AIM exit topic questions Flashcards
Accidental hypothermia
- Defined as core temp < 35ºC
- Mild hypothermia 32-35 ºC, mod hypothermia 28-32ºC, severe hypothermia <28ºC
- Check cortisol and thyroid
- check blood gas, CK, toxicology and CTB
- Maintain ABC, may need fluid resuscitation and inotropes
- consider broad spectrum Abx and empirical hydrocortisone, especially if there is failure to rewarm
- Mild hypothermia - External rewarming
- Moderate hypothermia - External rewarming of truncal area only
- For severe hypothermia, for active external and internal rewarming
- warm IVF 38-42ºC , warm O2 42-46ºC
- endovascular rewarming catheter
- Aim rewarm till 35ºC
- consider not for rewarming of post-shockable arrest patients with spontaneous mild hypothermia >33ºC
AML-M3 management and complications
- high LDH, urate +/- DIC
- look for hyperleucostasis and tumor lysis
- ATRA + arsenic
- allopurinol to reduce urate levels (consider rasburicase if high risk)
- PCP prophylaxis
- aggressive transfusion as required (Plt / FFP / cryoprecipitate)
- antibiotics if fever
[] Hyperleukostasis
- WCC >100
- look for end-organ dysfunction - eg chest pain / SOB / hypoxia / MI / acute limb / acute bowel ischemia
- leukopheresis + HU if end-organ symptoms
- HU (+/- cytarabine) if no symptoms
- no transfusion until WCC <100
[] Tumor lysis
- hyperPO4 / urate / K, hypoCa (change >25%)
- aggressive fluid
- rasburicaase for established TLS
- may require dialysis
[] Differentiation syndrome / cytokine storm
(fever, APO, hypotension, AKI)
- Dexamethasone and supportive management
Anaphylaxis overview
Presentation
- acute mucocutaneous reaction + respiratory compromise / GI symptom / hypotension and shock
- or exposure to allergen + above symptoms
Management
- 0.5ml 1:1000 im adrenaline, repeat in 5min
- IVF and ABC
- consider iv adrenaline if refractory hypotension
- consider antihistamine (for mucocutaneous symptoms only)
- consider steroid to prevent late phase reaction
Blood x tryptase within 4h + >24h as baseline
Epipen before discharge
Conditions that prolong QTc
- HyopK, HyopMg, HypoCa
- Myocardial ischemia, post-arrest
- Hypothermia, raised ICP
- congenital long QT
- drugs
Drugs:
[] antiarrhythmics
- class IA - quinidine, procainamide
- class IC - flecainide
- class III - amiodarone
[] Psy meds
- antipsychotics (eg haloperidol, quetiapine, olanzapine, amisulpride)
- TCA (eg amitriptyline)
- other antidepressants (eg citalopram, bupropion, venlafaxine)
[] antibiotics
- quinines (hydroxychloroquine)
- quinolones
- macrolides (erythromycin, clarithromycin)
[] antihistamine (eg loratadine)
Anticholinergic poisoning and management
Eg with diphenhydramine, atropine / hyoscine, TCA, Artane (benzhexol) and benztropine, oxybutynin
Flushing (red as a beet)
Dry mouth, anhidrosis (dry as a bone)
Hyperthermia (hot as a hare)
Confusion (mad as a hatter)
Mydriasis (blind as a bat)
AROU (full as a flask)
TCA will also have signs of serotonin syndrome and widened QRS
Mx
- phytostigmine (AChE inhibitor) 0.5mg slow iv
(cf also used in MG)
- !! CI in TCA poisoning and asthma
For TCA - GL, AC if within time window; MDAC and urine alkalinization to reverse arrhythmia
Brain death prerequisites, timing of tests and personnel to conduct tests
