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Clinical Parkinsonism Related Disorders最新文献

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Too little or too much nocturnal movements in Parkinson’s disease: A practical guide to managing the unseen 帕金森病患者夜间活动过少或过多:管理不可见现象的实用指南
Q3 CLINICAL NEUROLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.prdoa.2024.100258
Jirada Sringean , Ornanong Udomsirithamrong , Roongroj Bhidayasiri

Nocturnal and sleep-related motor disorders in people with Parkinson’s disease (PD) have a wide spectrum of manifestations and present a complex clinical picture. Problems can arise due to impaired movement ability (hypokinesias), e.g. nocturnal hypokinesia or early-morning akinesia, or to excessive movement (hyperkinesias), e.g. end-of-the-day dyskinesia, parasomnias, periodic limb movement during sleep and restless legs syndrome. These disorders can have a significant negative impact on the sleep, daytime functional ability, and overall quality of life of individuals with PD and their carers. The debilitating motor issues are often accompanied by a combination of non-motor symptoms, including pain and cramping, which add to the overall burden. Importantly, nocturnal motor disorders encompass a broader timeline than just the period of sleep, often starting in the evening, as well as occurring throughout the night and on awakening, and are not just limited to problems of insomnia or sleep fragmentation. Diagnosis can be challenging as, in many cases, the ‘gold standard’ assessment method is video polysomnography, which may not be available in all settings. Various validated questionnaires are available to support evaluation, and alternative approaches, using wearable sensors and digital technology, are now being developed to facilitate early diagnosis and monitoring. This review sets out the parameters of what can be considered normal nocturnal movement and describes the clinical manifestations, usual clinical or objective assessment methods, and evidence for optimal management strategies for the common nocturnal motor disorders that neurologists will encounter in people with PD in their clinical practice.

帕金森病(PD)患者夜间和睡眠相关运动障碍的表现范围很广,临床表现也很复杂。出现问题的原因可能是运动能力受损(运动机能减退),如夜间运动机能减退或清晨运动失调,也可能是运动过度(运动机能亢进),如日间运动障碍、寄生虫症、睡眠中周期性肢体运动和不宁腿综合征。这些障碍会对帕金森氏症患者及其照顾者的睡眠、日间功能能力和整体生活质量产生严重的负面影响。使人衰弱的运动问题往往伴随着疼痛和痉挛等非运动症状,加重了整体负担。重要的是,夜间运动障碍的时间范围比睡眠时间更广,通常从傍晚开始,也会在整晚和醒来时出现,并不仅限于失眠或睡眠片段问题。诊断可能具有挑战性,因为在许多情况下,"金标准 "评估方法是视频多导睡眠图,但并非所有环境都能提供这种方法。目前有各种经过验证的问卷可用于支持评估,而使用可穿戴传感器和数字技术的替代方法也正在开发中,以促进早期诊断和监测。本综述列出了可被视为正常夜间运动的参数,并描述了临床表现、常用的临床或客观评估方法,以及神经科医生在临床实践中会遇到的常见夜间运动障碍的最佳管理策略证据。
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引用次数: 0
Coupling neurologic music therapy with immersive virtual reality to improve executive functions in individuals with Parkinson’s disease: A Quasi-Randomized Clinical Trial 将神经音乐疗法与沉浸式虚拟现实相结合,改善帕金森病患者的执行功能:准随机临床试验
IF 1.9 Q3 CLINICAL NEUROLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.prdoa.2024.100277
Federica Impellizzeri , Maria Grazia Maggio , Paolo De Pasquale , Mirjam Bonanno , Lilla Bonanno , Rosaria De Luca , Giuseppe Paladina , Angela Alibrandi , Demetrio Milardi , Michael Thaut , Corene Hurt , Angelo Quartarone , Rocco Salvatore Calabrò

Introduction

Parkinson’s disease (PD) is one the most common neurodegenerative movement disorder, leading to motor and non-motor symptoms, including deficits in executive functions (EF), memory, visuospatial abilities, and psychomotor speed. Current treatments are primarily symptomatic, involving pharmacological, surgical strategies. Neurologic Music Therapy (NMT) has gained recognition for its effectiveness in neurorehabilitation of PD patients and improving motor and cognitive domains, such as EF. This study combines NMT with the virtual reality (VR) platform Computer-Assisted Rehabilitation Environment (CAREN), offering customizable environments for rhythmic cue practice to provide an innovative approach to Parkinson’s rehabilitation.

