AI Article Synopsis

  • This study aimed to compare the outcomes of single chamber (SC) versus dual chamber (DC) implantable cardioverter-defibrillators (ICDs) in preventing sudden cardiac death, focusing on factors like mortality and complications.
  • The researchers analyzed data from eight studies involving 2,087 patients, finding no significant differences in mortality rates or inappropriate ICD therapies between SC and DC devices after an average follow-up of about 16 months.
  • The conclusion suggests that both types of ICDs perform similarly in terms of patient outcomes, but future research should explore long-term effects and specific patient groups to provide more insights.

Article Abstract

Aims: Implantable cardioverter-defibrillators (ICDs) are key in the prevention of sudden cardiac death, but outcomes may vary by type of device or programming [single chamber (SC) vs. dual chamber (DC)] in patients without a bradycardia pacing indication. We sought to meta-analyse patient outcomes of randomized trials of SC vs. DC devices or programming.

Methods And Results: We searched PubMed, Embase, Scopus, Web of Science, and Cochrane trials databases for relevant studies excluding those published before 2000, involving children, or not available in English. Endpoints included mortality, inappropriate ICD therapies, and implant complications. Endpoints with at least three reporting studies were meta-analysed. We identified eight studies meeting inclusion criteria representing 2087 patients with 16.1 months mean follow-up. Mean age was 62.7 years (SD 1.92); in six studies reporting sex, most patients were male (85%). Comparing patients with a SC or DC ICD or programming, we found similar rates of mortality [odds ratio (OR) 0.95, 95% confidence interval (CI) 0.54-1.68; P = 0.86] and inappropriate therapies (OR 1.46, 95% CI 0.97-2.19; P = 0.07) in five and six studies, respectively. In three studies of SC vs. DC ICDs (but not programming) rates of pneumothorax and lead dislodgement were not different (OR 2.12, 95% CI 0.18-24.72; P = 0.55 and OR 0.87, 95% CI 0.32-2.47; P = 0.83, respectively).

Conclusion: In this meta-analysis of randomized controlled trials comparing SC vs. DC ICD device or programming, there was no significant difference in inappropriate therapies, mortality, pneumothorax, or lead dislodgement. Future studies should compare these devices over longer follow-up and in specific patient populations.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182310PMC
http://dx.doi.org/10.1093/europace/euy183DOI Listing

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