Helicobacter pylori eradication protocols
Helicobacter pylori eradication protocols is a standard name for all treatment protocols for peptic ulcers and gastritis; the primary goal is not only temporary relief of symptoms, but also total elimination of Helicobacter pylori infection.Patients with active duodena or gastric ulcers and those with a prior ulcer history should be tested for H. pylori. Appropriate therapy should be given for eradication. Patients with MALT lymphoma should also be tested and treated for H. pylori since eradication of this infection can induce remission in many patients when the tumor is limited to the stomach. Several consensus conferences, including the Maastricht Consensus Report, recommend testing and treating several other groups of patients but there is limited evidence of benefit. This includes patients diagnosed with gastric adenocarcinoma (especially those with early-stage disease), patients found to have atrophic gastritis or intestinal metaplasia, as well as first-degree relatives of patients with gastric adenocarcinoma since the relatives themselves are at increased risk of gastric cancer partly due to the intrafamilial transmission of H. pylori. To date, it remains controversial whether to test and treat all patients with functional dyspepsia, gastroesophageal reflux disease, or other non-GI disorders as well as asymptomatic individuals.
The success of H. pylori cure depends on the type and duration of therapy, patient compliance and bacterial factors such as antibiotic resistance. Patients most often fail to respond to initial H. pylori eradication therapy because of noncompliance or antibiotic resistance. Patients should be queried about any side effects, missed doses, and completion of therapy. As culture with antibiotic sensitivities is not routinely performed when H pylori infection is diagnosed, it is generally recommended that different antibiotics be given at higher doses for 14 days. 
Regimens for Helicobacter pylori therapy
Eradication of H pylori has proved difficult. Combination regimens that use two or three antibiotics with a proton pump inhibitor or bismuth are required to achieve adequate rates of eradication and to reduce the number of failures due to antibiotic resistance. In the United States, up to 50% of strains are resistant to metronidazole and 13% are resistant to clarithromycin. At present, experts disagree on the optimal regimen.
First-line therapy: triple therapy
In areas of low clarithromycin resistance, including the United States, a 14-day course of “triple therapy, ” with an oral proton pump inhibitor, clarithromycin 500 mg, and amoxicillin 1 g (or, if penicillin allergic, metronidazole 500 mg), all given twice daily for 14 days, is still recommended for first-line therapy. Unfortunately, this regimen only achieves rates of eradication > 75%.
Second-line therapy: quadruple therapy
with a proton pump inhibitor, bismuth, tetracycline, and metronidazole or tinidazole for 14 days is a more complicated but also more effective regimen. In a 2011 randomized, controlled trial, the per protocol eradication rates were 93% with quadruple therapy and 70% with triple therapy. Bismuth-based quadruple therapy is recommended as first line therapy for patients in areas with high clarithromycin resistance (> 20%), in patients who have previously been treated with a macrolide antibiotic, or as second-line therapy for patients whose infection persists after an initial course of triple therapy. Several studies reported eradication rates of > 90% using a 10-day sequential regimen consisting of four drugs: a proton pump inhibitor and amoxicillin for 5 days, followed by a proton pump inhibitor, clarithromycin, and tinidazole for 5 days. However, subsequent studies confirmed equivalent or superior efficacy when all four drugs were given concomitantly for 10 days (non-bismuth quadruple therapy). 
Unfortunately, recent studies have reported lower eradication rates with sequential therapy, and a 2013 meta-analysis did not detect superiority compared with 14-day triple therapy or bismuth-based therapy, except in patients with organisms exhibiting clarithromycin resistance. Most recently, a 2013 large multicenter European controlled trial conducted in regions of high clarithromycin resistance reported 92% eradication with a 14-day quadruple therapy consisting of a proton pump inhibitor, amoxicillin, clarithromycin, and nitroimidazole (the latter not available in the United States). 
Role of Probiotics
Some studies have recently evaluated the role of the Saccharomyces boulardii as a coadjutant in the eradication of H. pylori and in the prevention of the secondary effects of antibiotic therapy. A meta-analysis showed that supplementation with S. boulardii significantly increased the H. pylori eradication rate and reduced the risk of overall H. pylori therapy-related adverse effects.49 In a cohort of patients in Korea who received S. boulardii for 4 weeks during and after a 1-week course of standard triple therapy, eradication rates were 10% higher than for those who did not receive the supplement.50 Other studies in which Bifidobacterium spp. and Lactobacillus acidophilus have been administered revealed no significant difference in eradication rates in patients who were infected with strains susceptible to both antibiotics and who were treated with standard triple therapy. Further studies will be necessary to clarify the exact role of the probiotics in the eradication treatment.
