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Efficacy and Safety of Electromyography-Guided Injection of Botulinum Toxin to Treat Retrograde Cricopharyngeus Dysfunction.
Wajsberg, Benjamin; Hoesli, Rebecca C; Wingo, Melissa L; Bastian, Robert W.
Afiliación
  • Wajsberg B; Bastian Voice Institute, Downers Grove, Illinois, USA.
  • Hoesli RC; Bastian Voice Institute, Downers Grove, Illinois, USA.
  • Wingo ML; Bastian Voice Institute, Downers Grove, Illinois, USA.
  • Bastian RW; Bastian Voice Institute, Downers Grove, Illinois, USA.
OTO Open ; 5(1): 2473974X21989587, 2021.
Article en En | MEDLINE | ID: mdl-33598599
ABSTRACT

OBJECTIVE:

To report the efficacy and safety of electromyography-guided percutaneous botulinum toxin injection into the cricopharyngeus muscle in an office setting for treatment of the inability to belch and associated symptoms caused by retrograde cricopharyngeus dysfunction (R-CPD). STUDY

DESIGN:

Retrospective case series of treated patients.

SETTING:

Tertiary care laryngology clinic.

METHODS:

A retrospective review was performed on 18 consecutive patients who were diagnosed syndromically with R-CPD. The combined diagnostic test and treatment-specifically, botulinum toxin injection into the cricopharyngeus muscle-was accomplished in an office setting by a single surgeon using electromyography guidance. Items assessed are efficacy, safety, complications, and duration of benefit.

RESULTS:

All 18 patients (100%) treated in the in-office setting gained the ability to burp with improvement in the associated symptoms of R-CPD at initial follow-up. Of those who had the in-office procedure performed initially, 80% maintained the ability to burp at 6 months with relief of all the associated symptoms of R-CPD. No patients experienced permanent complications from the injection, but 7 patients experienced varying degrees of noisy breathing within 1 week after the procedure, which was managed with breathing techniques and resolved.

CONCLUSION:

In a case series of 18 patients with R-CPD, all patients gained the ability to burp with improvement in the majority of their symptoms of R-CPD at the time of their initial follow-up at 1 week. None experienced severe complications, and 7 experienced transient noisy breathing, which resolved.
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: OTO Open Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: OTO Open Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos