Search results for "Informed consent"
showing 10 items of 109 documents
Genomic Testing for Human Health and Disease Across the Life Cycle: Applications and Ethical, Legal, and Social Challenges
2019
The expanding use of genomic technologies encompasses all phases of life, from the embryo to the elderly, and even the posthumous phase. In this paper, we present the spectrum of genomic healthcare applications, and describe their scope and challenges at different stages of the life cycle. The integration of genomic technology into healthcare presents unique ethical issues that challenge traditional aspects of healthcare delivery. These challenges include the different definitions of utility as applied to genomic information; the particular characteristics of genetic data that influence how it might be protected, used and shared; and the difficulties applying existing models of informed con…
Il consenso informato ai trattamenti sanitari sui minori e decisioni di fine vita. Riflessioni comparatistiche
2019
The essay deals with the informed consent to allow or to refuse medical treatment for pediatric patients, in a comparative law perspective. The first part focuses on the principle of personal autonomy and the rights to health and to life for patiens who lack capacity, as enshrined in Italian legislation. In determining care and treatment in relation to their child, parents have to take into account the physical and mental well-being, life and dignity of the person, as fully as possible (art. 3, L. 219/2017). The second part of the paper investigates the consequences of parents' refusal to interrupt or continue life-sustaining treatment in relation to infants suffering from serious and incur…
Protocol of a multicenter international randomized controlled manikin study on different protocols of cardiopulmonary resuscitation for laypeople (MA…
2018
IntroductionOut-of-hospital cardiac arrest is one of the leading causes of death in industrialised countries. Survival depends on prompt identification of cardiac arrest and on the quality and timing of cardiopulmonary resuscitation (CPR) and defibrillation. For laypeople, there has been a growing interest on hands-only CPR, meaning continuous chest compression without interruption to perform ventilations. It has been demonstrated that intentional interruptions in hands-only CPR can increase its quality. The aim of this randomised trial is to compare three CPR protocols performed with different intentional interruptions with hands-only CPR.Methods and analysisThis is a prospective randomise…
Issues of Ethics and Methods in Studying Social Media
2016
The Editorial raises some challenging ethical and methodological aspects of Internet based research (such as protection of informational privacy, informed consent, general ethical guidelines vs case-based approach), which are further discussed in the five articles of this special issue.
Perceived influence of oral health upon quality of life in heart transplant patients
2011
Objective: A study was made of heart transplant patient perception of the influence of oral health upon quality of life, based on the Oral Health Impact Profile (OHIP-49) questionnaire validated for Spanish speaking subjects. Design: A cross-sectional evaluation was made of the heart transplant patients followed-up on in the Heart Transplantation Unit of Reina Sofía University Hospital (Spain), using the OHIP-49 questionnaire. The included patients were all over age 18 and signed the corresponding informed consent to participation in the study. The data were entered in a database and analyzed using the SPSS statistical package. Results: A total of 150 heart transplant patients (118 males an…
Informed consent and minors: hiv testing in italian legislation.
2008
Bioethics and power: Informed consent procedures in post-socialist Latvia
2013
This paper explores two lines of development in the donor consent procedures in post-Soviet Latvia. The paper is based on secondary analysis of interview, focus group discussion data, and media and legal text material collected throughout three previously conducted research projects on organ transplantation, population genome project and xenotransplantation focusing on the historical development of the issues of donor consent across these three fields of medical technologies. The paper argues that the quality of consent depends not as much on political and legal change per se as on the strengthening of the position of both medical specialists and donors, facilitating bonds between the two.
Mapping of activation frequencies during ventricular fibrillation in isolated perfused healthy human heart
2013
dentity Narrative in informal family and non-family caregivers of people on dialysis
2019
Objetivo. Explorar la identidad narrativa de las cuidadoras informales familiares o no, de personas en diálisis. Método. Entrevistas en profundidad a 9 cuidadoras de personas de programas de Hemodiálisis o Diálisis Peritoneal del Hospital General Universitario. Se obtuvo autorización del Comité de Ética y los consentimientos informados de los participantes. El análisis se hizo desde la Teoría Fundamentada. Las narraciones transcritas y codificadas fueron sometidas a reflexión hermenéutica. Resultados. La enfermedad genera un impacto y las cuidadoras asumen el cuidado como pueden. Surge el sentimiento de “cuidado como destino” y como dotación intrínseca de “ser mujer”, percibido como una esp…
Il lascito del proprio corpo a fini didattici e di ricerca. Il nobile (ma vano) intento della legge 10/2020
2021
The essay gives a sharp outline of the recent Italian law ruling body donation to science after death, as a personal choice exclusively founds on a conscious and free act of will. The statute, however, has not been met its aim, lacking of supporting the donor in making his consent fully effective. Indeed, as one of the highest displays of human solidarity, this issue would have required a balance between scientific research interests and individual autonomy protection.