Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 10 de 10
Filter
1.
Toxicon ; 238: 107587, 2024 Feb 01.
Article in English | MEDLINE | ID: mdl-38142904

ABSTRACT

BACKGROUND: Foot dystonia occurs in patients with Parkinson's disease (PD) and leads to pain, malformation, and difficulty with walking. Botulinum toxin injections may be effective for foot dystonia, but the extent of improvement and effects on motor function are unclear. METHODS: In this study, we performed botulinum toxin injections for foot dystonia in 25 patients with PD. At 3 weeks and 3 months post-infection, we assessed changes in plantar pressure distribution utilizing the Pressure Plate system; dystonia using the Modified Ashworth Spasm score; pain using the visual analog scale (VAS) score; and lower extremity function using the Calf-raise Senior (CRS) test, Timed Up and Go (TUG) test, and gait parameters (eg, stride length, step length). RESULTS: We found improved Modified Ashworth Spasm score (p < 0.01) and VAS score (p < 0.01) post-injection. CRS test score (3 weeks, p = 0.006; 3 months, p = 0.068), stride length (3 weeks, p = 0.012; 3 months, p = 0.715), and step length (3 weeks, p = 0.011; 3 months, p = 0.803) also improved. Plantar pressure distribution improved after botulinum toxin injection (metatarsal 1, 3 weeks, p = 0.031; 3 months, p = 0.144; metatarsal 2, 3 weeks, p = 0.049; 3 months, p = 0.065; metatarsal 3, 3 weeks, p = 0.002; 3 months, p = 0.017; metatarsal 4, 3 weeks, p = 0.017; 3 months, p = 0.144; medial heel, 3 weeks, p = 0.01; 3 months, p = 0.395; lateral heel, 3 weeks, p = 0.035; 3 months, p = 0.109). CONCLUSION: Botulinum toxin injection for foot dystonia in patients with PD can reduce spasms and pain and normalize plantar pressure distribution, which improves balance and lower extremity function.


Subject(s)
Botulinum Toxins, Type A , Dystonia , Neuromuscular Agents , Parkinson Disease , Humans , Botulinum Toxins, Type A/therapeutic use , Dystonia/drug therapy , Dystonia/etiology , Parkinson Disease/complications , Parkinson Disease/drug therapy , Neuromuscular Agents/therapeutic use , Pain/drug therapy , Spasm , Treatment Outcome
3.
Toxins (Basel) ; 15(2)2023 01 17.
Article in English | MEDLINE | ID: mdl-36828396

ABSTRACT

This review provides an up-to-date literature account on the efficacy of Botulinum toxin treatment for common motor disorders of Parkinson Disease. The reviewed disorders include the common motor disorders in PD such as tremor, focal foot dystonia, rigidity and freezing of gait (FOG). In the area of Parkinson tremor, two newly described evaluation/injection techniques (Yale method in USA and Western University method in Canada) offer efficacy with low incidence of hand and finger weakness as side effects. Blinded studies conducted on foot dystonia of PD indicate that botulinum toxin injections into toe flexors are efficacious in alleviating this form of dystonia. Small, blinded studies suggest improvement of Parkinson rigidity after botulinum toxin injection; proof of this claim, however, requires information from larger, blinded clinical trials. In FOG, the improvement reported in open label studies could not be substantiated in blinded investigations. However, there is room for further controlled studies that include the proximal lower limb muscles in the injection plan and/or use higher doses of the injected toxin for this indication.


Subject(s)
Botulinum Toxins, Type A , Botulinum Toxins , Dystonia , Dystonic Disorders , Gait Disorders, Neurologic , Motor Disorders , Parkinson Disease , Humans , Botulinum Toxins/therapeutic use , Parkinson Disease/drug therapy , Dystonia/drug therapy , Tremor/drug therapy , Motor Disorders/chemically induced , Motor Disorders/complications , Motor Disorders/drug therapy , Gait Disorders, Neurologic/drug therapy , Dystonic Disorders/drug therapy , Botulinum Toxins, Type A/therapeutic use , Treatment Outcome
4.
Can J Neurol Sci ; 49(1): 123-128, 2022 01.
Article in English | MEDLINE | ID: mdl-33685541

