北京大学学报(医学版) ›› 2023, Vol. 55 ›› Issue (5): 934-938. doi: 10.19723/j.issn.1671-167X.2023.05.024
Xue-li TIAN,Zhi-qiang SONG*(),Bao-jun SUO,Li-ya ZHOU,Cai-ling LI,Yu-xin ZHANG
摘要:
目的: 以琼脂稀释法为金标准, 评价Epsilometer试验(Epsilometer test, E-test)法检测幽门螺杆菌(Helicobacter pylori, H. pylori)对甲硝唑敏感性的一致性。方法: 纳入2018年8月至2020年7月因消化不良症状就诊于北京大学第三医院行胃镜检查的H. pylori感染初治患者, 取胃黏膜组织活检行H. pylori培养, 分别采用E-test法和琼脂稀释法检测H. pylori对甲硝唑的敏感性, 比较两种方法检测结果的一致性和相关性。结果: 成功培养105株H. pylori, 将最小抑菌浓度≥ 8 mg/L定义为耐药。琼脂稀释法检测甲硝唑耐药菌株68株, 耐药率64.8%, E-test法检测耐药菌株66株, 耐药率62.9%, 其中, 琼脂稀释法和E-test法检测均为耐药的菌株66株, 均为敏感的菌株37株, 两种方法的一致率为98.1%。2例菌株被琼脂稀释法评价为耐药, 而E-test法评价为敏感, 非常严重错误率为1.9%。没有菌株被琼脂稀释法评价为敏感, 而E-test法评价为耐药(严重错误率为0%)。以琼脂稀释法为金标准, E-test法检测甲硝唑耐药的灵敏度为97.1%(95%CI: 0.888~0.995), 特异度为100%(95%CI: 0.883~1.000)。Cohen’s kappa系数为0.959 (95%CI: 0.902~1.016, P < 0.001), Spearmans相关性检测r=0.807(P < 0.001)。采用Bland-Altman法进行一致性评价, 结果提示较好, 未出现一致性区间外的测值。E-test法比琼脂稀释法的成本更低, 平均完成1例试验两者的成本分别为269.8元和356.6元。结论: E-test法检测H. pylori对甲硝唑的药敏试验与琼脂稀释法相比具有较强的一致性, E-test法省时、省力、价廉, 可以作为H. pylori药敏试验的优选检测方法。
中图分类号:
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