Keller Roberta L, Eichenwald Eric C, Hibbs Anna Maria, Rogers Elizabeth E, Wai Katherine C, Black Dennis M, Ballard Philip L, Asselin Jeanette M, Truog William E, Merrill Jeffrey D, Mammel Mark C, Steinhorn Robin H, Ryan Rita M, Durand David J, Bendel Catherine M, Bendel-Stenzel Ellen M, Courtney Sherry E, Dhanireddy Ramasubbareddy, Hudak Mark L, Koch Frances R, Mayock Dennis E, McKay Victor J, Helderman Jennifer, Porta Nicolas F, Wadhawan Rajan, Palermo Lisa, Ballard Roberta A
Department of Pediatrics, University of California San Francisco, San Francisco, CA.
Department of Pediatrics, University of Texas, Houston, TX.
J Pediatr. 2017 Apr;183:19-25.e2. doi: 10.1016/j.jpeds.2016.12.059. Epub 2017 Jan 16.
To determine the effects of late surfactant on respiratory outcomes determined at 1-year corrected age in the Trial of Late Surfactant (TOLSURF), which randomized newborns of extremely low gestational age (≤28 weeks' gestational age) ventilated at 7-14 days to late surfactant and inhaled nitric oxide vs inhaled nitric oxide-alone (control).
Caregivers were surveyed in a double-blinded manner at 3, 6, 9, and 12 months' corrected age to collect information on respiratory resource use (infant medication use, home support, and hospitalization). Infants were classified for composite outcomes of pulmonary morbidity (no PM, determined in infants with no reported respiratory resource use) and persistent PM (determined in infants with any resource use in ≥3 surveys).
Infants (n = 450, late surfactant n = 217, control n = 233) were 25.3 ± 1.2 weeks' gestation and 713 ± 164 g at birth. In the late surfactant group, fewer infants received home respiratory support than in the control group (35.8% vs 52.9%, relative benefit [RB] 1.28 [95% CI 1.07-1.55]). There was no benefit of late surfactant for No PM vs PM (RB 1.27; 95% CI 0.89-1.81) or no persistent PM vs persistent PM (RB 1.01; 95% CI 0.87-1.17). After adjustment for imbalances in baseline characteristics, relative benefit of late surfactant treatment increased: RB 1.40 (95% CI 0.89-1.80) for no PM and RB 1.24 (95% CI 1.08-1.42) for no persistent PM.
Treatment of newborns of extremely low gestational age with late surfactant in combination with inhaled nitric oxide decreased use of home respiratory support and may decrease persistent pulmonary morbidity.
ClinicalTrials.gov: NCT01022580.
在晚期表面活性剂试验(TOLSURF)中,确定晚期表面活性剂对出生后1年矫正年龄时呼吸结局的影响。该试验将孕龄极低(≤28周)且在7 - 14天接受机械通气的新生儿随机分为晚期表面活性剂联合吸入一氧化氮组和单纯吸入一氧化氮组(对照组)。
在矫正年龄3、6、9和12个月时,以双盲方式对照顾者进行调查,收集呼吸资源使用情况(婴儿用药、家庭支持和住院情况)的信息。根据肺部疾病复合结局对婴儿进行分类(无肺部疾病,在未报告有呼吸资源使用的婴儿中确定;持续性肺部疾病,在≥3次调查中有任何资源使用的婴儿中确定)。
婴儿(n = 450,晚期表面活性剂组n = 217,对照组n = 233)出生时孕龄为25.3 ± 1.2周,出生体重为713 ± 164克。晚期表面活性剂组中,接受家庭呼吸支持的婴儿少于对照组(35.8%对52.9%,相对获益[RB] 1.28 [95% CI 1.07 - 1.55])。晚期表面活性剂对无肺部疾病与有肺部疾病(RB 1.27;95% CI 0.89 - 1.81)或无持续性肺部疾病与有持续性肺部疾病(RB 1.01;95% CI 0.87 - 1.17)均无益处。在对基线特征的不平衡进行调整后,晚期表面活性剂治疗的相对获益增加:无肺部疾病时RB为1.40(95% CI 0.89 - 1.80),无持续性肺部疾病时RB为1.24(95% CI 1.08 - 1.42)。
对孕龄极低的新生儿使用晚期表面活性剂联合吸入一氧化氮治疗可减少家庭呼吸支持的使用,并可能降低持续性肺部疾病的发生率。
ClinicalTrials.gov:NCT01022580。