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RESEARCH AND PRACTICE |
Kristina M. Zierold is with the Department of Environmental Health Sciences, Arnold School of Public Health, University of South Carolina, Columbia. Henry Anderson is with the Wisconsin Division of Public Health, Bureau of Environmental Health, Madison.
Correspondence: Requests for reprints should be sent to Kristina M. Zierold, PhD, Department of Environmental Health Sciences, Arnold School of Public Health, 800 Sumter St, University of South Carolina, Columbia, SC 29208 (e-mail: zierold{at}gwm.sc.edu).
| ABSTRACT |
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We analyzed data from the Wisconsin Childhood Lead Poisoning Prevention Program to examine the distribution of and trends in elevated blood lead levels among WIC-enrolled children from 1996 until 2000. Higher blood lead levels were seen among WIC-enrolled children, and although not statistically significant, the rate of blood lead level decline among WIC-enrolled children was greater than among non-WIC-enrolled children.
| INTRODUCTION |
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The blood lead level decline represents an environmental public health success story. However, vulnerable populations remain in which lead poisoning continues to present significant public health problems. Unfortunately, the communities in which children are most at risk for elevated blood lead levels are communities that are poor and underserved. In an effort to target blood lead level reduction in children in these vulnerable populations, the Wisconsin Childhood Lead Poisoning Prevention Program has developed a unique partnership with the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) to provide screening for lead as part of the required examination for WIC enrollees.
WIC is a state-based, federally funded program administered by the Food and Nutrition Service of the US Department of Agriculture. WIC provides supplement foods, nutrition education, and heath care referrals to pregnant and postpartum women, their infants, and their children aged younger than 6 years who are income eligible and at nutritional risk. In general, WIC guidelines require that during a free health screening, blood samples be taken, analyzed, and recorded as one method of determining nutritional risk. The Wisconsin Childhood Lead Poisoning Prevention Program and WIC determined that such existing blood sampling provides a perfect opportunity to expand blood testing to include collection for lead testing.
The objective of this study was to examine the distribution of and trends in elevated blood lead levels among WIC-enrolled children from 1996 until 2000, as a measure of success at increasing screening and prevention efforts in this population.
| METHODS |
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Any WIC-enrolled child aged younger than 6 years screened with a venous blood test during 1996 through 2000 was included in the study (n = 52 407). As a comparison, all other children aged younger than 6 years screened with a venous blood test during 1996 through 2000 but not enrolled in WIC were included (n = 58 789).
| RESULTS |
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Although the WIC-enrolled childrens blood lead levels declined more quickly during 1996 to 2000, the difference between the slopes of the WIC-enrolled and non-WIC-enrolled children was not statistically significant (P = .25).
To further evaluate the blood lead level decline in the WIC-enrolled children, the data were stratified by race/ethnicity and are shown in Figure 2
. WIC-enrolled Black children had an average blood lead level decline of 0.70 µg/dL per year (95% CI = 0.41, 1.00), Hispanic children had an average blood lead level decline of 0.36 µg/dL per year (95% CI = 0.14, 0.59), and White children had an average blood lead level decline of 0.28 µg/dL per year (95% CI = 0.20, 0.37). Black children had a significantly quicker decline compared with White children (P = .03).
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| DISCUSSION |
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Initially, the Wisconsin Childhood Lead Poisoning Prevention Program worked with WIC as a convenient access point to promote child blood lead testing because WIC participants had a high-risk profile (low income, poor nutritional status). However, after evaluating the data, we noticed that the blood lead levels in the WIC-enrolled children seemed to be declining more quickly than in the other children. The blood lead level decline among the WIC-enrolled children was greater than that among the non-WIC-enrolled children (0.64 µg/dL per year vs 0.42 µg/dL per year).
WIC-enrolled children have shown a quicker blood lead level decline for several reasons: (1) some WIC programs provide information and clinical follow-up; (2) the dietary supplements and management of anemia reduce lead absorption; and (3) WIC qualifications standards have changed; thus, "higher-income" individuals are eligible, even though they may not have a "high-risk" profile.
The major limitation of the study was that we could not identify the racial/ethnic distribution of the non-WIC-enrolled children. Although race has never been identified as a risk factor for blood lead poisoning, it is a surrogate of low income, poor housing, and so forth, which are risk factors for blood lead poisoning. We do know that the racial profile of the WIC-enrolled children changed dramatically during 1996 to 2000. In 1996, more than half (53%) of the WIC-enrolled children were Black, but by 2000, the racial demographics had changed to one-third Black children and 57% White or Hispanic children.
Programs like WIC are in an excellent position to identify children with elevated blood lead levels. Most childhood lead poisoning is asymptomatic, so blood lead screening in children is an inexpensive and effective method for early detection of lead poisoning. WIC programs, which include blood collection as part of a health examination, should be encouraged to provide blood lead testing to help identify children with elevated blood lead levels. Our observation of a more rapid blood lead level decline in the WIC population deserves further investigation to determine whether the dietary supplements, treatment of irondeficiency anemia, and frequent contact with a health professional may contribute and are an unanticipated benefit of partnering with WIC.
| Acknowledgments |
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Human Participant Protection
No protocol approval was needed for this study.
| Footnotes |
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Accepted for publication January 12, 2004.
| References |
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2. Fraust D, Brown J. Moderately elevated blood lead levels: effects on neurophysiologic functioning in children. Pediatrics. 1987;80:623629.
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4. Bellinger DC, Leviton A, Waternaux C, et al. Longitudinal analysis of prenatal and postnatal lead exposure and cognitive development. N Engl J Med. 1987;316:10371043.[Abstract]
5. Measuring Lead Exposure in Infants, Children, and Other Sensitive Populations, Report of the Committee on Measuring Lead in Critical Populations, Board of Environmental Studies and Toxicology, Commission of Life Sciences, National Academy of Sciences. Washington, DC: National Academy Press; 1993.
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