SCOUT - SARCOIDOSIS OUTCOMES TASKFORCE. A SYSTEMATIC REVIEW OF OUTCOMES TO INFORM THE DEVELOPMENT OF A CORE OUTCOME SET FOR PULMONARY SARCOIDOSIS

被引:3
|
作者
Harman, Nicola L. [1 ]
Gorst, Sarah L. [1 ]
Williamson, Paula R. [1 ]
Barnathan, Elliot S. [2 ]
Baughman, Robert P. [3 ]
Judson, Marc A. [4 ]
Junks, Heidi [5 ]
Kampstre, Nynke A. [6 ,11 ]
Sullivan, Eugene J. [7 ]
Victorson, David E. [8 ]
Walton, Marc [9 ]
AL-Hakim, Tamara [10 ]
Nabulsi, Hana [10 ]
Singh, Noopur [10 ]
Grutters, Jan C. [11 ,12 ]
Culver, Daniel A. [13 ]
机构
[1] Univ Liverpool, Dept Hlth Data Sci, Liverpool, Merseyside, England
[2] Janssen Res & Dev LLC, Raritan, NJ USA
[3] Univ Cincinnati, Med Ctr, Dept Med, Cincinnati, OH 45267 USA
[4] Albany Med Coll, Dept Med, Div Pulm & Crit Care Med, Albany, NY USA
[5] Patient Advocate Fdn Sarcoidosis Res, Nieuwegein, Netherlands
[6] St Antonius Hosp, Dept Value Based Healthcare, Nieuwegein, Netherlands
[7] Radboud Univ Nijmegen, Sci Ctr Qual Healthcare IQ Healthcare, Radboud Inst Hlth Sci, Med Ctr, Nijmegen, Netherlands
[8] Insmed Inc, Bridgewater, NJ USA
[9] Northwestern Univ, Feinberg Sch Med, Evanston, IL USA
[10] Janssen Res & Dev, Titusville, NJ USA
[11] Fdn Sarcoidosis Res, Chicago, IL USA
[12] St Antonius Hosp, Dept Pulmonol, Interstitial Lung Dis Ctr Excellence, Nieuwegein, Netherlands
[13] Univ Med Ctr Utrecht, Div Heart & Lungs, Utrecht, Netherlands
关键词
Pulmonary sarcoidosis; Systematic review; Core outcome set; Outcomes;
D O I
10.36141/svdld.v38i3.10737
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Clinical trials evaluating different management strategies for pulmonary sarcoidosis may measure different outcomes. This heterogeneity in outcomes can lead to waste in research due to the inability to compare and combine data. Core outcome sets (COS) have the potential to address this issue and here we describe a systematic review of outcomes as the first step in the development of a COS for pulmonary sarcoidosis research. Methods: A search of clinical trial registries for phase II, III and IV trials of pulmonary sarcoidosis was undertaken along with a rapid review of the patient perspective literature. Each study was screened for eligibility and outcomes extracted verbatim from the registry entry or publication then reviewed, grouped and categorised using the COMET taxonomy. Results: 36 trial registry entries and 6 studies on patients' perspective of pulmonary sarcoidosis were included reporting 56 and 82 unique outcomes respectively across 23 domains. The most frequently reported outcome domain was "respiratory, thoracic and mediastinal outcomes". However, the patients' perspective literature identified outcomes in the "personal circumstances" and "societal/carer burden" domains that were not reported in any of the included trial registrations. Conclusions: Using both clinical trial registry data and published literature on patients' perspective has allowed rapid review of outcomes measured and reported in pulmonary sarcoidosis research. The use of multiple sources has led to the development of a comprehensive list of outcomes that represents the first step in the development of a COS for use in future pulmonary sarcoidosis research.
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页数:14
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