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ORIGINAL RESEARCH article

Front. Public Health, 07 July 2020
Sec. Children and Health
This article is part of the Research Topic Effective Delivery of Integrated Interventions in Early Childhood: Innovations in Evidence Use, Monitoring, Evaluation and Learning View all 32 articles

How Effective Is Iron Supplementation During Pregnancy and Childhood in Reducing Anemia Among 6–59 Months Old Children in India?

  • Gerald and Patricia Turpanjian School of Public Health, American University of Armenia, Yerevan, Armenia

Objectives: The study sought to identify whether iron and folic acid supplementation of pregnant women and preschool children is associated with child's anemia status and the predictors of anemia among children in India.

Design: Secondary data analysis was performed using the National Family Health Survey 4 data. Multivariable logistic regression was used to identify the adjusted associations between child's anemia status and iron supplementation, both during pregnancy and childhood. Also, a model of significant predictors of anemia among children was fitted.

Setting: India.

Participants: Youngest children (6-59 months) in families.

Results: The adjusted association between supplementation during pregnancy and child's anemia status was significant (p = 0.010), whereas the adjusted association between supplementation during childhood and child's anemia status was insignificant (p = 0.16). The variables independently associated with anemia status of the child included younger age (95% CI 2.67–2.86), child's recent diarrhea (95% CI 1.02–1.14), low birth weight (95% CI 1.17–1.27), current underweight (95% CI 1.14–1.28), diet diversity score (95% CI 0.96–0.98), higher birth order (95% CI 1.01–1.05), mother's current anemia (95% CI 1.68–1.81), months of breastfeeding (95% CI 0.99–1.00), no/primary education (95% CI 1.23–1.35), family's low wealth index (95% CI 1.11–1.23), and backward caste (95% CI 1.04–1.14).

Conclusions: The National Iron Plus Initiative strategy of child's iron supplementation should be evaluated to identify the reasons of its ineffectiveness in anemia reduction. In addition, vulnerable groups of children, i.e., children from poor and less educated families and those with low birth weight, higher birth order, and poor nutritional status, should be targeted first with anemia reduction interventions.

Introduction

Burden

The prevalence of anemia among children under five was 41.7% worldwide in 2016. In India, this rate was 57.3% (1) and the prevalence of anemia among children 6–59 months of age was 58.5% (2); thus indicating a major public health problem. Compared to other age groups, children under five have a disproportionately higher level of anemia (3). Iron deficiency is considered to be a major cause of anemia in childhood (4). Iron deficiency anemia is associated with a number of other health conditions among children, like behavioral problems, cognitive impairment, stunted growth, and psychomotor development (57). Studies from different parts of the world have often found different sets of determinants for iron deficiency anemia, suggesting possible variations in the risk factors across countries.

Prevention Strategies

Iron supplementation is a part of World Health Organization (WHO) (4) guidelines in combating anemia, which has been successfully implemented in many countries to treat and prevent anemia (8). In 2013, the National Iron Plus Initiative (NIPI) was launched in India to combat the increasing prevalence of anemia (9). It replaced the National Nutritional Anemia Control (NNAC) program which existed since 1991 (10). According to NIPI recommendations, children aged 6–59 months should receive a preparation containing 20 mg elemental iron and 100 mcg folic acid twice a week (9). For pregnant women, the recommendation is using 100 mg elemental iron and 500 mcg folic acid daily for 100 days beginning at 14–16 weeks of gestation (9). It should be noted that the NIPI's iron and folic acid (IFA) supplementation schedule differs in some extent from the WHO recommendations in both the dosage and duration.

Study Rationale and Aim

Despite the ongoing NIPI program, the prevalence of childhood anemia continues to be alarmingly high in India, and no study has yet evaluated the effectiveness of the NIPI program nationally. The current study aimed to fill in this gap and provide evidence that can be used by policymakers to improve the NIPI program and specifically target the most vulnerable groups of children with anemia reduction interventions. Hence, the study objectives were (1) to identify whether there is difference in anemia rates between those children whose mothers followed the iron supplementation schedule during pregnancy and those children whose mothers did not follow it, (2) to identify whether there is significant difference in anemia rates between those children who follow the iron supplementation schedule and those who do not follow it, and (3) to find the predictors of anemia among 6–59-month-old children in India.

Methods

Study Design

Secondary data analysis was performed using the data from the National Family Health Survey 2015–16 (NFHS-4). NFHS-4 was carried out by the International Institute for Population Sciences, Mumbai, under the supervision of the Government of India (2). It was a household survey collecting data on the characteristics of population and their health and nutrition (2). The survey was accompanied with anthropometric measurements of children and testing of adults and young children for blood hemoglobin level, using the HemoCue instrument (11). The NFHS 4 used the HemoCue Hb 201+ instrument because of the rapid results, simplicity of operation, and known precision and accuracy (12). It is based on the cyanomethemoglobin method and thus proven to be “stable and durable in field settings” (13). The NFHS-4 samples were nationally representative and included 601,509 households, 103,525 men (15–54 years), and 699,686 women (15–49 years). The fieldwork for NFHS-4 was carried out from January 2015 to December 2016 (2). The study dataset can be downloaded by registering at the DHS program (14), and the questionnaire can be accessed at the national family health survey website (http://rchiips.org/NFHS/nfhs4.shtml) (15).

