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BMC Pregnancy and Childbirth logoLink to BMC Pregnancy and Childbirth
. 2023 Apr 18;23:260. doi: 10.1186/s12884-023-05593-7

Individual and contextual-level factors associated with iron-folic acid supplement intake during pregnancy in Ethiopia: a multi-level analysis

Melaku Yalew 1,2,, Shiferaw Getachew 3, Keriya Mohammed 4, Hailu Hankarso 5, Adane Bayile 6, Shambel Dessale Asmamaw 7, Mesfin Getahun Assefa 8, Getaw Walle Bazie 9, Wondwosen Mebratu 9, Bereket Kefale 2, Yitayish Damtie 2,10, Mastewal Arefaynie 2, Tesfaye Birhane 2, Reta Dewau 9, Nigus Cherie 2, Elsabeth Addisu 2, Kefale Mitiku 11, Fentaw Tadese 9, Teklehaimanot Fentie Wendie 12, Adane Habtie 13, Tefera Chane Mekonnen 14, Sisay Eshete Tadesse 14, Getachew Tadesse Bedane 15, Yitbarek Wasihun 16, Tilahun Degu Tsega 1, Mekuanint Taddele 17, Zenebe Tefera 18, Bezawit Adane 1, Birhanu Wagaye 14, Fanos Yeshanew Ayele 14, Aregash Abebayehu Zerga 14, Abebaw Molla 19, Biruk Desalegn 20, Mengesha Birkie 21, Bekalu Bewket 22, Belete Kassa Alemu 23, Segenet Zewdie 23, Meseret Kefale Tsegaye 24, Abebayehu Bitew 25, Kassu Mehari 15, Lemma Derseh 26
PMCID: PMC10111777  PMID: 37072714

Abstract

Background

Anemia is still one of the major public health problems in many developing countries including Ethiopia. Thus, this study aimed to assess individual and contextual-level factors associated with iron-folic acid supplement intake during pregnancy in Ethiopia.

Methods

A secondary analysis was done on the 2019 mini-Ethiopian Demographic and Health Survey (EDHS) dataset. A total of 3,927 pregnant women who gave birth five years before the survey were included in the analysis. Multi-level mixed-effect logistic regression analysis was done by STATA/SE version 14.0 to identify individual and contextual-level factors. Adjusted Odds Ratio (AOR) with 95% Confidence Interval (CI) was used to show the strength and direction of the association. The level of statistical significance was declared at a P value less than 0.05.

Results

Those primary educated [AOR = 1.83, 95% CI: (1.24, 2.74)], secondary educated [AOR = 2.75, 95% CI: (1.57, 4.824)], women who had greater than 5 living children [AOR = 2.02, 95% CI: (1.25, 3.27)], women who had ANC visit [AOR = 21.26, 95% CI: (13.56, 33.32)] and women who lived in a cluster with high proportion of women had ANC visit [AOR = 1.72, 95% CI: (1.17, 2.54)] and women who lived in Somali [AOR = 0.44 0.73, 95% CI: (0.22, 0.87)] were significantly associated with iron-folic acid intake during pregnancy.

Conclusions

Both individual and contextual-level factors were significantly associated with iron-folic acid intake during pregnancy. From individual-level factors: education status of women, the total numbers of living children, and ANC follow-up are significant and from contextual-level factors: region and living in a high proportion of women who had ANC follow-up were found to have a statistically significant association. Promoting women’s education and maternal health services like ANC and intervention targeting the Somali region would be the recalled area of the government.

Keywords: Iron intake, Iron supplement, Anemia, Pregnant women, Ethiopia

Background

The global estimate indicated that nearly 42% of pregnant women and 30% of non-pregnant women are found to be anemic [1, 2]. In Sub-Sahara Africa, 20% of maternal mortality was directly attributed to anemia [1]. According to 2016, Ethiopia Demographic and Health Survey, 24% of reproductive-age women were anemic [3]. Anemia among reproductive-age women who reside in rural and urban areas was 25% and 17%, respectively [4]. In several low-income countries, the cause of anemia during pregnancy is multi-factorial. It includes nutrition deficiencies of folate, vitamin B12, iron, and parasitic diseases such as malaria and hookworm [5].

Anemia develops as a result of ineffective or deficient erythropoiesis or loss of red blood cells and iron deficiency anemia (IDA) and anemia of red blood cell morphology is types of anemia that have different biological mechanisms of causation. Iron in the human body is regulated by the iron cycle and most of the storage iron human body is used for new red blood cell (RBC) synthesis or erythropoiesis and the lack of iron stored in the body limits the erythropoiesis process which leads to a reduction in the number of circulating RBCs lower than normal and insufficient oxygen-carrying capacity to meet physiological demands subsequently results in the development of IDA [6, 7]. On the other hand, folate has a crucial role in the DNA synthesis pathway and the deficiency of folate or vitamin B12 affects DNA synthesis and cell division in the bone marrow (megaloblastic changes). This deficiency leads to nuclear division without significant alteration in the cytoplasmic maturation cycle and nucleated precursor cells in the bone marrow develop immature or morphologically abnormal nuclei and giant metamyelocytes, with macrocytic red blood cells called megaloblastic anemia [8].

