El Panico Flashcards

1
Q

No exclusion

A

Conjunctivitis
Fifth disease (slapped cheek)
Roseola
Infectious mononucleosis
Head lice
Threadworms
Hand, foot and mouth

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2
Q

What is the school exclusion time for scarlet fever?

A

24 hours after commencing antibiotics

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3
Q

What is the school exclusion for whooping cough?

A

2 days after commencing antibiotics

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4
Q

What is the school exclusion criteria for measles?

A

4 days from onset of rash

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5
Q

What is the school exclusion criteria for rubella?

A

5 days from the onset of rash?

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6
Q

What is the school exclusion criteria for chicken pox?

A

All lesions crusted over

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7
Q

What is the school exclusion criteria for mumps?

A

5 days from onset of swollen glands

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8
Q

What is the school exclusion criteria for impetigo?

A

Lesions crusted and healed

or

48 hours after commencing antibiotics

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9
Q

What is the school exclusion criteria for scabies?

A

Until treated

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10
Q

What is the school exclusion criteria for influenza?

A

Until recovered

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11
Q

What are the vaccinations that you receive at 2 months?

A

‘6-1 vaccine’ (diphtheria, tetanus, whooping cough, polio, Hib and hepatitis B)
Oral rotavirus vaccine
Men B

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12
Q

Vaccinations at three months?

A

‘6-1 vaccine’ (diphtheria, tetanus, whooping cough, polio, Hib and hepatitis B)
Oral rotavirus vaccine
PCV

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13
Q

Vaccination schedule at 4 months?

A

‘6-1 vaccine’ (diphtheria, tetanus, whooping cough, polio, Hib and hepatitis B)
Men B

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14
Q

Vaccination schedule

12 - 13 months

A

Hib/Men C
MMR
PCV
Men B

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15
Q

2-8 years vaccination schedule?

A

Flu vaccine

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16
Q

3-4 years

A

‘4-in-1 pre-school booster’ (diphtheria, tetanus, whooping cough and polio)
MMR

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17
Q

Vaccination schedule 12-13 years?

A

HPV vaccination

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18
Q

Vaccination schedule 13-18 years?

A

‘3-in-1 teenage booster’ (tetanus, diphtheria and polio)
Men ACWY

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19
Q

RR, SBP and HR for less than 1 year of age?

A

RR = 30-40

SBP = 70-90

HR = 110 - 160

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20
Q

RR, SBP and HR for 2-5 years of age?

A

RR = 25-30

SBP = 80-100

HR = 95-140

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21
Q

RR, SBP and HR for 5-12 years of age

A

RR = 20-25

SBP = 90-110

HR = 80-120

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22
Q

RR, SBP and HR forover 12 years?

A

RR= 15-20

SBP = 100-120

Pulse = 60-100

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23
Q

What is the weight of a macrosomic baby?

A

over 4000g

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24
Q

What is normal birth weight?