Diagnosis of severe irremediable brain injury, with diagnosis of that underlying disorder
Exclusion of:
- CNS depressants / drugs
- hypothermia core temp <35’C
- severe metabolic and endocrine disturbances
- arterial hypotension
- locked in syndrome
Done by:
- 1x specialist with skill and knowledge in certifying brain death - ICU, CCM, Neurologist, NS
- 1x specialist, ideally with same qualification, should be at least 6y after registration
- Personnel certifying brain death should not be related to organ removal
Timing of tests
- 1st exam performed after all prerequisite criteria met, at least 4h after reaching GCS 3
- 2nd exam can be performed any time after 1st exam, so that the total period of observation is at least 4 hours
- Need at least 24 hours after an arrest
- Delay for at least 72h after rewarming if therapeutic hypothermia has been used
- time of death = when 2nd exam is completed, or after the confirmatory investigation
Brain death tests
- Both pupils fixed, >4mm, non-reactive to light
- Absence of bilateral corneal reflexes
- Absence of vestibulo-ocular reflexes (cold water to ear)
- No motor response within trigeminal nerve by pain sensation of any somatic area
- Absence of gag reflex
- Absence of cough reflex (suction catheter)
- Apnea - no resp movements when patient is disconnected from IMV, with oxygenation during the process
(ABG - PaCO2 >8kPa, pH <7.3; suggest PaCO2 rise >2.7 kPa above baseline
Brugada Syndrome
Autosomal dominant, present with LOC / SCD
Type 1 - coved ST elevation over V2/3
Type 2 - saddle ST elevation
Type 3 - ST elevation <2mm
Exacerbated by fever, hypoK, drugs incl flecainide, TCA, lithium, propofol, alcohol
Flecainide test for asymptomatic type 2 pattern ECG
Management
- avoid fever / contraindicated drugs
- ICD if aborted arrest
- genetic screening / family screening
Carboxyhemoglobin
- elevated COHb level in VBG (levels do not correlate with severity), test by co-oximetry
- PO2 levels may be normal (but HbO2 is profoundly reduced)
- symptoms - headache, nausea, dizziness; chest pain (can have MI), syncope, tachycardia, SOB, confusion and seizures
Mx
- 100% O2 with NRM
- HBOT if LOC, COHb >25%, metabolic acidosis pH <7.25, end-organ ischemia (eg MI, confusion, resp failure)
Causes of cerebellar dysfunction
- tumor, stroke (localized)
- alcohol
- B12, thiamine, Wilson’s
- inflammatory - MS
- paraneoplastic
- degeneratie (SCA)
Causes of high AG metabolic acidosis
L - lactic acidosis (metformin, severe shock)
U - Uremia
K - ketoacidosis (DKA, alcoholism, starvation)
E - exogenous (salicylate, ethylene glycol, methanol, paraldehyde)
(Also includes CO, theophylline, cyanide)
Causes of hyperCa
High PTH
- 1’ hyperPTH
- 3’ hyperPTH
- consider Lithium and exclude FHH
Suppressed PTH
- Myeloma
- Malignancy - humoral hyperCa of malignancy, bone mets, ectopic vitamin D / PTH production
- Dehydration
- Drugs - Teriparatide, Thiazide
- Granulomatous disease (ectopic vitamin D)
Causes of hypoCa
- Drugs - bisphosphonates, denosumab, cinacalcet
- HypoPTH - post-op, hypoMg, congenital (ADH, autoimmune polyglandular type 1 (APECED), DiGeorge)
- Low vit D / active vit D (2’ hyperPTH)
