Drug-Resistant Helicobacter pylori: Diagnosis and Evidence-Based Approach

Author:

Jearth Vaneet1,Rath Mitali Madhumita2,Chatterjee Abhirup1,Kale Aditya3,Panigrahi Manas Kumar4ORCID

Affiliation:

1. Post Graduate Institute Medical Education and Research, Chandigarh 160012, India

2. Hi-Tech Medical College and Hospital, Bhubaneswar 751010, India

3. Tata Memorial Hospital, Mumbai 400012, India

4. All India Institute of Medical Sciences, Bhubaneswar 751019, India

Abstract

Helicobacter pylori (H. pylori) is the most common chronic bacterial infection, affecting approximately half of the world’s population. H. pylori is a Class I carcinogen according to the World Health Organization, and the International Agency for Research on Cancer (IARC) has linked it to 90% of stomach cancer cases worldwide. The overall pattern points to a yearly reduction in eradication rates of H. pylori with the likelihood of success further decreasing after each unsuccessful therapeutic effort. Antimicrobial resistance in Helicobacter pylori is a major public health concern and is a predominant cause attributed to eradication failure. As a result, determining H. pylori’s antibiotic susceptibility prior to the administration of eradication regimens becomes increasingly critical. Detecting H. pylori and its antimicrobial resistance has traditionally been accomplished by time-consuming culture and phenotypic drug susceptibility testing. The resistance of H. pylori to different antibiotics is caused by various molecular mechanisms, and advances in sequencing technology have greatly facilitated the testing of antibiotic susceptibility to H. pylori. This review will summarize H. pylori antibiotic resistance patterns, mechanisms, and clinical implications. We will also review the pros and cons of current antibiotic susceptibility testing methods. Along with a comparison of tailored susceptibility-guided regimens and empirical therapy based on the latest evidence, an evidence-based approach to such situations will be explored.

Publisher

MDPI AG

Subject

Clinical Biochemistry

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