Evidence map›Paper›PMID 39742032›Full record

ArticleInternational journal of general medicine2024

Web-Based Educational Resources for Patients with Sickle Cell Disease: Availability and Reliability.

Dalal Mahmoud Alabdulmohsen, Sarah Khalid Alfuhaydi, Abdullah Mohamed Al Saloum, Bayan Alomair, Mohannad Yousuf Alhindi, Ruba Yosof Alsulami, Mortadah Hadi Alsalman

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Article in International journal of general medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Dalal Mahmoud AlabdulmohsenDepartment of Medicine, College of Medicine, King Faisal University, Alahsa, Saudi Arabia.ORCID 0009-0003-4721-2481
Sarah Khalid AlfuhaydiDepartment of Medicine, King Fahad Medical City, Riyadh, Saudi Arabia.
Abdullah Mohamed Al SaloumDepartment of Medicine, College of Medicine, International University of Africa, Khartoum, Sudan.
Bayan AlomairDepartment of Medicine, College of Medicine, King Faisal University, Alahsa, Saudi Arabia.
Mohannad Yousuf AlhindiDepartment of Medicine, College of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID 0009-0008-0234-3177
Ruba Yosof AlsulamiDepartment of Medicine, College of Medicine, University of Jeddah, Jeddah, Saudi Arabia.ORCID 0009-0005-7337-9319
Mortadah Hadi AlsalmanDepartment of Medicine, College of Medicine, King Faisal University, Alahsa, Saudi Arabia.ORCID 0000-0003-3975-5550

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Arabic is the primary language used in the Middle East, where sickle cell disease (SCD) is prevalent. This study aims to quantify Arabic web educational materials for patients with SCD and provide a descriptive standardized assessment. Methods and Materials: This retrospective, descriptive study aimed to analyze Arabic websites on SCD through the Discern instrument and JAMA benchmark. Results: We evaluated the quality and reliability of 27 Arabic SCD-related websites. Regarding website content, all 27 (100%) defined sickle cell disease, whereas 25 (96.30%) and 24 (92.59%) illustrated its manifestations and treatments, respectively. However, only 12 (44.44%) discussed the prevention of the disease through premarital genetic screening and counseling. According to the Discern score, 11 (40.74%) websites were of low quality, while 16 (59.26%) were of moderate quality. On the other hand, the JAMA score reveals that only 2 (7.41%) websites were high reliability, while the majority 25 (92.59%) were low reliability. Additionally, analysis revealed a weak positive correlation between the Discern and JAMA scores (correlation coefficient of 0.19). There were no statistically significant differences in the Discern and JAMA scores between websites on the first page of the search results and those on other pages ( Conclusion: Empowering patients with comprehensive knowledge about various disease aspects is a pivotal component in the effective management of SCD and, consequently, improving its outcomes. Regrettably, there is a notable scarcity of credible and high-quality written web-based health resources available in Arabic despite significant advancements in other clinical aspects of SCD. Augmenting the existing online resources in Arabic patients' native language could yield substantial enhancements in patient care across various dimensions.

Indexed as

Arabic languageeducationsickle cell disease

Identifiers

PMID39742032
PMCPMC11687319

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.