Calcium Disturbance Flashcards
Normal range of Calicum
2.2-2.6
What are the causes of hypercalcaemia
PTH suppressed
- Malignancy
- Sarcoidosis
- vit D excess
- Thyrotoxicosis
- Thiazide diuretics
- Hypoadrenalism
- milk alkali syndrome (excess of Rennie sweet consumption)
PTH not suppressed
- Primary hyperparathyroidism (most common community cause of hyperCa)
- Familial hypocalciuric hypercalcaemia
What are the causes of primary hyperparathyroidism
Parathyroid adenoma (80%)
Parathyroid hyperplasia
Parathyroid carcinoma (0/%)
MEN1 (adenoma) MEN2 (hyperplasia)
Why might people with sarcoidosis get hypercalcaemia
1-alpha hydroxylase can be expressed unregulated in lung cells of sarcoid tissue → increases renal and intestinal abs. of Ca
What are the symptoms of hypercalcaemia
Polyuria/polydipsia (osmotic diuretic effect) + dehydration
Constipation (slows nerves/muscles)
Calcium >3.0mmol/L: Neuro - confusion/seizures/coma
Describe familial benign/hypocalciuric hypercalcaemia (FBH/FHH)
Mutation in CaSR which usually detects the level of Ca for the parathyroid gland
This increases the set point for PTH release → mild hypercalcaemia
Benign condition - do not form kidney stones + reduced urine calcium
Gland removal will not cure it - surgery not required
What are the causes of Hypercalcaemia of malignancy
- Humoral e.g. sq lung cancer releasing PTHrp → dissolves bone
- Bone mets e.g. breast cancer causing local bone osteolysis (most common)
- Haem. malignancy e.g. myeloma
How is hypercalcaemia managed
- Fluid resus (pt will be dehydrated)
- 0.9% saline 1L over the first 1-2 h
- re-measure → 4-6L over 24h - Bisphosphonates if the cause is known to be cancer
- Treat underlying cause e.g. surgery
How are causes of hypercalcaemia differentiated on investigation
Albumin raised → unlikely to be true hyperCa
Urea raised = dehydration
Urea normal = cuffed specimen
Albumin normal/low:
Phosphate low → primary or tertiary hyperparathyroidism
Phosphate high:
ALP raised: bone mets, thyrotoxicosis, sarcoidosis
ALP normal: myeloma, excess vit D, sarcoidosis, milk alkali syndrome
What are the causes of hypocalcaemia
PTH driven (low PTH)
Surgical e.g. post thyroidectomy
Auto-immune hypoparathyroidism
Congenital absence of parathyroids e.g. DiGeorge syndrome
Mg deficiency (PTH regulation)
non-PTH driven
vitamin D deficiency - dietary, malabsorption, lack of sunlight
CKD (1a-hydroxylase not produced → reduced Ca resorption → hypoCa → PTH stimulated → secondary hyperPTH → hyperCa → tertiary hyperPTH )
PTH resistance (pseudohypoparathyroidism)
What are the clinical features of hypocalcaemia
Neuro-muscular excitability
- Chvosteks sign (fascial nerve excitability, twitching of facial muscles in response to tapping over the facial nerve – 29% sensitive)
- Trousseaus sign (carpopedal spasm induced by pressure - latent tetany – 94% sensitive)
- Hyperreflexia
- Convulsions
- Laryngeal spasm → stridor
- Choked optic disk
- Prolonged QT
- Peri-oral paraesthesia
What is the management for hypocalcaemia
symptomatic, Ca <1.875 → 10% Calcium gluconate IV
Asymptomatic, mild → oral supplementation e.g. SandoCal
Low vit D → vit D supplementation with alfacalcidol (CKD) or vit D2/D3