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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.
RapidNIVBiPAPacute hypercapnic respiratory failureCOPDIPAPEPAPventilation

Non-invasive ventilation

Essential points for quick revision.

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Escalate

NIV must not delay intubation in a patient who cannot protect the airway, is peri-arrest, has severe worsening acidosis, uncontrolled vomiting, refractory hypoxaemia or haemodynamic instability. Call critical care early and document whether invasive ventilation is appropriate before the mask is applied.

Synopsis

Start, optimise and monitor acute NIV safely in patients with a reversible ventilatory failure, with a clear ceiling, failure criteria and route to invasive ventilation when needed.

  • For acute COPD, consider NIV when pH remains below 7.35 with PaCO2 above 6.5 kPa and tachypnoea after about 1 hour of optimal medical treatment.
  • NICE calls NIV the treatment of choice for persistent hypercapnic ventilatory failure during a COPD exacerbation despite optimal medical therapy.
  • Start acute NIV within 60 minutes of the qualifying blood-gas result and, for patients presenting with AHRF, within 120 minutes of hospital arrival where possible.

Key red flags

Evidence-based COPD indication

Persistent pH below 7.35 and PaCO2 above 6.5 kPa with tachypnoea after controlled oxygen, bronchodilators, steroids and cause treatment.

Investigation priorities

01
Pre-NIV ABGFirst step

Confirm acute hypercapnic failure and establish severity.

Management branches

PrepareOne-hour optimisation and decision

Suspected COPD-related acute hypercapnic respiratory failure.

  1. Give controlled oxygen to 88–92%, nebulised bronchodilators, systemic steroid and antibiotics when indicated; stop/reverse respiratory depressants and manage secretions.
  2. Obtain/repeat ABG after initial treatment. If pH remains below 7.35 with PaCO2 above 6.5 kPa and tachypnoea, decide on NIV promptly.

Key medicines

Salbutamol nebuliser2.5 mg nebulised, increasing to 5 mg in severe bronchospasm and repeating according to response; use compressed air to drive in hypercapnia risk while oxygen is delivered separately to target.
Ipratropium bromide nebuliser500 micrograms nebulised, commonly every 4–6 hours during a severe COPD exacerbation, alongside short-acting beta2 agonist.
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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