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成为一名心力衰竭患者。

Becoming a patient with heart failure.

作者信息

Stull D E, Starling R, Haas G, Young J B

机构信息

Department of Sociology, The University of Akron, Ohio 44325-1905, USA.

出版信息

Heart Lung. 1999 Jul-Aug;28(4):284-92. doi: 10.1016/s0147-9563(99)70075-0.

Abstract

OBJECTIVE

The purpose of this study was to gain a better understanding of the process of becoming a patient with heart failure, a process of identity formation. Are there clues in the patients' stories about heart failure that might give us a better idea of how patients adjust to heart failure and what heart failure means to them? Meanings that individuals attach to events or situations are central to development of identity and subsequent behaviors.

DESIGN AND SETTING

Qualitative methods involving detailed interviews and grounded theory method were used in an outpatient cardiology department of a large health care facility in northeast Ohio.

PATIENTS

Twenty-one patients with a diagnosis of heart failure were conveniently selected and interviewed for this research. Patients were selected on the basis of having a left ventricular ejection fraction of 35% or less and New York Heart Association class II, III, or IV. Other possible selection criteria (eg, VO(2Max ), walk test, or dyspnea) were not available for all patients and thus did not constitute consistent selection criteria. A broad net was cast for patients with varying characteristics to see if common processes and experiences existed regardless of the differences in clinical indicators.

METHODS

Patients were interviewed in the examining room as part of a regularly scheduled visit with their cardiologists. All interviews were tape recorded and fully transcribed. Field notes and relevant patient chart data (eg, age, sex, race, marital status, cause of heart failure, comorbidities, history of hospitalization, New York Heart Association functional class, left ventricular ejection fraction) were included in the transcribed interviews. The transcribed interview was read and responses were given initial conceptual codes. These coded passages were categorized according to more abstract categories or concepts and underlying processes that encompass them. This process continues until all relevant passages have been categorized and subsumed under higher-order (more abstract or general) categories.

RESULTS

The process of becoming a patient with heart failure involves a gradual process of taking on a new identity. Five distinct phases of this process of identity formation emerged from the data: a crisis event, the diagnosis, the patient's and family's response to the diagnosis, their acceptance and adjustment to life with this condition, and making the decision to get on with life.

CONCLUSIONS

Most research on heart failure has focused on patients or their families farther along in the trajectory of this condition. We know little about the psychosocial experience of the early phases of this condition. Becoming a patient with heart failure is a process of searching for a meaning to this condition (what is it? what does it mean for the future?) and a process of taking on a new identity and appropriate role behaviors. This process takes place over a period of time. This suggests that the formation of individual identities evolve as new information becomes available, as meanings are attached to the new circumstances, and as a process of negotiating new roles among family members (and among patient, family members, and clinicians) takes place. The findings of this study suggest possible interventions that may positively affect the patient's condition and the quality of family life.

摘要

目的

本研究旨在更好地理解成为心力衰竭患者这一身份形成过程。在患者关于心力衰竭的故事中,是否存在线索能让我们更清楚地了解患者如何适应心力衰竭以及心力衰竭对他们意味着什么?个体赋予事件或情境的意义对于身份发展及后续行为至关重要。

设计与背景

在俄亥俄州东北部一家大型医疗机构的门诊心脏病科,采用了涉及详细访谈和扎根理论方法的定性研究方法。

患者

本研究方便选取了21名诊断为心力衰竭的患者进行访谈。入选患者的左心室射血分数为35%或更低,且纽约心脏协会心功能分级为II级、III级或IV级。并非所有患者都具备其他可能的入选标准(如最大摄氧量、步行试验或呼吸困难情况),因此这些标准未构成一致的入选标准。我们广泛纳入了具有不同特征的患者,以探究无论临床指标存在何种差异,是否存在共同的过程和经历。

方法

患者在检查室接受访谈,这是他们定期与心脏病专家就诊的一部分。所有访谈均进行录音并完整转录。转录的访谈内容中包含现场记录和相关患者病历数据(如年龄、性别、种族、婚姻状况、心力衰竭病因、合并症、住院史、纽约心脏协会心功能分级、左心室射血分数)。阅读转录的访谈内容并对回答赋予初始概念编码。这些编码段落根据更抽象的类别或概念以及涵盖它们的潜在过程进行分类。这一过程持续进行,直到所有相关段落都被分类并归入更高层次(更抽象或更一般)的类别。

结果

成为心力衰竭患者的过程涉及逐渐形成新身份的过程。从数据中浮现出这一身份形成过程的五个不同阶段:危机事件、诊断、患者及其家人对诊断的反应、他们对这种状况下生活的接受和调整,以及决定继续生活。

结论

大多数关于心力衰竭的研究都聚焦于病情发展轨迹中处于更后期阶段的患者或其家人。我们对这种疾病早期阶段的心理社会经历了解甚少。成为心力衰竭患者是一个探寻这种疾病意义(它是什么?对未来意味着什么?)的过程,也是一个形成新身份并采取适当角色行为的过程。这个过程会持续一段时间。这表明个体身份的形成会随着新信息的出现、新情况被赋予意义以及家庭成员(以及患者、家庭成员和临床医生之间)协商新角色的过程而演变。本研究结果提示了可能对患者病情和家庭生活质量产生积极影响的干预措施。

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