A

2500-4000

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25
What is low birth weight?
Less than 2500 g
26
What is very low borth weight?
Less than 1500 g
27
What is extremely low birth weight?
Less than 1000g
28
What is impossibly low birth weight?
less than 750g
29
What is avergae weekly weight gain of baby from 0-3 months?
200g
30
What is average weekly weight gain from 3-6 months?
150g
31
What is avergae weight gain from 6-9 months?
100g
32
What is average weekly weight gain from 9-12 months?
75-50g
33
How do you calculate weight of a baby that is less than 1 year old?
0.5 x age in months plus 4
34
How do you calculate the weight of a child that is 1-5 years old?
2 x age + 8
35
How do you calculate the weight of a child that is 6-10 years olf?
3 x age plus 7
36
What is blood volume in a baby\>
80 mls/kg
37
What is urine output for a child?
0.5-1ml/kg/hour
38
What is the insensible fluid loss for a child per day?
20ml/kg/day
39
What is the golden rule for fluid managmement in children (maintenance fluids)?
4ml/kg for the first 10 kg 2ml/kg for the next 10 kg 1ml/kilo for the next 10kg (0.9% NaCl / 5% dextrose +/- 0.15%KCL)
40
Blood pressure flow chart
41
How do thiazide diuretics work?
inhibiting **sodium** reabsorption at the beginning of the **distal** convoluted tubule (DCT) by blocking the thiazide-sensitive Na+-Cl− symporter. Since more sodium reaches the collecting duct then more potassium lost
42
What are the side effects of thiazide diuretics (10)?
* dehydration * postural hypotension * hyponatraemia, hypokalaemia, hypercalcaemia\* * gout * impaired glucose tolerance * impotence **_Rare adverse effects_** * thrombocytopaenia * agranulocytosis * photosensitivity rash * pancreatitis
43
What is stage 1 hypertension?
Clinic BP = 140/90 ABPM = 135/85
44
What is stage 2 hypertension?
160/100 150/95
45
What is severe hypertension?
Clinic values over 180 110
46
Whan do we start treating hypertension?
47
What is the choice of hypertensive in afrocarribean patient already on CCB?
ARB
48
What are the blood pressure targets for people under 80?
140/90 135/85
49
What are the blood pressure targets for people over 80?
150/90 145/85 (these are just 10 values more than the targets for people less than 80)
50
What can a GP do if meningococcal meningitis is suspected?
IM benzylpenicillin
51
What is baseline meningitis treatment?
IV cefotaxime
52
Under what circumstances do we not give IV cefotaxime?
Under 3 months or over 50 years we give IV cefotaxime plus amoxicillin If meningococcal we give IV benzylpenicillin or IV cefotaxime If listeria we give IV amoxicillin + gent
53
What are the components of a qSOFA?
Resp rate over 22 Altered mentition Systolic BP less than 100
54
What does a sofa score of 2 indicate?
overall mortality risk of approximately 10% in a general hospital population with suspected infection
55
What are the likely causative organisms for neonatal sepsis?
Group B strep (strep agalacticae) E.Coli Late-onset sepsis usually occurs via the transmission of pathogens from the environment post-delivery, coagulase-negative staphylococcal species such as Staphylococcus epidermidis, Gram-negative bacteria such as Pseudomonas aeruginosa, Klebsiella and Enterobacter, and fungal species
56
What is typical antibiotic therapy for neonatal sepsis?
Benzylpenicillin and gent are first line
57
What is antibiotic therapy for neutropenic sepsis?
Tazocin if patients are still febrile and unwell after 48 hours an alternative antibiotic such as meropenem is often prescribed +/- vancomycin
58
CURB 65
Patients with a CURB-65 score of 0 should be managed in the community. Patients with a CURB-65 score of 1 should have their Sa02 assessed which should be \>92% to be safely managed in the community and a CXR performed. If the CXR shows bilateral/multilobar shadowing hospital admission is advised. Patients with a CURB-65 score of 2 or more should be managed in hospital as this represents a severe community acquired pneumonia.
59
Management of pneumonia?
Management of low-severity community acquired pneumonia ## Footnote **amoxicillin** is first-line if penicillin allergic then use a macrolide or tetracycline NICE now recommend a 5 day course of antibiotics for patients with low severity community acquired pneumonia Management of moderate and high-severity community acquired pneumonia dual antibiotic therapy is recommended with **amoxicillin** and a **macrolide** a 7-10 day course is recommended NICE recommend considering a beta-lactamase stable penicillin such as **co-amoxiclav, ceftriaxone or piperacillin with tazobactam** and a macrolide in high-severity community acquired pneumonia
60
What are the causative bacteria for pneumonia?
Community acquired pneumonia (CAP) may be caused by the following infectious agents: Streptococcus pneumoniae (accounts for around 80% of cases) Haemophilus influenzae = COPD patients Staphylococcus aureus: commonly after influenza infection atypical pneumonias (e.g. Due to Mycoplasma pneumoniae) viruses Klebsiella pneumoniae is classically in alcoholics
61
Treatment for LUTI
Trimethoprim or nitrofurantoin. Alternative: amoxicillin or cephalosporin
62
Treatment for acute pyelonephritis
Broad-spectrum cephalosporin or quinolone
63
Treatment for acute prostatitis?
Quinolone or trimethoprim
64
Treatment for impetigo?
Topical hydrogen peroxide, topical fusidic acid oral flucloxacillin or erythromycin if widespread
65
Treatment for cellulitis and erysipelas
Flucloxacillin (clarithromycin, erythromycin or doxycycline if penicillin-allergic)
66
Treatment for cellulitis near the eyes or nose / animal bite?
Co-amoxiclav (doxycycline + metronidazole if penicillin-allergic)
67
Mastitis treatment (antibiotic)
Flucloxacillin
68
Throat infections / sinusitis antibiotic?
Phenoxymethylpenicillin
69
Otitis media anti-biotic?
Amoxicillin Erythromycin if allergic
70
Otitis externa antibiotic
Flucloxicillin | (plus steroid)
71
Peri-apical or peridontal abscess?
Amoxicillin
72
Gingivitis antibiotic
Metronidazole
73
Gonorrhoea antibiotic
IM ceftriaxone
74
Antibiotic for chlamydia
doxycycline (7 days) or azithromycin (1g od for one day, then 500mg od for two days)
75
Antibiotic therapy for PID
Oral ofloxacin + oral metronidazole OR intramuscular ceftriaxone + oral doxycycline + oral metronidazole
76
What is the antibiotic management for bacterial vaginosis?
Oral or topical metro or topical clindamycin
77
ABX for c.diff
First episode: metronidazole Second or subsequent episode of infection: vancomycin
78
Life threatening c.diff
for life-threatening infections a combination of oral vancomycin and intravenous metronidazole should be used
79
Campylobacter enteritis
Clari
80
Salmonella and shigellosis abx
Cipro
81
ECG changes for anteroseptal MI Coronary artery for anteroseptal
V1-V4 Left-anterior descending
82
ECG changes for inferior MI Coronary artery for inferior MI
2,3, aVF Right coronary artery
83
ECG changes for anterolaterl MI Coronary artery for anterolateral MI
1, AVL V4-6 LAD Left circumflex
84
Lateral MI ECG changes and artery
1, AVL, +/- V5-V6
85
Posterior MI ECG changes and coronary artery
Tall R waves V1-V2 Usually left circumflex, also right coronary artery
86
What are the ejection systolic murmurs?
louder on expiration * aortic stenosis * hypertrophic obstructive cardiomyopathy louder on inspiration * pulmonary stenosis * atrial septal defect also: tetralogy of Fallot
87
Holosystolic murmurs
Holosystolic (pansystolic) mitral/tricuspid regurgitation (high-pitched and 'blowing' in character) * tricuspid regurgitation becomes louder during inspiration, unlike mitral stenosis * during inspiration, the venous blood flow into the right atrium and ventricle are increased → increases the stroke volume of the right ventricle during systole ventricular septal defect ('harsh' in character)
88
Late systolic murmurs
Late systolic mitral valve prolapse coarctation of aorta
89
Early diastolic murmurs
Aortic regurgitation Graham steel murmur (pulmonary regurgitation)
90
Mid-late diastolic murmur
Mitral stenosis Austin flint murmur (severe aortic regurgitation 'rumbling in character'
91
Contunous machine like murmur
PDA
92
Describe venous hum
Continous hum below clavicles
93
Describe stills murmur
Low-pitched sound heard at lower left sternal edge
94
Describe heart sounds of TOGA
No murmur Loud S2 Prominent right ventricular impulse
95
describe murmur of tetralogy
Ejection systolic Upper left sternal edge (above stills murmur) Radiates to axilla
96
Describe tricuspid atresia murmur
Left upper sternal edge (same place as tetralogy, above stills) Prominent apical pulse
97
What does S1 correlate with?
Closure of mitral and tricuspid valves
98
What causes a soft S1?
Long PR or mitral regurgitation
99
What causes a loud S1?
Mitral stenosis
100
What does S2 correlate with?
Closure of the aortic and pulmonary valves
101
What causes a soft S2?
Aortic stenosis
102
What is a physiological cause of splitting of S2?
Inspiration
103
What correlates with S3?
Diastolic filling of the ventricle
104
When is a third heart sound considered normal
If under 30 May persist in women up to 50 years old
105
What are causes of S3?
Left ventricular failure (dilated cardiomyopathy) Constrictive pericarditis Mitral regurgitation
106
When might you hear S4
Aortic stenosis HOCM Hypertension
107
What causes the sound of S4
Atrial contraction against stiff ventrical (P wave)
108
What might you feel on the chest wall if they have a S4 heart sound?
Double apical impulse
109
What is the management of angina?
= beta blocker or calcium channel blocker first line. If CCB monotherapy, use **verapamil** or **diltiazem**. If using beta blocker and want to add ccb, add nifedipine/amlodipine/felodipine. If you can't tolerate these two drugs and want to better control add an adjunct. So prescribe 1 Then add another to make combination of beta blocker and nifedipine. If this combo isn't tolerated, try adding; long-acting **nitrate, ivabradine, nicorandil or ranolazine** Nicorandil is associated with ulcers that can occur anywhere along the gastrointestinal tract Nitrates require a nitrate-free interval each day to prevent tolerance
110
Post MI medications
Satan playing double bass Statin Dual antiplatelet therapy Beta blocker Ace inhibitor
111
Read over STEMI/NSTEMI
112
What is rate control for AF?
Beta blockers CCBs Digoxin (useful if coexistant heart failure)
113
Rhythm control in AF drug therapy
Sotalol Amiodarone Flecainide
114
Factors favouring rate control
Over 65 History of IHD
115
Factors favouring rhythm control
Under 65 Symptomatic First presentation Lone AF or AF secondary to corrected precipitant (e.g alcohol) Congestive heart failure
116
If CHA2DS2-VASc score suggests no need for anticoagulation what investigation is necessary?
echo to exclude valvular heart disease
117
Heart failure drug management
Ace inhibitor and Beta blocker Spironolactone Third-line treatment should be initiated by a specialist. Options include ivabradine, sacubitril-valsartan, hydralazine in combination with nitrate, digoxin and cardiac resynchronisation therapy
118
When is cardioversion indicated in VT?
If systolic BP is less than 90
119
What is drug therapy for VT?
Amiodarone Lidocaine Procainamide **VERAPAMIL SHOULD NOT BE USED**
120
Ventricular tachycardia with broad QRS. What is the formulation of amiodarone?
300mg IV over 20-60minutes 900mg over 24 hours
121
What are differentials for irregular broad QRS tachycardia?
AF with bundle branch block Pre-excited AF Polymorphic VT (torsades de pointes)
122
What is the treatment for narrow complex tachycardia with regular rhythm?
Vagal manouvres Adenosine 6mg, 12mg, 12mg
123
What is management of irregular narrow complex tachycardia?
Probably AF Control rate with beta blocker or diltiazem Consider digoxin or amiodarone
124
What is the most common cause of death after MI?
Ventricular fibrillation
125
What type of MI might cause AV block | (causes bradycardia)
Inferior
126
WHen does pericarditis occur after an MI?
Within the first 48 hours
127
When does dresslers syndrome occur after MI?
2-6 weeks after
128
What are the features of dresslers syndrome?
Fever Pleuritic pain Pericardial effusion Raised ESR
129
What is the cause of persistent ST elevation after MI?
Left verntricular aneurysm
130
What are the features of left ventricular free wall rupture?
Occurs 1-2 weeks after MI Acute heart failure Cardiac tamponade Raised JVP Pulsus paridoxus Diminished heart sounds
131
Pansystolic murmur post-MI
VSD Also has features of acute heart failure
132
Acute hypotension and pulmonary oedema after MI
Acute mitral regurgitation More common in infero=posterior infarction. May be due to ischaemia or rupture of papillary muscle
133
Blind therapy for IE
**_Native valve_** amoxicillin, consider adding low-dose gentamicin **_If penicillin allergic, MRSA or severe sepsis_** vancomycin + low-dose gentamicin **_If prosthetic valve_** vancomycin + rifampicin + low-dose gentamicin
134
What are the indications for surgery in IE?
* severe valvular incompetence * aortic abscess (often indicated by a lengthening PR interval) * infections resistant to antibiotics/fungal infections * cardiac failure refractory to standard medical treatment * recurrent emboli after antibiotic therapy
135
General rules for IE ABX therapy
If staph use flucloxacillin If strep use benzylpenicillin If prosthetic valve use rifampicin Back up always involves vancomycin and usually low-dose gent
136
Major bleeding with warfarin
Stop warfarin Give intravenous vitamin K 5mg Prothrombin complex concentrate - if not available then FFP\*
137
INR \> 8.0 Minor bleeding
Stop warfarin Give intravenous vitamin K 1-3mg Repeat dose of vitamin K if INR still too high after 24 hours Restart warfarin when INR \< 5.0
138
INR \> 8.0 No bleeding
Stop warfarin Give vitamin K 1-5mg by mouth, using the intravenous preparation orally Repeat dose of vitamin K if INR still too high after 24 hours Restart when INR \< 5.0
139
INR 5.0-8.0 Minor bleeding
Stop warfarin Give intravenous vitamin K 1-3mg Restart when INR \< 5.0
140
INR 5.0-8.0 No bleeding
Withhold 1 or 2 doses of warfarin Reduce subsequent maintenance dose
141
General rules for warfarin managment with high INR
Prothrombin complex concentrate only used when there is major bleeding If bleeding the vitamin K will be IV You always stop warfarin unless INR is 5-8 and no bleeding (in this case you withold 1-2 doses) Restart warfarin when INR less less than 5 Standard dose of vit K is 1-3mg (major bleeding dose is 5mg, oral dose is 1-5mg)
142
p450
143
