Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research

被引:150
作者
Kraft, Stephanie A. [1 ]
Cho, Mildred K. [2 ]
Gillespie, Katherine [3 ]
Halley, Meghan [3 ]
Varsava, Nina [2 ]
Ormond, Kelly E. [2 ]
Luft, Harold S. [3 ]
Wilfond, Benjamin S. [1 ]
Lee, Sandra Soo-Jin [2 ]
机构
[1] Seattle Childrens Res Inst, Seattle, WA 98101 USA
[2] Stanford Univ, Stanford, CA 94305 USA
[3] Palo Alto Med Fdn, Res Inst, Palo Alto, CA 94301 USA
关键词
genetic research; research ethics; informed consent; precision medicine; biobank; electronic medical records; PATIENT ADVOCACY ORGANIZATIONS; INDIVIDUAL RESEARCH; AFRICAN-AMERICANS; HEALTH-CARE; ATTITUDES; RETURN; RACE; PARTICIPATION; WILLINGNESS; BIOBANKING;
D O I
10.1080/15265161.2018.1431322
中图分类号
B82 [伦理学(道德学)];
学科分类号
摘要
With the growth of precision medicine research on health data and biospecimens, research institutions will need to build and maintain long-term, trusting relationships with patient-participants. While trust is important for all research relationships, the longitudinal nature of precision medicine research raises particular challenges for facilitating trust when the specifics of future studies are unknown. Based on focus groups with racially and ethnically diverse patients, we describe several factors that influence patient trust and potential institutional approaches to building trustworthiness. Drawing on these findings, we suggest several considerations for research institutions seeking to cultivate long-term, trusting relationships with patients: (1) Address the role of history and experience on trust, (2) engage concerns about potential group harm, (3) address cultural values and communication barriers, and (4) integrate patient values and expectations into oversight and governance structures.
引用
收藏
页码:3 / 20
页数:18
相关论文
共 64 条
  • [1] Anderson Nick., 2010, GTIP, P15, DOI DOI 10.1145/1920320.1920323
  • [2] [Anonymous], 2022, DED WEB APPL MAN AN
  • [3] [Anonymous], 2014, EMERGE NETWORK ELECT
  • [4] [Anonymous], 2015, QUICKFACTS
  • [5] [Anonymous], 2016, ALL US RES PROGR
  • [6] ETHICS AND CLINICAL RESEARCH
    BEECHER, HK
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1966, 274 (24) : 1354 - &
  • [7] Race and trust in the health care system
    Boulware, LE
    Cooper, LA
    Ratner, LE
    LaVeist, TA
    Powe, NR
    [J]. PUBLIC HEALTH REPORTS, 2003, 118 (04) : 358 - 365
  • [8] Race, medical researcher distrust, perceived harm, and willingness to participate in cardiovascular prevention trials
    Braunstein, Joel B.
    Sherber, Noelle S.
    Schulman, Steven P.
    Ding, Eric L.
    Powe, Neil R.
    [J]. MEDICINE, 2008, 87 (01) : 1 - 9
  • [9] Two large-scale surveys on community attitudes toward an opt-out biobank
    Brothers, Kyle B.
    Morrison, Daniel R.
    Clayton, Ellen W.
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2011, 155A (12) : 2982 - 2990
  • [10] Community leaders' perspectives on engaging African Americans in biobanks and other human genetics initiatives
    Buseh A.G.
    Stevens P.E.
    Millon-Underwood S.
    Townsend L.
    Kelber S.T.
    [J]. Journal of Community Genetics, 2013, 4 (4) : 483 - 494