab may need referral for micro-suction. If a patient fails to respond to topical antibiotics then the patient should be referred to ENT.
41
Anterior uveitis presentation
Features acute onset ocular discomfort & pain (may increase with use) pupil may be irregular and small photophobia (often intense) blurred vision red eye lacrimation ciliary flush hypopyon; describes pus and inflammatory cells in the anterior chamber, often resulting in a visible fluid level visual acuity initially normal → impaired ``` Associated conditions ankylosing spondylitis reactive arthritis ulcerative colitis, Crohn's disease Behcet's disease sarcoidosis: bilateral disease may be seen ```
42
Anterior uveitis management
Management urgent review by ophthalmology cycloplegics (dilates the pupil which helps to relieve pain and photophobia) e.g. Atropine, cyclopentolate steroid eye drops
43
Subacute thyroiditis
occur following viral infection and typically presents with hyperthyroidism. ``` There are typically 4 phases; phase 1 (lasts 3-6 weeks): hyperthyroidism, painful goitre, raised ESR phase 2 (1-3 weeks): euthyroid phase 3 (weeks - months): hypothyroidism phase 4: thyroid structure and function goes back to normal ``` Investigations thyroid scintigraphy: globally reduced uptake of iodine-131 Management usually self-limiting - most patients do not require treatment thyroid pain may respond to aspirin or other NSAIDs in more severe cases steroids are used, particularly if hypothyroidism develops
44
Pulsus paradoxus
greater than the normal (10 mmHg) fall in systolic blood pressure during inspiration → faint or absent pulse in inspiration - severe asthma, cardiac tamponade
45
Slow-rising/plateau
aortic stenosis
46
Pulsus alternans
regular alternation of the force of the arterial pulse | severe LVF
47
Bisferiens pulse
'double pulse' - two systolic peaks | mixed aortic valve disease
48
'Jerky' pulse
hypertrophic obstructive cardiomyopathy*
49
Legionnaire's disease
Legionella pneumophilia. It typically colonizes water tanks and hence questions may hint at air-conditioning systems or foreign holidays. Person-to-person transmission is not seen ``` Features flu-like symptoms including fever (present in > 95% of patients) dry cough relative bradycardia confusion lymphopaenia hyponatraemia deranged liver function tests pleural effusion: seen in around 30% of patients ``` iagnosis urinary antigen Management treat with erythromycin/clarithromycin
50
Superficial spreading melanoma
70% of cases Arms, legs, back and chest, young people A growing moles flat patch of pigmented skin which grows slowly, often taking months or years to be recognised. It can be recognised by an ABCDE approach (asymmetry, border irregularity, colour variation, diameter >6mm and evolving)
51
routine manintance fluids adult
NICE guidelines from 2013 state for routine maintenance fluids the water requirement is approximately 25-30 ml/kg/day.
52
Osteogenesis imperfecta Features Investigations
Overview autosomal dominant abnormality in type 1 collagen due to decreased synthesis of pro-alpha 1 or pro-alpha 2 collagen polypeptides ``` Features presents in childhood fractures following minor trauma blue sclera deafness secondary to otosclerosis dental imperfections are common ``` Investigations adjusted calcium, phosphate, parathyroid hormone and ALP results are usually normal in osteogenesis imperfecta
53
Smudge or smear cells
CLL
54
Reed-Sternberg cells
Hodgkin's lymphoma.
55
Rouleaux formation
multiple myeloma.
56
Auer rods
a feature of AML.
57
Pseudo Pelger-Huet cells
CML
58
Hypothermia on ECG
J Wave
59
reverse tick sign ECG
dioxin
60
PE management
the use of direct oral anticoagulants (DOACs) as first-line treatment for most people with VTE the use of DOACs in patients with active cancer, as opposed to low-molecular weight heparin as was the previous recommendation outpatient treatment in low-risk pulmonary embolism (PE) patients routine cancer screening is no longer recommended following a VTE diagnosis if neither apixaban or rivaroxaban are suitable then either LMWH followed by dabigatran or edoxaban OR LMWH followed by a vitamin K antagonist (VKA, i.e. warfarin) if the patient has active cancer previously LMWH was recommended the new guidelines now recommend using a DOAC, unless this is contraindicated Anticoag for at least three months if provoked Thrombolysis thrombolysis is now recommended as the first-line treatment for massive PE where there is circulatory failure (e.g. hypotension) other invasive approaches should be considered where appropriate facilities exist
61
Toxic epidermal necrolysis
``` Drugs known to induce TEN phenytoin sulphonamides allopurinol penicillins carbamazepine NSAIDs ```
62
Pericarditis Features
Features chest pain: may be pleuritic. Is often relieved by sitting forwards other symptoms include non-productive cough, dyspnoea and flu-like symptoms pericardial rub tachypnoea tachycardia
63
Pericarditis causes
``` Causes viral infections (Coxsackie) tuberculosis uraemia (causes 'fibrinous' pericarditis) trauma post-myocardial infarction, Dressler's syndrome connective tissue disease hypothyroidism malignancy ```
64
Pericarditis Investigations & Management
Investigations ECG changes the changes in pericarditis are often global/widespread, as opposed to the 'territories' seen in ischaemic events 'saddle-shaped' ST elevation PR depression: most specific ECG marker for pericarditis all patients with suspected acute pericarditis should have transthoracic echocardiography Management treat the underlying cause a combination of NSAIDs and colchicine is now generally used for first-line for patients with acute idiopathic or viral pericarditis
65
Type 1 RTA
distal) inability to generate acid urine (secrete H+) in distal tubule causes hypokalaemia complications include nephrocalcinosis and renal stones causes include idiopathic, rheumatoid arthritis, SLE, Sjogren's, amphotericin B toxicity, analgesic nephropathy
66
absolute contraindication to the use of regional anaesthesia such as spinal, epidural or plexus block?
Therapeutic anticoagulation is an absolute contraindication to the use of regional anaesthesia due to the risk of bleeding and the severity of a hematoma within the rigid space of the central nervous system.
67
Ankylosing spondylitis
Features typically a young man who presents with lower back pain and stiffness of insidious onset stiffness is usually worse in the morning and improves with exercise the patient may experience pain at night which improves on getting up Clinical examination reduced lateral flexion reduced forward flexion - Schober's test - a line is drawn 10 cm above and 5 cm below the back dimples (dimples of Venus). The distance between the two lines should increase by more than 5 cm when the patient bends as far forward as possible reduced chest expansion
68
lithium toxciity precipitated by
Toxicity may be precipitated by: dehydration renal failure drugs: diuretics (especially thiazides), ACE inhibitors/angiotensin II receptor blockers, NSAIDs and metronidazole.
69
Diclofenac NSAID - contraindications
Diclofenac is now contraindicated with any form of cardiovascular disease
70
Degenerative cervical myelopathy
DCM symptoms can include any combination of [1]: Pain (affecting the neck, upper or lower limbs) Loss of motor function (loss of digital dexterity, preventing simple tasks such as holding a fork or doing up their shirt buttons, arm or leg weakness/stiffness leading to impaired gait and imbalance Loss of sensory function causing numbness Loss of autonomic function (urinary or faecal incontinence and/or impotence) - these can occur and do not necessarily suggest cauda equina syndrome in the absence of other hallmarks of that condition Hoffman's sign: is a reflex test to assess for cervical myelopathy. It is performed by gently flicking one finger on a patient's hand. A positive test results in reflex twitching of the other fingers on the same hand in response to the flick. (GOLD Standard - MRI of cervical spine if cervical suspected )
71
primary hyperparathyroidism | features
Features - 'bones, stones, abdominal groans and psychic moans' polydipsia, polyuria peptic ulceration/constipation/pancreatitis bone pain/fracture renal stones depression hypertension
72
primary hyperparathyroidism investigations
Investigations raised calcium, low phosphate PTH may be raised or (inappropriately, given the raised calcium) normal technetium-MIBI subtraction scan pepperpot skull is a characteristic X-ray finding of hyperparathyroidism Treatment the definitive management is total parathyroidectomy conservative management may be offered if the calcium level is less than 0.25 mmol/L above the upper limit of normal AND the patient is > 50 years AND there is no evidence of end-organ damage calcimimetic agents such as cinacalcet are sometimes used in patients who are unsuitable for surgery
73
Ottawa Rules with for ankle x-rays
The Ottawa Rules with for ankle x-rays have a sensitivity approaching 100% An ankle x-ray is required only if there is any pain in the malleolar zone and any one of the following findings: bony tenderness at the lateral malleolar zone (from the tip of the lateral malleolus to include the lower 6 cm of posterior border of the fibular) bony tenderness at the medial malleolar zone (from the tip of the medial malleolus to the lower 6 cm of the posterior border of the tibia) inability to walk four weight bearing steps immediately after the injury and in the emergency department
74
New York Heart Association (NYHA) classification
NYHA Class I no symptoms no limitation: ordinary physical exercise does not cause undue fatigue, dyspnoea or palpitations NYHA Class II mild symptoms slight limitation of physical activity: comfortable at rest but ordinary activity results in fatigue, palpitations or dyspnoea NYHA Class III moderate symptoms marked limitation of physical activity: comfortable at rest but less than ordinary activity results in symptoms NYHA Class IV severe symptoms unable to carry out any physical activity without discomfort: symptoms of heart failure are present even at rest with increased discomfort with any physical activity
75
DDX breathing difficulty in children
``` Infection (ie croup, URTI) If stridor present - Larynomalcia, asthma Allergy Cardiac (malformation in young children) ```
76
croup | presentation
Parainfluenza viruses ``` Features stridor barking cough (worse at night) fever coryzal symptoms ```
77
croup | when to admit
CKS suggest admitting any child with moderate or severe croup. Other features which should prompt admission include: < 6 months of age known upper airway abnormalities (e.g. Laryngomalacia, Down's syndrome) uncertainty about diagnosis (important differentials include acute epiglottitis, bacterial tracheitis, peritonsillar abscess and foreign body inhalation)
78
croup investigations
the vast majority of children are diagnosed clinically however, if a chest x-ray is done: a posterior-anterior view will show subglottic narrowing, commonly called the 'steeple sign' in contrast, a lateral view in acute epiglottis will show swelling of the epiglottis - the 'thumb sign'
79
croup management
Management CKS recommend giving a single dose of oral dexamethasone (0.15mg/kg) to all children regardless of severity prednisolone is an alternative if dexamethasone is not available Emergency treatment high-flow oxygen nebulised adrenaline
80
Acute epiglottitis
Haemophilus influenzae type B. Prompt recognition and treatment is essential as airway obstruction may develop. Epiglottitis generally occurs in children between the ages of 2 and 6 years. The incidence of epiglottitis has decreased since the introduction of the Hib vaccine ``` Features rapid onset unwell, toxic child stridor drooling of saliva ```
81
Acute epiglottitis | management
Management immediate senior involvement, including those able to provide emergency airway support (e.g. anaesthetics, ENT) endotracheal intubation may be necessary to protect the airway if suspected do NOT examine the throat due to the risk of acute airway obstruction the diagnosis is made by direct visualisation but this should only be done by senior staff who are able to intubate if necessary oxygen intravenous antibiotics
82
Parainfluenza virus
croup
83
Rhinovirus
cold
84
Streptococcus pneumoniae
he most common cause of community-acquired pneumonia
85
Haemophilus influenzae
Community-acquired pneumonia Most common cause of bronchiectasis exacerbations Acute epiglottitis
86
Staphylococcus aureus
Pneumonia, particularly following influenza
87
Mycoplasma pneumoniae
Atypical pneumonia Flu-like symptoms classically precede a dry cough. Complications include haemolytic anaemia and erythema multiforme
88
Pneumocystis jiroveci
Common cause of pneumonia in HIV patients. Typically patients have few chest signs and develop exertional dyspnoea
89
Mycobacterium tuberculosis
Causes tuberculosis. A wide range of presentations from asymptomatic to disseminated disease are possible. Cough, night sweats and weight loss may be seen
90
Wheeze questions
- Infection - systemic illness - Associated symptoms -Associated with excersies Associated with environment (pet, dust, smoking, mould, damp, _ Imms
91
Ddx Cyanosis
- Illness and infection - cardiac (TOF, ebsteins, tricuspid atresia, transposition) Medications (quinones) Resp - choanal atresia, Pierre Robin Sequence, airway hemangioma, vascular rings/slings, cystic hygroma, and micrognathia Blood related disorders - Polycythemia, Methemoglobinemia
92
pansystolic murmur at his lower left sternal edge and a loud P2.
