Abstract
Introduction
Helicobacter pylori infection is encountered in more than 50% of the world population. A high rate of clarithromycin resistance is observed among Helicobacter pylori strains in some regions because clarithromycin is a drug commonly used for the treatment of other infections.
Aim
To identify an efficient eradication protocol for patients infected with H. pylori and to suggest an alternative first-line therapy particularly in countries with high clarithromycin resistance.
Material and methods
Patients (18–75 years old) having dyspeptic complaints in a 1-year period and diagnosed with H. pylori infection by gastric biopsy were included and randomised to three groups, each receiving different sequential eradication therapy (LAM-B: lansoprazole, amoxicillin, metronidazole, bismuth: LAM-T: lansoprazole, amoxicillin, metronidazole, tetracycline; LAM-BT: lansoprazole, amoxicillin, metronidazole, bismuth, tetracycline). Eradication was evaluated via urea breath test.
Results
This study included 166 patients (mean age: 40 ±12 years; female, 68.7%) with H. pylori infection. Among them, 50 (30.1%) were in the LAM-B group, 59 (35.5%) were in the LAM-T group, and 57 (34.3%) were in the LAM-BT group. The non-steroidal anti-inflammatory drug use was the lowest in the LAM-BT group. Eradication rates were over 80% and similar in each group, with the highest rate in the LAM-BT group (93%). Adverse event rate was the highest in the LAM-T group. Helicobacter pylori eradication was achieved in 143 (86.1%) patients.
Conclusions
The combination regimens without clarithromycin achieved an eradication rate over 80% in all groups. Knowing and monitoring the regional antibiotic resistance rates is important for successful treatment of H. pylori infections.
Keywords: Helicobacter pylori eradication, clarithromycin resistance
Introduction
Helicobacter pylori (H. pylori) is a microorganism that is estimated to cause infection in more than 50% of the world population despite its varying prevalence among geographical regions, and thereby it is responsible for significant morbidity and mortality [1]. Helicobacter pylori is associated with active chronic gastritis, peptic ulcer disease, gastric cancer, and gastric mucosa-associated lymphoid tissue lymphoma and is reported to enhance the risk of developing ulceration and gastric bleeding in individuals using non-steroidal anti-inflammatory drugs (NSAIDs) [1]. Nearly 5% of the total annual cancer cases worldwide have been attributed to H. pylori [2].
Urea breath test and endoscopy with biopsy are the major diagnostic tools used to detect H. pylori infection [1]. Various combinations of antibiotics are used as eradication treatment. The most common therapeutic recommendations include 1-week triple therapy with proton pump inhibitor (PPI), amoxicillin, and clarithromycin. There are second-line therapies recommended in case the first-line therapy fails. The presence of pre-treatment antimicrobial resistance, nonadherence to treatment, and smoking have been reported among the factors contributing to treatment failure [1].
It has been emphasised that response to the first-line standard treatment of H. pylori infection has decreased in recent years. While the eradication rate was over 90% in the beginning, it has been reduced to below 70% in time [3]; one of the reasons for this is the resistance to antibiotics, particularly to clarithromycin. A high rate of clarithromycin resistance is encountered among H. pylori strains in some regions because clarithromycin is a drug commonly used for the treatment of other infections [1, 3]. The reported prevalence of clarithromycin resistance in H. pylori ranges from 12.5% to 76.2% in different regions of the world [4–8].
In a study from Turkey, which screened the population via urea breath test, the prevalence of H. pylori infection was found to be as high as 82.5% [9]. In the studies, the rates of clarithromycin resistance in Turkey have been reported to be 36.7% [10], 47.5% [11], and 48.2% [12].
Aim
The aim of the present study was to identify an efficient eradication protocol for patients infected with H. pylori and to suggest an alternative first-line therapy, particularly in countries with high clarithromycin resistance, such as Turkey. In addition, it was aimed to investigate the factors that may have an effect on eradication.
Material and methods
Patients
Patients aged between 18 and 75 years, who presented with dyspeptic complaints in a 1-year period and in whom H. pylori was determined by gastric biopsy, were enrolled in the present study in three centres in Ankara. Patients with gastric or duodenal ulcer, those with chronic liver/kidney disease or history of malignancy, those having previous treatment for H. pylori infection, and those with a history of PPI, histamine-2 (H2) receptor antagonist, or antibiotic use within the last four weeks were excluded. The present study was approved by the Ethics Committee of Dışkapı Yıldırım Beyazıt Training and Research Hospital.
