Screening for Iron Deficiency Anemia - Including Iron Supplementation for Children and Pregnant Women: United States Preventive Services Task Force
United States Preventive Services Task Force
guidelines, iron deficiency anemia, prevention, u.s. preventive services task force
United States Preventive Services Task Force. Screening for Iron Deficiency Anemia - Including Iron Supplementation for Children and Pregnant Women: United States Preventive Services Task Force. The Internet Journal of Nutrition and Wellness. 2006 Volume 3 Number 1.
Summary of Screening Recommendations
Screening Children and Pregnant Women for Iron Deficiency Anemia
The U.S. Preventive Services Task Force (USPSTF) concludes that evidence is insufficient to recommend for or against routine screening for iron deficiency anemia in asymptomatic children aged 6 to 12 months. I recommendation
The USPSTF recommends routine screening for iron deficiency anemia in asymptomatic pregnant women. B recommendation
Summary of Supplementation Recommendations
Iron Supplementation for Children and Pregnant Women
The U.S. Preventive Services Task Force (USPSTF) recommends routine iron supplementation for asymptomatic children aged 6 to 12 months who are at increased risk for iron deficiency anemia (see Clinical Considerations for a discussion of increased risk). B recommendation
The USPSTF concludes that evidence is insufficient to recommend for or against routine iron supplementation for asymptomatic children aged 6 to 12 months who are at average risk for iron deficiency anemia. I recommendation
The USPSTF concludes that evidence is insufficient to recommend for or against routine iron supplementation for non-anemic pregnant women. I recommendation
These USPSTF recommendations address screening for iron deficiency anemia and iron supplementation in children aged 6 to 12 months who are at increased risk and average risk, in asymptomatic pregnant women, and in non-anemic pregnant women. Infants younger than 6 months of age, older children, non-pregnant women, and men are not addressed.
Iron deficiency anemia can be defined as iron deficiency (abnormal values for serum ferritin, transferrin saturation, and free erythrocyte protoporphyrin) with a low hemoglobin or hematocrit value. Iron deficiency is much more common than iron deficiency anemia and is part of a continuum that ranges from iron depletion to iron deficiency anemia. Many of the negative health outcomes of iron deficiency are associated with its extreme manifestation, iron deficiency anemia. Iron deficiency has also been associated with negative neurodevelopmental outcomes in children.
Other causes of anemia vary by population and include other nutritional deficiencies, abnormal hemoglobin (e.g., thalassemia), enzyme defects, and anemia associated with acute and chronic infections.
In the U.S., race, income, education, and other socioeconomic factors are associated with iron deficiency and iron deficiency anemia. Individuals considered to be at high risk for iron deficiency include adult females, recent immigrants and, among adolescent females, fad dieters, and those who are obese. Premature and low birth weight infants are also at increased risk for iron deficiency.
Venous hemoglobin is more accurate than capillary hemoglobin for identifying anemia. Ferritin has the highest sensitivity and specificity for diagnosing iron deficiency in anemic patients.
Iron deficiency anemia is usually treated with oral iron preparations. The likelihood that iron deficiency anemia identified by screening will respond to treatment is unclear because many families do not adhere to treatment and because the rate of spontaneous resolution is high. 97% of infant formula sold in the U.S. is iron-fortified. Substantial reductions in the incidence of iron deficiency and iron deficiency anemia have been demonstrated in healthy infants fed iron-fortified formula or iron-fortified cereal, compared with infants fed cow's milk or unfortified formula.
Iron supplements accounted for 30% of fatal pediatric pharmaceutical overdoses occurring between 1983 and 1990, and iron poisoning has been observed even in the context of controlled trials in which parents were instructed in the safe storage and use of iron products. A reduction in deaths of children due to iron overdose was observed when unit-dose packaging was required between 1998 and 2002; this requirement was overturned by the courts in 2003.
