BMC Cancer (Apr 2018)

Cost of Medical Care of Patients with Advanced Serious Illness in Singapore (COMPASS): prospective cohort study protocol

  • Irene Teo,
  • Ratna Singh,
  • Chetna Malhotra,
  • Semra Ozdemir,
  • Rebecca A. Dent,
  • Nesaretnam Barr Kumarakulasinghe,
  • Wee Lee Yeo,
  • Yin Bun Cheung,
  • Rahul Malhotra,
  • Ravindran Kanesvaran,
  • Alethea Chung Pheng Yee,
  • Noreen Chan,
  • Huei Yaw Wu,
  • Soh Mun Chin,
  • Hum Yin Mei Allyn,
  • Grace Meijuan Yang,
  • Patricia Soek Hui Neo,
  • Nivedita V. Nadkarni,
  • Richard Harding,
  • Eric A. Finkelstein

DOI
https://doi.org/10.1186/s12885-018-4356-z
Journal volume & issue
Vol. 18, no. 1
pp. 1 – 8

Abstract

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Abstract Background Advanced cancer significantly impacts quality of life of patients and families as they cope with symptom burden, treatment decision-making, uncertainty and costs of treatment. In Singapore, information about the experiences of advanced cancer patients and families and the financial cost they incur for end-of-life care is lacking. Understanding of this information is needed to inform practice and policy to ensure continuity and affordability of care at the end of life. The primary objectives of the Cost of Medical Care of Patients with Advanced Serious Illness in Singapore (COMPASS) cohort study are to describe changes in quality of life and to quantify healthcare utilization and costs of patients with advanced cancer at the end of life. Secondary objectives are to investigate patient and caregiver preferences for diagnostic and prognostic information, preferences for end-of-life care, caregiver burden and perceived quality of care and to explore how these change as illness progresses and finally to measure bereavement adjustment. The purpose of this paper is to present the COMPASS protocol in order to promote scientific transparency. Methods This cohort study recruits advanced cancer patients (n = 600) from outpatient medical oncology clinics at two public tertiary healthcare institutions in Singapore. Patients and their primary informal caregiver are surveyed every 3 months until patients’ death; caregivers are followed until 6 months post patient death. Patient medical and billing records are obtained and merged with patient survey data. The treating medical oncologists of participating patients are surveyed to obtain their beliefs regarding care delivery for the patient. Discussion The study will allow combination of self-report, medical, and cost data from various sources to present a comprehensive picture of the end-of-life experience of advanced cancer patients in a unique Asian setting. This study is responsive to Singapore’s National Strategy for Palliative Care which aims to identify opportunities to meet the growing need for high quality care for Singapore’s aging population. Results will also be of interest to policy makers and researchers beyond Singapore who are interested to understand and improve the end-of-life experience of cancer patients. Trial registration NCT02850640 (Prospectively registered on June 9, 2016).

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