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Effect of a modified fluid therapy on renal function during indomethacin therapy for persistent ductus arteriosus

J U Leititis1, R Burghard, N Gordjani

  • 1Department of Paediatrics, Philipps-University, Marburg, FRG.

Insights

Preterm infants receiving a specific fluid rehydration before indomethacin treatment showed preserved renal function. This approach also aided in closing the persistent ductus arteriosus, minimizing adverse effects in neonates.

Area of Science:

  • Neonatal Medicine
  • Pediatric Nephrology
  • Pharmacology

Background:

  • Persistent ductus arteriosus (PDA) is common in premature infants.
  • Indomethacin is frequently used to treat PDA but can cause adverse renal effects.
  • Neonatal renal function is sensitive to hemodynamic changes and medications.

Purpose of the Study:

  • To evaluate the effect of a pre-administration fluid regimen on indomethacin's renal toxicity in premature infants with PDA.
  • To assess renal function and ductal closure rates with the modified fluid protocol.

Main Methods:

  • Premature infants with PDA received a 6-hour pre-treatment rehydration (7 ml/kg/h).
  • Indomethacin was administered post-rehydration, with a 36-hour observation period.
  • Renal function markers (serum creatinine, electrolytes, urinary flow, creatinine clearance, fractional sodium excretion) were monitored.

Main Results:

  • The fluid regimen prevented adverse renal effects of indomethacin.
  • No significant changes in serum creatinine, sodium, or potassium were observed.
  • A reduction in fractional sodium excretion was the primary significant finding, suggesting suppressed vasoconstriction.
  • Ductal closure was achieved in 7 out of 10 treatment courses without cardiovascular side effects.

Conclusions:

  • A pre-administration fluid load effectively mitigates indomethacin-induced renal dysfunction in preterm neonates with PDA.
  • This modified fluid regimen supports ductal closure while preserving renal function and avoiding cardiovascular complications.
  • The findings suggest a potential role for fluid management in optimizing indomethacin therapy for PDA.

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