Evidence map›Paper›PMID 41088538›Full record

ArticleHelicobacter

Empirical Rescue Eradication Therapy for Helicobacter pylori Infection in Second and Subsequent Treatment Lines: Experience From 500 Cases of the Brazilian Registry on H. pylori Management (Hp-BrazilReg).

B S F Sanches, O P Nyssen, S R Chaves, J S Veloso, L S Silva, J R Marinho, H Okamoto, G C Couto, H P Breyer, C S Alencar and 41 more

Abstract readMulticenter Study
In one paragraph

Article in Helicobacter. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Tetracycline for Helicobacter pylori eradication: a narrative review from quadruple to dual therapy.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Review
  2. Article
  3. Article
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

51 authors.

B S F SanchesUniversidade Federal de Minas Gerais, Belo Horizonte, Brazil.ORCID https://orcid.org/0000-0003-0193-6292
O P NyssenGastroenterology Unit, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Universidad Autónoma de Madrid (UAM), and Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain.
S R ChavesUniversidade Federal de Minas Gerais, Belo Horizonte, Brazil.
J S VelosoHospital Santa Helena, Brasilia, Brazil.
L S SilvaHospital Adventista de Manaus, Manaus, Brazil.
J R MarinhoUniversidade Estadual de Ciências da Saúde de Alagoas, Maceio, Brazil.
H OkamotoCentro Medico Oxford, São Bento do Sul, Brazil.
G C CoutoCentro de Consultas Especializadas, Contagem, Brazil.
H P BreyerHospital de Clinicas/Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
C S AlencarClinicas Reunidas São Victor, Rio de Janeiro, Brazil.
E ComelliClinica Castromed, Castro, Brazil.
L S SousaCoopclin, Recife, Brazil.
M HornClinica Endocentro, Florianopolis, Brazil.
M G MassoteUnidade de Saúde, Santos, Brazil.
M T R LouresHospital Nossa Senhora das Graças, Curitiba, Brazil.
M P VidalHospital Ana Costa, Santos, Brazil.
R V PaulaPrivate Practice, Aracaju, Brazil.
L T RibeiroHospital Universitário Prof. Alberto Antunes, Maceio, Brazil.
H O GalizziHepscan, Belo Horizonte, Brazil.
D A A TerraInstituto Alfa de Gastroenterologia/Hospital das Clínicas/Ebserh-UFMG, Belo Horizonte, Brazil.
G G L CançadoHospital Militar de Minas Gerais, Belo Horizonte, Brazil.
B P BurmannMedPlus, Porto Alegre, Brazil.
J S CaetanoHospital São Rafael, Salvador, Brazil.
L F PenaSocor, Belo Horizonte, Brazil.
M A DecanioHospital Português, Salvador, Brazil.
H S SouzaUniversidade Federal Do Rio de Janeiro, Belo Horizonte, Brazil.ORCID https://orcid.org/0000-0002-3647-7324
A S O KuniyoshiUniversidade Estadual de Maringá, Maringá, Brazil.
L R GuedesRede Mater Dei de Saude, Belo Horizonte, Brazil.
M C F PassosInstituto Alfa de Gastroenterologia/Hospital das Clínicas/Ebserh-UFMG, Belo Horizonte, Brazil.
F P MarinhoInstituto Alfa de Gastroenterologia/Hospital das Clínicas/Ebserh-UFMG, Belo Horizonte, Brazil.
I Z BombassaroSanta Casa de Misericordia de Porto Alegre, Porto Alegre, Brazil.
A G DominguesPrivate Practice, Rio de Janeiro, Brazil.
J G BarbosaSanta Casa de Barretos, Barretos, Brazil.
I M NogueiraPrivate Practice, São Paulo, Brazil.
A F P RamosGrupo Santa Casa de Belo Horizonte, Belo Horizonte, Brazil.
D R KormanHospital Militar de Minas Gerais, Belo Horizonte, Brazil.
T B SouzaFaculdades Integradas de Patos, Patos, Brazil.
M C BarbosaPrivate Practice, Arapiraca, Brazil.
D ChinzonUniversidade de São Paulo, São Paulo, Brazil.
L L SilvaMonte Sinai Hospital e Maternidade, Juiz de Fora, Brazil.
A MantovaniUniversidade Do Vale Do Rio dos Sinos, Porto Alegre, Brazil.
A H A FreitasUnimed Sul Capixaba, Cachoeiro Do Itapemirim, Brazil.
C S PoncinelliBiogastro, Belo Horizonte, Brazil.
M A FrancatoHospital Municipal Antonio Giglio, Osasco, Brazil.
J N GoncalvesUniversidade Federal de Minas Gerais, Belo Horizonte, Brazil.
P ParraGastroenterology Unit, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Universidad Autónoma de Madrid (UAM), and Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain.
A Cano-CatalàGastrointestinal Oncology, Endoscopy and Surgery (GOES) Research Group, Althaia Xarxa Assistencial Universitària de Manresa, Institut de Recerca i Innovació en Ciències de la Vida i de la Salut de la Catalunya Central (IRIS-CC), Manresa, Spain.
L MoreiraDepartment of Gastroenterology, Hospital Clínic de Barcelona, Centro de Investigación Biomédica en Red en Enfermedades Hepáticas y Digestivas (CIBERehd), Institut D'investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.
J P GisbertGastroenterology Unit, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Universidad Autónoma de Madrid (UAM), and Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain.ORCID https://orcid.org/0000-0003-2090-3445
Luiz Gonzaga Vaz CoelhoInstituto Alfa de Gastroenterologia/Hospital das Clínicas/Ebserh-UFMG, Belo Horizonte, Brazil.
Hp‐BrazilReg

