Revision Flashcards

1
Q

when should you never prescribe the combined oral contraceptive pill

A

FHx of thrombophilia

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2
Q

when should you never prescribe doxycycline

A

if patient< 12

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3
Q

what condition should you consider before prescribing furosemide

A

gout

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4
Q

what condition should you consider before prescribing an NSAID

A

hypertension

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5
Q

what should you consider before considering prochlorperazine

A

if patient pregnant

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6
Q

when should you not prescribe naproxen

A

if patient on warfarin- increased risk of GI bleeding

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7
Q

when in pregnancy is trimethoprim contraindicated

A

first trimester- folate antagonist

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8
Q

what antibiotic is first line for UTI in pregnancy

A

nitrofuratoin

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9
Q

give examples drugs you should monitor (4)

A

ACEi (BP, renal function, electrolytes)
warfarin
DMARDs
chemotherapy

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10
Q

how long is exclusive breastfeeding recommended for

A

first 6 months

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11
Q

what supplements should babies get

A

vit d from birth (not if on formula)

vit A,C and D from 6 months

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12
Q

what BMI decile would mean a child is overweight

A

> 91st
98th obese
99.6th clinically obese

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13
Q

what is the treatment for a baby with a suspected cows milk intolerance

A

2-4week lactose exclusion with extensively hydrolysed infant formula followed by a reintroduction of cows milk (if symptoms return then confirms diagnosis)

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14
Q

what condition is dermatitis herpetiformis associated with

A

coeliac disease

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15
Q

what percentage weight loss is recommended for BMIs of 25-35

A

5-10%

>35 15-20%

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16
Q

what does an insulin ratio mean

A

insulin to carb

e.g. 1:10 will need 1 unit for 10g of CHO

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17
Q

should T1DM patients carb count alcohol

A

no as increased risk of hypo following consumption of alcohol

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18
Q

does high fibre reduce CVD risk

A

yes

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19
Q

how does fibre reduce colon cancer risk

A

fibre fermentation creates short chain fatty acids which have anti-proliferative effect

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20
Q

what GI condition can exclusive enteral nutrition induce remission

A

crohns disease in paediatric patient

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21
Q

what is parenteral nutrition

A

the provision of all nutrients, fluids and electrolytes directly into a central or peripheral vein (indicated for an inadequate or unsafe oral and/or enteral nutritional intake or a no functional inaccessible or perforated GI tract.

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22
Q

what are the red flags for spinal pain

A
thoracic pain 
fever and unexpected weight loss 
bladder of bowel dysfunction 
ill health/ presence of other medical illness progressive neurological deficit 
disturbed gait, saddle anaesthesia 
age of onset <20 or >55
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23
Q

what are the yellow flags of pain

A

psychosocial factors shown to be indicative of long term chronicity and disability (predictors of response to treatment)

  • negative attitude that back pain is harmful or potentially severely disabling
  • fear avoidance behaviour and reduced activity levels
  • expectation that passive treatment will be beneficial rather than active treatment
  • tendency to depression, low morale, and social withdrawal
  • social or financial problems
  • compensation issues
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24
Q

what are the reds flags for cauda equina

A

bilateral sciatica
severe/ progressive neurological deficit of the legs (major weakness)
difficulty initiating micturition or impaired sensation of urinary flow- may lead to irreversible retention with overflow incontinence
loss of sensation of rectal fullness- may lead to reversible faecal incontinence
perianal, perineal or genital sensory loss (saddle anaesthesia/ paraesthesia)
laxity of anal sphincter

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25
Q

what are the red flags for a spinal fracture

A

sudden onset severe central spinal pain which is relieved by lying down
Hx of trauma/ strenuous lifting in people with osteoporosis/ corticosteroid users
structural deformity
point tenderness

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26
Q

what are the red flags for cancer associated spinal pain

A

> 55y/o
gradual onset of symptoms
severe unremitting paint hat remains when supine, aching night pain that prevents/ disturbs sleep and aggravated by straining
thoracic pain
localised tenderness
no symptomatic improvement after four-six weeks of conservative low back pain therapy
unexplained weight loss
PHx of cancer (esp breast, lung, prostate, GI, renal, thryoid)

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27
Q

what are the red flags for infection associated back pain

A
fever 
TB 
recent UTI 
diabetes 
Hv of IVDU
HIV infection 
immunosuppressants
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28
Q

what are the trigger words for neuropathic pain

A
shooting 
numb 
stabbing 
electric feel pain 
tingling 
burning 
traditional pain killers don't help emotional impact
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29
Q

what is anticholinergic syndrome

A

when antocholinergic drugs (e.g. amitriptyline) blocks M3 muscarinic receptors (parasympathic nervous system) causing anorexia, blurry vision, constipation/ confusion, dry mouth, sedation/ stasis of urine, drowsiness and QT prolongation

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30
Q

what dosing technique should you use with anticholinergic drugs

A

start low go slow and be aware of side effects

dont use post MI or in the manic stage of BPAD

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31
Q

when is creatine most effective in showing kidney function

A

when patient underweight or elderly

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32
Q

what BP medication can cause a cough

A

ACEi (e.g. lisinopril- increases bradykinin levels)

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33
Q

name a side effect of amlodipine

A

ankle swelling

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34
Q

what is edoxaban

A

anti-coagulant: inhibits factor 10a

prescribed based on patient weight

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35
Q

what is a coagulopathy

A

tendency to bleed due to inability to coagulate blood

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36
Q

doacs vs warfarin go

A

doacs cause less major bleeds, dont need monitoring and have faster onset

but cant be reversed unlike warfarin (vit K) and cant be given to patients with mechanical heart valves

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37
Q

name the doacs

A

dabigatran
apixaban
edoxaban
rivoroxaban

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38
Q

what is leucopenia

A

reduction in leukocytes (WBC)

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39
Q

what happens when steroids are stopped too quickly

A

adrenal insufficiency/ crisis

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40
Q

how is gentamicin given

A

IV only

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41
Q

how could you clinically differentiate intracranial heamorrhages

A

subdural- subclinical, slow deterioration
extradural- lucid period, quick deterioration
subarachnoid- thunderclap headache

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42
Q

treatment pathway asthma

A

SABA as required
consider low dose ICS to diagnose- if helps symptoms prescribe as regular
if >3 times a week use of SABA or disturbing sleep add in LABA to ICS and SABA
increase ICS or add LTRA

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43
Q

when should you do peak flow

A

3-4x a day to look for diurnal variation, low value usually in morning, cough at night

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44
Q

can you give SAMA and LAMA at the same time

A

no

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45
Q

how many puff of salbutamol should you take in suspected asthma attack

A

10

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46
Q

what does PRHrP released by Sqclc cause

A

hypercalcaemia with normal PTH

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47
Q

what can pancoast tumour cause

A

SVC syndrome, horners, vocal cord palsy (recurrent larhyngeal nerve)

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48
Q

how long should you give DOACs in DVTS

A

provoked- 3 months
unprovoked 6 months
more than 2 unprovoked lifelong
if renal impairement give LMWH

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49
Q

what scoring system for DVT and PE

A

wells score (>2 DVT >4 PE)

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50
Q

Tx for PE

A

calculate wells score (if <4 do d dimer, if +ve immediate CTPA)
if >4 admit for CTPA with interim DOAC if needed

if unstable unfractionated heparin and thrombolysis (alteplase/ streptokinase)
if stable CTPA and DOAC

continue anticoagulation for at least 3 months (DOAC)

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51
Q

what are the features of horners

A

anhidrosis
ptosis
miosis

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52
Q

what is in the paediatric sepsis 6

A

give high flow oxygen
obtain IV or IO access for: blood cultures, blood glucose (treat if low), blood lactate/ gas
give IV/IO abx

if shocked
fluid resus
consider early inotropic support
involve seniors early

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53
Q

how should you start child CPR

A

5 rescue breaths then 15 to 2

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54
Q

what drugs do you stop in AKIs

A

nephrotoxics- ACEi, ARBs, NSAIDs, aminoglycosides (gent, -micins)
drugs that increase comps: duiretics, metformin, anti-hypertensives

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55
Q

what are the indications for anticoagulants

A

venous thrombosis, AF, prophylaxis

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56
Q

what factors is def the haemophilias

A

a- 8

b- 9

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57
Q

what does APPT measure and what raises it

A
intrinsic system (8+9) 
raised in heparin, haemophilias, DIC and liver dissease
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58
Q

what does PT measure and what raises it

A

extrinsic (2,7)
measured as INR (0.9-1.2)
raised by warfarin, vit k def, liver disease and DIC

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59
Q

what is the anticoagulation after DVT or PE

A

offer apixaban or rivaroxaban for at least 3 months
if provoking factor no longer presence can stop after 3
if active cancer 6 months
if unprovoked or risk factors remain then calculate has bled score (stop anticoag if >4) and chadvasc score if risk of stroke to decide on lifelong anticoagulation

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60
Q

what drugs should be stopped before surgery

A

acei, arbs
nsaids,
warfarin 5 days before (INR<1.5)
DOACS- 24hrs if low risk, 48hrs if high bleeding- dont stop if op no bleeding risk)
all diabetic meds (except long acting insulin)
contraceptive pill and HRT if major op

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61
Q

what antiemetics are best post op

A

5HT3 receptor antagonists (odansetron)
dexamethasone, prochlorperazine
Cyclizine for opioid nausea

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62
Q

what antiemetic is best for chemo

A

ondansetron

dexamethasone

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63
Q

what antiemetics for motion sickness

A

cyclizine
hyoscine hydobromide
promethazine (sedating)

