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Back to the 16 September 2026 edition

Practice changer · 06 of 06

Routine CT coronary angiography after MI rule-out did not reduce later events

After ruling out MI, do not send intermediate-risk patients for routine CT coronary angiography; target testing to symptoms and optimise prevention.

Design
Multicentre randomised controlled trial
Population
3170 emergency department patients with MI ruled out and troponin >5 ng/L, UK
Primary outcome
Myocardial infarction or cardiac death
Effect
7.1% vs 7.3% at median 3 years, HR 0.95 (95% CI 0.73–1.23)

TARGET-CTCA enrolled 3170 patients at 14 UK emergency departments in whom myocardial infarction had been ruled out, but whose high-sensitivity troponin was above 5 ng/L, marking intermediate risk. They were randomised to outpatient CT coronary angiography-guided care or standard care. The primary outcome was myocardial infarction or cardiac death. It was published at the end of August 2026.

Almost all of the CT group (92%) had the scan. After a median of 3 years, the primary outcome occurred in 7.1% with CT-guided care and 7.3% with standard care (HR 0.95). Complications from CT were uncommon, at 0.4%.

This is a clear negative result from a large, well-conducted trial. Testing everyone with a low-positive troponin after MI rule-out found disease but did not prevent events. CT still has a role when symptoms suggest angina or the diagnosis is uncertain. As a reflex test for every intermediate-risk patient discharged from the emergency department, it does not pay off.

  • Do not order CT coronary angiography routinely after MI is ruled out
  • Base further testing on symptoms and clinical judgement, not troponin level alone
  • Start or optimise preventive therapy for patients with risk factors before discharge
  • Arrange follow-up for recurrent or typical symptoms

Why it matters

It removes the case for routine further imaging in patients whose troponin is low but detectable after MI rule-out.

The statistics, in plain English

HR 0.95 (95% CI 0.73–1.23) crosses 1, so no reduction in events was shown; the interval makes a large benefit unlikely. The trial reached its prespecified event count and nearly all patients received the allocated test, so this is a genuine negative, not an underpowered one.

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