Ítem
Acceso Abierto

La familia del paciente en Unidad de Cuidado Intensivo (UCI)

Mostrar el registro sencillo de la publicación
dc.contributor.advisorPalacios Espinosa, Ximena
dc.creatorTarquino Díaz, Larry Julián
dc.creator.degreePsicólogo(a)
dc.date.accessioned2015-01-14T16:35:50Z
dc.date.available2015-01-14T16:35:50Z
dc.date.created2013-12-09
dc.date.issued2013
dc.descriptionIntroducción: Ingresar a la UCI no es una experiencia exclusiva del paciente; implica e involucra directamente a la familia, en aspectos generadores de estrés, estrategias de afrontamiento, temores, actitudes y expectativas, la participación de la familia en el cuidado y el rol del psicólogo. Objetivo: Revisar de los antecedentes teóricos y empíricos sobre la experiencia de la familia en UCI. Metodología: Se revisaron 62 artículos indexados en bases de datos. Resultados: la UCI es algo desconocido tanto para el paciente como para la familia, por esto este entorno acentúa la aparición de síntomas ansiosos, depresivos y en algunos casos estrés post traumático. La muerte es uno de los principales temores que debe enfrentar la familia. Con el propósito de ajustarse a las demandas de la UCI, los familiares exhiben estrategias de afrontamiento enfocadas principalmente en la comunicación, el soporte espiritual y religioso y la toma de decisiones. El cuidado centrado en la familia permite una mejor comunicación, relación con el paciente y personal médico. El papel del psicólogo es poco explorado en el espacio de la UCI, pero este puede promover estrategias de prevención y de rehabilitación en el paciente y su grupo familiar. Discusión: es importante tener en cuenta que la muerte en UCI es una posibilidad, algunos síntomas como ansiedad, depresión pueden aparecer y mantenerse en el tiempo, centrar el cuidado en la familia permite tomar las decisiones basados en el diagnóstico y pronóstico y promueve expectativas realistas. Conclusiones: temores, expectativas, actitudes, estrategias de afrontamiento, factores generadores de estrés permiten explicar y comprender la experiencia de la familia del paciente en UCI.spa
dc.description.abstractIntroduction: Joining the ICU is not exclusively a patient’s experience; it involves directly his family, in stress generator factors, confrontation strategies, fears, attitudes and expectations, families’ involvement during care and the psychologist role. Goal: To review the theoretical and empirical precedents about the family’s experience in the ICU. Methodology: 62 data base indexed articles were reviewed. Results: The ICU is an unknown place to the patient and his family, therefore this surroundings stresses the anxiety, depressive and in some cases post-traumatic stress symptoms sprout. Death is one of the main fears that the family has to endure. With the purpose to adjust themselves to the ICUs’ demands, relatives present confrontation strategies focused mainly on communication, spiritual and religious support and decision making. Care focused on family allows a better communication and treat with patient and medical staff. The role of the psychologist is hardly explored inside the ICU, but he can promote prevention and rehabilitation strategies for the patient and his relatives. Debate: It is important to take into account that death in the ICU is a possibility, some symptoms such as anxiety or depression may appear and remain for a while, to centre the care on family allows making decisions based on diagnosis and forecast, and it provides realistic expectations. Conclusions: Fears, expectations, attitudes, confrontation strategies, stress generator factors allow the explanation and comprehension of the family’s experience in the ICU.eng
dc.format.mimetypeapplication/pdf
dc.format.tipoDocumentospa