Burden of Illness
Iron deficiency anemia is uncommon in the United States. Overall, the prevalence of iron deficiency anemia has remained stable over the past decade at 7% in children aged 1 to 2 years; 9% in adolescent females; and 2%–5% in non-pregnant females. More detailed data on the prevalence of iron deficiency anemia in infants of different ages has not been identified. The prevalence among pregnant women is uncertain. (1)
Iron deficiency, the most common nutritional deficiency in the world, can be caused by a number of factors. In infants, such factors are rapid growth, inadequate dietary intake, blood loss, decreased absorption, and prematurity. In women of childbearing age, such factors are heavy menstrual blood loss and pregnancy. (1)
In children, iron deficiency anemia has been associated with psychomotor and cognitive abnormalities, poor school performance, and mental retardation. Longitudinal studies indicate that anemic children diagnosed in infancy continue to be developmentally delayed after 10 years of follow-up. It is difficult to establish a causal relationship between anemia and developmental abnormalities in longitudinal studies due to environmental, socioeconomic, and other nutritional confounding factors. Iron deficiency anemia in pregnancy has been associated with an increased risk of low birth weight, preterm delivery, and perinatal mortality, as well as decreased parental interaction and poorer developmental outcomes in infants. Reduced work productivity, endurance, and exercise capacity have been associated with anemia in adults. Adults with severe anemia are at risk for cardiopulmonary complications. (1)
The USPSTF examined new evidence addressing 1) the overarching question of whether screening for iron deficiency anemia results in improved neurodevelopmental outcomes and 2) the effectiveness of interventions since the publication of its 1996 recommendation, Screening for Iron Deficiency Anemia-Including Iron Prophylaxis in Children and Pregnancy. (2) The Task Force also examined the literature addressing other evidence linking screening (e.g., prevalence, the accuracy of screening tests, and harms of screening and interventions) to improved health outcomes.
Accuracy of Tests
Serum hemoglobin or hematocrit is the primary screening test for identifying anemia. Hemoglobin is sensitive for iron deficiency anemia; however, it is not sensitive for iron deficiency because mild deficiency states may not affect hemoglobin levels. Hemoglobin is also nonspecific, since many cases of anemia are due to causes other than iron deficiency. The positive predictive value of low hemoglobin for iron deficiency in children 12 months of age has been shown to range from 10% to 40%. (1) In infants, particularly before 12 months of age, iron deficiency and iron deficiency anemia often resolve spontaneously, reducing the positive predictive value of any screening test. The sensitivity and specificity of using other single tests (e.g., serum ferritin, transferrin saturation, and erythrocyte protoporphyrin) as primary screening tools for iron deficiency anemia have not been well studied. There was insufficient evidence (no studies) to specifically address the accuracy of screening tests in asymptomatic pregnant women.
The USPSTF found poor evidence (conflicting studies) that treatment of iron deficiency anemia results in improved neurodevelopmental outcomes. In a randomized control trial in an Indonesian clinic, 12- to 18-month-old infants treated for iron deficiency anemia demonstrated a significant improvement in Bayley developmental scores compared with a control group at 4 months of follow-up.(3) A Cochrane review, published in 2001 found 7 trials of treatment in children up to 3 years of age; the review concluded that there was a lack of clear evidence that treatment of iron deficiency anemia has a beneficial effect on psychomotor development. (4)
Previous randomized and nonrandomized controlled trials, observational studies, and time series studies have demonstrated a substantial decrease in the incidence of iron deficiency and iron deficiency anemia in healthy infants as a result of iron supplementation (e.g., iron-fortified formula, iron-fortified cereal) compared with infants fed cow's milk or unfortified formula. Three randomized controlled trials published since the 1996 USPSTF review measure motor, cognitive, or behavioral outcomes in average-risk infants (2 fair-quality studies) and infants at increased risk for iron deficiency anemia (1 fair-quality study). (1)
