MedElevator Войти в исследования
← Поиск публикаций

DOI 10.3389/fneur.2015.00177

Медицинская библиотека · Frontiers in neurology · 2015

A Prospective Pilot Trial for Pallidal Deep Brain Stimulation in Huntington's Disease.

Wojtecki Lars, Groiss Stefan J, Ferrea Stefano, Elben Saskia, Hartmann Christian J, Dunnett Stephen B, Rosser Anne, Saft Carsten, Südmeyer Martin, Ohmann Christian, Schnitzler Alfons, Vesper Jan, Surgical Approaches Working Group of the European Huntington's Disease Network (EHDN)

СтатьяПеревод пока не подготовлен

Аннотация

BACKGROUND

Movement disorders in Huntington's disease are often medically refractive. The aim of the trial was assessment of procedure safety of deep brain stimulation, equality of internal- and external-pallidal stimulation and efficacy followed-up for 6 months in a prospective pilot trial.

METHODS

In a controlled double-blind phase six patients (four chorea-dominant, two Westphal-variant) with predominant movement disorder were randomly assigned to either the sequence of 6-week internal- or 6-week external-pallidal stimulation, or vice versa, followed by further 3 months chronic pallidal stimulation at the target with best effect-side-effect ratio. Primary endpoints were changes in the Unified Huntington's Disease Rating Scale motor-score, chorea subscore, and total motor-score 4 (blinded-video ratings), comparing internal- versus external-pallidal stimulation, and 6 months versus baseline. Secondary endpoints assessed scores on dystonia, hypokinesia, cognition, mood, functionality/disability, and quality-of-life.

RESULTS

Intention-to-treat analysis of all patients (n = 3 in each treatment sequence): Both targets were equal in terms of efficacy. Chorea subscores decreased significantly over 6 months (-5.3 (60.2%), p = 0.037). Effects on dystonia were not significant over the group due to it consisting of three responders (>50% improvement) and three non-responders. Westphal patients did not improve. Cognition was stable. Mood and some functionality/disability and quality-of-life scores improved significantly. Eight adverse events and two additional serious adverse events - mostly internal-pallidal stimulation-related - resolved without sequalae. No procedure-related complications occurred.

CONCLUSION

Pallidal deep brain stimulation was demonstrated to be a safe treatment option for the reduction of chorea in Huntington's disease. Their effects on chorea and dystonia and on quality-of-life should be examined in larger controlled trials.

Для цитирования: Wojtecki Lars, Groiss Stefan J, Ferrea Stefano, Elben Saskia, Hartmann Christian J, Dunnett Stephen B, Rosser Anne, Saft Carsten, Südmeyer Martin, Ohmann Christian, Schnitzler Alfons, Vesper Jan, Surgical Approaches Working Group of the European Huntington's Disease Network (EHDN). A Prospective Pilot Trial for Pallidal Deep Brain Stimulation in Huntington's Disease.. Frontiers in neurology. 2015. DOI: 10.3389/fneur.2015.00177.
Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.