dc.identifier.doihttps://doi.org/10.48713/10336_9613
dc.identifier.urihttp://repository.urosario.edu.co/handle/10336/9613
dc.language.isospa
dc.publisherUniversidad del Rosariospa
dc.publisher.departmentEscuela de Medicina y Ciencias de la Saludspa
dc.publisher.programPsicologíaspa
dc.rights.accesRightsinfo:eu-repo/semantics/openAccess
dc.rights.accesoAbierto (Texto completo)spa
dc.rights.ccAtribución-SinDerivadas 2.5 Colombiaspa
dc.rights.licenciaEL AUTOR, manifiesta que la obra objeto de la presente autorización es original y la realizó sin violar o usurpar derechos de autor de terceros, por lo tanto la obra es de exclusiva autoría y tiene la titularidad sobre la misma. PARGRAFO: En caso de presentarse cualquier reclamación o acción por parte de un tercero en cuanto a los derechos de autor sobre la obra en cuestión, EL AUTOR, asumirá toda la responsabilidad, y saldrá en defensa de los derechos aquí autorizados; para todos los efectos la universidad actúa como un tercero de buena fe. EL AUTOR, autoriza a LA UNIVERSIDAD DEL ROSARIO, para que en los términos establecidos en la Ley 23 de 1982, Ley 44 de 1993, Decisión andina 351 de 1993, Decreto 460 de 1995 y demás normas generales sobre la materia, utilice y use la obra objeto de la presente autorización. -------------------------------------- POLITICA DE TRATAMIENTO DE DATOS PERSONALES. Declaro que autorizo previa y de forma informada el tratamiento de mis datos personales por parte de LA UNIVERSIDAD DEL ROSARIO para fines académicos y en aplicación de convenios con terceros o servicios conexos con actividades propias de la academia, con estricto cumplimiento de los principios de ley. Para el correcto ejercicio de mi derecho de habeas data cuento con la cuenta de correo habeasdata@urosario.edu.co, donde previa identificación podré solicitar la consulta, corrección y supresión de mis datos.spa
dc.rights.urihttp://creativecommons.org/licenses/by-nd/2.5/co/
dc.source.bibliographicCitationAlcaldía Mayor de Bogotá. (s.f.). Ley 73 de 1988. Por la cual se adiciona la Ley 09 de 1979 y se dictan otras disposiciones en materia de donación y trasplante de órganos y componentes anatómicos para fines de trasplantes u otros usos terapéuticos. Congreso de Colombia. Recuperado el 10 de 09 de 2014, de Bogotá Juridica: http://www.alcaldiabogota.gov.co/sisjur/normas/Norma1.jsp?i=14524
dc.source.bibliographicCitationAmerican Academy of Pediatrics. (2003). Family-Centered Care and the Pediatrician’s Role. Pediatrics, 112(3): 691 -696. URL: http://pediatrics.aappublications.org/content/112/3/691.full.pdf+html
dc.source.bibliographicCitationBailey, J., Sabbagh, M., Loiselle, C., Boileau, J. & Mcvey, L. (2010). Supporting families in the ICU: A descriptive correlational study of informational support, anxiety and satisfaction with care. Intensive and Critical Care Nursing, 26(2): 114-122. doi: 10.1016/j.iccn.2009.12.006
dc.source.bibliographicCitationBarreto da Costa, J., Felicetti, C.R., de Macedo Costa, C.R., Miglioranza, D.C., Osaku, E.F., et al. (2010). Fatores estressantes para familiares de pacientes criticamente enfermos de uma Unidade de Terapia Intensiva. J bras Psiquiatria, 59 (3): 182-189. http://dx.doi.org/10.1590/S0047-20852010000300003
dc.source.bibliographicCitationBennun, I. (2001). Intensive Care Unit Syndrome: A Consideration of Psychological Interventions. British Journal of Medical Psychology, 54(Pt3): 369-377. DOI: 10.1348/000711201161046Bennun, I. (2001). Intensive Care Unit Syndrome: A Consideration of Psychological Interventions. British Journal of Medical Psychology, 54(Pt3): 369-377. DOI: 10.1348/000711201161046
dc.source.bibliographicCitationBedsworth, J. & Molen, M. (1982). Psychological stress in spouses of patients with myocardial infarction. Hearth and Lung , 11(4), 450-456.
dc.source.bibliographicCitationBishop, S., Walker, M. & Spivak, M. (2013). The family presence in the adult burn Intensive Care Unit during dressing changes. Critical Care Nurse, 33(1): 14-24. doi: 10.4037/ccn2013116.
dc.source.bibliographicCitationBlack, P., Boore, J. R. P. & Parahoo, K. (2011). The effect of a nurse-facilitated family participation in psychological care of critically ill patient. Journal of Advanced Nursing 67(5): 1091-1101. doi: 10.1111/j.1365-2648.2010.0558.x
dc.source.bibliographicCitationBouman, C. (1984). Identifying priority concerns of families of ICU patients. Dimens Crit Care Nurs. 3(5): 313-319.
dc.source.bibliographicCitationBreitbart, W., Gibson, C. & Tremblay, A. (2002). The delirium experience: Delirium recall and Delirium-related distress in hospitalized patients with cancer, their spouses/caregivers, and their nurses. Psichosomatics, 43 (3): 183-194. doi: 10.1176/appi.psy.43.3.183
dc.source.bibliographicCitationBrazil, K., Bainbridge, D., Ploeg, J., Krueger, P., Taniguchi, A. & Marshall, D. (2012). Family caregiver views on patient-centred care at the end of life. Scandinavian Journal of Caring Science, 26(3): 513-518. DOI:10.1111/j.1471-6712.2011.00956
dc.source.bibliographicCitationBrooks, R., Kerridge, R., Hillman, K., Baumann, A. & Daffurn, K. (1997). Quality of life outcomes after intensive care. Intensive Care Med, 23 (5): 581-586. DOI: 10.1007/s001340050376
dc.source.bibliographicCitationChaboyer, W; Thalib, L; Alcorn, K; & Foster, M. (2007). The effect of an ICU liaison nurse on patients and family´s anxiety prior to transfer to the ward: An intervention study. Intensive and Critical Care Nursing, 23: 362- 369. DOI:10.1016/j.iccn.2007.04.005
dc.source.bibliographicCitationChan, K.S. & Twinn, S. (2006). An analysis of the stressors and coping strategies of Chinese adults with a partner admitted to an intensive care unit in Hong Kong: an exploratory study. Journal of Clinical Nurse, 16(1): 185-193. DOI: 10.1111/j.1365-2702.2005.01452.x
dc.source.bibliographicCitationCheng, Y.C. (2005). Caregiver Burnout: A Critical Review of the Literature. California.
dc.source.bibliographicCitationChoi, J., Hoffman, L. A., Schulz, R., Ren, D., Danohe, M. P., Given, B. & Sherwood, P.R. (2013). Health Risk Behaviors InThe Family Caregivers During Patients Stay In Intensive Care Units. A pilot Analysis. American Journal of Critical Care, 22(1): 40-45. doi: 10.4037/ajcc2013830
dc.source.bibliographicCitationChoi, J., Tate, J., Hoffman, L.A.,Schulz, R., Ren, D., Donahoe, M.P., Given, B. & Sherwood, PR. (2013). Fatigue in Family Caregivers of Adult Intensive Care Unit Survivors. Journal of Pain and Symptom Management, 48(3): 1-11. Doi: 10.1016/j.jpainsymman.2013.09.018.
dc.source.bibliographicCitationContreras Moreno, A. M. y Palacios-Espinosa, X. (2014). Contribuciones de la psicología al manejo interdisciplinario del paciente en Unidad de Cuidados Intensivos (UCI). Rev. Univ. Ind. Santander. Salud, 46(1): 47-60.
