Pediatric Palliative Care: A Qualitative Study of Physicians’ Perspectives in a Tertiary Care University Hospital

Author:

St-Laurent-Gagnon Thérèse1,Carnevale Franco A.2,Duval Michel3

Affiliation:

1. Centre de réadaptation Marie-Enfant and Université de Montréal, Montreal

2. Montreal Children's Hospital and McGill University, Montreal

3. Hôpital Sainte-Justine and Université de Montréal, Montreal, Quebec, Canada

Abstract

The objective of this study was to assess the concept of palliative care for a group of physicians in a tertiary care pediatric university hospital. Grounded theory methodology was used. Data included 12 semi-structured interviews, field notes, research consent forms, research protocols, and articles published by the participants. Physicians involved in both research and clinical care of severely ill children were interviewed. Data analysis identified three principal themes. First, physicians limited their concept of palliative care to the relief of physical symptoms, equating palliative care with comfort care. Second, there was variation regarding the appropriate moment to introduce palliative care for children. Finally, many physicians were not comfortable using the term “palliative care”. Although this study was conducted in one Canadian centre, the results raise questions that should be examined in other settings. A vague concept of palliative care may delay the provision of palliative care to children.

Publisher

SAGE Publications

Subject

General Medicine

Reference19 articles.

1. Royal College of Paediatrics and Child Health. A Guide to the Development of Children's Palliative Care Service. UK: RCPCH, 1997.

2. Ethical Aspects of Pediatric Palliative Care

3. GoldmanA, HainR, LibenS (eds). Oxford Textbook of Palliative Care for Children. Oxford: Oxford University Press, 2006.

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