GP Flashcards

1
Q

what happens when you take clozapine (antipsychotic) and carbamazepine - BAM ZAP

A

agranulocytosis

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2
Q

drug causes of gastric ulcers

A

nsaids
ssri’s
alendronic acid
steroids

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3
Q

order of potency of topical steroids

A

least

hydrocortisone
betamethasone 0.025%, butyrate (eumovate)
betamethasone 0.1%
propionate (Dermovate)

most

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4
Q

side effects of bisphosphonates

A
GI and headache
reflux and indigestion
alopecia 
anaemia 
arthraliga/myaglia 
asthenia (lack of energy)
peripheral Aedema
atypical fractures - new onset hip pain 
osteonecrosis of jaw - should maintain good physical hygiene
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5
Q

should you stop statins if suffereing from muscle pain

A

if ck is 5x upper limit of normal

or if raised but not that much but are severely impacted by the muscle pain

NB it is common to have muscle pain, but uncommon overall for CK to be so high that they have to stop it

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6
Q

dose of statin for primary vs secondary prevention

and when is it used for primary prevention

A

atorvastatin 20mg for primary
atorvastatin 80mg for secondary

QRISK ≥10% - risk of heart attack or stroke in 10 years
most T1DM
CKD if eGFR <60
increase dose if non-HDL has not reduced by >40%

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7
Q

statins interactions

A
  • CI in pregnancy
  • Macrolides (azithromycin etc.) are an important interaction - statins should be stopped until patient has completed the course
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8
Q

which diabetic drugs cause weight gain

A

sulphylureas - gliclazide

pioglitazone

insulin

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9
Q

which diabetic drugs cause weight loss

A

GLP-1 agonist - given by weekly injection e.g. exenatide

sglt-2 inhibitors (flozin)

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10
Q

side effects of sulphonulureas (NB are good for rapid glucose correction)

A
hypoglycaemia 
weight gain 
GI side effects 
SIADH - low sodium
peripheral neuropathy

should take in morning to reduce risk of nocturnal hypo

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11
Q

side effects of metformin

A
lactic acidosis 
GI effects
altered taste 
anorexia 
decreased b12 absorption

can switch metformin to modified release if getting bad GI effects (as opposed to immediate release)

The symptoms of lactic acidosis include abdominal or stomach discomfort, decreased appetite, diarrhea, fast, shallow breathing, a general feeling of discomfort, muscle pain or cramping, and unusual sleepiness, tiredness, or weakness

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12
Q

side effects of pioglitazone

A
weight gain 
fluid retenion (not good in HF)
liver impairement
bladder cancer - report dysuria
anaemia
increase risk of fractures

CI = haematuria

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13
Q

side effects of dpp-4 inhibitors (sitagliptin)

A
GI upset 
Headache 
painful muscles - Myalgia 
pulmonary - Interstitial lung disease
Pancreatitis
peripheral oedema 

is liscensed in liver and kidney failure

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14
Q

side effects of sglt-2 inhibitors

A
GI - constipation
Euglycemia DKA
UTI + thrush risk 
Increased thirst 
Dyslipidaemia 
Ineffective if eGFR<60 
Affects genitalia

very cardioprotective

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15
Q

example of long acting insulins

A

lantus - glargine
levemir - detemir

onset in 30 mins - 1 hour and last for 24 hours

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16
Q

example of short acting insulins

A

human - actrapid

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17
Q

DMARD side effects examples

A

methotrexate - pulmonary fibrosis
leflunamide - HTN, peripheral neuropathy
hydroxchlorquirne - nightmares, reduced visual acuity
rituximab - night sweats, low platelets
sulfalazine - male infertiliy

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18
Q

effect of drinking alcohol with warfarin

A

a binge increases INR so increases chance of bleeding

chronic alcohol use decreases INR

if drinkning - should be occassional and limited amount
should stick to guidelines of 14 units a week - spread over at least 3 days

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19
Q

missed warfarin dose

A

do not double to make up for a missed dose

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20
Q

what things enhance effect of warfain

A
wight loss
smoking cessation 
acute illness 
cranberry juice 
grapefruit juice
alcohol binge 

avoid st johns wart, aspirin and ibuprofen due to increased bleeding risk

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21
Q

what things decrease effect of warfarin

A

diarrhoea
vomiting
green leafy vegetables and green tea

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22
Q

can you take paracetamol on wafarin

A

o But only take 1 tablet (500mg) at a time
o Do not take more than 4 tablets over a 24 hours period
o Taking more = increases bleeding risk / higher INR

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23
Q

RIPE for tb management

A

rifampicin
isoniazid
pyrazinamide
ethambutol

NICe recommend treatment in those <65 w evidece of latent tb and been in contact w someone - treat w 6m of isoniazid or 3m of isoniazid and rifampicin

ACTIVE TB
notfiable disease - public health
no CNS involvemtn - then RIPE for 2 months then RI for 4 months
with CNS involvement - RIPE for 2 months, then RI for 10 months
patients with CNS may also have adujavent steroids for first 1-2 months
directly observed therapy to improve adherence in those that would benefit eg alcoholics, homeless

isoniazide is given with pyridoxine to reduce the risk of polyneuropathy

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24
Q

why chose apixaban over rivaroxaban

A

rivaroxaban has to be taken with food

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25
Q

when do DOACs vs warfarin reach therapeutic levels

A
doacs = 3-4 hours 
warfarin = 3-7 days 

BUT effects fade after 12-24 hours with DOACs vs 48-72 hours with warfarin (something to think about w poor adherence)

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26
Q

side effect of ethambutol

A

optic neuritis

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27
Q

drugs at risk of toxic build up in AKI

A
ACEi, ARB
diuretics
stop statins if aki due to rhabdomyolsis or muscle pain
metofrmin 
lithium
digoxin - reduce dose
trimethoprim and co-amox
aciclovir - reduce dose
morphine 
consider witholoding DOACs

should either reduce doses or stop

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28
Q

sick day rules for preventing AKI

A
  • When vomiting of diarrhoea (unless minor) should stop certain triggering medication to avoid an AKI
  • ACEi/ARBs, NSAIDs, diuretics
  • Note - not one fits all, should be stated on an individual basis
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29
Q

conversion of oral morphine to SC morphine or SC oxycodone

A

divide by 2

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30
Q

example of bulk forming laxative

A

fybogel - ispaghula husk

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31
Q

blood pressure targets

A

<140/90
if >80 then <150/90

T1DM <135/85 (if accompanied by albuminuria (kidney disease) or 2+ features of metabolic syndrome then ≤130/80)

CKD <140/90 (if also accompanied by CVD or diabetes or high urine creat ratio then lower than this)

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32
Q

3 stages of htn

A
  • Stage 1 hypertension - BP in surgery/clinic is ≥140/90 mm Hg AND ambulatory blood pressure monitoring (ABPM) or home blood pressure monitoring (HBPM) from 135/85 mm Hg
  • Stage 2 hypertension - BP in surgery/clinic is ≥160/100 mm Hg AND ABPM or HBPM is ≥150/95 mm Hg
  • Stage 3 or severe hypertension - systolic BP in surgery/clinic is 180 mm Hg or higher or diastolic BP is 120 mm Hg or higher

I.e. confirm readings with ABPM OR HBPM for stage 1 and 2!!

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33
Q

<55 or with type 2 diabetes first and second line for anti-HTN

A

ace or arb

then a + c OR a + d

(then a plus c plus d)

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34
Q

> 55 or black first and second line for anti-HTN

A

CCB

then c + a OR c + d

(then a plus c plus d)

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35
Q

4th line anti-htn management

A

spironolactone if potassium <4.5

alpha or beta blocker if potassium >4.5

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36
Q

what stage to start anti-htn treatment

A

STAGE 1
treat if <80 AND any of following apply organ damage, established CV disease, renal disease, diabetes, QRISK >10

STAGE 2
offer regardless of age

STAGE 3
investigate for end-organ damage
urine dip, urine ACR, HbA1c, UE, creatiine, eGFR, opthalm, ECG
if all normal, repeat BP in 7 days

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37
Q

ABPM vs HBPM

A

abpm measures at least 2 per hour in persons normal waking hours - if not tolerated or declined then offer hbpm

hbpm - 2 readings taken 1 min apart with person seated - at least twice daily - ideally for 7 days

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38
Q

when to take first dose of acei

A

before bed because of first dose hypotension

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39
Q

monitoring and stopping acei

A

measure renal function and electrolytes before starting

POTASSIUM
if rises to 5 - investigate and treat other causes like stop potassium sparing drugs (amiloride, spironolactone) or nephrotoxic drugs
if persists 5-5.9 - reduce dose and recheck in 5-7 days
if >6 - stop and switch to amlodopine
can also do ECG if raised

OVERALL - refer immediately to A+E if K >6.5 or >5.5 with ECG changes

EGFR AND CREATININE
o If >25% reduction in eGFR or rise of >30% of creatinine - check for another cause, then stop or reduce for a week then recheck
o If >15% reduce in eGFR or rise of >20% in creatinine - remeasure in 2 weeks

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40
Q

ACEi SEs

A
  • Dry cough
  • High potassium
  • Angioedema
  • GI discomfort, nausea, constipation, vomiting
  • Renal artery stenosis
  • Low glucose
  • First dose hypotension
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41
Q

DHP CCBs

A

amlodipine

nifedipine

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42
Q

side effects of CCBs

A
peripheral oedema
flushing 
palpitaitons 
headaches 
constipation
HF 
bradycardia or heart block for verapamil 
HF (verapamil and diltiazem can worsen HF)
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43
Q

interactions with CCBs

A

non-dhps (diltiazem and verapamil) with BB - can cause brady or heart block (are both negative inotropic and chronotropic)

lower dose of simvastatin - they increase dose

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44
Q

sodium and potassium levels with thiazide or indapamide use and loop diuretic use

A

low sodium and low potassium

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45
Q

side effects of thiazide like diuretics

A
  • GI
  • Hypokalaemia – as a result of low sodium
  • Hyponatraemia
  • Can exacerbate diabetes
  • Impotence

may precipitate gout attakes - reduces uric acid excretion

their effectiveness can be reduced by NSAIDs

increases liklihood of digoxin toxicity

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46
Q

best time to take diuretics

A

morning so not awaken to go to loo in night

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47
Q

side effects of beta blockers

A
fatigue
cold extremities
bradycardia
erectile dysfunction 
can cause hypo or hyperglycaemia - beware in diabetics with frequent hypos

beware in COPD - can cause bronchospasm - not on BNF CI list

CI in asthma

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48
Q

does high or low potasium precipitate digoxin toxicity

A

low

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49
Q

digoxin toxicity

A

confusion
nausea
arrhtymias
yellow vision or haloes

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50
Q

time of day to take warfarin

A

should take at 6pm every day so if their dose is changed it can be actioned on the same day (i.e. blood test in morning, then change dose for their evening time)