(inadequate diet intake and sunlight exposure, liver disease, antiepileptics (25-OHD), low 1a-OHD - CKD, FGF23, hypoPTH and VDDR, end-organ resistance to vit D (VDDR2)) - Pancreatitis (saponification of Ca salts by FFA), tumor lysis (sequestered by PO4)
- Malabsorption syndromes (eg IBD)
- PseudohypoPTH
Causes of hypoK
1) Transcellular Shift
- insulin, thyrotoxicosis, refeeding
2) non-renal loss
- diarrhoea (acidosis) and vomiting (alkalosis)
- TTKG <3
3) Renal loss
- Acidosis - Type 1/2 RTA
- Normotensive - Barter, Gitelman
- drugs - steroids, liquorice, diuretics
- hypoMg
- Primary aldosteronism
- 2’ aldo
RAS, renin secreting tumor
Malignant HT, CHF (renal ischemia) - Suppressed aldo axis
Fluid overload
Causes of hypoMg
GI loss (renal FEMg <2.5%)
- PPI
- diarrhoea, malabsorption
Renal wasting
- loop diuretics and thiazide
- alcoholism
- uncontrolled DM
- other drugs - digoxin, amioglycosides, cisplatin
Causes of hypopit
- Pituitary adenoma with mass effect / Tx (TSS / RT)
- Other tumors with mass effect: RCC, craniopharyngioma, lymphoma, germ cell, metastases
- Hx of trauma / surgery / RT
- Vascular: apoplexy, sheehan (pituitary infarction after postpartum hemorrhage)
- Inflammatory: hypophysitis, sarcoidosis, histiocytosis, hemochromatosis
- Rare infections incl bacterial / TB / fungal
Causes of hypoPO4
1) Transcellular shift - refeeding, resp alkalosis, insulin
2) Non-renal cause
- malabsorption
- vitamin D deficiency
- alcoholism
3) Renal loss (high FEPO4, low TMP/GFR)
- FGF23 mediated - TIO, iv iron, congenital (XLHR)
- non-FGF23 mediated - 1’ hyperPTH, Fanconi, HHRH
Causes of Pericarditis and Pericardial effusion
Pericarditis
- Infection - Cox, adenovirus
- TB, fungal
- uremia
- SLE
- isoniazid, hydralazine
- Dressler
Pericardial effusion
- Pericarditis - Cox, adenovirus, TB, fungal, uremia, SLE
- Malignancy
- Hypothyroid
Myocarditis
- Cox, adenovirus, flu
- bacterial - mycoplasma, leptospira, rickettsia
- SLE, Kawasaki
- eosinophilic myocarditis
- clozapine, amphetamine
Causes of proteinuria and Ix
- Transient (eg orthostatic, exercise)
- UTI
- Secondary to DM, SLE
- Nephritic picture - IgA nephropathy, HSP, membranoproliferative, post-strep GN; ANCA, anti-GBM; SLE
- Nephrotic picture - Minimal change, membranous, focal segmental glomerulosclerosis; DM, SLE
Nephrotic:
- ANA dsDNA ENA C3 C4
- A1C
- HBsAg, anti-HCV (membranous)
- malignancy screen
Nephritic
- Similarly screen SLE
- ANCA anti-GBM
- hepatitis and cyroglobulin (membranoproliferative)
- ASOT
- Ig pattern (IgA)
24h urine protein
urine multistix, c/st, cast, dysmorphic cells
KUB for stones
USG and renal Bx
Cholinergic crisis
Agents
- insecticide (organophosphate)
- AChE inhibitors - Aricept (Donepezil), Rivastigmine patch, Pyridostigmine in MG
Presentation
- water from orifices - sweating, tearing, rhinorrhoea, salivation, urination, diarrhea, vomiting
- bradycardia, pinpoint pupils
- seizures and bronchoconstriction
Mx
- atropine to reverse toxicity
- consider pralidoxime to prevent aging of AChE
- consult Psy for suicide attempt (if appropriate)
Contraindications to lytics
[] Contraindications:
- Hx of ICH, malignant intracranial tumor, AVM / other structural lesion;
- active bleeding
- recent ischemic stroke / significant head trauma in 3m
- intracranial / spinal surgery in 2m
- aortic dissection (beware in inferior MI!)