Funding

Núcleo Brasileiro para estudo do Helicobacter pylori e Microbiota 01.817.342/0001-61
6 · The paper itself

Abstract

backgroundThe effectiveness of anti-H. pylori treatment diminishes with therapy failure, making regional performance understanding crucial.

objectiveTo evaluate the effectiveness of empirical therapy in second-line and subsequent treatments in Brazil.

methodsA multicenter, prospective, noninterventional registry assessed H. pylori management outcomes by Brazilian gastroenterologists (Hp-BrazilRe, Hp-WorldReg's partner). Data were registered at e-CRF AEG-ReCap from March 2022 to October 2024 and analyzed via modified intention-to-treat (mITT) methodology. Data were subject to quality review.

results572 patients (mean age 52 years, 64% women) were included. The primary treatment indications were dyspepsia (64%) and gastroduodenal ulcer (9.2%). Among them, 67% underwent second-line therapy, while 33% received third-line or subsequent treatments. Proton-pump inhibitors (PPIs) were administered at low (40%), standard (10%), and high doses (24%), with vonoprazan used in 26% of cases. The overall eradication rate for second-line treatment was 74%, with the most common regimen being triple therapy (PPI + amoxicillin + levofloxacin), achieving 73% eradication for 14 days and 57% for 10 days. Adding bismuth to the 14-day regimen increased effectiveness to 100% (p = 0.016). In third-line therapy, a regimen of PPI-bismuth-tetracycline-metronidazole yielded an 87% cure rate. The fourth-line dual therapy with amoxicillin-vonoprazan achieved 100% eradication, while bismuth-quadruple therapy showed similar results. Dual therapy with vonoprazan and amoxicillin was also effective in fifth-line treatments, achieving 100% effectiveness. Mild adverse events occurred in 23% of patients, with nausea being the most common (14%), and compliance was 99%.

conclusionIn Brazil, the overall effectiveness of second-line therapy was suboptimal (< 90%); however, the combination of bismuth-amoxicillin-levofloxacin prescribed for 14 days reported successful cure rates. In the third-line, the classical bismuth-quadruple therapy with metronidazole-tetracycline provided acceptable results (87%). Alternatively, dual therapy with vonoprazan and amoxicillin and rifabutin-based bismuth-quadruple therapy showed promising results in third- and fifth-line rescue treatment.

Indexed as

Anti-Bacterial AgentsHelicobacter InfectionsHelicobacter pyloriAdultAgedAmoxicillinBrazilDrug Therapy, CombinationFemaleHumansMaleMiddle AgedProspective StudiesProton Pump InhibitorsPyrrolesRegistries1-(5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl)-N-methylmethanamineAmoxicillinAnti-Bacterial AgentsProton Pump InhibitorsPyrrolesSulfonamidesempirical treatmentHelicobacter pyloriregistryretreatmenttreatment failure

Identifiers

PMID41088538
PMCPMC12521799

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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.