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51
Q

when to double dose of levonelle

A

if BMI >26 or weight >70kg or if taking enzyme inducer

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52
Q

missed pop

A

if >3 horus or >12 then take a pill asap

need extra contraception for next 2 days

if you have unprotected sex in the 2 days after you start taking it reliably again, you may need emergency contraception (it takes 2 days for the POP to thicken cerical mucus so sperm cannot get through)

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53
Q

when do you need EC when missing 2 or more combined pill

A

only if in first week of pack and had unprotected sex in previous 7 days

(if later then will just need extra contraception for 7 days

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54
Q

when to stop combined pill prior to surgery

A

4 weeks before major and restart 2 weeks after due to increased VTE risk

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55
Q

if vomit while taking combined pill

A

if within 3 hours of taking then take another

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56
Q

side effects of combined pill

A
  • Mood swings, nausea, breast tenderness, headaches, change of periods - usually settle in a few months
  • May have spotting in between periods
  • No evidence for weight gain
  • Serious side effects - blood clots, cervical and breast cancer
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57
Q

starting contraception after levonelle vs ellaone

A

levonella - immediate quick start but will need additional contraception for 7 days if COC or 2 days if POP

ellaone - wait 5 days before restarting contraception then same as above

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58
Q

ovulation with leveonella and ellaone and iud

A

levelonelle has to be >48 hours before ovulation

ellaone can be right up until ovulation

IUD can be 5 days after ovulation

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59
Q

symptoms and management of temporomandibular joint dysfunction

A

restricted jaw function
joint noise
facial pain

may have locking episodes - unable to open their mouth

manage by avoid yawning, singing and chewing gum, bite guards for bruxism (grinding teeth and clenching jaw), analgesia, steroid injection for some, or surgery for some

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60
Q

ankylosing spondylitis presentation

A

o Pain at night that is not relieved when person is supine
 The spinal disease starts in the sacroiliac joints and may be felt as diffuse non-specific buttock pain
 OE there is often tenderness of sacroiliac joints or limited range of spinal motion - later stages will get lumbar lordosis, buttock atrophy, question mark posture
o Stiffness in morning that is relieved with movement/exercise - characteristic
o Gradual onset of symptoms
o Symptoms develop over 3 months
o Usually presents before the age of 30
o Most patients have mild chronic disease or intermittent flares with periods of remission
o Systemic features are common - fever, weight loss may occur in active disease
o Peripheral enthesitis and peripheral arthritis each occur in about 1/3 (e.g. plantar fasciitis)
o Extra-articular occur in 20-30% e.g. anterior uveitis, aortic regurgitation secondary to aortitis of ascending aorta, pulmonary fibrosis…

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61
Q

how is pain relieved in a spinal fracture

A

lying down

whereas pain due to cancer typically remains when supine

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62
Q

symptoms of cauda equina

A
bilateral sciatica
lower back pain
neurological deficit of the legs
impairment in micturition or faecal incontinence
laxity of anal sphincter
saddle anaesthesia
sexual dysfunction
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63
Q

sciatica symptoms

A

o Unilateral pain radiating below knee
o Low back may also be present - if so, is less severe than leg pain (often though, is pain in legs without co-existing back pain)
o Numbness, tingling and muscles weakness in the distribution is suggestive of nerve root compression

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64
Q

types of tendinopathy

A
  • De Quervain’s tenosynovitis
    o Affects tendons that extend the thumb
    o The typical symptom is pain over your wrist at the base of your thumb that is made worse by activity and eased by rest
  • Trigger finger
    o This most commonly affects your ring finger. The condition prevents your finger from straightening fully
  • Tennis elbow (lateral epicondylitis)
    o It is usually due to overuse of your forearm muscles
  • Golfer’s elbow (medial epicondylitis)
  • Achilles tendinopathy
  • Rotator cuff tendinopathy
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65
Q

management of tendinopathy

A
rest
ice packs 
ibuprofen, paracetamol, co-codamol
physiotherapy
steroid injection 
rarely - surgical release of the tendon
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66
Q

plantar fasciitis

A

under surface heel pain
is a misnomer as pathologyi is actually degenerative
thorught to be a traction and overuse injury
damage is usually in the form of micro-tears
can be bilateral

risk factors = spending time on feet, running, jumping, wearing worn-out trainers, obesity, flat feet

reproduction of pain when pressing on plantar surface - or when patient stands on toes or passive dorsiflexion

rule out referred pain from S1/s2 lesion via straight leg raise

manage with weight loss, run on a softer surface, update shoes reguarly, takes 6-8w w conservative management, deep massage of sole and foot, heal and arch support may help, night splints to keep ankle dorsiflexed and toes extended to help stretch the plantar fascia

limited evidence for steroid injection

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67
Q

viral vs bacterial vs allergic conjunctivitis

A

VIRAL
more likely watery discharge
pre-auricular lymphadenopathy

BACTERIAL
purulent discharge
more likely unilateral

ALLERGIC
itchiness more common
might be redder around the eye
may be swelling

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68
Q

investigations and management of conjuncitivits

A

visual acuity, fundocsopy if unsure (look for clouding of the anterior chamber), can swab for HSV if longer lasting

VIRAL
usually resolves within 7 days, dont share towels, cool compresses, lubricating drops, avoid contacts, avoid close contact with others (dont have to exclude from school), wash hands frequently

BACTERIAL
most resolve within 7 days wihtout treatment, same self care as above, if severe or needs rapid resolution then can use topical antibiotics , or can do a delayed strategy saying to take if not resolved in 3 days - chloramphenicol drops or fusidic acid second line, dont exclude from school, explain red flags of reduced visual acuity or photophobia

ALLERGIC
avoid allergens like pets or mould, avoid eye rubbing, cold compress, artifical tears, if non-pharmacological measures dont provide relief then topical antihistamine like antazoline drops (mast cell stabiliser second line, topical steroids if v severe)

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69
Q

herniated disc management

A

90% will resolve spontaneously – the herniatied material will become dehydrated, and be reabsorbed - within a few weeks
Encourage return to normal activities as soon as possible
Short frequent walks
Swimming is beneficial
Advise analgesics and NSAIDs - 10-14 days of regular NSAIDs
In more severe cases, physiotherapy may be beneficial
In very severe cases, you can give local steroid injections, which will provide pain relief, but do not alter the longer term course of the illness

In cases lasting longer than 12 weeks:

Further investigation may be necessary
X-ray is of virtually no use!
MRI – is the investigation of choice. It can directly show the herniation, allowing you to assess its location, size, and view any impinged structures
CT – may also be useful, but provides a lower resolution image, and has been mainly superceeded by MRI
Most cases are still managed conservatively
Consider some of the treatment options for chronic pain
e.g. Amitriptyline 10-25mg nocte, increasing to a maximum of 75-100mg daily
Operative treatment is given in some cases. The main procedure is called microdiscectomy. It is performed thrugh a small inscisional windows cut in the laminae and ligamentum flavum. In 90% of cases, patients can return to work within 6 weeks

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70
Q

presentation of glandular fever

A

low-grade fever, fatigue, headache, tired all the time, myalgia and prolonged malaise
may have nausea or vomiting
sore throat
tonsillar enlargement (often meet in midline) - classically exudative
palatal petechiae and uvular oedema
bilateral cervical lymphadenopathy
snoring or even sleep apnoea due to significant tonsillar enlargement
neck may be swollen
may seen splenomegaly (+/- abdo pain) and even hepatmegaly

feverish/tired symptoms/swollen lymph glands may persist for several months after acute infection has resolveed, whereas the sore throat typically lasts 7-10 days

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71
Q

investigations for glandular fever (EBV)

A

FBC - atypical lymphocytosis - i.e. a relative raised lymphocyte count within the raised WCC
ESR - raised
LFTs - mildly raised in around 75%

monospot test is primary technique but relies on generation of non-specific heterophile IgM autoantibodies which may take a week to appear (NICE say to do this in second week of illness)

repeat this a week later if negative and suspicions are high

patients who remain heterophile-neg after 6 weeks with IM are considered to be heterophile-negative and should be tested for EBV specific antibodies (also useful if a false positive monospot is suspected) - via ELISA for IgM viral capsid antigen

abdominal US may be required to assess for splenomegaly

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72
Q

management for glandular fever

A

arrange hospital admission if stridor, dehydration or difficulty swallowing, suspected splenic rupture
avoid contact sports for 4 weeks because of splenic rupture risk - risk is highest 14 days after
avoid alcohol for illness duration - can feel much worse than usual due to effect of glandular fever on the liver
paracetamol for fever and pain

bacterial superinfection is present in as many as 30% and so penicillin-based antibiotics (usually benzylpenicillin/penicillin V) are often prescribed - remember to avoid ampicillin and amoxicillin

advise that symptoms usually last 2-4w
tiredness is common and often last thing to resoslve
dont have to exclude from work or school
avoid kissing and sharing eating utensils

advise to seek medical help if develop stridor, become systemicall yunwell, develop abdo pain (may indicate splenic rupture)

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73
Q

assessing breathlessness in COPD

A

mrc dyspnoea scale

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74
Q

2 types of chest infection

A
ACUTE BRONCHITIS
normal cxr
less unwell 
may or may not have temp 
may or may not have sputum, wheeze, breathlessness

PNEUMONIA
fever
more fatigue
more productive cough

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75
Q

management of acute bronchitis

A

increase fluids, paracetamol, ibuprofen
seek medical help if symptoms worsen rapidly or do not improve after 3 to 4 weeks
do not routinely offer an antibiotic in people who are not systemically very unwell
–> advise people that antibiotics do not make a large difference to the duration of symptoms, only shortening cough duration by about half a day on average + about adverse effects including diarrhoea and nausea
offer an immediate antibiotic prescription if the person is systemically very unwell
consider an immediate antibiotic prescription or a back-up antibiotic prescription for a person at higher risk of complication e.g. comorbid lung condition or something or elderly using steroids etc

if CRP has been done can be a guide to abx prescribing
o CRP less than 20 mg/L — do not routinely offer antibiotics
o CRP 20–100 mg/L — consider a delayed antibiotic prescription
o CRP greater than 100 mg/L — offer antibiotic therapy

  • If antibiotics are indicated, for adults 18 years of age and older:
    o First-line choice is oral doxycycline
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76
Q

causes of palpitations

A
-	Arrhythmias 
o	SVT, AF, bradyarrhythmias (AV block, sinus bradycardia) 
-	Structural heart disease
o	Mitral valve prolapses, aortic or mitral regurgitation, cardiomegaly, HF 
-	Psychosomatic 
o	Anxiety, depression 
-	Systemic causes
o	Hyperthyroidism, hypoglycaemia, fever, anaemia, pregnancy, menopause, hypovolaemia
-	Medication, recreational drugs
o	Beta-2 agonists, vasodilators
o	Withdrawal of beta blockers 
o	Alcohol
o	Nicotine 
o	Cocaine, MDMA, cannabis, speed, heroin
o	Caffeine - cola, coffee, tea, red bull
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77
Q

histroy/investigations for palpitations

A
  • Ask the patient to tap out the beat
  • Ask if accompanying chest pain - = more sinister
  • Onset associated with exercise is a red flag
  • Ask about family history of sudden cardiac death <40 years
  • General exam, BP
  • Gold standard is ECG taken at the time of the palpitations
  • Blood tests - FBC, U&Es, TFTs, LFTs and HbA1c
  • 24-hour or 48-hour Holter monitor (types of ambulatory ECGs) - if not can use an event monitor or self-activated recorder for less frequent symptoms
  • Echo if cardiomyopathy is suspected
  • Exercise testing: if the problem is related to exercise then a treadmill ECG or stress echocardiogram is required
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78
Q

diagnosis of T2DM

A

HbA1c >48
random blood glucose >11.1
fasting blood glucose >7

should be confirmed with repeat testing - esp if asymptomatic - is prudent for symptomatic - usually taken in 2 weeks time

pre-diabetes = 42-47 mmol/l

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79
Q

management of t2dm

A

DESMOND programme (a group of educational programmes for diabetics)
X-PERT diabetes programme (a 6w course for anyone living with a longterm health disorder inc diabetes)
lifestyle - consider dietician - it is essential that these modifications continue once antidiabetic drugs are introduced
o Control amount of carbohydrates and high-fat foods, increase fibre
o Exercise can lower blood glucose as it increases glucose use by the muscles
o Exercise daily with at least 150 minutes of moderate intensity activity over a weekly period - do strengthening activities that work all the major muscles (legs, hips, back, abdomen, chest, shoulders and arms) on at least 2 days a week
o Smoking and alcohol (alcohol can exacerbate hypoglycaemia as well)

48
metofrmin - if not then DPP-4, pioglitazone, SU, SGLT-2
aim for 48, if associated with hypo then 53

58
dual therapy
aim for 53

STILL NOT DECREASING
add a third or consider insulin (if >58 and not if obese)

STILL NOT
if on triple - consider combination of metformin, SU and GLP-1
if on insulin - seek specialist advise

BP management
<140/90, but if kidney, eye or CV damage then <130/80

GLP1 agonist can be added w su and metformin in obese patients (or where weight loss would benefit weight related comorbidites like HTN, OA, sleep apnoea) or where insulin would lead to occupational restrictions like HGV drivers

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80
Q

how is metformin given - how do you take it/how many times

A

starts just breakfast, then breakfast and tea etc. etc. to TDS - start at 500mg

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81
Q

example of DPP inhibitor

A

sitagliptin

linagliptin

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82
Q

things other than unusal rbcs that can affect hba1c reading

A

Vitamin B12/folic acid deficiency
Iron-deficiency anaemia
Splenectomy

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83
Q

differentiating between T1DM and T2

A

in some cases, it may be indicated to differentiate between T1DM and T2DM in a newly presenting patient

this involves testing for C-peptide (low in T1DM) and Autoantibodies (+ve in T1DM)

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84
Q

sick day rules on insulin

A

o Cortisol released during illness –> higher glucose levels
o Increase frequency of blood glucose monitoring and consider ketone monitoring
 If no ketones, then test glucose and ketones every 2-4 hours, if ketones present or glucose is high (>15) then test glucose and ketones every 2 hours
o Never stop taking insulin - you may need an increased dose/additional doses of fast acting (even if not able to eat)
o Try keep a normal meal pattern - meals may be replaced by carbohydrate-based drinks
o Good hydration - as well as sugary drinks, also drink clear sugar free fluids to avoid dehydration
o Seek urgent medical attention if unable to tolerate oral intake, drowsy or sustained vomiting, rapid breathing (sign of DKA)
o If blood glucose is 10-13 then increase usually insulin by 10%
o If >13 or not responded to increasing insulin then give extra dose of quick acting insulin (approximately 10% of total daily insulin)

type 2
sometimes need to hold your medications - when ill still produce some insulin w type 2 so may be at risk of hypo
drink a lot of fluids and montior levels
seek help if vomiting

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85
Q

educational programme for t1dm

A

DAFNE - dose adjustment for normal eating educational programme

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86
Q

type 1 diabetes cap glucose targets and self monitroign

A

should perform at least 4 capillary blood glucoses per day - including one before each meal and one before bed
increase monitoring if frequency of hypos increases, during periods of illness, before, during and after sport, when planning pregnancy, during pregnancy and while breastfeeding

o Should be 4-7 before meals/at other times of day
o 5-9 at least 90 minutes after eating
o 5-7 on waking

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87
Q

type 1 diabetes hba1c target and monitoring

A
  • HbA1c should be 48 - measured 3-6 monthly - consider more if blood glucose control is changing rapidly
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88
Q

management of type 1 diabetes

A
  • DAFNE - dose adjustment for normal eating education programme
  • Life-long insulin is needed to prevent complications like DKA and CKD, IHD, retinopathy
  • 3 types of insulin regime
    o Basal bolus
     One to offer first
     Injection of rapid or short-acting before meals, with 1 or more separate daily injections of intermediate or long-acting per day
     Thought to best mimic physiological function of the pancreas
    o Continuous subcutaneous insulin infusion (insulin pump therapy)
     Patient can activate pre-meal boluses
     As well as it given a regular amount of short or rapid acting
     May be used in those having troubling hypoglycaemic episodes
    o One, two or three injections per day
     These are usually injections of short acting insulin or rapid acting insulin analogue mixed with intermediate acting insulin (or injected separately)
     It may be difficult to achieve optimal glycaemic control and the regimen can be complicated by hypoglycaemic episodes

E.g. 4 units for small meal, 8 for large

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89
Q

how does metformin work

A

lowers blood glucose levels through inhibition of hepatic gluconeogenesis whilst increasing peripheral insulin sensitivity and enhancing peripheral uptake of glucose

CI in CKD and those at risk of lactic acidosis or not tolerated

90
Q

monitoring hba1c in t2dm

A
  • Patients with poor glycaemic control require measurement of the HbA1c every 3 months
  • Patients with stable disease can have their HbA1c measured every 6 months
91
Q

monitoring for complications with t2dm

A
  • At least on an annual basis
  • During each review - BMI, smoking status, assess for any anxiety or depression
  • Annually …
    o Retinopathy: annual retinal screening and eye check
    o Nephropathy: renal function (eGFR) and albumin:creatinine ratio (ACR)
    o Neuropathy and diabetic foot: assessment for peripheral neuropathy, autonomic neuropathy, full examination including footwear, monofilament assessment of neuropathy, vascular assessment +/- dopplers
    o Cardiovascular risk factors: primary/secondary prevention strategy with optimisation of blood pressure and lipids
92
Q

insulin regimes for t2dm

A
  • Once or twice daily intermediate-acting insulin (NPH)
    o Often started on this in early stages - then if bad may start on mixed
  • Intermediate-acting insulin along-side a short-acting insulin as separate injections or a pre-mixed formula
  • Once daily long-acting insulin therapy (glargine, determir)
    o Usually reserved for when hypoglycaemia is a problem with NPH or patient relies on carers for infections
  • Basal-bolus regimes
    o Finally, patients on a pre-mixed insulin regime that still have inadequate blood glucose control should be assessed for conversion to a basal bolus regime
93
Q

jod-basedow effect

A

hyperthyroidism following administrating of iodine or iodide like contrast

94
Q

presentation of osteoporosis

A
  • Asymptomatic with the exception of fracture

- Common fragility fractures include vertebral crush fractures and proximal wrist and proximal femur fractures

95
Q

who to assess for fragility fracture risk

A
  • All women >65
  • All men >75
  • All aged 50+ who have any of the following risk factors:
    o A previous osteoporotic fragility fracture
    o Current use or frequent recent use of oral corticosteroids
    o History of falls
    o Low BMI (less than 18.5 kg/m2)
    o Smoker
    o Alcohol intake of more than 14 units per week
    o A secondary cause of osteoporosis such as hypogonadism, DM, hyperthyroidism, hyperparathyroidism, ceoliac, MM, CKD, immobility, RA, IBD, cushings…

AND<50 if taking steroids or premature menopause of histroy of fragility fractures

AND <40 taking steroids or previous fractures

also consider if on SSRIs, anti-epilpetics, PPIs, pioglitaozne, GnRH agonists or aromatase inhibitors

96
Q

when to go straight to DXA before doing a risk calculation

A

o Over 50 years of age with a history of fragility fractures — a DXA scan should be offered
o Under 40 years of age who have a major risk factor for fragility fracture — a DXA scan should be offered
o With vertebral or hip fractures — starting treatment without undertaking DXA should be considered if this is inappropriate or impractical

97
Q

investigations for osteoporosis

A

NICE recommend having a DEXA if the 10-year fracture risk is 10% or more
o T score -≤2.5 = osteoporosis
o -≤2.5 + previous fragility fracture = severe or established osteoporosis
o -1 to-2.5 = osteopenia

bloods - calcium, phosphate and PTH and ALP should be normal (low calcium could be osteomalacia, hypercalcaemia could be hyperparathyroidism)

can also consider doing radiographs if 
o	≥4cm height loss
o	Kyphosis
o	Recent or current long-term steroids 
o	BMD ≤2.5
98
Q

management of osteoporoiss

A

treat any secondary cause
offer treatment if -<2.5 T score and repeat DXA every 2 years (1 if changes to treatment)
if <2.5 then dont treat but repeat DXA every 2 years

lifestyle - alcohol, smoking, diet, supplementation if needed, falls assess inc med review, weight bearing exericses, balance training

bisphosphonates - alendonic acid usually frst line (remember good dental hygiene and report thigh or hip pain) - others inlcude risedronate (PO) or zoledronic acid (IV injection annually)
CI in low calcium and uveitis

denosumab- monoclonal antibody given 6 monthly SC - SE hypocalciaemia so may have to monitor - it may be a suitable option in women who are unable to comply with instructions for alendronate

raloxifene - selective oestrogen receptor modulator

HRT - noramlyl reserved for younger - longterm not recommended

99
Q

ET vs PD tremor

A
ET bilateral, PD unilateral 
PD occurs at rest 
PD affects arms, legs, jaw
ET affects arms, head, voice 
ET is a postural/action tremor
alcohol relieves ET tremor

