Inhaled bronchodilators for the prevention and treatment of chronic lung disease in preterm infants.

G. Ng, Matteo Bruschettini, John Ibrahim, Orlando da Silva
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This is an update of the 2016 Cochrane review.\n\n\nOBJECTIVES\nTo determine the effect of inhaled bronchodilators given as prophylaxis or as treatment for chronic lung disease (CLD) on mortality and other complications of preterm birth in infants at risk for or identified as having CLD.\n\n\nSEARCH METHODS\nAn Information Specialist searched CENTRAL, MEDLINE, Embase, CINAHL and three trials registers from 2016 to May 2023. In addition, the review authors undertook reference checking, citation searching and contact with trial authors to identify additional studies.\n\n\nSELECTION CRITERIA\nWe included randomised and quasi-randomised controlled trials involving preterm infants less than 32 weeks old that compared bronchodilators to no intervention or placebo. CLD was defined as oxygen dependency at 28 days of life or at 36 weeks' postmenstrual age. Initiation of bronchodilator therapy for the prevention of CLD had to occur within two weeks of birth. Treatment of infants with CLD had to be initiated before discharge from the neonatal unit. The intervention had to include administration of a bronchodilator by nebulisation or metered dose inhaler. The comparator was no intervention or placebo.\n\n\nDATA COLLECTION AND ANALYSIS\nWe used the standard methodological procedures expected by Cochrane. Critical outcomes included: mortality within the trial period; CLD (defined as oxygen dependency at 28 days of life or at 36 weeks' postmenstrual age); adverse effects of bronchodilators, including hypokalaemia (low potassium levels in the blood), tachycardia, cardiac arrhythmia, tremor, hypertension and hyperglycaemia (high blood sugar); and pneumothorax. We used the GRADE approach to assess the certainty of the evidence for each outcome.\n\n\nMAIN RESULTS\nWe included two randomised controlled trials in this review update. Only one trial provided useable outcome data. This trial was conducted in six neonatal intensive care units in France and Portugal, and involved 173 participants with a gestational age of less than 31 weeks. The infants in the intervention group received salbutamol for the prevention of CLD. The evidence suggests that salbutamol may result in little to no difference in mortality (risk ratio (RR) 1.08, 95% confidence interval (CI) 0.50 to 2.31; risk difference (RD) 0.01, 95% CI -0.09 to 0.11; low-certainty evidence) or CLD at 28 days (RR 1.03, 95% CI 0.78 to 1.37; RD 0.02, 95% CI -0.13 to 0.17; low-certainty evidence), when compared to placebo. The evidence is very uncertain about the effect of salbutamol on pneumothorax. The one trial with usable data reported that there were no relevant differences between groups, without providing the number of events (very low-certainty evidence). Investigators in this study did not report if side effects occurred. We found no eligible trials that evaluated the use of bronchodilator therapy for the treatment of infants with CLD. We identified no ongoing studies.\n\n\nAUTHORS' CONCLUSIONS\nLow-certainty evidence from one trial showed that inhaled bronchodilator prophylaxis may result in little or no difference in the incidence of mortality or CLD in preterm infants, when compared to placebo. The evidence is very uncertain about the effect of salbutamol on pneumothorax, and neither included study reported on the incidence of serious adverse effects. We identified no trials that studied the use of bronchodilator therapy for the treatment of CLD. Additional clinical trials are necessary to assess the role of bronchodilator agents in the prophylaxis or treatment of CLD. Researchers studying the effects of inhaled bronchodilators in preterm infants should include relevant clinical outcomes in addition to pulmonary mechanical outcomes.","PeriodicalId":515753,"journal":{"name":"The Cochrane database of systematic reviews","volume":"61 11","pages":"CD003214"},"PeriodicalIF":0.0000,"publicationDate":"2024-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Cochrane database of systematic reviews","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/14651858.CD003214.pub4","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

