Complications associated with the current sequential pharmacological management of early postnatal hypotension in

Rita P Verma1, Shaeequa Dasnadi2, Yuan Zhao3

  • 1Division of Neonatology, Department of Pediatrics, Nassau University Medical CenterEast MeadowNew York.

Proceedings (Baylor University. Medical Center)
|August 7, 2019
PubMed

Insights

Treating hypotension in premature infants with vasopressor-inotropes (VI) or hydrocortisone (HCVI) increases risks for serious complications. These infants face higher rates of intraventricular hemorrhage, bronchopulmonary dysplasia, and patent ductus arteriosus.

Area of Science:

  • Neonatal Medicine
  • Pediatric Pharmacology
  • Critical Care Pediatrics

Background:

  • Early postnatal hypotension is common in extremely low-birth-weight infants (ELBWIs).
  • Standard treatment involves vasopressor-inotropes (VI), with hydrocortisone (HCVI) added if VI fails.
  • Adverse effects of these treatments are not well-documented.

Purpose of the Study:

  • To compare complications of VI and HCVI treatments in ELBWIs.
  • To identify risks associated with hypotension management in premature infants.

Main Methods:

  • Retrospective case-control study.
  • Compared ELBWIs (≤1000 g) receiving VI or HCVI with medication-naïve controls.
  • Utilized univariate and multivariate analyses.

Main Results:

  • VI treatment was associated with increased risks of patent ductus arteriosus, intraventricular-periventricular hemorrhage, spontaneous intestinal perforation, ventriculomegaly, and bronchopulmonary dysplasia.
  • HCVI treatment also showed higher risks for intraventricular-periventricular hemorrhage, bronchopulmonary dysplasia, air leaks, and patent ductus arteriosus compared to controls.
  • Maternal diabetes mellitus was linked to increased hypotension, while maternal hypertension showed a trend towards lower VI-refractory hypotension.

Conclusions:

  • Hypotensive ELBWIs treated with VI or HCVI are susceptible to intraventricular-periventricular hemorrhage, bronchopulmonary dysplasia, and patent ductus arteriosus.
  • VI therapy is further associated with risks of spontaneous intestinal perforation and ventriculomegaly.
  • Understanding these risks is crucial for optimizing hypotension management in premature infants.

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