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.
2 min synopsisUK scopeSources checked 27 Aug 2026Clinical review pending
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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.
Call the cardiac-arrest team, start high-quality CPR and attach a defibrillator.
Treat VF/pulseless VT with unsynchronised shocks under the 2025 RCUK ALS algorithm, resuming CPR immediately after each shock.
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.
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.