Zraick Richard I, Risner Brandy Y, Smith-Olinde Laura, Gregg Brent A, Johnson Felicia L, McWeeny Elizabeth K
University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205, USA.
J Voice. 2007 Jul;21(4):485-94. doi: 10.1016/j.jvoice.2006.06.006. Epub 2006 Sep 6.
The primary purpose of this study was to compare patient's and communication partner's perceptions of handicap secondary to dysphonia. A secondary purpose was to compare patient health-related quality of life (HRQOL) to that of speakers with normal voice. Participants were 20 adults (mean age=69.15 years) with dysphonia and their communication partners. Patients completed the Voice Handicap Index (VHI), a questionnaire of self-perceived voice handicap, and the Short-Form 36 (SF-36), a general health questionnaire. Partners completed the Voice Handicap Index-Partner (VHI-P), a questionnaire derived from the VHI for this pilot study, to gauge partner perception of voice handicap. Patients in this study viewed themselves as only moderately handicapped by their dysphonia and their partners were in close agreement. Patients and their partners were also in close agreement on each of three VHI subscales (physical, functional, and emotional), and in all cases the physical domain was perceived by both patients and their partners to be most handicapped. Patients had lower SF-36 mean scores than those of persons with normal voice from the general U.S. population on scales assessing physical functioning, physical role, general health, vitality, social functioning, emotional role, and mental health. The results of this study are consistent with previous studies examining patient-partner agreement, which consider proxy ratings to be a useful alternative or collaborative source of patient's self-perception. Further research regarding the reliability of patient and partner agreement is necessary to most effectively assess and manage patients with dysphonia.
本研究的主要目的是比较患者及其交流伙伴对发音障碍所致残疾的认知。次要目的是将患者的健康相关生活质量(HRQOL)与嗓音正常者的健康相关生活质量进行比较。研究对象为20名患有发音障碍的成年人(平均年龄 = 69.15岁)及其交流伙伴。患者完成了嗓音障碍指数(VHI),这是一份自我感知嗓音障碍的问卷,以及简短健康调查问卷36项版本(SF - 36),这是一份一般健康状况问卷。伙伴们完成了嗓音障碍指数 - 伙伴版(VHI - P),这是为本项初步研究从VHI衍生而来的问卷,用于衡量伙伴对嗓音障碍的认知。本研究中的患者认为自己仅因发音障碍而有中度残疾,且他们的伙伴也持相近看法。患者及其伙伴在VHI的三个分量表(身体、功能和情感)上的看法也相近,在所有情况下患者及其伙伴都认为身体方面的残疾最为严重。在评估身体功能、身体角色、总体健康、活力、社会功能、情感角色和心理健康的量表上,患者的SF - 36平均得分低于美国普通人群中嗓音正常者的得分。本研究结果与之前考察患者 - 伙伴一致性的研究一致,这些研究认为代理评级是患者自我认知的一种有用的替代方式或协作来源。有必要进一步研究患者与伙伴一致性的可靠性,以便最有效地评估和管理发音障碍患者。