Acta Bioethica
https://revistapuntogenero.uchile.cl/index.php/AB
<p>Acta Bioethica is a biannual publication by the Interdisciplinary Center for Studies in Bioethics of the University of Chile (ISSN 0717-5906, press edition, y 1726-569-X, electronic edition), which publishes in three languages: Spanish, English and Portuguese.</p> <p>Indexed in Science Citation Index (SCI), Scopus, Lilacs, SciELO y Latindex, and in database from several Institutions; it constitutes a pluralistic source of perspectives and an important tribune which accepts the contributions of authors compromised with the interdisciplinary study of ethical determinants and consequences of techno scientific research.</p> <p>The journal edits a main topic per issue, with articles asked by an invited editor (specialist in the topic chosen), and it also includes a section of articles not solicited of various nature (interfaces), reviews of recent bioethical publications and other significant documents for the inter discipline. It also counts with an International Advisory Committee and a system of arbitration of manuscripts based on peer review.</p> <p>The journal is published on HTML and PDF format in SciELO (Scientific Electronic Library Online) and in PDF in the web site for journals of the University of Chile.</p>Universidad de Chile. Centro Interdisciplinario de Estudios en Bioéticaen-USActa Bioethica0717-5906<p>Acta Bioethica is edited by the Interdisciplinary Center for Bioethical Studies of the University of Chile and published under a Creative Commons Attribution Share Alike 4.0 International license.Intellectual property::The submission and evaluation of the manuscripts received implies that the author (s) declare that they are original and exclusive owners of the author's economic and moral rights over the article, in accordance with the provisions of Law 17.336 on Intellectual Property (Chile) In case of having used outside works in the creation of the article, in whole or in part, they declare that they have the respective authorizations or licenses of use of their respective owners or that their use is expressly protected by law.The author expressly releases from any subsequent responsibility to the Interdisciplinary Center of Studies in Bioethics of the University of Chile, for any legal, regulatory or contractual infraction that eventually commits or has committed in relation to the work, being obliged to repair any damage that results from the Infringement of these or other rights.The author authorizes the Interdisciplinary Center of Studies in Bioethics of the University of Chile, in order that, by itself or through third parties expressly authorized by it, exercise the rights that are specified below, with respect to the article sent:Publication, edition, reproduction, adaptation, distribution and sale of reproduced copies, including making available to the public online by electronic or digital means, of the article, in Castilian language, in any known territory, And for all types of printed edition in paper and electronic or digital, by its inclusion in the journal Acta Bioethica or another publication that publishes the Center.This authorization is conferred on a non-exclusive, free, indefinite, perpetual and non-revocable basis, as long as the corresponding rights subsist and release the Interdisciplinary Center for Bioethical Studies of the University of Chile from any payment or remuneration for the exercise of Rights.The authors retain their copyright on their works, being able to reuse them as they decide.</p>Revisiting the Conceptual Aspects of Humanization and Dignified Treatment in Healthcare from an Ethical Perspective: A systematic review of the literature
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76133
Background: The attainment of humanization and dignified treatment in healthcare has proven to be a challenging endeavor, notwithstanding the advancements made in initiatives aimed at their implementation. One approach to addressing this issue is to direct reflection towards its ethical and conceptual foundations, as well as exploring the potential integration of the various dimensions involved in its management and approach. Objectives: The aim of this study is to conduct a systematic review of original articles focusing on humanization and dignified treatment in healthcare from an ethical and bioethical standpoint, with two specific research objectives: 1. To identify key conceptualizations related to humanization and dignified treatment, taking into account the perspectives of the various stakeholders at contextual, institutional, interpersonal, and personal levels. 2. To propose a relational model that facilitates the visualization of the dimensions, agents, and practices involved in humanization. Methods: A systematic search was performed in the Web of Science (WoS) database, following bibliometric procedures and the PRISMA methodology. Results: A total of 8 articles were selected from the WoS indexing categories of “Ethics” and “Religion,” published between 2010 and 2022. The analysis revealed that ethics and bioethics play a fundamental role in shaping the discourse on humanization and dignified treatment in healthcare. Key themes included respect for individuals' integrity, relational ethics, associated ethical principles, and concrete institutional practices. Discussion: The implications of considering ethical notions as foundations for humanization and dignified treatment in healthcare, as well as the proposal of a relational model in humanization applicable to healthcare practices, are discussed.Paola Andreucci-AnnunziataAugusto MelladoAlejandro Vega-MuñozFrancisco León-Correa