ET can be treated with propranolol or primidone (antiepileptic)

100
Q

symptoms of parkinsons

A
  • Resting tremor - usually improve with moving
  • Rigidity - cogwheeling and lead pipe
  • Bradykinesia
  • Postural instability
  • Masked facies
  • Shuffling gait
  • Hypophonia
  • Micrographia
101
Q

investigations for PD

A
  • Diagnosis is based on clinical criteria and exclusion of other disorders
  • DAT scan or SPECT if unclear
  • CT or MRI if thinking secondary cause like stroke
102
Q

management of PD core symptoms

A

(currently no disease-modifying treatments so key is symptom control - treatment should be initiated early following diagnosis)

physiotherapy, speech and language (help with hypophonia), OT

FIRST LINE TREATMENTS
levodopa - usually given with a dopa decarboxylase inhibitor - is usually given in early stages of the disease when motor symptoms effect QoL - BUT only lasts for 4-6 years before longterm motor complications may arise so younger pts are often given dopamine agonists instead in earlier phases
oral or transdermal dopamine agoinsts like pramipexole or ropinirole
MAO-B inhibitors like selegiline - not as good for motor symptoms - so maybe good for early stages where motor not as pominent

ADJUVANTS
many pts will require additional therapy - this may mean combining some of the above or addigng the following
COMT inhibitors like entacapone (in combo w levodopa for dyskinesia or motor fluctuations)
amantadine a nicotininc antagonist (if dyskinesia not adequately controlled)
sc apomorphine a dopamine agonist
duodopa pump refractory to oral
DBS of subthalamic nucleus if refractory to medical (via insretion of electrodes into deep nuclei of the biran then pulse generator is inserted into the chest wall)

review every 6-12 m

103
Q

management of PD non-motor symptoms

A

constipation - increase fibre, laxatives
pain
n+v - avoid metoclopramide and prochlorperazine - consider low dose domperidone
bladder dysfunction - catheter

104
Q

problem in PD

A

loss of dopaminergic neurones

105
Q

motor complications in PD

A

Motor ‘on-off’ fluctuations - switch from dyskinesia to immobility in a few minutes - can be helped with a dopamine agonist
Dyskinesia - hyperkinetic movement due to dosing of medications - relieved by reducing dose or adding a long-acting dopamine agonist
Freezing of gait - complete inability to move
‘Wearing off’ phenomenon - towards end of dose - can be helped by introducing other drug ontop of Levodopa
Falls

106
Q

management of insomnia

A

hygeiene - avoid caffine smoking alcohol at night, regular exercise, relaxing activities, avoid heavy meals before bed, avoid screens, only use room to sleep, routine

if fail - try short course 3-7 day course of z drugs - zopiclone, zaleplon, zolpidem

if unlikely to reoslve soon then
CBT for insomina - typically includes behavioural interventions (such as stimulus control and sleep restriction), cognitive therapy and relaxation training
consider need for hypnotic medicaitions like short term z drug or melatonin if >55 for 3 weeks

107
Q

presentation of bell’s palsy

A
  • Symptoms
    o One-sided facial weakness that comes on over hours (<72 hours)
    o Difficulty chewing food on that side +/- drooling
    o Unable to close eye on affected side
    o Unable to wrinkle forehead
    o May have speech difficulties
    o Post-auricular/ear pain in 50%
    o Loss of taste on one side of tongue
    o Hyperacusis - loud noises may become uncomfortable - this occurs due to weakness of the strapedius muscle (strapedius nerve comes off facial nerve)
  • Signs
    o Loss of nasolabial fold
    o Drooping of the face on that side - corner of mouth, eyebrow, asymmetrical smile
    o Bell’s sign - upward movement of the eye maintained on attempt to close the eye
108
Q

cause of bell’s palsy

A

thought to be related to infalmmation and oedema of the facial nerve secondary to a viral infection or autoimmunity - most commonly due to herpes simplex of varicella zoeter

most common in pregnant women and diabetics

109
Q

differentials of bells palsy

A
  • Ramsay hunt syndrome
    o Results from reactivation of the latent VZV within the geniculate ganglion
    o Facial nerve palsy that is associated with a vesicular rash at the ear, ipsilateral hard palate, and anterior 2/3 of the tongue - other than that has same symptoms as Bell’s
    o Treatment is with antivirals and steroids and appropriate eyecare
  • Stroke
  • Cerebral tumour
  • If bilateral - needs specialist input as this is very rare and often secondary to something like lyme disease, sarcoid, GBS, HIV
110
Q

investigations for bells palsy

A
  • Clinical diagnosis

- May involve routine bloods, neuroimaging or special tests like LP, lyme serology

111
Q

management of bells palsy

A

prednisolone for 10 days if presenting <72 hours of symptom onset
antiviral may be combined with this but only small benefit and specialist advise should be sought
eye protection with eye drops, tape shut at night, wear sunglasses outdoors, avoid swimming and dusty environments

if eating is affected - can use a straw for liquids and a soft diet

advise that prognosis is good but may take several months to recover

refer to neurology or ENT if no improvement after 3 weeks of treatment

112
Q

sick day rules for t2dm

A
  • If becoming really dehydrated, may have to stop metformin - the GP or diabetic team will guide you
  • In general, may need to increase your medication depending on the glucose results
  • If on insulin - same as T1DM but increase insulin by 20% instead of 10%
113
Q

presentation of giant cell arteritis

A

unilateral temporal pain - occassionally diffuse and bilateral
headache
tenderness over scalp e.g. pain on combining hair
intermittent jaw claudication +/- tongue claudication
visual disturabnce in 50% - bluured vision, amaurosis fugax, transietn or permanent visual loss or diplopia - if untreated second eye is likely to be affected within 1-2 weeks
systemic features like PMR - fever, fatigue, anorexia, weight loss, night sweats, anorexia, depression

Thoracic aorta and aortic root involvement: occur in about 15%. This is more common in women and younger patients. Thoracic aneurysms can develop as late as 15 years after the diagnosis and successful treatment of GCA

NB features of polymyalgia rheumatica – bilateral upper arm stiffness, neck and shoulder pain, aching, tenderness, pelvic girdle pain

114
Q

investigations for GCA

A

examine area - temporal artereies may be prominent, beaded, tender, pulsenss
listen for bruits
temporal artery biopsy under LA - positive confirms but negative doesnt always run out due to skip lesions
start steroids while awiting biopsy in high suspicion
fbc, lfts, esr (often greater >50mm/hour), crp also typically elevated
fudoscopy for eye changes = e.g. may see anterior ischaemic optic neuritis
other - colour duplex US is being increasingly used but doesnt replace temporal biopsy

115
Q

management of gca

A

oral prednisolone - 60mg if claudication symptoms, 40mg if not - assess response in 48 hours, will be rapid
once symptoms resolve then reduce dose by 10mg every 2 weeks
for people w visual symptoms admit for treatment with IV methylpred
course of 1-2 years of steriods is often necessary but can be longer - osteoporosis prophylaxis for longterm
disease settles after 12-36m in 75% of cases
aspirin 75mg to reduce thrombotic even in affected arteries - is uncertain how long for
PPI for steroid and aspirin use

116
Q

follow up for gca

A

o Every 2–8 weeks during the first 6 months of diagnosis — close monitoring of BP and blood glucose (cos of steroids)
o Then decrease to every 12-24 weeks

monitor bloods and side effect

117
Q

complications of gca

A
  • Vision loss
  • Large artery complications (such as aortic aneurysm, aortic dissection, large artery stenosis, and aortic regurgitation)
  • Cardiovascular disease (such as MI, HF, stroke, peripheral arterial disease)
  • Peripheral neuropathy
  • Deafness
  • If the internal carotid arteries are affected there may be TIA or stroke
118
Q

chronic tension headaches define

A

> 15 days per month

119
Q

management of tension headache

A

consider keeping a headache diary to monitor for triggers
reassure
explain they are more common in sedentary people and regular exercise can benefit
ibuprofen fist line - paracetamol seems to be less effective - other options = naproxen or aspirn

TCAs - amitriptyline alternative

120
Q

what is trigeminal neuralgia and what causes it

A

pain in distribution of trigeminal nerve - typically mandibular and maxillary branches (ophthalmic not so much affected)

is due to vascular compression of the trigeminal nerve in most cases - other rarer causes include MS, tumours, AV malformations

121
Q

presentation of trigeminal nerualgia

A

pain in distribution of trigeminal nerve - cheek or lower jaw
severe, electric shock like, unilateral, short lived (seconds-2 minutes, stopping suddenly)
pain may occur infrequently - e.g. periods of remission may last years , or have a frquency of up to 100 times a day

pain can be triggered by touching the face, talking, cold wind, vibration, brushing teeth

atypical trigeminal nerualgia occurs when there is a persistent discomfort between pain episodes

122
Q

age of onset of trigeminal neuralgia

A

50-60

rare under 40

123
Q

investigations for trigeminal neuralgia

A

diagnosis is clinical

MRI if in doubt or underlying cause like a mass is supected - or occuring <40 or if surgery is being considered as a treatment

124
Q

management of trigeminal nerualgia

A

carbamazepine - start at 100mg up to 2x daily and titrate in steps of 100-200 until pain has resolsved
once pain is in remission, dosage should be gradually reduced until maintenance level, or drug can be discontinued until a further attack occurs

alternatives = gabapentin, baclofen, lamotrigine

if not reponding to meds - botulinum toxin type A, deep brain stimulation surgery (decompression surgery or ablative surgery)

