目的：分析Phadiatop检测的应用价值。方法：选取湖北省人民医院2022年1月——2024年5月500例哮喘患者和500名健康体检者，入选者均行混合吸入性过敏原sIgE检测以及Phadiatop检测，比较两种方法诊断结果以及检查费用与检查时间的差异。结果：本组500例哮喘患者混合吸入性过敏原sIgE检测的阳性率为45.0%，Phadiatop检测的阳性率为47.0%；500例健康体检者混合吸入性过敏原sIgE检测的阳性率为8.0%，Phadiatop检测的阳性率为8.6%，两种方法检查结果的差异无意义（P＞0.05），两种方法存在较高的一致性（kappa值为0.785）；Phadiatop检测的检查费用与检查时间低于混合吸入性过敏原sIgE检测，差异有意义（P＜0.05）。结论：Phadiatop检测具有较好的筛查价值，且具有检查费用低、检查速度快的优点，可推广使用。

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