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Quality of care in cystic fibrosis: assessment protocol of the French QIP PHARE-M
BACKGROUND: The PHARE-M care quality improvement program, modeled on the US Cystic Fibrosis Quality Improvement Program, was introduced at 14 cystic fibrosis centers (CFCs) in the French Cystic Fibrosis Network between 2011 and 2013. The pilot phase assessments attested the progressive adherence of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6225544/ https://www.ncbi.nlm.nih.gov/pubmed/29799381 http://dx.doi.org/10.1186/s13023-017-0749-3 |
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author | Pougheon Bertrand, Dominique Nowak, Emmanuel Dehillotte, Clémence Lemmonier, Lydie Rault, Gilles |
author_facet | Pougheon Bertrand, Dominique Nowak, Emmanuel Dehillotte, Clémence Lemmonier, Lydie Rault, Gilles |
author_sort | Pougheon Bertrand, Dominique |
collection | PubMed |
description | BACKGROUND: The PHARE-M care quality improvement program, modeled on the US Cystic Fibrosis Quality Improvement Program, was introduced at 14 cystic fibrosis centers (CFCs) in the French Cystic Fibrosis Network between 2011 and 2013. The pilot phase assessments attested the progressive adherence of the teams and improvements in care management. The PHARE-M Performance research project aims at assessing in 2015 the impact of the PHARE-M program on patient health indicators at trained versus untrained centers. It also sought to identify contextual factors that could account for variability in the performance of the PHARE-M among the trained centers. METHODS: A mixed methodology combining: a quantitative experimental study: a comparison, using a mixed model for repeated data (from 2011 to 2015), of the average changes over time in forced expiratory volume in 1 s (FEV1) and body mass index (BMI) between two groups of patients included in a closed cohort (non-transplant patients, continuous follow-up at one participating CFC, and a CF-causing mutation), one having benefitted from the PHARE-M program and the other not having done so, and a realistic study: a characterization of the impact on care management and an identification of mechanisms through which the PHARE-M intervention improved the team’s effectiveness in different CFC contexts; this required modeling the intervention, context, and impact on care management with respect to the criteria of the chronic care model (CCM); this was done using a self-administered questionnaire given to professionals and patients/parents supplemented with focus groups. CONCLUSION: Although the study population was controlled, it may be difficult to establish a causal relationship between the differences in the changes over time in patient health indicators in the two groups of patients and the PHARE-M intervention as it is often the case in complex interventions rolled out in adaptive environments. The analysis of factors associated with variations in the impact of the PHARE-M at the different trained CFCs required the adoption of instruments validated in other contexts; these could be useful for assessing the performance of other interventions in healthcare practices at CFCs in France. |
format | Online Article Text |
id | pubmed-6225544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62255442018-11-19 Quality of care in cystic fibrosis: assessment protocol of the French QIP PHARE-M Pougheon Bertrand, Dominique Nowak, Emmanuel Dehillotte, Clémence Lemmonier, Lydie Rault, Gilles Orphanet J Rare Dis Research BACKGROUND: The PHARE-M care quality improvement program, modeled on the US Cystic Fibrosis Quality Improvement Program, was introduced at 14 cystic fibrosis centers (CFCs) in the French Cystic Fibrosis Network between 2011 and 2013. The pilot phase assessments attested the progressive adherence of the teams and improvements in care management. The PHARE-M Performance research project aims at assessing in 2015 the impact of the PHARE-M program on patient health indicators at trained versus untrained centers. It also sought to identify contextual factors that could account for variability in the performance of the PHARE-M among the trained centers. METHODS: A mixed methodology combining: a quantitative experimental study: a comparison, using a mixed model for repeated data (from 2011 to 2015), of the average changes over time in forced expiratory volume in 1 s (FEV1) and body mass index (BMI) between two groups of patients included in a closed cohort (non-transplant patients, continuous follow-up at one participating CFC, and a CF-causing mutation), one having benefitted from the PHARE-M program and the other not having done so, and a realistic study: a characterization of the impact on care management and an identification of mechanisms through which the PHARE-M intervention improved the team’s effectiveness in different CFC contexts; this required modeling the intervention, context, and impact on care management with respect to the criteria of the chronic care model (CCM); this was done using a self-administered questionnaire given to professionals and patients/parents supplemented with focus groups. CONCLUSION: Although the study population was controlled, it may be difficult to establish a causal relationship between the differences in the changes over time in patient health indicators in the two groups of patients and the PHARE-M intervention as it is often the case in complex interventions rolled out in adaptive environments. The analysis of factors associated with variations in the impact of the PHARE-M at the different trained CFCs required the adoption of instruments validated in other contexts; these could be useful for assessing the performance of other interventions in healthcare practices at CFCs in France. BioMed Central 2018-02-08 /pmc/articles/PMC6225544/ /pubmed/29799381 http://dx.doi.org/10.1186/s13023-017-0749-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Pougheon Bertrand, Dominique Nowak, Emmanuel Dehillotte, Clémence Lemmonier, Lydie Rault, Gilles Quality of care in cystic fibrosis: assessment protocol of the French QIP PHARE-M |
title | Quality of care in cystic fibrosis: assessment protocol of the French QIP PHARE-M |
title_full | Quality of care in cystic fibrosis: assessment protocol of the French QIP PHARE-M |
title_fullStr | Quality of care in cystic fibrosis: assessment protocol of the French QIP PHARE-M |
title_full_unstemmed | Quality of care in cystic fibrosis: assessment protocol of the French QIP PHARE-M |
title_short | Quality of care in cystic fibrosis: assessment protocol of the French QIP PHARE-M |
title_sort | quality of care in cystic fibrosis: assessment protocol of the french qip phare-m |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6225544/ https://www.ncbi.nlm.nih.gov/pubmed/29799381 http://dx.doi.org/10.1186/s13023-017-0749-3 |
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