Procedures
Gastric biopsy was taken from the gastric antrum and corpus of the patients during endoscopic examination of the upper gastrointestinal system. The patients were diagnosed with H. pylori infection based on histopathological examination, and histopathological grading was performed.
The patients infected with H. pylori were randomised to three groups, and each group received different sequential eradication therapy. The treatment schedule of the study groups is presented in Table I. Eradication was evaluated via carbon 14-labeled urea breath test (14C-UBT) performed 6 weeks after the completion of treatment.
Table I.
Week | Treatment groups | ||
---|---|---|---|
LAM-B | LAM-T | LAM-BT | |
1 | Lansoprazole 2 × 30 mg | Lansoprazole 2 × 30 mg | Lansoprazole 2 × 30 mg |
Amoxicillin 2 × 1000 mg | Amoxicillin 2 × 1000 mg | Amoxicillin 2 × 1000 mg | |
2 | Lansoprazole 2 × 30 mg | Lansoprazole 2 × 30 mg | Lansoprazole 2 × 30 mg |
Metronidazole 4 × 500 mg | Metronidazole 4 × 500 mg | Metronidazole 4 × 500 mg | |
Bismuth 4 × 500 mg | Tetracycline 4 × 500 mg | Bismuth 4 × 500 mg | |
Tetracycline 4 × 500 mg |
Factors (age, gender, body mass index, alcohol consumption, smoking, non-steroidal anti-inflammatory drug use, localisation of H. pylori, H. pylori load, severity of inflammation, degree of activation, and presence of atrophy and intestinal metaplasia) that might have an effect on eradication were assessed.
Histopathological examination
Helicobacter pylori load, severity of inflammation, and degree of activation were graded by the modified Sydney classification [13] using visual analogue scales as follows: 0, normal; 1+, mild; 2+, moderate; and 3+, marked. Moreover, presences of atrophy and intestinal metaplasia were also recorded.
Statistical analysis
Data analyses were performed using PASW Statistics for Windows version 18.0 (SPSS Inc., Chicago, IL, USA). Descriptive statistics were expressed as mean, standard deviation, median, minimum, and maximum for numerical variables. Normal distribution of variables was analysed using visual (histogram and probability graphics) and analytical methods (Kolmogorov-Smirnov/Shapiro-Wilk test). Two- and multiple-group comparisons between categorical variables were performed by χ2 test or by Fisher’s exact test. χ2 test with Bonferroni correction was used for subgroup comparisons. Multiple independent group comparisons were performed using analysis of variance (ANOVA) test for normally distributed numerical variables and using Kruskal-Wallis test for non-normally distributed numerical variables. Comparison of numerical variables between two independent groups was performed using t-test for normally distributed variables and using Mann-Whitney U test for non-normally distributed variables. The level of significance was determined as p < 0.05.
Results
The present study included 166 patients (mean age: 40 ±12 years) with H. pylori infection. Of the patients, 68.7% were female, 27.1% were smokers, and 33.7% had a history of NSAID use. The general characteristics of the patients are shown in Table II.
Table II.
Characteristics | Value |
---|---|
Age [years], mean ± SD | 40 ±12 |
Gender, n (%): | |
Male | 52 (31.3) |
Female | 114 (68.7) |
BMI [kg/m2], n (%): | |
< 18.5 | 2 (1.2) |
18.5–< 25 | 58 (34.9) |
25–< 30 | 65 (39.2) |
≥30 | 41 (24.7) |
Alcohol consumption, n (%) | 1 (0.6) |
Smoking, n (%) | 45 (27.1) |
NSAIDs use, n (%) | 56 (33.7) |
Localization of H. pylori infection, n (%): | |
Antrum | 28 (16.9) |
Corpus | 22 (13.3) |
Antrum + corpus | 116 (69.9) |
SD – standard deviation, BMI – body mass index, NSAIDs – non-steroidal anti-inflammatory drugs.
Of the H. pylori infections, 144 were in the antrum and 138 were in the corpus. The characteristics according to the localisations (antrum and corpus) are shown in Table III.
Table III.
