Shah S S, Ohlsson A, Halliday H, Shah V S
Cochrane Database Syst Rev. 2007 Oct 17(4):CD002057. doi: 10.1002/14651858.CD002057.pub2.
Chronic lung disease (CLD) remains a serious and common problem among very low birth weight infants despite the use of antenatal steroids and postnatal surfactant therapy to decrease the incidence and severity of respiratory distress syndrome. Due to their anti-inflammatory properties, corticosteroids have been widely used to treat or prevent CLD. However, the use of systemic steroids has been associated with serious short and long-term adverse effects. Administration of corticosteroids topically through the respiratory tract might result in beneficial effects on the pulmonary system with fewer undesirable systemic side effects.
To determine the effect of inhaled versus systemic corticosteroids administered to ventilator dependent preterm neonates with birth weight < 1500 g or gestational age < 32 weeks after two weeks of life for the treatment of evolving CLD.
Randomized and quasi-randomized trials were identified by searching the Cochrane Central Register of Controlled Trials (CENTRAL, The Cochrane Library, Issue 3, 2007), MEDLINE (1966 - June 2007), EMBASE (1980 - June 2007), CINAHL (1982 - June 2007), reference lists of published trials and abstracts published in Pediatric Research or electronically on the Pediatric Academic Societies website (1990 - April 2007).
Randomized or quasi-randomized trials comparing inhaled versus systemic corticosteroid therapy (irrespective of the dose and duration of therapy) starting after the first two weeks of life in ventilator dependent very low birth weight preterm infants.
Data were extracted regarding clinical outcomes including CLD at 28 days or 36 weeks postmenstrual age (PMA), mortality, combined outcome of death or CLD at 28 days of age or 36 weeks PMA, other pulmonary outcomes and adverse effects. All data were analyzed using RevMan 4.2.10. When appropriate, meta-analysis was performed using relative risk (RR), risk difference (RD), and weighted mean difference (WMD) along with their 95% confidence intervals (CI). If RD was statistically significant, the number needed to treat (NNT) was calculated.
Data from one additional trial were available for inclusion in this update. Thus, five trials comparing inhaled versus systemic corticosteroids in the treatment of CLD were identified. Two trials were excluded as both included non-ventilator dependent patients and three trials qualified for inclusion in this review. Halliday et al (Halliday 2001) randomized infants at < 72 hours, while Rozycki et al (Rozycki 2003) and Suchomski et al (Suchomski 2002) randomized at 12 - 21 days. The data from the two trials of Rozycki et al and Suchmoski et al are combined using meta-analytic techniques. The data from the trial by Halliday et al are reported separately, as outcomes were measured over different time periods from the age at randomization. In none of the trials was there a statistically significant difference between the groups in the incidence of CLD at 36 weeks PMA among all randomized infants. The estimates for the trial by Halliday et al (Halliday 2001) were RR 1.10 (95% CI 0.82, 1.47), RD 0.03 (95% CI -0.08, 0.15); number of infants (n = 292). For the trials by Rozycki et al (Rozycki 2003) and Suchomski et al (Suchomski 2002) the typical RR was 1.02 (95% CI 0.83, 1.25) and the typical RD 0.01 (95% CI -0.11, 0.14); (number of infants = 139 ). There were no statistically significant differences between the groups in either trial for oxygen dependency at 28 days of age, death by 28 days or 36 weeks PMA, the combined outcome of death by or CLD at 28 days or 36 weeks PMA, duration of intubation, duration of oxygen dependence, or adverse effects. Information on the long-term neurodevelopmental outcomes was not available.
AUTHORS' CONCLUSIONS: This review found no evidence that inhaled corticosteroids confer net advantages over systemic corticosteroids in the management of ventilator dependent preterm infants. Neither inhaled steroids nor systemic steroids can be recommended as standard treatment for ventilated preterm infants. There was no evidence of difference in effectiveness or side-effect profiles for inhaled versus systemic steroids. A better delivery system guaranteeing selective delivery of inhaled steroids to the alveoli might result in beneficial clinical effects without increasing side-effects. To resolve this issue, studies are needed to identify the risk/benefit ratio of different delivery techniques and dosing schedules for the administration of these medications. The long-term effects of inhaled steroids, with particular attention to neurodevelopmental outcome, should be addressed in future studies.
