Search Results - "Pougheon Bertrand, D"

Collaborative research protocol to define patient-reported experience measures of the cystic fibrosis care pathway in France: the ExPaParM study by Pougheon Bertrand, D, Fanchini, A, Lombrail, P, Rault, G, Chansard, A, Le Breton, N, Frenod, C, Milon, F, Heymes-Royer, C, Segretain, D, Silber, M, Therouanne, S, Haesebaert, J, Llerena, C, Michel, P, Reynaud, Q

“…In France, the cystic fibrosis (CF) care pathway is coordinated by multidisciplinary teams from specialised CF centres or transplant centres. It includes the…”
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A conceptual framework to develop a patient-reported experience questionnaire on the cystic fibrosis journey in France: the ExPaParM collaborative study by Pougheon Bertrand, D, Fanchini, A, Lombrail, P, Rault, G, Chansard, A, Le Breton, N, Frenod, C, Milon, F, Royer, C Heymes, Segretain, D, Silber, M, Therouanne, S, Haesebaert, J, Llerena, C, Michel, P, Reynaud, Q

“…The objective of the study was to elaborate a conceptual framework related to the domains of patient experience along the cystic fibrosis (CF) journey from the…”
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WS16.2 Adolescence and cystic fibrosis: improving the median FEV1 of adolescents by patient education linked with a quality improvement program by David, V, Pougheon-Bertrand, D, Rault, G, Perrin, A, Bihouee, T

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Provision of information on transplantation to cystic fibrosis patients and their relatives: Overview of French practices and recommendations by David, V., Perrin, A., Le Rhun, A., Pougheon-Bertrand, D., Kanaan, R., Grenet, D., Moret, L.

“…How health-care professionals inform cystic fibrosis patients and their relatives about transplantation is not well known. Such information may not be provided…”
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252 Recognition of pulmonary exacerbation (PEX) in adult patients with CF: An educational process to overcome barriers by David, V, Pougheon-Bertrand, D, Vion, V, Scalbert, M, Dury, S, Jollivet, D

“…Objectives PEX are the main cause of lung function worsening. Early recognition of PEX by patients should improve the management of the disease. The objective…”
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342 Therapeutic patient education and quality improvement program: What synergy? by David, V, Rault, G, Pougheon-Bertrand, D, Dorenlot, E

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WS19.4 CF quality improvement program: a pilot phase to experiment the US QIP approach in France by Rault, G, Pougheon Bertrand, D, Guéganton, L, Minguet, G, Lombrail, P

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283 Sizing and financing multidisciplinary resources for CF care in the French healthcare system by Rault, G, Bellon, G, Pougheon Bertrand, D, Kletz, F, Moisdon, J.-C

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824 Implementation of patient experience surveys to improve CF care: the ExPaParM-ACTION research study by Bertrand, D. Pougheon, Bellis, G., Lombrail, P., Taillandier, L., de Carli, P.

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Parent et coordinatrice du programme PHARE-M d'amélioration de la qualité des soins dans la mucoviscidose by Bertrand, D. Pougheon, Raultb, G.

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Collaborative research protocol to define patient-reported experience measures of the cystic fibrosis care pathway in France: the ExPaParM study by Pougheon Bertrand, D., Fanchini, A., Lombrail, P., Rault, G., Chansard, A., Le Breton, N., Frenod, C., Milon, F., Heymes-Royer, C., Segretain, D., Silber, M., Therouanne, S., Haesebaert, J., Llerena, C., Michel, P., Reynaud, Q.

“…Abstract Introduction In France, the cystic fibrosis (CF) care pathway is coordinated by multidisciplinary teams from specialised CF centres or transplant…”
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Parents and the program coordinator of PHARE-M help to improve the quality of care of cystic fibrosis by Bertrand, D Pougheon, Raultb, G

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