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RapidMLAMSRAFoundationspirometryFEV1FVCPEF

Spirometry, bronchodilator reversibility and peak flow

Essential points for quick revision.

Synopsis

Obtain and interpret quality-assured airflow measurements, distinguish obstruction from possible restriction, and use variability or reversibility as evidence without confusing a test result with a diagnosis.

  • Check identity, age, sex, height, indication, contraindications, current symptoms and recent bronchodilator use before testing.
  • FEV1 is the volume expired in the first second; FVC is the total forced expiratory volume; the FEV1/FVC ratio identifies airflow obstruction.
  • Interpret against appropriate reference values and the lower limit of normal where available; a fixed ratio below 0.70 supports COPD only in the right clinical context and can overdiagnose older adults.

Key red flags

Unsafe or invalid test setting

Acute cardiorespiratory instability, active significant haemoptysis, recent relevant thoracic/abdominal/eye surgery, untreated pneumothorax, severe infection-control risk or inability to follow instructions requires deferral or specialist assessment.

Investigation priorities

01
Pre-test clinical and medicine checkFirst step

Decide whether testing is safe and whether bronchodilator washout is appropriate.

Management branches

PatternFrom numbers to a physiological statement

Any acceptable spirometry result.

  1. 1. Confirm acceptability, repeatability, reference equation and whether result is pre- or post-bronchodilator.
  2. 2. Read FEV1/FVC first: below LLN indicates obstruction; then use FEV1 to describe impairment without equating it to symptom burden.

Key medicines

Salbutamol for bronchodilator reversibility testing400 micrograms inhaled through a spacer (typically 4 actuations of a 100 microgram metered-dose inhaler), then repeat spirometry after the protocol interval, commonly about 15 minutes.
Ipratropium as an alternative reversibility agent in specialist protocolsA common protocol uses 160 micrograms inhaled (for example 8 actuations of a 20 microgram inhaler) with repeat testing after about 30 minutes; follow the physiology laboratory protocol and product licence.
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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