TY - JOUR
T1 - The Impact of Peripheral Artery Disease in Chronic Total Occlusion Percutaneous Coronary Intervention (Insights From PROGRESS-CTO Registry)
AU - Xenogiannis, Iosif
AU - Gkargkoulas, Fotis
AU - Karmpaliotis, Dimitri
AU - Alaswad, Khaldoon
AU - Krestyaninov, Oleg
AU - Khelimskii, Dmitrii
AU - Choi, James W.
AU - Jaffer, Farouc A.
AU - Patel, Mitul
AU - Mahmud, Ehtisham
AU - Khatri, Jaikirshan J.
AU - Kandzari, David E.
AU - Doing, Anthony H.
AU - Dattilo, Phil
AU - Toma, Catalin
AU - Koutouzis, Michalis
AU - Tsiafoutis, Ioannis
AU - Uretsky, Barry
AU - Yeh, Robert W.
AU - Tamez, Hector
AU - Wyman, R. Michael
AU - Jefferson, Brian K.
AU - Patel, Taral
AU - Jaber, Wissam
AU - Samady, Habib
AU - Sheikh, Abdul M.
AU - Malik, Bilal A.
AU - Holper, Elizabeth
AU - Potluri, Srinivasa
AU - Moses, Jeffrey W.
AU - Lembo, Nicholas J.
AU - Parikh, Manish
AU - Kirtane, Ajay J.
AU - Ali, Ziad A.
AU - Hall, Allison B.
AU - Vemmou, Evangelia
AU - Nikolakopoulos, Ilias
AU - Dargham, Bassel Bou
AU - Rangan, Bavana Venkata
AU - Abdullah, Shuaib
AU - Garcia, Santiago
AU - Banerjee, Subhash
AU - Burke, M. Nicholas
AU - Brilakis, Emmanouil S.
N1 - Funding Information:
Study data were collected and managed using Research Electronic Data Capture (REDCap) electronic data capture tools hosted at the Minneapolis Heart Institute Foundation (MHIF), Minneapolis, Minnesota. REDCap is a secure, web-based application designed to support data capture for research studies, providing (1) an intuitive interface for validated data entry, (2) audit trails for tracking data manipulation and export procedures, (3) automated export procedures for seamless data downloads to common statistical packages, and (4) procedures for importing data from external sources. Declaration of Conflicting Interests The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: Dr. Karmpaliotis: speaker honoraria: Abbott Vascular, Boston Scientific, Medtronic, Vascular Solutions. Dr. Alaswaad: consulting fees from Terumo and Boston Scientific; consultant, no financial, Abbott Laboratories. Dr. Jaffer: consultant: Abbott Vascular, Boston Scientific and Siemens. Research grant: Canon, Siemens and National Institutes of Health. Dr. M. Patel: speakers’ bureau for Astra Zeneca. Dr. Mahmud: consulting fees from Medtronic and Corindus; speaker’s fees from Medtronic, Corindus, and Abbott Vascular; educational program fees from Abbott Vascular; and clinical events committee fees from St. Jude. Dr. Khatri: Asahi Intecc. Speaker/Proctor: Abbott Vascular. Dr. Kandzari: research grant: Boston Scientific and Medtronic Cardiovascular, Abbott. Consultant/Advisory Board: Boston Scientific and Medtronic Cardiovascular. Dr. Yeh: career development award (1K23HL118138) from the National Heart, Lung, and Blood Institute. Dr. Wyman: Speaker’s bureau: Boston Scientific, Abbott Vascular, and Asahi. Honoraria: Boston Scientific, Abbott Vascular, and Asahi. Consultant/Advisory Board: Boston Scientific, Abbott Vascular, and Asahi. Dr. Jefferson: honoraria/consulting/speaking fees from Abbott, Boston Scientific, CSI, Medtronic. Dr. Moses: consultant to Boston Scientific and Abiomed. Dr. Lembo: speaker bureau: Medtronic. Consultant/Advisory Board: Abbott Vascular and Medtronic. Dr. Parikh: speaker bureau: Abbot Vascular, Medtronic, CSI, BSC, Trireme; advisory boards: Medtronic, Abbott Vascular, Philips. Dr. Kirtane: Institutional research grants to Columbia University from Boston Scientific, Medtronic, Abbott Vascular, Abiomed, St. Jude Medical, Vascular Dynamics, Glaxo SmithKline, and Eli Lilly. Dr. Ali: consultant fees/honoraria from St. Jude Medical, and AstraZeneca Pharmaceuticals; ownership interest/partnership/principal in Shockwave Medical and VitaBx Inc; and research grants from Medtronic and St. Jude Medical. Dr. Rangan: research grants from InfraReDx, Inc., and The Spectranetics Corporation. Dr. Garcia: consulting fees from Medtronic. Dr. Banerjee: research grants from Gilead and the Medicines