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REASONING GP · Clinical algorithm · Quick reference
Hypocalcaemia in adults — triage and diagnostic approachCorrect for albumin, then decide urgency on symptoms and speed of fall. Vitamin D deficiency and post-surgical hypoparathyroidism are the common causes; check the magnesium, or replacement fails.
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| Trigger / red flag | Leading concern · destination | Do now · do not delay |
|---|---|---|
| Adjusted Ca²⁺ below 1.90 mmol/L, however well the patient seems; or any level with tetany, carpopedal spasm, seizure, laryngospasm, stridor, bronchospasm or confusion. | Severe symptomatic hypocalcaemia · needs IV calcium gluconate with monitoring Emergency admission now |
Oral calcium does not work fast enough here. Do an ECG and send it with the patient. Test and record Chvostek and Trousseau signs. Do not give IV calcium in the community unless trained and equipped with cardiac monitoring. Send the adjusted calcium with albumin, magnesium, phosphate and U&E. |
| Prolonged QT on ECG, arrhythmia, bradycardia, hypotension, new heart failure, or the patient takes digoxin or a QT-prolonging drug. | Ventricular arrhythmia · torsades de pointes Emergency admission now |
The prolonged QT is what makes hypocalcaemia lethal, and it is invisible without an ECG — do one in every symptomatic patient. Review QT-prolonging drugs (macrolides, quinolones, antipsychotics, citalopram, ondansetron). Hypocalcaemia reduces the effect of digoxin, so the dose may become excessive once calcium is corrected — flag it. |
| Within days to weeks of thyroid, parathyroid or radical neck surgery, with a falling calcium, new perioral or fingertip tingling, or cramps — including after a recent discharge. | Post-surgical hypoparathyroidism · hungry bone syndrome Emergency admission if symptomatic or below 1.90 Same-day assessment and surgical team contact |
The commonest cause of acute symptomatic hypocalcaemia, and the fall can be steep and early. Contact the operating team directly — they hold the calcium and alfacalcidol protocol. Do not start a supplement and review in a month. Perioral tingling after thyroidectomy is never "anxiety". |
| Acute precipitant: massive transfusion, acute pancreatitis, rhabdomyolysis, tumour lysis, severe sepsis, or a recent IV bisphosphonate or denosumab given without vitamin D repletion. | Acute chelation or sequestration · drug-induced severe hypocalcaemia Emergency admission now |
Denosumab and IV bisphosphonates cause severe, sometimes life-threatening hypocalcaemia when vitamin D is deficient or eGFR is low — correct vitamin D and check calcium before giving them, and again after (MHRA). In tumour lysis and rhabdomyolysis the phosphate is high and calcium must not be replaced casually. |
| Adjusted Ca²⁺ 1.90–2.09 mmol/L in an alert patient without tetany or a long QT. | Moderate hypocalcaemia — assessment today Same-day assessment, ECG and bloods |
Assess face to face: Chvostek and Trousseau signs, GCS, and an ECG for the QT. Send PTH with a paired calcium, magnesium, phosphate, vitamin D, U&E, albumin and ALP the same day. Start oral calcium if symptomatic, and repeat within 24–48 hours with a named person to check it. |
| Low magnesium, or a cause for it: proton pump inhibitor use, alcohol excess, diuretics, diarrhoea, malabsorption, refeeding, or a patient whose calcium fails to rise on adequate replacement. | Hypomagnesaemia blocking PTH secretion and action Same-day magnesium replacement and review of the cause |
Hypocalcaemia will not correct while the magnesium is low, because magnesium is required for PTH release and end-organ response — this is the single commonest reason replacement appears to fail. Replace magnesium first or alongside. Long-term PPI use is a frequent and reversible cause; review the indication. |
| Malabsorption or nutritional cause: coeliac disease, IBD, bariatric or bowel surgery, chronic pancreatitis, alcohol excess, eating disorder, housebound or covered-skin vitamin D deficiency; or a high PTH with low vitamin D. | Severe vitamin D deficiency · osteomalacia · malabsorption Urgent investigation; admission if severe or symptomatic |
Send coeliac serology, vitamin D, ALP, phosphate and PTH. A raised ALP with bone pain and proximal weakness suggests osteomalacia, which needs loading-dose vitamin D and follow-up, not a maintenance dose. Look for the malabsorption rather than treating the vitamin D level in isolation. |
| Hypocalcaemia with a cancer feature: unexplained bone pain, pathological fracture, weight loss, anaemia, unexplained renal impairment, a raised ALP, or hypocalcaemia during or after cancer treatment — particularly with a high phosphate or after denosumab. | Osteoblastic bone metastases · myeloma · tumour lysis Very urgent FBC, calcium, plasma viscosity/ESR and protein electrophoresis with Bence Jones protein — within 48 hours; urgent suspected-cancer referral if positive · NICE NG12 |