Copyright (c) 2024 Paola Andreucci-Annunziata, Augusto Mellado, Alejandro Vega-Muñoz, Francisco León-Correa
2024-09-252024-09-25302177192Exploring ethical principles and values in the surgical care of the geriatric patient: a humanized and emergent approach
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76134
The objective of this research is to describe the meanings and practices from the values and principles that emerge during the humanized care provided by the surgical team to the geriatric patient scheduled for surgery. Through the qualitative and interpretive paradigm, and from an objectivist and methodological epistemic framework, the perception existing among surgeons on how humanized care should be towards the elderly is reflected. Ten surgeons were interviewed through semi-structured sessions, and the analysis was carried out using the matrix of categories with the support of the ATLAS Ti 8.0 ® program. The perception of surgeons regarding humanized care considers that care is strengthened during the higher education they receive at the university and is fortified through the norms that govern the profession, in the sense of always aiming for the well-being and respect for the dignity of patients, especially the most vulnerable.Anderson Díaz PérezAlbeis Castro NovoaAndrea Carolina Villegas PachecoZuleima Yáñez TorregrosaYoliseth Cabarcas TeheranAngélica Roca PérezWendy Acuña Pérez
Copyright (c) 2024 Anderson Díaz Pérez, Albeis Castro Novoa, Andrea Carolina Villegas Pacheco, Zuleima Yáñez Torregrosa, Yoliseth Cabarcas Teheran, Angélica Roca Pérez, Wendy Acuña Pérez
2024-09-252024-09-25302193206Comprehensive Methodology for Ethical-Clinical Analysis (CMECA): A new paradigm for resolving end-of-Life dilemmas
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76135
End-of-life care management presents significant ethical challenges, especially in complex clinical cases such as that of a patient with severe head trauma and multiple complications. Ethical decision-making involves considering the rights, dignity, and preferences of the patient and his or her family, as well as quality of life and relief from suffering. The objective of this research is to design and implement a comprehensive methodology to provide a care plan that respects the dignity and improves the quality of life of patients at the end of life, aligned with their wishes and those of their family. The approach used was the Comprehensive Methodology of Clinical-Ethical Analysis (CMECA), which included a continuous evaluation, pain and symptom management, supportive care, limitations of medical interventions, and preparation for the end of life, with the active participation of the family from a palliative care approach. The resolution of the case was achieved through a shared decision between the parents and the medical team, proceeding with a gradual disconnection of life support. The importance and relevance of the Comprehensive Methodology of Ethical-Clinical Analysis (CMECA) is highlighted, due to its comprehensive approach focused on the patient and in accordance with medical ethics. This method stands out for considering legal and ethical aspects, empathy, and respect for human dignity at all times.Anderson Díaz Pérez
Copyright (c) 2024 Anderson Díaz Pérez
2024-09-252024-09-25302207218The right to be forgotten regarding genetic data: A legal and ethical analysis
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76137
This article investigates an under-discussed provision of the European Union's (EU's) General Data Protection Regulation (GDPR) regarding genetic data, i.e., the right to be forgotten. The debate on this right came from the commerce-related side of data protection instead of the medical side. Thus, this article addresses the implications of the RTBF for the lawful processing of familial genetic data. The article develops a normative, ethically focused principles argument about interpreting genetic data’s right to be forgotten. It gives due consideration to autonomy, privacy, and human dignity. It argues that the individualistic approach of genetic privacy materialised through the extreme solution of data erasure is challenging to combine with familial and scientific research interests. The article suggests an interpretation of the GDPR according to bioethical principles and the inclusion of a specific exception regarding genetic data to prevent patients from claiming the right to be forgotten. Keywords: bioethics, data protection, genetic data, privacy, right to be forgotten.Mónica CorreiaGuilhermina RegoRui Nunes
Copyright (c) 2024 Mónica Correia, Guilhermina Rego, Rui Nunes
2024-09-252024-09-25302231243What “evidence” does Evidence-Based Medicine (EBM) refer to?
