Streamlining quantification of age-related vocal atrophy

被引:0
|
作者
Al-Awadi, Hamzah A. [1 ]
Zughni, Lisa [1 ]
Knutson, Madeline [1 ]
Carlson, Abbey [2 ]
Aboueisha, Mohamed A. [1 ]
Jaleel, Zaroug A. [1 ]
Merati, Albert L. [1 ]
Bhatt, Neel K. [1 ,3 ]
机构
[1] Univ Washington, Sch Med, Dept Otolaryngol Head & Neck Surg, Div Laryngol, Seattle, WA USA
[2] Community Hosp, Dept Speech Language Pathol, Munster, IN USA
[3] 1959 NE Pacific St, Seattle, WA 98195 USA
来源
关键词
age-related vocal atrophy; presbylaryngis; presbyphonia; vocal fold bowing; AUDITORY-PERCEPTUAL EVALUATION;
D O I
10.1002/lio2.1241
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
ObjectivesAge-related vocal atrophy (ARVA) has a significant impact on voice, communication, and quality of life. Vocal folds are bowed with incomplete glottic closure during phonation. Efficient quantification of vocal fold atrophy and collection of voice recordings in clinic remains challenging. The primary focus of this study is to describe a novel method for quantifying vocal atrophy and obtaining voice recordings in clinic among patients with ARVA.MethodsPatients with ARVA were included. Voice recordings were collected during the clinic visit, and acoustic analysis was subsequently performed. A novel mobile application was used to quantify the bowing index (BI).ResultsThe study included 10 patients with ARVA, with a mean age of 72.7 +/- 6.8 years and body mass index (BMI) of 24.9 +/- 2.4 kg/m2. Calculation of BI was feasible with a mean of 9.9 +/- 1.8 units. On average, the audio recording took 2.6 +/- 0.4 min, and subsequent analysis required 7.1 +/- 1.8 min. Mean continuous speech f0 was 212.1 +/- 10.1 and 134.2 +/- 31.5 Hz for male and female patients, respectively. Smoothed cepstral peak prominence was 8.9 +/- 1.5 dB (male) and 8.5 +/- 0.3 dB (female), and maximum phonation time between male and female patients was 16.7 +/- 9.8 and 13.8 +/- 1.9 s, respectively.ConclusionWe present a feasible and streamlined method for quantification of vocal fold atrophy in the clinic among patients with ARVA. The accuracy and reliability of this new method are areas of ongoing investigation. Quantification of vocal atrophy may help with clinical decisions, including diagnosing vocal atrophy and tracking treatment progress. Moreover, this method may improve research data acquisition without burdening patients and clinicians with additional time-consuming tasks. Level of evidence: 4.ConclusionWe present a feasible and streamlined method for quantification of vocal fold atrophy in the clinic among patients with ARVA. The accuracy and reliability of this new method are areas of ongoing investigation. Quantification of vocal atrophy may help with clinical decisions, including diagnosing vocal atrophy and tracking treatment progress. Moreover, this method may improve research data acquisition without burdening patients and clinicians with additional time-consuming tasks. Level of evidence: 4. Quantification of age-related vocal atrophy is difficult in clinic. This study presents a novel and practical method for quantifying endoscopic and acoustic data in patients with this condition. image
引用
收藏
页数:6
相关论文
共 50 条
  • [41] Age-related differences in apoptosis with disuse atrophy in soleus muscle
    Leeuwenburgh, C
    Gurley, CM
    Strotman, BA
    Dupont-Versteegden, EE
    AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2005, 288 (05) : R1288 - R1296
  • [42] Measuring geographic atrophy in advanced age-related macular degeneration
    Sunness, JS
    Bressler, NM
    Tian, Y
    Alexander, J
    Applegate, CA
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1999, 40 (08) : 1761 - 1769
  • [43] Progression of Geographic Atrophy and Genotype in Age-Related Macular Degeneration
    Klein, Michael L.
    Ferris, Frederick L., III
    Francis, Peter J.
    Lindblad, Anne S.
    Chew, Emily Y.
    Hamon, Sara C.
    Ott, Jurg
    OPHTHALMOLOGY, 2010, 117 (08) : 1554 - U117
  • [44] Hippocampal and temporal lobe atrophy and age-related decline in memory
    Ylikoski, R
    Salonen, O
    Mäntylä, R
    Ylikoski, A
    Keskivaara, P
    Leskelä, M
    Erkinjuntti, T
    ACTA NEUROLOGICA SCANDINAVICA, 2000, 101 (04): : 273 - 278
  • [45] Microperimetry for geographic atrophy secondary to age-related macular degeneration
    Csaky, Karl G.
    Patel, Praveen J.
    Sepah, Yasir J.
    Birch, David G.
    Do, Diana, V
    Ip, Michael S.
    Guymer, Robyn H.
    Luu, Chi D.
    Gune, Shamika
    Lin, Hugh
    Ferrara, Daniela
    SURVEY OF OPHTHALMOLOGY, 2019, 64 (03) : 353 - 364
  • [46] Precursors to Geographic Atrophy in Age-Related Macular Degeneration (AMD)
    Taylor, Kenneth
    Cleland, Spencer
    Pak, Jeong
    Banghart, Mark
    Blodi, Barbara
    Domalpally, Amitha
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2021, 62 (08)
  • [47] Macular atrophy development in neovascular age-related macular degeneration
    Calugaru, Dan
    Calugaru, Mihai
    EUROPEAN JOURNAL OF OPHTHALMOLOGY, 2022, 32 (01) : NP307 - NP308
  • [48] Microperimetry of Nascent Geographic Atrophy in Age-Related Macular Degeneration
    Wu, Zhichao
    Ayton, Lauren N.
    Luu, Chi D.
    Guymer, Robyn H.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2015, 56 (01) : 115 - 121
  • [49] Geographic atrophy severity and mortality in age-related macular degeneration
    Ahluwalia, Aneesha
    Shen, Liangbo L.
    Chen, Evan M.
    Sun, Mengyuan
    Park, Michael M.
    Young, Benjamin K.
    Del Priore, Lucian V.
    GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2021, 259 (09) : 2643 - 2651
  • [50] NSAIDs may protect against age-related brain atrophy
    Bendlin, Barbara B.
    Newman, Lisa M.
    Ries, Michele L.
    Puglielli, Luigi
    Carlsson, Cynthia M.
    Sager, Mark A.
    Rowley, Howard A.
    Gallagher, Catherine L.
    Willette, Auriel A.
    Alexander, Andrew L.
    Asthana, Sanjay
    Johnson, Sterling C.
    FRONTIERS IN AGING NEUROSCIENCE, 2010, 2