Fifteen-Year Nationwide Trend in Antiplatelet Treatment among Drug-Eluting Stent Recipients in Korea: Many Patients Receive Very Prolonged Dual-Antiplatelet Treatment, and Newer Drugs Are Replacing the Older Ones

Author:

Kim Sunwon1ORCID,Lee Jong-Seok1,Lee Jungkuk2ORCID,Kim Yong-Hyun1,Kim Jin-Seok1ORCID,Lim Sang-Yup1,Kim Seong Hwan1,Ahn Jeong-Cheon1,Song Woo-Hyuk1ORCID

Affiliation:

1. Cardiovascular Center, Korea University Ansan Hospital, Ansan-si 15355, Republic of Korea

2. Hanmi Pharmaceuticals, Songpa-gu, Seoul 05545, Republic of Korea

Abstract

Drug-eluting stent (DES) recipients require 6–12 months of dual antiplatelet treatment (DAPT) and long-term aspirin mono-antiplatelet treatment (MAPT). Given the diversity of contemporary antiplatelet agents, antiplatelet treatment (APT) selection is becoming more complicated. We evaluated 15-year APT trends based on nationwide prescription data of 79,654 patients who underwent percutaneous coronary intervention (PCI) using DESs from 2002 to 2018 in Korea. DAPT (80.7%) was the most preferred initial APT post-PCI. Many DES recipients received prolonged DAPT (post-PCI 3 years: 41.0%; 10 years: 27.7%). There was a noticeable delay in DAPT-to-MAPT conversion from the mid to late 2000s (after the late-stent thrombosis concerns of first-generation DESs raised); the conversion after that was similar during the 2010s, occurring most robustly at 12–18 months post-PCI. Clopidogrel had long and increasingly been used for MAPT, surpassing aspirin. The recent increase in newer P2Y12 inhibitor prescriptions was noted. The patients treated with newer P2Y12 inhibitors were more likely younger men and presented with acute myocardial infarction. Real-world APT is evolving, and guideline–practice gaps exist. Further studies exploring the impact of diverse APT strategies on patient outcomes are expected to provide insights into optimal APT that can sophisticatedly balance the ischemic and bleeding risks.

Funder

the National Research Foundation

Korea University Research Fund

Publisher

MDPI AG

Subject

General Medicine

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