Pneumothorax guidelines
144
COPD management
Essentially the patient will be on SABA and LABA if no steroid responsive features then add LAMA If steroid responsive then give inhjaled corticosteroids Then all of these medications as last line therapy
145
What are the features of severe asthma?
PEFR 33 - 50% best or predicted Can't complete sentences RR \> 25/min Pulse \> 110 bpm
146
What are the features of life threatening asthma?
* PEFR \< 33% best or predicted * Oxygen sats \< 92% * Silent chest, cyanosis or feeble respiratory effort * Bradycardia, dysrhythmia or hypotension * Exhaustion, confusion or coma Normal PCO2
147
Asthma management
In child under 5 SABA Then 8 week trial of moderate dose ICS Then final line therapy is SABA low dose ICS and LTRA - after that you refer to specialist In child 5-12 SABA Plus low dose ICS Plus LTRA Plus LABA (stop LTRA) Then increase steroids Then add theophyline
148
What is a classic history of bronchopulmonary aspergillosis?
bronchiectasis and eosinophilia bronchoconstriction: wheeze, cough, dyspnoea. Patients may have a previous label of asthma
149
What are investigations for allergic bronchopulmonary aspergillosis?
* eosinophilia * flitting CXR changes * positive radioallergosorbent (RAST) test to Aspergillus * positive IgG precipitins (not as positive as in aspergilloma) * raised IgE
150
What organism causes allergic bronchopulmonary aspergillosis?
Aspergillus spores
151
What is the management of allergic bronchopulmonary aspergillosis?
oral glucocorticoids itraconazole is sometimes introduced as a second-line agent
152
What is the new name for hypersensitivity pheumonitis?
Extrinsic allergic alveolitis
153
What type of hypersensitivity reaction is EAA?
Type 3 and type 4
154
What are examples of allergens that provoke EAA
* bird fanciers' lung: avian proteins from bird droppings * farmers lung: spores of Saccharopolyspora rectivirgula from wet hay (formerly Micropolyspora faeni) * malt workers' lung: Aspergillus clavatus * mushroom workers' lung: thermophilic actinomycetes\*
155
What is the presentation of EAA?
acute (occurs 4-8 hrs after exposure) * dyspnoea * dry cough * fever chronic (occurs weeks-months after exposure) * lethargy * dyspnoea * productive cough * anorexia and weight loss
156
What is the investigation for EAA?
Investigation ## Footnote imaging: upper/mid-zone fibrosis bronchoalveolar lavage: lymphocytosis serologic assays for specific IgG antibodies blood: NO eosinophilia (this is in contrast to allergic bronchopulmonary aspergillosis) (additionally, imaging shows bronchiectasis on bronchopulmonary aspergillosis)
157
Management of EAA
avoid precipitating factors oral glucocorticoids
158
What causes fibrosis of upper lobes?
Fibrosis of upper lobes: C- Coal worker's pneumoconiosis H - Histiocytosis/ hypersensitivity pneumonitis A - Ankylosing spondylitis R - Radiation T - Tuberculosis S - Silicosis/sarcoidosis
159
Which COPD patients are offered long-term oxygen therpay?
Assess patients if any of the following: * very severe airflow obstruction (FEV1 \< 30% predicted). Assessment should be 'considered' for patients with severe airflow obstruction (FEV1 30-49% predicted) * cyanosis * polycythaemia * peripheral oedema * raised jugular venous pressure * oxygen saturations less than or equal to 92% on room air Assessment is done by measuring arterial blood gases on 2 occasions at least 3 weeks apart in patients with stable COPD on optimal management. Offer LTOT to patients with a pO2 of \< 7.3 kPa or to those with a pO2 of 7.3 - 8 kPa and one of the following: * secondary polycythaemia * peripheral oedema * pulmonary hypertension Cannot be given to people who smoke Risk assessment should include falls assessment and risk of burns/fires
160
Features of 21-hydroxylase deficiency
virilisation of female genitalia precocious puberty in males 60-70% of patients have a salt-losing crisis at 1-3 wks of age
161
Features of 11-beta hydroxylase deficiency
virilisation of female genitalia precocious puberty in males hypertension hypokalaemia
162
Features of 17 hydroxylase deficiency
non-virilising in females inter-sex in boys hypertension
163
Features of androgen insensitivity?
Androgen insensitivity syndrome is an X-linked recessive condition due to end-organ resistance to testosterone causing genotypically male children (46XY) to have a female phenotype. Complete androgen insensitivity syndrome is the new term for testicular feminisation syndrome Features 'primary amennorhoea' undescended testes causing groin swellings breast development may occur as a result of conversion of testosterone to oestradiol
164
Management of androgen insensitivity?
Management ## Footnote counselling - raise child as female bilateral orchidectomy (increased risk of testicular cancer due to undescended testes) oestrogen therapy
165
What is the pathophysiology of kallmans?
X-linked Hypogonadotrophic hypogonadism
166
What are the features of kallmans?
* 'delayed puberty' * hypogonadism, cryptorchidism * anosmia * sex hormone levels are low * LH, FSH levels are inappropriately low/normal * patients are typically of normal or above average height
167
What are the features of kartagener's syndrome?
Primary ciliary dyskinesia Features * dextrocardia or complete situs inversus * bronchiectasis * recurrent sinusitis * subfertility (secondary to diminished sperm motility and defective ciliary action in the fallopian tubes)
168
What are the levels of sex hormones in klinefelters?
elevated gonadotrophin levels but low testosterone
169
What are the features of klinefelters?
* 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
170
What is the value of impaired fasting glucose?
A fasting glucose greater than or equal to 6.1 but less than 7.0 mmol/l implies impaired fasting glucose (IFG)
171
How to differentiate between secondary and tertiary hyperparathyroidism?
Secondary hyperthyroidism = high phosphate, Calcium is porportionatel MUCH lower than PTH Tertiary hyperthyroidism = high ALP Remember that secondary hyperparathyroidism is due to CKD. In response to PTH kidney should REABSORB calcium, EXCRETE phosphate and Start making vitamin D. However in CKD the kidneys suck, so it can't do these things. Hence, low calcium, high phosphate and low vit D.
172
Causes og hypoglycaemia in non-diabetic patients
* Exogenous drugs such alcohol, aspirin poisoning, pentamidine, quinine sulfate, ACE-inhibitor * Pituitary insufficiency * Liver failure * Addison's disease * Islet cell tumours eg insulinoma * Non-pancreatic neoplasms
173
Side effects of SGLT-2 inhibitors
genital infections, diabetic ketoacidosis, fourniers gangrene
174
Side effects of metformin
GI upset Lactic acidosis
175
What are the side effects of GLP-1 mimetics?
Nause Vomitting Pancreatitis
176
What are the side effects of insulin
weight gain, hypoglycaemia, lipodystrophy
177
Side effects of thiazolidinones
* weight gain * liver impairment: monitor LFTs * fluid retention - therefore contraindicated in heart failure. The risk of fluid retention is increased if the patient also takes insulin * recent studies have indicated an increased risk of fractures * bladder cancer: recent studies have shown an increased risk of bladder cancer in patients taking pioglitazone (hazard ratio 2.64)
178
How to pick your T2 diabetes medication?
Try lifestyle, if above 48 add metformin. If above 58 after adding metformin then add another drug. If still above 58 with two drugs then add a third (insulin therapy can be considered instead of adding a third drug) Target is 48 mmol with metformin If two drugs the target is now 53 _​Small tips:_ * Drugs that cause weight gain = sulphonylureas and thiazolidinones * Weight neutral = DPPIV * Weight loss = GLP-1 anologues and SGLT2 inhibitors * If heart failure then don't use thiazolidenones * Only ones really used in pregnancy is metformin and insulin * Gliptin in triple therapy can only be used with sulfonylurea * GLP-1's are last line if metformin tolerated * SGLT-1's are not used if metformin is not tolerated
179
What are the criteria for GLP-1 anologues?
Criteria for glucagon-like peptide1 (GLP1) mimetic (e.g. exenatide) ## Footnote if triple therapy is not effective, not tolerated or contraindicated then NICE advise that we consider combination therapy with metformin, a sulfonylurea and a glucagon-like peptide1 (GLP1) mimetic if: BMI \>= 35 kg/m² and specific psychological or other medical problems associated with obesity or BMI \< 35 kg/m² and for whom insulin therapy would have significant occupational implications or weight loss would benefit other significant obesity-related comorbidities **(basically people who need to lose weight and people who can't take insulin)** only continue if there is a reduction of at least 11 mmol/mol [1.0%] in HbA1c and a weight loss of at least 3% of initial body weight in 6 months. **Probably because they are very expensive! - Need to make sure they are working to justify using them.**
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Multiple endocrine neoplasia
181
What does MODY stand for?
Maturity-onset diabetes of the young
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What are the features of MODY?
development of type 2 diabetes mellitus in patients \< 25 years old ## Footnote typically develops in patients \< 25 years a family history of early onset diabetes is often present ketosis is not a feature at presentation patients with the most common form are very sensitive to sulfonylureas, insulin is not usually necessary
183
Side effects of thyroxine
* hyperthyroidism: due to over treatment * reduced bone mineral density * worsening of angina * atrial fibrillation
184
What is the most common type of thyroid cancer?
Papillary 65%, generally young females. Metastasis to cervical lymph nodes. Thyroglobulin can be used as a tumour marker. Characteristic Orphan Annie eyes on light microscopy. Good prognosis
185
What type of thyroid tumour presents as a solitary thyroid nodule?
Follicular adenoma
186
How do you differentiate between follicular adenoma and follicular carcinoma
Capsular invasion Follicular carcinoma = 20%, generally women \>50 years old. Metastasis to lung and bones. Thyroglobulin can be used as a tumour marker. Moderate prognosis
187
What thyroid cancer is predominantly comprised of C cells derived from neural crest tissue, raised serum calcitonin and has a genetic component?
Medullary thyroid
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If this thyroid cancer were to occur, it would most likely occur in elderly females
Anaplastic carcinoma Not responsive to treatment, can cause pressure symptoms
189
What type of thyroid cancer is associated with hashimotot's thyroiditis?
Lymphoma
190
What are the causes of primary hyperparathyroidism?
Solitary adenoma Hyperplasia Multiple adenoma Carcinoma
191
What conditions cause lower than expected HbA1c?
Sickle-cell anaemia GP6D deficiency Hereditary spherocytosis
192
What conditions may cause higher than expected HbA1c?
Vitamin B12/folic acid deficiency Iron-deficiency anaemia Splenectomy
193
What conditions will cause an increased total gas transfer (rate at which gas will diffuse from alveoli into the blood.
* asthma * pulmonary haemorrhage (Wegener's, Goodpasture's) * left-to-right cardiac shunts * polycythaemia * hyperkinetic states * male gender, exercise
194
Causes of decreased TLCO?
* pulmonary fibrosis * pneumonia * pulmonary emboli * pulmonary oedema * emphysema * anaemia * low cardiac output
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KCO also tends to increase with age. Some conditions may cause an increased KCO with a normal or reduced TLCO corrected for lung volume (transfer coefficient, KCO)
* pneumonectomy/lobectomy * scoliosis/kyphosis * neuromuscular weakness * ankylosis of costovertebral joints e.g. ankylosing spondylitis
196
Antibodies in Graves and Hashimotos?
Graves = TSH receptor stimulating antibodies and anti thyroid peroxidase antibodies Hashimotos = Anti-thyroid peroxidase and anti thyroglobulin antibodies
197
What are the features of De Quervains thyroiditis?
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**
198
What are causes of adrenal failure?
* Autoimmune * tuberculosis * metastases (e.g. bronchial carcinoma) * meningococcal septicaemia (Waterhouse-Friderichsen syndrome) * HIV * antiphospholipid syndrome
199
Causes of gynaecomastia?
* physiological: normal in puberty * syndromes with androgen deficiency: Kallman's, Klinefelter's * testicular failure: e.g. mumps * liver disease * testicular cancer e.g. seminoma secreting hCG * ectopic tumour secretion * hyperthyroidism * haemodialysis * drugs: see below * spironolactone (most common drug cause) * cimetidine * digoxin * cannabis * finasteride * GnRH agonists e.g. goserelin, buserelin * oestrogens, anabolic steroids
200
What type of metabolic disturbance does cushings cause?
Hypokalaemic metabolic alkalosis
201
What is a neuroblastoma?
Neuroblastoma is one of the top five causes of cancer in children, accounting for around 7-8% of childhood malignancies. The tumour arises from neural crest tissue of the adrenal medulla (the most common site) and sympathetic nervous system.
202
What are the features of a neuroblastoma?
* abdominal mass * pallor, weight loss * bone pain, limp * hepatomegaly * paraplegia * proptosis
203
What are the investigations for a neuroblastoma?
* raised urinary vanillylmandelic acid (VMA) and homovanillic acid (HVA) levels * calcification may be seen on abdominal x-ray * biopsy
204
What does nuclear scintigraphy show for a toxic multinodular goitre
Patchy uptake Treatment is radioiodine therapy
205
What is the AKI criteria?
increase in serum creatinine by 26.5 mol/l within 48 hours, increase in serum creatinine to 1.5 times baseline, or urine volume \< 0.5 ml/kg/h for 6 hours.
206
What is protocol for DC cardioversion in a patient with AF lasting longer than 48 hours?
* anticoagulation should be given for at least 3 weeks prior to cardioversion. * An alternative strategy is to perform a transoesophageal echo (TOE) to exclude a left atrial appendage (LAA) thrombus. If excluded patients may be heparinised and cardioverted immediately * If there is a high risk of cardioversion failure (e.g. Previous failure or AF recurrence) then it is recommend to have at least 4 weeks amiodarone or sotalol prior to electrical cardioversion * Following electrical cardioversion patients should be anticoagulated for at least 4 weeks. After this time decisions about anticoagulation should be taken on an individual basis depending on the risk of recurrence
207
What is the nephrotic syndrome triad?
Triad of: ## Footnote 1. Proteinuria (\> 3g/24hr) causing 2. Hypoalbuminaemia (\< 30g/L) and 3. Oedema
208
Why does nephrotic syndrome lead to predisposition to thrombosis?
Loss of antithrombin-III, proteins C and S and an associated rise in fibrinogen levels predispose to thrombosis. Loss of thyroxine-binding globulin lowers the total, but not free, thyroxine levels.
209
Exampleas of nephritic vs Nephrotic syndromes
210
What are causes of rapidly progressive glomerulonephritis?
Goodpasture's syndrome Wegener's granulomatosis others: SLE, microscopic polyarteritis
211
What structure is formed in the majority of glomeruli in RPGN?
Crescents
212
What are features of RPGN?
* nephritic syndrome: haematuria with red cell casts, proteinuria, hypertension, oliguria * features specific to underlying cause (e.g. haemoptysis with Goodpasture's, vasculitic rash or sinusitis with Wegener's)
213
What is the classic presentation of IgA nephropathy?
macroscopic haematuria in young people following an upper respiratory tract infection.
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How you differentiate between IgA nephropathy and Post-strep glomerulonephritis?
Differentiating between IgA nephropathy and post-streptococcal glomerulonephritis * post-streptococcal glomerulonephritis is associated with low complement levels * main symptom in post-streptococcal glomerulonephritis is proteinuria (although haematuria can occur) * there is typically an interval between URTI and the onset of renal problems in post-streptococcal glomerulonephritis
215
Histology findings for IgA nephropathy?
histology: mesangial hypercellularity, positive immunofluorescence for IgA & C3
216
What are causes of type 1 membranoproliferative glomerulonephritis?
Type 1 ## Footnote accounts for 90% of cases cause: **cryoglobulinaemia, hepatitis C** renal biopsy electron microscopy: subendothelial and mesangium immune deposits of electron-dense material resulting in a 'tram-track' appearance
217
Type 2 membranoproliferative glomerulonephritis on histology
electron microscopy: intramembranous immune complex deposits with 'dense deposits'
218
What causes post-strep glomerulonephritis?
Post-streptococcal glomerulonephritis typically occurs 7-14 days following a group A beta-haemolytic Streptococcus infection (usually Streptococcus pyogenes). It is caused by immune complex (IgG, IgM and C3) deposition in the glomeruli. Young children are most commonly affected. C3 deposited hence low C3
219
What are renal biopsy features of post-strep glomerulonephritis?
* post-streptococcal glomerulonephritis causes acute, diffuse proliferative glomerulonephritis * endothelial proliferation with neutrophils * electron microscopy: subepithelial 'humps' caused by lumpy immune complex deposits * immunofluorescence: granular or 'starry sky' appearance
220
What are the common causes of minimal change disease?
The majority of cases are idiopathic, but in around 10-20% a cause is found: drugs: NSAIDs, rifampicin Hodgkin's lymphoma, thymoma infectious mononucleosis
221
What does renal biopsy show for minimal change disease?
normal glomeruli on light microscopy electron microscopy shows fusion of podocytes and effacement of foot processes
222
What is blood pressure in minimal change
normotension - hypertension is rare
223
What is the commonest cause of glomerulonephritis in adults?
Membranous glomerulonephritis
224
What does renal biopsy show for membranous glomerulonephritis?
electron microscopy: the basement membrane is thickened with subepithelial electron dense deposits. This creates a 'spike and dome' appearance
225
What are causes of membranous glomerulonephritis?
* idiopathic: **due to anti-phospholipase A2 antibodies** * infections: hepatitis B, malaria, syphilis * malignancy (in 5-20%): prostate, lung, lymphoma, leukaemia * drugs: gold, penicillamine, NSAIDs * autoimmune diseases: systemic lupus erythematosus (class V disease), thyroiditis, rheumatoid
226
What is the management of membranous glomerulonephritis?
Management * all patients should receive an ACE inhibitor or an angiotensin II receptor blocker (ARB): * these have been shown to reduce proteinuria and improve prognosis * immunosuppression * as many patients spontaneously improve only patient with severe or progressive disease require immunosuppression * corticosteroids alone have not been shown to be effective. A combination of corticosteroid + another agent such as cyclophosphamide is often used * consider anticoagulation for high-risk patients
227
What are the features of FSGS on renal biopsy?
* focal and segmental sclerosis and hyalinosis on light microscopy * effacement of foot processes on electron microscopy
228
What are indications for dialysis in AKI?
Indications for dialysis in acute kidney injury: Acute renal dialysis indications- HAVEPEE * H- hyperkalaemia (refractory) * A-acidosis (refractory) * V- volume overload * E- elevated urea * P- pericarditis * E- encephalopathy * E- (o)Edema (pulmonary)
229
What type of reaction occurs after erythromycin and simvastatin?
Rhabdomyolysis
230
What drug can cause acute interstitial nephritis?
Penicillin
231
If kidneys can no longer concentrate urine, what is the urine osmolality and urine sodium?
Urine osmolality is low, urine sodium is high (because kidneys try to retain sodium)
232
Core features of churg strauss
Features ## Footnote asthma blood eosinophilia (e.g. \> 10%) paranasal sinusitis mononeuritis multiplex pANCA positive in 60%
233
What are the core features of granulomatosis with polyangitis?
Features * upper respiratory tract: epistaxis, sinusitis, nasal crusting * lower respiratory tract: dyspnoea, haemoptysis * rapidly progressive glomerulonephritis ('pauci-immune', 80% of patients) * saddle-shape nose deformity * also: vasculitic rash, eye involvement (e.g. proptosis), cranial nerve lesions
234
What are the variables for eGFR?
eGFR variables - CAGE - Creatinine, Age, Gender, Ethnicity
235
Causes of cranial DI?
* idiopathic * post head injury * pituitary surgery * craniopharyngiomas * histiocytosis X * DIDMOAD is the association of cranial Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy and Deafness (also known as Wolfram's syndrome) * haemochromatosis
236
What are causes of nephrogenic DI?
* genetic: the more common form affects the vasopression (ADH) receptor, the less common form results from a mutation in the gene that encodes the aquaporin 2 channel * electrolytes: hypercalcaemia, hypokalaemia * lithium * lithium desensitizes the kidney's ability to respond to ADH in the collecting ducts * demeclocycline * tubulo-interstitial disease: obstruction, sickle-cell, pyelonephritis
237
What are the rules for drivin gafter an MI?
Driving Post-MI * For a car/motorcycle licence, you do not need to tell the DVLA * Can recommence driving after 1 week if successfully treated with coronary angioplasty * If not successfully treated with coronary angioplasty, can commence driving after 4 weeks * For a bus, coach or lorry licence - must tell DVLA and stop driving for 6 weeks. Assessment with doctor after 6 weeks to see if meet medical standard to start driving again.
238
What are the rules for driving with an arrhythmia?
* Must not drive if arrythmia has caused or is likely to cause incapacity * Drive 4 weeks after underlying cause of arrythmia has been found and the arrythmia has been controlled * If they drive a bus, coach or lorry, licence will be revoked and only be reinstated after an underlying cause has been identified, the arrythmia has been controlled for 3 months, and they have an LV ejection fraction of \>40%. So cars = drive after 1 month of control Buses = drive after 3 months of control
239
What are the neurological symptoms that can present via Wilsons disease?
Neurological problems may manifest as dementia, tremor or dyskinesias. - Wilson’s disease
240
Features of wilsons disease?
Features result from excessive copper deposition in the tissues, especially the brain, liver and cornea: ## Footnote liver: hepatitis, cirrhosis neurological: basal ganglia degeneration: in the brain, most copper is deposited in the basal ganglia, particularly in the putamen and globus pallidus speech, behavioural and psychiatric problems are often the first manifestations also: asterixis, chorea, dementia, parkinsonism Kayser-Fleischer rings green-brown rings in the periphery of the iris due to copper accumulation in Descemet membrane present in around 50% of patients with isolated hepatic Wilson's disease and 90% who have neurological involvement renal tubular acidosis (esp. Fanconi syndrome) haemolysis blue nails
241
What are the levels of serum caeruloplasmin, total serum copperin and free serum copper in Wilson's disease?
* reduced serum caeruloplasmin * reduced total serum copper (counter-intuitive, but 95% of plasma copper is carried by ceruloplasmin) * free (non-ceruloplasmin-bound) serum copper is increased * increased 24hr urinary copper excretion
242
What electron changes are typical of refeeding syndrome?
low potassium, low magnesium and low phosphate and fluid shifts
243
What is the management of H.Pylori?
a proton pump inhibitor + amoxicillin + (clarithromycin OR metronidazole)
244
RUQ pain- colic RUQ pain plus fever- cholecystitis RUQ pain plus fever plus jaundice (charcot triad)- cholangitis epigastric pain- more likely pancreatitis RUQ pain plus jaundice (no fever) - choledocholithiasis
245
How do you interpret ABPI?
246
What does a raised SAAG of over 11 g/L indicate?
portal hypertension that has caused the ascites
247
What are causes of ascites with SAAG over 11?
Liver disorders are the most common cause * cirrhosis/alcoholic liver disease * acute liver failure * liver metastases Cardiac * right heart failure * constrictive pericarditis Other causes * Budd-Chiari syndrome * portal vein thrombosis * veno-occlusive disease * myxoedema
248
Causes of SAAG less than 11
Hypoalbuminaemia * nephrotic syndrome * severe malnutrition (e.g. Kwashiorkor) Malignancy * peritoneal carcinomatosis Infections * tuberculous peritonitis Other causes * pancreatitisis * bowel obstruction * biliary ascites * postoperative lymphatic leak * serositis in connective tissue diseases
249
TACS
involves middle and anterior cerebral arteries all 3 of the criteria are present 1. unilateral hemiparesis and/or hemisensory loss of the face, arm & leg 2. homonymous hemianopia 3. higher cognitive dysfunction e.g. dysphasia
250
PACs
involves smaller arteries of anterior circulation e.g. upper or lower division of middle cerebral artery 2 of the criteria are present 1. unilateral hemiparesis and/or hemisensory loss of the face, arm & leg 2. homonymous hemianopia 3. higher cognitive dysfunction e.g. dysphasia
251
Lacunar Infarcts
involves perforating arteries around the internal capsule, thalamus and basal ganglia presents with 1 of the following: 1. unilateral weakness (and/or sensory deficit) of face and arm, arm and leg or all three. 2. pure sensory stroke. 3. ataxic hemiparesis
252
Posterior circulation infarct
involves vertebrobasilar arteries presents with 1 of the following: 1. cerebellar or brainstem syndromes 2. loss of consciousness 3. isolated homonymous hemianopia
253
Stroke affecting anterior cerebral artery?
Contralateral hemiparesis and sensory loss, **lower extremity \> upper**
254
Middle cerebral artery
Contralateral hemiparesis and sensory loss, upper extremity \> lower Contralateral homonymous hemianopia Aphasia
255
Posterior cerebral artery
Contralateral homonymous hemianopia with macular sparing Visual agnosia (Notice pure visual)
256
Weber's Syndrome (branches of the posterior cerebral artery that supply the midbrain)
Ipsilateral CN III palsy Contralateral weakness of upper and lower extremity
257
Wallenberg syndrome? (posterior inferior cerebellar artery)
Ipsilateral: facial pain and temperature loss Contralateral: limb/torso pain and temperature loss Ataxia, nystagmus
258
Anterior inferior cerebellar artery
Symptoms are similar to Wallenberg's (see above), but: Ipsilateral: facial paralysis and deafness
259
Stroke in retinal / ophthalmic artery?
Amaurosis fugax
260
Stroke in what location causes locked in syndrome?
Basilar artery
261
What is another term used to describe 1. Wallenberg syndrome (posterior inferior cerebellar artery) 2. Anterior inferior cerebellar artery stroke?
1. Lateral medullary syndrome 1. Lateral pontine syndrome
262
Surgical management of achalasia
Heller cardiomyotomty
263
a surgical procedure used to strengthen and tighten the lower oesophageal sphincter in patients suffering from severe gastro-oesophageal reflux disease (GORD).
Nissen fundoplication
264
What is involved in whipple procedure?
A Whipple procedure is a surgical procedure used for the treatment of pancreatic cancers. It removes the head of the pancreas, the duodenum, the gallbladder and the bile duct.
265
What is the Sister Mary Joseph node
Sister Mary Joseph node is a palpable nodule in the umbilicus due to metastasis of malignant cancer within the pelvis or abdomen
266
Why does thrombocytopenia occur in liver cirrhosis?
'Multiple factors, including splenic sequestration, reduced activity of the hematopoietic growth factor thrombopoietin, bone marrow suppression by chronic hepatitis C virus infection and anti-cancer agents, and antiviral treatment with interferon-based therapy, can contribute to the development of thrombocytopenia in cirrhotic patients'.
267
What is the investigation for pancreatic cancer?
High Res CT
268
What is first line management for constipation in patients with IBS?
Isphagula husk
269
Where would you find signet ring cells?
Gastric adenocarcinoma - signet ring cells
270
What causes carcinoid syndrome?
usually occurs when metastases are present in the liver and release serotonin into the systemic circulation may also occur with lung carcinoid as mediators are not 'cleared' by the liver
271
What are the features of carcinoid syndrome?
* flushing (often earliest symptom) * diarrhoea * bronchospasm * hypotension * right heart valvular stenosis (left heart can be affected in bronchial carcinoid) * other molecules such as ACTH and GHRH may also be secreted resulting in, for example, Cushing's syndrome * pellagra can rarely develop as dietary tryptophan is diverted to serotonin by the tumour Carcinoid syndrome can affect the right side of the heart. The valvular effects are tricuspid insufficiency and pulmonary stenosis
272
What are the grades of hepatic encephalopathy?
Grade I: Irritability Grade II: Confusion, inappropriate behaviour Grade III: Incoherent, restless Grade IV: Coma
273
What are the electrolyte abnormalities seen in tumour lysis syndrome?
It leads to a high potassium and high phosphate level in the presence of a low calcium
274
What are complications of tumour lysis syndrome?
Complications of tumour lysis syndrome: * hyperkalaemia * hyperphosphataemia * hypocalcaemia * hyperuricaemia * acute renal failure
275
General rules for DVT management
Wells of 2 or more * Skip D-Dimer * Do doppler - if positive then start DOAC, if negative do D-dimer * If D-dimer comes back positive (scan negative) stop any DOACs, repeat doppler 6-8 days later * If doppler is going to take a 4 hours or more - do D-dimer and start DOAC Wells of 1 or less * Do D-dimer * DOAC if D-dimer is going to take more than 4 hours * if D-dimer is positive then do doppler * If doppler is going to take more than 4 hours then DOAC should be started
276
General rules for PE management
DOAC LMWH followed by VKA (warfarin) for Severe renal impairment and antiphospholipid syndrome. 3 months of anticoagulation for provoked 6 months of anticoagulation for unprovoked
277
What disease is this? * monoclonal IgM paraproteinaemia * systemic upset: weight loss, lethargy * hyperviscosity syndrome e.g. visual disturbance * the pentameric configuration of IgM increases serum viscosity * hepatosplenomegaly * lymphadenopathy * cryoglobulinaemia e.g. Raynaud's
Waldenstorm's macroglubulinaemia
278
In sickle cell, what causes; 1. Low reticulocyte count 2. High reticulocyte count
1. Parvovirus 2. Acute sequestration and haemolysis
279
What is the diagnostic criteria for myeloma?
**one major and one minor criteria or three minor criteria in an individual who has signs or symptoms of multiple myeloma.** **_Major criteria_** Plasmacytoma (as demonstrated on evaluation of biopsy specimen) 30% plasma cells in a bone marrow sample Elevated levels of M protein in the blood or urine **_Minor criteria_** 10% to 30% plasma cells in a bone marrow sample. Minor elevations in the level of M protein in the blood or urine. Osteolytic lesions (as demonstrated on imaging studies). Low levels of antibodies (not produced by the cancer cells) in the blood.
280
What is the definition of normocytic anaemia?
normocytic anaemia, leukopenia and thrombocytopenia is the definition of aplastic anaemia
281
How does Rivaroxaban, Apixaban, Dabigatran and Heparin work?
Rivaroxaban is a direct factor Xa inhibitor. Apixaban is also a direct factor Xa inhibitor. Dabigatran is a direct thrombin inhibitor. Heparin activates antithrombin III.
282
How does beta thalassaemia show up on lab results?
Mild anaemia with big reduction in MCV = beta thalassaemia
283
Intravascular hemolysis occurs when erythrocytes are destroyed in the blood vessel itself, whereas extravascular hemolysis occurs in the hepatic and splenic macrophages within the reticuloendothelial system. Intravascular hemolysis is often dramatic, with free hemoglobin released into the plasma leading to hemoglobinuria (positive blood on urine dipstick but few erythrocytes on microscopic examination). Examples of intravascular hemolysis include enzyme defects such as glucose-6-phosphate dehydrogenase (G6PD) deficiency or certain immune-mediated processes. Extravascular hemolysis usually results from more subtle RBC destruction, typically with chronic splenic enlargement and jaundice. Extravascular hemolysis is more common with RBC membrane disorders such as hereditary spherocytosis.
284
What are the features of hodgkin lymphoma?
Reed-sternberg cell Bimodal age distribution (3rd and 7th decades) * lymphadenopathy (75%) - painless, non-tender, asymmetrical * systemic (25%): weight loss, pruritus, night sweats, fever (Pel-Ebstein) * alcohol pain in HL * normocytic anaemia, eosinophilia * LDH raised B-symptoms with blood findings and alcohol pain
285
What are the histological classifications of Hodgkin's lymphoma?
286
Describe a reed-sternberg cell
Reed-sterberg cell: either multinucleated or have a bilobed nucleus with prominent eosinophilic inclusion-like nucleoli (thus resembling an "owl's eye" appearance).
287
What are thresholds for platelet transfusion?
30 with clinically significant bleeding 100 for severe bleeding or bleeding at critical sites such as the CNS Platelet transfusion for thrombocytopenia before surgery/ an invasive procedure. Aim for plt levels of: * \> 50×109/L for most patients * 50-75×109/L if high risk of bleeding * \>100×109/L if surgery at critical site A threshold of 10 x 109 except where platelet transfusion is contradindicated or there are alternative treatments for their condition For example, do not perform platelet transfusion for any of the following conditions: * Chronic bone marrow failure * Autoimmune thrombocytopenia * Heparin-induced thrombocytopenia, or * Thrombotic thrombocytopenic purpura.
288
What are the live attenuated vaccines?
BCG MMR Influenza (intranasal) Oral rotavirus Oral Polio Yellow Fever Oral typhoid
289
what are inactivated preparations of vaiccine
Rabies Hepatitis A Influenza (IM)
290
Which vaccinations are toxoid?
Tetanus Diptheria Pertussis
291
Which bacteria have the following incubation periods? 1. 1-6 hours 2. 12-48 hours 3. 48-72 hours 4. \> 7 days
1-6 hrs: Staphylococcus aureus, Bacillus cereus\* 12-48 hrs: Salmonella, Escherichia coli 48-72 hrs: Shigella, Campylobacter \> 7 days: Giardiasis, Amoebiasis
292
What type of HPV causes genital warts?
Genital warts, They are caused by the many varieties of the human papillomavirus HPV, especially types **6 & 11**. It is now well established that HPV (primarily types 16,18 & 33) predisposes to cervical cancer.
293
Descriptions of genital ulcers 1. Herpes 2. Syphillis 3. Chancroid (haemophylus ducreyi) 4. LGV
1. Herpes = painful ulcers 2. Syphillis = Painless ulcer (chancre). Local non-tender lymphadenopathy. 3. Chancroid = Painful ulcer, unilateral painful inguinal lymphadenopathy 4. LGV = Painless ulcer, painful inguinal lymphadenopathy
294
What are primary, secondary and tertiary features of syphillis?
Primary = chancre, non-tender lymphadenopathy Secondary = Fever, rash, buccal snail track ulcers, condylomata lata (painless warty lesions on the genitalia) Tertiary = Gummas, ascending aortic aneurysms, generaly paralysis of the insane, tabes dorsales, Argyll - Robertson Pupil
295
Features of Congenital Syphilis?
* blunted upper incisor teeth (Hutchinson's teeth), 'mulberry' molars * rhagades (linear scars at the angle of the mouth) * keratitis * saber shins * saddle nose * deafness
296
How does pneumocystis jiroveci present?
This is a fungal infection which classically affects patients with HIV. It classically presents with a dry cough, exercise-induced desaturations and the absence of chest signs.
297
What are high-risk tetanus prone wounds?
* heavy contamination with material likely to contain tetanus spores e.g. soil, manure * wounds or burns that show extensive devitalised tissue * wounds or burns that require surgical intervention
298
What are the tetanus rules?
Patient has had a full course of tetanus vaccines, with the last dose \< 10 years ago * no vaccine nor tetanus immunoglobulin is required, regardless of the wound severity Patient has had a full course of tetanus vaccines, with the last dose \> 10 years ago * if tetanus prone wound: reinforcing dose of vaccine * high-risk wounds (e.g. compound fractures, delayed surgical intervention, significant degree of devitalised tissue): reinforcing dose of vaccine + tetanus immunoglobulin If vaccination history is incomplete or unknown * reinforcing dose of vaccine, regardless of the wound severity * for tetanus prone and high-risk wounds: reinforcing dose of vaccine + tetanus immunoglobulin In short. Grade 2 wound = tetanus booster. Grade 3 wound = Add Immunoglobulin If vaccination history is unknown then your threshold is lowered by 1. Grade 1 wound = tetanus booster Grade 2 wound = add Immunogloblin I you have had vaccine in the last 10 years then you need no extra intervention.
299
What causes kaposi's sarcoma?
caused by HHV-8 (human herpes virus 8)
300
What are the features of leptospirosis?
Leptospirosis - conjunctival suffusion plus muscle tenderness (localised in the calves and possibly the paraspinal muscles)
301
What are the features of typhoid/paratyphoid?
* initially systemic upset as above (fever, headache, arthralgia) * relative bradycardia * abdominal pain, distension * constipation: although Salmonella is a recognised cause of diarrhoea, constipation is more common in typhoid * rose spots: present on the trunk in 40% of patients, and are more common in paratyphoid
302
Features of legionella
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
303
Features of mycoplasma pneumonaie
Haemolytic anaemia and thrombocytopenia Erythema multiforme Ecephalitis / GBS Peri/myocarditis Bullous myringitis
304
What is treatment for diarrhoea?
Invasive diarrhoea (bloody diarrhoea + fever) then give ciprofloxacin, otherwise give clairithromycin
305
What is the most common cause of viral meningitis?
Coxsackie
306
Cellulitis treatment if allergic to penicillin
clarithromycin, erythromycin (in pregnancy) or doxycyline
307
What are the complications of mycoplasma pneumoniae
* cold agglutins (IgM): may cause an haemolytic anaemia, thrombocytopenia * erythema multiforme, erythema nodosum * meningoencephalitis, Guillain-Barre syndrome and other immune-mediated neurological diseases * bullous myringitis: painful vesicles on the tympanic membrane * pericarditis/myocarditis * gastrointestinal: hepatitis, pancreatitis * renal: acute glomerulonephritis
308
What is the most common cause of viral meningitis?
Herpes simplex virus
309
What does hookworm show on blood tests?
Iron deficiency anaemia Eosinophilia
310
How do you treat legionella and mycoplasma pneumoniae
Macrolides (clari)
311
How can trimethoprim affect the kidneys?
Trimethoprim can cause tubular dysfunction, leading to hyperkalaemia and increased serum creatinine
312
The antibiotic always used in pregnancy
Erythromycin
313
Incubation period of salmonella typhi
10-20 days
314
What is UTI management in pregnant women?
Nitro Amoxicillin or cefalexin if near term
315
What is Mrizzi syndrome?
Mirizzi syndrome described common hepatic duct obstruction by an impacted gallstone.
316
What are the types of renal stones?
Calcium oxalate Cystine Uric acid Calcium phosphate Struvite (staghorn calculi) Xanthine
317
What are risk factors for calcium oxalate stones?
Hypercalciuria Hyperoxaluria Hypocitraturia
318
What are risk factors for uric acid stones?
urinary pH low Extensive tissue breakdown
319
What are risk factors for calcium phosphate stones?
Renal tubular acidosis (1 and 3) High pH
320
What is a risk factor for struvite stones?
Urease producing bacteria
321
Which stones are opaque/semi-opaque/lucent?
Opague: * Calcium oxalate * Calcium phosphate Lucent: * Uric Acid Others: Struvite = slightly radiolucent Cystine = radiodense
322
Symptomatic AAA have high rupture risk and should undergo endovascular repair (EVAR)
323
What is the triad of turp syndrome?
Hyponatraemia Fluid overload GLycine toxicity
324
Ultrasound findings for liver cysts
Haemangioma = hyperechoic Liver abscess = hyperechoic Liver cell adnoma = mixed echoity and heterogeneous texture Cystadenoma = anechoic Amoebic abscess = fluid filled structure with poorly defined boundaries Hyatid cysts = septa, hyatid sand or daughter cysts
325
Features of haemangioma
Incidental finding Hyperechoic
326
What are the features of liver cell adenoma?
3-5th decade Women Link with OCP
327
What are the features of liver abscess?
fever, right upper quadrant pain. Jaundice may be seen in 50% Ultrasound will usually show a fluid filled cavity, hyperechoic walls may be seen in chronic abscesses
328
Features of ameobic abscess in liver?
Fever RUQ (this is a mimic of cholecystitis) FLuid filled structure with poorly defined borders Anchovy paste consistency Metronidazole
329
Features of hyatid cysts?
Echinococcus infection Malaise and RUQ Eosinophilia Do not aspirate Mebendazole followed by surgical resection
330
Pain after eating with increased lactate
Mesenteric ischaemia
331
How long is PSA elevated for 1. prostate biopsy 2. proven UTI 3. DRE 4. vigorous exercise 5. ejaculation
1. 6 weeks of a prostate biopsy 2. 4 weeks following a proven UTI 3. 1 week after DRE 4. 48 hours after vigorous exercise 5. 48 hours after ejaculation
332
What causes acute epididymo orchitis
Acute epididymo-orchitis is most commonly caused by Chlamydia E. coli is the most common cause of epididymo-orchitis in men over 35 years of age.
333
What type of chemotherapy is used in patients with breast cancer node+
FEC-D
334
What is Stauffer syndrome / paraneoplastic hepatic dysfunction syndrome?
Cholestasis Hepatosplenomegaly in response to increased levels of IL-6
335
What is the treatment for renal cell carcinoma?
**alpha-interferon** and **interleukin-2** have been used to reduce tumour size and also treat patients with metatases receptor **tyrosine kinase inhibitors** (e.g. sorafenib, sunitinib) have been shown to have superior efficacy compared to interferon-alpha
336
What is the parkland fluid formula?
The Parkland formula for fluid resuscitation in burns is: * Volume of fluid = total body surface area of the burn % x weight (Kg) x 4ml * 50% given in first 8 hours * 50% given in next 16 hours
337
Abdominal signs of pancreatitis
periumbilical discolouration (Cullen's sign) and flank discolouration (Grey-Turner's sign) is described but rare - acute pancreatitis.
338
What is the retinopathy assocaited with pancreatitis?
ischaemic (Purtscher) retinopathy - may cause temporary or permanent blindness
339
Investigations for acute pancreatitis vs chronic pancreatitis
Acute = can usually be made clinically (raised amylase, lipase) Ultrasound may be used to determeine cause Contrast enhanced CT is another option Chronic = Abdo CT showing pancreatic calcification Faecal elastase may be used to determine exocrine function
340
Systemic complication of pancreatitis?
ARDS
341
What is the glasgow score for pancreatitis?
342
What type of drugs are etomidate and propofol?
Sedation agents
343
What type of drug is suxamethonium
Depolarising muscle relaxant. Short lasting Rapid action
344
What type of drug are vecuronium and atracurium
Non-depolarizing muscle relaxant
345
What are the side effects of suxamethonium
