Persons using assistive technology might not be able to fully access information in this file. For assistance, please send e-mail to: mmwrq@cdc.gov. Type 508 Accommodation and the title of the report in the subject line of e-mail.

Recommendations to Prevent and Control Iron Deficiency in the United States

Summary

Iron deficiency is the most common known form of nutritional deficiency. Its prevalence is highest among young children and women of childbearing age (particularly pregnant women). In children, iron deficiency causes developmental delays and behavioral disturbances, and in pregnant women, it increases the risk for a preterm delivery and delivering a low-birthweight baby. In the past three decades, increased iron intake among infants has resulted in a decline in childhood iron-deficiency anemia in the United States. As a consequence, the use of screening tests for anemia has become a less efficient means of detecting iron deficiency in some populations. For women of childbearing age, iron deficiency has remained prevalent.

To address the changing epidemiology of iron deficiency in the United States, CDC staff in consultation with experts developed new recommendations for use by primary health-care providers to prevent, detect, and treat iron deficiency. These recommendations update the 1989 "CDC Criteria for Anemia in Children and Childbearing-Aged Women" (MMWR 1989;38(22):400-4) and are the first comprehensive CDC recommendations to prevent and control iron deficiency. CDC emphasizes sound iron nutrition for infants and young children, screening for anemia among women of childbearing age, and the importance of low-dose iron supplementation for pregnant women. INTRODUCTION

In the human body, iron is present in all cells and has several vital functions -- as a carrier of oxygen to the tissues from the lungs in the form of hemoglobin (Hb), as a facilitator of oxygen use and storage in the muscles as myoglobin, as a transport medium for electrons within the cells in the form of cytochromes, and as an integral part of enzyme reactions in various tissues. Too little iron can interfere with these vital functions and lead to morbidity and mortality.

In the United States, the prevalence of iron-deficiency anemia among children declined during the 1970s in association with increased iron intake during infancy (1-3). Because of this decline, the value of anemia as a predictor of iron deficiency has also declined, thus decreasing the effectiveness of routine anemia screening among children. In contrast, the rate of anemia among low-income women during pregnancy is high, and no improvement has been noted since the 1970s (4). These findings, plus increased knowledge about screening for iron status, raised questions about the necessity and effectiveness of existing U.S. programs to prevent and control iron deficiency. CDC requested the Institute of Medicine to convene an expert committee to develop recommendations for preventing, detecting, and treating iron-deficiency anemia among U.S. children and U.S. women of childbearing age. The committee met throughout 1992, and in 1993 the Institute of Medicine published the committee's recommendations (5). These guidelines are not practical for all primary health-care and public health settings, however, because they require serum ferritin testing during pregnancy (6). This testing may be appropriate in practices where women consistently visit their physician throughout pregnancy, but it is less feasible when analysis of serum ferritin concentration is unavailable or when prenatal care visits are sporadic. The CDC recommendations in this report -- including those for pregnant women -- were developed for practical use in primary health-care and public health settings.

Beside the Institute of Medicine (5,7), the American Academy of Pediatrics (8,9), the U.S. Preventive Services Task Force (10), the American College of Obstetricians and Gynecologists (9,11), the Federation of American Societies for Experimental Biology (12), and the U.S. Public Health Service (13) have all published guidelines within the past 9 years for health-care providers that address screening for and treatment of iron deficiency in the United States. Preventing and controlling iron deficiency are also addressed in Nutrition and Your Health: Dietary Guidelines for Americans (14).

The CDC recommendations differ from the guidelines published by the U.S. Preventive Services Task Force (10) in two major areas. First, the Task Force recommended screening for anemia among infants at high risk for anemia and pregnant women only. The CDC recommends periodic screening for anemia among high-risk populations of infants and preschool children, among pregnant women, and among nonpregnant women of childbearing age. Second, the Task Force stated there is insufficient evidence to recommend for or against iron supplementation during pregnancy, but the CDC recommends universal iron supplementation to meet the iron requirements of pregnancy. The CDC recommendations for iron supplementation during pregnancy are similar to the guidelines issued by the American Academy of Pediatrics and the American College of Obstetricians and Gynecologists (9).

This report is intended to provide guidance to primary health-care providers and emphasizes the etiology and epidemiology of iron deficiency, the laboratory tests used to assess iron status, and the screening for and treatment of iron deficiency at all ages. The recommendations in this report are based on the 1993 Institute of Medicine guidelines; the conclusions of an expert panel convened by CDC in April 1994; and input from public health nutrition program personnel, primary health-care providers, and experts in hematology, biochemistry, and nutrition.

National health objective 2.10 for the year 2000 is to "reduce iron deficiency to less than 3% among children aged 1-4 and among women of childbearing age" (15). The recommendations in this report for preventing and controlling iron deficiency are meant to move the nation toward this objective. BACKGROUND Iron Metabolism

Total body iron averages approximately 3.8 g in men and 2.3 g in women, which is equivalent to 50 mg/kg body weight for a 75-kg man (16,17) and 42 mg/kg body weight for a 55-kg woman (18), respectively. When the body has sufficient iron to meet its needs, most iron (greater than 70%) may be classified as functional iron; the remainder is storage or transport iron. More than 80% of functional iron in the body is found in the red blood cell mass as Hb, and the rest is found in myoglobin and intracellular respiratory enzymes (e.g., cytochromes) (Table_1). Iron is stored primarily as ferritin, but some is stored as hemosiderin. Iron is transported in blood by the protein transferrin. The total amount of iron in the body is determined by intake, loss, and storage of this mineral (16). Iron Intake

Regulation of iron balance occurs mainly in the gastrointestinal tract through absorption. When the absorptive mechanism is operating normally, a person maintains functional iron and tends to establish iron stores. The capacity of the body to absorb iron from the diet depends on the amount of iron in the body, the rate of red blood cell production, the amount and kind of iron in the diet, and the presence of absorption enhancers and inhibitors in the diet.

The percentage of iron absorbed (i.e., iron bioavailability) can vary from less than 1% to greater than 50% (19). The main factor controlling iron absorption is the amount of iron stored in the body. The gastrointestinal tract increases iron absorption when the body's iron stores are low and decreases absorption when stores are sufficient. An increased rate of red blood cell production can also stimulate iron uptake severalfold (16,20).

Among adults, absorption of dietary iron averages approximately 6% for men and 13% for nonpregnant women in their childbearing years (19). The higher absorption efficiency of these women reflects primarily their lower iron stores as a result of menstruation and pregnancy. Among iron-deficient persons, iron absorption is also high (21). Absorption of iron increases during pregnancy, but the amount of the increase is not well defined (6); as iron stores increase postpartum, iron absorption decreases.

Iron bioavailability also depends on dietary composition. Heme iron, which is found only in meat, poultry, and fish, is two to three times more absorbable than non-heme iron, which is found in plant-based foods and iron-fortified foods (19,20). The bioavailability of non-heme iron is strongly affected by the kind of other foods ingested at the same meal. Enhancers of iron absorption are heme iron (in meat, poultry, and fish) and vitamin C; inhibitors of iron absorption include polyphenols (in certain vegetables), tannins (in tea), phytates (in bran), and calcium (in dairy products) (16,22). Vegetarian diets, by definition, are low in heme iron. However, iron bioavailability in a vegeterian diet can be increased by careful planning of meals to include other sources of iron and enhancers of iron absorption (14). In the diet of an infant, before the introduction of solid foods, the amount of iron absorbed depends on the amount and bioavailability of iron in breast milk or formula (8) (Table_2). Iron Turnover and Loss

Red blood cell formation and destruction is responsible for most iron turnover in the body. For example, in adult men, approximately 95% of the iron required for the production of red blood cells is recycled from the breakdown of red blood cells and only 5% comes from dietary sources. In contrast, an infant is estimated to derive approximately 70% of red blood cell iron from the breakdown of red blood cells and 30% from the diet (23).

In adults, approximately 1 mg of iron is lost daily through feces and desquamated mucosal and skin cells (24). Women of childbearing age require additional iron to compensate for menstrual blood loss (an average of 0.3-0.5 mg daily during the childbearing years) (18) and for tissue growth during pregnancy and blood loss at delivery and postpartum (an average of 3 mg daily over 280 days' gestation) (25). In all persons, a minute amount of iron is lost daily from physiological gastrointestinal blood loss. Pathological gastrointestinal iron loss through gastrointestinal bleeding occurs in infants and children sensitive to cow's milk and in adults who have peptic ulcer disease, inflammatory bowel syndrome, or bowel cancer. Hookworm infections, although not common in the United States (26), are also associated with gastrointestinal blood loss and iron depletion (27). Iron Stores

Iron present in the body beyond what is immediately needed for functional purposes is stored as the soluble protein complex ferritin or the insoluble protein complex hemosiderin (16,17). Ferritin and hemosiderin are present primarily in the liver, bone marrow, spleen, and skeletal muscles. Small amounts of ferritin also circulate in the plasma. In healthy persons, most iron is stored as ferritin (an estimated 70% in men and 80% in women) and smaller amounts are stored as hemosiderin (Table_1). When long-term negative iron balance occurs, iron stores are depleted before iron deficiency begins.

Men store approximately 1.0-1.4 g of body iron (17,28), women approximately 0.2-0.4 g (18,28), and children even less (23). Full-term infants of normal or high birthweight are born with high body iron (an average of 75 mg/kg body weight), to which iron stores contribute approximately 25% (23). Preterm or low-birthweight infants are born with the same ratio of total body iron to body weight, but because their body weight is low, the amount of stored iron is low too. Manifestations of Iron Deficiency

Iron deficiency is one of the most common nutritional deficiencies worldwide (29) and has several causes (Exhibit 1) (Table_1B). Iron deficiency represents a spectrum (Table_3) ranging from iron depletion, which causes no physiological impairments, to iron-deficiency anemia, which affects the functioning of several organ systems. In iron depletion, the amount of stored iron (e.g., as measured by serum ferritin concentration) is reduced but the amount of functional iron may not be affected (30,31). Persons who have iron depletion have no iron stores to mobilize if the body requires more iron. In iron-deficient erythropoiesis, stored iron is depleted and transport iron (e.g., as measured by transferrin saturation) is reduced further; the amount of iron absorbed is not sufficient to replace the amount lost or to provide the amount needed for growth and function. In this stage, the shortage of iron limits red blood cell production and results in increased erthryocyte protoporphyrin concentration. In iron-deficiency anemia, the most severe form of iron deficiency, the shortage of iron leads to underproduction of iron-containing functional compounds, including Hb. The red blood cells of persons who have iron-deficiency anemia are microcytic and hypochromic (30,31).

