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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.
RapidPCICABGrevascularisationSTEMIcoronary disease

Coronary revascularisation: PCI and CABG

Essential points for quick revision.

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Escalate

STEMI, refractory ischaemia, haemodynamic instability or cardiogenic shock requires immediate interventional-cardiology activation; do not delay transfer for non-essential testing.

Synopsis

Choose the urgent or elective revascularisation route, explain PCI versus CABG trade-offs and manage the immediate antithrombotic and follow-up priorities.

  • Primary PCI is the preferred STEMI reperfusion strategy when it can be delivered within the NICE time window; if it cannot, assess promptly for fibrinolysis and the pharmaco-invasive pathway.
  • For NSTEMI/unstable angina, the timing of angiography follows clinical instability and calculated risk; unstable patients need immediate invasive assessment.
  • In stable angina, revascularisation is primarily for symptoms not controlled by optimal medical therapy; prognostic benefit depends on anatomy and clinical context.

Key red flags

STEMI requiring reperfusion

Persistent ST elevation or equivalent with compatible acute ischaemia requires immediate PPCI network activation and a documented symptom/ECG timeline.

Investigation priorities

01
12-lead ECG and serial ECGsFirst step

Define acute ischaemic territory and detect dynamic change or post-procedure occlusion.

Management branches

First-lineSTEMI reperfusion

STEMI within the reperfusion window

  1. Activate the regional primary-PCI pathway immediately and give ACS antithrombotic treatment unless contraindicated.
  2. Offer coronary angiography with primary PCI when this can be delivered within 120 minutes of when fibrinolysis could have been given under NICE NG185.
Third-lineStable disease choice

Angina despite optimal medical therapy or prognostically important anatomy

Key medicines

AspirinFor long-term post-revascularisation prevention, typically 75 mg orally once daily after the acute loading dose.
TicagrelorACS: 180 mg oral loading dose then 90 mg twice daily, generally with low-dose aspirin, for the planned course up to 12 months unless adjusted.
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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