Evidence map›Paper›PMID 42707434›Full record

SynthesisFrontiers in microbiology2026

Comparative efficacy and safety of vonoprazan-based dual therapy vs. bismuth-based quadruple therapy for

Alejandro Chen Liang, Yeison Cruz Castillo, Lorena M Murrieta Bruciaga, Barbara Abreu Lopez, Salma Beltrán Covarrubias, Hector Jonan Flores Uribe, Vanessa Pamela Salolin-Vargas, Gabriela Flores Monar, José García-Corella, Ishaan Kalha and 1 more

Abstract readSystematic Review
In one paragraph

Synthesis in Frontiers in microbiology, 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

11 authors.

Alejandro Chen LiangCentro de Estudios Universitarios Xochicalco, Campus Tijuana, Tijuana, México.
Yeison Cruz CastilloUniversidad Autónoma de Santo Domingo, Santo Domingo, República Dominicana.
Lorena M Murrieta BruciagaUniversidad del Valle de México, Hermosillo, México.
Barbara Abreu LopezMaimonides Medical Center, New York, NY, United States.
Salma Beltrán CovarrubiasUniversidad de Guadalajara, Guadalajara, México.
Hector Jonan Flores UribeCentro de Estudios Universitarios Xochicalco, Campus Tijuana, Tijuana, México.
Vanessa Pamela Salolin-VargasFacultad de Medicina, Universidad Westhill, Ciudad de México, México.
Gabriela Flores MonarUniversity of Miami/Jackson Health System, Miami, FL, United States.
José García-CorellaDepartment of Medicine, UCLA-Kern Medical, Bakersfield, CA y David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
Ishaan KalhaDivision of Gastroenterology, Department of Medicine, UCLA-Kern Medical, Bakersfield, CA y David Geffen School of Medicine at UCLA, Los Angeles, CA, United States.
Ernesto Calderon MartinezTexas Tech University Health Sciences Center El Paso, El Paso, TX, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Methods: A systematic search of PubMed/MEDLINE, EMBASE, Web of Science, CINAHL, Google Scholar, and the Cochrane Library was conducted through April 2026 (PROSPERO: CRD420251108849) for randomized controlled trials (RCTs). All comparator arms were restricted to conventional PPI-based BQT. Outcomes included eradication rate, total adverse events (AE), nausea, diarrhea, treatment compliance, and bitter taste. Certainty of evidence was assessed using the GRADE approach and trial sequential analysis. Meta-analysis was performed using R software. Results: From 17,661 screened articles, 15 RCTs comprising 4,410 patients were included. Pooled eradication rates were 86.4% with VA and 85.0% with BQT, with no statistically significant difference (RR 1.03, 95% CI 1.00-1.07; Conclusion: VA dual therapy achieves eradication rates comparable to PPI-based BQT while offering a significantly more favorable tolerability profile, driven by fewer total AEs, less nausea, and less bitter taste. As all included trials were conducted in China, generalizability requires further investigation. These findings support VA dual therapy as a viable alternative for first-line

Indexed as

adverse eventsbismuth quadruple therapycomplianceeradication ratevonoprazan–amoxicillin dual therapy

Identifiers

PMID42707434
PMCPMC13547320

What OpenQuestion holds

Textmetadata
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.