dc.source.bibliographicCitationDaffurn, K., Bishop, G., Hillman, K. & Bauman, A. (1994). A problems following discharge after intensive care. Intensive Crit care Nurs, 10(4): 244-251. doi:10.1016/0964-3397(94)90032-9
dc.source.bibliographicCitationDavidson, J.E., Powers, K., Hedayat, K.M., Tieszen, M., Kon, A.A., Shepard, E., Spuhler, V., Todres, I.D., Levy, M., Barr, J., Ghandi, R., Hirsch, G. & Armstrong, D. (2007). Clinical practice guidelines for support of the family in the patient-centered intensive care unit . Crit Care Med, 35(2): 605-622. URL: http://www.learnicu.org/docs/guidelines/patient-centeredintensive.pdf
dc.source.bibliographicCitationDavidson, J., Jones, C. & Bienvenu, J. (2012). Family Response To Critical Illness: Postintensive Care Syndrome-Family. Critical Care Medicine, 40(2): 618-625. doi: 10.1097/CCM.0b013e318236ebf9
dc.source.bibliographicCitationFlodén, A., Persson, L.O., Rizell, M., Sanner, M. & Forsberg, A. (2011). Attittudes to argan donation among Swedish ICU nurses. Journal of CLinical Nursing , 20 (21-22): 3183-3195. DOI: 10.1111/j.1365-2702.2011.03756.x
dc.source.bibliographicCitationFoster, M. & Chaboyer, W. (2003). Family carers of ICU survivors: A survey of the burden the experience. Nordic College of Caring Science, 17(3): 205-2014. DOI: 10.1046/j.1471-6712.2003.00230.x
dc.source.bibliographicCitationFranzoi, S. (2007). Psicologia Social. En S. Franzoi, Psicologia Social (Vol. IV, pp. 167-202). México: Mc Graw Hill.
dc.source.bibliographicCitationFridh, S., Forsberg, A. & Bergbom, I. (2007). End Of Life care in intensive care units. Family routines and enviromental factors. Scandinavian Journal of Caring Science, 21(1): 25-31. DOI: 10.1111/j.1471-6712.2007.00470.x
dc.source.bibliographicCitationGómez-Carretero, P., Monsalve, V., Soriano, J. y de Andrés, J. (2007). Alteraciones Emocionales y Necesidades Psicológicas de Pacientes en una Unidad de Cuidados Intensivos. Sociedad Española de Medicina Intensiva, Critica y Unidades Coronarias, 31(6): 318-325. URL: http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S0210-56912007000600006&lng=es.
dc.source.bibliographicCitationGoméz-Carretero, P., Soriano, J., Monsalve, V. y de Andrés, J. (2009 ). Satisfaccion con la información: posible variable interviniente en el estado de ánimo de cuidadores primarios de pacientes críticos. Clínica y Salud, 20(1): 91-105. URL: http://scielo.isciii.es/pdf/clinsa/v20n1/v20n1a08.pdf
dc.source.bibliographicCitationHupcey, J. E. (2000). Feeling safe: The psychosocial meed of ICU patients . Journal of Nursing Scolarship, 32(4): 361-367. DOI: 10.1111/j.1547-5069.2000.00361.x
dc.source.bibliographicCitationJohansson, I., Hildingh, C., Wenneberg, S., Fridlund, B. & Ahlström, G. (2006). Theorical model of coping among relatives of patients n intensive care units a simultaneous concepts analysis. Journal of Advanced Nursing, 56(5): 463-471. DOI: 10.1111/j.1365-2648.2006.04040.x
dc.source.bibliographicCitationKhalaila, R. (2014). Meetings the needs of patients´families in intensive care units. Nursing Standar, 28(43): 34-44. http://dx.doi.org/10.7748/ns.28.43.37.e8333
dc.source.bibliographicCitationKubler-Röss, E. (2000). Sobre la muerte y los moribundos. España: Grijalbo Mondadori.
dc.source.bibliographicCitationKnussen, C., Tolson, D., Brogan, C., Swan, I.R.C., Stott, D.J. & Sullivan, F. (2008). Family caregivers of older relatives: ways of coping and change in distress. Psychology Health & Medicine, 13(3): 274-290. doi: 10.1080/13548500701405483
dc.source.bibliographicCitationKoenig, H. G., Pargament, K. & Nielsen, J. (1998). Religious Coping and Health Status in Medically Ill Hospitalized Older Adults . The Journal of Nervous & Mental Disease, 186(9): 513-521. URL: http://journals.lww.com/jonmd/Abstract/1998/09000/Religious_Coping_and_Health_Status_in_Medically.1.aspx
dc.source.bibliographicCitationLatour, J. (2005). Is Family-Centred Care in critical care units that difficult? A view from Europe. Nursing in Critical Care, 10 (2): 51-53. DOI: 10.1111/j.1362-1017.2005.0108b.
