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Related Subjects: |Calcium Physiology |Calcitonin |Hypocalcaemia |Hypercalcaemia |Hypomagnesaemia |Hypermagnesaemia |Primary Hyperparathyroidism |Familial hypocalciuric hypercalcaemia (FHH) |Sarcoidosis
⚠️ Always check magnesium in hypocalcaemia. Hypomagnesaemia can both reduce PTH secretion and cause end-organ resistance to PTH, making hypocalcaemia refractory until Mg²⁺ is corrected.
| 🚨 Acute / Severe Hypocalcaemia: Initial Management
Always ask: Is the patient symptomatic? Are they on digoxin? Is magnesium low? |
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| Category | Adjusted Ca (mmol/L) |
|---|---|
| ✅ Normal | About 2.20–2.60 |
| ⬇️ Mild hypocalcaemia | 1.90–2.19 and asymptomatic |
| 🚨 Severe hypocalcaemia | <1.90 or symptomatic at any level below normal |
📌 Use adjusted calcium for routine interpretation, but consider ionised calcium in critical illness, major acid–base disturbance, or when albumin makes total calcium misleading.
| Cause | Typical Clues | Biochemistry Pattern | Management Principles |
|---|---|---|---|
| Hypoparathyroidism
(post-thyroid/parathyroid surgery, autoimmune, infiltrative) |
Perioral tingling, tetany, post-op neck surgery | Low Ca, low or inappropriately normal PTH, often high phosphate | Calcium ± alfacalcidol/calcitriol; treat acute episodes with IV calcium if severe |
| Vitamin D deficiency | Bone pain, proximal myopathy, osteomalacia/rickets risk | Low/low-normal Ca, low vitamin D, raised PTH, often low phosphate | Vitamin D replacement ± calcium |
| CKD / reduced 1α-hydroxylation | Renal disease, CKD-MBD features | Low Ca, high phosphate, raised PTH, reduced active vitamin D | Manage CKD-MBD, phosphate control, active vitamin D analogues, calcium as needed |
| Hypomagnesaemia | Alcohol excess, diarrhoea, PPIs, diuretics, aminoglycosides | Low Mg, low Ca, PTH low or inappropriately normal | Replace Mg first / alongside Ca |
| Acute pancreatitis | Severe epigastric pain, vomiting | Low Ca, raised amylase/lipase | Supportive pancreatitis care; calcium if severe/symptomatic |
| Pseudohypoparathyroidism | Possible Albright hereditary osteodystrophy phenotype | Low Ca, high PTH, high phosphate | Calcium + active vitamin D; endocrine follow-up |
| Drugs
(bisphosphonates, denosumab, cisplatin, foscarnet, anticonvulsants, cinacalcet) |
Temporal relationship to treatment | Variable, depending on mechanism | Stop/review culprit drug, replace calcium ± Mg/vitamin D |
| Sepsis / critical illness | Shock, organ dysfunction | Low Ca in context of severe illness | Treat underlying illness; reserve IV calcium for severe/symptomatic cases |
| Hungry bone syndrome | After parathyroid surgery, high bone turnover states | Marked/prolonged low Ca ± low Mg ± low phosphate | Aggressive calcium replacement + active vitamin D |
| Massive transfusion / citrate load | Major haemorrhage / blood product exposure | Low ionised calcium | Correct as part of major haemorrhage management |