Ventricular septal defect
93
typical features of heart failure in child
breathlessness, difficulty feeding, poor growth at an early age
94
VSD presentation | associations
classically a pan-systolic murmur which is louder in smaller defects chromosomal disorders (e.g. Down's syndrome, Edward's syndrome, Patau syndrome) and single gene disorders such as Non-congenital causes include post myocardial infarction
95
VSD complications
``` Complications aortic regurgitation* infective endocarditis Eisenmenger's complex right heart failure pulmonary hypertension: pregnancy is contraindicated in women with pulmonary hypertension as it carries a 30-50% risk of mortality ```
96
ostium secundum
stium secundum (70% of ASDs) associated with Holt-Oram syndrome (tri-phalangeal thumbs) ECG: RBBB with RAD
97
Ostium primum
present earlier than ostium secundum defects associated with abnormal AV valves ECG: RBBB with LAD, prolonged PR interval
98
Coarctation of the aorta presentation
infancy: heart failure adult: hypertension radio-femoral delay mid systolic murmur, maximal over back apical click from the aortic valve notching of the inferior border of the ribs (due to collateral vessels) is not seen in young children
99
Coarctation of the aorta associations
``` Associations Turner's syndrome bicuspid aortic valve berry aneurysms neurofibromatosis ```
100
hypertrophic obstructive cardiomyopathy associated pulse
bisferiens pulse (double pulse).
101
Aortic stenosis management
VR if symptomatic, otherwise cut-off is gradient of 40 mmHg
102
Features of severe aortic stenosis
``` narrow pulse pressure slow rising pulse delayed ESM soft/absent S2 S4 thrill duration of murmur left ventricular hypertrophy or failure ```
103
Aortic regurgitation features
ifficulty breathing at night, occasional palpitations and tight chest pain. On examination, he has a collapsing pulse and a laterally shifted apex beat murmur = early diastolic
104
Abdominal pain ddx in children
- infection (Gastroenteritis) -Constipation _ Appendcitis Merkles adentisi - Hernia Intussception Allergery Hischsprung IBS coalic -
105
Attention Deficit Hyperactivity Disorder presentaion
- inattentiveness hyperactivity and impulsiveness associated mood or behaviour disorders
106
Attention Deficit Hyperactivity Disorder management
watch and wait (CAMHS ref needed) Drug therapy should be seen as a last resort and is only available to those aged 5 years or more Methylphenidate is first line in children f there is inadequate response, switch to lisdexamfetamine;
107
Methylphenidate side effects
ide-effects include abdominal pain, nausea and dyspepsia. In children, weight and height should be monitored every 6 months
108
Features Bronchiolitis
eatures coryzal symptoms (including mild fever) precede: dry cough increasing breathlessness wheezing, fine inspiratory crackles (not always present) feeding difficulties associated with increasing dyspnoea are often the reason for hospital admission
109
Bronchiolitis - NICE recommend immediate referral (usually by 999 ambulance) if they have any of the following:
apnoea (observed or reported) child looks seriously unwell to a healthcare professional severe respiratory distress, for example grunting, marked chest recession, or a respiratory rate of over 70 breaths/minute central cyanosis persistent oxygen saturation of less than 92% when breathing air.
110
Bronchiolitis- management
Management is largely supportive humidified oxygen is given via a head box and is typically recommended if the oxygen saturations are persistently < 92% nasogastric feeding may be needed if children cannot take enough fluid/feed by mouth suction is sometimes used for excessive upper airway secretions
111
causes Cerebral palsy
Causes antenatal (80%): e.g. cerebral malformation and congenital infection (rubella, toxoplasmosis, CMV) intrapartum (10%): birth asphyxia/trauma postnatal (10%): intraventricular haemorrhage, meningitis, head-trauma
112
presentations Cerebral palsy
``` Possible manifestations include: abnormal tone early infancy delayed motor milestones abnormal gait feeding difficultie. ```
113
Cerebral palsy
Management as with any child with a chronic condition a multidisciplinary approach is needed treatments for spasticity include oral diazepam, oral and intrathecal baclofen, botulinum toxin type A, orthopaedic surgery and selective dorsal rhizotomy anticonvulsants, analgesia as required
114
Exanthems
eruptive skin rashes associated with a fever or other constitutional symptoms
115
Causes of maculopapular eruptions
``` Measles (rubeola) Rubella Erythema infectiosum (slapped cheek) Exanthum subitum (roseola) Lyme disease Pityriasis Drug-related eruptions Erythema multiforme ```
116
Causes of diffuse erythema with desquamation
Scarlet fever Toxic shock syndrome Staphylococcal scaled skin syndrome Kawasaki disease
117
Measles rash
erythematous maculopapular rash beginning on the head, with a cephalocaudad progression. Blue-white Kopliks spots occurring on the buccal mucosa opposite the second molar and lasting around 1-2 day
118
Measles management
Measles is a notifiable illness and notification is required based on clinical suspicion. Children diagnosed with measles should be kept off school until 5 days after the appearance of the rash. The treatment of measles is largely symptomatic and the majority of children will recover uneventfully.
119
Meckel's diverticulum | presentation
Presentation (usually asymptomatic) abdominal pain mimicking appendicitis rectal bleeding Meckel's diverticulum is the most common cause of painless massive GI bleeding requiring a transfusion in children between the ages of 1 and 2 years intestinal obstruction secondary to an omphalomesenteric band (most commonly), volvulus and intussusception
120
Anaphylaxis presentation
Anaphylaxis may be defined as a severe, life-threatening, generalised or systemic hypersensitivity reaction. Common identified causes of anaphylaxis: food (e.g. nuts) - the most common cause in children drugs venom (e.g. wasp sting)
121
Anaphylaxis management
Adrenaline is by far the most important drug in anaphylaxis and should be given as soon as possible. also give Hydrocortisone and Chlorphenamine Adrenaline can be repeated every 5 minutes if necessary. The best site for IM injection is the anterolateral aspect of the middle third of the thigh. Management following stabilisation: patients who have had emergency treatment for anaphylaxis should be observed for 6–12 hours from the onset of symptoms, as it is known that biphasic reactions can occur in up to 20% of patients sometimes it can be difficult to establish whether a patient had a true episode of anaphylaxis. Serum tryptase levels are sometimes taken in such patients as they remain elevated for up to 12 hours following an acute episode of anaphylaxis.v
122
Anaphylaxis test after episode to confirm
serum tryptase levels rise following an acute episode
123
Acute exacerbations of COPD features
Features increase in dyspnoea, cough, wheeze there may be an increase in sputum suggestive of an infective cause patients may be hypoxic and in some cases have acute confusion
124
The most common bacterial organisms that cause infective exacerbations of COPD are:
Haemophilus influenzae (most common cause) Streptococcus pneumoniae Moraxella catarrhalis
125
Infective exacerbations of COPD managements
NICE guidelines from 2010 recommend the following: increase frequency of bronchodilator use and consider giving via a nebuliser give prednisolone 30 mg daily for 5 days it is common practice for all patients with an exacerbation of COPD to receive antibiotics. NICE do not support this approach. They recommend giving oral antibiotics 'if sputum is purulent or there are clinical signs of pneumonia' the BNF recommends one of the following oral antibiotics first-line: amoxicillin or clarithromycin or doxycycline.
126
pneumonia causes
bacterial pneumonia is by far the most common type of pneumonia Streptococcus pneumoniae = most common Haemophilus influenzae = COPD Staphylococcus aureus = occurs in patient following influenza infection Klebsiella pneumoniae = alcoholics
127
Pneumonia Bloods
Bloods full blood count: would usually show a neutrophilia in bacterial infections urea and electrolytes: check for dehydration (remember the 'U' for urea in CURB-65, see below) and also other changes seen with some atypical pneumonias CRP: raised in response to infection
128
Pneumonia management
Patients with pneumonia require the following: antibiotics: to treat the underlying infection supportive care: for example oxygen therapy if the patients is hypoxaemic, intravenous fluids if the patient is hypotensive or shows signs of dehydration CURB- 65 score
129
Pneumonia - Discharge criteria and advice post-discharge
Discharge criteria and advice post-discharge ``` NICE recommend that patients are not routinely discharged if in the past 24 hours they have had 2 or more of the following findings: temperature higher than 37.5°C respiratory rate 24 breaths per minute or more heart rate over 100 beats per minute systolic blood pressure 90 mmHg or less oxygen saturation under 90% on room air abnormal mental status inability to eat without assistance. ``` They also recommend delaying discharge if the temperature is higher than 37.5°C.
130
Pneumothorax risk factors
Risk factors pre-existing lung disease: COPD, asthma, cystic fibrosis, lung cancer, Pneumocystis pneumonia connective tissue disease: Marfan's syndrome, rheumatoid arthritis ventilation, including non-invasive ventilation catamenial pneumothorax is the cause of 3-6% of spontaneous pneumothoraces occurring in menstruating women. It is thought to be caused by endometriosis within the thorax
131
Pneumothorax symptoms
``` Symptoms tend to come on suddenly. Features include: dyspnoea chest pain: often pleuritic sweating tachypnoea tachycardia ```
132
Primary pneumothorax | management
Recommendations include: if the rim of air is < 2cm and the patient is not short of breath then discharge should be considered otherwise, aspiration should be attempted if this fails (defined as > 2 cm or still short of breath) then a chest drain should be inserted patients should be advised to avoid smoking to reduce the risk of further episodes - the lifetime risk of developing a pneumothorax in healthy smoking men is around 10% compared with around 0.1% in non-smoking men
133
Secondary pneumothorax management
Recommendations include: if the patient is > 50 years old and the rim of air is > 2cm and/or the patient is short of breath then a chest drain should be inserted. otherwise aspiration should be attempted if the rim of air is between 1-2cm. If aspiration fails (i.e. pneumothorax is still greater then 1cm) a chest drain should be inserted. All patients should be admitted for at least 24 hours if the pneumothorax is less the 1cm then the BTS guidelines suggest giving oxygen and admitting for 24 hours regarding scuba diving, the BTS guidelines state: 'Diving should be permanently avoided unless the patient has undergone bilateral surgical pleurectomy and has normal lung function and chest CT scan postoperatively.'
