Evidence map›Paper›PMID 39131120›Full record

ArticleGastro hep advances2022

Two-dimension Tailor-made Therapy: A New Salvage Therapy After Multiple Eradication Failures for

Shigemi Nakajima, Hisayuki Inoue, Hiroshi Satake, Rena Chatani, Mariko Ohara, Yuki Tsubakimoto, Makoto Fujii, Hiroshi Hasegawa, Keiko Takahashi, Kiyoyuki Hayafuji and 1 more

Abstract read
In one paragraph

Article in Gastro hep advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Observational
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.

Shigemi NakajimaConsortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Hisayuki InoueInoue Clinic, Moriyama, Shiga, Japan.
Hiroshi SatakeSatake Clinic, Kusatsu, Shiga, Japan.
Rena ChataniConsortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Mariko OharaConsortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Yuki TsubakimotoConsortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Makoto FujiiConsortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Hiroshi HasegawaConsortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Keiko TakahashiConsortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Kiyoyuki HayafujiConsortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.
Yoshihide FujiyamaConsortium for Community Medicine, Shiga University of Medical Science, Otsu, Shiga, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Vonoprazan-based eradication therapies have a higher eradication rate than usual proton pump inhibitor (PPI)-based therapies in treating Methods: Patients who failed twice or more PPI-based triple therapies were recruited. Patients underwent CYP2C19 genotype and antibiotic susceptibility tests (ASTs). PPI doses per day were decided as per the CYP2C19 genotype: twice for poor and 4 times for extensive metabolizers (dimension 1). Two antibiotics were selected as per the results of the AST in each patient (dimension 2). Regimens of 2dTMT included 2 susceptible antibiotics and a PPI. For those who could not have enough information with the AST, tailor-made PPI dosing was indicated with empirically selected 2 antibiotics (one-dimension tailor-made therapy [1dTMT]). Results: Of 51 candidates with multiple eradication failures, 37 patients underwent the genotype test and AST, and 24 succeeded to obtain sufficient information to select 2 susceptible antibiotics. Of them, 22 patients accepted to receive 14-day 2dTMT. Of the residual patients, 12 accepted to receive 14-day 1dTMT. The mean eradication rate of 2dTMT was 86.4% (95% confidence interval [CI]: 65.1%-98.8%) in intention-to-treat and 90.5% (95% CI: 69.6%-98.8%) in per-protocol analyses, whereas that of 1dTMT was 75.0% (95% CI: 42.8%-94.5%) in intention-to-treat and 90.0% (95% CI: 55.5%-99.7%) in per-protocol analyses. Conclusion: Without vonoprazan, 14-day 2dTMT could be one of the salvage therapies for patients with multiple eradication failures. In cases of insufficient information with the AST, 14-day 1dTMT could be an alternative therapy. Clinical Trials Registry number, UMIN000022154 (https://www.umin.ac.jp/icdr/index.html).

Indexed as

Antibiotics Susceptibility TestCYP2C19 GenotypeProton Pump InhibitorThird-line TherapyVonoprazan

Identifiers

PMID39131120
PMCPMC11308230

What OpenQuestion holds

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Registered trials

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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.