The recently published real-world study on Helicobacter pylori treatment, revealing that female (odds ratio 2.41 \[95% confidence interval (CI) 1.16-5.03\], P = 0.02) and age-Charlson Comorbidity Index ≥ 2 (odds ratio 3.16 \[1.05-9.48\], P = 0.04) were two independent factors for the failure of sequential therapy in eradicating Helicobacter pylori. The main cause of eradication failure is antibiotic resistance of the bacteria. Previous studies have found that females had more antibiotic-resistant Helicobacter pylori infections as compared with males did. In Australia and Italy, female was a predictor of metronidazole resistance; in Japan and Korea, female was a predictor of clarithromycin resistance; and among Alaskan Natives and in China, female predicted resistance to both metronidazole and clarithromycin.
The recent clinical trial found that the efficacy of a 10-day bismuth quadruple therapy was non-inferior to a 14-day bismuth quadruple therapy (Intention-to-treat analyses, 92.4% \[95% (CI): 88.2%-96.5%\] vs. 92.9% \[95% CI: 88.9%-97.0%\], absolute difference: -0.6%, lower boundary of the one-sided 97.5% CI: -6.7%, P = 0.020). However, subgroup analyses for males and females showed that while the 10-day therapy remained non-inferior to the 14-day therapy in males (95.2% \[95% CI: 90.6%-99.8%\] vs. 94.0% \[95% CI: 88.4%-99.7%\], absolute difference: 1.2%, lower boundary of the one-sided 97.5% CI: -6.8%, P = 0.022), it could not be demonstrated as non-inferior in females (89.2% \[95% CI: 82.1%-96.3%\] vs. 92.1% \[95% CI: 86.5%-96.3%\], absolute difference: -3.0%, lower boundary of the one-sided 97.5% CI: -12.3%, P = 0.198).
Previous research has identified female as a factor in the failure of 7-day clarithromycin-based triple therapy or concomitant therapy for Helicobacter pylori eradication. However, it is still uncertain whether female is a factor for Helicobacter pylori eradication failure with bismuth quadruple therapy.
In recent years, analyzing research results separately for females and males has become a trend. Historically, gender and sex differences were often overlooked in research design, conduct, and reporting, limiting the generalizability and applicability of findings to clinical practice. Heidari et al. have also advocated for the establishment of basic principles for international guidelines to encourage interdisciplinary research to systematically report sex and gender differences. The Sex and Gender Equity in Research (SAGER) guidelines recommend that researchers provide information on sex and gender in research design, data analysis, and result interpretation.
Given consecutive findings that females may have lower Helicobacter pylori eradication rates than males, designing a study to compare the efficacy of different durations of bismuth quadruple therapy between sexes is of significant clinical importance and aligns with current research trends.
This study hypothesizes that the rate of antibiotic resistance is higher in females compared to males. Consequently, the 10-day bismuth quadruple therapy will have a lower eradication rate in females compared to males. Because of the higher level of antibiotic resistance, females may require a longer treatment duration of 14 days to achieve the optimal eradication rate.
The patients with Helicobacter pylori infection are enrolled from National Cheng Kung University Hospital and Tainan Hospital, Ministry of Health and Welfare. Enrolled male participants received 10-day bismuth quadruple therapy. Enrolled female participants were randomly assigned into 10- or 14-day bismuth quadruple therapy with a 1:1 allocation ratio. Females and males are defined by biological attributes based on external body characteristics.
Sample size assessment: Using a Chi-square test to compare the 10-day bismuth quadruple therapy in females (experimental group) with the 10-day bismuth quadruple therapy in males (control group), where the efficacy in the control group is 96%. The null hypothesis is that there is no difference in efficacy between the experimental and control groups, with a margin of difference set at 7% (Helicobacter pylori eradication rate must be at least 90%). If the efficacy difference between the two groups is ≥ 7% (experimental group efficacy \< 90%), the null hypothesis will be rejected, indicating a difference between females and males in efficacy of the 10-day bismuth quadruple therapy. If the efficacy difference between the two groups is \< 7% (experimental group efficacy ≥ 90%), the null hypothesis cannot be rejected; however, there is no evidence to suggest that the 10-day therapy in females is as effective as in males. Based on this, each group needs 221 patients to achieve 80% power and a two-sided 95% confidence interval to reject the null hypothesis of a ≥ 7% difference in efficacy between the two groups.
Additionally, a superiority trial will compare the 14-day bismuth quadruple therapy in females (experimental group) with the 10-day bismuth quadruple therapy in females (control group), where the efficacy in the control group is 89%. The null hypothesis is that the experimental group is the same as or worse than the control group, with a margin of difference set at 7% (past research shows bismuth quadruple therapy efficacy at 96%). If the experimental group is superior to the control group with a difference of ≥ 7% (experimental group efficacy ≥ 96%), the null hypothesis will be rejected, indicating that the 14-day therapy is superior to the 10-day therapy in females. If the efficacy difference between the two groups is \< 7% (experimental group efficacy \< 96%), the null hypothesis cannot be rejected; however, there is no evidence to suggest that the 14-day therapy is as effective as or worse than the 10-day therapy in females. Based on this, each group needs 219 patients to achieve 80% power and a two-sided 95% confidence interval to reject the null hypothesis of a \< 7% difference in efficacy between the two groups.
Primary Endpoint: The primary endpoint of the study is the successful eradication rate of Helicobacter pylori. All enrolled participants will be included in the overall analysis, incorporating intention-to-treat, per-protocol, and modified intention-to-treat analyses. All enrolled participants are included in the intention-to-treat analysis; those who are lost to follow-up, take less than 80% of the study medications, or have any protocol violation are excluded from the per-protocol analysis. The modified intention-to-treat analysis is similar to the intention-to-treat analysis, but patients with missing primary outcome data are excluded.
Secondary Endpoints: The secondary endpoints include the incidence of adverse events and medication adherence. There are 14 adverse events recorded, including dizziness, skin rash, headache, taste alteration, abdominal pain, nausea, diarrhea, constipation, bloating, vomiting, tongue discoloration, darkened stool, fatigue, and anorexia. Adverse events are assessed by a physician and a format questionnaire survey after the end of treatment. Serious adverse events are defined as daily activities restricted or participant unable to work. Medication adherence is assessed using a medication diary to record the number of days the medication was taken.
Statistical analysis: The statistical analysis is performed with SPSS software (SPSS 17, Chicago, IL, USA). The Student's t-test, Pearson's χ2 test, and Mann-Whitney U test are conducted to identify the statistical differences between the two comparison groups.
Antibiotic resistance that might affect the eradication rate, is assessed by H pylori culture.