134
triad of PE | and clinical signs
pleuritic chest pain, dyspnoea and haemoptysis. The relative frequency of common clinical signs is shown below: Tachypnea (respiratory rate >20/min) - 96% Crackles - 58% Tachycardia (heart rate >100/min) - 44% Fever (temperature >37.8°C) - 43%
135
PE suspected
If a PE is suspected a 2-level PE Wells score should be performed: linical probability simplified scores PE likely - more than 4 points PE unlikely - 4 points or less If a PE is 'likely' (more than 4 points) arrange an immediate computed tomography pulmonary angiogram (CTPA). If there is a delay in getting the CTPA then interim therapeutic anticoagulation should be given until the scan is performed. interim therapeutic anticoagulation used to mean giving low-molecular weight heparin NICE updated their guidance in 2020. They now recommend using an anticoagulant that can be continued if the result is positive. this means normally a direct oral anticoagulant (DOAC) such as apixaban or rivaroxaban
136
test in PE
CTPA is now the recommended initial lung-imaging modality for non-massive PE. Advantages compared to V/Q scans include speed, easier to perform out-of-hours, a reduced need for further imaging and the possibility of providing an alternative diagnosis if PE is excluded if the CTPA is negative then patients do not need further investigations or treatment for PE V/Q scanning may be used initially if appropriate facilities exist, the chest x-ray is normal, and there is no significant symptomatic concurrent cardiopulmonary disease. V/Q scanning is also the investigation of choice if there is renal impairment (doesn't require the use of contrast unlike CTPA)
137
Pulmonary embolism and renal impairment →
V/Q scan is the investigation of choice
138
Massive PE + hypotension
- thrombolyse
139
bloods PE
Pulmonary embolism causes hyperventilation, causing a drop in arterial carbonic dioxide partial pressure and thus alkalosis.
140
Features of pulmonary oedema on a chest x-ray may include:
Features of pulmonary oedema on a chest x-ray may include: interstitial oedema bat's wing appearance upper lobe diversion (increased blood flow to the superior parts of the lung) Kerley B lines pleural effusion cardiomegaly may be seen if there is cardiogenic cause
141
Tricuspid regurgitation signs
Pan systolic mumur JVP increase Hepatomegaly Heave
142
Tricuspid regurgitation causes
Right V INFARCT Pulmonary hypertension Rheumatic heart disease Infective endo Ébstekns
143
NSTEMI
All patients should receive aspirin 300mg nitrates or morphine to relieve chest pain if required Clopidogrel
144
optic neuritis causes
Causes multiple sclerosis diabetes syphilis
145
optic neuritis features
Features unilateral decrease in visual acuity over hours or days poor discrimination of colours, 'red desaturation' pain worse on eye movement relative afferent pupillary defect central scotoma
146
optic neuritis management
Management high-dose steroids recovery usually takes 4-6 weeks Prognosis MRI: if > 3 white-matter lesions, 5-year risk of developing multiple sclerosis is c. 50%
147
abdo signs
A number of eponymous abdominal signs are noted. These include: Rovsings sign- appendicitis Boas sign -cholecystitis Murphys sign- cholecystitis Cullens sign- pancreatitis (other intraabdominal haemorrhage) Grey-Turners sign- pancreatitis (or other retroperitoneal haemorrhage)
148
BV causes and treatment
Bacterial vaginosis (BV) describes an overgrowth of predominately anaerobic organisms such as Gardnerella vaginalis Features vaginal discharge: 'fishy', offensive asymptomatic in 50% Amsel's criteria for diagnosis of BV - 3 of the following 4 points should be present thin, white homogenous discharge clue cells on microscopy: stippled vaginal epithelial cells vaginal pH > 4.5 positive whiff test (addition of potassium hydroxide results in fishy odour) ``` Management oral metronidazole for 5-7 days 70-80% initial cure rate relapse rate > 50% within 3 months the BNF suggests topical metronidazole or topical clindamycin as alternatives. ```
149
BV in pregnancy
Bacterial vaginosis in pregnancy results in an increased risk of preterm labour, low birth weight and chorioamnionitis, late miscarriage it was previously taught that oral metronidazole should be avoided in the first trimester and topical clindamycin used instead. Recent guidelines however recommend that oral metronidazole is used throughout pregnancy. The BNF still advises against the use of high dose metronidazole regimes
150
hypocalcaemia causes
auses vitamin D deficiency (osteomalacia) chronic kidney disease hypoparathyroidism (e.g. post thyroid/parathyroid surgery) pseudohypoparathyroidism (target cells insensitive to PTH) rhabdomyolysis (initial stages) magnesium deficiency (due to end organ PTH resistance) massive blood transfusion acute pancreatitis
151
hypocalcaemia Management
Management acute management of severe hypocalcaemia is with intravenous replacement. The preferred method is with intravenous calcium gluconate, 10ml of 10% solution over 10 minutes intravenous calcium chloride is more likely to cause local irritation ECG monitoring is recommended further management depends on the underlying cause
152
Bells palsy presentation
Features lower motor neuron facial nerve palsy - forehead affected* patients may also notice post-auricular pain (may precede paralysis), altered taste, dry eyes, hyperacusis
153
Bells palsy management
prednisolone 1mg/kg for 10 days should be prescribed for patients within 72 hours of onset of Bell's palsy. Adding in aciclovir gives no additional benefit eye care is important - prescription of artificial tears and eye lubricants should be considered
154
large fluid volumes risk
hyperchloraemic acidosis
155
stroke post coag
Aspirin 300 mg daily for 2 weeks should be given immediately after an ischaemic stroke is confirmed by brain imaging. Following this, clopidogrel 75 mg daily should be given long-term -if it can be tolerated and is not contraindicated. If clopidogrel is contraindicated or not tolerated, then the patient should be given modified-release dipyridamole alongside low dose aspirin.
156
Age-related macular degeneration presentation
Patients typically present with a subacute onset of visual loss with: a reduction in visual acuity, particularly for near field objects difficulties in dark adaptation with an overall deterioration in vision at night fluctuations in visual disturbance which may vary significantly from day to day they may also suffer from photopsia, (a perception of flickering or flashing lights), and glare around objects
157
Age-related macular degeneration treatment
zinc with anti-oxidant vitamins A,C and E reduced progression of the disease by around one third. anti-VEGF agents (wet) - instituted within the first two months of diagnosis of wet ARMD if possible. Laser photocoagulation does slow progression of ARMD where there is new vessel formation, although there is a risk of acute visual loss after treatment, which may be increased in patients with sub-foveal ARMD. For this reason anti-VEGF therapies are usually preferred.
158
Central retinal vein occlusion presentation
Features sudden, painless reduction or loss of visual acuity, usually unilaterally severe retinal haemorrhages are usually seen on fundoscopy
159
Herpes simplex keratitis presentation
``` Features red, painful eye photophobia epiphora visual acuity may be decreased fluorescein staining may show an epithelial ulcer ```
160
Herpes simplex keratitis management
Management immediate referral to an ophthalmologist topical aciclovir
161
Rentral retinal artery occlusion
causes sudden unilateral visual loss due to thromboembolism (from atherosclerosis) or arteritis (e.g. temporal arteritis) features include afferent pupillary defect, 'cherry red' spot on a pale retina
162
retinal detachment presentaition
Peripheral curtain over vision + spider webs + flashing lights in vision (painless loss of vision)
163
amaurosis fugax
Painless, transient monocular blindness together with the description of a 'black curtain coming down'
164
Tunnel vision is the concentric diminution of the visual fields Causes
``` Causes papilloedema glaucoma retinitis pigmentosa choroidoretinitis optic atrophy secondary to tabes dorsalis hysteria ```
165
Acute angle closure glaucoma is associated with ?
hypermetropia,
166
primary open-angle glaucoma is associated with
myopia
167
Acyanotic heart disease
most common causes (blood contains oxygen) ``` ventricular septal defects (VSD) - most common, accounts for 30% atrial septal defect (ASD) patent ductus arteriosus (PDA) coarctation of the aorta aortic valve stenosis ```
168
Cyanotic heart disease
Cyanotic - most common causes tetralogy of Fallot transposition of the great arteries (TGA) tricuspid atresia
169
Anti-dsDNA
SLE
170
Anti-CCP
RA
171
Anti-La
Sjogren's syndrome. It can also be found in patients with SLE, however, it is not very specific.
172
ANCA
ANCA is an antibody targeted against neutrophils. It is seen in patients with autoimmune vasculitis.
173
Anti-centromere
Anti-centromere antibodies are characteristic of the CREST syndrome which is the cutaneous form of systemic sclerosis. CREST stands for calcinosis, Raynaud's, oesophageal dysmotility, sclerodactyly and telangiectasia.
174
metoclopramide avoid when
bowel obstruction | as could cause a perforation in bowel obstruction.
175
Osteochondritis dissecans presentation
Patients typically present with a subacute onset of: Knee pain and swelling, typically after exercise Knee catching, locking and/or giving way - more constant and severe symptoms are associated with the presence of loose bodies Feeling a painful 'clunk' when flexing or extending the knee - indicating the involvement of the lateral femoral condyle
176
Osteochondritis dissecans signs
Joint effusion Full range of movement in the joint without signs of ligamentous instability External tibial rotation when walking - if medial femoral involvement Tenderness on palpation of the articular cartilage of the medial femoral condyle, when the knee is flexed Wilson's sign for detecting medial condyle lesion - with the knee at 90° flexion and tibia internally rotated, the gradual extension of the joint leads to pain at about 30°, external rotation of the tibia at this point relieves the pain
177
Osteochondritis dissecans investigations
Investigations: X-ray (anteroposterior, lateral and tunnel views) - may show the subchondral crescent sign or loose bodies MRI - used to evaluate cartilage, visualise loose bodies, stage and assess the stability of the lesion CT - may be used in preoperative planning and in cases where MRI is not available or contraindicated Scintigraphy - may be used to guide treatment as it may show increased uptake in the fragments - a sign of osteoblastic activity
178
treatments have not been shown to improve mortality in patients with chronic heart failure?
furosemide
179
Heart failure management
The first-line treatment for all patients is both an ACE-inhibitor and a beta-blocker Second-line treatment is an aldosterone antagonist Third-line treatment should be initiated by a specialist. Options include ivabradine, sacubitril-valsartan, hydralazine in combination with nitrate, digoxin and cardiac resynchronisation therapy
180
antibiotics for Exacerbations of chronic bronchitis
Amoxicillin or tetracycline or clarithromycin
181
antibiotics for Uncomplicated community-acquired pneumonia
Amoxicillin (Doxycycline or clarithromycin in penicillin allergic, add flucloxacillin if staphylococci suspected e.g. In influenza)
182
antibiotics for Pneumonia possibly caused by atypical pathogens
Clarithromycin
183
antibiotics for Hospital-acquired pneumonia
Within 5 days of admission: co-amoxiclav or cefuroxime More than 5 days after admission: piperacillin with tazobactam OR a broad-spectrum cephalosporin (e.g. ceftazidime) OR a quinolone (e.g. ciprofloxacin)
184
Impetigo treatment
Topical hydrogen peroxide, oral flucloxacillin or erythromycin if widespread
185
Cellulitis treatment
Flucloxacillin (clarithromycin, erythromycin or doxycycline if penicillin-allergic) Co-amoxiclav (clarithromycin, + metronidazole if penicillin-allergic)
186
Animal or human bite treat
Co-amoxiclav (doxycycline + metronidazole if penicillin-allergic)
187
Salicylate poisoning presentation
present with nausea, vomiting, tinnitus and headache. In more severe overdoses, hyperventilation and a secondary respiratory alkalosis develops. give IV sodium bicarb
188
benzodiazepine overdose.
