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患者对决策制定沟通的报告差异:DECISIONS 调查。

Disparities in patient reports of communications to inform decision making in the DECISIONS survey.

机构信息

Department of Health Behavior and Health Education, University of Michigan, Ann Arbor, MI 48109-2029, USA.

出版信息

Patient Educ Couns. 2012 May;87(2):198-205. doi: 10.1016/j.pec.2011.08.002. Epub 2011 Sep 3.

Abstract

OBJECTIVE

To identify patient- and decision-type predictors of two key aspects of informed decision making: discussing the cons (not just the pros) of medical interventions and asking patients what they want to do.

METHODS

Using data from 2473 members of the DECISIONS survey, a nationally representative sample of U.S. adults age 40+, we used logistic regression analysis to identify which patient characteristics predicted patient reports of healthcare providers discussing cons or eliciting preferences about one of 9 common medical decisions.

RESULTS

Multiple demographic characteristics predicted both discussions of cons and elicitations of preferences, although the specific characteristics varied between decision contexts. In particular, African-American respondents reported being more likely to receive a discussion of the cons of cancer screening (OR=1.69, p<0.05) yet less likely to have been asked their opinion about either getting a cancer screening test (OR=0.56, p<0.05) or initiating medications (OR=0.53, p<0.05). Significant cross-decision variations remained even after controlling for patient characteristics.

CONCLUSIONS

Important disparities in patient communication and involvement appear to exist both between different types of medical decisions and between different types of patients.

PRACTICE IMPLICATIONS

Providers must make sure to consistently discuss the cons of treatment and to solicit input from all patients, especially African-Americans.

摘要

目的

确定患者和决策类型的预测因子,这些预测因子与知情决策的两个关键方面有关:讨论医疗干预的弊端(不仅仅是益处)和询问患者他们想做什么。

方法

使用来自 DECISIONS 调查的 2473 名美国成年人的数据,该调查是一项具有全国代表性的 40 岁以上成年人样本,我们使用逻辑回归分析来确定哪些患者特征预测了医疗服务提供者讨论弊端或询问患者对 9 种常见医疗决策之一的偏好。

结果

多种人口统计学特征预测了讨论弊端和征求偏好,尽管在不同的决策情境中具体特征有所不同。特别是,非裔美国受访者报告说更有可能收到癌症筛查弊端的讨论(OR=1.69,p<0.05),但不太可能被问及他们对接受癌症筛查测试(OR=0.56,p<0.05)或开始服用药物(OR=0.53,p<0.05)的意见。即使在控制了患者特征后,跨决策的显著差异仍然存在。

结论

在不同类型的医疗决策之间以及不同类型的患者之间,似乎存在重要的患者沟通和参与差距。

实践意义

提供者必须确保始终讨论治疗的弊端,并向所有患者征求意见,尤其是非裔美国人。

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