Department of Cardiovascular Medicine, Shinshu University School of Medicine.
Department of Cardiovascular Medicine, Kyoto University Graduate School of Medicine.
Circ J. 2023 Dec 25;88(1):33-42. doi: 10.1253/circj.CJ-22-0712. Epub 2023 Aug 4.
Hyperpolypharmacy is associated with adverse outcomes in older adults, but because literature on its association with cardiovascular (CV) outcomes after acute decompensated heart failure (ADHF) is sparse, we investigated the relationships among hyperpolypharmacy, medication class, and death in patients with HF.
We evaluated the total number of medications prescribed to 884 patients at discharge following ADHF. Patients were categorized into nonpolypharmacy (<5 medications), polypharmacy (5-9 medications), and hyperpolypharmacy (≥10 medications) groups. We examined the relationship of polypharmacy status with the 2-year mortality rate. The proportion of patients taking ≥5 medications was 91.3% (polypharmacy, 55.3%; hyperpolypharmacy, 36.0%). Patients in the hyperpolypharmacy group showed worse outcomes than patients in the other 2 groups (P=0.002). After multivariable adjustment, the total number of medications was significantly associated with an increased risk of death (hazard ratio [HR] per additional increase in the number of medications, 1.05; 95% confidence interval [CI], 1.01-1.10; P=0.027). Although the number of non-CV medications was significantly associated with death (HR, 1.07; 95% CI, 1.02-1.13; P=0.01), the number of CV medications was not (HR, 1.01; 95% CI, 0.92-1.10; P=0.95).
Hyperpolypharmacy due to non-CV medications was associated with an elevated risk of death in patients after ADHF, suggesting the importance of a regular review of the prescribed drugs including non-CV medications.
在老年人中,药物过量与不良结局相关,但由于急性失代偿性心力衰竭(ADHF)后药物过量与心血管(CV)结局相关的文献很少,因此我们研究了 HF 患者药物过量、药物类别与死亡之间的关系。
我们评估了 884 例 ADHF 患者出院时开具的药物总数。患者分为非药物过量组(<5 种药物)、药物过量组(5-9 种药物)和药物过量组(≥10 种药物)。我们检查了药物过量状态与 2 年死亡率的关系。服用≥5 种药物的患者比例为 91.3%(药物过量组 55.3%;药物过量组 36.0%)。药物过量组患者的预后较其他两组患者差(P=0.002)。多变量调整后,药物总数与死亡风险增加显著相关(每增加一种药物的风险比[HR]为 1.05;95%置信区间[CI],1.01-1.10;P=0.027)。虽然非 CV 药物的数量与死亡显著相关(HR,1.07;95%CI,1.02-1.13;P=0.01),但 CV 药物的数量与死亡无关(HR,1.01;95%CI,0.92-1.10;P=0.95)。
非 CV 药物引起的药物过量与 ADHF 后患者死亡风险升高相关,提示定期审查包括非 CV 药物在内的处方药物的重要性。