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Spontaneous closure of the patent ductus arteriosus in very low birth weight infants following discharge from the neonatal unit
  1. K Herrman,
  2. C Bose,
  3. K Lewis,
  4. M Laughon
  1. Department of Pediatrics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA
  1. Matthew Laughon, Division of Neonatal-Perinatal Medicine, CB # 7596, UNC Hospital, Chapel Hill, North Carolina 27599-7596, USA; matt_laughon{at}med.unc.edu

Abstract

Objective: To determine the incidence of spontaneous closure of the patent ductus arteriosus (PDA) and the use of medical therapies for treatment of PDA-related conditions among very low birth weight (VLBW) infants with ductal patency at the time of initial hospital discharge.

Study design: We conducted a single-centre, retrospective, observational study of VLBW infants (birth weight <1500 g) born during 2004 and 2005 and discharged with a PDA. PDA was defined by echocardiographic and/or clinical criteria. We identified the related discharge needs, subsequent interventions, and the post-menstrual age (PMA) at which there was no longer evidence of a PDA.

Results: Three hundred and ninety one VLBW infants were admitted; 310 survived to discharge. Ninety five were diagnosed with a PDA during their hospitalisations; 21 had a PDA at discharge (10 received indomethacin, 11 were never treated). Among these, mean gestational age was 28 weeks, mean birth weight was 998 g, and median duration of hospitalisation was 73 days. Two infants were discharged on oxygen, two on diuretics, and two on both. None had congestive heart failure, and none died during infancy. Spontaneous closure occurred in 18 of 21 infants at a median PMA of 48 weeks (range 34–76; interquartile range 46–56). Two infants had coil occlusion at 11 months of age. One patient had a PDA at 14 months of age.

Conclusions: Among a select group of VLBW infants with a PDA at initial hospital discharge, spontaneous closure during early infancy occurred in most infants.

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Footnotes

  • Funding: Funded in part by a research grant received as part of a Professional Development Award by Pediatrix Medical Group.

  • Competing interests: None.

  • Ethics approval: This study was approved by the Biomedical Institutional Review Board of the University of North Carolina at Chapel Hill.

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