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COPD-Lower Respiratory Tract Infection Visual Analogue Score (c-LRTI-VAS) validation in stable and exacerbated patients with COPD.
Prins, Hendrik Johannes; Duijkers, Ruud; Daniels, Johannes M A; van der Molen, Thys; van der Werf, Tjip S; Boersma, Wim.
Afiliación
  • Prins HJ; Department Pulmonary Diseases, Noordwest Ziekenhuisgroep, Alkmaar, Noord-Holland, The Netherlands.
  • Duijkers R; Department Pulmonary Diseases, Noordwest Ziekenhuisgroep, Alkmaar, Noord-Holland, The Netherlands.
  • Daniels JMA; Pulmonary Diseases, Vrije Universiteit Amsterdam, Amsterdam, Noord-Holland, The Netherlands.
  • van der Molen T; Department of Pulmonary Diseases & Tuberculosis, University Medical Centre Groningen, Groningen, Groningen, The Netherlands.
  • van der Werf TS; Infectious diseases Service and Tuberculosis unit, University of Groningen Faculty of Medical Sciences, Groningen, Groningen, The Netherlands t.s.van.der.werf@umcg.nl.
  • Boersma W; pulmonary disease, Noordwest Ziekenhuisgroep, Alkmaar, Noord-Holland, The Netherlands.
BMJ Open Respir Res ; 8(1)2021 02.
Article en En | MEDLINE | ID: mdl-33593795
ABSTRACT

BACKGROUND:

We developed the chronic obstructive pulmonary disease (COPD)-Lower Respiratory Tract Infection-Visual Analogue Score (c-LRTI-VAS) in order to easily quantify symptoms during exacerbations in patients with COPD. This study aimed to validate this score.

METHODS:

In our study, patients with stable COPD as well as those with an acute exacerbations of COPD (AECOPD) were included. The results of c-LRTI-VAS were compared with other markers of disease activity (lung function parameters, oxygen saturation and two health related quality of life questionnaires (St Georges Respiratory Questionnaire (SGRQ) and Clinical COPD Questionnaire (CCQ)) and validity, reliability and responsiveness were assessed.

RESULTS:

Eighty-eight patients with clinically stable COPD and 102 patients who had an AECOPD completed the c-LRTI-VAS questionnaire. When testing on two separate occasions for repeatability, no statistically significant difference between total scores was found 0.143 (SD 5.42) (p=0.826). Internal consistency was high across items (Cronbach's apha 0.755). Correlation with SGRQ and CCQ total scores was moderate to high. After treatment for hospitalised AECOPD, the mean c-LRTI-VAS total score improved 8.14 points (SD 9.13; p≤0.001).

CONCLUSIONS:

c-LRTI-VAS showed proper validity, responsiveness to change and moderate to high correlation with other questionnaires. It, therefore, appears a reliable tool for symptom measurement during AECOPD. TRIAL REGISTRATION NUMBER NCT01232140.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones del Sistema Respiratorio / Enfermedad Pulmonar Obstructiva Crónica Tipo de estudio: Diagnostic_studies Aspecto: Patient_preference Límite: Humans Idioma: En Revista: BMJ Open Respir Res Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones del Sistema Respiratorio / Enfermedad Pulmonar Obstructiva Crónica Tipo de estudio: Diagnostic_studies Aspecto: Patient_preference Límite: Humans Idioma: En Revista: BMJ Open Respir Res Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM