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Updated: Apr 11, 2026

A Controlled Mouse Model for Neonatal Polymicrobial Sepsis
Published on: January 27, 2019
Risk factors for sepsis-related death in children and adolescents with hematologic and malignant diseases
Hirozumi Sano1, Ryoji Kobayashi1, Akihiro Iguchi2
1Department of Pediatrics, Sapporo Hokuyu Hospital, Sapporo, Japan.
Insights
Pediatric patients with hematologic malignancies experiencing sepsis have higher mortality risk if their disease has relapsed, is refractory, or shows high C-reactive protein levels. Early vancomycin may improve survival in these high-risk sepsis cases.
Area of Science:
- Pediatric Hematology
- Oncology
- Infectious Diseases
- Critical Care Medicine
Background:
- Sepsis poses a significant mortality risk in pediatric patients with hematologic and malignant disorders.
- Identifying specific risk factors is crucial for improving outcomes in this vulnerable population.
Purpose of the Study:
- To elucidate the risk factors associated with mortality in pediatric patients diagnosed with sepsis and underlying hematologic or malignant conditions.
- To identify clinical and laboratory features that predict sepsis-related death in this patient cohort.
Main Methods:
- A retrospective analysis of 134 sepsis episodes in 90 pediatric patients (June 2006-March 2014) with hematologic/malignant diseases.
- Comparison of clinical and laboratory features between patients who died within 14 days of sepsis onset (sepsis-related death) and survivors.
- Univariate and multivariate analyses were employed to identify significant risk factors for mortality.
Main Results:
- Relapsed or refractory underlying disease and high C-reactive protein (CRP) levels (≥50 mg/L) at fever onset were significant predictors of sepsis-related death (p<0.01).
- Hematopoietic stem cell transplantation and changes in initial antibiotic therapy were also associated with increased mortality risk.
- Gram-positive cocci resistant to beta-lactam antibiotics, but sensitive to vancomycin, accounted for over half of sepsis-related deaths.
Conclusions:
- A history of relapse, refractory disease state, and elevated CRP levels at fever onset are key risk factors for sepsis mortality in pediatric cancer patients.
- Early administration of vancomycin may enhance survival rates for pediatric patients with hematologic malignancies who develop sepsis and present with identified risk factors.
Background:
The aim of this study was to elucidate risk factors for mortality after developing sepsis in pediatric patients with hematologic and malignant disorders.
Methods:
A total of 90 patients (43 boys, 47 girls) with various hematologic and malignant diseases who experienced sepsis between June 2006 and March 2014 were enrolled. Clinical and laboratory features of 134 episodes of sepsis observed in the 90 patients were compared between those with and without sepsis-related death which was defined as death within 14 days after sepsis.
Results:
Age at hospitalization, sex, and type of underlying disease did not differ between patients with and without sepsis-related death. Sepsis episode-based univariate analysis identified patients with a history of relapse or in a refractory state of underlying disease (p<0.01), those with high C-reactive protein concentrations (≥50 mg/L) at the beginning of fever (p<0.01), those who had undergone hematopoietic stem cell transplantation (p<0.01), and those who were forced to change initial antibiotics (p = 0.02) because of being at high risk of sepsis-related death. The former two factors were further confirmed by multivariate analysis. More than half (52.9%) the isolates from sepsis-related death were Gram-positive cocci resistant to β-lactam antibiotics, but susceptible to vancomycin.
Conclusion:
It was found that a history of relapse, a refractory state of underlying disease, and high C-reactive protein concentrations at the beginning of fever were significant risk factors for mortality after developing sepsis. Survival rate of patients with risk factors raised in this study might be improved by early introduction of vancomycin.
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