In assessing iron supplementation in average risk infants, the USPSTF found poor evidence (conflicting studies) that supplementation results in improved outcomes. In a fair quality randomized controlled trial average risk infants who received oral iron supplementation had increased Bayley psychomotor scores at 13 months compared with the control group (100 ± 12 vs. 93 ± 9; normal range 85 to 115); Bayley mental developmental scores did not differ between the groups. (5) Another fair-quality RCT conducted in average risk infants found no differences in Bayley mental and psychomotor scores at 18 months. (6) The USPSTF found fair evidence that iron supplementation (e.g., iron–fortified formula or iron supplements) provides moderate benefits in children at increased risk. In a fair quality randomized control trial conducted in England, a smaller decrease in Griffith's global developmental quotient at 24 months of age was demonstrated in infants at increased risk for iron deficiency anemia who were fed iron-fortified formula compared with the control group of infants who received unmodified cows' milk. (7)
Harms of Screening and Treatment
The USPSTF found no new evidence regarding the potential harms of screening for iron deficiency anemia in infants and children. Potential harms of screening include false-positive results, anxiety, and cost. Unintentional overdose is a known potential harm of treatment with oral iron, as are gastrointestinal symptoms. Given appropriate protection against overdose, these harms are small. Cohort studies have reported no important adverse effects with iron-fortified formula, nor were serious side effects reported in the clinical trials of iron fortified food or formula.
The USPSTF found poor evidence (poor quality studies) that treatment of asymptomatic pregnant women with iron deficiency anemia improves health outcomes for the mother. While most studies of treatment found no effect on birth outcomes, a recent but flawed RCT found a substantial increase in the birthweight of infants whose mothers received treatment. (1)
There is good evidence that iron supplements improve the hematological indices of pregnant women. However, the USPSTF found poor evidence (poor quality studies) that iron supplementation in non-anemic pregnant women improves health outcomes for mother or neonate. A Cochrane review found that iron supplementation prevents low hemoglobin at birth or at 6 weeks post-partum in the neonate, but concluded there were no reliable data from controlled trials about the pregnancy outcomes for either mother or baby. (8)
Harms of Screening and Treatment
The USPSTF found no evidence on the harms of screening for iron deficiency anemia in asymptomatic pregnant women. Potential harms are the same as those found in children. There is poor evidence (poor quality studies) on the potential harms of iron supplementation in non-anemic pregnant women. Unintentional overdose of young children in the home is a known potential harm of supplementation with oral iron. Another potential harm of iron supplementation is higher Caesarean section rates. In one Finnish trial of pregnant women, routine iron supplementation led to higher rates of Cesarean sections and post partum blood transfusions. Study investigators attributed the increased cesarean sections and blood transfusion rates to possible anxiety by midwives and obstetricians about low hematocrit values in the selectively supplemented group. (9)
Iron deficiency anemia in infancy is a marker for subsequent poor neurocognitive development; however, screening and early treatment have not consistently improved neurocognitive outcomes. It is possible that prevention of neurodevelopmental consequences of iron deficiency anemia may require the prevention of iron deficiency rather than the detection and treatment of existing iron deficiency. Another possibility is that the prevention of neurodevelopmental consequences may require screening and early treatment of multiple nutritional deficiencies, rather than iron deficiency anemia alone. At present there is little evidence to support these hypotheses, but additional studies, particularly in developing countries, may confirm them (1).
Recommendations of Others
The Centers for Disease Control and Prevention (CDC) recommends screening for iron deficiency anemia in high-risk infants, high-risk preschool children, pregnant women, and non-pregnant women of childbearing age. The CDC also recommends universal iron supplementation to meet the iron requirements of pregnancy.(10)
The American Academy of Pediatricians (AAP) recommends screening for all infants between the ages of 9 to 12 months and then 6 months later; for children at high risk, screen once a year from ages 2 to 5 years. The 2005 AAP breastfeeding guidelines recommend continuing breastfeeding for at least the first year of life and beyond, while introducing complementary foods rich in iron beginning around 6 months of age; breastfed infants weaned before 12 months of age should receive iron-fortified infant formula. AAP recommends that preterm and low birth weight infants receive iron supplementation before 6 months of age.(11,12)
The American Academy of Family Physicians (AAFP) recommends screening for iron deficiency anemia in high-risk infants aged 6 to 12 and in infants whose principal dietary intake is unfortified cow's milk.
