Virginia Commonwealth University School of Pharmacy, Richmond, VA.
Department of Pharmacy Services, Virginia Commonwealth University Health System, Richmond, VA; and.
J Cardiovasc Pharmacol. 2024 Oct 1;84(4):451-456. doi: 10.1097/FJC.0000000000001623.
Guidelines recommend intravenous loop diuretics as first-line therapy for patients hospitalized with acute heart failure (AHF) and volume overload. Additional agents can be used for augmentation, but there is limited guidance on agent selection. The study objective was to determine if chlorothiazide or metolazone is associated with differences in diuretic efficacy or safety in loop diuretic-resistant patients with AHF and renal dysfunction (eGFR <45 mL/min/1.73 m²). We conducted a multicenter, retrospective cohort study of patients hospitalized with AHF and renal dysfunction who received metolazone or chlorothiazide in addition to intravenous loop diuretics. The primary end point was a comparison of 24-hour urine output (UOP) between the 24 hours before and after thiazide administration. Secondary and safety end points included weight change, requirement for vasopressors or inotropes, electrolyte abnormalities, and changes in renal function. A total of 221 patients were included. The mean daily diuretic doses were chlorothiazide 632 mg and metolazone 7 mg. The mean 24-hour UOP increased more among chlorothiazide-treated (from 1668 mL to 3826 mL) versus metolazone-treated patients (from 1672 mL to 2834 mL) ( P < 0.001) after the addition of the second diuretic. Statistically significant reductions in serum creatinine were observed in the chlorothiazide group following 72 hours of treatment ( P = 0.016). More hypomagnesemia was observed in the chlorothiazide group; no differences in other electrolytes or changes in weight were observed. Overall, chlorothiazide was associated with a greater increase in 24-hour UOP than metolazone without an excess of potassium or serum creatinine derangements. However, weight changes did not differ significantly between groups. Future prospective studies are needed to confirm potential differences in diuretic response and safety.
指南建议静脉注射袢利尿剂作为急性心力衰竭(AHF)和容量超负荷住院患者的一线治疗药物。可以使用其他药物进行增强治疗,但关于药物选择的指导有限。本研究的目的是确定在伴有肾功能障碍(eGFR<45mL/min/1.73m²)的袢利尿剂抵抗的 AHF 患者中,氯噻嗪或美托拉宗是否与利尿剂疗效或安全性的差异相关。我们进行了一项多中心、回顾性队列研究,纳入了在接受静脉注射袢利尿剂治疗的同时接受美托拉宗或氯噻嗪治疗的伴有肾功能障碍的 AHF 住院患者。主要终点是比较噻嗪类药物治疗前后 24 小时尿量(UOP)的变化。次要终点和安全性终点包括体重变化、血管加压素或正性肌力药物的需求、电解质异常以及肾功能变化。共纳入 221 例患者。氯噻嗪的平均日剂量为 632mg,美托拉宗的平均日剂量为 7mg。与美托拉宗治疗组(从 1672mL 增加到 2834mL)相比,氯噻嗪治疗组(从 1668mL 增加到 3826mL)的 24 小时 UOP 增加更多(P<0.001)。在氯噻嗪治疗组中,在治疗 72 小时后观察到血清肌酐显著降低(P=0.016)。在氯噻嗪组中观察到更多的低镁血症,但其他电解质或体重变化无差异。总的来说,氯噻嗪在不增加钾或血清肌酐异常的情况下,与美托拉宗相比,可使 24 小时 UOP 增加更多。然而,两组间的体重变化无显著差异。需要进一步的前瞻性研究来证实利尿剂反应和安全性的潜在差异。