Platelet Transfusion for PDA Closure in Preterm Infants: A Randomized Controlled Trial

Jogender Kumar1, Sourabh Dutta2, Venkataseshan Sundaram1

  • 1Newborn Unit, Departments of Pediatrics.

Pediatrics
|April 4, 2019
PubMed

Insights

Liberal platelet transfusions did not speed up patent ductus arteriosus (PDA) closure in preterm infants with low platelets. This approach also increased the risk of intraventricular hemorrhage in these neonates.

Area of Science:

  • Neonatal Medicine
  • Pediatric Cardiology
  • Hematology

Background:

  • Thrombocytopenia, a common complication in preterm infants, is linked to delayed closure of patent ductus arteriosus (PDA).
  • Limited research exists on the efficacy of platelet transfusions for treating PDA in this vulnerable population.

Purpose of the Study:

  • To compare the effectiveness of liberal versus standard platelet transfusion criteria in achieving earlier closure of hemodynamically significant PDA (hs-PDA).
  • To evaluate the impact of liberal platelet transfusion on time to PDA closure in thrombocytopenic preterm neonates.

Main Methods:

  • A randomized controlled trial involving thrombocytopenic preterm neonates (<35 weeks' gestation) with hs-PDA.
  • Patients were assigned to either liberal (platelet count >100,000/µL) or standard transfusion groups.
  • Echocardiography monitored PDA closure, with survival analysis used for primary outcome comparison.

Main Results:

  • Median time to PDA closure was similar between liberal (72 hours) and standard (72 hours) transfusion groups (P=.697).
  • Liberal platelet transfusion did not significantly hasten PDA closure.
  • A higher incidence of intraventricular hemorrhage was observed in the liberal transfusion group (41%) compared to the standard group (4.5%, P=.009).

Conclusions:

  • Liberal platelet transfusion strategies do not accelerate PDA closure in thrombocytopenic preterm neonates.
  • The findings suggest that liberal platelet transfusions may increase the risk of adverse events like intraventricular hemorrhage without providing clinical benefit for PDA closure.
Abstract

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