Methods

In our single-blind quasi-randomized controlled trial, forty patients were assigned to either an experimental group (EG = 20) or a control group (CG = 20). Both groups underwent two months of training with CAREN scenarios (three times a week for 24 sessions). The experimental group additionally received NMT applied to the selected scenarios. Participants were evaluated by a neuropsychologist at baseline and immediately after training.

Results

Intra-group analysis showed significant improvements in the EG for MOCA (p = 0.007), FAB (p = 0.008), Stroop Error (p = 0.003), Stroop Time (p < 0.001), and Visual Search (p < 0.001). The CG showed a significant difference only in Stroop Error (p = 0.02).

Conclusions

This pilot study is the first to combine NMT with CAREN in PD patients. Our findings suggest that NMT, within an immersive VR environment, effectively improves cognitive and EF in PD. Music structured within NMT techniques, coupled with advanced audio-visual feedback from VR, offers an innovative and potentially more effective approach for managing cognitive and executive deficits associated with PD.
导言帕金森病(PD)是最常见的神经退行性运动障碍之一,可导致运动和非运动症状,包括执行功能(EF)、记忆、视觉空间能力和精神运动速度的缺陷。目前的治疗方法主要是对症治疗,包括药物治疗和手术治疗。神经音乐疗法(NMT)因其在帕金森病患者神经康复和改善运动和认知领域(如EF)方面的有效性而获得认可。本研究将 NMT 与虚拟现实(VR)平台 "计算机辅助康复环境"(CAREN)相结合,为节奏提示练习提供了可定制的环境,为帕金森病康复提供了一种创新方法。方法在我们的单盲准随机对照试验中,40 名患者被分配到实验组(EG = 20)或对照组(CG = 20)。两组患者均接受为期两个月的 CAREN 情景训练(每周三次,共 24 次)。实验组还接受了针对所选情景的 NMT 训练。结果组内分析显示,EG 在 MOCA (p = 0.007)、FAB (p = 0.008)、Stroop 错误 (p = 0.003)、Stroop 时间 (p < 0.001) 和视觉搜索 (p < 0.001) 方面均有显著改善。CG仅在Stroop错误(p = 0.02)方面显示出明显差异。我们的研究结果表明,在身临其境的 VR 环境中进行 NMT 可有效改善帕金森病患者的认知能力和 EF。NMT 技术中的音乐结构与 VR 先进的视听反馈相结合,为控制与帕金森病相关的认知和执行缺陷提供了一种创新且可能更有效的方法。
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引用次数: 0
Practitioner perspectives on the implementation of the Lee Silverman Voice Treatment BIG® program 从业人员对实施李-西尔弗曼嗓音治疗 BIG® 计划的看法
IF 1.9 Q3 CLINICAL NEUROLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.prdoa.2024.100268
Leah Botkin, Rachel Proffitt

Background

The Lee Silverman Voice Treatment BIG® (LSVT BIG®) intervention, originally designed for the patients with Parkinson’s disease, is a high amplitude, high repetition therapy protocol that encourages bigger, more quality movements. The purpose of this study was to understand practitioner utilization and perspectives of the LSVT BIG® intervention as there is no published work in this area.

Methods

An electronic survey with optional debriefings was distributed to LSVT BIG® certified practitioners via the Facebook page run by parent company, LSVT Global Inc.

Results

Forty-seven practitioners engaged in this study. Practitioners were largely in the outpatient setting. Forty-seven percent reported utilizing the LSVT BIG® intervention for patient populations outside of the Parkinson’s disease diagnosis. Sixty-one percent of respondents reported using the same assessment tools and ninety-five percent reported billing insurance for their services. Twenty-three percent reported offering the LSVT BIG® intervention via telehealth. Debriefings identified barriers to implementation.

Conclusion

Practitioners are implementing the LSVT BIG® intervention across settings and are most likely to be in the outpatient setting, serving patients who possess a neurological diagnosis, and focus their assessment on lower extremity, gait, and balance. When billing insurance, practitioners routinely select the three CPT® codes: Neuromuscular Re-Education, Therapeutic Activity, and Therapeutic Procedure/Exercise. Practitioners identified several barriers to implementing the LSVT BIG® program, such as the high frequency of in-clinic visits. Practitioners are currently unsystematically modifying the program to meet patient and practitioner needs. Further research should continue to explore the practitioner perspectives on implementation of the LSVT BIG® intervention.

