Endocrine Flashcards
(43 cards)
Management of hypocalcaemia
Acute:
Calcium gluconate
Maintenance:
Calcitriol + calcium carbonate/citrate
Management of hyperkalaemia
Calcium gluconate
Sodium bicarbonate (used in metabolic acidosis)
Insulin + glucose (used in CKD)
Sodium/calcium polystyrene sulfonate (to remove from bowel lumen)
Management of hyperphosphataemia
Calcium carbonate
Management of hypercalcaemia
Sodium chloride (for rehydration)
Bisphosphonates
Prednisolone (in vitamin D toxicity)
Management of hypokalaemia
Oral potassium supplements
IV potassium chloride
Potassium-sparing diuretics – spironolactone, amiloride (for maintenance)
Management of hyponatraemia
Fluid restriction
Sodium chloride
Management of hypernatraemia
Oral fluid replacement
5% dextrose infusion
Management of Addisonian crisis
Hydrocortisone + IV fluids
What is Addison’s disease?
Primary adrenal insufficiency
What is Conn’s disease?
Primary hyperaldosteronism
Causes of Conn’s disease
Adrenal adenoma (80%)
Bilateral adrenal hyperplasia (10%)
Adrenal carcinoma
Unilateral adrenal hyperplasia
What is Cushing’s syndrome?
Hypercortisolism
Causes of Cushing’s syndrome
Iatrogenic
ACTH-secreting pituitary adenoma (Cushing’s disease)
Cortisol-secreting adrenal adenoma/hyperplasia/carcinoma
ACTH-secreting ectopic tumour (e.g. SCLC)
Signs of Cushing’s syndrome
CUSHINGOID: Cataracts Ulcers Skin – striae, thinning, bruising, acne Hirsutism, hypertrichosis, buffalo hump Increased blood pressure Necrosis Glucose intolerance Osteoporosis, central obesity Immunosuppression Different face (moon-like facies, plethora)
Dexamethasone suppression test
Low dose:
Suppression = normal
No suppression = Cushing’s syndrome
High dose:
Suppression = Cushing’s disease
No suppression = other cause
Causes of hypercalcaemia
Metabolic:
- Hyperparathyroidism (primary - parathyroid adenoma, secondary - response to hypercalcaemia in CKD)
- Vitamin D intoxication
- Hyperthyroidism
- Sarcoidosis
- Milk-alkali syndrome
Malignant:
- Breast cancer
- SCC of lung
- Multiple myeloma
- Bone metastases
Congenital:
-Familial hypocalciuric hypercalcaemia
Drugs:
- Lithium
- Thiazides
Clinical features of hypercalcaemia
- Stones - polyuria, polydipsia, nephrolithiasis
- Bones - bone pain, osteoporosis, arthritis
- Abdominal moans - constipation, N/V, peptic ulcers, abdominal pain, anorexia, pancreatitis
- Psychic groans - depression, lethargy, weakness, confusion, coma, impaired memory
Clinical features of hyperthyroidism
GTFO THYROIDISM:
- Goitre
- Tremor
- Fine, brittle hair
- Ophthalmoplegia - NO SPECS:
- No signs
- Only signs - lid lag, lid retraction
- Soft tissue - periorbital swelling, conjunctival infection, chemosis
- Proptosis
- Extraocular (diplopia)
- Corneal abrasions
- Sight loss
- Thirst
- Heart - tachycardia, AF, palpitations, hypertension
- Yawning (fatigue)
- Reduced weight with increased appetite
- Oligo/amenorrhoea
- Intolerance to heat
- Diarrhoea
- Irritability, restlessness
- Sweating
- Muscle weakness
Signs of thyroid malignancy on U/S
Hypoechogenicity Microcalcifications Increased vascular flow Irregular borders Absence of halo
Causes of hypocalcaemia
Metabolic:
- Vitamin D deficiency
- Hypoparathyroidism (iatrogenic, congenital, autoimmune, infiltrative)
- Hypomagnesaemia (malnutrition, PPI/thiazides/loop diuretics, alcohol, IBD, coeliac disease, DKA)
- Hypermagnesaemia (renal failure)
- Hyperphosphataemia (renal failure, hypoparathyroidism)
Systemic:
- Sepsis
- Burns
- Renal failure
- Acute pancreatitis
- Rhabdomyolysis
- Tumour lysis syndrome
- Hyperventilation
- Blood transfusions
Drugs:
- Bisphosphonates
- Calcitonin
Order of pituitary hormone loss
GH, LH, FSH, TSH, ACTH, prolactin
Myxoedema coma
- Decompensated hypothyroidism, usually in older women with long-standing, undiagnosed or undertreated hypothyroidism
- Precipitated by infection, cold, disease or drugs
- Causes altered mental state and hypothermia
- Treated with T3 and active warming
Stages of diabetic retinopathy
Early - microaneurysms, blot haemorrhages, hard exudates
Diabetic maculopathy - macular involvement
Background retinopathy - macular sparing
Pre-proliferative retinopathy - cotton-wool spots, venous loops and beading
Proliferative retinopathy - neovascularisation
Frequency of eye monitoring in DM
If normal - every 2 years
Identified retinopathy, long duration DM or high HbA1c - every year