Abstract

This study aimed at validating an existing health-related quality of life questionnaire for patients with facial palsy for implementation in the Dutch language and culture. The Facial Clinimetric Evaluation Scale was translated into the Dutch language using a forward–backward translation method. A pilot test with the translated questionnaire was performed in 10 patients with facial palsy and 10 normal subjects. Finally, cross-cultural adaption was accomplished at our outpatient clinic for facial palsy. Analyses for internal consistency, test–retest reliability, construct validity and responsiveness were performed. Ninety-three patients completed the Dutch Facial Clinimetric Evaluation Scale, the Dutch Facial Disability Index, and the Dutch Short Form (36) Health Survey. Cronbach’s α, representing internal consistency, was 0.800. Test–retest reliability was shown by an intraclass correlation coefficient of 0.737. Correlations with the House–Brackmann score, Sunnybrook score, Facial Disability Index physical function, and social/well-being function were −0.292, 0.570, 0.713, and 0.575, respectively. The SF-36 domains correlate best with the FaCE social function domain, with the strongest correlation between the both social function domains (r = 0.576). The FaCE score did statistically significantly increase in 35 patients receiving botulinum toxin type A (P = 0.042, Student t test). The domains ‘facial comfort’ and ‘social function’ improved statistically significantly as well (P = 0.022 and P = 0.046, respectively, Student t-test). The Dutch Facial Clinimetric Evaluation Scale shows good psychometric values and can be implemented in the management of Dutch-speaking patients with facial palsy in the Netherlands. Translation of the instrument into other languages may lead to widespread use, making evaluation and comparison possible among different providers.

Highlights

  • Patients experiencing peripheral facial palsy experience both functional and psychosocial consequences

  • We approached the developers of the FaCE Scale and obtained permission to use the instrument for translation and validation [8]

  • Ten patients with peripheral facial palsy completed the pilot version of the translated questionnaire as well

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Summary

Introduction

Patients experiencing peripheral facial palsy experience both functional and psychosocial consequences. The self-assessment of patients using questionnaires gives an impression of the influence of disease on quality of life. For this purpose, nondisease-specific questionnaires exist [6, 7], as well as disease-specific questionnaires, though very few of them are adapted in regular clinical practice. Kahn et al [8] developed an instrument which covers both the functional and psychosocial aspect of facial palsy, the Facial Clinimetric Evaluation Scale (FaCE Scale). This questionnaire consists of 15 questions with a 5-point Likert scale. Total and domain scores range from 0 (worst) to 100 (best)

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