Abstract
PURPOSE:
Satisfaction
with care is important for quality assurance in oncology, but may
differ between patients and caregivers. We aimed to assess satisfaction
with cancer care in paired analyses of these groups, examine differences between them, and identify areas for potential intervention.
METHODS:
Patients with advanced cancer
and their caregivers were recruited from 24 medical oncology outpatient
clinics......
RESULTS:
Satisfaction ratings
in the 191 patient-caregiver pairs were high, but patients were more
satisfied (p = 0.02). Both groups were least satisfied with information
regarding prognosis and pain management. Caregivers were significantly
less satisfied than patients regarding coordination of care (p = 0.001)
and family inclusion in treatment/care decisions (p < 0.0001). In
both groups, higher education was associated with lower satisfaction
(p ≤ 0.01), while better QOL predicted greater satisfaction
(p < 0.0001).
CONCLUSIONS:
Communication regarding
pain control and prognosis were identified as key areas for improvement.
Caregivers seem to desire greater involvement in treatment decisions,
though this must be balanced with patient autonomy.
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