Am J Perinatol 2018; 35(02): 120-126
DOI: 10.1055/s-0037-1606189
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Role of Early Pulmonary Hypertension as a Risk Factor for Late Pulmonary Hypertension in Extremely Preterm Infants

Dinushan C. Kaluarachchi
1   Department of Pediatrics, University of Wisconsin-Madison, Madison, Wisconsin
,
Kaitlin M. Woo
2   Department of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, Wisconsin
,
Tarah T. Colaizy
3   Department of Pediatrics, University of Iowa, Iowa City, Iowa
› Author Affiliations
Further Information

Publication History

11 April 2017

21 July 2017

Publication Date:
24 August 2017 (online)

Abstract

Objective The evidence on the role of early pulmonary vascular disease (PVD) in the development of late pulmonary hypertension (PH) in the extremely preterm infants is limited. Objectives were to determine the incidence of early and late PH in extreme preterm infants and to evaluate the role of early PH as a risk factor for development of clinically detected late PH.

Methods It was a retrospective analysis of early echocardiograms (day of life 5–14) in preterm infants, 22 to 27 weeks' gestation, admitted to the University of Iowa NICU between July 01, 2012 to June 30, 2015. Late echocardiograms performed for clinical suspicion of PH were also analyzed.

Results A total of 154 infants were included in the study. Early PH was diagnosed in 31 (20%) infants. Twenty-four (16%) infants were evaluated for clinically suspected PH. Eight (5%) infants were diagnosed with late PH. Infants with early PH had echocardiograms performed earlier than infants without the evidence of early PH. Early PH was not associated with the development of late PH (p = 0.99).

Conclusion Early PH is common among extremely preterm infants (20%). Five percent of infants had clinically detected late PH. Infants with early PH had echocardiograms performed earlier than infants without the evidence of early PH. Early PH was not associated with the development of clinically detected late PH.

Funding

None.


 
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