Development and validation of prediction algorithm to identify tuberculosis in two large California health systems.

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Titel: Development and validation of prediction algorithm to identify tuberculosis in two large California health systems.
Autoren: Fischer H; Department of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA. Heidi.Fischer@kp.org., Qian L; Department of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA., Li Z; Department of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA., Bruxvoort K; Department of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.; Department of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA., Skarbinski J; Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA.; Department of Infectious Diseases, Oakland Medical Center, Kaiser Permanente Northern California, Oakland, CA, USA., Ni Y; Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA., Ku JH; Department of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA., Lewin B; Department of Family Medicine, Kaiser Permanente Los Angeles Medical Center, Los Angeles, CA, USA.; Department of Clinical Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, CA, USA., Garba S; Department of Health Systems Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, CA, USA., Mahale P; Department of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA., Shaw SF; Department of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA., Spence B; Department of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA., Tartof SY; Department of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.; Department of Health Systems Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, CA, USA.
Quelle: Nature communications [Nat Commun] 2025 Apr 10; Vol. 16 (1), pp. 3385. Date of Electronic Publication: 2025 Apr 10.
Publikationsart: Journal Article; Validation Study
Sprache: English
Info zur Zeitschrift: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
Imprint Name(s): Original Publication: [London] : Nature Pub. Group
MeSH-Schlagworte: Regional Health Planning* , Tuberculosis*/diagnosis , Tuberculosis*/epidemiology , Prediction Algorithms*, Humans ; Male ; Female ; Adolescent ; Young Adult ; Adult ; Middle Aged ; Aged ; California/epidemiology ; Mass Screening ; Risk Factors ; Electronic Health Records ; Datasets as Topic
Abstract: Competing Interests: Competing interests: The authors declare no competing interests.
California data demonstrate failures in latent tuberculosis screening to prevent progression to tuberculosis disease. Therefore, we developed a clinical risk prediction model for tuberculosis disease using electronic health records. This study included Kaiser Permanente Southern California and Northern California members ≥18 years during 2008-2019. Models used Cox proportional hazards regression, Harrell's C-statistic, and a simulated TB disease outcome accounting for cases prevented by current screening which includes both observed and simulated cases. We compared sensitivity and number-needed-to-screen for model-identified high-risk individuals with current screening. Of 4,032,619 and 4,051,873 Southern and Northern California members, tuberculosis disease incidences were 4.1 and 3.3 cases per 100,000 person-years, respectively. The final model C-statistic was 0.816 (95% simulation interval 0.805-0.824). Model sensitivity screening high-risk individuals was 0.70 (0.68-0.71) and number-needed-to-screen was 662 (646-679) persons-per tuberculosis disease case, compared to a sensitivity of 0.36 (0.34-0.38) and number-needed-to-screen of 1632 (1485-1774) with current screening. Here, we show our predictive model improves tuberculosis screening efficiency in California.
(© 2025. The Author(s).)
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Grant Information: R01 AI151072 United States AI NIAID NIH HHS; 5R01AI151072 Foundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.)
Entry Date(s): Date Created: 20250409 Date Completed: 20250418 Latest Revision: 20250418
Update Code: 20250418
PubMed Central ID: PMC11982269
DOI: 10.1038/s41467-025-58775-6
PMID: 40204727
Datenbank: MEDLINE
Beschreibung
Abstract:Competing Interests: Competing interests: The authors declare no competing interests.<br />California data demonstrate failures in latent tuberculosis screening to prevent progression to tuberculosis disease. Therefore, we developed a clinical risk prediction model for tuberculosis disease using electronic health records. This study included Kaiser Permanente Southern California and Northern California members ≥18 years during 2008-2019. Models used Cox proportional hazards regression, Harrell's C-statistic, and a simulated TB disease outcome accounting for cases prevented by current screening which includes both observed and simulated cases. We compared sensitivity and number-needed-to-screen for model-identified high-risk individuals with current screening. Of 4,032,619 and 4,051,873 Southern and Northern California members, tuberculosis disease incidences were 4.1 and 3.3 cases per 100,000 person-years, respectively. The final model C-statistic was 0.816 (95% simulation interval 0.805-0.824). Model sensitivity screening high-risk individuals was 0.70 (0.68-0.71) and number-needed-to-screen was 662 (646-679) persons-per tuberculosis disease case, compared to a sensitivity of 0.36 (0.34-0.38) and number-needed-to-screen of 1632 (1485-1774) with current screening. Here, we show our predictive model improves tuberculosis screening efficiency in California.<br /> (© 2025. The Author(s).)
ISSN:2041-1723
DOI:10.1038/s41467-025-58775-6