Parameter | Localisation | |
---|---|---|
Antrum (n = 144) | Corpus (n = 138) | |
H. pylori load, n (%): | ||
Normal | 22 (13.3) | 28 (16.9) |
Mild | 43 (25.9) | 50 (30.1) |
Moderate | 72 (43.4) | 70 (42.2) |
Marked | 29 (17.5) | 18 (10.8) |
Severity of inflammation, n (%): | ||
Normal | 0 (0.0) | 1 (0.6) |
Mild | 41 (24.7) | 68 (41.0) |
Moderate | 83 (50.0) | 87 (52.4) |
Marked | 42 (25.3) | 10 (6.0) |
Degree of activation, n (%): | ||
Normal | 21 (12.7) | 35 (21.1) |
Mild | 38 (22.9) | 46 (27.7) |
Moderate | 90 (54.2) | 78 (47.0) |
Marked | 17 (10.2) | 7 (4.2) |
Atrophy, n (%) | 26 (15.7) | 5 (3.0) |
Metaplasia, n (%) | 30 (18.1) | 3 (1.8) |
Among the patients, 50 (30.1%) were in the LAM-B group, 59 (35.5%) were in the LAM-T group, and 57 (34.3%) were in the LAM-BT group. The general characteristics of the treatment groups are shown in Table IV. The treatment groups were similar in terms of demographic and lesion characteristics. The rate of patients receiving NSAIDs was the lowest in the LAM-BT group. Eradication rates were over 80% and similar in each group. Although statistically not significant, the LAM-BT group had the highest clinical eradication rate at 93%. The rate of adverse events was the highest in the LAM-T group, and no adverse event was observed in the LAM-B group.
Table IV.
Parameter | Treatment groups | P-value | ||
---|---|---|---|---|
LAM-B (n = 50) | LAM-T (n = 59) | LAM-BT (n = 57) | ||
Age [year], mean ± SD | 38 ±10 | 40 ±12 | 40 ±13 | 0.533 |
Gender, n (%): | ||||
Male | 12 (24.0) | 23 (39.0) | 17 (29.8) | 0.233 |
Female | 38 (76.0) | 36 (61.0) | 40 (70.2) | |
BMI [kg/m2], n (%): | ||||
< 18.5–24.9 | 22 (44.0) | 21 (35.6) | 17 (29.8) | 0.210 |
25.0–29.9 | 15 (30.0) | 21 (35.6) | 29 (50.9) | |
≥30.0 | 13 (26.0) | 17 (28.8) | 11 (19.3) | |
Alcohol consumer, n (%) | 0 (0.0) | 0 (0.0) | 1 (1.8) | – |
Smoking, n (%) | 15 (30.0) | 16 (27.1) | 14 (24.6) | 0.819 |
NSAIDs use, n (%) | 25 (50.0)c | 17 (28.8) | 14 (24.6)a | 0.013 |
Localisation of lesion, n (%): | ||||
Antrum | 6 (12.0) | 13 (22.0) | 9 (15.8) | 0.508 |
Corpus | 8 (16.0) | 5 (8.5) | 9 (15.8) | |
Antrum + corpus | 36 (72.0) | 41 (69.5) | 39 (68.4) | |
H. pylori load*, median (min.–max.) | 2 (1–3) | 2 (1–3) | 2 (1–3) | 0.918 |
Severity of inflammation*, median (min.–max.) | 2 (1–3) | 2 (1–3) | 2 (1–3) | 0.537 |
Degree of activation*, median (min.–max.) | 2 (0–3) | 2 (0–3) | 2 (1–3) | 0.824 |
Presence of atrophy**, n (%) | 8 (16.0) | 12 (20.3) | 10 (17.5) | 0.835 |
Presence of metaplasia**, n (%) | 9 (18.0) | 13 (22.0) | 10 (17.5) | 0.798 |
Presence of eradication, n (%) | 41 (82.0) | 49 (83.1) | 53 (93.0) | 0.180 |
Presence of adverse event, n (%) | 0 (0.0)b | 6 (10.2)a | 2 (3.5) | 0.034 |
SD – standard deviation, BMI – body mass index, NSAIDs – non-steroidal anti-inflammatory drugs, min.–max. – minimum–maximum.
The region with higher score was evaluated in the patients with localisation in the antrum + corpus.
The region with change was evaluated in the patients with localisation in the antrum + corpus.
Different from the LAM-B group
Different from the LAM-T group
Different from the LAM-BT group.
Helicobacter pylori eradication was achieved in 143 (86.1%) patients. The characteristics of the patients with and without eradication of H. pylori were compared (Table V). No significant difference was determined between the groups in terms of demographic or histopathological features.
Table V.
Parameter | Patients | P-value | |
---|---|---|---|
Without eradication (n = 23) | With eradication (n = 143) | ||
Age [years], mean ± SD | 37 ±10 | 40 ±12 | 0.220 |
Gender, n (%): | |||
Male | 8 (34.8) | 44 (30.8) | 0.700 |
Female | 15 (65.2) | 99 (69.2) | |
BMI [kg/m2], n (%): | |||
< 18.5–24.9 | 9 (39.1) | 51 (35.7) | 0.312 |
25.0–29.9 | 6 (26.1) | 59 (41.3) | |
≥30.0 | 8 (34.8) | 33 (23.1) | |
Alcohol consumer, n (%) | 0 (0.0) | 1 (0.7) | – |
Smoking, n (%) | 5 (21.7) | 40 (28.0) | 0.533 |
NSAIDs use, n (%) | 6 (26.1) | 50 (35.0) | 0.403 |
Localization of H. pylori, n (%): | |||
Antrum | 1 (4.3) | 27 (18.9) | 0.213 |
Corpus | 3 (13.0) | 19 (13.3) | |
Antrum + corpus | 19 (82.6) | 97 (67.8) | |
H. pylori load*, median (min.–max.) | 2 (1–3) | 2 (1–3) | 0.179 |
Severity of inflammation*, median (min.–max.) | 2 (1–3) | 2 (1–3) | 0.404 |
Degree of activation*, median (min.–max.) | 2 (1–3) | 2 (0–3) | 0.638 |
Presence of atrophy**, n (%) | 5 (21.7) | 25 (17.5) | 0.571 |
Presence of metaplasia**, n (%) | 3 (13.0) | 29 (20.3) | 0.573 |
Treatment group, n (%): | |||
LAM-B | 9 (39.1) | 41 (28.7) | 0.180 |
LAM-T | 10 (43.5) | 49 (34.3) | |
LAM-BT | 4 (17.4) | 53 (37.1) | |
Adverse event, n (%) | 0 (0.0) | 8 (5.6) | 0.601 |
SD – standard deviation, BMI – body mass index, NSAIDs – non-steroidal anti-inflammatory drugs, min.–max. – minimum-maximum.
The region with higher score was evaluated in the patients with localisation in the antrum + corpus.
The region with change was evaluated in the patients with localisation in the antrum + corpus.
Discussions
In recent years the eradication rate of H. pylori infection has been gradually decreasing with standard first-line triple therapy [14]. Although an eradication rate of over 90% is still being achieved with seven-day triple therapy options for H. pylori infection in regions with low antibiotic resistance, [15] the eradication rate has been reduced to below 80% in regions with the problem of antibiotic resistance [14]. Alternative methods of first-line therapy such as increasing drug dose [16], prolonging treatment period [17], sequential administration of drugs [18], or using different drug combinations [19–21] have emerged to achieve a successful eradication.
In a systematic review with meta-analysis in which studies on first-line therapy in eradicating H. pylori infection were evaluated, 14-day sequential treatment, but not 10-day treatment, was concluded to be more effective as compared with triple therapy given for 14 days as first-line treatment [22]. Liou et al. [23] determined the eradication rate of H. pylori to be 90.4% with bismuth-based first-line quadruple therapy (300 mg of bismuth tripotassium dicitrate four times a day, 30 mg of lansoprazole two times a day, 500 mg of tetracycline four times a day, and 500 mg of metronidazole three times a day). The rate of adverse events with that treatment modality was 67%, and the rate of adverse events causing drug discontinuation was 10%. Uygun et al. [24] reported the eradication rate to be 82.3% with the same treatment modality. Alboraie et al. [25] compared the first-line treatment modality of 10-day triple therapy containing omeprazole, amoxicillin, and clarithromycin with 10-day quadruple therapy containing omeprazole, bismuth, tetracycline, and metronidazole. They found a higher eradication rate with bismuth-based quadruple therapy as compared to clarithromycin-based triple therapy (88% vs. 68.6%). In light of the above-mentioned information, we also achieved an eradication rate of over 80% by implementing bismuth-based (without clarithromycin) treatment regimens sequentially for 14 days. All treatment groups were similar in terms of demographical, clinical, and histopathological features. Although the eradication rate showed no significant difference among the three groups, the highest eradication rate was clinically observed in the LAM-BT group, at 93%. The rate of adverse events was the highest in the LAM-T group (10.2%). Comparison of the characteristics of patients with and without eradication of H. pylori revealed no difference in terms of demographical, clinical, or histopathological features.