[] Relative contraindications:
- uncontrolled hypertension
- other major surgery in 3 wks; recent internal bleeding in 2-4 wks; active PUD
- history of ischemic stroke >3m
- prolonged CPR >10min
- on oral anticoagulation (in the past 24h)
- pregnancy
Common organisms for IE and Abx regime
iv Ampicillin 2g Q4H + Gentamicin 1mg/kg Q8H as initial antibiotic regime
- covers HACEK (Hemophilus and 4 other bacteria), viridans Strep, Strep bovis, MSSA and other enterococci
IVDA
- Staph aureus, may be MSSA or MRSA
- iv ampicillin for MSSA
- iv vancomycin 15-20mg/kg/dose
Prosthetic valves
- also likely to be MSSA or MRSA
- need consider adding Gentamicin and Rifampicin (900mg/day in 3 divided doses) as well
Common parki meds and their SE
1) L-dopa
- N/V, constipation if taken before meals
- postural hypotension
- on-off phenomenon
- long-term dyskinesia
2) Peripheral decarboxylase inhibitors
- eg Carbidopa
- add on to L-dopa (included in Sinemet)
3) Dopamine agonists
- non-ergot - ropinirole, rotigotine; ergot - Bct
- N/V, constipation, postural hypotension
- pathological gambling
4) MAO-Bi
- eg Selegiline, rasagiline
- neuroprotective effect in younger patients
- SE insomnia; risk serotonin syndrome
Other meds
- anticholinergics (eg benzhexol) for rest tremor
- Amantadine (NMDA receptor (antagonist) for L dopa dyskinesia
Complete heart block - how to calculate ventricular rate & how to manage
HR = 300 / number of big squrares
or number of QRS x6
Causes
- beta-blockers, digoxin
- hypothyroid, HyperK
- MI
- injury during cardiac surgery
Management
- stabilize patient
- atropine 0.6mg x1, repeat in 3-5min if necessary
- consider dopamine infusion
- transcutaneous / transvenous pacing
PPM indications
- sinus node dysfunction with bradycardia symptoms, or symptomatic chronotropic incompetence
- CHB, advanced 2’ AVB (2+ consecutive p waves), mobitz type 2
- symptomatic mobitz type 1
- exercise-induced 2’ or 3’ heart block
- consider if trifascicular block with syncope
- consider CRT if wide QRS and poor LVEF
Criteria for IE diagnosis
Duke’s criteria
Major criteria include
- 2x blood culture with typical organism (includes HACEK, Staph aureus, Viridans Strep, Strep bovis, or other enterococci)
- Persistently +ve blood cultures drawn more than 12h apart
- Single +ve culture for Coxiella burnetii
- Positive echo for IE
- Oscillating mass suggestive of vegetation, without other explanation
- Abscess
- New dehiscence of prosthetic valve
- New valvular regurgitation
Minor criteria include
- fever
- predisposing condition (heart condition, IVDA)
- vascular phenomena - janeway lesions, septic emboli (eg pulmonary infarct, mycotic aneurysm)
- immunologic phenomena - osler’s nodes, roth spots, GN, RF
- +ve blood culture but not fit major criteria
Crohn’s disease features, measurement of severity and management
Cobblestone mucosa, deep linear ulcers, skip lesions, rectal sparing, fistulating disease
CDAI
- fever, general wellbeing
- abd pain, mass
- extracolonic - arthritis, uveitis, erythema nodosum
- anal complications - fistula and fissure
General management
- CRP, fecal calprotectin
- rule out infection (CDT, CMV, TB)
- calcium, ADEK vitamins, iron, B12
Management
- steroid to induce remission
- Thiopurines to maintain remission (eg AZA)
- may consider MTX
biologics
- anti-TNF - infliximab
- ustekinumab, vedolizumab, upadacitinib
CYP inducers and inhibitor
Inducers
- phenytoin, carbamazepine, oxcarbazepine, topiramate, phenobarbitone
- rifampin
- mitotane
- chronic alcoholism
Inhibitors
- clarithromycin, ketoconazole
- isoniazid
- verapamil and diltiazem
- Paxlovid
Diagnosis for Autoimmune neuro conditions
1) GBS
2) Miller Fisher
3) MS
4) NMOSD
5) MG
1) GBS
- LP cytoalbuminologic dissociation (high protein, normal WCC)
- anti-ganglioside Ab
- NCS slow conduction / neuropathy
2) MFS
- LP cystoalbuminologic dissociation
- anti-GQ1B
3) MS
- CSF oligoclonal band
- McDonald criteria - attacks disseminated in time and space
4) NMOSD
- anti-AQP4
- Wingerchuk criteria; not fulfill MS criteria
5) MG
- anti-AChR
- anti-MuSK, anti-LRP4
- Tensilon test (risk bradycardia / asystole) / ice pack test
-fatigability in repetitive nerve stimulation
Diagnosis of AS and Ax-SpA
Modified new york criteria
