Evidence mapPaperPMID 41787387Full record

Observational studyBMC infectious diseases2026

Omicron infection alters the profile of organ failure in severe COVID-19: a multicenter study comparing Omicron and the wild-type strain.

Ruixuan Yu, Ruiqiang Zheng, Xufeng Chen, Huiying Zhao, Jun Jin, Changsong Wang, Shulin Xiang, Man Huang, Hongsheng Zhao, Yi Wang and 5 more

Abstract readMulticenter StudyObservational StudyComparative Study
In one paragraph

Observational study in BMC infectious diseases, 2026. 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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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

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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

15 authors.

Ruixuan Yu *Jiangsu Provincial Key Laboratory of Critical Care Medicine, Department of Critical Care Medicine, School of Medicine, Zhongda Hospital, Southeast University, Nanjing, Jiangsu, China.
Ruiqiang Zheng *Department of Critical Care Medicine, Clinical Medical School, Northern Jiangsu People's Hospital, Yangzhou University, Yangzhou, Jiangsu, China.
Xufeng Chen *Department of Emergency Medicine, Emergency Department, Nanjing Medical University First Affiliated Hospital and Jiangsu Province Hospital, Nanjing, Jiangsu, China.
Huiying ZhaoDepartment of Critical Care Medicine, Peking University People's Hospital, Peking University, Beijing, China.
Jun JinDepartment of Critical Care Medicine, The First Affiliated Hospital of Soochow University, Soochow University, Suzhou, Jiangsu, China.
Changsong WangDepartment of Critical Care Medicine, Harbin Medical University Cancer Hospital, Harbin, China.
Shulin XiangDepartment of Intensive Care Unit, The Peoples Hospital of Guangxi Zhuang Autonomous Region, Nanning, Guangxi Zhuang Autonomous Region, China.
Man HuangGeneral Intensive Care Unit, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Hongsheng ZhaoDepartment of Critical Care Medicine, Affiliated Hospital of Nantong University, Nantong, Jiangsu, China.
Yi WangDepartment of Critical Care Medicine, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang Uyghur Autonomous Region, China.
Nan ShiJiangsu Provincial Key Laboratory of Critical Care Medicine, Department of Critical Care Medicine, School of Medicine, Zhongda Hospital, Southeast University, Nanjing, Jiangsu, China.
Hui ChenJiangsu Provincial Key Laboratory of Critical Care Medicine, Department of Critical Care Medicine, School of Medicine, Zhongda Hospital, Southeast University, Nanjing, Jiangsu, China.
Yi YangJiangsu Provincial Key Laboratory of Critical Care Medicine, Department of Critical Care Medicine, School of Medicine, Zhongda Hospital, Southeast University, Nanjing, Jiangsu, China.
Jianfeng XieJiangsu Provincial Key Laboratory of Critical Care Medicine, Department of Critical Care Medicine, School of Medicine, Zhongda Hospital, Southeast University, Nanjing, Jiangsu, China.
Haibo QiuJiangsu Provincial Key Laboratory of Critical Care Medicine, Department of Critical Care Medicine, School of Medicine, Zhongda Hospital, Southeast University, Nanjing, Jiangsu, China. haiboq2000@163.com.

Funding

Jiangsu Provincial Key Research and Development Program BE2023602National Key Research and Development Program of China 2022YFC2504405National Natural Science Foundation of China 82341032National Natural Science Foundation of China 82402565Noncommunicable Chronic Diseases-National Science and Technology Major Project 2023ZD0506500Noncommunicable Chronic Diseases-National Science and Technology Major Project 2023ZD0506506
6 · The paper itself

Abstract

introductionThe Omicron variant of SARS-CoV-2 has exhibited altered transmissibility and virulence compared with the Wild-type strain. Currently, no research has focused on the differences in organ failure caused by the two strains. Understanding the clinical characteristics and organ failure patterns of Omicron infection is essential to improve management strategies for severe cases.

methodsThis multicenter retrospective observational study included two cohorts: the Omicron cohort, consisting of 7,000 COVID-19 patients admitted to 10 national research centers in China from December 2022 to January 2023, and the Wild-type cohort, consisting of 733 patients from designated hospitals during the early outbreak in 2020. Demographic, clinical, laboratory, and treatment data were collected and analyzed. We compared the differences in patient characteristics, developments of organ dysfunction and outcomes between the two cohorts. Multivariate logistic regression models were employed to identify risk factors for severe COVID-19 and death.

resultsThe Omicron cohort included 7000 patients, 1551 (22.2%) of whom had severe cases. The median age of the patients was 73.0 [60.0, 84.0] years, with 4319 male patients (61.7%). Regarding underlying comorbidities, 5305 patients (75.7%) presented with at least one chronic condition, most frequently hypertension (46.0%) and diabetes mellitus (26.3%). The overall in-hospital mortality rate was 15.5%, and 5666 patients (80.9%) experienced at least one organ dysfunction, with respiratory failure being the most prevalent (72.6%). Compared with the Wild-type cohort, severe Omicron patients were older, had a greater proportion of males, and more comorbidities. Severe Omicron cases showed a distinct pattern characterized by a higher prevalence of extrapulmonary organ dysfunction, particularly kidney failure. Multivariate analysis identified older age, male sex, lack of vaccination, preadmission corticosteroid use, and comorbidities as independent predictors of severe disease. Among severe patients, older age, malignancy, hypoxemia, thrombocytopenia, and elevated troponin were independent predictors of mortality.

conclusionAfter the widespread emergence of Omicron, severe COVID-19 predominantly affected older patients with multiple comorbidities and showed a different organ failure spectrum, with greater extrapulmonary involvement, particularly kidney failure, in the early phase of hospitalization. These findings highlight the evolving clinical and pathophysiological features of COVID-19 in the Omicron era. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

COVID-19Multiple Organ FailureSARS-CoV-2AgedAged, 80 and overChinaComorbidityFemaleHumansMaleMiddle AgedRetrospective StudiesRisk FactorsSeverity of Illness IndexCOVID-19MortalityOmicron variantOrgan failureRisk factorsSevere COVID-19

Identifiers

PMID41787387
PMCPMC13078076

What Socratic holds

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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.