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Updated: Mar 28, 2026

A Neonatal Imaging Model of Gram-Negative Bacterial Sepsis
Published on: August 12, 2020
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.
Abstract:
We report a case of early onset sepsis caused by (CTX for cefotaximase and M for Munich)-type extended-spectrum β-lactamase-producing Escherichia coli (ESBL E. coli) in a preterm infant weighing 601 g. He was given meropenem and treated for endotoxin absorption with polymyxin B-immobilized fibers with only 8 mL of priming volume. The patient survived without any short-term neurological or respiratory sequelae. The choice of antibiotics is particularly important in seriously ill neonates with sepsis due to ESBL-producing organisms. Polymyxin B hemoperfusion might be an innovative therapy for severe neonatal sepsis and could improve outcome even in an extremely low-birthweight infant.
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