MRCP(UK) Part 1 flashcards
MRCP(UK) Part 1 · Build recall with a focused review session.
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- STEMI ECG criteria
- ST elevation of at least 1 mm in two contiguous limb leads, or at least 2 mm in leads V2-V3 in men, with reciprocal changes and a compatible clinical syndrome.
- Cardiac tamponade features
- Hypotension, raised jugular venous pressure and muffled heart sounds (Beck's triad), with pulsus paradoxus above 10 mmHg, electrical alternans on ECG and a large pericardial effusion.
- Severe aortic stenosis criteria
- Aortic valve area below 1.0 cm2, peak jet velocity of 4 m/s or more, or mean gradient of at least 40 mmHg; symptoms and left ventricular function determine timing of valve replacement.
- Light's criteria
- Pleural fluid is an exudate if the protein ratio to serum exceeds 0.5, the LDH ratio exceeds 0.6, or pleural LDH exceeds two-thirds of the serum upper limit of normal.
- CURB-65 score components
- Confusion, urea above 7 mmol/L, respiratory rate 30 or more, systolic blood pressure under 90 or diastolic 60 or less, and age 65 or over; each scores one point.
- Obstructive sleep apnoea diagnosis
- An apnoea-hypopnoea index of 5 or more per hour combined with typical symptoms, or an index of 15 or more alone, confirmed on a sleep study.
- Wilson disease findings
- Low caeruloplasmin, high urinary copper, Kayser-Fleischer rings, Coombs-negative haemolytic anaemia and neuropsychiatric features; ATP7B mutations cause impaired biliary copper excretion.
- Hepatitis B serology markers
- HBsAg indicates current infection, anti-HBs immunity, HBeAg high infectivity, and anti-HBc IgM acute or recent infection; anti-HBc IgG persists for life after exposure.
- Child-Pugh score components
- Bilirubin, albumin, INR, ascites and encephalopathy, each graded 1 to 3, giving class A (5-6), B (7-9) or C (10-15) with progressively worsening prognosis.
- Short Synacthen test interpretation
- Serum cortisol measured at 0, 30 and 60 minutes after 250 micrograms of tetracosactide; a peak below 500 nmol/L indicates adrenal insufficiency and requires confirmatory testing.
- Diagnostic criteria for diabetes
- HbA1c of 48 mmol/mol or more, fasting glucose 7.0 mmol/L or more, or two-hour glucose 11.1 mmol/L or more on OGTT; repeat to confirm unless symptoms are typical.
- SIADH diagnostic criteria
- Euvolaemic hyponatraemia with low plasma osmolality, inappropriately concentrated urine above 100 mOsm/kg, urine sodium above 30 mmol/L, and normal thyroid and adrenal function.
- KDIGO AKI definition
- Rise in creatinine of 26 micromol/L or more within 48 hours, or to 1.5 times baseline within 7 days, or urine output below 0.5 mL/kg/h for 6 hours.
- Treatment of hyperkalaemia
- Calcium gluconate for cardiac membrane stabilisation, insulin with dextrose and nebulised salbutamol to shift potassium intracellularly, then removal with dialysis or potassium binders.
- Nephrotic syndrome definition
- Proteinuria above 3.5 g per 24 hours with hypoalbuminaemia, oedema and hyperlipidaemia; causes include minimal change disease, membranous nephropathy and diabetic nephropathy.
- Albuminocytological dissociation
- Raised cerebrospinal fluid protein with a normal cell count, classically seen in Guillain-Barre syndrome and also in chronic inflammatory demyelinating polyneuropathy.
- McDonald criteria concept
- Diagnosis of multiple sclerosis requires demyelinating lesions disseminated in space and time, supported by MRI, cerebrospinal fluid oligoclonal bands and exclusion of alternative diagnoses.
- Wernicke encephalopathy triad
- Ophthalmoplegia or nystagmus, ataxia and confusion caused by thiamine deficiency; give parenteral thiamine immediately before glucose to prevent progression to Korsakoff syndrome.
- Gout crystal appearance
- Needle-shaped, negatively birefringent monosodium urate crystals under polarised light microscopy of joint aspirate; pseudogout crystals are rhomboid and positively birefringent.
- Antibodies in systemic sclerosis
- Anti-centromere antibodies associate with limited cutaneous disease and pulmonary hypertension; anti-topoisomerase (anti-Scl-70) antibodies associate with diffuse disease and interstitial lung disease.
- Giant cell arteritis features
- Age over 50, new headache, jaw claudication, scalp tenderness, visual loss and ESR usually above 50; give high-dose corticosteroids immediately before temporal artery biopsy.
- Findings in iron deficiency
- Low ferritin, low serum iron and raised total iron-binding capacity with microcytic hypochromic anaemia; ferritin is an acute phase reactant and may be normal during inflammation.
- Philadelphia chromosome
- Reciprocal translocation t(9;22) producing the BCR-ABL1 fusion tyrosine kinase, diagnostic of chronic myeloid leukaemia and treated with tyrosine kinase inhibitors such as imatinib.
- TTP pathophysiology
- Severe deficiency of ADAMTS13 causes platelet-rich microthrombi with microangiopathic haemolytic anaemia, thrombocytopenia, neurological and renal features; treat with urgent plasma exchange.
- Severe falciparum malaria treatment
- Intravenous artesunate is first line for severe disease, defined by impaired consciousness, acidosis, renal failure, pulmonary oedema or parasitaemia above 2 percent.
- Jarisch-Herxheimer reaction
- Fever, rigors and hypotension within hours of starting treatment for syphilis, caused by release of treponemal antigens; managed supportively without stopping penicillin.
- Cytochrome P450 inducers
- Rifampicin, carbamazepine, phenytoin, phenobarbital and St John's wort increase enzyme activity, lowering concentrations of warfarin, oral contraceptives and many other drugs.
- Zero-order drug kinetics
- Elimination at a constant rate independent of plasma concentration, so small dose increases cause large rises in level; phenytoin, ethanol and high-dose salicylates behave this way.
- Nikolsky sign
- Extension of blistering when lateral pressure is applied to skin, positive in pemphigus vulgaris and toxic epidermal necrolysis, indicating intraepidermal or full-thickness epidermal cleavage.
- Dermatitis herpetiformis
- Intensely itchy vesicles on extensor surfaces with granular IgA deposits in the dermal papillae; strongly associated with coeliac disease and responds to a gluten-free diet.
- Hypoactive delirium features
- Withdrawal, reduced movement and slowed speech that is easily mistaken for depression or dementia; occurs in older patients and carries a higher mortality than the hyperactive subtype.
- STOPP and START criteria
- Screening tools listing potentially inappropriate medicines to stop and beneficial medicines omitted, used to structure medication review in older adults and reduce adverse drug events.