Parameter | Mean | Source |
Mortality | ||
Monthly probability for general population | Age and sex-specific | US Centers for Disease Control16 |
HR for cardiac vs no syncope | 2.01 | Soteriades et al 20022 |
HR for vasovagal vs no syncope | 1.08 | Soteriades et al 20022 |
Cardiac cause of syncope | ||
Proportion of unexplained syncope patients with arrhythmia | 60.4% | Solbiati et al, 201718; meta-analysis of 4381 patients |
Proportion of arrhythmia patients with bradycardia* | 68.7% | |
Proportion of arrhythmia patients with ventricular tachycardia and ventricular fibrillation* | 10.2% | |
Proportion of arrhythmia patients with supraventricular tachycardia or atrial fibrillation* | 21.1% | |
Syncope recurrence | ||
Monthly probability of syncope recurrence | 5.1% | EaSyAS15; monthly risk corresponding to event rate of 0.6 events/year |
Injury due to syncope | ||
Probability of major injury per syncope event | 4.8% | Bartoletti et al, 200819 |
Probability of minor injury per syncope event | 24.7% | Bartoletti et al, 200819 |
Probability of ECG capture | ||
Conventional testing | 18.9% | Farwell et al, 200643 |
Reveal LINQ ICM | Month 0=70% Month 1=82% Month 2=78% Month 3=87% Month 4=90% Month 5 onward=97% | Musat et al, 201744 |
Battery life | ||
Reveal LINQ ICM | 3.0 years | |
Adverse events | ||
Risk of AE requiring ICM explant | First cycle=0.00734 Subsequent cycles=0 | Pooled data from LINQ ICM usability and registry studies |
Probability of ICM removal (explant) | ||
Probability of removal on diagnosis of arrhythmic syncope | 80% | Assumption |
Probability of removal on diagnosis of non-arrhythmic syncope | 100% | Assumption |
*See online supplemental files for a breakdown of how these probabilities were calculated.
AE, adverse event; EaSyAS, Eastbourne Syncope Assessment Study; ECG, electrocardiogram; HR, hazard ratio; ICM, insertable cardiac monitor; US, United States.