1) Sacroilitis grade 3-4, AND at least 1 of:
2) (i) LBP >3 months improving with exercise
(ii) Limitation of LS movement in sagittal & frontal planes
(iii) Limitation of chest expansion
Ax-SpA
- sacroilitis / HLA B27 +
- inflammatory back pain / arthritis / dactylitis / enthesitis / uveitis / psoriasis / IBD / FHx / elevated CRP / good response to NSAID
Diagnosis of DKA, difference from HHS and management
DKA:
- pH ≤7.30, HCO3 ≤15, AG >12
- presence of ketones (urine / beta-hydroxybutyrate)
- +/- RG >14
HHS
- POsm >320 (2xNa + glucose)
Management
- ICU care
- iv insulin (0.1U/kg/h)
- IVF with K+
- NaHCO3 50mmol if pH 6.9-7.0; 100 mmol if pH <6.9
- search for ppt (infection, MI)
- switch to sc insulin after resolution of ketoacidosis and patient can eat
NMS and Serotonin Syndrome - difference
NMS
- use of dopamine antagonists (eg antipsychotics such as olanzapine, risperidone) or withdrawal of dopamine agonists (eg Bct, L-dopa)
- 2 of: fever, rigidity, mental status change, dysautonomia
SS
- use of serotoninergic agents + 1 of:
i) spontaneous clonus
ii) inducible clonus / ocular clonus with agitation / diaphoresis
iii) ocular / inducible clonus with fever and hypertonia
iv) tremor and hyperreflexia
- other features also include agitation, confusion, tachycardia, tachypnea, dry mucous membranes, ataxia, autonomic dysfunction
- SSRI - citalopram, fluoxetine; sertraline
- SNRI - venlafaxine, duloxetine
- TCA - amitriptyline, imipramine
- MAOi - selegiline, rasagiline (MAOBi); other inhibitors incl methylene blue, linezolid
- Stimulants - Amphetamines, mirtazapine (remeron) (increase serotonin production)
- Others - Tramadol, fentanyl, codeine, dextromethorphan, trazodone, bupropion, ondansetron, Triptans, lamotrigine
Digoxin toxicity
Presentation, risk factors and Management
Presentation
- Digoxin use - reverse tick sign / scooped ST depression
- Digoxin toxicity - frequent PVC (most common) (including bigeminy), high grade AV block, bidirectional VT, AF with CHB / slow regular AF
- loss of appetite, N/V/D, blurred vision, halo, yellow-green discolouration
Risk factors - old age, renal impairment, hypoK
Management
- ABC, cardiac monitor, stop offending agent
- blood for digoxin level, RFT
- consider GL and activated charcoal (within 2h)
- Digifab (see below)
- HD may be necessary
- AVOID BB and TCP (may trigger more severe arrhythmias)
- atropine if bradycardia, lignocaine if tachycardia (0.5mg/kg iv push) and may consider MgSO4 (but most tachyarrhythmias are refractory to treatment if digifab is not given)
Digifab indications
- Digoxin level >10ng/mL, or injection >10mg
- hyperK >5
- brady/tachyarrhythmia not responsive to medical Tx
Pemphigus vs Pemphigoid
Pemphigus
- intra-epidermal lesions (more shallow)
- flaccid blisters
- more mucosal lesions
- associated with malignancy
- anti-desmoglein
- steroid + rituximab
Pemphigoid
- subepidermal lesions (deeper)
- tense blisters wtih urticarial plaques
- dermoepidermal junction Ig deposition
- can treat with super potent topical steroid (clobetasol propionate 0.05% cream)
- also consider systemic steroids, doxycycline, and other immunosuppressants
Pre-Tx and general management
- non-adhesive dressing
- fresh skin biopsy of lesion edge with immunofluorescence staining
- screening - G6PD, HBV / HCV, DM
CXR, Mantoux test / IGRA, TPMT / NUDT for AZA
Flaccid paraparesis causes
[] Myopathy (fasciculation, no sensory)
- myositis
- thyroid / cushing
- drug-induced (statin)
- congenital conditions
[] Neuropathy (sensory)
- DM, hypothyroid, uremia
- B12, B6
- drugs - isoniazid, platin chemo, alcohol, colchicine
- CMT
- vasculitis (eg SLE, PAN)
- paraproteinemia
- GBS (no sensory)
[] DDx - MG, MND
Four key elements of informed consent
- Competence (be aware of cognitive function and consciousness)
- Voluntariness (free will, independent decision making)
- Disclosure of information: pros and cons of choices including alternatives
- Understanding and acceptance of information and consequence
Assessing mental competence
1. Patient receive and understand information(s) – capable to comprehend.
2. Patient is asked to paraphrase – in order for the clinician to evaluate his/her understanding of the information, and correct any misconceptions.
