Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Am Heart J. 2010 Aug;160(2):264-271.e1. doi: 10.1016/j.ahj.2010.05.032.
The array of outcomes according to longitudinal furosemide doses in heart failure (HF) have not been evaluated. We examined the relationship of dynamic furosemide dose with mortality and hospitalizations for cardiovascular disease and renal dysfunction.
Among elderly patients with HF (>or=65 years) newly discharged from hospital, dynamic furosemide exposure was determined by examining dose fluctuations up to 5 years of follow-up using the Ontario Drug Benefit pharmacare database. Dynamic furosemide exposures were classified as low dose (LD; 1-59 mg/d), medium dose (MD; 60-119 mg/d), or high dose (HD; >or=120 mg/d). Outcomes were assessed by modeling furosemide exposure as a time-dependent covariate.
Among 4,406 patients (78.4 +/- 7.0 years; 50.5% male), 46% changed furosemide dose categories within 1 year, and 63% changed dose categories over the follow-up period. High-dose furosemide patients were younger, were mostly male, and exhibited more ischemic or valvular disease, diabetes, atrial fibrillation, hypotension, hyponatremia, and higher baseline creatinine than LD. Compared with LD, MD exposure was associated with increased mortality with adjusted hazard ratio 1.96 (95% CI 1.79-2.15), whereas HD exposure conferred greater mortality risk with hazard ratio 3.00 (95% CI 2.72-3.31) after multiple covariate adjustment (both P < .001). Adjusted risks of hospitalization for HF (MD: 1.24 [95% CI 1.12-1.38] and HD: 1.43 [95% CI 1.26-1.63]), renal dysfunction (MD: 1.56 [95% CI 1.38-1.76] and HD: 2.16 [95% CI 1.88-2.49]), and arrhythmias (MD: 1.15 [95% CI 1.03-1.30] and HD: 1.45 [95% CI 1.27-1.66]) were also higher with increasing furosemide exposure.
Exposure to higher furosemide doses is associated with worsened outcomes and is broadly predictive of death and morbidity.
心力衰竭(HF)中根据纵向呋塞米剂量的结果各不相同尚未得到评估。我们检查了动态呋塞米剂量与死亡率以及心血管疾病和肾功能障碍住院之间的关系。
在新出院的老年 HF 患者(>或=65 岁)中,使用安大略省药物福利处方药数据库检查了长达 5 年的随访中呋塞米剂量波动情况,以确定动态呋塞米暴露情况。将动态呋塞米暴露分为低剂量(LD;1-59mg/d)、中剂量(MD;60-119mg/d)或高剂量(HD;>或=120mg/d)。通过将呋塞米暴露建模为时间依赖性协变量来评估结果。
在 4406 名患者中(78.4+/-7.0 岁;50.5%为男性),46%的患者在 1 年内改变了呋塞米剂量类别,63%的患者在随访期间改变了剂量类别。高剂量呋塞米患者更年轻,主要为男性,并且比 LD 患者具有更多的缺血性或瓣膜疾病、糖尿病、心房颤动、低血压、低钠血症和更高的基线肌酐。与 LD 相比,MD 暴露与调整后的死亡率风险增加相关,风险比为 1.96(95%CI 1.79-2.15),而 HD 暴露在进行多次协变量调整后,死亡率风险更高,风险比为 3.00(95%CI 2.72-3.31)(均<0.001)。HF(MD:1.24[95%CI 1.12-1.38]和 HD:1.43[95%CI 1.26-1.63])、肾功能障碍(MD:1.56[95%CI 1.38-1.76]和 HD:2.16[95%CI 1.88-2.49])和心律失常(MD:1.15[95%CI 1.03-1.30]和 HD:1.45[95%CI 1.27-1.66])的住院风险也随着呋塞米暴露的增加而升高。
较高的呋塞米剂量暴露与不良结局相关,并广泛预测死亡和发病率。