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Joseph Tsui


jtsui@interchange.ubc.ca

Journal articles

2007
Zelma H T Kiss, Kristina Doig-Beyaert, Michael Eliasziw, Joseph Tsui, Angela Haffenden, Oksana Suchowersky (2007)  The Canadian multicentre study of deep brain stimulation for cervical dystonia.   Brain 130: Pt 11. 2879-2886 Nov  
Abstract: Deep brain stimulation (DBS) of the globus pallidus pars interna (GPi) is an effective treatment for generalized dystonia. Its role in the management of other types of dystonia is uncertain. Therefore we performed a prospective, single-blind, multicentre study assessing the efficacy and safety of bilateral GPi-DBS in 10 patients with severe, chronic, medication-resistant cervical dystonia. Two blinded neurologists assessed patients before surgery and at 6 and 12 months post-operatively using the Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS). The primary outcome measure was the severity subscore (range 0-30, higher scores indicating greater impairment). Secondary outcomes included disability (0 to 30), pain (0 to 40) subscores and total scores of the TWSTRS, Short Form-36 and Beck depression inventory. Swallowing and neuropsychological assessment were also performed at baseline and 12 months. One-way repeated measures analysis of variance was used to analyse the data. The TWSTRS severity score improved from a mean (SD) of 14.7 (4.2) before surgery to 8.4 (4.4) at 12 months post-operatively (P = 0.003). The disability and pain scores improved from 14.9 (3.8) and 26.6 (3.6) before surgery, to 5.4 (7.0) and 9.2 (13.1) at 12 months, respectively (both P < 0.001). General health and physical functioning as well as depression scores improved significantly. Complications were mild and reversible in four patients. Some changes in neuropsychological tests were observed, although these did not impact daily life or employment. Our results support the efficacy and safety of GPi-DBS for the treatment of patients with severe and prolonged cervical dystonia who have failed medical management.
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J Jankovic, J Tsui, C Bergeron (2007)  Prevalence of cervical dystonia and spasmodic torticollis in the United States general population.   Parkinsonism Relat Disord 13: 7. 411-416 Oct  
Abstract: PURPOSE: To examine the prevalence of cervical dystonia (CD) in the US population. METHOD: A survey consisting of relevant demographic and CD-related questions was e-mailed to 2 million people selected from the Shopper's Voice database. RESULTS: Across a census-weighted sample, 0.280% of 60,062 respondents (79% female, 92% Caucasian) reported a diagnosis of CD and 0.170% reported a diagnosis of ST, indicating possible prevalence of 0.390% of either/both diagnoses. Less than half (42.7%) of those who reported either diagnosis were receiving treatment. CONCLUSIONS: CD is potentially under-diagnosed and under-treated; approaches to increase awareness of CD and its treatments are needed.
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2005
C L Comella, J Jankovic, K M Shannon, J Tsui, M Swenson, S Leurgans, W Fan (2005)  Comparison of botulinum toxin serotypes A and B for the treatment of cervical dystonia.   Neurology 65: 9. 1423-1429 Nov  
Abstract: OBJECTIVE: To directly compare two serotypes of botulinum toxin (BoNTA and BoNTB) in cervical dystonia (CD) using a randomized, double-blind, parallel-arm study design. METHODS: Subjects with CD who had a previous response from BoNTA were randomly assigned to BoNTA or BoNTB and evaluated in a blinded fashion at baseline, 4 weeks, 8 weeks, and 2-week intervals thereafter until loss of 80% of clinical effect or completion of 20 weeks of observation. CD severity was measured with the Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS), and adverse events were assessed by structured interview. Statistical analysis included Wilcoxon rank sum test, log rank tests, and Kaplan-Meier survival curves for duration of effect. RESULTS: A total of 139 subjects (BoNTA, n = 74; BoNTB, n = 65) were randomized at 19 study sites. Improvement in TWSTRS score was found at 4 weeks after injection and did not differ between serotypes. Dysphagia and dry mouth were more frequent with BoNTB (dysphagia: BoNTA 19% vs BoNTB 48%, p = 0.0005; dry mouth (BoNTA 41% vs BoNTB 80%, p < 0.0001). In clinical responders, BoNT A had a modestly longer duration of benefit (BoNTA 14 weeks, BoNTB 12.1 weeks, p = 0.033). CONCLUSION: Both serotypes of botulinum toxin (BoNTA and BoNTB) had equivalent benefit in subjects with cervical dystonia at 4 weeks. BoNTA had fewer adverse events and a marginally longer duration of effect in subjects showing a clinical response.