The American College of Obstetricians and Gynecologists (ACOG) recommends prenatal screening for all women at the earliest prenatal visit and early in the third trimester.
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U.S. Preventive Services Task Force
Corresponding Author: Ned Calonge, MD, MPH, Chair, U.S. Preventive Services Task Force, c/o Program Director, USPSTF, Agency for Healthcare Research and Quality, 540 Gaither Road, Rockville, MD 20850, e-mail: firstname.lastname@example.org.
Members of the U.S. Preventive Services Task Force* are Ned Calonge, MD, MPH, Chair, USPSTF (Chief Medical Officer and State Epidemiologist, Colorado Department of Public Health and Environment, Denver, CO); Diana B. Petitti, MD, MPH , Vice-chair, USPSTF (Senior Scientific Advisor for Health Policy and Medicine, Regional Administration, Kaiser Permanente Southern California, Pasadena, CA); Thomas G. DeWitt, MD (Carl Weihl Professor of Pediatrics and Director of the Division of General and Community Pediatrics, Department of Pediatrics, Children's Hospital Medical Center, Cincinnati, OH); Leon Gordis, MD, MPH, DrPH (Professor, Epidemiology Department, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD); Kimberly D. Gregory, MD, MPH (Director, Women's Health Services Research and Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Cedars-Sinai Medical Center, Los Angeles, CA); Russell Harris, MD, MPH (Professor of Medicine, Sheps Center for Health Services Research, University of North Carolina School of Medicine, Chapel Hill, NC); Kenneth W. Kizer, MD, MPH (President and CEO, National Quality Forum, Washington, DC); Michael L. LeFevre, MD, MSPH (Professor, Department of Family and Community Medicine, University of Missouri School of Medicine, Columbia, MO); Carol Loveland-Cherry, PhD, RN (Executive Associate Dean, Office of Academic Affairs, University of Michigan School of Nursing, Ann Arbor, MI); Lucy N. Marion, PhD, RN (Dean and Professor, School of Nursing, Medical College of Georgia, Augusta, GA); Virginia A. Moyer, MD, MPH (Professor, Department of Pediatrics, University of Texas Health Science Center, Houston, TX); Judith K. Ockene, PhD (Professor of Medicine and Chief of Division of Preventive and Behavioral Medicine, University of Massachusetts Medical School, Worcester, MA); George F. Sawaya, MD (Associate Professor, Department of Obstetrics, Gynecology, and Reproductive Sciences and Department of Epidemiology and Biostatistics, University of California, San Francisco, CA); Albert L. Siu, MD, MSPH (Professor and Chairman, Brookdale Department of Geriatrics and Adult Development, Mount Sinai Medical Center, New York, NY); Steven M. Teutsch, MD, MPH (Executive Director, Outcomes Research and Management, Merck & Company, Inc., West Point, PA); and Barbara P. Yawn, MD, MSc (Director of Research, Olmstead Research Center, Rochester, MN).
*Members of the Task Force at the time this recommendation was finalized. For a list of current Task Force members, go to http://www.ahrq.gov/clinic/uspstfab.htm.
U.S. Preventive Services Task Force Recommendations and Ratings
The Task Force grades its recommendations according to one of 5 classifications (A, B, C, D, I) reflecting the strength of evidence and magnitude of net benefit (benefits minus harms):
U.S. Preventive Services Task Force Strength Of Overall Evidence
The USPSTF grades the quality of the overall evidence for a service on a 3-point scale (good, fair, poor):