长期哌醋甲酯单药治疗帕金森病:生化分析和17年病例研究

R. Townsend
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引用次数: 0

摘要

背景:本研究的信息可以改善1000多万帕金森病患者的健康和生活质量。本文介绍了长期使用哌醋甲酯治疗帕金森氏症的安全性和有效性,以取代传统的抗帕金森氏症药物,如卡比多巴-左旋多巴和普拉克索,这些药物会导致增强(神经损伤)、过度镇静、突然昏迷和认知减慢。哌醋甲酯加强和保护神经组织,维持正常的警觉性和认知。方法:在查阅已发表的400余篇研究和指南的基础上,分析哌甲酯治疗与抗帕金森治疗的神经生化差异。这篇文章还介绍了一个案例研究,涉及一个病例主体,他患有非常严重的帕金森病,有充分记录的9年抗帕金森治疗和8年哌甲酯治疗。病例主体是一名66岁的男性,拥有博士学位,是一名已发表论文的神经生物化学研究员。55岁时,他被医学记录为残疾,需要药物来维持身体机能。在58岁时,他的疾病和APs的不良影响共同导致了完全残疾,没有已知的治疗方法。因此,他构思并设计了世界上第一个长期治疗帕金森病的哌醋甲酯,并在一位开处方的医生的合作下实施了它。结果:每日辅助服用30mg哌甲酯克服了抗帕金森药物的不良反应。每日20mg剂量的哌醋甲酯单药治疗比抗帕金森药更好地控制帕金森病。3小时给药计划可使哌甲酯在不同剂量间和不同剂量间的疗效平稳且不间断。每3小时顺序给药可将药效持续时间延长至16小时。睡前持续服用大剂量的抗帕金森药能让人睡得很好。结论:作者建议临床医生利用这些发现,用哌醋甲酯代替每日服用抗帕金森药物,以提供更安全、更有效的帕金森病长期治疗。
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Long-term Methylphenidate Monotherapy for Parkinson’s: Biochemistry Analysis and 17 Year Case Study
Background: Information in this study can improve the health and quality of life of over ten million people with Parkinson’s. This paper presents long-term treatment of Parkinson’s with Methylphenidate that was found safe and effective to use instead of traditional anti-Parkinsonians such as Carbidopa-Levodopa and Pramipexole that cause augmentation (neural damage), excessive sedation, sudden passing out and slowed cognition. Methylphenidate strengthens and protects neural tissues and sustains normal alertness and cognition. Methods: This article analyzes the neurobiochemistry of Methylphenidate-therapy vs. AntiParkinsonian-therapy based on this author’s review of over 400 published studies and guidelines. This article also presents a Case Study involving a case-subject who has a very severe Parkinson’s disorder with a well-documented nine years of AntiParkinsonian-therapy followed by eight years of Methylphenidate-therapy. The case-subject is a 66 year-old male with a PhD who is a published Neurobiochemistry Researcher. At age-55 he was medically documented as disabled and needing medications to function. At age-58 his illness and the adverse effects of APs jointly caused total disability for which there was no known remedy. Thus he conceived and designed the world’s first long-term Methylphenidate treatment of Parkinson’s and implemented it with the cooperation of a prescribing Physician. Results: Adjunctive 30 mg doses of diurnal Methylphenidate overcame adverse effects of AntiParkinsonians. 20 mg doses of diurnal Methylphenidate monotherapy controlled Parkinson’s illness better than AntiParkinsonians. A 3-hour dosing schedule resulted in smooth and uninterrupted efficacy between and across doses of Methylphenidate. Sequential doses every three hours extended efficacy duration to 16 hours. Continued high-dose AntiParkinsonians at bedtime gave good sleep. Conclusion: This author recommends that clinicians use these findings to replace diurnal AntiParkinsonians with diurnal Methylphenidate in order to provide safer and more effective long-term treatment of Parkinson’s illnesses.
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