125
Q

prognosis of trigeminal neuralgia

A
  • Of a new diagnosis
    o 66% will have a further episode in 5 years
    o 77% will have a further episode in 10 years
  • The majority will have remission with medical therapy although 10% will not respond
126
Q

investigations for epidiymo-orchitis

A

urethral swab can diagnose urethritis (>5 polymorphonuclear cells per high power field) and gonorrhea culture and NAAT for chlamydia (or first pass urine)

microscopy and cluture midstream urine for bacteria

when considering mumps as a possible diagnosis - IgM/IgG serology

127
Q

management for epididymo orchitis

A
  • Empirical therapy should be given to all patients with epididymo-orchitis before culture/NAAT results are available
    o If most likely due to STI
     Ceftriaxone IM + doxycycline for 10-14 days
    o For epididymo-orchitis most probably due to enteric organisms
     Ofloxacin 200 mg by mouth twice daily for 14 days or ciprofloxacin 500 mg by mouth twice daily for 10 days
128
Q

investigations for BPH

A

IPSS to give assessment of quality of life - the score from the first 7 q’s which are about the symptoms classes the disease in mild, moderate, severe (the 8th q is about quality of life)
examine abdomen for palpable bladder
DRE - note tone of anal sphincter/pelvic floor as may be poor with neurogenic bladder - and assess prostate
urine dipstick - MSU for microscopy and culture
bloods - may be deranged in mets e.g. lfts
PSA - avoid vigarous exercise and ejaculation for 48 hours prior
post-void residual bladder volume via catheter or bladder scan
US via abdomen or transreactal can be done to evaulate prostate size also evaluate for hydronephorisis in urinary retention
MRI for malignnacy
urodynamic studies - Qmax and flow pattern

other = pressure studies but invasive (type of invasive urodynamic study) or cystoscopy if sticture is suspected

129
Q

management of BPH

A

acute retention - catheter then TWOC

minimal symptoms - watch and wait provided malignancy has been excluded - med and surgical therapies have comps which can be avoided

MEDICAL
alpha blocker reduce tone of muscle in bladder neck - tamsulosin - postural hypotension may limit use for some, and can sometimes cause ejaculatory dysfunction
5-alpha reductase inhibitos - reduce synthesis of testosteorne - can take longer to take effect (months rather than days) - finasteride - can cause reduced libido, erectile dysfunction
can combine

SURGERY - large prostate failed to respond
TURP - can cause infection, retrograde ejaculation and may need catheter after
holmium laser enucleation of prostate (HoLEP) - similar SE to TURP
transurethral vaporisation of prostate
transurethral incision of prostate (smaller ones)
open prostaectomy for larger ones - no ejaculate can be produced and may have urinary frequency

130
Q

causes of erectile dysfunction

A
  • Vascular - CVD, atherosclerosis, HTN, DM, smoking, surgery or radiotherapy
  • Neuro - PD, stroke, MS, tumours, spinal cord disease, alcoholism, peripheral neuropathy
  • Hormonal - hypogonadism, high prolactin
  • Drugs - antihypertensives, BB, diuretics, antidepressants
  • Psychosexual factors
  • Psychiatric illness
131
Q

management of cold sores

A

avoid touching, wash hands after, avoid kissing
paracetamol and ibuprofen
choline salicylate gel (bonjela) (CI<16)
lidocaine gel
topical antiviral agents like aciclovir 5% but benefits are small and usually resolve in 7-10 days without treatment

for immunocompromised - oral antiviral

132
Q

management of impetigo (typically Staph aureus or step pyogenes - bullous usually occurs on top of other diseases like atopic eczema)

A

hygiene measures - avoid touching, avoid sharing towels
children should stay off school until lesions are dry and scabbed over or person has been on Abx for 48 hours

LOCALISED NON-BULLOUS
hydrogen peroxide cream
fusidic acid 2nd line

WIDESPREAD NON-BULLOUS
flucloxacillin oral - plus can do topical things as above

BULLOUS
oral fluxclox

133
Q

shingles cause and presentation

A

caused by varicella zoster (HHV-3) - after chickenpox it lies dormant in sensory root ganglia (if facial nerve is affected it causes ramsay hunt syndrome)

presents with
pre-eruptive phase - burning, itching or paraesthesia in one dermatome, may feel unwell
eruptive phase - skin lesion apperas, may have neuritic pain, vesicular erythematous rash, resolves at 14-21 days
chronic pain/postherpetic neuraliga - persistent pain

134
Q

shingles management

A

ophthalmic is a danger to sight so should see an ophthalmologist the same day for antiviral therapy

rash should be kept clean to avoid secondary bacterial infection
if the rash is weeping and not in a covered part of skin, then the person should stay off work or school
oral aciclovir preferable within 72 hours of onset for anyone w non-truncal involvement or where moderate pain or immunocompomised
and consider if >50 to reduce incidence of post-herpetic neuralgia as this is common in this age group

if it is not possible to initiate treatment within 72 hours, consider starting an antiviral drug up to one week after rash onset, especially if the person is at higher risk of severe shingles or complications (e.g. continued vesicle formation, older age or severe pain)

longer IV treatment may be required in elderly and the immunocompromised

use of steroids is debated - must combine w aciclovir if used

analgesia - can try TCAs, gabapentin or pregabalin or opiods if first line fails like NSAIDs

135
Q

general treatment for irritating rashes

A

calamine lotion

non-sedating antihistmaines

136
Q

risk factors for acne

A
age 
genetic predisposition 
increased sebum productin/oily skin 
medication - steroids, antiepileptics 
use of cosmetics - should try paraben free
pcos 
thyroid dysfunction
137
Q

patholophysiology of acne

A

abnormal follicluar differentiation
sebaceous gland hyperplasia and excess sebum production
propionibacterium acnes colonisation
inflammation

138
Q

management of acne

A

patient education
conservative - dont overwash face, use fragrance free products, SPF, role of diet not understood but data suggests high GI diets may exacerbate, avoid picking spots due to scarring risk

MILD-MOD
topical retinoid (tretinoin - skin more sensitive to light so apply at night - CI in pregnancy) alone or in combo with benzoyl peroxide (may bleech clothing - apply once daily wash off several hours after)
OR topical antibiotic (clindamycin) always in comb w benzoyl peroxide
OR azelaic acid
OR salicyclic acid

creams or lotions for dry or sensitive skin, gels for oily skin

MODERATE
consider adding lymecycline or doxycycline taken for at least 2m - co prescribed w topical retinoid or benzoyl peroxide
OR COC

REFER TO DERM IF 
multiple treatments fail, sig distress, severe variant, diagnostic uncertainty, scarring
consider isotretinoin (Roaccutane)

light treatments can be used but research not as good atm

139
Q

presentation + diagnosis of scabies

A
  • In primary infestation, signs and symptoms only develop after 3-4 weeks
  • Generalised and intense pruritus, typically worse at night and when the person is warm
  • Burrows
  • Papules, vesicles, excoriations

diagnosis is clinical - magnifying lens can help identify burrows, and can do ink burrow test - skin scraping can confirm (can site mite or eggshell under micorscope)

140
Q

management of scabies

A

treat all members of household w topical application on whole body with permethrin cream

wash clothing and beeding at 50 degrees

141
Q

pathophysiology of eczema

A

combo of genetics and environment

mutations in a gene that controls the skin barrier is thought to lead to impaired barrier function
thus this means increased exposure and sensitisation to antigens
once antigens are allowed in they trigger an inflammotory response

142
Q

presentation of eczema

A

scaly, itchy and erythematous patches commonly affecting the flexures (elbow, knees, wrists)
infants often present with rash affecting the cheeks

those of black ethnicity may demonstrate a different distribution with rashes affecting the extensor surfaces

affected skin can develop patches of both hypo and hyperpigmentation

itchiness leading to scratching can be evidenced by excoriations and with time lichenification (thickening) of the skin develops

143
Q

management of eczema

A

screening tools like POEM
conservative - avoid allergens e.g. animals, soap, food, avoid tight clothing, avoid fragraces/soap, keep house cool, cut fingernails (more so for children)

MILD
emollients - frequent and liberal use
consider mild topical steroid like hydrocortisone for areas of red angry skin

MODERATIE
emollients
moderaly potent steroid for inflammed skin like betamethasone 0.025%
severe itch then non-sedating antihistamine
between flares can consider prescribing a maintenance regime of topical steroids to skin prone to flares
2nd line to topical steroids would be calcineurin inhibitor like tracrolimus

SEVERE
emollients
potent topical steroid for inalmmed skin e.g. betamethasone 0.1%
non-sedating histamine for itch
severe eczema causing lots of distress then short course of oral steroid
consider topical steroid between flares as above
phototherapy
immunosuppressants
biologics

can use bandages to stop scratching

Local side effects of steroids are common and may include a burning sensation, thinning of skin, contact dermatitis, acne and depigmentation

144
Q

wart management

A

watchful waiting, debridement w pummel stone then salicyclic acid, duct tape occlusion as an adjunct, cyrotherapy, silver nitrate solution

145
Q

anal fissure management

A
  • Keep stools soft - lots of fluid, increase fibre, consider a laxative (bulk forming for adults - ispaghula husk/Fybogel) or osmotic (lactulose) for children)
  • Pain relief - paracetamol/ibuprofen, warm baths, GTN ointment (for adults with a fissure for over a week)
  • Consider a topical anaesthetic e.g. lidocaine for adults with extreme pain
  • Treat underlying cause
  • Refer adults with ongoing pain that has not resolved within 6-8 weeks
  • Secondary care
    o Topical diltiazem or nifedipine
    o Botulinum toxin
    o Surgery - sphincterotomy
146
Q

haemorrhoids presentation and investigations

A
internal haemorrhoids are painless cos upper anal canal has no pain fibres - only painful if strangulated
external may be painful and itchy
bright red bleeding with defectation 
feeling of rectal fullness 
impaired continenence 

investigations - ask pt to sprain may become visible, protoscopy to view inside, flex sig may be done to exclude other pathology, FBC anaemia

147
Q

management of haemorrhoids

A

increase fibre, bulk forming laxative like fibrogel
analgeisa
topical therapies like anaesthetics or topical steroids
avoid straining
non-surgical - rubber band ligation (becomes necrotic then falls off), infrared coagulation, injection sclerotheapy leads to atrophy, bipolar diathermy (heat leads to fibrosis)

surgical - haemorrhoidectomy under GA, haemorrhoidal artery ligation

148
Q

define CKD

A

definition of CKD is the presence of either of the following for 3 months or more

Marker of kidney damage:

  • Albuminuria (> 3 mg/mmol, i.e. A2/3)
  • Abnormalities (including electrolyte derangement) secondary to tubular disorders
  • Structural abnormalities
  • Abnormalities on histology
  • History of kidney transplant

