• Glenna Bradshaw, Pamela S Hinds, Shelly Lensing, Jami S Gattuso, and Bassem I Razzouk.
• Baptist Memorial Hospital-East, Memphis, Tennessee, USA.
• J Palliat Med. 2005 Feb 1;8(1):86-95.

BackgroundTo add to the data regarding the quality of care given to dying children and their families.ObjectiveTo develop baseline of end-of-life care at a single pediatric facility to evaluate institution-wide palliative care initiative.DesignRetrospective chart review of all known deaths during an 18-month time period.Setting/SubjectsOne hundred forty-five charts of patients from a single pediatric cancer facility who died during designated time period.MeasurementsVariables included: cause and place of death; CPR/DNR status prior to death; length of end of life care prior to death; sibling counseling and bereavement counseling offered to family after death; and wishes or preferences of patient/family regarding the death experience.ResultsResults included: solid tumor patients more likely to die of progressive disease than leukemia or bone marrow transplant patients; bone marrow transplant patients 2-3 times more likely to die of cardiopulmonary or cardiovascular complications; solid tumor patients were more likely to die at home than leukemia patients; solid tumor/brain tumor patients had a median time in end of life or palliative care of 29 days compared to leukemia patients' median of 11 days; 48% of DNRs completed 11 days prior to death.ConclusionsRelationship exists between diagnosis, cause and place of death in this population; findings replicate findings of 4 similar studies; accurate and consistent quality standards of care need to be established for this population as well as methods of documentation before reviewing/accrediting agencies impose standards that are not evidence based.

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