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Botulinum Toxin in Secondarily Nonresponsive Patients with Spasmodic Dysphonia
Niv Mor1, Christopher Tang2, Andrew Blitzer3
1Voice and Swallowing Disorders, Division of Otolaryngology-Head and Neck Surgery, Maimonides Medical Center, Brooklyn, New York, USA Department of Otolaryngology-Head and Neck Surgery, Mount Sinai Roosevelt Hospital, New York, New York, USA nivmor73@gmail.com.
Secondary nonresponse to botulinum toxin type A (BoNT-A) is rare in spasmodic dysphonia (SD) patients, with low doses potentially reducing immunoresistance. Patients who stopped treatment could resume BoNT-A without recurrence of nonresponse.
Area of Science:
- Neurology
- Pharmacology
Background:
- Chemodenervation using botulinum toxin (BoNT) is a long-established treatment for dystonia.
- Secondary nonresponse to BoNT can occur in patients with various dystonia types.
Purpose of the Study:
- To investigate the incidence and characteristics of secondary nonresponse to botulinum toxin type A (BoNT-A) in patients with spasmodic dysphonia (SD).
- To assess the possibility of resuming BoNT-A treatment after a period of nonresponse.
Main Methods:
- Retrospective review of patients with SD treated with BoNT-A.
- Analysis of secondary nonresponse rates and outcomes after treatment cessation and reinitiation.
Main Results:
- A low rate of secondary nonresponse to BoNT-A (0.57%) was observed in SD patients, lower than in other dystonias.
- Four out of four patients who resumed BoNT-A after cessation did not experience recurrence of immunoresistance.
- SD patients typically receive significantly lower doses of BoNT-A compared to other dystonias.
Conclusions:
- The low incidence of secondary nonresponse in SD may be attributed to the extremely low doses of BoNT-A used.
- Small antigen exposure could contribute to reduced immunoresistance and sustained efficacy upon reinitiation of BoNT-A in SD patients.
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