Improved vocal quality and decreased vocal effort after botulinum toxin treatment for laryngeal dystonia

Leung, Jai-sen; Rosenbaum, Andres; Holmberg, Jorge; Villarroel, Pablo; Napolitano, Carla; Badia, Pedro I.; Lagos-Villaseca, Antonia

Abstract

Objectives: Laryngeal dystonia (LD) is characterized by irregular and involuntary task-specific spasms of the intrinsic laryngeal muscles. There is no curative treatment for it, however, laryngeal botulinum neurotoxin injections (BoNT-I) are considered the standard of care therapy. This study aims to characterize the population of LD patients and to assess the results of laryngeal BoNT-I. Methods: A Retrospective cohort study was conducted. Medical records were reviewed for all the patients with LD diagnosis seen in the Voice Unit of the Red de Salud UC-Christus between January 2013 and October 2021. Biodemographic, clinical and treatment data were collected. Additionally, a telephonic survey was completed by the patients that underwent laryngeal BoNTI, including self-reported voice outcomes and Voice Handicap Index 10 (VHI-10). Results: Of the 34 patients with LD included in the study, 23 received a total of 93 laryngeal BoNT-I and 19 completed the telephone survey. The majority (97%) of the injections corresponded to patients with adductor LD and 3% to abductor LD. Patients received a median of 3 (1-17) injections, with a more frequent cricothyroid approach (94.4%), while the thyrohyoid approach accounted for 5.6% of cases. Most injections were bilateral (96.8%). A significant improvement in the vocal quality and effort was noted after the last injection and the overall BoNT-I treatment ( P < 0.001). Similarly, the VHI-10 score improved from a median of 31 (7-40) to 2 (0-19) ( P < 0.001) after the last injection. A post-treatment breathy voice was reported in 95% of patients, and dysphagia to liquids and solids in 68% and 21%, respectively. Conclusions: Laryngeal BoNT-I is an effective treatment for LD, achieving an improvement in self-reported vocal quality and VHI-10 scores, and a reduction of the self-reported vocal effort. Adverse effects are mild in the majority of cases, constituting a safe and effective therapy for these patients.

Más información

Título según WOS: ID WOS:001165901500001 Not found in local WOS DB
Título de la Revista: AURIS NASUS LARYNX
Volumen: 51
Número: 1
Editorial: ELSEVIER SCI LTD
Fecha de publicación: 2024
Página de inicio: 106
Página final: 112
DOI:

10.1016/j.anl.2023.06.004

Notas: ISI