- Research article
- Open Access
Pharmacological regimens for eradication of Helicobacter pylori: an overview of systematic reviews and network meta-analysis
BMC Gastroenterology volume 16, Article number: 80 (2016)
Approximately half of the world’s population is infected with Helicobacter pylori (H.pylori), a bacterium shown to be linked with a series of gastrointestinal diseases. A growing number of systematic reviews (SRs) have been published comparing the effectiveness of different treatments for H.pylori infection but have not reached a consistent conclusion. The objective of this study is to provide an overview of SRs of pharmacological therapies for the eradication of H.pylori.
Major electronic databases were searched to identify relevant SRs published between 2002 and February 2016. Studies were considered eligible if they included RCTs comparing different pharmacological regimens for treating patients diagnosed as H.pylori infected and pooled the eradication rates in a meta-analysis. A modified version of the ‘A Measurement Tool to Assess Systematic Reviews’ (AMSTAR) was used to assess the methodological quality. A Bayesian random effects network meta-analysis (NMA) was conducted to compare the different proton pump inhibitors (PPI) within triple therapy.
30 SRs with pairwise meta-analysis were included. In triple therapy, the NMA ranked the esomeprazole to be the most effective PPI, followed by rabeprazole, while no difference was observed among the three old generations of PPI for the eradication of H.pylori. When comparing triple and bismuth-based therapy, the relative effectiveness appeared to be dependent on the choice of antibiotics within the triple therapy; moxifloxacin or levofloxacin-based triple therapy were both associated with greater effectiveness than bismuth-based therapy as a second-line treatment, while bismuth-based therapy achieved similar or greater eradication rate compared to clarithromycin-based therapy. Inconsistent findings were reported regarding the use of levofloxacin/moxifloxacin in the first-line treatment; this could be due to the varied resistant rate to different antibiotics across regions and populations. Critical appraisal showed a low-moderate level of overall methodological quality of included studies.
Our analysis suggests that the new generation of PPIs and use of moxifloxacin or levofloxacin within triple therapy as second-line treatment were associated with greater effectiveness. Given the varied antibiotic resistant rate across regions, the appropriateness of pooling results together in meta-analysis should be carefully considered and the recommendation of the choice of antibiotics should be localized.
Helicobacter pylori (H.pylori) is one of the most common human infections with a worldwide prevalence of approximately 50 %. In the United States (US) and Europe, the prevalence of H.pylori is estimated to be 20 % to 50 %, varying in different socioeconomic, age and ethnic groups and geography [1, 2]. In developing countries, the prevalence has been reported to be as high as 70 % . H.pylori is usually latent and asymptomatic; however, increasing evidence has demonstrated the link between H.pylori infection and the pathogenesis of a series of upper gastrointestinal diseases: functional dyspepsia, chronic gastritis, peptic ulcer disease, gastric cancer and gastric mucosa-associated lymphoid-tissue lymphoma [4–9].
Eradication of H.pylori has been shown to be associated with increased rate of peptic ulcer healing and reduced risk of gastric cancer [10, 11]. Standard triple therapy, which includes a proton pump inhibitor (PPI), clarithromycin, and amoxicillin or metronidazole, is recommended as first-line eradication therapy for H.pylori infection in clinical guidelines worldwide [12–15]. A treatment alternative also widely recommended is bismuth-based quadruple therapy, which contains a PPI or H2 receptor antagonist (H2RA), bismuth, metronidazole, and tetracycline. Other treatment options include varying individual drugs within the triple therapy and quadruple therapy based regimens. More recently, sequential therapy of these multiple treatment options also has been introduced. In the US, the American College of Gastroenterology guideline (2007) recommends clarithromycin-based triple therapy for first-line eradication in patients who have not previously been treated with clarithromycin and are not allergic to penicillin. For patients who are allergic to penicillin or have previously received a macrolide antibiotic, a bismuth quadruple therapy is preferred .
Although these recommendations specified the type of antibiotics in the regimen, the choice of PPIs was not specified. Based on the available evidence at the time when the guidelines were produced, the relative effectiveness of PPIs was assumed to be comparable. Furthermore, in recent years, a decline in the effectiveness of the treatment regimens has been observed due to increasing clarithromycin resistance; this may have an impact on the relative effectiveness of these treatment strategies . A 12-year retrospective study published in 2008 showed that the eradication rate of standard therapy decreased from 90.6 % in 1997 to 74.8 % .
In the past decade, several systematic reviews have evaluated the effectiveness of individual specific pharmacological regimens for H.pylori eradication. These reviews compared the eradication rate by different PPIs and antibiotics, triple versus quadruple therapy, or PPI versus H2RA, but the conclusions of these reviews were not always consistent.
The Scottish Intercollegiate Guidelines Network (SIGN) published their recommendations on H.pylori eradication in the dyspepsia guideline in 2003 and is due to update their guidance . This study aims to systematically evaluate the current evidence (since 2003) on the effectiveness of H.pylori eradication therapies for the patients diagnosed as H.pylori infection through an overview of systematic reviews.
An overview of systematic reviews was carried out according to the general principles of systematic reviewing methodology . A Bayesian network meta-analysis (NMA) was conducted to compare the eradication rates by using different PPIs within triple therapy.
All systematic reviews comparing different drug therapies for the eradication of H.pylori infection that fulfilled the following criteria were included:
Patient — studies of adult patients who were naïve to treatment (first-line therapy) or have previous treatment failures (second-line therapy).
Intervention/Comparator — studies comparing any pharmacological regimens.
Outcome measure — studies reporting pooled eradication rates measured by urea breathe testing or gastric mucosal biopsy four weeks after completion of treatment, as the primary outcome. Secondary outcome measures may include adverse events rates and rates of discontinuation of therapy due to severe adverse events.
Design — systematic reviews and meta-analyses of data from randomized controlled trials (RCTs).
Studies were excluded if they focused on comparing the variation of dose or duration of the same drug combination; if no meta-analysis was conducted; meta-analysis included observational studies; or the included RCTs in the meta-analysis were not clearly specified. Conference abstracts were excluded due to lack of details for data extraction and quality assessment. Studies on furazolidone were excluded because it is no longer available in the US and the United Kingdom (UK) due to severe side effects. No language exclusions were applied. As this work was initiated by the SIGN guideline update, studies published prior to 2002 were excluded.
Four major electronic databases were searched: MEDLINE, EMBASE, the Cochrane Library and the Database of abstracts of review of effects. Relevant keywords were used to develop appropriate search strategies; these are shown in the Additional file 1. The primary search was carried out in November 2012 and updated in March 2016.
Two reviewers (JM and YX) independently reviewed the titles and abstracts of all retrieved studies for identification of potentially relevant systematic reviews. After the initial screening, the full texts of studies deemed relevant were obtained and reviewed in detail. The discrepancy was addressed by discussion or a third reviewer (OW). Reference list of included studies was also checked to identify any potentially relevant studies that may not have been identified by the electronic searching.
For each included systematic review, the following data were extracted by two reviewers independently: first author, publication year and country; objective; search database and selection criteria; number of included studies in the review and meta-analysis; number of patients in the meta-analysis; patient characteristics; intervention and comparison; outcomes including eradication rate, adverse events rate, therapy discontinuation rate. In addition, as the resistant rate to antibiotics differs across regions, the country of the RCTs included in the meta-analysis was also extracted when the focus of the comparison was involved with antibiotics. To conduct the NMA, we also extracted data from the individual RCTs in the included systematic reviews, including: interventions in comparison, the total number of people in each arm and the number of people of which H.pylori had been eradicated.
To assess methodological quality of the included systematic reviews, a modified version of the ‘A Measurement Tool to Assess Systematic Reviews’ (AMSTAR) checklist  was used by two reviewers (JM and YX) independently to examine the following 11 aspects: (1) clearly defined research question; (2) study selection and data extraction carried out by two independent reviewers; (3) comprehensive literature search; (4) clear selection criteria; (5) list of included and excluded studies; (6) study characteristics appropriately extracted; (7) quality assessment documented; (8) results of quality assessment appropriately considered in reaching conclusions; (9) results combined appropriately; (10) publication bias assessed; (11) conflicts of interest declared. Studies were graded as “high quality (++)”, “acceptable (+)” or “low quality (0)”, based on the overall risk of bias and the likelihood that results may be changed by further research.
Network meta-analysis (NMA)
A Bayesian random effect NMA was conducted to compare and rank all the PPIs within the triple therapy based on the eradication rates. When more than two interventions are being evaluated, conventional pairwise meta-analysis is limited in that it requires direct head-to-head evidence between interventions. In contrast, NMA allows the estimation of relative effects between multiple alternative interventions by incorporating both direct and indirect evidence [21, 22]. The NMA model used in this study is shown in Additional file 2. The odds ratios (ORs) for all pairwise comparisons of each treatment were calculated and presented in an interval plot. The median of the posterior distribution along with 95 % credible intervals (95%CrI) was reported. In addition, the PPIs were ranked based on their probability to be considered the best for the outcome of eradication rate of H.pylori.
Two sets of vague priors, uniform and inverse Gamma, were used for the Bayesian model, which were burned-in for 27,000 and 8,000 Markov Chain Monte Carlo iterations respectively until the convergence was met based on the Gelman-Rubin-Brooke statistic (within 1+/− 0.05). A further approximately 40,000 iterations were run until the MC error became lower than 5 % standard error and the results became stable. The median of the posterior distribution and credible intervals for ORs was reported. The analysis was performed using WinBUGS 1.4.3 .
Results of search and selection
The search identified 1690 studies, of which 30 studies were included in this overview of systematic reviews. The flowchart of the screening process is shown in Fig. 1. The excluded studies at full-text screening stage are listed in Additional file 3: Table S1 with reasons for exclusion.
Systematic reviews included in analysis
All the included studies were published between 2002 and 2015 in English, with the exception of three studies, which were published in Chinese [24–26]. Six studies exclusively evaluated second-line treatment for patients with at least one prior course of treatment failure [27–32]; 12 studies focused on treatment naive patients [25, 26, 33–42]; the remaining systematic reviews included RCTs for both first-line and second-line treatment. 13 studies evaluated treatments in patients with comorbid gastric diseases including peptic ulcer disease, duodenal ulcer, functional dyspepsia, chronic gastritis or other non-ulcer diseases [24, 27, 37–40, 43–49] (the remaining studies did not provide such data). In addition to the eradication rate, 15 systematic reviews also compared adverse events rates [25, 28–38, 41, 47, 50] and six compared the discontinuity rate (compliance rate) [25, 29–31, 37, 50]. The pooled eradication rates of different regimens in all of the included systematic reviews ranged between 47 % (data from three RCTs relating to standard triple therapy ) and 94 % (data from one RCT relating to esomeprazole-based triple therapy ) by intention to treat (ITT) analysis.
