Safety and efficacy of botulinum toxin type B (Myobloc) in adductor spasmodic dysphonia.
Identifieur interne : 003351 ( PubMed/Corpus ); précédent : 003350; suivant : 003352Safety and efficacy of botulinum toxin type B (Myobloc) in adductor spasmodic dysphonia.
Auteurs : Charles H. Adler ; Stephen F. Bansberg ; Kari Krein-Jones ; Joseph G. HentzSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2004.
English descriptors
- KwdEn :
- Adult, Botulinum Toxins (administration & dosage), Botulinum Toxins (therapeutic use), Dose-Response Relationship, Drug, Female, Humans, Injections, Male, Middle Aged, Neuromuscular Agents (administration & dosage), Neuromuscular Agents (therapeutic use), Severity of Illness Index, Vocal Cords (physiopathology), Voice Disorders (diagnosis), Voice Disorders (drug therapy), Voice Disorders (physiopathology).
- MESH :
- chemical , administration & dosage : Botulinum Toxins, Neuromuscular Agents.
- chemical , therapeutic use : Botulinum Toxins, Neuromuscular Agents.
- diagnosis : Voice Disorders.
- drug therapy : Voice Disorders.
- physiopathology : Vocal Cords, Voice Disorders.
- Adult, Dose-Response Relationship, Drug, Female, Humans, Injections, Male, Middle Aged, Severity of Illness Index.
Abstract
This single-site, open-label, dose-finding study evaluated the safety and efficacy of botulinum toxin type B (BoNT-B; Myobloc) for the treatment of adductor spasmodic dysphonia (AdSD) in 13 patients. Three patients received a total of 50 U (25 U per vocal fold); the same three subsequently received 100 U, and then 10 more received 200 U. The primary measure of efficacy was the patient's rating of the change in the severity of spasms on a scale from -3 to +3. There were seven secondary measures of efficacy, including blinded ratings of the sound of voice recorded on audiotape. At Week 8 after injection, spasms improved in 0 of 3 patients who received 50 U, 1 of 3 patients who received 100 U, and 8 of 10 patients who received 200 U. The mean (+/- standard deviation [SD]) score for the change in spasm severity at Week 8 in the 200 U group was 1.4 (+/-1.2) points (P = 0.004). All seven secondary measures also showed improvement. Breathiness was the most common side effect but was mild in intensity and of short duration. We conclude that BoNT-B is safe and effective for the treatment of adductor spasmodic dysphonia.
DOI: 10.1002/mds.20098
PubMed: 15372600
Links to Exploration step
pubmed:15372600Le document en format XML
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<author><name sortKey="Adler, Charles H" sort="Adler, Charles H" uniqKey="Adler C" first="Charles H" last="Adler">Charles H. Adler</name>
<affiliation><nlm:affiliation>Parkinson's Disease and Movement Disorders Center, Department of Neurology, Mayo Clinic Scottsdale, 13400 E. Shea Blvd., Scottsdale, AZ 85259, USA. calder@mayo.edu</nlm:affiliation>
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<author><name sortKey="Bansberg, Stephen F" sort="Bansberg, Stephen F" uniqKey="Bansberg S" first="Stephen F" last="Bansberg">Stephen F. Bansberg</name>
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<author><name sortKey="Krein Jones, Kari" sort="Krein Jones, Kari" uniqKey="Krein Jones K" first="Kari" last="Krein-Jones">Kari Krein-Jones</name>
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<author><name sortKey="Hentz, Joseph G" sort="Hentz, Joseph G" uniqKey="Hentz J" first="Joseph G" last="Hentz">Joseph G. Hentz</name>
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<front><div type="abstract" xml:lang="en">This single-site, open-label, dose-finding study evaluated the safety and efficacy of botulinum toxin type B (BoNT-B; Myobloc) for the treatment of adductor spasmodic dysphonia (AdSD) in 13 patients. Three patients received a total of 50 U (25 U per vocal fold); the same three subsequently received 100 U, and then 10 more received 200 U. The primary measure of efficacy was the patient's rating of the change in the severity of spasms on a scale from -3 to +3. There were seven secondary measures of efficacy, including blinded ratings of the sound of voice recorded on audiotape. At Week 8 after injection, spasms improved in 0 of 3 patients who received 50 U, 1 of 3 patients who received 100 U, and 8 of 10 patients who received 200 U. The mean (+/- standard deviation [SD]) score for the change in spasm severity at Week 8 in the 200 U group was 1.4 (+/-1.2) points (P = 0.004). All seven secondary measures also showed improvement. Breathiness was the most common side effect but was mild in intensity and of short duration. We conclude that BoNT-B is safe and effective for the treatment of adductor spasmodic dysphonia.</div>
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<Abstract><AbstractText>This single-site, open-label, dose-finding study evaluated the safety and efficacy of botulinum toxin type B (BoNT-B; Myobloc) for the treatment of adductor spasmodic dysphonia (AdSD) in 13 patients. Three patients received a total of 50 U (25 U per vocal fold); the same three subsequently received 100 U, and then 10 more received 200 U. The primary measure of efficacy was the patient's rating of the change in the severity of spasms on a scale from -3 to +3. There were seven secondary measures of efficacy, including blinded ratings of the sound of voice recorded on audiotape. At Week 8 after injection, spasms improved in 0 of 3 patients who received 50 U, 1 of 3 patients who received 100 U, and 8 of 10 patients who received 200 U. The mean (+/- standard deviation [SD]) score for the change in spasm severity at Week 8 in the 200 U group was 1.4 (+/-1.2) points (P = 0.004). All seven secondary measures also showed improvement. Breathiness was the most common side effect but was mild in intensity and of short duration. We conclude that BoNT-B is safe and effective for the treatment of adductor spasmodic dysphonia.</AbstractText>
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