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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-8775796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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