Underuse of heart failure medications and poor long-term prognosis in chronic heart failure patients with polypharmacy - A report from the CHART-2 study

被引:1
|
作者
Fujihashi, Takahide [1 ]
Nochioka, Kotaro [1 ]
Yasuda, Satoshi [1 ]
Sakata, Yasuhiko [2 ]
Hayashi, Hideka [1 ]
Shiroto, Takashi [1 ]
Takahashi, Jun [1 ]
Miyata, Satoshi [3 ]
Shimokawa, Hiroaki [1 ,4 ]
机构
[1] Tohoku Univ, Grad Sch Med, Dept Cardiovasc Med, 1-1 Seiryo Machi,Aoba Ku, Sendai, Miyagi 9808574, Japan
[2] Natl Cerebral & Cardiovasc Ctr, 6-1 Kishibe Shinmachi, Suita, Osaka 5648565, Japan
[3] Teikyo Univ, Grad Sch Publ Hlth, 2-11-1 Kaga,Itabashi Ku, Tokyo 1738605, Japan
[4] Int Univ Hlth & Welf, 4-3 Kozunomori, Chiba 2868686, Japan
来源
IJC HEART & VASCULATURE | 2024年 / 50卷
关键词
Heart failure; Polypharmacy; Prognosis; ALL-CAUSE MORTALITY; CLINICAL CHARACTERISTICS; AMERICAN-COLLEGE; FOCUSED UPDATE; ASSOCIATION; MANAGEMENT; GUIDELINE; DIAGNOSIS; SURVIVAL; PEOPLE;
D O I
10.1016/j.ijcha.2024.101345
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In patients with chronic heart failure (CHF), comorbidities are often managed with multiple medications, characterized by polypharmacy, leading to increased risk of potentially inappropriate medication and adverse effects. Methods: We studied 4,876 consecutive patients with CHF (Stage C/D, age 69.0 +/- 12.3 years) in the CHART-2 study to evaluate the association among polypharmacy, underuse of HF medications, and all-cause death. Polypharmacy was defined as the daily use of >= 8 medications for the survival classification and regression tree analysis. Results: The average number of medications was 10 in the polypharmacy group and 5 in the non-polypharmacy group, respectively. Over a median of 8.3 (4.1-11.7) years, the incidence rate of all-cause death was significantly higher in the polypharmacy group (n = 2,108) than in the non-polypharmacy group (57.3 % vs. 40.6 %; adjusted hazard ratio [aHR] 1.34 (95 %CI, 1.22-1.48), P < 0.001), even in age < 55 years (26.6 % vs. 14.3 %; adjusted hazard ratio [aHR] 1.61 (95 %CI, 1.04-2.50), P = 0.033). In patients with polypharmacy, those without reninangiotensin system inhibitors (RAS -I) and/or beta-blockers (N =1,023) were associated with increased incidence of all-cause death as compared with those with both medications (aHR 1.18; 95 %CI 1.04-1.35, P = 0.012). Conclusions: Polypharmacy was associated with poor long-term prognosis, even in younger patients with CHF. Among 4,876 patients with CHF, 1023 (20.9%) with polypharmacy and underuse of RAS -I and/or beta-blocker were associated with increased risk of all-cause death.
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页数:6
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