Division of Gastroenterology, Department of Internal Medicine, Incheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Incheon, Korea.
Division of Gastroenterology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
Gut Liver. 2023 Sep 15;17(5):722-730. doi: 10.5009/gnl220256. Epub 2022 Sep 28.
BACKGROUND/AIMS: Dual priming oligonucleotide-based multiplex polymerase chain reaction (DPO-PCR) has recently been used for both the detection of and the identification of 23S ribosomal RNA point mutations that cause clarithromycin resistance. The aim of this study was to investigate the duration of effective standard triple therapy in a clarithromycin susceptible group and of bismuth-based quadruple therapy in a resistant group based on DPO-PCR.
We retrospectively analyzed the electronic medical records of 184 patients who, between September 2019 and December 2020, received eradication therapy following detection of , and the subsequent identification of the clarithromycin susceptibility of their using DPO-PCR. Patients were treated with 7- or 14-day standard triple therapy in the clarithromycin susceptible group, whereas 7- or 14-day bismuth-based quadruple therapy in the clarithromycin resistance group.
In the clarithromycin susceptible group, per-protocol analyses showed eradication rates of 87.5% (42/48; 95% confidence interval [CI], 77.1% to 95.8%) for 7-day therapy and 87.2% (41/47; 95% CI, 78.7% to 95.7%) for 14-day therapy (p=0.969). The eradication rates in the clarithromycin resistance group were 91.4% (32/35; 95% CI, 80.0% to 100.0%) for 7-day therapy and 90.3% (28/31; 95% CI, 77.4% to 100.0%) for 14-day therapy (p=0.876). There was no significant difference in the eradication rates, patient compliance, or rate of adverse events between the 7- and 14-day therapies for both groups.
Compared to the 14-day therapy, 7-day eradication therapy is sufficient after DPO-PCR-based clarithromycin susceptibility testing.
背景/目的:基于双重引物寡核苷酸的多重聚合酶链反应(DPO-PCR)最近被用于检测和鉴定导致克拉霉素耐药的 23S 核糖体 RNA 点突变。本研究的目的是基于 DPO-PCR 研究克拉霉素敏感组中有效标准三联疗法的持续时间和耐药组中铋基四联疗法的持续时间。
我们回顾性分析了 2019 年 9 月至 2020 年 12 月期间,184 例接受检测 的电子病历,通过 DPO-PCR 检测 克拉霉素敏感性,随后对其 进行鉴定。克拉霉素敏感组患者接受 7 或 14 天标准三联疗法治疗,克拉霉素耐药组患者接受 7 或 14 天铋基四联疗法治疗。
在克拉霉素敏感组中,根据方案分析,7 天治疗的根除率为 87.5%(42/48;95%置信区间[CI],77.1%至 95.8%),14 天治疗的根除率为 87.2%(41/47;95%CI,78.7%至 95.7%)(p=0.969)。克拉霉素耐药组中,7 天治疗的根除率为 91.4%(32/35;95%CI,80.0%至 100.0%),14 天治疗的根除率为 90.3%(28/31;95%CI,77.4%至 100.0%)(p=0.876)。两组患者的根除率、患者依从性或不良反应发生率在 7 天和 14 天治疗之间均无显著差异。
与 14 天治疗相比,基于 DPO-PCR 的克拉霉素敏感性检测后,7 天的根除治疗是足够的。