Medicine Flashcards
Crohns vs UC?
Crohns: non-bloody diarrhoea, abdominal pain (often right-sided), weight loss, and extraintestinal manifestations like oral ulcers or skin lesions; pei-anal disease eg skin tags
UC: Tender LLQ, bloody diarrhoea, abdominal pain, and a feeling of incomplete evacuation after defecation (tenesmus), urgency.
In a patient on long term hydrocortisone and fludrocortisone who has N+V what should you do re their medications
A person with Addisons’ who vomits should take IM hydrocortisone until vomiting stops
Fludrocortisone is a mineralocorticoid that is used to manage Addison’s. However, it is extra glucocorticoid (hydrocortisone) that is required in this situation
What signs are associated with mitral stenosis?
malar flush on cheeks.
regular, low-volume pulse
mid-diastolic murmur loudest with the patient leaning to left-hand side.
Thinks ARMS - atrial regurg early murmur, followed by MS with mid murmur
WHat is the most common cause of inherited thrombophilia?
Activated protein C resistance (Factor V Leiden) is the most common inherited thrombophilia
At what ages and how often are FITs done as part of the colorectal screening programme?
Faecal immunochemical tests are sent every 2 years to all patients aged 60-74 years in England, 50-74 years in Scotland.
ACA vs MCA vs PCA stroke?
ACA:
contralateral sensory and motor loss
Lower> upper
MCA: (most common)
Contralateral sensory and motor loss
Upper> lower
aphasia
contralateral homonymous hemianopia
PCA:
Contralateral homonymous hemianopia with macular sparing
Visual agnosia (can’t recognise objects seen)
Webers syndrome vs posterior inferior cerebellar artery stroke vs anterior infectior cerebellar artery stroke vs basilar artery stroke vs lacunar stroke?
Webers:
Affects branches of PCA which supply midbrain
Ipsilateral CN III palsy
Contralateral weakness of upper and lower extremity
Posterior inferior cerebellar AKA wallenberg syndrome : Ipsilateral: facial pain and temperature loss
Contralateral: limb/torso pain and temperature loss
Ataxia, nystagmus
Anterior inferior cerebllar AKA lateral pontine syndrome: Symptoms are similar to Wallenberg’s (see above), but:
Ipsilateral: facial paralysis and deafness
Basilar artery: Locked in syndrome
Lacunar stroke: either isolated hemiparesis, hemisensory loss or hemiparesis with limb ataxia
common sites include the basal ganglia, thalamus and internal capsule
Management of ischaemic stroke?
A combination of thrombolysis AND thrombectomy is recommend for patients with an acute ischaemic stroke who present within 4.5 hours
aspirin 300mg orally or rectally should be given as soon as possible if a haemorrhagic stroke has been excluded
What signs are associated with aortic regurgitation?
early diastolic murmur: intensity of the murmur is increased by the handgrip manoeuvre
collapsing pulse
wide pulse pressure
Quincke’s sign (nailbed pulsation)
De Musset’s sign (head bobbing)
Management of suspected temporal arteritis with visual loss and without visual loss?
- Steroids: give urgent high dose steroids as soon as suspected, before biopsy.
If visual loss IV methylprednisolone is given prior to PO steroids as above.
there should be a dramatic response, if not the diagnosis should be reconsidered - urgent ophthalmology review
- bone protection with bisphosphonates due to high dose steroids
What skin changes do you get in dermatomyosis?
Get weakness + skin changes:
photosensitive
macular rash over back and shoulder
heliotrope rash in the periorbital region
Gottron’s papules - roughened red papules over extensor surfaces of fingers
‘mechanic’s hands’: extremely dry and scaly hands with linear ‘cracks’ on the palmar and lateral aspects of the fingers
nail fold capillary dilatation
What are the most common types of HPV? which types are linked to cervical cancer?
Most common: Types 6 and 11 are responsible for 90% of genital warts cases
Link to cancer: 16,18 & 33 predisposes to cervical cancer.
Cushings disease vs syndrome?