In infants (persons aged 0-12 months) and preschool children (persons aged 1-5 years), iron-deficiency anemia results in developmental delays and behavioral disturbances (e.g., decreased motor activity, social interaction, and attention to tasks) (32,33). These developmental delays may persist past school age (i.e., 5 years) if the iron deficiency is not fully reversed (32-34). In these studies of development and behavior, iron-deficiency anemia was defined as a Hb concentration of less than or equal to 10.0 g/dL or less than or equal to 10.5 g/dL; further study is needed to determine the effects of mild iron-deficiency anemia (for example, a Hb concentration of greater than 10.0 g/dL but less than 11.0 g/dL in children aged 1- less than 2 years) on infant and child development and behavior. Iron-deficiency anemia also contributes to lead poisoning in children by increasing the gastrointestinal tract's ability to absorb heavy metals, including lead (35). Iron-deficiency anemia is associated with conditions that may independently affect infant and child development (e.g., low birthweight, generalized undernutrition, poverty, and high blood level of lead) that need to be taken into account when interventions addressing iron-deficiency anemia are developed and evaluated (34).

In adults (persons aged greater than or equal to 18 years), iron-deficiency anemia among laborers (e.g., tea pickers, latex tappers, and cotton mill workers) in the developing world impairs work capacity; the impairment appears to be at least partially reversible with iron treatment (36,37). It is not known whether iron-deficiency anemia affects the capacity to perform less physically demanding labor that is dependent on sustained cognitive or coordinated motor function (37).

Among pregnant women, iron-deficiency anemia during the first two trimesters of pregnancy is associated with a twofold increased risk for preterm delivery and a threefold increased risk for delivering a low-birthweight baby (38). Evidence from randomized control trials indicates that iron supplementation decreases the incidence of iron-deficiency anemia during pregnancy (10,39-42), but trials of the effect of universal iron supplementation during pregnancy on adverse maternal and infant outcomes are inconclusive (10,43,44). Risk for and Prevalence of Iron Deficiency in the United States

A rapid rate of growth coincident with frequently inadequate intake of dietary iron places children aged less than 24 months, particularly those aged 9-18 months, at the highest risk of any age group for iron deficiency (3). The iron stores of full-term infants can meet an infant's iron requirements until ages 4-6 months, and iron-deficiency anemia generally does not occur until approximately age 9 months. Compared with full-term infants of normal or high birthweight, preterm and low-birthweight infants are born with lower iron stores and grow faster during infancy; consequently, their iron stores are often depleted by ages 2-3 months (5,23) and they are at greater risk for iron deficiency than are full-term infants of normal or high birthweight. Data from the third National Health and Nutrition Examination Survey (NHANES III), which was conducted during 1988-1994, indicated that 9% of children aged 12-36 months in the United States had iron deficiency (on the basis of two of three abnormal values for erythrocyte protoporphyrin concentration, serum ferritin concentration, and transferrin saturation) and that 3% also had iron-deficiency anemia (Table_4). The prevalence of iron deficiency is higher among children living at or below the poverty level than among those living above the poverty level and higher among black or Mexican-American children than among white children (45).

Evidence from the Continuing Survey of Food Intakes by Individuals (CSFII), which was conducted during 1994-1996, suggests that most infants meet the recommended dietary allowance for iron through diet (Table_5; these data exclude breast-fed infants). However, the evidence also suggests that more than half of children aged 1-2 years may not be meeting the recommended dietary allowance for iron through their diet (Table_5; these data do not include iron intake from supplemental iron).

An infant's diet is a reasonable predictor of iron status in late infancy and early childhood (23,48). For example, approximately 20%-40% of infants fed only non-iron-fortified formula or whole cow's milk and 15%-25% of breast-fed infants are at risk for iron deficiency by ages 9-12 months (23,48). Infants fed mainly iron-fortified formula (greater than or equal to 1.0 mg iron/100 kcal formula) (8) are not likely to have iron deficiency at age 9 months (48). Another study has documented that intake of iron-fortified cereal protects against iron deficiency: among exclusively breast-fed infants who were fed cereal starting at age 4 months, 3% of infants who were randomized to receive iron-fortified cereal compared with 15% of infants who were randomized to receive non-iron-fortified cereal had iron-deficiency anemia at age 8 months (49). The effect of prolonged exclusive breast feeding on iron status is not well understood. One nonrandomized study with a small cohort suggested that exclusive breast feeding for greater than 7 months is protective against iron deficiency compared with breast feeding plus the introduction of non-iron-fortified foods at age less than or equal to 7 months (50); infants weaned to iron-fortified foods were not included in this study.

Early introduction (i.e., before age 1 year) of whole cow's milk and consumption of greater than 24 oz of whole cow's milk daily after the 1st year of life are risk factors for iron deficiency because this milk has little iron, may replace foods with higher iron content, and may cause occult gastrointestinal bleeding (8,48,51,52). Because goat's milk and cow's milk have similar compositions (53,54), infants fed goat's milk are likely to have the same risk for developing iron deficiency as do infants fed cow's milk. Of all milks and formulas, breast milk has the highest percentage of bioavailable iron, and breast milk and iron-fortified formulas provide sufficient iron to meet an infant's needs (55). Iron-fortified formulas are readily available, do not cost much more than non-iron-fortified formulas, and have few proven side effects except for darker stools (56,57). Controlled trials and observational studies have indicated that iron-fortified formula causes no more gastrointestinal distress than does non-iron-fortified formula (56-58), and there is little medical indication for non-iron-fortified formula (59).

After age 24 months, when the growth rate of children slows and the diet becomes more diversified, the risk for iron deficiency drops (28,45,47). In children aged greater than 36 months, dietary iron and iron status are usually adequate (45,47). For these older children, risks for iron deficiency include limited access to food (e.g., because of low family income (45) or because of migrant or refugee status), a low-iron or other specialized diet, and medical conditions that affect iron status (e.g., inflammatory or bleeding disorders) (3).

During adolescence (ages 12- less than 18 years), iron requirements (46) and hence the risk for iron deficiency increase because of rapid growth (60,61). Among boys, the risk subsides after the peak pubertal growth period. Among girls and women, however, menstruation increases the risk for iron deficiency throughout the childbearing years. An important risk factor for iron-deficiency anemia among nonpregnant women of childbearing age is heavy menstrual blood loss (greater than or equal to 80 mL/month) (18), which affects an estimated 10% of these women in the United States (17,18). Other risk factors include use of an intrauterine device (which is associated with increased menstrual blood loss), high parity, previous diagnosis of iron-deficiency anemia, and low iron intake (45,60). Use of oral contraceptives is associated with decreased risk for iron deficiency (18,62).

Data from CSFII suggest that only one fourth of adolescent girls and women of childbearing age (12-49 years) meet the recommended dietary allowance for iron through diet (Table_5). Indeed, data from the complete NHANES III indicated that 11% of nonpregnant women aged 16-49 years had iron deficiency and that 3%-5% also had iron-deficiency anemia (Table_4).

Among pregnant women, expansion of blood volume by approximately 35% and growth of the fetus, placenta, and other maternal tissues increase the demand for iron threefold in the second and third trimesters to approximately 5.0 mg iron/day (18,46). Although menstruation ceases and iron absorption increases during pregnancy, most pregnant women who do not take iron supplements to meet increased iron requirements during pregnancy cannot maintain adequate iron stores, particularly during the second and third trimesters (63). After delivery, the iron in the fetus and placenta is lost to the woman, but some of the iron in the expanded blood volume may be returned to the woman's iron stores (18).

The prevalence of anemia in low-income, pregnant women enrolled in public health programs in the United States has remained fairly stable since 1979 (4). In 1993, the prevalence of anemia among these women was 9%, 14%, and 37% in the first, second, and third trimesters, respectively (4). Comparable data for the U.S. population of all pregnant women are unavailable. The low dietary intake of iron among U.S. women of childbearing age (47), the high prevalence of iron deficiency and iron-deficiency anemia among these women (45), and the increased demand for iron during pregnancy (18,46) suggest that anemia during pregnancy may extend beyond low-income women.

Published data on iron supplement use by a representative sample of pregnant U.S. women are limited. In the 1988 National Maternal and Infant Health Survey of a nationally representative sample of U.S. women who delivered a child in that year, 83% of respondents reported that they took supplements with multiple vitamins and minerals greater than or equal to 3 days/week for 3 months after they found out they were pregnant (64). Significantly smaller percentages of black women; Eskimo, Aleut, or American Indian women; women aged less than 20 years; and women having less than a high school education reported taking these supplements. In this survey, self-reported use of supplementation was within the range (55%-95%) found in a review of studies using objective measures to estimate adherence (e.g., pill counts and serum ferritin concentration) (65). The survey results suggest that the groups of women at high risk for iron deficiency during nonpregnancy are less likely to take supplements with multiple vitamins and minerals during pregnancy. This survey did not question respondents about changes in supplement use during pregnancy or what dose of iron supplements was consumed.

In the United States, the main reasons for lack of a recommended iron supplementation regimen during pregnancy may include lack of health-care provider and patient perceptions that iron supplements improve maternal and infant outcomes (65), complicated dose schedules (5,65), and uncomfortable side effects (e.g., constipation, nausea, and vomiting) (66,67). Low-dose supplementation regimens that meet pregnancy requirements (i.e., 30 mg iron/day) (46) and reduce unwanted side effects are as effective as higher dose regimens (i.e., 60 or 120 mg iron/day) in preventing iron-deficiency anemia (66). Simplified dose schedules (e.g., 1 dose/day) may also improve compliance (65). Methods to improve compliance among pregnant women at high risk for iron deficiency require further study.

Among men (males aged greater than or equal to 18 years) and postmenopausal women in the United States, iron-deficiency anemia is uncommon. Data from NHANES III indicated that less than or equal to 2% of men aged greater than or equal to 20 years and 2% of women aged greater than or equal to 50 years had iron-deficiency anemia (Table_4). Data from CFSII indicate that most men and most women aged greater than or equal to 50 years meet the recommended dietary allowance for iron through diet (Table_5). In a study of adults having iron-deficiency anemia, 62% had clinical evidence of gastrointestinal bleeding as a result of lesions (e.g., ulcers and tumors) (68). In NHANES I, which was conducted during 1971-1975, about two thirds of anemia cases among men and postmenopausal women were attributable to chronic disease or inflammatory conditions (69). The findings of these studies suggest that, among these populations, the primary causes of anemia are chronic disease and inflammatory conditions and that low iron intake should not be assumed to be the cause of the anemia. TESTS USED TO ASSESS IRON STATUS

Iron status can be assessed through several laboratory tests. Because each test assesses a different aspect of iron metabolism, results of one test may not always agree with results of other tests. Hematological tests based on characteristics of red blood cells (i.e., Hb concentration, hematocrit, mean cell volume, and red blood cell distribution width) are generally more available and less expensive than are biochemical tests. Biochemical tests (i.e., erythrocyte protoporphyrin concentration, serum ferritin concentration, and transferrin saturation), however, detect earlier changes in iron status.