ABSTRACT

We investigated the effects of botulinum toxin on gait in Parkinson's disease (PD) patients with foot dystonia. Six patients underwent onabotulinum toxin A injection and were assessed by Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS), visual analog scale (VAS) of pain, Timed Up and Go (TUG), Berg Balance Test (BBT), and 3D gait analysis at baseline, 1 month, and 3 months. BFMDRS (p = 0.002), VAS (p = 0.024), TUG (p = 0.028), and BBT (p = 0.034) were improved. Foot pressures at Toe 1 (p = 0.028) and Midfoot (p = 0.018) were reduced, indicating botulinum toxin's effects in alleviating the dystonia severity and pain and improving foot pressures during walking in PD.


Subject(s)
Botulinum Toxins, Type A , Dystonia , Parkinson Disease , Botulinum Toxins, Type A/therapeutic use , Dystonia/drug therapy , Gait , Humans , Parkinson Disease/complications , Parkinson Disease/drug therapy , Treatment Outcome
5.
Bone Joint J ; 103-B(6): 1127-1132, 2021 Jun.
Article in English | MEDLINE | ID: mdl-34058886

ABSTRACT

AIMS: To assess the characteristic clinical features, management, and outcome of patients who present to orthopaedic surgeons with functional dystonia affecting the foot and ankle. METHODS: We carried out a retrospective search of our records from 2000 to 2019 of patients seen in our adult tertiary referral foot and ankle unit with a diagnosis of functional dystonia. RESULTS: A total of 29 patients were seen. A majority were female (n = 25) and the mean age of onset of symptoms was 35.3 years (13 to 71). The mean delay between onset and diagnosis was 7.1 years (0.5 to 25.0). Onset was acute in 25 patients and insidious in four. Of the 29 patients, 26 had a fixed dystonia and three had a spasmodic dystonia. Pain was a major symptom in all patients, with a coexisting diagnosis of chronic regional pain syndrome (CRPS) made in nine patients. Of 20 patients treated with Botox, only one had a good response. None of the 12 patients who underwent a surgical intervention at our unit or elsewhere reported a subjective overall improvement. After a mean follow-up of 3.2 years (1 to 12), four patients had improved, 17 had remained the same, and eight reported a deterioration in their condition. CONCLUSION: Patients with functional dystonia typically presented with a rapid onset of fixed deformity after a minor injury/event and pain out of proportion to the deformity. Referral to a neurologist to rule out neurological pathology is advocated, and further management should be carried out in a movement disorder clinic. Response to treatment (including Botulinum toxin (Botox) injections) is generally poor. Surgery in this group of patients is not recommended and may worsen the condition. The overall prognosis remains poor. Cite this article: Bone Joint J 2021;103-B(6):1127-1132.


Subject(s)
Ankle/physiopathology , Complex Regional Pain Syndromes/physiopathology , Dystonia/physiopathology , Foot/physiopathology , Adolescent , Adult , Aged , Comorbidity , Complex Regional Pain Syndromes/diagnosis , Dystonia/diagnosis , Dystonia/therapy , Female , Humans , London , Male , Middle Aged , Prognosis , Retrospective Studies
7.
Toxins (Basel) ; 10(12)2018 12 12.
Article in English | MEDLINE | ID: mdl-30545078

ABSTRACT

Foot dystonia (FD) is a disabling condition causing pain, spasm and difficulty in walking. We treated fourteen (14) adult patients experiencing FD with onabotulinum toxin A injection into the dystonic foot muscles. We analyzed the spatiotemporal gait utilizing the GaitRite system pre- and 3 weeks post-botulinum toxin injection along with measuring dystonia by the Fahn⁻Marsden Dystonia Scale (FMDS), pain by the Visual Analog Scale (VAS) and other lower limb functional outcomes such as gait velocity, the Berg Balance Scale (BBS), the Unified Parkinson's Disease Rating Scale⁻Lower Limb Score (UPDRS⁻LL), the Timed Up and Go (TUG) test and the Goal Attainment Scale (GAS). We found that stride length increased significantly in both the affected (p = 0.02) and unaffected leg (p = 0.01) after treatment, and the improvement in stride length was roughly the same in each leg. Similar results were found for step length (p = 0.02) with improvement in the step length differential (p = 0.01). The improvements in the lower limb functional outcomes were also significant-FMDS, VAS, TUG, and UPDRS⁻LL decreased significantly after treatment (all p < 0.001), and BBS (p = 0.001), GAS (p < 0.001) except cadence (p = 0.37). BT injection improved walking in foot dystonia as evidenced through gait analysis, pain and lower limb functional outcomes. Main study limitations were small sample size and lack of control.