Reduced GFR: GFR < 60 ml/min/1.73 m2 (i.e. G3a-G5)

149
Q

what 2 things determine stage of CKD

A

eGFR

ACR (degree of albuminuria)

150
Q

management of CKD

A

RENOPROTECTION
smoking cessation
target bp <140/90 (<130/80 if also diabetic or ACR >70)
statin 20mg
antiplatelet
diet - K restriction if hyperkalaemic, avoidance of high phosphate food e.g. milk, egg, cheese

SECONDARY HYPERPARATHYROIDISM
phosphate binders, vitamin D analogues

ANAEMIA
replace iron/b12/folate as necessary, consdier recombinant EPO

ACIDOSIS
sodium bicarb supplements

OEDEMA
loop diuretics

RESLETSS LEGS/ CRAMPA
quinine

dialysis, kidney transplant at end stage <30 egfr, uncontrolled complications

151
Q

define UTI

A

the presence of characteristic symptoms (e.g. dysuria, frequency) and significant bacteriuria (presence of bacteria in urine). Significant bacteriuria is defined as > 105 colony forming units (CFU)/ml. In the absence of symptoms, this level of bacteriuria is termed asymptomatic bacteriuria

152
Q

diagnosis of UTI

A

in young, non-pregnant females, typical clinical features (e.g. dysuria, suprapubic pain) in the absence of vaginal symptoms, is highly suggestive of a UTI. In this patient group, the probability of a UTI is > 90%. Further laboratory testing offers little to the diagnosis, however as a minimum, the majority of clinicians would do a urine dip

In the presence of complicating factors (e.g. systemic upset, diabetes, pregnancy, recurrent UTIs), further laboratory testing is necessary. Urinalysis, involving a urine dipstick and urinary microscopy, culture & sensitivity, (MC&S), is key

for complicated - can do bloods, US or CT to assess for abscess, haemorrhage, calculi, obsrtuction and emphysematous pyelonephritis

consider cystoscopy if haematuria present or recurrent infections not responding to abx

153
Q

management of UTI

A

conservative - avoid risk factors, drink lots of fluids, avoid wiping back to front, post-coital urination, avoid occlusive underwear - cranberry juice isnt recommended (benefit is limited surggestive of studies)

uncomplicated UTI - trimetho or nitro for 3 days in women and childen, 7 days for men, 7 days for catheter-associated
NB a delayed script can be considered instead of immediate abx if symptoms are mild and no risk factors for complicatino - 48 hours

uncomplicated pylonephritis - ciprofloxacin 14 days from home

complicated UTI - oral ciprofloxacin and will need MSU (complicated = occurs where anatomical, functional, or pharmacological factors predispose the person to persistent infection, recurrent infection or treatment failure - e.g. diabetes, catheter, anatomy)

recurrent
if associated with sex can take trimethoprim 2 hours before sex
if not associated with sex then 6m course of low dose abx (nitro or trimetho)
in postmenopausal women consider vaginal oestrogen

Safety-netting

  • Tell the patient that most UTIs respond to antibiotics within 24-48 hours - seek help if not repsonding
  • Red flags - if pain is increasing and travelling up towards the loins, they may be developing pyelonephritis which needs treating with cephalexin +/- admission if becoming septic so they must see the GP, or call NHS 111, or 999/A&E
154
Q

UTI abx - when to avoid

A

avoid trimethoprim in pregn - is a folate antagonist - esp avoid in 1st trimester
avoid nitro in renal impairement -egfr <45 and avoid at term due to risk of neonatal haemolysis

155
Q

management of UTI w haematuria

A

re-test urine after antibiotic - if haematuria persists then consider possible underlying causes

e.g. CKD, urological cancer, gynaecological cancer

156
Q

causes of vertigo

A

peripheral/vestibular - BPPV, vestibular neuronitis, labyrinthisis, meniere’s disease

central - acoustic neuroma, CVA, brainstem lesion, MS

NB in peripheral - if nystagmus is associaed this is NEVER vertical
also can differentiate with the dix-hallpike maneouvre - in central there is no lag between it and nystagmus and nystagmus lasts <1min - whereas in peripheral - there is a 2-4 second lag and lasts <1 min
And with central - neurological symptoms/signs, auditory features are uncommon, prolonged vertigo >24 hours

also the vertigo provoked is more likely to be severe with peripheral after the manoeuvre

157
Q

BPPV - all

A

specific and predictable changes in head position eg getting out of bed causes vertigo that lasts 30 seconds to 1 minute
nausea commonly associated

is due to debris in the canal which is disturbed by head movement, then (debris could be there cos of idiopathic, infection, ageing or trauma) resettles causing vertigo due to interrpting flow of endolymph

signs = nystagmus when preforming dix-hallpike is diagnostic
o Turn head to 45 degrees to the horizontal. Patients are lowered quickly to a supine position with the neck extended around 30 degrees below horizontal (so hanging off the bed) – will experience vertigo and see nystagmus

treat with epley manoeruvres to clear the debris - can be taught modified one to do themselves
can also advise to avoid suddent head movements and to lie and sit in stages

generally is self limiting - if lasting >4w then should refer as is unlikely BPPV

158
Q

meniere’s disease -all

A

most common in 40-50

triad of vertigo, unilateral hearing loss and tinnitus (additional = aural fullness)
not related to head movements like bppv
abrupt onset

is due to dilation of endolymphatic spaces by fluid - overproduction - causes rupture of membrane separating endolymph from perilymph

vertigo attacks last >20 minutes but <24 hours (patients will have nystagmus during the attacks) - acute episodes may occur in clusters of about 6-10 a year - remission between

may develop bilateral symptoms years later

MRI is advised for unilateral cases to exclude acoustic neuroma

should inform dvla, limit salt caffeien fatigue, consider saftey w heights, dangerous machinery
acute attack treat with propchloperazine or cyclizine
or antihistamines
for severe may need hospital to maintain hydration

prophylaxis with betahistine
diuretics may be started in secondary care
may also need counselling or relaxation therapy - can be distressing

prognosis - vertigo may resolve if the condition ‘burns out’, which can happen after 5-15 years. However, tinnitus, unilateral hearing loss, and sensations of aural pressure and a sense of general imbalance may persist

159
Q

describe vertigo cause

A

mismatch between sensory inputs - vision, proprioception and vestibular system

160
Q

acute labyrinthitis and vestivbular neuronitis

A

infection of the vestibular nerve/labyrinth usually following an upper respiratory infection that leads to an inner ear infection (usually caused by viruses)
hearing is not affected in vestibular neuronitis

acute, isolated, spontaneous vertigo lasting several days - head movements worsen but can occur at rest, no specific position
with nausea and vomiting. No deafness or tinnitus. But there may be hearing loss in labyrinthisis
also have nystagmus

reassure the person that symptoms will usually settle over several weeks – even if no treatment is given
o Advise that factors such as alcohol, tiredness, or intercurrent illness may have a greater than usual effect on their balance
o Advise that bed rest may be necessary if symptoms are particularly severe during the acute phase, but that activity should be resumed as soon as possible (even if vertigo becomes more prominent during movement)
o Advise the person not to drive when they are dizzy, or if they are likely to experience an episode of vertigo while driving
o The person should inform their employer if their vertigo poses a risk in the workplace

if severe - anthistamines or antiemetics to suppress vestibular system

161
Q

investigations and treatment for tinnitus

A

examine ear to look for otitis, tympanic membrane perforation and cholesteatoma
pure tone audiogram may help diagnose a cause although some wont have hearing loss
mri for unilateral tinnitus
if pulsatile, examine head and neck and check peronns bp and bruits

treat underlying cause if found
may benefit from sound enrichment therapy - low-level background noice
hearing loss w hearing aids
psychological support
cbt 
relaxation techniques
162
Q

causes of tinntius

A

unilateral w sensorineural hearing loss = menieres disease, acoustic neuroma

bilateral w sensorineural hearing loss = age releated hearing loss, noise-induced hearing loss, drug-induced ototoxicity e.g. gentamicin, aspirin, nsaidds, loop duiretics, cytotoxic drugs

unilateral or bilateral w conduction hearing loss = impacted wax, otitis media, cholesteatoma, otosclerosis

163
Q

presentation and management for acute rhinosinusitis aka sinusitis

A

diagnosed by presence of nasal blockage or discharge w facial pain/pressure (headache) and or reduction of sense of smell
maxillofacial area swollen/tender
can also do anteiror rhinoscopy (use largest speculum of an otoscope)

treat in hospital if systemically unwell or has complications e.g. periorbital oedema or cellulitis

analgesia for pain, anitpyretics
trial of nasal saline or decongestants
avoid abx - most resolve by 14 days - is usually caused by a virus and only complicated by bacteria in 2 in 100 cases
only give abx if high risk ocmplications

if symptoms >10 days then consider high-dose nasal steroid for 14 days or consider back-up abx prescribption with phenoxymethylpenicillin

if symptoms suggest neoplasm (for example, unilateral polyp or mass, bloody nasal discharge)

164
Q

things that suggest bacterial rather than viral rhinosinusitus

A
  • Symptoms for more than 10 days
  • Discoloured or purulent nasal discharge (with unilateral predominance)
  • Severe local pain (with unilateral predominance)
  • A fever greater than 38°C
  • A marked deterioration after an initial milder form of the illness (so-called ‘double-sickening’)
  • Elevated ESR/CRP (although the practicality of this criterion is limited)

treat with phenoxymethylpenicillin

165
Q

management of allergic rhinitis

A

allergen avoidance
intranasal antihistamines
possible use of nasal irrigation w saline
oral antihistamines where nasal discharge or sneezing is predominant
topical intranasal steroids where predominant symptom is nasal blockage or where polyps are present
nasal saline washouts

surgery may be indicated e.g. polyp removal

166
Q

otitis externa v media presentaiton

A
EXTERNA
erythema, oedema on otoscopy
pain w movement of tragus or auricle
pre-auricular lymphadneopathy 
more severe cases - hearing loss, discharge, fever, cellulitis spreading beyond ear 

MEDIA
middle ear fluid - red/yellow/cloudy/bulging tympanic membrane
earache - if perforation occurs this will less

167
Q

management of otitis externa (usually a bacterial cause)

A

topical drops for 7 days with acetic acid for mild cases
if anything more than mild then topical antibiotics with neomycin or clioquinol (avoid gent if perforated membrane)
can combine with steroids if ear is inflamed e.g. otomize spray or sofradex drops (both are dex combined w an abx)
if cellulitis or systemically unwell then oral fluclox
if extensive swelling of ear canal then consider inserting an ear wick impregnanted with the medication changed 2-3 days