Based on the treatment regimens under comparison, the included studies were classified into the following five categories:
Triple therapy with different PPIs
Triple therapy with different antibiotics
Triple therapy versus bismuth-based therapy
PPI versus H2RA in triple therapy
Other drug therapies
Triple therapy with different PPIs
Seven studies evaluated the impact of different PPIs within a triple therapy regimen on H.pylori eradication rate (Table 1) [24, 42–46, 51]. These included both new (esomeprazole, rabeprazole) and older generations of PPIs (omeprazole, pantoprazole, lansoprazole); overall, the results were mixed, but a time trend was observed that studies published from 2006 onwards [24, 42, 46] suggested consistently that new generation of PPIs achieved greater eradication rate than the older generations. Amongst the new PPIs, the reported eradication rates ranged from 77 % (data from nine RCTs relating to rabeprazole-based triple therapy ) to 94 % (data from one RCT relating to esomeprazole-based triple therapy ); for the older generation PPIs, the reported eradication rates ranged from 75 % (data from four RCTs relating to omeprazole-based triple therapy ) to 88 % (data from two RCTs relating to omeprazole-based triple therapy ). Five studies compared esomeprazole with older generation PPIs in the triple therapy, of which, three reported a statistically significant benefit of esomeprazole in H.pylori eradication with OR of approximately 1.3 [24, 42, 46]. A similar effect was reported in one of the three studies comparing the effectiveness of the rabeprazole with the older generation PPIs (OR 1.21; 95%CI 1.02–1.42) . Only one study compared the effectiveness of esomeprazole with rabeprazole and found no difference in eradication rate (OR 0.90; 95%CI 0.70–1.17) . Similarly, no difference was observed when comparing within older generation PPIs [45, 51].
A diagram of the PPI network is given in Fig. 2. Overall, 57 trials were included in the NMA analysis. None of the trials compared rabeprazole with pantoprazole, or lansoprazole with esomeprazole. In contrast, esomeprazole was compared with omeprazole in 15 trials. In our analysis omeprazole was used as the reference treatment since direct trials existed comparing omeprazole and each of the other PPIs and it was the most commonly used PPI in the triple therapy for H.pylori eradication. Esomeprazole was ranked first in the probability best test, with OR to be 1.29 (95 % credible interval 1.08–1.56) when compared with omeprazole, followed by rabeprazole (Table 2). The three old generations of PPIs showed similar effectiveness. The OR and interval plot for each pair of the mixed comparisons of different PPIs is shown in Fig. 3.
Triple therapy with different antibiotics
Seven studies evaluated the impact of different antibiotics within a triple therapy for the first-line treatment [25, 26, 33–37] and one study evaluated the antibiotics for both first-line and second-line treatment  (Table 3). Clarithromycin was used as a comparator in all the studies while the intervention antibiotics included levofloxacin [25, 26, 35–37], azithromycin  and moxifloxacin . Five studies compared levofloxacin-based triple therapy with standard triple therapy for first-line treatment [25, 26, 35–37], among which two studies reported improved eradication rates with levofloxacin [25, 26] while the other three studies showed no difference between the two regimens [35–37]. Similarly, for moxifloxacin, two systematic reviews reached conflict conclusions when comparing it with standard triple therapy for first-line treatment [34, 47]. The two systematic reviews included three same RCTs while one of them included an additional RCT from China . With the inclusion of this RCT, the pooled result showed moxifloxacin was associated with greater eradication rate for the naïve patient (OR 1.13; 95%CI 1.01–1.27)  while no difference was shown in another study (OR 1.80; 95%CI 0.71–4.55) . The use of moxifloxacin as second-line treatment was evaluated in one study which showed that the moxifloxacin-based triple therapy achieved greater eradication rate than the clarithromycin-based therapy (OR 1.78; 95%CI 1.16–2.73) . In addition to levofloxacin and moxifloxacin, one study evaluated azithromycin-based triple therapy versus standard triple therapy as first-line treatment and did not find a difference .
In addition to the eradication rates, adverse events rates were also compared in seven studies, such as nausea, metallic taste and other gastrointestinal tract discomforts [25, 33–37, 47]. Compared to clarithromycin, the risk of adverse events was approximately halved with azithromycin (OR 0.58; 95%CI 0.41–0.82) . Two studies compared the adverse events between moxifloxacin and clarithromycin containing triple therapy; one showed lower adverse events rate associated with moxifloxacin (OR 0.45; 95%CI 0.26–0.77)  while the other did not show any difference . For levofloxacin, one study showed there were reduced adverse events rate (OR 0.57; 95%CI 0.44–0.74)  while three studies reported no difference when comparing to the standard therapy [35–37].
