A North American perspective of content and quality of websites in the English language on childhood-onset lupus erythematosus. (April 2018)

• Record Type: Journal Article
• Authors: Cutler, C; Peng, T; Stinson, J; Tucker, L; Boneparth, A; Klein Gitelman, M; Moorthy, L Nandini
• Is Part Of: Lupus. Volume 27:Number 5(2018)
• Page Start: 762
• Page End: 770
• Publication Date: 2018-04
• Subjects: Systemic lupus erythematosus -- internet -- website -- pediatrics -- transition -- readability; Systemic lupus erythematosus -- Periodicals; 616.772005
• DOI: 10.1177/0961203317746246
• Languages: English
• ISSNs: 0961-2033

Abstract

Objective: The objective of this article is to examine the quality, content, and readability of information and resources in the English language and accessible on the internet by pediatric patients with systemic lupus erythematosus (SLE) and their families in North America. Methods: Keywords relevant to SLE were generated by an undergraduate student, a first-year medical student, and a third-year pediatric resident, and a search was conducted across five commonly used search engines. Quality of information found was evaluated independently by an undergraduate student, a graduate student, a first-year medical student, and a third-year pediatric resident using the DISCERN tool. Two pediatric rheumatologists assessed website accuracy and completeness. Readability of websites was determined using the Flesch-Kincaid grade level and Reading Ease score. Results: Out of 2000 websites generated in the search, only 34 unique websites met inclusion criteria. Only 16 of these websites had DISCERN scores above 50% (fair quality). Overall quality of website information was fair with mean ±standard deviation (SD) DISCERN quality score of 44 ± 7 (range: 30–56). Only nine websites of 34 had DISCERN scores above 50 (>66%, indicating greater quality) and were further assessed for completeness. Flesch-Kincaid grade level was 11 ± 1 (mean±SD) and reading ease score was 39 ± 10 (mean±SD, range of 11–61). Conclusion: Our study highlights the need for more complete, readable information regarding the unique needs of pediatric patients with childhood-onset SLE and their families.