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"If we don't speak the language, we aren't offered the same opportunities": Qualitative perspectives of palliative care access for women of color living with advanced breast cancer.
Krishnamurthy, Nithya; David, Daniel; Odom, J Nicholas; Mathelier, Krystina; Lin, Jenny J; Smith, Cardinale; Peralta, Maria; Moorehead, Dolores; Mazor, Melissa.
Afiliação
  • Krishnamurthy N; Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • David D; NYU Rory Meyers College of Nursing, New York, NY, USA.
  • Odom JN; School of Nursing, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Mathelier K; Pace University, Lienhard School of Nursing, New York, NY, USA.
  • Lin JJ; Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Smith C; Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Peralta M; Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Moorehead D; Women's Cancer Resource Center, Berkeley, CA, USA.
  • Mazor M; Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Article em En | MEDLINE | ID: mdl-38957483
ABSTRACT
Context Despite efforts to enhance equity, disparities in early palliative care (PC) access for historically minoritized patients with advanced breast cancer (ABC) persist. Insight into patient and clinician perspectives are needed to inform future models aimed at improving equity in PC access and outcomes.

Objectives:

To explore qualitative barriers and facilitators to early PC access in an urban setting with Black and Latina women with ABC.

Methods:

In this qualitative descriptive study, we conducted one-on-one interviews with Black and Latina women with ABC (N = 20) and interdisciplinary clinicians (N = 20) between February 2022 and February 2023. Participants were recruited from urban academic and community cancer clinics. Transcripts were analyzed using an inductive coding and thematic analysis approach.

Results:

Barriers identified by both patients and clinicians included lack of communication between oncology, PC, and primary care teams, limited understanding of PC among patients and non-PC clinicians, language and health literacy-related communication challenges, and racism and marginalization, including implicit bias and lack of diverse racial/ethnic representation in the supportive care workforce. Facilitators identified by both patients and clinicians included patient-to-patient referrals, support groups breaking cultural stigma on topics including self-advocacy and PC, referrals from trusted providers, and community organizations' abilities to overcome challenges related to social determinants of health, most specifically logistical and financial support.

Conclusions:

Patients and clinicians reported similar barriers and facilitators to PC access, most commonly through the lens of care coordination and communication. These findings will inform future adaptation of a culturally and linguistically care model to improve access to early PC services for Black and Latina women with ABC.

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: SSM Qual Res Health Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: SSM Qual Res Health Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos