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IIR 03-126
 
 
Intervention to Improve Care at Life's End in VA Medical Centers
Kathryn L. Burgio PhD MA BA
Brimingham VA Medical Center
Birmingham, AL
Funding Period: July 2005 - June 2012

BACKGROUND/RATIONALE:
Currently 28,000 veterans die each year within VA Medical Centers. In acute care units, patients near the end of life are frequently not identified, and as a result, their suffering may not be properly appreciated or managed, and may even be exacerbated by standard medical care. The primary goal of this study is to evaluate an intervention designed to improve the quality of end-of-life care provided in VA Medical Centers.

OBJECTIVE(S):
The objective of this study is to transfer the best practices of traditionally home-based hospice and palliative care into the VA inpatient setting. Specific aims are: (1) to evaluate the effectiveness of a Comfort Care intervention for improving processes of care at life's end, and (2) conduct qualitative analyses of after-death interviews with families and caregivers.

METHODS:
The study is a pre-post intervention trial in 5 VA Medical Centers. The Comfort Care intervention targets physician, nursing, and ancillary staff, training them to identify veterans who are dying and to implement care plans appropriate for the last days or hours of life. Applying Comfort Care to dying patients in the acute care setting involves altering the trajectory of care to treatment pathways oriented more toward meeting the needs of dying patients, including pain control, DNR planning, transfer from ICUs to medical units, and elimination of instrumentation and restraints. Through intensive on-site staff training and follow-up consultation, staff will be trained to identify patients who are near the end of life and implement Comfort Care interventions. To facilitate the use of these interventions, an electronic Comfort Care Order Set will be integrated into the Computerized Patient Record System (CPRS).

Data extracted from the CPRS records of veterans who have died during a 12-month period before and after intervention will be used to determine the impact of the intervention on 5 process of care indicators: presence of an order for opioid pain medication at the time of death, DNR orders, location of death, nasogastric tubes/intravenous lines, and restraints. Analyses will account for clustering of patients within facilities and staggered implementation of intervention across facilities will allow for examination of secular trends.

Semi-structured after-death interviews will be used to elicit family members' attitudes, beliefs and feelings about the care received at the end of life. They will also complete questionnaires assessing their perceptions of the intensity and frequency of the loved one's pain at the end of life, satisfaction with care, and impact of the death on the family/caregiver. Data from qualitative analyses will be compared with quantitative measures of processes of care to help in developing concurrency between the issues of importance to families and patients and those of the medical system.

FINDINGS/RESULTS:
Data collection is ongoing. There are no results at this time.

IMPACT:
In February 2003, Palliative Care Consult Teams (PCCT) were mandated by VHA at all VA facilities. PCCT teams are functioning at many different levels of maturity and effectiveness at different VAMCs. This project builds on this new and developing infrastructure by providing the PCCT teams at the targeted facilities with training and technical support to help accomplish their mission to improve care at life's end for the veterans they serve. In the final year of the project, training materials will be posted on the VA website and a training manual will be prepared to facilitate broader dissemination of the Comfort Care interventions.

PUBLICATIONS:

Journal Articles

  1. Williams BR, Woodby LL, Bailey FA, Burgio KL. Identifying and Responding to Ethical and Methodological Issues in After-Death Interviews with Next-of-Kin. Death Studies. 2008; 32(3): 197-236.


DRA: Aging and Age-Related Changes, Health Services and Systems
DRE: Quality of Care, Communication and Decision Making
Keywords: End-of-life, Hospice, Pain
MeSH Terms: none