Mental Sciences II. Posters
Földesi, Enikő
Pedagogical Professional Services, Pest County
+36 30 3899265
foldesie@gmail.com
Parents’ Perspective on Medical Communication During the Transition to Palliative Care in Pediatric Oncology
Enikő Földesi1, Szilvia Zörgő2, Péter Hauser3, Judit Nyirő3, Katalin Hegedűs2
1 Pedagogical Professional Services, Pest County
2 Semmelweis University, Faculty of Medicine, Institute of Behavioural Sciences
3 Semmelweis University, 2nd Dept of Pediatrics
Mental Sciences II. Posters
Hungarian
Mental Sciences
Health Sciences
Introduction: The treatment of pediatric malignant diseases with poor prognosis affects the whole family. Several models have been developed that address the timing of curative and palliative elements in the treatment process. Literature suggests that in instances of poor prognosis, communication about the integration of palliative care should begin early, yet everyday practice and experiences of doctors and parents may differ.
Aim: To explore the parents’ perspective on features and circumstances of medical communication during the transition to palliative care, in order to develop recommendations for more effective doctor-parent communication.
Methods: Semi-structured interviews comprised of 18 questions were conducted with parents who had lost their child to cancer within the past 1-5 years. Questions explored parents’ experiences and the circumstances of the transition to palliative care; demographic data of each participant was also recorded. Recruitment occurred by phone via main centers of Hungarian pediatric oncology care; a clinical psychologist conducted all interviews. Transcribed and narratives were scrutinized with Interpretative Phenomenological Analysis.
Results: As of now, preliminary analysis has been performed on 23 interviews. Free (inductive) coding, the first step in our analytical process, yielded the following codes that will be used to develop the final code tree: Participants of the conversation (subcodes: psychologist, spouse/partner, other), Language (subcodes: positive/negative appraisal of communication, use of word “death”), Institutional support in grief (subcodes: needed, not needed, needed from other resources) and Behavior towards child (subcodes: changed, not changed). Coding suggests that the presence of a psychologist during conversations about palliative care and institutional support in grief are favored by parents, appraisal of direct communication and use of the word “death” is varied.
Conclusions: According to our preliminary results, ensuring psychological support throughout the treatment process would be beneficial to doctor-parent communication. The salience and reasons behind preference for direct and indirect communication need to be explored further to formulate recommendations.
Supervisors:
Katalin Hegedűs
Péter Hauser
hegedus.katalin@med.semmelweis-univ.hu
hausepeti@yahoo.com
Poszter
Szabad
elfogadva
poszter
nem rendelkezett róla
4122
12:28
12:31
Enikő Földesi1, Szilvia Zörgő2, Péter Hauser3, Judit Nyirő3, Katalin Hegedűs2
1 Pedagogical Professional Services, Pest County
2 Semmelweis University, Faculty of Medicine, Institute of Behavioural Sciences
3 Semmelweis University, 2nd Dept of Pediatrics