Author
Listed:
- Zhikai Wan
- Mengyan Wang
- Weiwei Zhang
- Yu Zhou
- Biao Zhu
Abstract
Background: Talaromycosis is an invasive fungal infection that predominantly affects immunocompromised individuals, with a particularly high incidence and mortality rate among HIV-infected patients. The purpose of this study was to develop and validate a novel nomogram model to predict mortality risk in HIV-associated talaromycosis (HTM) patients. Method: The authors retrospectively analyzed HTM patients from January 2013 to December 2023 at three research centers. The research participants were randomly divided into the training and validation sets at a ratio of 7:3. To determine the crucial variables for establishment of the predictive model, the study sequentially applied univariate logistic regression, lasso regression, stepwise logistic regression. The validation set was used to assess the performance of the established prediction model, with its efficacy evaluated through receiver operating characteristics curve, clinical decision curves, and calibration curves. Result: A total of 431 subjects were enrolled in the study with 55/431 (12.76%) patients dying during hospitalization. Statistical analysis shows that there was no difference between training set and validation set in the baseline demographic and clinical characteristics. Five factors including breathlessness, elevated TB, APRI, CRP and decreased Hb were identified as predictive factors for HTM mortality. A nomogram model was built and the area under the curve (AUC) for the nomogram in predicting death was 0.83 (95% CI: 0.76-0.90) in the training set and 0.81 (95% CI: 0.70-0.93) in the validation set. The H-L test and calibration curves showed a strong alignment between predicted and actual results in both sets. Additionally, the decision curve analysis (DCA) indicated that the model provided significant net benefits for patients experiencing poor outcomes. Conclusion: The nomogram model developed in this study integrating easily accessible clinical indicators and symptoms is effective in predicting in-hospital mortality in patients with HTM, which will greatly assist clinicians in the individual management of HTM patients. Author summary: Human immunodeficiency virus (HIV)-associated talaromycosis is a life-threatening invasive fungal infection that remains a major cause of mortality among immunocompromised individuals, yet tools for identifying those at highest risk remain limited. In this multicenter retrospective study of 431 hospitalized patients, we sought to address this gap by developing a practical predictive tool. Using routine clinical and laboratory parameters readily available at the bedside—namely, the presence of breathlessness, elevated total bilirubin, elevated aspartate aminotransferase-to-platelet ratio index (APRI) score, elevated C-reactive protein, and decreased hemoglobin—we constructed a nomogram model to estimate the risk of in-hospital death. The model exhibited good discrimination in both the training and validation cohorts. Given that all included variables are routinely accessible at the time of admission, this nomogram may support clinicians in early risk stratification and individualized patient management.
Suggested Citation
Zhikai Wan & Mengyan Wang & Weiwei Zhang & Yu Zhou & Biao Zhu, 2026.
"Multivariate predictive model for predicting in-hospital mortality in HIV-associated talaromycosis: a multicenter retrospective study,"
PLOS Neglected Tropical Diseases, Public Library of Science, vol. 20(6), pages 1-14, June.
Handle:
RePEc:plo:pntd00:0014432
DOI: 10.1371/journal.pntd.0014432
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pntd00:0014432. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosntds (email available below). General contact details of provider: https://journals.plos.org/plosntds/ .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.