Department of Gastroenterology, Assistance publique-Hôpitaux de Paris (AP-HP), Paris Est Creteil University (UPEC), Henri-Mondor Hospital, 51, avenue du Maréchal-de-Lattre-de-Tassigny, 94010 Creteil, France.
Department of Gastroenterology, Assistance publique-Hôpitaux de Paris (AP-HP), Paris Est Creteil University (UPEC), Henri-Mondor Hospital, 51, avenue du Maréchal-de-Lattre-de-Tassigny, 94010 Creteil, France; Laboratory of Clinical Investigation (LIC, EA 4393), Paris Est Creteil University (UPEC), 94010 Creteil, France.
Clin Res Hepatol Gastroenterol. 2016 Sep;40(4):517-24. doi: 10.1016/j.clinre.2015.12.012. Epub 2016 Feb 2.
The emergence of H. pylori strains that are resistant to clarithromycin, metronidazole and fluoroquinolone requires the evaluation of new and effective salvage therapies.
To test the efficacy of a new formulation of a bismuth-containing quadruple therapy as a rescue therapy in patients who were infected with a H. pylori strain resistant to metronidazole, clarithromycin and fluoroquinolone or who failed multiple lines of treatment using these three antibiotics.
A total of 103 patients with confirmed H. pylori infection with a resistance profile described above were treated with Pylera(®) (3-in-1 capsules containing bismuth subcitrate potassium 140mg, metronidazole 125mg and tetracycline 125mg) 3 capsules four times a day plus omeprazole 20mg two times a day for 10 days in a named patient program. Eradication was confirmed using a urea breath test at least 28 days after the end of treatment. Efficacy and safety were studied.
A total of 103 patients were prospectively included from June 2010 to October 2011. The eradication rate for the intent-to-treat analysis was 83% (CI95%[75-89%]); an 87% eradication rate (CI95%[80-94%]) was found for the per-protocol analysis and 81% (CI95%[80-82%]) for the intent-to-treat analysis in patients with proven resistance to metronidazole. Nine patients discontinued treatment, all due to adverse events. Two serious adverse events (AEs) were reported (memory disorders of unknown significance). Fifty-six (54%) patients reported at least one AE.
This bismuth-containing quadruple therapy achieved a remarkable eradication rate as a salvage therapy in patients infected with metronidazole-resistant H. pylori strain, despite the frequent occurrence of mild-to-moderate adverse events.
幽门螺杆菌对克拉霉素、甲硝唑和氟喹诺酮耐药菌株的出现,要求评估新的有效补救治疗方法。
检测一种新的含铋四联疗法治疗对甲硝唑、克拉霉素和氟喹诺酮耐药或对上述三种抗生素联合治疗失败的幽门螺杆菌感染者的疗效。
在一项名为患者的方案中,共 103 例经确认的对上述三种抗生素耐药的幽门螺杆菌感染者,采用 Pylera(®)(三联胶囊,每粒含枸橼酸铋钾 140mg、甲硝唑 125mg 和四环素 125mg),每天 4 次,每次 3 粒,同时每天 2 次口服奥美拉唑 20mg,治疗 10 天。治疗结束后至少 28 天,采用尿素呼气试验确认根除。研究疗效和安全性。
2010 年 6 月至 2011 年 10 月,共前瞻性纳入 103 例患者。意向治疗分析的根除率为 83%(95%可信区间[75-89%]);符合方案分析的根除率为 87%(95%可信区间[80-94%]),甲硝唑耐药患者的意向治疗分析的根除率为 81%(95%可信区间[80-82%])。9 例患者因不良事件停药。报告了 2 例严重不良事件(AE)(原因不明的记忆障碍)。56 例(54%)患者报告了至少 1 例 AE。
尽管发生了轻度至中度不良事件,但这种含铋的四联疗法作为补救治疗,在甲硝唑耐药的幽门螺杆菌感染者中,达到了显著的根除率。