Target Population and Variables

The target population for this study comprised a subsample of the youngest children in surveyed families aged 6–59 months taken from the NFHS-4 dataset. The youngest children in families were chosen, as the information on certain study variables (folic acid and iron supplementation during pregnancy, child's diet diversity, and blood sample given by mother during pregnancy) was available only for them.

The outcome variable was the presence or absence of anemia in a child. The criterion used to determine anemic children was the hemoglobin level <110 grams per liter at the sea level (16). This is the cutoff value for identifying anemia among 6–59 months old children recommended by WHO, which is adopted and used in India as well (13, 17, 18). The exposures of interest were IFA supplementation of mother during pregnancy (whether she was supplemented at least 50 days) and IFA supplementation of the child (at the time of the survey). The covariates and potential confounders considered were age and gender of the child, education of parents, family's wealth index, caste of the household, current anemia of the mother (hemoglobin adjusted for sea level below 120 g/L) (13, 17), blood sample given by the mother during pregnancy (as the only available proxy for pregnancy anemia), mother's young age (<18 years old) at child's birth, child's breastfeeding duration, diet diversity of the child, recent diarrhea in the child, child's undernutrition (stunting, wasting, and underweight), type of household heating and cooking fuel (low-quality biofuel such as straw/shrubs/grass, agricultural crops, and animal dung vs. other fuels), child's birth order, and birth weight.

Data Analysis

The analysis was done using SPSS 23 statistical software package. Descriptive data analysis of the selected characteristics was done comparing the groups of 6–59-month-old children with and without anemia. The analysis took into account the survey design (clustering and stratification) and applied sampling weights. The statistical significance of the difference between the selected characteristics was measured using chi-square test for categorical variables and student t-test for continuous variables. For logistic regression analysis, the categorical variables with more than two categories were transformed into dummy variables. All the variables with p < 0.25 in the descriptive analyses were entered into univariate logistic regression analyses (done in complex samples package) with the dependent variable, anemia status of the child. Then, multivariable logistic regression for the weighted data was applied to evaluate the adjusted associations of interest while controlling for all available potential confounders. The large sample size of this study resulted in ample significant associations, therefore, in addition to the statistical significance; an effect size was calculated by comparing the change of the odds ratio of the main association when adding each identified confounder in the multivariable model. Only those categorical variables that produced at least 5.0% change of the odds ratio of the main association were included in the final multivariable logistic regression models. As the last step, a logistic regression model of independent predictors of anemia in 6–59-month-old children was fitted and the model fit evaluated via the Hosmer–Lemeshow goodness-of-fit test and the area under the ROC curve.

Ethical Review

The study protocol did not require any approval by the Institutional Review Board as it was a secondary analysis of a de-identified dataset.

Results

Descriptive Findings

In total, 145,904 last-born 6–59-month-old children were included in the analysis. Among the children, 39.9% were non-anemic (≥11 g/dL), 27.8% mildly anemic (10–10.9 g/dL), 30.7% moderately anemic (7–9.9 g/dL), and 1.6% severely anemic (<7 g/dL).

As Table 1 shows, the sample consisted of 54.7% male and 45.3% female children. Of all the 16 variables analyzed, gender was the only variable that was not statistically significantly related with the anemia status in crude comparisons. Younger age, low birth weight (<2,500 g), recent (within the last 2 weeks) diarrhea, and all the three types of under-nutrition (stunting, wasting, and underweight) were more prevalent in the group of anemic children as compared to those without anemia. The mean dietary diversity score was lower among anemic children than among those without anemia (2.26 vs. 2.45 of the maximum score of 12). Children in the anemic group had higher mean birth order as compared to those in the non-anemic group.

TABLE 1
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Table 1. Descriptive analysis of the selected characteristics among the last born 6–59-month-old children in India by “anemia status” (based on National Family Health Survey 2015–2016 data).

Of mothers of the studied children, 65.3% used IFA supplements during pregnancy, while only 26.6% of the studied children were taking IFA supplements at the time of interview. Mothers and fathers of children in the anemia group were less educated compared to parents of children without anemia. Mothers of children with anemia were younger, suffered from anemia (blood hemoglobin <120 g/dL at the sea level) more frequently, and breastfed for fewer months than mothers of non-anemic children.

Families of anemic children had lower wealth index as compared to families of non-anemic children. Children who belonged to a scheduled caste or tribe or other backward caste had a higher prevalence of anemia. High-quality fuel (electricity, LPG, natural gas, and biogas) usage was more prevalent in the non-anemic group as compared to the anemic group (41.0 vs. 34.0%), while families in the anemic group used lower quality biofuel more frequently (18.0 vs. 15.0%).

