S1436 From Bleeding to Healing: Unveiling the Efficacy and Safety of UI-EWD Hemostatic Powder in Gastrointestinal Bleeding—A Systematic Review and Meta-Analysis

Introduction: A novel endoscopic hemostatic adhesive powder (UI-EWD) was developed to cope with the high rebleeding rates associated with the current endoscopic hemostatic options for gastrointestinal bleeding. This meta-analysis aimed to assess the safety and effectiveness of UI-EWD hemostatic adhesive powder as a salvage treatment modality for upper and lower gastrointestinal bleeding. Methods: Electronic databases like PubMed, Cochrane Central and ScienceDirect were searched from inception to January 2025. This review followed the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines. The proportions were pooled with 95% Confidence Intervals (CI) using R version 4.2.3 and employing the “metaprop” package for the dichotomous outcomes. The primary and secondary outcomes of interest were clinical success, overall rebleeding, early rebleeding, delayed rebleeding, time to rebleeding, mortality and adverse events. The quality assessment was done through the Cochrane Risk of Bias (RoB) 2.0 tool and the Newcastle Ottawa Scale. The risk of publication bias was assessed visually through funnel plots and statistically through Egger’s regression test. Results: Three studies (including 2 trials and one cohort) with a total of 211 patients were included in this meta-analysis. The pooled clinical success rate was 98% (95% confidence interval [CI]: [85-100%]; I2 = 0%). The overall rebleeding rate was 11% (95% confidence interval: [0-93%]; I2 = 11.5%). The pooled rates of early and delayed rebleeding were 10% (95% CI: [1-51%]; I2 = 70.5%) and 9% (95% CI: [3-22%]; I2 = 0%) respectively. Conclusion: UI-EWD hemostatic adhesive powder demonstrates a high clinical success rate and relatively low overall rebleeding rates, making it an effective salvage treatment for gastrointestinal bleeding. The early and delayed rebleeding rates are manageable, with minimal heterogeneity observed in delayed rebleeding outcomes. These findings suggest UI-EWD is a promising and safe option for managing challenging bleeding cases.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001133204.35135.35
Primary Topic
Hemostasis and retained surgical items
Type
article
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0.00
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article

S1436 From Bleeding to Healing: Unveiling the Efficacy and Safety of UI-EWD Hemostatic Powder in Gastrointestinal Bleeding—A Systematic Review and Meta-Analysis

The American Journal of Gastroenterology
Hemostasis and retained surgical items
article

S1436 From Bleeding to Healing: Unveiling the Efficacy and Safety of UI-EWD Hemostatic Powder in Gastrointestinal Bleeding—A Systematic Review and Meta-Analysis

article en

Abstract

Introduction: A novel endoscopic hemostatic adhesive powder (UI-EWD) was developed to cope with the high rebleeding rates associated with the current endoscopic hemostatic options for gastrointestinal bleeding. This meta-analysis aimed to assess the safety and effectiveness of UI-EWD hemostatic adhesive powder as a salvage treatment modality for upper and lower gastrointestinal bleeding. Methods: Electronic databases like PubMed, Cochrane Central and ScienceDirect were searched from inception to January 2025. This review followed the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines. The proportions were pooled with 95% Confidence Intervals (CI) using R version 4.2.3 and employing the “metaprop” package for the dichotomous outcomes. The primary and secondary outcomes of interest were clinical success, overall rebleeding, early rebleeding, delayed rebleeding, time to rebleeding, mortality and adverse events. The quality assessment was done through the Cochrane Risk of Bias (RoB) 2.0 tool and the Newcastle Ottawa Scale. The risk of publication bias was assessed visually through funnel plots and statistically through Egger’s regression test. Results: Three studies (including 2 trials and one cohort) with a total of 211 patients were included in this meta-analysis. The pooled clinical success rate was 98% (95% confidence interval [CI]: [85-100%]; I2 = 0%). The overall rebleeding rate was 11% (95% confidence interval: [0-93%]; I2 = 11.5%). The pooled rates of early and delayed rebleeding were 10% (95% CI: [1-51%]; I2 = 70.5%) and 9% (95% CI: [3-22%]; I2 = 0%) respectively. Conclusion: UI-EWD hemostatic adhesive powder demonstrates a high clinical success rate and relatively low overall rebleeding rates, making it an effective salvage treatment for gastrointestinal bleeding. The early and delayed rebleeding rates are manageable, with minimal heterogeneity observed in delayed rebleeding outcomes. These findings suggest UI-EWD is a promising and safe option for managing challenging bleeding cases.

The American Journal of GastroenterologyVol. 120(10S2)
Good health and well-being
Openalex Percentile: Top 27%
Hemostasis and retained surgical items
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S1436 From Bleeding to Healing: Unveiling the Efficacy and Safety of UI-EWD Hemostatic Powder in Gastrointestinal Bleeding—A Systematic Review and Meta-Analysis · The American Journal of Gastroenterology (2025) | TGRS Research Map | TGRS