Brion L P, Primhak R A
Pediatrics, Division of Neonatology, Albert Einstein College of Medicine and Montefiore Medical Center, Weiler Hospital Room 725, 1825 Eastchester Road, Bronx, NY, USA, 10461.
Cochrane Database Syst Rev. 2000(4):CD001453. doi: 10.1002/14651858.CD001453.
Lung disease in preterm infants is often complicated with lung edema.
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.
We used the standard search method of the Cochrane Neonatal Review Group. We used the following keywords: [
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).
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.
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.
早产儿肺部疾病常并发肺水肿。
本综述旨在评估在患有或正发展为慢性肺部疾病(CLD)的早产儿中使用作用于髓袢的利尿剂(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。
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>]和<袢利尿剂>,限定为<人类>且限定为<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。
我们纳入本分析的试验为,患有或正发展为慢性肺部疾病且至少5日龄的早产儿被随机分配接受肠内或静脉内袢利尿剂治疗。符合条件的研究需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)。
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。两名研究者分别提取、评估并编码每项研究的所有数据,使用专门为此综述设计的表格。任何分歧通过讨论解决。我们合并了平行试验和交叉试验,并尽可能使用Follmann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。
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,也未评估利尿剂治疗的潜在并发症。在小于3周龄且正发展为CLD的早产儿中,使用呋塞米的效果不一致或未发现可检测到的效果。在大于3周龄且患有CLD的婴儿中,单次静脉注射1 mg/kg呋塞米可使肺顺应性和气道阻力在1小时内得到改善。长期使用呋塞米可改善氧合和肺顺应性。
在大于3周龄且患有CLD的早产儿中,急性和长期使用呋塞米可改善肺顺应性。静脉内或肠内长期使用呋塞米可改善氧合。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使用呋塞米对生存、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。