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64
Q

what are mild opioids

A

codeine

dihydrocodeine

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65
Q

what are strong opioids

A

morphine

oxycodone

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66
Q

what score for DVT

A

wells (calculate before doing dimer)
if 2 or more DVT likely do USS then d dimer if that is negative. if cant to USS in 4 hours do d dimer then intermin coagulation.
if d dimer +ve scan negative stop any interim coag and repeat USS in a week
if wells score 1 or less DVT unlikely do a d dimer, if thats +ve do USS

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67
Q

what score for PE

A

wells
>4 PE likely do CTPA, if CI offer anticoagulation
if 4 or less do d dimer, if positive do CTPA

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68
Q

what anticoagulation for DVT and PE

A

apixaban or rivaroxaban

if APS or renal impairment LMWH

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69
Q

what is acute cholecystitis

A

impaction of stone in neck of gallbladder

continuous RUQ/ epigastric pain, fever, vomiting, murphys sign positive

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70
Q

what causes biliary colic, how is it different to acute cholecystitis

A

cause by stone in cystic duct or common bile duct

doesnt have inflammatory component to cholecystitis (local peritonism, fever, increased WCC)

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71
Q

what are the features of chronic cholecystitis

A

chronic inflammation + colic
flatulent dyspepsia, nausea, distension, fat intolerance
treatment- cholecystectomy

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72
Q

what is ascending cholangitis

A

infection of bile duct

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73
Q

what are the features of ascending cholangitis

A

RUQ, fever and jaundice
rigors
tx- piperacillin, tazobactm

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74
Q

when is ERCP used

A

common bile duct clearance- stone in CBD

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75
Q

when should you consider antibiotics in sinusitis

A

when symptoms lasting for >10 days or symptoms of bacterial infection (purulent discharge, severe pain, fever) or systemically unwell

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76
Q

what is the centor criteria

A
tonsilitis: 3 or more bacterial 
fever 
anterior cervincal tender nodes 
no cough 
tonsilar exudates
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77
Q

what are the urgent referalls for red eye

A

acute closed angle glaucoma
anterior uvetitis
scleritis
acute iritis

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78
Q

what causes of red eye also cause decreased visual acuity

A

acute glaucoma

anterior uveitis

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79
Q

what cause of red eye causes painful eye movements

A

scleritis

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80
Q

what is the pupil like in anterior uveitis

A

small, may have synechiae which distort pupil via adhesions

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81
Q

how do you diagnose ant uveitis

A

slit lamp- leukocytes in anterior chamber

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82
Q

what is the uvea

A

iris, cillary body, choroid

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83
Q

what is the eye like in acute angle closure glaucoma

A

hard, fixed dilated pupil, hazy cornea

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84
Q

what is the treatment for acute angle closed glaucoma

A

urgent referal, avoid darkness (dilates pupil more)
beta blocker (timolol) - decreases aqeous production
pilocarpine- constricts pupil, opens angle
IV acetazolamide- decreases aqueous production
analgesia, antiemetic
once IOP controlled peripheral iridectomy

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85
Q

treatment for herpes simplex corneal ulcer

A

aciclovir (NOT steroids as this causes full thickness involvement)

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86
Q

treatment for GCA

A

40mg
if visual involvement 60mg pred
tapered over a year,

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87
Q

what is the treatment for optic neuritis

A

high dose methylpred for 72 hours then pred for 11 days

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88
Q

white retina W/ cherry red spot=?

A

central retinal artery occlusion

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89
Q

tx for crao

A

occular massage, surgical removal of aqueous, treat RF

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90
Q

signs of CRVO

A

dot and flame haemorrhages
cotton wool spots
macular oedema
swelling of optic disc

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91
Q

treatment for open angle glaucoma

A

prostaglandins, pilocapine, sympathetmetics, trabeculoplasty: latanoprost increase outflow
beta blockers, alpha adrenergics (-nidine), carbonic anhydrase (azetazolamide)- decrease aqueous production

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92
Q

normal IOP

A

<21

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93
Q

what biochemical signs does pagets have

A

isolated rise of ALP

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94
Q

treatment for psoriasis

A

potent steroid + vit d once daily 4 weeks
vit d twice daily 8-12 weeks
potent steroid + vit d 2x daily/ coal tar
v potent
dithranol, phototherapy (PUVA), systemic tx (methotrexate, ciclosporin, acritrenin (oral retinoid), biologics)
(if face, flexures or genitals use mild-mod steroid)

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95
Q

list steroids mild to mod

A

hydrocortisone
betnovate
dermovate

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96
Q

acne treatment

A

mild: topical retinoid (adapalene, tretinoin) or BP or clindamycin
mod: combo of 2 of above, oral abx (doxy, tetra, erythrcycline) with topical BP
severe: isotretoin

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97
Q

treatment for rosacea

A

avoid sun and alcohol, soap substitutes
mild- topical metronidazole or azelaic acid
mod to severe: oral tetra- doxycycline, isotretinoin
lasers

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98
Q

what laxative for hard stools

A

osmotic- lactulose, laxido

softeners- docusate

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99
Q

what laxatives for stimulant issue

A

senna

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100
Q

what can be used to reduce ammonia is hepatic encephaopathy

A

lactulose

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101
Q

how do you take bisphosphonates

A

on empty stomach, sit up for thirty minutes

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102
Q

convert 40mg of oxycodone to morphine

A

80mg morphine

oxycodone is 2 times as potent as morphine, need to divide the daily dose of morphine by 2 to get oxycodone dose

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103
Q

daily dose of 120mg morphine, how much is breakthrough dose

A

20mg

breakthrough dose is 1/6th daily dose

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104
Q

what type of infusion is a syringe driver

A

subcut

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105
Q

500mg of morphine oral, covert this to subcut morphine

A

250mg

divide oral doses by 2 to get subcut doses

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106
Q

what electrolyte abnormality do PPIs cause

A

hyponatraemia

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107
Q

what should you prescribe is someone who is diabetic with proteinuria

A

ACEi

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108
Q

anticholinergic side effects

A

constipation, dry mouth, dry eyes, blurred vision, urinary retention, tachycardia, cog impairment, falls

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109
Q

examples of anticholinergic drugs

A

oxybutin, ipatopium, tolteridine, amitriptyline

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110
Q

what electrolyte imbalance can thiazides cause

A

hyponatraemia

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111
Q

what electrolyte imbalance can SSRIs cause

A

hyponatraemia

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112
Q

what drugs for acute confusion

A

haloperidol

if alcohol withdrawal benzos long acting: chlordiazepoxide

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113
Q

how long is an emergency detention and who can authorise it

A

72 hrs
fy2 and above
does not authorise tx, no right of appeal

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114
Q

how long is a short term detention, what does it allow and who can do it

A

28 days
assessment and treatment
approved mental practitioner and MHO
right of appeal

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115
Q

how long is a compulsory treatment order, what does it allow and who can authorise it

A

6 months
one medical practitioner, one MHO then report from 2 independent doctors (2x AMP or AMP + GP) who make care plan
mandatory tribunal
reviewed at 6 months, right to appeal

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116
Q

what does bronchial breathing suggest

A

consolidation or fibrosis

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117
Q

what electrolyte abnormalities happen in refeeding syndrome

A

hypophosphataemia (rhabdomyolysis, leucocyte dysfunction, respiratory failure, cardiac failure, hypotension, arrhythmias, seizures, coma, and sudden death)
hypomagnesium and hypopotassium

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118
Q

what order should you replace calcium and phosphate

and magnesium and potassium

A

replace calcium before phosphate (or will cause hypocalcaemia)
replace magnesium before potassium as potassium needs calcium to go up

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119
Q

what is HHS

A

hyperosmolar hyperglycaemic state
happens in type 2
presents with polydipsia, polyuria, dry, shock, acute cos impairment
hyperglycaemia, hyper serum osmolality, volume depletion
NO KETOACIDOSIS

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120
Q

treatment for HHS

A

IV fluids with potassium replacement
insulin
thromboprophylaxis

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121
Q

treatment for alzheimers

A

anticholinesterase inhibitors: donepezil, rivastigamine, galantamine
memantine (NMDA antagonist) in late stage
antipsychotics

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122
Q

what medications for incontinence should you avoid in eldery

A

tolterodine and oxybutin

use mirabegron

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123
Q

management for parkinsons

A

avoid levodopa as long as possible
DA ropinirole and pramipexole
antichoingerics in young, MAO-B inhibitors (-giline)
levodopa- given as co-beneldopa or co-careldopa to prevent nause and vomiting

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124
Q

what are the signs of spinal cord compression

A

pain: in spine, worse on straining, radicular (band like burning e.g. around rib cage, precedes weakness)
weakness: bi or unilateral
altered sensation: proprioception, light tough
urinary problems: retention
bowel problems: constipation

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125
Q

Ix for Spinal cord compression

A

urgent MRI of spine

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126
Q

Treatment for spinal cord compression

A

16mg IV dexamethaxone, followed by 8mg po bd (to reduce vasogenic oedema)
radiotherapy mainstay of tx
surgery if appropriate
chemo

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127
Q

if you suspect spinal cord compression what should you do

A

arrange urgent MRI and start dexamethasone 8mg bd

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128
Q

radicular pain= ?

