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Clinical Voice Outcomes for Two Voice Rest Protocols after Phonomicrosurgery.
Fan, Ruiqing Stephanie; Yiu, Yin; Kulesz, Paulina A; Dueppen, Abigail; Procter, Teresa; Goodwin, Maurice E; Thekdi, Apurva A; Joshi, Ashwini.
Afiliação
  • Fan RS; Dept. of Communication Sciences and Disorders, University of Houston, Houston, Texas, U.S.A.
  • Yiu Y; Texas Voice Center, Houston Methodist Department of Otolaryngology-Head & Neck Surgery, Houston, Texas, U.S.A.
  • Kulesz PA; Department of Psychology, Texas Institute for Measurement, Evaluation, and Statistics, University of Houston, Houston, Texas, U.S.A.
  • Dueppen A; Dept. of Communication Sciences and Disorders, University of Houston, Houston, Texas, U.S.A.
  • Procter T; Texas Voice Center, Houston Methodist Department of Otolaryngology-Head & Neck Surgery, Houston, Texas, U.S.A.
  • Goodwin ME; Texas Voice Center, Houston Methodist Department of Otolaryngology-Head & Neck Surgery, Houston, Texas, U.S.A.
  • Thekdi AA; Texas Voice Center, Houston Methodist Department of Otolaryngology-Head & Neck Surgery, Houston, Texas, U.S.A.
  • Joshi A; Texas Voice Center, Houston Methodist Department of Otolaryngology-Head & Neck Surgery, Houston, Texas, U.S.A.
Laryngoscope ; 134(6): 2812-2818, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38217412
ABSTRACT

OBJECTIVES:

Voice rest is commonly recommended for patients with benign vocal fold lesions (BVFLs) after phonomicrosurgery. The study compares the clinical voice outcomes of two protocols, 7-day complete voice rest (CVR) and 3-day CVR followed by 4-day relative voice rest (CVR + RVR), for patients with BVFLs after phonomicrosurgery. STUDY

DESIGN:

Prospective, randomized controlled trial.

METHOD:

Patients with BVFLs undergoing phonomicrosurgery were recruited prospectively and randomly assigned to either protocol. Outcomes were assessed on objective measures of acoustics (fundamental frequency, frequency range, mean intensity, cepstral peak analysis) and aerodynamics (vital capacity, airflow rate, subglottal pressure, phonation threshold pressure), as well as subjective measures, both provider-reported through the Consensus Auditory-Perceptual Evaluation of Voice (CAPE-V), and patient-reported through the Voice Handicap Index (VHI). Clinical measures were collected at three-time points preoperatively, 1-week postoperatively (on voice rest), and 1-month postoperatively. In addition, adherence was estimated using a vocal dosimeter.

RESULTS:

Twenty-five patients were recruited and randomized to 7-day CVR (n = 13) and CVR + RVR regimen (n = 12). Statistically significant changes were found within both groups for subglottal pressure (p = 0.03) and VHI score (p < 0.001) comparing pre-operative baseline to 1-month postoperative follow-up. There were no statistically significant differences between the groups. Regardless of group assignment, a significant decrease in overall severity ratings for the CAPE-V was found by comparing the preoperative scores to postoperative scores at 1-week (p < 0.001) and 1-month (p < 0.001).

CONCLUSION:

Both groups improved their overall voice quality comparably 1 month after undergoing phonomicrosurgery as measured by objective and subjective parameters. LEVELS OF EVIDENCE 2. Laryngoscope, 1342812-2818, 2024.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prega Vocal / Qualidade da Voz / Microcirurgia Tipo de estudo: Clinical_trials / Guideline Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Laryngoscope Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prega Vocal / Qualidade da Voz / Microcirurgia Tipo de estudo: Clinical_trials / Guideline Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Laryngoscope Ano de publicação: 2024 Tipo de documento: Article