dc.source.bibliographicCitationLazarus, R. & Folkman, S. (1984). Stress, appraisal and coping. New York: Springer.
dc.source.bibliographicCitationLeske, J. S. & Jiricka, M. K. (1998). Impact of Family Demands and Family Strengths and Capabilities on Family Well-Being and Adaptation After Critical Injury. American Journal of Critical Care, 7(5): 383-392. URL http://search.proquest.com.ez.urosario.edu.co/docview/227892988?accountid=50434
dc.source.bibliographicCitationLeung, N. Y. & Chow, S. K. (2012). Attitudes of healthcare staff and patients´ family members towards family presence during resucitation in adult critical care units . Journal of Critical Nursing, 21 (13-14): 2083-2093. doi: 10.1111/j.1365-2702.2011.04013.x
dc.source.bibliographicCitationMacDougall, D.S. (2007 ). Incorporate Family Members in the Care of ICU Patients. Healthcare Professionals Network. Disponible en URL: http://www.hcplive.com/publications/internal-medicine-world-report/2007/2007-06/2007-06_35
dc.source.bibliographicCitationMarosti, C. & Dantas, R. (2006 ). Relaçao entre estressores e caracteristicas sócio-demográficas de pacientes internados em uma unidade coronaria. Rev. Latino-am. Enfermagem, 14(5): 713-719. http://dx.doi.org/10.1590/S0104-11692006000500012
dc.source.bibliographicCitationMartins, M.V., Gonzaga, J., Bronzato, C.H., Trevizani, M.J. & Leite, S.R. (2013). Experience of family members as a result of children's hospitalization at the Intensive Care Unit. Investigacion & Educacion En Enfermeria , 31(2): 191-200. Disponible en URL: http://www.scielo.org.co/scielo.php?pid=S012053072013000200004&script=sci_arttext
dc.source.bibliographicCitationMasri, C., Farrell, C.A., Lacroix, J., Rocker, G. & Shemie, S. (2000). Decision Making and End-of-Life Care in Critically Ill Children. Journal of Palliative Care, 16(suppl): S45-S52.
dc.source.bibliographicCitationMathes, M. & Miles, M. (1991). Preparation of parents for the ICU experience: What are we missing? Child Health Care, 20(3): 132-137. DOI:10.1207/s15326888chc2003_1
dc.source.bibliographicCitationMedland, J. J. & Ferrans, C. E. (1998). Effectiveness of a structured communication program for family members of patients in ICU. American Journal of Critical Care, 7(1): 24-29. URL http://search.proquest.com.ez.urosario.edu.co/docview/227899430?accountid=50434
dc.source.bibliographicCitationMeyer, E., Snelling, L. & Myren-Manbeck, L. (1998). Pediatric Intensive Care: The Parents Experience. AACN Clin Issues , 9(1): 64-74. URL http://www.ncbi.nlm.nih.gov/pubmed/9505573
dc.source.bibliographicCitationMutran, E., Danis, M., Bettron, K., Sudha, S. & Hanson,L. (1997). Attitudes of the critically ill toward prolonging life: The role of social support. The Gerontologist, 37(2): 192-199. DOI: 10.1093/geront/37.2.192
dc.source.bibliographicCitationNovaes, M.A.F.P., Aronovich, A., Ferraz, M.B. & Knobel, E. (1997). Stressors in ICU: patients´evaluation. Intensive Care Medicine, 23(12): 1282-1285. DOI 10.1007/s001340050500
dc.source.bibliographicCitationNovoa, M. & Ballesteros, B.P. (2006). The role of the psychologist in an intesive care unit. Univ. Psychol. Bogotá (Colombia), 5(3): 599-612. URL http://www.scielo.org.co/pdf/rups/v5n3/v5n3a14.pdf
dc.source.bibliographicCitationNúñez Herrejón, J.L. y Ortíz Salinas, M. (2010). APA diccionario conciso de psicología. Mexico DF: Manual Moderno.
