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American journal of Alzheimer's disease and other dementias最新文献

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Practicalities and possibilities 实用性和可能性
Pub Date : 2004-05-01 DOI: 10.1177/153331750401900301
C. Rowland
: This paper discusses the historical context of the NSW AECG and the NSW Aboriginal Education Policy, and emphasises the need for culturally inclusive policies and effective implementation strategies. It also highlights the relationship between Indigenous educational disadvantage and colonisation, demonstrating the need for dominant educational frameworks to be inclusive of Indigenous ways of knowing, being and doing.
本文讨论了新南威尔士州AECG和新南威尔士州土著教育政策的历史背景,并强调了文化包容性政策和有效实施策略的必要性。它还突出了土著教育劣势与殖民之间的关系,表明主流教育框架需要包容土著的认识、存在和行动方式。
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引用次数: 0
Book review: Dementia Practice Guidelines for Treating Disturbing Behaviors 书评:痴呆症实践指南治疗令人不安的行为
Pub Date : 2004-03-01 DOI: 10.1177/153331750401900206
N. Richeson
The disturbing behaviors associated with dementia are a significant problem for older adults, their families, and their caregivers. By the year 2050, the incidence of dementia in the US is expected to climb to 14 million, according to the Alzheimer’s Association. The associated rise in disturbing behaviors will further affect the afflicted’s interpersonal relationships and quality of life, as well as opportunities to experience leisure. Dementia Practice Guidelines for Treating Disturbing Behaviors, a 400-page document, provides a long overdue systematic approach that will help recreational therapists treat these disturbing behaviors. The authors’ focus on the importance of including the best available evidence when formatting treatment decisions distinguishes this text from previous approaches to treatment in recreational therapy. The foundation of the dementia practice guidelines (DPG) is the merging of the Need-Driven DementiaCompromised Behavior (NDB) model and the Neurodevelopmental Sequencing Theory of Prescription (NDSP). The NDB model suggests that the disturbing behaviors of persons with dementia are not a symptom of the disease but rather an unmet need. The NDSP, developed by Buettner in the 1980s, is a comprehensive approach for treating the disturbing behaviors of frail older adults with dementia. While the Omnibus Budget Reconciliation Act of 1987 has long promoted a nonpharmacologic approach to treatment, little has been done to promote alternative treatment interventions. The DPG promotes recreational therapy as the first line of defense, ahead of prescribed psychoactive medication, with its negative side effects. The section on recreational therapy outlines the 10 steps in treating disturbing behaviors, referencing them with appendix materials such as behavior checklists, physician order forms, and evaluation materials. The tools provided in the appendices will ensure a place for the DPG on the practitioner’s desk. Also helpful is a chart of more than 80 protocols that can help the practitioner select the appropriate intervention based on factors such as behavior, stage, level of dementia, and research findings. The criteria for selecting an intervention to decrease a behavior illustrates the application of evidence-based practice. DPG’s literature review incorporates an evidencebased grading system that lets the reader determine the strength of the research. The reference section includes a key to inform the reader if the article is research, literature, national guidelines, or theory. The life work of two researchers, the DPG demonstrates a groundbreaking contribution not just to the therapeutic recreation profession but also to healthcare in general. The focus on evidence-based practice using a nonpharmological approach to treating disturbing behaviors for persons with dementia is an important one. As the authors note, there are many unanswered questions, and for that reason, Dementia Practice Guidelines for Treating Disturbing
