A Prescription for Wellness in Early PD: Just What the Doctor Ordered.

IF 2.9 4区 医学 Q2 CLINICAL NEUROLOGY Journal of Geriatric Psychiatry and Neurology Pub Date : 2023-11-01 Epub Date: 2023-03-13 DOI:10.1177/08919887231164358
Bradley McDaniels, Gregory M Pontone, Adrienne M Keener, Indu Subramanian
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引用次数: 1

Abstract

Background: Being diagnosed with a neurodegenerative disease is a life-changing event and a critical time to help patients cope and move forward in a proactive way. Historically, the main focus of Parkinson's disease (PD) treatment has been on the motor features with limited attention given to non-motor and mental health sequelae, which have the most impact on quality of life. Although depression and anxiety have been described at the time of PD diagnosis, demoralization, intolerance of uncertainty, decreased self-efficacy, stigma and loneliness can also present and have negative effects on the trajectory of the disease. Hence, understanding the psychological impact of the diagnosis and how to provide better counselling at this critical time point may be the key to a better long-term trajectory and quality of life.

Focus: There has been a paradigm shift in the treatment of chronic illness moving beyond the medical model, which focuses on fighting illness with the physician being in charge of the treatment process and the patient being the passive recipient, toward a more holistic (i.e., physical, psychological, social, and spiritual health) biopsychosocial approach that emphasizes behavioral factors with the patient being an active collaborator in their treatment. Hence, we propose that fostering resilience, social support, and psychological flexibility offer promise toward attenuating negative reactions and improving overall well-being.

Conclusion: Through a proactive wellness approach incorporating lifestyle choices, people with PD (PwP) can not only achieve improved states of health, well-being, and quality of life, but actually thrive.

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早期帕金森病患者的健康处方:正是医生所吩咐的。
背景:被诊断为神经退行性疾病是一个改变生活的事件,也是帮助患者以积极主动的方式应对和前进的关键时刻。从历史上看,帕金森病(PD)治疗的主要焦点一直是运动特征,而对非运动和心理健康后遗症的关注有限,这些后遗症对生活质量的影响最大。尽管在诊断PD时已经描述了抑郁和焦虑,但士气低落、对不确定性的不容忍、自我效能感下降、耻辱感和孤独感也会对疾病的发展轨迹产生负面影响。因此,了解诊断的心理影响,以及如何在这个关键时刻提供更好的咨询,可能是改善长期轨迹和生活质量的关键。焦点:慢性病治疗的范式发生了转变,超越了医学模式,医学模式侧重于与疾病作斗争,医生负责治疗过程,患者是被动接受者,更全面的(即身体、心理、社会和精神健康)生物心理社会方法,强调行为因素,患者在治疗中是积极的合作者。因此,我们提出,培养韧性、社会支持和心理灵活性有望减少负面反应,提高整体幸福感。结论:通过结合生活方式选择的积极健康方法,帕金森病患者不仅可以改善健康、幸福感和生活质量,而且可以茁壮成长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
40
审稿时长
>12 weeks
期刊介绍: Journal of Geriatric Psychiatry and Neurology (JGP) brings together original research, clinical reviews, and timely case reports on neuropsychiatric care of aging patients, including age-related biologic, neurologic, and psychiatric illnesses; psychosocial problems; forensic issues; and family care. The journal offers the latest peer-reviewed information on cognitive, mood, anxiety, addictive, and sleep disorders in older patients, as well as tested diagnostic tools and therapies.
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