Triple therapy versus bismuth-based therapy
Nine studies compared the effectiveness, adverse events rate and therapy discontinuation rates between triple therapy and bismuth-based therapy [27–32, 38, 39, 50]. The study characteristics are presented in Table 4. For the bismuth-based therapies, seven studies evaluated bismuth-based quadruple therapy [29–32, 38, 39, 50], one evaluated ranitidine bismuth citrate (RBC)  and another one evaluated both quadruple therapy and RBC . Overall, the quadruple therapy was associated with similar or greater eradication rate than standard triple therapy; however when levofloxacin or moxifloxacin was contained in the triple therapy, the reverse was observed.
Two of the nine studies focused on treatment naive patients, and no difference in eradication rates was found between triple and quadruple therapy. The primary antibiotics used in both studies was clarithromycin [38, 39]. The remaining seven studies compared second-line therapy for patients with previous treatment failures [27–32, 50]. The primary antibiotics used in triple therapy varied: two studies evaluated clarithromycin [27, 50], one study with moxifloxacin , three studies with levofloxacin [28, 29, 32], and one study compared all of the three . Clarithromycin-containing triple therapy was associated with lower eradication rates than bismuth-based therapy in two studies [27, 30] while one study showed no difference . In contrast, moxifloxacin-containing triple therapy was suggested to achieve greater effectiveness than bismuth-based therapy [30, 31]. Similar to moxifloxacin, triple therapy with levofloxacin appeared to be more effective than bismuth-based therapy, however statistically significant finding was only reported in one of the four studies (OR 1.18; 95%CI 1.08–1.29) .
The adverse events around the bismuth-based therapy included diarrhea, abdominal pain, dark stools, dizziness, headache, nausea, metallic taste and nausea . Seven studies reported adverse events of the compared regimens [28–32, 38, 50]. The pooled adverse event rates of clarithromycin-based triple therapy ranged from 35.4 %  to 37 % , 10.1 %  to 16.75 %  for levofloxacin or moxifloxacin-based triple therapy, and 27.8 %  to 44 %  for bismuth-based therapy. Five studies showed a lower risk of adverse events of levofloxacin/moxifloxacin compared with the bismuth-based regimen with ORs ranging from 0.27 to 0.51 [28–32], and one study favoured bismuth when comparing with clarithromycin triple therapy . One study classified adverse events by severity and reported much lower risk favouring levofloxacin compared with bismuth therapy when including only severe adverse events (OR 0.20; 95%CI 0.06–0.67) . Furthermore, the discontinuation rate of triple therapy using moxifloxacin and levofloxacin was statistically significantly lower than bismuth-based therapy in three of the four studies [29–31].
PPI versus H2RA in triple therapy
Three studies compared the effectiveness of PPI versus H2RA within a triple therapy (Table 5) [40, 41, 53]. One systematic review based on 20 RCTs with 2374 patients showed PPI was associated with greater effectiveness than H2RA (OR 1.31; 95%CI 1.09–1.58) . Another study of 12 RCTs did not show any difference between the two, but its subgroup analysis based on six RCTs suggested PPI-based triple therapy reached higher eradication rates than H2RA when clarithromycin was not contained . A recent systematic review of three RCTs compared lafutidine versus lansoprazole-containing triple therapy and reported no difference between the two regimens .
Other drug therapies
One study evaluated the impact of adding metronidazole or tinidazole (concomitant quadruple therapy) on standard triple therapy and reported greater eradication rates with concomitant therapy (OR 2.36; 95%CI 1.67–3.34) . One study based on 14 RCTs assessed the combination of tetracycline and amoxicillin in triple therapy/quadruple therapy and found no difference in eradication rate when compared to other regimens when the two drugs were not combined . One Japanese study evaluated the effectiveness of supplementation with rebamipide and found it was associated with greater eradication rate compared to rebamipide not-containing regimens (OR 1.59; 95%CI 1.14–2.22) . The characteristics of these studies are presented in Table 6.
The overall quality of the included systematic reviews was graded as low to moderate with a higher risk of bias (Fig. 4). This was primarily due to insufficient reporting and poor methodological approaches. The majority of the reviews met five to eight criteria out of the 11 total AMSTAR criteria. The criteria that were frequently not fulfilled included: (1) transparent study selection process and reference of excluded studies; (2) adequate reporting of the population characteristics; (3) using quality appropriately in making conclusions; (4) assessing publication bias when applicable. The detailed assessment for each of the included studies is presented in Additional file 4: Table S2.
Summary of findings
This overview of systematic reviews evaluated the effectiveness of pharmacological regimens for the eradication of H.pylori by searching and analysing the existing systematic reviews from 2002 to present. In triple therapy, regarding the use of different PPIs, we found that the results of studies were inconsistent; however more recently published studies tend to suggest new generation PPIs were associated with greater eradication rates than the old generation. The NMA suggested that esomeprazole was the most effective PPI with the highest probability to be the best among the five PPIs after incorporating evidence of both direct and indirect comparisons. Regarding the use of antibiotics, conflicting results exist between the studies to some extent; however this could be due to the varied resistant rate to different antibiotics across regions. This leads to the limited transferability of RCT results across countries and population and thus, there exist issues of fundamental heterogeneity when pooling results together in the meta-analysis. Concerning the comparison between triple therapy and bismuth-based therapy, there was no difference between the two regimens overall, but the antibiotics within the triple therapy may have an impact on the overall effectiveness of the drug regimen. Moxifloxacin or levofloxacin based triple therapy were associated with greater eradication rates, lower risk of adverse events and lower discontinuation rate than bismuth-based therapy for second-line treatment. With regard to the comparison between triple therapies and H2 receptor antagonist and others, no definite conclusion could be reached due to limited available evidence.