Subject(s)
Botulinum Toxins/therapeutic use , Dystonia/drug therapy , Aged , Aged, 80 and over , Dystonia/physiopathology , Female , Foot/physiopathology , Gait Analysis , Humans , Lower Extremity , Male , Middle Aged , Pilot Projects
8.
Parkinsonism Relat Disord ; 46: 9-15, 2018 01.
Article in English | MEDLINE | ID: mdl-29102441

ABSTRACT

INTRODUCTION: Plantar flexion of toe dystonia is very painful and leads to difficulties in walking. The objective of this study was to investigate the effect of incobotulinum toxin A (Xeomin) in the treatment of this type of dystonia in parkinsonian patients, using a randomized, double blind, placebo-controlled trial. METHODS: 45 parkinsonian patients with painful dystonic plantar flexion of toes were injected either with incobotulinum toxin A (Btx group), or with placebo in two muscle targets: the Flexor digitorum longus and the Flexor digitorum brevis. Three groups were compared: the first group received placebo in the Flexor digitorum longus and 100UI of Btx in the Flexor digitorum brevis (n = 16); the second group received 100 UI of Btx in the Flexor digitorum longus and placebo in the Flexor digitorum brevis (n = 13); and the third group, 2 injections of placebo (n = 16). The patients were injected in the same way twice with an interval of 3 months. The primary endpoint was measured six weeks after injections with the Clinical Global Impression (CGI) of change. Dystonia severity and associated pain were also assessed. RESULTS: Mean CGI was improved in the Btx group compared to the placebo group (P = 0.039). A significant reduction of pain and dystonia severity were observed in patients treated with Btx compared to baseline but no improvement was noted when compared to placebo group. No difference of efficacy was highlighted between the two injection sites. CONCLUSIONS: Btx injections are effective for improving clinical state of parkinsonian patients with plantar flexion of toe dystonia.


Subject(s)
Botulinum Toxins, Type A/pharmacology , Dystonia/drug therapy , Forefoot, Human/physiopathology , Muscle, Skeletal/drug effects , Neuromuscular Agents/pharmacology , Outcome Assessment, Health Care , Parkinson Disease/drug therapy , Aged , Botulinum Toxins, Type A/administration & dosage , Double-Blind Method , Dystonia/etiology , Female , Humans , Male , Middle Aged , Muscle, Skeletal/physiopathology , Neuromuscular Agents/administration & dosage , Parkinson Disease/complications
9.
Mov Disord Clin Pract ; 2(3): 291, 2015 Sep.
Article in English | MEDLINE | ID: mdl-30363488
10.
Mov Disord Clin Pract ; 2(3): 295-298, 2015 Sep.
Article in English | MEDLINE | ID: mdl-30363530

ABSTRACT

The most common presentation of foot dystonia in patients with Parkinson's disease (PD) or dystonia is inversion of the foot accompanied by flexion of the toes, with or without extension of the hallux. Less commonly, foot dystonia may mimic foot drop, as occurs with weakness of the dorsiflexors muscles, resulting in a pseudo foot drop. This has rarely been reported in the literature and has been poorly recognized, often leading to misdiagnosis and unnecessary investigations and treatment. We report 5 patients with dystonic pseudo foot drop, one of them diagnosed with early-onset PD, 2 with sporadic PD, and 2 with dystonia. Despite the steppage gait, their physical exam revealed normal strength, and no other explanation for a "foot drop" was found. It is important to recognize this phenomenology, which can be a clue to the diagnosis of early-onset PD, and may be responsive to levodopa in selected patients.

SELECTION OF CITATIONS
SEARCH DETAIL