Esps manuscript no: 18744 Manuscript Type: topic highlight 2015 Advances in Helicobacter pylori



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UPDATED H.PYLORI THERAPY

Successful eradication of H. pylori is a major component in treating these conditions[95]. However, the rate of H. pylori eradication after triple therapy is decreasing, with standard amoxicillin plus clarithromycin-based triple therapy achieving eradication rates of only approximately 75% in many series[96-97]. Apart from the conventional first-line regimen (triple therapy), other therapies have been proposed (sequential, concomitant, quadruple, and miscellaneous) to face the growing problem of antibiotic resistance. Although unsuccessful eradication can be caused by increasing antimicrobial resistance, an additional critical contributor is the treatment-related side effects and resultant incomplete therapy. New treatment regimens for H. pylori infections should be optimized to achieve an eradication rate of ≥ 95%[98]. Patient allergies and the local availability of drugs should be considered when selecting a treatment. H. pylori eradication should be confirmed after treatment, and, if second-line therapy is required, clarithromycin or a fluoroquinolone should not be reused[99].


Sequential therapy

First developed in Italy in the 1990s, sequential therapy (5-d PPI and amoxicillin, followed by 5-d PPI, clarithromycin, and metronidazole), is a regimen that has proven more effective in eradicating H. pylori than has triple therapy in many studies[100-104]. Recent multicenter randomized trials conducted in Taiwan have shown the superiority of sequential therapy over standard triple therapy. These findings also support that the most effective eradication regimen should be chosen on the basis of the prevalence of antibiotic-resistant H. pylori in a region[105]. The ability of sequential therapy to eradicate clarithromycin-resistant bacteria has been demonstrated, and sequential therapy has been included in a recent consensus report as a valid first-line option for eradicating H. pylori in geographic regions with high clarithromycin resistance[106].


Hybrid and concomitant therapy

Two novel eradication regimens, namely concomitant and hybrid therapy, have proven more effective than triple and sequential therapy in the last few years, particularly in patients with dual- (clarithromycin- and metronidazole-) resistant H. pylori strains[107-111]. Meta-analyses have shown that the outcome of concomitant therapy is duration-dependent[112]. Molina-Infante et al[113] proposed that optimized nonbismuth quadruple hybrid (consisting of omeprazole 40 mg twice daily and amoxicillin 1 g twice daily for 14 d, plus clarithromycin 500 mg twice daily and nitroimidazole 500 mg twice daily for the final 7 d as a quadruple therapy) and concomitant (consisting of omeprazole 40 mg twice daily, amoxicillin 1 g twice daily, clarithromycin 500 mg twice daily, and nitroimidazole 500 mg twice daily, all concurrently for 14 d) therapies cured more than 90% of patients with H. pylori infections in areas of high clarithromycin and metronidazole resistance. In concomitant therapy, all four drugs are administered for the entire therapy duration, indicating that this regimen is less complex than sequential therapy because it does not involve changing the number or type of drugs halfway through the therapy. A recently proposed hybrid therapy has proven as effective as a 14-d concomitant regimen in a pilot study[106].


High-dose amoxicillin therapy

The efficacy of treatment for H. pylori infection has decreased steadily because of increasing resistance to clarithromycin, metronidazole, and levofloxacin. Resistance to amoxicillin is generally low, and high intragastric pH increases the efficacy of amoxicillin. Therefore, Yang et al[114] proposed that a combination of a high-dose PPI and amoxicillin (dual therapy), consisting of rabeprazole (20 mg, four times daily) and amoxicillin (750 mg, four times daily) for 14 d, is superior to standard regimens as empirical first-line or rescue therapies for H. pylori infection and has similar safety profiles and tolerability.


Bismuth-based quadruple therapy

During the initial development of bismuth quadruple therapy, the dose and duration of bismuth therapy were shown to be crucial variables, particularly in regions where metronidazole resistance was common[115]. However, many studies on these regimens have used suboptimal doses and durations of bismuth therapy, producing relatively poor results[116]. Bismuth-containing quadruple therapy is an alternative to standard triple therapy in areas with low clarithromycin resistance and the main first-line therapeutic option in areas with high prevalence of clarithromycin resistance. Using this regimen at full doses for 14 d produces a 95% or greater treatment success rate, irrespective of the level of metronidazole resistance[117].


Salvage therapy

Tailored antimicrobial therapy for an infectious disease is typically selected on the basis of susceptibility testing[99,118]. The treatment of H. pylori infection differs from that of most common infectious diseases because culture and susceptibility testing is generally not offered for H. pylori infections by hospital laboratories. In addition, many H. pylori infections can be identified using noninvasive testing (such as UBT or stool antigen testing), indicating that endoscopies are neither necessary nor acceptable to patients, and clinicians must choose treatment empirically. Therefore, culture and susceptibility testing should be performed before third-line treatment[106]. Salvage therapy (after multiple treatment failures) should be chosen on the basis of susceptibility testing whenever possible[101].


Probiotic therapy

Song et al[119] proposed that supplementation with Saccharomyces boulardii could be effective for improving H. pylori eradication rates by reducing side effects, thus facilitating completion of eradication therapy. Probiotics are mostly administered by modulating the balance of its microflora[120]. Probiotic adjunct therapy is particularly useful in patients with a history of GI intolerance to antibiotic treatment[121]. These effects have been demonstrated for several species of probiotics, including Lactobacillus acidophilus, Lactobacillus salivarius, Lactobacillus rhamnosus, and Bifidobacterium bifidum, among others[122-124]. Proposed mechanisms include modulating the colonization of the gastric mucosa and the direct killing of H. pylori through secreted metabolites with antimicrobial properties[95]. The lack of protocol standardization is problematic, and interpreting the various results is difficult.


CONCLUSION

Although other factors influence the onset of peptic ulcer and recurrent peptic ulcer in ESRD and cirrhotic patients, H. pylori eradication therapy is the primary method of treating ESRD and cirrhotic patients with peptic ulcers. Culture susceptibility testing before first- or second-line therapy is unadvisable. The known obstacles to culture susceptibility testing include the need for endoscopic examination and the fact that culture is time-consuming, costly, and not 100% sensitive. Using highly effective empiric first-line and rescue regimens can yield acceptable results[100,97,125]. In the near future, in vivo and in vitro studies may possibly be grouped according to geographic area to identify the most effective therapy for eradicating H. pylori, which relates to the local habitat.


ACKNOWLEDGEMENTS

We wish to thank the Taiwan Ministry of Education for their support for this work through its “Aim for the Top University Plan.”




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