Evidence map›Paper›PMID 41941725›Full record

ReviewJMIR pediatrics and parenting2026

mHealth-Enabled Stroke Screening for Pediatric Sickle Cell Disease in Low-Resource Settings: Systematic Literature Review of Critical Barriers, Emerging Technologies, and AI-Driven Solutions.

Nursat Jahan, Seung Yup Lee, Nafisa Anjum, Monica Swahn, Sangsun Choi, Andrew Peachey, Sweta Sneha, Chitalu Kabwe, Nazmus Sakib

Abstract readReview
In one paragraph

Review in JMIR pediatrics and parenting, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Nursat JahanCollege of Computing and Software Engineering, Kennesaw State University, Marietta Campus, J3218 Atrium Building, Marietta, GA, 30060, United States, 1-470-578-3803.ORCID http://orcid.org/0009-0003-7709-6370
Seung Yup LeeDepartment of Electrical and Computer Engineering, Kennesaw State University, Marietta Campus, Marietta, GA, United States.ORCID http://orcid.org/0000-0002-0530-8464
Nafisa AnjumCollege of Computing and Software Engineering, Kennesaw State University, Marietta Campus, J3218 Atrium Building, Marietta, GA, 30060, United States, 1-470-578-3803.ORCID http://orcid.org/0009-0001-4176-9014
Monica SwahnSchool of Public Health, Virginia Commonwealth University, Richmond, VA, United States.ORCID http://orcid.org/0000-0002-6663-3885
Sangsun ChoiSchool of Communication & Media, Kennesaw State University, Kennesaw Campus, Kennesaw, GA, United States.ORCID http://orcid.org/0009-0007-4170-8979
Andrew PeacheyDepartment of Health Promotion and Physical Education, Kennesaw State University, Kennesaw Campus, Kennesaw, GA, United States.ORCID http://orcid.org/0009-0007-8960-4327
Sweta SnehaWright School of Business, Dalton State College, Dalton, GA, United States.ORCID http://orcid.org/0000-0002-7892-5236
Chitalu KabweMichael A. Leven School of Management, Kennesaw State University, Kennesaw Campus, Kennesaw, GA, United States.ORCID http://orcid.org/0000-0002-6231-9565
Nazmus SakibCollege of Computing and Software Engineering, Kennesaw State University, Marietta Campus, J3218 Atrium Building, Marietta, GA, 30060, United States, 1-470-578-3803.ORCID http://orcid.org/0000-0002-7008-1120

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sickle cell disease (SCD) is a genetic blood disorder affecting millions globally, with life-threatening complications, and most patients live in sub-Saharan Africa. Particularly, children with SCD have a high risk of stroke. Although early screening for stroke could help prevent many cases, access to effective stroke screening remains limited in low-resource settings (LRS). Existing traditional approaches are highly operator-dependent, costly, resource-intensive, or difficult to deploy at scale in pediatric care. These limitations highlight the urgent need for accessible, scalable, and child-appropriate stroke screening and assessment tools suitable for low-resource health care contexts. Objective: The aims of this systematic literature review are to (1) uncover system-level barriers affecting stroke screening accessibility for patients with pediatric sickle cell disease (PSCD) in LRS, including underserved contexts within high-income countries; (2) identify existing and emerging stroke screening and assessment technologies and their implementation characteristics, such as feasibility, scalability, portability, and training requirements; and (3) propose a user-centered mobile health (mHealth) framework for stroke screening that improves accessibility and feasibility in resource-constrained health care settings. Methods: PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines were followed to organize the search process. A systematic search was conducted using an advanced query and defined eligibility criteria in the academic databases of PubMed, IEEE Xplore, Wiley Online Library, and Google Scholar. Studies published in English between January 1, 2021, and October 31, 2025, were selected. Collected data were arranged in a preformatted Microsoft Excel spreadsheet for analysis. Risk-of-bias assessment was performed using various risk-of-bias assessment tools because of the heterogeneity of the included studies. Narrative synthesis was used for data synthesis. Results: The literature search initially identified 1465 studies, of which 28 (2%) were selected for analysis. Among the 28 studies, 10 (36%) focused on stroke screening accessibility for patients with PSCD in either low- and middle-income countries or other income-level countries for LRS, and 18 (64%) outlined key features and the feasibility of stroke screening technologies. Identified barriers were organized into 4 major categories (workforce and training constraints, health care system and infrastructure barriers, sociocultural and awareness factors, and economic and logistical constraints), emphasizing difficulties in accessing stroke screening in LRS. Additionally, existing and emerging stroke screening technologies were classified into 5 groups: nonimaging, imaging, light-based optical spectroscopy, biomarker-based, and artificial intelligence- and machine learning-based mHealth wearable approaches. Finally, a comprehensive mHealth app is proposed for an easy-to-use screening experience to address stroke screening challenges for patients with PSCD in LRS. Conclusions: This study contributes to identifying major barriers to stroke screening in LRS and highlights key characteristics of stroke screening solutions that can be used in the future. It also contributes to the design of a holistic mHealth solution for implementing stroke screening clinical care for patients with PSCD in LRS.

Indexed as

low-resource settingmHealthmobile healthpediatric strokePreferred Reporting Items for Systematic Reviews and Meta-AnalysesPRISMAsickle cell diseasestroke preventionstroke screening

Identifiers

PMID41941725
PMCPMC13053000

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.