Cushing’s syndrome is a collection of signs and symptoms due to prolonged exposure to cortisol and Cushing’s disease is a specific type of Cushing’s syndrome characterised by increased ACTH production of because of a pituitary adenoma
What are all MI patients discharged on?
beta blocker
aspirin
ticagrelor / second line anti-platelet (DAPT - this is stopped at 12 months post MI
ACE inhibitor
statin
What is limited vs diffuse cutaneous systemic sclerosis?
Limited cutaneous systemic sclerosis
scleroderma affects face and distal limbs predominately
associated with anti-centromere antibodies
a subtype of limited systemic sclerosis is CREST syndrome: Calcinosis, Raynaud’s phenomenon, oEsophageal dysmotility, Sclerodactyly, Telangiectasia
Diffuse cutaneous systemic sclerosis
scleroderma affects trunk and proximal limbs predominately
associated with anti scl-70 antibodies
the most common cause of death is now respiratory involvement, which is seen in around 80%: interstitial lung disease (ILD) and pulmonary arterial hypertension (PAH)
other complications include renal disease and hypertension
poor prognosis
What is hyperaldosteronism
Primary hyperaldosteronism was previously thought to be most commonly caused by an adrenal adenoma, termed Conn’s syndrome. However, recent studies have shown that bilateral idiopathic adrenal hyperplasia is the most common cause. Differentiating between the two is important as this determines treatment.
Causes
bilateral idiopathic adrenal hyperplasia: the cause of around 60-70% of cases
adrenal adenoma: 20-30% of cases
unilateral hyperplasia
familial hyperaldosteronism
adrenal carcinoma
Features
hypertension, hypokalaemia, metabolic alkalosis
Investigations
plasma aldosterone/renin ratio -
should show high aldosterone levels alongside low renin levels (negative feedback due to sodium retention from aldosterone)
following this a high-resolution CT abdomen and adrenal vein sampling is used to differentiate between unilateral and bilateral sources of aldosterone excess
if the CT is normal adrenal venous sampling (AVS) can be used to distinguish between unilateral adenoma and bilateral hyperplasia
Management
adrenal adenoma: surgery (laparoscopic adrenalectomy)
bilateral adrenocortical hyperplasia: aldosterone antagonist e.g. spironolactone
What is Pagets disease of the bone? Sx? management and ix (and blds)?
Paget’s disease is a disease of osteoclasts -> increased + uncontrolled bone turnover.
Presentation: typically older male with bone pain and an isolated raised ALP, (e.g. pelvis, lumbar spine, femur), untreated features: Bowing of tibia, Bossing of skull
Investigations: Raised ALP, normal Ca and Phosphate.
x-rays- osteolysis in early disease → mixed lytic/sclerotic lesions later
skull x-ray: thickened vault, osteoporosis circumscripta
Management: only treat if sx/ fracture/ deformity.
bisphosphonate (either oral risedronate or IV zoledronate)
Management of UC flare? severe vs mild-mod
definition of severe UC: >6 bloody stools per day + features of systemic upset (pyrexia, tachycardia, anaemia, raised inflammatory markers)
In mild/moderate: topical (rectal) aminosalicylate. –> PO aminosalicylate (eg Sulfasalazine)–> steroid
Severe: hospital. IV steroids –> IV ciclosporin –> surgery
1st, 2nd line and 3rd line mx of HF?
1st - BB (carvedilol or bisoprolol) + ACE-i
2nd - spironolactone (also think of SGLT-2 inhib if diabetic) - in hfref
3rd- initiated by a specialist. Options include ivabradine, sacubitril-valsartan, hydralazine in combination with nitrate, digoxin and cardiac resynchronisation therapy
How often are women with HIV meant to have smears?
Annually
What is pyoderma gangrenosum?
Inflammatory, not infection. An uncommon cause of very painful skin ulceration.
Associated with IBD.
Starts as pustule then ulcerates
Treat with steroids
WHat is used for prevenetion of variceal high risk bleeds?
A non-cardioselective B-blocker (NSBB) is used for the prophylaxis of oesophageal bleeding eg carvedilol, propranolol