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生物制剂治疗前常规胸部X线检查在CRSwNP中的有限价值

Limited value of routine chest X-rays before biologic therapy in CRSwNP.

临床研究鼻科IF 1.3Q3

文献信息

中文摘要

引言: 自2022年起,丹麦已批准生物制剂用于治疗慢性鼻窦炎伴鼻息肉(CRSwNP)。全球气道指导小组将胸部X线(CXR)作为治疗前筛查手段,以识别肺部疾病并监测不良反应。本研究评估了在CRSwNP患者开始生物治疗前常规CXR筛查的效用。
方法: 基线数据,包括胸部X线,在全国性全球气道注册中心(经丹麦研究伦理委员会批准,编号:H-21020685)前瞻性收集,并于2025年5月进行分析。
结果: 共识别并纳入511例患者(男性335例,女性176例;平均年龄46.5 ± 14.6岁);其中247例患者开始接受生物制剂治疗。在治疗组中,136例(55%)CXR正常,12例(5%)有异常发现。在264例未接受生物制剂治疗的患者中,143例(54%)CXR正常,10例(4%)显示异常发现。
结论: 在CRSwNP患者生物治疗前进行常规基线CXR筛查发现的异常结果很少。因此,常规CXR可能提供的临床获益有限。
资助: 全球气道数据库由葛兰素史克、赛诺菲和阿斯利康资助。任何制药公司均无权访问数据。
试验注册: 不相关。

英文摘要

INTRODUCTION: Biologic therapies for chronic rhinosinusitis with nasal polyps (CRSwNP) have been approved in Denmark since 2022. Chest X-ray (CXR) was implemented by the Global Airways Steering Group as pre-treatment screening to identify pulmonary conditions and monitor adverse effects. This study evaluates the utility of routine CXR screening before initiating biological therapy in patients with CRSwNP.
METHODS: Baseline data, including chest X-ray, were collected prospectively in the nationwide Global Airways Registry (approved by the Danish Research Ethics Committee R. no.: H-21020685) and analysed in May 2025.
RESULTS: A total of 511 patients (335 males, 176 females; mean age 46.5 ± 14.6) years were identified and included in this study; 247 patients were initiated on biologic therapy. In the treatment group, 136 (55%) had normal CXRs, and 12 (5%) had abnormal findings. Among the 264 patients who did not receive biologic treatment, 143 (54%) had normal CXRs and ten (4%) demonstrated abnormal findings.
CONCLUSIONS: Routine baseline CXR screening before biologic therapy in patients with CRSwNP identified few abnormal findings. Accordingly, routine CXR is likely to offer limited clinical benefit.
FUNDING: The Global Airways database is funded by GlaxoSmithKline, Sanofi and Astra Zeneca. None of the pharmaceutical companies has access to data.
TRIAL REGISTRATION: Not relevant.