Relation Between Iron Supplementation and Childhood Anemia

Table 2 shows the results of multivariable logistic regression analysis with “anemia status” as the outcome and supplementation during pregnancy as the independent variable controlled for all the available potential confounders, including all the continuous variables regardless of their effect size and those categorical variables that produced over 5.0% change in the odds ratio of the main association when being included in the model. As demonstrated, there is significant independent negative relation between the variables of interest indicating that children of mothers who used IFA supplements for at least 50 days during pregnancy are 10.0% less likely to have anemia.

TABLE 2
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Table 2. Controlled associations between “anemia status of the child” and the two independent variables: “mother's IFA supplementation during pregnancy” and “iron supplementation during childhood” among the last born 6–59-month-old children in India (based on NFHS-4 data).

The multivariable logistic regression with “anemia status” as the outcome and child's supplementation as the independent variable, controlled for all the available potential confounders, including all the continuous variables regardless of their effect size and those categorical variables that produced over 5.0% change in the odds ratio of the main association, found no significant relation between child's IFA supplementation and his/her anemia status (Table 2).

Predictors of Childhood Anemia

The fitted multivariable logistic regression model (Table 3) identified 11 independent predictors of anemia among 6–59-month-old children in India. Among these, age was a protective factor for anemia with 6–23-month-old children having 2.77 times higher odds and 24–41-month-old children 1.73 times higher odds of suffering from anemia compared to the oldest age group of 42–59-month-old children. An episode of recent diarrhea (within last 2 weeks) increased the odds of the child being anemic by 8.0%. Children whose birth weight was <2.5 kg had 22.0% increased odds of being anemic as compared to children whose birth weight was more than 2.5 kg. An underweight child had a 21.0% increased chance of being anemic as compared to a normal-weight child. Each one-unit increase of diet diversity score decreased the risk of the child's anemia by 3.0%. With each unit increase in the birth order, a child was at a 3.0% increased likelihood of being anemic. Current anemia of the mother increased the likelihood of the child being anemic by 74.0%. With every 1-month increase in breastfeeding duration, the odds of a child being anemic decreased by 1.0%. Mothers with no or primary education had 29.0% higher odds for their child being anemic as compared to mothers with secondary or higher education. Children from households with poor and middle wealth index had, respectively, 1.17 and 1.11 times higher odds of being anemic as compared to children from households with rich wealth index. Scheduled caste, scheduled tribe, and other backward caste households had 9.0% higher odds of the child being anemic as compared to any other caste households.

TABLE 3
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Table 3. Multivariate logistic regression model of anemia predictors among the last born 6–59-month-old children in India (based on NFHS-4 data; valid n = 49,162).

Discussion

Prevalence and Dynamics of Childhood Anemia

According to this study results, the prevalence of anemia among 6–59-month-old children in India was 60.1%, which reflects a significant decrease from the prevalence of 69.4% found by NFHS-3 in 2005–06 (19). This decrease can be due to the measures undertaken in the scope of the NIPI Program. However, the observed decrease is far from the ultimate goal of the program to combat childhood anemia in the country. Moreover, the current rate of anemia among under-five children in India still represents a “severe public health problem” according to WHO criteria (20). It is comparable to that in Pakistan (59.0%) and is considerably higher than in Bangladesh (40.0%) and the world average (41.7%) (21). Anemia rates are equally high among both genders, which is consistent with a study conducted using the Ghana demographic and health survey that found no significant difference in anemia prevalence among boys and girls (22).

Iron Supplementation and Childhood Anemia

This study found no significant association between IFA supplementation during preschool years and child's anemia status, even though in many countries a significant association has been found (23, 24). Potential explanations for this could include compliance and logistics-related challenges in the NIPI program (9) as well as other shortcomings that this program might have inherited from the prior NNAC program. As to the latter, a study evaluating the NNAC program in Andhra Pradesh found that only 19.0% of the pregnant women and 1.0% of the child beneficiaries had received their supplementations (25). The main reasons for the poor coverage included inadequate and irregular supplies of the supplements and incomplete registration of beneficiaries by the health centers (25). The chemical analysis of the supplements also found out that 30.0% of them had less than recommended iron levels and none of them had the recommended folic acid levels (25). A study that evaluated the NNAC program in the Dharwad taluk also found an issue of irregular supply of the supplements (26). A cross-sectional study evaluating the compliance of the NIPI program among a group of reproductive aged (15–49 years) females in Puducherry found that only 45.7% of them were receiving the supplements under the NIPI program (27). Among the women who received supplementation, only 61% reported compliance (27). A qualitative study in Odisha showed the necessity of monitoring and evaluation to strengthen the implementation of the NIPI program (28). Another possible reason of ineffectiveness of iron supplementation in reducing anemia among Indian children could be an underlying multiple micronutrient deficiency, as found in a study done among Mexican preschoolers (29).

