Barriers and Needs in Paediatric Palliative Home Care in Germany: a Qualitative Interview Study with Professional Experts

Overview

Journal BMC Palliat Care

Publisher Biomed Central

Specialty Critical Care

Date 2010 Jun 8

PMID 20525166

Citations 15

Authors

Saskia Junger

Tania Pastrana

Martina Pestinger

Martina Kern

Boris Zernikow

Lukas Radbruch

Affiliations

Soon will be listed here.

Abstract

Background: In North-Rhine Westphalia (Germany) a pilot project for an extensive service provision of palliative care for children and adolescents has been implemented. Accompanying research was undertaken with the aim to assess the status quo of service delivery at the outset of the project and to evaluate the effects of the pilot project. As part of the research, barriers and needs with respect to paediatric palliative home care in the target region were explored.

Methods: Semi-structured interviews with 24 experts in the field of paediatrics, palliative and hospice care have been conducted and were analysed by qualitative content analysis.

Results: Four main categories emerged from the interviews: (1) specific challenges and demands in palliative care for children and adolescents, (2) lack of clear legal and financial regulations, (3) gaps in the existing care delivery, and (4) access to services. Generally the interviews reflected the observation that the whole field is currently expanding and that certain deficits are temporary barriers that will be resolvable in the medium-term perspective.

Conclusions: Predominant barriers were seen in the lack of clear legal and financial regulations which take into account the specific challenges of palliative care in children and adolescents, as well as in a shortcoming of specialist services for a local based care provision throughout the federal country.

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