Disease
Treatment
H. pylori eradication therapy is a matter of continuing debate. The number and type of combinations are innumerable. The data accumulated in this area is a matter of much confusion for a practitioner faced with such a common problem. The first rule is not to use a single agent for treatment. All single agents have given eradication rates below 50% and are not acceptable in clinical management. The second rule is to use a strong acid suppressant drug along with antibiotic combination. Hypochlorhydria during antibiotic therapy enhances H. pylori eradication rates. Of great importance is the data that strong acid suppressant therapy, particularly with proton pump inhibitors (PPIs), overcomes resistance to metronidazole and possibly other antibiotics. Thirdly, antibiotic sensitivity pattern of H. pylori in the geographical region of practice needs to be kept in mind.87-98

Over the years, the two combinations, which have shown consistently high eradication rates are shown. Most European studies use one-week triple therapy while North American studies use two -week therapy for high eradication rates. A recently introduced combination popularly named the RBC-based triple therapy combines ranitidine and bismuth and two antibiotics, namely, clarithromycin and amoxicillin. This combination has given consistently high eradication rate comparable to standard triple therapy (Table 2). Antibiotic resistance to H. pylori is a problem, which shall become of great significance in future. To date, metronidazole resistance is seen in a high percentage of patients particularly in developing countries.

Clarithromycin resistance occurs from 1%-12% of patients and amoxicillin resistance is rare. Is antibiotic resistance of clinical importance as of today? Data show that when there is no resistance, eradication rates approach 100%. When there is resistance to one antibiotic, the risk of treatment failure increases, but eradication rates remain high and clinically acceptable. Resistance to two agents drops the eradication rate to less than 50%. Of significance is the data that PPI therapy does overcome a high degree resistance to metronidazole and clarithromycin. Metronidazole resistance is defined as minimal inhibitory concentration (MIC) of 8 ug/mL or more. However, there is no clear association between resistance and treatment failures until MIC is above 32 ug/mL. Clarithromycin resistance is defined as MIC of 1 ug/mL or more. Treatment failures occur only when clarithromycin resistance reaches a high grade with MIC of 128 ug/mL.87

The high prevalence of H. pylori infection in the world, its implications in the appearance of gastric malignancies and the emergence of antibiotic resistance demand that prophylactic and new measures are developed against this infection. Two types of oral vaccines are being intensely studied. Candidate preventive vaccines include crude sonicates of Helicobacter felis and recombinant subunits of enzyme urease and catalase. A human vaccine using urease and heat labile enterotoxin of E. coli is already under field trial. Candidate treatment vaccine has had success in infected mice and clears the infection by hosting an immune response. The oral antigens used in these two types of vaccines have been shown to result in T-helper cell-2 driven immune response, which in turn stimulates Blymphocytes. Natural immunity to H. pylori in contrast is a T-helper-1 driven response, which has no value in clearing or preventing the infection.99-100 H pylori status in the Middle East
The prevalence of H. pylori in the Middle Eastern population is around 60%. The epidemiology of the infection in this region resembles those of many other developing countries.101 It is significant that standard PPIbased triple therapy for one or two weeks gives H. pylori eradication rate of 65% at best. This low eradication rate was exclusively related to high percentage and high-grade resistance to first-line antibiotics used in the therapy (Figure 5). In view of the above, newer drug combinations need to be explored for H. pylori eradication therapy in this region.102
 
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