Different Statin Effects of ST-elevation Versus Non-ST-Elevation Acute Myocardial Infarction After Stent Implantation.


Journal

The American journal of the medical sciences
ISSN: 1538-2990
Titre abrégé: Am J Med Sci
Pays: United States
ID NLM: 0370506

Informations de publication

Date de publication:
03 2020
Historique:
received: 26 07 2019
revised: 02 12 2019
accepted: 05 12 2019
entrez: 25 2 2020
pubmed: 25 2 2020
medline: 1 5 2020
Statut: ppublish

Résumé

Intensive statin therapy reduces cardiovascular events in acute coronary syndrome. The data concerning the long-term clinical impacts of statin therapy between ST-segment elevation myocardial infarction (STEMI) and non-STEMI (NSTEMI) after drug-eluting stent implantation are limited. We compared the 2-year clinical outcomes between these 2 groups after statin therapy. A total of 30,616 Korean patients with acute myocardial infarction (AMI) were enrolled. Among them, 13,686 patients were classified as group A (STEMI statin user), 3,824 patients were as group B (STEMI statin nonuser), 10,398 patients were as group C (NSTEMI statin user), and 2,708 patients were as group D (NSTEMI statin nonuser). The major clinical endpoint was the occurrence of major adverse cardiac events (MACE) defined as all-cause death, recurrent myocardial infarction (re-MI), and any repeat revascularization during a 2-year follow-up period. After adjustment, the cumulative risks of MACE (adjusted hazard ratio [aHR] = 1.112 [1.002-1.235]; P = 0.047), all-cause death (aHR = 1.271 [1.054-1.532]; P = 0.012), and target vessel revascularization (TVR, aHR = 1.262 [1.049-1.518]; P = 0.014) in group C were significantly higher than group A. The cumulative risks of MACE, all-cause death, and cardiac death of the statin nonuser group (groups B and D) were significantly higher compared with statin user group (groups A and C). Statin therapy was more effective in reducing the cumulative risks of MACE, all-cause death, and TVR in the STEMI group than NSTEMI group in Korean patients with AMI after successful drug-eluting stent implantation.

Sections du résumé

BACKGROUND
Intensive statin therapy reduces cardiovascular events in acute coronary syndrome. The data concerning the long-term clinical impacts of statin therapy between ST-segment elevation myocardial infarction (STEMI) and non-STEMI (NSTEMI) after drug-eluting stent implantation are limited. We compared the 2-year clinical outcomes between these 2 groups after statin therapy.
MATERIALS AND METHODS
A total of 30,616 Korean patients with acute myocardial infarction (AMI) were enrolled. Among them, 13,686 patients were classified as group A (STEMI statin user), 3,824 patients were as group B (STEMI statin nonuser), 10,398 patients were as group C (NSTEMI statin user), and 2,708 patients were as group D (NSTEMI statin nonuser). The major clinical endpoint was the occurrence of major adverse cardiac events (MACE) defined as all-cause death, recurrent myocardial infarction (re-MI), and any repeat revascularization during a 2-year follow-up period.
RESULTS
After adjustment, the cumulative risks of MACE (adjusted hazard ratio [aHR] = 1.112 [1.002-1.235]; P = 0.047), all-cause death (aHR = 1.271 [1.054-1.532]; P = 0.012), and target vessel revascularization (TVR, aHR = 1.262 [1.049-1.518]; P = 0.014) in group C were significantly higher than group A. The cumulative risks of MACE, all-cause death, and cardiac death of the statin nonuser group (groups B and D) were significantly higher compared with statin user group (groups A and C).
CONCLUSIONS
Statin therapy was more effective in reducing the cumulative risks of MACE, all-cause death, and TVR in the STEMI group than NSTEMI group in Korean patients with AMI after successful drug-eluting stent implantation.

Identifiants

pubmed: 32089157
pii: S0002-9629(19)30428-8
doi: 10.1016/j.amjms.2019.12.004
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

156-167

Informations de copyright

Copyright © 2019 Southern Society for Clinical Investigation. Published by Elsevier Inc. All rights reserved.

Auteurs

Yong Hoon Kim (YH)

Division of Cardiology, Department of Internal Medicine, Kangwon National University School of Medicine, Chuncheon, Republic of Korea. Electronic address: yhkim02@kangwon.ac.kr.

Ae-Young Her (AY)

Division of Cardiology, Department of Internal Medicine, Kangwon National University School of Medicine, Chuncheon, Republic of Korea.

Myung Ho Jeong (MH)

Department of Cardiology, Cardiovascular Center, Chonnam National University Hospital, Gwangju, Republic of Korea.

Byeong-Keuk Kim (BK)

Division of Cardiology Severance Cardiovascular Hospital, Yonsei University College of Medicine, Republic of Korea.

Sung-Jin Hong (SJ)

Division of Cardiology Severance Cardiovascular Hospital, Yonsei University College of Medicine, Republic of Korea.

Seunghwan Kim (S)

Division of Cardiology, Inje University College of Medicine, Haeundae Paik Hospital, Busan, Republic of Korea.

Chul-Min Ahn (CM)

Division of Cardiology Severance Cardiovascular Hospital, Yonsei University College of Medicine, Republic of Korea.

Jung-Sun Kim (JS)

Division of Cardiology Severance Cardiovascular Hospital, Yonsei University College of Medicine, Republic of Korea.

Young-Guk Ko (YG)

Division of Cardiology Severance Cardiovascular Hospital, Yonsei University College of Medicine, Republic of Korea.

Donghoon Choi (D)

Division of Cardiology Severance Cardiovascular Hospital, Yonsei University College of Medicine, Republic of Korea.

Myeong-Ki Hong (MK)

Division of Cardiology Severance Cardiovascular Hospital, Yonsei University College of Medicine, Republic of Korea.

Yangsoo Jang (Y)

Division of Cardiology Severance Cardiovascular Hospital, Yonsei University College of Medicine, Republic of Korea.

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