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2003
2001
W J Hwang, D B Calne, J K Tsui, R de la Fuente-Fernández (2001)  The long-term response to levodopa in dopa-responsive dystonia.   Parkinsonism Relat Disord 8: 1. 1-5 Sep  
Abstract: We report the long-term response to levodopa in 20 patients with dopa-responsive dystonia (DRD). We found an inverse correlation between the daily dose of levodopa and duration of treatment (r=-0.59, P<0.01). Mild dyskinesias were present in 20% of our patients. Dyskinetic patients were on a higher dose of levodopa than non-dyskinetics. Dyskinesias responded to a reduction in levodopa, with no deterioration in motor function. We propose that the dopamine turnover might decrease with time, which would lead to a decrease in the requirement for levodopa and the occurrence of dyskinesias late in the course of DRD.
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2000
P K Pal, A Samii, M Schulzer, E Mak, J K Tsui (2000)  Head tremor in cervical dystonia.   Can J Neurol Sci 27: 2. 137-142 May  
Abstract: OBJECTIVE: To compare the clinical characteristics, natural history, and therapeutic outcome of patients with cervical dystonia (CD) with head tremor (HT+) and without head tremor (HT-). METHODS: We prospectively evaluated 114 consecutive patients of CD over a 9-month period with a detailed questionnaire. Chi-square and t-tests were employed for statistical analysis. RESULTS: Seventy-eight (68.4%) patients had head tremor and 27 of them (34.6%) had tremor as one of the first symptoms. Age at onset of symptoms were similar in HT+ and HT- groups; however there was a higher prevalence in women in the former group (66.7% vs. 41.7%; p=0.01). HT+ patients had more frequent positive family history of essential-like hand/head tremor (21.8% vs. 5.5%; p<0.05), associated neck pain (92.3% vs. 77.8%: p<0.05), and essential-like hand tremor (40% vs. 8.3%; p<0.001). They also appeared to have more frequent history of preceding head/neck trauma (14.1% vs. 8.3%), frequent head rotation (88.5% vs. 69.4%) and antecollis (12.8% vs. 5.5%) but less often head tilt (37.2% vs. 47.2%) and gestes antagonistes (60.2% vs. 75%) than the HT- patients; however these differences were not statistically significant. The frequency of prior psychiatric illnesses, the incidence of dystonias in other parts of the body, frequency of retrocollis and shoulder elevation, and spontaneous remission were similar in the two groups. CONCLUSION: Head tremor is common in CD and is more commonly associated with hand tremor and family history of tremor or other movement disorders. This supports a possible genetic association between CD and essential tremor (ET). Linkage studies are required to evaluate the genetic association between CD and ET.
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A Samii, P K Pal, M Schulzer, E Mak, J K Tsui (2000)  Post-traumatic cervical dystonia: a distinct entity?   Can J Neurol Sci 27: 1. 55-59 Feb  
Abstract: BACKGROUND/OBJECTIVE: The incidence of head/neck trauma preceding cervical dystonia (CD) has been reported to be 5-21%. There are few reports comparing the clinical characteristics of patients with and without a history of injury. Our aim was to compare the clinical characteristics of idiopathic CD (CD-I) to those with onset precipitated by trauma (CD-T). METHODS: We evaluated 114 consecutive patients with CD over a 9-month period. All patients were interviewed using a detailed questionnaire and had a neurological examination. Their clinical charts were also reviewed. RESULTS: Fourteen patients (12%) had mild head/neck injury within a year preceding the onset of CD. Between the two groups (CD-I and CD-T), the gender distribution (F:M of 3:2), family history of movement disorders (32% vs. 29%), the prevalence of gestes antagonistes (65% vs. 64%), and response to botulinum toxin were similar. There were non-specific trends, including an earlier age of onset (mean ages 43.3 vs. 37.6), higher prevalence of neck pain (86% vs. 100%), head tremor (67% vs. 79%), and dystonia in other body parts (23% vs. 36%) in CD-T. CONCLUSIONS: CD-I and CD-T are clinically similar. Trauma may be a triggering factor in CD but this was only supported by non-significant trends in its earlier age of onset.
