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218. Development of a Simple Score for Diagnosis Melioidosis
BACKGROUND: Melioidosis is a common gram-negative bacterial infection in northeastern Thailand. Patients with melioidosis infections often experience severe conditions and high mortality rates. This study aims to develop a clinical prediction model to estimate the risk of melioidosis septicemia. MET...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677673/ http://dx.doi.org/10.1093/ofid/ofad500.291 |
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author | Khaejawat, Kanjana Panichote, Anupol Meesing, Atibordee |
author_facet | Khaejawat, Kanjana Panichote, Anupol Meesing, Atibordee |
author_sort | Khaejawat, Kanjana |
collection | PubMed |
description | BACKGROUND: Melioidosis is a common gram-negative bacterial infection in northeastern Thailand. Patients with melioidosis infections often experience severe conditions and high mortality rates. This study aims to develop a clinical prediction model to estimate the risk of melioidosis septicemia. METHODS: This retrospective case-control study included patients with positive hemoculture for Burkholderia pseudomallei (BP) and other gram-negative bacteria (Escherichia coli, and Klebsiella pneumoniae) admitted to Srinagarind Hospital between January 2015 and December 2020. Logistic regression analyses were used to determine the calculation of a score for diagnosing melioidosis infection. RESULTS: A total of 426 patients with positive hemoculture were included: 132 patients for BP and 294 patients for other gram-negative bacteria. The clinical prediction model for diagnosing melioidosis utilized seven variables: age ≥ 60 years (-2 points), male gender (3 points), duration of symptom onset to hospitalization ≥ 7 days (5 points), occupation as a farmer (3 points), presence of diabetes mellitus (2 points), presence of cancer (-5 points), and platelet count (x 10(9)/L) (200-399.9: 1 point, ≥400: 3 points). The model demonstrated good discrimination (area under the curve: 0.89; 95% CI: 0.86-0.93) and acceptable calibration (Hosmer and Lemeshow goodness of fit test: P-value of 0.252). A cut-off point of the melioidosis score ≥ 5 points (maximum score = 16 and minimum score = -7) resulted in an accuracy of 84.3% (95%CI 80.5-87.6), a sensitivity of 78.8%, and a specificity of 86.7%. [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: The melioidosis score exhibited high performance and clinical utility in predicting melioidosis infection. DISCLOSURES: All Authors: No reported disclosures |
format | Online Article Text |
id | pubmed-10677673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106776732023-11-27 218. Development of a Simple Score for Diagnosis Melioidosis Khaejawat, Kanjana Panichote, Anupol Meesing, Atibordee Open Forum Infect Dis Abstract BACKGROUND: Melioidosis is a common gram-negative bacterial infection in northeastern Thailand. Patients with melioidosis infections often experience severe conditions and high mortality rates. This study aims to develop a clinical prediction model to estimate the risk of melioidosis septicemia. METHODS: This retrospective case-control study included patients with positive hemoculture for Burkholderia pseudomallei (BP) and other gram-negative bacteria (Escherichia coli, and Klebsiella pneumoniae) admitted to Srinagarind Hospital between January 2015 and December 2020. Logistic regression analyses were used to determine the calculation of a score for diagnosing melioidosis infection. RESULTS: A total of 426 patients with positive hemoculture were included: 132 patients for BP and 294 patients for other gram-negative bacteria. The clinical prediction model for diagnosing melioidosis utilized seven variables: age ≥ 60 years (-2 points), male gender (3 points), duration of symptom onset to hospitalization ≥ 7 days (5 points), occupation as a farmer (3 points), presence of diabetes mellitus (2 points), presence of cancer (-5 points), and platelet count (x 10(9)/L) (200-399.9: 1 point, ≥400: 3 points). The model demonstrated good discrimination (area under the curve: 0.89; 95% CI: 0.86-0.93) and acceptable calibration (Hosmer and Lemeshow goodness of fit test: P-value of 0.252). A cut-off point of the melioidosis score ≥ 5 points (maximum score = 16 and minimum score = -7) resulted in an accuracy of 84.3% (95%CI 80.5-87.6), a sensitivity of 78.8%, and a specificity of 86.7%. [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: The melioidosis score exhibited high performance and clinical utility in predicting melioidosis infection. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10677673/ http://dx.doi.org/10.1093/ofid/ofad500.291 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstract Khaejawat, Kanjana Panichote, Anupol Meesing, Atibordee 218. Development of a Simple Score for Diagnosis Melioidosis |
title | 218. Development of a Simple Score for Diagnosis Melioidosis |
title_full | 218. Development of a Simple Score for Diagnosis Melioidosis |
title_fullStr | 218. Development of a Simple Score for Diagnosis Melioidosis |
title_full_unstemmed | 218. Development of a Simple Score for Diagnosis Melioidosis |
title_short | 218. Development of a Simple Score for Diagnosis Melioidosis |
title_sort | 218. development of a simple score for diagnosis melioidosis |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677673/ http://dx.doi.org/10.1093/ofid/ofad500.291 |
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