背景李-西尔弗曼嗓音治疗 BIG®(LSVT BIG®)干预最初是为帕金森病患者设计的,它是一种高振幅、高重复的治疗方案,可鼓励患者做出更大、更有质量的动作。本研究的目的是了解从业人员对 LSVT BIG® 干预疗法的使用情况和看法,因为在这一领域还没有公开发表的研究成果。研究方法通过母公司 LSVT Global Inc.Facebook 页面向 LSVT BIG® 认证从业人员发放电子调查问卷,并可选择听取汇报。大部分从业人员都在门诊工作。47%的受访者表示,在帕金森病诊断之外的患者群体中使用了 LSVT BIG® 干预疗法。61%的受访者表示使用相同的评估工具,95%的受访者表示为其服务向保险机构付费。23%的受访者表示通过远程医疗提供LSVT BIG®干预。结论从业人员正在不同的环境中实施 LSVT BIG® 干预,最有可能在门诊环境中实施,服务对象是拥有神经系统诊断的患者,评估重点是下肢、步态和平衡。在向保险公司收费时,医生通常会选择这三种 CPT® 代码:神经肌肉再教育、治疗活动和治疗程序/运动。从业人员指出了实施 LSVT BIG® 项目的几个障碍,如门诊就诊频率高。目前,从业人员还没有系统地修改该计划,以满足患者和从业人员的需求。进一步的研究应继续探讨从业人员对实施 LSVT BIG® 干预的看法。
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引用次数: 0
Treatment of task-specific dystonia in sports: A systematic review 运动中任务特异性肌张力障碍的治疗:系统回顾
Q3 CLINICAL NEUROLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.prdoa.2024.100245
B. Nijenhuis , E. van Wensen , M. Smit , T. van Zutphen , J. Zwerver , M.A.J. Tijssen

Introduction

Task specific dystonia is a movement disorder only affecting a highly practiced skill and is found in a broad set of expert movements including in sports. Despite affecting many sports, there is no comprehensive review of treatment options, which is in contrast to better studied forms of task specific dystonia in musicians and writers. For this reason, studies involving an intervention to treat task specific dystonia in sports were systematically reviewed, with special attention for the quality of outcome measures.

Methods

The PICO systematic search strategy was employed on task-specific dystonia, and all synonyms. Inclusion criteria were peer reviewed published studies pertaining to sports, studies with a measurement and/or intervention in TSD, all in English. We excluded abstracts, expert opinions, narrative review articles, unpublished studies, dissertations and studies exclusively relating to choking. We included case reports, case studies and case-control studies.

Results

In April 2022 Pubmed, Embase, Web of Science, and Psychinfo were searched. Of the 7000 articles identified, 31 were included that described psychological and invasive and/or pharmacological interventions. There was a lack of formal standardized outcome measures in studies resulting in low quality evidence for the effectiveness of treatment options. A descriptive synthesis showed emotional regulation was effective, but was exclusively tried in golfers. Interventions like botulinum toxin or pharmacology had a similar effectiveness compared to studies in musicians dystonia, however there was almost no formal evidence for these treatments.

Conclusion

The quality of studies was low with a lack of standardized outcome measures. Future studies with larger cohorts and quantitative outcome measures are needed to improve understanding of treatments for task specific dystonia in athletes.

导言特异性肌张力障碍是一种仅影响高度练习技能的运动障碍,在包括体育运动在内的一系列专业运动中均可发现。尽管这种疾病影响着许多体育运动,但目前还没有全面的治疗方案,这与研究较多的音乐家和作家的任务型肌张力障碍形成了鲜明对比。为此,我们对涉及干预治疗体育运动中特定任务肌张力障碍的研究进行了系统性回顾,并对结果测量的质量给予了特别关注。方法采用 PICO 系统性检索策略对特定任务肌张力障碍及所有同义词进行检索。纳入标准为同行评审发表的与体育有关的研究、对 TSD 进行测量和/或干预的研究,所有研究均为英文。我们排除了摘要、专家意见、叙述性综述文章、未发表的研究、学位论文以及仅与窒息有关的研究。结果 2022 年 4 月,我们检索了 Pubmed、Embase、Web of Science 和 Psychinfo。在确定的 7000 篇文章中,有 31 篇描述了心理干预、侵入性干预和/或药物干预。这些研究缺乏正式的标准化结果测量,因此治疗方案的有效性证据质量较低。一项描述性综述显示,情绪调节是有效的,但只在高尔夫球运动员中试用。与针对蕈样肌张力障碍的研究相比,肉毒杆菌毒素或药物治疗等干预措施具有相似的效果,但这些治疗方法几乎没有正式的证据。未来的研究需要更大规模的队列和量化的结果测量,以提高对运动员特定任务肌张力障碍治疗方法的认识。
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引用次数: 0
Inter-rater reliability of hand motor function assessment in Parkinson’s disease: Impact of clinician training 帕金森病患者手部运动功能评估的评分者间可靠性:临床医师培训的影响
IF 1.9 Q3 CLINICAL NEUROLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.prdoa.2024.100278
Lorna Kenny , Zahra Azizi , Kevin Moore , Megan Alcock , Sarah Heywood , Agnes Jonsson , Keith McGrath , Mary J. Foley , Brian Sweeney , Sean O’Sullivan , John Barton , Salvatore Tedesco , Marco Sica , Colum Crowe , Suzanne Timmons
Medication adjustments in Parkinson’s disease (PD) are driven by patient subjective report and clinicians’ rating of motor feature severity (such as bradykinesia and tremor).

Objective

As patients may be seen by different clinicians at different visits, this study aims to determine the inter-rater reliability of upper limb motor function assessment among clinicians treating people with PD (PwPD).

Methods

PwPD performed six standardised hand movements from the Movement Disorder Society’s Unified Parkinson’s Disease Rating Scale (MDS-UPDRS), while two cameras simultaneously recorded. Eight clinicians independently rated tremor and bradykinesia severity using a visual analogue scale. We compared intraclass correlation coefficient (ICC) before and after a training/calibration session where high-variance participant videos were reviewed and MDS-UPDRS instructions discussed.

Results

In the first round, poor agreement was observed for most hand movements, with best agreement for resting tremor (ICC 0.66 bilaterally; right hand 95 % CI 0.50–0.82; left hand: 0.50–0.81). Postural tremor (left hand) had poor agreement (ICC 0.14; 95 % CI 0.04–0.33), as did wrist pronation-supination (right hand ICC 0.34; 95 % CI 0.19–0.56). In post-training rating exercises, agreements improved, especially for the right hand. Best agreement was observed for hand open-close ratings in the left hand (ICC 0.82, 95 % CI 0.64–0.94) and resting tremor in the right hand (ICC 0.92, 95 % CI 0.83–0.98). Discrimination between right and left hand features by raters also improved, except in resting tremor (disimprovement) and wrist pronation-supination (no change).

