Are we underestimating the clinical efficacy of botulinum toxin (type A)? Quantifying changes in spasticity, strength and upper limb function after injections of Botox® to the elbow flexors in a unilateral stroke population

2002 ◽  
Vol 16 (6) ◽  
pp. 654-660 ◽  
Author(s):  
Anand D Pandyan ◽  
Philippe Vuadens ◽  
Frederike MJ van Wijck ◽  
Sandra Stark ◽  
Garth R Johnson ◽  
...  
2009 ◽  
Vol 90 (9) ◽  
pp. 1462-1468 ◽  
Author(s):  
Chia-Lin Chang ◽  
Michael C. Munin ◽  
Elizabeth R. Skidmore ◽  
Christian Niyonkuru ◽  
Lynne M. Huber ◽  
...  

2019 ◽  
Vol 70 (10) ◽  
pp. 3490-3494

The present study quantifies the effect of the two botulinum toxin type A products, Xeomin and Dysport, with approval from the National Agency for Medicines and Medical Devices of Romania (ANMDMR), for the treatment of the spastic upper limb following a stroke. The results obtained in the present study show a good efficiency of using both products in the spasticity of the upper limb, and a maintenance of the results obtained for both products for a minimum period of 3 months. Also, at higher doses, the results of the study show better improvement of spasticity and upper limb function on the evaluation scales, but the local effect is not maintained for a longer period. Keywords: toxinum botulinum type A, Xeomin, Dysport, spasticity


2019 ◽  
Vol 70 (10) ◽  
pp. 3490-3494
Author(s):  
Marius Nicolae Popescu ◽  
Razvan Cosmin Petca ◽  
Cristina Beiu ◽  
Mihai Cristian Dumitrascu ◽  
Aida Petca ◽  
...  

The present study quantifies the effect of the two botulinum toxin type A products, Xeomin and Dysport, with approval from the National Agency for Medicines and Medical Devices of Romania (ANMDMR), for the treatment of the spastic upper limb following a stroke. The results obtained in the present study show a good efficiency of using both products in the spasticity of the upper limb, and a maintenance of the results obtained for both products for a minimum period of 3 months. Also, at higher doses, the results of the study show better improvement of spasticity and upper limb function on the evaluation scales, but the local effect is not maintained for a longer period.


2014 ◽  
Vol 51 (1) ◽  
pp. 38-46 ◽  
Author(s):  
Toru TAKEKAWA ◽  
Takatoshi HARA ◽  
Wataru KAKUDA ◽  
Kazushige KOBAYASHI ◽  
Yousuke SASE ◽  
...  

Brain Injury ◽  
2010 ◽  
Vol 24 (9) ◽  
pp. 1108-1112 ◽  
Author(s):  
Andrea Santamato ◽  
Francesco Panza ◽  
Serena Filoni ◽  
Maurizio Ranieri ◽  
Vincenzo Solfrizzi ◽  
...  

Toxins ◽  
2020 ◽  
Vol 12 (7) ◽  
pp. 440
Author(s):  
Heli Sätilä

Botulinum toxin type A (BTXA) has been used for over 25 years in the management of pediatric lower and upper limb hypertonia, with the first reports in 1993. The most common indication is the injection of the triceps surae muscle for the correction of spastic equinus gait in children with cerebral palsy. The upper limb injection goals include improvements in function, better positioning of the arm, and facilitating the ease of care. Neurotoxin type A is the most widely used serotype in the pediatric population. After being injected into muscle, the release of acetylcholine at cholinergic nerve endings is blocked, and a temporary denervation and atrophy ensues. Targeting the correct muscle close to the neuromuscular junctions is considered essential and localization techniques have developed over time. However, each technique has its own limitations. The role of BTXA is flexible, but limited by the temporary mode of action as a focal spasticity treatment and the restrictions on the total dose deliverable per visit. As a mode of treatment, repeated BTXA injections are needed. This literature reviewed BTXA injection techniques, doses and dilutions, the recovery of muscles and the impact of repeated injections, with a focus on the pediatric population. Suggestions for future studies are also discussed.


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