There are numerous factors that influence treatment for H. pylori eradication. In addition to antibiotic resistance, these factors include personal, genetic, and environmental factors [14]. While some studies have reported gender difference for response to the eradication therapy [25, 26], some have found no difference [27]. In the present study, the eradication rates were not different between males and females. Smoking has also been reported as one of the factors unfavourably influencing eradication [26, 28]. In the present study, the rate of smoking was similar in the patient groups with and without successful eradication.
In gastroduodenal pathology, there is a complex relation between H. pylori infection and NSAIDs. Both H. pylori infection and nonselective use of NSAIDs have been reported as independent risk factors for peptic ulcer development and ulcer bleeding. These factors probably show additive or synergistic effect, as well [29, 30]. Therefore, clinicians want to test the presence of H. pylori and to treat it if present, to reduce development and complications of ulcers in individuals receiving NSAIDs [30]. In the present study, 33.7% of the patients were using NSAIDs. The rate of NSAID use was the lowest (24.6%) in the LAM-BT group, in which the eradication rate was 93%. Nevertheless, no significant difference was found between the groups with and without successful eradication in terms of NSAID use.
In their study, Onal et al. [31] investigated the effect of H. pylori density, which was determined by histological grading, on the success of eradication therapy and reported that H. pylori density negatively affected triple therapy (lansoprazole, clarithromycin, amoxicillin) but not quadruple therapy (colloidal bismuth subcitrate, lansoprazole, tetracycline, metronidazole). Shah et al. [32] determined a correlation between H. pylori density and complications such as duodenal ulcer, reflux esophagitis, and antral erosions and found a significantly lower eradication rate in the patients with higher H. pylori density. In the present study, no significant difference was determined between the patients with and without eradication in terms of graded histopathological features, including H. pylori density.
Conclusions
Based on the knowledge that clarithromycin resistance is high in Turkey, the present study tested the combination regimens without clarithromycin as the first-line therapy and achieved an eradication rate of over 80% in all treatment groups with an eradication rate of 93% achieved in the LAM-BT group. Knowing and monitoring the rates of regional antibiotic resistance, which is among the factors that influence eradication, are important to overcome this problem for successful treatment of H. pylori infections.
Conflict of interest
The authors declare no conflict of interest.
References
- 1.Mitchell H, Katelaris P. Epidemiology, clinical impacts and current clinical management of Helicobacter pylori infection. Med J Aust. 2016;204:376–80. doi: 10.5694/mja16.00104. [DOI] [PubMed] [Google Scholar]
- 2.Plummer M, Franceschi S, Vignat J, et al. Global burden of gastric cancer attributable to Helicobacter pylori. Int J Cancer. 2015;136:487–90. doi: 10.1002/ijc.28999. [DOI] [PubMed] [Google Scholar]
- 3.O’Connor A, Gisbert JP, McNamara D, et al. Treatment of Helicobacter pylori infection 2010. Helicobacter. 2010;15(Suppl 1):46–52. doi: 10.1111/j.1523-5378.2010.00774.x. [DOI] [PubMed] [Google Scholar]
- 4.Martins GM, Sanches BS, Moretzsohn LD, et al. Molecular detection of clarithromycin and fluoroquinolones resistance in Helicobacter pylori infection, directly applied to gastric biopsies, in an urban Brazilian population. Arq Gastroenterol. 2016;53:113–7. doi: 10.1590/S0004-28032016000200012. [DOI] [PubMed] [Google Scholar]
