Virkud Arti V, Chang Patricia P, Funk Michele Jonsson, Kshirsagar Abhijit V, Edwards Jessie K, Pate Virginia, Kosorok Michael R, Gower Emily W
School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Am J Cardiol. 2024 Jan 1;210:208-216. doi: 10.1016/j.amjcard.2023.08.162. Epub 2023 Nov 14.
Loop diuretics are a standard pharmacologic therapy in heart failure (HF) management. Although furosemide is most frequently used, torsemide and bumetanide are increasingly prescribed in clinical practice, possibly because of superior bioavailability. Few real-world comparative effectiveness studies have examined outcomes across all 3 loop diuretics. The study goal was to compare the effects of loop diuretic prescribing at HF hospitalization discharge on mortality and HF readmission. We identified patients in Medicare claims data initiating furosemide, torsemide, or bumetanide after an index HF hospitalization from 2007 to 2017. We estimated 6-month risks of all-cause mortality and a composite outcome (HF readmission or all-cause mortality) using inverse probability of treatment weighting to adjust for relevant confounders. We identified 62,632 furosemide, 1,720 torsemide, and 2,389 bumetanide initiators. The 6-month adjusted all-cause mortality risk was lowest for torsemide (13.2%), followed by furosemide (14.5%) and bumetanide (15.6%). The 6-month composite outcome risk was 21.4% for torsemide, 24.7% for furosemide, and 24.9% for bumetanide. Compared with furosemide, the 6-month all-cause mortality risk was 1.3% (95% confidence interval [CI]: -3.7, 1.0) lower for torsemide and 1.0% (95% CI: -1.2, 3.2) higher for bumetanide, and the 6-month composite outcome risk was 3.3% (95% CI: -6.3, -0.3) lower for torsemide and 0.2% (95% CI: -2.5, 2.9) higher for bumetanide. In conclusion, the findings suggested that the first prescribed loop diuretic following HF hospitalization is associated with clinically important differences in morbidity in older patients receiving torsemide, bumetanide, or furosemide. These differences were consistent for the effect of all-cause mortality alone, but were not statistically significant.
袢利尿剂是心力衰竭(HF)管理中的标准药物治疗方法。虽然呋塞米最为常用,但托拉塞米和布美他尼在临床实践中的处方量越来越大,这可能是因为它们具有更高的生物利用度。很少有实际的比较有效性研究对所有这三种袢利尿剂的疗效进行过考察。本研究的目的是比较HF住院出院时开具袢利尿剂对死亡率和HF再入院率的影响。我们在医疗保险索赔数据中识别出2007年至2017年首次因HF住院后开始使用呋塞米、托拉塞米或布美他尼的患者。我们使用治疗权重的逆概率来调整相关混杂因素,估计全因死亡率和复合结局(HF再入院或全因死亡率)的6个月风险。我们识别出62,632名开始使用呋塞米的患者、1,720名开始使用托拉塞米的患者和2,389名开始使用布美他尼的患者。托拉塞米的6个月调整后全因死亡率风险最低(13.2%),其次是呋塞米(14.5%)和布美他尼(15.6%)。托拉塞米的6个月复合结局风险为21.4%,呋塞米为24.7%,布美他尼为24.9%。与呋塞米相比,托拉塞米的6个月全因死亡率风险低1.3%(95%置信区间[CI]:-3.7, 1.0),布美他尼高1.0%(95% CI:-1.2, 3.2);托拉塞米的6个月复合结局风险低3.3%(95% CI:-6.3, -0.3),布美他尼高0.2%(95% CI:-2.5, 2.9)。总之,研究结果表明,HF住院后首次开具的袢利尿剂与接受托拉塞米、布美他尼或呋塞米的老年患者的发病率在临床上存在重要差异。这些差异在单独的全因死亡率影响方面是一致的,但无统计学意义。