GI Division, Shanghai Jiao-Tong University School of Medicine Renji Hospital, Shanghai Institution of Digestive Disease, Key Laboratory of Gastroenterology and Hepatology, Ministry of Health, Shanghai, China.
Clin Gastroenterol Hepatol. 2013 Jul;11(7):802-7.e1. doi: 10.1016/j.cgh.2013.01.008. Epub 2013 Jan 29.
BACKGROUND & AIMS: We assessed the efficacy and safety of 4 bismuth-containing quadruple regimens as empiric therapies for Helicobacter pylori infections in patients who did not respond to previous treatment.
We performed a prospective single-center study of 424 patients with H pylori infection that was not eradicated by previous therapies. Patients were assigned randomly to groups given lansoprazole (30 mg twice daily) and bismuth potassium citrate (220 mg twice daily), along with 500 mg tetracycline and 400 mg metronidazole 4 times daily (LBTM), 500 mg tetracycline and 100 mg furazolidone 3 times daily (LBTF), 1000 mg amoxicillin 3 times and 500 mg tetracycline 4 times daily (LBAT), or 1000 mg amoxicillin and 100 mg furazolidone 3 times daily (LBAF). Eradication was assessed by a (13)C-urea breath test. Antimicrobial susceptibility was assessed in 188 patients by the agar dilution method.
Per-protocol rates of H pylori eradication were greater than 90% for all regimens: 93.1% for LBTM (95% confidence interval [CI], 88.1%-98.0%), 96.1% for LBTF (95% CI, 92.4%-99.8%), 94.6% for LBAT (95% CI, 90.0%-99.2%), and 99.0% for LBAF (95% CI, 97.0%-100%). The intention-to-treat response rates were 87.9% for LBTM (95% CI, 81.7%-94.0%), 91.7% for LBTF (95% CI, 87.1%-96.3%), 83.8% for LBAT (95% CI, 76.8%-90.9%), and 95.2% for LBAF (95% CI, 91.1%-99.3%). Significantly more patients had infections eradicated by furazolidone-containing regimens than nonfurazolidone regimens (P = .01). Side effects occurred in 33.6% of subjects and occurred significantly more frequently in the LBTM group than the other 3 groups (vs LBTF, P = .006; vs LBAT, P = .003; vs LBAF, P = .02). Metronidazole resistance was 96.8%; no isolates were resistant to amoxicillin, tetracycline, or furazolidone.
Four bismuth-containing quadruple therapies achieved greater than 90% eradication of H pylori in patients who did not respond to previous treatment, including patients with metronidazole resistance. For patients allergic to penicillin, tetracycline and either metronidazole- or furazolidone-containing regimens are recommended. ClincialTrials.gov number, NCT01668927.
我们评估了 4 种含铋四联方案作为既往治疗失败的幽门螺杆菌感染经验性治疗的疗效和安全性。
我们进行了一项前瞻性单中心研究,纳入 424 例既往治疗未根除的幽门螺杆菌感染患者。患者被随机分为以下 4 组:兰索拉唑(30 mg,每日 2 次)和枸橼酸铋钾(220 mg,每日 2 次),联合四环素 500 mg 和甲硝唑 400 mg,每日 4 次(LBTM);四环素 500 mg 和痢特灵 100 mg,每日 3 次(LBTF);阿莫西林 1000 mg,每日 3 次和四环素 500 mg,每日 4 次(LBAT);或阿莫西林 1000 mg 和痢特灵 100 mg,每日 3 次(LBAF)。通过(13)C-尿素呼气试验评估根除情况。在 188 例患者中通过琼脂稀释法评估了抗菌药物敏感性。
所有方案的幽门螺杆菌根除率均大于 90%:LBTM 组为 93.1%(95%置信区间[CI]:88.1%-98.0%),LBTF 组为 96.1%(95%CI:92.4%-99.8%),LBAT 组为 94.6%(95%CI:90.0%-99.2%),LBAF 组为 99.0%(95%CI:97.0%-100.0%)。意向治疗的应答率分别为 LBTM 组 87.9%(95%CI:81.7%-94.0%)、LBTF 组 91.7%(95%CI:87.1%-96.3%)、LBAT 组 83.8%(95%CI:76.8%-90.9%)和 LBAF 组 95.2%(95%CI:91.1%-99.3%)。含痢特灵的方案根除率显著高于不含痢特灵的方案(P=0.01)。33.6%的患者出现不良反应,LBTM 组明显多于其他 3 组(与 LBTF 相比,P=0.006;与 LBAT 相比,P=0.003;与 LBAF 相比,P=0.02)。甲硝唑耐药率为 96.8%;无分离株对阿莫西林、四环素或痢特灵耐药。
4 种含铋四联疗法对既往治疗失败的幽门螺杆菌感染患者的根除率均大于 90%,包括对甲硝唑耐药的患者。对于对青霉素过敏的患者,建议使用含有四环素和/或甲硝唑的方案。临床试验注册号:NCT01668927。