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用于患有(或正在发展为)慢性肺病的早产儿的静脉或肠内袢利尿剂。

Intravenous or enteral loop diuretics for preterm infants with (or developing) chronic lung disease.

作者信息

Brion L P, Primhak R A

机构信息

Pediatrics, Division of Neonatology, Albert Einstein College of Medicine and Montefiore Medical Center, Weiler Hospital Room 725, 1825 Eastchester Road, Bronx, NY 10461, USA.

出版信息

Cochrane Database Syst Rev. 2000(2):CD001453. doi: 10.1002/14651858.CD001453.

Abstract

BACKGROUND

Lung disease in preterm infants is often complicated with lung edema.

OBJECTIVES

The aim of this review was to assess the risks and benefits of administration of a diuretic acting on the loop of Henle (loop diuretic) in preterm infants with or developing chronic lung disease (CLD). Primary objectives were to assess changes in need for oxygen or ventilatory support and effects on long-term outcome, and secondary objectives were to assess changes in pulmonary mechanics and potential complications of therapy.

SEARCH STRATEGY

We used the standard search method of the Cochrane Neonatal Review Group. We used the following keywords: ¿ or ¿ and , limited to and limited to <infant, newborn> or . We searched Medline (1966-1998), Embase (1974-1998) and the Cochrane Controlled Trials Register (CCTR) from the Cochrane Library (1998, issue 4). In addition, we hand searched several abstract books of national and international American and European Societies.

SELECTION CRITERIA

We included in this analysis trials in which preterm infants with or developing chronic lung disease and at least 5 days of age were all randomly allocated to receive a loop diuretic either enterally or intravenously. Eligible studies needed to assess at least one of the outcome variables defined a priori for this systematic review. Primary outcome variables included important clinical outcomes, and secondary outcome variables included toxicity and pulmonary mechanics (e.g., lung compliance and airway resistance).

DATA COLLECTION AND ANALYSIS

We used the standard method for the Cochrane Collaboration which is described in the Cochrane Collaboration Handbook. Two investigators extracted, assessed and coded separately all data for each study, using a form that was designed specifically for this review. Any disagreement was resolved by discussion. We combined parallel and cross-over trials and, whenever possible, transformed baseline and final outcome data measured on a continuous scale into change scores using Follmann's formula.

MAIN RESULTS

The only loop diuretic used in the studies which met the selection criteria was furosemide. Most studies focused on pathophysiological parameters and did not assess effects on important clinical outcomes defined in this review, or the potential complications of diuretic therapy. In preterm infants < 3 weeks of age developing CLD, furosemide administration has either inconsistent effects or no detectable effect. In infants > 3 weeks of age with CLD, a single intravenous dose of 1 mg/kg of furosemide improves lung compliance and airway resistance for 1 hour. Chronic administration of furosemide improves both oxygenation and lung compliance.

REVIEWER'S CONCLUSIONS: In preterm infants > 3 weeks of age with CLD, acute and chronic administration of furosemide improve lung compliance. Chronic administration of intravenous or enteral furosemide improves oxygenation. In view of the lack of data from randomized trials concerning effects on important clinical outcomes, routine or sustained use of systemic loop diuretics in infants with (or developing) CLD cannot be recommended based on current evidence. Randomized trials are needed to assess the effects of furosemide administration on survival, duration of ventilatory support and oxygen administration, length of hospital stay, potential complications and long-term outcome.

摘要

背景

早产儿肺部疾病常并发肺水肿。

目的

本综述旨在评估在患有或正在发展为慢性肺部疾病(CLD)的早产儿中使用作用于髓袢升支粗段的利尿剂(袢利尿剂)的风险和益处。主要目的是评估对氧气或通气支持需求的变化以及对长期预后的影响,次要目的是评估肺力学的变化以及治疗的潜在并发症。

检索策略

我们采用了Cochrane新生儿综述小组的标准检索方法。我们使用了以下关键词:“<支气管肺发育不良> 或 <慢性肺部疾病>”以及 “<袢利尿剂>”,限定为 “<人类>”,并限定为 “<婴儿,新生儿>” 或 “<婴儿>”。我们检索了Medline(1966 - 1998年)、Embase(1974 - 1998年)以及Cochrane图书馆(1998年第4期)中的Cochrane对照试验注册库(CCTR)。此外,我们还手工检索了美国和欧洲国家及国际学会的几本摘要书籍。

入选标准

我们纳入本分析的试验为,患有或正在发展为慢性肺部疾病且至少5日龄的早产儿被随机分配经肠道或静脉给予袢利尿剂。符合条件的研究需要评估为本系统综述预先定义的至少一个结局变量。主要结局变量包括重要的临床结局,次要结局变量包括毒性和肺力学(如肺顺应性和气道阻力)。

数据收集与分析

我们采用了Cochrane协作网的标准方法,该方法在《Cochrane协作网手册》中有描述。两名研究人员分别提取、评估并对每项研究的所有数据进行编码,使用专门为本综述设计的表格。任何分歧都通过讨论解决。我们合并了平行试验和交叉试验,并尽可能使用福尔曼公式将以连续尺度测量的基线和最终结局数据转换为变化分数。

主要结果

符合入选标准的研究中使用的唯一袢利尿剂是呋塞米。大多数研究关注病理生理参数,未评估对本综述中定义的重要临床结局的影响或利尿剂治疗的潜在并发症。在3周龄以下发展为CLD的早产儿中,给予呋塞米的效果要么不一致,要么未检测到效果。在3周龄以上患有CLD的婴儿中,单次静脉注射1mg/kg呋塞米可使肺顺应性和气道阻力改善1小时。长期给予呋塞米可改善氧合和肺顺应性。

综述作者结论

在3周龄以上患有CLD的早产儿中,急性和长期给予呋塞米可改善肺顺应性。静脉或肠道长期给予呋塞米可改善氧合。鉴于缺乏关于对重要临床结局影响的随机试验数据,基于当前证据,不建议在患有(或正在发展为)CLD的婴儿中常规或持续使用全身性袢利尿剂。需要进行随机试验来评估给予呋塞米对生存、通气支持和吸氧持续时间、住院时间、潜在并发症以及长期预后的影响。

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