Shiotani Akiko, Roy Priya, Lu Hong, Graham David Y
Department of Internal Medicine, Kawasaki Medical School, Okayama, Japan.
Department of Medicine, Baylor College of Medicine, Houston, TX, USA.
Therap Adv Gastroenterol. 2021 Dec 21;14:17562848211064080. doi: 10.1177/17562848211064080. eCollection 2021.
The diagnosis and therapy of infection have undergone major changes based on the use the principles of antimicrobial stewardship and increased availability of susceptibility profiling. gastritis now recognized as an infectious disease, as such there is no placebo response allowing outcome to be assessed in relation to the theoretically obtainable cure rate of 100%. The recent recognition of as an infectious disease has changed the focus to therapies optimized to reliably achieve high cure rates. Increasing antimicrobial resistance has also led to restriction of clarithromycin, levofloxacin, or metronidazole to susceptibility-based therapies. Covid-19 resulted in the almost universal availability of polymerase chain reaction testing in hospitals which can be repurposed to utilize readily available kits to provide rapid and inexpensive detection of clarithromycin resistance. In the United States, major diagnostic laboratories now offer culture and susceptibility testing and American Molecular Laboratories offers next-generation sequencing susceptibility profiling of gastric biopsies or stools for the six commonly used antibiotics without need for endoscopy. Current treatment recommendations include (a) only use therapies that are reliably highly effective locally, (b) always perform a test-of-cure, and (c) use that data to confirm local effectiveness and share the results to inform the community regarding which therapies are effective and which are not. Empiric therapy should be restricted to those proven highly effective locally. The most common choices are 14-day bismuth quadruple therapy and rifabutin triple therapy. Prior guidelines and treatment recommendations should only be used if proven locally highly effective.
基于抗菌药物管理原则的应用以及药敏分析的更多可得性,感染的诊断和治疗发生了重大变化。胃炎现在被认为是一种传染病,因此不存在安慰剂反应,无法根据理论上可达到的100%治愈率来评估治疗结果。最近胃炎被认定为传染病,这使得重点转向优化治疗方法以可靠地实现高治愈率。日益增加的抗菌药物耐药性也导致将克拉霉素、左氧氟沙星或甲硝唑限制用于基于药敏的治疗。新冠疫情使得医院几乎普遍能够进行聚合酶链反应检测,这些检测可以重新利用现成的试剂盒来快速、廉价地检测克拉霉素耐药性。在美国,主要诊断实验室现在提供培养和药敏检测,美国分子实验室提供对胃活检或粪便中六种常用抗生素的下一代测序药敏分析,无需进行内镜检查。当前的治疗建议包括:(a) 仅使用在局部可靠地高度有效的治疗方法;(b) 始终进行治疗效果检测;(c) 利用该数据确认局部有效性,并分享结果以告知社区哪些治疗方法有效,哪些无效。经验性治疗应限于那些在当地已被证明高度有效的方法。最常见的选择是14天铋剂四联疗法和利福布汀三联疗法。只有在当地被证明高度有效时,才应使用先前的指南和治疗建议。