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Research · 03 of 05

Fourteen-day ECG monitoring after unexplained syncope did not reduce further syncope at a year

Do not order extended ECG monitoring routinely after unexplained syncope; target it at patients with features of an arrhythmic cause.

Design
Multicentre, open-label randomised trial
Population
2,234 adults with unexplained syncope after ED assessment, 45 UK hospitals
Primary outcome
Mean patient-reported syncope episodes at 1 year
Effect
1.37 vs 1.58; IRR 0.89 (95% CI 0.68 to 1.18)

ASPIRED, an open-label randomised trial in the New England Journal of Medicine (August 2026), enrolled 2,234 adults at 45 UK hospitals whose syncope remained unexplained after emergency department assessment. Half had a 14-day ambulatory ECG patch immediately; half had the usual local care.

The mean number of patient-reported syncope episodes at one year was 1.37 against 1.58 (incidence rate ratio 0.89, 95% CI 0.68 to 1.18). Adverse events were reported 49 times in the monitoring group against 8, with one serious event in each.

The primary outcome was recurrence, not diagnosis, and a monitor can find an arrhythmia without reducing episodes if most recurrences are reflex syncope. About 12% had no follow-up and were excluded from the primary analysis.

For most patients the history and ECG remain the investigation that matters; extended monitoring belongs to those with features suggesting an arrhythmic cause.

  • Take a careful history of the prodrome, posture and triggers — most syncope is reflex
  • Reserve extended ECG monitoring for red flags: exertional syncope, syncope while supine, palpitations first, or an abnormal ECG
  • Do not order routine 14-day monitoring for every unexplained faint
  • Tell patients that monitoring brought more minor adverse events than standard care

Why it matters

It questions the reflex to monitor everyone after an unexplained faint, a common and resource-heavy default.

Don't overread it

The trial measured recurrence, not diagnostic yield, and did not test targeted monitoring in high-risk patients.

The statistics, in plain English

An incidence rate ratio of 0.89 suggests 11% fewer episodes, but the interval from 0.68 to 1.18 includes no difference, and the large standard deviations mean a few patients with many episodes drove the averages.

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