dc.source.bibliographicCitationPlaszewka-Zywoko, L. & Gazda, D. (2012). Emotional reactions and needs of family members of ICU patients. Anaesthesiology Intensive Therapy, 44(3): 145-149. URL http://czasopisma.viamedica.pl/ait/article/view/19823/15534
dc.source.bibliographicCitationQuinn, J., Schmitt, M., Gedney Baggs, J., Norton, S. & Dombeck, M. & Sellers, C.R. (2012). Family members informal roles in end of life decision making in adult intensive care units. American Journal of Critical Care, 21(1): 43-49. doi: 10.4037/ajcc2012520.
dc.source.bibliographicCitationRedinbaugh, E. M., Baum, A., DeMoss, C., Fello, M. & Arnold, R. (2002). Factors Associated with the Accuracy of Family Caregiver Estimates of Patient Pain. Journal of Pain and Symptom Management, 23(1): 31-38. doi:10.1016/S0885-3924(01)00372-4
dc.source.bibliographicCitationRuíz-Benítez De Lugo, M.A. y Coca, M. (2008). El pacto de silencio en los familiares de los pacientes oncológicos terminales. Psicooncología, 5(1): 53-69. URL: http://revistas.ucm.es/index.php/PSIC/article/view/PSIC0808130053A/15496
dc.source.bibliographicCitationSchenker, Y., White, D., Crowley-Matoka, M., Dohan, D., Tiver, G. & Arnold, R. (2013). It hurts to know... and it helps: exploring how surrogates in the ICU cope with prognostic information. Journal of Palliantive Medicine, 16(3): 243-249. doi: 10.1089/jpm.2012.0331.
dc.source.bibliographicCitationSchenker, Y., Crowley-Matoka, M., Dohan, D., Tiver, G.A., Arnold, R.M. & White D.B. (2012) I don't want to be the one saying 'we should just let him die': intrapersonal tensions experienced by surrogate decision makers in the ICU. J Gen Intern Med, 27(12): 1657-1665. doi: 10.1007/s11606-012-2129-y
dc.source.bibliographicCitationSchleder, L. P., Parejo, L. S., Puggina, A. C. & da Silva, M.J.P. (2013). Spirituality of relatives of patients hospitalized in intensive care unit/Espiritualidade dos familiares de pacientes internados em unidade de terapia intensiva. Acta Paulista De Enfermagem, 26(1): 71-78. http://dx.doi.org/10.1590/S0103-21002013000100012
dc.source.bibliographicCitationScott, A. (2004). Managing anxiety in ICU patients: the role of pre-operative information provision. Nursing in critical care, 9(2): 72-79. Disponible en URL: https://www.365healthcare.com/wp-content/uploads/2013/03/Managing-Anxiety-ICU-Patients_Preoperative-Teaching.pdf
dc.source.bibliographicCitationSewitch, M.J., McCusker, J., Dendukuri, N. & Yaffe, M.J. (2004). Depression in frail elders: impact on family caregivers. International journal of geriatric psychiatry , 19(7): 655-665. DOI: 10.1002/gps.1135
dc.source.bibliographicCitationSiddiqui, S. & Sheikh, F. & Kamal, R. (2011). What families want an assessment of family expectations in the ICU. International Archives of Medicine, 4(21): 1-5. doi:10.1186/1755-7682-4-21
dc.source.bibliographicCitationSiegel, M. (2009). End of life decision making in the ICU. Clin Chest Med, 30: 181-194. Disponible en URL: http://palliativecare.yale.edu/student/361_37173_EOLDecisionMakingClinicsinChestMed0309.pdf
dc.source.bibliographicCitationSöderströn, I.M., Saveman, B.I., Hagberg, M., & Benzein, E. (2009). Family adaptation in relation to a family member´s stay in ICU. Intensive and Critical Care Nursing, 25(5): 250-257. doi: 10.1016/j.iccn.2009.06.006
dc.source.bibliographicCitationStickney, C., Ziniel, S., Brett, M.S. & Troug, R. (2014). Family participation during Intensive Care Units rouds: Attitudes and experiences of parents and healthcare providers in a tertiary Pediatric Intensive Care Unit. The Journals of Pediatrics , 164(2): 402-406. doi: 10.1016/j.jpeds.2013.09.037.