Conclusions

Clinicians vary in rating video-recorded PD upper limb motor features, especially bradykinesia, but this can be improved somewhat with training.
帕金森病(PD)的用药调整取决于患者的主观报告和临床医生对运动特征严重程度(如运动迟缓和震颤)的评分。由于患者可能在不同的就诊时间由不同的临床医生接诊,本研究旨在确定治疗帕金森病患者(PwPD)的临床医生对上肢运动功能评估的互评可靠性。方法帕金森病患者进行运动障碍协会统一帕金森病评定量表(MDS-UPDRS)中的六项标准化手部运动,同时由两台摄像机进行记录。八名临床医生使用视觉模拟量表独立评定震颤和运动迟缓的严重程度。我们比较了培训/校准课程前后的类内相关系数(ICC),在培训/校准课程中,我们查看了高方差参与者的视频,并讨论了 MDS-UPDRS 的使用说明。结果在第一轮中,大多数手部运动的一致性较差,静止性震颤的一致性最好(双侧 ICC 为 0.66;右手 95 % CI 为 0.50-0.82;左手:0.50-0.81)。姿势性震颤(左手)的一致性较差(ICC 0.14;95 % CI 0.04-0.33),腕关节前伸和上举的一致性也较差(右手 ICC 0.34;95 % CI 0.19-0.56)。在训练后的评分练习中,一致性有所改善,尤其是右手。左手开合评分(ICC 0.82,95 % CI 0.64-0.94)和右手静止震颤评分(ICC 0.92,95 % CI 0.83-0.98)的一致性最好。结论临床医生对视频记录的帕金森病患者上肢运动特征(尤其是运动迟缓)的评分不尽相同,但通过培训可以得到一定程度的改善。
{"title":"Inter-rater reliability of hand motor function assessment in Parkinson’s disease: Impact of clinician training","authors":"Lorna Kenny ,&nbsp;Zahra Azizi ,&nbsp;Kevin Moore ,&nbsp;Megan Alcock ,&nbsp;Sarah Heywood ,&nbsp;Agnes Jonsson ,&nbsp;Keith McGrath ,&nbsp;Mary J. Foley ,&nbsp;Brian Sweeney ,&nbsp;Sean O’Sullivan ,&nbsp;John Barton ,&nbsp;Salvatore Tedesco ,&nbsp;Marco Sica ,&nbsp;Colum Crowe ,&nbsp;Suzanne Timmons","doi":"10.1016/j.prdoa.2024.100278","DOIUrl":"10.1016/j.prdoa.2024.100278","url":null,"abstract":"<div><div>Medication adjustments in Parkinson’s disease (PD) are driven by patient subjective report and clinicians’ rating of motor feature severity (such as bradykinesia and tremor).</div></div><div><h3>Objective</h3><div>As patients may be seen by different clinicians at different visits, this study aims to determine the inter-rater reliability of upper limb motor function assessment among clinicians treating people with PD (PwPD).</div></div><div><h3>Methods</h3><div>PwPD performed six standardised hand movements from the Movement Disorder Society’s Unified Parkinson’s Disease Rating Scale (MDS-UPDRS), while two cameras simultaneously recorded. Eight clinicians independently rated tremor and bradykinesia severity using a visual analogue scale. We compared intraclass correlation coefficient (ICC) before and after a training/calibration session where high-variance participant videos were reviewed and MDS-UPDRS instructions discussed.</div></div><div><h3>Results</h3><div>In the first round, poor agreement was observed for most hand movements, with best agreement for resting tremor (ICC 0.66 bilaterally; right hand 95 % CI 0.50–0.82; left hand: 0.50–0.81). Postural tremor (left hand) had poor agreement (ICC 0.14; 95 % CI 0.04–0.33), as did wrist pronation-supination (right hand ICC 0.34; 95 % CI 0.19–0.56). In post-training rating exercises, agreements improved, especially for the right hand. Best agreement was observed for hand open-close ratings in the left hand (ICC 0.82, 95 % CI 0.64–0.94) and resting tremor in the right hand (ICC 0.92, 95 % CI 0.83–0.98). Discrimination between right and left hand features by raters also improved, except in resting tremor (disimprovement) and wrist pronation-supination (no change).</div></div><div><h3>Conclusions</h3><div>Clinicians vary in rating video-recorded PD upper limb motor features, especially bradykinesia, but this can be improved somewhat with training.</div></div>","PeriodicalId":33691,"journal":{"name":"Clinical Parkinsonism Related Disorders","volume":"11 ","pages":"Article 100278"},"PeriodicalIF":1.9,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142572472","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Orthostatic hypotension and subjective symptomatic orthostasis in Parkinson’s disease: Associations and correlations 帕金森病患者的直立性低血压和主观症状性直立性低血压:关联性和相关性
IF 1.9 Q3 CLINICAL NEUROLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.prdoa.2024.100262
Jillian M. Heisler , Jon Toledo-Atucha , Chih-Chun Lin , Harsh N. Patel , William G. Ondo

Background

Both measured orthostatic hypotension and symptomatic orthostasis are common in PD but their relationship is unclear.

Objective

We aim to determine clinical predictors of both measured orthostatic hypotension and reported symptomatic orthostasis in PD, including the impact of “on”/“off” status and seasons, and to determine the correlation between measured OH and subjective orthostasis.

Methods

We analyzed BP readings, demographic and disease state predictors for both 1. Measured blood pressure OH criteria and 2. The subjective report of orthostatic symptoms, using logistic regression analyses from an initial “on” motor state clinical visit in all PD patient visits. We then correlated subjective orthostasis symptoms with BP measurements. We also compared intra-subject BP measures in PD patients seen in both “on” and “off” states, and when seen “on” in both summer and winter.

Results

723 consecutive visits over 2 years identified 250 unique PD individuals. Subjective orthostasis was reported by 44 % and “on” measured OH (>20 drop in SBP or 10 DBP upon standing) was seen in 30 %. Measured OH did not significantly correlate with any assessed clinical feature or specific medicine. Subjective orthostasis correlated most with older age, dementia, and L-dopa use. Subjective orthostasis correlated equally with absolute lower measured standing SBP and the drop in SBP from sitting to standing. Compared to the “off” state, “on” state showed lower sitting and standing SBP, more than DBP, but no significant change in BP drop upon standing. Seasons did not impact measured BP.

Conclusions

Both OH and symptomatic orthostasis are common. Dopaminergic medications did not cause traditionally defined OH but lowered all SBP (sitting and standing) and thus reduced pulse pressure, possibly by increasing arteriole compliance simply by reducing motor tone, as this BP-lowering effect may be specific to Parkinsonism.

