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Development and validation of the Exercise-Induced Laryngeal Obstruction Dyspnea Index (EILODI).
Olin, James Tod; Shaffer, Monica; Nauman, Emily; Durso, Catherine S; Fan, Elizabeth M; Staudenmayer, Herman; Christopher, Kent L; Gartner-Schmidt, Jackie.
Afiliação
  • Olin JT; Department of Pediatrics, National Jewish Health, Denver, Colo; Department of Medicine, National Jewish Health, Denver, Colo. Electronic address: olint@njhealth.org.
  • Shaffer M; Department of Rehabilitation Medicine, National Jewish Health, Denver, Colo.
  • Nauman E; Department of Rehabilitation Medicine, National Jewish Health, Denver, Colo.
  • Durso CS; Department of Computer Science, University of Denver, Denver, Colo.
  • Fan EM; Department of Pediatrics, National Jewish Health, Denver, Colo.
  • Staudenmayer H; Department of Psychiatry, University of Colorado School of Medicine, Aurora, Colo.
  • Christopher KL; Department of Medicine, University of Colorado School of Medicine, Aurora, Colo.
  • Gartner-Schmidt J; Department of Otolaryngology, University of Pittsburgh Medical Center, Pittsburgh, Pa.
J Allergy Clin Immunol ; 149(4): 1437-1444, 2022 04.
Article em En | MEDLINE | ID: mdl-34619181
ABSTRACT

BACKGROUND:

Exercise-induced laryngeal obstruction (EILO) causes exertional dyspnea and is important for its effect on quality of life, diagnostic confusion with exercise-induced asthma, and health care resource utilization. There is no validated patient-reported outcome measure specific to EILO.

OBJECTIVE:

We sought to develop, validate, and define a minimal clinically important difference for a patient-reported outcome measure to be used with adolescents and young adults with EILO.

METHODS:

A multidisciplinary group created a preliminary measure, modified by a 10-member participant focus group, with 20 items scored along a 5-point Likert scale. A subsequent cohort of participants recruited from a clinic, aged 12 to 21 years, with confirmed EILO by continuous laryngoscopy during exercise testing (1) completed the measure at 3 points in time over 28 days and (2) provided anchoring data in the form of a daily exercise log and categorical self-assessments of clinical improvement. Thirty additional participants without exertional dyspnea served as controls.

RESULTS:

Two hundred nineteen subjects with mild to severe EILO participated in the exploratory factor analysis, which identified 7 factors within the preliminary outcome measure. After a process of item reduction, a 12-item metric with a total score ranging from 0 to 48 was developed. Mean scores of patients with EILO and healthy controls at baseline were 28.8 ± 7.4 and 4.5 ± 7.4, respectively. A minimal clinically important difference of 6 was determined by comparison of index change with changes in categorical self-assessments of improvement.

CONCLUSIONS:

This is the first patient-reported outcome measure specifically designed for adolescents and young adults with EILO.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma Induzida por Exercício / Doenças da Laringe / Obstrução das Vias Respiratórias Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Qualitative_research Limite: Adolescent / Adult / Humans Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma Induzida por Exercício / Doenças da Laringe / Obstrução das Vias Respiratórias Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Qualitative_research Limite: Adolescent / Adult / Humans Idioma: En Revista: J Allergy Clin Immunol Ano de publicação: 2022 Tipo de documento: Article