Table 3.
Quality assessment criteria | Acceptable (*) | Kuroki et al. [15] | Cochet et al. [13] | Nakatani et al. [14] | Blockhause et al. [16] | Maurhofer et al. [16] |
---|---|---|---|---|---|---|
Selection | ||||||
Representativeness of the exposed cohort? | Truly or somewhat representative of the average patient referred for ablation | * | * | * | * | * |
Selection of the non-exposed cohort? | Drawn from the same community as the exposed cohort | * | * | * | * | * |
Ascertainment of exposure? | Secure record | * | * | * | * | * |
Demonstration that outcome of interest was not present at start of study? | Yes | * | * | * | * | * |
Comparability | ||||||
Study controls for antiarrhythmic drug use? | Yes | - | - | - | - | - |
Study controls for at least 3 additional factors? | Age, sex, HTN, HLD, DM, CAD, CVA/TIA | - | - | - | - | * |
Outcome | ||||||
Assessment of outcome? | Independent blind assessment or record linkage | - | - | - | - | - |
Was follow-up long enough for outcomes to occur? | Yes | - | * | * | * | * |
Adequacy of follow up of cohorts? | Complete follow up or subjects lost to follow up unlikely to introduce bias | * | * | * | * | * |
Overall quality score (maximum = 9) | 5 | 6 | 6 | 6 | 7 |
Abbreviations: AF, atrial fibrillation; CAD, coronary artery disease; CVA, cerebral vascular accident; DM, diabetes mellitus; HLD, hyperlipidemia; HTN, hypertension; TIA, transient ischemic attack