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Haemophilia in France: Modelisation of the Clinical Pathway for Patients

Process-of-care studies participate in improving the efficiency of the care pathway for patient with haemophilia (CPPH) and rationalize the multidisciplinary management of patients. Our objective is to establish a current overview of the different actors involved in the management of patients with h...

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Autores principales: Beny, Karen, du Sartz de Vigneulles, Benjamin, Carrouel, Florence, Bourgeois, Denis, Gay, Valérie, Negrier, Claude, Dussart, Claude
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775796/
https://www.ncbi.nlm.nih.gov/pubmed/35055467
http://dx.doi.org/10.3390/ijerph19020646
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author Beny, Karen
du Sartz de Vigneulles, Benjamin
Carrouel, Florence
Bourgeois, Denis
Gay, Valérie
Negrier, Claude
Dussart, Claude
author_facet Beny, Karen
du Sartz de Vigneulles, Benjamin
Carrouel, Florence
Bourgeois, Denis
Gay, Valérie
Negrier, Claude
Dussart, Claude
author_sort Beny, Karen
collection PubMed
description Process-of-care studies participate in improving the efficiency of the care pathway for patient with haemophilia (CPPH) and rationalize the multidisciplinary management of patients. Our objective is to establish a current overview of the different actors involved in the management of patients with haemophilia and to provide an accurate description of the patient trajectory. This is a qualitative exploratory research based on interviews of the principal health professionals of four haemophilia services, between November 2019 and February 2020, in France. Mapping of the CPPH processes within the different institutions and/or services, as well as the rupture zones, were identified. Treatment delivery and biological analyses were carried out exclusively in healthcare institutions. The main liberal health professionals solicited were nurses, physiotherapists and general practitioner. Obstacles and barriers within the specialized service, with other hospital services and external hospital or private services, community health care providers et community environment and individual one was complex and multiples. Our research identified potential concerns that need to be addressed to improve future studies to identify influential elements. Similarly, other qualitative studies will have to be conducted on the perceptions and literacy of patients with haemophilia to develop a global interactive mapping of their trajectories.
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spelling pubmed-87757962022-01-21 Haemophilia in France: Modelisation of the Clinical Pathway for Patients Beny, Karen du Sartz de Vigneulles, Benjamin Carrouel, Florence Bourgeois, Denis Gay, Valérie Negrier, Claude Dussart, Claude Int J Environ Res Public Health Article Process-of-care studies participate in improving the efficiency of the care pathway for patient with haemophilia (CPPH) and rationalize the multidisciplinary management of patients. Our objective is to establish a current overview of the different actors involved in the management of patients with haemophilia and to provide an accurate description of the patient trajectory. This is a qualitative exploratory research based on interviews of the principal health professionals of four haemophilia services, between November 2019 and February 2020, in France. Mapping of the CPPH processes within the different institutions and/or services, as well as the rupture zones, were identified. Treatment delivery and biological analyses were carried out exclusively in healthcare institutions. The main liberal health professionals solicited were nurses, physiotherapists and general practitioner. Obstacles and barriers within the specialized service, with other hospital services and external hospital or private services, community health care providers et community environment and individual one was complex and multiples. Our research identified potential concerns that need to be addressed to improve future studies to identify influential elements. Similarly, other qualitative studies will have to be conducted on the perceptions and literacy of patients with haemophilia to develop a global interactive mapping of their trajectories. MDPI 2022-01-06 /pmc/articles/PMC8775796/ /pubmed/35055467 http://dx.doi.org/10.3390/ijerph19020646 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Beny, Karen
du Sartz de Vigneulles, Benjamin
Carrouel, Florence
Bourgeois, Denis
Gay, Valérie
Negrier, Claude
Dussart, Claude
Haemophilia in France: Modelisation of the Clinical Pathway for Patients
title Haemophilia in France: Modelisation of the Clinical Pathway for Patients
title_full Haemophilia in France: Modelisation of the Clinical Pathway for Patients
title_fullStr Haemophilia in France: Modelisation of the Clinical Pathway for Patients
title_full_unstemmed Haemophilia in France: Modelisation of the Clinical Pathway for Patients
title_short Haemophilia in France: Modelisation of the Clinical Pathway for Patients
title_sort haemophilia in france: modelisation of the clinical pathway for patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775796/
https://www.ncbi.nlm.nih.gov/pubmed/35055467
http://dx.doi.org/10.3390/ijerph19020646
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