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首页> 外文期刊>BMJ Open >Using probabilistic record linkage methods to identify Australian Indigenous women on the Queensland Pap Smear Register: the National Indigenous Cervical Screening Project
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Using probabilistic record linkage methods to identify Australian Indigenous women on the Queensland Pap Smear Register: the National Indigenous Cervical Screening Project

机译:使用概率记录链接方法在昆士兰巴氏涂片检查登记册上识别澳大利亚土著妇女:国家土著宫颈筛查项目

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Objective To evaluate the feasibility and reliability of record linkage of existing population-based data sets to determine Indigenous status among women receiving Pap smears. This method may allow for the first ever population measure of Australian Indigenous women's cervical screening participation rates. Setting/participants A linked data set of women aged 20–69 in the Queensland Pap Smear Register (PSR; 1999–2011) and Queensland Cancer Registry (QCR; 1997–2010) formed the Initial Study Cohort. Two extracts (1995–2011) were taken from Queensland public hospitals data (Queensland Hospital Admitted Patient Data Collection, QHAPDC) for women, aged 20–69, who had ever been identified as Indigenous (extract 1) and had a diagnosis or procedure code relating to cervical cancer (extract 2). The Initial Study Cohort was linked to extract 1, and women with cervical cancer in the initial cohort were linked to extract 2. Outcome measures The proportion of women in the Initial Cohort who linked with the extracts (true -pairs) is reported, as well as the proportion of potential pairs that required clerical review. After assigning Indigenous status from QHAPDC to the PSR, the proportion of women identified as Indigenous was calculated using 4 algorithms, and compared. Results There were 28?872 women (2.1%) from the Initial Study Cohort who matched to an ever Indigenous record in extract 1 (n=76?831). Women with cervical cancer in the Initial Study Cohort linked to 1385 (71%) records in extract 2. The proportion of Indigenous women ranged from 2.00% to 2.08% when using different algorithms to define Indigenous status. The Final Study Cohort included 1?372?823 women (PSR n=1?374?401; QCR n=1955), and 5?062?118 records. Conclusions Indigenous status in Queensland cervical screening data was successfully ascertained through record linkage, allowing for the crucial assessment of the current cervical screening programme for Indigenous women. Our study highlights the need to include Indigenous status on Pap smear request and report forms in any renewed and redesigned cervical screening programme in Australia.
机译:目的评估现有基于人群的数据集进行记录链接以确定接受子宫颈抹片检查妇女的土著地位的可行性和可靠性。这种方法可能允许对澳大利亚土著妇女的宫颈筛查参与率进行首次人口统计。设置/参与者昆士兰巴氏涂片涂片登记册(PSR; 1999-2011)和昆士兰癌症登记处(QCR; 1997-2010)中20-69岁女性的链接数据集构成了初始研究队列。从昆士兰州公立医院的数据(昆士兰医院入院患者数据收集,QHAPDC)中提取了两份摘录(1995-2011年),这些摘录用于20-69岁的女性,这些女性曾被确定为土著居民(摘录1)并且具有诊断或程序代码与子宫颈癌有关(摘录2)。初始研究队列与提取物1相关,而在初始队列中患有宫颈癌的女性与提取物2相关。结果衡量方法也报告了初始队列中与提取物相关的女性比例(真对)。作为需要笔迹复查的潜在对的比例。在将QHAPDC中的土著身份分配给PSR之后,使用4种算法来计算被确定为土著的妇女比例,并进行比较。结果初始研究队列中有28?872名女性(占2.1%)与提取物1中的原住民记录相匹配(n = 76?831)。初始研究队列中患有宫颈癌的女性与提取物2中的1385条记录相关。使用不同的算法定义土著身份时,土著女性的比例在2.00%至2.08%之间。最终研究队列包括1 372 823名女性(PSR n = 1 374 401; QCR n = 1955)和5 0 062 118名记录。结论通过记录联系成功地确定了昆士兰州宫颈筛查数据中的土著状况,从而可以对当前针对土著妇女的宫颈筛查计划进行重要评估。我们的研究强调,在澳大利亚任何经过更新和重新设计的子宫颈普查计划中,需要在子宫颈抹片检查请求和报告表格中包括土著身份。

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