IFA supplementation of the mother during pregnancy is found to have a preventive effect on anemia status of the child in this study. According to a number of studies, the mechanism of this effect is that routine supplementation of the mother during pregnancy prevents a bunch of conditions associated with increased risk of childhood anemia, including maternal anemia (3032), low birth weight (33), and preterm birth (3437). An interesting finding of the study was that during the analysis, the initial controlled association between pregnancy supplementation and child's anemia was positive, meaning that pregnancy supplementation acted as a “risk factor” for child's anemia. As there was no available data on woman's anemia status during pregnancy, the research team suspected that this finding might be the reflection of a practice of prescribing supplements specifically to those pregnant women with known anemia. In this case, pregnancy supplementation could indirectly point out the women with anemia during pregnancy. This suspicion was confirmed by the fact that the relation between pregnancy supplementation and childhood anemia became protective after including in the model “giving blood sample during pregnancy,” the only available proxy variable for pregnancy anemia. The practical implication of this finding is the need to reinforce the compliance with the recommended pattern of universal preventive prescription of IFA supplements to all pregnant women regardless of their anemia status. Another inference that can be made from this finding is that the actual protective effect of iron supplementation during pregnancy on child's likelihood of developing anemia could be even stronger if the data on pregnancy anemia status was available and controlled for.

Predictors of Childhood Anemia

Literature reports the following common determinants of childhood anemia: age of the child (30, 3841), exclusive breastfeeding duration (31), literacy of parents (31, 40), household income (31, 32, 38, 40), caste of the household (42, 43), geographical location (32, 40), anemia of mother (3032), nutritional status of the child (3032, 38, 41), and diarrhea (31). This study found 11 independent predictors of anemia among under-five children. Child-related predictors included younger age of the child, child's recent diarrhea, low birth weight, underweight, low diet diversity score, and higher birth order. In a number of studies, as in this study, the age group of 24 months and below was strongly associated with anemia in the child (30, 38). This is due to the high-iron requirements of the child because of high growth speed during this age (44), often combined with poor dietary diversity resulting in consumption of a diet which doesn't include iron rich foods (45). An episode of recent diarrhea (within the past 2 weeks) in a child was found to be positively associated with child's anemia status in other studies as well (31, 46). According to these studies, poor absorption of nutrients and decreased food consumption of the child during diarrhea could be among the underlying mechanisms of this association (31, 47, 48). The findings of this study on child's low birth weight and current underweight predicting anemia are also consistent with the literature. A study conducted in a rural area in China found that anemia was significantly associated with low birth weight and malnutrition (underweight, stunting, and wasting) (33). The mechanism underlying the relation between low birth weight and anemia is that hemoglobin and ferritin concentrations are found to be positively correlated to the birth weight of a child (49, 50). Poor dietary diversity is also a known predictor of anemia (51, 52), due to its direct relation with inadequate micronutrient intake (52). Higher birth order is another factor positively associated with anemia in a child not only in this study, but in a number of other studies (53, 54).

In this study, the identified predictors related to maternal factors included current anemia of mother, months of breastfeeding, and educational level of mother. A study conducted in Timor Leste found that the severity of anemia of mothers was directly correlated to the severity of anemia in children (31), showing that anemia of mother is a predictor of anemia status of children. This is due to the correlation of maternal hemoglobin with cord blood hemoglobin concentrations and breast milk iron levels (55, 56). Consistent with this study, a study conducted in Eastern Cuba showed that lack of breastfeeding is a predictor of anemia (57). The underlying mechanism is the presence of highly bioavailable iron in breast milk (58). The finding that children of mothers with higher education are at lower risk of anemia is again consistent with other studies (40). This is due to ensuring better dietary practices of children, including consumption of iron rich foods, by those mothers having higher educational level (59).

The household-related predictors included wealth index and type of caste or tribe of the household. The wealth index of the household was associated with anemia status of the child with a dose-response relationship, as the poorest households had the highest risk and the middle households had higher risk of the child being anemic as compared to the rich households. This relationship is seen in other countries as well, which is due to better nutrition and health services to children from richer households (60). Children of scheduled caste, scheduled tribe, and other backward castes have increased risk of anemia both in this and other (42) studies, which is due to substandard living conditions, unfavorable behaviors (maternal smoking, poor dietary habits), and inefficient healthcare use among these castes (42).

Study Strengths and Limitations

This study had a number of limitations. Similar to most secondary data analysis studies, the current study was limited to the variables covered in the NFHS-4 survey and did not have any control over the data collection process (61). The NFHS-4 questionnaire collected no information on the dosage or duration of the child's supplementation. The only question on this matter was whether the child was taking supplements currently, which might have introduced an instrumentation error, making it impossible to identify children who received supplements according to the existing recommendations. For women's supplementation, we only took those women who had taken the supplements for at least 50 days out of the 100-day criteria. The NFHS-4 survey used the HemoCue Hb 201+ instrument which has a sensitivity of 75–91% and specificity of 88–100% for anemia (62). This instrument is mainly used for screening of anemia and requires a full blood count for confirmation (62). The test results do not differentiate types of anemia. Data on the anemia status of mothers during pregnancy was not available, and a proxy variable of “whether blood sample was collected during pregnancy” had to be used instead. Also, the study lacked information on the actual content of supplements, their quality and availability, and whether they were prescribed in accordance with the current recommendations of the NIPI program.