尽管使用了产前类固醇和产后表面活性剂疗法来降低呼吸窘迫综合征的发病率和严重程度,但慢性肺部疾病(CLD)在极低出生体重儿中仍然是一个严重且常见的问题。由于其抗炎特性,皮质类固醇已被广泛用于治疗或预防CLD。然而,全身使用类固醇与严重的短期和长期不良反应相关。通过呼吸道局部给予皮质类固醇可能会对肺部系统产生有益影响,同时减少不良的全身副作用。
确定出生体重<1500g或胎龄<32周、依赖呼吸机的早产儿在出生后两周开始吸入与全身使用皮质类固醇治疗进展性CLD的效果。
通过检索Cochrane对照试验中心注册库(CENTRAL,Cochrane图书馆,2007年第3期)、MEDLINE(1966 - 2007年6月)、EMBASE(1980 - 2007年6月)、CINAHL(1982 - 2007年6月)、已发表试验的参考文献列表以及发表在《儿科研究》上的摘要或在儿科学术协会网站上以电子方式发表的内容(1990 - 2007年4月),识别随机和半随机试验。
随机或半随机试验,比较出生后两周开始,在依赖呼吸机的极低出生体重早产儿中吸入与全身皮质类固醇疗法(无论治疗剂量和疗程)。
提取有关临床结局的数据,包括出生后28天或孕龄36周时的CLD、死亡率、出生后28天或孕龄36周时死亡或CLD的综合结局、其他肺部结局和不良反应。所有数据均使用RevMan 4.2.10进行分析。在适当情况下,使用相对风险(RR)、风险差异(RD)和加权平均差(WMD)及其95%置信区间(CI)进行荟萃分析。如果RD具有统计学意义,则计算治疗所需人数(NNT)。
本次更新纳入了一项额外试验的数据。因此,共识别出五项比较吸入与全身皮质类固醇治疗CLD的试验。两项试验被排除,因为它们均纳入了非依赖呼吸机的患者,三项试验符合本综述的纳入标准。Halliday等人(Halliday 2001)在<72小时时对婴儿进行随机分组,而Rozycki等人(Rozycki 2003)和Suchomski等人(Suchomski 2002)在12 - 21天时进行随机分组。Rozycki等人和Suchmoski等人的两项试验数据使用荟萃分析技术进行合并。Halliday等人试验的数据单独报告,因为结局是在随机分组年龄后的不同时间段测量的。在所有随机分组的婴儿中,各试验组在孕龄36周时CLD的发生率均无统计学显著差异。Halliday等人(Halliday 2001)试验的估计值为RR 1.10(95%CI 0.82,1.47),RD 0.03(95%CI -0.08,0.15);婴儿数量(n = 292)。对于Rozycki等人(Rozycki 2003)和Suchomski等人(Suchomski 2002)的试验,典型RR为1.02(95%CI 0.83,1.25),典型RD为0.01(95%CI -0.11,0.14);(婴儿数量 = 139)。在任何一项试验中,两组在出生后28天时的氧依赖、出生后28天或孕龄36周时的死亡、出生后28天或孕龄36周时死亡或CLD的综合结局、插管持续时间、氧依赖持续时间或不良反应方面均无统计学显著差异。关于长期神经发育结局的信息不可用。
本综述未发现证据表明在依赖呼吸机的早产儿管理中,吸入皮质类固醇比全身皮质类固醇具有净优势。吸入类固醇和全身类固醇均不能推荐作为依赖呼吸机早产儿的标准治疗方法。没有证据表明吸入与全身类固醇在有效性或副作用方面存在差异。一种能保证吸入类固醇选择性输送到肺泡的更好给药系统可能会产生有益的临床效果而不增加副作用。为解决这一问题,需要开展研究以确定这些药物不同给药技术和给药方案的风险/效益比。未来研究应关注吸入类固醇的长期影响,尤其要关注神经发育结局。