Evidence map›Paper›PMID 40153553›Full record

ArticleCritical care explorations2025

Performance of Pediatric Risk of Mortality IV in Brazilian PICUs: A Multicenter Prospective Study.

Gustavo Rodrigues-Santos, Arnaldo Prata-Barbosa, Fernanda Lima-Setta, Pedro Henrique Nunes Costa Silami, Mariana Barros Genuíno de Oliveira, Jaqueline Rodrigues Robaina, José Colleti Júnior, Felipe Rezende Caino de Oliveira, Luís Fernando Andrade de Carvalho, Mariana Digiovanni and 11 more

Abstract readMulticenter Study
In one paragraph

Article in Critical care explorations, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Gustavo Rodrigues-SantosDepartment of Epidemiology, Institute of Social Medicine, State University of Rio de Janeiro, Brazil.ORCID 0000-0001-7947-8207
Arnaldo Prata-BarbosaDepartment of Pediatrics, D'Or Institute for Research and Education (IDOR), Rio de Janeiro, RJ, Brazil.
Fernanda Lima-SettaDepartment of Pediatrics, D'Or Institute for Research and Education (IDOR), Rio de Janeiro, RJ, Brazil.
Pedro Henrique Nunes Costa SilamiDepartment of Pediatrics, D'Or Institute for Research and Education (IDOR), Rio de Janeiro, RJ, Brazil.
Mariana Barros Genuíno de OliveiraDepartment of Pediatrics, D'Or Institute for Research and Education (IDOR), Rio de Janeiro, RJ, Brazil.
Jaqueline Rodrigues RobainaDepartment of Pediatrics, D'Or Institute for Research and Education (IDOR), Rio de Janeiro, RJ, Brazil.
José Colleti JúniorPediatric Intensive Care Unit, Hospital Assunção, São Bernardo do Campo, SP, Brazil.
Felipe Rezende Caino de OliveiraPediatric Intensive Care Unit, Hospital Alvorada Moema, Moema, SP, Brazil.
Luís Fernando Andrade de CarvalhoPediatric Intensive Care Unit, Hospital João Paulo II, Belo Horizonte, MG, Brazil.
Mariana DigiovanniPediatric Intensive Care Unit, Hospital Universitario Evangélico Mackenzie, Curitiba, PR, Brazil.
Ana Paula Novaes BellinatPediatric Intensive Care Unit, Hospital Martagão Gesteira, Salvador, BA, Brazil.
Thiago Peres da SilvaPediatric Intensive Care Unit, Hospital Oeste D`Or, Rio de Janeiro, RJ, Brazil.
Taisa Roberta Ramos Nantes de CastilhoPediatric Intensive Care Unit, Hospital Anália Franco, São Paulo, SP, Brazil.
Simone Camera GregoryPediatric Intensive Care Unit, Hospital Estadual da Criança, Rio de Janeiro, RJ, Brazil.
Ana Carolina Cabral Pinheiro ScarlatoPediatric Intensive Care Unit, Hospital Rios D`Or, Rio de Janeiro, RJ, Brazil.
Paula Marins RiveiroPediatric Intensive Care Unit, Hospital Caxias D`Or, Rio de Janeiro, RJ, Brazil.
José Oliva Proença FilhoPediatric Intensive Care Unit, Hospital e Maternidade Brasil, Santo André, SP, Brazil.
Antonio José Ledo Alves da CunhaDepartment of Pediatrics, D'Or Institute for Research and Education (IDOR), Rio de Janeiro, RJ, Brazil.
Maria Clara de Magalhães-BarbosaDepartment of Pediatrics, D'Or Institute for Research and Education (IDOR), Rio de Janeiro, RJ, Brazil.
Claudia de Souza LopesDepartment of Epidemiology, Institute of Social Medicine, State University of Rio de Janeiro, Brazil.
Brazilian Research Network in Pediatric Intensive Care (BRnet-PIC)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

importanceThis is the first Brazilian study evaluating the performance of Pediatric Risk of Mortality (PRISM) IV and the first to use the calibration belt technique.

objectivesThis study aimed to evaluate the performance of PRISM IV in a large cohort of patients admitted to Brazilian PICUs. DESIGN, SETTING AND

participantsThis is a longitudinal, prospective, multicenter study conducted in 36 Brazilian PICUs with children between 29 days and 18 years old admitted from March 2020 to March 2022. MAIN OUTCOMES AND MEASURES: PRISM IV's performance was assessed using the standardized mortality ratio (SMR), the area under the receiver operating characteristic curve (AUROC) with 95% CI, and the calibration belt with 80% and 95% CI.

resultsA total of 12,046 patients from 36 PICUs were included. Observed overall in-hospital mortality was higher than predicted: observed = 249 (2.1%) × predicted = 188.1 (1.56%) (SMR = 1.32 [95% CI, 1.16-1.50]); discrimination was good (AUROC = 0.86 [95% CI, 0.83-0.89]), and calibration was poor, underestimating mortality over a wide range of predicted mortality (2-61%). To explore the impact of the COVID-19 pandemic on PRISM IV's performance, we divided the study period into prevaccine and postvaccine. In the prevaccine period, the SMR was 1.38 (95% CI, 1.17-1.62), the AUROC was 0.84 (95% CI, 0.80-0.88), and the range of miscalibration was broader than in the total cohort (underestimation in the 2-98% range). In the postvaccine period, the SMR was 1.26 (95% CI, 1.03-1.51), the AUROC was 0.90 (95% CI, 0.86-0.94), and the calibration belt underestimated mortality in a narrower range of 3-46% of predicted mortality. CONCLUSIONS AND RELEVANCE: PRISM IV showed good discrimination but miscalibration across a wide range of predicted mortality and different COVID-19 pandemic periods in a large cohort. Further research with subgroup analyses are needed to develop strategies to improve the performance of PRISM IV in different and heterogeneous Brazilian healthcare contexts.

Indexed as

Hospital MortalityIntensive Care Units, PediatricAdolescentBrazilChildChild, PreschoolCOVID-19FemaleHumansInfantInfant, NewbornLongitudinal StudiesMaleProspective StudiesRisk AssessmentROC Curve

Identifiers

PMID40153553
PMCPMC11957651

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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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 Socratic graph.