Although all of these tests can be used to assess iron status, no single test is accepted for diagnosing iron deficiency (70). Detecting iron deficiency in a clinical or field setting is more complex than is generally believed.

Lack of standardization among the tests and a paucity of laboratory proficiency testing limit comparison of results between laboratories (71). Laboratory proficiency testing is currently available for measuring Hb concentration, hematocrit, red blood cell count, serum ferritin concentration, and serum iron concentration; provisional proficiency testing was added in 1997 for total iron-binding capacity in the College of American Pathologists survey and was added to the American Association of Bioanalysts survey in 1998. As of April 1998, three states (New York, Pennsylvania, and Wisconsin) had proficiency testing programs for erthrocyte protoporphryin concentration. Regardless of whether test standardization and proficiency testing become routine, better understanding among health-care providers about the strengths and limitations of each test is necessary to improve screening for and diagnosis of iron-deficiency anemia, especially because the results from all of these tests can be affected by factors other than iron status.

Only the most common indicators of iron deficiency are described in this section. Other indicators of iron deficiency (e.g., unbound iron-binding capacity and the concentrations of transferrin receptor, serum transferrin, and holo-ferritin) are less often used or are under development. Hb Concentration and Hematocrit

Because of their low cost and the ease and rapidity in performing them, the tests most commonly used to screen for iron deficiency are Hb concentration and hematocrit (Hct). These measures reflect the amount of functional iron in the body. The concentration of the iron-containing protein Hb in circulating red blood cells is the more direct and sensitive measure. Hct indicates the proportion of whole blood occupied by the red blood cells; it falls only after the Hb concentration falls. Because changes in Hb concentration and Hct occur only at the late stages of iron deficiency, both tests are late indicators of iron deficiency; nevertheless, these tests are essential for determining iron-deficiency anemia.

Because iron deficiency is such a common cause of childhood anemia, the terms anemia, iron deficiency, and iron-deficiency anemia are often used interchangeably (3). The only cases of anemia that can be classified as iron-deficiency anemia, however, are those with additional evidence of iron deficiency. The concept of a close association between anemia and iron deficiency is closest to correct when the prevalence of iron deficiency is high. In the United States, the prevalence and severity of anemia have declined in recent years; hence, the proportion of anemia due to causes other than iron deficiency has increased substantially. As a consequence, the effectiveness of anemia screening for iron deficiency has decreased in the United States.

Iron deficiency may be defined as absent bone marrow iron stores (as described on bone marrow iron smears), an increase in Hb concentration of greater than 1.0 g/dL after iron treatment, or abnormal values on certain other biochemical tests (17). The recent recognition that iron deficiency seems to have general and potentially serious negative effects (32-34) has made identifying persons having iron deficiency as important as identifying persons having iron-deficiency anemia.

The case definition of anemia recommended in this report is less than 5th percentile of the distribution of Hb concentration or Hct in a healthy reference population and is based on age, sex, and (among pregnant women) stage of pregnancy (45,72). This case definition for anemia was shown to correctly identify 37% of women of childbearing age and 25% of children aged 1-5 years who were iron deficient (defined as two of three positive test results {i.e., low mean cell volume, high erythrocyte protoporphyrin, or low transferrin saturation}) (sensitivity) and to correctly classify 93% of women of childbearing age and 92% of children aged 1-5 years as not having iron deficiency (specificity) (73). Lowering the Hb concentration or Hct cut-off would result in identifying fewer people who have anemia due to causes other than iron deficiency (false positives) but also in overlooking more people with iron deficiency (true positives) (74).

The distributions of Hb concentration and Hct and thus the cutoff values for anemia differ between children, men, nonpregnant women, and pregnant women and by age or weeks of gestation (Table_6). The distributions also differ by altitude, smoking status, and race.

Among pregnant women, Hb concentration and Hct decline during the first and second trimesters because of an expanding blood volume (18,39-42). Among pregnant women who do not take iron supplements, Hb concentration and Hct remain low in the third trimester, and among pregnant women who have adequate iron intake, Hb concentration and Hct gradually rise during the third trimester toward the prepregnancy levels (39,40). Because adequate data are lacking in the United States, the cutoff values for anemia are based on clinical studies of European women who had taken iron supplementation during pregnancy (39-42,72). For pregnant women, a test result greater than 3 standard deviations (SD) higher than the mean of the reference population (i.e., a Hb concentration of greater than 15.0 g/dL or a Hct of greater than 45.0%), particularly in the second trimester, likely indicates poor blood volume expansion (72). High Hb concentration or Hct has been associated with hypertension and poor pregnancy outcomes (e.g., fetal growth retardation, fetal death, preterm delivery, and low birthweight) (75-78). In one study, women who had a Hct of greater than or equal to 43% at 26-30 weeks' gestation had more than a twofold increased risk for preterm delivery and a fourfold increased risk for delivering a child having fetal growth retardation than did women who had a Hct of 33%-36% (76). Hence, a high Hb concentration or Hct in the second or third trimester of pregnancy should not be considered an indicator of desirable iron status.

Long-term residency at high altitude (greater than or equal to 3,000 ft) (79) and cigarette smoking (80) cause a generalized upward shift in Hb concentration and Hct (Table_7). The effectiveness of screening for anemia is lowered if the cutoff values are not adjusted for these factors (72,79,80). Adjustment allows the positive predictive value of anemia screening to be comparable between those who reside near sea-level and those who live at high altitude and between smokers and nonsmokers (72).

In the United States, the distribution of Hb concentration values is similar among whites and Asian Americans (81), and the distribution of Hct values is similar among whites and American Indians (82). The distributions are lower among blacks than whites, however, even after adjustment for income (83,84). These different distributions are not caused by a difference in iron status indicators (e.g., iron intake, serum ferritin concentration, or transferrin saturation); thus, applying the same criteria for anemia to all races results in a higher rate of false-positive cases of iron deficiency for blacks (84). For example, in the United States during 1976-1980, 28% of nonpregnant black women but only 5% of nonpregnant white women had a Hb concentration of less than 12 g/dL and, according to the anemia criteria, would be classified as iron deficient, even though other tests for iron status suggested these women were not iron deficient (84). For this reason, the Institute of Medicine recommends lowering Hb concentration and Hct cutoff values for black children aged less than 5 years by 0.4 g/dL and 1%, respectively, and for black adults by 0.8 g/dL and 2%, respectively (5). Because the reason for this disparity in distributions by race has not been determined, the recommendations in this report do not provide race-specific cutoff values for anemia. Regardless, health-care providers should be aware of the possible difference in the positive predictive value of anemia screening for iron deficiency among blacks and whites and consider using other iron status tests (e.g., serum ferritin concentration and transferrin saturation) for their black patients.

Accurate, low-cost, clinic-based instruments have been developed for measuring Hb concentration and Hct by using capillary or venous blood (85,86). Small diurnal variations are seen in Hb concentration and Hct measurements, but these variations are neither biologically nor statistically significant (87,88). A potential source of error of using capillary blood to estimate Hb concentration and Hct in screening is improper sampling technique. For example, excessive squeezing (i.e., "milking") of the finger contaminates the blood with tissue fluid, leading to false low readings (89). Confirmation of a low reading is recommended by obtaining a second capillary blood sample from the finger or by venipuncture.

Although measures of Hb concentration and Hct cannot be used to determine the cause of anemia, a diagnosis of iron-deficiency anemia can be made if Hb concentration or Hct increases after a course of therapeutic iron supplementation (23,51). Alternatively, other laboratory tests (e.g., mean cell volume, red blood cell distribution width, and serum ferritin concentration) can be used to differentiate iron-deficiency anemia from anemia due to other causes.

In the United States in recent years, the usefulness of anemia screening as an indicator of iron deficiency has become more limited, particularly for children. Studies using transferrin saturation (a more sensitive test for iron deficiency) have documented that iron deficiency in most subpopulations of children has declined such that screening by Hb concentration no longer efficiently predicts iron deficiency (3,45,51,90). Data from NHANES II, which was conducted during 1976-1980, indicated that less than 50% of children aged 1-5 years and women in their childbearing years who had anemia (as defined by Hb concentration less than 5th percentile) were iron deficient (i.e., had at least two of the following: low mean cell volume, high erythrocyte protoporphyrin concentration, or low transferrin saturation) (70,73,83). Causes of anemia other than iron deficiency include other nutritional deficiencies (e.g., folate or vitamin B12 deficiency), hereditary defects in red blood cell production (e.g., thalassemia major and sickle cell disease), recent or current infection, and chronic inflammation (91). The current pattern of iron-deficiency anemia in the United States (28,45) indicates that selective anemia screening of children at known risk for iron deficiency or additional measurement of indicators of iron deficiency (e.g., erythrocyte protoporphyrin concentration and serum ferritin concentration) to increase the positive predictive value of screening are now suitable approaches to assessing iron deficiency among most U.S. children (3,73). The costs and feasibility of screening using additional indicators of iron deficiency may preclude the routine use of these indicators. Mean Cell Volume

Mean cell volume (MCV), the average volume of red blood cells, is measured in femtoliters (10-15 liters). This value can be calculated as the ratio of Hct to red blood cell count or measured directly using an electronic counter. MCV is highest at birth, decreases during the first 6 months of life, then gradually increases during childhood to adult levels (23,51). A low MCV corresponds with the 5th percentile for age for the reference population in NHANES III (28).

Some anemias, including iron-deficiency anemia, result in microcytic red blood cells; a low MCV thus indicates microcytic anemia (Table_8). If cases of lead poisoning and the anemias of infection, chronic inflammatory disease, and thalassemia minor can be excluded, a low MCV serves as a specific index for iron-deficiency anemia (28,87,94,95). Red Blood Cell Distribution Width

Red blood cell distribution width (RDW) is calculated by dividing the SD of red blood cell volume by MCV and multiplying by 100 to express the result as a percentage:

RDW (%) = {SD of red blood cell volume (fL)/MCV (fL)} x 100

A high RDW is generally set at greater than 14.0%, which corresponds to the 95th percentile of RDW for the reference population in NHANES III (20). The RDW value obtained depends on the instrument used (51,95).

