Evidence map›Paper›PMID 42438862›Full record

ArticlePediatrics international : official journal of the Japan Pediatric Society

Mortality Stratification With Pediatric SOFA and Persistent Inflammation, Immunosuppression, and Catabolism Syndrome.

Shin Tsubokura, Norihiko Tsuboi, Saki Endo, Eisaku Nashiki, Soichiro Tanimura, Shotaro Matsumoto

Abstract read
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Article in Pediatrics international : official journal of the Japan Pediatric Society. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Shin TsubokuraCritical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4343-8654
Norihiko TsuboiCritical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.ORCID https://orcid.org/0000-0002-7444-8137
Saki EndoCritical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.
Eisaku NashikiCritical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.
Soichiro TanimuraCritical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.ORCID https://orcid.org/0009-0004-4666-2437
Shotaro MatsumotoCritical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.ORCID https://orcid.org/0000-0002-4995-8442

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn 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.

methodsWe 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.

resultsThe 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.

conclusionIntegration 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.

Indexed as

InflammationOrgan Dysfunction ScoresAdolescentChildChild, PreschoolCritical IllnessFemaleHumansInfantInfant, NewbornIntensive Care Units, PediatricMaleMultiple Organ FailurePrognosisRetrospective StudiesRisk Assessmentchild mortalitycritical illnessintensive care unitsorgan dysfunction scoresprediction algorithms

Identifiers

PMID42438862
PMCPMC13358464

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.