endocrinology Flashcards
addisons disease mx in illness
double hydrocortisone dose and keep fludrocortisone the same
dequervains thyroidirtis iodine uptake scane
globally reduced
painful goitre
Men1 3 ps
men2a 2 ps
men 2b 1 p
parathyroid pituitary pancreas men 1 gene
parathyroid phaeo ret oncogene
phaeo
mx of DKA
fluid replacement: most patients with DKA are deplete around 5-8 litres. Isotonic saline is used initially. Please see an example fluid regime below.
insulin: an intravenous infusion should be started at 0.1 unit/kg/hour. Once blood glucose is < 15 mmol/l an infusion of 5% dextrose should be started
correction of hypokalaemia
long-acting insulin should be continued, short-acting insulin should be stopped
whipples triad of insulinom
Symptoms and signs of hypoglycemia
Plasma glucose < 2.5 mmol/L
Reversibility of symptoms on the administration of glucose
pioglitazone c/i
Pioglitazone can cause fluid retention and is therefore contraindicated in patients with heart failure.
and c/i in history of bladder cancer
drug causes of gynaecomastia
C: cirrhosis. O: obesity. D: digoxin. E: estrogen. S: spironolactone.
sick euthyroid syndrome
In sick euthyroid syndrome (now referred to as non-thyroidal illness) it is often said that everything (TSH, thyroxine and T3) is low. In the majority of cases however the TSH level is within the >normal range (inappropriately normal given the low thyroxine and T3).
waterhouse friderichsen syndrome
adrenal gland failure due to bleeding into the adrenal glands, commonly caused by severe bacterial infection. Typically, it is caused by Neisseria meningitidis
t1dm bm targets
Blood glucose targets
5-7 mmol/l on waking and
4-7 mmol/l before meals at other times of the day
when to give bisphosphonate in high calcium low bone density
ca above 3 iv bisphos
cause
neuropathy of nervous system
when to add drug 2 in t2dm mx
HbA1c more than 58 on metformin
thyroid storm
Precipitating events: thyroid or non-thyroidal surgery trauma infection acute iodine load e.g. CT contrast media
Clinical features include: fever > 38.5ºC tachycardia confusion and agitation nausea and vomiting hypertension heart failure abnormal liver function test - jaundice may be seen clinically
Management:
symptomatic treatment e.g. paracetamol
treatment of underlying precipitating event
beta-blockers: typically IV propranolol
anti-thyroid drugs: e.g. methimazole or propylthiouracil
Lugol’s iodine
dexamethasone - e.g. 4mg IV qds - blocks the conversion of T4 to T3
mody fx
MODY 3
60% of cases
due to a defect in the HNF-1 alpha gene
is associated with an increased risk of HCC
Features of MODY
typically develops in patients < 25 years
a family history of early onset diabetes is often present
ketosis is not a feature at presentation
patients with the most common form are very sensitive to sulfonylureas, insulin is not usually necessary
kallmans syndrome
secondary hypogonadism
characteristically suffer from anosmia and would not exhibit gynaecomastia.
criteria for glp-1 mimetic
BMI >= 35 kg/m² in people of European descent and there are problems associated with high weight, or
BMI < 35 kg/m² and insulin is unacceptable because of occupational implications or weight loss would benefit other comorbidities.