Jornal Brasileiro de Pneumologia (Apr 2019)

Translation of the quality-of-life measure for adults with primary ciliary dyskinesia and its application in patients in Brazil

  • Ana Paula Lima de Queiroz,
  • Rodrigo Abensur Athanazio,
  • Mary Anne Kowal Olm,
  • Bruna Rubbo,
  • Yuri Reis Casal,
  • Jane Lucas,
  • Laura Behan

DOI
https://doi.org/10.1590/1806-3713/e20170358
Journal volume & issue
Vol. 45, no. 3

Abstract

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ABSTRACT Primary ciliary dyskinesia (PCD) is a genetic disorder that is typically inherited in an autosomal recessive manner. It is clinically characterized by recurrent respiratory infections. However, its repercussions for patient quality of life should not be overlooked. Studies have shown that PCD has a significant impact on the lives of patients, although there are as yet no PCD-specific markers of quality of life. To address that problem, researchers in the United Kingdom developed a quality-of-life questionnaire for patients with PCD. The present communication focuses on the process of translating that questionnaire into Brazilian Portuguese, through a partnership between researchers in Brazil and those in the United Kingdom, as well as its subsequent application in patients in Brazil.

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