- 5.Ji Z, Han F, Meng F, et al. The association of age and antibiotic resistance of Helicobacter pylori: a study in Jiaxing City, Zhejiang Province, China. Medicine (Baltimore) 2016;95:e2831. doi: 10.1097/MD.0000000000002831. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Hakemi Vala M, Eyvazi S, Goudarzi H, et al. Evaluation of clarithromycin resistance among Iranian Helicobacter pylori isolates by E-Test and real-time polymerase chain reaction methods. Jundishapur J Microbiol. 2016;9:e29839. doi: 10.5812/jjm.29839. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Alsohaibani F, Al Ashgar H, Al Kahtani K, et al. Prospective trial in Saudi Arabia comparing the 14-day standard triple therapy with the 10-day sequential therapy for treatment of Helicobacter pylori infection. Saudi J Gastroenterol. 2015;21:220–5. doi: 10.4103/1319-3767.161647. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Tongtawee T, Dechsukhum C, Matrakool L, et al. High prevalence of Helicobacter pylori resistance to clarithromycIn: a hospital-based cross-sectional study in Nakhon Ratchasima Province, Northeast of Thailand. Asian Pac J Cancer Prev. 2015;16:8281–5. doi: 10.7314/apjcp.2015.16.18.8281. [DOI] [PubMed] [Google Scholar]
- 9.Ozaydin N, Turkyilmaz SA, Cali S. Prevalence and risk factors of Helicobacter pylori in Turkey: a nationally-representative, cross-sectional, screening with the ¹³C-urea breath test. BMC Public Health. 2013;13:1215. doi: 10.1186/1471-2458-13-1215. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Caliskan R, Tokman HB, Erzin Y, et al. Antimicrobial resistance of Helicobacter pylori strains to five antibiotics, including levofloxacin, in Northwestern Turkey. Rev Soc Bras Med Trop. 2015;48:278–84. doi: 10.1590/0037-8682-0027-2015. [DOI] [PubMed] [Google Scholar]
- 11.Kaya AD, Oztürk CE, Akcan Y, et al. Prevalence of Helicobacter pylori in symptomatic patients and detection of clarithromycin resistance using melting curve analysis. Curr Ther Res Clin Exp. 2007;68:151–60. doi: 10.1016/j.curtheres.2007.06.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Onder G, Aydin A, Akarca U, et al. High Helicobacter pylori resistance rate to clarithromycin in Turkey. J Clin Gastroenterol. 2007;41:747–50. doi: 10.1097/MCG.0b013e31802e7ee7. [DOI] [PubMed] [Google Scholar]
- 13.Dixon MF, Genta RM, Yardley JH, et al. Classification and grading of gastritis. The updated Sydney System. International Workshop on the Histopathology of Gastritis, Houston 1994. Am J Surg Pathol. 1996;20:1161–81. doi: 10.1097/00000478-199610000-00001. [DOI] [PubMed] [Google Scholar]
- 14.Zhang M. High antibiotic resistance rate: a difficult issue for Helicobacter pylori eradication treatment. World J Gastroenterol. 2015;21:13432–7. doi: 10.3748/wjg.v21.i48.13432. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Tong YF, Lv J, Ying LY, et al. Seven-day triple therapy is a better choice for Helicobacter pylori eradication in regions with low antibiotic resistance. World J Gastroenterol. 2015;21:13073–9. doi: 10.3748/wjg.v21.i46.13073. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Franceschi F, Ojetti V, Gabrielli M, et al. High dose amoxicillin-based first line regimen is equivalent to sequential therapy in the eradication of H. pylori infection. Eur Rev Med Pharmacol Sci. 2016;20:297–300. [PubMed] [Google Scholar]
- 17.Chen YI, Fallone CA. A 14-day course of triple therapy is superior to a 10-day course for the eradication of Helicobacter pylori: a Canadian study conducted in a ‘real world’ setting. Can J Gastroenterol Hepatol. 2015;29:e7–10. doi: 10.1155/2015/659390. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Haider RB, Brennan DE, Omorogbe J, et al. A randomized-controlled study to compare the efficacy of sequential therapy with standard triple therapy for Helicobacter pylori eradication in an Irish population. Eur J Gastroenterol Hepatol. 2015;27:1265–9. doi: 10.1097/MEG.0000000000000457. [DOI] [PubMed] [Google Scholar]
