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Characterizing COPD Symptom Variability in the Stable State Utilizing the Evaluating Respiratory Symptoms in COPD Instrument.
Krishnan, Jamuna K; Ancy, Kayley M; Oromendia, Clara; Hoffman, Katherine L; Easthausen, Imaani; Leidy, Nancy K; Han, MeiLan K; Bowler, Russell P; Christenson, Stephanie A; Couper, David J; Criner, Gerard J; Curtis, Jeffrey L; Dransfield, Mark T; Hansel, Nadia N; Iyer, Anand S; Paine Iii, Robert; Peters, Stephen P; Wedzicha, Jadwiga A; Woodruff, Prescott G; Ballman, Karla V; Martinez, Fernando J.
Afiliación
  • Krishnan JK; Pulmonary and Critical Care Medicine, Weill Cornell Medicine, New York, New York, United States.
  • Ancy KM; Department of Medicine, Weill Cornell Medicine, New York, New York, United States.
  • Oromendia C; Division of Biostatistics, Department of Population Health Sciences, Weill Cornell Medical College, New York, New York, United States.
  • Hoffman KL; Division of Biostatistics, Department of Population Health Sciences, Weill Cornell Medical College, New York, New York, United States.
  • Easthausen I; Division of Biostatistics, Department of Population Health Sciences, Weill Cornell Medical College, New York, New York, United States.
  • Leidy NK; Evidera, Bethesda, Maryland, United States.
  • Han MK; Internal Medicine, University of Michigan Health System, Ann Arbor, Michigan, United States.
  • Bowler RP; Department of Medicine, National Jewish Medical and Research Center, Denver, Colorado, United States.
  • Christenson SA; Pulmonary and Critical Care, University of California San Francisco, San Francisco, California, United States.
  • Couper DJ; University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States.
  • Criner GJ; Pulmonary and Critical Care Medicine, Temple University Hospital, Philadelphia, Pennsylvania, United States.
  • Curtis JL; Internal Medicine, University of Michigan Health System, Ann Arbor, Michigan, United States.
  • Dransfield MT; Medical Service, VA Ann Arbor Healthcare System, Ann Arbor, Michigan, United States.
  • Hansel NN; Pulmonary, Allergy and Critical Care, University of Alabama at Birmingham, , Birmingham, Alabama, United States.
  • Iyer AS; Division of Pulmonary and Critical Care Medicine, Johns Hopkins University, Baltimore Maryland, United States.
  • Paine Iii R; Pulmonary, Allergy and Critical Care, University of Alabama at Birmingham, , Birmingham, Alabama, United States.
  • Peters SP; Division of Pulmonary and Critical Care Medicine, Department of Veterans Affairs Medical Center, University of Utah, Salt Lake City, Utah, United States.
  • Wedzicha JA; Section on Pulmonary, Critical Care, Allergy and Immunological Diseases, Wake Forest School of Medicine Medical Center, Winston-Salem, North Carolina, United States.
  • Woodruff PG; National Heart and Lung Institute, Imperial College London, United Kingdom.
  • Ballman KV; Pulmonary and Critical Care, University of California San Francisco, San Francisco, California, United States.
  • Martinez FJ; Division of Biostatistics, Department of Population Health Sciences, Weill Cornell Medical College, New York, New York, United States.
Chronic Obstr Pulm Dis ; 9(2): 195-208, 2022 Apr 29.
Article en En | MEDLINE | ID: mdl-35403414
Rationale: It has been suggested that patients with chronic obstructive pulmonary disease (COPD) experience considerable daily respiratory symptom fluctuation. A standardized measure is needed to quantify and understand the implications of day-to-day symptom variability. Objectives: To compare standard deviation with other statistical measures of symptom variability and identify characteristics of individuals with higher symptom variability. Methods: Individuals in the SubPopulations and InteRmediate Outcome Measures In COPD Study (SPIROMICS) Exacerbations sub-study completed an Evaluating Respiratory Symptoms in COPD (E-RS) daily questionnaire. We calculated within-subject standard deviation (WS-SD) for each patient at week 0 and correlated this with measurements obtained 4 weeks later using Pearson's r and Bland Altman plots. Median WS-SD value dichotomized participants into higher versus lower variability groups. Association between WS-SD and exacerbation risk during 4 follow-up weeks was explored. Measurements and Main Results: Diary completion rates were sufficient in 140 (68%) of 205 sub-study participants. Reproducibility (r) of the WS-SD metric from baseline to week 4 was 0.32. Higher variability participants had higher St George's Respiratory Questionnaire (SGRQ) scores (47.3 ± 20.3 versus 39.6 ± 21.5, p=.04) than lower variability participants. Exploratory analyses found no relationship between symptom variability and health care resource utilization-defined exacerbations. Conclusions: WS-SD of the E-RS can be used as a measure of symptom variability in studies of patients with COPD. Patients with higher variability have worse health-related quality of life. WS-SD should be further validated as a measure to understand the implications of symptom variability.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies Aspecto: Patient_preference Idioma: En Revista: Chronic Obstr Pulm Dis Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies Aspecto: Patient_preference Idioma: En Revista: Chronic Obstr Pulm Dis Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos