Drotrecogin alpha (activated) in neonatal septic shock

David Frommhold1, Alexandra Birle, Otwin Linderkamp

  • 1Division of Neonatology, Department of Paediatrics, University of Heidelberg Medical School, Heidelberg, Germany. david_frommhold@med.uni-heidelberg.de

Insights

Recombinant human activated protein C (rhAPC) effectively treated group B streptococcal septic shock in a neonate. The infant recovered fully within 14 days with no adverse effects from the treatment.

Area of Science:

  • Neonatal intensive care
  • Pharmacology
  • Hematology

Background:

  • Group B Streptococcus (GBS) is a leading cause of neonatal sepsis and septic shock.
  • Septic shock in neonates carries a high mortality rate.
  • Activated protein C (APC) plays a crucial role in regulating coagulation and inflammation.

Observation:

  • A 12-day-old neonate presented with severe GBS septic shock.
  • The neonate received an infusion of recombinant human activated protein C (rhAPC) at a dose of 24 microg/kg/h for 96 hours.
  • Protein C activity levels increased significantly from 5% to 53% during rhAPC therapy.

Findings:

  • The neonate demonstrated a complete clinical recovery within 14 days of rhAPC treatment.
  • No adverse events or complications were observed during or after the rhAPC infusion.
  • rhAPC therapy normalized protein C activity, suggesting restoration of anticoagulant pathways.

Implications:

  • This case suggests that rhAPC may be a safe and effective therapeutic option for neonates with GBS septic shock.
  • Further research is warranted to explore the efficacy and safety of rhAPC in larger neonatal populations with sepsis.
  • Targeting coagulation pathways with rhAPC could offer a novel treatment strategy for severe neonatal infections.

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