TY  - JOUR
AU  - Annesi, Thomas
AU  - Steinway, Caren
AU  - Oluwole, Toyosi
AU  - Shilly, Steffi
AU  - Szalda, Dava
AU  - Myers, Regina
AU  - Chen, Jack
AU  - Jan, Sophia
PY  - 2023
DA  - 2023/12/13
TI  - Quality of Web-Based Sickle Cell Disease Resources for Health Care Transition: Website Content Analysis
JO  - JMIR Pediatr Parent
SP  - e48924
VL  - 6
KW  - sickle cell
KW  - health care transition
KW  - readability
KW  - Flesch Reading Ease
KW  - health care information
KW  - adulthood
KW  - sickle cell disease
KW  - online resource
KW  - quality
KW  - adolescent
KW  - transition
KW  - health care service
KW  - website quality
KW  - online information
KW  - Ensuring Quality Information for Patients
KW  - EQIP
KW  - FRE
AB  - Background: Adolescents and young adults with sickle cell disease (SCD) transitioning from pediatric to adult health care face a high-risk period associated with increased use of acute health care services and mortality. Although 59% of American citizens report using the internet for health care information, the quality of web-based, patient-facing resources regarding transition in SCD care has not been evaluated. Objective: This study aimed to evaluate the quality and readability of web-based health information on SCD, especially as it pertains to the transition to adulthood for inidividuals with SCD. The study also compared the readability and content scores of websites identified in 2018 to those from 2021 to assess any change in quality over time. Methods: Keywords representing phrases adolescents may use while searching for information on the internet regarding transition in SCD care, including “hydroxyurea” and “SCD transition,” were identified. A web-based search using the keywords was conducted in July 2021 using Google, Yahoo, and Bing. The top 20 links from each search were collected. Duplicate websites, academic journals, and websites not related to SCD health care transition were excluded. Websites were categorized based on the source: health department, hospital or private clinician, professional society, and other websites. Websites were assessed using Health On the Net Foundation code of conduct (HONcode), Flesch Reading Ease (FRE), Flesch-Kincaid Grade Level (FGL), Ensuring Quality Information for Patients (EQIP), and a novel SCD content checklist (SCDCC). EQIP and SCDCC scores range from 0- to 100. Each website was reviewed by 2 research assistants and assessed for interrater reliability. Descriptive statistics were calculated. Results: Of the 900 websites collected, 67 (7.4%) met the inclusion criteria: 13 health department, 7 hospital or private clinician, 33 professional society, and 14 other websites. A total of 15 (22%) out of 67 websites had HONcode certification. Websites with HONcode certification had higher FRE and EQIP scores and lower FGL scores than those without HONcode certification, reflecting greater readability. Websites without HONcode certification had higher SCDCC scores, reflecting greater clinical content. Only 7 (10%) websites met the National Institutes of Health recommendation of a seventh-grade or lower reading level. Based on EQIP scores, 6 (9%) websites were of high quality. The mean SCDCC score was 20.60 (SD 22.14) out of 100. The interrater reliability for EQIP and SCDCC ratings was good (intraclass correlation: 0.718 and 0.897, respectively). No source of website scored significantly higher mean EQIP, FRE, FGL, or SCDCC scores than the others (all P<.05). Conclusions: Although seeking health care information on the web is very common, the overall quality of information about transition in SCD care on the internet is poor. Changes to current web-based health care information regarding SCD care transitions would benefit transitioning youth by providing expectations, knowledge, skills, and tools to increase self-efficacy. 
SN  - 2561-6722
UR  - https://pediatrics.jmir.org/2023/1/e48924
UR  - https://doi.org/10.2196/48924
UR  - http://www.ncbi.nlm.nih.gov/pubmed/38100579
DO  - 10.2196/48924
ID  - info:doi/10.2196/48924
ER  -