Endo Flashcards
Acromegaly comp
Comp - HTN, DM, Cardiomyopathy, colorectal Ca
Acromegaly Ix
Ix - GH fluctuate - not reliable
Raised Serum IGF-1 levels - also to monitor
GH not suppressed after OGTT
MRI - pit tumour
Acromegal Tx
Trans-sphenoidal surgery = 1st line
If inoperable-
Somatostatin analogues (octreotide)
DA agonist (bromocriptine)
lethargy, weakness, anorexia, nausea & vomiting, weight loss, pigmented palm creased
primary hypoaldosteronism (addisons)
hypotension, hyponat, hyperkal, metabolic acidosis
Addisons bloods
Ix for addisons
Short synACTHen test
Give 250ug ACTH IM - measure plasma cortisol 30 mins after
Normal response = increase of cortisol >500
If cortisol < 500 - adrenal insuff
Tx for addisons
Hydrocortisone + fludro
(sick day rules, double H)
Obesity, hypokalaemic metabolic alkalosis, imparied glucose tolerance
Cushings syndrome
Causes of cushing syndro
ACTH dep: #
Cushings disease = ACTH sec pituitart adenoma
Ectopic ACTH (SCLC)
ACTH indep:
steroids
Adrenal adenoma
Cushings Ix
Overnight low-dose dex suppression test for Dx
High dose Dex suppression test for differentiating - fails to suppress in cushings syndro (ectopic ACTH sec or other abn), suceeds to suppress in Cushings disease
- Cortisol up, ACTH up - Ectopic ACTH cushings syndro (SCLC)
- Cortisol up, ACTH down - cushions syndro due to other causes (adrenal adenoma)
- Cortisol down, ACTH down - cushings disease (pit adenoma)
Glucose tollerance interpretation
HbA1c >48 = DM,
41-47 = pre-D
Fasting BM
<6 = normal
6.1-7 = impaired fasting glucose
7+ = DM
Impaired glucose tolerance = OGTT > 7.8 but < 11.1
Tx for DKA
- IVF - 5-8L isotonic saline
- IV insulin inf at 0.1u/kg/hr
- Start 10% destrose “ 125ml/hr once BM < 14
Continue long acting insulin, stop short acting
DKA diagnostic and resolution criteria
Dx - Glucose > 11 / known DM, pH < 7.3, Bicarb < 15, Ket > 3
Resolution - pH > 7.3, ketones < 0.6, bicarb > 15
Tx for diabetic neuropathy
amitriptyline, duloxetine, gabapentin or pregabalin
Causes fo lower or higher than expected HbA1c
Lower:
Sickle-cell anaemia, GP6D deficiency, Hereditary spherocytosis, Haemodialysis
Higher:
Vitamin B12/folic acid deficiency, Iron-deficiency anaemia, Splenectomy
Tx for Graves disease
Propranolol helps with symptom control initially
CBZ = 1st line - start at 40 then gradually reduce
Radioiodine if resistant to anti-thyroid therapy
Causes of gynecomastia
Due to inc oestrogen:androgen ration
testicular failure, liver disease
Drugs;
Spironolactine, cimetidine, digoxin, finasteride, GnRH ago (gosrelin)
Causes of hypercalcaemia
Primary hyperparathy
Malig (myeloma, SQLC, bone mets)
Sarcoidosis
Vit D intox
Acromegaly
Thyrotoxicosis
Dehydration
Addisons
Thiazides
Dehydrated, altered consciousness + neurological deficits Raised serum osmo, Ketones <3,no sinificant acidosis
HHS
Hypergly >30
Tx - fluid rep, insulin
VTE prophylaxis (due to hyperviscosity)
Investigation and causes of hypogly
Check insulin and C peptide levels
High insulin, high C pep = exogenous insulin prod - insulinoma, excess sulphonylurea
High insulin, low C pep - excess insulin administration
Low insulin, low c pep - non insulin related cause - alcohol induced, sepsis, adrenal insuff, fasting
muscle twitching, perioral paraesthesia, long QT, depression
Hypocal
Trousseau’s sign: carpal spasm if inflated BP cuff on arm
Chvostek’s sign: tapping over parotid causes facial muscles to twitch
Causes of hypothyroidism
Hashimotos (AI) - most common cause in UK
Iodine def (most common cause worldwide)
DQT, post thyroidectomy
Lithium, CBZ, Amiodarone
Delayed puberty in boy, low sex hormones, low LH/FHS, cleft lip/palate, anosmia
Kallmans (hypogonadotropic hypogonadism)
X linked rec
Tx = testosterone supp
delayed puberty, lack of secondary sexual charachteristics, tall, small/firm testes, gynaecomastia
Kleinfelters (XXY)