Validation and Test-Retest Reliability of Acoustic Voice Quality Index Version 02.06 in the Turkish Language.

OBJECTIVES: The aim of the present study was to investigate the validity (both concurrent and diagnostic) and test-retest reliability of Acoustic Voice Quality Index (AVQI) version 2 (AVQI 02.06) in Turkish speaking population. MATERIALS AND METHODS: Two hundred and fifty five native Turkish subjects with normal voices (n = 128) and with voice disorders (n = 127) were asked to sustain the vowel [a:] and read aloud the Turkish phonetically balanced text. To determine the test-retest reliability of AVQI, 20 dysphonic (ie, around 15% of the group), and 20 normophonic (ie, around 15% of the group) were reassessed 15 minutes after the first AVQI determination. A three middle seconds of sustained vowel [a:] and a sentence with 25 syllables was concatenated, and AVQI analysis was conducted. The auditory-perceptual evaluation was performed by five experienced raters with Grade (G) from GRBAS Protocol. RESULTS: There was a statistically significant correlation between AVQI scores and auditory-perceptual evaluation of overall voice quality (rs = 0.717, P < 0.001). AVQI gave a threshold of 2.98 for the dysphonic voice. The values of intraclass correlation coefficient with two-way mixed-effects model, single-measures type, absolute agreement definition showed an excellent test-retest reliability for AVQI in Turkish language (intraclass correlation coefficient = 0.986). CONCLUSION: AVQI v.02.06 is a valid and robust tool in differentiating dysphonic and normal voice, and has excellent test-retest reliability in Turkish language

The Turkish version of the consensus auditory-perceptual evaluation of voice (CAPE-V): A reliability and validity study

Objective: The Consensus Auditory-Perceptual Evaluation of Voice (CAPE-V) was developed to assess voice quality. The aim of this study was to develop a Turkish adaptation of CAPE-V and to evaluate the reliability and validity of the Turkish version. Methods: To adapt the CAPE-V protocol to Turkish, six sentences were constructed to meet the phonetic requirements. The validity of the Turkish version of the CAPE-V was tested with inter-rater reliability, intrarater reliability, and GRBAS versus the CAPE-V judgments. Ninety-nine dysphonic and 83 healthy subjects were enrolled. Results: High inter-rater and intrarater reliability (ICC > 0.88, r > 0.81, respectively) were obtained for all vocal parameters. The differences in the six CAPE-V parameters between healthy and dysphonic subjects were statistically significant (P < 0.0001). The correlations between CAPE-V and GRBAS scales were high in overall severity-grade and roughness parameters (r = 0.85, r = 0.82, respectively), the lowest correlation was the strain parameter (r = 0.66). Conclusion: The Turkish version of CAPE-V is a reliable and valid instrument for auditory-perceptual evaluation of the Turkish speaking population

Quantum molecular resonance-assisted phonomicrosurgery: Preliminary experience

WOS: 000347066300029PubMed ID: 25214549The objective of this study was to evaluate the use of quantum molecular resonance (QMR) energy in phonomicrosurgery. Quantum molecular resonance energy (QMRE) is an innovative technology that provides low temperature cutting and coagulation of tissues and causes minimal tissue damage during the procedure. Because of these features, this technology may offer new possibilities in phonomicrosurgery. Twelve patients with vocal fold polyps underwent QMR-assisted phonomicrosurgery. The patients were evaluated before and after surgery at 1 and 3 months postoperatively by using the voice handicap index, laryngeal stroboscopy rating, acoustic voice analysis, and perceptual voice evaluation. The subjects were also evaluated by a patient self-assessment questionnaire at 3 months postoperatively. All parameters significantly improved after QMR-assisted phonomicrosurgery (P < .05). All of the patients also subjectively improved by self-rating. These results suggest that QMRE is a safe and potentially promising treatment in phonomicrosurgery. Yet, further studies should be conducted to confirm these results