Primary Care Provider Visits Among Cancer Survivors 5-7 Years Postdiagnosis

Author:

Birken Sarah A.1ORCID,Peluso Alexandra G.2,Shalowitz David I.34ORCID,Isom Scott5,Wagi Cheyenne R.6,Randazzo Aliza6,Falk Derek7ORCID,Strom Carla8,Bell Ronny9ORCID,Weaver Kathryn E.10ORCID

Affiliation:

1. Department of Implementation Science, Wake Forest School of Medicine, Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC

2. Department of Implementation Science, Wake Forest School of Medicine, Winston-Salem, NC

3. West Michigan Cancer Center, Kalamazoo, MI

4. Collaborative on Equity in Rural Cancer Care, Kalamazoo, MI

5. Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, NC

6. Department of Implementation Science, Wake Forest University School of Medicine, Winston-Salem, NC

7. Department of Population and Quantitative Health Science, Case Western Reserve University School of Medicine, Cleveland, OH

8. Office of Cancer Health Equity, Comprehensive Cancer Center, Atrium Health Wake Forest Baptist, Winston-Salem, NC

9. Division of Pharmaceutical Outcomes and Policy, UNC Eshelman School of Pharmacy, UNC Chapel Hill, Chapel Hill, NC

10. Department of Social Sciences and Health Policy, Wake Forest University School of Medicine, Winston-Salem, NC

Abstract

PURPOSE Cancer survivors experience better outcomes when primary care providers (PCPs) are engaged in their care. Nearly all survivors have a PCP engaged in their care in the initial 5 years postdiagnosis, but little is known about sustained PCP engagement. We assessed PCP engagement in survivors' care 5-7 years postdiagnosis and characterized survivors most vulnerable to loss to PCP follow-up. METHODS We linked electronic health record ambulatory care and cancer registry data from an National Cancer Institute–Designated Comprehensive Cancer Center to identify eligible survivors (≥18 years; diagnosed with breast, colorectal, or uterine cancer; had an in-network PCP). We used multiple logistic regression to assess associations between survivor demographics, clinical factors, and health care utilization and odds of sustained PCP engagement. RESULTS In 5-7 years postdiagnosis, PCPs were engaged in care for 43% of survivors. Survivors with sustained PCP-engagement were on average 4.6 years older than those without ( P < .0001); survivors had 1.36 greater odds of having regular PCP visits for each decade increase in age on cancer diagnosis ( P = .0030). Survivors were less likely to be lost to PCP follow-up if diagnosed at an earlier stage with odds at 0.57 and 0.10 for stage I and stage IV, respectively ( P = .0005), and had 2.70 greater odds of engagement in care with at least one oncology visit annually 5-7 years postdiagnosis ( P < .0001). CONCLUSION Sustained PCP engagement is endorsed as critical by survivors, PCPs, and oncologists. We found most survivors were lost to PCP follow-up 5-7 years postdiagnosis. Our study is among the first to contribute empirical evidence of survivors being lost in transition. Findings from this study demonstrate the need to bridge gaps in long-term care for cancer survivors.

Publisher

American Society of Clinical Oncology (ASCO)

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