Validity and Reliability of a French Version of Reflux Symptom Index

被引:19
作者
Lechien, Jerome R. [1 ,2 ,3 ]
Huet, Kathy [2 ]
Finck, Camille [4 ]
Khalife, Mohamad [3 ]
Fourneau, Anne-Francoise [3 ]
Delvaux, Veronique [2 ]
Piccaluga, Myriam [2 ]
Harmegnies, Bernard [2 ]
Saussez, Sven [1 ,3 ]
机构
[1] Univ Mons UMONS, UMONS Res Inst Hlth Sci & Technol, Fac Med, Lab Anat & Cell Biol, Ave Champ de Mars 6, B-7000 Mons, Belgium
[2] Univ Mons UMONS, Res Inst Language Sci & Technol, Fac Psychol, Lab Phonet, Mons, Belgium
[3] EpiCURA Hosp, RIIMS Baudour, Dept Otorhinolaryngol & Head & Neck Surg, Baudour, Belgium
[4] Univ Liege, Dept Otorhinolaryngol & Head & Neck Surg, CHU Liege, Liege, Belgium
关键词
Laryngopharyngeal; Reflux; RSI; Voice; Validation; LARYNGOPHARYNGEAL REFLUX; ACID; HOARSENESS; DISEASE; PEPSIN; VOICE;
D O I
10.1016/j.jvoice.2016.11.020
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
Objective. To develop a French version of the Reflux Symptom Index (Fr-RSI) and to assess its internal consistency, reliability, and clinical validity. Study Design. Controlled, prospective trial. Materials and Methods. Forty-four patients with a reflux finding score > 7 and an Fr-RSI > 13 were enrolled and treated with 20 mg of pantoprazole twice daily and diet changes for 3 months. Ninety asymptomatic subjects were also included in the study. To assess reliability, Fr-RSI was completed twice within a 7-day period. Validity was assessed by comparing Fr-RSI scores with scores from the Voice Handicap Index (VHI) in 24 of 44 patients, at baseline and at 3 months posttherapy. Results. The mean values of Fr-RSI at baseline and after 7 days were 20.17 +/- 5.76 and 19.75 +/- 7.08, respectively, for patients with laryngopharyngeal reflux (LPR) and 4.02 +/- 3.49 and 3.71 +/- 3.82, respectively, for controls. The test-retest reliability was high in patients with LPR (r(BP) = 0.78) and in healthy subjects (r(BP) = 0.80). Cronbach's alpha was 0.85, indicating high internal consistency. The mean Fr-RSI score significantly improved from a baseline of 20.17 +/- 5.76 to 5.58 +/- 3.65 after 3 months of treatment (P = 0.001), and the initial mean VHI total score significantly improved from 20.29 +/- 19.62 to 12.87 +/- 12.04 after treatment (P = 0.029), indicating validity of the results. However, of the subcategories of the VHI, only the mean physical score improved from a baseline of 11.19 +/- 9.22 to 7.35 +/- 5.96 after treatment (P = 0.016). Conclusion. The Fr-RSI developed in this study demonstrated both reliability and validity. It can be easily administered to assist in diagnosing and monitoring of LPR in French-speaking patients.
引用
收藏
页码:512.e1 / 512.e7
页数:7
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