{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,17]],"date-time":"2026-04-17T11:28:26Z","timestamp":1776425306674,"version":"3.51.2"},"reference-count":16,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2023,11,5]],"date-time":"2023-11-05T00:00:00Z","timestamp":1699142400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Clinical Otolaryngology"],"published-print":{"date-parts":[[2024,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Objectives<\/jats:title><jats:p>To validate and test the reliability of the 10\u2010Item Unilateral Vocal Fold Paralysis\u2010Voice Handicap Index (UVFP\u2010HI\u201010) quality of life (QoL) questionnaire for patients with UVFP.<\/jats:p><\/jats:sec><jats:sec><jats:title>Design<\/jats:title><jats:p>Prospective describe study based on perceptive surveys.<\/jats:p><\/jats:sec><jats:sec><jats:title>Participants<\/jats:title><jats:p>We recruited 61 patients with UVFP and 53 healthy individuals comprised the control group.<\/jats:p><\/jats:sec><jats:sec><jats:title>Main Outcome Measures<\/jats:title><jats:p>Both the patients and controls completed the UVFP\u2010HI\u201010 questionnaire. A statistical analysis was performed to assess the internal consistency and validity of the survey. In addition, maximum phonation time (MPT) was used to objectively measure patient QoL.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Internal consistency was high (<jats:italic>\u03b1<\/jats:italic>\u2009=\u2009.914) and the correlation with MPT was significant (<jats:italic>r<\/jats:italic>s\u2009=\u2009\u22120.722). The estimated marginal mean in the discriminant validity study was around seven times higher in the UVFP group compared to the controls. The UVFP\u2010HI\u201010 cut\u2010off value was more than 0.9 and the sensitivity and specificity were more than 0.8.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>The UVFP\u2010HI\u201010 is a self\u2010administered patient\u2010reported outcome questionnaire with a high reliability and excellent criterion\u2010based validity. This questionnaire can be used to evaluate specific clinical complaints (e.g., vocalisation, swallowing, and breathing) in terms of their impact on QoL in patients with UVFP. Thus, its use is appropriate as a basic assessment tool as part of a specific UVFP treatment protocol.<\/jats:p><\/jats:sec>","DOI":"10.1111\/coa.14120","type":"journal-article","created":{"date-parts":[[2023,11,6]],"date-time":"2023-11-06T02:10:08Z","timestamp":1699236608000},"page":"185-190","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Validation of the <scp>10\u2010Item<\/scp> Unilateral Vocal Fold Paralysis\u2010Handicap Index quality of life questionnaire"],"prefix":"10.1111","volume":"49","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-7591-4953","authenticated-orcid":false,"given":"Rosa","family":"Hern\u00e1ndez\u2010Sandemetrio","sequence":"first","affiliation":[{"name":"ENT Department University General Hospital of Valencia, Valencia School of Medicine  Valencia 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