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Lactose intolerance and carbohydrate malabsorption

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Synopsis

Separate lactose malabsorption from clinical intolerance and milk allergy, recognise secondary mucosal disease, use breath testing or structured dietary challenge appropriately, and preserve calcium, vitamin D and dietary diversity.

  • Lactase non-persistence causes reduced lactose absorption, but symptoms depend on dose, meal context, transit, colonic adaptation and visceral sensitivity; malabsorption is not identical to intolerance.
  • Bloating, cramp, flatus and watery diarrhoea after lactose reflect osmotic retention and bacterial fermentation, not intestinal inflammation.
  • Cow's-milk protein allergy is an immune reaction with a different history; urticaria, wheeze, angioedema or anaphylaxis needs urgent allergy assessment.

Key red flags

Immediate milk allergy

Rapid hives, swelling, wheeze, vomiting, hypotension or collapse after milk protein is an immune emergency, not lactose intolerance.

Investigation priorities

01
Structured lactose exclusion and reintroductionFirst step

Change lactose exposure alone for a defined short period, record symptoms, then reintroduce a measured amount in a usual meal.

Management branches

TrialLikely lactose intolerance

Meal-linked symptoms occur without allergy or organic alarm features.

  1. Quantify lactose portions and associated foods, then reduce lactose alone for a short predefined interval while maintaining calcium-rich alternatives.
  2. Reintroduce a measured amount with food and record symptom threshold; use breath testing if the result remains unclear or major restriction is contemplated.

Key medicines

Lactase enzymeUse the product-specific oral dose with the first mouthful of a lactose-containing meal, adjusted to portion size and individual response.
Colecalciferol and calcium supplementationUse dietitian and BNF-guided supplementation only when dietary intake or measured vitamin D is inadequate, accounting for age, pregnancy, renal function and bone risk.
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Sources and review status5 sources · checked 27 Aug 2026 · clinical review pending
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom