Evaluation of a respiratory symptom diary for clinical studies of idiopathic pulmonary fibrosis

被引:10
|
作者
Bacci, Elizabeth Dansie [1 ]
O'Quinn, Sean [2 ]
Leidy, Nancy Kline [3 ]
Murray, Lindsey [3 ]
Vernon, Margaret [3 ]
机构
[1] Evidera, 1417 Fourth Ave,Suite 510, Seattle, WA 98101 USA
[2] AstraZeneca, Gaithersburg, MD USA
[3] Evidera, Bethesda, MD USA
关键词
Idiopathic pulmonary fibrosis; Patient-reported outcome; Psychometric; Reliability; Validity; Responsiveness; QUALITY-OF-LIFE; UCSD SHORTNESS; QUESTIONNAIRE; COUGH; VALIDATION; VALIDITY; COPD; EXACERBATIONS; INSTRUMENTS; TRIALS;
D O I
10.1016/j.rmed.2017.11.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: There are no validated patient diaries for evaluating respiratory symptoms in idiopathic pulmonary fibrosis (IPF). Purpose: To evaluate the performance properties of the chronic obstructive pulmonary disease (COPD) Evaluating Respiratory Symptoms (TM) (E-RS (TM): COPD) measure in patients with IPF. Methods: Concept elicitation and cognitive interviews were conducted with IPF patients to evaluate content validity, including comprehensiveness, relevance, and interpretability of E-RS (TM) items in this patient population. Secondary analyses of IPF clinical study data were performed to evaluate the scoring structure of the tool. With modifications, reliability, validity, and responsiveness of the instrument (E-RS (TM) : IPF) were evaluated. Results: Qualitative interviews (n = 30) were conducted. During the elicitation interviews (n = 20), concept saturation for IPF respiratory symptoms was achieved; all respiratory symptoms covered by the E-RS (TM) were endorsed by >= 30% of the sample. During cognitive interviews (n = 10), all participants found the items interpretable and relevant. Factor analyses conducted via secondary analysis of IPF clinical study data identified no total score and four symptom scales: Chest, Breathlessness, Cough, and Sputum. Reliability of each scale was high (internal consistency [alpha]> 0.85); 2-day reproducibility (ICC > 0.88). Validity was supported through significant (P < 0.0001) relationships with the St. George's Respiratory Questionnaire (SGRQ), the University of California, San Diego Shortness of Breath Questionnaire (UCSD-SOBQ), and other variables. The scales were responsive to change when evaluated using SGRQ Symptoms, UCSD-SOBQ, and Patient Global Impression of Change as anchors (P < 0.01 to P < 0.0001). Conclusion: The E-RS (TM) : IPF is a valid, reliable, and responsive tool for evaluating respiratory symptoms in patients with IPF.
引用
收藏
页码:130 / 138
页数:9
相关论文
共 50 条
  • [21] Clinical Features and Outcomes in Combined Pulmonary Fibrosis and Emphysema in Idiopathic Pulmonary Fibrosis
    Ryerson, Christopher J.
    Hartman, Thomas
    Elicker, Brett M.
    Ley, Brett
    Lee, Joyce S.
    Abbritti, Marta
    Jones, Kirk D.
    King, Talmadge E., Jr.
    Ryu, Jay
    Collard, Harold R.
    CHEST, 2013, 144 (01) : 234 - 240
  • [22] The clinical course of patients with idiopathic pulmonary fibrosis
    Martinez, FJ
    Safrin, S
    Weycker, D
    Starko, KM
    Bradford, WZ
    King, TE
    Flaherty, KR
    Schwartz, DA
    Noble, PW
    Raghu, G
    Brown, KK
    ANNALS OF INTERNAL MEDICINE, 2005, 142 (12) : 963 - 967
  • [23] Clinical Predictors of a Diagnosis of Idiopathic Pulmonary Fibrosis
    Fell, Charlene D.
    Martinez, Fernando J.
    Liu, Lyrica X.
    Murray, Susan
    Han, Meilan K.
    Kazerooni, Ella A.
    Gross, Barry H.
    Myers, Jeffrey
    Travis, William D.
    Colby, Thomas V.
    Toews, Galen B.
    Flaherty, Kevin R.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2010, 181 (08) : 832 - 837
  • [24] Prevalence And Clinical Characteristics Of Idiopathic Pulmonary Fibrosis
    Raimundo, K.
    Chang, E.
    Broder, M.
    Carrigan, G.
    Zazzali, J.
    Swigris, J. J.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2015, 191
  • [25] THE CLINICAL ROLE OF BAL IN IDIOPATHIC PULMONARY FIBROSIS
    HASLAM, PL
    POULTER, LW
    ROSSI, GA
    BAUER, W
    DEROSE, V
    ECKERT, H
    OLIVIERI, D
    TESCHLER, H
    EUROPEAN RESPIRATORY JOURNAL, 1990, 3 (08) : 940 - 942
  • [26] Genetics in Idiopathic Pulmonary Fibrosis: A Clinical Perspective
    Papiris, Spyros A. A.
    Kannengiesser, Caroline
    Borie, Raphael
    Kolilekas, Lykourgos
    Kallieri, Maria
    Apollonatou, Vasiliki
    Ba, Ibrahima
    Nathan, Nadia
    Bush, Andrew
    Griese, Matthias
    Dieude, Philippe
    Crestani, Bruno
    Manali, Effrosyni D. D.
    DIAGNOSTICS, 2022, 12 (12)
  • [27] Severe idiopathic pulmonary fibrosis: A clinical approach
    Lipsi, R.
    Mazzola, D.
    Caminati, A.
    Elia, D.
    Lonati, C.
    Harari, S.
    EUROPEAN JOURNAL OF INTERNAL MEDICINE, 2018, 50 : 20 - 27
  • [28] The Future of Clinical Trials in Idiopathic Pulmonary Fibrosis
    Podolanczuk, Anna J.
    Richeldi, Luca
    Martinez, Fernando J.
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2023, 329 (18): : 1554 - 1555
  • [29] The clinical relevance of autoimmunity in idiopathic pulmonary fibrosis
    Tomassetti, Sara
    Gurioli, Christian
    Ravaglia, Claudia
    Piciucchi, Sara
    Casoni, Gian Luca
    Romagnoli, Micaela
    Gurioli, Carlo
    Poletti, Venerino
    EUROPEAN RESPIRATORY JOURNAL, 2012, 40
  • [30] Clinical course and management of idiopathic pulmonary fibrosis
    Quinn, Caitlin
    Wisse, Amy
    Manns, Stephenie T.
    MULTIDISCIPLINARY RESPIRATORY MEDICINE, 2019, 14 (01)