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dc.rights.licenseLicencia de Creative Commons Reconocimiento-NoComercial-CompartirIgual 4.0 Internacionalspa
dc.contributor.authorDíaz-Pérez, Anderson
dc.contributor.authorVega Ochoa, Arley Denisse
dc.contributor.authorRomero Oñate, Zoraima
dc.date.accessioned2018-08-06T15:02:54Z
dc.date.available2018-08-06T15:02:54Z
dc.date.issued2018-07-25
dc.identifier.issn19169744
dc.identifier.urihttp://hdl.handle.net/20.500.12442/2221
dc.description.abstractIt is necessary to recognize the child as an active moral subject in making decision process related to his health or his participation in research. The taking of informed consent as a communication process should tend to respect the autonomy and dignity of the child considered mature or not, taking their decisions seriously and not just an assent as a normative principle of mere legal aspect. It describes theoretical elements that can be used as tools to have an approach to the moral development of the child from the principle of responsibility according to the degree of emancipation. The objective is to provide a description of the most relevant aspects about the informed consent process in the mature child and their right to be informed to agree or consent. We searched the databases such as: PROQUEST, MEDLINE, LILACS and PUBMED, analyzing 51 articles. For the organization of the information, the SLIDING methodology was used: sort, label, integrate and prioritize. It was concluded that the ability to assent of the child considered mature or not should be evaluated under objective parameters and not simply under the perception of the doctor or researcher. Finally, it is necessary to design strategies to promote the autonomy, respect and dignity of the child based on the same practices at the time of informed consent.eng
dc.language.isoengeng
dc.publisherCanadian Center of Science and Educationeng
dc.sourceGlobal Journal of Health Scienceeng
dc.sourceVol. 10, No.8 (2018)spa
dc.source.urihttps://www.researchgate.net/publication/326627218_The_Informed_ConsentAssent_from_the_Doctrine_of_the_Mature_Minoreng
dc.subjectConsent/informed assenteng
dc.subjectChildreneng
dc.subjectAdolescentseng
dc.subjectMoral developmenteng
dc.subjectCapacityeng
dc.subjectDilemmaseng
dc.subjectBioethicseng
dc.subjectDignityeng
dc.subjectRespecteng
dc.subjectAutonomyeng
dc.titleThe Informed Consent/Assent from the Doctrine of the Mature Minoreng
dc.typearticleeng
dcterms.referencesAierbe, A., Cortés, A., & Medrano, C. (2001). Una visión integradora de la teoría kohlberiana a partir de las críticas contextuales: implicaciones para la educación y la investigación en el ámbito moral. Cultura y Educación, 13(2), 147-177. https://doi.org/10.1174/113564001750425123eng
dcterms.referencesAlderson, P. (2007). Competent children? Minors’ consent to health care treatment and research. Social science & medicine, 65(11), 2272-2283. https://doi.org/10.1016/j.socscimed.2007.08.005eng
dcterms.referencesAppelbaum, P. S., & Roth, L. H. (1982). Competency to consent to research: A psychiatric overview. Archives of General Psychiatry, 39(8), 951-958. https://doi.org/10.1001/archpsyc.1982.04290080061009eng
dcterms.referencesAresté, M. E., Paradero, J. P., & Fernández, E. M. (2013). La capacidad de decisión en el menor. Aspectos particulares de la información en el niño y en el joven. Anales de Pediatría Continuada, 11(4), 204-211. https://doi.org/10.1016/S1696-2818(13)70139-2spa
dcterms.referencesBarbero, J. (2006). El derecho del paciente a la información: el arte de comunicar. En Anales del sistema sanitario de Navarra (Vol. 29, pp. 19-27). SciELO Espana. https://doi.org/10.4321/S1137-66272006000600003spa
dcterms.referencesBioethics, C. on, & others. (1995). Informed consent, parental permission, and assent in pediatric practice. Pediatrics, 95(2), 314-317.eng
dcterms.referencesBlázquez, F. O. (2014). El menor maduro ante el derecho. Competencia, capacidad, autonomía. https://doi.org/10.13184/eidon.41.2014.28-52spa
dcterms.referencesBruskas, D. (2008). Children in foster care: A vulnerable population at risk. Journal of Child and Adolescent Psychiatric Nursing, 21(2), 70-77. https://doi.org/10.1111/j.1744-6171.2008.00134.xeng
dcterms.referencesBueno, M., & Ramos, F. J. (2000). Bioética, genética y pediatría. An Esp Pediatr, 52(551), 30-33.spa
dcterms.referencesCaldwell, P. H., Murphy, S. B., Butow, P. N., & Craig, J. C. (2004). Clinical trials in children. The Lancet, 364(9436), 803-811. https://doi.org/10.1016/S0140-6736(04)16942-0eng
dcterms.referencesCardoso, P. C., & Calabró, P. D. (2005). Investigación clínica farmacológica en pediatría:?` Es ético y legal experimentar en niños?(Parte 1). Archivos argentinos de pediatría, 103(1), 46-50.spa
dcterms.referencesCortés, N. (2009). El pronóstico: un compromiso ético fundamental para el consentimiento informado. Revista Facultad de Odontología Universidad de Antioquia, 18(1). Retrieved from https://aprendeenlinea.udea.edu.co/revistas/index.php/odont/article/view/3099eng
dcterms.referencesDerish, M. T., & Heuvel, K. V. (2000). Mature minors should have the right to refuse life-sustaining medical treatment. The Journal of Law, Medicine & Ethics, 28(2), 109-124. https://doi.org/10.1111/j.1748-720X.2000.tb00001.xeng
dcterms.referencesDíaz, B. O., & Pérez, C. G. (2007). Consentimiento informado y capacidad para decidir del menor maduro. Pediatría integral, 10, 877-883.spa
dcterms.referencesDíaz, F. A. G. (2009). Aspectos bioéticos del consentimiento informado en investigación biomédica con población vulnerable. Revista Latinoamericana de bioética, 9(17), 8-27.spa
dcterms.referencesDomínguez, M. E. (2006). El consentimiento informado en la clínica con niños. Paradigmas, Métodos y Técnicas. Memorias XIII Jornadas de Investigación. Facultad de Psicología, Universidad de Buenos Aires. Buenos Aires, 10(11), 388-391.spa
dcterms.referencesDrane, J. F. (1999). Las múltiples caras de la competencia. En Bioética para clínicos (pp. 163-176). Editorial Triacastela.spa
dcterms.referencesEcoffey, C., & Dalens, B. (2003). Informed consent for children. Current Opinion in Anesthesiology, 16(2), 205-208. https://doi.org/10.1097/00001503-200304000-00015eng
dcterms.referencesFlaskerud, J. H., & Winslow, B. J. (1998). Conceptualizing vulnerable populations health-related research. Nursing research, 47(2), 69-78. https://doi.org/10.1097/00006199-199803000-00005eng
dcterms.referencesFluke, J. D., Baumann, D. J., Dalgleish, L. I., & Kern, H. D. (2014). Decisions to protect children: A decision making ecology. En Handbook of child maltreatment (pp. 463-476). https://doi.org/10.1007/978-94-007-7208-3_25eng
dcterms.referencesGonzález, J. J. Z. (1996). Creencias sobre la madurez psicológica y desarrollo adulto. Anales de psicología, 12(1), 41.spa
dcterms.referencesGoodwin, M., & Duke, N. (2011). Capacity and autonomy: a thought experiment on minors’ access to assisted reproductive technology. Retrieved from https://papers.ssrn.com/soL3/papers.cfm?abstract_id=1933829eng
dcterms.referencesGracia, D., Jarabo, Y., Espíldora, N. M., Ríos, J., & others. (2001). Toma de decisiones en el paciente menor de edad. Medicina clínica, 117(5), 179-190. https://doi.org/10.1016/S0025-7753(01)72054-4spa
dcterms.referencesGuillén, D. G. (1997). Bioética y pediatría. Rev Esp Pediatr, 53(2), 99-106.spa
dcterms.referencesGuirao-Goris, J. A., Olmedo Salas, A., & Ferrer Ferrandis, E. (2008). El artículo de revisión. Revista Iberoamericana de Enfermería Comunitaria, 1(1), 1-25.spa
dcterms.referencesHansen, T. W. R. (2016). Patient autonomy–what does it mean for clinical decision-making in children and adolescents? INTERNATIONAL ADVISORS, 3.eng
dcterms.referencesHurley, J. C., & Underwood, M. K. (2002). Children’s understanding of their research rights before and after debriefing: Informed assent, confidentiality, and stopping participation. Child development, 73(1), 132-143. https://doi.org/10.1111/1467-8624.00396eng
dcterms.referencesJacob, M. S. (2005). El menor maduro. Boletín de Pediatría, 45(193), 156-160.spa
dcterms.referencesKaser-Boyd, N., Adelman, H. S., Taylor, L., & Nelson, P. (1986). Children’s understanding of risks and benefits of psychotherapy. Journal of Clinical Child Psychology, 15(2), 165-171. https://doi.org/10.1207/s15374424jccp1502_9eng
dcterms.referencesKing, N. M., & Cross, A. W. (1989). Children as decision makers: guidelines for pediatricians. The Journal of pediatrics, 115(1), 10-16. https://doi.org/10.1016/S0022-3476(89)80321-Xeng
