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eISSN: 2581-9615 || CODEN: WJARAI || Impact Factor 8.2 ||  CrossRef DOI

Research and review articles are invited for publication in March 2026 (Volume 29, Issue 3) Submit manuscript

Therapies for Inherited Epidermolysis Bullosa in Indonesia, 2015–2025: A Systematic Review

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  • Therapies for Inherited Epidermolysis Bullosa in Indonesia, 2015–2025: A Systematic Review

Kinesha Kostya 1, Yuri Widia 2, *, Pepy Dwi Endraswari 3 and Sawitri 4

1 Medical Programme, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.

2 Department/Functional Medical Staff of Dermatology and Venereology, Faculty of Medicine Universitas Airlangga/ Universitas Airlangga Teaching Hospital Surabaya, Indonesia.

3 Department/Functional Medical Staff of Clinical Microbiology, Faculty of Medicine Universitas Airlangga/Dr. Soetomo General Academic Hospital, Surabaya, Indonesia.

4 Department/Functional Medical Staff of Dermatology and Venereology, Faculty of Medicine Universitas Airlangga/Dr. Soetomo General Academic Hospital, Surabaya, Indonesia.

Review Article

World Journal of Advanced Research and Reviews, 2025, 28(02), 2513-2523

Article DOI: 10.30574/wjarr.2025.28.2.3982

DOI url: https://doi.org/10.30574/wjarr.2025.28.2.3982

Received 15 October 2025; revised on 26 November 2025; accepted on 29 November 2025

Background: Inherited epidermolysis bullosa (EB) is a genetic disorder that involves skin fragility caused by structural damage of the sin. In Indonesia, the multidisciplinary care and advanced wound therapies are still limited. A systematic evaluation of published Indonesian EB management strategies is needed to understand current practices and identify gaps in care.

Methods: This is a systematic review gathers case reports, case series, and observational studies from both Indonesian and international databases regarding inherited EB published from 2015 to 2025. Data were taken from each study based on variables such as study design, demographics, EB subtype, clinical features, treatments, and outcomes. Some findings such as clinical features, therapy given and outcomes are extracted narratively because of heterogenicity of the data. Study selection followed PRISMA guidelines.

Results: Thirteen studies were found and reported cases of EBS, DEB, JEB and unclassified EB with clinical findings of extensive blistering, chronic wounds, malnutrition, anemia, infections, and mucosal involvement. Most treatments of wound care (saline compress, petroleum jelly application, cold compresses, and non-adhesive or tulle dressings) resulted in improvements in pain, wound drying, and infection prevention. However, no studies reported the use of advanced wound products, genetic testing, or structured multidisciplinary care. Limited resource constraints and lack of standardized outcome measures were consistent challenges across all reports.

Conclusion: EB management in Indonesia mostly relies on supportive wound care, which is symptomatic treatment, but is still limited compared to international standards that usually prefer advanced dressings, genetic testing, and multidisciplinary care. Improving access to specialized wound-care materials, and developing national EB management pathways are important to bring better results. Future research should focus on cost-effective interventions, long-term monitoring, and standardized evaluation methods.

Epidermolysis Bullosa; Indonesia; Therapy; Systematic Review

https://wjarr.com/sites/default/files/fulltext_pdf/WJARR-2025-3982.pdf

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Kinesha Kostya, Yuri Widia, Pepy Dwi Endraswari and Sawitri. Therapies for Inherited Epidermolysis Bullosa in Indonesia, 2015–2025: A Systematic Review. World Journal of Advanced Research and Reviews, 2025, 28(2), 2513-2523. Article DOI: https://doi.org/10.30574/wjarr.2025.28.2.3982

Copyright © Author(s). All rights reserved. This article is published under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0), which permits use, sharing, adaptation, distribution, and reproduction in any medium or format, as long as appropriate credit is given to the original author(s) and source, a link to the license is provided, and any changes made are indicated.


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