- 19.Gokcan H, Oztas E, Onal IK. Different bismuth-based therapies for eradicating Helicobacter pylori: randomized clinical trial of efficacy and safety. Clin Res Hepatol Gastroenterol. 2016;40:124–31. doi: 10.1016/j.clinre.2015.06.014. [DOI] [PubMed] [Google Scholar]
- 20.Songür Y, Senol A, Balkarli A, et al. Triple or quadruple tetracycline-based therapies versus standard triple treatment for Helicobacter pylori treatment. Am J Med Sci. 2009;338:50–3. doi: 10.1097/MAJ.0b013e31819c7320. [DOI] [PubMed] [Google Scholar]
- 21.Zhang W, Chen Q, Liang X, et al. Bismuth, lansoprazole, amoxicillin and metronidazole or clarithromycin as first-line Helicobacter pylori therapy. Gut. 2015;64:1715–20. doi: 10.1136/gutjnl-2015-309900. [DOI] [PubMed] [Google Scholar]
- 22.Liou JM, Chen CC, Lee YC, et al. Taiwan Gastrointestinal Disease and Helicobacter Consortium. Systematic review with meta-analysis: 10- or 14-day sequential therapy vs. 14-day triple therapy in the first line treatment of Helicobacter pylori infection. Aliment Pharmacol Ther. 2016;43:470–81. doi: 10.1111/apt.13495. [DOI] [PubMed] [Google Scholar]
- 23.Liou JM, Fang YJ, Chen CC, et al. Taiwan Gastrointestinal Disease and Helicobacter Consortium. Concomitant, bismuth quadruple, and 14-day triple therapy in the first-line treatment of Helicobacter pylori: a multicentre, open-label, randomised trial. Lancet. 2016;388:2355–65. doi: 10.1016/S0140-6736(16)31409-X. [DOI] [PubMed] [Google Scholar]
- 24.Uygun A, Kadayifci A, Safali M, et al. The efficacy of bismuth containing quadruple therapy as a first-line treatment option for Helicobacter pylori. J Dig Dis. 2007;8:211–5. doi: 10.1111/j.1751-2980.2007.00308.x. [DOI] [PubMed] [Google Scholar]
- 25.Alboraie M, Saad M, Al-Ali J, et al. Quadruple therapy versus standard triple therapy for eradication of Helicobacter pylori in Kuwait. Arab J Gastroenterol. 2015;16:131–5. doi: 10.1016/j.ajg.2015.09.007. [DOI] [PubMed] [Google Scholar]
- 26.Kim SE, Park MI, Park SJ, et al. Trends in Helicobacter pylori eradication rates by first-line triple therapy and related factors in eradication therapy. Korean J Intern Med. 2015;30:801–7. doi: 10.3904/kjim.2015.30.6.801. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Apostolopoulos P, Koumoutsos I, Ekmektzoglou K, et al. Concomitant versus sequential therapy for the treatment of Helicobacter pylori infection: a Greek randomized prospective study. Scand J Gastroenterol. 2016;51:145–51. doi: 10.3109/00365521.2015.1079646. [DOI] [PubMed] [Google Scholar]
- 28.Koivisto TT, Rautelin HI, Voutilainen ME, et al. First-line eradication therapy for Helicobacter pylori in primary health care based on antibiotic resistance: results of three eradication regimens. Aliment Pharmacol Ther. 2005;21:773–82. doi: 10.1111/j.1365-2036.2005.02398.x. [DOI] [PubMed] [Google Scholar]
- 29.Malfertheiner P, Megraud F, O’Morain C, et al. Current concepts in the management of Helicobacter pylori infection: the Maastricht III Consensus Report. Gut. 2007;56:772–81. doi: 10.1136/gut.2006.101634. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Chey WD, Wong BC. Practice Parameters Committee of the American College of Gastroenterology. American College of Gastroenterology guideline on the management of Helicobacter pylori infection. Am J Gastroenterol. 2007;102:1808–25. doi: 10.1111/j.1572-0241.2007.01393.x. [DOI] [PubMed] [Google Scholar]
- 31.Onal IK, Gokcan H, Benzer E, et al. What is the impact of Helicobacter pylori density on the success of eradication therapy: a clinico-histopathological study. Clin Res Hepatol Gastroenterol. 2013;37:642–6. doi: 10.1016/j.clinre.2013.05.005. [DOI] [PubMed] [Google Scholar]
- 32.Shah DK, Jain SS, Mohite A, et al. Effect of H. pylori density by histopathology on its complications and eradication therapy. Trop Gastroenterol. 2015;36:101–6. doi: 10.7869/tg.261. [DOI] [PubMed] [Google Scholar]