PMID- 22534249 OWN - NLM STAT- MEDLINE DCOM- 20120904 LR - 20220409 IS - 1941-3084 (Electronic) IS - 1941-3149 (Print) IS - 1941-3084 (Linking) VI - 5 IP - 3 DP - 2012 Jun 1 TI - Meta-analysis of bleeding complications associated with cardiac rhythm device implantation. PG - 468-74 LID - 10.1161/CIRCEP.111.969105 [doi] AB - BACKGROUND: Many patients receiving cardiac rhythm devices have conditions requiring antiplatelet (AP) and/or anticoagulant (AC) therapy. Current guidelines recommend a heparin-bridging strategy (HBS) for anticoagulated patients with moderate/high risk for thrombosis. Several studies reported lower bleeding risk with continued oral anticoagulation rather than HBS. The best strategy for perioperative management of patients on AP therapy is less clear. The present study was designed as a meta-analysis of device implantation-associated bleeding complications using different AC/AP therapies. METHODS AND RESULTS: PubMed and Cochrane Database searches identified articles based on design, outcomes, and available data. Device recipients were grouped as follows: no therapy, aspirin only, AC held, AC continued, dual AP, and HBS. The primary outcome was defined as a bleeding complication including hematoma, transfusion, or prolonged hospital stay. Thirteen articles were identified for analysis including 5978 patients. The combined incidence of bleeding complications was 274 of 5978 (4.6%), ranging from 2.2% (no therapy) to 14.6% (HBS). The estimated odds of bleeding were increased by 8.3 (95% CI, 5.5-12.9) times in the HBS group, 5.0 (95% CI, 3.0-8.3) for dual AP therapy, 1.7 (95% CI, 1.0-3.1) for AC held, 1.6 (95% CI, 0.9-2.6) for AC continued, and 1.5 (95% CI, 0.9-2.3) for aspirin only relative to the no therapy group. HBS significantly increased bleeding events compared with holding or continuing AC. Continuing AC did not increase bleeding events compared with no therapy. CONCLUSIONS: Continuing AC appears safer than HBS for device implantation. Dual AP therapy but not continuing AC carries a significant risk of bleeding. FAU - Bernard, Michael L AU - Bernard ML AD - Division of Cardiology, Medical University of South Carolina, Charleston, SC 29425, USA. FAU - Shotwell, Matthew AU - Shotwell M FAU - Nietert, Paul J AU - Nietert PJ FAU - Gold, Michael R AU - Gold MR LA - eng GR - UL1 RR029882/RR/NCRR NIH HHS/United States GR - UL1RR029882/RR/NCRR NIH HHS/United States PT - Journal Article PT - Meta-Analysis PT - Research Support, N.I.H., Extramural PT - Review DEP - 20120424 PL - United States TA - Circ Arrhythm Electrophysiol JT - Circulation. Arrhythmia and electrophysiology JID - 101474365 RN - 0 (Anticoagulants) SB - IM MH - Anticoagulants/administration & dosage/*adverse effects MH - Arrhythmias, Cardiac/*therapy MH - *Defibrillators, Implantable MH - Hemorrhage/*chemically induced/epidemiology MH - Humans MH - *Pacemaker, Artificial MH - Practice Guidelines as Topic MH - Prevalence MH - Risk Factors MH - Thrombosis/prevention & control PMC - PMC3626087 MID - NIHMS385362 EDAT- 2012/04/27 06:00 MHDA- 2012/09/05 06:00 PMCR- 2013/06/01 CRDT- 2012/04/27 06:00 PHST- 2012/04/27 06:00 [entrez] PHST- 2012/04/27 06:00 [pubmed] PHST- 2012/09/05 06:00 [medline] PHST- 2013/06/01 00:00 [pmc-release] AID - CIRCEP.111.969105 [pii] AID - 10.1161/CIRCEP.111.969105 [doi] PST - ppublish SO - Circ Arrhythm Electrophysiol. 2012 Jun 1;5(3):468-74. doi: 10.1161/CIRCEP.111.969105. Epub 2012 Apr 24.