An RDW measurement often follows an MCV test to help determine the cause of a low MCV. For example, iron-deficiency anemia usually causes greater variation in red blood cell size than does thalassemia minor (96). Thus, a low MCV and an RDW of greater than 14.0% indicates iron-deficiency anemia, whereas a low MCV and an RDW less than or equal to 14.0% indicates thalassemia minor (51). Erythrocyte Protoporphyrin Concentration

Erythrocyte protoporphyrin is the immediate precursor of Hb. The concentration of erythrocyte protoporphyrin in blood increases when insufficient iron is available for Hb production. A concentration of greater than 30 ug/dL of whole blood or greater than 70 ug/dL of red blood cells among adults and a concentration of greater than 80 ug/dL of red blood cells among children aged 1-2 years indicates iron deficiency (28,45,91). The normal range of erythrocyte protoporphyrin concentration is higher for children aged 1-2 years than for adults, but no consensus exists on the normal range for infants (28,90). The sensitivity of free erythrocyte protoporphyrin to iron deficiency (as determined by response to iron therapy) in children and adolescents aged 6 months-17 years is 42%, and the estimated specificity is 61% (74).

Infection, inflammation, and lead poisoning as well as iron deficiency can elevate erythrocyte protoporphyrin concentration (23,92). This measure of iron status has several advantages and disadvantages relative to other laboratory measures. For example, the day-to-day variation within persons for erythrocyte protoporphyrin concentration is less than that for serum iron concentration and transferrin saturation (87). A high erythrocyte protoporphyrin concentration is an earlier indicator of iron-deficient erythropoiesis than is anemia, but it is not as early an indicator of low iron stores as is low serum ferritin concentration (30). Inexpensive, clinic-based methods have been developed for measuring erythrocyte protoporphyrin concentration, but these methods can be less reliable than laboratory methods (92). Serum Ferritin Concentration

Nearly all ferritin in the body is intracellular; a small amount circulates in the plasma. Under normal conditions, a direct relationship exists between serum ferritin concentration and the amount of iron stored in the body (97), such that 1 ug/L of serum ferritin concentration is equivalent to approximately 10 mg of stored iron (98). In the United States, the average serum ferritin concentration is 135 ug/L for men (28), 43 ug/L for women (28), and approximately 30 ug/L for children aged 6-24 months (23).

Serum ferritin concentration is an early indicator of the status of iron stores and is the most specific indicator available of depleted iron stores, especially when used in conjunction with other tests to assess iron status. For example, among women who test positive for anemia on the basis of Hb concentration or Hct, a serum ferritin concentration of less than or equal to 15 ug/L confirms iron deficiency and a serum ferritin concentration of greater than 15 ug/L suggests that iron deficiency is not the cause of the anemia (93). Among women of childbearing age, the sensitivity of low serum ferritin concentration (less than or equal to 15 ug/L) for iron deficiency as defined by no stainable bone marrow iron is 75%, and the specificity is 98%; when low serum ferritin concentration is set at less than 12 ug/L, the sensitivity for iron deficiency is 61% and the specificity is 100% (93). Although low serum ferritin concentration is an early indicator of low iron stores, it has been questioned whether a normal concentration measured during the first or second trimester of pregnancy can predict adequate iron status later in pregnancy (6).

The cost of assessing serum ferritin concentration and the unavailability of clinic-based measurement methods hamper the use of this measurement in screening for iron deficiency. In the past, methodological problems have hindered the comparability of measurements taken in different laboratories (87), but this problem may be reduced by proficiency testing and standardized methods. Factors other than the level of stored iron can result in large within-individual variation in serum ferritin concentration (99). For example, because serum ferritin is an acute-phase reactant, chronic infection, inflammation, or diseases that cause tissue and organ damage (e.g., hepatitis, cirrhosis, neoplasia, or arthritis) can raise its concentration independent of iron status (97). This elevation can mask depleted iron stores. Transferrin Saturation

Transferrin saturation indicates the extent to which transferrin has vacant iron-binding sites (e.g., a low transferrin saturation indicates a high proportion of vacant iron-binding sites). Saturation is highest in neonates, decreases by age 4 months, and increases throughout childhood and adolescence until adulthood (23,28). Transferrin saturation is based on two laboratory measures, serum iron concentration and total iron-binding capacity (TIBC). Transferrin saturation is calculated by dividing serum iron concentration by TIBC and multiplying by 100 to express the result as a percentage:

Transferrin saturation (%) = {serum iron concentration (ug/dL)/TIBC (ug/dL)} x 100

Serum iron concentration is a measure of the total amount of iron in the serum and is often provided with results from other routine tests evaluated by automated, laboratory chemistry panels. Many factors can affect the results of this test. For example, the concentration of serum iron increases after each meal (71), infections and inflammations can decrease the concentration (69), and diurnal variation causes the concentration to rise in the morning and fall at night (100). The day-to-day variation of serum iron concentration within individuals is greater than that for Hb concentration and Hct (88,101).

TIBC is a measure of the iron-binding capacity within the serum and reflects the availability of iron-binding sites on transferrin (94). Thus, TIBC increases when serum iron concentration (and stored iron) is low and decreases when serum iron concentration (and stored iron) is high. Factors other than iron status can affect results from this test. For example, inflammation, chronic infection, malignancies, liver disease, nephrotic syndrome, and malnutrition can lower TIBC readings, and oral contraceptive use and pregnancy can raise the readings (87,102). Nevertheless, the day-to-day variation is less than that for serum iron concentration (87,101). TIBC is less sensitive to iron deficiency than is serum ferritin concentration, because changes in TIBC occur after iron stores are depleted (17,31,94).

A transferrin saturation of less than 16% among adults is often used to confirm iron deficiency (93). Among nonpregnant women of childbearing age, the sensitivity of low transferrin saturation (less than 16%) for iron deficiency as defined by no stainable bone marrow iron is 20%, and the specificity is 93% (93).

The factors that affect serum iron concentration and TIBC, such as iron status, diurnal variation (87,103), and day-to-day variation within persons (101), can affect the measured transferrin saturation as well. The diurnal varation is larger for transferrin saturation than it is for Hb concentration or Hct (87,103). Transferrin saturation is an indicator of iron-deficient erythropoiesis rather than iron depletion; hence, it is less sensitive to changes in iron stores than is serum ferritin concentration (30,31). The cost of assessing transferrin saturation and the unavailability of simple, clinic-based methods for measuring transferrin saturation hinder the use of this test in screening for iron deficiency. JUSTIFICATION FOR RECOMMENDATIONS

These recommendations are intended to guide primary health-care providers in preventing and controlling iron deficiency in infants, preschool children, and women of childbearing age (especially pregnant women). Both primary prevention through appropriate dietary intake and secondary prevention through detecting and treating iron-deficiency anemia are discussed. Primary Prevention

Primary prevention of iron deficiency means ensuring an adequate intake of iron. A reliable source of dietary iron is essential for every infant and child's growth and development, because a rapid rate of growth and low dietary iron may predispose an infant to exhaustion of iron stores by ages 4-6 months (23). Primary prevention of iron deficiency is most important for children aged less than 2 years, because among all age groups they are at the greatest risk for iron deficiency caused by inadequate intake of iron (28,45,47,48,91). The adequacy of the iron content of an infant's diet is a major determinant of the iron status of the infant as a young child, as indicated by declines in the prevalence of iron-deficiency anemia that correspond with improvements in infant feeding practices (1-3). In infants and young children, iron deficiency may result in developmental and behavioral disturbances (33,34).

The evidence for the effectiveness of primary prevention among pregnant women is less clear. Although iron-deficiency anemia during pregnancy is associated with preterm delivery and delivering a low-birthweight baby (38), well designed, randomized control trials are needed to evaluate the effectiveness of universal iron supplementation on mitigating adverse birth outcomes. Some studies have indicated that adequate iron supplementation during pregnancy reduces the prevalence of iron-deficiency anemia (6,10,39-42,66,104), but over the last few decades, the recommendation by the Council on Foods and Nutrition and other groups to supplement iron intake during pregnancy has not resulted in a reduced prevalence of anemia among low-income, pregnant women (4,9,105). Evidence on iron supplement use is limited, however, so it is not known how well the recommendation has been followed. Conclusive evidence of the benefits of universal iron supplementation for all women is lacking, but CDC advocates universal iron supplementation for pregnant women because a large proportion of women have difficulty maintaining iron stores during pregnancy and are at risk for anemia (6,18,63), iron-deficiency anemia during pregnancy is associated with adverse outcomes (38), and supplementation during pregnancy is not associated with important health risks (10,65,66). Potential Adverse Effects of Increasing Dietary Iron Intake

Approximately 3.3 million women of childbearing age and 240,000 children aged 1-2 years have iron-deficiency anemia (45); conversely, up to one million persons in the United States may be affected by iron overload due to hemochromatosis (106,107). Hemochromatosis is a genetic condition characterized by excessive iron absorption, excess tissue iron stores, and potential tissue injury. If undetected and untreated, iron overload may eventually result in the onset of morbidity (e.g., cirrhosis, hepatomas, diabetes, cardiomyopathy, arthritis or athropathy, or hypopituitarism with hypogonadism), usually between ages 40 and 60 years. Clinical expression of iron overload depends on the severity of the metabolic defect, the presence of sufficient quantities of absorbable iron in the diet, and physiological blood loss from the body (e.g., menstruation) (16). Transferrin saturation is the recommended screening test for hemochromatosis; a repeated high value indicates hemochromatosis (108). Preventing or treating the clinical signs of hemochromatosis involves repeated phlebotomy to remove excess iron from the body (108).

Although increases in iron intake would seem contraindicated in persons with hemochromatosis, there is no evidence that iron fortification of foods or the use of a recommended iron supplementation regimen during pregnancy is associated with increased risk for clinical disease due to hemochromatosis (16). Even when their dietary intake of iron is approximately average, persons with iron overload due to hemochromatosis will require phlebotomy to reduce their body's iron stores (108). Secondary Prevention

Secondary prevention involves screening for, diagnosing, and treating iron deficiency. Screening tests can be for anemia or for earlier indicators of iron deficiency (e.g., erythrocyte protoporphyrin concentration or serum ferritin concentration). The cost, feasibility, and variability of measurements other than Hb concentration and Hct currently preclude their use for screening. The decision to screen an entire population or to screen only persons at known risk for iron deficiency should be based on the prevalence of iron deficiency in that population (73).

