» Articles » PMID: 36458050

Update on the First-line Treatment of Infection in Areas with High and Low Clarithromycin Resistances

Overview
Publisher Sage Publications
Specialty Gastroenterology
Date 2022 Dec 2
PMID 36458050
Authors
Affiliations
Soon will be listed here.
Abstract

Current international consensuses on eradication therapy recommend that only regimens that reliably produce eradication rates of ⩾90% should be used for empirical treatment. The Real-world Practice & Expectation of Asia-Pacific Physicians and Patients in Eradication Survey also showed that the accepted minimal eradication rate in -infected patients was 91%. According to efficacy prediction model, the per-protocol eradication rates of 7-day and 14-day standard triple therapies fall below 90% when clarithromycin resistance rate ⩾5%. Several strategies including bismuth-containing, non-bismuth-containing quadruple therapies (including sequential, concomitant, hybrid and reverse hybrid therapies), high-dose dual therapy and vonoprazan-based triple therapy have been proposed to increase the eradication rate of infection. According to efficacy prediction model, the eradication rate of 14-day concomitant therapy, 14-day hybrid therapy and 7-day vonoprazan-based triple therapy is less than 90% if the frequency of clarithromycin-resistant strains is higher than 90%, 58% and 23%, respectively. To meet the recommendation of the consensus report and patients' expectation, local surveillance networks for resistance of to clarithromycin are required to select appropriate eradication regimens in each geographic region. In areas with low (<5%) clarithromycin resistance (e.g. Sweden, Philippine, Myanmar and Bhutan), 7-day and 14-day standard triple therapies can be adopted for the first-line treatment of infection with eradication rates of ⩾90%. In areas with high (⩾5%) clarithromycin resistance (most other countries worldwide) or unknown clarithromycin resistance, 14-day hybrid, 14-day reverse hybrid, 14-day concomitant and 10- to 14-day bismuth quadruple therapy can be used to treat infection.

Citing Articles

In Silico Identification of Potential Clovibactin-like Antibiotics Binding to Unique Cell Wall Precursors in Diverse Gram-Positive Bacterial Strains.

Sierra-Hernandez O, Saurith-Coronell O, Rodriguez-Macias J, Marquez E, Mora J, Paz J Int J Mol Sci. 2025; 26(4).

PMID: 40004190 PMC: 11855776. DOI: 10.3390/ijms26041724.


Genomic insights into the antimicrobial resistance and virulence of Helicobacter pylori isolates from gastritis patients in Pereira, Colombia.

Alvarez-Aldana A, Ikhimiukor O, Guaca-Gonzalez Y, Montoya-Giraldo M, Souza S, Buiatte A BMC Genomics. 2024; 25(1):843.

PMID: 39251950 PMC: 11382513. DOI: 10.1186/s12864-024-10749-6.


Efficacy and safety of vonoprazan-amoxicillin dual therapy for first-line treatment: a single-center, randomized, controlled trial.

Wang X, Teng G, Dong X, Dai Y, Wang W Therap Adv Gastroenterol. 2023; 16:17562848231190976.

PMID: 37664169 PMC: 10469240. DOI: 10.1177/17562848231190976.


Targeted delivery of a short antimicrobial peptide (CM11) against Helicobacter pylori gastric infection using concanavalin A-coated chitosan nanoparticles.

Moosazadeh Moghaddam M, Bolouri S, Golmohammadi R, Fasihi-Ramandi M, Heiat M, Mirnejad R J Mater Sci Mater Med. 2023; 34(9):44.

PMID: 37650975 PMC: 10471652. DOI: 10.1007/s10856-023-06748-w.


The Efficacy and Safety of 14-day Rabeprazole Plus Amoxicillin High Dose Dual Therapy by Comparing to 14-day Rabeprazole-Containing Hybrid Therapy for the Naïve Helicobacter pylori Infection in Taiwan: A Randomized Controlled Trial.

Tai W, Yang S, Yao C, Wu C, Liu A, Lee C Infect Dis Ther. 2023; 12(5):1415-1427.

PMID: 37133673 PMC: 10229508. DOI: 10.1007/s40121-023-00811-3.


References
1.
Tepes B, Vujasinovic M, Seruga M, Stefanovic M, Forte A, Jeverica S . Randomized clinical trial comparing 10-day sequential, 7-day concomitant and 7-day standard triple therapies for Helicobacter pylori eradication. Eur J Gastroenterol Hepatol. 2016; 28(6):676-83. DOI: 10.1097/MEG.0000000000000590. View

2.
Kuo Y, Liou J, El-Omar E, Wu J, Leow A, Goh K . Primary antibiotic resistance in Helicobacter pylori in the Asia-Pacific region: a systematic review and meta-analysis. Lancet Gastroenterol Hepatol. 2017; 2(10):707-715. DOI: 10.1016/S2468-1253(17)30219-4. View

3.
Sardarian H, Fakheri H, Hosseini V, Taghvaei T, Maleki I, Mokhtare M . Comparison of hybrid and sequential therapies for Helicobacter pylori eradication in Iran: a prospective randomized trial. Helicobacter. 2012; 18(2):129-34. DOI: 10.1111/hel.12017. View

4.
Sugimoto M, Furuta T, Shirai N, Kajimura M, Hishida A, Sakurai M . Different dosage regimens of rabeprazole for nocturnal gastric acid inhibition in relation to cytochrome P450 2C19 genotype status. Clin Pharmacol Ther. 2004; 76(4):290-301. DOI: 10.1016/j.clpt.2004.06.008. View

5.
De Francesco V, Margiotta M, Zullo A, Hassan C, Troiani L, Burattini O . Clarithromycin-resistant genotypes and eradication of Helicobacter pylori. Ann Intern Med. 2006; 144(2):94-100. DOI: 10.7326/0003-4819-144-2-200601170-00006. View