与痴呆症相关的令人不安的行为对老年人、他们的家人和他们的照顾者来说是一个重大问题。根据阿尔茨海默氏症协会的数据,到2050年,美国的痴呆症发病率预计将攀升至1400万。相关的不安行为的增加将进一步影响受折磨者的人际关系和生活质量,以及体验休闲的机会。一份长达400页的文件《痴呆症治疗令人不安行为实践指南》提供了一种姗姗姗姗来的系统方法,将帮助娱乐治疗师治疗这些令人不安的行为。作者的重点是,在格式化治疗决策时,包括最好的可用证据的重要性,将这篇文章与以前的娱乐疗法治疗方法区分开来。痴呆实践指南(DPG)的基础是需求驱动痴呆妥协行为(NDB)模型和处方神经发育测序理论(NDSP)的合并。NDB模型表明,痴呆症患者令人不安的行为并不是该疾病的症状,而是一种未满足的需求。由Buettner在20世纪80年代开发的NDSP是一种综合方法,用于治疗患有痴呆症的体弱老年人的令人不安的行为。尽管1987年的《综合预算和解法案》(Omnibus Budget Reconciliation Act)长期以来一直提倡非药物治疗方法,但在促进替代治疗干预方面做得很少。DPG提倡娱乐疗法作为第一道防线,而不是处方精神活性药物,因为它有负面的副作用。关于娱乐疗法的部分概述了治疗令人不安行为的10个步骤,并参考了附录材料,如行为检查表、医生处方和评估材料。附录中提供的工具将确保在从业者的办公桌上为DPG提供一个位置。还有一张包含80多种治疗方案的图表也很有帮助,它可以帮助医生根据行为、阶段、痴呆水平和研究结果等因素选择适当的干预措施。选择干预措施以减少行为的标准说明了循证实践的应用。DPG的文献综述结合了一个基于证据的评分系统,让读者确定研究的强度。参考部分包括一个关键,告知读者如果文章是研究,文献,国家指导方针,或理论。作为两位研究人员的终身工作,DPG不仅对治疗性娱乐行业,而且对一般的医疗保健行业都有开创性的贡献。关注以证据为基础的实践,使用非药物方法来治疗痴呆症患者的不安行为是一个重要的方面。正如作者所指出的,有许多悬而未决的问题,因此,《痴呆症实践指南治疗令人不安的行为》可能被认为是一项正在进行的工作…但是非常有用。
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引用次数: 2
Book Review: Design for Assisted Living: Guidelines for Housing the Physically and Mentally Frail 书评:《辅助生活的设计:为身体和精神脆弱的人提供住房的指南》
Pub Date : 2004-03-01 DOI: 10.1177/153331750401900207
Elizabeth Hirshom
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引用次数: 0
Behaviors and concepts 行为和观念
Pub Date : 2004-03-01 DOI: 10.1177/153331750401900201
C. Rowland
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引用次数: 0
Memantine, ethics, and behavioral matters 美金刚,道德和行为问题
Pub Date : 2004-01-01 DOI: 10.1177/153331750401900101
C. Rowland
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引用次数: 0
Accepting the Challenge 接受挑战
Pub Date : 2004-01-01 DOI: 10.1177/153331750401900113
Jan Sharrow
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引用次数: 0
Book Review: Staying Connected While Letting Go: The Paradox of Alzheimer's Caregiving 书评:在放手的同时保持联系:阿尔茨海默氏症护理的悖论
Pub Date : 2004-01-01 DOI: 10.1177/153331750401900112
S. Albrecht
Studying Greek tragedies, Nelson Mandela noticed that characters were measured upon dealing with difficult situations and that a hero was a person who did not break even under difficult circumstances. This book is about optimism in the face of the tragedy of Alzheimer disease. It illustrates how caregivers become heroes through struggling and transcending the chaos caused by dementia, into a situation in which the dignity of both the patient and the caregiver is preserved. The authors illustrate how in the actual phases of care for a demented patient caregivers can cope with the problems they are confronted with, starting with dealing with the first signs until recovery after the patient’s death. They use the principles of cognitive reframing to illustrate how untapped individual potentials can be used to deal with difficult situations. In the beginning, there is the ambivalence of getting a diagnosis, the “wanting to know” versus the “not wanting to know.” The actual information on the diagnosis causes dual feelings of upsetting on the one hand and relief and validation of expectations on the other hand. The disclosure of the diagnosis is considered to be essential to come to terms with the illness. The patient’s changed behavior can now be defined as an illness, out