Nonbismuth Quadruple (Concomitant) Therapy: Empirical and Tailored Efficacy versus Standard Triple Therapy for Clarithromycin-Susceptible Helicobacter pylori and versus Sequential Therapy for Clarithromycin-Resistant Strains

被引:79
作者
Molina-Infante, Javier [1 ]
Pazos-Pacheco, Carmen [2 ]
Vinagre-Rodriguez, Gema [1 ]
Perez-Gallardo, Belen [1 ]
Duenas-Sadornil, Carmen [1 ]
Hernandez-Alonso, Moises [1 ]
Gonzalez-Garcia, Guadalupe [1 ]
Mateos-Rodriguez, Jose M. [1 ]
Fernandez-Bermejo, Miguel [1 ]
Gisbert, Javier P. [3 ,4 ]
机构
[1] Hosp San Pedro de Alcantara, Dept Gastroenterol, Caceres 10003, Spain
[2] Hosp San Pedro de Alcantara, Dept Microbiol, Caceres 10003, Spain
[3] Hosp Univ Princesa, Dept Gastroenterol, Inst Invest Sanitaria Princesa IP, Madrid, Spain
[4] CIBEREHD, Madrid, Spain
关键词
Helicobacter pylori; nonbismuth quadruple therapy; concomitant therapy; clarithromycin resistance; sequential therapy; triple therapy; ANTIBIOTIC-RESISTANCE; ERADICATION THERAPY; RANDOMIZED-TRIAL; INFECTION; METAANALYSIS; METRONIDAZOLE; LEVOFLOXACIN; MANAGEMENT; REGIMENS; 4-DRUG;
D O I
10.1111/j.1523-5378.2012.00947.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background:similar to Using quadruple clarithromycin-containing regimens for Helicobacter pylori eradication is controversial with high rates of macrolide resistance. Aim:similar to To evaluate antibiotic resistance rates and the efficacy of empirical and tailored nonbismuth quadruple (concomitant) therapy in a setting with cure rates <80% for triple and sequential therapies. Methods:similar to 209 consecutive naive H.similar to pylori-positive patients without susceptibility testing were empirically treated with 10-day concomitant therapy (proton pump inhibitors (PPI), amoxicillin 1 g, clarithromycin 500 mg, and metronidazole 500 mg; all drugs b.i.d.). Simultaneously, 89 patients with positive H.similar to pylori culture were randomized to receive triple versus concomitant therapy for clarithromycin-susceptible H.similar to pylori, and sequential versus concomitant therapy for clarithromycin-resistant strains. Eradication was confirmed with 13C-urea breath test or histology 8 weeks after completion of treatment. Results:similar to Per-protocol (PP) and intention-to-treat eradication rates after empirical concomitant therapy without susceptibility testing were 89% (95%CI:8493%) and 87% (8392%). Antibiotic resistance rates were: clarithromycin, 20%; metronidazole, 34%; and both clarithromycin and metronidazole, 10%. Regarding clarithromycin-susceptible H.similar to pylori, concomitant therapy was significantly better than triple therapy by per protocol [92% (82100%) vs 74% (5891%), p = 0.05] and by intention to treat [92% (82100%) vs 70% (5790%), p = 0.02]. As for antibiotic-resistant strains, eradication rates for concomitant and sequential therapies were 100% (5/5) vs 75% (3/4), for clarithromycin-resistant/metronidazole-susceptible strains and 75% (3/4) vs 60% (3/5) for dual-resistant strains. Conclusions:similar to Empirical 10-day concomitant therapy achieves good eradication rates, close to 90%, in settings with multiresistant H.similar to pylori strains. Tailored concomitant therapy is significantly superior to triple therapy for clarithromycin-susceptible H.similar to pylori and at least as effective as sequential therapy for resistant strains.
引用
收藏
页码:269 / 276
页数:8
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