NB administering the drops - remove any substantial exudate first with a cotton bud or twist of cotton wool. Then warm the drops with your hands (prevents dizziness that can occur if cold drops are given). Person should lie laterally. Remain in that position for 3-5 minutes

swab if treatment failure or looks atypical

168
Q

what is malignant otitis externa

A

spread of otitis externa into the bone surrounding the ear canal (the mastoid and temporal bones)

without treatment, is a fatal condition

169
Q

management of otitis media (usually caused by bacteria)

A

advise usual course is 3 days but can be up to 1 week
analgesia/antipyretic
many people will not require Abx because symptoms usually resolve spontaneously within a few days
usually advice that antibiotics are unlikely to make a difference
can do a delayed prescribing strategy – to take after 4 days if not improving

immediate abx if systemically unwell, no improvement after 4 days, <2 years with bilateral, perforation, high risk of comps like immunocomprmoseid

5-7 days of amoxicillin

Take account of evidence that acute complications such as mastoiditis are rare with or without antibiotics, and the possible adverse effects of antibiotics

170
Q

define otitis media with effusion

A

characterised by fluid in the middle ear, but is not associated with symptoms and signs of an acute ear infection

AKA GLUE EAR – this is an important differential

cause unknwon - but over 50% are thought to follow an episode of acute otitis media
if persistent may be due to impiared eustachian tube fucntion or low-grad infection

can present with significant hearing loss but can just be asymptomatic - mild intermittent ear pain w fullness or popping may occur

171
Q

diagnosis of glue ear

A

otosocpy - no signs of inflammation or discharge but will find abnormal colour of drum (yellow red or blue), loss of light reflex and may see air bublles or air/fluid level and bulging drum

perform hearing test - mild conductive hearing loss
pure tone audiometry

nice recommends a 2nd hearing loss 3m after the first

172
Q

management of otits media w effusion

A

spontaneous resolution of OME is common, so for most children a period of active observation over 6–12 weeks is appropriate
90% of children will have complete resolution within one year (although recurrence is common)
during this period - should re-evaluate signs of the effusion and concerns regarding child’s hearing or language development - 2 hearing tests with pure tone audiometry at least 3 months apart as well as tympanometry

consider ENT referral depending on amount of hearing loss

persistent bilateral OME or bad hearing loss may benefit from surgery with grommet insertion (SE = tympanoscerosis and infectoin)

173
Q

diagnosis of thrush

A
  • Examination is not routinely required in primary care if history suggests uncomplicated thrush
  • If examination is indicated - signs suggestive include erythema usually localised to vagina and vulva, vaginal fissuring and/or oedema, excoriation of the vulva

investigations are not usually required but can include
o pH <4.5 (>4.5 suggests bacterial vaginosis or trichomonas)
o Routine vaginal swabs
• High vaginal swab (HVS) but 10-20% women are asymptomatic vaginal carriers and their symptoms may not be due to the candida isolated
o MSU if symptoms could be due to UTI
o HbA1c to exclude DM as a cause of recurrent thrush

174
Q

management of thrush

A

if no symptoms do not treat
recommended regimen = antifungal pessary +/- cream for external areas like clotrimazole
alternative = oral fluconazole or itraconazole (oral is CI in pregnancy)

consider associated precipitants (e.g. soaps, shower gels, sanitary towels) or conditions like DM, steroid or abx use

return if symptoms not resolved in 7-14 days

for recurrent provide prescription as required or a 6m maintenance regime

175
Q

diagnosis of chlamydia

A

NAAT - vulvovaginal swab in women, first catch or urethral sampling in men

will see pus cells on slide

176
Q

management of chlamydia

A

doxycycline 2x daily 7 days or single dose of 1g azithromycin if doxy not tolerated or ci (e.g. in pregnancy)

advise that sex should be avoided until person has completed treatment

NB complications = PID, reactive arthritis, perihepatitis

177
Q

gonorrhoea diagnosis

A

culture or NAAT - depends on setting

fast pass urine for men or urethral swab, and high vaginal in women or endocervical

a culture should be taken in all people who are NAAT positive to work out abx susceptibility

178
Q

managemenet of gonorrheoa

A

ceftriaxone 1g IM - but if antibioitc susceptibility is known then cirpofloxacin single oral dose

in pregn = ceftriaxone

do test of cure at least 2 weeks after treatment is finished

179
Q

amsel’s criteria

A

pH >4.5
thin grey/white discharge
positive amine test (release of fishy odour on adding alkali/10% KOH)
clue cells on microscopy

180
Q

score used to measure micorscopic appearance in BV

A

hay-ison score

Grade 0 = epithelial cells only with no bacteria
Grade 1 = normal vaginal flora (predominance of lactobacillus morphotypes)
Grade 2 = intermediate vaginal flora (reduced number of lactobacilli with mixed bacterial flora)
Grade 3 = mixed bacterial flora only
Grade 4 = gram positive cocci only

2 and 3 = BV

181
Q

managmenet of BV

A

metronidazole 400mg twice daily for 5-7 days or 2g stat (avoid single dose in pregnancy)

182
Q

TV - all

A

women - can be asymptomatic, or frothy yellow discharge and can have fishy odor, vulval itching, pain in sex
men - usually asymptomatic but can have dysuria and discharge

diagnosed via high vaginal swab w NAAT - men w culture of first void urine

treat with metronidazole single dose of 5-7 days

dont have alcohol on this and for 48 hours after due to possibility of disulfiram reaction

183
Q

presentation of herpes

A

febrile illness prodrome for a week in first episode only - may also have a tingling sensation over the area - this is for all episodes

dysuria - can be so painful that they could go into urinary retention
multiple painful genital ulcers
lymphadenopathy
discharge
untreated episode may last 3w or more
future episodes may last 3-4 days - on average they have 4-5 attacks a year

may have had a clinical infection for years

184
Q

investigations and management of herpes

A

take a swab from base of lesion - pop blister if necessary - for viral culture or PCR (negative does not rule out as may have been taken too late in an attack)

management - first episode treat within 5 days with oral aciclovir for 5-10 days
self care - clean area w plain or saltwater, apply vaseline or topical anaesthetic, increase fluid intake to dilute urine, aovid tight clothes, analgesia, dont share towels, abstain from sex until lesions gone

can have episodic antiviral thearpy for future attacks but reduction is onyl about 1-2 days

can have suppressive antiviral if >6 attacks a year with aciclovir daily - then discontinue after a year to reassess attack frequency

185
Q

pathology and cause - polymyalgia rheumatica

A

predominant site of inflammation includes bursae and tendons - despite the name implying a myopathic process, the muscles are actually normal on histopathological assessment

o Bursae are fluid filled sacs that counteract the friction associated with tendons

cause = genetics and environemntal - the cyclical pattern of cases and peak incidence in winter months suggests an infectious trigger

186
Q

presentation of polymyalgia rheumatica

A

> 2 weeks duration of symptoms
bilateral shoulder or pelvic girdle arching or both
mornign stiffness >45 minutes in duration
worse on waking

may have flu like features on onset, associated with fatigue, fever, weight loss, anorexia and depression

reduced ROM, synovitis and swelling, power normal

peripheral symptoms like features of arthritis, swelling and carpal tunnel syndrome (10-15%) may be identified

187
Q

investigaitons for polymyalgia rheumatica

A

raised crp and esr
CK normal
do autoimmune screen like ASA
anti-ccp and rf
screen for GCA - temporal biopsy if needed
imaging like US can assess for synovitis, rotator cuff tears or joint swelling/bursitis

188
Q

management of polymyalgia rheumatica

A

prednisolone 15mg daily
review at 1 week - should have dramatic response
decrease dose slowly once symptoms fully controleld (usually after 3-4 weeks) - tapering may be requried over a long period (1-2 years) due to risk fo relapse if stopped too early

arrange regular reviews to assess crp, esr and glucose due to risk of steroid-induced diabetes

bisphosphates, PPI +/- calcium and vitamin D

saftey net about gca

methotrexate occassionally used as steroid-sparing agent

189
Q

risk factors for gout

A
high levels of uric acid in the blood 
foods high in purines (which are broken down into uric acid) - red meat, seafood like sardines and anchovies, alcohol, sugary drinks
things that affect excretion of uric acid e.g. diuretics, ace inhibitors 
otehr drugs - bb, chemothearpy agents 
male
older age 
genetic factors 
high cell turnover states e.g. lymphoma
high cholesterol, DM
menopause
190
Q

presentation of gout

A

The deposition of crystals within joints and soft tissue may occur asymptomatically such as in chronic gout with the formation of small gouty tophi on the skin. However, during acute attacks, crystals trigger an acute inflammatory reaction leading to acutely painful swollen joints

typically first metatarsophalangeal joint (big toe) - can affect any joint - others inlucde knee, midfoot, fingers
usually monoarticualr
severe pain with swelling, redness, warmth, tenderness - max intensity within 24 hours
tophi - asymmetric swellings with a chalky appearance producign firm noduels - at ear, achilles tendons and upper kimbs

191
Q

investigations for gout

A

no investigations needed if no suspicion of other conditions like septic arthritis

joint micorcsopy and culture if unsure about septic arthritis - gold standard but not practial - presence of negatively birefringement needle shaped crystals

do serum uric acid 4-6 weeks after an acute attack to confirm hyperuricaemia- if normal does not rule out (usual cut off is 360)

Xray if suspecting other things - will be normal in gout

screen for CV risk factors and renal disease e.g. lipids and glucose in meatbolic syndrome

192
Q

management of gout - acute attacks last about a week

A

conservative - rest and elevate, avoid trauma to jiont, discuss lifestyle issues, ice pack, keep exposed

medical
NSAID (naproxen, indometacin or diclofenac) - continue until 1-2 days after resolved w a PPI
OR colchicine
2nd line = oral or injected steroid

consider paracetamol as adjunct
advise to return if symptoms get worse or no improvement in 1-2 days

193
Q

prevention of gout

A

medication is normally lifelong and regular monitoring is needed
allopurinol is first line urate lowering agent
used in all people but particuarly if 2 or more attacks in 12m, otphi present, chronic gouty arthritis, join damange, eGFR<6-, history of stones, young age, diuretic use
start at low dose and titrate up every 4w until serum uric acid is <300
start 1-2w after attack settled as can actually trigger gout - so co-prescribe colchicine for 6m to prevent acute flair

