Low-dose lansoprazole and clarithromycin plus metronidazole vs. full-dose lansoprazole and clarithromycin plus amoxicillin for eradication of Helicobacter pylori injection

被引:14
作者
Bazzoli, F
Zagari, RM
Pozzato, P
Fossi, S
Ricciardiello, L
Nicolini, G
De Luca, L
Barretti, D
Alampi, G
Di Pietro, C
Morelli, P
Roda, E
机构
[1] Univ Bologna, Policlin S Orsola, Dipartimento Med Interna & Gastroenterol, I-40138 Bologna, Italy
[2] Univ Bologna, Ist Anat & Istol Patol, I-40138 Bologna, Italy
关键词
D O I
10.1046/j.1365-2036.2002.01141.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim: To compare, in a randomized controlled trial, the efficacy and tolerability of two 1-week triple therapies for Helicobacter pylori eradication. Methods: One hundred and thirty-four consecutive patients with non-ulcer dyspepsia and H. pylori infection were randomized to receive lansoprazole 30 mg once daily, clarithromycin 250 mg twice daily, and metronidazole 500 mg twice daily (LCM group), or lansoprazole 30 mg twice daily, clarithromycin 500 mg twice daily, and amoxicillin 1000 mg twice daily (LCA group). H. pylori status was assessed by rapid urease test, histology and 13 C-urea breath test before and after therapy. Results: At 3 months, H. pylori eradication (intention-to-treat/per protocol analysis) was 92.4%/93.8% in the LCM group and 83.1%/85.7% in the LCA group (P = N.S.). Side-effects were more frequently reported in the LCA group (37.9%) than in the LCM group (19.7%) (P < 0.05). Conclusions: In this open, randomized controlled trial, eradication of H. pylori by low-dose lansoprazole and clarithromycin plus metronidazole was higher with significantly less side-effects than by full-dose lansoprazole and clarithromycin plus amoxicillin. This finding may be related to the stronger synergism of clarithromycin plus metronidazole, even at lower doses, than of clarithromycin plus amoxicillin. Considering the lower cost as well, LCM should be preferred to LCA in the eradication of H. pylori.
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页码:153 / 158
页数:6
相关论文
共 29 条
[21]   Antimicrobial susceptibility testing of Helicobacter pylori in a large multicenter trial:: the MACH 2 study [J].
Mégraud, F ;
Lehn, N ;
Lind, T ;
Bayerdörffer, E ;
O'Morain, C ;
Spiller, R ;
Unge, P ;
Van Zanten, SV ;
Wrangstadh, M ;
Burman, CF .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (11) :2747-2752
[22]  
MEYER JM, 2000, GASTROENTEROLOGY, V118, pA3702
[23]  
Miehlke S, 2000, GUT, V47, pA99
[24]  
MOAYYEDI P, 1995, EUR J GASTROEN HEPAT, V7, P835
[25]   Prevalence of Helicobacter pylori resistance to antibiotics in Northeast Italy:: a multicentre study [J].
Pilotto, A ;
Rassu, M ;
Leandro, G ;
Franceschi, M ;
Di Mario, F .
DIGESTIVE AND LIVER DISEASE, 2000, 32 (09) :763-768
[26]   Accurate prediction of macrolide resistance in Helicobacter pylori by a PCR line probe assay for detection of mutations in the 23S rRNA gene:: Multicenter validation study [J].
van Doorn, LJ ;
Glupczynski, Y ;
Kusters, JG ;
Mégraud, F ;
Midolo, P ;
Maggi-Solcà, N ;
Queiroz, DMM ;
Nouhan, N ;
Stet, E ;
Quint, WGV .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (05) :1500-1504
[27]   Mutations in 23S rRNA are associated with clarithromycin resistance in Helicobacter pylori [J].
Versalovic, J ;
Shortridge, D ;
Kibler, K ;
Griffy, MV ;
Beyer, J ;
Flamm, RK ;
Tanaka, SK ;
Graham, DY ;
Go, MF .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (02) :477-480
[28]   HISTOLOGICAL DIAGNOSIS OF CHRONIC GASTRITIS IN FIBEROPTIC GASTROSCOPE BIOPSY SPECIMENS [J].
WHITEHEAD, R ;
TRUELOVE, SC ;
GEAR, MWL .
JOURNAL OF CLINICAL PATHOLOGY, 1972, 25 (01) :1-+
[29]  
Wong BCY, 2000, ALIMENT PHARM THER, V14, P217