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Feasibility and Effect of Physiological-Based CPAP in Preterm Infants at Birth.
Martherus, Tessa; Kuypers, Kristel L A M; Böhringer, Stefan; Dekker, Janneke; Witlox, Ruben S G M; Hooper, Stuart B; Te Pas, Arjan B.
Afiliación
  • Martherus T; Division of Neonatology, Department of Pediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, Netherlands.
  • Kuypers KLAM; Division of Neonatology, Department of Pediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, Netherlands.
  • Böhringer S; Department of Biomedical Data Sciences, Leiden University Medical Center, Leiden, Netherlands.
  • Dekker J; Division of Neonatology, Department of Pediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, Netherlands.
  • Witlox RSGM; Division of Neonatology, Department of Pediatrics, Willem-Alexander Children's Hospital, Leiden University Medical Center, Leiden, Netherlands.
  • Hooper SB; The Ritchie Centre, Hudson Institute of Medical Research, Melbourne, VIC, Australia.
  • Te Pas AB; Department of Obstetrics and Gynecology, Monash University, Melbourne, VIC, Australia.
Front Pediatr ; 9: 777614, 2021.
Article en En | MEDLINE | ID: mdl-34926350
ABSTRACT

Background:

Preterm infants are commonly supported with 5-8 cmH2O CPAP. However, animal studies demonstrate that high initial CPAP levels (12-15 cmH2O) which are then reduced (termed physiological based (PB)-CPAP), improve lung aeration without adversely affecting cardiovascular function. We investigated the feasibility of PB-CPAP and the effect in preterm infants at birth.

Methods:

Preterm infants (24-30 weeks gestation) were randomized to PB-CPAP or 5-8 cmH2O CPAP for the first 10 min after birth. PB-CPAP consisted of 15 cmH2O CPAP that was decreased when infants were stabilized (heart rate ≥100 bpm, SpO2 ≥85%, FiO2 ≤ 0.4, spontaneous breathing) to 8 cmH2O with steps of ~2/3 cmH2O/min. Primary outcomes were feasibility and SpO2 in the first 5 min after birth. Secondary outcomes included physiological and breathing parameters and short-term neonatal outcomes. Planned enrollment was 42 infants.

Results:

The trial was stopped after enrolling 31 infants due to a low inclusion rate and recent changes in the local resuscitation guideline that conflict with the study protocol. Measurements were available for analysis in 28 infants (PB-CPAP n = 8, 5-8 cmH2O n = 20). Protocol deviations in the PB-CPAP group included one infant receiving 3 inflations with 15 cmH2O PEEP and two infants in which CPAP levels were decreased faster than described in the study protocol. In the 5-8 cmH2O CPAP group, three infants received 4, 10, and 12 cmH2O CPAP. During evaluations, caregivers indicated that the current PB-CPAP protocol was difficult to execute. The SpO2 in the first 5 min after birth was not different [61 (49-70) vs. 64 (47-74), p = 0.973]. However, infants receiving PB-CPAP achieved higher heart rates [121 (111-130) vs. 97 (82-119) bpm, p = 0.016] and duration of mask ventilation was shorter [042 (034-222) vs. 258 (136-603) min, p = 0.020]. Infants in the PB-CPAP group required 636 (549-1103) min to stabilize, compared to 957 (658-1506) min in the 5-8 cmH2O CPAP group (p = 0.256). There were no differences in short-term outcomes.

Conclusion:

Stabilization of preterm infants with PB-CPAP is feasible but tailoring CPAP appeared challenging. PB-CPAP did not lead to higher SpO2 but increased heart rate and shortened the duration of mask ventilation, which may reflect faster lung aeration.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Front Pediatr Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: Front Pediatr Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos