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Blood Lead Levels in a Continuity Clinic Population
Abstract Introduction: Lead toxicity is well recognized as a significant cause of morbidity in children, especially those under the age of six years. While lead toxicity has not been recognized as a public health problem in Houston, it is possible that children in the area suffer from low-level lead...
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Published in: | Clinical toxicology (Philadelphia, Pa.) Pa.), 1997, Vol.35 (2), p.181-186 |
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Introduction: Lead toxicity is well recognized as a significant cause of morbidity in children, especially those under the age of six years. While lead toxicity has not been recognized as a public health problem in Houston, it is possible that children in the area suffer from low-level lead effect on the central nervous system. Objectives: To detect asymptomatic cases of lead toxicity in one population of Houston children and to assess the effectiveness of the lead risk questionnaire. Design: Venous blood samples for quantitative lead were analyzed utilizing the Anodic Stripping Voltameter. The Centers for Disease Control's lead risk assessment questionnaire was administered to each patient. Setting: Baylor College of Medicine Continuity Clinic at Texas Children's Hospital. Subjects: All patients, age 9-72 months, seen for routine care between December 1992 and June 1994 were screened once. Results: Blood lead levels were obtained on 801 children; all but 47 completed lead risk questionnaires. The mean age of the study group was 2.37 years (SD 1.84) and they were 54% male. They were 39% Hispanic, 39% Black, and 18% White. Eighty-eight percent reported an annual income of >$20,000. They lived in 127 separate zip codes. Twenty-five (3.1%) patients had elevated blood lead, 21 between 10-14 μ/dL and 4 between 15-19 μ/dL. No patients had blood lead levels of 20μ/dL. No statistically significant differences were found between patients with blood lead > 10μ/dL and those with 10μ/dL when comparing for age, sex, ethnicity, income, and zip code. Only those children living in or regularly visiting a pre-1960 home with peeling or chipping paint were significantly more likely to have elevated blood lead (p=. 045). Conclusion: Although the majority of children in our setting were poor and urban, the prevalence of blood lead > 10 μ/dL was 3.1%, well below the estimated 17% quoted by the Centers for Disease Control in recommending stringent screening guidelines. The lead risk assessment questionnaire failed to identify 32% of children with elevated blood lead levels. Since this questionnaire is critical to screening populations at low risk for lead toxicity, it is important to determine whether a revised questionnaire or a more careful elicitation of parental responses will improve identification of those children at risk |
doi_str_mv | 10.3109/15563659709001190 |
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Introduction: Lead toxicity is well recognized as a significant cause of morbidity in children, especially those under the age of six years. While lead toxicity has not been recognized as a public health problem in Houston, it is possible that children in the area suffer from low-level lead effect on the central nervous system. Objectives: To detect asymptomatic cases of lead toxicity in one population of Houston children and to assess the effectiveness of the lead risk questionnaire. Design: Venous blood samples for quantitative lead were analyzed utilizing the Anodic Stripping Voltameter. The Centers for Disease Control's lead risk assessment questionnaire was administered to each patient. Setting: Baylor College of Medicine Continuity Clinic at Texas Children's Hospital. Subjects: All patients, age 9-72 months, seen for routine care between December 1992 and June 1994 were screened once. Results: Blood lead levels were obtained on 801 children; all but 47 completed lead risk questionnaires. The mean age of the study group was 2.37 years (SD 1.84) and they were 54% male. They were 39% Hispanic, 39% Black, and 18% White. Eighty-eight percent reported an annual income of >$20,000. They lived in 127 separate zip codes. Twenty-five (3.1%) patients had elevated blood lead, 21 between 10-14 μ/dL and 4 between 15-19 μ/dL. No patients had blood lead levels of 20μ/dL. No statistically significant differences were found between patients with blood lead > 10μ/dL and those with 10μ/dL when comparing for age, sex, ethnicity, income, and zip code. Only those children living in or regularly visiting a pre-1960 home with peeling or chipping paint were significantly more likely to have elevated blood lead (p=. 045). Conclusion: Although the majority of children in our setting were poor and urban, the prevalence of blood lead > 10 μ/dL was 3.1%, well below the estimated 17% quoted by the Centers for Disease Control in recommending stringent screening guidelines. The lead risk assessment questionnaire failed to identify 32% of children with elevated blood lead levels. Since this questionnaire is critical to screening populations at low risk for lead toxicity, it is important to determine whether a revised questionnaire or a more careful elicitation of parental responses will improve identification of those children at risk</description><identifier>ISSN: 1556-3650</identifier><identifier>ISSN: 0731-3810</identifier><identifier>EISSN: 1556-9519</identifier><identifier>EISSN: 1097-9875</identifier><identifier>DOI: 10.3109/15563659709001190</identifier><identifier>PMID: 9120888</identifier><language>eng</language><publisher>Monticello, NY: Informa UK Ltd</publisher><subject>Biological and medical sciences ; Chemical and industrial products toxicology. Toxic occupational diseases ; Child ; Child, Preschool ; Continuity of Patient Care ; Female ; Humans ; Infant ; Internship and Residency ; Lead - adverse effects ; Lead - blood ; Male ; Medical sciences ; Metals and various inorganic compounds ; Outpatient Clinics, Hospital ; Primary Health Care ; Risk Assessment ; Surveys and Questionnaires ; Toxicology ; Urban Population</subject><ispartof>Clinical toxicology (Philadelphia, Pa.), 1997, Vol.35 (2), p.181-186</ispartof><rights>1997 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1997</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c461t-e5242c16b11f9c48cd213ab68f39e4cea0c093709faceb8f8020880d5b4367573</citedby><cites>FETCH-LOGICAL-c461t-e5242c16b11f9c48cd213ab68f39e4cea0c093709faceb8f8020880d5b4367573</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2607985$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9120888$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Holmes, Susan E.</creatorcontrib><creatorcontrib>Drutz, Jan E.</creatorcontrib><creatorcontrib>Buffone, Gregory J.</creatorcontrib><creatorcontrib>Rice, Teresa Duryea</creatorcontrib><title>Blood Lead Levels in a Continuity Clinic Population</title><title>Clinical toxicology (Philadelphia, Pa.)</title><addtitle>J Toxicol Clin Toxicol</addtitle><description>Abstract
Introduction: Lead toxicity is well recognized as a significant cause of morbidity in children, especially those under the age of six years. While lead toxicity has not been recognized as a public health problem in Houston, it is possible that children in the area suffer from low-level lead effect on the central nervous system. Objectives: To detect asymptomatic cases of lead toxicity in one population of Houston children and to assess the effectiveness of the lead risk questionnaire. Design: Venous blood samples for quantitative lead were analyzed utilizing the Anodic Stripping Voltameter. The Centers for Disease Control's lead risk assessment questionnaire was administered to each patient. Setting: Baylor College of Medicine Continuity Clinic at Texas Children's Hospital. Subjects: All patients, age 9-72 months, seen for routine care between December 1992 and June 1994 were screened once. Results: Blood lead levels were obtained on 801 children; all but 47 completed lead risk questionnaires. The mean age of the study group was 2.37 years (SD 1.84) and they were 54% male. They were 39% Hispanic, 39% Black, and 18% White. Eighty-eight percent reported an annual income of >$20,000. They lived in 127 separate zip codes. Twenty-five (3.1%) patients had elevated blood lead, 21 between 10-14 μ/dL and 4 between 15-19 μ/dL. No patients had blood lead levels of 20μ/dL. No statistically significant differences were found between patients with blood lead > 10μ/dL and those with 10μ/dL when comparing for age, sex, ethnicity, income, and zip code. Only those children living in or regularly visiting a pre-1960 home with peeling or chipping paint were significantly more likely to have elevated blood lead (p=. 045). Conclusion: Although the majority of children in our setting were poor and urban, the prevalence of blood lead > 10 μ/dL was 3.1%, well below the estimated 17% quoted by the Centers for Disease Control in recommending stringent screening guidelines. The lead risk assessment questionnaire failed to identify 32% of children with elevated blood lead levels. Since this questionnaire is critical to screening populations at low risk for lead toxicity, it is important to determine whether a revised questionnaire or a more careful elicitation of parental responses will improve identification of those children at risk</description><subject>Biological and medical sciences</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Continuity of Patient Care</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Internship and Residency</subject><subject>Lead - adverse effects</subject><subject>Lead - blood</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metals and various inorganic compounds</subject><subject>Outpatient Clinics, Hospital</subject><subject>Primary Health Care</subject><subject>Risk Assessment</subject><subject>Surveys and Questionnaires</subject><subject>Toxicology</subject><subject>Urban Population</subject><issn>1556-3650</issn><issn>0731-3810</issn><issn>1556-9519</issn><issn>1097-9875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNp9kE9LxDAQxYMoq65-AA9CD-KtmjRNm6AXLf6DBT3oOaRpwmbJJmvSKvvtbdm6IMJeJsPM7w0vD4AzBK8wguwaEVLggrASMggRYnAPHA2zlBHE9se-B-AhOI5xASGmOUMTMGEog5TSI4DvrfdNMlNiKF_KxsS4RCSVd61xnWnXSWWNMzJ586vOitZ4dwIOtLBRnY7vFHw8PrxXz-ns9emlupulMi9QmyqS5ZlERY2QZjKnsskQFnVBNWYql0pACRnurWshVU01hYMn2JA6x0VJSjwFl5u7q-A_OxVbvjRRKmuFU76LHJFeTvIBRBtQBh9jUJqvglmKsOYI8iEo_i-oXnM-Hu_qpWq2ijGZfn8x7kWUwuognDRxi2UFLBklPXa7wYzTPizFtw-24a1YWx9-NXiXi5s_8rkStp1LERRf-C64Pt4df_gBhgWTGA</recordid><startdate>1997</startdate><enddate>1997</enddate><creator>Holmes, Susan E.