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The Randomized, Controlled Trial of Late Surfactant: Effects on Respiratory Outcomes at 1 Year Corrected Age

R. Keller, E. Eichenwald, A. Hibbs, E. Rogers, Katherine C. Wai, D. Black, P. Ballard, J. Asselin et al.

Jornal de Pediatria, 2017

450 participants · 29 citations

Abstract

Objective 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). Study design 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). Results 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. Conclusion Treatment of newborns of extremely low…

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Evidence Hub reads this as a randomized trial, done in people. Its evidence level is 2 of 5 (High · randomized trial). Randomized trials of a reasonable size are the strongest single-study design. Reported size: 450 participants or records.

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