Compounding or confounding?—addressing context-specific disparities in access to outpatient specialty palliative care

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Authors: Hannah Nettelblad, Rubina Ratnaparkhi, Sharon Fitzgerald Wolff, Elaine Pope, Ian C. Cook, Melissa Javellana, Andrea Jewell, Christian T. Sinclair, Lori Ann Spoozak
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Abstract

BACKGROUND: Despite proven benefit of outpatient specialty palliative care on symptom burden, quality-of-life, and survival, only 20-30% of eligible patients with gynecologic cancers receive a referral, even in high-resource health systems. Socioeconomically disadvantaged and culturally marginalized populations face inequitable access to specialty palliative care. However, the relationships between social determinants of health (SDOH) and palliative care utilization remain understudied. We evaluated rates of outpatient specialty palliative care referral and assessed disparities associated with SDOH. METHODS: A single institution retrospective cohort quality improvement study evaluated gynecologic oncology patients receiving care in Kansas City, Kansas (midwestern United States) who met American Society of Clinical Oncology (ASCO) criteria for referral to outpatient specialty palliative care from 2019-2022. Eligible patients were stratified based on whether or not they were referred to an outpatient specialty palliative care provider. Groups were compared based on clinical factors [age, cancer site, stage, primary versus recurrent disease status, body mass index (BMI)], and SDOH (race, ethnicity, primary language, insurance status, having a primary care provider (PCP), distance from the hospital, rurality, and Area Deprivation Index (ADI). Descriptive statistics and multivariable logistic regression were performed, and odds ratios were calculated. RESULTS: During the study period, 432 gynecologic oncology patients were eligible for referral to outpatient specialty palliative care, of which 191 (44%) were referred and 146 (34%) ultimately saw a palliative care provider. Patients who received a palliative care referral more frequently had recurrent disease and lower BMI. Patients were referred to a palliative care provider less commonly if they lived in a rural or disadvantaged (>70th percentile ADI) county, lived further from a National Cancer Institute (NCI)-designated cancer center, or if they were established with a PCP. On multivariable logistic regression evaluating rurality, distance, deprivation, and primary care access, only rurality and primary care access remained significant. Rural patients were less likely to be referred to a palliative care provider [odds ratio (OR) 0.3, 95% confidence interval (CI): 0.17-0.54, P

Fields of Study & Subjects

Palliative Care and End-of-Life Issues Palliative and Oncologic Care Pain Management and Opioid Use

Publication details

Journal / source
Annals of Palliative Medicine
Volume
15
Issue
1
Pages
4–4
Publication date
1 January 2026
Language
EN