</creator><creator>Drutz, Jan E.</creator><creator>Buffone, Gregory J.</creator><creator>Rice, Teresa Duryea</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><general>Dekker</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T2</scope><scope>7U2</scope><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>1997</creationdate><title>Blood Lead Levels in a Continuity Clinic Population</title><author>Holmes, Susan E. ; Drutz, Jan E. ; Buffone, Gregory J. ; Rice, Teresa Duryea</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c461t-e5242c16b11f9c48cd213ab68f39e4cea0c093709faceb8f8020880d5b4367573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Biological and medical sciences</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Continuity of Patient Care</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Internship and Residency</topic><topic>Lead - adverse effects</topic><topic>Lead - blood</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metals and various inorganic compounds</topic><topic>Outpatient Clinics, Hospital</topic><topic>Primary Health Care</topic><topic>Risk Assessment</topic><topic>Surveys and Questionnaires</topic><topic>Toxicology</topic><topic>Urban Population</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Holmes, Susan E.</creatorcontrib><creatorcontrib>Drutz, Jan E.</creatorcontrib><creatorcontrib>Buffone, Gregory J.</creatorcontrib><creatorcontrib>Rice, Teresa Duryea</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Safety Science and Risk</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Clinical toxicology (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Holmes, Susan E.</au><au>Drutz, Jan E.</au><au>Buffone, Gregory J.</au><au>Rice, Teresa Duryea</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Blood Lead Levels in a Continuity Clinic Population</atitle><jtitle>Clinical toxicology (Philadelphia, Pa.)</jtitle><addtitle>J Toxicol Clin Toxicol</addtitle><date>1997</date><risdate>1997</risdate><volume>35</volume><issue>2</issue><spage>181</spage><epage>186</epage><pages>181-186</pages><issn>1556-3650</issn><issn>0731-3810</issn><eissn>1556-9519</eissn><eissn>1097-9875</eissn><abstract>Abstract
Introduction: Lead toxicity is well recognized as a significant cause of morbidity in children, especially those under the age of six years. While lead toxicity has not been recognized as a public health problem in Houston, it is possible that children in the area suffer from low-level lead effect on the central nervous system. Objectives: To detect asymptomatic cases of lead toxicity in one population of Houston children and to assess the effectiveness of the lead risk questionnaire. Design: Venous blood samples for quantitative lead were analyzed utilizing the Anodic Stripping Voltameter. The Centers for Disease Control's lead risk assessment questionnaire was administered to each patient. Setting: Baylor College of Medicine Continuity Clinic at Texas Children's Hospital. Subjects: All patients, age 9-72 months, seen for routine care between December 1992 and June 1994 were screened once. Results: Blood lead levels were obtained on 801 children; all but 47 completed lead risk questionnaires. The mean age of the study group was 2.37 years (SD 1.84) and they were 54% male. They were 39% Hispanic, 39% Black, and 18% White. Eighty-eight percent reported an annual income of >$20,000. They lived in 127 separate zip codes. Twenty-five (3.1%) patients had elevated blood lead, 21 between 10-14 μ/dL and 4 between 15-19 μ/dL. No patients had blood lead levels of 20μ/dL. No statistically significant differences were found between patients with blood lead > 10μ/dL and those with 10μ/dL when comparing for age, sex, ethnicity, income, and zip code. Only those children living in or regularly visiting a pre-1960 home with peeling or chipping paint were significantly more likely to have elevated blood lead (p=. 045). Conclusion: Although the majority of children in our setting were poor and urban, the prevalence of blood lead > 10 μ/dL was 3.1%, well below the estimated 17% quoted by the Centers for Disease Control in recommending stringent screening guidelines. The lead risk assessment questionnaire failed to identify 32% of children with elevated blood lead levels. Since this questionnaire is critical to screening populations at low risk for lead toxicity, it is important to determine whether a revised questionnaire or a more careful elicitation of parental responses will improve identification of those children at risk</abstract><cop>Monticello, NY</cop><pub>Informa UK Ltd</pub><pmid>9120888</pmid><doi>10.3109/15563659709001190</doi><tpages>6</tpages></addata></record> |
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subjects | Biological and medical sciences Chemical and industrial products toxicology. Toxic occupational diseases Child Child, Preschool Continuity of Patient Care Female Humans Infant Internship and Residency Lead - adverse effects Lead - blood Male Medical sciences Metals and various inorganic compounds Outpatient Clinics, Hospital Primary Health Care Risk Assessment Surveys and Questionnaires Toxicology Urban Population |
title | Blood Lead Levels in a Continuity Clinic Population |
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