My Lived Experiences Are More Important Than Your Probabilities: The Role of Individualized Risk Estimates for Decision Making about Participation in the Study of Tamoxifen and Raloxifene (STAR)
被引:37
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作者:
Holmberg, Christine
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机构:
Charite, Berlin Sch Publ Hlth, D-13347 Berlin, GermanyCharite, Berlin Sch Publ Hlth, D-13347 Berlin, Germany
Holmberg, Christine
[1
]
Waters, Erika A.
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机构:
Washington Univ, Sch Med, Dept Surg, St Louis, MO 63110 USACharite, Berlin Sch Publ Hlth, D-13347 Berlin, Germany
Waters, Erika A.
[2
]
Whitehouse, Katie
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机构:
Charite, Berlin Sch Publ Hlth, D-13347 Berlin, GermanyCharite, Berlin Sch Publ Hlth, D-13347 Berlin, Germany
Whitehouse, Katie
[1
]
Daly, Mary
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机构:
Fox Chase Canc Ctr, Philadelphia, PA 19111 USACharite, Berlin Sch Publ Hlth, D-13347 Berlin, Germany
individualized risk information;
lived experiences;
narrative interviews;
decision making;
chemoprevention;
breast cancer risk;
BREAST-CANCER CHEMOPREVENTION;
SURGICAL ADJUVANT BREAST;
BOWEL PROJECT;
PRIMARY-CARE;
P-2;
TRIAL;
US WOMEN;
PREVENTION;
HEALTH;
INFORMATION;
PERCEPTIONS;
D O I:
10.1177/0272989X15594382
中图分类号:
R19 [保健组织与事业(卫生事业管理)];
学科分类号:
摘要:
Background: Decision-making experts emphasize that understanding and using probabilistic information are important for making informed decisions about medical treatments involving complex risk-benefit tradeoffs. Yet empirical research demonstrates that individuals may not use probabilities when making decisions. Objectives: To explore decision making and the use of probabilities for decision making from the perspective of women who were risk-eligible to enroll in the Study of Tamoxifen and Raloxifene (STAR). Methods: We conducted narrative interviews with 20 women who agreed to participate in STAR and 20 women who declined. The project was based on a narrative approach. Analysis included the development of summaries of each narrative, and thematic analysis with developing a coding scheme inductively to code all transcripts to identify emerging themes. Results: Interviewees explained and embedded their STAR decisions within experiences encountered throughout their lives. Such lived experiences included but were not limited to breast cancer family history, a personal history of breast biopsies, and experiences or assumptions about taking tamoxifen or medicines more generally. Conclusions: Women's explanations of their decisions about participating in a breast cancer chemoprevention trial were more complex than decision strategies that rely solely on a quantitative risk-benefit analysis of probabilities derived from populations In addition to precise risk information, clinicians and risk communicators should recognize the importance and legitimacy of lived experience in individual decision making.