Eradication Therapy for Helicobacter pylori Infection in Patients Receiving Hemodialysis: Review

Author:

Sahara Shu1ORCID,Sugimoto Mitsushige2,Murata Masaki3ORCID,Iwata Eri4,Kawai Takashi4,Murakami Kazunari5ORCID,Yamaoka Yoshio6ORCID,Shimoyama Tadashi7

Affiliation:

1. Department of Gastroenterology Hamamatsu Medical Center Hamamatsu Japan

2. Division of Genome‐Wide Infectious Diseases, Research Center for GLOBAL and LOCAL Infectious Disease Oita University Yufu Japan

3. Department of Gastroenterology National Hospital Organization Kyoto Medical Center Kyoto Japan

4. Department of Gastroenterological Endoscopy Tokyo Medical University Hospital Shinjuku Japan

5. Department of Gastroenterology Oita University Yufu Japan

6. Department of Environmental and Preventive Medicine Oita University Yufu Japan

7. Aomori General Health Examination Center Aomori Japan

Abstract

ABSTRACTPatients receiving hemodialysis (HD) often develop gastrointestinal diseases. Recently, although in general population, clinical guidelines for Helicobacter pylori have strongly recommended its eradication in patients to prevent gastric cancer, optimal eradication regimen and optimal dosage of drugs for patients receiving HD have not been established, due to possible incidence of adverse events. Some antimicrobial agents used in eradication therapy, particularly amoxicillin, can exacerbate renal dysfunction. Given the delayed pharmacokinetics of drugs in patients receiving HD compared with those in healthy individuals, drug regimen and dosage should be considered to minimize adverse effects. Although previous studies have investigated the benefits of eradication therapy for patients receiving HD, because most studies were small in terms of the number of enrolled patients, it is hard to show evidence. The numbers of eradication in HD patients have recently increased, and it is important to provide an optimal regimen. The consideration of eradication in patients undergoing HD with a reduction in the drug dose by 1/2–1/3 may prevent adverse events. Additionally, another important consideration is whether adverse events can be prevented while maintaining a similar eradication rate with reduced drug dosages. Recent meta‐analysis findings indicate comparable eradication rates in patients receiving HD and healthy individuals, both with the same dosage regimen and at a reduced dosage regimen, with no significant differences (relative risk [RR] for successful eradication: 0.85 [95% confidence interval (CI): 0.48–1.50]). Unlike with the same dosage regimen (RR for adverse events: 3.15 [95% CI: 1.93–5.13]), the adverse events in the dosage reduction regimen were similar to those in healthy individuals (RR: 1.26 [95% CI: 0.23–6.99]). From a pharmacological perspective, the eradication regimen in patients receiving HD should consider the dosage (1/2–1/3 dosage), dosing number (bid), dosing timing of drugs (after HD), and susceptibility to antimicrobial agents.

Publisher

Wiley

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