A

cord compression

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129
Q

symptoms of superior vena cava obstruction

A
swelling of face, neck, one or both arms 
distended veins 
SOB 
HA 
lethargy 
late- injected conjunctiva, sedation
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130
Q

Ix for SVC obstruction

A

cxr- is there a mass/ foreign body
venogram- is there a clot
CT chest

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131
Q

treatment for SVC obstruction

A

clot- thrombolysis with alteplase, anticoagulation (LMWH, warfarin)
extrinsic compression- steroids, chemo, radio, stent

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132
Q

what side of lung tumour causes SVC obstruction

A

right

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133
Q

what can cause hypercalcaemia in cancer pt

A

humoural (PTHrP)
bone destruction
tumour production of vit D (lymphomas)

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134
Q

symptoms of hypercalcaemia

A
nausea, anorexia 
thirsty 
polydipsia, polyuria 
constipated 
confused 
poor concentration, drowsy
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135
Q

Ix for hypercalcaemia

A

U+Es to look for dehydration
phosphate (low in hyperparathryoidism)
if no known malignancy myeloma screen

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136
Q

ts for hypercalcaemia

A

rehydrate first - several L of saline

bisphosphonates (pamidronate after rehydrated)

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137
Q

symptoms + signs of cardiac tamponade

A

SOB
fatigue, palpitations, pericarditis (chest pain improved by sitting forward), symptoms of advanced cancer
JVP distention, pulsus paradoxus (fall in pressure during inspiration), soft heart sounds/ pericardial rub, tachycardia with low BP

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138
Q

IX for tamponade

A

CXR
ECG
echo (rim of pericardial fluid)
cytology of fluid

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139
Q

tx for tamponade

A

pericadiocentesis

pericardial window

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140
Q

does perciardial tamponade cause systolic or diastolic heart failure

A

diastolic

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141
Q

what is neutropenic sepsis

A

sepsis in a patient with a neutrophil count less than 0.5 or <1 in cancer patients or who have had chemo in the last 21 days

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142
Q

tx for neutropenic sepsis

A

antibiotics within 1 hr of admission

give immediately before septic screen/ blood tests

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143
Q

what is CO2 like in a PE

A

low (blowing it off with tachypnoea)

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144
Q

Ix for Pe

A
CTPA 
ABGs 
O2 sats 
ECG 
bloods
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145
Q

tx for PE in malignancy

A

LWMH for 6 months

consider rivaroaban if recurrent DVTs/PE

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146
Q

what is 8/500 co-codamol

A

8mg codeine with 500 mg paracetamol

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147
Q

100mg of codeine = ? morphine

A

10

morphine is 10 times as strong as codeine

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148
Q

what is the pain ladder

A

mild- paracetamol
mod- co-codamol 30/500, dihydrocodeine, tramadol
severe- morphine, diamorphine, oxycodone, hydromorphine, methadone
adjuvants: NSAIDs, TCAs, anticonvulsants. steroids, anxiolytics, muscle relaxants, antimuscarinics

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149
Q

what should you prescribe with opioid

A

anti-emetic and laxative

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150
Q

what drugs can be used as muscle relaxants

A

diazepam, baclofen

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151
Q

what drugs can be used as antimuscarinics (for colicky pain)

A

hyoscine butylbromide

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152
Q

how do you convert oral tramadol dose to oral morphine dose

A

divide tramadol dose by 10

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153
Q

how do you convert oral morphine to SC diamorphine

A

divide by 3

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154
Q

what are the anticipatory care medications

A

Opioid for pain and/or breathlessness: morphine 2mg SC
anxiolytic or sedative for anxiety, agitation or breathlessness: midazolam 2mg sc
anti-secretory medications for resp secretions: hyoscine butylbromide 20mg sc
anti-emetic for n+v: levomepromazine 2.5-5mg sc

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155
Q

what are the dexa results meaning

A

t scores
1- -1 normal
-1 to -2.5 osteopenia
-2.5 or less osteoporosis

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156
Q

talk me through the bone protection guidelines girly xx

A

calculate Qfracture/frax score (10 year risk of fragility fracture) for all high risk (>65 women, >75 men, RFs)
if score 10% or more do DEXA
if -1 to -2.5 modify risk factors
if less than -2,5 bone protection (once weeklr bisphosphonate)
consider bone protection in those taking steroids
offer HRT to young post menopausal women

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157
Q

rank these from least to most potent:

methyl pred, betamethason, hyrocortisone, cortisone, prednisolone, dexamethasone

A

cortisone, hydrocortisone, methyl pred, pred, dex

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158
Q

what drug first line for delirium

A

haloperidol

benzos if have PD

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159
Q

what can be used to treat acute pulmonary oedema

A

high flow oxygen
IV furosemide
IV diamorphine (vasodiltor, reduces CO)
digoxin

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160
Q

what is a modified release preparation

A

12 hourly tablets

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161
Q

who should adenosine not be given to

A

asthmatics

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162
Q

what are the signs of brugada syndrome on ECG

A

st change - coved/ saddle

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163
Q

which brain bleed has a period of lucidity

A
extradural 
lemon shaped (lens shaped), MMA, associated with skull fractures, young men, LOC following lucidity after injury
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164
Q

who gets subdural haematomas

A

old people on blood thinners, slow decline in cognition

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165
Q

what is laryngomalacia

A

congenital cause of stridor in infants

resolves usually by 12-24 months

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166
Q

what are the features of epiglottitis

A

dsypnoea, dysphagia, drooling, dysphonia (muffled voice)
stridor is a late sign
tripod position
distinguished from retropharyngeal abscess by xray

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167
Q

what is seen on cray in croup

A

steeple sign of subglottis

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168
Q

what is quinsy

A

peritonsilar abscess

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169
Q

what occurs sooner physiological or breast feeding jaundice

A

physiological- after 24 hours
breast feeding- usually in 2-3 weeks, can be in first
in sufficient intake- first week not getting enough calories

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170
Q

what are the alarm symptoms of dyspepsia

A
anaemia 
loss of wight 
anorexia 
recent progression 
malaena/ haematemesis 
swallowing difficulties (dysphagia) 
(think malignancy)
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171
Q

how does phenytoin affect COCP

A

induces liver enzymes, reduces efficacy of CoCP

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172
Q

what are the features of osteomalacia

A

bony pain
vit d and calcium def (calcium can be normal)
high PTH

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173
Q

what is the most important step in HHS

A

IV fluids first

insulin when rehydrated

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174
Q

what contraception for dysmenorrhoea

A

COCP

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175
Q

what causes CNIII palsies

A

intracranial anuerisms, diabetes and extradural haematomas

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176
Q

difference between somatosism and conversion disorder

A

Conversion disorder is characterised by voluntary motor or sensory function deficits that suggest neurological or medical conditions but are rather associated with clinical findings that are not compatible with such conditions. Somatic symptom disorder is characterised by one or more somatic symptoms that are distressing or result in significant disruption of daily life.

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177
Q

tender mass in RIF- UC or crohns

A

crohns

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178
Q

how do you tell the difference between an indirect and a direct inguinal hernia

A

indirect goes down towards scrotum
direct above pubic tubercle
indirect can be controlled by pressure at the internal ring (halfway between pubic tubercle and ASIS)

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179
Q

what type of incontinence does oxybutin help with

A

OAB

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180
Q

what type of incontinence does duloxetine help with

A

stress

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181
Q

treatment for STEMI

A

300 mg aspirin - continue indefinitely unless CI
presenting in 12 hours: reperfusion therapy (PCI or fibrinolysis)
-PCI available in 120 mins: prasugrel if not on AC, clopidogrel if on anti coagulant, if >75 and high bleeding risk offer tricagrelor or clopidogrel instead of prasugrel
- PCI not available in 120 mins: fibrinolysis= alteplase, streptokinase, antithrombin (fondaparinux) at same time, ECG 60-90 mins after fibrinolysis, give tricagrelor (or clopidorgrel if high bleeding risk)

medical management:
-tricagrelor or clopidogrel if high bleeding risk

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182
Q

treatment for NSTEMI/ unstable angina

A

300mg aspirin and continue indefinitely
antithrombin (fondaparinux) unless high bleeding risk or immediate angiography
calculate grace score (6 month mortality), ECG, troponin I/ T
intermediate or high risk (>3%): if unstable offer immediate angiography +/- PCI, if stable offer in 72 hours
give prasugrel with aspirin (or clopidogrel if on AC), give unfractionated heparin if getting PCI

low risk: <3%
(young people may still benefit from PCI)
tricagrelor (or clopigrel if high bleeding risk)

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183
Q

what drugs used for secondary prevention following an MI

A
ACEi (arb if intolerant) indefinitely 
dual antiplatelet (aspirin + another e.g. clopidogrel) for 12 months 
beta blockers 12 months/ indefinitely if LVEF reduced 
statin (atorvastatin 80mg) 

if LVEF reduced start aldosterone antagonist 3-14 days after MI

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184
Q

what lifestyle changes for secondary prevention following an MI

A

exercise, stress, Mediterranean diet, alcohol, smoking
cant drive with unstable angina
stop driving for a week after PCI

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185
Q

when should a statin be started for primary prevention

A

in those with a QRISK2 score >10%, CKD, T1DM, >85 who smoke/ HPTN, severe obesity
(atorvastatin 20mg)

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186
Q

management of AF

A

if unstable DC cardioversion (+ amiodarone if unsuccessful)
heparin for anticoagulation in the acute setting
treat underlying cause: HPTN, valvular disease, HF, IHD, infection, cancer, alcohol, hyperthyroid, electrolytes
if <48 hrs: rate (BB, RL CCB (verapamil/ diltiazem), digoxin if sedentary)/ rhythm (cardioversion, flecainide, amiodarone)
if >48 hours: rate control, need to be anticoagulated for 3 weeks before rhythm control

assess CHA2DS2VASc score (stroke risk) and ORBIT bleeding risk
anticoagulation if CV score 2 or more, 1 if man: apixaban, dabigatran, rivaroxaban (if DOAC CI warfarin) (do not offer anticoagulation to those <65 with 0 (men) or 1 (women) CHV score)
rate control: beta blocker or diltiazem/ verapamil or digoxin if sedentary
(do not offer amiodarone long term)
rhythm control if rate control unsuccessful: flecainide, amiodarone, electrical cardioversion, ablation

amiodarone not flecainide if ischaemic or structural HD

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187
Q

what can you not prescribe verapamil and ditiazem with

A

alpha blockers, ACEis, arbs, antipyschotics, amiodarone, beta blockers, digoxin, NSAIDS LOADS

