Diplophonia

  • 文章类型: Comparative Study
    OBJECTIVE: The objective of this study was to investigate the ability of a two-stage method of cepstral peak identification to effectively discriminate rough vs breathy vs typical voice in sustained vowel productions. It was hypothesized that a dual-stage search for cepstral peak prominences (CPP\'s) above and below specified quefrency/F0 cutoffs would result in a CPP difference that would be characteristic of the rough, diplophonic voice type.
    METHODS: Central one-second portions of sustained vowel /a/ productions were obtained from 90 subjects (rough, breathy, and normophonic voices). All voice samples were analyzed using a a two-stage cepstral analysis process in which a CPPHigh-Low difference value was obtained by identifying cepstral peaks above and below a lower limit for expected F0 (150 Hz for females and 90 Hz for males), called CPPHigh and CPPLow respectively.
    RESULTS: The CPPHigh-Low difference value was observed to be a highly significant predictor, with negative values for this parameter characteristic of a dominant subharmonic in the voice signal and the perception of diplophonic, rough voice. Correct classification of rough vs nonrough voice samples was 82.2% (sensitivity 0.80 and specificity 0.833). In the consideration of three group classification (breathy vs. normophonic vs. rough), models incorporating two predictors (the CPP obtained from a single search through a 60 to 300 Hz frequency range (CPPDefault) and the CPPHigh-Low difference value) correctly classified 78.88% of the voice samples.
    CONCLUSIONS: Rough, diplophonic voices were consistently observed to have a subharmonic peak that was greater in amplitude than the cepstral peak obtained within the region of the expected F0, resulting in a negative value for the CPPHigh-Low difference. The two-stage cepstral analysis process described herein is visually intuitive from the graphical display of a cepstrum and is a simple extended calculation derived from cepstral analysis procedures that have been recommended as essential in the acoustic description of vocal quality.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Sci-hub)

  • 文章类型: Journal Article
    息肉患者可能会出现双音,萎缩,瘫痪或疤痕。它的振动模式尚未得到很好的表征。高速视频(HSV)分析有助于他们的理解。HSV研究了20名具有双音语音质量的受试者。文凭是由于医学原因,包括声带麻痹(n=7),声带萎缩(n=5),息肉(n=5),和疤痕/沟(n=3)。使用多切片数字视频记录(DKG)分析HSV。对DKG跟踪进行定性分析,然后将其转换为振动图波形信号进行频率分析。结果:在HSV上看到的振动异常解释了双音。可以通过DKG可视化基频的次谐波。没有一个可以通过频闪镜检查解决。可以根据一个或两个声带的参与,将双音音分层为对称或不对称。疤痕和萎缩表现出对称的次谐波产生,每4-10次跳动一次异位跳动。一些受试者显示了前后独立的声带振荡器。不对称的原因在瘫痪患者中很常见。每个声带的两个不同的振荡频率在两侧之间产生相位相互作用。振动图分析记录了高于主要基频的谐波间能量峰的频繁存在。20个受试者中有18个具有明显的次谐波峰。结论:复音患者存在声带引起的振动异常。HSV和振动图分析,然后对振动图进行频率分析,可以将振动异常分解为对称和非对称原因,并可以记录振动异常的类型。
    Diplophonia can occur in patients with polyps, atrophy, paralysis, or scars. Its vibratory patterns have not been well characterized. High-speed video (HSV) analysis can contribute to their understanding. Twenty subjects with a diplophonic voice quality were studied by HSV. Diplophonia was due to medical causes including vocal fold paresis (n = 7), vocal atrophy (n = 5), polyps (n = 5), and scars/sulci (n = 3). The HSV was analyzed using a multislice digital videokymography (DKG). The DKG tracing was analyzed qualitatively and then transformed into a vibrogram waveform signal for frequency analysis. RESULTS: Vibratory abnormalities seen on HSVs explained the diplophonia. Subharmonics to the fundamental frequency can be visualized by DKG. None could be resolved by stroboscopy. One can stratify diplophonia as symmetric or asymmetric based on the involvement of one or both vocal folds. Scars and atrophy showed symmetric subharmonic production with ectopic beats every 4-10 beats. Some subjects showed anterior and posterior independent vocal fold oscillators. Asymmetric causes of diplophonia are common in patients with paralysis. Two different oscillation frequencies of each vocal fold generate in and then out of phase interaction between the two sides. Vibrogram analysis documents the frequent presence of interharmonic energy peaks above the dominant fundamental frequency. Eighteen of the 20 subjects have obvious subharmonic peaks. CONCLUSION: Patients with diplophonia have vibratory abnormalities arising from the vocal folds. HSV and vibrogram analysis followed by frequency analysis of the vibrogram can resolve vibratory abnormality into symmetric versus asymmetric causes and can document the type of vibratory abnormality.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Sci-hub)

  • 文章类型: Case Reports
    OBJECTIVE: Automatic acoustic measures of voice quality in people with Down syndrome (DS) do not reliably reflect perceived voice qualities. This study used acoustic data and visual spectral data to investigate the relationship between perceived voice qualities and acoustic measures.
    METHODS: Participants were four young adults (two males, two females; mean age 23.8 years) with DS and severe learning disabilities, at least one of whom had a hearing impairment.
    METHODS: Participants imitated sustained /i/, /u/, and /a/ vowels at predetermined target pitches within their vocal range. Medial portions of vowels were analyzed, using Praat, for fundamental frequency, harmonics-to-noise ratio, jitter, and shimmer. Spectrograms were used to identify the presence and the duration of subharmonics at onset and offset, and mid-vowel. The presence of diplophonia was assessed by auditory evaluation.
    RESULTS: Perturbation data were highest for /a/ vowels and lowest for /u/ vowels. Intermittent productions of subharmonics were evident in spectrograms, some of which coincided with perceived diplophonia. The incidence, location, duration, and intensity of subharmonics differed between the four participants.
    CONCLUSIONS: Although the acoustic data do not clearly indicate atypical phonation, diplophonia and subharmonics reflect nonmodal phonation. The findings suggest that these may contribute to different perceived voice qualities in the study group and that these qualities may result from intermittent involvement of supraglottal structures. Further research is required to confirm the findings in the wider DS population, and to assess the relationships between voice quality, vowel type, and physiological measures.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Sci-hub)

  • 文章类型: Evaluation Study
    OBJECTIVE: Diplophonia is an often misinterpreted symptom of disordered voice, and needs objectification. An audio signal processing algorithm for the detection of diplophonia is proposed. Diplophonia is produced by two distinct oscillators, which yield a profound physiological interpretation. The algorithm\'s performance is compared with the clinical standard parameter degree of subharmonics (DSH).
    METHODS: This is a prospective study.
    METHODS: A total of 50 dysphonic subjects with (28 with diplophonia and 22 without diplophonia) and 30 subjects with euphonia were included in the study. From each subject, up to five sustained phonations were recorded during rigid telescopic high-speed video laryngoscopy. A total of 185 phonations were split up into 285 analysis segments of homogeneous voice qualities. In accordance to the clinical group allocation, the considered segmental voice qualities were (1) diplophonic, (2) dysphonic without diplophonia, and (3) euphonic. The Diplophonia Diagram is a scatter plot that relates the one-oscillator synthesis quality (SQ1) to the two-oscillator synthesis quality (SQ2). Multinomial logistic regression is used to distinguish between diplophonic and nondiplophonic segments.
    RESULTS: Diplophonic segments can be well distinguished from nondiplophonic segments in the Diplophonia Diagram because two-oscillator synthesis is more appropriate for imitating diplophonic signals than one-oscillator synthesis. The detection of diplophonia using the Diplophonia Diagram clearly outperforms the DSH by means of positive likelihood ratios (56.8 versus 3.6).
    CONCLUSIONS: The diagnostic accuracy of the newly proposed method for detecting diplophonia is superior to the DSH approach, which should be taken into account for future clinical and scientific work.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Sci-hub)

公众号