The importance of the general practitioner as an information source for patients with hereditary haemochromatosis

Detalhes bibliográficos
Autor(a) principal: Teixeira, Emerência
Data de Publicação: 2014
Outros Autores: Borlido-Santos, Júlio, Brissot, Pierre, Butzeck, Barbara, Courtois, Françoise, Evans, Robert W., Fernau, Janet, Nunes, João Arriscado
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/27916
https://doi.org/10.1016/j.pec.2014.04.017
Resumo: Objective To explore hereditary haemochromatosis (HH) patients’ perspectives on genetic information, namely the types of sources used, preferred or trusted. Methods A survey online was conducted by the European Federation of Associations of Patients with Haemochromatosis (EFAPH) and applied to members of nine National Associations. Results From a total of 1019 validated questionnaires, 895 respondents had performed a genetic testing for HH. From these, 627 self-declared that they were sufficiently informed about the implications of the genetic test to their health. The majority (66%) obtained the information from a specialist doctor, but would like to obtain it from the family doctor. However, the specialist was still the one they trusted more (69%). Regarding the 298 respondents who did not feel sufficiently informed, the majority (78%) also would like to have information from the family doctor although they also trusted the specialist more (75%). A different perspective was reported when patients were asked about the implications of the genetic testing to their family members, where the majority of respondents preferred obtaining information from a specialist (69%). Conclusion This study elucidates the patients’ needs for information and identifies the general practitioner (GP) as the preferred source to obtain information about HH. Practice implications These results may have important implications in future strategies for HH awareness, giving a special emphasis on GPs as the main players.
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spelling The importance of the general practitioner as an information source for patients with hereditary haemochromatosisHereditary haemochromatosisPatient communicationSources of informationGeneral practitionerObjective To explore hereditary haemochromatosis (HH) patients’ perspectives on genetic information, namely the types of sources used, preferred or trusted. Methods A survey online was conducted by the European Federation of Associations of Patients with Haemochromatosis (EFAPH) and applied to members of nine National Associations. Results From a total of 1019 validated questionnaires, 895 respondents had performed a genetic testing for HH. From these, 627 self-declared that they were sufficiently informed about the implications of the genetic test to their health. The majority (66%) obtained the information from a specialist doctor, but would like to obtain it from the family doctor. However, the specialist was still the one they trusted more (69%). Regarding the 298 respondents who did not feel sufficiently informed, the majority (78%) also would like to have information from the family doctor although they also trusted the specialist more (75%). A different perspective was reported when patients were asked about the implications of the genetic testing to their family members, where the majority of respondents preferred obtaining information from a specialist (69%). Conclusion This study elucidates the patients’ needs for information and identifies the general practitioner (GP) as the preferred source to obtain information about HH. Practice implications These results may have important implications in future strategies for HH awareness, giving a special emphasis on GPs as the main players.Elsevier2014-07info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/27916http://hdl.handle.net/10316/27916https://doi.org/10.1016/j.pec.2014.04.017engTEIXEIRA, Emerência [et. al] - The importance of the general practitioner as an information source for patients with hereditary haemochromatosis. "Patient Education and Counseling". ISSN 0738-3991. Vol. 96 Nº. 1 (2014) p. 86–920738-3991http://www.sciencedirect.com/science/article/pii/S0738399114001785Teixeira, EmerênciaBorlido-Santos, JúlioBrissot, PierreButzeck, BarbaraCourtois, FrançoiseEvans, Robert W.Fernau, JanetNunes, João Arriscadoinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2021-07-14T09:38:00Zoai:estudogeral.uc.pt:10316/27916Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:50:34.340112Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv The importance of the general practitioner as an information source for patients with hereditary haemochromatosis
title The importance of the general practitioner as an information source for patients with hereditary haemochromatosis
spellingShingle The importance of the general practitioner as an information source for patients with hereditary haemochromatosis
Teixeira, Emerência
Hereditary haemochromatosis
Patient communication
Sources of information
General practitioner
title_short The importance of the general practitioner as an information source for patients with hereditary haemochromatosis
title_full The importance of the general practitioner as an information source for patients with hereditary haemochromatosis
title_fullStr The importance of the general practitioner as an information source for patients with hereditary haemochromatosis
title_full_unstemmed The importance of the general practitioner as an information source for patients with hereditary haemochromatosis
title_sort The importance of the general practitioner as an information source for patients with hereditary haemochromatosis
author Teixeira, Emerência
author_facet Teixeira, Emerência
Borlido-Santos, Júlio
Brissot, Pierre
Butzeck, Barbara
Courtois, Françoise
Evans, Robert W.
Fernau, Janet
Nunes, João Arriscado
author_role author
author2 Borlido-Santos, Júlio
Brissot, Pierre
Butzeck, Barbara
Courtois, Françoise
Evans, Robert W.
Fernau, Janet
Nunes, João Arriscado
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Teixeira, Emerência
Borlido-Santos, Júlio
Brissot, Pierre
Butzeck, Barbara
Courtois, Françoise
Evans, Robert W.
Fernau, Janet
Nunes, João Arriscado
dc.subject.por.fl_str_mv Hereditary haemochromatosis
Patient communication
Sources of information
General practitioner
topic Hereditary haemochromatosis
Patient communication
Sources of information
General practitioner
description Objective To explore hereditary haemochromatosis (HH) patients’ perspectives on genetic information, namely the types of sources used, preferred or trusted. Methods A survey online was conducted by the European Federation of Associations of Patients with Haemochromatosis (EFAPH) and applied to members of nine National Associations. Results From a total of 1019 validated questionnaires, 895 respondents had performed a genetic testing for HH. From these, 627 self-declared that they were sufficiently informed about the implications of the genetic test to their health. The majority (66%) obtained the information from a specialist doctor, but would like to obtain it from the family doctor. However, the specialist was still the one they trusted more (69%). Regarding the 298 respondents who did not feel sufficiently informed, the majority (78%) also would like to have information from the family doctor although they also trusted the specialist more (75%). A different perspective was reported when patients were asked about the implications of the genetic testing to their family members, where the majority of respondents preferred obtaining information from a specialist (69%). Conclusion This study elucidates the patients’ needs for information and identifies the general practitioner (GP) as the preferred source to obtain information about HH. Practice implications These results may have important implications in future strategies for HH awareness, giving a special emphasis on GPs as the main players.
publishDate 2014
dc.date.none.fl_str_mv 2014-07
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/27916
http://hdl.handle.net/10316/27916
https://doi.org/10.1016/j.pec.2014.04.017
url http://hdl.handle.net/10316/27916
https://doi.org/10.1016/j.pec.2014.04.017
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv TEIXEIRA, Emerência [et. al] - The importance of the general practitioner as an information source for patients with hereditary haemochromatosis. "Patient Education and Counseling". ISSN 0738-3991. Vol. 96 Nº. 1 (2014) p. 86–92
0738-3991
http://www.sciencedirect.com/science/article/pii/S0738399114001785
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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