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188
Q

how is heart failure diagnosed

A

HX, exam, ECG, NT-proBNP, if high echo (>2000 in 2 weeks, 400-2000 in 6 weeks)

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189
Q

management for chronic HF

A
diuretics- mineralocorticoid receptor antagonist (spironolactone) 
if reduced ejection fraction: 
-ACEi (or ARB) (if intolerant to both hydralazine and nitrate) 
-BB 
if still symptoms: 
-sacubitril if EF <35% 
or 
-ivabridine sinus rhythm EF<35% 
or 
-hydralazine and nitrate 
or 
-digoxin
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190
Q

treatment for stable angina

A

GTN (2nd dose after 5 mins, ambulance 5 mins after 2nd dose)
BB/ CCB (combo of two if not helped- must be -dipine ones (dihydropyridine))
if not helping: long acting nitrate (isosorbide), ivabradine, nicorandil
if still not helping referral for revascularisation surgery (CBG)

consider aspirin 75 mg
consider ACEi
Statin

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191
Q

what should you do for people with BPs in clinic between 140/90- 179/119

A

ABPM
if 135/85-149/94 : lifestyle advice + tx if >80 or CVD/ organ damage/ high CVD risk (>10%)
150/95 lifestyle + tx

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192
Q

what should you so for people with BP in clinic of 180/120

A

refer same day if papilloedema/ life threatening symptoms or suspected pheochromocytoma
anti hypertensives immediately

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193
Q

what are the BP targets

A

<80 140/90 clinic 135/95 ABPM

>/= 80 150/90 clinic 145/95 ABPM

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194
Q

what is the tx pathway for HPTN

A

hypertension with type two diabetes or <55: ACEi/ ARB -> A + CCB or thiazide (indapamide) -> A + C + T
>55 or black african or african-caribean : CCB + C + A/T -> C + A + T

resistant: spironolactone if potassium <4.5
alpha (sin) or beta blocker if >4.5

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195
Q

what bugs usually cause infective endocarditis

A

commonest- staph aureus: amox + gent / fluclox if sepsis
prosthetic valve/ abnormal valves/ IVDU- staph epidermidis: vancomycin and gent
dental- viridans ( beta lactam (penicillin, cephalosporins) +/- gent, vancomycin

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196
Q

what is S1

A

closure of mitral and tricuspid valves

start of systole, pulse felt at same time

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197
Q

what is S2

A

closure of aortic and pulmonary valves

start of diastole

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198
Q

what causes a split S2

A

inspiration, pulmonary stenosis

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199
Q

what grade of murmer has a thrill

A

4-6

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200
Q

Murmur: ejection systolic, crescendo decrescendo, radiates to carotids, loudest on expiration when patient sitting forward, slow rising pulse

A

AS

most common cause calcification, bicuspid valve, rheumatic heart disease

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201
Q

Murmur: pansystolic, radiating to axilla, loudest on expiration lying on left side

A

MR

Ax- IE, MI, rheumatic HD

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202
Q

murmur: early diastolic, crescendo decrescendo, left sternal border 3/4th ICS

A

AR

bicuspid valve, RHD, IE, aortic dissection

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203
Q

collapsing pulse

A

AR

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204
Q

murmur: mid diastolic, rumbling, opening click, low volume pulse, heard loudest over…

A

MS
congenital
… apex

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205
Q

mid systolic click, late systolic murmur

A

mitral prolapse

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206
Q

pan systolic murmur over left 4th ICS

A

tricuspid regurg

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207
Q

what sided murmurs are loudest on inspiration

A

right- tricupsid regurg, pulmonary stenosis

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208
Q

soft diastolic murmur, loudest at 3/4th ICS at left sternal edge, loudest on inspiration

A

TS

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209
Q

ejection systolic, loudest on inspiration, a waves

A

pulmonary stenosis

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210
Q

does smoking make UC or crohns worse

A

crohns

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211
Q

treatment for crohns

A

inducing remission:
- monotherapy if 1 epsiode in 12 months: steroid/ budesonide (sulfsalazine or mesalazine (5-ASA) - less effective)
- add azathioprine if 2 or more episodes (or methotrexate if CI)
-infliximab/ adalimumab if severe
maintenance:
-azathioprine/ metacaptopurine monptherapy
-methotrexate

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212
Q

treatment of UC

A
inducing remission: 
mild mod (max 6 stools a day, no pyrexia, pulse <90, no anaemia, ESR<30)- topical (proctitis/ proctosiggmoiditis/ left sided UC)/ oral aminosysalicylate (5-ASA/  sulfasalazine) (or both)
-steroid short term
-biologics 
severe acute: 
-Iv steroids/ ciclosporin/ surgery (if no improvement at 72 hours or worsening symptoms: stools >8x/day, pyrexia, tachycardia, colonic dilatation, abnormal bloods) 
maintaining remission: 
-topical/ oral aminosalicylate (5-ASA) 
-azathioprine
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213
Q

where does UC affect

A

distal to ileocecal valve (end of large intestine)

left sided UC common

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214
Q

who should you test for H pylori

A

uncontrolled dyspepsia with no alarm symptoms (no response to lifestyle changes, antacids, one month course of PPI)
patients at high risk, previous ulcer/bleed, unexplained IDA after endoscopy exclude malignancy

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215
Q

what tests for h pylori

A

urea 13c breath test
stool helicobacter antigen test
(not within 2 weeks of ppi and 4 weeks of abx)

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216
Q

treatment for H pylori

A

triple therapy: PPI and 2 abx (consider previous ones tried)
1st line: amoxicillin + clarithromycin/ metronidazole (depending on previous use) for 7 days
if that doesn’t work try the other one for another 7 days
if penicillin allergic
- PPI + clarithromycin + metronidazole

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217
Q

tx for dyspepsia

A

weight loss, eating (alcohol, coffee, chocolate, fatty foods), smoking

  • PPI for 4 weeks, h pylori test if this doesnt help
  • endoscopy if alarm symptoms/ GI bleed
  • offer H2RA if still inadequate response (-tidines)
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218
Q

what drugs can cause dyspepsia

A

calcium antagonists, nitrates, theophyllines, bisphosphonates, cortitosteroids, NSAIDs

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219
Q

what are the alarm symptoms

A

nice 2 weeks:
dysphagia
>55+ weight loss with: upper abdo pain/reflux/ dyspepsia

anaemia 
loss of weight 
anorexia 
recent progression 
malaena/haematemesis
swallowing difficulties
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220
Q

what laxatives for diverticulosis

A

bulk forming (high fibre diet, lots of water)

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221
Q

when should you suspect diverticular disease

A

(diverticulosis asymptomatic)
DD- intermittent abdo pain in left lower quadrant with constipation, diarrhoea and occasional large rectal bleeds
-pain triggered by eating and relieved by passage of stool/ flatus

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222
Q

what are the symptoms of acute diverticulitis

A

constant abdo pain, severe and localising to left lower quadrant with:
fever
or
sudden change in bowel habit and significant rectal bleeding/ mucus
or
Tender LLQ, Hx of DD

complicated if:

  • mass palpable- abscess
  • adbo rigidity and guarding- perforation
  • signs of sepsis
  • signs of fistula
  • signs of obstruction
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223
Q

Ix for acute complicated diverticulitis

A

if inflam markers raised contrast CT within 24 hours

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224
Q

tx for acute diverticulitis

A

systemically well- paractamol
unwell/ cormorbid- abx (co-amoxiclav/ cefalexin + met)
complicated- IV abx (same as above)
surgery if continuing symptoms

225
Q

what antibiotics cause C diff

A

clindamycin, cephalosporins, co-amoxiclav, ciprofloxacin

Cephalosporins: ceph or cefts

226
Q

what are the severities if c diff infection

A

mild- normal WCC, <3 loose stools
mod- wcc <15, 3-5 stools/ day
severe- wcc >15, increased serum creatinine, temp >38.5, evidence of severe colitis
life threatening- hypotension, partial/ complete ileus, toxic megacolon

227
Q

tx for c diff

A

mid/ mod/ severe- oral vanc for 10 days (2nd line fidaxomicin)
if that ineffective- oral vanc IV met 10 days
further episodes (<12 weeks fidaxomicin, >12 weejs oral vanc, both 10 days)
life threatening: vanc + IV met 10 days

228
Q

what scan for renal stones

A

non contrast CT

229
Q

what abdo stuff do you use USS for

A

gall bladder and biliary tree
renal tract
appendicitis
chronic pancreatitis

230
Q

duodenal biopsy endoscopy or colonscopy

A

endoscopy

231
Q

imaging for pancreatitis

A

ct

232
Q

what bug:
incubation 1-6 hours
starchy food (rice)

A

baciluus cereus

233
Q

what bug: 1-6 hours
rood temp food
milk/ meat/ fish/ cream

A

staph aureus

234
Q

what bug: bloody diarrhoea

beef, raw milk, petting zoos

A

ecoli 0157 (causes HUS)
notify health protection unit
stool toxin

235
Q

what bug: 2-5 days, most common cause, raw poultry, GBS

A

campylobacter

236
Q

what bug: poultry, meat, raw eggs, 12-48 hours

A

salmonella

237
Q

travellers diarrhoea

A

e coli

238
Q

what bug: kids, mild watery, not bloody

A

rotavirus

239
Q

what bug: winter vomiting big, explosive D+V, cruise ships

A

noravirus

240
Q

treatment for hepatic encephalopathy

A

lactulose

if persistent symptoms add rifaximin

241
Q

what prophylatic antibiotic in acute variceal bleed

A

ceftriaxone IV

242
Q

what prophylatic treatment to prevent bleeds in oesophageal varcies

A

small- diagnostic and annual andoscopy

medium to large- beta blocker +/- band ligation

243
Q

what is wernickes encephalopathy

A

reversible thiamine def that causes: confusion, ataxia and opthalmoplegia
tx with thiamine and magnesium replacement