3. Capable to analyse the decision(s) to make – seeing both sides of argument and appreciating consequence(s).
4. Patient make his/her own choice(s) with reasoning.
5. Patient has to express his decision(s) by means of communication understandable by others.
6. Capable to retain the information and decision, at least for a short period.
GCA diagnosis and management
GCA Diagnostic criteria
- age >50
- headache
- high ESR +/- CRP
- temporal artery abnormalities (tenderness to palpitation, decreased pulse amplitude, presence of nodules)
- biopsy suggestive of GCA
Other features
- jaw claudication, sudden visual disturbance (AION)
- unexplained fever, anemia, other constitutional symptoms
- associations with PMR (symmetrical aching of shoulders and proximal muscle with elevated CRP / ESR and normal CK)
Workup
- elevated ESR
- consult eye - AION
- CTB - no lesion
- consult NS - temporal artery bx
- USG doppler temporal artery - halo sign (ddx ANCA vasculitis / severe atherosclerosis)
- high res MRI of cranial arteries if USG inconclusive
Management:
- consider treatment with high dose steroid (prednisolone or iv MP) while awaiting temporal artery biopsy result
- MTX ay be used as adjunctive therapy for large vessel vasculitis
- may consider Tocilizumab in specific cases
- PMR also shows dramatic improvement with steroids
HBV post exposure prophylaxis
Source HBsAg +ve or unknown
Transmission risk 6-30%
- HCW vaccinated and anti-Hbs+ => no need Tx
- HCW vaccinated but known non-responder (anti-HBs<10) => HBIG within 24h and repeat within 1 month
HBV vaccine is offered if anti-Hbs -ve
FU check HBsAg + anti-HBc at 24 weeks post exposure
HCM features
- FHx (Autosomal dominant)
- PE: double apex, double carotid impulse, ESM over LLSB
- ECG: precordial leads LVH (V1+V5/6 >35mm) and deep Q over inf / lateral leads
- Echo: asymmetric septal hypertrophy, SAM of mitral valve, LVOT gradient >50 = serious (at rest or provoked)
- should also do holter to look for ventricular arrhythmias
HCM management
Adequate hydration
Avoid competitive sports
Avoid vasodilators (ACEi, nitrates)
Give beta-blockers / nondihydropyridine CCB
Avoid +ve inotropes (incl digoxin)
ICD if ventricular arrhythmias, or if massive LVH / unexplained LOC / apical aneurysm / EF <50% / FHx SCD
Surgical Tx (alcohol septal ablation / surgical myomectomy) if LVOT >50
Genetic counseling and family screening
HCV post-exposure management
no PEP available
check HCV RNA (not anti-HCV Ab) at 6-8 weeks, 24 weeks
transmission risk 2%
Headache ddx
- worst ever / thunderclap - SAH
- injury - SDH, artery dissection
- vision - GCA, PCOM aneurysm
- raised ICP (tumor)
- fever / meningitis
- chronic tension type headache, migraine, cluster headache, trigeminal headache
- Other areas - acute glaucoma, sinusitis, dental pain, cervical spondylosis
Hemolytic Anemia Causes
(high retic, high indirect bili / LDH / urate)
DAT -
- TTP / HUS / DIC picture (see Plt +/- clotting)
- Malaria
- Mechanical valves
- PNH
- G6PD deficiency
- Spherocytosis
- Methemoglobinemia
DAT +
- ABOi
- Warm AIHA (40% idiopathic)
Infection (EBV, HIV), Lymphoproliferative (CLL, lymphoma), Autoimmune (SLE), Drugs (quinine, penicillin)
- Cold agglutinin
Infection (Mycoplasma, HIV), Lymphoproliferative (CLL, lymphoma), Autoimmune less common (SLE)
Hemoptysis, massive hemoptysis causes and management
Causes
- malignancy
- TB
- pneumonia (eg Klebsiella, MRSA)
- bronchiectasis
- pulmonary embolism, pulmonary artery rupture
- vasculitis (eg Anti-GBM, ANCA associated)
Management
- Protect airway
- Correct coagulopathy
- Antibiotics & transamin
- Bronchoscopy
- Urgent bronchial arterial embolisation
(Risk: Spinal cord infarction )
- Surgical resection