Context
Knowledge is limited regarding pain assessment and management
practices, as well as pain-related outcomes in hospice care.
Objectives
To generate national estimates of pain assessment and management
practices and outcomes of pain control among patients 65 years or older
receiving hospice care in the U.S. and identify hospice discharge and agency
characteristics predicting study outcomes.
Methods
The 2007 National Home Health and Hospice Care Survey was analyzed.
Multivariate logistic regressions were estimated to identify discharge and
agency characteristics predicting guideline-concordant pain assessment and
management practices and pain control outcomes.
Results
A high percentage of discharges had pain assessment at admission
(97%) and before discharge (93%); use of valid pain rating
scales was relatively low (69% and 54% for first and last
assessments, respectively). Almost 95% of patients received pain
medication, but only 42% received nonpharmacologic therapies. About
70% of patients assessed with a valid pain scale saw improvement in
the level of pain or remained free of pain from admission to discharge.
Non-Hispanic blacks were less likely to have pain assessments, and Hispanics
were less likely to receive opioid analgesics or to have pain-free status at
discharge, compared with non-Hispanic whites. Patients receiving care from
for-profit (vs. nonprofit) agencies were more likely to receive pain
assessment with a valid scale before discharge but less likely to experience
pain control or improvement.
Conclusion
Greater use of valid pain assessment scales and nonpharmacologic
therapies constitutes areas for improvement in hospice care. Targeted
interventions are needed to address disparities in pain care by patient race
and/or ethnicity and agency ownership status.