Bibliographic citations
Aparcana, D., Ascencio, E. (2023). Enfermedad renal crónica en países de bajos y medianos ingresos: una revisión sistemática de modelos diagnósticos y pronósticos [Universidad Peruana Cayetano Heredia]. https://hdl.handle.net/20.500.12866/15059
Aparcana, D., Ascencio, E. Enfermedad renal crónica en países de bajos y medianos ingresos: una revisión sistemática de modelos diagnósticos y pronósticos []. PE: Universidad Peruana Cayetano Heredia; 2023. https://hdl.handle.net/20.500.12866/15059
@misc{renati/911112,
title = "Enfermedad renal crónica en países de bajos y medianos ingresos: una revisión sistemática de modelos diagnósticos y pronósticos",
author = "Ascencio Yuncaccallo, Edson Jesus",
publisher = "Universidad Peruana Cayetano Heredia",
year = "2023"
}
Objective: To summarise available chronic kidney disease (CKD) diagnostic and prognostic models in low-income and middle-income countries (LMICs). Method: Systematic review (Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines). We searched Medline, EMBASE, Global Health (these three through OVID), Scopus and Web of Science from inception to 9 April 2021, 17 April 2021 and 18 April 2021, respectively. We first screened titles and abstracts, and then studied in detail the selected reports; both phases were conducted by two reviewers independently. We followed the CHecklist for critical Appraisal and data extraction for systematic Reviews of prediction Modelling Studies recommendations and used the Prediction model Risk Of Bias ASsessment Tool for risk of bias assessment. Results: The search retrieved 14 845 results, 11 reports were studied in detail and 9 (n=61 134) were included in the qualitative analysis. The proportion of women in the study population varied between 24.5% and 76.6%, and the mean age ranged between 41.8 and 57.7 years. Prevalence of undiagnosed CKD ranged between 1.1% and 29.7%. Age, diabetes mellitus and sex were the most common predictors in the diagnostic and prognostic models. Outcome definition varied greatly, mostly consisting of urinary albumin-to-creatinine ratio and estimated glomerular filtration rate. The highest performance metric was the negative predictive value. All studies exhibited high risk of bias, and some had methodological limitations. Conclusion: There is no strong evidence to support the use of a CKD diagnostic or prognostic model throughout LMIC. The development, validation and implementation of risk scores must be a research and public health priority in LMIC to enhance CKD screening to improve timely diagnosis.
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