244
Q

what is korsakoffs

A

irreversible hypothalamic damage and cerebral atrophy due to thiamine deficiency
confabulation due to retrograde amnesia, unable to make new memories, lack of insight and apathy

245
Q

tx for withdrawal

A

chlordiazepoxide
acamprosate after acute withdrawal to reduce cravings
disulfram for chronic dependence

246
Q

what are the CAGE questions

A

ever tried to/ felt like you should cut down
angry at criticism
guilt over drinking
eye opener

247
Q

what does HBsAg mean

A

surface antigen
first thing to arise after infection
converted to anti-HBs and HBsAg cleared in resolved infections
presence for >6 months = chronic infection

248
Q

HBeAG

A

positive and chronic

shows high viral replication and infectiousness

249
Q

Anti-HBe

A

inactive, carrier disease

immunity from previous infection

250
Q

anti-HBc

A

current or previous infection

persists for life

251
Q

anti-HBc IgM

A

infection in last 6 months

252
Q

anti-HBc IgG

A

chronic or past infection

253
Q

anti-Hbs

A

previous vaccination or cleared infection

254
Q

HBV DNA

A

viral replication

increased risk of cirrhosis and hepatocellular cancer

255
Q

HBV DNA

A

viral replication

increased risk of cirrhosis and hepatocellular cancer

256
Q

what is positive in previous hep B vaccination

A

anti-HBs only

257
Q

when is HbsAg -ve

A

vaccination

cleared infection

258
Q

when is HbeAg -ve

A

vaccination
cleared infection (anti-HBe +ve)
chronic infection inactive carrier (anti-HBe +ve)

259
Q

treatment for PBC

A

ursodeoxycholic acid

colestyramine for itch

260
Q

treatment for PSC

A

transplant

colestyramine for itch

261
Q

hypertension + hypokalaemia=?

A

primary hyperaldosteronism

  • 2/3rds due to aldosterone producing adenoma (conns syndrome), surgery
  • 1/3rd due to bilateral adrenal hyperplasia, treated with spironolactone
262
Q

commonest cause of pneumoniae

A

strep pneumoniae

263
Q

describe what happens in barretts

A

intestinal metaplasia

squamous to columnar with goblet and paneth cells

264
Q

is bicarb an acid or a base

A

base

265
Q

what does a high base excess mean

A

alkalotic

266
Q

what is the rate of insulin infusion for DKA

A

0.1 units /kg/hr

267
Q

what does SSRI + statin risk

A

GI bleed- give PPI

268
Q

when can you insert a copper IUD after birth

A

within 48 hours or after 28 days

269
Q

a bishops score of 5 or less indicates what

A

labour is unlikely to start without induction

270
Q

how should you alter medication in addisonian patients with intercurrent illness

A

double hydrocortisone, same fludrocortisone

271
Q

how do you tell small from large bowel

A

small has valvulae conniventes that go whole way across bowel
large bowel has haustra

272
Q

what are the size limits for the bowels

A

small 3cm
colon 6cm
caecum 9cm

273
Q

where is the ceacum

A

start of large bowel,

RIF

274
Q

what does a small bowel obstruction look like

A

coiled spring
central
can see valvulae conniventes

275
Q

what does a large bowel obstruction look like

A

haustra

276
Q

what does a sigmoid vovulus look like

A

coffee bean in left lower quadrant
ahaustral
as distal bowel ascending, transverse and descending bowel may be dilated

277
Q

what does a caecal volvulus look like

A

right lower quadrant
haustra
distal colon collapsed
looks like a fetus

278
Q

what is riglers sign

A

can see both sides of bowel

means theres air in abdomen

279
Q

what are the features of IBD on a-xray

A

thumbprinting: thickening of haustra
lead pipe colon: loss of normal haustral marking secondary to chornic colitis
toxic megacolon: dilatation of colon

280
Q

is a subcapital hip # intra or extra capsular

A

intra

281
Q

what surgery should you stop the COCP/HRT 28 days prior to

A

any lasting over 30 mins
emergency surgery
(dont need to do it for e.g. tooth extractions or varicose vein surgery)

282
Q

what causes osteomalacia

A

vit D def

283
Q

what biochem is seen in osteomalacia

A

low vit D, low calcium, low phosphate

high ALk phos and PTH

284
Q

what is the empirical tx for gonorrhoea

A

IM ceftriaxone

285
Q

what does gonorrhoea look like on gram stain

A

gram -ve diplococci

286
Q

what is the anticoagulation in a DVT

A

LMWH for 5 days then DOAC

if active cancer then DOAC

287
Q

what causes a cavitating pneumonia in the upper lobes, seen in diabetics and alcoholics

A

klebsiella

288
Q

what is pseudomonas aeruginosa like

A

commin in bronchiectasis and CF patients

causes ground glass on CT

289
Q

symptoms of mycoplasma pneumoniae

A

flu like, HA, arthalgia, dry cough

290
Q

what is legionella pneumonia like

A

flu like symptoms, dry cough, fever, myalgia, hepatitis, diarrhoea and vomiting
bi basal consolidation

291
Q

who gets staph areus pneumonia

A

IVDU, young, elderly, comorbid

people after the flu

292
Q

blood stained nipple discharge= ?

A

duct papilloma (malignant potential so gets removed)

293
Q

what will duct ectasia have

A

green brown discharge
abscess
smoking

294
Q

how long should people eat gluten for before testing TTG

A

6 weeks

295
Q

what is the management for acute upper urinary tract obstruction

A

nephrostomy

296
Q

best test for liver function

A

PT

297
Q

pain when exposed to cold

A

vasoclusive crises in sickle cell

298
Q

what does FFP contain and help with

A

blood proteins and CFs

when low INR/ PT

299
Q

what does CLL transformin to

A

non hodgkins lymphoma (richters transformation)

300
Q

what med should you stop beofre coronary angioplasty

A

metformin

lactic acidosis

301
Q

can you attempt external cephalic version after membranes have ruptured

A

no

302
Q

Tx for suspected PE

A

admit immediately if unstable or pregnant/ post partum. everyone else calculate wells score and admit if >4
CTPA, DOAC for interim

if <4 do d dimer, DOAC if cant be done in 4 hours
if positive do CTPA, if -ve stop DOAC

(LMWH if renal impairment or pregnant)

303
Q

tx for confirmed PE

A

DOAC
LMWH if CI ot APS
3 months if provoked, 6 months if unprovoked or cancer
if patient unstable thrombolysis (alteplase)

304
Q

difference between schizoid and schizotypal PD

A

schizotypal had ideas of refence, odd beliefs and behaviours

305
Q

when should patients with a mild diverticulitis flare be admitted

A

if symptoms dont improve in 72 hours

306
Q

what iron study results in Haemochromatosis

A

high transferrin sats
raised transferrin
low TIBC

307
Q

difference between acute and critical limb ischaemia

A

acute: pale, pulseless, pain, paralysis, paraesthesia, perishingly cold
critical: pain at rest for >2 weeks aften at night not helped by analgesia

308
Q

what prophylaxis following spontaneous bacterial peritonitis

A

ciprofloxacin

309
Q

what antiemetic for intracranial tumours

A

dexamethasone

310
Q

do you need to x-ray an ng tube with apsiriate <5.5

A

no

311
Q

treatment for thrush

A

oral fluconazole
clotrimazole pessart
topical imidazole if vulval symptoms

312
Q

when is mastectomy preferred to WLE

A

mutlifocal tumour
large, central tumour
DCIS >4cm

313
Q

treatment after breast surgery

A

radiotherapy for all WLE and mastectomy for T3-4 tumours
if hormone receptor positive:
-tamoxifen for pre and perimenopausal (blocks oestrogen receptors in breast)
-aromatase inhibitors for post menopausal (anastrozole) (prevent peripheral conversion of oestrogen)
HER2 +ve: trastuzumab

314
Q

how do the glaucoma drugs work: B blockers

A

reduce aqueous secretion

315
Q

how do the glaucoma drugs work: prostglandins

A

increase aqueous outflow through uveoscleral route

316
Q

how do the glaucoma drugs work: sympathomimetics (brimonidine)

A

reduce secretion and increase outflow

317
Q

how do the glaucoma drugs work: miotics (pilocarpine)

A

opening aqeous drainage in trabecular meshwork

318
Q

how do the glaucoma drugs work: laser cycloablation

A

destroys secreting bit of ciliary body

319
Q

what treatment should be offered first in open angle glaucoma

A

prostaglandin analogue (latanoprost)
(2nd line beta blocker, CAinhibitors, symps)
more advanced laser

320
Q

how do the glaucoma drugs work: carbonic anhydrase (dorzolamide)

