Stevens T P, Harrington E W, Blennow M, Soll R F
University of Rochester, Pediatrics, Dept of Pediatrics (Neonatology), Box 651, 601 Elmwood Ave, Rochester, NY 14642, USA.
Cochrane Database Syst Rev. 2007 Oct 17;2007(4):CD003063. doi: 10.1002/14651858.CD003063.pub3.
BACKGROUND: Both prophylactic and early surfactant replacement therapy reduce mortality and pulmonary complications in ventilated infants with respiratory distress syndrome (RDS) compared with later selective surfactant administration. However, continued post-surfactant intubation and ventilation are risk factors for bronchopulmonary dysplasia (BPD). The purpose of this review was to compare outcomes between two strategies of surfactant administration in infants with RDS; prophylactic or early surfactant administration followed by prompt extubation, compared with later, selective use of surfactant followed by continued mechanical ventilation. OBJECTIVES: To compare two treatment strategies in preterm infants with or at risk for RDS: early surfactant administration with brief mechanical ventilation (less than one hour) followed by extubation vs. later selective surfactant administration, continued mechanical ventilation, and extubation from low respiratory support. Two populations of infants receiving early surfactant were considered: spontaneously breathing infants with signs of RDS (who receive surfactant administration during evolution of RDS prior to requiring intubation for respiratory failure) and infants at high risk for RDS (who receive prophylactic surfactant administration within 15 minutes after birth). SEARCH STRATEGY: Searches were made of the Oxford Database of Perinatal Trials, MEDLINE (1966 - December 2006), CINAHL (1982 to December Week 2, 2006), EMBASE (1980 - December 2006), Cochrane Central Register of Controlled Trials (CENTRAL, The Cochrane Library, Issue 4, 2006), Pediatric Research (1990 - 2006), abstracts, expert informants and hand searching. No language restrictions were applied. SELECTION CRITERIA: Randomized or quasi-randomized controlled clinical trials comparing early surfactant administration with planned brief mechanical ventilation (less than one hour) followed by extubation vs. selective surfactant administration continued mechanical ventilation, and extubation from low respiratory support. DATA COLLECTION AND ANALYSIS: Data were sought regarding effects on the incidence of mechanical ventilation (ventilation continued or initiated beyond one hour after surfactant administration), incidence of bronchopulmonary dysplasia (BPD), chronic lung disease (CLD), mortality, duration of mechanical ventilation, duration of hospitalization, duration of oxygen therapy, duration of respiratory support (including CPAP and nasal cannula), number of patients receiving surfactant, number of surfactant doses administered per patient, incidence of air leak syndromes (pulmonary interstitial emphysema, pneumothorax), patent ductus arteriosus requiring treatment, pulmonary hemorrhage, and other complications of prematurity. Stratified analysis was performed according to inspired oxygen threshold for early intubation and surfactant administration in the treatment group: inspired oxygen within lower (FiO2< 0.45) or higher (FiO2 > 0.45) range at study entry. Treatment effect was expressed as relative risk (RR) and risk difference (RD) for categorical variables, and weighted mean difference (WMD) for continuous variables. MAIN RESULTS: Six randomized controlled clinical trials met selection criteria and were included in this review. In these studies of infants with signs and symptoms of RDS, intubation and early surfactant therapy followed by extubation to nasal CPAP (NCPAP) compared with later selective surfactant administration was associated with a lower incidence of mechanical ventilation [typical RR 0.67, 95% CI 0.57, 0.79], air leak syndromes [typical RR 0.52, 95% CI 0.28, 0.96] and BPD [typical RR 0.51, 95% CI 0.26, 0.99]. A larger proportion of infants in the early surfactant group received surfactant than in the selective surfactant group [typical RR 1.62, 95% CI 1.41, 1.86]. The number of surfactant doses per patient was significantly greater among patients randomized to the early surfactant group [WMD 0.57 doses per patient, 95% CI 0.44, 0.69]. In stratified analysis by FIO2 at study entry, a lower threshold for treatment (FIO2< 0.45) resulted in lower incidence of airleak [typical RR 0.46 and 95% CI 0.23, 0.93] and BPD [typical RR 0.43, 95% CI 0.20, 0.92]. A higher treatment threshold (FIO2 > 0.45) at study entry was associated with a higher incidence of patent ductus arteriosus requiring treatment [typical RR 2.15, 95% CI 1.09, 4.13]. AUTHORS' CONCLUSIONS: Early surfactant replacement therapy with extubation to NCPAP compared with later selective surfactant replacement and continued mechanical ventilation with extubation from low ventilator support is associated with less need mechanical ventilation, lower incidence of BPD and fewer air leak syndromes. A lower treatment threshold (FIO2< 0.45) confers greater advantage in reducing the incidences of airleak syndromes and BPD; moreover a higher treatment threshold (FIO2 at study > 0.45) was associated with increased risk of PDA. These data suggest that treatment with surfactant by transient intubation using a low treatment threshold (FIO2< 0.45) is preferable to later, selective surfactant therapy by transient intubation using a higher threshold for study entry (FIO2 > 0.45) or at the time of respiratory failure and initiation of mechanical ventilation.
