Burani Rossella, Caimi Francesco, Maggioni Carlo, Marinoni Guia, Pellizzoni Romana, Pirola Maria Elena, Villa Roberto, Ciatto Stefano
Azienda Sanitaria Locale Provincia Milano, Milan.
Radiol Med. 2005 Mar;109(3):260-7.
To evaluate the sensitivity of the mammographic screening programme and the causes of diagnostic fault in cases surfacing as interval cancers.
Interval cancers (CI) were identified by linkage of the screening database for the years 2000-2002 to the database of hospital discharge records (HDR) for breast cancer during 2000-2002. Linkage between screening attenders during 2000-2001 and HDR (biennial follow-up for year 2000, one year follow-up for year 2001) was used to calculate the proportional rate of observed/expected IC. The observed/ expected rate was compared with international standards and literature data. Screening mammograms followed by IC, randomly admixtured with negative controls, underwent blind review by an independent radiologist, using the recommended classification criteria to evaluate causes of error (occult, minimal signs, screening error).
The analysis of HDR during 2000-2002 allowed us to identify 31 out of 89 expected IC. Proportional observed/expected IC rate in the first or second year of screening interval was 26 or 67%, respectively. Screening mammograms for radiological review were available in 38 of 61 total IC: 20 cases (52.6%) were classified as occult, whereas minimal signs or screening errors were 2 (5.2%) or 16 (42.1%), respectively. Diagnostic suspicion had been reported at screening in 7 of 16 cases classified as screening error, but were not diagnosed at the subsequent diagnostic assessment.
Proportional IC rate was higher than reported in the literature or currently recommended (<30% in the 1st, <50% in the 2nd year). The analysis of error causes shows an excess of screening errors with respect to current recommendations (<20% of IC should be classified as screening error at review), but also an excess of IC suspected at screening but misdiagnosed at assessment (7/38=18.4 %). Overall the analysis revealed a reduced sensitivity of the screening programme, as often observed in service screening as compared to excellence centres, and suggests proper action to improve diagnostic accuracy. Analysis and critical review of IC is an early indicator of screening efficacy which is not currently used in Italian screening programmes. Using HDR for this purpose may have limited drawbacks, but gives the advantage of earlier identification of IC as compared to cancer registries and is the most reliable source of information in areas lacking a cancer registry. The present study methodology might be currently applied in screening programmes.
评估乳腺钼靶筛查项目的敏感性以及作为间期癌出现的病例中诊断失误的原因。
通过将2000 - 2002年筛查数据库与2000 - 2002年乳腺癌医院出院记录(HDR)数据库相链接来识别间期癌(CI)。利用2000 - 2001年筛查参与者与HDR之间的链接(2000年进行两年随访,2001年进行一年随访)来计算观察到的/预期的CI比例率。将观察到的/预期的比率与国际标准和文献数据进行比较。对随后出现间期癌的筛查乳腺钼靶片,随机混入阴性对照,由一名独立放射科医生进行盲法审查,使用推荐的分类标准来评估错误原因(隐匿性、微小征象、筛查错误)。
对2000 - 2002年HDR的分析使我们在89例预期的间期癌中识别出31例。筛查间期第一年或第二年观察到的/预期的CI比例率分别为26%或67%。在总共61例间期癌中有38例可获得用于放射学审查的筛查乳腺钼靶片:20例(52.6%)被分类为隐匿性,而微小征象或筛查错误分别为2例(5.2%)或16例(42.1%)。在被分类为筛查错误的16例病例中有7例在筛查时曾报告有诊断怀疑,但在随后的诊断评估中未被诊断出来。
间期癌比例率高于文献报道或目前推荐的水平(第一年<30%,第二年<50%)。对错误原因的分析显示,与当前推荐相比筛查错误过多(在审查中间期癌应被分类为筛查错误的比例<20%),但也存在筛查时怀疑为间期癌但在评估时误诊的情况过多(7/38 = 18.4%)。总体而言,分析显示筛查项目的敏感性降低,这在服务性筛查中与优秀中心相比经常观察到,并建议采取适当行动以提高诊断准确性。对间期癌的分析和批判性审查是筛查效果的早期指标,目前意大利的筛查项目未使用。为此目的使用HDR可能有有限的缺点,但与癌症登记处相比具有更早识别间期癌的优势,并且在缺乏癌症登记处的地区是最可靠的信息来源。本研究方法目前可能适用于筛查项目。