Despite these limitations, the study produced very interesting results that could be used for developing better targeted strategies to reduce childhood anemia in India. This study was the first attempt of measuring the impact of the NIPI program on anemia status of children using an impressive nationwide sample and an analytical approach that applied sampling weights, thus making the findings nationally representative. Also, the study results delineated areas for further research, including investigation of the lack of relation between child's iron supplementation and anemia status, investigation of the content and quality of the supplements for children, the extent of compliance with the recommended regimen of administration and the actual coverage of pregnant women and preschool children with the supplements, and investigation of the possible relation between pregnancy anemia and prescription of IFA supplements during pregnancy. The questionnaire of NFHS-5 needs to be revised to include questions on child supplementation and maternal anemia to get a better idea of the problem in future.

Recommendations

This study identified areas that can be of short- and long-term targets for the Indian government. The short-term objectives include addressing the challenges of NIPI in every state and prioritizing anemia as a major public health problem. A study conducted in India showed that the “estimated yearly costs of iron deficiency anemia in 6–59 months old children amount to intangible costs of 8.3 million disability adjusted life years and production losses of 24,001 million USD, equal to 1.3% of gross domestic product” (63). A randomized, double-blinded study done among Indian school children showed that iron-fortified flour significantly improved body iron stores and reduced iron deficiency anemia (64). A study conducted in 10 developing countries showed that long-term iron fortification programs have a median cost benefit ratio of 6:1, which becomes 36:1 if the impact on cognitive improvements are also included (65), clearly showing that this is an efficient solution. Thus, in the long term, if anemia continues to remain a prevalent issue, food fortification can be another option for combating it. Based on this study findings, the vulnerable groups of children, i.e., children from poor and less educated families, those with low birth weight, higher birth order, and poor nutritional status, should be targeted first with anemia reduction interventions in India.

The study also measured the effect of the nationwide iron and folic acid supplementation program in India on children's anemia status while the NIPI program is still ongoing, thus creating a knowledge base for refining the program. Therefore, our results may contribute to learning and decision-making through the course of the program implementation to achieve better performance, compliance, and hence, better outcomes.

Data Availability Statement

The datasets generated for this study are available on request to the corresponding author.

Author Contributions

MT formulated the research question, analyzed the data, and had primary responsibility for the final content. AD, VK, and MT designed and carried out the research and wrote the paper. All authors contributed to the article and approved the submitted version.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Abbreviations

LPG, liquefied petroleum gas; NFHS, National Family Health Survey; NIPI, National Iron Plus Initiative; NNAC, National Nutritional Anemia Control; ROC, receiver operating characteristic; SPSS, Statistical Package for the Social Sciences; USD, United States Dollar; WHO, World Health Organization.

References

1. Prevalence, of Anemia Among Children (% of Children Under 5) | Data,. Available online at: https://data.worldbank.org/indicator/SH.ANM.CHLD.ZS?end=2016&start=1990&year_high_desc=true (accessed February 10, 2018).

Google Scholar

2. International Institute for Population Sciences. India Fact Sheet. Natl Fam Heal Surv. (2016) 2016:1–6.

Google Scholar

3. McLean E, Cogswell M, Egli I, Wojdyla D, de Benoist B. Worldwide prevalence of anaemia, WHO vitamin and mineral nutrition information system, 1993–2005. Public Health Nutr. (2009) 12:444–54. doi: 10.1017/S1368980008002401

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Kassebaum NJ, Jasrasaria R, Naghavi M, Wulf SK, Johns N, Lozano R, et al. A systematic analysis of global anemia burden from 1990 to 2010. Blood. (2014) 123:615–24. doi: 10.1182/blood-2013-06-508325

PubMed Abstract | CrossRef Full Text | Google Scholar

5. What Are the Signs Symptoms of Iron-Deficiency Anemia? NHLBI NIH. Available online at: https://www.nhlbi.nih.gov/health/health-topics/topics/ida/signs (accessed May 28, 2017).

Google Scholar

6. Walter T, de Andraca I, Chadud P, Perales CG. Iron deficiency anemia: adverse effects on infant psychomotor development. Pediatrics. (1989) 84:7–17.

PubMed Abstract | Google Scholar

7. Lozoff B, Beard J, Connor J, Felt B, Georgieff M, Schallert T. Long-lasting neural and behavioral effects of iron deficiency in infancy. Nutr Rev. (2006) 64(5 Pt 2):S34–43. doi: 10.1301/nr.2006.may.S34-S43

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Pasricha SR, Hayes E, Kalumba K, Biggs BA. Effect of daily iron supplementation on health in children aged 4-23 months: a systematic review and meta-analysis of randomised controlled trials. Lancet Glob Heal. (2013) 1:e77–86. doi: 10.1016/S2214-109X(13)70046-9

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Deb S. Emplementation of National iron plus initiative for child health: challanges ahead. Indian J Public Health. (2015) 59:1–2. doi: 10.4103/0019-557X.152844

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Sciences P. Clinical Anthropometric Biochemical (Cab) Manual. Mumbai (2014).

Google Scholar

12. Bäck SE, Magnusson CGM, Norlund LK, von Schenck HH, Menschik ME, Lindberg PES. Multiple-site analytic evaluation of a new portable analyzer, HemoCue Hb 201+, for point-of-care testing. Plast Surg Nurs. (2004) 3:60–5. doi: 10.1097/01.poc.0000127152.03809.87

CrossRef Full Text | Google Scholar

13. VMNIS. Haemoglobin Concentrations for the Diagnosis of Anaemia and Assessment of Severity. Geneva: WHO (2011). p. 1–6.

