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HSTAT: Guide to Clinical Preventive Services, 3rd Edition: Recommendations and Systematic Evidence Reviews, Guide to Community Preventive Services U.S. Preventive Services Task Force Evidence Syntheses, formerly Systematic Evidence Reviews 40. Screening for Iron Deficiency Anemia in Childhood and Pregnancy: Update of the 1996 U.S. Preventive Task Force Review Prepared for: Agency for Healthcare Research and Quality U.S. Department of Health and Human Services 540 Gaither Road Rockville, MD 20850 Contract Number 290-02-0024 Prepared by: Oregon Evidence-based Practice Center Oregon Health and Science University 3181 SW Sam Jackson Park Road Portland, Oregon 97239 AHRQ Publication No. 06-0590-EF-1 April 21, 2006 AbstractBackground. To update its 1996 guidelines, the U.S. Preventive Services Task Force (USPSTF) commissioned this brief update of the evidence on selected questions about screening for iron deficiency anemia (IDA) in children, adolescents, and pregnant women. METHODS: We searched relevant databases, Web sites, journals, and reference lists for systematic reviews, epidemiologic surveys, and controlled trials published in 1995 or later that contained new information about the prevalence, diagnosis, natural course, or treatment of iron deficiency anemia in asymptomatic persons in developed countries. One investigator rated the quality of included trials and summarized their results in tables. RESULTS: In the U.S., the average prevalence IDA in target groups is: Infants 12 years (6 to 17 per 1000), teenage girls (1.5%), nonpregnant females of reproductive age (2% to 5%). Factors associated with a higher prevalence include prematurity and low birth weight, black or Mexican-American race, Alaskan native heritage, recent immigration, poverty and, among teenage girls, fad dieting or obesity. The prevalence among pregnant women is not known. For cognitive and school outcomes, trials of iron supplementation for iron deficiency anemia have had mixed results. Most trials conducted in high-risk groups within developed countries did not demonstrate any benefit for infants and preschool children, but one trial in high-risk infants demonstrated a transient benefit. |