Schenck Ulrich, Hantschke-Zerbich Heike, Woellner Frank, Michel Frank
Institut für Allgemeine Pathologie und Pathologische Anatomie, Technische Universität München, München, Germany.
Dezernat Versorgungsqualität, Kassenärztliche Bundesvereinigung KdöR, Berlin, Germany.
Geburtshilfe Frauenheilkd. 2023 Sep 22;83(10):1235-1249. doi: 10.1055/a-2134-6740. eCollection 2023 Oct.
Cervical cancer screening, which was introduced into the programme of medical care covered by statutory health insurance in Germany in 1971 and has since been constantly updated through quality assurance measures, was fundamentally revised and developed in 2008 through the Cervical Cytology Quality Assurance Agreement pursuant to Section 135(2) of the German Social Code Book V [SGB V]. Since 2015 it has been mandatory for cytology facilities to record annual statistics based on the Munich Nomenclature III. The aim of this article is to present the results of the annual statistics for 2019, which was the last year before the introduction of the cervical cancer screening programme in accordance with the Federal Joint Committee's guideline on organised cancer screening programmes 1 .
The annual statistics of the laboratories, including histology analyses performed up until 30 June the following year, are reported to the Regional Associations of Statutory Health Insurance Physicians. The laboratories receive benchmark reports from their Regional Associations of Statutory Health Insurance Physicians, and these statistics are transmitted anonymously to the National Association of Statutory Health Insurance Physicians (KBV).
In 2019, 17609082 smears from 15608413 women were examined in Germany. Of these smears, 97.49% were normal and 2.51% showed atypical or suspicious changes, consisting mostly of minor squamous epithelial changes in groups II-p (0.81%) and IIID1 (0.735%).Histology specimens are available for "Dysplasia findings with higher probability of regression" in group IIID1 (4.89% of initial IIID1 cytology findings), group IIID2 (18.60%), "unclear or doubtful findings" in group III-p to x (20.7%), and "immediate precursors to cervical carcinoma" in group IV (83.1%) and group V (77.19%).In the cytology findings for group IVa-p, which corresponds to CIN 3 target lesions, the cytology correlated with the histology finding in 80.48% of cases.Lesions found in 2019: 23463 CIN 3 lesions, 668 adenocarcinomas in situ, 3891 malignant tumours, including 2342 cervical carcinomas of which 1743 were squamous cell carcinomas and 599 were cervical adenocarcinomas (25.57%); 1549 endometrial carcinomas and other malignancies.
INFERENCE/CONCLUSION: The data demonstrate the good practicability of cervical cancer screening in 2019. Higher grade lesions were reliably clarified histologically.
宫颈癌筛查于1971年被纳入德国法定医疗保险覆盖的医疗保健计划,并通过质量保证措施不断更新。2008年,根据德国社会法典第五编[SGB V]第135(2)条的宫颈细胞学质量保证协议,对其进行了根本性修订和完善。自2015年起,细胞学检查机构必须根据慕尼黑命名法III记录年度统计数据。本文旨在介绍2019年的年度统计结果,这是根据联邦联合委员会关于有组织癌症筛查计划1的指南引入宫颈癌筛查计划的前一年。
实验室的年度统计数据,包括截至次年6月30日进行的组织学分析,上报给法定医疗保险医师区域协会。实验室从其法定医疗保险医师区域协会收到基准报告,这些统计数据被匿名传输给法定医疗保险医师全国协会(KBV)。
2019年,德国对15608413名女性的17609082份涂片进行了检查。其中,97.49%的涂片正常,2.51%显示非典型或可疑变化,主要包括II-p组(0.81%)和IIID1组(0.735%)的轻度鳞状上皮变化。对于IIID1组中“回归可能性较高的发育异常发现”(初始IIID1细胞学发现的4.89%)、IIID2组(18.60%)、III-p至x组中“不明确或可疑发现”(20.7%)以及IV组(83.1%)和V组(77.19%)中“宫颈癌的直接前体”,有组织学标本可用。在对应于CIN 3目标病变的IVa-p组细胞学发现中,80.48%的病例细胞学与组织学发现相关。2019年发现的病变:23463例CIN 3病变、668例原位腺癌、3891例恶性肿瘤,包括2342例宫颈癌,其中1743例为鳞状细胞癌,599例为宫颈腺癌(25.57%);1549例子宫内膜癌和其他恶性肿瘤。
推论/结论:数据表明2019年宫颈癌筛查具有良好的实用性。高级别病变通过组织学得到了可靠的明确诊断。