TY - JOUR
T1 - Genetic counseling and testing for Asian Americans
T2 - a systematic review
AU - Young, Jennifer L.
AU - Mak, Julie
AU - Stanley, Talia
AU - Bass, Michelle
AU - Cho, Mildred K.
AU - Tabor, Holly K.
N1 - Funding Information:
J.Y. was supported by National Institutes of Health grant T32HG00895301.
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics.
PY - 2021/8
Y1 - 2021/8
N2 - Purpose: Asian Americans have been understudied in the literature on genetic and genomic services. The current study systematically identified, evaluated, and summarized findings from relevant qualitative and quantitative studies on genetic health care for Asian Americans. Methods: A search of five databases (1990 to 2018) returned 8,522 unique records. After removing duplicates, abstract/title screening, and full text review, 47 studies met inclusion criteria. Data from quantitative studies were converted into “qualitized data” and pooled together with thematic data from qualitative studies to produce a set of integrated findings. Results: Synthesis of results revealed that (1) Asian Americans are under-referred but have high uptake for genetic services, (2) linguistic/communication challenges were common and Asian Americans expected more directive genetic counseling, and (3) Asian Americans’ family members were involved in testing decisions, but communication of results and risk information to family members was lower than other racial groups. Conclusion: This study identified multiple barriers to genetic counseling, testing, and care for Asian Americans, as well as gaps in the research literature. By focusing on these barriers and filling these gaps, clinical genetic approaches can be tailored to meet the needs of diverse patient groups, particularly those of Asian descent.
AB - Purpose: Asian Americans have been understudied in the literature on genetic and genomic services. The current study systematically identified, evaluated, and summarized findings from relevant qualitative and quantitative studies on genetic health care for Asian Americans. Methods: A search of five databases (1990 to 2018) returned 8,522 unique records. After removing duplicates, abstract/title screening, and full text review, 47 studies met inclusion criteria. Data from quantitative studies were converted into “qualitized data” and pooled together with thematic data from qualitative studies to produce a set of integrated findings. Results: Synthesis of results revealed that (1) Asian Americans are under-referred but have high uptake for genetic services, (2) linguistic/communication challenges were common and Asian Americans expected more directive genetic counseling, and (3) Asian Americans’ family members were involved in testing decisions, but communication of results and risk information to family members was lower than other racial groups. Conclusion: This study identified multiple barriers to genetic counseling, testing, and care for Asian Americans, as well as gaps in the research literature. By focusing on these barriers and filling these gaps, clinical genetic approaches can be tailored to meet the needs of diverse patient groups, particularly those of Asian descent.
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U2 - 10.1038/s41436-021-01169-y
DO - 10.1038/s41436-021-01169-y
M3 - Review article
C2 - 33972720
AN - SCOPUS:85105887634
SN - 1098-3600
VL - 23
SP - 1424
EP - 1437
JO - Genetics in Medicine
JF - Genetics in Medicine
IS - 8
ER -