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
  • [41] PULMONARY HYPERTENSION IN IDIOPATHIC PULMONARY FIBROSIS: PREVALENCE AND CLINICAL PROGRESS
    Castria, D.
    Refini, R. M.
    Bargagli, E.
    Mezzasalma, F.
    Pierli, C.
    Rottoli, P.
    INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 2012, 25 (03) : 681 - 689
  • [42] Pulmonary hypertension in idiopathic pulmonary fibrosis: Epidemiology and clinical correlates
    Shorr, AF
    Cors, C
    Lettieri, CJ
    Helman, DL
    Nathan, SD
    CHEST, 2005, 128 (04) : 218S - 218S
  • [43] A comparison of respiratory oscillometry and spirometry in idiopathic pulmonary fibrosis: performance time, symptom burden and test-retest reliability
    Patel, Suhani
    Sylvester, Karl P.
    Wu, Zhe
    Rhamie, Serena
    Dickel, Peter
    Maher, Toby M.
    Molyneaux, Philip L.
    Calverley, Peter M. A.
    Man, William D. -C.
    ERJ OPEN RESEARCH, 2024, 10 (04)
  • [44] Diagnosis and management of idiopathic pulmonary fibrosis: Implications for respiratory care
    Hospenthal, MAC
    RESPIRATORY CARE, 2006, 51 (04) : 382 - 391
  • [45] Risk Factors for Acute Respiratory Deterioration in Idiopathic Pulmonary Fibrosis
    Choi, W.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2024, 209
  • [46] DRIVE AND TIMING OF THE RESPIRATORY CYCLE IN SARCOIDOSIS AND IDIOPATHIC PULMONARY FIBROSIS
    RENZI, GD
    AMERICAN REVIEW OF RESPIRATORY DISEASE, 1979, 119 (04): : 351 - 351
  • [47] Prevalence of respiratory viruses in Iranian patients with idiopathic pulmonary fibrosis
    Keyvani, Hossein
    Moghoofei, Mohsen
    Bokharaei-Salim, Farah
    Mostafaei, Shayan
    Mousavi, Seyed-Ali Javad
    Monavari, Seyed Hamidreza
    Esghaei, Maryam
    JOURNAL OF MEDICAL MICROBIOLOGY, 2017, 66 (11) : 1602 - 1606
  • [48] Respiratory Polygraphy Features From Patients With Idiopathic Pulmonary Fibrosis
    Ernst, Glenda
    Borsini, Eduardo
    Bosio, Martin
    Decima, Tamara
    Chertcoff, Felipe
    Quadrelli, Silvia
    Salvado, Alejandro
    CHEST, 2015, 148 (04)
  • [49] 2022 update on clinical practice guidelines for idiopathic pulmonary fibrosis and progressive pulmonary fibrosis
    Tzilas, Vasilios
    Tzouvelekis, Argyrios
    Ryu, Jay H.
    Bouros, Demosthenes
    LANCET RESPIRATORY MEDICINE, 2022, 10 (08): : 729 - 731
  • [50] Characterization of Idiopathic Pulmonary Fibrosis (IPF) and Combined Pulmonary Fibrosis and Emphysema (CPFE) using Respiratory Oscillometry
    Wu, J.
    Xu, J. J.
    Nohra, C.
    Vasileva, A.
    Binnie, W. M.
    Shapera, S.
    Fisher, J.
    Ryan, C.
    Mcinnis, M.
    Hantos, Z.
    Chow, C.
    EUROPEAN RESPIRATORY JOURNAL, 2022, 60