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Rapidbroad-complex tachycardiaventricular tachycardiacardioversionprocainamideamiodaronetorsades

Broad-complex tachycardia

Essential points for quick revision.

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Escalate

Pulseless VT is a cardiac arrest requiring immediate defibrillation and ALS. With a pulse, shock, severe hypotensive syncope, myocardial ischaemia, pulmonary oedema or post-ROSC status requires synchronised cardioversion.

Synopsis

Treat broad-complex tachycardia safely as ventricular tachycardia unless a more secure diagnosis supports a specific alternative.

  • A tachycardia with QRS duration 120 ms or more is broad complex; sustained regular broad tachycardia should be treated as VT when uncertain.
  • Structural heart disease, previous myocardial infarction and older age increase the prior probability of VT.
  • AV dissociation, capture beats, fusion beats and precordial concordance strongly support VT, but their absence does not exclude it.

Key red flags

Irregular broad rhythm

Consider pre-excited AF, AF with bundle-branch block, frequent ventricular ectopy and polymorphic VT; inspect QT and beat-to-beat QRS morphology before giving drugs.

Investigation priorities

01
Continuous monitoring and 12-lead ECGFirst step

Define regularity, QRS morphology and adverse evolution while preserving a diagnostic tracing.

Management branches

pulselessPulseless broad tachycardia

No signs of life or definite pulse.

  1. Call the cardiac-arrest team, start high-quality CPR and attach a defibrillator.
  2. Treat VF/pulseless VT with unsynchronised shocks under the 2025 RCUK ALS algorithm, resuming CPR immediately after each shock.
stable-regularStable regular broad-complex tachycardia

A pulse is present and no life-threatening adverse feature is identified.

Key medicines

Procainamide10-15 mg/kg IV over 20 minutes, maximum 1 g.
AmiodaroneRCUK stable broad-tachycardia alternative: 300 mg IV over 10-60 minutes then 900 mg IV over 24 hours; after failed cardioversion in an unstable patient, 300 mg IV over 10-20 minutes before another shock.
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Sources and review status6 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