The percentage of anemic persons who are truly iron deficient (i.e., the positive predictive value of anemia screening for iron deficiency) increases with increasing prevalence of iron deficiency in the population (73). In the United States, children from low-income families, children living at or below the poverty level, and black or Mexican-American children are at higher risk for iron deficiency than are children from middle- or high-income families, children living above the poverty level, and white children, respectively (2,3,45). Routine screening for anemia among populations of children at higher risk for iron deficiency is effective, because anemia is predictive of iron deficiency. In populations having a low prevalence of anemia or a prevalence of iron deficiency less than 10% (e.g., children from middle- or high-income families and white children) (2,3,45), anemia is less predictive of iron deficiency (73), and selectively screening only the persons having known risk factors for iron deficiency increases the positive predictive value of anemia screening (3,70). Because the iron stores of a full-term infant of normal or high birthweight can meet the body's iron requirements up to age 6 months (23), anemia screening is of little value before age 6 months for these infants. Anemia among pregnant women and anemia among all nonpregnant women of childbearing age should be considered together, because childbearing increases the risk for iron deficiency (both during and after pregnancy) (41,42), and iron deficiency before pregnancy likely increases the risk for iron deficiency during pregnancy (109). Periodic screening for anemia among adolescent girls and women of childbearing age is indicated for several reasons. First, most women have dietary intake of iron below the recommended dietary allowance (46,47). Second, heavy menstrual blood loss, which increases iron requirements to above the recommended dietary allowance, affects an estimated 10% of women of childbearing age (17,18). Finally, the relatively high prevalence of iron deficiency and iron-deficiency anemia among nonpregnant women of childbearing age (45) and of anemia among low-income, pregnant women (4) suggests that periodic screening for anemia is indicated among adolescent girls and nonpregnant women of childbearing age during routine medical examinations (73) and among pregnant women at the first prenatal visit. Among men and postmenopausal women, in whom iron deficiency and iron-deficiency anemia are uncommon (45), anemia screening is not highly predictive of iron deficiency. RECOMMENDATIONS Infants (Persons Aged 0-12 Months) and Preschool Children (Persons Aged 1-5 Years)

Primary prevention of iron deficiency in infants and preschool children should be achieved through diet. Information on diet and feeding is available in the Pediatric Nutrition Handbook (8), Guide to Clinical Preventive Services (10), Nutrition and Your Health: Dietary Guidelines for Americans (14), Breastfeeding and the Use of Human Milk (110), and Clinician's Handbook of Preventive Services: Put Prevention into Practice (111). For secondary prevention of iron deficiency in this age group, screening for, diagnosing, and treating iron-deficiency anemia are recommended. Primary Prevention Milk and Infant Formulas

Encourage breast feeding of infants.
Encourage exclusive breast feeding of infants (without supplementary liquid, formula, or food) for 4-6 months after birth.
When exclusive breast feeding is stopped, encourage use of an additional source of iron (approximately 1 mg/kg per day of iron), preferably from supplementary foods.
For infants aged less than 12 months who are not breast fed or who are partially breast fed, recommend only iron-fortified infant formula as a substitute for breast milk.
For breast-fed infants who receive insufficient iron from supplementary foods by age 6 months (i.e., less than 1 mg/kg per day), suggest 1 mg/kg per day of iron drops.
For breast-fed infants who were preterm or had a low birthweight, recommend 2-4 mg/kg per day of iron drops (to a maximum of 15 mg/day) starting at 1 month after birth and continuing until 12 months after birth.
Encourage use of only breast milk or iron-fortified infant formula for any milk-based part of the diet (e.g., in infant cereal) and discourage use of low-iron milks (e.g., cow's milk, goat's milk, and soy milk) until age 12 months.
Suggest that children aged 1-5 years consume no more than 24 oz of cow's milk, goat's milk, or soy milk each day. Solid Foods
At age 4-6 months or when the extrusion reflex disappears, recommend that infants be introduced to plain, iron-fortified infant cereal. Two or more servings per day of iron-fortified infant cereal can meet an infant's requirement for iron at this age.
By approximately age 6 months, encourage one feeding per day of foods rich in vitamin C (e.g., fruits, vegetables, or juice) to improve iron absorption, preferably with meals.
Suggest introducing plain, pureed meats after age 6 months or when the infant is developmentally ready to consume such food. Secondary Prevention Universal Screening
In populations of infants and preschool children at high risk for iron-deficiency anemia (e.g., children from low-income families, children eligible for the Special Supplemental Nutrition Program for Women, Infants, and Children {WIC}, migrant children, or recently arrived refugee children), screen all children for anemia between ages 9 and 12 months, 6 months later, and annually from ages 2 to 5 years. Selective Screening
In populations of infants and preschool children not at high risk for iron-deficiency anemia, screen only those children who have known risk factors for the condition. These children are described in the next three bulleted items.
Consider anemia screening before age 6 months for preterm infants and low-birthweight infants who are not fed iron-fortified infant formula.
Annually assess children aged 2-5 years for risk factors for iron-deficiency anemia (e.g., a low-iron diet, limited access to food because of poverty or neglect, or special health-care needs). Screen these children if they have any of these risk factors.
At ages 9-12 months and 6 months later (at ages 15-18 months), assess infants and young children for risk factors for anemia. Screen the following children:

Preterm or low-birthweight infants
Infants fed a diet of non-iron-fortified infant formula for greater than 2 months
Infants introduced to cow's milk before age 12 months
Breast-fed infants who do not consume a diet adequate in iron after age 6 months (i.e., who receive insufficient iron from supplementary foods)
Children who consume greater than 24 oz daily of cow's milk
Children who have special health-care needs (e.g., children who use medications that interfere with iron absorption and children who have chronic infection, inflammatory disorders, restricted diets, or extensive blood loss from a wound, an accident, or surgery).

Diagnosis and Treatment

Check a positive anemia screening result by performing a repeat Hb concentration or Hct test. If the tests agree and the child is not ill, a presumptive diagnosis of iron-deficiency anemia can be made and treatment begun.
Treat presumptive iron-deficiency anemia by prescribing 3 mg/kg per day of iron drops to be administered between meals. Counsel the parents or guardians about adequate diet to correct the underlying problem of low iron intake.
Repeat the anemia screening in 4 weeks. An increase in Hb concentration of greater than or equal to 1 g/dL or in Hct of greater than or equal to 3% confirms the diagnosis of iron-deficiency anemia. If iron-deficiency anemia is confirmed, reinforce dietary counseling, continue iron treatment for 2 more months, then recheck Hb concentration or Hct. Reassess Hb concentration or Hct approximately 6 months after successful treatment is completed.
If after 4 weeks the anemia does not respond to iron treatment despite compliance with the iron supplementation regimen and the absence of acute illness, further evaluate the anemia by using other laboratory tests, including MCV, RDW, and serum ferritin concentration. For example, a serum ferritin concentration of less than or equal to 15 ug/L confirms iron deficiency, and a concentration of greater than 15 ug/L suggests that iron deficiency is not the cause of the anemia. School-Age Children (Persons Aged 5- less than 12 Years) and Adolescent Boys (Males Aged 12- less than 18 Years)

Among school-age children and adolescent boys, only those who have a history of iron-deficiency anemia, special health-care needs, or low iron intake should be screened for anemia. Age-specific anemia criteria should be used (Table_6). Treatment for iron-deficiency anemia includes one 60-mg iron tablet each day for school-age children and two 60-mg iron tablets each day for adolescent boys and counseling about dietary intake of iron. Follow-up and laboratory evaluation are the same for school-age children and adolescent boys as they are for infants and preschool children. Adolescent Girls (Females 12- less than 18 Years) and Nonpregnant Women of Childbearing Age

Primary prevention of iron deficiency for adolescent girls and nonpregnant women of childbearing age is through diet. Information about healthy diets, including good sources of iron, is available in Nutrition and Your Health: Dietary Guidelines for Americans (14). Screening for, diagnosing, and treating iron-deficiency anemia are secondary prevention approaches. Age-specific anemia criteria should be used during screening (Table_6). Primary Prevention

Most adolescent girls and women do not require iron supplements, but encourage them to eat iron-rich foods and foods that enhance iron absorption.
Women who have low-iron diets are at additional risk for iron-deficiency anemia; guide these women in optimizing their dietary iron intake. Secondary Prevention Screening
Starting in adolescence, screen all nonpregnant women for anemia every 5-10 years throughout their childbearing years during routine health examinations.
Annually screen for anemia women having risk factors for iron deficiency (e.g., extensive menstrual or other blood loss, low iron intake, or a previous diagnosis of iron-deficiency anemia). Diagnosis and Treatment
Confirm a positive anemia screening result by performing a repeat Hb concentration or Hct test. If the adolescent girl or woman is not ill, a presumptive diagnosis of iron-deficiency anemia can be made and treatment begun.
Treat adolescent girls and women who have anemia by prescribing an oral dose of 60-120 mg/day of iron. Counsel these patients about correcting iron deficiency through diet.
Follow up adolescent girls and nonpregnant women of childbearing age as is done for infants and preschool children, except that for a confirmed case of iron-deficiency anemia, continue iron treatment for 2-3 more months.
If after 4 weeks the anemia does not respond to iron treatment despite compliance with the iron supplementation regimen and the absence of acute illness, further evaluate the anemia by using other laboratory tests, including MCV, RDW, and serum ferritin concentration. In women of African, Mediterranean, or Southeast Asian ancestry, mild anemia unresponsive to iron therapy may be due to thalassemia minor or sickle cell trait. Pregnant Women

Primary prevention of iron deficiency during pregnancy includes adequate dietary iron intake and iron supplementation. Information about healthy diets, including good sources of iron, is found in Nutrition and Your Health: Dietary Guidelines for Americans (14). More detailed information for pregnant women is found in Nutrition During Pregnancy and Lactation: An Implementation Guide (112). Secondary prevention involves screening for, diagnosing, and treating iron-deficiency anemia. Primary Prevention

Start oral, low-dose (30 mg/day) supplements of iron at the first prenatal visit.
Encourage pregnant women to eat iron-rich foods and foods that enhance iron absorption.
Pregnant women whose diets are low in iron are at additional risk for iron-deficiency anemia; guide these women in optimizing their dietary iron intake. Secondary Prevention Screening
Screen for anemia at the first prenatal care visit. Use the anemia criteria for the specific stage of pregnancy (Table_6). Diagnosis and Treatment
Confirm a positive anemia screening result by performing a repeat Hb concentration or Hct test. If the pregnant woman is not ill, a presumptive diagnosis of iron-deficiency anemia can be made and treatment begun.
If Hb concentration is less than 9.0 g/dL or Hct is less than 27.0%, refer the patient to a physician familiar with anemia during pregnancy for further medical evaluation.
Treat anemia by prescribing an oral dose of 60-120 mg/day of iron. Counsel pregnant women about correcting iron-deficiency anemia through diet.
If after 4 weeks the anemia does not respond to iron treatment (the woman remains anemic for her stage of pregnancy and Hb concentration does not increase by 1 g/dL or Hct by 3%) despite compliance with an iron supplementation regimen and the absence of acute illness, further evaluate the anemia by using other tests, including MCV, RDW, and serum ferritin concentration. In women of African, Mediterranean, or Southeast Asian ancestry, mild anemia unresponsive to iron therapy may be due to thalassemia minor or sickle cell trait.
When Hb concentration or Hct becomes normal for the stage of gestation, decrease the dose of iron to 30 mg/day.
During the second or third trimester, if Hb concentration is greater than 15.0 g/dL or Hct is greater than 45.0%, evaluate the woman for potential pregnancy complications related to poor blood volume expansion. Postpartum Women

