Efficacy of Helicobacter pylori eradication regimens in Rwanda: a randomized controlled trial

被引:17
|
作者
Kabakambira, Jean Damascene [1 ]
Hategeka, Celestin [2 ,3 ]
Page, Cameron [4 ]
Ntirenganya, Cyprien [5 ]
Dusabejambo, Vincent [1 ]
Ndoli, Jules [5 ]
Ngabonziza, Francois [1 ]
Hale, DeVon [6 ]
Bayingana, Claude [5 ]
Walker, Tim [5 ,7 ]
机构
[1] Kigali Univ Teaching Hosp CHUK, Kigali, Rwanda
[2] Univ British Columbia, Sch Populat & Publ Hlth, Fac Med, Ctr Hlth Serv & Policy Res, Vancouver, BC, Canada
[3] Univ British Columbia, Fac Pharmaceut Sci, Collaborat Outcomes Res & Evaluat, Vancouver, BC, Canada
[4] Univ Hosp Brooklyn, Dept Med, New York, NY USA
[5] Butare Univ Teaching Hosp CHUB, Huye, Rwanda
[6] Univ Utah, Sch Med, Dept Med, Salt Lake City, UT USA
[7] Univ Newcastle, Fac Hlth & Med, Sch Med & Publ Hlth, Newcastle, NSW, Australia
来源
BMC GASTROENTEROLOGY | 2018年 / 18卷
关键词
H. pylori eradication; Dyspepsia; Clinical trial; Rwanda; PROTON PUMP INHIBITOR; QUALITY-OF-LIFE; PYLORI INFECTION; FUNCTIONAL DYSPEPSIA; ANTIBIOTIC-RESISTANCE; CLINICAL-IMPLICATIONS; ERADICATION THERAPY; TRIPLE THERAPY; STRAINS; SUSCEPTIBILITY;
D O I
10.1186/s12876-018-0863-2
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Successful H. pylori treatment requires the knowledge of local antimicrobial resistance. Data on the efficacy of H. pylori eradication regimens available in sub-Saharan Africa are scant, hence the optimal treatment is unknown. Our goals were to determine the efficacy of available regimens in Rwanda as well as evaluate the effect of treatment on health-related quality of life (HRQoL) in patients undergoing esophagogastroduodenoscopy. Methods: This is a randomized controlled trial conducted from November 2015 to October 2016 at a tertiary hospital in Rwanda. Enrollees were 299 patients (35% male, age 42 +/- 16 years (mean +/- SD)) who had a positive modified rapid urease test on endoscopic biopsies. After a fecal antigen test (FAT) and HRQoL assessment by the Short Form Nepean Dyspepsia Index (SF-NDI) questionnaire, patients were randomized 1:1:1:1 to either a triple therapy combining omeprazole, amoxicillin and one of clarithromycin/ciprofloxacin/metronidazole or a quadruple therapy combining omeprazole, amoxicillin, ciprofloxacin and doxycycline. All therapies were given for a duration of 10 days. The outcome measures were the persistence of positive FAT (treatment failure) 4 to 6 weeks after treatment and change in HRQoL scores. Results: The treatment success rate was 80% in the total population and 78% in patients with a history of prior triple therapy. Significant improvement in HRQoL in the total group (HRQoL mean scores before and after treatment respectively: 76 +/- 11 and 32 +/- 11, p < 0.001) and the group with functional dyspepsia (HRQoL mean scores before and after treatment respectively: 73 +/- 11 and 30 +/- 9, P < 0.001) was observed across all treatment groups. Using clarithromycin based triple therapy (standard of care) as a reference, the group treated with metronidazole had worse HRQoL (p = 0.012) and had a trend towards worse treatment outcome (p = 0.086) compared to the ciprofloxacin based combination therapies. Conclusion: Clarithromycin and ciprofloxacin based combination therapies are effective and safe to use alternatively for H. pylori eradication and improve HRQoL. Among the regimens studied, metronidazole based triple therapy is likely to be clinically inferior.
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页数:9
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