Healthcare Experiences Are Associated with Colorectal Cancer Mortality but only for Specific Racial Groups

A Seer-CAHPS Study

Bibliographic Data

ID2073009
AuthorsCarol Y Ochoa-Dominguez (0000-0002-6946-3287, University of Southern California), Trevor A Pickering (0000-0002-2281-641X, University of Southern California), Stephanie Navarro (0000-0003-3220-852X, University of Southern California), Claudia Rodríguez (0009-0007-4764-3627, University of Southern California), Albert J Farias (0000-0002-6463-7831, University of Southern California, corresponding author)
Year2024
Volume11
Issue4
Pages2224-2235
Publication date2024-08-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueJournal of Racial and Ethnic Health Disparities (JOURNAL)
Journal identifiersISSN: 2196-8837 • E-ISSN: 2197-3792
PublisherSpringer Science and Business Media LLC (PUBLISHER)
DOI10.1007/s40615-023-01690-7
PMID37369914
OpenAlexW4382318115
LanguageEN
Citations received2
References cited30

Background The objective of this study was to determine whether racial/ethnic disparities exist in patient-reported experiences with care after colorectal cancer diagnosis and whether they are associated with mortality. Methods We conducted a retrospective cohort study of colorectal cancer patients diagnosed from 1997 to 2011, ≥ 65 years, and completed a Consumer Assessment of Healthcare Providers and Systems (CAHPS) survey at least 6 months after a cancer diagnosis. We leverage the National Cancer Institute's SEER-CAHPS dataset of Medicare beneficiaries. CAHPS survey responses were used to generate four composite measures of patient experiences with 1) getting needed care, 2) getting needed prescription drugs, 3) getting care quickly, and 4) physician communication. We used multivariable linear regression models to examine racial differences in patient experiences with aspects of their care and multivariable Cox proportional hazards models to identify the risk of mortality associated with each composite score by racial group. Results Of the 5135 patients, 76.86% were non-Hispanic White, 7.58% non-Hispanic Black, 8.30% Hispanic, and 7.26% non-Hispanic Asian. Overall, patients reported the highest scores for composite measures regarding "getting all needed prescriptions" and the lowest score for "getting care quickly." In our adjusted models, we found that Hispanics, non-Hispanic Black, and non-Hispanic Asian patients reported significantly lower scores for getting needed prescription drugs (B = − 4.34, B = − 4.32, B = − 5.66; all p < 0.001) compared to non-Hispanic Whites. Moreover, non-Hispanic Black patients also reported lower scores for getting care quickly (B = − 3.44, p < 0.05). We only found one statistically significant association between composite scores of patient experience and mortality. For non-Hispanic Black patients, a 3-unit increase in getting needed care was associated with 0.97 times the hazard of mortality (p = 0.003). Conclusion Our research underscores that CAHPS patient experiences with care are an important patient-centered quality-of-care metric that may be associated with cancer outcomes and that there may be differences in these relationships by race and ethnicity. Thus, highlighting how patients' perceptions of their healthcare experiences can contribute to disparities in colorectal cancer outcomes

Cancer · Colorectal cancer · Family medicine · Health care · Pathology · Political science · Public health · Quality of Life Research · Colorectal Cancer Screening and Detection · Global Cancer Incidence and Screening · Healthcare Policy and Management · Medicine · Epidemiology · Gerontology · Internal Medicine · Oncology