Women at risk for anemia at 4-6 weeks postpartum should be screened for anemia by using a Hb concentration or Hct test. The anemia criteria for nonpregnant women should be used (Table_6). Risk factors include anemia continued through the third trimester, excessive blood loss during delivery, and a multiple birth. Treatment and follow-up for iron-deficiency anemia in postpartum women are the same as for nonpregnant women. If no risk factors for anemia are present, supplemental iron should be stopped at delivery. Men (Males Aged greater than or equal to 18 Years) and Postmenopausal Women

No routine screening for iron deficiency is recommended for men or postmeno-pausal women. Iron deficiency or anemia detected during routine medical examinations should be fully evaluated for its cause. Men and postmenopausal women usually do not need iron supplements. CONCLUSION

In the United States, iron deficiency affects 7.8 million adolescent girls and women of childbearing age and 700,000 children aged 1-2 years (45). Primary health-care providers can help prevent and control iron deficiency by counseling individuals and families about sound iron nutrition during infancy and beyond and about iron supplementation during pregnancy, by screening persons on the basis of their risk for iron deficiency, and by treating and following up persons with presumptive iron deficiency. Implementing these recommendations will help reduce manifestations of iron deficiency (e.g., preterm births, low birthweight, and delays in infant and child development) and thus improve public health.

