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非裔美国患者对医疗决策的看法。

African American patients' perspectives on medical decision making.

作者信息

Torke Alexia M, Corbie-Smith Giselle M, Branch William T

机构信息

Division of General Medicine, Emory University School of Medicine, Atlanta, GA 30303, USA.

出版信息

Arch Intern Med. 2004 Mar 8;164(5):525-30. doi: 10.1001/archinte.164.5.525.

Abstract

BACKGROUND

The medical literature offers little information about how older African Americans view the medical decision-making process. We sought to describe the perspectives of older African American patients in a primary care clinic as they consider a medical decision.

METHODS

We interviewed 25 African American patients older than 50 years who had discussed flexible sigmoidoscopy with their primary care provider. Interviews were analyzed using qualitative methods.

RESULTS

Patients listed concerns about cancer and health, risks and benefits, their own understanding of the test, and the recommendation of the provider as the most important factors in their decision. Most patients wanted information about medical tests and procedures to increase their understanding and to provide reassurance rather than to guide decision making. Most patients explained that they wanted the provider to make medical decisions because of his or her training and experience. Despite this, many expressed a sense of ownership or control over one's own body. Patients thought trust was built by a health care provider's honesty, patience, kindness, interest, and continuity of care.

CONCLUSIONS

Although traditional models of informed consent have emphasized providing patients with information to guide autonomous decision making, patients may want this information for other reasons. Fully informing patients about their medical condition increases understanding and provides reassurance. Because many of these patients want their provider to participate in making medical decisions, he or she should not only provide information but should also provide guidance to the patient.

摘要

背景

医学文献中关于老年非裔美国人如何看待医疗决策过程的信息较少。我们试图描述一家初级保健诊所中年龄较大的非裔美国患者在考虑医疗决策时的观点。

方法

我们采访了25名年龄超过50岁且与初级保健提供者讨论过乙状结肠镜检查的非裔美国患者。采用定性方法对访谈进行分析。

结果

患者将对癌症和健康的担忧、风险和益处、他们自己对检查的理解以及提供者的建议列为决策中最重要的因素。大多数患者希望获得有关医学检查和程序的信息,以增进理解并获得安心,而非用于指导决策。大多数患者解释说,由于提供者的培训和经验,他们希望由提供者做出医疗决策。尽管如此,许多患者表达了对自己身体的自主感或掌控感。患者认为医疗保健提供者的诚实、耐心、善良、关心和持续护理能够建立信任。

结论

尽管传统的知情同意模式强调向患者提供信息以指导自主决策,但患者可能出于其他原因需要这些信息。向患者充分告知其病情可增进理解并提供安心。由于这些患者中的许多人希望提供者参与医疗决策,提供者不仅应提供信息,还应为患者提供指导。

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