Flumazenil
189
CLL is associated with
warm autoimmune haemolytic anaemia
190
The Mackler triad for Boerhaave syndrome:
vomiting, thoracic pain, subcutaneous emphysema. It typically presents in middle aged men with a background of alcohol abuse. = oesphgealo perforation
191
Plummer-Vinson syndrome
Triad of: dysphagia (secondary to oesophageal webs) glossitis iron-deficiency anaemia Treatment includes iron supplementation and dilation of the webs
192
Orlistat
weight loss | inhibiting gastric and pancreatic lipase to reduce the digestion of fat
193
Features suggestive of hypernatraemic dehydration:
``` jittery movements increased muscle tone hyperreflexia convulsions drowsiness or coma ```
194
X-linked recessive inheritance
males only effected X-linked recessive disorders are transmitted by heterozygote females (carriers) and male-to-male transmission is not seen. ie haemophilia A
195
life treating asthma attack
``` SpO2 <92% PEF <33% best or predicted Silent chest Poor respiratory effort Agitation Altered consciousness Cyanosis ```
196
risk factors for erectile dysfunction
Other than increasing age, risk factors include: cardiovascular disease risk factors: obesity, diabetes mellitus, dyslipidaemia, metabolic syndrome, hypertension, smoking alcohol use drugs: SSRIs, beta-blockers
197
assessment for erectile dysfunction
t all men have their 10-year cardiovascular risk calculated by measuring lipid and fasting glucose serum levels. Free testosterone should also be measured in the morning between 9 and 11am. If free testosterone is low or borderline, it should be repeated along with follicle-stimulating hormone, luteinizing hormone and prolactin levels. If any of these are abnormal refer to endocrinology for further assessment.
198
erectile dysfunction management
PDE-5 inhibitors (such as sildenafil, 'Viagra') Vacuum erection devices are recommended as first-line treatment in those who can't/won't take a PDE-5 inhibitor. Other points for a young man who has always had difficulty achieving an erection, referral to urology is appropriate people with erectile dysfunction who cycle for more than three hours per week should be advised to stop
199
normocytic anaemia with low serum iron, low TIBC but raised ferritin
anaemia of chronic disease
200
Sideroblastic anaemia
a microcytic anaemia with raised serum iron levels.
201
a microcytic anaemia, low ferritin and a raised TIBC, not the current clinical picture.
iron def
202
Subcapsular cataracts may be associated with what medication
steroids (Allopurinol less strong link )
203
) Myotonic dystrophy is associated with what eye problem
dot cataracts
204
Whipple’s triad of symptoms of for insluinoma
) hypoglycaemia with fasting or exercise, 2) reversal of symptoms with glucose, and 3) recorded low BMs at the time of symptoms is hallmark for an insulinoma
205
insluinoma features
Features of hypoglycaemia: typically early in morning or just before meal, e.g. diplopia, weakness etc rapid weight gain may be seen high insulin, raised proinsulin:insulin ratio high C-peptide
206
Rhabdomyolysis causes
Causes seizure collapse/coma (e.g. elderly patients collapses at home, found 8 hours later) ecstasy crush injury McArdle's syndrome drugs: statins (especially if co-prescribed with clarithromycin)
207
Hypothyroidism causes a euvolaemic hyponatraemia | blood results
Plasma osmolality low | NA in urine = high
208
The recommended dose of adrenaline to give during advanced ALS
1mg
209
Hodgkin's lymphoma - best prognosis =
lymphocyte predominant
210
Intramuscular ceftriaxone is the treatment of choice for
gonnorhoae
211
Bifascicular block
combination of RBBB with left anterior or posterior hemiblock e.g. RBBB with left axis deviation
212
Trifascicular block
Trifascicular block | features of bifascicular block as above + 1st-degree heart block
213
metformin not tolerated GI
If metformin is not tolerated due to GI side-effects, try a modified-release formulation before switching to a second-line agent
214
Lithium monitoring
When checking lithium levels, the sample should be taken 12 hours post-dose after starting lithium levels should be performed weekly and after each dose change until concentrations are stable once established, lithium blood level should 'normally' be checked every 3 months after a change in dose, lithium levels should be taken a week later and weekly until the levels are stable.
215
Lithium SE
Adverse effects nausea/vomiting, diarrhoea fine tremor nephrotoxicity: polyuria, secondary to nephrogenic diabetes insipidus thyroid enlargement, may lead to hypothyroidism ECG: T wave flattening/inversion weight gain idiopathic intracranial hypertension leucocytosis hyperparathyroidism and resultant hypercalcaemia
216
GCS
Motor response 6. Obeys commands 5. Localises to pain 4. Withdraws from pain 3. Abnormal flexion to pain (decorticate posture) 2. Extending to pain 1. None Verbal response 5. Orientated 4. Confused 3. Words 2. Sounds 1. None Eye opening 4. Spontaneous 3. To speech 2. To pain 1. None
217
autoimmune hep - presentation
Features may present with signs of chronic liver disease acute hepatitis: fever, jaundice etc (only 25% present in this way) amenorrhoea (common) ANA/SMA/LKM1 antibodies, raised IgG levels liver biopsy: inflammation extending beyond limiting plate 'piecemeal necrosis', bridging necrosis
218
duloxetine
duloxetine. This acts as a serotonin/norepinephrine reuptake inhibitor and its common side effects include nausea, dizziness and insomnia.
219
Lacunar strokes can present with
unilateral motor disturbance affecting the face, arm or leg or all 3. complete one sided sensory loss. ataxia hemiparesis.
220
patient refuses IM ceftriaxone in gonorrhoea
oral cefixime + oral azithromycin
221
optimal treatment in HNF1A-MODY.
Sulfonylureas (e.g. gliclazide)
222
live attenuated vaccines which should not be given in immunocompromised patients are:
``` Yellow fever Oral polio Intranasal influenza Varicella Measles, mumps and rubella (MMR) BCG ```
223
most frequent malaria
Falciparum malaria is the commonest type of malaria
224
recent parovirus in pregnancy immunology | Rubella
IgG positive & IgM negative - shows immunity to parvovirus. Reassure, no further action. IgG negative & IgM positive - non-immune. Recent parvovirus infection in last 4 weeks. Refer immediately for further tests/fetal medicine. IgG negative & IgM negative - repeat test in 4 weeks. If both tests still negative, this confirms susceptibility, but no recent infection. Reassure, further action required only if subsequent exposure occurs.
225
Dupuytren's contracture
``` Specific causes include: manual labour phenytoin treatment alcoholic liver disease diabetes mellitus trauma to the hand ```
226
Orbital cellulitis présentation
``` Presentation Redness and swelling around the eye Severe ocular pain Visual disturbance Proptosis Ophthalmoplegia/pain with eye movements Eyelid oedema and ptosis Drowsiness +/- Nausea/vomiting in meningeal involvement (Rare) ```
227
Orbital cellulitis investigations
nvestigations Full blood count – WBC elevated, raised inflammatory markers. Clinical examination involving complete ophthalmological assessment – Decreased vision, afferent pupillary defect, proptosis, dysmotility, oedema, erythema. CT with contrast – Inflammation of the orbital tissues deep to the septum, sinusitis. Blood culture and microbiological swab to determine the organism. Most common bacterial causes – Streptococcus, Staphylococcus aureus, Haemophilus influenzae B.
228
Felty's syndrome
RA + splenomegaly + low white cell count)
229
Irradiated blood products when
Irradiated blood products are used to avoid transfusion-associated graft versus host disease Neonates up to 28 days post expected date of delivery Pregnancy: Elective transfusions during pregnancy (not during labour or delivery) Immunocompromised (e.g. chemotherapy or congenital) Patients with/previous Hodgkins Disease HIV
230
Injury to the AC joint - injury
AC joint injuries are graded I to VI depending on the degree of separation. Grade I and II injuries are very common and are typically managed conservatively including resting the joint using a sling. Grade IV, V and VI are rare and require surgical intervention. The management of grade III injuries is a matter of debate and often depends on individual circumstances.
231
sialadenitis
inflammation of the salivary gland likely secondary to obstruction by a stone impacted in the duct. The duct from the submandibular gland drain into the floor of the mouth and purulent discharge from this duct causes a foul taste in the mouth.
232
Oesophageal adenocarcinoma is associated with
GORD or Barrett's
233
Constipation in children history
poor diet and fluid intake history of cerebral palsy learning difficulties, or spinal cord problems; psychological factors (e.g., depression, abuse, ADHD, autism, oppositional disorder), weaning, toilet training, start of schooling or other causes of stress may be present; vague abdominal pain, painful defecation (infants may extend their legs and squeeze anal and buttock muscles to prevent stooling;
234
constipation in children exam
examination findings may be minimal (mild abdominal tenderness, stool in rectum); abdominal distension in severe cases or in small children; faecal mass palpable on abdominal or rectal examination
235
constipation in children management
1. Dietary changes remain a common initial recommendation, particularly increased intake of fluids and dietary fibre. 2. osmotic agents ie lactulose or polyethylene glycol (PEG) (quicker response, over 1) 3. Some children may require the addition of a short-term stimulant laxative (e.g., senna) to achieve regular bowel movements. If impaction present given osmotic lax 1st line
236
Appendicitis history
history of sharp or stabbing periumbilical pain that migrates to the right lower quadrant (RLQ); anorexia, fever, vomiting, and/or diarrhoea may be present; occurs in all age groups but is rare in infants
237
Appendicitis exam
positive McBurney's sign (RLQ pain and tenderness to palpation at a point two-thirds along a line from the umbilicus to the anterior superior iliac spine); positive Rovsing's sign (pain in the RLQ in response to left-sided palpation, suggesting peritoneal irritation); positive psoas sign (pain in the RLQ when child placed on left side and right hip gently hyperextended, suggesting irritation to the psoas fascia and muscle); positive obturator sign (RLQ pain on internal rotation of the flexed right thigh);
238
Appendicitis management
Seek immediate surgical input and consider involving critical care for any patient with suspected appendicitis and signs of shock or sepsis. Think fluids, abx and access - consider if patient is acutely unwell and in shock. Laparoscopic appendicectomy is the first choice for most adults
239
Gastroenteritis history
vague abdominal pain with nausea and vomiting; diarrhoea with or without mucus in stool; recent travel or contact with sick individual(s) or ingestion of suspected food and drink; >10 days suggests parasitic or non-infectious cause; fever, chills, myalgia, rhinorrhoea, upper respiratory symptoms
240
Gastroenteritis on exam
diffuse abdominal pain without evidence of peritonitis (no guarding or rebound tenderness); abdominal distension; hyperactive bowel sounds; mucus in stool (bacterial or parasitic); signs of volume depletion (tachycardia, hypotension, dry mucous membranes, poor capillary refill, sunken fontanelle in infants); low-grade fever, lethargy and/or irritability, reduced response to noxious stimuli, abnormal temperature
241
Gastroenteritis management
access dehydration rehydrate if needed Daily fluid maintenance requirement is 100 mL/kg for the first 10 kg body weight, 50 mL/kg for the next 10 kg, and 20 mL/kg for each subsequent 1 kg over 20 kg. This is usually supplied by the age-appropriate diet. For infants who are breast-fed, breastfeeding should be continued. ondansetron should be considered when vomiting interferes with ORT.
242
UTI in children management
age dependant Neonates under 6 weeks - IV abx infants >6 weeks to <2 years children and adolescents : systemically stable - oral cefixime if unstable - need IV abx
243
Intussuspection presentation / history
usually infant between 3 months and 12 months of age presenting with colicky abdominal pain, flexing of the legs, fever, lethargy, and vomiting; Henoch-Schonlein purpura (HSP) may be initiating factor in an older child (usually <11 years of age); vague abdominal complaints; severe, cramp-like abdominal pain; child may be inconsolable
244
Intussuspection exam
may see gross or occult blood that may be mixed with mucus and have 'red currant jelly ' appearance, abdominal tenderness, and palpable abdominal mass; signs of HSP may be present in older child (rash of palpable purpura, blood in the stools) confirm with USS
245
Intussuspection treatment
1st line - fluid resuscitation Reduction should be first attempted by contrast enema 2nd (when contrast enema is contra ie in peritonitis, perforation, and hypovolaemic shock) - surgical reduction
246
merkles diverticulum history
typically aged <2 years; may present with abdominal pain (may be intermittent or mimic acute appendicitis), and/or painless passage of bright red blood per rectum (haematochezia); often asymptomatic
247
merkles diverticulum exam
dark red, maroon, or 'red currant jelly' stools; abdominal tenderness with guarding and rebound (may suggest diverticulitis);
248
merkles diverticulum investigation
Pertechnetate scan is best | ectopic focus or 'hot spot'; enhancement of diverticulum
249
merkles diverticulum management
symptomatic - surgical excision of the diverticulum
250
crohns disease history
crampy abdominal pain, intermittent diarrhoea, bloody diarrhoea if colitis a feature (blood less common in Crohn's disease than in ulcerative colitis), weight loss, fatigue, family history of inflammatory bowel disease
251
crohns disease exam
ulcers, evidence of weight loss, pallor, abdominal tenderness, abdominal mass, perianal fistula, perirectal abscess, anal fissure, perianal skin tags; extraintestinal manifestations including iritis, arthritis, sacroiliitis, erythema nodosum, pyoderma gangrenosum
252
crohns disease investigation
FBC: leukocytosis, anaemia, thrombocytosis CRP and ESR - raised colonoscopy with biopsy: may demonstrate inflammation, friability, ulcer formation, and oedema
253
crohns disease management
budesonide - a modified-release corticosteroid, which is active particularly at the terminal ileum prednisolone: 0.5 to 0.75 mg/kg/day orally, taper gradually according to response (consider adverse effect profile) immunmodulator therapy ie azathioprine or mercaptopurine: or methotrexate (with folic acid) biological therapy TNF-alpha inhibitors infliximab and adalimumab
254
testicular torsion history
acute-onset testicular pain; nausea, and vomiting; history of recurrent episodes suggests repeated episodes of testicular torsion followed by spontaneous detorsion; history of trauma may be present
255
testicular torsion exam
tender, oedematous testicle; affected testicle may appear higher than unaffected testicle with horizontal lie; associated scrotal erythema and oedema; absent cremasteric reflex; usually no pain relief with elevation of the scrotum
256
testicular torsion investigations
duplex Doppler ultrasound of scrotum: presence of fluid and the whirlpool sign (the swirling appearance of the spermatic cord from torsion as the ultrasound probe scans downwards perpendicular to the spermatic cord); absent or decreased blood flow in the affected testicle
257
giardiasis history
history of travel, contaminated water/food, IgA deficiency, foul-smelling watery/fatty stools, abdominal pain, bloating, or weight loss
258
giardiasis investigation
giardiasis - stool culture - This remains the most definitive investigation. Inexpensive, but requires microscopic expertise and specialised laboratories.
259
giardiasis treatment
metronidazole 1st line Nitroimidazoles (e.g., metronidazole and tinidazole) are first choice for these patients and bind with parasite DNA causing death of the trophozoite. paromomycin in pregnancy (1st Trimenster`0
260
Labyrinthitis history
history of vertigo, dizziness, hearing loss, tinnitus, otalgia, and flu-like symptoms; irritation of the vestibular system can be secondary to trauma, central nervous system or ear infection, or vestibular neuritis
261
Labyrinthitis risk factors
Key risk factors include viral infections, acute or chronic otitis media, meningitis, cholesteatoma, and inner ear malformations.
262
Labyrinthitis treatment
Symptoms of acute vertigo episodes can be treated with vestibular suppressants and anti-emetics ie promethazine:
263
malrotation history
onset <1 month age with bilious vomiting; more concerning symptoms include haematochezia, abdominal distension, and shock; for older children, presents as chronic vomiting and poor weight gain
264
malrotation exam
examination initially normal but may demonstrate rapid progression to acute abdomen secondary to bowel necrosis; there is a high risk of midgut volvulus and intestinal necrosis
265
malroation investigation
plain abdominal x-ray: obstruction: dilatation of the stomach and duodenum needs emergency surgery
266
aaa screening
In England, abdominal aortic aneurysm screening (AAA) is offered to men during the year they turn 65. If normal (<3cm) the patient will require no further future scans as the chances of developing a AAA after 65 years old is small.
267
Carbimazole
hyrotoxicosis. It is typically given in high doses for 6 weeks until the patient becomes euthyroid before being reduced. Mechanism of action blocks thyroid peroxidase from coupling and iodinating the tyrosine residues on thyroglobulin → reducing thyroid hormone production in contrast propylthiouracil as well as this central mechanism of action also has a peripheral action by inhibiting 5'-deiodinase which reduces peripheral conversion of T4 to T3 Adverse effects agranulocytosis crosses the placenta, but may be used in low doses during pregnancy
268
Argyll-Robertson pupil
Argyll-Robertson pupil is one of the classic pupillary syndrome. It is sometimes seen in neurosyphilis. A mnemonic used for the Argyll-Robertson Pupil (ARP) is Accommodation Reflex Present (ARP) but Pupillary Reflex Absent (PRA) Features small, irregular pupils no response to light but there is a response to accommodate Causes diabetes mellitus syphilis
269
Orthostatic hypotension
Orthostatic hypotension can be diagnosed when there is: a. A drop in systolic BP of 20mmHg or more (with or without symptoms) b. A drop to below 90mmHg on standing even if the drop is less than 20mmHg (with or without symptoms) c. A drop in diastolic BP of 10mmHg with symptoms (although clinically much less significant than a drop in systolic BP).
270
SSRI + NSAID = =
GI bleeding risk - give a PPI
271
Genital warts
90% are caused by HPV 6 & 11 Management topical podophyllum or cryotherapy are commonly used as first-line treatments depending on the location and type of lesion. Multiple, non-keratinised warts are generally best treated with topical agents whereas solitary, keratinised warts respond better to cryotherapy imiquimod is a topical cream which is generally used second line genital warts are often resistant to treatment and recurrence is common although the majority of anogenital infections with HPV clear without intervention within 1-2 years
272
Venous leg ulcers | presentation
Most due to venous hypertension, secondary to chronic venous insufficiency (other causes include calf pump dysfunction or neuromuscular disorders) Ulcers form due to capillary fibrin cuff or leucocyte sequestration Features of venous insufficiency include oedema, brown pigmentation, lipodermatosclerosis, eczema Location above the ankle, painless Deep venous insufficiency is related to previous DVT and superficial venous insufficiency is associated with varicose veins Doppler ultrasound looks for presence of reflux and duplex ultrasound looks at the anatomy/ flow of the vein Management: 4 layer compression banding after exclusion of arterial disease or surgery If fail to heal after 12 weeks or >10cm2 skin grafting may be needed
273
Marjolin's ulcer presentation
Squamous cell carcinoma Occurring at sites of chronic inflammation e.g; burns, osteomyelitis after 10-20 years Mainly occur on the lower limb
274
Arterial ulcers presentation
``` Occur on the toes and heel Painful There may be areas of gangrene Cold with no palpable pulses Low ABPI measurements ```
275
Neuropathic ulcers presentation
Commonly over plantar surface of metatarsal head and plantar surface of hallux The plantar neuropathic ulcer is the condition that most commonly leads to amputation in diabetic patients Due to pressure Management includes cushioned shoes to reduce callous formation
276
Pyoderma gangrenosum presentation
Associated with inflammatory bowel disease/RA Can occur at stoma sites Erythematous nodules or pustules which ulcerate
277
retractile testis
testis that appears in warm conditions or which can be brought down on clinical examination and does not immediately retract
278
neoplastic spinal cord compression is suspected
high-dose oral dexamethasone should be given whilst awaiting investigations
279
benign prostatic hyperplasia management
Alpha-1 antagonists
280
BPH typically presents with lower urinary tract symptoms (LUTS), which may be categorised into:
``` voiding symptoms (obstructive): weak or intermittent urinary flow, straining, hesitancy, terminal dribbling and incomplete emptying storage symptoms (irritative) urgency, frequency, urgency incontinence and nocturia post-micturition: dribbling complications: urinary tract infection, retention, obstructive uropathy ```
281
prophylaxis for contacts of patients with meningococcal meningitis
``` Oral ciprofloxacin (preferred ) ( or rifampicin) ```
282
most useful prognostic marker in paracetamol overdose?
An elevated prothrombin time signifies liver failure in paracetamol overdose and is a marker of poor prognosis.
283
acute pericarditis management
1. combination of NSAID and colchicine
284
Otosclerosis describes the replacement of normal bone by vascular spongy bone. It causes a progressive conductive deafness due to fixation of the stapes at the oval window. Otosclerosis is autosomal dominant and typically affects young adults features
``` Onset is usually at 20-40 years - features include: conductive deafness tinnitus normal tympanic membrane* positive family history ```
285
Otosclerosis management
hearing aid
286
bstructive urinary calculi and signs of infection
urgent renal decompression and IV antibiotics due to the risk of sepsis
287
Sarcoidosis is a multisystem disorder of unknown aetiology characterised by non-caseating granulomas. It is more common in young adults and in people of African descent Features
acute: erythema nodosum, bilateral hilar lymphadenopathy, swinging fever, polyarthralgia insidious: dyspnoea, non-productive cough, malaise, weight loss skin: lupus pernio hypercalcaemia: macrophages inside the granulomas cause an increased conversion of vitamin D to its active form (1,25-dihydroxycholecalciferol)
288
Lyme disease management
Management of suspected/confirmed Lyme disease doxycycline if early disease. Amoxicillin is an alternative if doxycycline is contraindicated (e.g. pregnancy) people with erythema migrans should be commenced on antibiotic without the need for further tests ceftriaxone if disseminated disease Jarisch-Herxheimer reaction is sometimes seen after initiating therapy: fever, rash, tachycardia after first dose of antibiotic (more commonly seen in syphilis, another spirochaetal disease)
289
OCD management
he most appropriate initial management would be a form of low-intensity psychological therapy. NICE guidelines recommend exposure and response prevention as a beneficial therapy for patients with OCD. The use of selective serotonin re-uptake inhibitors is also recommended by NICE guidelines, but is typically commenced following a stepwise approach where non-pharmacological interventions are recommended first.
290
Chronic insomnia
may be diagnosed after three months, if a person has trouble falling asleep or staying asleep at least three nights per week
291
medication in insomnia
hypnotics: The hypnotics recommended for treating insomnia are short-acting benzodiazepines or non-benzodiazepines (zopiclone, zolpidem and zaleplon). Diazepam is not recommended but can be useful if the insomnia is linked to daytime anxiety. Use the lowest effective dose for the shortest period possible. If there has been no response to the first hypnotic, do not prescribe another. You should make the patient aware that repeat prescriptions are not usually given. It is important to review after 2 weeks and consider referral for cognitive behavioural therapy (CBT).