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76138
This article examines the use of the concept of “evidence” in the current movement known as “Evidence-Based Medicine” (EBM). The article includes some historical milestones of the concept, in which Aristotle, André Lalande and Michel Foucault are the main references. Then, the process through which EBM was born is reviewed, going through Cochrane, Guyatt, Sackett and Woolf. It is explained that EBM understands evidence as facts, where controlled and randomized clinical studies, as well as systematic reviews, are the most appropriate means to obtain evidence. We propose that EBM may not be aware that the concept of “evidence” used is crypto-normative, which makes this concept contain a strong axiological load. The article does not intend to simply dismiss the concept of “evidence”, but rather to review its univocality and open it to an analogous understanding that could improve clinical practices and the theoretical scope that serve as their foundation. A central part of the arguments used in this paper consists of reviewing the supposed epistemic neutrality of EBM, which is a movement in formation that requires various adjustments. Among them, an in-depth review of the concept that gives it its name and meaning, for the benefit of the generators and users of EBM (clinicians and patients).Karina Ordóñez TorresJorge Martínez Barrera
Copyright (c) 2024 Karina Ordóñez Torres, Jorge Martínez Barrera
2024-09-252024-09-25302245252Ethical aspects in telemedicine. Literature review
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76139
This paper analyzes the ethical aspects related to telemedicine. A literature search on the topic was conducted, based on a systematic review of the specific ethical aspects of telemedicine using thirteen articles selected from the Web of Science and PubMed databases. The findings were grouped into the following categories: access; principles; quality of care; privacy, confidentiality, cybersecurity; commercialization, conflict of interest; trust and doctor-patient relationship; education, training and licensing; professional malpractice, telenegligence; virtual prescription of medications; shared decisions, patient empowerment; informed consent; governance and policies. The ethical aspects of telemedicine are important not only for adequate health care, but also for the construction of adequate public policies.Francisco Rosero-VillarrealGalo Sánchez del Hierro
Copyright (c) 2024 Francisco Rosero-Villarreal, Galo Sánchez del Hierro
2024-09-252024-09-25302253261Computing addiction: Epistemic injustice challenges in the culture of computational psychiatry
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76142
Computational psychiatry (CP), based on artificial intelligence technology, plays an increasingly important role in scientific research and medical diagnosis. Epistemic concerns in the ethics of artificial intelligence have also been at the center of debate in CP, but the different epistemic forms of injustice caused by the internal cultures of CP remain unexplained. We distinguish between data-driven and theory-driven cultures and their research purposes via practical examples of CP models deployed in addiction. A data-driven culture may advance medical understanding of biological categories of mental illness, whereas a theory-driven culture provides better explanatory mechanisms between symptoms and biology. We discuss testimonial injustice caused by the silencing of patient voices in a data-driven culture, and hermeneutic injustice caused by the non-sharing of hermeneutic resources in theory-driven culture based on Miranda Fricker's account of epistemic injustice. We analyze the factors underlying nuances in epistemic forms between the two, such as naturalistic-dominated medical understanding and the system's epistemic privileging. The above epistemic risks all indicate the intricacies of mental disorders and require that success be assessed in terms of actual benefit to patients. Finally, we emphasize the importance of the patient's phenomenology and call for greater inclusion of patients in psychiatric decision-making processes.Min WangZhoukang WuLiangjiecheng HuangXiaochu ZhangXiaosong He
Copyright (c) 2024 Min Wang, Zhoukang Wu, Liangjiecheng Huang, Xiaochu Zhang, Xiaosong He
2024-09-252024-09-25302263272Evaluation of moral intelligence in prehospital emergency healthcare employees: The case of Bolu-Düzce
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76143