Google Scholar

14. Wado YD, Sully EA, Mumah JN. The DHS Program - Request Access To Datasets. Available online at: https://dhsprogram.com/data/new-user-registration.cfm (accessed April 12, 2020).

Google Scholar

15. National Family Health Survey. Available online at: http://rchiips.org/NFHS/nfhs4.shtml (accessed April 12, 2020).

Google Scholar

16. World Development Indicators. 5th ed. Washington, DC (2011).

Google Scholar

17. IIPS. National Family Health Survey (NFHS-4), 2015-16: India. Available online at: http://rchiips.org/nfhs/NFHS-4Reports/India.pdf (accessed April 10, 2020).

Google Scholar

18. Anemia Mukt Bharat—Vikaspedia. Available online at: https://vikaspedia.in/health/health-campaigns/anemia-mukt-bharat (accessed April 10, 2020).

Google Scholar

19. IIPS. National Family Health Survey. Mumbai (2015).

Google Scholar

20. World Health Organization. Interpretation Guide Nutrition Landscape Information System (NLIS). Geneva: WHO (2010).

Google Scholar

21. Prevalence, of Anemia Among Children (% of Children Under 5) | Data,. Available online at: https://data.worldbank.org/indicator/SH.ANM.CHLD.ZS?view=chart (accessed April 15, 2018).

Google Scholar

22. Ewusie JE, Ahiadeke C, Beyene J, Hamid JS. Prevalence of anemia among under-5 children in the Ghanaian population: estimates from the Ghana demographic and health survey. BMC Public Health. (2014) 14:626. doi: 10.1186/1471-2458-14-626

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Coutinho GG, Cury PM, Cordeiro JA. Cyclical iron supplementation to reduce anemia among Brazilian preschoolers: a randomized controlled trial. BMC Public Health. (2013) 13:21. doi: 10.1186/1471-2458-13-21

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Palupi L, Schultink W, Achadi E, Gross R. Effective community intervention to improve hemoglobin status in preschoolers receiving once-weekly iron supplementation. Am J Clin Nutr. (1997) 65:1057–61. doi: 10.1093/ajcn/65.4.1057

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Vijayaraghavan K, Brahmam GN, Nair KM, Akbar D, Rao NP. Evaluation of national nutritional anemia prophylaxis programme. Indian J Pediatr. (2017) 57:183–90. doi: 10.1007/BF02722084

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Malagi U, Reddy M, Naik RK. Evaluation of National nutritional anaemia control programme in Dharwad (Karnataka). J Hum Ecol. (2006) 20:279–81. doi: 10.1080/09709274.2006.11905939

CrossRef Full Text | Google Scholar

27. Gayathri S, Manikandanesan S, Venkatachalam J, Gokul S, Yashodha A, Premarajan KC. Coverage of and compliance to iron supplementation under the National Iron Plus Initiative among reproductive age-group women in urban Puducherry - A cross-sectional study. Int J Adolesc Med Health. (2019). doi: 10.1515/ijamh-2018-0094. [Epub ahead of print].

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Bhatia V, Mahajan P, Parida SP, Bhattacharjee S, Sahoo SS. Challenges in supervision, monitoring, and reporting in anemia programme implementation in Odisha, India: a qualitative process documentation. J Fam Med Prim Care. (2019) 8:1365–9. doi: 10.4103/jfmpc.jfmpc_68_19

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Allen LH, Rosado JL, Casterline JE, López P, Muñoz E, Garcia OP, et al. Lack of hemoglobin response to iron supplementation in anemic Mexican preschoolers with multiple micronutrient deficiencies. Am J Clin Nutr. (2000) 71:1485–94. doi: 10.1093/ajcn/71.6.1485

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Ayoya MA, Ngnie-Teta I, Séraphin MN, Mamadoultaibou A, Boldon E, Saint-Fleur JE, et al. Prevalence and risk factors of anemia among children 6–59 months old in Haiti. Anemia. (2013) 2013:502968. doi: 10.1155/2013/502968

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Agho KE, Dibley MJ, D'Este C, Gibberd R. Factors associated with haemoglobin concentration among Timor-Leste children aged 6-59 months. J Heal Popul Nutr. (2008) 26:200–9.

PubMed Abstract | Google Scholar

32. Khan JR, Awan N, Misu F. Determinants of anemia among 6–59 months aged children in Bangladesh: evidence from nationally representative data. BMC Pediatr. (2016) 16:3. doi: 10.1186/s12887-015-0536-z

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Yang W, Li X, Li Y, Zhang S, Liu L, Wang X, et al. Anemia, malnutrition and their correlations with socio-demographic characteristics and feeding practices among infants aged 0-18 months in rural areas of Shaanxi province in northwestern China: a cross-sectional study. BMC Public Health. (2012) 12:1127. doi: 10.1186/1471-2458-12-1127

CrossRef Full Text | Google Scholar

34. WHO. Daily Iron and Folic Acid Supplementation During Pregnancy. Geneva: WHO (2017).

Google Scholar

35. Haider BA, Olofin I, Wang M, Spiegelman D, Ezzati M, Fawzi WW, et al. Anaemia, prenatal iron use, and risk of adverse pregnancy outcomes: systematic review and meta-analysis. BMJ. (2013) 346:f3443. doi: 10.1136/bmj.f3443

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Imdad A, Bhutta ZA. Routine iron/Folate supplementation during pregnancy: effect on maternal anaemia and birth outcomes. Paediatr Perinat Epidemiol. (2012) 26:168–77. doi: 10.1111/j.1365-3016.2012.01312.x

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Menendez C, Todd J, Alonso PL, Francis N, Lulat S, Ceesay S, et al. The effects of iron supplementation during pregnancy, given by traditional birth attendants, on the prevalence of anaemia and malaria. Trans R Soc Trop Med Hyg. (1994) 88:590–3. doi: 10.1016/0035-9203(94)90176-7

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Gebreegziabiher G, Etana B, Niggusie D. Determinants of Anemia among children aged 6–59 months living in Kilte Awulaelo Woreda, Northern ethiopia. Anemia. (2014) 2014:245870. doi: 10.1155/2014/245870

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Osório MM, Lira PI, Ashworth A. Factors associated with Hb concentration in children aged 6–59 months in the State of Pernambuco, Brazil. Br J Nutr. (2004) 91:307–15. doi: 10.1079/BJN20031042

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Bharati S, Pal M, Chakrabarty S, Bharati P. Socioeconomic determinants of iron-deficiency Anemia among children aged 6 to 59 months in India. Asia Pacific J Public Heal. (2015) 27:NP1432–43. doi: 10.1177/1010539513491417

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Barreto ML. Childhood anemia prevalence and associated factors in Salvador, Bahia, Brazil Prevalência e fatores associados à ocorrência da anemia em pré-escolares na cidade de Salvador, Bahia, Brasil. Cad Saude Publica. (2004). 20:1633–41. doi: 10.1590/s0102-311x2004000600022

CrossRef Full Text | Google Scholar

42. Vart P, Jaglan A, Shafique K. Caste-based social inequalities and childhood anemia in India: results from the National Family Health Survey (NFHS) 2005–2006. BMC Public Health. (2015) 15:537. doi: 10.1186/s12889-015-1881-4

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Goswmai S, Das KK. Socio-economic and demographic determinants of childhood anemia. J Pediatr. (2015) 91:471–7. doi: 10.1016/j.jped.2014.09.009

PubMed Abstract | CrossRef Full Text | Google Scholar

44. VMINS Serum Ferritin Concentrations for Assessment of Iron Status and Iron Deficiency in Populations Scope and Purpose. Available online at: http://www.who.int/vmnis/indicators/serum_ferritin.pdf (accessed April 23, 2018).

Google Scholar

45. Uddin M, Sardar M, Hossain M, Alam MM, Bhuya MF, Uddin MM, et al. Prevalence of Anaemia in children of 6 months to 59 months in Narayanganj, Bangladesh. J Dhaka Med Coll. (2011) 19:126. doi: 10.3329/jdmc.v19i2.7084

CrossRef Full Text | Google Scholar

46. Howard CT, de Pee S, Sari M, Bloem MW, Semba RD. Association of diarrhea with anemia among children under age five living in rural areas of Indonesia. J Trop Pediatr. (2007) 53:238–44. doi: 10.1093/tropej/fmm011

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Desai MR, Terlouw DJ, Kwena AM, Phillips-Howard PA, Kariuki SK, Wannemuehler KA, et al. Factors associated with hemoglobin concentrations in pre-school children in western Kenya: cross-sectional studies. Am J Trop Med Hyg. (2005) 72:47–59. doi: 10.4269/ajtmh.2005.72.47

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Semba RD, de Pee S, Ricks MO, Sari M, Bloem MW. Diarrhea and fever as risk factors for anemia among children under age five living in urban slum areas of Indonesia. Int J Infect Dis. (2008) 12:62–70. doi: 10.1016/j.ijid.2007.04.011

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Emond AM, Hawkins N, Pennock C, Golding J. Haemoglobin and ferritin concentrations in infants at 8 months of age. Arch Dis Child. (1996) 74:36–9. doi: 10.1136/adc.74.1.36

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Sherriff A, Emond A, Hawkins N, Golding J. Haemoglobin and ferritin concentrations in children aged 12 and 18 months. ALSPAC children in focus study team. Arch Dis Child. (1999) 80:153–7. doi: 10.1136/adc.80.2.153

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Gwetu TP, Chhagan MK, Martin CJ, Myra Taylor MC. Anemia, iron deficiency and diet independently influence growth patterns of school aged children in South Africa. Acad J Pediatr Neonatol. (2016) 1:1–8. doi: 10.19080/AJPN.2016.03.555565

CrossRef Full Text | Google Scholar

52. Woldie H, Kebede Y, Tariku A. Factors associated with Anemia among children aged 6–23 months attending growth monitoring at Tsitsika health center, Wag-Himra zone, Northeast Ethiopia. J Nutr Metab. (2015) 2015:1–9. doi: 10.1155/2015/928632

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Rivera Damm R, Ruiz Astorga MR, Carrillo de Jiménez H, Hernández Alvarado AB, Sosa Curiel S. Prevalence of anemia in a sample of school children in Durango City. Bol Med Hosp Infant Mex. (1979) 36:507–17.