dc.source.bibliographicCitationSukantarat, K., Greer, S., Brett, S. & Williamson, R. (2007). Physical and psychological sequelae of critical illness. British Journal of Health Psychology,12 (Pt1): 65-74. DOI:10.1348/135910706X94096
dc.source.bibliographicCitationTwibell, R.S. (1998). Family coping during critical illness. Dimension of critical care nursing, 17(2): 100-112. Disponible en URL: http://www.bmhlibrary.info/9624951.pdf
dc.source.bibliographicCitationWaldrop, D P; Meeker, M A. (2011). Crisis in caregiving: when home-based end -of-life care is no longer possible. Journal of Palliative Care, 27(2): 117-125
dc.source.bibliographicCitationWall, R., Curtis, R. & Cooke, C. R. (2007). Family Satisfaction in the ICU: differences between families of survivors and nonsurvivors. Critical Care Medicine, 132(5): 1425-1435. DOI 10.1378/chest.07-0419
dc.source.bibliographicCitationZaider, T. & Kissane, D. (2009). The Assesment And Management Of Family Distress During Paliative Care. Curr Opin Support Palliat Care, 3(1): 67-71. doi: 10.1097/SPC.0b013e328325a5ab.
dc.source.bibliographicCitationZanetti, T. G., Stumm, E. M. F. & Ubessi, L. D. (2013). Stress and coping in families of patients in an intensive care unit. Revista de Pesquisa: Cuidado é Fundamental, 5(2): 3608-3619. DOI: http://dx.doi.org/10.9789/2175-5361.2013.v5i2.3608-3619
dc.source.instnameinstname:Universidad del Rosariospa
dc.source.reponamereponame:Repositorio Institucional EdocURspa
dc.subjectAfrontamientospa
dc.subjectComunicaciónspa
dc.subjectCuidadoresspa
dc.subjectEstrésspa
dc.subjectFamiliaspa
dc.subjectRol del Psicólogospa
dc.subjectTemoresspa
dc.subjectToma de decisionesspa
dc.subjectUCIspa
dc.subject.ddcPsicología diferencial & del desarrollo
dc.subject.decsUnidad de cuidados intensivosspa
dc.subject.decsEstrésspa
dc.subject.decsPsicologíaspa
dc.subject.keywordCaregiverseng
dc.subject.keywordCommunicationeng
dc.subject.keywordCopingeng
dc.subject.keywordDecision makingeng
dc.subject.keywordFamilyeng
dc.subject.keywordFearseng
dc.subject.keywordICUeng
dc.subject.keywordPsychologist Role Playeng
dc.subject.keywordStresseng
dc.titleLa familia del paciente en Unidad de Cuidado Intensivo (UCI)spa
dc.typebachelorThesiseng
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersion
dc.type.spaTrabajo de gradospa
local.department.reportEscuela de Medicina y Ciencias de la Saludspa
Archivos
Bloque original
Mostrando1 - 1 de 1
Miniatura
Nombre:
TarquinoDiaz-LarryJulian-2013.pdf
Tamaño:
429.7 KB
Formato:
Adobe Portable Document Format
Descripción:
Articulo Principal
Descargar
Colecciones
Pregrado en Psicología