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BiDil in the Clinic: An Interdisciplinary Investigation of Physicians' Prescription Patterns of a Race-Based Therapy

机译:诊所的竞标者:对基于种族治疗的医师处方模式的跨学科调查

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Background: The African American Heart Failure Trial (A-HeFT) and the Food and Drug Administration (FDA) approval of BiDil for race-specific prescription have stirred the debate about the scientific and medical status of race. Yet there is no assessment of the potential fallout of this dispute on physicians' willingness to prescribe the drug. We present here an analysis of the factors influencing physicians' prescription of BiDil and investigate whether exposure to the controversy has an impact on their therapeutic judgments about the drug. Methods: We conducted an electronic survey with physicians in the department of internal medicine at the University of Cincinnati. Participants were randomly assigned to two groups, with one group receiving information about the controversy over BiDil. We used various statistical tests, including a linear mixed effects model, to analyze the results. Results: Twenty-seven percent of the participants reported using patients' race as a major factor in making treatment decisions. Thirty-three percent reported the inefficacy of standard therapies, 25% the severity of the disease, and 15% other unspecified factors as primary determining criteria in prescribing BiDil. With respect to the controversy, 68% of physicians reported that they were not aware of any controversy surrounding BiDil. Physicians' willingness to prescribe BiDil as a therapy was associated with their awareness of the controversy surrounding A-HeFT (p <.003). But their willingness to prescribe the therapy along racial lines did not vary significantly with exposure to the controversy. Conclusions: Overall, physicians prescribe and are willing to prescribe BiDil more to black patients than to white patients. However, physicians' lack of awareness about the controversial scientific status of A-HeFT suggests the need for more efficient ways to convey scientific information about BiDil to clinicians. Furthermore, the uncertainties about the determination of clinical utility of BiDil for the individual patient raise questions about whether this specific race-based therapy is in patients' best interests.
机译:背景:非洲裔美国心力衰竭试验(A-HEFT)和食品药品监督管理局(FDA)批准比德本体以进行种族特定的处方已激起了关于种族的科学和医学地位的辩论。然而,对医生开毒药愿意的这种争议的潜在影响没有评估。我们在这里展示了影响BIDIL的医生处方的因素分析,并调查是否对争议的暴露对其对药物的治疗判断产生影响。方法:我们在辛辛那提大学内科医生进行了电子调查。参与者被随机分配到两组,一个集团接收关于竞争对手的争议的信息。我们使用了各种统计测试,包括线性混合效果模型,分析结果。结果:二十七名参与者报告使用患者的竞赛作为制定治疗决策的主要因素。 33%的人报告标准疗法的低效率,疾病的严重程度为25%,以及15%的其他未指明因素作为处方竞标中的主要确定标准。关于争议,68%的医生报告说,他们没有意识到贝迪尔周围的任何争议。医生愿意向竞标作为治疗的意愿与他们对围绕A-HEFT周围的争议的认识有关(P <.003)。但他们愿意沿着种族线规定治疗的意愿并没有因争议而显着变化。结论:总体而言,医生规定并愿意向黑人患者开出竞标,而不是白人患者。然而,医生对A-HEFT的争议科学地位缺乏意识表明需要更有效的方法来向临床医生传达有关BIDIL的科学信息。此外,关于贝迪尔临床效用的不确定性为个体患者提出了关于这种特定种族的治疗是否有患者最佳利益的问题。

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