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Racial and Ethnic Differences in Psychosocial Care Use Among Adults With Metastatic Breast Cancer: A Retrospective Analysis Across Six New York City Health Systems.
Pinheiro, Laura C; An, Anjile; Zeng, Caroline; Walker, Desiree; Mercurio, Anne Marie; Hershman, Dawn L; Rosenberg, Shoshana M.
Afiliação
  • Pinheiro LC; Division of General Internal Medicine, Department of Medicine, Weill Cornell Medicine, New York, NY.
  • An A; Division of Epidemiology, Department of Population Health Sciences, Weill Cornell Medicine, New York, NY.
  • Zeng C; Division of Biostatistics, Department of Population Health Sciences, Weill Cornell Medicine, New York, NY.
  • Walker D; Division of General Internal Medicine, Department of Medicine, Weill Cornell Medicine, New York, NY.
  • Mercurio AM; Patient Research Advocate, New York, NY.
  • Hershman DL; Patient Research Advocate, Ponte Vedra Beach, FL.
  • Rosenberg SM; Division of Medical Oncology, Columbia University Medical Center, New York, NY.
JCO Oncol Pract ; 20(7): 984-991, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38466926
ABSTRACT

PURPOSE:

A metastatic breast cancer (mBC) diagnosis can affect physical and emotional well-being. However, racial and ethnic differences in receipt of outpatient psychosocial care and supportive care medications in adults with mBC are not well described.

METHODS:

Adults with mBC were identified in the INSIGHT-Clinical Research Network, a database inclusive of >12 million patients receiving care across six New York City health systems. Outpatient psychosocial care was operationalized using Common Procedure Terminology codes for outpatient psychotherapy or counseling. Psychosocial/supportive care medications were defined using Rx Concept Unique Identifier codes. Associations between race/ethnicity and outpatient care and medication use were evaluated using logistic regression.

RESULTS:

Among 5,429 adults in the analytic cohort, mean age was 61 years and <1% were male; 53.6% were non-Hispanic White (NHW), 21.4% non-Hispanic Black (NHB), 15.9% Hispanic, 6.1% Asian/Native Hawaiian/Pacific Islander (A/NH/PI), and 3% other or unknown. Overall, 4.1% had ≥one outpatient psychosocial care visit and 63.4% were prescribed ≥one medication. Adjusted for age, compared with NHW, Hispanic patients were more likely (odds ratio [OR], 2.14 [95% CI, 1.55 to 2.92]) and A/NH/PI patients less likely (OR, 0.35 [95% CI, 0.12 to 0.78]) to have an outpatient visit. NHB (OR, 0.59 [95% CI, 0.51 to 0.68]) and Asian (OR, 0.36 [95% CI, 0.29 to 0.46]) patients were less likely to be prescribed medications.

CONCLUSION:

Despite the prevalence of depression, anxiety, and distress among patients with mBC, we observed low utilization of psychosocial outpatient care. Supportive medication use was more prevalent, although differences observed by race/ethnicity suggest that unmet needs exist.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Aceitação pelo Paciente de Cuidados de Saúde / Serviços de Saúde Mental Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: JCO Oncol Pract Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Aceitação pelo Paciente de Cuidados de Saúde / Serviços de Saúde Mental Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: JCO Oncol Pract Ano de publicação: 2024 Tipo de documento: Article