Axillary vein puncture versus cephalic vein cutdown for cardiac implantable electronic device implantation: A meta‐analysis

Author:

Vetta Giampaolo1ORCID,Magnocavallo Michele2,Parlavecchio Antonio1,Caminiti Rodolfo1,Polselli Marco2,Sorgente Antonio3,Cauti Filippo Maria2,Crea Pasquale1,Pannone Luigi3,Marcon Lorenzo3,Savio Armando Lo1,Pistelli Lorenzo1,Vetta Francesco4,Chierchia Gian‐Battista3,Rossi Pietro2,Bianchi Stefano2,Natale Andrea5,de Asmundis Carlo3,Rocca Domenico G. Della53

Affiliation:

1. Cardiology Unit Department of Clinical and Experimental Medicine University of Messina Messina Italy

2. Cardiology Division Arrhythmology Unit S. Giovanni Calibita Hospital Isola Tiberina Rome Italy

3. Heart Rhythm Management Centre Postgraduate Program in Cardiac Electrophysiology and Pacing Universitair Ziekenhuis Brussel‐Vrije Universiteit Brussel European Reference Networks Guard‐Heart Brussels Belgium

4. Saint Camillus International University of Health Sciences Rome Italy

5. Texas Cardiac Arrhythmia Institute St. David's Medical Center Austin Texas USA

Abstract

AbstractIntroductionCephalic vein cutdown (CVC) and axillary vein puncture (AVP) are both recommended for transvenous implantation of leads for cardiac implantable electronic devices (CIEDs). Nonetheless, it is still debated which of the two techniques has a better safety and efficacy profile.MethodsWe systematically searched Medline, Embase, and Cochrane electronic databases up to September 5, 2022, for studies that evaluated the efficacy and safety of AVP and CVC reporting at least one clinical outcome of interest. The primary endpoints were acute procedural success and overall complications. The effect size was estimated using a random‐effect model as risk ratio (RR) and relative 95% confidence interval (CI).ResultsOverall, seven studies were included, which enrolled 1771 and 3067 transvenous leads (65.6% [n = 1162] males, average age 73.4 ± 14.3 years). Compared to CVC, AVP showed a significant increase in the primary endpoint (95.7 % vs. 76.1 %; RR: 1.24; 95% CI: 1.09–1.40; p = .001) (Figure 1). Total procedural time (mean difference [MD]: −8.25 min; 95% CI: −10.23 to −6.27; p < .0001; I2 = 0%) and venous access time (MD: −6.24 min; 95% CI: −7.01 to −5.47; p < .0001; I2 = 0%) were significantly shorter with AVP compared to CVC. No differences were found between AVP and CVC for incidence overall complications (RR: 0.56; 95% CI: 0.28–1.10; p = .09), pneumothorax (RR: 0.72; 95% CI: 0.13−4.0; p = .71), lead failure (RR: 0.58; 95% CI: 0.23–1.48; p = .26), pocket hematoma/bleeding (RR: 0.58; 95% CI: 0.15–2.23; p = .43), device infection (RR: 0.95; 95% CI: 0.14–6.60; p = .96) and fluoroscopy time (MD: −0.24 min; 95% CI: −0.75 to 0.28; p = .36).ConclusionOur meta‐analysis suggests that AVP may improve procedural success and reduce total procedural time and venous access time compared to CVC.

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine,General Medicine

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