292
oculogyric crisis
oculogyric" refers to the bilateral elevation of the visual gaze, but several other responses are associated with the crisis. = dsytonia
293
Tricyclic antidepressants (TCAs) ie imipramine side effects
``` Common side-effects drowsiness dry mouth blurred vision constipation urinary retention lengthening of QT interval ``` antimuscarinic side-effects are more common with imipramine than other types of tricyclic antidepressants.
294
Akathisia
sense of inner restlessness and inability to keep still
295
Metformin should be stopped f when
following a myocardial infarction due to the risk of lactic acidosis.
296
typical carboxyhaemoglobin levels
3% non-smokers < 10% smokers 10 - 30% symptomatic: headache, vomiting > 30% severe toxicity
297
Drug-induced thrombocytopenia (probable immune-mediated)
quinine abciximab NSAIDs diuretics: furosemide antibiotics: penicillins, sulphonamides, rifampicin anticonvulsants: carbamazepine, valproate heparin
298
Ethylene glycol toxicity management (antifreeze)
Fomepizole (IV), an inhibitor of alcohol dehydrogenase, is used as the first-line treatment for ethylene glycol toxicity. Fomepizole is superior antidote than ethanol because it is safer and easy to dose and administer.
299
Contraindications of metformin
chronic kidney disease: NICE recommend that the dose should be reviewed if the creatinine is > 130 µmol/l (or eGFR < 45 ml/min) and stopped if the creatinine is > 150 µmol/l (or eGFR < 30 ml/min) metformin may cause lactic acidosis if taken during a period where there is tissue hypoxia. Examples include a recent myocardial infarction, sepsis, acute kidney injury and severe dehydration iodine-containing x-ray contrast media: examples include peripheral arterial angiography, coronary angiography, intravenous pyelography (IVP); there is an increasing risk of provoking renal impairment due to contrast nephropathy; metformin should be discontinued on the day of the procedure and for 48 hours thereafter alcohol abuse is a relative contraindication
300
Drugs to avoid in renal failure
antibiotics: tetracycline, nitrofurantoin NSAIDs lithium metformin
301
Drugs likely to accumulate in chronic kidney disease - need dose adjustment in renal failure
``` most antibiotics including penicillins, cephalosporins, vancomycin, gentamicin, streptomycin digoxin, atenolol methotrexate sulphonylureas furosemide opioids ```
302
Rifampicin tb
mechanism of action: inhibits bacterial DNA dependent RNA polymerase preventing transcription of DNA into mRNA potent liver enzyme inducer hepatitis, orange secretions flu-like symptoms
303
Isoniazid tb
mechanism of action: inhibits mycolic acid synthesis peripheral neuropathy: prevent with pyridoxine (Vitamin B6) hepatitis, agranulocytosis liver enzyme inhibitor
304
Pyrazinamide | tb
mechanism of action: converted by pyrazinamidase into pyrazinoic acid which in turn inhibits fatty acid synthase (FAS) I hyperuricaemia causing gout arthralgia, myalgia hepatitis
305
Ethambutol tb
mechanism of action: inhibits the enzyme arabinosyl transferase which polymerizes arabinose into arabinan optic neuritis: check visual acuity before and during treatment dose needs adjusting in patients with renal impairment
306
Methotrexate monitoring
FBC, LFT, U&E
307
Caution should always be exercised when combining diuretics. However, which one of the following combinations is always contraindicated?
Amiloride and spironolactone a | hyperkalemia
308
Steroid responsiveness COPD
Asthmatic features/features suggesting steroid responsiveness in COPD: previous diagnosis of asthma or atopy a higher blood eosinophil count substantial variation in FEV1 over time (at least 400 ml) substantial diurnal variation in peak expiratory flow (at least 20%)
309
Acromegaly: management
Trans-sphenoidal surgery is the first-line treatment for acromegaly in the majority of patients Dopamine agonists for example bromocriptine the first effective medical treatment for acromegaly, however now superseded by somatostatin analogues effective only in a minority of patients ``` Somatostatin analogue directly inhibits the release of growth hormone for example octreotide effective in 50-70% of patients may be used as an adjunct to surgery ``` Pegvisomant GH receptor antagonist - prevents dimerization of the GH receptor once daily s/c administration very effective - decreases IGF-1 levels in 90% of patients to normal doesn't reduce tumour volume therefore surgery still needed if mass effect
310
Drug-induced urinary retention
The following drugs may cause urinary retention: tricyclic antidepressants e.g. amitriptyline anticholinergics opioids NSAIDs disopyramide
311
Thyrotoxic storm treatment
beta blockers, propylthiouracil and hydrocortisone
312
ACR results
NICE recommendations for referral to a nephrologist: a urinary albumin:creatinine ratio (ACR) of 70 mg/mmol or more, unless known to be caused by diabetes and already appropriately treated a urinary ACR of 30 mg/mmol or more, together with persistent haematuria (two out of three dipstick tests show 1+ or more of blood) after exclusion of a urinary tract infection consider referral to a nephrologist for people with an ACR between 3-29 mg/mmol who have persistent haematuria and other risk factors such as a declining eGFR, or cardiovascular disease Management ACE inhibitors (or angiotensin II receptor blockers) are key in the management of proteinuria they should be used first-line in patients with coexistent hypertension and CKD if the ACR > 70 mg/mmol they are indicated regardless of the patient's blood pressure
313
open angle glaucoma treatment
NICE guidelines: first line: prostaglandin analogue (PGA) eyedrop second line: beta-blocker, carbonic anhydrase inhibitor, or sympathomimetic eyedrop if more advanced: surgery or laser treatment can be tried2
314
open angle glaucoma features
Features severe pain: may be ocular or headache decreased visual acuity symptoms worse with mydriasis (e.g. watching TV in a dark room) hard, red-eye haloes around lights semi-dilated non-reacting pupil corneal oedema results in dull or hazy cornea systemic upset may be seen, such as nausea and vomiting and even abdominal pain
315
Metformin predisposes to lactic acidosis
should therefore be used with caution in patients with acute kidney injury
316
adverse effects if metformin
dverse effects gastrointestinal upsets are common (nausea, anorexia, diarrhoea), intolerable in 20% reduced vitamin B12 absorption - rarely a clinical problem lactic acidosis* with severe liver disease or renal failure
317
Nerve at risk during a total hip replacement
Sciatic nerve
318
MRSA management
uppression of MRSA from a carrier once identified nose: mupirocin 2% in white soft paraffin, tds for 5 days skin: chlorhexidine gluconate, od for 5 days. Apply all over but particularly to the axilla, groin and perineum The following antibiotics are commonly used in the treatment of MRSA infections: vancomycin teicoplanin linezolid
319
Headache: red flags
compromised immunity, caused, for example, by HIV or immunosuppressive drugs age under 20 years and a history of malignancy a history of malignancy known to metastasis to the brain vomiting without other obvious cause worsening headache with fever sudden-onset headache reaching maximum intensity within 5 minutes - 'thunderclap' new-onset neurological deficit new-onset cognitive dysfunction change in personality impaired level of consciousness recent (typically within the past 3 months) head trauma headache triggered by cough, valsalva (trying to breathe out with nose and mouth blocked), sneeze or exercise orthostatic headache (headache that changes with posture) symptoms suggestive of giant cell arteritis or acute narrow-angle glaucoma a substantial change in the characteristics of their headache
320
mild to moderate dementia management
Acetylcholinesterase (AChE) inhibitors (donepezil, galantamine, and rivastigmine) [NICE, 2006; NICE, 2011]: These drugs can be used for mild to moderate Alzheimer's disease but must only be prescribed by healthcare professionals with expertise in this area ... Memantine is an option for managing Alzheimer's disease for people with: Moderate Alzheimer's disease who are intolerant of, or have a contraindication to, AChE inhibitors or Severe Alzheimer's disease.
321
tonsilitis criteria
``` The criteria are as follows: • Temperature >38ºC • Tender anterior cervical lymphadenopathy • Absence of a cough • Exudate present on tonsils ```
322
TURP syndrome what is this
TURP syndrome is a rare and life-threatening complication of transurethral resection of the prostate surgery. It is caused by irrigation with large volumes of glycine, which is hypo-osmolar and is systemically absorbed when prostatic venous sinuses are opened up during prostate resection. This results in hyponatremia, and when glycine is broken down by the liver into ammonia, hyper-ammonia and visual disturbances.
323
RF TURP syndrome
``` There are risk factors for developing TURP syndrome are : surgical time > 1 hr height of bag > 70cm resected > 60g large blood loss perforation large amount of fluid used poorly controlled CHF ```
324
Adhesive capsulitis presents
painful stiff shoulder with restriction of active and passive range of motion in abduction, internal and external rotation.
325
Sensineural hearing loss
t has a diverse range of pathologies including common causes such as: Presbycusis (most common) Noise-induced hearing loss Congenital infections (e.g. rubella, CMV) Neonatal complications (e.g. kernicterus or meningitis) Drug induced deafness (aminoglycosides). Vascular pathology (stroke, transient ischaemic attacks)
326
Pharmacodynamic interactions with Methotrexate
Trimethoprim and Methotrexate are anti-folate agents. This means that there is an increased risk of Methotrexate toxicity,
327
AKI following contrast risks
An increased risk of AKI is associated with: chronic kidney disease, diabetes with chronic kidney disease, heart failure, renal transplant, age 75 or over, hypovolaemia, increasing volume of contrast agent, and intra-arterial administration of contrast agent.
328
Pharmacological management of chronic COPD
Step 1 Starting with a Short acting B2 agonist (SABA)/ short acting muscarinic antagonist (SAMA). These are continued as the patient goes up the management steps. Step 2 For patients with persistent exacerbations but no asthmatic features (e.g. asthma/atopy history, raised eosinophils, reduced FEV1 or diurnal variations in peak flow) or evidence of steroid responsiveness then add a long acting B2 agonist (LABA) AND a long acting muscarinic antagonist (LAMA). For patients with persistent exacerbations with asthmatic features or evidence of steroid responsiveness increase management to long acting B2 agonist (LABA) and inhaled corticosteroid in combination (ICS). Step 3 If patients on a LABA + LAMA combination are still getting daily symptoms that affect their activities of daily living then a 3 month trial of LAMA + LABA + ICS should be considered. If this does not work then it should be reverted back to LABA + LAMA. If any patient on Step 2 is getting more than one severe or two moderate exacerbations in a year then LAMA + LABA + ICS should be started. Step 4 If patients are still symptomatic consider specialist referral.
329
drug induced lupus
Drug induced lupus (DIL) typically presents as a less severe form of systemic lupus erythematosus (SLE) which starts while taking an offending medication, and completely resolves after it is discontinued. Although DIL can present with any feature of SLE, the most common features are: Systemic upset (fever / fatigue / myalgia). Arthritis (non-erosive) or arthralgia. Serositis in the form of pleurisy or pericarditis. check for
330
Acquired melanocytic naevus
Acquired melanocytic naevus Occur in childhood and evolve through a number of steps: Junctional: flat + pigmented (due to melanocytes at the basal layer of the epidermis) Compound: raised + pigmented (due to melanocytes at the basal layer of the epidermis + deep in the dermis) Intradermal: raised + pale (due to melanocytes deep in the dermis)
331
Antibodies associated with dermatomyositis
constitutional symptoms, symmetrical muscle weakness and a characteristic rash (heliotrope rash, shawl rash, mechanic's hands). Creatine kinase is markedly raised and Anti-Jo1 antibodies are characteristically raised as well. A muscle biopsy will show evidence of Dermatomyositis.