194
Q

joints affected in OA of hand and signs in the hand

A

PIP and DIP - MCP joints are spared

bouchards nodes are proximal, heberdens are distal

in advanced disease there may be squaring at CMC joint caused by subluxation, formation of osteophytes and bone remodelling

may also be radial or ulnar deviation

195
Q

features of OA in the knee

A

giving way due to altered patella tracking - the patella shifts out the way when legs bends or straightends
locking - suggests loose meniscal cartilage in the joint
crepitus
tenderness along joint line
small-to-moderate effusions

196
Q

features of OA in spine

A

in the spine there can be osteophyte formation and loss of disc space leading to neuro symptoms e.g. cervical spondylosis e.g. vague numbness, tingling or weakness in the upper limbs.(cervical spondylosis = cervical OA)

197
Q

diagnosis of OA

A

NICE say can diagnose if 45 or older, has activity related joint pain, has no morning joint-related stiffness or stiffness that lasts no longer than 30 mins

can calculate BMI - weight loss if needed
consider xray to exclude other conditions or diagnostic uncertainty but x ray changes do not really correlate with symptoms (NICE say can diagnose without)
bloods including crp/esr to rule out inflammation
check UE as a baseline before medication
joint aspiration if needing to rule out gout and septic arthritis
MRI good at ruling out soft tissue injuries

X ray changes = joint space narrowing, osteophytes, subchondral sclerosis, subchondral cysts (look black)

198
Q

differentials of OA

A

greater trochanteric pain syndrome - a common cause of lateral hip pain due to tedinopathy of gluteal medius or minimus - this can be a differential for hip or knee OA

ganglion of the hand
trigger thumb
sciatica
spinal stenosis

199
Q

management of OA

A

conservative - appropriate footwear (podiatry referal), local heat or cold packs, TENS can help reduce reliance on oral analgesia and offers significant pain relief , weight loss, exercise - swimming and static bike cycling are really good options for muscle strengthening

phsyiotherapy

OT assesmment and help with psychological aspect of the disease

paracetamol, w or without topical NSAIDs
then oral NSAIDs
then opiods like codeiene ot topical capsaicin
intra-articualr steroid
surgery - arhtroscopy w debridement, osteotomy (surgery that reshapes bones), partial or total joint replacement
arthodesis is an option for base of thumb OA

pain clinic referral is an option

200
Q

achilles tendon rupture

A

usually occurs with a pushing-off motion – in contact to ankle sprain, which is often due to impact on landing

Sudden onset Achilles tendon pain. Initially sharp pain, often settles within hours to days to more of a dull ache
A loud “snap” or “bang” is sometimes heard when the tendon ruptures!

Calf squeeze (aka Thomson’s calf squeeze test) – in a normal, intact Achilles tendon, a calf squeeze should cause plantar flexion of the ankle. In Achilles tendon rupture, there will be minimal or no plantar flexion

ofter clinical diagnosis but can do US and MRI

manage w no weight bearing and refer to ortho immediately then rehabiliation - may take months to get back to normal

Conservative management is an option for older more sedentary patients – but decision should be made by orthopaedic specialist
Plaster cast for 2 weeks
Can be changed to immobilising boot from 2 weeks
Weight bear as pain allows from 4-6 weeks

201
Q

carpal tunnel syndrome management

A
avoid repetitive movements 
consider adaptation of their workplace 
wrist splinting in a neutral position can help with nighttime symptoms in particular
steroid injection 
do not prescribe NSAIDs to treat

refer to specialist like rheumatologist or orthopaedic surgeon if not getting better

surgery - involves cutting the ligament - most people return to work after 12 days average

other treatments - acupuncture has shown some benefit, or physio

202
Q

managemnet of RA

A

analgeisa commonly NSAIDS or newer cox2 inhibitors like celecoxib w a PPI
physiotherapy
podiatry input
while awaiting rheum referral to start dmards - gp’s can start them on nsaids

DMARD first line - methotrexate, leflunamide, sulfalazine usually in combo with bridging steroid therapy (2-3m) which allows time for DMARD to take effect
failure to respond then combine dmards
safteynet - report sx of infection esp sore throat w methotrexate

still ongoing active disease then consider biologic therapy (either in combination w DMARD or used initialy in patietns with severely active and progressive disease) - e.g. adalimumab, infliximab…

manage flairs with steroids e.g. prednisolone

surgery is occasionalyl needed

203
Q

disease activity score for RA

A

DAS28

involves assessment of 28 joints for swelling and tenderness in combination with inflammatory markers (e.g. CRP/ESR) and global assessment of health scale

204
Q

systems review for rheumatoid history

A

systemic - fevers (discitis, septic arthritis), weight change in malignany
CV - chest pain (pericarditis or myocarditits)
resp - dysnpoea, cough (ILD, sarcoid), pleuritic checkt pain (pleuritis)
gastro - nausea, dyspepsia, abdo pain (SLE)
GU - dysuria (urethritis)
neuro - seizures (SLE)
derm - rashes (psorosis), buterrfly rash (SLE)

205
Q

acne severity

A
mild = open and closed comedones predominate
moderate= inflammatory lesions predominate - papules and pustules 
severe = visible scarring or risk of scarring of hyperpigmentatin
206
Q

red flags for dyspepsia - ALARMS

A
A – Anorexia
L – Loss of weight
A - Anaemia (IDA)
R – Recent onset of persistent symptoms
M – Melaena
S – Swallowing difficulty
other
>55 years old
Dysphagia/ odynophagia
Persistent vomiting
Palpable epigastric mass
FH of upper GI malignancy 1st degree relative
207
Q

2w referal for OGD

A

dysphagia OR
>55 and weight loss with any of
upper abdo pain, reflux, dyspepsia

non-urgent = heamatemesis, treatment resistant dyspepsia and >55, dyspepsia with nausea or vomiting…

208
Q

red flags for urinary incontinence

A
  • Heamaturia
  • Persistent UTI - UTIs can resemble bladder cancer
  • Constant leakage
  • Associated faecal incontinence
  • Constitutional symptoms
  • Poor renal function
  • Abnormal neurology
  • Saddle anaesthesia
  • Recent back trauma
  • Recent pelvic surgery
209
Q

cut off for chadvas and hasbled

A

chadvas - consider 1, prescribe 2

hasbled - consider still anticoagulating if 2, alternatives should be found if 3 (anyone 3 or above have high risk for major bleeding)

210
Q

which abx should be avoided in eldery due to risk of c diff

A

ciprofloxacin

co-amox

211
Q

why is doxy avoided in children

A

teeth discolouration

212
Q

which abx have cross-sensitivity w penicillines

A

Cephalosporins (0.17-0.7% in observational studies (10% is commonly quoted from early studies)) - cefuroxamine, ceftiaxone
Carbapenems (<3%) e.g. meropenam

213
Q

SPIKES

A

Setting - make sure is informal and appropriate
Perception - assess the patients perception on their current situation, understanding of recent tests
Invitation - ask if they are ready to receive their results and ask if they want anyone else to join
Knowledge - Explain what results mean, let them know the results weren’t what they hoped for, then break the news
Emotions - recognise and respond to emotions
Strategy and summarise - Organise a time to discuss next steps in treatment and referral, summarise findings for patient and answer any questions

Can give details of our clinical nurse specialist if have more questions
Offer assistance to tell others
Point towards sources of support
Offer written materials
Consider asking about religious preferences

214
Q

examples of GLP-1 agonists and SEs

A

liraglutide
exenatide

note - GI upset, decreased appetiete, rare reports of pancreatitis and improved CV outcomes

215
Q

testing for frailty

A

Prisma-7 - walking aids, how much help you require
time get up and go - measure time in seconds for person to rise from chair to walk 3m then walk back and sit down again - 10 seconds is normal, >20 high risks of falls and frailty
rockwood frailty scale

216
Q

diagnosis of TB

A

SCREENING
mantoux test - intradermal injection of purified tb protein - hypersntivity reaction will deevelop if they’ve had exposure (previous bcg can affect restuls)
interferon gamma release asseay (unaffected by prev bcg vaccine - tests fot t cell interferon gamma response to tb antigens)
if postiive screening then need to exclude active tb w clinical review and CXR
in general patients with latent TB should be treated to prevent the development of post-primary TB

DIAGNOSING ACTIVE
CXR
where possible 3 sputum samples should be taken for tb microscopy and culture (bronchoalveolar lavage can be taken if not)
for rapid testing can use NAAT but is expensive and only advised in certian settings e.g. v young or patient has hiv

can start treatment without culture results if clinical sigsns

samples are analysed with ZN stain, then micorsocpy for acid fast bacillin then culture on LJ slope -takes up to 8 weeks

217
Q

drug to combine with isoniazid to prevent peripheral neuropathy

A

pyridoxine

218
Q

things to add in a bleeding hitsory e.g. LGIB

A

consider lifestyle changes like increasing iron rich foods, avoid NSAIDs

ask about amount of iron rich food in diet like red meat and beans

219
Q

prostate cancer

A

DRE - many men will have normal tho
PSA - no UTI in last 6w, no ejaculaton for 48 hours, no vigorous exercise for 48 hours, no urological interention in past 6w (PSA can be offered to men >50 that request it) (DRE can make it raised, as can exercise, ejaculation, UTI, BPH, prostatits

refer people w abnormal prostate on DRE or PSA elevated for 2ww

multiparametric MRI is first line - generate a likert score from this
then offer biopsy guided by US
a negative biopsy does not completely exclude and should take into accont previous investigations - can have a repeat done

further imaging = ct or another mri to identify spread

TNM and gleason for histological grade

MANAGEMENT
localised = active surveillance (associated w reduce incidence of urianry incontinence and erectile dysfunction), radical prosatectomy or radical radiotherapy (radicla options reduce risk of recurrence)
androgen deprivation therapy may be combined - particuarly those w high risk disease

locally advanced = radical prostatectomy and radical radio - chemo may also be used

metastatic = chemo and androgen deprivation may be used

220
Q

monitoring in T2DM vs T1

remember t1 targets = 5-9 90 mins after eating, then 4-7 at other tiems of day

A

TYPE 2
- Patients with poor glycaemic control require measurement of the HbA1c every 3 months
- Patients with stable disease can have their HbA1c measured every 6 months
annually for complications - eyes, nephropathy w egfr and acr, diabetic foot exam, nerve exam, cv exam and bp and lipids

TYPE 1
same - should be done 3-6 monthly
also screen for complications AND thyroid disease annually