TY - JOUR
T1 - Outcomes in women and minorities compared with white men 1 year after everolimus-eluting stent implantation
T2 - Insights and results from the PLATINUM diversity and PROMUS element plus post-approval study pooled analysis
AU - Batchelor, Wayne
AU - Kandzari, David E.
AU - Davis, Scott
AU - Tami, Luis
AU - Wang, John C.
AU - Othman, Islam
AU - Gigliotti, Osvaldo S.
AU - Haghighat, Amir
AU - Singh, Sarabjeet
AU - Lopez, Mario
AU - Giugliano, Gregory
AU - Horwitz, Phillip A.
AU - Chandrasekhar, Jaya
AU - Underwood, Paul
AU - Thompson, Craig A.
AU - Mehran, Roxana
N1 - Publisher Copyright:
© 2017 American Medical Association. All rights reserved.
PY - 2017/12
Y1 - 2017/12
N2 - IMPORTANCE There exist limited outcomes data for women and minorities after contemporary percutaneous coronary intervention (PCI). OBJECTIVE To examine 1-year outcomes in women and minorities vs white men after PCI with everolimus-eluting stents. DESIGN, SETTINGS, AND PARTICIPANTS The PLATINUM Diversity studywas a single-arm study enrolling women and minorities. Patient-level pooling with the PROMUS Element Plus Post-Approval Study was prespecified. Data on social determinants of health and language were collected in the PLATINUM Diversity cohort, which included 1501 patients at 52 US sites. The PROMUS Element Plus Post-Approval study enrolled 2681 patients at 52 US sites with some site overlap and included an 'all-comers' population. All patients were enrolled beginning in October 2014 and were followed for 12 months. Analyses began in August 2016. INTERVENTIONS Patients received 1 or more everolimus-eluting stent implantation. MAIN OUTCOMES AND MEASURES The primary end pointwas 1-year major adverse cardiac events (MACE), which included death/myocardial infarction (MI)/target vessel revascularization. Secondary ischemic end points were also evaluated. RESULTS The pooled study consisted of 4182 patients: 1635 white men (39.1%), 1863 women (white and minority) (44.5%), and 1059 minority patients (women and men) (25.3%). Women and minorities had a higher prevalence of diabetes, prior stroke, hypertension, renal disease, and congestive heart failure than white men but lower rates of multivessel disease, prior coronary artery bypass graft surgery, prior MI, and smoking. Unadjusted 1-year MACE rates (white men, 7.6%; women, 8.6%; minorities, 9.6%) were similar between groups with no significant differences after risk adjustment. The adjusted risk of death/MI was higher among women (odds ratio, 1.6; 95%CI, 1.1-2.4) and minorities (odds ratio, 1.9; 95%CI, 1.2-2.8) compared with white men and the adjusted risk of MI was higher in minorities (odds ratio, 2.6; 95%CI, 1.4-4.8). These differences were driven primarily by nonstent-related MIs. Within the PLATINUM Diversity cohort, the independent predictors of MACE were cardiogenic shock, renal disease, history of peripheral vascular disease, multivessel disease, widowhood, and lack of private insurance. CONCLUSIONS AND RELEVANCE After contemporary everolimus-eluting stent implantation, women and minorities experience a similar risk of 1-year MACE but a higher adjusted risk of recurrent ischemic events primarily because of nonstent-related MIs. Both clinical and angiographic factors and social determinants of health, including widowhood and insurance status, contribute to 1-year MACE among women and minorities.
AB - IMPORTANCE There exist limited outcomes data for women and minorities after contemporary percutaneous coronary intervention (PCI). OBJECTIVE To examine 1-year outcomes in women and minorities vs white men after PCI with everolimus-eluting stents. DESIGN, SETTINGS, AND PARTICIPANTS The PLATINUM Diversity studywas a single-arm study enrolling women and minorities. Patient-level pooling with the PROMUS Element Plus Post-Approval Study was prespecified. Data on social determinants of health and language were collected in the PLATINUM Diversity cohort, which included 1501 patients at 52 US sites. The PROMUS Element Plus Post-Approval study enrolled 2681 patients at 52 US sites with some site overlap and included an 'all-comers' population. All patients were enrolled beginning in October 2014 and were followed for 12 months. Analyses began in August 2016. INTERVENTIONS Patients received 1 or more everolimus-eluting stent implantation. MAIN OUTCOMES AND MEASURES The primary end pointwas 1-year major adverse cardiac events (MACE), which included death/myocardial infarction (MI)/target vessel revascularization. Secondary ischemic end points were also evaluated. RESULTS The pooled study consisted of 4182 patients: 1635 white men (39.1%), 1863 women (white and minority) (44.5%), and 1059 minority patients (women and men) (25.3%). Women and minorities had a higher prevalence of diabetes, prior stroke, hypertension, renal disease, and congestive heart failure than white men but lower rates of multivessel disease, prior coronary artery bypass graft surgery, prior MI, and smoking. Unadjusted 1-year MACE rates (white men, 7.6%; women, 8.6%; minorities, 9.6%) were similar between groups with no significant differences after risk adjustment. The adjusted risk of death/MI was higher among women (odds ratio, 1.6; 95%CI, 1.1-2.4) and minorities (odds ratio, 1.9; 95%CI, 1.2-2.8) compared with white men and the adjusted risk of MI was higher in minorities (odds ratio, 2.6; 95%CI, 1.4-4.8). These differences were driven primarily by nonstent-related MIs. Within the PLATINUM Diversity cohort, the independent predictors of MACE were cardiogenic shock, renal disease, history of peripheral vascular disease, multivessel disease, widowhood, and lack of private insurance. CONCLUSIONS AND RELEVANCE After contemporary everolimus-eluting stent implantation, women and minorities experience a similar risk of 1-year MACE but a higher adjusted risk of recurrent ischemic events primarily because of nonstent-related MIs. Both clinical and angiographic factors and social determinants of health, including widowhood and insurance status, contribute to 1-year MACE among women and minorities.
UR - http://www.scopus.com/inward/record.url?scp=85040021190&partnerID=8YFLogxK
U2 - 10.1001/jamacardio.2017.3802
DO - 10.1001/jamacardio.2017.3802
M3 - Article
C2 - 29049508
AN - SCOPUS:85040021190
SN - 2380-6583
VL - 2
SP - 1303
EP - 1313
JO - JAMA Cardiology
JF - JAMA Cardiology
IS - 12
ER -