Hypocalcaemia is less often malignant than hypercalcaemia, but osteoblastic metastases (prostate, breast) and tumour lysis both consume calcium, and myeloma presents with bone pain, anaemia and renal impairment at any calcium level. NG12: in anyone 60 or over with a presentation consistent with possible myeloma, arrange a very urgent FBC, calcium, plasma viscosity or ESR and serum protein electrophoresis with urinary Bence Jones protein within 48 hours, and refer on the urgent suspected-cancer route if they suggest myeloma. Unexplained bone pain with a raised ALP also needs imaging. |
REASONING GP · Hypocalcaemia in adults — triage and diagnostic approach |
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| Vitamin D deficiency and malabsorption PTH high, vitamin D low | The commonest cause in the community: limited sun exposure, covered or darker skin, housebound or care-home residence, obesity, pregnancy, malabsorption (coeliac, IBD, bariatric surgery, pancreatitis), anticonvulsants. Phosphate low or normal; a raised ALP with bone pain and proximal weakness means osteomalacia. |
| Hypoparathyroidism PTH low or inappropriately normal | Post-surgical (thyroid, parathyroid, neck) is much the commonest, transient or permanent — check the operation date. Also autoimmune, infiltration, radiation, and magnesium-related, which is reversible. A low PTH with a high phosphate is the classic pattern; needs endocrine input. |
| Hypomagnesaemia | Blocks PTH secretion and its end-organ effect, so calcium will not correct until magnesium does — the commonest reason replacement fails. Causes: proton pump inhibitors (long-term and forgotten), alcohol, diuretics, diarrhoea, malabsorption, refeeding. Replace magnesium first or alongside. |
| CKD, drugs and acute precipitants | CKD — PTH high, phosphate high: reduced 1-alpha-hydroxylation with phosphate retention, managed with alfacalcidol or calcitriol, not plain colecalciferol alone which cannot be activated, alongside phosphate control under renal guidance (NG203). Drugs: denosumab and IV bisphosphonates — severe hypocalcaemia if vitamin D is deficient or eGFR low, so correct and check before giving (MHRA) · PPIs via magnesium · loop diuretics, foscarnet, phenytoin. Acute: massive transfusion (citrate), pancreatitis, rhabdomyolysis, tumour lysis, sepsis, hyperventilation. |
| Artefact, and what not to conclude | Artefact: a low albumin with a normal ionised calcium — no treatment · a contaminated or EDTA sample · respiratory alkalosis. Do not conclude: "vitamin D deficiency" without a PTH and magnesium · "post-surgical, settled" without a recheck · "anxiety" for tingling after neck surgery. |
| Confirm on the adjusted value, then send four tests and an ECG | Repeat the calcium with albumin, and send PTH with a paired calcium, magnesium, phosphate and vitamin D together — not sequentially over months. Add U&E, ALP, FBC, coeliac serology where indicated, and an ECG if there is any symptom. A low total with a low albumin and no symptoms needs no treatment. |
| Replace magnesium first, then the vitamin D | Magnesium first: if it is low, correct it before expecting any calcium response — oral for mild deficiency, IV via the acute route if severe — and review the cause, stopping or reducing the proton pump inhibitor where the indication no longer holds. Then the vitamin D: a loading regimen of colecalciferol (about 300,000 units total over 6–10 weeks in divided doses) then maintenance, per local formulary — a maintenance dose alone corrects deficiency too slowly. Add oral calcium if dietary intake is poor or symptoms are present. Recheck at 4–8 weeks and look for the malabsorption behind it. Before denosumab or an IV bisphosphonate, every time: check calcium and correct vitamin D before each dose and check calcium after, particularly where eGFR is reduced (MHRA) — never give the next dose with an uncorrected calcium. |
| Recheck and the escalation rule — write it down | Repeat adjusted calcium, magnesium and U&E at 1–2 weeks after starting replacement, then 4–8 weeks, then widening intervals. Write the triggers down: below 1.90, or any tetany, spasm, seizure, stridor or long QT → emergency admission; 1.90–2.09, or new symptoms → same-day assessment. |
| What not to do | Do not act on a total calcium with a low albumin, start calcium without checking magnesium and PTH, give plain colecalciferol alone in CKD (it cannot be activated), manage confirmed hypoparathyroidism in primary care, attribute post-thyroidectomy tingling to anxiety, or skip the ECG. |