The importance of the general practitioner as an information source for patients with hereditary haemochromatosis
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , , , |
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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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 |
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reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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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1799133787129380865 |