背景测量到的直立性低血压和症状性直立性低血压在帕金森病中都很常见,但它们之间的关系尚不清楚。目的我们旨在确定帕金森病中测量到的直立性低血压和报告的症状性直立性低血压的临床预测因素,包括 "开"/"关 "状态和季节的影响,并确定测量到的 OH 和主观直立性低血压之间的相关性。所有帕金森病患者就诊时的初始 "开启 "运动状态临床就诊结果的逻辑回归分析。然后,我们将主观静立症状与血压测量值进行了关联。我们还比较了在 "开 "和 "关 "两种状态下以及在夏季和冬季 "开 "状态下就诊的帕金森病患者的受试者内血压测量值。44%的患者报告了主观正位,30%的患者报告了 "开启 "测量的OH(站立时SBP下降20或DBP下降10)。测量的OH与任何评估的临床特征或特定药物均无明显相关性。主观正位与老年人、痴呆症和左旋多巴的使用相关性最大。主观正位与测量到的站立 SBP 绝对值较低以及 SBP 从坐姿到站立的降幅同样相关。与 "关闭 "状态相比,"开启 "状态显示坐位和站位 SBP 更低,DBP 更低,但站立时血压下降无显著变化。结论OH和症状性正位都很常见。多巴胺能药物不会导致传统意义上的OH,但会降低所有SBP(坐位和站位),从而降低脉压,这可能是通过降低运动张力来增加动脉顺应性,因为这种降压效果可能是帕金森病特有的。
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引用次数: 0
Apomorphine titration with and without anti-emetic pretreatment in patients with Parkinson’s disease experiencing OFF episodes: A modified Delphi panel 阿朴吗啡滴定治疗帕金森病患者的 "关断 "发作,有无止吐预处理?改良德尔菲小组
IF 1.9 Q3 CLINICAL NEUROLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.prdoa.2024.100264
Stuart H. Isaacson , Richard Dewey , Robert A. Hauser , Daniel Kremens , Rajeev Kumar , Mark Lew , William Ondo , Fernando Pagan , Kelly E. Lyons , Rajesh Pahwa

Introduction

In the United States (US), prophylactic treatment with the antiemetic trimethobenzamide has been used before initiating apomorphine therapy. However, US trimethobenzamide stores have been depleted, leaving uncertainty regarding whether antiemetic pretreatment is needed.

Methods

This modified Delphi panel aimed to inform circumstances when apomorphine is initiated without antiemetic pretreatment. During Round 1, a panel of 9 US movement disorder specialists rated the appropriateness of prescribing apomorphine therapy with and without antiemetic pretreatment across 192 patient scenarios and were able to review their scores in relation to other scores. During the Round 2, consensus was defined for each scenario as either strong (>75 % agreement) or moderate (66 % agreement).

Results

There was strong consensus on 118 of 192 scenario’s (97 as appropriate and 21 as inappropriate), moderate consensus on 29 scenarios, some agreement on 32 scenarios, and lack of agreement on 13 scenarios. In the absence of an antiemetic, there was strong consensus that titration schedules should be flexible and based on dose response. However, the group only reached moderate consensus on the speed of titration, highlighting the need for more systematic information on this area. In the presence of an antiemetic, panelists considered usual initial dosing and flexible titration to be appropriate in most scenarios except for when the patient is already experiencing dopaminergic adverse events.

Conclusions

Experts generally reached consensus that apomorphine can usually be prescribed without antiemetic pretreatment. Recommendations described here reflect the areas of greatest agreement among a panel of experts based on current available evidence.

导言在美国,在开始阿扑吗啡治疗前一直使用止吐药曲美苄胺进行预防性治疗。然而,美国的曲美苄胺库存已经耗尽,因此在是否需要止吐预处理的问题上存在不确定性。方法本改良德尔菲小组旨在告知在何种情况下可以在不进行止吐预处理的情况下使用阿朴吗啡。在第一轮讨论中,由 9 位美国运动障碍专家组成的小组对 192 种患者情况下使用阿扑吗啡治疗和不使用止吐药预处理的适当性进行了评分,并将他们的评分与其他评分进行对比。结果在 192 个方案中,有 118 个方案达成了高度共识(97 个方案认为合适,21 个方案认为不合适),29 个方案达成了中度共识,32 个方案达成了部分共识,13 个方案未达成共识。在没有止吐药的情况下,专家组达成了强烈共识,即滴定时间应具有灵活性,并以剂量反应为基础。然而,专家组仅就滴注速度达成了中等程度的共识,这凸显了在这一领域需要更多系统性信息的必要性。在存在止吐药的情况下,专家组成员认为,除了患者已经出现多巴胺能不良反应的情况外,在大多数情况下,一般的初始剂量和灵活的滴定都是合适的。本文所述的建议反映了专家小组在现有证据基础上达成最大共识的领域。
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引用次数: 0
Characteristics of Creutzfeldt-Jakob disease at Siriraj Hospital, Thailand: Case series and literature review 泰国Siriraj医院克雅氏病的特点:病例系列和文献回顾
IF 1.9 Q3 CLINICAL NEUROLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.prdoa.2024.100281
Chaisak Dumrikarnlert , Nuttapong Kanokkawinwong , Chatchawan Rattanabannakit , Vorapun Senanarong