References

Yip R, Walsh KM, Goldfarb MG, Binkin NJ. Declining prevalence of anemia in childhood in a middle-class setting: a pediatric success story? Pediatrics 1987;80(3):330-4.
Yip R, Binkin NJ, Fleshood L, Trowbridge FL. Declining prevalence of anemia among low-income children in the United States. JAMA 1987;258(12):1619-23.
Yip R. The changing characteristics of childhood iron nutritional status in the United States. In: Filer LJ Jr, ed. Dietary iron: birth to two years. New York, NY: Raven Press, 1989:37-61.
Perry GS, Yip R, Zyrkowski C. Nutritional risk factors among low-income pregnant US women: the Centers for Disease Control and Prevention (CDC) Pregnancy Nutrition Surveillance System, 1979 through 1993. Semin Perinatol 1995;19(3):211-21.
Earl R, Woteki CE, eds. Iron deficiency anemia: recommended guidelines for the prevention, detection, and management among U.S. children and women of childbearing age. Washington, DC: National Academy Press, 1993.
Allen LH. Pregnancy and iron deficiency: unresolved issues. Nutr Rev 1997;55(44):91-101.
Institute of Medicine. Nutrition during pregnancy. Washington, DC: National Academy Press, 1990.
Barness LA, ed. Pediatric nutrition handbook. 3rd ed. Elk Grove Village, IL: American Academy of Pediatrics, 1993.
Hauth John C, Merenstein BB, eds. Guidelines for perinatal care. 4th ed. Elk Grove Village, IL: American Academy of Pediatrics and American College of Obstetricians and Gynecologists, 1997.
U.S. Preventive Services Task Force. Screening for iron deficiency anemia -- including iron prophylaxis. In: Guide to clinical preventive services. 2nd ed. Alexandria, VA: International Medical Publishing, 1996:231-46.
International Federation of Gynecology and Obstetrics. Nutrition during pregnancy. Int J Gynecol Obstet 1993;43:67-74. (ACOG Technical Bulletin no. 179.)
Anderson SA, ed. Guidelines for the assessment and management of iron deficiency in women of childbearing age. Bethesda, MD: U.S. Department of Health and Human Services, Food and Drug Administration, Center for Food Safety and Applied Nutrition, 1991.
Public Health Service. Caring for our future: the content of prenatal care. A report of the Public Health Service Expert Panel on the Content of Prenatal Care. Washington, DC: U.S. Department of Health and Human Services, Public Health Service, 1989.
U.S. Department of Agriculture and U.S. Department of Health and Human Services. Nutrition and your health: dietary guidelines for Americans. 4th ed. Washington, DC: U.S. Department of Agriculture and U.S. Department of Health and Human Services, 1995. (Home and Garden Bulletin no. 232.)
Public Health Service. Healthy people 2000: national health promotion and disease prevention objectives. Washington, DC: U.S. Department of Health and Human Services, Public Health Service, 1991. DHHS publication no. (PHS) 91-50212.
Bothwell TH. Overview and mechanisms of iron regulation. Nutr Rev 1995;53(9):237-45.
Bothwell TH, Charlton RW, Cook JD, Finch CA. Iron metabolism in man. Oxford, UK: Blackwell Scientific Publications, 1979.
Bothwell TH, Charlton RW. Iron deficiency in women. Washington, DC: The Nutrition Foundation, 1981.
Hallberg L. Bioavailability of dietary iron in man. Annu Rev Nutr 1981;1:123-47.
Skikne B, Baynes RD. Iron absorption. In: Brock JH, Halliday JW, Pippard MJ, Powell LW, eds. Iron metabolism in health and disease. London, UK: W.B. Saunders, 1994:151-87.
Finch CA, Cook JD. Iron deficiency. Am J Clin Nutr 1984;39:471-7.
Siegenberg D, Baynes RD, Bothwell TH, et al. Ascorbic acid prevents the dose-dependent inhibitory effects of polyphenols and phytates on nonheme-iron absorption. Am J Clin Nutr 1994;53:537-41.
Dallman PR, Siimes MA, Stekel A. Iron deficiency in infancy and childhood. Am J Clin Nutr 1980;33:86-118.
Green R, Charlton R, Seftel H, et al. Body iron excretion in man: a collaborative study. Am J Med 1968;45:336-53.
Hallberg L. Iron balance in pregnancy. In: Berger H, ed. Vitamins and minerals in pregnancy and lactation. New York, NY: Raven Press, 1988:115-27.
Kappus KD, Lundgren RG Jr, Juranek DD, Roberts JM, Spencer HC. Intestinal parasitism in the United States: update on a continuing problem. Am J Trop Med Hyg 1994;50(6):705-13.
Stoltzfus RJ, Chwaya HM, Tielsch JM, Schulze KJ, Albonico M, Savioli L. Epidemiology of iron deficiency anemia in Zanzibari schoolchildren: the importance of hookworms. Am J Clin Nutr 1997;65:153-9.
Dallman PR, Looker AC, Johnson CL, Carroll M. Influence of age on laboratory criteria for the diagnosis of iron deficiency anemia and iron deficiency in infants and children. In: Hallberg L, Asp NG, eds. Iron nutrition in health and disease. London, UK: John Libby & Co., 1996:65-74.
DeMaeyer EM. Preventing and controlling iron deficiency anaemia through primary health care: a guide for health administrators and programme managers. Geneva, Switzerland: World Health Organization, 1989.
Herbert V. Everyone should be tested for iron disorders. J Am Diet Assoc 1992;92(12):1502-9.
Baynes RD. Iron deficiency. In: Brock JH, Halliday JW, Pippard MJ, Powell LW, eds. Iron metabolism in health and disease. London, UK: W.B. Saunders, 1994:189-225.
Pollitt E. Iron deficiency and cognitive function. Annu Rev Nutr 1993;13:521-37.
Idjradinata P, Pollitt E. Reversal of developmental delays in iron-deficient anaemic infants treated with iron. Lancet 1993;341(8836):1-4.
Lozoff B, Jimenez E, Wolf AW. Long-term developmental outcome of infants with iron deficiency. N Engl J Med 1991;325(10):687-94.
Goyer RA. Nutrition and metal toxicity. Am J Clin Nutr 1995;61(suppl):646S-650S.
Li R, Chen X, Yan H, Deurenberg P, Garby L, Hautvast JG. Functional consequences of iron supplementation in iron deficient female cotton mill workers in Beijing, China. Am J Clin Nutr 1994;59(4):908-13.
Cook JD, Skikne BS, Baynes RD. Iron deficiency: the global perspective. In: Hershko C, Konijn AN, Aisen P, eds. Progress in iron research. New York, NY: Plenum Press, 1994:219-28.
Scholl TO, Hediger ML, Fischer RL, Shearer JW. Anemia vs iron deficiency: increased risk of preterm delivery in a prospective study. Am J Clin Nutr 1992;55:985-8.
Svanberg B, Arvidsson B, Norrby A, Rybo G, S�lvell L. Absorption of supplemental iron during pregnancy: a longitudinal study with repeated bone-marrow studies and absorption measurements. Acta Obstet Gynecol Scand Suppl 1975;48:87-108.
Sjostedt JE, Manner P, Nummi S, Ekenved G. Oral iron prophylaxis during pregnancy: a comparative study on different dosage regimens. Acta Obstet Gynecol Scand Suppl 1977;60:3-9.
Puolakka J, Janne O, Pakarinen A, Jarvinen A, Vihko R. Serum ferritin as a measure of iron stores during and after normal pregnancy with and without iron supplements. Acta Obstet Gynecol Scand Suppl 1980;95:43-51.
Taylor DJ, Mallen C, McDougall N, Lind T. Effect of iron supplementation on serum ferritin levels during and after pregnancy. Br J Obstet Gynaecol 1982;89:1011-7.
Hemminki E, Rimpela U. A randomized comparison of routine versus selective iron supplementation during pregnancy. J Am Coll Nutr 1991;10(1):3-10.
Hemminki E, Merilainen J. Long-term follow-up of mothers and their infants in a randomized trial on iron prophylaxis during pregnancy. Am J Obstet Gynecol 1995;173(1):205-9.
Looker AC, Dallman PR, Carroll MD, Gunter EW, Johnson CL. Prevalence of iron deficiency in the United States. JAMA 1997;277(12):973-6.
National Research Council. Recommended dietary allowances. 10th ed. Washington, DC: National Academy Press, 1989.
U.S. Department of Agriculture, Agricultural Research Service. Data tables: results from USDA's 1994-96 Continuing Survey of Food Intakes by Individuals and 1994-96 Diet and Health Knowledge Survey {online}. Riverdale, MD: U.S. Department of Agriculture, Agricultural Research Service, Beltsville Human Nutrition Research Center, December 1997. Available at: http://www.barc.usda.gov/bhnrc/foodsurvey/home.htm. Accessed January 14, 1998.
Pizarro F, Yip R, Dallman PR, Olivares M, Hertrampf E, Walter T. Iron status with different infant feeding regimens: relevance to screening and prevention of iron deficiency. J Pediatr 1991;118:687-92.
Walter T, Dallman PR, Pizarro F, et al. Effectiveness of iron-fortified infant cereal in prevention of iron deficiency anemia. Pediatrics 1993;91(5):976-82.
Pisacane A, De Vizia B, Valiente A, et al. Iron status in breast-fed infants. J Pediatr 1995; 127(3):429-31.
Oski FA. Iron deficiency in infancy and childhood. N Engl J Med 1993;329(3):190-3.
Boutry M, Needlman R. Use of diet history in the screening of iron deficiency. Pediatrics 1996;98(6):1138-42.
Sawaya WN, Khalil JK, Al-Shalhat AF. Mineral and vitamin content of goat's milk. J Am Diet Assoc 1984;84(4):433-5.
USDA Nutrient Database for Standard Reference {database online}. Riverdale, MD: United States Department of Agriculture, Agricultural Research Service, Beltsville Human Research Center, September 1996. Available at: http://www.nal.usda.gov/fnic/cgi-bin/nut_search.pl. Accessed January 16, 1998.
Yip R. Iron deficiency: contemporary scientific issues and international programmatic approaches. J Nutr 1994;124:1479S-1490S.
Oski FA. Iron-fortified formulas and gastrointestinal symptoms in infants: a controlled study. Pediatrics 1980;66(2):168-70.
Nelson SE, Ziegler EE, Copeland AM, Edwards BB, Fomon SJ. Lack of adverse reactions to iron-fortified formula. Pediatrics 1988;81(3):360-4.
Scariati PD, Grummer-Strawn LM, Fein SB, Yip R. Risk of diarrhea related to iron content of infant formula: lack of evidence to support the use of low-iron formula as a supplement for breastfed infants. Pediatrics {serial online}. March 1997;99(3). Available at: http://www.pediatrics.org/cgi/content/full/99/3/e2.
American Academy of Pediatrics Committee on Nutrition. Iron-fortified infant formulas. Pediatrics 1989;84(6):1114-5.
Yip R, Dallman PR. Iron. In: Ziegler EE, Filer LJ Jr, eds. Present knowledge in nutrition. 7th ed. Washington, DC: International Life Sciences Institute Press, 1996:277-92.
Hallberg L. Iron requirements: comments on methods and some crucial concepts in iron nutrition. Biol Trace Elem Res 1992:35:25-45.
Mooij PNM, Thomas CMG, Doesburg WH, Eskes TKAB. The effects of oral contraceptives and multivitamin supplementation on serum ferritin and hematological parameters. Int J Clin Pharmacol Ther Toxicol 1992;30(2):57-62.
Thomsen JK, Prien-Larsen JC, Devantier A, Fogh-Andersen N. Low dose iron supplementation does not cover the need for iron during pregnancy. Acta Obstet Gynecol Scand 1993;72:93-8.
Yu SM, Keppel KG, Singh GK, Kessel W. Preconceptional and prenatal multivitamin-mineral supplement use in the 1988 National Maternal and Infant Health Survey. Am J Public Health 1996;86(2):240-2.
Galloway R, McGuire J. Determinants of compliance with iron supplementation: supplies, side effects, or psychology? Soc Sci Med 1994;39(3):381-90.
Chanarin I, Rothman D. Further observations on the relation between iron and folate status in pregnancy. Br Med J 1971;2:81-4.
Hemminki E, Uski A, Koponen P, Rimpela U. Iron supplementation during pregnancy -- experiences of a randomized trial relying on health service personnel. Controlled Clin Trials 1989;10:290-8.
Rockey DC, Cello JP. Evaluation of the gastrointestinal tract in patients with iron-deficiency anemia. N Engl J Med 1993;329(23):1691-5.
Yip R, Dallman PR. The roles of inflammation and iron deficiency as causes of anemia. Am J Clin Nutr 1988;48:1295-300.
Yip R. Iron nutritional status defined. In: Filer LJ Jr, ed. Dietary iron: birth to two years. New York, NY: Raven Press, 1989:19-36.
Tietz NW, ed. Clinical guide to laboratory tests. 3rd ed. Philadelphia, PA: W.B. Saunders, 1995.
CDC. CDC criteria for anemia in children and childbearing-aged women. MMWR 1989; 38(22):400-4.
Binkin NJ, Yip R. When is anemia screening of value in detecting iron deficiency? In: Hercberg S, Galan P, Dupin H, eds. Recent knowledge on iron and folate deficiencies in the world. Vol. 197. Paris, France: L'Institut National de la Sante et de la Recherche Medicale, 1990:137-45.
Margolis HS, Hardison HH, Bender TR, Dallman PR. Iron deficiency in children: the relationship between pretreatment laboratory tests and subsequent hemoglobin response to iron therapy. Am J Clin Nutr 1981;34(10):2158-68.
Steer P, Alam MA, Wadsworth J, Welch A. Relation between maternal haemoglobin concentration and birth weight in different ethnic groups. Br Med J 1995;310:489-91.
Lu ZM, Goldenberg RL, Cliver SP, Cutter G, Blankson M. The relationship between maternal hematocrit and pregnancy outcome. Obstet Gynecol 1991;77:190-4.
Garn SM, Ridella SA, Petzold AS, Falkner F. Maternal hematologic levels and pregnancy outcomes. Semin Perinatol 1981;5(2):155-62.
Murphy JF, O'Riordan J, Newcomb RG, Coles EC, Pearson JF. Relation of haemoglobin levels in first and second trimesters to outcome of pregnancy. Lancet 1986;1(8488):992-5.
Dirren H, Logman MHGM, Barclay DV, Freire WB. Altitude correction for hemoglobin. Eur J Clin Nutr 1994;48:625-32.
Nordenberg D, Yip R, Binkin NJ. The effect of cigarette smoking on hemoglobin levels and anemia screening. JAMA 1990;264(12):1556-9.
Dallman PR, Barr GD, Allen CM, Shinefield HR. Hemoglobin concentration in white, black, and Oriental children: is there a need for separate criteria in screening for anemia? Am J Clin Nutr 1978;31:377-80.
Yip R, Schwartz S, Deinard AS. Hematocrit values in white, black, and American Indian children with comparable iron status: evidence to support uniform diagnostic criteria for anemia among all races. Am J Dis Child 1984;138:824-7.
Johnson-Spear MA, Yip R. Hemoglobin difference between black and white women with comparable iron status: justification for race-specific anemia criteria. Am J Clin Nutr 1994; 60:117-21.
Perry GS, Byers T, Yip R, Margen S. Iron nutrition does not account for the hemoglobin differences between blacks and whites. J Nutr 1992;122:1417-24.
Bridges N, Parvin RM, van Assendelft OW. Evaluation of a new system for hemoglobin measurement. Am Clin Products Rev 1987;6(4):22-25.
Bartfield JM. Robinson D, Lekas J. Accuracy of microcentrifuged hematocrits in the emergency department. J Emerg Med 1993;11:673-6.
Beaton GH, Corey PN, Steele C. Conceptual and methodological issues regarding the epidemiology of iron deficiency and their implications for studies of the functional consequences of iron deficiency. Am J Clin Nutr 1989;50:575-88.
Borel MJ, Smith SM, Derr J, Beard JL. Day-to-day variations in iron-status indices in healthy men and women. Am J Clin Nutr 1991;54:729-35.
Thomas WJ, Collins TM. Comparison of venipuncture blood counts with microcapillary measurements in screening for anemia in one-year-old infants. J Pediatr 1982;101(1):32-5.
Pilch SM, Senti FR, eds. Assessment of the iron nutritional status of the U.S. population based on data collected in the second National Health and Nutrition Examination Survey, 1976-1980. Bethesda, MD: Federation of American Societies for Experimental Biology, Life Sciences Research Office, 1984.
Dallman PR, Yip R, Johnson C. Prevalence and causes of anemia in the United States, 1976 to 1980. Am J Clin Nutr 1984;39:437-45.
Piomelli S. The diagnostic utility of measurements of erythrocyte porphyrins. Hematol Oncol Clin North Am 1987;1(3):419-30.
Hallberg L, Bengtsson C, Lapidus L, Lindstedt G, Lundberg P-A, Hulten L. Screening for iron deficiency: an analysis based on bone-marrow examinations and serum ferritin determinations in a population sample of women. Br J Haematol 1993;85:787-98.
Gibson RS. Principles of nutritional assessment. New York, NY: Oxford University Press, 1990.
Oski FA, Brugnara C, Nathan DG. A diagnostic approach to the anemic patient. In: Nathan DG, Orkin SH, eds. Nathan and Oski's hematology of infancy and childhood. 5th ed. Philadelphia, PA: W.B. Saunders Co., 1998:375-84.
Novak RW. Red blood cell distribution width in pediatric microcytic anemias. Pediatrics 1987;80(2):251-4.
Lipschitz DA, Cook JD, Finch CA. A clinical evaluation of serum ferritin as an index of iron stores. N Engl J Med 1974;290(22):1213-6.
Cook JD, Finch CA. Assessing iron status of a population. Am J Clin Nutr 1979;32:2115-9.
Cooper MJ, Zlotkin SH. Day-to-day variation of transferrin receptor and ferritin in healthy men and women. Am J Clin Nutr 1996;64:738-42.
Hamilton LD, Gubler CJ, Cartwright GE, Wintrobe MM. Diurnal variation in the plasma iron level of man. Proc Soc Exp Biol Med 1950;75(1):65-8.
Looker AC, Sempos CT, Liu K, Johnson CL, Gunter EW. Within person variance in biochemical indicators of iron status: effects on prevalence estimates. Am J Clin Nutr 1990;52:541-7.
Brittenham GM. Disorders of iron metabolism: iron deficiency and overload. In: Hoffman R, Benz EJ Jr, Shattil SJ, Furie B, Cohen HJ, eds. Hematology: basic principles and practice. 2nd ed. New York, NY: Churchill Livingstone, 1995:492-523.
Looker AC, Gunter EW, Johnson CL. Methods to assess iron status in various NHANES surveys. Nutr Rev 1995;53(9):246-54.
Simmons WK, Cook JD, Bingham KC, et al. Evaluation of a gastric delivery system for iron supplementation in pregnancy. Am J Clin Nutr 1993;58:622-6.
Council on Foods and Nutrition Committee on Iron Deficiency. Iron deficiency in the United States. JAMA 1968;203(6):119-24.
Edwards CQ, Kushner JP. Screening for hemochromatosis. N Engl J Med 1993;328(22):1616-20.
Bradley LA, Haddow JE, Palomaki GE. Population screening for haemochromatosis: a unifying analysis of published intervention trials. J Med Screening 1996;3:178-84.
Witte DL, Crosby WH, Edwards CQ, Fairbanks VF, Mitros FA. Hereditary hemochromatosis. Clin Chim Acta 1996;245:139-200.
Viteri FE. Effective iron supplementation does not happen in isolation. Am J Clin Nutr 1997;65:889-90.
American Academy of Pediatrics Work Group on Breastfeeding. Breastfeeding and the use of human milk. Pediatrics 1997;100(6):1035-9.
Public Health Service. Clinician's handbook of preventive services: put prevention into practice. Washington, DC: U.S. Department of Health and Human Services, Public Health Service, Office of Disease Prevention and Health Promotion, 1994.
Institute of Medicine. Nutrition during pregnancy and lactation: an implementation guide. Washington, DC: National Academy Press, 1992.

