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. 2022 Jan 15;23:42. doi: 10.1186/s13063-022-06000-w

Table 1.

Characteristics of included publications

Characteristics Inflammatory conditions
ALL RA* JIA AS PsA SS CD** UC Uv SLE*** (jSLE)
Total number included 44 10 2 4 8 2 7 2 1 6 (2)
Type of publication:
 Collaborative reports 34 8 1 3 7 2 6 0 1 4 (2)
Regulatory guidance 10 2X 1e 1e 1e 0 1e 2X 0 2X (0)
Patient population:
Adults 37ap 10ap 4 8 2 5ap 2ap 0 6ap
Paediatric specific 7 0 2 0 0 0 2 0 1 2
Purpose:
Trials and LOS 43 10 2 3 8 2 7 2 1 6 (2)
Routine practice 8 2 0 2 2 0 1 0 0 0 (0)
Registries 4 0 0 3 1 0 0 0 0 0 (0)
Methods:
 Initial literature or systematic review/database search 22 6 0 3 3 1 5 0 1 3 (0)
 Surveys 9 2 1 1 2 1 0 0 1 0 (1)
 Interviews/focus groups 4 0 0 1 2 0 1 0 0 0 (0)
 Delphi/ NGT/other consensus group meeting 32 8 1 2 6 2 6 0 1 4 (2)
 Patient involvement 14 5 0 2 4 0 3 0 0 0 (0)
 HCP involvement 34 8 1 3 7 2 6 0 1 4 (2)

AS ankylosing spondylitis, CD Crohn’s disease, EMA European Medicines Agency, FDA Food and Drug Administration, HCP health care professionals, ICHOM International Consortium for Health Outcomes Measurement, JIA juvenile idiopathic arthritis, LOS longitudinal observation studies, NGT nominal group technique, PsA psoriatic arthritis, RA rheumatoid arthritis, SLE systemic lupus erythematosus, jSLE juvenile SLE, SS Sjogren’s syndrome, UC ulcerative colitis, uV uveitis

*ICHOM 2018 document for inflammatory arthritis covers RA, PsA, AS and JIA

**Kim 2018 and Ruemmele 2014 referred to both CD and UC (inflammatory bowel disease). To avoid confusion, these have been recorded under CD

***Values in brackets represent the subsets relating to jSLE (under SLE)

eDenotes an EMA publication whilst f represents an FDA document

xSignifies that both EMA and FDA produced documents for the condition

apSignifies the inclusion of publications with mixed patient populations