Effect of PMX-DHP for sepsis due to ESBL-producing E. coli in an extremely low-birthweight infant

Naoto Nishizaki1, Mayu Nakagawa1, Satoshi Hara1

  • 1Department of Pediatrics, Juntendo University Urayasu Hospital, Chiba, Japan.

Insights

A preterm infant with early-onset sepsis caused by extended-spectrum β-lactamase-producing Escherichia coli survived. Treatment included meropenem and polymyxin B hemoperfusion, showing potential for severe neonatal sepsis.

Area of Science:

  • Neonatal Medicine
  • Infectious Diseases
  • Pharmacology

Background:

  • Early-onset sepsis in preterm infants poses significant mortality risks.
  • Extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae infections present treatment challenges due to antibiotic resistance.
  • Extremely low-birthweight infants are particularly vulnerable to severe infections.

Observation:

  • A case of early-onset sepsis in a preterm infant (601g) caused by ESBL-producing Escherichia coli (CTX-M type) is presented.
  • The infant received meropenem for antibiotic treatment.
  • Polymyxin B-immobilized fiber treatment was administered for endotoxin absorption with a minimal priming volume (8 mL).

Findings:

  • The patient survived the severe sepsis without short-term neurological or respiratory complications.
  • Successful management highlights the importance of appropriate antibiotic selection for ESBL infections in neonates.
  • Polymyxin B hemoperfusion demonstrated potential efficacy in managing severe neonatal sepsis.

Implications:

  • This case suggests polymyxin B hemoperfusion may be an innovative therapeutic option for severe neonatal sepsis.
  • The treatment approach could improve outcomes in extremely low-birthweight infants with multidrug-resistant organism infections.
  • Further research into polymyxin B hemoperfusion for neonatal sepsis is warranted.

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