332
Imatinib
Imatinib is a tyrosine kinase inhibitor treatment of chronic myeloid leukaemia (CML) in 2001. Common side effects include fluid retention, headache, diarrhoea, loss of appetite, weakness, nausea and vomiting, abdominal distension, oedema, rash, dizziness, and muscle cramps. Serious side effects may include myelosuppression, heart failure, and liver function abnormalities.
333
Causes of high output cardiac failure
auses of high output cardiac failure can be remembered by the mnemonic AAPPTT: ``` Anaemia Arteriovenous malformation Paget's disease Pregnancy Thyrotoxicosis Thiamine deficiency (wet Beri-Beri) ```
334
Complications of nephrotic syndrome
lose immunoglobulins in their urine. This is because the damage to the glomerular capillary walls causes increased permeability to proteins. This means that these patients are at an increased susceptibility to infection. In particular they are susceptible to staphylococcal and pneumococcal infections.
335
Peri-operative Management of Insulin Dependent Diabetes
Peri-operative management principles of insulin use are: Put the patient as early on the theatre list as possible minimising the amount of time the patient is nil by mouth. Stop long acting insulin the night before. Stop any other insulin and begin sliding scale insulin infusion from when the patient is placed nil by mouth. Continue infusion until patient is able to eat post-operatively. Switch to normal insulin regimen around their first meal.
336
broad complex tachycardia
A broad complex tachycardia will have a heart rate of more than 100 and widened QRS complexes. These patients can be stable or unstable. Patients with a broad complex tachycardia should be managed according to the ALS algorithm. All patients should be maintained on high flow oxygen and IV access obtained. Adverse signs are: ``` Blood pressure <90mmHg (systolic) Heart rate >150 Chest pain Heart failure If a patient displays adverse signs, the patient should be prepared for DC cardioversion. ``` If the patient is stable, they should be started on 300mg IV amiodarone over 1h followed by an infusion of 900mg amiodarone over 24h. The patient should be urgently reviewed by cardiology and intensive care.
337
Haemofiltration should be considered if the following are present;
``` Pulmonary oedema Refractory hyperkalaemia Severe metabolic acidosis Uraemia Drug overdose e.g. aspirin overdose ```
338
Muscle spasm pain in palliative care
The management of pain in palliative care patients in important but can be challenging, and a history is key to ascertaining the best course of treatment. Simple, conservative measures such as heat, massage and relaxation should always be considered. Transcutaneous electric nerve stimulation can be used if there is a specific trigger point. PO diazepam is the first line treatment for spasmodic pain, titrated to effect. Baclofen is a GABA receptor agonist may also be used as a second line.
339
Torsades de points
orsades de points is a polymorphic ventricular tachycardia, a heart rhythm that may arise in a patient with a prolonged QT interval. Patients present with feeling generally unwell, palpitations, chest pain, dizziness and syncope. Sudden cardiac death may also occur. Causes of torsades de points include; Abnormal electrolytes Drugs - clarithromycin, anti-psychotics, fluoxetine, cimetidine, lithium, sotalol Genetic conditions Treatment of torsades de points is primarily supportive using the ABCDE algorithm. DC cardioversion is indicated if the patient is unstable. Isoprenaline and pacing can be used if the patient is stable, and advice should be sought from a specialist.
340
chronic mesenteric ischaemia
Chronic mesenteric ischaemia typically presents in elderly patients. Patients have risk factors for arterial disease (smoking, diabetes, high cholesterol, previous MI etc.) or embolic disease (such as atrial fibrillation). Patients typically present with diffuse, colicky abdominal pain which is worse after eating. Weight loss is a common feature, as patients avoid eating due to the pain. There may be associated diarrhoea and melaena or haematochezia (secondary to mucosal sloughing). On physical examination there is commonly abdominal tenderness. An epigastric bruits may be present (secondary to turbulent flow in the narrowed vessels).
341
Management of narrow complex tachycardias (regular)
``` ABCDE adverse features (shock, syncope, heart failure, or myocardial ischaemia), emergency synchronised direct current (DC) cardioversion is indicated ``` trial vagal manoeuvres (carotid sinus massage or Valsalva manoeuvre). If vagal manoeuvres fail, adenosine should be administered (initially as a 6 mg intravenous bolus, and if this fails 12 mg followed by a further 12 mg is trialled).
342
Management of narrow complex tachycardias (irregular)
``` ABCDE adverse features (shock, syncope, heart failure, or myocardial ischaemia), emergency synchronised direct current (DC) cardioversion is indicated ``` Atrial fibrillation with onset less than 48 hours is typically managed with rhythm control (LMWH followed by flecainide if there is no structural heart disease, or amiodarone if there is structural heart disease). Atrial fibrillation with onset more than 48 hours is typically managed with rate control (i.e. metoprolol or bisoprolol or verapamil, or digoxin if there are signs of heart failure) and anticoagulation
343
investigation for aortic dissection diagnosis
CT angiogram is used to diagnose dissection
344
Acute causes of AR
Infective endocarditis, with valve destruction and leaflet perforation. It can also cause perivalvular abscesses, which can rupture into the left ventricle Aortic dissection, which can cause regurgitation by primarily impeding valve closure Traumatic rupture of the valve leaflets, caused by blunt chest trauma or deceleration injury Iatrogenic causes include balloon valvotomy or trans catheter aortic valve implantation (TAVI)
345
Chronic causes of AR
Chronic valvular causes of AR include: Calcific aortic valve disease (age related) Myxomatous degeneration Congenital disease e.g. bicuspid aortic valve Rheumatic heart disease - most common cause in the developing world Infective endocarditis Rheumatic causes e.g. rheumatoid arthritis, antiphospholipid syndrome Marfan's syndrome
346
Presentation of Acute AR
``` Sudden cardiovascular collapse Pulmonary oedema Pallor Sweating Peripheral vasoconstriction ``` (Early diastolic murmur)
347
Presentation of Chronic AR
Exertional dyspnoea Orthopnoea Paroxysmal nocturnal dyspnoea Stable angina can also develop in some patients with severe AR, even in the absence of coronary artery disease. This is due to reduction in diastolic coronary perfusion. (Early diastolic murmur)
348
Investigations for AR
Echocardiogram is the definitive investigation for aortic regurgitation (AR).
349
Surgical intervention in aortic regurgitation (AR) is indicated in the following situations
Significant enlargement of the ascending aorta Symptomatic AR Asymptomatic AR with the following parameter findings: Poor left ventricular ejection fraction (<= 50%) Left ventricular end diastolic diameter more than 70mm or left ventricular end systolic diameter mote than 50mm Infective endocarditis refractory to medical therapy
350
Aortic stenosis (AS) is associated with a classic triad of symptoms:
Heart failure Syncope Angina
351
ECG findings for AS
Increased QRS complex voltage Left axis deviation Poor R-wave progression
352
AS can be judged to be severe via the following parameters
Peak gradient > 40 mmHg (note, in severe left ventricular dysfunction, a low peak gradient can be falsely reassuring) Valve area < 1.0 cm^2 Aortic jet velocity >4 m/s
353
ndications for intervention in AS
All patients with symptomatic aortic stenosis Asymptomatic patients with a left ventricular ejection fraction (LVEF) < 50% Asymptomatic patients with an LVEF > 50% who are physically active, and who have symptoms or a fall in blood pressure during exercise testing Aortic valve peak velocity > 5.5 m/s^2 Severe calcification and peak velocity progression >= 0.3 m/s^2 Markedly elevated BNP levels without other explanation Severe pulmonary hypertension (pulmonary artery systolic pressure > 60mmHg)
354
intervention in AS
TAVI is favoured with patients with severe comorbidities, previous heart surgery, frailty, restricted mobility, and those older than 75 years of age. SAVR is favoured for patients who are low risk and less than 75 years of age.
355
CHADS2VASc score components
C: 1 point for congestive cardiac failure. H: 1 point for hypertension. A2: 2 points if the patient is aged 75 or over. D: 1 point if the patient has diabetes mellitus. S2: 2 points if the patient has previously had a stroke or transient ischaemic attack (TIA). V: 1 point if the patient has known vascular disease. A: 1 point if the patient is aged 65-74. Sc: 1 point if the patient is female.
356
Management of VF
Management is according to the Advanced Life Support guidelines: The initial priorities will be as for the Basic Life Support: ensure the airway is patent, check for signs of life (pulse and breathing), and commence CPR. Ventricular fibrillation is a shockable rhythm: the next step is to administer defibrillation (unsynchronised cardioversion using a 200 J biphasic shock). Chest compressions should then be resumed. 1 mg adrenaline (10 ml 1:10 000) plus 300 mg amiodarone should be administered after the 3rd shock. Adrenaline should subsequently be administered every 3-5 mins (after every alternate shock).
357
Management of pulseless Ventricular tachycardia (VT)
If there is no pulse the patient should be managed according to the Advanced Life Support algorithm: VT is a shockable rhythm so a 200 J bi-phasic (unsynchronised) shock should be administered. CPR should be resumed for 2 minutes before re-checking the rhythm. Intravenous adrenaline (1 mg of 10 ml 1:10 000 solution) and amiodarone (300 mg) should be administered after delivery of the 3rd shock. Adrenaline should be administered every 3-5 minutes thereafter (after every alternate shock).
358
Management of Ventricular tachycardia with a pulse with adverse features
If there is a pulse but the patient shows adverse features (shock, syncope, myocardial ischaemia, or heart failure) the patient should be managed according to the Resuscitation Council tachyarrhythmia algorithm: Administer a synchronised DC shock (up to 3 attempts). After seeking expert help amiodarone (300 mg intravenously over 10-20 minutes followed by 900 mg over 24 hours) should be administered.
359
Management of Ventricular tachycardia with a pulse with no adverse feature
Management of Ventricular tachycardia with a pulse with no adverse features Management is with amiodarone (300 mg intravenously over 20-60 minutes followed by 900 mg over 24 hours)
360
Signs of Cardiac Tamponade can be remembered by Beck's Triad.
Signs of Cardiac Tamponade can be remembered by Beck's Triad. Hypotension Quiet heart sounds Raised JVP
361
Bradyarrhythmias requiring pacemakers
Complete heart block (whether asymptomatic or symptomatic) Mobitz type 2 heart block (whether asymptomatic or symptomatic) Symptomatic sick sinus syndrome Permanent bradyarrhythmias caused by a myocardial infarct (typically anterior infarcts - arrhythmias caused by inferior infarcts tend to be temporary)
362
Tachyarrhythmias requiring pacemakers
Tachyarrhythmias requiring permanent pacing are those that are resistant to pharmacological therapy. These forms of permanent pacing are typically dual chamber (with one lead in the right atrium and one lead in the right ventricle). Bi-ventricular pacemaker (in which a 3rd wire is placed in a branch of the coronary sinus, to allow left ventricular pacing and ventricular synchronisation) is an option if the left ventricular ejection fraction is <35%.
