2009
DOI: 10.1038/eye.2009.192
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Long-term efficacy of botulinum toxin A for treatment of blepharospasm, hemifacial spasm, and spastic entropion: a multicentre study using two drug-dose escalation indexes

Abstract: Purpose To investigate the long-term effectiveness and safety of botulinum neurotoxin A (BoNT-A) treatment in patients with blepharospasm (BEB), hemifacial spasm (HFS), and entropion (EN) and to use for the first time two modified indexes, 'botulin toxin escalation index-U' (BEI-U) and 'botulin toxin escalation index percentage' (BEI-%), in the dose-escalation evaluation. Methods All patients in this multicentre study were followed for at least 10 years and main outcomes were clinical efficacy, duration of rel… Show more

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Cited by 67 publications
(48 citation statements)
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“…These findings corroborate those published studies. 16,17,18,19,20,21,22,23,24 . The success rate in the present study was 94.73% when injections that did not produce any effect or produced a short-term or minor effect were excluded.…”
Section: Discussionmentioning
confidence: 99%
“…These findings corroborate those published studies. 16,17,18,19,20,21,22,23,24 . The success rate in the present study was 94.73% when injections that did not produce any effect or produced a short-term or minor effect were excluded.…”
Section: Discussionmentioning
confidence: 99%
“…Botulinum neurotoxin, although a less invasive treatment than surgery, can result in potentially life-threatening allergic reactions and systemic manifestation of toxin adverse effects. 3,7 Because HFS is a disabling condition, the choice to receive repeated noninvasive local injections of botulinum neurotoxin appears to be more acceptable before MVD surgery is considered. In the present study, we analyzed and compared 2 patients groups, one that underwent botulinum neurotoxin treatment prior to MVD, and another that did not.…”
Section: Discussionmentioning
confidence: 99%
“…Benefit from aboBoNT-A or onaBoNT-A was sustained for at least 15 years in 128 patients, 11 onaBoNT-A for 10 years in 83 patients, 12 and incoBoNT-A for 69 weeks in 82 patients. 13 In 288 patients arbitrarily assigned to toxin formulation, similar degrees of benefit were sustained for at least 10 years (onaBoNT-A), 15 years (aboBoNT-A), and 5 years (incoBoNT-A).…”
mentioning
confidence: 99%