Evidence map›Paper›PMID 42036712›Full record

ArticleCritical care (London, England)2026

Performance of sequential organ failure assessment 1 versus 2 for sepsis identification in patients with suspected infection: a multicenter retrospective cohort study.

Rong Liufu, Xiao-Yun Fu, Xian-Qing Shi, Feng Shen, Yao Wu, Maomao Cao, Yi-Fan Wang, Jin-Min Peng, Wei Jiang, Xiao-Yun Hu and 5 more

Abstract readComparative StudyMulticenter Study
In one paragraph

Article in Critical care (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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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

1 citing paper in PubMed.

  1. Article
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

15 authors.

Rong LiufuMedical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.
Xiao-Yun FuDepartment of Critical Care Medicine, Affiliated Hospital of Zunyi Medical University, Zunyi, China.
Xian-Qing ShiDepartment of Critical Care Medicine, Guizhou Provincial People's Hospital, Guiyang, China.
Feng ShenDepartment of Intensive Care Unit, The Affiliated Hospital of Guizhou Medical University, Guiyang, China.
Yao WuMedical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.
Maomao CaoMedical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.
Yi-Fan WangMedical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.
Jin-Min PengMedical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.
Wei JiangMedical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.
Xiao-Yun HuMedical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.
Yang-Yan-Qiu WangMedical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China.
Li WengMedical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China. wengli@gmail.com.
Xiang ZhouDepartment of Critical Care Medicine, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 073100, China. zx_pumc@163.com.
Bin DuMedical Intensive Care Unit, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences, 1 Shuai Fu Yuan, Beijing, 100730, China. dubin98@gmail.com.
China Critical Care Clinical Trials Group (CCCCTG)

Funding

National Key R&D Program of China from Ministry of Science and Technology of the People's Republic of China 2025ZD01903003Noncommunicable Chronic Diseases-National Science and Technology Major Projec 2024ZD0526700Noncommunicable Chronic Diseases-National Science and Technology Major Project 2023ZD0506505
6 · The paper itself

Abstract

objectiveThe revised Sequential Organ Failure Assessment (SOFA-2) score was recently developed to update definitions of acute organ dysfunction in intensive care units (ICU). This study aimed to evaluate performance between SOFA-1 and SOFA-2 definition for sepsis identification in patients with suspected infection.

methodsWe analyzed 24,510 patients with suspected infection in Chinese multicenter cohort and validated in the MIMIC-IV database. Patients were divided into four categories based on concordance between SOFA versions: SOFA-1(-)/SOFA-2(-), SOFA-1(+)/SOFA-2(+), SOFA-1(-)/SOFA-2(+), and SOFA-1(+)/SOFA-2(-). Kaplan-Meier analyses and cox proportional hazards models assessed the associations with in-hospital mortality.

resultsMost patients met sepsis criteria under both SOFA versions (18,179/24,510; 74.2%[95% confidential interval (CI), 73.6%-74.7%]), while 9.9% (95% CI, 9.53%-10.2%) were classified as SOFA-1(+)/SOFA-2(-), 5.5% (95% CI, 5.2%-5.8%) as SOFA-1(-)/SOFA-2(+), and 10.2% (95% CI, 9.8%-10.6%) as SOFA-1(-)/SOFA-2(-). Patients in SOFA-1(-)/SOFA-2(+) group were younger, more often male, higher rates of pneumonia, gastrointestinal infection, and neurologic infection. Superior discrimination for in-hospital mortality was observed in SOFA-2 [area under the receiver operating characteristic curve (AUROC) 0.746; 95% confidence interval (CI) 0.737-0.756] compared with SOFA-1 (0.679; 95% CI 0.668-0.689). In-hospital mortality was markedly higher in SOFA-2 (+) groups [2.9% in SOFA-1(-)/SOFA-2(-), 3.3% in SOFA-1(+)/SOFA-2(-), 10.6% in SOFA-1(-)/SOFA-2(+), and 14.3% in SOFA-1(+)/SOFA-2(+); p < 0.001]. Compared with SOFA-1(-)/SOFA-2(-), the hazard ratios for in-hospital mortality were 0.99 (95% CI, 0.72-1.36) for SOFA-1(+)/SOFA-2(-), 3.52 (95% CI, 2.66-4.67) for SOFA-1(-)/SOFA-2(+), and 4.44 (95% CI, 3.52-5.60) for SOFA-1(+)/SOFA-2(+). These patterns were consistent in sensitivity analyses.

conclusionSOFA-2-based sepsis identified a clinically meaningful higher-risk subgroup, with consistent results across sensitivity analyses. Nevertheless, cohort-specific differences emphasize the need for cautious interpretation and further validation in diverse clinical settings.

Indexed as

Organ Dysfunction ScoresSepsisAgedChinaCohort StudiesFemaleHospital MortalityHumansIntensive Care UnitsMaleMiddle AgedMultiple Organ FailureRetrospective StudiesPredictive validityReclassificationSepsisSequential organ failure assessment (SOFA-2) score

Identifiers

PMID42036712
PMCPMC13188382

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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.