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General practitioner residents and patients end-of life: involvement and consequences
BACKGROUND: The ageing of the population and the increased number of chronic diseases are associated with an increased frequency of end of life care in hospital settings. Residents rotating in hospital wards play a major part in their care, regardless of their specialty. General practitioner (GP) re...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719227/ https://www.ncbi.nlm.nih.gov/pubmed/36463158 http://dx.doi.org/10.1186/s12910-022-00867-9 |
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author | Haardt, Victoire Cambriel, Amélie Hubert, Sidonie Tran, Marc Bruel, Cédric Philippart, Francois |
author_facet | Haardt, Victoire Cambriel, Amélie Hubert, Sidonie Tran, Marc Bruel, Cédric Philippart, Francois |
author_sort | Haardt, Victoire |
collection | PubMed |
description | BACKGROUND: The ageing of the population and the increased number of chronic diseases are associated with an increased frequency of end of life care in hospital settings. Residents rotating in hospital wards play a major part in their care, regardless of their specialty. General practitioner (GP) residents are confronted to such activities in hospital settings during their training. Our aim was to know how they feel about taking care of dying patients, as end-of-life care are very different from the clinical activity they are trained to. METHODS: We surveyed all GP trainees of “Ile de France”. The survey was made of 41 questions regarding advanced directives divided in 7 sections about patients’ care, communication, mentoring and repercussion on personal life. The survey was done one time, during two pre-specified days. RESULTS: 525 residents (53.8%) accepted to fulfill the survey. 74.1% of the residents thought that palliative care could have been better. Possible ways of improvements were: a reduction of unreasonable obstinacy (or therapeutic overkill, two terms defined in French law as curative treatment without reasonable hope of efficiency) (59.6%), patient’s (210 answers, 40%) and relative’s communication (information of patients and relatives about the severity of the disease and risk of death) (199 answers 37.9%). Residents also reported a lack of knowledge regarding end-of-life care specific treatments (411 answers, 79.3%) and 298 (47.2%) wished for better mentoring. Those difficulties were associated with repercussion on their private life (353 answers, 67.2%), particularly with their close relatives (55.4%). Finally, 56.2% of trainees thought that a systematic psychologic follow up should be instituted for those working in “at risk” hospital settings. CONCLUSION: Self-perception management of dying patients by GP resident emphasize their lack of training and supervision. The feeling of suboptimal care is associated with consequences on personal life. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12910-022-00867-9. |
format | Online Article Text |
id | pubmed-9719227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97192272022-12-04 General practitioner residents and patients end-of life: involvement and consequences Haardt, Victoire Cambriel, Amélie Hubert, Sidonie Tran, Marc Bruel, Cédric Philippart, Francois BMC Med Ethics Research Article BACKGROUND: The ageing of the population and the increased number of chronic diseases are associated with an increased frequency of end of life care in hospital settings. Residents rotating in hospital wards play a major part in their care, regardless of their specialty. General practitioner (GP) residents are confronted to such activities in hospital settings during their training. Our aim was to know how they feel about taking care of dying patients, as end-of-life care are very different from the clinical activity they are trained to. METHODS: We surveyed all GP trainees of “Ile de France”. The survey was made of 41 questions regarding advanced directives divided in 7 sections about patients’ care, communication, mentoring and repercussion on personal life. The survey was done one time, during two pre-specified days. RESULTS: 525 residents (53.8%) accepted to fulfill the survey. 74.1% of the residents thought that palliative care could have been better. Possible ways of improvements were: a reduction of unreasonable obstinacy (or therapeutic overkill, two terms defined in French law as curative treatment without reasonable hope of efficiency) (59.6%), patient’s (210 answers, 40%) and relative’s communication (information of patients and relatives about the severity of the disease and risk of death) (199 answers 37.9%). Residents also reported a lack of knowledge regarding end-of-life care specific treatments (411 answers, 79.3%) and 298 (47.2%) wished for better mentoring. Those difficulties were associated with repercussion on their private life (353 answers, 67.2%), particularly with their close relatives (55.4%). Finally, 56.2% of trainees thought that a systematic psychologic follow up should be instituted for those working in “at risk” hospital settings. CONCLUSION: Self-perception management of dying patients by GP resident emphasize their lack of training and supervision. The feeling of suboptimal care is associated with consequences on personal life. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12910-022-00867-9. BioMed Central 2022-12-03 /pmc/articles/PMC9719227/ /pubmed/36463158 http://dx.doi.org/10.1186/s12910-022-00867-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Haardt, Victoire Cambriel, Amélie Hubert, Sidonie Tran, Marc Bruel, Cédric Philippart, Francois General practitioner residents and patients end-of life: involvement and consequences |
title | General practitioner residents and patients end-of life: involvement and consequences |
title_full | General practitioner residents and patients end-of life: involvement and consequences |
title_fullStr | General practitioner residents and patients end-of life: involvement and consequences |
title_full_unstemmed | General practitioner residents and patients end-of life: involvement and consequences |
title_short | General practitioner residents and patients end-of life: involvement and consequences |
title_sort | general practitioner residents and patients end-of life: involvement and consequences |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9719227/ https://www.ncbi.nlm.nih.gov/pubmed/36463158 http://dx.doi.org/10.1186/s12910-022-00867-9 |
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