Introduction

Creutzfeldt-Jakob disease (CJD) is a rare, rapidly progressive, fatal, neurodegenerative disease classified as prion diseases. There are many subtypes of this disease, but information about clinical presentation and investigation findings in Thailand is scarce.

Objective

To describe the clinical presentation, radiological and electroencephalographic characteristics of CJD encountered at Siriraj hospital in the past 10 years (between January 1, 2006 and December 31, 2015).

Materials and Methods

This was descriptive epidemiological data (retrospective, observational study). Patients with rapidly progressive dementia who met the diagnostic criteria for sporadic CJD (sCJD) and variant CJD (vCJD) were included. All were investigated in detail to find any other possible treatable cause including brain magnetic resonance imaging (MRI), electroencephalography (EEG), and cerebrospinal fluid (CSF) analysis.

Results

Of the 18 cases, they were classified as sCJD 15 cases and possible vCJD 3 cases. The mean age of the patients was 60.72 years (range: 24‐77) and 10 patients were male. The main clinical manifestations were cognitive disturbance (100 %) and myoclonus (14 out of 18 cases, 77 %). Brain imaging abnormalities were observed in 17 patients: Hyperintensities in diffusion weight imaging (DWI) in the cortical regions (temporal, parietal, and occipital) were observed in 94 % of the patients. Classical EEG of periodic epileptiform discharges were observed in 83.33 % of patients.

Conclusions

CJD is a rare but fatal disease that needs to be considered in the patient with cognitive, neuropsychiatric, and movement disorders. Findings of specific abnormalities on brain imaging and/or EEG can support the diagnosis in suspicious cases.
克雅氏病(CJD)是一种罕见、进展迅速、致死性神经退行性疾病,属于朊病毒疾病。该病有许多亚型,但有关泰国临床表现和调查结果的信息很少。目的:描述近10年来(2006年1月1日至2015年12月31日)在Siriraj医院就诊的CJD患者的临床表现、影像学和脑电图特征。材料和方法:采用描述性流行病学资料(回顾性、观察性研究)。符合散发性CJD (sCJD)和变异型CJD (vCJD)诊断标准的快速进展性痴呆患者被纳入研究。对所有患者进行详细调查,以发现任何其他可能的可治疗原因,包括脑磁共振成像(MRI)、脑电图(EEG)和脑脊液(CSF)分析。结果:18例患者中,sCJD 15例,疑似vCJD 3例。患者平均年龄60.72岁(24 ~ 77岁),男性10例。主要临床表现为认知障碍(100%)和肌阵挛(18例中14例,77%)。17例患者观察到脑成像异常:94%的患者在皮质区(颞、顶叶和枕部)观察到弥散加权成像(DWI)高信号。83.33%的患者有典型的周期性癫痫样放电脑电图。结论:CJD是一种罕见但致命的疾病,在认知、神经精神和运动障碍患者中需要考虑。在可疑病例中,脑成像和/或脑电图的特殊异常可以支持诊断。
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引用次数: 0
Meaning in life and Parkinson’s disease in the UK Biobank 英国生物数据库中的生命意义与帕金森病
Q3 CLINICAL NEUROLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.prdoa.2023.100231
Angelina R. Sutin , Martina Luchetti , Yannick Stephan , Antonio Terracciano

Introduction

Meaning in life is an aspect of eudaimonic well-being associated with lower dementia risk. This research examines whether this protective association extends to Parkinson’s disease (PD).

Methods

Participants (N = 153,569) from the UK Biobank reported on their meaning in life. Cases of PD were identified through health records.

