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速尿、口服氯化钠和液体限制治疗抗利尿激素不适当分泌综合征(SIAD)的疗效:一项开放标签随机对照研究(EFFUSE-FLUID 试验)。

Efficacy of Furosemide, Oral Sodium Chloride, and Fluid Restriction for Treatment of Syndrome of Inappropriate Antidiuresis (SIAD): An Open-label Randomized Controlled Study (The EFFUSE-FLUID Trial).

机构信息

Division of Nephrology, Department of Internal Medicine, Chiang Mai University, Chiang Mai, Thailand.

Department of Anesthesiology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand; Pharmacoepidemiology and Statistics Research Center, Faculty of Pharmacy, Chiang Mai University, Chiang Mai, Thailand.

出版信息

Am J Kidney Dis. 2020 Aug;76(2):203-212. doi: 10.1053/j.ajkd.2019.11.012. Epub 2020 Mar 19.

Abstract

RATIONALE & OBJECTIVE: First-line therapy for syndrome of inappropriate antidiuresis (SIAD) is fluid restriction. Additional treatment for patients who do not respond to fluid restriction are water restriction with furosemide or water restriction with furosemide and salt supplementation. However, the efficacy of these treatments has never been tested in a randomized controlled study. The objective of this study was to investigate whether, combined with fluid restriction, furosemide with or without sodium chloride (NaCl) supplementation was more effective than fluid restriction alone in the treatment of hyponatremia in SIAD.

STUDY DESIGN

Open-label randomized controlled study.

SETTING & PARTICIPANTS: Patients with serum sodium concentrations ([Na]) ≤ 130mmol/L due to SIAD.

INTERVENTION(S): Random assignment to 1 of 3 groups: fluid restriction alone (FR), fluid restriction and furosemide (FR+FM), or fluid restriction, furosemide, and NaCl (FR+FM+NaCl). Strictness of fluid restriction (<1,000 or<500mL/d) was guided by the urine to serum electrolyte ratio. Furosemide dosage was 20 to 40mg/d. NaCl supplements were 3g/d. All treatments were continued for 28 days.

OUTCOMES

The primary outcome was change in [Na] at days 4, 7, 14, and 28 after randomization.

RESULTS

92 patients were recruited (FR, n=31; FR+FM, n=30; FR+FM+NaCl, n=31). Baseline [Na] was 125±4mmol/L, and there were no significant differences between groups. Mean [Na] on day 4 in all treatment groups was significantly increased from baseline by 5mmol/L (P<0.001); however, the change in [Na] was not significantly different across groups (P=0.7). There was no significant difference in percentage of patients or time to reach [Na] ≥ 130 or≥135mmol/L across the 3 groups. Acute kidney injury and hypokalemia (potassium≤3.0mmol/L) were more common in patients receiving furosemide.

LIMITATIONS

Open-label treatment.

CONCLUSIONS

In patients with SIAD, furosemide with NaCl supplement in combination with fluid restriction did not show benefits in correction of [Na] compared with treatment with fluid restriction alone. Incidences of acute kidney injury and hypokalemia were increased in patients receiving furosemide.

FUNDING

None.

TRIAL REGISTRATION

Registered at the Thai Clinical Trial Registry with study number TCTR20170629004.

摘要

目的

治疗抗利尿激素不适当分泌综合征(SIAD)的一线疗法是限制液体摄入。对于那些对液体限制没有反应的患者,可以进行水限制加呋塞米或水限制加呋塞米和盐补充治疗。然而,这些治疗方法的疗效从未在随机对照研究中得到过验证。本研究的目的是探讨在 SIAD 患者中,与单独限制液体摄入相比,联合使用呋塞米加或不加氯化钠(NaCl)补充是否更能有效治疗低钠血症。

研究设计

开放标签随机对照研究。

设置和参与者

血清钠浓度([Na])≤130mmol/L 的 SIAD 患者。

干预措施

随机分为 3 组:单独限制液体摄入(FR)、限制液体摄入加呋塞米(FR+FM)或限制液体摄入、呋塞米和 NaCl(FR+FM+NaCl)。液体限制的严格程度(<1000 或<500mL/d)由尿电解质比指导。呋塞米剂量为 20-40mg/d。NaCl 补充剂为 3g/d。所有治疗均持续 28 天。

主要结局

随机分组后第 4、7、14 和 28 天[Na]的变化。

结果

共招募了 92 名患者(FR 组 31 例,FR+FM 组 30 例,FR+FM+NaCl 组 31 例)。基线时[Na]为 125±4mmol/L,各组间无显著差异。所有治疗组在第 4 天的平均[Na]与基线相比均显著升高 5mmol/L(P<0.001);然而,各组间[Na]的变化无显著差异(P=0.7)。三组间达到[Na]≥130 或≥135mmol/L的患者比例或时间无显著差异。在接受呋塞米治疗的患者中,急性肾损伤和低钾血症(血钾≤3.0mmol/L)更为常见。

局限性

开放性治疗。

结论

在 SIAD 患者中,与单独限制液体摄入相比,呋塞米加 NaCl 补充治疗在纠正[Na]方面没有显示出优势。接受呋塞米治疗的患者急性肾损伤和低钾血症的发生率增加。

资金来源

无。

试验注册

在泰国临床试验注册中心注册,注册号 TCTR20170629004。

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