The evidence on the effectiveness of PPI has evolved over time. Contrary to existing guidance, recent studies have shown that the new generation PPIs have achieved statistically significant greater effectiveness rate than the old generations. There is a clear time trend when evaluating the systematic reviews – systematic reviews published before 2006 reported no difference, while 2006 onwards, the statistical significant difference was shown in the pooled results. This can be explained by more recent RCTs and a more complete evidence base included in the recent systematic reviews (Additional file 5: Table S3). When comparing between triple therapy and bismuth-based therapy, the results were mixed. However, there seems to be a trend according to the choice of antibiotics in triple therapy – triple therapy achieved greater eradication rates than bismuth-based therapy when moxifloxacin or levofloxacin was used as a substitute of clarithromycin for second-line treatment. Although generally the results of comparing triple therapy and bismuth-based therapy failed to show statistical significance, it is possible this is a sample size issue. Our results support the current guidance on the recommendations of moxifloxacin or levofloxacin as the second-line treatment for previous treatment failures of H.pylori. However, its role as a first-line therapy was found to be controversial. Two studies showed the use of levofloxacin or moxifloxacin for treating naïve patients was associated with improved eradication rate [25, 26], while three studies found no difference [35–37]. This was further investigated by two subgroup analyses from two included studies which both suggested that levofloxacin achieved statistically greater eradication rates in European countries where the resistant rates were much lower than the global average [35, 37]. Therefore, the discrepancy of the results could be attributed to the varied resistant rates to different antibiotics across regions or populations. This could also possibly explain that the two meta-analyses which pooled RCTs mostly from China showed the improved effectiveness of levofloxacin as first-line treatment [25, 26] – the resistant rate to clarithromycin could be possibly much higher than that to levofloxacin in the regions where the included RCTs were conducted.
Comparison with current guidelines
Based on current guidelines from the American College of Gastroenterology, Canadian Helicobacter Study Group and National Institute for Health and Care Excellence (NICE), a triple regimen consisting of a PPI, clarithromycin with either metronidazole or amoxicillin is recommended as first-line treatment [13–15]. In addition, both of the American and Canadian guidelines recommend the combination of PPI, bismuth, tetracycline and metronidazole as an alternative for first-line therapy [13, 14]. The alternative of bismuth quadruple therapy is raised due to the increasing clarithromycin resistance rate which has lowered the efficacy of triple therapy to 70–85 %. The American guideline also recommends to consider levofloxacin-based triple therapy when bismuth or clarithromycin-based therapies are not an option in some circumstances . In 2009, the Asia–Pacific H.pylori Consensus Conference agreed that the first-line treatment should consist of either clarithromycin-based triple or bismuth quadruple therapy, and further proposed four options for second-line treatment: (i) standard triple therapy that has not been previously used; (ii) bismuth-based quadruple therapy; (iii) levofloxacin-based triple therapy; and (iv) rifabutin-based triple therapy .
The European Helicobacter Study Group published their latest guideline in 2012 – the Maastricht IV report  recommending specific H.pylori eradication strategies according to different clarithromycin resistance rates. The threshold for classifying clarithromycin resistance to the high/low area is set as 15 % –20 %. In regions with low clarithromycin resistance rates, clarithromycin-based triple therapy remains the first-line treatment, with the alternative of bismuth quadruple therapy. Where there is higher clarithromycin resistance, the bismuth-based therapy is recommended as the first-line treatment. In both circumstances, levofloxacin is recommended for second-line therapy rather than first-line for the reason of ’rapid acquisition of resistance’.
The World Gastroenterology Organization published their H.pylori guideline for developing countries in 2011, which is consistent with the above guidelines. However, it states that, due to its low cost, furazolidone may be served as an alternative option by developing countries, such as Brazil and China, despite being withdrawn in the US and the European Union due to the severe adverse events .
It is worth noting that the type of PPI is not specified in any of the current guidelines, which may be due to the limited availability of reliable evidence from studies when those guidelines were published. However, our review showed that the esomeprazole could achieve greater eradication rate than the older generation of PPIs. Despite the relatively high cost of newer generation of PPI, this difference in effectiveness between the generations of PPIs should be taken into account in the recommendations. Our finding supported the recommendation of bismuth-based therapy as a first-line alternative to standard triple therapy in a high clarithromycin resistant area. For the second-line treatment, our findings are consistent with the current guidelines; both moxifloxacin/levofloxacin containing triple therapy and bismuth-based therapy can achieve higher eradication rates than clarithromycin-containing triple therapy. Moreover, the former appeared to be superior to the latter in terms of eradication rates and adverse events rates.
There are a few limitations of this study. As this is an overview of systematic reviews, our results are dependent on what has been reported in the included systematic reviews and on the methodological rigour applied in their development. For instance, similar search strategy across systematic reviews has turned out to include difference RCTs. The low-moderate overall quality of included studies may affect the impact of this overview of systematic reviews on clinical decision making. However, it is difficult to judge whether the low internal validity of the individual systematic reviews resulted from insufficient reporting or certain methodological flaws. In addition, there were some heterogeneity issues in this overview. The systematic reviews have included a mixture of population characteristics, countries of origin and comorbidities, infection epidemiology and antibiotics resistance type and thus the eradication rates varied with those factors. This may not be appropriately considered and addressed in some of the included meta-analysis, leading to the inconsistent results in our findings.
