Thiazide diuretics versus loop diuretics in stage 3-5 CKD: impact on cardiorenal outcomes.

Postgraduate medicine Pub Date : 2024-09-01 Epub Date: 2024-08-27 DOI:10.1080/00325481.2024.2396796
Li-Chin Sung, Hui-Wen Chiu, Samuel Mon-Wei Yu, Liam Li-An Tsou, Yung-Ho Hsu, Mai-Szu Wu, Cheng-Li Lin, Fuu-Jen Tsai, Chu-Lin Chou
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Abstract

Objectives: The association between diuretic use and cardiorenal outcomes remains limited in patients with stage 3-5 chronic kidney disease (CKD) and hypertension. To address this gap, we aim to investigate the long-term clinical impact of diuretic use with its pharmacological classification in Taiwanese patients with stage 3-5 CKD and hypertension who were concurrently received angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin II receptor blockers (ARBs).

Methods: Using data from the National Health Insurance Research Database (January 2008 to December 2019), we focused on individuals with stage 3-5 CKD receiving ACEIs/ARBs between 2010 and 2018. We categorized the cohort into non-diuretic, loop diuretic (furosemide), thiazide diuretic, and combination diuretic groups. We used a Cox proportional hazards regression model with propensity score matching to analyze the influence of diuretics on all-cause mortality, cardiovascular (CV) death, and cardiorenal adverse outcomes.

Results: The study included 59,719 patients, with 17,585 in the non-diuretic group and 42,134 in the diuretic group. Diuretics including furosemide use was significantly associated the risks of hospitalization for decompensated congestive heart failure (CHF), acute renal failure (ARF), end-stage renal disease (ESRD) requiring dialysis, CV mortality, and all-cause mortality (p-value <0.001). Thiazide diuretics showed no such adverse outcomes associations. The group receiving both thiazide and furosemide was more associated with all-cause mortality than the nondiuretic, thiazide, and furosemide monotherapy groups (all p-value <0.001).

Conclusion: Among stage 3-5 CKD patients on ACEIs/ARBs, loop diuretics exposure was associated with increased mortality and hospitalization for cardiorenal events, while thiazide diuretics exposure in isolation had no such associations. In the present data, we cannot evaluate the relationship between furosemide-associated adverse outcomes and worse renal function. These findings highlight the need for randomized controlled trials to assess the safety of loop diuretics in this population, urging caution in their prescription without a clear clinical indication.

噻嗪类利尿剂与襻利尿剂在 3-5 期慢性肾脏病中的应用:对心肾功能预后的影响。
目的:在 3-5 期慢性肾脏病(CKD)和高血压患者中,利尿剂的使用与心衰结果之间的关系仍然有限。为了填补这一空白,我们旨在研究同时接受血管紧张素转换酶抑制剂(ACEIs)或血管紧张素II受体阻滞剂(ARBs)治疗的台湾3-5期慢性肾脏病和高血压患者使用利尿剂的长期临床影响及其药理分类:利用全国健康保险研究数据库(2008 年 1 月至 2019 年 12 月)的数据,我们重点研究了 2010 年至 2018 年期间接受 ACEIs/ARBs 治疗的 3-5 期 CKD 患者。我们将队列分为非利尿剂组、襻利尿剂组(呋塞米)、噻嗪类利尿剂组和联合利尿剂组。我们使用倾向得分匹配的 Cox 比例危险回归模型分析了利尿剂对全因死亡率、心血管(CV)死亡和心肾不良结局的影响:研究共纳入 59719 名患者,其中非利尿剂组 17585 人,利尿剂组 42134 人。包括呋塞米在内的利尿剂的使用与失代偿性充血性心力衰竭(CHF)、急性肾功能衰竭(ARF)、需要透析的终末期肾病(ESRD)住院风险、心血管疾病死亡率和全因死亡率显著相关(p-value p-value 结论):在使用 ACEIs/ARBs 的 3-5 期 CKD 患者中,襻利尿剂暴露与死亡率和心肾事件住院率增加有关,而单独使用噻嗪类利尿剂则没有这种关联。根据目前的数据,我们无法评估呋塞米相关不良后果与肾功能恶化之间的关系。这些发现突出表明,有必要进行随机对照试验,以评估襻利尿剂在这一人群中的安全性,并敦促在没有明确临床指征的情况下谨慎处方襻利尿剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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