PubMed Abstract | Google Scholar

54. Sinha N, Deshmukh PR, Garg BS. Epidemiological correlates of nutritional anemia among children (6-35 months) in rural Wardha, Central India. Indian J Med Sci. (2008) 62:45–54. doi: 10.4103/0019-5359.39366

PubMed Abstract | CrossRef Full Text | Google Scholar

55. El-Farrash RA, Ismail EA, Nada AS. Cord blood iron profile and breast milk micronutrients in maternal iron deficiency anemia. Pediatr Blood Cancer. (2012) 58:233–8. doi: 10.1002/pbc.23184

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Kumar A, Rai AK, Basu S, Dash D, Singh JS. Cord blood and breast milk iron status in maternal Anemia. Pediatrics. (2008) 121:e673–7. doi: 10.1542/peds.2007-1986

PubMed Abstract | CrossRef Full Text | Google Scholar

57. Pita GM, Jiménez S, Basabe B, García RG, Macías C, Selva L, et al. Anemia in children under five years old in Eastern Cuba, 2005-2011. MEDICC Rev. (2014) 16:16–23.

PubMed Abstract | Google Scholar

58. Saarinen UM, Siimes MA, Dallman PR. Iron absorption in infants: high bioavailability of breast milk iron as indicated by the extrinsic tag method of iron absorption and by the concentration of serum ferritin. J Pediatr. (1977) 91:36–9. doi: 10.1016/S0022-3476(77)80439-3

PubMed Abstract | CrossRef Full Text | Google Scholar

59. Choi HJ, Lee HJ, Jang HB, Park JY, Kang JH, Park KH, et al. Effects of maternal education on diet, anemia, and iron deficiency in Korean school-aged children. BMC Public Health. (2011) 11:870. doi: 10.1186/1471-2458-11-870

PubMed Abstract | CrossRef Full Text | Google Scholar

60. Balarajan Y, Ramakrishnan U, Ozaltin E, Shankar AH, Subramanian SV. Anaemia in low-income and middle-income countries. Lancet. (2011) 378:2123–35. doi: 10.1016/S0140-6736(10)62304-5

PubMed Abstract | CrossRef Full Text | Google Scholar

61. Cheng HG, Phillips MR. Secondary analysis of existing data: opportunities and implementation. Shanghai Arch Psychiatry. (2014) 26:371–5. doi: 10.11919/j.issn.1002-0829.214171

PubMed Abstract | CrossRef Full Text | Google Scholar

62. Tp G MkC, Craib M, Kauchali S. Hemocue validation for the diagnosis of Anaemia in children: a semi-systematic review. Pediat Ther. (2013) 4:1. doi: 10.4172/2161-0665.1000187

CrossRef Full Text | Google Scholar

63. Plessow R, Arora NK, Brunner B, Tzogiou C, Eichler K, Brügger U, et al. Social costs of iron deficiency Anemia in 6-59-month-old children in India. PLoS ONE. (2015) 10:e0136581. doi: 10.1371/journal.pone.0136581

PubMed Abstract | CrossRef Full Text | Google Scholar

64. Muthayya S, Thankachan P, Hirve S, Amalrajan V, Thomas T, Lubree H, et al. Iron fortification of whole wheat flour reduces iron deficiency and iron deficiency Anemia and increases body iron stores in Indian school-aged children. J Nutr. (2012) 142:1997–2003. doi: 10.3945/jn.111.155135

PubMed Abstract | CrossRef Full Text | Google Scholar

65. Horton S, Ross J. The economics of iron deficiency. Food Policy. (2003) 28:51–75. doi: 10.1016/S0306-9192(02)00070-2

CrossRef Full Text | Google Scholar

Keywords: anemia in children, predictors, iron supplementation, India, National Iron Plus Initiative

Citation: Thomas MS, Demirchyan A and Khachadourian V (2020) How Effective Is Iron Supplementation During Pregnancy and Childhood in Reducing Anemia Among 6–59 Months Old Children in India? Front. Public Health 8:234. doi: 10.3389/fpubh.2020.00234

Received: 03 December 2019; Accepted: 18 May 2020;
Published: 07 July 2020.

Edited by:

Zahiruddin Quazi Syed, Datta Meghe Institute of Medical Sciences, India

Reviewed by:

Monika Sharma, Christian Medical College & Hospital, India
Eduardo Daniel Rosas-Blum, Texas Tech University Health Sciences Center, United States

Copyright © 2020 Thomas, Demirchyan and Khachadourian. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Monica Steffi Thomas, dG1vbmljYXN0ZWZmaSYjeDAwMDQwO2dtYWlsLmNvbQ==

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