Morphine and Hospice
4
This article is consistent with this authors PICO(T) question in that it proposes an
intervention to relieve family concerns regarding pain management beginning with hospice
admission which can lead to better quality of life of the hospice patient.
Oliver, D. P., Wittenberg-Lyles, E., Washington, K., Kruse, R. L., Albright, D. L.,
Baldwin, P. K., . . . Demiris, G. (2013). Hospice caregivers' experiences with pain
management: "I'm not a doctor, and I don't know if I helped her go faster
or.slower".
Journal of Pain and Symptom Management,
46
(6), 846-858.
doi:10.1016/j.jpainsymman.2013.02.011
The purpose of this study was to understand the experience of caregivers to hospice
patient’s pain management.
The study consisted of interviews of 146 caregivers which resulted
in five themes: administration, side effects, insecurity with assessment, communication and
unrelieved pain.
The study concluded that effective planning for pain control needs to include
values and beliefs of patients and families.
This study is important to this writers’ research because it finds many caregivers (37%)
are concerned about side effects of medications (Oliver et al., 2013).
Further results indicate that
family caregivers can feel guilt, thinking they overmedicated the patient.
The authors of this
study feel that a formal assessment of caregiver beliefs and values can assist staff in planning
care.
They conclude that “Early in the admission while the patient is more likely to be able to
communicate coherently, hospice staff would be well served to facilitate family discussions
between caregivers and patients as part of the pain control plan
(Oliver et al., 2013).”
