Background: Cancer patients are receiving a greater
proportion of their care on an outpatient basis. The impact of this change in
oncology care patterns on Emergency Department (ED) and palliative care (PC) utilization
is poorly understood.
Objectives: To examine the rate of use of ED and PC services by adult
cancer patients; and demographic and psychosocial predictors of
each type of service use in the year following diagnosis.
Methods: Between July 2007 and March 2009, newly diagnosed adult cancer
patients attending a tertiary care cancer centre were recruited into a longitudinal
study examining distress. Patients were followed prospectively until March 2010.
Collected demographic and psychosocial data was linked to administrative data
on ED and PC visit and admission rates, ED diagnoses and consults ordered.
Results: 4329 (68% of eligible population) agreed to participate in the
study. 1283 patients (30%) made 2349 ED visits in the year following diagnosis.
58% of patients made 1 visit, 42% made 2-12 visits. 13% of ED visits required
an oncology consultation; 77% of these resulted in an admission. 691 patients
(16%) made 1316 visits to a palliative care service (including consultation,
inpatient, hospice or community). 58% of patients made 2-7 visits. People with lung cancer, older patients and
patients reporting higher distress, anxiety, pain and fatigue had higher ED
utilization.