Prehospital emergency healthcare employees are frequently faced with ethical problems. Moral intelligence, which is seen as a rising value in the field of health, is very important for prehospital emergency health employees to choose the best and right action ethically. This study aims to evaluate the moral intelligence of prehospital emergency healthcare employees and to determine whether moral intelligence parameters differ according to various socio-demographic characteristics. This study was conducted with 261 emergency medical personnel working in the ambulance service between November 2021 and February 2022. Participants showed high sensitivity to equality, empathy, moral intelligence, justice, tolerance, self-control, and kindness in the delivery of healthcare services. There were no significant differences between the groups in the scale dimensions in terms of gender, educational level, working hours, working systems, income level and having children. Single/widowed/divorced/separated participants had significantly higher levels of empathy (p=0.004), justice (p=0.039) and self-control (p=0.009) than married participants. The self-control levels of paramedics were found to be higher than those of health officers/nurses/midwives/others (p=0.015). The high sensitivity of employees towards moral intelligence parameters can play an effective role in solving both ethical issues and problems related to other moral intelligence parameters in the field of prehospital healthcare.Ramazan GüneşerNurdan Kırımlıoğlu
Copyright (c) 2024 Ramazan Güneşer, Nurdan Kırımlıoğlu
2024-09-252024-09-25302273283Bioethics in public university education in health sciences in Perú
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76160
The purpose of this research lies in evaluating the current state of higher university education about bioethics studies in the faculties of health sciences in the Peruvian territory. The methodological design adopts a descriptive level with a mixed approach that is divided into two stages: The first consists of a qualitative theoretical-analytical-rational analysis, followed by a subsequent empirical analysis with a quantitative, descriptive, and cross-sectional approach. The main discoveries refer to the existence of nineteen licensed public universities in Peru that offer the Human Medicine degree. However, it was found that the Bioethics course is only available in nine of these institutions. In summary, it can be affirmed that in the educational programs of careers related to health sciences, attempts are made to address ethical principles from different perspectives, for example, through courses on general ethics or deontology. However, this strategy is not considered adequate. In addition, it is imperative to promote an educational policy within the faculties of health sciences that mandates the mandatory inclusion of a bioethics course in the curricula of health sciences programs.Ana Alondra Paredes CohailaAmérico Alca GómezOmar Pezo Jiménez
Copyright (c) 2024 Ana Alondra Paredes Cohaila, Américo Alca Gómez, Omar Pezo Jiménez
2024-09-252024-09-25302285292The use of informed consent in dental practice in southern Peru
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76161
The objective of this research is to determine how informed consent is used in dental practice in southern Peru in the year 2023. The methodological design adopts a descriptive level with a mixed approach that is divided into two stages: The first consisted of a qualitative theoretical-analytical-rational analysis, followed by a subsequent empirical analysis with a quantitative, descriptive and cross-sectional approach. The study was carried out in a population of dentists who practice the dental profession in southern Peru in the year 2023 with a non-probabilistic convenience sample of 131 dentists. The main results were that the use of informed consent (14.5%) states that they do not use it in their daily consultation and (59.5%) use it in an erroneous way, due to different factors that influence this procedure and that the non-use of informed consent in its highest percentage arguing "lack of time" on the part of dentists It was concluded that there is a high rate of dental professionals who do not use informed consent in their professional practice, even more so that there is a high percentage that does not use consent correctly reported as an ethical-legal document.Astridh Semiramis Quenaya GarayUlises Massino Peñaloza De La TorreOlga Elizabeth Salazar PacoAlejandro Aldana CáceresOmar Pezo Jiménez
Copyright (c) 2024 Astridh Semiramis Quenaya Garay, Ulises Massino Peñaloza De La Torre, Olga Elizabeth Salazar Paco, Alejandro Aldana Cáceres, Omar Pezo Jiménez
2024-09-252024-09-25302293302Temporal and spatial changes and equity of nursing human resources configuration in Sichuan province, China
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76164
