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190504 r ||| eng |
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|a Pohar, Ron
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|a Switching botulinum toxin A products for patients with upper limb spasticity or cervical dystonia
|h Elektronische Ressource
|b a review of clinical effectiveness
|c Ron Pohar, Danielle Rabb
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|a Ottawa (ON)
|b CADTH
|c 2018, February 9, 2018
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|a 1 PDF file (24 pages)
|b illustration
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|a Includes bibliographical references
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|a Muscle Spasticity / drug therapy
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|a Drug Substitution
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|a Dystonia / drug therapy
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|a Treatment Outcome
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653 |
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|a Botulinum Toxins, Type A / therapeutic use
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|a Rabb, Danielle
|e [author]
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|a Canadian Agency for Drugs and Technologies in Health
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|a eng
|2 ISO 639-2
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|b NCBI
|a National Center for Biotechnology Information
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|a CADTH rapid response report: summary with critical appraisal
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|u https://www.ncbi.nlm.nih.gov/books/NBK531716
|3 Volltext
|n NLM Bookshelf Books
|3 Volltext
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|a 610
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|a The four Botulinum neurotoxin type A (BoNT-A) products have different complex protein structures and differ in their molecular weights, pharmacologic profiles, and potency. Because each BoNT-A product has a different potency, they are not considered interchangeable by Health Canada and dosages may not covert directly on a 1 to 1 basis. Each BoNT-A has a different nonproprietary name (generic name) to make it more clear that the products are not interchangeable. However, switching may be necessary for patients who experience secondary nonresponse, develop side effects, or are required to do so for reasons related to drug coverage. For these reasons, it is important to be aware of the evidence to support the efficacy of switching between different BoNT-A products in experienced users. This report will review the evidence of clinical effectiveness of switching BoNT-A products for patients with upper limb spasticity (ULS) and cervical dystonia (CD)
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