A

reduce aqueous

321
Q

treatment for acute angle closure glaucoma

A
pilocarpine drops
acetazolamide IV 
beta blockers 
steroids 
analgesia and anti-emetic 
surgery: iridotomy
322
Q

first line antiplatelet following a stroke

A

clopidogrel

323
Q

can acute pancreatitis cause hyper or hypocalcemia

A

hypo

324
Q

tx for thredworm

A

oral mebendazole

325
Q

what Das 28 score to qualify for biologics

A

> 5.1

326
Q

what should you give instead of morphine in patients with renal impairment

A

oxycodone

327
Q

what should be the first test in reduced fetal movements

A

doppler

328
Q

do no need to stop ARBs in ACEis

A

yes

329
Q

what is used as prophylaxis for meningitis

A

ciprofloxacin

330
Q

test for Achilles rupture

A

USS

331
Q

tx for chronic vestibular neuronitis

A

vestibular rehab

prochlorperazine for symptom control in acute setting

332
Q

what is the main risk factor for cholangiocarcinoma

A

PSC

333
Q

vision worse going down stairs

A

trochlear nerve palsy

334
Q

do patients >75 with fragility # need a dexa

A

no start bisphosphonates

335
Q

when do you give amiodarone in CPR

A

when its a shockable rhythm after 3rd shock and then after every 2nd shock

336
Q

what weeks if you miss 2 pills should you consider emergency contraception

A

pill free week

week 1

337
Q

what happens if you miss 1 pill

A

take asap, even if its 2 in one day

338
Q

what happens if you miss 2 pills in week 2

A

no need for emergency contraception

339
Q

what happens if you miss 2 pills in week 3

A

finish current pack, start next pack right with no pill free interval

340
Q

what general advice for missing 2 pills

A

use condoms until pills taken for 7 days in a row

341
Q

chlamydia psittaci pneumonia

A

birds, dry cough

342
Q

pneumocystitis pneumonia

A

immunosuppressed

343
Q

common HAP bugs

A

staph aureus, pseudomonas, klebsiella

344
Q

when should you consider an antibiotic in an acute exacerbation of COPD

A

signs of infection, change in volume or colour of sputum

give amoxicillin/ doxy

345
Q

COPD treatment pathway

A

SABA/SAMA
if no response stop SAMA, add LABA + LAMA
if asthmatic features (asthma, atopy, high eosinophils, diurnal peak flow variation, variation in FEV1) then LABA + ICS
LAMA+ LABA + ICS (+SABA)

346
Q

paediatric asthma pathway

A

SABA
ICS
LTRA
LABA

347
Q

what does a protein content of 45 in a pleural effusion mean

A

exudative, effusions >30 exudate, <30 transudate

348
Q

what causes transudative effusions

A

congestive HF
liver cirrhosis
severe hypoalbuminemia
nephrotic syndrome

349
Q

what causes exudative effusions

A
malignancy 
infection, if purulent empyema 
trauma - can be bloody, food particles oesophageal rupture 
pulmonary infarction 
pulmonary embolism
350
Q

what are the normal BM levels

A

4 -> 7 (fasting) 11.1 (random)

HbA1C <42 (6%)

351
Q

what blood sugars should diabetics aim for

A

4-7 before meals
5-9 2 hrs after
4-7 bed time
HbA1C <48 (6.5%), if on hypoglycaemic drugs <53 (7%)
if goes above 58 (7.5%) lifestyle advice and add another drug aim for 53

352
Q

what is a pre diabetic HBA1C

A

42-47

353
Q

when can you diagnose T2DM

A

HBa1C of 48 or more
random of 11 or more, fasting of 7 or more
if symptomatic can diagnose off one result, if not repeat test
dont use HBA1c on children, pregnant women, acutely unwell…

354
Q

what are the gliptins

A

DPP-4 inhibitors

355
Q

what weight effect does piaglitazone have

A

gain

356
Q

what are the gliflozins

A

SGLT2 inhibitors

357
Q

what effect do GLTT2 inhibs have on weight

A

loss

358
Q

what are: glimepiride, glipizide, tolbutamide

what weight effect do they have

A

sulfonylureas (also glicalzide) #gain

359
Q

what is renin like in primary and secondary hyperaldosteronism

A

primary low, adrenals making too much aldosterone

secondary high, BP in kidneys low so body making more renin

360
Q

what causes hyperaldosteronism

A

primary: conns syndrome (adrenal adenoma) , bilateral adrenal hyperplasia
secondary: renal artery stenosis

361
Q

screening tool for hyperalsosteronism

A

renin: angiotensin ratio

low renin primary, high renin secondary

362
Q

treatment for hyperadlosteronism

A

primary: spironolactone, removal of adenoma, angioplasty for stenosis

363
Q

tx for acromegaly

A

transphenoidal surgery
somatostatin analogues: ocreotide
pegvisomant (GH antagonist) if resistant

364
Q

what causes SIADH

A

too much ADH (vasopressin):

SCLC, too much from post pit: infection, post op, menigitis, medications (thiazides, carbamazepine)

365
Q

features and tx for SIADH

A

hyponatraemia, high urine osmolarity, high urine sodium

correct sodium slowly to prevent central pontine myelinolysis

366
Q

features of diabetes insipidus

A

lack of response to ADH- nephrogenic (lithium) or cranial (tumours, injury, infections)
polydipsia, polyuria, hypERnatraemia

367
Q

Ix for diabetes insipidus

A

water deprivation test: (desmopressin stimulation test)
avoid fluids for 8 hours and measure urine osmolality
give desmopressin and 8 hours later measure urine osmolality again:
-cranial will concentrate after desmopressin
-nephrogenic will not concentrate

368
Q

management for DI

A

demopressin

369
Q

tx for hyperprolactinaemia

A

if <10mm bromocriptide

if >10mm bromocriptide then surgery

370
Q

treatment for pheochromocytoma

A
alpha blockade (phenoxybenzamine) then beta blockade 
then surgery
371
Q

what scan for suspected pancreatic cancer

A

CT

372
Q

what test for stomach cancer

A

upper GI endoscopy

373
Q

what scan for gall bladder and liver cancer

A

USS

374
Q

what age do unexaplined breast lumps get referred on suspected cancer pathway

A

30

375
Q

what test if CA125 if higher than expected

A

USS

376
Q

What are the minor and major criteria for suspected melanoma referall

A

major : change in size, irregular shape or colour

minor: diameter 7mm or more, inflammation, oozing, change in sensation

377
Q

how urgent do SCC and BCCs need to be referred

A
BCC routine 
SCC Urgent (2 weeks)
378
Q

when is ulceration in mouth worrying

A

if there for >3 weeks

379
Q

how quick should you refer children with new neuro signs

A

very urgent- MRI in 48 hours

380
Q

how urgent is a suspected adult and child leukaemia referal

A

very - under 48 hours

381
Q

referal for lymphadenopathy and spenlomegaly, fever, nightweats, SOB, pruitus or weight loss (lymphoma) in adults and children

A

adults 2 weeks, children 48 hours

382
Q

referral for bone and soft tissue sarcomas adults and children

A

adults 2 weeks

children 48 hours

383
Q

referal for child wilms tumour (haematuria, abdo mass)

A

48 hours

384
Q

what is CK in rhabdomyolysis

A

> 10,000

385
Q

how to tell primary from tertiary hyperparathyroidism

A

tertiary may have abnormal renal function- seen in chronic renal failure
PTH can be high or inappropriately normal in primary, always high in tertiary

386
Q

perineal ulcer, tender lymphadenopathy and proctitis

A

lymphogranuloma venereum

387
Q

is the lymphadenopathy tender in herpes

A

yes

388
Q

features of pernicious anaemia

A

AI atrophic gastritis
anti gastric parietal cell antibodies
B12 def- macrocytic anaemia

389
Q

does coeliac cause a micro or macro cytic anaemia

A

micro

390
Q

how to tell the difference between IgA and post infectious GN

A

IgA- haematuria few days after URTI

PI- 2 weeks after infection

391
Q

are duodenal ulcer better or worse after eating

A

relieved by eating

392
Q

treatment for prolonged QRSs followinf tricyclic OD

A

sodium bicarb

393
Q

amiodarione can cause pulmonary fibrosis, what would the diagnostic test be

A

CT chest

394
Q

when should LP be done to diagnose SAH

A

at least 12 hours after symptom onset to look for xanthochromia

395
Q

treatment for SLE

A

NSAIDs- joint stiffness and pain (naproxen), avoid in hypertension
hydroxychloroquine: constitutional and cutaneous symptoms
IV methylpred for immediate relief, oral steroids for a short a time as possible
if not responding: methotrexate, azathioprine, mycophenolate, biologic agents

396
Q

signs of rheumatoid arthritis on x ray

A

reduced joint space
articular erosions
periarticular osteopenia
soft tissue swelling

397
Q

tx for RA

A

dmard within 3 months: methotrexate, lefunomide, sulfasalazine
bridging steroids

398
Q

features of PMR

A

elderly, myalgia of hip and shoulder girdle with morning stiffness
15% have GCA
raised CRP and PV/ESR
responds to 15 mg steroids tapered over 18 months

399
Q

treatment for GCA

A

40mg pred, 60mg if visual involvement

400
Q

features of polymyositis

A

symmetrical proximal muscle weakness
dysphagia may occur
anti Jo-1, SRP, ANA and RNP
ILD commoner in those with Jo-1

inflam markers raised, CK 10x normal
EMG
pred 40mg with immunosuppressants: methotrexate/azathioprine

401
Q

features of dermatomyosis

A

those of PM but with gottrons paules, V shaped rash, heliotrope rasg
management and Ix as for PM

402
Q

what are the ANCA positive vasculitis

A

microscopic polyagnitis
granulomatosis with polyangiitis
eosinophilic granulomatosis with polyangitis

403
Q

what are the large vessel vasculitis

A
giant cell (temporal) 
takayasu arteritis 

symps- low grade fever, weight loss, arthralgia and fatigue
ESR, PV and CRP raised
Tx steroids, steroid sparing agents (methotrexate, azapthioprine)

404
Q

features of granulomatosis with polyangitis

A

nose bleeds, deafness, recurrent sinusitis, nasal crusting (collapse of nose), haemoptysis, cavitating lesions on x ray
cANCA

405
Q

features of eosinophllic granulomatosis with polyangitis

A

late onset asthma, rhinitis and raised peripheral blood eosinophil count

406
Q

features of eosinophllic granulomatosis with polyangitis

A

late onset asthma, rhinitis and raised peripheral blood eosinophil count

407
Q

microscopic polyangitis causes what

A

GN

408
Q

tx for anca vasculitis

A

Iv steroids and cyclophosphamide

409
Q

what mediated HSP

A

IgA

410
Q

features of HSP

A

URTI
few weeks later purpuric rash over bottocks and legs, abdo pain, vomiting and joint pain
self limiting

