
Detecting atrial fibrillation (AFib) following an ischemic stroke (IS) is important, but in patients who suffer IS without a history of AFib, the optimal duration of electrocardiographic monitoring is unknown.
In the recent PER DIEM randomized clinical trial, Dr. Derek V. Exner and colleagues randomized 300 patients who suffered IS without a history AFib to monitoring with an implantable loop recorder (ILR) for 12 months or an external wearable loop recorder (ELR) for 4 weeks. The primary endpoint was definite or highly probable AFib lasting two minutes or longer over the 12 months following randomization. In an intent-to-treat analysis, detection of AFib was significantly higher in the ILR group (23/150, 15.3%) than the ELR group (7/150, 4.7%). This translated to an absolute increase in AF detection events of 10.7% (95% CI, 4.0%-17.3%), meaning that for every 10 patients monitored with ILR versus ELR, 1 additional patient was diagnosed with AFib.
Roughly 795,000 Americans suffer a stroke each year, and 87% of strokes are ischemic.1 Approximately 15-30% of IS can be attributed to AFib, and patients who suffer an IS in the context of AFib have worse outcomes.2,3 Detection of AFib is important because treatment with anticoagulation may reduce the risk of recurrent stroke. Current AHA guidelines state that prolonged rhythm monitoring after a stroke is reasonable, but do not comment on whether longer monitoring is warranted.4 Prior work has demonstrated that longer monitoring detects more AFib, but this is the first randomized trial comparing ambulatory rhythm monitoring modalities and duration.5