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Methods of competing risks flexible parametric modeling for estimation of the risk of the first disease among HIV infected men
BACKGROUND: Patients infected with the Human Immunodeficiency Virus (HIV) are susceptible to many diseases. In these patients, the occurrence of one disease alters the chance of contracting another. Under such circumstances, methods for competing risks are required. Recently, competing risks analyse...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6990537/ https://www.ncbi.nlm.nih.gov/pubmed/31996148 http://dx.doi.org/10.1186/s12874-020-0900-z |
Sumario: | BACKGROUND: Patients infected with the Human Immunodeficiency Virus (HIV) are susceptible to many diseases. In these patients, the occurrence of one disease alters the chance of contracting another. Under such circumstances, methods for competing risks are required. Recently, competing risks analyses in the scope of flexible parametric models have risen to address this requirement. These lesser-known analyses have considerable advantages over conventional methods. METHODS: Using data from Multi Centre AIDS Cohort Study (MACS), this paper reviews and applies methods of competing risks flexible parametric models to analyze the risk of the first disease (AIDS or non-AIDS) among HIV-infected patients. We compared two alternative subdistribution hazard flexible parametric models (SDH(FPM)1 and SDH(FPM)2) with the Fine & Gray model. To make a complete inference, we performed cause-specific hazard flexible parametric models for each event separately as well. RESULTS: Both SDH(FPM)1 and SDH(FPM)2 provided consistent results regarding the magnitude of coefficients and risk estimations compared with estimations obtained from the Fine & Gray model, However, competing risks flexible parametric models provided more efficient and smoother estimations for the baseline risks of the first disease. We found that age at HIV diagnosis indirectly affected the risk of AIDS as the first event by increasing the number of patients who experience a non-AIDS disease prior to AIDS among > 40 years. Other significant covariates had direct effects on the risks of AIDS and non-AIDS. DISCUSSION: The choice of an appropriate model depends on the research goals and computational challenges. The SDH(FPM)1 models each event separately and requires calculating censoring weights which is time-consuming. In contrast, SDH(FPM)2 models all events simultaneously and is more appropriate for large datasets, however, when the focus is on one particular event SDH(FPM)1 is more preferable. |
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