Literature DB >> 32979072

The St. George's Respiratory Questionnaire in Pulmonary Sarcoidosis.

K H Lo1, J Donohue2, M A Judson3, Y Wu1, E S Barnathan1, R P Baughman4.   

Abstract

RATIONALE: The Saint George's Respiratory Questionnaire (SGRQ) is a frequently used tool to assess health status in pulmonary disease patients. However, its performance characteristics in sarcoidosis patients are not well characterized.
METHODS: Data from a clinical trial of 138 symptomatic adults with sarcoidosis were used to examine the performance characteristics of SGRQ. Data were available at both baseline and week 24. Other assessments included FVC, FEV1, ATS dyspnea score, Borg's CR 10 dyspnea score, 6-min walk distance (6MWD), and Short Form-36 Physical Component Summary (SF-36 PCS) score.
RESULTS: Baseline SGRQ was 46.8, indicating impaired health status. At baseline, SGRQ total score correlated significantly with % predicted FVC, FEV1, ATS dyspnea score, Borg's CR 10 dyspnea score, 6MWD, and SF-36 PCS (r =  - 0.37, - 0.32, 0.57, 0.40, - 0.55, and - 0.80, respectively, p < 0.001). Change from baseline in SGRQ score also statistically significantly correlated with change from baseline in these parameters at week 24: r =  - 0.25, - 0.20, 0.30, 0.22, - 0.20, - 0.45, respectively (p < 0.05).
CONCLUSIONS: The SGRQ correlated with other outcome measures in sarcoidosis initially and with treatment. Improvement in FVC % predicted correlated with improvement in SGRQ. These data suggest the SGRQ may function as a reliable endpoint in clinical sarcoidosis trials.

Entities:  

Keywords:  Quality of life; SF-36; SGRQ; Sarcoidosis; Short form 36

Year:  2020        PMID: 32979072     DOI: 10.1007/s00408-020-00394-7

Source DB:  PubMed          Journal:  Lung        ISSN: 0341-2040            Impact factor:   2.584


  4 in total

1.  Ambrisentan for sarcoidosis associated pulmonary hypertension.

Authors:  M A Judson; K B Highland; S Kwon; J F Donohue; R Aris; N Craft; S Burt; H J Ford
Journal:  Sarcoidosis Vasc Diffuse Lung Dis       Date:  2011-10       Impact factor: 0.670

2.  Inhaled iloprost for sarcoidosis associated pulmonary hypertension.

Authors:  R P Baughman; M A Judson; E E Lower; K Highland; S Kwon; N Craft; P J Engel
Journal:  Sarcoidosis Vasc Diffuse Lung Dis       Date:  2009-07       Impact factor: 0.670

3.  Psychophysical bases of perceived exertion.

Authors:  G A Borg
Journal:  Med Sci Sports Exerc       Date:  1982       Impact factor: 5.411

Review 4.  Endpoints for clinical trials of sarcoidosis.

Authors:  R P Baughman; M Drent; D A Culver; J C Grutters; T Handa; M Humbert; M A Judson; E E Lower; J Mana; C A Pereira; A Prasse; R Sulica; D Valyere; V Vucinic; A U Wells
Journal:  Sarcoidosis Vasc Diffuse Lung Dis       Date:  2012-10       Impact factor: 0.670

  4 in total
  3 in total

1.  Tofacitinib as a Steroid-Sparing Therapy in Pulmonary Sarcoidosis, an Open-Label Prospective Proof-of-Concept Study.

Authors:  Marcia A Friedman; Brian Le; Janelle Stevens; Julianna Desmarais; Daniel Seifer; Kimberly Ogle; Dongseok Choi; Christina A Harrington; Peter Jackson; James T Rosenbaum
Journal:  Lung       Date:  2021-04-07       Impact factor: 2.584

2.  Symptoms, impacts, and suitability of the Pulmonary Arterial Hypertension-Symptoms and Impact (PAH-SYMPACT™) questionnaire in patients with sarcoidosis-associated pulmonary hypertension (SAPH): a qualitative interview study.

Authors:  Brooke M Currie; Evan W Davies; Amélie Beaudet; Larissa Stassek; Leah Kleinman; Robert P Baughman
Journal:  BMC Pulm Med       Date:  2021-11-12       Impact factor: 3.317

3.  Riociguat for Sarcoidosis-Associated Pulmonary Hypertension: Results of a 1-Year Double-Blind, Placebo-Controlled Trial.

Authors:  Robert P Baughman; Oksana A Shlobin; Rohit Gupta; Peter J Engel; Jeffrey I Stewart; Elyse E Lower; Franck F Rahaghi; Joyce Zeigler; Steven D Nathan
Journal:  Chest       Date:  2021-08-04       Impact factor: 9.410

  3 in total

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