Helicobacter pylori eradication protocols is a standard name for all treatment protocols for peptic ulcers and gastritis in the presence of Helicobacter pylori infection. The primary goal of the treatment is not only temporary relief of symptoms but also total elimination of H. pylori infection. Patients with active duodenal 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.[1]
Antibiotic resistance edit
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 a H. pylori infection is diagnosed, it is generally recommended that different antibiotics be given at higher doses for 14 days.[2]
Regimens for Helicobacter pylori therapy edit
Achieving optimal eradication of H. pylori has proven difficult. Combination regimens that use two or three antibiotics with a proton pump inhibitor and/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.[3]
First-line therapy: triple therapy edit
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 recommended for first-line therapy. This regimen can achieve rates of eradication in up to 70% of cases.[4]
Second-line therapy: quadruple therapy edit
A 14-day course of "quadruple therapy" with a proton pump inhibitor, bismuth, tetracycline, and metronidazole or tinidazole 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).[5][6]
Sequential therapy edit
Sequential therapy is a newer approach that combines a 5-day course of a "dual therapy" using a proton pump inhibitor in combination with amoxicillin, with a sequential second 5-day course of the standard "triple therapy".[3] Although initial studies promisingly reported higher eradication rates,[3] a 2013 meta-analysis did not detect superiority compared to the other therapies except in the presence of clarithromycin resistant organisms. Another 2013, large multi–center European, controlled trial 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).[4]
Other proposed regimes edit
A number of other eradication regimens have been proposed. In the Table below they are compared to with standard regimes.
| Regimen | Duration, days | Drugs used | Notes |
|---|---|---|---|
| Vonoprazan-amoxicillin dual therapy | 7-14 | vonoprazan 20 mg bid and amoxicillin 750 mg bid | As successful as bismuth-containing quadruple therapy[9] |
| Triple therapy | 7–14 | PPI (standard dose) bid, amoxicillin 1 g bid and clarithromycin 0.5 g bid | First line therapy in areas with low clarithromycin resistance |
| Sequential therapy | 10 | 1st 5 days: PPI (standard dose) bid and amoxicillin 1 g bid 2nd 5 days: metronidazole 0.5 g bid and clarithromycin 0.5 g bid |
First line therapy |
| Concomitant therapy | 7–10 | PPI (standard dose bid), amoxicillin 1 g bid, metronidazole 0.5 g bid and clarithromycin 0.5 g bid | First line therapy |
| Hybrid therapy | 14 | 1st week: PPI (standard dose) and amoxicillin 1 g bid 2nd week: PPI (standard dose), amoxicillin 1 g, metronidazole 0.5 g and clarithromycin 0.5 g bid |
First line therapy |
| Bismuth-containing quadruple therapy | 10–14 | PPI (standard dose) bid, tetracycline 0.5 g qid, metronidazole 0.25 g qid and bismuth standard dose qid | First line or second line therapy |
| Levofloxacin-based triple therapy | 10 | PPI (standard dose) bid, levofloxacin 0.5 g qid and amoxicillin 1 g bid | Second line therapy if there is no fluoroquinolone resistance |
| Culture-guided therapy | 10 | PPI (standard dose) bid, bismuth standard dose qid and two antibiotics selected by sensitivity tests | Third line therapy if there is no fluoroquinolone resistance |
| Levofloxacin-based quadruple therapy | 10 | PPI (standard dose) bid, bismuth standard dose qid, levofloxacin 0.5 g qid and amoxicillin 1 g bid | Third line therapy |
| High-dose dual PPI therapy | 14 | PPI (high dose) qid and amoxicillin 0.5 g qid | Third line therapy |
| Rifabutin triple therapy | 14 | PPI (standard dose) bid, rifabutin 0.15 g bid and amoxicillin 1 g bid | Third line therapy |
| Furazolidone-based quadruple therapy | 10-14 | PPI (standard dose) bid, bismuth standard dose qid, tetracycline 0.5 g bid and furazolidone 200 mg bid | First line for penicillin-allergic patients |
Note: bid – twice daily, qid – four times a day
Adjuvant therapies edit
Recent meta-analyses have proposed two adjuvant therapies which may help in the eradication of H. pylori. Periodontal therapy or what is known as scaling and root planing and probiotics both need further studies to confirm their adjuvant role.[citation needed]
Role of periodontal therapy edit
