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Subcutaneous versus transvenous implantable cardioverter defibrillator in hypertrophic cardiomyopathy: a systematic review and meta-analysis.
da Silva Menezes Júnior, Antônio; Oliveira, Izadora Caiado; de Sousa, André Maroccolo; Paro Piai, Ricardo Figueiredo; Oliveira, Vinícius Martins Rodrigues.
Affiliation
  • da Silva Menezes Júnior A; Department of Medicine, Federal University of Goiás, Goiânia, GO, Brazil.
  • Oliveira IC; Internal Medicine Department, Pontifical Catholic University of Goiás, Goiânia, GO, Brazil.
  • de Sousa AM; Department of Medicine, Federal University of Goiás, Goiânia, GO, Brazil.
  • Paro Piai RF; Department of Medicine, Federal University of Goiás, Goiânia, GO, Brazil.
  • Oliveira VMR; Department of Medicine, Federal University of Goiás, Goiânia, GO, Brazil.
Cardiovasc Diagn Ther ; 14(3): 318-327, 2024 Jun 30.
Article in En | MEDLINE | ID: mdl-38975009
ABSTRACT

Background:

A subcutaneous implantable cardioverter-defibrillator (S-ICD) is an alternative to a transvenous implantable cardio defibrillator (TV-ICD). An S-ICD reduces the risk of transvenous lead placement. However, further research is required to determine how S-ICDs affect patients with hypertrophic cardiomyopathy (HCM). In this study, we investigated the comparative efficacy and safety of S-ICDs versus TV-ICDs in HCM.

Methods:

On December 6th, 2023, we performed a comprehensive search of the PubMed, Embase, Scopus, and Cochrane databases to identify randomized clinical trials (RCTs) and observational studies comparing S-ICDs with TV-ICDs in HCM patients published from 2004 until 2023. No language restrictions were applied. The primary outcome was appropriate shocks (AS), with inappropriate shocks (IAS), and device-related complications considered as secondary outcomes. Odds ratios (ORs) and 95% confidence intervals (CIs) were pooled using a random effects model. The ROBINS-I tool was used to assess the risk of bias of the studies.

Results:

The search yielded 1,114 records. Seven studies comprising 4,347 HCM patients were included, of whom 3,325 (76.0%) had TV-ICDs, and 1,022 (22.6%) had S-ICDs. There were 2,564 males (58.9%). The age range was from 39.1 to 49.4 years. Compared with the TV-ICD group, the S-ICD cohort had a significantly lower incidence of device-related complications (OR 0.52; 95% CI 0.30-0.89; P=0.02; I2=4%). Contrastingly, there were no statistically significant differences in the occurrences of AS (OR 0.49; 95% CI 0.22-1.08; P=0.08; I2=75%) and IAS (OR 1.03; 95% CI 0.57-1.84; P=0.93; I2=65%) between the two device modalities. In the analysis of the overall risk of bias in the studies, we found 42% of them with several, 28% with moderate, and 14% with low risk of bias.

Conclusions:

In HCM patients, S-ICDs were associated with a lower incidence of device-associated problems than TV-ICDs. AS and IAS incidence rates were similar between groups. These findings may assist clinicians in determining the most suitable device for treating patients with HCM.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cardiovasc Diagn Ther Year: 2024 Document type: Article Affiliation country: Brazil

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cardiovasc Diagn Ther Year: 2024 Document type: Article Affiliation country: Brazil