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Patent ductus arteriosus, tracheal ventilation, and the risk of bronchopulmonary dysplasia.
Clyman, Ronald I; Hills, Nancy K; Cambonie, Gilles; Debillon, Thierry; Ligi, Isabelle; Gascoin, Geraldine; Patkai, Juliana; Beuchee, Alain; Favrais, Geraldine; Durrmeyer, Xavier; Flamant, Cyril; Rozé, Jean Christophe.
  • Clyman RI; Department of Pediatrics and Cardiovascular Research Institute, University of California San Francisco, San Francisco, CA, USA. clymanr@peds.ucsf.edu.
  • Hills NK; Departments of Epidemiology and Biostatistics, and Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Cambonie G; Neonatal Medicine, Montpellier University Hospital, Montpellier, France.
  • Debillon T; Department of Neonatalogy, University Hospital of Grenoble, Grenoble, France.
  • Ligi I; Department of Neonatalogy, Assitance Publique Hôpitaux de Marseille, Marseille, France.
  • Gascoin G; Neonatal Medicine, Angers University Hospital, Angers, France.
  • Patkai J; Neonatal Intensive Care Unit, Cochin Hospital Maternity of Port-Royal, Paris, France.
  • Beuchee A; Department of Neonatalogy, Rennes University Hospital, Rennes, France.
  • Favrais G; Department of Neonatalogy, Tours University Hospital, Tours, France.
  • Durrmeyer X; Department of Neonatalogy, Centre Hospitalier Intercommunal de Créteil, Créteil, France.
  • Flamant C; Faculté de Médecine de Créteil, Université Paris Est Créteil, IMRB, GRC CARMAS, Créteil, France.
  • Rozé JC; Department of Neonatalogy, Nantes University Hospital, Nantes, France.
Pediatr Res ; 91(3): 652-658, 2022 02.
Article en En | MEDLINE | ID: mdl-33790415
ABSTRACT

BACKGROUND:

An increased risk for bronchopulmonary dysplasia (BPD) exists when moderate-to-large patent ductus arteriosus shunts (hsPDA) persist beyond 14 days. GOAL To examine the interaction between prolonged exposures to tracheal ventilation (≥10 days) and hsPDA on the incidence of BPD in infants <28 weeks gestation. STUDY

DESIGN:

Predefined definitions of prolonged ventilation (≥10 days), hsPDA (≥14 days), and BPD (room air challenge test at 36 weeks) were used to analyze deidentified data from the multicenter TRIOCAPI RCT in a secondary analysis of the trial.

RESULTS:

Among 307 infants who survived >14 days, 41 died before 36 weeks. Among survivors, 93/266 had BPD. The association between BPD and hsPDA depended on the length of intubation. In multivariable analyses, prolonged hsPDA shunts were associated with increased BPD (odds ratio (OR) (95% confidence interval (CI)) = 3.00 (1.58-5.71)) when infants required intubation for ≥10 days. In contrast, there was no significant association between hsPDA exposure and BPD when infants were intubated <10 days (OR (95% CI) = 1.49 (0.98-2.26)). A similar relationship between prolonged hsPDA and length of intubation was found for BPD/death (n = 307) infants intubated ≥10 days OR (95% CI) = 2.41 (1.47-3.95)); infants intubated <10 days OR (95% CI) = 1.37 (0.86-2.19)).

CONCLUSIONS:

Moderate-to-large PDAs were associated with increased risks of BPD and BPD/death-but only when infants required intubation ≥10 days. IMPACT Infants with a moderate-to-large hsPDA that persist beyond 14 days are only at risk for developing BPD if they also receive prolonged tracheal ventilation for ≥10 days. Infants who receive less ventilatory support (intubation for <10 days) have the same incidence of BPD whether the ductus closes shortly after birth or whether it persists as a moderate-to-large shunt for several weeks. Early PDA closure may be unnecessary in infants who require short durations of intubation since the PDA does not seem to alter the incidence of BPD in infants who require intubation for <10 days.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Displasia Broncopulmonar / Conducto Arterioso Permeable Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Infant / Newborn Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Displasia Broncopulmonar / Conducto Arterioso Permeable Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Infant / Newborn Idioma: En Año: 2022 Tipo del documento: Article