PMID- 15565402 OWN - NLM STAT- MEDLINE DCOM- 20050118 LR - 20181201 IS - 0944-1174 (Print) IS - 0944-1174 (Linking) VI - 39 IP - 9 DP - 2004 Sep TI - Results of triple eradication therapy in Japanese children: a retrospective multicenter study. PG - 838-43 AB - BACKGROUND: Large-scale clinical trials in children are lacking concerning Helicobacter pylori eradication therapies. The purpose of this study was to assess the efficacy of proton pump inhibitor (PPI)-based triple therapies in Japanese children. METHODS: This was a retrospective analysis of the first- and second-line PPI-based triple therapies from pediatric gastrointestinal units between 1996 and 2003. Data collected included doses and duration of regimens, drug compliance, success or failure of eradication, ulcer healing, and symptom response of those with dyspepsia and no ulcers. The results of antibiotic susceptibility tests were also reported in cases where these were performed. RESULTS: A total of 149 pediatric patients (mean age, 12.6 years) were studied, including 123 patients who received first-line therapy: 115 received a PPI plus amoxicillin and clarithromycin (PAC) and 8 received a PPI plus amoxicillin and metronidazole (PAM). Overall eradication rates of the first-line PAC and PAM therapies were 77.4% and 87.5%, respectively ( P = 0.68). All 14 patients with failed PAC therapy received the second-line PAM regimen, resulting in an eradication rate of 100%. Mild side effects were reported only in PAC regimens (13.8%). Primary resistance to amoxicillin, clarithromycin, and metronidazole was detected in 0%, 34.7%, and 12.5% of the strains, respectively. The PAC regimen showed a high eradication rate for clarithromycin-susceptible strains (91.7%), but was relatively ineffective for resistant strains (40.0%) ( P < 0.01). Eradication of H. pylori was associated with ulcer healing and symptomatic improvement among those with gastritis only (both; P < 0.001). Among 17 patients with iron-deficiency anemia, post-treatment hemoglobin levels were higher than the pretreatment levels ( P < 0.001). CONCLUSIONS: The PAC regimen is effective in children. Clarithromycin resistance is associated with eradication failure. Metronidazole is a good substitute for clarithromycin as the second-line option for children. FAU - Kato, Seiichi AU - Kato S AD - Department of Pediatrics, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, 980-8574 Sendai, Japan. FAU - Konno, Mutsuko AU - Konno M FAU - Maisawa, Shun-Ichi AU - Maisawa S FAU - Tajiri, Hitoshi AU - Tajiri H FAU - Yoshimura, Norikazu AU - Yoshimura N FAU - Shimizu, Toshiaki AU - Shimizu T FAU - Toyoda, Shigeru AU - Toyoda S FAU - Nakayama, Yoshiko AU - Nakayama Y FAU - Iinuma, Kazuie AU - Iinuma K LA - eng PT - Journal Article PT - Multicenter Study PL - Japan TA - J Gastroenterol JT - Journal of gastroenterology JID - 9430794 RN - 0 (2-Pyridinylmethylsulfinylbenzimidazoles) RN - 0 (Anti-Ulcer Agents) RN - 0 (Benzimidazoles) RN - 0 (Proton Pump Inhibitors) RN - 0 (Sulfoxides) RN - 0K5C5T2QPG (Lansoprazole) RN - 140QMO216E (Metronidazole) RN - 32828355LL (Rabeprazole) RN - 804826J2HU (Amoxicillin) RN - D8TST4O562 (Pantoprazole) RN - H1250JIK0A (Clarithromycin) RN - KG60484QX9 (Omeprazole) SB - IM MH - 2-Pyridinylmethylsulfinylbenzimidazoles MH - Adolescent MH - Amoxicillin/therapeutic use MH - Anti-Ulcer Agents/*therapeutic use MH - Benzimidazoles/therapeutic use MH - Child MH - Child, Preschool MH - Clarithromycin/pharmacology/therapeutic use MH - Drug Resistance, Microbial MH - Drug Therapy, Combination MH - Helicobacter Infections/*drug therapy MH - Humans MH - Infant MH - Lansoprazole MH - Metronidazole/pharmacology/therapeutic use MH - Microbial Sensitivity Tests MH - Omeprazole/*analogs & derivatives/therapeutic use MH - Pantoprazole MH - *Proton Pump Inhibitors MH - Rabeprazole MH - Retrospective Studies MH - Sulfoxides/therapeutic use EDAT- 2004/11/27 09:00 MHDA- 2005/01/19 09:00 CRDT- 2004/11/27 09:00 PHST- 2003/10/02 00:00 [received] PHST- 2004/02/13 00:00 [accepted] PHST- 2004/11/27 09:00 [pubmed] PHST- 2005/01/19 09:00 [medline] PHST- 2004/11/27 09:00 [entrez] AID - 10.1007/s00535-004-1398-6 [doi] PST - ppublish SO - J Gastroenterol. 2004 Sep;39(9):838-43. doi: 10.1007/s00535-004-1398-6.