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心力衰竭患者对个性化生存估计沟通的看法。

Patient Perspectives on Communication of Individualized Survival Estimates in Heart Failure.

作者信息

Narayan Madhav, Jones Jacqueline, Portalupi Laura B, McIlvennan Colleen K, Matlock Daniel D, Allen Larry A

机构信息

University of Colorado School of Medicine, Aurora, Colorado.

University of Colorado College of Nursing, Aurora, Colorado.

出版信息

J Card Fail. 2017 Apr;23(4):272-277. doi: 10.1016/j.cardfail.2016.12.008. Epub 2016 Dec 21.

Abstract

BACKGROUND

Despite the availability of validated risk scores for survival in heart failure (HF), individualized estimates are not typically provided directly to patients.

METHODS AND RESULTS

We explored patient perspectives regarding conveyance of individualized Seattle Heart Failure Model (SHFM) survival estimates. In 2014 and 2015, 24 HF patients completed a semistructured interview at the initial offering of SHFM survival estimates (baseline) and a follow-up interview. Themes emerging from questions of interest were identified: 1) preferences for receiving estimates: patients generally wished to see their SHFM estimates (acceptors; n = 17, and ideally would have received such information early after HF "diagnosis"; 2) reactions: viewing their personalized estimates restored some control and hope for most patients and rarely increased anxiety; 3) application: some acceptors found the information to be helpful in considering future plans, but its usefulness in specific decisions was restricted owing to perceived model limitations; 4) understanding uncertainty: participants contextualized estimates through observations that uncertainty is pervasive in life; acceptors qualitatively understood the population-based nature of the estimates.

CONCLUSIONS

The majority of patients valued receiving individualized prognostic survival estimates. Acceptors generally understood the nature of the information and found it to provide clarity, control, and hope rather than invoking confusion or anxiety.

摘要

背景

尽管已有经过验证的心力衰竭(HF)生存风险评分,但通常不会直接向患者提供个体化的评估。

方法与结果

我们探讨了患者对传达西雅图心力衰竭模型(SHFM)个体化生存评估的看法。在2014年和2015年,24名HF患者在首次提供SHFM生存评估时(基线)完成了一次半结构化访谈,并进行了一次随访访谈。确定了从感兴趣的问题中浮现出的主题:1)接收评估的偏好:患者普遍希望看到他们的SHFM评估结果(接受者;n = 17),并且理想情况下希望在HF“诊断”后尽早获得此类信息;2)反应:查看他们的个性化评估结果使大多数患者恢复了一些掌控感和希望,并且很少增加焦虑;3)应用:一些接受者发现该信息有助于考虑未来计划,但由于认为模型存在局限性,其在特定决策中的有用性受到限制;4)理解不确定性:参与者通过观察到生活中普遍存在不确定性来将评估结果置于情境中;接受者从定性角度理解了评估结果基于人群的性质。

结论

大多数患者重视接受个体化的预后生存评估。接受者通常理解信息的性质,并发现它能提供清晰度、掌控感和希望,而不是引起困惑或焦虑。

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