Side effects. Side effects include malignant hyperthermia, muscle pains, acute rhabdomyolysis with high blood levels of potassium, transient ocular hypertension, constipation and changes in cardiac rhythm, including slow heart rate, and cardiac arrest.
346
What is the reversal agent for non-depolarising muscle relaxants?
Neostigmine
347
How is local anaesthetic toxicity treated?
20% lipid emulsion
348
If a UC patient needs a panproctocolectomy, but is systemically unwell, what is the surgical alternative?
Ileoanal pouch with defunctioning ileostomy Subtotal colectomy
349
What are complications of SAH?
Complications of SAH: * 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
350
How do we prevent vasospasm in SAH?
Nimodipine
351
What type of breast lump mimics cancer and can have teathering
Fat necrosis
352
When would you perform: 1. Anterior resection 2. Hartmann's 3. Abdominoperineal excision of the rectum?
Mid/high rectal tumours can be managed with anterior resection. Hartmann's procedure is generally for sigmoid tumours, and abdominoperineal excision of rectum is for low rectal or anal tumours.
353
Boas sign
Cholecystitis Hyperaesthesia between 9th and 11th ribs on posterior right side
354
What diabetic medications require changing in preparation for surgery (not insulin for this question)
Metformin Sulfonylureas SGLT-2 inhibitors
355
What change is required to insulin in preparation of surgery?
Lantus/levemir = 20/20/20 Novomix / Humilin M3 = 0/halve/halve
356
Strongest risk factor for anal cancer
HPV infection
357
What are the features of renal adenocarcinoma?
Hypertension, haematuria, polycythaemia and renal mass = renal adenocarcinoma
358
Renal pelvis = transitional cell carcinoma
359
What is subfalcine herniation?
Displacement of the cingulate gyrus under the falx ceribri
360
Describe central herniation
Downwards displacement of the brain
361
Describe transtentorial/uncal herniation
Displacement of the uncus of the temporal lobe under the tentorium cerebelli. Clinical consequences include an ipsilateral fixed, dilated pupil (due to parasympathetic compression of the third cranial nerve) and contralateral paralysis (due to compression of the cerebral peduncle)
362
Describe tonsillar herniation
Displacement of the cerebellar tonsils through the foramen magnum. This is called ‘coning’. In raised ICP this causes compression of the cardiorespiratory centre. In Chiari 1 malformation, tonsillar herniation is seen without raised ICP
363
Describe transcalvarial
Occurs when brain is displaced through a defect in the skull (e.g. a fracture or craniotomy site)
364
What are the signs of lateral cutaneous nerve lesion
Burning over anterior thigh which worsens on walking, positive tinel sign over inguinal ligament
365
Inability to dorsiflex foot after total hip replacement?
Sciatic nerve injury
366
Signs of ilioinguinal nerve injury?
Pfannelstein incision + pain over inguinal ligament, and tenderness when inguinal nerve is compressed
367
Femoral nerve lesion
Weak hip flexion, weak knee extension, impaired quadriceps reflex, sensory deficit over anterior-medial aspect of thigh.
368
What are the 6 tests for brain death?
* Fixed pupils which do not respond to sharp changes in the intensity of incident light * No corneal reflex * Absent oculo-vestibular reflexes - no eye movements following the slow injection of at least 50ml of ice-cold water into each ear in turn (the caloric test) * No response to supraorbital pressure * No cough reflex to bronchial stimulation or gagging response to pharyngeal stimulation * No observed respiratory effort in response to disconnection of the ventilator for long enough (typically 5 minutes) to ensure elevation of the arterial partial pressure of carbon dioxide to at least 6.0 kPa (6.5 kPa in patients with chronic carbon dioxide retention). Adequate oxygenation is ensured by pre-oxygenation and diffusion oxygenation during the disconnection (so the brain stem respiratory centre is not challenged by the ultimate, anoxic, drive stimulus)
369
When should women be prescribed cyclical combined HRT?
If their last menstrual period was less than 1 year ago
370
When should continuous combined HRT begin?
if they have: * taken cyclical combined for at least 1 year or * it has been at least 1 year since their LMP or * it has been at least 2 years since their LMP, if they had premature menopause (menopause below the age of 40)
371
effect of antiphospholipid syndrome on APTT?
Paradoxical rise
372
Triad of disseminated gonococcal disease How does this compare to reactive arthritis
Triad of tenosynovitis, migratory polyarthritis and dermatitis Whereas reactive arthritis is urethritis, arthritis and conjunctivitis. Can’t see, pee or climb a tree
373
Bone disease with isolated ALP?
Pagets disease
374
Gout vs pseudogout crystals
Gout- monosodium urate crystals that are needle-shaped that are **negatively** birefringent under polarised light Pseudogout- calcium pyrophosphate crystals are rhombic/brick shaped that are **positively** birefringent under polarised light
375
Buttock claudication and impotence (not cauda equina!)
Leriche syndrome Also has atrophy of the legs
376
Behcets disease features?
Behcet's disease is an autoimmune small vessel vasculitis that targets venules. It is a type 3 hypersensitivity reaction induced by immune complex deposition in small vessels. Its main clinical presentation is with recurrent **oral and genital ulcers**, **anterior uveitis**, and skin lesions (such as **erythema nodosum**). It is most commonly seen in people of East Mediterranean descent. Flares may be precipitated by parvovirus or herpes simplex virus.
377
What is the Garden system?
Grades hip facture severity Type I: Stable fracture with impaction in valgus Type II: Complete fracture but undisplaced Type III: Displaced fracture, usually rotated and angulated, but still has boney contact Type IV: Complete boney disruption Just remember that 3 is displaced but with bony contact
378
What is management for intracapsular fracture - undisplaced?
Internal fixation Hemiarthroplasty if unfit
379
What is management of intracapsular hip fracture displaced?
Total hip replacement Hemiarthroplasty if unfit
380
Management of extracapsular fracture intertrochanteric?
Dynamic hip screw
381
Management of extracapsular subtrochanteric fracture?
Intramedullary device
382
Osteomalacia findings 1. Calcium 2. Phosphate 3. ALP 4. PTH
1. Calcium - decreased 2. Phosphate - decreased 3. ALP - increased 4. PTH - increased
383
Osteoporosis findings 1. Calcium 2. Phosphate 3. ALP 4. PTH
All normal
384
Primary Hyperparathyroidism findings 1. Calcium 2. Phosphate 3. ALP 4. PTH
1. Calcium = High 2. Phosphate = Low 3. ALP = High 4. PTH = High
385
Secondary Hyperparathyroidism findings 1. Calcium 2. Phosphate 3. ALP 4. PTH
1. Calcium = Low 2. Phosphate = High 3. ALP = High 4. PTH = High
386
What test should be done prior to starting hydroxychloroquine?
Ophthalmic examination
387
What does hyperparathyoidism predispose you to?
Pseudogout Chondrocalcinosis
388
Inflammatory arthritis involving DIP swelling and dactylitis points to a diagnosis of psoriatic arthritis
389
Which two tendons are affected by de-quervains tenosynovitis?
De Quervain's tenosynovitis is a common condition in which the sheath containing the **extensor pollicis brevis and abductor pollicis** longus tendons is inflamed
390
When does scaphoid fractures become more susceptible to AVN?
More proximal
391
How to tell the difference between meralgia paraesthetica and trochanteric bursitis?
present very similarly with pain over the anterior aspect of the thigh. However, with meralgia paraesthetica you can also get numbness/paraesthesia. Meralgia paraesthetic is the same is lateral cutaneous nerve of thigh lesion (Burning over anterior thigh which worsens on walking, positive tinel sign over inguinal ligament)
392
First line investigation for suspected osteoporotic vertebral fracture?
X-ray
393
Salter Harris scoring system
Physis = 1 point Metaphysis = 1 point Epiphysis = 2 points 5 = crush
394
Function of the following nerves 1. Femoral 2. Obturator 3. Lateral cutaneous nerve of thigh 4. Tibial 5. Common peroneal 6. Superior gluteal 7. Inferior gluteal nerve
1. Femoral = hip flexion and knee extension 2. Obturator = thigh adduction 3. Lateral cutaneous nerve of thigh = Lateral and posterior surfaces of the thigh 4. Tibial - Plantarflexion and inversion 5. Common peroneal = dorsiflexion and eversion (and extensor hallucis longus) 6. Superior gluteal = Hip abduction 7. Inferior gluteal nerve = Hip extension and lateral rotation
395
What nerve is damaged after anterior hip dislocation?
Obturator nerve
396
What nerve injury would a popliteal laceration/posterior knee cause?
Tibial nerve
397
What causes damage to the common peroneal nerve?
Injury often occurs at the neck of the fibula Tightly applied lower limb plaster cast Injury causes foot drop
398
What things can damage the superior gluteal nerve?
Misplaced intramuscular injection Hip surgery Pelvic fracture Posterior hip dislocation
399
What nerve injusry would result in a positive trendelenberg sign?
Superior gluteal nerve
400
What nerve is commonly injured alongside the inferior gluteal nerve?
Sciatic nerve
401
What is the manifestation of injury of the inferior gluteal nerve?
Injury results in difficulty rising from seated position. Can't jump, can't climb stairs
402
What movement is associated with anterior shoulder dislocation?
External rotation and abduction
403
What injuries is the anterior shoulder dislocation assocaited with?
Greater tuberosity fracture Bankart lesion Hill-Sachs deformity
404
What signs are seen on posterior shoulder dislocation?
Rim's sign, light bulb sign. Associated with Trough sign
405
What is a hill-sachs deformity vs bankart lesion
Hill-Sachs = Compression fracture of posterolateral humeral head due to compression against glenoid Bankart lesion = labral tear on anterior inferior glenoid
406
Description of anterior vs posterior shoulder x-ray
Anterior dislocation description: On examination, the right arm is abducted and externally rotated, and she resists all movement. The acromion appears prominent. The humeral head is seen in a subcoracoid position in anteroposterior view on X-ray Posterior dislocation = arm held in internal rotation
407
Crystals seen in osteoarthritis vs rheumatoid arthritis?
* Osteoarthritis- **calcium phosphate** crystals associated with degeneration of cartilage, coffin-lid shaped with no birefringence * Rheumatoid arthritis- **cholesterol crystals**, these are rhombic/brick-shaped with a negative birefringence
408
Adverse effects of phenytoin?
Phenytoin adverse effects: P= p450 interactions H = hirsutism E= enlarged gums N = nystagmus Y= yellow skin ie jaundice T = teratogen O = osteomalacia I = intereference with b12 metabolism - causing megaloblastic anaemia N = neuropathies Can also cause DUPYTREN's
409
Elderly people becomming clumsy with their hands Positive hoffmans sign?
Degenerative cervical myelopathy
410
Definition of orthostatic hypotension?
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).
411
What does the drug memantine act on?
NMDA receptor antagonist
412
What is involved in a confusion screen?
B12/folate: macrocytic anaemias, B12/folate deficiency worsen confusion TFTs: confusion is more commonly seen in hypothyroidism Glucose: hypoglycaemia can commonly cause confusion Bone Profile (Calcium): hypercalcaemia can cause confusion
413
What type of dementia is assocaited with motor neurones disease?
Frontotemporal
414
How does respiratory alkalosis impact calcium?
Hypocalcaemia can be seen secondary to respiratory alkalosis as the higher pH lowers the amount of ionised calcium seen in the blood
415
What are the first line drugs for spasticity in MS?
Baclofen Gabapentin
416
How can syringe drivers be used to manage respiratory secretions and bowel colic?
Syringe drivers: respiratory secretions & bowel colic may be treated by hyoscine hydrobromide, hyoscine butylbromide, or glycopyrronium bromide. If bowel colic, assume it’s an obstruction - use hyoscine butyl bromide. Metoclopramide is contraindicated in bowel obstruction.
417
What is pellagra?
Niacin deficiency Vitamin B3 * Pellagra * dermatitis * diarrhoea * dementia
418
What are the features of vitamin B6 deficiency?
Anaemia, irritability, seizures B6 is called pyridoxine
419
What are the features of B7 deficiency?
Dermatitis Seborrhoea B7 is called biotin
420
What is vitamin B9 called What does deficiency in this vitamin cause?
Folic acid Megaloblastic anaemia, deficiency during pregnancy - neural tube defects
421
What is the name for vitamin B12?
Cyanocobalamin Megaloblastic anaemia, peripheral neuropathy
422
What is ascorbic acid?
Vitamin C Scurvy gingivitis bleeding
423
What is the name of vitamin E What does deficiency of this vitamin cause?
Tocopherol, tocotrienol Mild haemolytic anaemia in newborn infants, ataxia, peripheral neuropathy
424
What is the name of vitamin K?
Naphthoquinone
425
What are risk factors for placental abruption?
Abruption previously; Blood pressure (i.e. hypertension or pre-eclampsia); Ruptured membranes, either premature or prolonged; Uterine injury (i.e. trauma to the abdomen); Polyhydramnios; Twins or multiple gestation; Infection in the uterus, especially chorioamnionitis; Older age (i.e. aged over 35 years old); Narcotic use (i.e. cocaine and amphetamines, as well as smoking)
426
Risk factors for endometrial cancer
* obesity * nulliparity * early menarche * late menopause * unopposed oestrogen. The addition of a progestogen to oestrogen reduces this risk (e.g. In HRT). The BNF states that the additional risk is eliminated if a progestogen is given continuously * diabetes mellitus * tamoxifen * polycystic ovarian syndrome * hereditary non-polyposis colorectal carcinoma
427
When does the Moror reflex dissappear?
4 months
428
Risk factors for DDH
* female sex: 6 times greater risk * breech presentation * positive family history * firstborn children * oligohydramnios * birth weight \> 5 kg * congenital calcaneovalgus foot deformity
429
Difference between lichen planus and lichen sclerosus
planus: purple, pruritic, papular, polygonal rash on flexor surfaces. Wickham's striae over surface. Oral involvement common sclerosus: itchy white spots typically seen on the vulva of elderly women
430
What do fibroids look like on ultrasound?
Hypoechoic mass
431
What does beads on a string refer to?
Chronic salpingitis
432
What sign is assocaited with ovarian torsio non ultrasound?
Whirlpool sign
433