Results

Meaning in life was associated with a 50 % lower likelihood of prevalent PD (OR = 0.68, 95 % CI = 0.59–0.78). Over the 5-year follow-up, meaning was associated with a 35 % lower risk of incident PD (HR = 0.74, 95 % CI = 0.65–0.83), an association robust to sociodemographic characteristics, depression, history of seeking mental health care, smoking, physical activity, and genetic risk and not moderated by age, sex, education, deprivation, or genetic risk.

Conclusions

Meaning in life is associated with lower risk of incident PD, an association independent of other major risk factors and generalizable across sociodemographic groups. Meaning is a promising target of intervention for common neurodegenerative diseases.

导言:人生意义是与降低痴呆症风险相关联的幸福感的一个方面。本研究探讨了这种保护性关联是否延伸至帕金森病(PD)。方法来自英国生物库的参与者(N = 153,569 人)报告了他们的生活意义。结果 生活意义与帕金森病发病率降低 50% 相关(OR = 0.68,95 % CI = 0.59-0.78)。在为期5年的随访中,"生活中的意义 "与帕金森病发病风险降低35%有关(HR = 0.74, 95 % CI = 0.65-0.83),这种关联与社会人口特征、抑郁、寻求心理保健的历史、吸烟、体育锻炼和遗传风险密切相关,且不受年龄、性别、教育程度、贫困程度或遗传风险的影响。对于常见的神经退行性疾病,意义是一个很有前景的干预目标。
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引用次数: 0
Effect of zonisamide on sleep and rapid eye movement sleep behavioral disorders in patients with Parkinson’s disease: A randomized control trial 唑尼沙胺对帕金森病患者睡眠和快速眼动睡眠行为障碍的影响:随机对照试验
IF 1.9 Q3 CLINICAL NEUROLOGY Pub Date : 2024-01-01 DOI: 10.1016/j.prdoa.2024.100285
Hiroshi Kataoka , Masahiro Isogawa , Hitoki Nanaura , Hiroyuki Kurakami , Miyoko Hasebe , Kaoru Kinugawa , Takao Kiriyama , Tesseki Izumi , Masato Kasahara , Kazuma Sugie

Introduction

Zonisamide is a medication developed in Japan that is effective for motor symptoms and wearing off in Parkinson’s disease (PD). Zonisamide has properties that may improve sleep disorders. The aim of this study is to verify the safety and efficacy of zonisamide for sleep disorders and rapid eye movement (REM) sleep behavioral disorders (RBD) using a mobile two-channel electroencephalography /electrooculography recording system in patients with PD.

Methods

The present study is a single-blind randomized placebo-controlled trial. The subjects in the treatment group took zonisamide (25 mg per day) before bedtime. The primary outcome was sleep efficiency. The secondary endpoints were assessed as followed; objective outcomes of TST, WASO, SOL, REM sleep/non-REM sleep ratio, deep sleep (N3) time, ratio of RWA to total REM sleep epochs, and subjective outcomes of the PDSS-2, Pittsburgh sleep questionnaire, and RBDSQ.

Results

Between the zonisamide and placebo groups, no significant differences were found in the primary outcome and secondary outcomes.

Conclusions

The objective and subjective sleep metrics in this clinical trial did not significantly demonstrate zonisamide efficacy for sleep disorder in patients with PD. Although not significant, improvement in WASO and SOL was observed when zonisamide was compared with the placebo.
简介唑尼沙胺是日本开发的一种药物,对帕金森病(PD)的运动症状和消退有效。唑尼沙胺具有改善睡眠障碍的特性。本研究旨在使用移动式双通道脑电图/脑电记录系统,验证唑尼沙胺治疗帕金森病患者睡眠障碍和快速眼动睡眠行为障碍(RBD)的安全性和有效性。治疗组受试者在睡前服用唑尼沙胺(每天 25 毫克)。主要结果是睡眠效率。次要终点评估如下:TST、WASO、SOL、快速动眼期睡眠/非快速动眼期睡眠比率、深度睡眠(N3)时间、RWA与快速动眼期睡眠总时间的比率等客观结果,以及PDSS-2、匹兹堡睡眠问卷和RBDSQ等主观结果。结果在唑尼沙胺组和安慰剂组之间,主要结果和次要结果均未发现显著差异。结论该临床试验中的客观和主观睡眠指标并未显著显示唑尼沙胺对帕金森病患者睡眠障碍的疗效。与安慰剂相比,唑尼沙胺对WASO和SOL的改善虽然不明显,但仍可观察到。
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引用次数: 0
期刊
Clinical Parkinsonism Related Disorders
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