背景:与后期选择性使用表面活性剂相比,预防性和早期表面活性剂替代疗法可降低患有呼吸窘迫综合征(RDS)的通气婴儿的死亡率和肺部并发症。然而,表面活性剂给药后持续插管和通气是支气管肺发育不良(BPD)的危险因素。本综述的目的是比较RDS婴儿两种表面活性剂给药策略的结果;预防性或早期给予表面活性剂后迅速拔管,与后期选择性使用表面活性剂后继续机械通气进行比较。 目的:比较RDS或有RDS风险的早产儿的两种治疗策略:早期给予表面活性剂并进行短暂机械通气(少于1小时)后拔管,与后期选择性给予表面活性剂、继续机械通气以及从低呼吸支持水平拔管。考虑了接受早期表面活性剂治疗的两类婴儿:有RDS体征的自主呼吸婴儿(在RDS进展过程中,在因呼吸衰竭需要插管之前接受表面活性剂给药)和RDS高危婴儿(出生后15分钟内接受预防性表面活性剂给药)。 检索策略:检索了牛津围产期试验数据库、MEDLINE(1966年至2006年12月)、CINAHL(1982年至2006年12月第2周)、EMBASE(1980年至2006年12月)、Cochrane对照试验中心注册库(CENTRAL,Cochrane图书馆,2006年第4期)、《儿科研究》(1990年至2006年)、摘要、专家信息提供者并进行了手工检索。未设语言限制。 选择标准:随机或半随机对照临床试验,比较早期给予表面活性剂并计划进行短暂机械通气(少于1小时)后拔管与选择性给予表面活性剂、继续机械通气以及从低呼吸支持水平拔管。 数据收集与分析:收集了关于以下方面的数据:对机械通气发生率(表面活性剂给药后通气持续或开始超过1小时)、支气管肺发育不良(BPD)发生率、慢性肺部疾病(CLD)、死亡率、机械通气持续时间、住院时间、氧疗持续时间、呼吸支持持续时间(包括持续气道正压通气和鼻导管吸氧)、接受表面活性剂治疗的患者数量、每位患者给予的表面活性剂剂量数量、气漏综合征(肺间质气肿、气胸)发生率、需要治疗的动脉导管未闭、肺出血以及其他早产并发症。根据治疗组早期插管和给予表面活性剂时的吸入氧阈值进行分层分析:研究开始时吸入氧在较低范围(FiO2<0.45)或较高范围(FiO2>0.45)。治疗效果以分类变量的相对风险(RR)和风险差值(RD)以及连续变量的加权平均差值(WMD)表示。 主要结果:六项随机对照临床试验符合选择标准并纳入本综述。在这些对有RDS体征和症状婴儿的研究中,插管并早期给予表面活性剂治疗后拔管至鼻持续气道正压通气(NCPAP)与后期选择性给予表面活性剂相比,机械通气发生率较低[典型RR 0.67,95%CI 0.57,0.79]、气漏综合征发生率较低[典型RR 0.52,95%CI 0.28,0.96]以及BPD发生率较低[典型RR 0.51,9%CI 0.26,0.99]。早期表面活性剂组接受表面活性剂治疗的婴儿比例高于选择性表面活性剂组[典型RR 1.62,95%CI 1.41,1.86]。随机分配至早期表面活性剂组的患者每位给予的表面活性剂剂量数量显著更多[WMD每位患者0.57剂,95%CI 0.44,0.69]。根据研究开始时的FiO2进行分层分析,较低的治疗阈值(FiO2<0.45)导致气漏发生率较低[典型RR 0.46,95%CI 0.23,0.93]以及BPD发生率较低[典型RR 0.43,95%CI 0.20,0.92]。研究开始时较高的治疗阈值(FiO2>0.45)与需要治疗的动脉导管未闭发生率较高相关[典型RR 2.15,95%CI 1.09,4.13]。 作者结论:与后期选择性表面活性剂替代治疗并继续机械通气以及从低通气支持水平拔管相比,早期表面活性剂替代治疗并拔管至NCPAP所需机械通气较少,BPD发生率较低且气漏综合征较少。较低的治疗阈值(FiO2<0.4=在降低气漏综合征和BPD发生率方面具有更大优势;此外,较高的治疗阈值(研究开始时FiO2>0.45)与动脉导管未闭风险增加相关。这些数据表明,使用低治疗阈值(FiO2<0.45)通过短暂插管给予表面活性剂治疗优于后期使用较高阈值(研究开始时FiO2>0.45)或在呼吸衰竭和开始机械通气时通过短暂插管进行的选择性表面活性剂治疗。
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