Company; consultant/speaker honoraria from Covidien and Medtronic; ownership in MDCARE Global (spouse); intellectual property in HygeiaTel. Dr. Burke: consulting and speaker honoraria from Abbott Vascular and Boston Scientific. Dr. Brilakis: consulting/speaker honoraria from Abbott Vascular, American Heart Association (associate editor Circulation), Boston Scientific, Cardiovascular Innovations Foundation (Board of Directors), CSI, Elsevier, GE Healthcare, and Medtronic; research support from Siemens, Regeneron, and Osprey. Shareholder: MHI Ventures. Board of Trustees: Society of Cardiovascular Angiography and Interventions. Funding The author(s) disclosed receipt of the following financial support for the research and/or authorship of this article: The Progress CTO registry has received support from the Abbott Northwestern Hospital Foundation, Minneapolis, MN. ORCID iDs Iosif Xenogiannis https://orcid.org/0000-0002-5004-6635 Emmanouil S. Brilakis https://orcid.org/0000-0001-9416-9701
Publisher Copyright:
© The Author(s) 2019.
PY - 2020/3/1
Y1 - 2020/3/1
N2 - The impact of peripheral artery disease (PAD) in patients undergoing chronic total occlusion (CTO) percutaneous coronary intervention (PCI) has received limited study. We reviewed 3999 CTO PCIs performed in 3914 patients between 2012 and 2018 at 25 centers, 14% of whom had a history of PAD. We compared the clinical and angiographic characteristics and procedural outcomes of patients with versus without history of PAD. Patients with PAD were older (67 ± 9 vs 64 ± 10 years, P <.001) and had a higher prevalence of cardiovascular risk factors. They also had more complex lesions as illustrated by higher Japanese CTO score (2.7 ± 1.2 vs 2.4 ± 1.3, P <.001). In patients with PAD, the final crossing technique was less often antegrade wire escalation (40% vs 51%, P <.001) and more often the retrograde approach (23 vs 20%, P <.001) and antegrade dissection/reentry (20% vs 16%, P <.001). Technical success was similar between the 2 study groups (84% vs 87%, P =.127), but procedural success was lower for patients with PAD (81% vs 85%, P =.015). The incidence of in-hospital major adverse cardiac events was higher among patients with PAD (3% vs 2%, P =.046). In conclusion, patients with PAD undergoing CTO PCI have more comorbidities, more complex lesions, and lower procedural success.
AB - The impact of peripheral artery disease (PAD) in patients undergoing chronic total occlusion (CTO) percutaneous coronary intervention (PCI) has received limited study. We reviewed 3999 CTO PCIs performed in 3914 patients between 2012 and 2018 at 25 centers, 14% of whom had a history of PAD. We compared the clinical and angiographic characteristics and procedural outcomes of patients with versus without history of PAD. Patients with PAD were older (67 ± 9 vs 64 ± 10 years, P <.001) and had a higher prevalence of cardiovascular risk factors. They also had more complex lesions as illustrated by higher Japanese CTO score (2.7 ± 1.2 vs 2.4 ± 1.3, P <.001). In patients with PAD, the final crossing technique was less often antegrade wire escalation (40% vs 51%, P <.001) and more often the retrograde approach (23 vs 20%, P <.001) and antegrade dissection/reentry (20% vs 16%, P <.001). Technical success was similar between the 2 study groups (84% vs 87%, P =.127), but procedural success was lower for patients with PAD (81% vs 85%, P =.015). The incidence of in-hospital major adverse cardiac events was higher among patients with PAD (3% vs 2%, P =.046). In conclusion, patients with PAD undergoing CTO PCI have more comorbidities, more complex lesions, and lower procedural success.
KW - chronic total occlusion
KW - percutaneous coronary intervention
KW - peripheral artery disease
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U2 - 10.1177/0003319719895178
DO - 10.1177/0003319719895178
M3 - Article
C2 - 31845593
AN - SCOPUS:85077371805
SN - 0003-3197
VL - 71
SP - 274
EP - 280
JO - Angiology
JF - Angiology
IS - 3
ER -