This overview of systematic reviews suggests that the new generation of PPIs and use of moxifloxacin or levofloxacin in triple therapy or bismuth-based therapy as second-line treatment were associated with greater effectiveness, while the comparative effectiveness of antibiotics is complex which probably depends on the resistant rate to different antibiotics in different regions. This should be explored in future research for updating the guidelines. In addition, considering the substantiated difference in the cost of treatment, estimating the cost-effectiveness of these treatments is of value to clinical decision making, especially in the area with high H.pylori prevalence. Given the variation in infection epidemiology and increasing antibiotics resistance, from a clinical perspective, the recommendations should be localized based on the specific prevalence of H.pylori infection and antibiotics resistance rate in the local region and population.
AMSTAR, A measurement tool to assess systematic reviews; CI, Confidence interval; CrI, Credible interval; H.pylori, Helicobacter pylori; H2RA, H2 receptor antagonist; ITT, Intention to treat; NICE, National Institute for Health and Care Excellence; NMA, Network meta-analysis; OR, Odds ratio; PPI, Proton pump inhibitor; RBC, Ranitidine bismuth citrate; RCT, Randomized controlled trial; SIGN, Scottish Intercollegiate Guidelines Network; UK, United Kingdom; US, United States
Everhart JE, Kruszon-Moran D, Perez-Perez GI, Tralka TS, McQuillan G. Seroprevalence and ethnic differences in Helicobacter pylori infection among adults in the United States. J Infect Dis. 2000;181:1359–63.
Ford AC, Axon AT. Epidemiology of Helicobacter pylori infection and public health implications. Helicobacter. 2010;15 Suppl 1:1–6.
Mandeville KL, Krabshuis J, Ladep NG, Mulder CJ, Quigley EM, Khan SA. Gastroenterology in developing countries: issues and advances. World J Gastroenterol. 2009;15:2839–54.
Parsonnet J, Hansen S, Rodriguez L, Gelb AB, Warnke RA, Jellum E, et al. Helicobacter pylori infection and gastric lymphoma. N Engl J Med. 1994;330:1267–71.
Qadri Q, Rasool R, Gulzar GM, Naqash S, Shah ZA. H. pylori Infection, Inflammation and Gastric Cancer. J Gastrointest Cancer. 2014;45:126–32.
Panic N, Mastrostefano E, Leoncini E, Persiani R, Arzani D, Amore R, et al. Susceptibility to Helicobacter pylori infection: results of an epidemiological investigation among gastric cancer patients. Mol Biol Rep. 2014;41:3637–50.
Hsu WY, Lin CH, Lin CC, Sung FC, Hsu CP, Kao CH. The relationship between Helicobacter pylori and cancer risk. Eur J Intern Med. 2014;25:235–40.
Chen YS, Xu SX, Ding YB, Huang XE, Deng B. Helicobacter pylori Infection and the Risk of Colorectal Adenoma and Adenocarcinoma: an Updated Meta-analysis of Different Testing Methods. Asian Pac J Cancer Prev. 2013;14:7613–9.
Peek Jr RM, Fiske C, Wilson KT. Role of innate immunity in Helicobacter pylori-induced gastric malignancy. Physiol Rev. 2010;90:831–58.
Gisbert JP, Calvet X, Cosme A, Almela P, Feu F, Bory F, et al. Long-term follow-up of 1,000 patients cured of Helicobacter pylori infection following an episode of peptic ulcer bleeding. Am J Gastroenterol. 2012;107:1197–204.
Ford AC, Forman D, Hunt RH, Yuan Y, Moayyedi P. Helicobacter pylori eradication therapy to prevent gastric cancer in healthy asymptomatic infected individuals: systematic review and meta-analysis of randomised controlled trials. BMJ. 2014;348:g3174.
Malfertheiner P, Megraud F, O'Morain CA, Atherton J, Axon AT, Bazzoli F, et al. Management of Helicobacter pylori infection--the Maastricht IV/Florence Consensus Report. Gut. 2012;61:646–64.
Hunt R, Fallone C, Veldhuyzan van Zanten S, Sherman P, Smaill F, Flook N, et al. Canadian Helicobacter Study Group Consensus Conference: Update on the management of Helicobacter pylori--an evidence-based evaluation of six topics relevant to clinical outcomes in patients evaluated for H pylori infection. Can J Gastroenterol. 2004;18:547–54.
Chey WD, Wong BC. American College of Gastroenterology guideline on the management of Helicobacter pylori infection. Am J Gastroenterol. 2007;102:1808–25.
National Institute for Health and Care Excellence. Dyspepsia: Managing Dyspepsia in Adults in Primary Care. CG17. London: National Institute for Health and Care Excellence; 2004. Newcastle upon Tyne UK: Crown 2004.
Giorgio F, Principi M, De Francesco V, Zullo A, Losurdo G, Di Leo A, et al. Primary clarithromycin resistance to Helicobacter pylori: Is this the main reason for triple therapy failure? World J Gastrointest Pathophysiol. 2013;4:43–6.
Sasaki M, Ogasawara N, Utsumi K, Kawamura N, Kamiya T, Kataoka H, et al. Changes in 12-Year First-Line Eradication Rate of Helicobacter pylori Based on Triple Therapy with Proton Pump Inhibitor, Amoxicillin and Clarithromycin. J Clin Biochem Nutr. 2010;47:53–8.
Scottish Intercollegiate Guidelines Network (SIGN). Dyspepsia. Edinburgh: SIGN; 2003. SIGN publication no.68.
Smith V, Devane D, Begley CM, Clarke M. Methodology in conducting a systematic review of systematic reviews of healthcare interventions. BMC Med Res Methodol. 2011;11:15.
Scottish Intercollegiate Guidelines Network (SIGN). Critical appraisal: notes and checklists. http://www.sign.ac.uk/methodology/checklists.html. Accessed 02 Feb 2014.
Lumley T. Network meta-analysis for indirect treatment comparisons. Stat Med. 2002;21:2313–24.
Mills EJ, Thorlund K, Ioannidis JP. Demystifying trial networks and network meta-analysis. BMJ. 2013;346:f2914.
Lunn DJ, Thomas A, Best N, Spiegelhalter D. WinBUGS - A Bayesian modelling framework: Concepts, structure, and extensibility. Stat Comput. 2000;10:325–37.
Wang Z, Xiong G, Wu S. Comparing the efficacy of esomeprazole and omeprazole combined with antibiotics in Helicobacter pylori eradication: A meta-analysis. Chin J Gastroenterol. 2006;11:598–601.
Zhang ZF, Zhao G, Liu LN. Effectiveness and safety of proton pump inhibitor and levofloxacin based first-line triple therapy in the eradication of Helicobacter pylori: a meta-analysis. Zhonghua Yi Xue Za Zhi. 2008;88:2722–5.
Gou QY, Shi RH, Yu RB. Levofloxacin containing triple therapy vs standard triple therapy for eradication of Helicobacter pylori: A Meta-analysis. [Chinese]. Shi Jie Hua Ren Xiao Hua Za Zhi. 2014;22:5207–11.
Gisbert JP, Gonzalez L, Calvett X. Systematic review and meta-analysis: Proton pump inhibitor vs. ranitidine bismuth citrate plus two antibiotics in Helicobacter pylori eradication. Helicobacter. 2005;10:157–71.
Gisbert JP, De La Morena F. Systematic review and meta-analysis: Levofloxacin-based rescue regimens after Helicobacter pylori treatment failure. Aliment Pharmacol Ther. 2006;23:35–44.
Saad RJ, Schoenfeld P, Kim HM, Chey WD. Levofloxacin-based triple therapy versus bismuth-based quadruple therapy for persistent Helicobacter pylori infection: a meta-analysis. Am J Gastroenterol. 2006;101:488–96.
Li Y, Huang X, Yao L, Shi R, Zhang G. Advantages of moxifloxacin and levofloxacin-based triple therapy for second-line treatments of persistent Helicobacter pylori infection: a meta analysis. Wien Klin Wochenschr. 2010;122:413–22.
Wu C, Chen X, Liu J, Li M-Y, Zhang Z-Q, Wang Z-Q. Moxifloxacin-containing triple therapy versus bismuth-containing quadruple therapy for second-line treatment of Helicobacter pylori infection: a meta-analysis. Helicobacter. 2011;16:131–8.
Di Caro S, Fini L, Daoud Y, Grizzi F, Gasbarrini A, De Lorenzo A, et al. Levofloxacin/amoxicillin-based schemes vs quadruple therapy for helicobacter pylori eradication in second-line. World J Gastroenterol. 2012;18:5669–78.
Dong J, Yu X-F, Zou J. Azithromycin-containing versus standard triple therapy for Helicobacter pylori eradication: a meta-analysis. World J Gastroenterol. 2009;15:6102–10.
Yuan W, Yang K, Ma B, Li Y, Guan Q, Wang D, et al. Moxifloxacin-based triple therapy versus clarithromycin-based triple therapy for first-line treatment of Helicobacter pylori infection: a meta-analysis of randomized controlled trials. Intern Med. 2009;48:2069–76.
Ye CL, Liao GP, He S, Pan YN, Kang YB, Zhang ZY. Levofloxacin and proton pump inhibitor-based triple therapy versus standard triple first-line therapy for Helicobacter pylori eradication. Pharmacoepidemiol Drug Saf. 2014;23:443–55.
Peedikayil MC, Alsohaibani FI, Alkhenizan AH. Levofloxacin-based first-line therapy versus standard first-line therapy for Helicobacter pylori eradication: meta-analysis of randomized controlled trials. PLoS One. 2014;9:e85620.
Xiao SP, Gu M, Zhang GX. Is levofloxacin-based triple therapy an alternative for first-line eradication of Helicobacter pylori? A systematic review and meta-analysis. Scand J Gastroentero. 2014;49:528–38.
Gene E, Calvet X, Azagra R, Gisbert JP. Triple vs. quadruple therapy for treating Helicobacter pylori infection: a meta-analysis. Aliment Pharmacol Ther. 2003;17:1137–43.
Venerito M, Krieger T, Ecker T, Leandro G, Malfertheiner P. Meta-analysis of bismuth quadruple therapy versus clarithromycin triple therapy for empiric primary treatment of Helicobacter pylori infection. Digestion. 2013;88:33–45.
Gisbert JP, Khorrami S, Calvet X, Gabriel R, Carballo F, Pajares JM. Meta-analysis: proton pump inhibitors vs. H2-receptor antagonists--their efficacy with antibiotics in Helicobacter pylori eradication. Aliment Pharmacol Ther. 2003;18:757–66.
Ren Q, Ma B, Yang K, Yan X. Lafutidine-based triple therapy for Helicobacter pylori eradication. Hepatogastroenterology. 2010;57:1074–81.
McNicholl AG, Linares PM, Nyssen OP, Calvet X, Gisbert JP. Meta-analysis: esomeprazole or rabeprazole vs. first-generation pump inhibitors in the treatment of Helicobacter pylori infection. Aliment Pharmacol Ther. 2012;36:414–25.
Gisbert JP, Khorrami S, Calvet X, Pajares JM. Systematic review: Rabeprazole-based therapies in Helicobacter pylori eradication. Aliment Pharmacol Ther. 2003;17:751–64.
Gisbert JP, Pajares JM. Esomeprazole-based therapy in Helicobacter pylori eradication: a meta-analysis. Dig Liver Dis. 2004;36:253–9.
Gisbert JP, Khorrami S, Calvet X, Pajares JM. Pantoprazole based therapies in Helicobacter pylori eradication: a systematic review and meta-analysis. Eur J Gastroenterol Hepatol. 2004;16:89–99.
Wang X, Fang JY, Lu R, Sun DF. A meta-analysis: comparison of esomeprazole and other proton pump inhibitors in eradicating Helicobacter pylori. Digestion. 2006;73:178–86.
Zhang G, Zou J, Liu F, Bao Z, Dong F, Huang Y, et al. The efficacy of moxifloxacin-based triple therapy in treatment of Helicobacter pylori infection: a systematic review and meta-analysis of randomized clinical trials. Braz J Med Biol Res. 2013;46:607–13.
Gisbert JP, Calvet X. Update on non-bismuth quadruple (concomitant) therapy for eradication of Helicobacter pylori. Clin Exp Gastroenterol. 2012;5:23–34.
Lv ZF, Wang FC, Zheng HL, Wang B, Xie Y, Zhou XJ, et al. Meta-analysis: is combination of tetracycline and amoxicillin suitable for Helicobacter pylori infection? World J Gastroenterol. 2015;21:2522–33.
Luther J, Higgins PDR, Schoenfeld PS, Moayyedi P, Vakil N, Chey WD. Empiric quadruple vs. triple therapy for primary treatment of Helicobacter pylori infection: Systematic review and meta-analysis of efficacy and tolerability. Am J Gastroenterol. 2010;105:65–73.
Vergara M, Vallve M, Gisbert JP, Calvet X. Meta-analysis: comparative efficacy of different proton-pump inhibitors in triple therapy for Helicobacter pylori eradication. Aliment Pharmacol Ther. 2003;18:647–54.
Ford AC, Malfertheiner P, Giguere M, Santana J, Khan M, Moayyedi P. Adverse events with bismuth salts for Helicobacter pylori eradication: systematic review and meta-analysis. World J Gastroenterol. 2008;14:7361–70.
Graham DY, Hammoud F, El-Zimaity HMT, Kim JG, Osato MS, El-Serag HB. Meta-analysis: proton pump inhibitor or H2-receptor antagonist for Helicobacter pylori eradication. Aliment Pharmacol Ther. 2003;17:1229–36.
Nishizawa T, Nishizawa Y, Yahagi N, Kanai T, Takahashi M, Suzuki H. Effect of supplementation with rebamipide for Helicobacter pylori eradication therapy: a systematic review and meta-analysis. J Gastroenterol Hepatol. 2014;29 Suppl 4:20–4.
Fock KM, Katelaris P, Sugano K, Ang TL, Hunt R, Talley NJ, et al. Second Asia-Pacific Consensus Guidelines for Helicobacter pylori infection. J Gastroenterol Hepatol. 2009;24:1587–600.
Hunt RH, Xiao SD, Megraud F, Leon-Barua R, Bazzoli F, van der Merwe S, et al. Helicobacter pylori in developing countries. World Gastroenterology Organisation Global Guideline. J Gastrointestin Liver Dis. 2011;20:299–304.
No funding source.
Availability of data and materials
OW designed the study. JM conducted the electronic database search. JM and YX performed the selection of eligible studies. YX, JM and OW performed data extraction and critical appraisal. YX and LG carried out the network meta-analysis. YX and OW drafted the manuscript with comments by JM, RH, JB and EW. All authors approved the final version of the article, including the authorship list.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
Search strategy. (DOCX 13 kb)
WinBUGS code for the network meta-analysis model. (DOCX 12 kb)
Excluded studies based on full-text review. (DOCX 14 kb)
Quality assessment of included studies based on revised AMSTAR checklist. (DOCX 17 kb)
Individual study check table. (DOCX 52 kb)
About this article
Cite this article
Xin, Y., Manson, J., Govan, L. et al. Pharmacological regimens for eradication of Helicobacter pylori: an overview of systematic reviews and network meta-analysis. BMC Gastroenterol 16, 80 (2016). https://doi.org/10.1186/s12876-016-0491-7
- Helicobacter pylori
- Systematic review
- Network meta-analysis