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Informed consent in clinical practice: patients’ experiences and perspectives following surgery

BACKGROUND: Informed consent during medical practice is an essential component of comprehensive medical care and is a requirement that should be sought all the time the doctor interacts with the patients, though very challenging when it comes to implementation. Since the magnitude and frequency of s...

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Autores principales: Ochieng, Joseph, Buwembo, William, Munabi, Ian, Ibingira, Charles, Kiryowa, Haruna, Nzarubara, Gabriel, Mwaka, Erisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675036/
https://www.ncbi.nlm.nih.gov/pubmed/26653100
http://dx.doi.org/10.1186/s13104-015-1754-z
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author Ochieng, Joseph
Buwembo, William
Munabi, Ian
Ibingira, Charles
Kiryowa, Haruna
Nzarubara, Gabriel
Mwaka, Erisa
author_facet Ochieng, Joseph
Buwembo, William
Munabi, Ian
Ibingira, Charles
Kiryowa, Haruna
Nzarubara, Gabriel
Mwaka, Erisa
author_sort Ochieng, Joseph
collection PubMed
description BACKGROUND: Informed consent during medical practice is an essential component of comprehensive medical care and is a requirement that should be sought all the time the doctor interacts with the patients, though very challenging when it comes to implementation. Since the magnitude and frequency of surgery related risk are higher in a resource limited setting, informed consent for surgery in such settings should be more comprehensive. This study set out to evaluate patients’ experiences and perspectives of informed consent for surgery. METHODS: This was a survey of post-operative patients at three university teaching hospitals in Uganda. The participants were interviewed using guided, semi-structured questionnaires. Patients from different surgical disciplines participated in the study. RESULTS: A total of 371 patients participated in the study. Eighty percent of the participants reported having been given explanations on the indication for their surgery, 56.1 % had all their questions answered before the operation, 17 % did not know the type of operation they had undergone and another 17 % did not give their consent for the operation. Additionally, more than 81 % of the participants reported giving their own permission for surgery, although only 23.7 % were able to identify the person who obtained consent from them and 22.4 % knew the names of the surgeons who conducted the surgical procedure on them. About 20 % of the participants were not satisfied with the information provided by both the doctor before and after the operation. However, there were varying responses on when doctors should explain to patients with the majority saying it should be done before treatment or surgery, while others thought it should be done on admission, others proposed that it be made immediately after the examination among other responses. On what should be done to improve communication between doctors and patients, a number of suggestions, including the need for a detailed explanation for the patient by the doctor about their disease conditions and treatment options were suggested. CONCLUSIONS: Patients’ perceptions of what constitutes informed consent are diverse and many patients undergo surgery without knowledge of the identity of the surgeon or the reason for the surgery. There is a need to improve on patients’ participation in informed decision making, and this can be achieved through continuing medical education for doctors.
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spelling pubmed-46750362015-12-11 Informed consent in clinical practice: patients’ experiences and perspectives following surgery Ochieng, Joseph Buwembo, William Munabi, Ian Ibingira, Charles Kiryowa, Haruna Nzarubara, Gabriel Mwaka, Erisa BMC Res Notes Research Article BACKGROUND: Informed consent during medical practice is an essential component of comprehensive medical care and is a requirement that should be sought all the time the doctor interacts with the patients, though very challenging when it comes to implementation. Since the magnitude and frequency of surgery related risk are higher in a resource limited setting, informed consent for surgery in such settings should be more comprehensive. This study set out to evaluate patients’ experiences and perspectives of informed consent for surgery. METHODS: This was a survey of post-operative patients at three university teaching hospitals in Uganda. The participants were interviewed using guided, semi-structured questionnaires. Patients from different surgical disciplines participated in the study. RESULTS: A total of 371 patients participated in the study. Eighty percent of the participants reported having been given explanations on the indication for their surgery, 56.1 % had all their questions answered before the operation, 17 % did not know the type of operation they had undergone and another 17 % did not give their consent for the operation. Additionally, more than 81 % of the participants reported giving their own permission for surgery, although only 23.7 % were able to identify the person who obtained consent from them and 22.4 % knew the names of the surgeons who conducted the surgical procedure on them. About 20 % of the participants were not satisfied with the information provided by both the doctor before and after the operation. However, there were varying responses on when doctors should explain to patients with the majority saying it should be done before treatment or surgery, while others thought it should be done on admission, others proposed that it be made immediately after the examination among other responses. On what should be done to improve communication between doctors and patients, a number of suggestions, including the need for a detailed explanation for the patient by the doctor about their disease conditions and treatment options were suggested. CONCLUSIONS: Patients’ perceptions of what constitutes informed consent are diverse and many patients undergo surgery without knowledge of the identity of the surgeon or the reason for the surgery. There is a need to improve on patients’ participation in informed decision making, and this can be achieved through continuing medical education for doctors. BioMed Central 2015-12-09 /pmc/articles/PMC4675036/ /pubmed/26653100 http://dx.doi.org/10.1186/s13104-015-1754-z Text en © Ochieng et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Ochieng, Joseph
Buwembo, William
Munabi, Ian
Ibingira, Charles
Kiryowa, Haruna
Nzarubara, Gabriel
Mwaka, Erisa
Informed consent in clinical practice: patients’ experiences and perspectives following surgery
title Informed consent in clinical practice: patients’ experiences and perspectives following surgery
title_full Informed consent in clinical practice: patients’ experiences and perspectives following surgery
title_fullStr Informed consent in clinical practice: patients’ experiences and perspectives following surgery
title_full_unstemmed Informed consent in clinical practice: patients’ experiences and perspectives following surgery
title_short Informed consent in clinical practice: patients’ experiences and perspectives following surgery
title_sort informed consent in clinical practice: patients’ experiences and perspectives following surgery
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675036/
https://www.ncbi.nlm.nih.gov/pubmed/26653100
http://dx.doi.org/10.1186/s13104-015-1754-z
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