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初始静脉利尿剂剂量对急性失代偿性心力衰竭的临床意义。

Clinical implication of initial intravenous diuretic dose for acute decompensated heart failure.

机构信息

Department of Cardiology, Kameda Medical Center, Chiba, Japan.

Department of Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

Sci Rep. 2022 Feb 8;12(1):2127. doi: 10.1038/s41598-022-06032-x.

Abstract

Although intravenous diuretics is a cornerstone of acute heart failure treatment (AHF), its optimal initial dose is unclear. This is a post-hoc analysis of the REALITY-AHF, a prospective multicentre observational registry of AHF. The initial intravenous diuretic dose used in each patient was categorised into below, standard, or above the recommended dose groups according to guideline-recommended initial intravenous diuretic dose. The recommended dose was individualised based on the oral diuretic dose taken at admission. We compared the study endpoints, including 60-day mortality, diuretics response within six hours, and length of hospital stay (HS). Of 1093 patients, 429, 558, and 106 were assigned to the Below, Standard, and Above groups, respectively. The diuretics response and HS were significantly greater in the Below group than in the Standard group after adjusting for covariates. Kaplan-Meier analysis indicated a significantly higher incidence of 60-day mortality in the Above group than the Standard group. This difference was retained after adjusting for other prognostic factors. Treatment with a lower than guideline-recommended intravenous diuretic dose was associated with longer HS, whereas above the guideline-recommended dose was associated with a higher 60-day mortality rate. Our results reconfirm that the guideline-recommended initial intravenous diuretic dose is feasible for AHF.

摘要

尽管静脉利尿剂是急性心力衰竭(AHF)治疗的基石,但最佳初始剂量仍不清楚。这是对 REALITY-AHF 的事后分析,REALITY-AHF 是一项针对 AHF 的前瞻性多中心观察性注册研究。根据指南推荐的初始静脉利尿剂剂量,将每位患者使用的初始静脉利尿剂剂量分为以下、标准或高于推荐剂量组。推荐剂量根据入院时口服利尿剂的剂量进行个体化。我们比较了研究终点,包括 60 天死亡率、六小时内利尿剂反应和住院时间(HS)。在 1093 名患者中,分别有 429、558 和 106 名患者被分配到以下、标准和高于标准组。在调整了协变量后,与标准组相比,低于标准组的利尿剂反应和 HS 显著更大。Kaplan-Meier 分析表明,高于标准组的 60 天死亡率显著更高。在调整了其他预后因素后,这种差异仍然存在。与指南推荐的静脉利尿剂剂量相比,使用低于指南推荐剂量的治疗方法与较长的 HS 相关,而高于指南推荐剂量与较高的 60 天死亡率相关。我们的结果再次证实,指南推荐的初始静脉利尿剂剂量对 AHF 是可行的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4b1/8825846/f5a536e1c891/41598_2022_6032_Fig1_HTML.jpg

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