THE WILLINGNESS OF CANCER OUTPATIENTS TO COMPLETE PATIENT-REPORTED OUTCOME MEASURES OUTSIDE OF THE CLINIC

Author(s)

Ho V1, Song Y1, Brown C2, Vennettilli A1, Eng L1, Zarrin A1, Dobriyal A1, Chen L1, Mirshams M1, Patel D1, Hon H1, Pat V1, Ho A1, Solomon H1, Tiessen K1, Thai H1, Irwin M1, Mahler M1, Xu W2, Liu G2, Howell D2
1Ontario Cancer Institute, Princess Margaret Cancer Centre, Toronto, ON, Canada, 2Princess Margaret Cancer Centre, Toronto, ON, Canada

OBJECTIVES: Patient reported outcome (PRO) tools at our institution have focused traditionally on in-clinic evaluation. In anticipation of real time home electronic reporting, we assessed whether patients were willing to complete symptom/toxicity PRO tools prior to their clinic visits. Such tools may be more accurate and reliable but depend on patient motivation. METHODS: One hundred and seventy-two cancer outpatients were recruited at the Princess Margaret Cancer Centre. Patients were surveyed on their preferences for completing a currently established institutional electronic symptom/toxicity PRO tool when administered outside the clinic on an electronic platform, such as on a tablet or smartphone.  RESULTS: The median participant age was 56.5 years and 58% were female. 74% were Caucasian and 67% had some post-secondary education; 58% had local disease. Of the participants, 48% (83/172) indicated that they would not wish to complete the PRO tool in advance of attending their clinic appointments and only 15% (25/172) agreed or strongly agreed. Fair to moderate agreement (weighted kappa=0.41) existed between willingness/unwillingness to complete the PRO tool in advance and willingness/unwillingness to fill it out electronically. Lack of willingness was not associated with any clinico-demographic factors. Patients generally felt that the tool was not difficult to use (91%) and did not take too long (81%) to complete.  CONCLUSIONS: Patients were not willing to fill out a PRO tool electronically in advance of clinic visits, even though they were completing it at their outpatient clinic. Such data collection must be tied to a transparent clinical purpose that patients see as an integral part of their health care. Other avenues for collecting outpatient drug toxicities outcomes should be investigated.

Conference/Value in Health Info

2015-11, ISPOR Europe 2015, Milan, Italy

Value in Health, Vol. 18, No. 7 (November 2015)

Code

PCN228

Topic

Patient-Centered Research

Topic Subcategory

Patient-reported Outcomes & Quality of Life Outcomes

Disease

Oncology

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