A 2016 systematic review has found that periodontal therapy may have a role as an added treatment for short- and long-term follow up. For these results to be confirmed with regards eradication and non-recurrence, larger studies need to be carried out.[10]
Role of probiotics edit
Some studies have recently evaluated the role of the yeast Saccharomyces boulardii as a coadjutant in the eradication of H. pylori and in the prevention of the secondary effects of antibiotic therapy such as antibiotic-associated diarrhea. 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.[11] 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.[citation needed]
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.[12]
History edit
One of the first "eradication protocols", if not the first, was used by J. Robin Warren and Barry Marshall. Barry Marshall treated 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. This is not the current eradication protocol.[citation needed]
One of the first "modern" eradication protocols was a one-week triple therapy, which the Sydney gastroenterologist Thomas Borody formulated in 1987.[13] As of 2006, a standard triple therapy is amoxicillin, clarithromycin, and a proton pump inhibitor such as omeprazole,[14] lansoprazole, pantoprazole, or esomeprazole. Protocols with metronidazole were also in use.[14] An example of a fixed-dose combination is PantoPac, containing pantoprazole, clarithromycin, and amoxicillin.[citation needed]
Research edit
Giving acetylcysteine before antibiotic treatment was effective in overcoming H. pylori antibiotic resistance in a study with 40 patients who had at least four eradication failures in their history. The researchers believe it works by inhibiting the formation of biofilm.[15]
References edit
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- ^ Sonnenberg A (June 2007). "Time trends of ulcer mortality in Europe". Gastroenterology. 132 (7): 2320–7. doi:10.1053/j.gastro.2007.03.108. PMID 17570207.
- ^ a b c 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. doi:10.1136/bmj.f4587. PMC 3736972. PMID 23926315.
- ^ a b 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 (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. hdl:1765/64813. PMID 22491499.
- ^ 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. doi:10.1053/j.gastro.2013.03.050. 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. doi:10.1136/gut.2006.101634. PMC 1954853. PMID 17170018.
- ^ Urgesi R, Cianci R, Riccioni ME (2012). "Update on triple therapy for eradication of Helicobacter pylori: current status of the art". Clinical and Experimental Gastroenterology. 5: 151–157. doi:10.2147/CEG.S25416. PMC 3449761. PMID 23028235.
- ^ Rimbara E, Fischbach LA, Graham DY (2011). "Optimal therapy for Helicobacter pylori infections". Nat. Rev. Gastroenterol. Hepatol. 8 (2): 79–88. doi:10.1038/nrgastro.2010.210. PMID 21293508. S2CID 23529476.
- ^ Zhou BG, Jiang X, Ding YB, She Q, Li YY (2024). "Vonoprazan-amoxicillin dual therapy versus bismuth-containing quadruple therapy for Helicobacter pylori eradication: A systematic review and meta-analysis". Helicobacter. 29 (1): e13040. doi:10.1111/hel.13040. PMID 37983865. S2CID 265308205.
- ^ Ren Q, Yan X, Zhou Y, Li WX (7 February 2016). "Periodontal therapy as adjunctive treatment for gastric Helicobacter pylori infection". The Cochrane Database of Systematic Reviews. 2016 (2): CD009477. doi:10.1002/14651858.CD009477.pub2. PMC 8255095. PMID 26852297.
- ^ Szajewska H, Horvath A, Piwowarczyk A (2010). "Meta-analysis: the effects of Saccharomyces boulardii supplementation on Helicobacter pylori eradication rates and side effects during treatment". Aliment Pharmacol Ther. 32 (9): 1069–1079. doi:10.1111/j.1365-2036.2010.04457.x. PMID 21039671.
- ^ B Y, H A (2010). "Efficacy of probiotics in Helicobacter pylori eradication therapy". Turk J Gastroenterol. 21 (3): 212–217. doi:10.4318/tjg.2010.0090. PMID 20931422.
- ^ Borody TJ, 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. doi:10.5694/j.1326-5377.1989.tb101251.x. PMID 2687668. S2CID 26066525.
- ^ a b Mirbagheri SA, 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. doi:10.3748/wjg.v12.i30.4888. PMC 4087627. PMID 16937475.
- ^ Cammarota G, Branca G, Ardito F, Sanguinetti M, Ianiro G, Cianci R, Torelli R, Masala G, Gasbarrini A, Fadda G, Landolfi R, Gasbarrini G (2010). "Biofilm Demolition and Antibiotic Treatment to Eradicate Resistant Helicobacter pylori: A Clinical Trial". Clinical Gastroenterology and Hepatology. 8 (9): 817–820.e3. doi:10.1016/j.cgh.2010.05.006. PMID 20478402.