Latinx attitudes, barriers, and experiences with genetic counseling and testing: A systematic review.

As genetics is increasingly used across clinical settings, there is a need to understand the impact and experiences of diverse patients. This review systematically examined research literature on Latinx experiences with genetic counseling and genetic testing (GC/GT) in the United States, synthesizin...

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Published in:Journal of Genetic Counseling Vol. 32; no. 1; pp. 166 - 182
Main Authors: Dron, Heather A., Bucio, Daiana, Young, Jennifer L., Tabor, Holly K., Cho, Mildred K.
Format: research systematic review tables/charts Journal Article
Published: Wiley-Blackwell Feb2023
Online Access:View this record in EBSCOhost
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      dt: Feb2023
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1002/jgc4.1632
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        atl: Latinx attitudes, barriers, and experiences with genetic counseling and testing: A systematic review.
      aug:
        au:
          Dron, Heather A.
          Bucio, Daiana
          Young, Jennifer L.
          Tabor, Holly K.
          Cho, Mildred K.
        affil: Stanford Center for Biomedical Ethics (SCBE), Stanford University, Stanford California,, USA
      sug:
        subj:
          Genetic Counseling
          Genetic Screening
          Health Services Accessibility
          Hispanic Americans
          Cancer Patients Psychosocial Factors
          Breast Neoplasms Familial and Genetic
          Ovarian Neoplasms Familial and Genetic
          Decision Making, Patient
          Human
          Systematic Review
          United States
          Thematic Analysis
          Health Knowledge
          Implicit Bias
          Acculturation
          Communication
          Healthcare Disparities
          Health Status Disparities
          Life Experiences
          Funding Source
      ab: As genetics is increasingly used across clinical settings, there is a need to understand the impact and experiences of diverse patients. This review systematically examined research literature on Latinx experiences with genetic counseling and genetic testing (GC/GT) in the United States, synthesizing key themes and knowledge gaps pertaining to both patient experience and hypothetical scenarios. Findings were based on a systematic search, inclusion, and thematic analysis of 81 empirical peer‐reviewed articles published from January 1990 to July 2019 pertaining to Latinx populations and GC/GT. Studies most commonly addressed Latinas' perspectives on GC/GT in prenatal settings or for hereditary breast and ovarian cancer (HBOC). Costs, referrals, and communication were significant barriers to accessing genetic services for many Latinx patients, particularly those with low English proficiency (LEP). Studies highlighted difficulties accessing and communicating in healthcare settings, and how medical context and prior experience with healthcare workers and institutions influenced GC/GT decision‐making. Providers' implicit biases about Latinx patients negatively impacted their care and impeded communication. Despite low awareness of cancer GT, Latinx patients often reported interest in learning more about GC/GT or unmet needs for GT discussion and provider involvement. This systematic review identified areas where providers can take action to improve Latinx experiences with GC/GT. Clinicians should elicit and respond to patient preferences about shared decision‐making. For patients with low numeracy or LEP, providers should consider tailored educational and communication techniques. Most studies focused on HBOC and prenatal testing, and Latinx patients are heterogeneous, leaving many research questions about Latinx experience with GT/GC in other clinical areas.
      pubtype: Academic Journal
      doctype:
        research
        systematic review
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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