Division of Gastroenterology and Hepatology, Key Laboratory of Gastroenterology and Hepatology, Ministry of Health, Renji Hospital, School of Medicine, Shanghai Institute of Digestive Disease, Shanghai Jiao Tong University, Shanghai, China.
Helicobacter. 2018 Jun;23(3):e12485. doi: 10.1111/hel.12485. Epub 2018 Apr 25.
Helicobacter pylori (H. pylori) eradication has become increasingly difficult especially for penicillin allergy patients.
To evaluate the efficacy of adding bismuth or high-dose metronidazole to an H. pylori eradication regimen containing a proton-pump inhibitor, clarithromycin, and metronidazole in patients allergic to penicillin.
Pilot study in which penicillin-allergic, treatment-naive subjects were randomized (1:1) to 14-day esomeprazole (20 mg q12h), clarithromycin (500 mg q12h), and high dose of metronidazole (400 mg q6h) with (BECM group) or without (ECM group) bismuth (600 mg q12h). Eradication was confirmed by C-urea breath test 6 weeks after therapy. Antimicrobial susceptibility was assessed by the agar dilution method. Adverse events were recorded.
Sixty-six subjects were randomized, four were lost to follow-up and eight violated the protocol. The eradication rates were 63.6% (95% CI: 47.2%-80.0%) for ECM vs 84.8% (95% CI 72.6%-97.1%) (p = .049) for BECM by intention-to-treat, 67.7% (95% CI 51.3%-84.2%) vs 90.3% (95% CI 79.9%-100%) (p = .029) by modified ITT, and 70% (95% CI 53.6%-86.4%) vs 96% (95% CI 88.3%-100%) (P = .033) by per-protocol. Metronidazole, clarithromycin, and dual-resistant rates were 74.2%, 24.2%, and 18.2%, respectively. The cure rates were significantly improved by the addition of bismuth for both clarithromycin-resistant isolates (100% vs 25%, P = .024) and metronidazole-resistant isolates (94.7% vs 63.6%, P = .043). Adverse events were reported by 45.5% of subjects in ECM group and 48.5% in the BECM group (P = .805).
This prospective trial demonstrated that while high-dose metronidazole could not completely overcome metronidazole resistance, bismuth was additive and improved the overall cure rates by 21%-26%.
幽门螺杆菌(H. pylori)的根除治疗变得越来越困难,尤其是对青霉素过敏的患者。
评估在对青霉素过敏的患者中,在质子泵抑制剂、克拉霉素和甲硝唑三联疗法中添加铋剂或高剂量甲硝唑对幽门螺杆菌根除治疗的疗效。
在这项前瞻性、随机、双盲、平行对照的临床试验中,将 66 名青霉素过敏、未经治疗的受试者随机(1:1)分为两组,分别接受为期 14 天的埃索美拉唑(20mg,q12h)、克拉霉素(500mg,q12h)和高剂量甲硝唑(400mg,q6h)治疗(BECM 组)或不添加铋剂(ECM 组)。治疗结束后 6 周通过 C-尿素呼气试验确认根除情况。采用琼脂稀释法检测抗菌药物敏感性。记录不良反应。
共 66 名受试者随机分组,4 名受试者失访,8 名受试者违反方案。意向治疗人群中 ECM 组的根除率为 63.6%(95%CI:47.2%-80.0%),BECM 组的根除率为 84.8%(95%CI:72.6%-97.1%)(p=0.049);改良意向治疗人群中 ECM 组的根除率为 67.7%(95%CI:51.3%-84.2%),BECM 组的根除率为 90.3%(95%CI:79.9%-100%)(p=0.029);按方案治疗人群中 ECM 组的根除率为 70%(95%CI:53.6%-86.4%),BECM 组的根除率为 96%(95%CI:88.3%-100%)(p=0.033)。甲硝唑、克拉霉素和双重耐药率分别为 74.2%、24.2%和 18.2%。添加铋剂可显著提高克拉霉素耐药菌株(100% vs 25%,P=0.024)和甲硝唑耐药菌株(94.7% vs 63.6%,P=0.043)的治愈率。ECM 组和 BECM 组分别有 45.5%和 48.5%的受试者报告了不良反应(P=0.805)。
这项前瞻性试验表明,高剂量甲硝唑虽然不能完全克服甲硝唑耐药,但添加铋剂可将总体治愈率提高 21%-26%。