This research aims to analyze the configuration, distribution, and equity of nursing human resources in Sichuan Province, China, providing a reference for the future development of nursing care in the region. A descriptive analysis was conducted to describe the configuration of nursing human resources in 2010, 2015, and 2020. The Lorenz curve, Gini coefficient, health resource density index, and distribution density maps were used as resources and methodology to evaluate the changes and equity in the configuration of nursing human resources. The result of this research determined that the nurse-to-population ratio was 1.17, 2.09, and 3.42 in 2010, 2015, and 2020, and nursing staff accounted for 24%, 49%, and 35% of technical health personnel. The nurse-to-physician ratio was 1:0.72, 1:1.05, and 1:1.22 in the three years. The Gini coefficients of nursing resource allocation for permanent population and area were 0.24, 0.20, and 0.12 and 0.74, 0.72, and 0.72, respectively. The nursing resource density index was 0.50, 0.91, and 1.42, respectively. In conclusion, the study shows that the equity of nursing resources based on population increased, while the equity based on region still showed disparity, with a sustained increase in nursing human resource density from 2010 to 2020. However, it is necessary to continue increasing the number of nurses and improving the geographical accessibility of nursing care.Huan YangYayun Song
Copyright (c) 2024 Huan Yang, Yayun Song
2024-09-252024-09-25302303310Brazilian physicians' attitudes and feelings towards palliative care in pediatrics
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76165
The aim of the article is to evaluate and understand the feelings and attitudes of Brazilian physicians regarding the implementation of palliative care in pediatric patients. Between July 2018 and December 2019, 236 questionnaires were sent to physicians on the National Academy of Palliative Care roster. The data collected through the planned questionnaires were analyzed using the IRAMUTEQ programs (Interface de R pour les Analyzes Multidimensionnelles de Textes et de Questionnaires). From the analysis performed by IRAMUTEQ, a dendrogram containing words with p<0.05 was obtained. Feelings of sadness, anguish, relief, regret and fulfillment were perceived as relevant. Attitudes such as understanding, communication, instructing, treating well, strategy, and multiprofessional conferences were also described. Thus, it was observed that these professionals experience different contradictory feelings and make use of different strategies so that they do not harm the treatment carried out, in addition to maintaining a good relationship with the patient's family. In the present study, we demonstrate that there are intrinsic characteristics of pediatric palliative care that are a source of mixed feelings for medical professionals. In this context, challenges still exist and it is essential to conduct new studies that address this issue. Paying attention to these feelings promotes better management of palliative care in pediatrics.Anderson de Almeida RochaBianca Gusmão MeirellesLaís Costa Lage de AssisRui Manuel Lopes Nunes
Copyright (c) 2024 Anderson de Almeida Rocha, Bianca Gusmão Meirelles, Laís Costa Lage de Assis, Rui Manuel Lopes Nunes
2024-09-252024-09-25302311318Humanización, humanismo, ética
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76131
Fernando Lolas Stepke
Copyright (c) 2024 Fernando Lolas Stepke
2024-09-252024-09-25302175176HERREROS, BENJAMÍN. Filosofía y Medicina. Una historia de amor
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76169
Fernando Lolas Stepke
Copyright (c) 2024 Fernando Lolas Stepke
2024-09-252024-09-25302329330PIÑAS-MESA, A. y POVEDA GARCÍA-NOBLEJAS, B. (eds). Juan Rof Carballo. Medicina, Psicología, Antropología
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76170
Nunzio Bombaci
Copyright (c) 2024 Nunzio Bombaci
2024-09-252024-09-25302331332Desafíos en la especialización para gestión de datos de investigación en un contexto ético
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76166
Este comentario explora los desafíos éticos y bioéticos asociados con la gestión responsable de datos de investigación en Chile, en el contexto de la implementación de regulaciones europeas como el Reglamento General de Protección de Datos (GDPR) y los principios FAIR (Findability, Accessibility, Interoperability, and Reusability). Se comentan los esfuerzos de instituciones chilenas y regionales, como La Referencia, CLACSO y UNESCO, en la promoción de prácticas de gestión de datos que se alinean con los criterios europeos, y se explicitan recomendaciones para integrar de mejor forma la gestión responsable de los datos en el contexto de la investigación.Ricardo Hartley BelmarJaviera Atenas
Copyright (c) 2024 Ricardo Hartley Belmar, Javiera Atenas
2024-09-252024-09-25302319322Octaviano Humberto Domínguez Márquez: incansable defensor de la dignidad de la vida
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76167
Octavio Márquez Mendoza
Copyright (c) 2024 Octavio Márquez Mendoza
2024-09-252024-09-2530232332412 Congreso Internacional de Educación en Ética: Desarrollo Sostenible y Ecología Integral
https://revistapuntogenero.uchile.cl/index.php/AB/article/view/76168
David Cerdio-DomínguezAntonio María Cabrera-Cabrera
Copyright (c) 2024 David Cerdio-Domínguez, Antonio María Cabrera-Cabrera
2024-09-252024-09-25302325327