急性失代偿性心力衰竭患者利尿剂抵抗的预测因素。

IF 2 Q2 MEDICINE, GENERAL & INTERNAL
Journal of clinical medicine research Pub Date : 2026-04-15 eCollection Date: 2026-04-01 DOI:10.14740/jocmr6391
Rarsari Soerarso, Dian Yaniarti Hasanah, Emir Yonas, Ahmad Pandu Pratama, Sunu Budhi Raharjo, Bambang Budi Siswanto, Maarten J M Cramer, Pim van der Harst, Marish I F J Oerlemans
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引用次数: 0

摘要

背景:急性失代偿性心力衰竭(ADHF)是世界上死亡率和发病率的主要原因。利尿剂耐药发生在20-30% ADHF患者中,是临床结果恶化、治疗后立即死亡和再入院事件的独立预测因子。本研究旨在:1)从ADHF患者的基础疾病、合并症、生命体征、左室射血分数、实验室参数等方面,找出影响ADHF患者利尿剂耐药发生的因素;2)探讨ADHF患者利尿剂耐药发生的临床特征指标。方法:对2019年1 - 12月收治的535例ADHF患者进行回顾性队列研究。利尿抵抗定义为在给予40mg静脉(IV)呋塞米(或同等药物)后24小时内利尿反应小于1400 mL。观察受试者在静脉滴注40 mg呋塞米后24小时是否出现利尿剂耐药。通过双因素和多因素分析,综合临床评分系统预测利尿剂耐药的发生。结果:68%的患者出现利尿剂耐药。多因素logistic回归分析获得的独立预测因子为:糖尿病史(DM, P = 0.013)、静脉袢利尿剂使用史> 6天(P = 0.002)、口服袢利尿剂剂量> 80 mg/天(P = 0.006)、左室射血分数(LVEF)≤49% (P = 0.002)、血尿素氮(BUN)≥21 mg/dL (P < 0.001)、血清氯< 98 mmol/L (P < 0.001)。此外,还根据最终模型制作了评分系统。结论:通过多因素分析,DM、静脉袢利尿剂史、每日袢利尿剂用量、LVEF < 49%、BUN > 21 mg/dL、血清氯化物< 98 mmol/L与利尿剂耐药的发生有统计学意义,可合成临床评分系统,帮助预测利尿剂耐药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors Predicting Diuretic Resistance in Patients With Acute Decompensated Heart Failure.

Background: Acute decompensated heart failure (ADHF) is a leading cause of mortality and morbidity in the world. Diuretic resistance occurs in 20-30% of patients with ADHF and is an independent predictor of worsening clinical outcomes, immediate post-treatment death, and re-admission events. This study aims to: 1) identify factors that influence the occurrence of diuretic resistance in ADHF patients based on the underlying disease, comorbidities, vital signs, left ventricular ejection fraction, and laboratory parameters, and 2) investigate the clinical characteristics that serve as indicators of diuretic resistance incidence in patients with ADHF.

Methods: A retrospective cohort study was conducted on 535 patients treated with ADHF during the period from January to December 2019. Diuretic resistance was defined as a diuresis response of less than 1,400 mL in the first 24 h after administration of 40 mg of intravenous (IV) furosemide (or equivalent). Subjects were observed for 24 h post 40 mg IV furosemide for occurrence of diuretic resistance. Bivariate and multivariate analyses were performed to synthesize clinical scoring system to predict occurrence of diuretic resistance.

Results: Diuretic resistance occurs in 68% of patients. Independent predictors obtained from multivariate logistic regression analysis were: history of diabetes mellitus (DM, P = 0.013), history of using IV loop diuretics > 6 days (P = 0.002), oral loop diuretic dose > 80 mg/day (P = 0.006), left ventricular ejection fraction (LVEF) ≤ 49% (P = 0.002), blood urea nitrogen (BUN) ≥ 21 mg/dL (P < 0.001), and serum chloride < 98 mmol/L (P < 0.001). In addition, a scoring system has been made from the final model.

Conclusion: DM, history of IV loop diuretic, daily loop diuretic dosage, LVEF < 49%, BUN > 21 mg/dL, and serum chloride < 98 mmol/L were found to be statistically significant in association with occurrence of diuretic resistance using multivariate analysis and can be synthesized into a clinical scoring system to help predict diuretic resistance.

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