Heart transplantation experiences: a phenomenological approach
Authors:
- Maria Lúcia Araújo SadalaMSMaria Lúcia Araújo Sadala
- Noedir Antônio Groppo StolfNSNoedir Antônio Groppo Stolf
- 10 June 2008
- journal article
- Published by Wiley in Journal of Clinical Nursing
- Vol. 17 (7b) , 217-225
Abstract
Aim. The aim of this study was to understand the heart transplantation experience based on patients’ descriptions.Background. To patients with heart failure, heart transplantation represents a possibility to survive and improve their quality of life. Studies have shown that more quality of life is related to patients’ increasing awareness and participation in the work of the healthcare team in the post‐transplantation period. Deficient relationships between patients and healthcare providers result in lower compliance with the postoperative regimen.Method. A phenomenological approach was used to interview 26 patients who were heart transplant recipients. Patients were interviewed individually and asked this single question: What does the experience of being heart transplanted mean? Participants’ descriptions were analysed using phenomenological reduction, analysis and interpretation.Results. Three categories emerged from data analysis: (i) the time lived by the heart recipient; (ii) donors, family and caregivers and (iii) reflections on the experience lived. Living after heart transplant means living in a complex situation: recipients are confronted with lifelong immunosuppressive therapy associated with many side‐effects. Some felt healthy whereas others reported persistence of complications as well as the onset of other pathologies. However, all participants celebrated an improvement in quality of life. Health caregivers, their social and family support had been essential for their struggle. Participants realised that life after heart transplantation was a continuing process demanding support and structured follow‐up for the rest of their lives.Conclusion. The findings suggest that each individual has unique experiences of the heart transplantation process. To go on living participants had to accept changes and adapt: to the organ change, to complications resulting from rejection of the organ, to lots of pills and food restrictions.Relevance to clinical practice. Stimulating a heart transplant patients spontaneous expression about what they are experiencing and granting them the actual status of the main character in their own story is important to their care.Keywords
This publication has 16 references indexed in Scilit:
- Depression and Quality of Life in Patients Living 10 to 18 Years Beyond Heart TransplantationThe Journal of Heart and Lung Transplantation, 2005
- Two-year follow-up of quality of life in patients referred for heart transplantHeart & Lung, 2005
- Prevalence and correlates of depression symptoms at 10 years after heart transplantation: continuous attention requiredTransplant International, 2004
- An internet-based intervention to improve psychosocial outcomes in heart transplant recipients and family caregivers: development and evaluationThe Journal of Heart and Lung Transplantation, 2004
- Psychosocial vulnerability, physical symptoms and physical impairment after lung and heart–lung transplantationThe Journal of Heart and Lung Transplantation, 2003
- The registry of the international society for heart and lung transplantation: twentieth official adult heart transplant report—2003The Journal of Heart and Lung Transplantation, 2003
- Noncompliance in Heart Transplantation: A Role for the Advanced Practice NurseProgress in Cardiovascular Nursing, 2003
- LONG-TERM EFFECTS OF HEART TRANSPLANTATION: THE GAP BETWEEN PHYSICAL PERFORMANCE AND EMOTIONAL WELL-BEINGJournal of Rehabilitation Medicine, 1999
- DOES TRANSPLANTATION PRODUCE QUALITY OF LIFE BENEFITS?Transplantation, 1997
- Avaliação da qualidade de vida de pacientes com doença de Chagas submetidos a transplante de coraçãoRevista da Sociedade Brasileira de Medicina Tropical, 1997