One of the first "eradication protocols", if not the first, was used by Barry Marshall to treat his own gastritis, which developed following intentional ingestion of H. pylori culture. He used bismuth salt and metronidazole. This treatment effectively cured his gastritis and eliminated the H. pylori infection, but in terms of modern eradication protocol definition, which requires not only occasional ability to cure the infection, but also at least 80% eradication rate, this protocol cannot be described as an "eradication protocol" and is not clinically reasonable.[original research?]
One of the first "modern" eradication protocols was a one-week triple therapy, which the Sydney gastroenterologist Thomas Borody formulated in 1987. As of 2006, a standard triple therapy is amoxicillin, clarithromycin, and a proton pump inhibitor such as omeprazole, lansoprazole, pantoprazole, or esomeprazole. Protocols with metronidazole were also in use.
An example of a fixed-dose combination is PantoPac, containing pantoprazole, clarithromycin, and amoxicillin.
- Chan, FK; To, KF; Wu, JC; Yung, MY; Leung, WK; Kwok, T; Hui, Y; Chan, HL; Chan, CS; Hui, E; Woo, J; Sung, JJ (5 January 2002). "Eradication of Helicobacter pylori and risk of peptic ulcers in patients starting long-term treatment with non-steroidal anti-inflammatory drugs: a randomised trial.". Lancet 359 (9300): 9–13. PMID 11809180.
- Sonnenberg, A (June 2007). "Time trends of ulcer mortality in Europe.". Gastroenterology 132 (7): 2320–7. PMID 17570207.
- Gatta, L; Vakil, N; Vaira, D; Scarpignato, C (7 August 2013). "Global eradication rates for Helicobacter pylori infection: systematic review and meta-analysis of sequential therapy.". BMJ (Clinical research ed.) 347: f4587. PMID 23926315.
- Malfertheiner, P.; Megraud, F.; O'Morain, C. A.; Atherton, J.; Axon, A. T. R.; Bazzoli, F.; Gensini, G. F.; Gisbert, J. P.; Graham, D. Y.; Rokkas, T.; El-Omar, E. M.; Kuipers, E. J. (5 April 2012). "Management of Helicobacter pylori infection--the Maastricht IV/ Florence Consensus Report". Gut 61 (5): 646–664. doi:10.1136/gutjnl-2012-302084.
- Molina-Infante, J; Romano, M; Fernandez-Bermejo, M; Federico, A; Gravina, AG; Pozzati, L; Garcia-Abadia, E; Vinagre-Rodriguez, G; Martinez-Alcala, C; Hernandez-Alonso, M; Miranda, A; Iovene, MR; Pazos-Pacheco, C; Gisbert, JP (July 2013). "Optimized nonbismuth quadruple therapies cure most patients with Helicobacter pylori infection in populations with high rates of antibiotic resistance.". Gastroenterology 145 (1): 121–128.e1. PMID 23562754.
- Malfertheiner, P; Megraud, F; O'Morain, C; Bazzoli, F; El-Omar, E; Graham, D; Hunt, R; Rokkas, T; Vakil, N; Kuipers, EJ (June 2007). "Current concepts in the management of Helicobacter pylori infection: the Maastricht III Consensus Report.". Gut 56 (6): 772–81. PMID 17170018.
- Malfertheiner, P; Megraud, F; O'Morain, CA; Atherton, J; Axon, AT; Bazzoli, F; Gensini, GF; Gisbert, JP; Graham, DY; Rokkas, T; El-Omar, EM; Kuipers, EJ; European Helicobacter Study, Group (May 2012). "Management of Helicobacter pylori infection--the Maastricht IV/ Florence Consensus Report.". Gut 61 (5): 646–64. PMID 22491499.
- B, Yaşar; H, Abut (2010). "Efficacy of probiotics in Helicobacter pylori eradication therapy.". Turk J Gastroenterol 21 (3): 212–217.
- Borody, Thomas J.; P. Cole; S. Noonan; A. Morgan; J. Lenne; L. Hyland; S. Brandl; E. G. Borody; L. L. George (October 16, 1989). "Recurrence of duodenal ulcer and Campylobacter pylori infection after eradication". Medical Journal of Australia 151 (8): 431–435. PMID 2687668.
- Mirbagheri, Seyed Amir; Mehrdad Hasibi; Mehdi Abouzari; Armin Rashidi (August 14, 2006). "Triple, standard quadruple and ampicillin–sulbactam-based quadruple therapies for H pylori eradication: A comparative three-armed randomized clinical trial". World Journal of Gastroenterology 12 (30): 4888–4891. PMID 16937475. Retrieved 2006-09-30.