Nj. Jarrett et al., Terminally ill patients' and lay-carers' perceptions and experiences of community-based services, J ADV NURS, 29(2), 1999, pp. 476-483
This paper reports on terminally ill patients' and their lay-carers' percep
tions and experiences of community-based services, It forms part of a large
r investigation which examined the extent of service provision and any perc
eived gaps and problems from the perspectives of both clients and providers
of community-based assistance for the? terminally ill. The participants we
re nine terminally ill patients and 12 lay-carers receiving community nursi
ng cafe, Fifteen face-to-face, semi-structured interviews were conducted to
elicit their experiences and perceptions of the care being provided, quali
tative, thematic analysis was carried out on the audio-taped interviews. On
the whole, respondents reported a high level of satisfaction and appreciat
ion for the help provided. Several areas appeared more problematic, however
, and warrant further consideration. These include perceptions of health pr
ofessionals, particularly their role domains, power and expertise, and some
of the practical disadvantages and problems faced by some patients and the
ir families. These are illustrated and the implications for dying patients,
their lay-carers and community-based health professionals are discussed.