TY - JOUR
T1 - Long-Term Outcomes in Women and Men Following Percutaneous Coronary Intervention
AU - Kosmidou, Ioanna
AU - Leon, Martin B.
AU - Zhang, Yiran
AU - Serruys, Patrick W.
AU - von Birgelen, Clemens
AU - Smits, Pieter C.
AU - Ben-Yehuda, Ori
AU - Redfors, Björn
AU - Madhavan, Mahesh V.
AU - Maehara, Akiko
AU - Mehran, Roxana
AU - Stone, Gregg W.
N1 - Publisher Copyright:
© 2020 American College of Cardiology Foundation
PY - 2020/4/14
Y1 - 2020/4/14
N2 - Background: Studies examining sex-related outcomes following percutaneous coronary intervention (PCI) have reported conflicting results. Objectives: The purpose of this study was to examine the sex-related risk of 5-year cardiovascular outcomes after PCI. Methods: The authors pooled patient-level data from 21 randomized PCI trials and assessed the association between sex and major adverse cardiac events (MACE) (cardiac death, myocardial infarction [MI], or ischemia-driven target lesion revascularization [ID-TLR]) as well as its individual components at 5 years. Results: Among 32,877 patients, 9,141 (27.8%) were women. Women were older and had higher body mass index, more frequent hypertension and diabetes, and less frequent history of surgical or percutaneous revascularization compared with men. By angiographic core laboratory analysis, lesions in women had smaller reference vessel diameter and shorter lesion length. At 5 years, women had a higher unadjusted rate of MACE (18.9% vs. 17.7%; p = 0.003), all-cause death (10.4% vs. 8.7%; p = 0.0008), cardiac death (4.9% vs. 4.0%; p = 0.003) and ID-TLR (10.9% vs. 10.2%; p = 0.02) compared with men. By multivariable analysis, female sex was an independent predictor of MACE (hazard ratio [HR:]: 1.14; 95% confidence interval [CI:]: 1.01 to 1.30; p = 0.04) and ID-TLR (HR: 1.23; 95% CI: 1.05 to 1.44; p = 0.009) but not all-cause death (HR: 0.91; 95% CI: 0.75 to 1.09; p = 0.30) or cardiac death (HR: 0.97; 95% CI: 0.73 to 1.29; p = 0.85). Conclusions: In the present large-scale, individual patient data pooled analysis of contemporary PCI trials, women had a higher risk of MACE and ID-TLR compared with men at 5 years following PCI.
AB - Background: Studies examining sex-related outcomes following percutaneous coronary intervention (PCI) have reported conflicting results. Objectives: The purpose of this study was to examine the sex-related risk of 5-year cardiovascular outcomes after PCI. Methods: The authors pooled patient-level data from 21 randomized PCI trials and assessed the association between sex and major adverse cardiac events (MACE) (cardiac death, myocardial infarction [MI], or ischemia-driven target lesion revascularization [ID-TLR]) as well as its individual components at 5 years. Results: Among 32,877 patients, 9,141 (27.8%) were women. Women were older and had higher body mass index, more frequent hypertension and diabetes, and less frequent history of surgical or percutaneous revascularization compared with men. By angiographic core laboratory analysis, lesions in women had smaller reference vessel diameter and shorter lesion length. At 5 years, women had a higher unadjusted rate of MACE (18.9% vs. 17.7%; p = 0.003), all-cause death (10.4% vs. 8.7%; p = 0.0008), cardiac death (4.9% vs. 4.0%; p = 0.003) and ID-TLR (10.9% vs. 10.2%; p = 0.02) compared with men. By multivariable analysis, female sex was an independent predictor of MACE (hazard ratio [HR:]: 1.14; 95% confidence interval [CI:]: 1.01 to 1.30; p = 0.04) and ID-TLR (HR: 1.23; 95% CI: 1.05 to 1.44; p = 0.009) but not all-cause death (HR: 0.91; 95% CI: 0.75 to 1.09; p = 0.30) or cardiac death (HR: 0.97; 95% CI: 0.73 to 1.29; p = 0.85). Conclusions: In the present large-scale, individual patient data pooled analysis of contemporary PCI trials, women had a higher risk of MACE and ID-TLR compared with men at 5 years following PCI.
KW - mortality
KW - outcomes
KW - percutaneous coronary intervention
KW - sex
UR - http://www.scopus.com/inward/record.url?scp=85082560279&partnerID=8YFLogxK
U2 - 10.1016/j.jacc.2020.01.056
DO - 10.1016/j.jacc.2020.01.056
M3 - Article
C2 - 32273029
AN - SCOPUS:85082560279
SN - 0735-1097
VL - 75
SP - 1631
EP - 1640
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 14
ER -