363
Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy is the commonest genetic heart condition. It is often the cause of sudden cardiac death in young people and athletes. (AD) ``` Many patient are asymptomatic Generally presents in young adults Exertional syncope Shortness of breath Chest pain Palpitations Heart failure Double apex pulse Ejection systolic murmur at the lower left sternal edge that may get louder during exercise and reduce if lying supine. ```
364
ECG findings in MR
P-mitrale (a broad notched P wave due to left atrial enlargement) Right ventricular hypertrophy Right axis deviation.m
365
Causes of right heart strain
Right heart strain is caused by pathologies affecting the pulmonary vasculature such as ``` Pulmonary emboli Pulmonary hypertension Chronic lung disease Pulmonary stenosis Pneumothorax ```
366
ECG features of right heart strain
``` Sinus tachycardia (most common) Right ventricular strain pattern (ST depression and T wave inversion in right ventricle and inferior leads) RBBB Right axis deviation P pulmonale S1Q3T3 Atrial arrhythmias ```
367
Managment of AF
1.Aspirin Statin Sublingual GTN Beta blocker or rate limiting calcium channel blocker 2. beta blocker and long-acting dihydropyridine calcium channel blocker. 3. A 3rd medication should only be added if the patient is symptomatic despite 2 anti-anginal drugs. Coronary angiography should be arranged unless contraindicated as PCI may be required.
368
Contraindications in WPW
Digoxin and NDP-CCBs (e.g. verapamil) are contraindicated for long term use because they may precipitate ventricular fibrillation. If the patient is experiencing supraventricular tachycardia the management depends on whether the patient is stable or unstable, and if stable the type of arrhythmia:
369
prevent pathological fractures in bone metastases
Bisphosphonates and denosumab can be used to prevent pathological fractures in bone metastases. If the eGFR < 30, denosumab is preferred
370
Medical management of a miscarriage
vaginal misoprostol alone
371
drugs should be avoided in breast feeding
``` antibiotics: ciprofloxacin, tetracycline, chloramphenicol, sulphonamides psychiatric drugs: lithium, benzodiazepines aspirin carbimazole methotrexate sulfonylureas cytotoxic drugs amiodarone ```
372
loop diuretic. where do they act
inhibits the Na-K-Cl cotransporter in the thick ascending limb of the loop of Henle
373
Acute angle closure glaucoma and priamry assocaitions
Acute angle closure glaucoma | is associated with hypermetropia, where as primary open-angle glaucoma is associated with myopia
374
Water deprivation test: cranial DI
urine osmolality after fluid deprivation: low | urine osmolality after desmopressin: high
375
Nephrogenic DI water dep
urine osmolality after fluid deprivation: low | urine osmolality after desmopressin: low
376
Symptoms of Hypoalbuminaemia
``` Peripheral oedema (due to reduced oncotic pressure, fluid moves to tissues) - starts in ankles and progresses up the body Ascites ```
377
certain circumstances when the creatine equation may not be accurate. Examples include:
Amputation - reduced muscle mass and body weight Pregnancy Very high or low BMI High protein meals Under 18s - never validated Extremely old patients - never validated and likely to have low muscle mass
378
Hypercalcaemia is defined as correct calcium >2.65mmol/L. Management
Aggressive IV fluids (corrects dehydration, protects the kidneys and increases calcium excretion) Bisphosphonates (inhibits osteoclast activity reducing calcium release) Further management to prevent recurrence (depending on the cause): Chemotherapy (malignancy) Surgical resection (malignancy) Radiotherapy (malignancy) Steroids (sarcoidosis) Calcitonin Furosemide
379
Hypernatraemia is defined as serum sodium concentration >145mmol/L. Clinical Features
Lethargy Weakness Signs; Confusion Agitation Seizures Coma treat with IV fluids
380
Hyperphosphataemia may be treated with
phsophate binders (eg. sevelamer 800mg TDS PO during meals)
381
Clinical features of hypocalcaemia can be remembered by the mnemonic 'SPASMODIC'.
SPASMODIC: ``` S – Spasms (Trousseau's sign) P – Perioral parasthaesia A – Anxiety/Irritability S – Seizures M – Muscle tone increase (colic, dysphagia) O– Orientation impairment (i.e. confusion) D – Dermatitis I – Impetigo herpetiformis C – Chvostek's sign ```
382
Management of severe hypokalaemia
Management of severe hypokalaemia Severe: Continuous cardiac monitoring Check and correct magnesium (low magnesium causes renal potassium wasting) IV infusion of 1L 0.9% saline containing 40mmol potassium chloride. Note that maximum peripheral potassium infusion rate is 10mmol/hour. If faster rates required, a central line will neeed to be inserted Avoid glucose and bicarbonate solutions Treat cause(s)
383
The management of hyponatraemia depends on the cause:
``` Hypovolaemic: IV normal saline Treat underlying cause Euvoleamic: SIADH Fluid restriction ADH receptor antagonists (e.g. tolvaptan, deomeclocycline) Oral sodium and furosemide Hypothyroidism Levothyroxine Hypervolaemic: Fluid restriction Treat underlying cause ```
384
Causes of lactic acidosis
``` Tissue hypoxia (Type A) Shock (e.g. cardiogenic, hypovolaemic, haemorrhagic) Hypoxia Acute mesenteric ischaemia Limb ischaemia Severe anaemia Seizures Vigorous exercise Abnormalities in metabolism of lactate (Type B) Diabetic ketoacidosis Cancer Liver disease Inborn errors in metabolism Drugs: Metformin - impairs liver metabolism of lactate Aspirin ```
385
Normal anion gap acidosis is the result of one of three pathologies:
Increased loss of HCO3-, such as; Diarrhoea High output ileostomy Ureterosigmoidostomy Impaired kidney resorption (e.g. acetazolamide treatment) Renal tubular acidosis type 2 Hypoaldosteronism Adrenal insufficiency Mineralocorticoid receptor block (e.g. spironolactone treatment) ``` Increased production of H+, such as; Toluene poisoning Lysine or arginine administration (found in total parental nutrition) Decreased excretion of H+, such as; Renal tubular acidosis types 1 and 4 ```
386
Management of osteomalcia
A vitamin D level of < 25 nmol/L = deficiency, requires high dose treatment initially followed by maintenance treatment. A vitamin D level of between 25-50 nmol/L = insufficiency, can be treated with long term maintenance therapy alone. Lifestyle advice: Safe sun exposure Dietary intake of vitamin D and calcium Long term maintenance supplements
387
SIADH managment
Management revolves around offloading this excess water: ``` Fluid restriction (up to 750ml/day) and treat underlying cause ADH antagonists (e.g. tolvaptan, deomeclocycline) Oral sodium and furosemide ```
388
vestibular schwannomas which cranial nerves effected
Cranial nerves V, VII and VIII
389
cardiogenic shock | PAP CO and SVR
Pulmonary artery occlusion pressure - high CO - Low Systemic vascular resistance - high
390
Hypovolaemia | PAP CO and SVR
Pulmonary artery occlusion pressure - low CO - Low (decreased preload) Systemic vascular resistance - high
391
Septic shock | PAP CO and SVR
Pulmonary artery occlusion pressure - low CO - high Systemic vascular resistance - low
392
prophylaxis of oesophageal bleeding
A non-cardioselective B-blocker (NSBB) is used for the prophylaxis of oesophageal bleeding ie Propranolol
393
e investigation of choice for reflux nephropathy
Micturating cystography
394
safer opioid to use in patients with moderate to end-stage renal failure
Oxycodone
395
Klinefelter's syndrome is associated with
karyotype 47, XXY. Features often taller than average lack of secondary sexual characteristics small, firm testes infertile gynaecomastia - increased incidence of breast cancer elevated gonadotrophin levels but low testosterone Diagnosis is by karyotype (chromosomal analysis).
396
Oesophageal cancer
Dysphagia may be associated with weight loss, anorexia or vomiting during eating Past history may include Barrett's oesophagus, GORD, excessive smoking or alcohol use
397
Hypertrophic obstructive cardiomyopathy (HOCM) Management
``` Management Amiodarone Beta-blockers or verapamil for symptoms Cardioverter defibrillator Dual chamber pacemaker Endocarditis prophylaxis* ```
398
Drugs to avoid in HOCM
Drugs to avoid nitrates ACE-inhibitors inotropes
399
The British Thoracic Society (BTS) state that the following are the main indications for placing a chest tube in pleural infection:
Patients with frankly purulent or turbid/cloudy pleural fluid on sampling should receive prompt pleural space chest tube drainage. The presence of organisms identified by Gram stain and/or culture from a non-purulent pleural fluid sample indicates that pleural infection is established and should lead to prompt chest tube drainage. Pleural fluid pH < 7.2 in patients with suspected pleural infection indicates a need for chest tube drainage.
400
confirm stone diagnosis imagine (renal colic)
non contrast CT
401
pontaneous bacterial peritonitis: most common organism
E. coli
402
HRT for women at risk of venous thromboembolism
transdermal
403
Bile-acid malabsorption may be treated with c
cholestyramine
404
Hyperemesis gravidarum, diagnostic criteria triad:
5% pre-pregnancy weight loss dehydration electrolyte imbalance
405
Left ventricular hypertrophy and deep ST depression and T-wave inversions
hypertrophic obstructive cardiomyopathy.
406
Charcot's cholangitis triad:
fever, jaundice and right upper quadrant pain
407
Beta-blockers are contraindicated in patients with asthma when managing atrial fibrillation what do you give instead?
CCB ie n. Diltiazem
408
Blepharitis may be associated with
seborrhoeic dermatitis, dry eye syndrome and acne rosacea
409
osmotic diuretic that may be used in patients with raised ICP
IV mannitol
410
otitis media - Indications for antibiotics in children are:
Indications for antibiotics in children are: Perforated eardrum <2 years old and bilateral Present for ≥4 days <3 months old
411
Examples of acyanotic heart disease
Ventricular septal defect Coarctation of the aorta Patent ductus arteriosus
412
Types of brain tumours in children include:
Craniopharyngioma: originates from the pituitary gland and presents with homonymous hemianopia from pressure on the optic chiasm. Astrocytoma: graded from 1 (pilocytic astrocytoma) to 4 (glioblastoma multiforme). Grade 1 tumours have an excellent prognosis (95% 5 year survival). Grade 4 tumours have a poor prognosis (20% 5 year survival). Grade 4 astrocytomas may cross the corpus callosum, giving a characteristic 'butterfly glioma' appearance on CT. Ependymomas (tumours of the cells of the ventricular system) Meningioma (tumours of arachnoid cells of the meninges)
413
bronchiolitis obliterans organism
Whilst bronchiolitis obliterans is a relatively rare complication of bronchiolitis it is most commonly associated with adenovirus infection.
414
complication of RSV
Hyponatraemia is commonly seen as a complication in bronchiolitis caused by respiratory syncytial virus (RSV).
415
Congenital Adrenal Hyperplasia (CAH)
s a genetic defect in an enzyme in the synthesis of steroid hormones. Patients can present within a few weeks of birth, with evidence of vomiting and dehydration - suggests that this is the most common and also most severe of the CAH syndromes: classical “salt-wasting” 21-hydroxylase deficiency.
416
Calculating paediatric doses using WETFLAG
``` Weight: (Age + 4) * 2 Energy: 4J/kg Tube size: (Age/4) + 4 Fluids: 20ml/kg normal saline bolus (10ml/kg if septic, trauma or in heart failure) Lorazepam: 0.1mg/kg Adrenaline: 10 micrograms/kg Glucose: 2ml/kg of 10% dextrose ```
417
Glandular fever
EBV illness worsened by antibiotics Risk of speenic rupture -
418
Meconium ileus is managed with
with 'drip and suck' (stomach drainage with an NG ryles tube, and IV fluids), along with enemas to remove the sticky meconium. In severe cases, surgery may be necessary.