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Bare-metal Stents(BMS) Versus Drug-eluting Stents(DES) in Patients Who Underwent Periprocedural Blood Transfusion : A Nationwide Longitudinal Cohort Study
Retrospective cohort study of Korean National Healthcare Insurance Database. To investigate clinical outcomes of bare metal stents versus drug eluting stents in patients who underwent periprocedural red blood cell transfusion.
A Korean nationwide, multi-center, retrospective observational cohort study. The receipt of red blood cell transfusion is at high risk of cardiac events or death. But little is know regarding the comparative outcomes of BMS and DES implantation in patients who underwent periprocedural red blood cell transfusion. Longitudinal data is collected from administrative claims in the national health insurance services of Korea. All Korean data(N=500,591) undergoing PCI from 2006 to 2015 is extracted. BMS or DES Patients(N=28,322) who received periprocedural red blood cell transfusion is investigate. Clinical outcomes until December 31, 2017 is investigate. Primary endpoint is a time to the first major adverse clinical event(MACE) defined as a composite of all-cause death, revascularization, critically ill cardiovascular status, or stroke.
Age
All ages
Sex
ALL
Healthy Volunteers
No
Samsung Medical Center
Seoul, Gang nam-Gu, Ilwon-Dong, South Korea
Start Date
January 3, 2018
Primary Completion Date
November 30, 2018
Completion Date
November 30, 2018
Last Updated
December 27, 2018
28,322
ACTUAL participants
Stent, red blood cell transfusion
DEVICE
Lead Sponsor
Samsung Medical Center
NCT07001332
NCT06909565
Data Source & Attribution
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