Related Experiment Videos
Mortality Stratification With Pediatric SOFA and Persistent Inflammation, Immunosuppression, and Catabolism Syndrome
Shin Tsubokura1, Norihiko Tsuboi1, Saki Endo1
1Critical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.
Insights
Combining the pediatric sequential organ failure assessment (pSOFA) score and persistent inflammation, immunosuppression, and catabolism syndrome in pediatrics (PIICS-p) criteria improves mortality risk stratification in critically ill children. This approach identifies high-risk patients early and predicts late mortality.
Area of Science:
- Pediatric critical care medicine
- Clinical risk stratification
- Prognostic modeling
Background:
- Persistent inflammation, immunosuppression, and catabolism syndrome in pediatrics (PIICS-p) criteria identify pediatric intensive care unit (PICU) patients with poor long-term prognosis.
- Pediatric sequential organ failure assessment (pSOFA) score is a validated predictor of short-term mortality in critically ill children.
Purpose of the Study:
- To evaluate the combined utility of pSOFA score and PIICS-p criteria for comprehensive risk stratification in critically ill children.
- To determine if integrating these measures improves prediction of mortality compared to using them individually.
Main Methods:
- A retrospective cohort study included 285 pediatric patients with prolonged PICU stays (≥15 days).
- Patients were assessed on PICU day 14 for high (>8) or low pSOFA scores and stratified by the presence or absence of PIICS-p criteria.
- Primary outcomes included in-hospital mortality and time from PICU day 14 to death.
Main Results:
- Overall mortality was 47% in the high pSOFA group, 32% in the low pSOFA/PIICS-p group, and 10% in the low pSOFA/non-PIICS-p group (p < 0.001).
- High pSOFA (HR 6.33) and low pSOFA/PIICS-p (HR 3.14) were significant independent risk factors for mortality.
- Kaplan-Meier survival analysis revealed significant differences among the three risk groups, with distinct early and late mortality patterns.
Conclusions:
- The integration of pSOFA score and PIICS-p criteria effectively stratifies critically ill children into three distinct mortality risk groups.
- This combined approach allows for early identification of patients at high risk for both short-term and late mortality, even among those initially appearing to have a low acute risk.
Background:
In the previous study, persistent inflammation, immunosuppression, and catabolism syndrome in pediatrics (PIICS-p) criteria identified a subgroup with poor long-term prognosis. Pediatric sequential organ failure assessment (pSOFA) score is a well-known predictor of short-term mortality. We hypothesized that combining the pSOFA score and PIICS-p criteria could provide more comprehensive risk stratification.
Methods:
We conducted a retrospective cohort study in a PICU. Included were 285 eligible patients aged zero to 19 years with 15 days or longer of PICU stay between January 2019 and December 2023. The primary outcomes were death during the observation period and time from PICU day 14 to death. Patients were classified on PICU day 14: high pSOFA (> 8) or low, subsequently stratified by PIICS-p or not.
Results:
The overall mortality rate was 47% (35/75) in high pSOFA, 32% (8/25) in low pSOFA/PIICS-p, and 10% (18/185) in low pSOFA/non-PIICS-p group (p < 0.001). In a multivariable Cox proportional hazards model, high pSOFA (HR 6.33, 95% CI 3.43-11.7, p < 0.001) and low pSOFA/PIICS-p (HR 3.14, 95% CI 1.28-7.69, p = 0.012) were identified as significant risk factors for mortality. The Kaplan-Meier curves showed significant differences among the three groups (p < 0.001). The high pSOFA group showed an early decline in survival. Survival in the low pSOFA/PIICS-p group was lower than that in the low pSOFA/non-PIICS-p group, and the difference widened over time.
Conclusion:
Integration of pSOFA and PIICS-p enables three-group mortality stratification in critically ill children and early recognition of late-mortality risk among those who appear low risk acutely.
Related Concept Videos
Immunodeficiency Diseases
There are three main causes of immunodeficiency disorders...
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Pulmonary Tuberculosis I
Causative Organism
The primary infectious agent causing tuberculosis is Mycobacterium tuberculosis, a slow-growing, acid-fast, aerobic rod that exhibits sensitivity to heat and ultraviolet light. Instances of Mycobacterium bovis and Mycobacterium avium contributing to the development of TB infection are rare.
Mode of...
Chronic Inflammation: Introduction
Inflammatory Bowel Disease III: Crohn's Disease
Chronic Obstructive Pulmonary Disease III: Chronic Bronchitis Features