Sensitising events: Potentially sensitising events in pregnancy: - Ectopic pregnancy - Evacuation of retained products of conception and molar pregnancy - Vaginal bleeding \< 12 weeks, only if painful, heavy or persistent - Vaginal bleeding \> 12 weeks - Chorionic villus sampling and amniocentesis - Antepartum haemorrhage - Abdominal trauma - External cephalic version - Intra-uterine death - Post-delivery (if baby is RhD-positive)
434
When do you use antibiotics in mastitis?
an infected nipple fissure, symptoms not improving after 12-24 hours despite effective milk removal and/or breast milk culture positive. If antibiotics are indicated, first line would be flucloxacillin for 10-14 days or erythromycin or clarithromycin if penicillin allergic.
435
Risk factors for PPH
* previous PPH * prolonged labour * pre-eclampsia * increased maternal age * polyhydramnios * emergency Caesarean section * placenta praevia, placenta accreta * macrosomia * ritodrine (a beta-2 adrenergic receptor agonist used for tocolysis)
436
Management of PPH
1st line (physical method) - bimanual uterine massage - empty bladder (catheter) 2nd line - oxytocin/syncitocin - carboprost - ergimetrine (not in hypertension) 3rd line (surgical) - balloon tamponade (do this first in surgical method) - B-Lynch suture - ligation of the uterine arteries or internal iliac arteries Last option hysterectomy
437
When are grommets used?
* recurrent acute otitis media * otitis media with effusion in both ears 3 months or one ear for 6 months * In patients with speech delays
438
What are the common causative organisms in acute otitis media?
whilst viral upper respiratory tract infections (URTIs) typically precede otitis media, most infections are secondary to bacteria, particularly Streptococcus pneumonaie, Haemophilus influenzae and Moraxella catarrhalis
439
When should antibiotics be prescribed for acute otitis media?
Antibiotics should be prescribed immediately if: * Symptoms lasting more than 4 days or not improving * Systemically unwell but not requiring admission * Immunocompromise or high risk of complications secondary to significant heart, lung, kidney, liver, or neuromuscular disease * Younger than 2 years with bilateral otitis media * Otitis media with perforation and/or discharge in the canal
440
According to NICE guidance 'a woman of reproductive age who has not conceived after 1 year of unprotected vaginal sexual intercourse, in the absence of any known cause of infertility, should be offered further clinical assessment and investigation along with her partner.'
441
What factors exacerbate psoriasis?
trauma alcohol drugs: beta blockers, lithium, antimalarials (chloroquine and hydroxychloroquine), NSAIDs and ACE inhibitors, infliximab withdrawal of systemic steroids
442
How to tell the difference between bullous pemphigoid and pemphigus vulgaris?
* no mucosal involvement (in exams at least\*): bullous pemphigoid * mucosal involvement: pemphigus vulgaris
443
One of the main clinical features of polymorphic eruption in pregnancy is periumbilical sparing
444
What are the discontinuation symptoms of SSRIs?
* increased mood change * restlessness * difficulty sleeping * unsteadiness * sweating * gastrointestinal symptoms: pain, cramping, diarrhoea, vomiting * paraesthesia
445
What drugs are ototoxic?
aminoglycosides (e.g. Gentamicin), furosemide, aspirin and a number of cytotoxic agents
446
When are APGAR scores measured?
1,5,10 minutes
447
What are the features of wet age related macular degeneration?
Decreasing vision over months with metamorphopsia and central scotoma should cause high suspicion of wet age-related macular degeneration
448
What is the diagnostic threshold for gestational diabetes vs the targets for gestational diabetes?
_Diagnosis_ fasting glucose is \>= 5.6 mmol/L 2-hour glucose is \>= 7.8 mmol/L
449
When is gestational diabetes screened for?
as soon as possible after booking and at 24-28 weeks
450
Summary of managment of gestational diabetes
If fasting glucose is less than 7 try exercise - add metformin if needed - add insulin if needed If over 7 go immediately to insulin
451
How do you manage gestational diabetes?
* weight loss for women with BMI of \> 27 kg/m^2 * stop oral hypoglycaemic agents, apart from metformin, and commence insulin * folic acid 5 mg/day from pre-conception to 12 weeks gestation * detailed anomaly scan at 20 weeks including four-chamber view of the heart and outflow tracts * tight glycaemic control reduces complication rates * treat retinopathy as can worsen during pregnancy Also having diabetes (type 1 or 2) is a high risk factor for pre-eclampsia, therefore women should take aspirin 75-150mg daily from 12 weeks gestation until the birth.
452
Risk factors for pre-eclampsia
453
What precipitates pompholyx eczema?
Precipitated by humidity and temperature Pompholyx eczema is a subtype of eczema characterised by an intensely pruritic rash on the palms and soles (basically, if the diagnosis seems like hand foot and mouth but it’s an adult.
454
What do they test during the heel prick of a baby with CF?
Newborns with a positive heel prick for CF, i.e. they have a raised immunoreactive trypsinogen (IRT) result, get a sweat test, which will be high if they have CF
455
What is the management of vaginal vault prolapse?
Sacrocolpoplexy
456
What is the management of cystocele/cystourethrocele?
anterior colporrhaphy, colposuspension
457
Management of uterin prolapse?
Hysterectomy Sacrohysteropexy
458
Management of rectocele
Posterior colporrhaphy
459
Management of chickenpox exposure in pregnancy, i.e. post-exposure prophylaxis (PEP)
**_PEP_** Woman less than 20 weeks pregnant and has EXPOSURE - Check immunity status - Give VZIG IMMEDIATELY Women over 20 weeks pregnant - Check iommunity status - Give VZIG or Aciclovir 7-14 days after the exposure **_Signs of varicella infection:_** Give oral aciclovir
460
How do we manage HIV increased risk of CIN?
Annual cervical cytology
461
What causes eczema herpeticum?
Eczema herpeticum is a primary infection of the skin caused by herpes simplex virus (HSV) and uncommonly coxsackievirus
462
What is the managment of ramsay hunt?
Oral aciclovir Oral steroids
463
When do cord prolapses often happen
After articficial rupture of membranes
464
What bacteria causes erythrasma?
Corynebacterium minutissimum Treated with erythromycin
465
What is Samter's triad?
asthma + aspirin sensitivity + nasal polyposis
466
What are the features of dermatomyosits?
Skin features * photosensitive * macular rash over back and shoulder * heliotrope rash in the periorbital region * Gottron's papules - roughened red papules over extensor surfaces of fingers * 'mechanic's hands': extremely dry and scaly hands with linear 'cracks' on the palmar and lateral aspects of the fingers * nail fold capillary dilatation Other features * proximal muscle weakness +/- tenderness * Raynaud's * respiratory muscle weakness * interstitial lung disease: e.g. Fibrosing alveolitis or organising pneumonia * dysphagia, dysphonia
467
What are the antibodies assocaited with dermatomyosits?
* the majority of patients (around 80%) are **ANA** positive * around 30% of patients have antibodies to aminoacyl-tRNA synthetases (**anti-synthetase** antibodies), including: * antibodies against histidine-tRNA ligase (also called Jo-1) * antibodies to signal recognition particle (SRP) * anti-Mi-2 antibodies
468
Features of polymyositis
* proximal muscle weakness +/- tenderness * Raynaud's * respiratory muscle weakness * interstitial lung disease: e.g. fibrosing alveolitis or organising pneumonia * dysphagia, dysphonia
469
Investigations for polymyositis
* elevated **creatine kinase - this helps distinguish the condition from PMR** * other muscle enzymes (lactate dehydrogenase (LDH), aldolase, AST and ALT) are also elevated in 85-95% of patients * EMG * muscle biopsy * anti-synthetase antibodies * anti-Jo-1 antibodies are seen in pattern of disease associated with lung involvement, Raynaud's and fever
470
General mnemonic for antisynthetase syndrome
RIM JOB Reynauds Interstitial lung disease Myositis (or mechanics hands with gottrons papules for dermatomyositis) JOB = jo-1 antibodies
471
What antibodies are assocaited with drug induced lupus?
ANA positive in 100%, dsDNA negative anti-histone
472
What drugs cause drug-induced lupus?
**_Most common causes_** procainamide hydralazine **_Less common causes_** **isoniazid** minocycline phenytoin
473
Most sensitive and most-specific antibodies for lupus?
99% are **ANA** positive this high **sensitivity** makes it a useful rule out test, but it has low specificity 20% are rheumatoid factor positive **anti-dsDNA: highly specific (\> 99%), but less sensitive (70%)** **anti-Smith: highly specific** (\> 99%), sensitivity (30%) also: anti-U1 RNP, SS-A (anti-Ro) and SS-B (anti-La)
474
What is the first line investigation for psoas abscess?
Abdominal CT
475
Antiphospholipid syndrome: (paradoxically) prolonged APTT + low platelets
476
Which artery is compromised in the fracture of the scaphoid?
**The dorsal carpal branch of the radial artery** is the main neurovascular structure that is compromised in a scaphoid fracture
477
What are the features of scleroderma renal crisis?
1- Abrupt onset of moderate to severe hypertension that is typically associated with an increase in plasma renin activity 2- Acute kidney injury (AKI) 3- Urinalysis that is normal or reveals only mild proteinuria with few cells or casts
478
What is the treatment for scleroderma renal crisis?
Ace inhibitors
479
Extra-genital features of behcets
Behcet's syndrome is associated with various dermatological symptoms including aphthous ulcers, genital ulcers, acne-like lesions and erythema nodosum.
480
What is the most common site of metatarsal stress fracture?
2nd metatarsal
481
What is the Z score of the DEXA scan adjusted for?
Age Gender Ethnic factors
482
What is the investigation for osteomyelitis vs septic arthritis
Osteomyelitis=MRI Septic arthritis = joint aspiration/bloodcultures/joint imaging
483
What is CK and ESR in PMR?
CK normal ESR raised
484
filter paper near conjunctival sac to measure tear formation
Schirmers test
485
Which medium vessel vasculitis is assocaited with hep-b
Polyarteritis nodoa
486
What is the test for meniscal tear?
Thelassey's test weight bearing at 20 degrees of knee flexion, patient supported by doctor, postive if pain on twisting knee (for meniscal tear)
487
What are causes of avascular necrosis of the hip?
* long-term steroid use * chemotherapy * alcohol excess * trauma
488
What is theinvestigation of choice for avascular necrosis of the hip?
MRI X-ray may show crescent sign
489
Features of OA in hands
OA of the hand: Usually bilateral: Usually one joint at a time is affected over a period of several years. The carpometacarpal joints (CMCs), distal interphalangeal joints (DIPJs) are affected more than the proximal interphalangeal joints (PIPJs). Squaring of thumb
490
Antibodies for scleroderma
ANA positive in 90% RF positive in 30% anti-scl-70 antibodies associated with diffuse cutaneous systemic sclerosis anti-centromere antibodies associated with limited cutaneous systemic sclerosis
491
What biochemical marker can be used to measure disease activity in patients with lupus?
Low complement = active disease
492
Methotrexate may cause mucositis
493
How to tell the difference between osteochondritis dissecans and chondromalacia patella?
Osteochondritis dissecans: = Pain after exercise, swelling, locking, giving way, clunking Chondromalacia patellae = Softening of the cartilage of the patella Common in teenage girls Characteristically anterior knee pain on walking up and down stairs and rising from prolonged sitting Usually responds to physiotherapy
494
Why is a chest x-ray important before starting biologics for RA?
Look for TB Biologics can cause re-activation of TB
495
Features of colles fracture?
Features of the injury 1. Transverse fracture of the radius 2. 1 inch proximal to the radio-carpal joint 3. Dorsal displacement and angulation
496
Features of smiths fracture
Volar angulation of distal radius fragment (Garden spade deformity) Caused by falling backwards onto the palm of an outstretched hand or falling with wrists flexed
497
Describe bennets fracture
* Intra-articular fracture at the base of the thumb metacarpal * Impact on flexed metacarpal, caused by fist fights * X-ray: triangular fragment at the base of metacarpal
498
Monteggia fracture
* Dislocation of the proximal radioulnar joint in association with an ulna fracture * Fall on outstretched hand with forced pronation * Needs prompt diagnosis to avoid disability
499
Galeazzi fracture
* Radial shaft fracture with associated dislocation of the distal radioulnar joint * Occur after a fall on the hand with a rotational force superimposed on it. * On examination, there is bruising, swelling and tenderness over the lower end of the forearm. * X Rays reveal the displaced fracture of the radius and a prominent ulnar head due to dislocation of the inferior radio-ulnar joint.
500
Description of Barton's fracture
* Distal radius fracture (Colles'/Smith's) with associated radiocarpal dislocation * Fall onto extended and pronated wrist
501
Features of radial head fracture
* Fracture of the radial head is common in young adults. * It is usually caused by a fall on the outstretched hand. * On examination, there is **marked local tenderness over the head of the radius, impaired movements at the elbow, and a sharp pain at the lateral side of the elbow at the extremes of rotation (pronation and supination).**
502
longitudinal compression of the thumb = scaphoid fracture
503
What can discitis be secondary to?
Infective endocarditis
504
what are the ottowa rules for ankle fracture?
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
505
What is a potts ankle fracture
Bimalleolar ankle fracture Forced foot eversion
506
What is weber classification of ankle fracture
Related to the level of the fibular fracture. ## Footnote Type A is below the syndesmosis Type B fractures start at the level of the tibial plafond and may extend proximally to involve the syndesmosis Type C is above the syndesmosis which may itself be damaged
507
General management of ankle fractures 1. Weber a / minimally displaced 2. Displaced 3. Unstable 4. Management prior to scan
1. Weber a / minimally displaced = cam boot 2. Displaced = casted 3. Unstable / weber c = ORIF 4. Management prior to scan = reduction **All ankle fractures should be promptly reduced to remove pressure on the overlying skin and subsequent necrosis**
508
RA drug therapy
NSAIDS Steroid DMARDS
509