Table_1
Note: To print large tables and graphs users may have to change their printer settings to landscape and use a small font size.


TABLE 1. Normal distribution of iron-containing
compounds in men (17 ) and women (18 ) (milligrams
of iron per kilogram of body weight)
====================================================
Compound               Men   Women
----------------------------------------------------
Storage complexes
 Ferritin                9      4
 Hemosiderin             4      1
Transport protein
 Transferrin             <1     <1
Functional compounds
 Hemoglobin              31     31
 Myoglobin               4      4
 Respiratory enzymes     2      2

Total                   50     42
====================================================

Return to top.

Table_2
Note: To print large tables and graphs users may have to change their printer settings to landscape and use a small font size.


TABLE 2. Iron absorption by infants fed formula or milk (8)
===============================================================================================
Substance                Iron content (mg/L)   Bioavailable iron (%)   Absorbed iron (mg/L)
-----------------------------------------------------------------------------------------------
Nonfortified formula           1.5-4.8*                 ~10                  0.15-0.48
Iron-fortified formula+       10.0-12.8*                ~ 4                  0.40-0.51
Whole cow's milk                 0.5                    ~10                    0.05
Breast milk                      0.5                    ~50                    0.25
-----------------------------------------------------------------------------------------------
* Values are given for commonly marketed infant formulas.
+ Iron-fortified formula contains >=1.0 mg iron/100 kcal formula (8). Most iron-fortified
  formulas contain approximately 680 kcal/L, which is equivalent to >=6.8 mg iron/L.
===============================================================================================

Return to top.

Table_3
Note: To print large tables and graphs users may have to change their printer settings to landscape and use a small font size.


TABLE 3. Spectrum of body iron content (17,30,31)
=================================================================================
Iron status                     Stored iron   Transport iron    Functional iron
---------------------------------------------------------------------------------
Iron-deficiency anemia          Low           Low               Low
Iron-deficient erythropoiesis   Low           Low               Normal
Iron depletion                  Low           Normal            Normal
Normal                          Normal        Normal            Normal
Iron overload                   High          High              Normal
=================================================================================

Return to top.

Table_4
Note: To print large tables and graphs users may have to change their printer settings to landscape and use a small font size.


TABLE 4. Prevalence (%) of iron deficiency and iron-deficiency anemia,
United States, third National Health and Nutrition Examination Survey,
1988-1994 (45)
=======================================================================
Sex and age (years)   Iron deficiency   Iron-deficiency anemia
-----------------------------------------------------------------------
Both sexes
 1-2                         9                    3*
 3-5                         3                    <1
 6-11                        2                    <1
Nonpregnant females
 12-15                       9                    2*
 16-19                      11*                   3*
 20-49                       11                   5*
 50-69                       5                    2
  >=70                       7*                   2*
Males
 12-15                       1                    <1
 16-19                       <1                   <1
 20-49                       <1                   <1
 50-69                       2                    1
  >=70                       4                    2
-----------------------------------------------------------------------
* Prevalence in nonblacks is 1 percentage point lower than prevalance
  in all races.

=======================================================================

Return to top.

Table_5
Note: To print large tables and graphs users may have to change their printer settings to landscape and use a small font size.


TABLE 5. 1989 Recommended dietary allowance (RDA) for iron and the proportion
of Americans having diets meeting 100% of the RDA for iron, 1994-1996
==============================================================================
Sex and age (years)   RDA (mg/day)*     Proportion of Americans
                                        meeting 100% of the 1989
                                           RDA for iron+ (%)
------------------------------------------------------------------------------
Both sexes
   <1                      6-10                   87.9&
   1-2                      10                    43.9
   3-5                      10                    61.7
Females
  6-11                      10                    60.9
 12-19                      15                    27.7
 20-29                      15                    25.9
 30-39                      15                    26.6
 40-49                      15                    22.1
 50-59                      10                    55.2
 60-69                      10                    59.3
  >=70                      10                    59.2
Males
  6-11                      10                    79.8
 12-19                      12                    83.1
 20-29                      10                    86.9
 30-39                      10                    88.9
 40-49                      10                    85.9
 50-59                      10                    83.8
 60-69                      10                    85.5
  >=70                      10                    78.5
------------------------------------------------------------------------------
* National Research Council (46). The age groups designated by the council
  are slightly different from those presented in this table.
+ Two-day average dietary intakes, from the U.S. Department of Agriculture
  Continuing Survey of Food Intakes by Individuals, 1994-1996 (47).
& Excludes breast-fed infants.
==============================================================================

Return to top.

Table_6
Note: To print large tables and graphs users may have to change their printer settings to landscape and use a small font size.


TABLE 6. Maximum hemoglobin concentration and hematocrit values for anemia* (45,72)
======================================================================================
                               Hemoglobin concentration          Hematocrit (<%)
                                        (<g/dL)
--------------------------------------------------------------------------------------
Children (age,in years)
   1-<2+                                 11.0                          32.9
   2-<5                                  11.1                          33.0
   5-<8                                  11.5                          34.5
  8-<12                                  11.9                          35.4
Men (age in years)
 12-<15                                  12.5                          37.3
 15-<18                                  13.3                          39.7
   >=18                                  13.5                          39.9
Nonpregnant women and
lactating women (age in
years)
 12-<15                                  11.8                          35.7
 15-<18                                  12.0                          35.9
   >=18                                  12.0                          35.7
Pregnant women
Weeks' gestation
     12                                  11.0                          33.0
     16                                  10.6                          32.0
     20                                  10.5                          32.0
     24                                  10.5                          32.0
     28                                  10.7                          32.0
     32                                  11.0                          33.0
     36                                  11.4                          34.0
     40                                  11.9                          36.0
Trimester
  First                                  11.0                          33.0
  Second                                 10.5                          32.0
  Third                                  11.0                          33.0
* Age- and sex-specific cutoff values for anemia are based on the 5th percentile from
  the third National Health and Nutrition Examination Survey (NHANES III), which
  excluded persons who had a high likelihood of iron deficiency by using the same
  methods described by Looker et al. (45). Maximum values for anemia during pregnancy
  are based on values from pregnant women who had adequate supplementation (39-42,72).
+ Although no data are available from NHANES III to determine the maximum hemoglobin
  concentration and hematocrit values for anemia among infants, the values listed for
  children aged 1-<2 years can be used for infants aged 6-12 months.
======================================================================================

Return to top.

Table_7
Note: To print large tables and graphs users may have to change their printer settings to landscape and use a small font size.


TABLE 7. Adjustment of maximum hemoglobin concentration and hematocrit
values for anemia (72,79,80)
=======================================================================
                              Hemoglobin       Hematocrit (%)
                             concentration
                                (=2.0 packs per day               0.7                2.0
 All smokers                       0.3                1.0
=======================================================================

Return to top.

Table_8
Note: To print large tables and graphs users may have to change their printer settings to landscape and use a small font size.


TABLE 8. Cutoff values for laboratory tests for iron deficiency
==================================================================================================
Test                              Cutoff value                           Reference
--------------------------------------------------------------------------------------------------
Hemoglobin concentration          See Table 6 for cutoffs for anemia     Looker et al. (45 ),
                                                                         CDC (72)

Hematocrit                        See Table 6 for cutoffs for anemia     Looker et al. (45 ),
                                                                         CDC (72)

Mean cell volume                  Cutoffs for microcytic anemia at       Dallman et al. (28 )
                                  age:
                                  1-2 years:     <77 fL
                                  3-5 years:     <79 fL
                                  6-11 years:    <80 fL
                                  12-15 years:   <82 fL
                                  >15 years:     <85 fL

Red blood cell distribution       Cutoff for iron-deficiency anemia*:    Dallman et al. (28 ),
width                             14.0%                                  Oski (51)

Erythrocyte protoporphyrin        Cutoffs for iron deficiency:           Dallman et al. (28 ),
concentration                     Adults:  30 u/dL of whole blood or     Piomelli (92)
                                  70 ug/dL of red blood cells Children
                                  aged 1-2 years:
                                           80 ug/dL of red blood cells

Serum ferritin concentration      Cutoff for iron deficiency in          Hallberg et al. (93 )
                                  persons aged >6 months: <=15 ug/L

Transferrin saturation            Cutoff for iron deficiency: <16%       Dallman et al. (23 ),
                                                                         Pilch and Senti (90)
--------------------------------------------------------------------------------------------------
* The cutoff is instrument specific and may not apply in all laboratories.
==================================================================================================

Return to top.

Table_1B
Note: To print large tables and graphs users may have to change their printer settings to landscape and use a small font size.


EXHIBIT 1. Causes of iron deficiency
===================================================================
Increased iron requirements  Inadequate iron absorption
-------------------------------------------------------------------
Blood loss                   Diet low in bioavailable iron
    Menstruation             Impaired absorption
    Gastrointestinal tract       Intestinal malabsorption
         Food sensitivity        Gastric surgery
         Hookworms               Hypochlorhydria
    Genitourinary tract
    Respiratory tract
    Blood donation
Growth
Pregnancy
===================================================================

Return to top.

Disclaimer All MMWR HTML versions of articles are electronic conversions from ASCII text into HTML. This conversion may have resulted in character translation or format errors in the HTML version. Users should not rely on this HTML document, but are referred to the electronic PDF version and/or the original MMWR paper copy for the official text, figures, and tables. An original paper copy of this issue can be obtained from the Superintendent of Documents, U.S. Government Printing Office (GPO), Washington, DC 20402-9371; telephone: (202) 512-1800. Contact GPO for current prices.

**Questions or messages regarding errors in formatting should be addressed to mmwrq@cdc.gov.

Page converted: 10/05/98

Morbidity and Mortality Weekly Report
Centers for Disease Control and Prevention
1600 Clifton Rd, MailStop E-90, Atlanta, GA 30333, U.S.A

Department of Health
and Human Services

This page last reviewed 5/2/01