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Development and evaluation of a brief self-completed family history screening tool for common chronic disease prevention in primary care.

机译:开发和评估一个简短的自我完成的家族史筛查工具,用于初级保健中常见的慢性疾病预防。

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摘要

BACKGROUND: Family history is an important risk factor for many common chronic diseases, but it remains underutilised for diagnostic assessment and disease prevention in routine primary care. AIM: To develop and validate a brief self-completed family history questionnaire (FHQ) for systematic primary care assessment for family history of diabetes, ischaemic heart disease, breast cancer, and colorectal cancer. DESIGN AND SETTING: Two-stage diagnostic validation study in 10 general practices in eastern England. Method Participants aged 18-50 years were identified via random sampling from electronic searches of general practice records. Participants completed a FHQ then had a three-generational 'gold standard' pedigree taken, to determine disease risk category. In stage 1, the FHQ comprised 12 items; in stage 2 the shorter 6-item FHQ was validated against the same 'gold standard'. RESULTS: There were 1147 participants (stage 1: 618; stage 2: 529). Overall, 32% were at increased risk of one or more marker conditions (diabetes 18.9%, ischaemic heart disease 13.3%, breast cancer 6.2%, colorectal cancer 2.2%). The shorter 6-item FHQ performed very well for all four conditions: pooled data from both stages show diabetes, sensitivity = 98%, specificity = 94%; ischaemic heart disease, sensitivity = 93%, specificity = 81%; breast cancer, sensitivity = 81%, specificity = 83%; colorectal cancer, sensitivity = 96%, specificity = 88%, with an area under the receiver operating characteristic curve of 0.90 for males and 0.89 for females. CONCLUSION: This brief self-completed FHQ shows good diagnostic accuracy for identifying people at higher risk of four common chronic diseases. It could be used in routine primary care to identify patients who would be most likely to benefit from a more detailed pedigree and risk assessment, and consequent management strategies.
机译:背景:家族病史是许多常见慢性病的重要危险因素,但在常规初级保健中仍未充分用于诊断评估和疾病预防。目的:开发并验证一份简短的自我填写的家族史调查表(FHQ),用于对糖尿病,缺血性心脏病,乳腺癌和结直肠癌的家族史进行系统的初级保健评估。设计与设置:在英格兰东部的10个一般实践中进行的两阶段诊断验证研究。方法通过电子检索普通实践记录中的随机样本来识别年龄在18至50岁之间的参与者。参与者完成了FHQ,然后采用了三代“金标准”谱系,以确定疾病风险类别。在第一阶段,总部包括12个项目;在第2阶段,较短的6项FHQ已针对相同的“黄金标准”进行了验证。结果:有1147名参与者(阶段1:618;阶段2:529)。总体而言,有32%的人患有一种或多种标志物疾病的风险增加(糖尿病18.9%,缺血性心脏病13.3%,乳腺癌6.2%,结直肠癌2.2%)。较短的6项FHQ在所有四个条件下均表现良好:两个阶段的汇总数据显示糖尿病,敏感性= 98%,特异性= 94%;缺血性心脏病,敏感性= 93%,特异性= 81%;乳腺癌,敏感性= 81%,特异性= 83%;结肠直肠癌,敏感性= 96%,特异性= 88%,接受者操作特征曲线下的面积为:男性0.90,女性0.89。结论:该简短的自我完成的FHQ显示出较高的诊断准确性,可识别出四种常见慢性病的高危人群。它可用于常规初级保健中,以识别最有可能从更详细的家谱和风险评估以及随之而来的管理策略中受益的患者。

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