of the patient’s control. Knowing the diagnosis also enables sharing this information with family and friends, thereby usually decreasing the risk of isolation by hiding the patient. As there is little knowledge about the impact of disclosure of the diagnosis dementia, the cases presented in this book provide insight into the patient’s world. Becoming a caregiver requires adaptations of the premorbid relationship. It is important that the caregiver sees himself or herself as a whole person, an individual with own rights, separate from the patient. Caregivers describe how they were confronted with negative thoughts about dealing with the patient’s illness. It is essential that the caregiver give himself or herself permission to be angry and resentful. These are natural and normal feelings. However, in the communication with the patient, it is better to preserve patient’s dignity instead of arguing. The acknowledgments of negative thoughts and the emotional and practical suggestions to deal with these feelings are very valuable for those involved in caregiving. In the middle stage, competence in memory and other activities is uneven; one moment the patient is quite well another less capable than ever. A major challenge for caregivers is to accommodate and adjust to this disease in such a way that adaptation includes compassion for both themself and the patient. Awareness of the increasing stress and alertness for symptoms of burnout are required. The authors manage to vividly describe this difficult balance, including both the struggle and the victories of the caregivers. The idea through all stages of caregiving, even the late middle stage, is that caregivers have a choice. To mainta
纳尔逊·曼德拉在研究希腊悲剧时注意到,性格是通过处理困难的情况来衡量的,英雄是在困难的情况下不收支平衡的人。这本书是关于面对阿尔茨海默病悲剧的乐观主义。它展示了护理人员如何通过挣扎和超越痴呆症造成的混乱,成为维护患者和护理人员尊严的英雄。作者说明了在实际的护理阶段,护理人员如何处理他们所面临的问题,从处理最初的迹象开始,直到病人死后恢复。他们使用认知重构的原则来说明如何利用未开发的个人潜力来处理困难的情况。一开始,得到诊断的时候会有一种矛盾的心理,“想知道”和“不想知道”。诊断上的实际信息会引起双重感受,一方面是沮丧,另一方面是期望的缓解和验证。诊断结果的披露被认为是与疾病妥协的必要条件。病人行为的改变现在可以被定义为一种疾病,病人无法控制。了解诊断还可以与家人和朋友分享这些信息,从而通常通过隐藏患者来降低隔离的风险。由于对痴呆症诊断披露的影响知之甚少,本书中提出的病例提供了对患者世界的洞察。成为照顾者需要适应发病前的关系。重要的是,护理人员将自己视为一个完整的人,一个拥有自己权利的个体,与患者分开。护理人员描述了他们如何面对处理病人疾病的消极想法。至关重要的是,照顾者允许自己生气和怨恨。这些都是自然和正常的感觉。但是,在与患者的沟通中,与其争吵,不如维护患者的尊严。对消极想法的承认以及处理这些情绪的情感和实际建议对那些参与照顾的人来说是非常有价值的。在中期,记忆能力和其他活动能力参差不齐;病人一会儿还很好,一会儿又变得更弱了。护理人员面临的一个主要挑战是适应和适应这种疾病,这种适应包括对自己和病人的同情。意识到不断增加的压力和对倦怠症状的警觉是必要的。作者设法生动地描述了这种艰难的平衡,包括照顾者的挣扎和胜利。在看护的所有阶段,甚至是中后期,看护人都有一个选择。为了保持平衡,照顾者可以说“我需要帮助”是至关重要的。在最后阶段,是在保持联系和放手之间挣扎。当面对衰退和死亡的威胁时,护理人员可能希望在努力放手的同时继续下去。这通常是对最终分离的预期。这本书以重新进入后关怀来纪念明天结束。在这一时期,积极的生活娱乐受到刺激,就像在照顾时期一样。激励人们采取负责任的行动,利用尚未开发的人类潜能,是本书的乐观色彩。作为一个人自己的代理人,使自尊得到优化,并赋予意义和希望。这可能有助于超越损失。适应力是战胜痴呆症的关键。由于我们对护理中的挫折了解得太多,而对安慰却知之甚少,这本书设法在不否认问题的情况下提供安慰。相反,由于其非正统的特征,它也增加了未知的问题和损失,如亲密关系,被照顾者感知到的损失。它也说明了持久的爱的力量。这本书对家庭、朋友和专业人士的价值在于,它展示了如何在照顾者的个人兴趣和照顾任务之间建立健康的界限。
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引用次数: 0
2003 Cumulative Subject Index 二零零三年累积学科指数
Pub Date : 2004-01-01 DOI: 10.1177/153331750401900116
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引用次数: 0
2003 Cumulative Author Index 2003年累计作者索引
Pub Date : 2004-01-01 DOI: 10.1177/153331750401900115
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引用次数: 0
Book Review: Losing My Mind: An Intimate Look at Life with Alzheimer's 书评:《失去理智:阿尔茨海默氏症患者的生活》
Pub Date : 2004-01-01 DOI: 10.1177/153331750401900111
Alta F. McDonald
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引用次数: 0
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American journal of Alzheimer's disease and other dementias
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