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      Nomogram predictive model for in-hospital mortality risk in elderly ICU patients with urosepsis

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          Abstract

          Background

          Urinary tract infection (UTI) is a common cause of sepsis. Elderly patients with urosepsis in intensive care unit (ICU) have more severe conditions and higher mortality rates owing to factors such as advanced age, immunosenescence, and persistent host inflammatory responses. However, comprehensive studies on nomograms to predict the in-hospital mortality risk in elderly patients with urosepsis are lacking. This study aimed to construct a nomogram predictive model to accurately assess the prognosis of elderly patients with urosepsis and provide therapeutic recommendations.

          Methods

          Data of elderly patients with urosepsis were extracted from the Medical Information Mart for Intensive Care (MIMIC) IV 2.2 database. Patients were randomly divided into training and validation cohorts. A predictive nomogram model was constructed from the training set using logistic regression analysis, followed by internal validation and sensitivity analysis.

          Results

          This study included 1,251 patients. LASSO regression analysis revealed that the Glasgow Coma Scale (GCS) score, red cell distribution width (RDW), white blood count (WBC), and invasive ventilation were independent risk factors identified from a total of 43 variables studied. We then created and verified a nomogram. The area under the receiver operating characteristic curve (AUC), net reclassification improvement (NRI), integrated discrimination improvement (IDI), and decision curve analysis (DCA) of the nomogram were superior to those of the traditional SAPS-II, APACHE-II, and SOFA scoring systems. The Hosmer-Lemeshow test results and calibration curves suggested good nomogram calibration. The IDI and NRI values showed that our nomogram scoring tool performed better than the other scoring systems. The DCA curves showed good clinical applicability of the nomogram.

          Conclusions

          The nomogram constructed in this study is a convenient tool for accurately predicting in-hospital mortality in elderly patients with urosepsis in ICU. Improving the treatment strategies for factors related to the model could improve the in-hospital survival rates of these patients.

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          Most cited references42

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          The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3).

          Definitions of sepsis and septic shock were last revised in 2001. Considerable advances have since been made into the pathobiology (changes in organ function, morphology, cell biology, biochemistry, immunology, and circulation), management, and epidemiology of sepsis, suggesting the need for reexamination.
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            Global, regional, and national sepsis incidence and mortality, 1990–2017: analysis for the Global Burden of Disease Study

            Summary Background Sepsis is life-threatening organ dysfunction due to a dysregulated host response to infection. It is considered a major cause of health loss, but data for the global burden of sepsis are limited. As a syndrome caused by underlying infection, sepsis is not part of standard Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) estimates. Accurate estimates are important to inform and monitor health policy interventions, allocation of resources, and clinical treatment initiatives. We estimated the global, regional, and national incidence of sepsis and mortality from this disorder using data from GBD 2017. Methods We used multiple cause-of-death data from 109 million individual death records to calculate mortality related to sepsis among each of the 282 underlying causes of death in GBD 2017. The percentage of sepsis-related deaths by underlying GBD cause in each location worldwide was modelled using mixed-effects linear regression. Sepsis-related mortality for each age group, sex, location, GBD cause, and year (1990–2017) was estimated by applying modelled cause-specific fractions to GBD 2017 cause-of-death estimates. We used data for 8·7 million individual hospital records to calculate in-hospital sepsis-associated case-fatality, stratified by underlying GBD cause. In-hospital sepsis-associated case-fatality was modelled for each location using linear regression, and sepsis incidence was estimated by applying modelled case-fatality to sepsis-related mortality estimates. Findings In 2017, an estimated 48·9 million (95% uncertainty interval [UI] 38·9–62·9) incident cases of sepsis were recorded worldwide and 11·0 million (10·1–12·0) sepsis-related deaths were reported, representing 19·7% (18·2–21·4) of all global deaths. Age-standardised sepsis incidence fell by 37·0% (95% UI 11·8–54·5) and mortality decreased by 52·8% (47·7–57·5) from 1990 to 2017. Sepsis incidence and mortality varied substantially across regions, with the highest burden in sub-Saharan Africa, Oceania, south Asia, east Asia, and southeast Asia. Interpretation Despite declining age-standardised incidence and mortality, sepsis remains a major cause of health loss worldwide and has an especially high health-related burden in sub-Saharan Africa. Funding The Bill & Melinda Gates Foundation, the National Institutes of Health, the University of Pittsburgh, the British Columbia Children's Hospital Foundation, the Wellcome Trust, and the Fleming Fund.
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              Assessment of Clinical Criteria for Sepsis: For the Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3).

              The Third International Consensus Definitions Task Force defined sepsis as "life-threatening organ dysfunction due to a dysregulated host response to infection." The performance of clinical criteria for this sepsis definition is unknown.
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                Author and article information

                Contributors
                11072@ahu.edu.cn
                lyujun2020@jnu.edu.cn
                yangmin@ahmu.edu.cn
                Journal
                BMC Infect Dis
                BMC Infect Dis
                BMC Infectious Diseases
                BioMed Central (London )
                1471-2334
                26 April 2024
                26 April 2024
                2024
                : 24
                : 442
                Affiliations
                [1 ]GRID grid.452696.a, ISNI 0000 0004 7533 3408, The Second Department of Critical Care Medicine, , The Second Affiliated Hospital of Anhui Medical University, ; 678 Furong Road, 230601 Hefei, Anhui Province China
                [2 ]GRID grid.452696.a, ISNI 0000 0004 7533 3408, Laboratory of Cardiopulmonary Resuscitation and Critical Care, , The Second Affiliated Hospital of Anhui Medical University, ; 678 Furong Road, 230601 Hefei, Anhui Province China
                [3 ]GRID grid.252245.6, ISNI 0000 0001 0085 4987, Key Laboratory of Intelligent Computing & Signal Processing, Ministry of Education, , Anhui University, ; 111 Jiulong Road, 230601 Hefei, Anhui Province China
                [4 ]School of Integrated Circuits, Anhui University, ( https://ror.org/05th6yx34) 111 Jiulong Road, 230601 Hefei, Anhui Province China
                [5 ]Laboratory of Molecular, Biology and Department of Biochemistry, Anhui Medical University, ( https://ror.org/03xb04968) 81 Meishan Road, 230022 Hefei, Anhui Province China
                [6 ]GRID grid.412601.0, ISNI 0000 0004 1760 3828, Department of Clinical Research, , The First Affiliated Hospital of Jinan University, ; 613 West Huangpu Avenue, Tianhe District, 510630 Guangzhou, Guangdong Province China
                Article
                9319
                10.1186/s12879-024-09319-8
                11046882
                38671376
                e8b215c1-970d-4050-b862-f2a9347dfa9d
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 28 February 2024
                : 14 April 2024
                Funding
                Funded by: the Basic and Clinical Improvement Program of Anhui Medical University
                Award ID: No.2023xkjT042
                Funded by: the National Natural Science Foundation of China
                Award ID: No.82072134
                Funded by: the Anhui University Excellent Young Talents Support Plan
                Award ID: No. gxyqZD2018026
                Categories
                Research
                Custom metadata
                © BioMed Central Ltd., part of Springer Nature 2024

                Infectious disease & Microbiology
                urinary tract infection,urosepsis,nomogram,mimic-iv
                Infectious disease & Microbiology
                urinary tract infection, urosepsis, nomogram, mimic-iv

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