411
Q

what are the nephritic GN

A

IgA (12-72 hours post infection, IgA deposits on mesangium, proteinuria)
post step (2-3 weeks post infection, oedema)
HSP (purpuric rash, abdo/ joint pain , IgA)
Anti-GBM (renal disease and pulmonary haemorrhage)
rapidly progressing (lots of causes, failure in weeks/days)

412
Q

treatment for nephritic syndrome

A

IgA- ACEi/ARB to reduce proteinuria, steroids if this doesnt help
HSP- steroids
PS-abx
Anti-GBM- plasma exchange, steroids and cyclophosphamide
rapidly progressing- steroids and cyclophosphamide

413
Q

what is nephrotic syndrome

A

proteinuria (>3g/24hrs)
hypoaluminaemia
oedema

414
Q

what can cause nephrotic syndrome

A

GN

pre-eclampsia, lupus, DM, myeloma, amyloid

414
Q

what can cause nephrotic syndrome

A

GN

pre-eclampsia, lupus, DM, myeloma, amyloid

415
Q

Tx for nephrotic syndrome

A

fluid and salt restriction, furosemide
treat cause
ACEi/ARB to reduce proteinuria
Abx, thromboprophylaxis

416
Q

what are the nephrotic GN

A

minimal change (idiopathic, NSAIDs, lithium, HL; light microscopy normal, electron podocyte effacement, pred)
focal segmental glomerulosclerosis- ACE/ARB, steroids in primary disease
membranous- (malignancy, infection, AI, drugs - gold, spikes of silver stain, thickened basement membrane)
membranoproliferative- immune complex of C3, electron dense deposits on membrane, ACEi/ARB

417
Q

what are the pre renal causes of AKI

A
hypoperfusion: 
decreased plasma volume 
decreased CO 
vasodilation
renal vasoconstriction (NSAIDs, ACEi, hepatorenal syndrome- concurrent liver cirrhosis/ failure)
418
Q

what are the renal causes of AKI

A
glomerular 
interstitial (drugs, infection, infiltration- sarcoid)
419
Q

what are the post renal causes of AKI

A

stone, malignancy, stricture, clot, extrinsic compression

420
Q

treatment for AKI

A
fluid resus 
monitor fluid balance, K+
assess for proteinuria 
USS in 24 hours 
check liver function 
check platelets - if low check film for haemolysis (TTP, HUS) 
treat cause
421
Q

stages of CKD

A
GFR: 
1= >90 and evidence of kidney damage 
2=60-89 and evidence of kidney damage 
3a= 45-59 
3b= 30-44
4= 15-29 
5=<15 failure
422
Q

management for CKD

A

refer when stage 4-5/ declining gf/ genetic cause/ proteinuria despite tx/ poor BP control
ACE/ARB for BP and proteinuria
glycaemic control
salt restriction <2g
treat: anaemia, renal bone dystrophy (high phosphate low vit D) (phospahte binders, diet low in phosphate, vit D supplements), iron for restless legs, antiplatelets, statins
RRT

423
Q

tx for gout

A

acute: NSAID, colchine, steroids if CI
lifestyle (low urate- alcohol, red meat)
prophylaxis: allopurinol/ febuxostat

424
Q

VTE prophylaxis for patients with renal impairment

A

LWMH or unfractionated heparin

425
Q

VTE prophylaxis in palliative care

A

LMWH

426
Q

what do you do for people with a negative USS but positive D dimer for DVT

A

stop interim anticoagulation and repeat USS 6-8 days later

427
Q

can you drive after stroke/ TIA

A

1 month after TIA, 3 months if multiple

stroke 1 month, notify DVLA if residual neuro deficit

428
Q

what is the secondary prevention following a stroke

A
antiplatelet (not if paroxysmal AF) : 
aspirin in first two weeks then clopidogrel 75mg (if CI 75mg with modified release dipyridamole 200mg). Dual therapy aspirin + clopidogrel if high risk of TIA for 90 days
statin: 80mg atorvastatin 
HPTN control 
anticoagulation: (for all inc AF) DOAC
429
Q

what are the iron studies like in IDA

A

decreased ferritin, increased total iron binding capacity

430
Q

what should you consider in microcytic anaemia that is not responding to iron

A

sideroblastic- will have high iron and sideroblasts

431
Q

what are howell jolly bodies seen in

A

hyposplenism (sickle cell, IBD, amyloid)

432
Q

what is rouleaux seen in

A

chronic inflammation, myeloma

433
Q

what are schistocytes seen in

A

intravascular haemolysis (DIC, HUS, TTP)

434
Q

what are spherocytes seen in

A

sherocytosis, autoimmune haemolytic anaemia

435
Q

what must you always check before giving folate

A

B12 levels as replacing folate without B12 may precipitate subacute combined degeneration of spinal cord

436
Q

what biochem markers in haemolytic anaemia

A

increased unconjugated bilirubin and urobilinogen

increased LDH

437
Q

how to tell intravascular from extravascular haemolysis

A

splenomegaly in extravascular

free plasma haemoglobin in intra

438
Q

what are the causes of haemolytic anaemia

A
acquired: 
coombs test +ve
-drug induced 
-AIHA (extravascular haemolysis, warm IgG steroids, cold IgM keep warm
coombs -ve: 
-autoimmune hepatitis 
-hep b/c 
-post infection, drugs 
microagiopathic haemolytic anaemia: mechanical damage, intra, Ax: DIC, HUS, TTP, pre-eclampsia, mechanical valve, 
infection 

hereditary:
- G6PD def, x linked,
- sherocytosis

439
Q

abx seen in autoimmune hepatitis

A

ASMA, ANA, LKM1

440
Q

tx for AI hepatitis

A

steroids
azathioprine for sparing
transplant if needed

441
Q

what is the inheritance of sickle cells

A

AR

442
Q

prevent for sickle cell crises

A

hydroxycarbamide

443
Q

what is the inheritance of beta thalassaemias

A

recessive
heterozygous- carrier, minor or trait
intermediate- moderate anaemia, homo/hetero
major- hetero, lifelong transplant, hair on end bones, bossing, extramedullary haemotpoesis

444
Q

is VwF def a coagulopathy or bleeding disorder

A

bleeding- VWF aggregates platelets

445
Q

what inheritance are the haemophilias

A

x linked recessive

446
Q

when do you give platelets and FFP

A

platelets when <20

FFP to replace clotting factors: DIC, warfarin OD hen vit k would be too slow e.g. liver disease TTP

447
Q

what is seen in TRALI

A

white out

448
Q

what does LMWH target

A

factor Xa

449
Q

what does warfarin target

A

vit K

450
Q

what malignancy:
uncontrolled immature blast proliferation, children
anaemia, infections, bleeding (marrow failure)
tx: fluids, allopurinol (TLS), transfusion, IV abx, chemo, marrow transplant

A

Acute lympoblastic leukaemia

451
Q

what blood malig:

auer rods

A

AML

452
Q

what blood malig:

40-60, philadelphia chromosome, imantinib

A

CML

453
Q

which blood malig:

rubbery nodes, often asymptomatic, progresive accumulation of functionally incompetant B cells

A

CLL

454
Q

what blood malignancy:

reed sternberg cells, young adults and elderly, alcohol induced node pain, ann arbour staging

A

HL

455
Q

what blood malignancy:

b cells, includes MALT

A

NHL

456
Q

what myeloproliferative:

JAK2, itchy after hot bath, venesection

A

PCV

457
Q

treatment for thrombocythaemia

A

aspirin

458
Q

which myeloproliferative disorder :

teardrop RBCs, marrow fibrosis, massive hepatosplenomegaly

A

myelofibrosis

459
Q

which blood malignancy:
IgG, paraprotein on urine/ electrophoresis, osteolytic bone lesions, hypercalcaemia, marrow failure, renal impairment (light chain deposition), roulaeux

A

myeloma

460
Q

what tests for myleoma

A

serum and urine electrophoresis

461
Q

Tx for myeloma

A

analgesia, bisphosphonate, chemo, transfusions

462
Q

which jaundice:

normal urine and normal stools

A

pre-hepatic cause

unconjugated bili is not water soluble

463
Q

which jaundice:

dark urine + normal stools

A

hepatic cause

conjugated bili, able to get into bowel

464
Q

which jaundice:

dark urine + pale stools

A

post hepatic obstructive

conjugated bili, unable to get into bowel

465
Q

abx for animal bite

A

co-amoxiclav

466
Q

most common side effect with POP

A

irregular bledding

467
Q

what should all patients with peripheral arterial disease be taking

A

antiplatelet (clopid) and a statin

468
Q

abx for neutropenic sepsis

A

piperacillin with tazobactam

469
Q

what test for post H pylori eradications therapy

A

urea breath test

470
Q

what is a comp of fluid resus in DKA

A

cerebral oedema- monitor kids and YA especially for it

471
Q

dose blockage of the cystic duct cause jaundice

A

no, neither dose blockage of the gall bladder

472
Q

why is mastoiditis an emergency

A

risk of meningitis, cranial nerve palsies, osteomyelitis, hearing loss, osteomyelitis, carotid artery spasm

473
Q

what drug for babies in womb to help prevent resp distress

A

dexamethasone

474
Q

normal nuchal translucency

A

<3.5mm at 11-14 weeks

475
Q

when is a postural drop in BP significant

A

20 or more systolic/ below 90/ >10 with symptoms

476
Q

what is anastrozole

A

aromatase inhibitor

477
Q

what is a normal FEV1

A

> 80%

478
Q

what is the breast cancer screening programme

A

mammography every 3 years for women aged 50-70

479
Q

what abx for GBS prophylaxis

A

benzylpenicillin

480
Q

can you take statins in pregnancy

A

no

481
Q

what drugs are bad in G6PD def

A

sulpha drugs (sulphasalazine, sulphonylureas)