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1999
C R Honey, A J Stoessl, J K Tsui, M Schulzer, D B Calne (1999)  Unilateral pallidotomy for reduction of parkinsonian pain.   J Neurosurg 91: 2. 198-201 Aug  
Abstract: OBJECT: The goal of this study was to determine whether unilateral pallidotomy reduces parkinsonian pain. METHODS: Twenty-one patients suffering from Parkinson's disease (PD) were followed prospectively for 1 year after they had undergone a unilateral pallidotomy to assess the procedure's effect on pain related to PD. Pain unrelated to PD was not studied. Patients scored the level of their PD pain on an ordinal scale (0-10 points) preoperatively and 6 weeks and 1 year postoperatively. The results were analyzed using Wilcoxon's paired-ranks test (with Bonferroni correction) and showed a significant reduction in overall pain scores at 6 weeks (p < 0.001) and 1 year (p = 0.001) following pallidotomy. Various types of PD pain are described and their possible pathophysiological mechanisms are presented. CONCLUSIONS: Unilateral pallidotomy significantly reduces pain attributable to Parkinson's disease.
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1997
J H Chan, J K Tsui (1997)  Idiopathic cervical dystonia: Report of discordance in a pair of monozygotic twins.   Parkinsonism Relat Disord 3: 3. 167-169 Nov  
Abstract: The gene for idiopathic torsion dystonia (ITD) has been located on chromosome 9q32-34. It remains controversial whether cervical dystonia (CD) is genetically determined or not. A previous report of a concordant expression of CD in a pair of monozygotic twins suggested a genetic role. We report discordance in a pair of monozygotic twins, one presenting with adult-onset idiopathic CD with duration of disease for 7 yr, while the other co-twin remained normal. Family history was negative for dystonia. The pair of twins spent all their life in the same environment. This argues against the role of genetics in the etiology of CD.
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1996
J K Tsui (1996)  Botulinum toxin as a therapeutic agent.   Pharmacol Ther 72: 1. 13-24  
Abstract: Botulinum toxin is a presynaptic neuromuscular blocking agent that, when injected intramuscularly in minute quantities, can produce selective muscle weakness. This property is employed therapeutically to provide symptomatic relief in conditions related to excessive muscle activities in strabismus, blepharospasm, hemifacial spasm, cervical dystonia, spasmodic dysphonia (adductor type), and jaw closing dystonia. It is investigational for a long list of medical conditions. It is a marketed drug in a number of countries in the world, but its use has only been approved by different regulatory agencies for use in a limited number of conditions. The long-term effects, appropriate dose for children, and in pregnancy, and maximum dose without causing toxicity remain unclear.
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1995
1993
J K Tsui, M Bhatt, S Calne, D B Calne (1993)  Botulinum toxin in the treatment of writer's cramp: a double-blind study.   Neurology 43: 1. 183-185 Jan  
Abstract: We treated 20 patients with writer's cramp in a double-blind, placebo-controlled study. Each patient received two treatments in tandem, one with botulinum-A toxin (BTX-A) injections and another with normal saline, separated by 3 months. Treatment order was randomized and unknown to the patient and physician. Patients were assessed before each treatment and 2 and 6 weeks after each treatment by objective measurements of pen control. Twelve patients had improvement in pen control after treatment with BTX-A, but only four had significant improvement in writing. BTX-A injections are effective in relieving symptoms in selected cases of writer's cramp, particularly in those with significant wrist-joint deviation.
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1988
1987
J K Tsui, R D Fross, S Calne, D B Calne (1987)  Local treatment of spasmodic torticollis with botulinum toxin.   Can J Neurol Sci 14: 3 Suppl. 533-535 Aug  
Abstract: Fifty-six patients with spasmodic torticollis were treated with local injections of botulinum toxin. The drop out rate was 21%. The remaining 44 patients were followed for a period of 3 to 21 months. Thirty-two patients (76%) had pain relief out of 42 presenting with pain; 37 (66%) improved in the amount of sustained movements of torticollis. The efficacy was reproducible after repeated injections.
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1986
J K Tsui, A Eisen, A J Stoessl, S Calne, D B Calne (1986)  Double-blind study of botulinum toxin in spasmodic torticollis.   Lancet 2: 8501. 245-247 Aug  
Abstract: In a double-blind trial in 21 patients with spasmodic torticollis botulinum-A toxin produced both subjective and objective improvement, including significant pain relief in 14 of the 16 patients presenting with pain. Side-effects were more frequently reported during placebo administration and no significant systemic adverse reactions were noted.
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1985
J K Tsui, A Eisen, E Mak, J Carruthers, A Scott, D B Calne (1985)  A pilot study on the use of botulinum toxin in spasmodic torticollis.   Can J Neurol Sci 12: 4. 314-316 Nov  
Abstract: Dystonic torticollis has been treated with local injections of botulinum toxin in a single blind study of 12 patients. A significant decrease of abnormal movements was recorded, and pain improved. Further studies are desirable to define the optimum dosage and site for injections, and the long term effects of repeated injections.
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