Sargent J D, Dalton M, Klein R Z
Department of Pediatrics, Dartmouth Medical School, Hanover, New Hampshire 03756, USA.
Pediatrics. 1999 Apr;103(4):e51. doi: 10.1542/peds.103.4.e51.
Recent statements from the American Academy of Pediatrics and Centers for Disease Control and Prevention recommend diagnostic venous blood lead testing within 90 days of a marginally elevated screening test (10-14 microg/dL).
To evaluate the ability of a marginally elevated capillary (CScr) or venous (VScr) blood lead screening test to predict venous diagnostic (VPb) blood lead (taken within 90 days of the screening test) that would prompt environmental evaluation (>/=20 microg/dL).
Population-based follow-up study comparing CScr and VScr with VPb drawn within 90 days of the screening sample. This study population was drawn from all children aged 0 to 4 years who were screened in Worcester County, Massachusetts, and Providence County, Rhode Island, with CScr and VScr during calendar year 1994.
To evaluate predictive validity, CScr and VScr were correlated with VPb. CScr, VScr, and VPb results were then separated into the following categories: <10, 10 to 14, 15 to 19, and >/=20 microg/dL. CScr and VScr categories were cross-tabulated against VPb categories, and logistic regression analysis was used to evaluate categorical elevations of CScr and VScr as predictors of VPb >/=20 microg/dL.
Of 31 904 children screened with CScr, 5450 (17.1%) were elevated and 1278 were followed up with VPb within 90 days. Of 14 623 children screened with VScr, 2979 (20.4%) were elevated and 614 were followed up with VPb within 90 days. CScr was only weakly correlated with VPb (r = 0.39), whereas VScr was more strongly correlated with VPb (r = 0.73). Compared with CScr <10 microg/dL, CScr in the 10 to 14 microg/dL range did not identify a higher percentage of children with VPb elevation in any category, and falsely misclassified as lead poisoned some 77% of children. Compared with VScr <10 microg/dL, VScr in the 10 to 14 microg/dL range identified higher percentages of children with VPb in the 10 to 19 microg/dL range but not with VPb >/=20 microg/dL, and falsely misclassified as lead poisoned 42% of children. Compared with screening tests <10 microg/dL, the odds of identifying a child with VPb >/=20 were no different from 1 for CScr of 10 to 14 microg/dL (adjusted odds ratio 1.4 [95% confidence interval 0.3, 6.6]), CScr of 15 to 19 microg/dL (3.2 [0.7, 15.7]), or VScr of 10 to 14 microg/dL (0.9 [0.3, 3.0]). CScr and VScr in the 15 to 19 microg/dL range were associated with significantly higher odds of having VPb >/=20 microg/dL when compared with screening tests <10 microg/dL.
These data indicate that special diagnostic testing within 90 days for children with CScr and VScr in the 10 to 14 microg/dL range does not result in greater identification of VPb >/=20. Raising the set point for diagnostic testing to 15 microg/dL in this sample would eliminate the unnecessary follow-up of 5162 children, of whom 3360 were falsely misclassified as having undue lead exposure.
美国儿科学会和疾病控制与预防中心近期声明建议,在筛查试验结果略高于正常范围(10 - 14微克/分升)后的90天内进行诊断性静脉血铅检测。
评估毛细血管血铅筛查试验(CScr)或静脉血铅筛查试验(VScr)结果略高于正常范围时,预测90天内静脉诊断性血铅检测(VPb)结果(≥20微克/分升,此结果会促使进行环境评估)的能力。
基于人群的随访研究,比较CScr和VScr与筛查样本90天内采集的VPb。本研究人群来自1994年日历年在马萨诸塞州伍斯特县和罗德岛州普罗维登斯县接受CScr和VScr筛查的所有0至4岁儿童。
为评估预测效度,将CScr和VScr与VPb进行相关性分析。然后将CScr、VScr和VPb结果分为以下类别:<10、10至14、15至19和≥20微克/分升。将CScr和VScr类别与VPb类别进行交叉制表,并采用逻辑回归分析评估CScr和VScr的分类升高情况作为VPb≥20微克/分升的预测指标。
在31904名接受CScr筛查的儿童中,5450名(17.1%)结果升高,其中1278名在90天内接受了VPb检测。在14623名接受VScr筛查的儿童中,2979名(20.4%)结果升高,其中614名在90天内接受了VPb检测。CScr与VPb的相关性较弱(r = 0.39),而VScr与VPb的相关性更强(r = 0.73)。与CScr<10微克/分升相比,CScr在10至14微克/分升范围内并未在任何类别中识别出更高比例的VPb升高儿童,且约77%的儿童被错误分类为铅中毒。与VScr<10微克/分升相比,VScr在10至14微克/分升范围内识别出了10至19微克/分升范围内更高比例的VPb升高儿童,但未识别出≥20微克/分升的儿童,且42%的儿童被错误分类为铅中毒。与<10微克/分升的筛查试验相比,CScr为10至14微克/分升(调整后的优势比为1.4[95%置信区间0.3, 6.6])、CScr为15至19微克/分升(3.2[0.7, 15.7])或VScr为10至14微克/分升(0.9[0.3, 3.0])时,识别出VPb≥20微克/分升儿童的几率与1无异。与<10微克/分升的筛查试验相比,CScr和VScr在15至19微克/分升范围内与VPb≥20微克/分升的几率显著更高相关。
这些数据表明,对于CScr和VScr在10至14微克/分升范围内的儿童,90天内进行特殊诊断检测并不能更多地识别出VPb≥20微克/分升的情况。将本样本中的诊断检测设定点提高到15微克/分升可避免对5162名儿童进行不必要的随访,其中3360名被错误分类为铅暴露过度儿童。