Am J Perinatol 2016; 33(07): 671-677
DOI: 10.1055/s-0035-1571201
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Pulmonary Vein Stenosis in Neonates with Severe Bronchopulmonary Dysplasia

Autoren

  • Natasha L. Swier

    1   Division of Neonatology, The Ohio State University Wexner Medical Center, Columbus, Ohio
  • Bernadette Richards

    2   The Heart Center at Nationwide Children's Hospital, Columbus, Ohio
  • Clifford L. Cua

    2   The Heart Center at Nationwide Children's Hospital, Columbus, Ohio
  • Susan K. Lynch

    1   Division of Neonatology, The Ohio State University Wexner Medical Center, Columbus, Ohio
  • Han Yin

    4   Department of Biostatistics, Nationwide Children's Hospital Research Center, Columbus, Ohio
  • Leif D. Nelin

    1   Division of Neonatology, The Ohio State University Wexner Medical Center, Columbus, Ohio
    3   Center for Perinatal Research, Research Institute at Nationwide Children's Hospital, Columbus, Ohio
  • Charles V. Smith

    5   Seattle Children's Research Institute, University of Washington School of Medicine, Seattle, Washington
  • Carl H. Backes

    1   Division of Neonatology, The Ohio State University Wexner Medical Center, Columbus, Ohio
    2   The Heart Center at Nationwide Children's Hospital, Columbus, Ohio
    3   Center for Perinatal Research, Research Institute at Nationwide Children's Hospital, Columbus, Ohio
Weitere Informationen

Publikationsverlauf

29. Juli 2015

25. November 2015

Publikationsdatum:
10. Februar 2016 (online)

Abstract

Objectives Pulmonary vein stenosis (PVS) is a rare, often lethal anomaly associated with poor outcomes. Given the association between bronchopulmonary dysplasia (BPD) and cardiovascular complications, we tested the hypotheses that (1) a subgroup of neonates with severe BPD develop PVS (BPD-PVS) and have worse outcomes than do neonates with severe BPD alone (BPD); (2) among a cohort of neonates with severe BPD-associated pulmonary hypertension (BPD-PH), PVS is an additional risk factor for adverse outcomes and mortality.

Study Design We performed a retrospective review of neonates with severe BPD, based on the Eunice Kennedy Shriver National Institute of Child Health and Development (NICHD) criteria, at our institution between June 1, 2009, and June 30, 2013. PVS was determined based on serial review of echocardiograms performed during their hospitalization. Neonates with congenital heart disease or chromosomal anomalies were excluded.

Results Of 213 patients with severe BPD, 10 (4.7%) were found to have PVS (BPD-PVS). Neonates with BPD-PVS had lower birth weight (634 ± 178 vs. 767 ± 165 g; p < 0.01) and were more likely to be intrauterine growth restricted (80 vs. 11%; p < 0.01) than neonates with BPD alone. Time on mechanical ventilation and length of hospitalization were longer in the BPD-PVS group than BPD group. Survival was lower in the BPD-PVS group than BPD group (5/10 [50%] vs. 196/203 [97%]; log-rank test p < 0.01). Among a subgroup of neonates with BPD-PH, survival was lower among infants with PVS than those without PVS (5/9 [56%] vs. 26/30 [86%]; log-rank test p = 0.01).

Conclusions Compared with neonates with severe BPD alone, those with acquired PVS are at increased risk for worse outcomes, including higher mortality. Evidence-based recommendations regarding screening protocols and surveillance are needed in this high-risk subgroup of BPD neonates.