PMID- 31618228 OWN - NLM STAT- MEDLINE DCOM- 20200316 LR - 20200316 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 14 IP - 10 DP - 2019 TI - Outcomes of acute coronary syndrome patients with concurrent extra-cardiac vascular disease in the era of transradial coronary intervention: A retrospective multicenter cohort study. PG - e0223215 LID - 10.1371/journal.pone.0223215 [doi] LID - e0223215 AB - BACKGROUND: Extra-cardiac vascular diseases (ECVDs), such as cerebrovascular disease (CVD) or peripheral arterial disease (PAD), are frequently observed among patients with acute coronary syndrome (ACS). However, it is not clear how these conditions affect patient outcomes in the era of transradial coronary intervention (TRI). METHODS AND RESULTS: Among 7,980 patients with ACS whose data were extracted from the multicenter Japanese percutaneous coronary intervention (PCI) registry between August 2008 and March 2017, 888 (11.1%) had one concurrent ECVD (either PAD [345 patients: 4.3%] or CVD [543 patients; 6.8%]), while 87 patients (1.1%) had both PAD and CVD. Overall, the presence of ECVD was associated with a higher risk of mortality (odds ratio [OR]: 1.728; 95% confidence interval [CI]: 1.183-2.524) and bleeding complications (OR: 1.430; 95% CI: 1.028-2.004). There was evidence of interaction between ECVD severity and procedural access site on bleeding complication on the additive scale (relative excess risk due to interaction: 0.669, 95% CI: -0.563-1.900) and on the multiplicative scale (OR: 2.105; 95% CI: 1.075-4.122). While the incidence of death among patients with ECVD remained constant during the study period, bleeding complications among patients with ECVD rapidly decreased from 2015 to 2017, in association with the increasing number of TRI. CONCLUSIONS: Overall, the presence of ECVD was a risk factor for adverse outcomes after PCI for ACS, both mortality and bleeding complications. In the most recent years, the incidence of bleeding complications among patients with ECVD decreased significantly coinciding with the rapid increase of TRI. FAU - Kodaira, Masaki AU - Kodaira M AUID- ORCID: 0000-0002-7293-617X AD - Department of Cardiology, Japanese Red Cross Ashikaga Hospital, Tochigi, Japan. FAU - Sawano, Mitsuaki AU - Sawano M AD - Department of Cardiology, Keio University School of Medicine, Tokyo, Japan. FAU - Kuno, Toshiki AU - Kuno T AD - Department of Cardiology, Japanese Red Cross Ashikaga Hospital, Tochigi, Japan. AD - Department of Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai Beth Israel, New York, New York, United States of America. FAU - Numasawa, Yohei AU - Numasawa Y AD - Department of Cardiology, Japanese Red Cross Ashikaga Hospital, Tochigi, Japan. FAU - Noma, Shigetaka AU - Noma S AD - Department of Cardiology, Saiseikai Utsunomiya Hospital, Tochigi, Japan. FAU - Suzuki, Masahiro AU - Suzuki M AD - Department of Cardiology, National Hospital Organization Saitama Hospital, Saitama, Japan. FAU - Imaeda, Shohei AU - Imaeda S AD - Department of Cardiology, Keio University School of Medicine, Tokyo, Japan. FAU - Ueda, Ikuko AU - Ueda I AD - Department of Cardiology, Keio University School of Medicine, Tokyo, Japan. FAU - Fukuda, Keiichi AU - Fukuda K AD - Department of Cardiology, Keio University School of Medicine, Tokyo, Japan. FAU - Kohsaka, Shun AU - Kohsaka S AD - Department of Cardiology, Keio University School of Medicine, Tokyo, Japan. LA - eng PT - Journal Article PT - Multicenter Study PT - Research Support, Non-U.S. Gov't DEP - 20191016 PL - United States TA - PLoS One JT - PloS one JID - 101285081 SB - IM MH - Acute Coronary Syndrome/complications/*surgery MH - Aged MH - Aged, 80 and over MH - Cerebrovascular Disorders/*complications/diagnosis MH - Female MH - Hospital Mortality MH - Humans MH - Incidence MH - Male MH - Middle Aged MH - Percutaneous Coronary Intervention/*adverse effects MH - Peripheral Vascular Diseases/*complications/diagnosis MH - Postoperative Hemorrhage/*epidemiology/etiology MH - Radial Artery/surgery MH - Registries MH - Retrospective Studies MH - Risk Factors MH - Severity of Illness Index MH - Treatment Outcome PMC - PMC6795465 COIS- Dr. Kohsaka has received grants from Bayer Yakuhin and Daiichi-Sankyo; has received lecture fees from Bayer Y.akuhin and Bristol-Myers Squibb. This does not alter our adherence to PLOS ONE policies on sharing data and materials. EDAT- 2019/10/17 06:00 MHDA- 2020/03/17 06:00 PMCR- 2019/10/16 CRDT- 2019/10/17 06:00 PHST- 2019/06/17 00:00 [received] PHST- 2019/09/16 00:00 [accepted] PHST- 2019/10/17 06:00 [entrez] PHST- 2019/10/17 06:00 [pubmed] PHST- 2020/03/17 06:00 [medline] PHST- 2019/10/16 00:00 [pmc-release] AID - PONE-D-19-17185 [pii] AID - 10.1371/journal.pone.0223215 [doi] PST - epublish SO - PLoS One. 2019 Oct 16;14(10):e0223215. doi: 10.1371/journal.pone.0223215. eCollection 2019.