dcterms.referencesKrauskopf, D. (2011). Enfoques y dimensiones para el desarrollo de indicadores de juventud orientados a su inclusión social y calidad de vida. Ultima década, 19(34), 51-70. https://doi.org/10.4067/S0718-22362011000100004spa
dcterms.referencesKunin, H. (1997). Ethical issues in pediatric life-threatening illness: dilemmas of consent, assent, and communication. Ethics & behavior, 7(1), 43-57. https://doi.org/10.1207/s15327019eb0701_4eng
dcterms.referencesKuther, T. L. (2003). Medical decision-making and minors: issues of consent and assent. Adolescence, 38(150), 343.eng
dcterms.referencesLevy, M. D. L., Larcher, V., Kurz, R., & others. (2003). Informed consent/assent in children. Statement of the Ethics Working Group of the Confederation of European Specialists in Paediatrics (CESP). European journal of pediatrics, 162(9), 629-633. https://doi.org/10.1007/s00431-003-1193-zeng
dcterms.referencesLyon, R.-M. (1987). Speaking for a Child: The Role of Independent Counsel for Minors. California Law Review, 75(2), 681-706. https://doi.org/10.2307/3480627eng
dcterms.referencesMartínez, J. L. C., & others. (2001). Ética a Nicómaco. Alianza Editorial. Retrieved from https://dialnet.unirioja.es/servlet/libro?codigo=292204spa
dcterms.referencesMeisel, A. (1979). The exceptions to the informed consent doctrine: striking a balance between competing values in medical decisionmaking. Wis. L. Rev., 413.eng
dcterms.referencesMorrow, V., & Richards, M. (1996). The ethics of social research with children: an overview. Children & society, 10(2), 90-105. https://doi.org/10.1002/(SICI)1099-0860(199606)10:2%3C90::AID-CHI14%3E3.0.CO;2-Zeng
dcterms.referencesOppliger, W., & Bascuñán, M. (2011). Consentimiento informado: Percepción de médicos, enfermeras y padres sobre el proceso comunicativo. Revista chilena de pediatría, 82(3), 204-210. https://doi.org/10.4067/S0370-41062011000300005spa
dcterms.referencesOwens, H. (1977). When is a voluntary commitment really voluntary? American Journal of Orthopsychiatry, 47(1), 104. https://doi.org/10.1111/j.1939-0025.1977.tb03250.xeng
dcterms.referencesPaling, J. (2003). Strategies to help patients understand risks. British Medical Journal, 327(7417), 745. https://doi.org/10.1136/bmj.327.7417.745eng
dcterms.referencesPerez-Mana, C., Llonch, C., & Farré, M. (2012). Transparencia en la investigación clínica: registro de los ensayos clínicos y publicación de resultados. Medicina Clínica, 139(13), 593-597. https://doi.org/10.1016/j.medcli.2012.06.009spa
dcterms.referencesPower, F. C., Higgins, A., & Kohlberg, L. (1991). Lawrence Kohlberg’s approach to moral education. Columbia University Press.eng
dcterms.referencesPrieto, P. (2015). Comités de ética en investigación con seres humanos: relevancia actual en Colombia. Experiencia de la Fundación Santa Fe de Bogotá. Acta Médica Colombiana, 40(2), 50-56.spa
dcterms.referencesReubi, D. (2012). The human capacity to reflect and decide: Bioethics and the reconfiguration of the research subject in the British biomedical sciences. Social Studies of Science, 42(3), 348-368. https://doi.org/10.1177/0306312712439457eng
dcterms.referencesRoth, L. H., Appelbaum, P. S., Sallee, R., Reynolds, C. F., & Huber, G. (1982). The dilemma of denial in the assessment of competency to refuse treatment. Am J Psychiatry, 139(7), 910-913. https://doi.org/10.1176/ajp.139.7.910eng
dcterms.referencesTealdi, J. C., & Mainetti, J. A. (1990). Los comités hospitalarios de ética. Retrieved from http://hist.library.paho.org/Spanish/BOL/v108n(5-6)p431.pdfspa
dcterms.referencesWeithorn, L. A., & Campbell, S. B. (1982). The competency of children and adolescents to make informed treatment decisions. Child development, 1589-1598. https://doi.org/10.2307/1130087eng
dcterms.referencesWendler, D., & Shah, S. (2003). Should children decide whether they are enrolled in nonbeneficial research? American Journal of Bioethics, 3(4), 1-7. https://doi.org/10.1162/152651603322614382eng
dcterms.referencesWitholding.pdf_40818793.pdf. (s. f.). Retrieved from http://www.gmc-uk.org/Witholding.pdf_40818793.pdeng
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