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抑郁症、精神病和痴呆症:对家庭的影响。

Depression, psychosis, and dementia: impact on the family.

作者信息

Ellgring J H

机构信息

Institute for Psychology (I), University of Wurzburg, Germany.

出版信息

Neurology. 1999;52(7 Suppl 3):S17-20.

Abstract

Similar to the setting of other chronic, debilitating diseases, considerable psychoeducational support of the patient's family and other caregivers represents an often-overlooked component of appropriately thorough care. Nearly three of four persons caring for an individual with PD report psychological stress and anxiety, which are exacerbated by concerns about progression of the disease. Counseling for PD caregivers can be dispensed particularly effectively through individual psychological counseling as well as PD support and community self-help groups that assist caregivers in sharing concerns and promote a sense they are understood by others. Through such measures, which may be delivered effectively by nurse practitioners, PD caregivers can develop effective coping strategies for disease related stressors. Empirical results show the most common stressors are: anxiety, concern about the future, impatience or intolerance, loss of autonomy, sleep disturbances, diminished time and opportunity for recreation and social contact, and anger. These sequelae often ensue when the PD patient evidences depression, advanced dementia, or psychosis, each of which can severely constrain communication. Caregivers often must also contend with two other adverse psychological phenomena: cognitive dissonance surrounding placement of the patient in a nursing home and learned helplessness, which may predispose to depressive states. Other often unmet needs of the "hidden victims" of PD include compromised immune function, social stigmata, and financial difficulties. Respite care may be useful in reducing the stress associated with these and other problems frequently affecting caregivers.

摘要

与其他慢性衰弱性疾病的情况类似,对患者家属和其他照料者给予大量心理教育支持是全面适当护理中一个常常被忽视的组成部分。近四分之三照料帕金森病患者的人报告有心理压力和焦虑,对疾病进展的担忧会加剧这些情况。针对帕金森病照料者的咨询可以通过个体心理咨询以及帕金森病支持和社区自助小组特别有效地进行,这些小组帮助照料者分享担忧,并让他们有被他人理解的感觉。通过这些措施(执业护士可以有效地提供这些措施),帕金森病照料者可以制定有效的应对策略来应对与疾病相关的压力源。实证结果表明,最常见的压力源有:焦虑、对未来的担忧、不耐烦或不宽容、自主性丧失、睡眠障碍、娱乐和社交接触的时间和机会减少,以及愤怒。当帕金森病患者出现抑郁、晚期痴呆或精神病时,这些后遗症常常会随之而来,每一种情况都会严重限制沟通。照料者通常还必须应对另外两种不良心理现象:围绕将患者安置在养老院的认知失调和习得性无助,这可能会导致抑郁状态。帕金森病“隐性受害者”的其他常常未得到满足的需求包括免疫功能受损、社会污名化和经济困难。临时护理可能有助于减轻与这些以及其他经常影响照料者的问题相关的压力。

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