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
For tachyarrhythmia with shock, severe hypotensive syncope, myocardial ischaemia, severe pulmonary oedema or immediately after ROSC, perform synchronised cardioversion. If the patient becomes pulseless, disable synchronisation and use the cardiac-arrest defibrillation pathway.
Synopsis
Deliver synchronised cardioversion safely, choose rhythm-specific energy and use emergency antiarrhythmics in their correct licensed or resuscitation context.
Synchronised cardioversion times the shock to the R wave to avoid energy delivery during ventricular repolarisation.
A conscious patient needs carefully titrated sedation or anaesthesia, but instability must not be allowed to worsen while waiting.
RCUK 2025 energies: AF at maximum defibrillator output; flutter/regular narrow tachycardia 70-120 J; VT with a pulse 120-150 J.
Key red flags
Unstable tachyarrhythmia
Shock, syncope with severe or ongoing hypotension, myocardial ischaemia, severe pulmonary oedema or immediately post-ROSC favours immediate electricity.
Investigation priorities
01
12-lead ECGFirst step
Define rhythm, regularity, QRS width, QT, pre-excitation and ischaemia.
Management branches
unstableImmediate synchronised cardioversion
A perfusing tachyarrhythmia causes a life-threatening adverse feature.
Call expert and anaesthetic help, perform ABCDE assessment, attach pads, monitor continuously and obtain IV access.
Sedate or anaesthetise a conscious patient with careful haemodynamic planning when feasible without dangerous delay.
narrowStable regular narrow tachycardia
QRS is under 120 ms, rhythm regular and no adverse feature is present.
Key medicines
AdenosineRCUK March 2026: 6 mg, then 12 mg, then 18 mg by very rapid IV bolus, each followed by a rapid flush. This algorithm-specific sequence differs from the cited product SmPC's licensed 3 mg, 6 mg, then 12 mg sequence.
Procainamide10-15 mg/kg IV over 20 minutes, maximum 1 g.
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.