BACKGROUND Chronic lung disease (CLD) occurs frequently in preterm infants and is associated with respiratory morbidity. Bronchodilators have the potential effect of dilating small airways with muscle hypertrophy. Increased compliance and tidal volume, and decreased airway resistance, have been documented with the use of bronchodilators in infants with CLD. Therefore, bronchodilators are widely considered to have a role in the prevention and treatment of CLD, but there remains uncertainty as to whether they improve clinical outcomes. This is an update of the 2016 Cochrane review. OBJECTIVES To determine the effect of inhaled bronchodilators given as prophylaxis or as treatment for chronic lung disease (CLD) on mortality and other complications of preterm birth in infants at risk for or identified as having CLD. SEARCH METHODS An Information Specialist searched CENTRAL, MEDLINE, Embase, CINAHL and three trials registers from 2016 to May 2023. In addition, the review authors undertook reference checking, citation searching and contact with trial authors to identify additional studies. SELECTION CRITERIA We included randomised and quasi-randomised controlled trials involving preterm infants less than 32 weeks old that compared bronchodilators to no intervention or placebo. CLD was defined as oxygen dependency at 28 days of life or at 36 weeks' postmenstrual age. Initiation of bronchodilator therapy for the prevention of CLD had to occur within two weeks of birth. Treatment of infants with CLD had to be initiated before discharge from the neonatal unit. The intervention had to include administration of a bronchodilator by nebulisation or metered dose inhaler. The comparator was no intervention or placebo. DATA COLLECTION AND ANALYSIS We used the standard methodological procedures expected by Cochrane. Critical outcomes included: mortality within the trial period; CLD (defined as oxygen dependency at 28 days of life or at 36 weeks' postmenstrual age); adverse effects of bronchodilators, including hypokalaemia (low potassium levels in the blood), tachycardia, cardiac arrhythmia, tremor, hypertension and hyperglycaemia (high blood sugar); and pneumothorax. We used the GRADE approach to assess the certainty of the evidence for each outcome. MAIN RESULTS We included two randomised controlled trials in this review update. Only one trial provided useable outcome data. This trial was conducted in six neonatal intensive care units in France and Portugal, and involved 173 participants with a gestational age of less than 31 weeks. The infants in the intervention group received salbutamol for the prevention of CLD. The evidence suggests that salbutamol may result in little to no difference in mortality (risk ratio (RR) 1.08, 95% confidence interval (CI) 0.50 to 2.31; risk difference (RD) 0.01, 95% CI -0.09 to 0.11; low-certainty evidence) or CLD at 28 days (RR 1.03, 95% CI 0.78 to 1.37; RD 0.02, 95% CI -0.13 to 0.17; low-certainty evidence), when compared to placebo. The evidence is very uncertain about the effect of salbutamol on pneumothorax. The one trial with usable data reported that there were no relevant differences between groups, without providing the number of events (very low-certainty evidence). Investigators in this study did not report if side effects occurred. We found no eligible trials that evaluated the use of bronchodilator therapy for the treatment of infants with CLD. We identified no ongoing studies. AUTHORS' CONCLUSIONS Low-certainty evidence from one trial showed that inhaled bronchodilator prophylaxis may result in little or no difference in the incidence of mortality or CLD in preterm infants, when compared to placebo. The evidence is very uncertain about the effect of salbutamol on pneumothorax, and neither included study reported on the incidence of serious adverse effects. We identified no trials that studied the use of bronchodilator therapy for the treatment of CLD. Additional clinical trials are necessary to assess the role of bronchodilator agents in the prophylaxis or treatment of CLD. Researchers studying the effects of inhaled bronchodilators in preterm infants should include relevant clinical outcomes in addition to pulmonary mechanical outcomes.
预防和治疗早产儿慢性肺病的吸入式支气管扩张剂。
背景早产儿常出现慢性肺部疾病(CLD),并与呼吸系统发病率相关。支气管扩张剂具有肌肉肥大扩张小气道的潜在作用。有记录显示,在使用支气管扩张剂后,CLD 婴儿的顺应性和潮气量增加,气道阻力降低。因此,人们普遍认为支气管扩张剂在预防和治疗 CLD 方面具有一定作用,但其是否能改善临床结果仍存在不确定性。本文是对2016年Cochrane综述的更新。目的确定吸入性支气管扩张剂作为慢性肺病(CLD)的预防或治疗药物,对有CLD风险或确定患有CLD的婴儿的死亡率和其他早产并发症的影响。检索方法一位信息专家检索了CENTRAL、MEDLINE、Embase、CINAHL以及2016年至2023年5月的三个试验登记册。此外,综述作者还进行了参考文献检查、引文检索以及与试验作者联系,以确定其他研究。筛选标准我们纳入了涉及 32 周以下早产儿的随机和准随机对照试验,这些试验对支气管扩张剂与无干预措施或安慰剂进行了比较。CLD定义为出生28天或月龄后36周时的氧依赖。预防 CLD 的支气管扩张剂治疗必须在婴儿出生后两周内开始。对 CLD 患儿的治疗必须在新生儿出院前开始。干预措施必须包括通过雾化或计量吸入器使用支气管扩张剂。数据收集与分析我们采用了 Cochrane 所要求的标准方法程序。关键结果包括:试验期内的死亡率;CLD(定义为出生 28 天或月龄后 36 周时的氧依赖);支气管扩张剂的不良反应,包括低钾血症(血液中钾含量低)、心动过速、心律失常、震颤、高血压和高血糖(血糖高);以及气胸。我们采用 GRADE 方法对每项结果的证据确定性进行了评估。主要结果我们在本次综述更新中纳入了两项随机对照试验。只有一项试验提供了可用的结果数据。该试验在法国和葡萄牙的六个新生儿重症监护室进行,共有 173 名胎龄小于 31 周的参与者。干预组的婴儿接受了沙丁胺醇治疗,以预防 CLD。证据表明,与安慰剂相比,沙丁胺醇可能导致的死亡率(风险比(RR)1.08,95% 置信区间(CI)0.50 至 2.31;风险差异(RD)0.01,95% CI -0.09 至 0.11;低确定性证据)或 28 天时的 CLD(RR 1.03,95% CI 0.78 至 1.37;RD 0.02,95% CI -0.13 至 0.17;低确定性证据)几乎没有差异。关于沙丁胺醇对气胸的影响,目前的证据还很不确定。一项有可用数据的试验报告称,组间没有相关差异,但没有提供事件的数量(确定性极低的证据)。这项研究的研究人员没有报告是否出现了副作用。我们没有发现符合条件的试验对使用支气管扩张剂治疗 CLD 婴儿进行评估。一项试验的低确定性证据显示,与安慰剂相比,吸入支气管扩张剂预防性治疗可能对早产儿的死亡率或 CLD 发生率几乎没有影响。关于沙丁胺醇对气胸的影响,目前的证据还很不确定,纳入的两项研究均未报告严重不良反应的发生率。我们没有发现使用支气管扩张剂治疗慢性阻塞性肺疾病的试验。有必要进行更多的临床试验,以评估支气管扩张剂在预防或治疗慢性阻塞性肺疾病中的作用。研究人员在研究吸入性支气管扩张剂对早产儿的影响时,除肺机械功能结果外,还应包括相关的临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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