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Cystic Fibrosis Point of Personalized Detection (CFPOPD): An Interactive Web Application

BACKGROUND: Despite steady gains in life expectancy, individuals with cystic fibrosis (CF) lung disease still experience rapid pulmonary decline throughout their clinical course, which can ultimately end in respiratory failure. Point-of-care tools for accurate and timely information regarding the ri...

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Autores principales: Wolfe, Christopher, Pestian, Teresa, Gecili, Emrah, Su, Weiji, Keogh, Ruth H, Pestian, John P, Seid, Michael, Diggle, Peter J, Ziady, Assem, Clancy, John Paul, Grossoehme, Daniel H, Szczesniak, Rhonda D, Brokamp, Cole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JMIR Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773511/
https://www.ncbi.nlm.nih.gov/pubmed/33325834
http://dx.doi.org/10.2196/23530
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author Wolfe, Christopher
Pestian, Teresa
Gecili, Emrah
Su, Weiji
Keogh, Ruth H
Pestian, John P
Seid, Michael
Diggle, Peter J
Ziady, Assem
Clancy, John Paul
Grossoehme, Daniel H
Szczesniak, Rhonda D
Brokamp, Cole
author_facet Wolfe, Christopher
Pestian, Teresa
Gecili, Emrah
Su, Weiji
Keogh, Ruth H
Pestian, John P
Seid, Michael
Diggle, Peter J
Ziady, Assem
Clancy, John Paul
Grossoehme, Daniel H
Szczesniak, Rhonda D
Brokamp, Cole
author_sort Wolfe, Christopher
collection PubMed
description BACKGROUND: Despite steady gains in life expectancy, individuals with cystic fibrosis (CF) lung disease still experience rapid pulmonary decline throughout their clinical course, which can ultimately end in respiratory failure. Point-of-care tools for accurate and timely information regarding the risk of rapid decline is essential for clinical decision support. OBJECTIVE: This study aims to translate a novel algorithm for earlier, more accurate prediction of rapid lung function decline in patients with CF into an interactive web-based application that can be integrated within electronic health record systems, via collaborative development with clinicians. METHODS: Longitudinal clinical history, lung function measurements, and time-invariant characteristics were obtained for 30,879 patients with CF who were followed in the US Cystic Fibrosis Foundation Patient Registry (2003-2015). We iteratively developed the application using the R Shiny framework and by conducting a qualitative study with care provider focus groups (N=17). RESULTS: A clinical conceptual model and 4 themes were identified through coded feedback from application users: (1) ambiguity in rapid decline, (2) clinical utility, (3) clinical significance, and (4) specific suggested revisions. These themes were used to revise our application to the currently released version, available online for exploration. This study has advanced the application’s potential prognostic utility for monitoring individuals with CF lung disease. Further application development will incorporate additional clinical characteristics requested by the users and also a more modular layout that can be useful for care provider and family interactions. CONCLUSIONS: Our framework for creating an interactive and visual analytics platform enables generalized development of applications to synthesize, model, and translate electronic health data, thereby enhancing clinical decision support and improving care and health outcomes for chronic diseases and disorders. A prospective implementation study is necessary to evaluate this tool’s effectiveness regarding increased communication, enhanced shared decision-making, and improved clinical outcomes for patients with CF.
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spelling pubmed-77735112021-01-07 Cystic Fibrosis Point of Personalized Detection (CFPOPD): An Interactive Web Application Wolfe, Christopher Pestian, Teresa Gecili, Emrah Su, Weiji Keogh, Ruth H Pestian, John P Seid, Michael Diggle, Peter J Ziady, Assem Clancy, John Paul Grossoehme, Daniel H Szczesniak, Rhonda D Brokamp, Cole JMIR Med Inform Original Paper BACKGROUND: Despite steady gains in life expectancy, individuals with cystic fibrosis (CF) lung disease still experience rapid pulmonary decline throughout their clinical course, which can ultimately end in respiratory failure. Point-of-care tools for accurate and timely information regarding the risk of rapid decline is essential for clinical decision support. OBJECTIVE: This study aims to translate a novel algorithm for earlier, more accurate prediction of rapid lung function decline in patients with CF into an interactive web-based application that can be integrated within electronic health record systems, via collaborative development with clinicians. METHODS: Longitudinal clinical history, lung function measurements, and time-invariant characteristics were obtained for 30,879 patients with CF who were followed in the US Cystic Fibrosis Foundation Patient Registry (2003-2015). We iteratively developed the application using the R Shiny framework and by conducting a qualitative study with care provider focus groups (N=17). RESULTS: A clinical conceptual model and 4 themes were identified through coded feedback from application users: (1) ambiguity in rapid decline, (2) clinical utility, (3) clinical significance, and (4) specific suggested revisions. These themes were used to revise our application to the currently released version, available online for exploration. This study has advanced the application’s potential prognostic utility for monitoring individuals with CF lung disease. Further application development will incorporate additional clinical characteristics requested by the users and also a more modular layout that can be useful for care provider and family interactions. CONCLUSIONS: Our framework for creating an interactive and visual analytics platform enables generalized development of applications to synthesize, model, and translate electronic health data, thereby enhancing clinical decision support and improving care and health outcomes for chronic diseases and disorders. A prospective implementation study is necessary to evaluate this tool’s effectiveness regarding increased communication, enhanced shared decision-making, and improved clinical outcomes for patients with CF. JMIR Publications 2020-12-16 /pmc/articles/PMC7773511/ /pubmed/33325834 http://dx.doi.org/10.2196/23530 Text en ©Christopher Wolfe, Teresa Pestian, Emrah Gecili, Weiji Su, Ruth H Keogh, John P Pestian, Michael Seid, Peter J Diggle, Assem Ziady, John Paul Clancy, Daniel H Grossoehme, Rhonda D Szczesniak, Cole Brokamp. Originally published in JMIR Medical Informatics (http://medinform.jmir.org), 16.12.2020. 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 use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Medical Informatics, is properly cited. The complete bibliographic information, a link to the original publication on http://medinform.jmir.org/, as well as this copyright and license information must be included.
spellingShingle Original Paper
Wolfe, Christopher
Pestian, Teresa
Gecili, Emrah
Su, Weiji
Keogh, Ruth H
Pestian, John P
Seid, Michael
Diggle, Peter J
Ziady, Assem
Clancy, John Paul
Grossoehme, Daniel H
Szczesniak, Rhonda D
Brokamp, Cole
Cystic Fibrosis Point of Personalized Detection (CFPOPD): An Interactive Web Application
title Cystic Fibrosis Point of Personalized Detection (CFPOPD): An Interactive Web Application
title_full Cystic Fibrosis Point of Personalized Detection (CFPOPD): An Interactive Web Application
title_fullStr Cystic Fibrosis Point of Personalized Detection (CFPOPD): An Interactive Web Application
title_full_unstemmed Cystic Fibrosis Point of Personalized Detection (CFPOPD): An Interactive Web Application
title_short Cystic Fibrosis Point of Personalized Detection (CFPOPD): An Interactive Web Application
title_sort cystic fibrosis point of personalized detection (cfpopd): an interactive web application
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7773511/
https://www.ncbi.nlm.nih.gov/pubmed/33325834
http://dx.doi.org/10.2196/23530
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