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Enteral tube feeding

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Synopsis

Select enteral access appropriately, confirm tube position without unsafe shortcuts, prescribe feed and water coherently, and prevent aspiration, metabolic, mechanical and medication-related harm.

  • Use enteral feeding when oral intake is unsafe or inadequate but the gastrointestinal tract is sufficiently accessible and functional; the indication and intended duration determine access.
  • Nasogastric tubes generally suit short-term gastric feeding, post-pyloric tubes help selected gastric-intolerance or aspiration situations, and gastrostomy or jejunostomy may serve longer-term needs.
  • Before first use of a nasogastric tube, accept only aspirate pH within the endorsed safe range or an appropriately obtained and interpreted X-ray; never use whoosh, bubble, litmus or fluid appearance tests.

Key red flags

Acute cough, cyanosis, desaturation or respiratory distress during tube use requires immediate cessation, airway assessment and confirmation that feeding access has not entered or migrated toward the airway.

Investigation priorities

01
Nasogastric aspirate pHFirst stepFirst line

Provide the first-line endorsed initial placement check when aspirate is obtainable.

Management branches

STARTInitiating enteral support

Oral intake is unsafe or insufficient and enteral feeding offers a proportionate benefit.

  1. Confirm indication, expected duration, gastrointestinal function, refeeding risk, capacity and the agreed goals of treatment.
  2. Choose gastric or post-pyloric access with the nutrition, endoscopy, radiology or surgical team according to anatomy and aspiration factors.

Key medicines

Prescribed enteral feed formulaDeliver the dietitian-approved volume by the specified continuous, intermittent or bolus schedule, with staged introduction where tolerance or refeeding risk requires it.
Thiamine for high refeeding riskGive immediately before and during early feeding using the current NICE-aligned local regimen and an absorbable route.
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Sources and review status4 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