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FINDRISC in Latin America: a systematic review of diagnosis and prognosis models

This review aimed to assess whether the FINDRISC, a risk score for type 2 diabetes mellitus (T2DM), has been externally validated in Latin America and the Caribbean (LAC). We conducted a systematic review following the CHARMS (CHecklist for critical Appraisal and data extraction for systematic Revie...

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Autores principales: Carrillo-Larco, Rodrigo M, Aparcana-Granda, Diego J, Mejia, Jhonatan R, Bernabé-Ortiz, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202717/
https://www.ncbi.nlm.nih.gov/pubmed/32327446
http://dx.doi.org/10.1136/bmjdrc-2019-001169
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author Carrillo-Larco, Rodrigo M
Aparcana-Granda, Diego J
Mejia, Jhonatan R
Bernabé-Ortiz, Antonio
author_facet Carrillo-Larco, Rodrigo M
Aparcana-Granda, Diego J
Mejia, Jhonatan R
Bernabé-Ortiz, Antonio
author_sort Carrillo-Larco, Rodrigo M
collection PubMed
description This review aimed to assess whether the FINDRISC, a risk score for type 2 diabetes mellitus (T2DM), has been externally validated in Latin America and the Caribbean (LAC). We conducted a systematic review following the CHARMS (CHecklist for critical Appraisal and data extraction for systematic Reviews of prediction Modelling Studies) framework. Reports were included if they validated or re-estimated the FINDRISC in population-based samples, health facilities or administrative data. Reports were excluded if they only studied patients or at-risk individuals. The search was conducted in Medline, Embase, Global Health, Scopus and LILACS. Risk of bias was assessed with the PROBAST (Prediction model Risk of Bias ASsessment Tool) tool. From 1582 titles and abstracts, 4 (n=7502) reports were included for qualitative summary. All reports were from South America; there were slightly more women, and the mean age ranged from 29.5 to 49.7 years. Undiagnosed T2DM prevalence ranged from 2.6% to 5.1%. None of the studies conducted an independent external validation of the FINDRISC; conversely, they used the same (or very similar) predictors to fit a new model. None of the studies reported calibration metrics. The area under the receiver operating curve was consistently above 65.0%. All studies had high risk of bias. There has not been any external validation of the FINDRISC model in LAC. Selected reports re-estimated the FINDRISC, although they have several methodological limitations. There is a need for big data to develop—or improve—T2DM diagnostic and prognostic models in LAC. This could benefit T2DM screening and early diagnosis.
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spelling pubmed-72027172020-05-13 FINDRISC in Latin America: a systematic review of diagnosis and prognosis models Carrillo-Larco, Rodrigo M Aparcana-Granda, Diego J Mejia, Jhonatan R Bernabé-Ortiz, Antonio BMJ Open Diabetes Res Care Epidemiology/Health Services Research This review aimed to assess whether the FINDRISC, a risk score for type 2 diabetes mellitus (T2DM), has been externally validated in Latin America and the Caribbean (LAC). We conducted a systematic review following the CHARMS (CHecklist for critical Appraisal and data extraction for systematic Reviews of prediction Modelling Studies) framework. Reports were included if they validated or re-estimated the FINDRISC in population-based samples, health facilities or administrative data. Reports were excluded if they only studied patients or at-risk individuals. The search was conducted in Medline, Embase, Global Health, Scopus and LILACS. Risk of bias was assessed with the PROBAST (Prediction model Risk of Bias ASsessment Tool) tool. From 1582 titles and abstracts, 4 (n=7502) reports were included for qualitative summary. All reports were from South America; there were slightly more women, and the mean age ranged from 29.5 to 49.7 years. Undiagnosed T2DM prevalence ranged from 2.6% to 5.1%. None of the studies conducted an independent external validation of the FINDRISC; conversely, they used the same (or very similar) predictors to fit a new model. None of the studies reported calibration metrics. The area under the receiver operating curve was consistently above 65.0%. All studies had high risk of bias. There has not been any external validation of the FINDRISC model in LAC. Selected reports re-estimated the FINDRISC, although they have several methodological limitations. There is a need for big data to develop—or improve—T2DM diagnostic and prognostic models in LAC. This could benefit T2DM screening and early diagnosis. BMJ Publishing Group 2020-04-22 /pmc/articles/PMC7202717/ /pubmed/32327446 http://dx.doi.org/10.1136/bmjdrc-2019-001169 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Epidemiology/Health Services Research
Carrillo-Larco, Rodrigo M
Aparcana-Granda, Diego J
Mejia, Jhonatan R
Bernabé-Ortiz, Antonio
FINDRISC in Latin America: a systematic review of diagnosis and prognosis models
title FINDRISC in Latin America: a systematic review of diagnosis and prognosis models
title_full FINDRISC in Latin America: a systematic review of diagnosis and prognosis models
title_fullStr FINDRISC in Latin America: a systematic review of diagnosis and prognosis models
title_full_unstemmed FINDRISC in Latin America: a systematic review of diagnosis and prognosis models
title_short FINDRISC in Latin America: a systematic review of diagnosis and prognosis models
title_sort findrisc in latin america: a systematic review of diagnosis and prognosis models
topic Epidemiology/Health Services Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202717/
https://www.ncbi.nlm.nih.gov/pubmed/32327446
http://dx.doi.org/10.1136/bmjdrc-2019-001169
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