Abstract

Rising demand on cancer system resources, alongside mounting evidence that demonstrates the safety and acceptability of primary care-led follow-up care, has resulted in some cancer centres discharging patients back to primary care after treatment. At the same time, the ways in which routine cancer follow-up care is provided across Canada continue to vary widely. The objectives of the present study were to investigate patterns of routine follow-up care at a cancer centre for breast, colorectal, gynecologic, and prostate cancer survivors; factors associated with receipt of follow-up care at a cancer centre; and changes in follow-up care at a cancer centre over time. We identified all people diagnosed in Nova Scotia with an invasive breast, colorectal, gynecologic, or prostate cancer between 1 January 2006 and 31 December 2013. We linked the resulting population-based dataset, at the patient level, to cancer centre or clinic data and to census data. We identified a nonmetastatic survivor cohort (n = 12,267) and developed decision rules to differentiate routine from non-routine visits during the follow-up care period (commencing 1 year after diagnosis). Descriptive statistics were computed to describe the patterns of routine follow-up care at a cancer centre. Negative binomial regression was used to examine factors associated with visits made and changes over time. Nearly half the survivors (48.4%) had at least 1 follow-up visit to the cancer centre, with variation by disease site (range: 30.2%-62.4%). Disease site and stage at diagnosis were associated with receipt of follow-up care at a cancer centre. For instance, compared with breast cancer survivors, survivors of gynecologic cancer had more visits [incidence rate ratio (irr): 1.48; 95% confidence interval (ci): 1.34 to 1.64], and survivors of colorectal cancer had fewer visits (irr: 0.45; 95% ci: 0.40 to 0.51). Year of diagnosis was associated with follow-up at a cancer centre, with each successive calendar year being associated with an 8% increase in visits made (irr: 1.08; 95% ci: 1.07 to 1.10). Despite evidence that follow-up care can be effectively and safely delivered in primary care, and despite intensifying demands on oncology services, many survivors continue to receive routine follow-up care at a cancer centre.

Highlights

  • Rising demand on cancer system resources, alongside mounting evidence that demonstrates the safety and acceptability of primary care–led follow-up care, has resulted in some cancer centres discharging patients back to primary care after treatment

  • This retrospective cohort study used linked administrative health data to examine routine follow-up visits to specialist cancer centres and clinics for all persons diagnosed in Nova Scotia with nonmetastatic breast, prostate, colorectal, or gynecologic cancer over an 8-year period

  • We investigated patterns of routine follow-up visits received by breast, colorectal, gynecologic, and prostate cancer survivors at cancer centres in Nova Scotia

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Summary

Introduction

Rising demand on cancer system resources, alongside mounting evidence that demonstrates the safety and acceptability of primary care–led follow-up care, has resulted in some cancer centres discharging patients back to primary care after treatment. The prevalence of cancer survivors is rapidly growing[1]: Considering all cancer types, two thirds of individuals diagnosed with cancer today will be long-term survivors, meaning that they will live for 5 years or more after diagnosis. For those patients, routine follow-up care marks the transition from intensive treatment to long-term survivorship[2]. As long-term survivors, those individuals require routine follow-up to detect disease recurrence or new primary cancers, to prevent and manage the late effects of the cancer and its treatment, to manage pre-existing chronic conditions, and to address general preventive care needs. Together with a mounting evidence base showing that primary care–led follow-up is a safe and acceptable alternative to oncology-led care[7,8,9], has resulted in some cancer centres transfering routine follow-up care back to a patient’s primary care provider (pcp) after treatment[10]

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