What are the drug therapies available for RA?
Steroids for flares (IM methylprednisolone, intra-articular steroids, oral prednisolone) NSAIDs for symptom relief DMARDs (methotrexate, sulfasalazine, hydroxychloroquine, leflunomide) Biologics: TNF = infliximab, etanercept, adalimumab Anti-CD20 - rituximab Anakinra = IL-1 IL-6 = Toclizumab
510
What are the side effects of methotrexate?
Pneumonitis Oral ulcers Heoatotoxicity
511
How often is methotrexate monitored?
Initially monthly then every three months
512
Whar are the side effects of sulfasalazine?
* oligospermia * Stevens-Johnson syndrome * pneumonitis / lung fibrosis * myelosuppression, Heinz body anaemia, megaloblastic anaemia * may colour tears → stained contact lenses
513
Side effects of hydroxychloroquine
Irreversible retinopathy
514
What are the side effects of leflunomide?
Increased BP Oral ulcers Hepatotoxicity Diarrhoea Male and female teratogenicity
515
What DMARDs are contraindicated in pregnancy?
**Methotrexate** women should avoid pregnancy for at least 6 months after treatment has stopped the BNF also advises that men using methotrexate need to use effective contraception for at least 6 months after treatment) **Leflunomide**
516
DMARDs that may be used during pregnancy?
Sulfasalazine Hydroxychloroquine
517
What are the drug interactions of methotrexate?
* avoid prescribing trimethoprim or co-trimoxazole concurrently - increases risk of marrow aplasia * high-dose aspirin increases the risk of methotrexate toxicity secondary to reduced excretion
518
What is methotrexate co-prescribed with?
Folic acid folic acid 5mg once weekly should be co-prescribed, taken more than 24 hours after methotrexate dose
519
What are the adverse effects of cyclophosphamide?
* Haemorrhagic cystitis * myelosuppression * transitional cell carcinoma
520
Bleomycin SE
Lung fibrosis
521
Anthracyclines (doxorubicin SE)
Cardiomyopathy
522
SE of fluoracil
Myelosuppression, mucositis, dermatitis
523
SE of cytarabine
ataxia
524
SE of vincristine
Peripheral neuropathy (reversible) , paralytic ileus
525
SE of docetaxel
Neutropenia
526
SE of cisplastin
Ototoxicity, peripheral neuropathy, hypomagnesaemia
527
Eye features of third nerve palsy?
Third nerve palsy: Eye will be abducted and depressed Ptosis Dilated pupil and absent light reflex - there will be intact consensual constriction
528
What are causes of third nerve palsy
* diabetes mellitus * vasculitis e.g. temporal arteritis, SLE * Uncal herniation * posterior communicating artery aneurysm (often associated pain) * cavernous sinus thrombosis * Weber's syndrome: ipsilateral third nerve palsy with contralateral hemiplegia -caused by midbrain strokes * amyloid, multiple sclerosis
529
What is autonomic dysreflexia?
This clinical syndrome occurs in patients who have had a spinal cord injury at, or above T6 spinal level. Briefly, afferent signals, most commonly triggered by faecal impaction or urinary retention (but many other triggers have been reported) cause a sympathetic spinal reflex via thoracolumbar outflow. The usual, centrally mediated, parasympathetic response however is prevented by the cord lesion. The result is an unbalanced physiological response, characterised by extreme hypertension, flushing and sweating above the level of the cord lesion, agitation, and in untreated cases severe consequences of extreme hypertension have been reported, e.g. haemorrhagic stroke. Management of autonomic dysreflexia involves removal/control of the stimulus and treatment of any life-threatening hypertension and/or bradycardia.
530
What are the different types of motor neurone disease?
Amytrophic lateral sclerosis Primary lateral sclerosis Progressive muscular atrophy Progressive bulbar palsy
531
What are the features of ALS?
* typically LMN signs in arms and UMN signs in legs * in familial cases the gene responsible lies on chromosome 21 and codes for superoxide dismutase
532
What are the features of primary lateral sclerosis?
UMN signs only
533
Signs of progressive muscular atrophy
LMN signs only affects distal muscles before proximal carries best prognosis
534
Signs of progressive bulbar palsy
* palsy of the tongue, muscles of chewing/swallowing and facial muscles due to loss of function of brainstem motor nuclei * carries worst prognosis
535
Adrenaline doses
536
Side effects of sodium valproate
* teratogenic * P450 inhibitor * gastrointestinal: nausea * increased appetite and weight gain * alopecia: regrowth may be curly * ataxia * tremor * hepatotoxicity * pancreatitis * thrombocytopaenia * hyponatraemia * hyperammonemic encephalopathy: L-carnitine may be used as treatment if this develops
537
Side effects of Carbemazepine
Adverse effects * P450 enzyme inducer * dizziness and ataxia * drowsiness * headache * visual disturbances (especially diplopia) * Steven-Johnson syndrome * leucopenia and agranulocytosis * hyponatraemia secondary to syndrome of inappropriate ADH secretion
538
What are the antibodies associated with diabetes?
Antibodies associated with diabetes. (Anti-GAD, islet cell antibodies, insulin autoantibodies)
539
Driving advice for type 1 diabetes
* Driving advice for type 1 diabetes: * If you have had more than 1 hypo in the last 12 months you must not drive and inform the DVLA * If you have had a hypo in the last 12 months you must not drive a lorry and you must notify the DVLA of every severe episode of hypoglycaemia * If severe hypoglycaemia occurs whilst driving - stop driving and inform the DVLA * Keep glucose treatments in car * Check blood glucose before driving and every two hours * Blood glucose should be more than 5 in order for you to drive
540
Where is BROCAs and Wernickes?
* Brocas is inferior frontal gyrus. It is typically supplied by the superior division of the left MCA. * Wernickes = Due to a lesion of the superior temporal gyrus. It is typically supplied by the inferior division of the left MCA
541
How do acute haematomas compare to chronic haematomas?
Acute = hyperdense Chronic = hypodense
542
How do you diagnose acromegaly?
Diagnosis of acromegaly = measure serum IGF1 levels (raised), then do glucose tolerance test - measuring GH (normal patients GH is suppressed to less than 1 microgram/L. Levels higher than this conform acromegaly. MRI of sella turcica needed as well. Remember to screen for other secretory effects of the tumour: They include thyroid stimulating hormone (TSH), gonadotropic hormones (FSH, LH), adrenocorticotropic hormone, and prolactin.
543
Jacksonian movements are a feature of frontal lobe epilepsy. Temporal lobe seizures are associated with aura, lip smacking and clothes plucking. Occipital seizures are associated with visual abnormalities. Parietal seizures are associated with sensory abnormalities.
544
Rapid correction of 1. Hyponatraemia 2. Hypernatraemia
1. Rapid correction of hyponatraemia can cause **osmotic demyelination syndrome** 2. Correction of chronic hypernatraemia too fast predisposes to **cerebral oedema**
545
What is management for intrapartum pyrexia?
Benzylpenizillin, to cover for BGS Vanc if penicillin allergic Erythromycin is given for premature rupture of membranes
546
What drugs can cause idiopathic intracranial hypertension?
ciclosporin, oral contraceptives, mineralocorticoids, amiodarone, antibiotics (tetracyclines, sulphonamides), retinoic acid
547
What is the most common brain tumour in adults?
Glioblastoma multiforme
548
How does glioblastoma look on imaging and histology?
Imaging: Central necrotic area, with enhanced rim Histology: Pleomorphic tumour cells border necrotic areas
549
Where do meningiomas arise from?
Dura matter
550
Histology of meningioma
Spindle cells in concentric whorls and calcified psammoma bodies
551
Histology of vestibular schwannomas
Antoni A or B patterns are seen. Verocay bodies (acellular areas surrounded by nuclear palisades)
552
What is the most common primary brain cancer in children?
Pilocytic astrocytoma
553
What are the histological features of astrocytoma?
Rosenthal fibres (corkscrew eosinophilic bundle)
554
What is the histology for medulloblastoma?
Small, blue cells. Rosette pattern of cells with many mitotic figures
555
Where are ependymomas commonly seen
4th ventricle
556
What are the histology findings for ependymoma?
perivascular pseudorosettes
557
Oligodendroma appearance on histology
Calcifications with 'fried-egg' appearance
558
Haemangioblastoma histology
foam cells and high vascularity
559
Histology of craniopharyngoma
Derived from remnants of Rathke pouch
560
Neuroleptic malignant syndrome blood findings
raised CK and leukocytosis
561
Squamous vs adenocarcinoma lung cancer location
Squamous = central Adenocarcinoma = peripheral
562
Which cranial nerves are affected in vestibular schwannomas
5'7'8
563
What is a marker of medullary thyroid cancer?
calcitonin
564
Painful third nerve palsy = posterior communicating artery aneurysm
565
Multi-system atrophy is just Parkinson’s symptoms plus autonomic disturbance
566
How to manage metastatic bone pain
Analgesia Bisphosphonates Radiotherapy
567
How do you manage acute hyponatraemia?
Hypertonic saline
568
How would you manage chronic hyponatraemia?
**_If a hypovolemic cause is suspected_** ## Footnote normal, i.e. isotonic, saline (0.9% NaCl) this may sometimes be given as a trial if the serum sodium rises this supports a diagnosis of hypovolemic hyponatraemia if the serum sodium falls an alternative diagnosis such as SIADH is likely **_If a euvolemic cause is suspected_** fluid restrict to 500–1000 mL/day consider medications: demeclocycline vaptans (see below) **_If a hypervolemic cause is suspected_** fluid restrict to 500–1000 mL/day consider loop diuretics consider vaptans
569
What type of dementia has fluctuating cognition?
Lewy body dimentia
570
Describe progressive supranuclear palsy
Parkinson’s plus falls plus vertical gaze palsy
571
What drugs cause SIADH?
Carbemazepine Sulfonylureas SSRIs Tricyclics
572
How do you treat hiccups in palliative care?
Chlorpromazine or haloperidol
573
Parkinson's plus dementia think Lewy body
574
Drugs for neuropathic pain are typically used as monotherapy, i.e. if not working then drugs should be switched, not added
575
If raised afp what testicular cancer is excluded
seminoma
576
Which nerves are frequently injured during axillary nerve dissection?
The intercostobrachial nerves are frequently injured during axillary dissection. These nerves traverse the axilla and supply cutaneous sensation.
577
How does subacute degeneration of the spinal cord present?
dorsal columns and lateral corticospinal tracts are affected. joint position and vibration sense lost first then distal paraesthesia.
578
What is weakness after a seizure called?
Todds paresis
579
Which drugs exacerbate myaesthenia gravis
The following drugs may exacerbate myasthenia: * penicillamine * quinidine, procainamide * **beta-blockers** * lithium * phenytoin * antibiotics: gentamicin, macrolides, quinolones, tetracyclines
580
What are the symptoms of digoxin toxicity?
gastrointestinal disturbance (nausea, vomiting, abdominal pain) dizziness confusion blurry or yellow vision arrhythmias.
581
Treatment for trigeminal neuralgia
Carbemazepine
582
The patient has a Klumpke's paralysis involving brachial trunks C8-T1. Classically there is weakness of the hand intrinsic muscles. Involvement of T1 may cause a Horner's syndrome. It occurs as a result of traction injuries or during delivery. The patient has an Erb's palsy involving brachial trunks C5-6.
583
Marfan syndrome + headache =
Intracranial hypotension
584
What are the side effects of levodopa
dyskinesia dry mouth anorexia palpitations postural hypotension psychosis drowsiness.
585
Side effects of bromocriptine and cabergoline?
pulmonary, retroperitoneal and cardiac fibrosis.
586
What are causes of hyperkalaemia?
* acute kidney injury * drugs\*: potassium sparing diuretics, ACE inhibitors, angiotensin 2 receptor blockers, spironolactone, ciclosporin, heparin\*\* * metabolic acidosis * Addison's disease * rhabdomyolysis * massive blood transfusion
587
What drug is used to treat magnesium sulphate driven respiratory depression?
Calcium gluconate
588
Sudden onset hearing loss management
Following referral to ENT, patients with sudden-onset sensorineural hearing loss are treated with high-dose oral corticosteroids
589
Which contraceptive does not interact with enzyme inducers
depo-provera
590
Constipation in children management
Constipation in children = movicol then add stimulant (Senna), then add osmotic such as lactulose
591
What can be used to promote PDA closure?
Indomethacin or ibuprofen
592
Which medical condition contraindicates ulipristal
Asthma Breastfeeding - have to stop for one week after taking ulipristal
593
What drugs most commonly cause TENS/SJS?
Penicillins Quinolones Sulfonamides Corticosteroids NSAIDs
594
What blood test might you need to do before starting SSRI?
U and E SSRI may invoke hyponatraemia, if patient is on a drug like omeprazole which also causes hyponatraemia you need to check U and E before starting SSRI
595
What organism causes tinea capitis?
Caused by trichopghyton tonsurans or Microsporum Canis (associated with cats and dogs, and fluoresce under woods lamp). Treatment for trichophyton tonsurans = oral terbinafine. Treatment for microsporum Canis = griseofulvin. Topical ketoconazole shampoo for first two weeks to reduce transmission.
596
What organism causes tinea corporis (ringworm)
Tinea corporis = trichophyton rubrum and trichophyton verrucosum. Treated with oral fluconazole. (BMJ says that this is treated with topical terbinafine adjunct is aluminium acetate topical. 2nd line is topical ‘azoles’. 3rd line is oral terbinafine/ oral itraconazole)
597
Antibiotic therapy for PID?
oral ofloxacin + oral metronidazole or intramuscular ceftriaxone + oral doxycycline + oral metronidazole
598
The first visit is from eight Check everything with mum is great Urine, bloods and rhesus state Give advice and educate From eleven to thirteen Is the best time to do the Down’s screen While you’re at it, check the dates At sixteen or ten plus six Do BP and multistix Second scan is at twenty To check the fingers and toes (Make sure there’s plenty(twenty).) Once again at twenty-eight Urine, blood and rhesus state Anti-D if appropriate Must give anti-D once more When the week is thirty-four And plan for the birth, what a chore Check the lie at thirty-six If breech offer a quick fix Last visit at thirty-eight All that is left it to wait
599
Causes of horners
600
Keith and Wagener classification of hypertensive retinopathy