Quality of written forms of informed consent in critically ill patients

Background: Informed Consent is the acceptance of a medical intervention by a patient, in a free, voluntary and conscious way, after the doctor has informed him of the nature of the intervention, risks, benefits and alternatives. Objective: to assess the quality of structure and content of the info...

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Main Authors: Anabel Hernández-Ruiz, Rebeca Iracema Delgado-Fernández, Carlos Omar Mitjans-Fuentes, Rosario González-Volta, Teresa Cuní-Rivera, Denis Díaz-González
Format: Article
Language:Spanish
Published: Universidad de Ciencias Médicas de Camagüey 2020-02-01
Series:Archivo Médico de Camagüey
Subjects:
Online Access:http://www.revistaamc.sld.cu/index.php/amc/article/view/6788
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author Anabel Hernández-Ruiz
Rebeca Iracema Delgado-Fernández
Carlos Omar Mitjans-Fuentes
Rosario González-Volta
Teresa Cuní-Rivera
Denis Díaz-González
author_facet Anabel Hernández-Ruiz
Rebeca Iracema Delgado-Fernández
Carlos Omar Mitjans-Fuentes
Rosario González-Volta
Teresa Cuní-Rivera
Denis Díaz-González
author_sort Anabel Hernández-Ruiz
collection DOAJ
description Background: Informed Consent is the acceptance of a medical intervention by a patient, in a free, voluntary and conscious way, after the doctor has informed him of the nature of the intervention, risks, benefits and alternatives. Objective: to assess the quality of structure and content of the informed consent forms in severe patients. Methods: cross-sectional retrospective descriptive study was carried out with 335 IC written forms applied to family members and/or patients admitted to the Intensive Care Unit of the Joaquín Albarrán Domínguez Hospital, Havana, Cuba, from September 30, 2017 to September 22, 2018. The Chi-square test was performed the frequencies of compliance. A value of p ≤ 0.05 was significant. Results: predominantly, the written formats in patients with a clinical profile complied with the completion of the document and the best were those of surgical profile. In compliance with the general data in the IC written format, there was an adequate compliance, in the forms of the clinical profile, they did not comply with writing the name and description of medical procedures. There was no consent forms to authorize medical researches and it was not delivered a copy of the written document to the interested persons. Conclusions: the quality of the formats was bad, we still have to improve the information offered, clarify the doubts, as well as the request for authorization for medical research and implement mechanisms that facilitate the delivery of a copy of the written document. DeCS: CONSENT FORMS; INFORMED CONSENT; PATIENT ACUITY; EPIDEMIOLOGY, DESCRIPTIVE; BIOMEDICAL RESEARCH.
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spelling doaj.art-6d7c2d63cdfb460e8a9c6e6f4da68fba2022-12-22T01:31:41ZspaUniversidad de Ciencias Médicas de CamagüeyArchivo Médico de Camagüey1025-02552020-02-012412139Quality of written forms of informed consent in critically ill patientsAnabel Hernández-Ruiz0Rebeca Iracema Delgado-FernándezCarlos Omar Mitjans-FuentesRosario González-VoltaTeresa Cuní-RiveraDenis Díaz-GonzálezMINSAPBackground: Informed Consent is the acceptance of a medical intervention by a patient, in a free, voluntary and conscious way, after the doctor has informed him of the nature of the intervention, risks, benefits and alternatives. Objective: to assess the quality of structure and content of the informed consent forms in severe patients. Methods: cross-sectional retrospective descriptive study was carried out with 335 IC written forms applied to family members and/or patients admitted to the Intensive Care Unit of the Joaquín Albarrán Domínguez Hospital, Havana, Cuba, from September 30, 2017 to September 22, 2018. The Chi-square test was performed the frequencies of compliance. A value of p ≤ 0.05 was significant. Results: predominantly, the written formats in patients with a clinical profile complied with the completion of the document and the best were those of surgical profile. In compliance with the general data in the IC written format, there was an adequate compliance, in the forms of the clinical profile, they did not comply with writing the name and description of medical procedures. There was no consent forms to authorize medical researches and it was not delivered a copy of the written document to the interested persons. Conclusions: the quality of the formats was bad, we still have to improve the information offered, clarify the doubts, as well as the request for authorization for medical research and implement mechanisms that facilitate the delivery of a copy of the written document. DeCS: CONSENT FORMS; INFORMED CONSENT; PATIENT ACUITY; EPIDEMIOLOGY, DESCRIPTIVE; BIOMEDICAL RESEARCH.http://www.revistaamc.sld.cu/index.php/amc/article/view/6788ética médica, consentimiento informado, autonomía, formatos escritos.
spellingShingle Anabel Hernández-Ruiz
Rebeca Iracema Delgado-Fernández
Carlos Omar Mitjans-Fuentes
Rosario González-Volta
Teresa Cuní-Rivera
Denis Díaz-González
Quality of written forms of informed consent in critically ill patients
Archivo Médico de Camagüey
ética médica, consentimiento informado, autonomía, formatos escritos.
title Quality of written forms of informed consent in critically ill patients
title_full Quality of written forms of informed consent in critically ill patients
title_fullStr Quality of written forms of informed consent in critically ill patients
title_full_unstemmed Quality of written forms of informed consent in critically ill patients
title_short Quality of written forms of informed consent in critically ill patients
title_sort quality of written forms of informed consent in critically ill patients
topic ética médica, consentimiento informado, autonomía, formatos escritos.
url http://www.revistaamc.sld.cu/index.php/amc/article/view/6788
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