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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>An open-label randomized controlled trial comparing the efficacy and safety of a 7-day triple therapy with bismuth versus 14-day standard triple therapy for Helicobacter pylori eradication in children and adolescents</dc:title><dc:creator>Šterbenc,	Anja	(Avtor)
	</dc:creator><dc:creator>Vratanar,	Bor	(Avtor)
	</dc:creator><dc:creator>Miler Mojškerc,	Eva	(Avtor)
	</dc:creator><dc:creator>Homan,	Matjaž	(Avtor)
	</dc:creator><dc:subject>treatment</dc:subject><dc:subject>eradication</dc:subject><dc:subject>Helicobacter pylori</dc:subject><dc:subject>bismuth</dc:subject><dc:subject>children</dc:subject><dc:description>Background: To achieve eradication rates &gt;90%, the ESPGHAN/NASPGHAN guidelines for pediatric Helicobacter pylori infection recommend tailored antimicrobial therapy using sufficiently high doses over 10–14days. However, prolonged treatment often leads to suboptimal compliance in children, which is a major contributor to reduced eradication rates. To address this, we evaluated the efficacy and safety of a shorter, 7day triple therapy with bismuth compared with the 14day standard triple therapy without bismuth in H. pylori infected children.
Materials and Methods: From 2020 to 2024, we carried out a randomized controlled trial involving treatment-naïve children and adolescents (5–18 years old) with confirmed H. pylori infection. Eligible participants were randomly allocated to receive either a 7day triple therapy with bismuth (bismuth subcitrate, a proton pump inhibitor [PPI], amoxicillin, plus clarithromycin/ metronidazole) or a 14day standard triple therapy (a PPI, amoxicillin, plus clarithromycin/metronidazole) without bismuth. Two months after completing therapy, treatment success was determined using either a two-step monoclonal stool antigen assay or a urea breath test. Any adverse events were documented using a structured questionnaire.
Results: Seventy-three children were enrolled in the study. In the intention-to-treat analysis, eradication was achieved in 91% of children treated with the 7day triple therapy with bismuth and 87% of those receiving the 14day standard triple therapy (p=0.695). Per-protocol eradication rates were 94% and 87%, respectively (p=0.418). No serious adverse events were reported, and most adverse events were mild to moderate. A metallic taste was significantly more frequent in the 14day standard triple therapy group, while other adverse events occurred with similar frequency.
Conclusions: Adding bismuth to a 7day triple regimen achieved high eradication rates and a safety profile similar to 14day standard triple therapy, supporting its use as an effective and safe treatment option for pediatric H. pylori infection.</dc:description><dc:date>2026</dc:date><dc:date>2026-01-12 13:19:23</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>177896</dc:identifier><dc:identifier>UDK: 616.3</dc:identifier><dc:identifier>ISSN pri članku: 1523-5378</dc:identifier><dc:identifier>DOI: 10.1111/hel.70103</dc:identifier><dc:identifier>COBISS_ID: 264152579</dc:identifier><dc:language>sl</dc:language></metadata>
