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Comparative Effectiveness and Safety of Ticagrelor and Clopidogrel in Patients With or Without Chronic Liver Disease: A Nationwide Cohort Study - 23/07/24

Doi : 10.1016/j.amjmed.2024.03.042 
Bin Hong, BS a, , Sungho Bea, PharmD, PhD a, b, , Seng Chan You, MD, PhD c, Yoosoo Chang, MD, PhD d, Won Kim, MD, PhD e, Ju-Young Shin, PhD a, f, g,
a School of Pharmacy, Sungkyunkwan University, Suwon, South Korea 
b Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women’s Hospital and Harvard Medical School, Boston, Massachusetts 
c Department of Biomedical Systems Informatics, Yonsei University College of Medicine, Seoul, South Korea 
d Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, South Korea 
e Department of Internal Medicine, Seoul National University College of Medicine, Seoul Metropolitan Government Boramae Medical Center, Seoul, South Korea 
f Department of Biohealth Regulatory Science, Sungkyunkwan University, Suwon, South Korea 
g Department of Clinical Research Design & Evaluation, Samsung Advanced Institute for Health Sciences & Technology, Sungkyunkwan University, Seoul, South Korea 

Requests for reprints should be addressed to Ju-Young Shin, PhD, School of Pharmacy, Sungkyunkwan University, 2066 Seobu-ro, Jangan-gu, Suwon-si, Gyeonggi-do 16419, South Korea.School of PharmacySungkyunkwan University2066 Seobu-ro, Jangan-guSuwon-si, Gyeonggi-do16419South Korea

Abstract

Background

Although the effectiveness and safety of ticagrelor versus clopidogrel may differ in patients with chronic liver disease, there is a scarcity of evidence comparing ticagrelor and clopidogrel in patients with chronic liver disease. We aimed to evaluate the risk of major adverse cardiovascular events (MACE) and major bleeding associated with ticagrelor versus clopidogrel in patients undergoing percutaneous coronary intervention (PCI) due to acute coronary syndrome by chronic liver disease status.

Methods

Using the Korean healthcare claim database, we included adult patients who underwent PCI and initiated ticagrelor or clopidogrel treatment within 7 days of an acute coronary syndrome diagnosis. Patients were classified into 2 mutually exclusive groups: patients with chronic liver disease and patients without chronic liver disease. Within each group, the hazard ratios (HRs) with 95% confidence intervals (CIs) of MACE and major bleeding associated with ticagrelor versus clopidogrel were calculated using a Cox proportional hazards model within a 1:1 propensity score (PS) matched cohort.

Results

The final cohort included 14,261 and 148,535 patients with and without chronic liver disease, respectively. After PS matching, the risk of MACE (with chronic liver disease, HR: 1.01, 95% CI: 0.91-1.13; without chronic liver disease, HR: 1.02, 95% CI: 0.98-1.05; P for homogeneity: 0.865) and major bleeding (with chronic liver disease, HR: 1.07, 95% CI: 0.71-1.61; without chronic liver disease, HR: 1.32, 95% CI: 1.15-1.53; P for homogeneity: 0.342) for ticagrelor versus clopidogrel do not vary with chronic liver disease status.

Conclusions

Among acute coronary syndrome patients undergoing PCI, the use of ticagrelor versus clopidogrel was associated with a similar risk of MACE and an increased risk of major bleeding, but these risks did not vary with chronic liver disease status.

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Keywords : Acute coronary syndrome, Ticagrelor, Clopidogrel, Chronic liver disease, Population-based cohort study


Plan


 Funding: This research was supported by a grant (21153MFDS607) from the Ministry of Food and Drug Safety, South Korea, in 2021-2025. This research was supported by a grant (22213MFDS486) from the Ministry of Food and Drug Safety, South Korea, in 2022. Dr. Bea was supported by the Health Fellowship Foundation (2022).
 Conflicts of Interest: The authors declare no conflict of interests relevant to this study. Dr. Shin received grants from the Ministry of Food and Drug Safety, Ministry of Health and Welfare, National Research Foundation of Korea, and Government-wide R&D Fund for Infectious Disease Research and Pharmaceutical Companies, including Amgen, Pfizer, SK Bioscience, Daiichi Sankyo, and GSK. Dr. You servers as the Chief Technology Officer of PHI Digital Healthcare. No other relationships or activities have influenced the submitted work.
 Authorship: BH: Conceptualization, Formal analysis, Investigation, Methodology, Visualization, Writing – original draft, Writing – review & editing. SB: Conceptualization, Investigation, Methodology, Writing – original draft, Writing – review & editing. SCY: Conceptualization, Investigation, Methodology, Writing – review & editing. YC: Conceptualization, Investigation, Methodology, Writing – review & editing. WK: Conceptualization, Investigation, Methodology, Writing – review & editing. J-YS: Conceptualization, Data curation, Funding acquisition, Investigation, Methodology, Supervision, Writing – review & editing.
 Data sharing: No additional data are available to the public.


© 2024  Elsevier Inc. Tous droits réservés.
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Vol 137 - N° 8

P. 742 - août 2024 Retour au numéro
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