Table 1

Characteristics of included studies

Trial name, published yearCRYSTAL AF, 20145PRE DIEM, 20216STROKE-AF, 20217
Population characteristicsPatients aged 40 years of age or older with cryptogenic stroke or TIAPatients aged 18 years or older with an arterial ischaemic strokePatients aged ≥60 years or aged 50 to 59 years with a stroke risk factor and stroke attributed to large- or small-vessel disease
Time from index stroke to enrollment≤90 days≤6 months≤10 days
Sample size (women, %)441 (37)300 (40)492 (38)
Mena age, years626467
CHA2DS2-VASC score, median (IQR)NA (CHADS2 score median: 3)4 (3–5)5 (4–6)
% of 24 hours Holter prior to enrolment7179NA
Duration of ILR12 months12 months12 months
Duration needed for qualified new-detected AFAF ≥2 minAF ≥2 minAF ≥2 min
Median (IQR) duration for the longest single episode of AF in the ILR, hours11.2 (0.7–19.6)NA1.5 (0.2–8.8)
Cardiac rhythm monitoring method in the control groupFollow-up visits scheduled at 1, 6 and 12 months and unscheduled visits in the event of symptom occurrenceConventional external loop recorder monitoring for 30 daysUsual care specific to each participating site.
  • AF, atrial fibrillation; CRYSTAL AF, the Cryptogenic Stroke and Underlying AF; ILR, implantable loop recorder; NA, not available; OAC, oral anticoagulant; PRE DIEM, the Post-Embolic Rhythm Detection with Implantable versus External Monitoring; STROKE-AF, the Stroke of Known Cause and Underlying Atrial Fibrillation; TIA, transient ischaemic attack.