482
Q

what eGFR is metformin CI

A

<30

483
Q

what Tx for fasting glucose >7 in pregnancy

A

insulin

if <7 lifestyle changes for 2 weeks then metformin if still high

484
Q

what does irradiating blood prevent

A

transfusion associate graft versus host disease

485
Q

what form of ventilation in acute COPD exacerbation

A

BiPAP

486
Q

when can hypertonic saline be given

A

acute severe hyponatraemia <120

487
Q

first line investigation for prostate cancer (after PR and PSA)

A

MRI

then TRUS biopsy

488
Q

tx for trichomonas vaginalis

A

oral metroniazole

489
Q

how long should you be faste for before surgery

A

6 hours

490
Q

what are the biochem markers of myleoma

A

calcium up, phosphate normal/up, ALP normal

491
Q

biochem markers of bone mets

A

calcium, phosphate and alp all up

492
Q

phosphate in primary hyperparathyroidism

A

down

493
Q

potassium up or down in cushings and addisions

A

cushings down

addisons up

494
Q

normal UO

A

1500, 200 in stool, 800 insensible

495
Q

can you use 5% dextrose for resus

A

no

496
Q

how to calculate the anion gap

A

(Na+ + K+) - (Cl- + HCO-)

497
Q

what do you need to be careful of when treating hyponatraemia

A

replacing too quickly can cause central pontine demyelination

498
Q

treatment for K>6.5 or >6 with ECG changes (tall tented T waves, increased RR, widened QRS, sine wave)

A

10ml of 10% calcium chloride (or 30ml 10% of calcium gluconate) IV over 5-10 mins (cardioprotective)
IV insulin (10u in 25g glucose- 50ml of 50%) over 30-60 mins (re-uptakes K)
salbutamol neb
renal replacement

499
Q

how to differentiate thyroid cancers

A

most common, young patients= papillary
middle aged, haem spread= follicular
MEN, calcitonin= medullary

500
Q

causes of hypocalcaemia with raised phosphate

A

CKD

hypoparathyroidism

501
Q

causes of hypocalcaemia with normal/ low phosphate

A

vit D def (helps absorb phosphate and calcium from gut)
osteomalacia (raised ALP)
acute pancreatitis

502
Q

tx for hypercalcaemia

A

rehydrate

bisphosphonates

503
Q

how much of ions and sugar and water do you need a day

A

1mmol/kg/day of sodium potassium and chloride
50-100g/kg/day glucose
25-30ml/kg/day water

504
Q

what ion can be raised by thiazides

A

hypercalcaemia

505
Q

what nerve does froments test test

A

ulnar

506
Q

tx for prolactinoma and acromegaly

A

prolactinoma- dopamine agonists (bromocriptide, cabergoline) for both macro >10mm and micro (surgery rarely needed)

acromegaly- transhenoidal surgery, somatostatin analogues (ocreotide), GH antagonist (pegvisomant)
(A= SS and surgery ASS)

507
Q

first line tx for superficial thrombophlebitis

A

NSAIDs

508
Q

what is used to reverse warfarin in emergency

A

prothrombin complex concentrate

509
Q

what is the desirable INR for invasive procedures

A

<1.5

510
Q

how should warfarin be managed before and after surgery

A

(low risk patients) withhold 5 days before, day before check INR and give vit K if >1.5
restart usual dose on day of procedure

511
Q

stop for surgery? loop diuretics

A

yes (omit morning of)

512
Q

stop for surgery? K sparing diuretics

A

yes (omit morning of)

513
Q

stop for surgery? beta blockers

A

no

514
Q

stop for surgery? acei and arbs

A

yes (omit morning of)

515
Q

stop for surgery? CCbs

A

no

516
Q

stop for surgery? DOACs

A

yes stop 48 hours before

517
Q

stop for surgery? clopidogrel

A

stop 7 days before

518
Q

stop for surgery? inhaled steroids

A

no

519
Q

stop for surgery? first gen antipsychotic

A

no

520
Q

stop for surgery? 2nd gen antipsuchotic

A

yes stop 12 hours before

521
Q

stop for surgery? bisphosphonates

A

omit on day

522
Q

stop for surgery? NSAIDs

A

stop 24 hours before, 72 if naproxen

523
Q

how do you change insulin for surgery

A

for multiple daily doses continue the daily long acting basal insulin subcut (glargine, determir, degludec)
for major surgery five VR IV insulin (actrapid)
aim for first on list, omit all medication and insulin expect long acting on morning of if AM, restart as usual with meal post op (if once daily regime or breakfast routine give half dose at lunch)
if PM 50% reduction in insulin dose at breakfast, omit oral meds at breakfast, fast after breakfast and omit lunchtime meds
VRII if major surgery

524
Q

how do you change oral diabetic meds for surgery

A

if poorly controlled or major surgery treat as insulin controlled diabetes (long acting + VRII)
give all usual day before except SUs
if AM omit all morning meds, take any missed drugs with lunch
if PM give morning doses, omit lunch time doses and give any missed doses with late lunch
if not eating/ drinking after op start VRII 2 hours before op and restart oral hypoglycaemics when eating

525
Q

what are the antihistamine anti-emetics

A

cyclizine, promethazine

526
Q

what anti-emetic for gastrointestinal or biliary disease

A

metoclopramide (prokinetic- stimulates gastric emptying, can cause tardive dyskinesia)

527
Q

what can domiperdone be used for

A

antiemetic for dopaminergic drugs (PD)

528
Q

what anti emetic for menieres

A

prochlorperazine

cyclizine

529
Q

what anti-emetic for migraines

A

metoclopramide or prochlorperazine

530
Q

what is the orbit score

A
>/= 75 1 point 
reduced Hb 2 points 
bleeding history 2 points 
eGFR <60 1 point 
on antiplatelet 1 point 

0-2 low risk
3 medium risk
4-7 high risk

531
Q

what is the chadvasc score

A
CHF 1 
HPTN 1 
age >/= 75 2 
Age 65-74 1 
DM 1 
stroke/tia/VTE 2 
vascular disease 1 
female 1
532
Q

can apixaban be used in CKD

A

yes

533
Q

what is the feverpain criteria

A
fever 
purulence 
attends rapidly (within 3 days) 
inflamed tonsils 
no cough or corzya 

score 0-1 do not offer an antibiotic, seek help if dont improve within a week
2-3 no antibiotic/ back up prescription (not needed immediately, use if no improvement in 3-5 days/ worsening (likely streptococcal)
4-5 immediate abx/ back up prescription

abx= phenoxymethylpenicillin

534
Q

what is the centor criteria

A

tonsilar exduate
tender anterior cervical lymphadenopathy
fever
absence of cough

0-2 no abx
3-4 immediate/ back up abx

abx phenoxymethylpencillin

535
Q

which is the most common cause of malaria

A

plasmodium falciparum - more likely if cerebral involvement

causes fever, cough, HA, malaise, diarrhoea,

536
Q

ix and tx for malaria

A

ix- giemsa stained thick and thin blood smears, rapid diagnostic test
tx: chloroquine or hydroxychloroquine

537
Q

difference between gram -ve and positive

A

-ve pink, has thin peptidoglycan cell wall

+ve purple, thick peptidoglycan wall

538
Q

is staph areus coagulase negative or positive

A

positive

539
Q

how to beta lactam antibiotics work

A

inhibit cell wall synthesis

540
Q

what antibiotics contain a beta lactam ring

A

(all cause penicillin allergy!)
penicillins
cephalosporins (ceph and cef)
clavulanic acid

541
Q

findings in LP in bacterial meningitis

A

cloudy, turbid
high pressure
>100 WBC (leukocytes)
glucose low, protein high

542
Q

findings in viral meningitis LP

A

clear, normal/ elevated pressure
WBC elevated, primarily lymphocytes
glucose normal (low in HSV), protein high

543
Q

findings in fungal meningitis (LP)

A

clear/ cloudy
elevated pressure
WB elevated, glucose low
protein elevated

544
Q

findings in tb meningitis LP

A

opaque, fibrin web
elevated pressure
WBC high, glucose low, protein high

545
Q

specificity

A

the ability of a test to correctly identify those withOUT the disease

546
Q

sensitivity

A

the ability of a test to correctly identify patients WITH a disease

547
Q

prevalence

A

the percentage of people in a population who have the condition of interest

548
Q

incidence

A

number of new cases over a period of time

549
Q

randomised control trial

A

gold standard of clinical trial, treatment vs placebo

550
Q

case control study

A

two groups identified on a differing characteristic (disease/condition) then explores retrospectively as to the cause of that characteristic

551
Q

cohort study

A

cohort of people followed to determine rate of disease/ risk factors prospective- people divided into two groups based on exposure to RF an then followed for several years to determine incidence
retrospective when cohort selected from the past and data is collected in past or present of how many people in that group were exposed to risk factor/ develop disease

552
Q

cross sectional study

A

data collected at specific time and point, don’t interfere, looking at incidence or prevalence of disease

553
Q

what is the bowel screening programme

A

people aged between 60 and 74 to return a faecal immunochemical test (FIT) kit every 2 years to detect the presence of blood in the stool.

554
Q

localising features of a temporal seizure

A

HEAD
hallucinations (auditory, gustatory, olfactory)
Epigastric rising/ emotional
Automatism (lip smacking, grapping, plucking)
Deja vu/ dysphagia post ictal

555
Q

localising features of the frontal lobe

A

head/leg movements, posturing, post-ictal weakness, jacksonian march
(motor)

556
Q

parietal localising features

A

(sensory) paraesthesia

557
Q

occipital localising features

A

(visual) floaters/ flashes

558
Q

what are the first rank symptoms of schizophrenia

A

auditory hallucinations (thoughts spoken aloud, third person, commentary)
though withdrawal/ insertion/ interruption
thought broadcasting
somatic hallucinations
delusional perceptions
passivity phenomena