Impact of hyper-polypharmacy due to non-cardiovascular medications on long-term clinical outcomes following endovascular treatment for lower limb artery disease: A sub-analysis of the I-PAD Nagano registry.

Endovascular therapy Lower extremity artery disease Major adverse cardiovascular events Peripheral artery disease Polypharmacy

Journal

Journal of cardiology
ISSN: 1876-4738
Titre abrégé: J Cardiol
Pays: Netherlands
ID NLM: 8804703

Informations de publication

Date de publication:
02 Jul 2024
Historique:
received: 14 07 2023
revised: 20 06 2024
accepted: 27 06 2024
medline: 5 7 2024
pubmed: 5 7 2024
entrez: 4 7 2024
Statut: aheadofprint

Résumé

Lower limb artery disease (LEAD) is accompanied by multiple comorbidities; however, the effect of hyperpolypharmacy on patients with LEAD has not been established. This study investigated the associations between hyperpolypharmacy, medication class, and adverse clinical outcomes in patients with LEAD. This study used data from a prospective multicenter observational Japanese registry. A total of 366 patients who underwent endovascular treatment (EVT) for LEAD were enrolled in this study. The primary endpoints were major adverse cardiac events (MACE), including myocardial infarction, stroke, and all-cause death. Of 366 patients with LEAD, 12 with missing medication information were excluded. Of the 354 remaining patients, 166 had hyperpolypharmacy (≥10 medications, 46.9 %), 162 had polypharmacy (5-9 medications, 45.8 %), and 26 had nonpolypharmacy (<5 medications, 7.3 %). Over a 4.7-year median follow-up period, patients in the hyperpolypharmacy group showed worse outcomes than those in the other two groups (log-rank test, p < 0.001). Multivariate analysis revealed that the total number of medications was significantly associated with an increased risk of MACE (hazard ratio per medication increase 1.078, 95 % confidence interval 1.02-1.13 p = 0.012). Although an increased number of non-cardiovascular medications was associated with an elevated risk of MACE, the increase in cardiovascular medications was not statistically significant (log-rank test, p = 0.002 and 0.35, respectively). Hyperpolypharmacy due to non-cardiovascular medications was significantly associated with adverse outcomes in patients with LEAD who underwent EVT, suggesting the importance of medication reviews, including non-cardiovascular medications.

Sections du résumé

BACKGROUND BACKGROUND
Lower limb artery disease (LEAD) is accompanied by multiple comorbidities; however, the effect of hyperpolypharmacy on patients with LEAD has not been established. This study investigated the associations between hyperpolypharmacy, medication class, and adverse clinical outcomes in patients with LEAD.
METHODS METHODS
This study used data from a prospective multicenter observational Japanese registry. A total of 366 patients who underwent endovascular treatment (EVT) for LEAD were enrolled in this study. The primary endpoints were major adverse cardiac events (MACE), including myocardial infarction, stroke, and all-cause death.
RESULTS RESULTS
Of 366 patients with LEAD, 12 with missing medication information were excluded. Of the 354 remaining patients, 166 had hyperpolypharmacy (≥10 medications, 46.9 %), 162 had polypharmacy (5-9 medications, 45.8 %), and 26 had nonpolypharmacy (<5 medications, 7.3 %). Over a 4.7-year median follow-up period, patients in the hyperpolypharmacy group showed worse outcomes than those in the other two groups (log-rank test, p < 0.001). Multivariate analysis revealed that the total number of medications was significantly associated with an increased risk of MACE (hazard ratio per medication increase 1.078, 95 % confidence interval 1.02-1.13 p = 0.012). Although an increased number of non-cardiovascular medications was associated with an elevated risk of MACE, the increase in cardiovascular medications was not statistically significant (log-rank test, p = 0.002 and 0.35, respectively).
CONCLUSIONS CONCLUSIONS
Hyperpolypharmacy due to non-cardiovascular medications was significantly associated with adverse outcomes in patients with LEAD who underwent EVT, suggesting the importance of medication reviews, including non-cardiovascular medications.

Identifiants

pubmed: 38964712
pii: S0914-5087(24)00128-X
doi: 10.1016/j.jjcc.2024.06.011
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Auteurs

Tamon Kato (T)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan. Electronic address: katot20110408@gmail.com.

Masatoshi Minamisawa (M)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Takashi Miura (T)

Department of Cardiology, Nagano Municipal Hospital, Nagano, Jaan, Japan.

Masafumi Kanai (M)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Yushi Oyama (Y)

Department of Cardiology, Shinonoi General Hospital, Nagano, Japan.

Naoto Hashizume (N)

Department of Cardiology, Nagano Red-Cross Hospital, Nagano, Japan.

Daisuke Yokota (D)

Department of Cardiology, Iida Hospital, Iida, Japan.

Minami Taki (M)

Department of Cardiology, Saku General Hospital, Saku, Japan.

Keisuke Senda (K)

Department of Cardiology, Aizawa Hospital, Matsumoto, Japan.

Ken Nishikawa (K)

Department of Cardiology, Joetsu General Hospital, Joetsu, Japan.

Tadamasa Wakabayashi (T)

Department of Cardiology, Suwa Central Hospital, Chino, Japan.

Koki Fujimori (K)

Department of Cardiology, Suwa Red-Cross Hospital, Suwa, Japan.

Kenichi Karube (K)

Department of Cardiology, Okaya City Hospital, Okaya, Japan.

Takahiro Sakai (T)

Department of Cardiology, Ina Central Hospital, Ina, Japan.

Minami Inoue (M)

Department of Cardiology, Ina Central Hospital, Ina, Japan.

Hidetsugu Yoda (H)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Daisuke Sunohara (D)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Yoshiteru Okina (Y)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Hidetomo Nomi (H)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Yusuke Kanzaki (Y)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Keisuke Machida (K)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Daisuke Kashiwagi (D)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Yasushi Ueki (Y)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Tatsuya Saigusa (T)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Soichiro Ebisawa (S)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Ayako Okada (A)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Hirohiko Motoki (H)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Koichiro Kuwahara (K)

Department of Cardiovascular Medicine, Shinshu University School of Medicine、Matsumoto, Japan.

Classifications MeSH