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1.
J Neurosurg ; 107(5): 1004-14, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17977274

ABSTRACT

OBJECT: The severity of Tourette syndrome (TS) typically peaks just before adolescence and diminishes afterward. In some patients, however, TS progresses into adulthood, and proves to be medically refractory. The authors conducted a prospective double-blind crossover trial of bilateral thalamic deep brain stimulation (DBS) in five adults with TS. METHODS: Bilateral thalamic electrodes were implanted. An independent programmer established optimal stimulator settings in a single session. Subjective and objective results were assessed in a double-blind randomized manner for 4 weeks, with each week spent in one of four states of unilateral or bilateral stimulation. Results were similarly assessed 3 months after unblinded bilateral stimulator activation while repeated open programming sessions were permitted. RESULTS: In the randomized phase of the trial, a statistically significant (p < 0.03, Friedman exact test) reduction in the modified Rush Video-Based Rating Scale score (primary outcome measure) was identified in the bilateral on state. Improvement was noted in motor and sonic tic counts as well as on the Yale Global Tic Severity Scale and TS Symptom List scores (secondary outcome measures). Benefit was persistent after 3 months of open stimulator programming. Quality of life indices were also improved. Three of five patients had marked improvement according to all primary and secondary outcome measures. CONCLUSIONS: Bilateral thalamic DBS appears to reduce tic frequency and severity in some patients with TS who have exhausted other available means of treatment.


Subject(s)
Deep Brain Stimulation/methods , Thalamus/physiology , Tourette Syndrome/therapy , Double-Blind Method , Female , Humans , Male , Prospective Studies , Quality of Life , Treatment Outcome , Video Recording
2.
Int J Psychiatry Med ; 32(4): 401-3, 2002.
Article in English | MEDLINE | ID: mdl-12779189

ABSTRACT

Neurosarcoidosis is a rare disorder in which psychosis and dementia may occur. They usually appear subsequently to the diagnosis of pulmonary sarcoidosis. We report on a 39-year-old patient who presented with long-term decline and acute onset of psychosis and delirium, and who was found to have neurosarcoidosis.


Subject(s)
Brain Diseases/complications , Cognition Disorders/etiology , Psychotic Disorders/etiology , Sarcoidosis/complications , Acute Disease , Adult , Antipsychotic Agents/therapeutic use , Brain/diagnostic imaging , Brain/pathology , Brain Diseases/diagnosis , Cognition Disorders/diagnosis , Diagnosis, Differential , Dibenzothiazepines/therapeutic use , Humans , Magnetic Resonance Imaging , Male , Neuropsychological Tests , Psychotic Disorders/diagnosis , Psychotic Disorders/drug therapy , Quetiapine Fumarate , Sarcoidosis/diagnosis , Tomography, X-Ray Computed
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