Iron and folic acid deficiencies are the most common causes of anemia among pregnant women in sub-Saharan Africa. Iron deficiency anemia contributes to adverse effects on maternal and child health. The maternal consequences include: low weight gain, preterm labor, placenta previa, premature rupture of membrane, cardiac arrest, hemorrhage, lowered resistance to infection, poor cognitive development, and reduced work capacity. But, it is not limited to the above-mentioned effects. Similarly, it has fetal and neonatal risks including prematurity, low birth weight, and fetal distress, which contributes to perinatal morbidity and mortality. Infants born to anemic women are more likely to become anemic [9, 10]. Folic acid (the synthetic form of Vitamin B9 or folate) deficiency at conception and in early pregnancy is also associated with an increased risk of neural tube defect, preeclampsia, fetal malformations, and preterm delivery [11, 12].

In Ethiopia, IFA supplementation is one of the main strategies for the prevention of anemia. The Ethiopian national guideline for the prevention of micronutrient deficiencies recommended the need for daily IFA supplementation during pregnancy and postpartum. However, the effectiveness and success of such interventions depend on the adherence to IFA tablets [13].

Even though iron-folic acid intake or supplementation among pregnant women was addressed in previous studies, most of them were taking on individual-level analysis by omitting the effect of clustering. In the classical logistic regression (individual-level analysis), the independent assumption among clustered individuals is violated. In addition, the association at the individual-level may not work at the cluster-level and vice versa. So, most of the previously published articles are subject to an atomistic or ecological fallacy [1419]. The factors associated with iron-folic acid supplement intake are area-specific which requires a different approach to analysis at a different level [20, 21]. Therefore, this study took into account those different levels of analysis and aimed to assess individual and contextual-level factors associated with iron-folic acid supplement intake among pregnant women in Ethiopia by using the mini-EDHS 2019 dataset.

Methods

Study area and data source

The study was conducted in Ethiopia, which is located in the North-Eastern part of Africa, which lies between 30 and 150 North latitude and 330 and 480 East longitudes. This study used the 2019 mini-EDHS dataset. It was collected by the Central Statistical Agency (CSA) in collaboration with the Federal Ministry of Health (FMoH) and the Ethiopian Public Health Institute (EPHI). Data were accessed from their URL: www.dhsprogram.com by contacting them through personal accounts after justifying the reason for requesting it [22]. A cross-sectional study design using secondary data from the 2019 mini-EDHS was conducted. A total of 3,927 weighted pregnant women were included in the analysis (Fig. 1).

Fig. 1.

Fig. 1

Sample size and sampling procedure to reach the study participants in mini-EDHS 2019, Ethiopia

Variable measurement, data processing, and analysis

The outcome variable for this study is dichotomized as iron-folic acid supplement intake (yes/no) which was generated from a constructed mini-EDHS variable. Wealth index is a composite variable that was calculated for urban and rural separately and it includes the following classification [3].

  • Poorest: Includes women whose wealth was less than or equal to 20 percentile.

  • Poorer: Includes women whose wealth ranged 21 to 40 percentile.

  • Middle: Includes women whose wealth ranged 41 to 60 percentile.

  • Richer: Includes women whose wealth ranged 61 to 80 percentile.

  • Richest: Includes women whose wealth ranged 81 to 100 percentile.

Contextual-level variables were created by taking aggregate measures from individual-level variables in each cluster. Data cleaning was conducted to check for consistency and missing value. Recoding, labeling, and exploratory analysis were performed by using Stata/SE version 14.0. Sample weight was used to compensate for the unequal probability of selection between the strata that were geographically defined, as well as for non-responses [23]. Descriptive statistics were used to present frequencies, with percentages in tables, graphs, and using texts. Multilevel analysis was conducted after checking that the data was eligible for multilevel analysis which means Intra-cluster Correlation Coefficient (ICC) was high (ICC = 32.04%). Since DHS data are hierarchical, i.e. individuals (level 1) were nested within communities (level 2 or cluster), a two-level mixed-effects logistic regression model was fitted to estimate both independent (fixed) effects of the explanatory variables and community-level random effects on iron-folic acid intake [24]. The log of the probability of iron-folic acid intake was modeled using a two-level multilevel model as follows:

graphic file with name M1.gif

Where, i and j are the level 1 (individual) and level 2 (contextual) units, respectively; X and Z refer to individual and contextual-level variables, respectively; πij is the probability of iron-folic acid intake for the ith women in the jth cluster; the β’s indicates the fixed coefficients. Whereas, β0 is the intercept-the probability of iron-folic acid intake in the absence of influence of predictors; and uj showed the random effect (effect of contextual factors on iron-folic acid intake for the jth cluster and eij showed random errors at the individual levels. By assuming each cluster had a different intercept (β0) and fixed coefficient (β), the clustered data nature and the within and between cluster variations were taken into account. During analysis first, bivariable multilevel logistic regression was fitted and variables with a p-value less than 0.25 were selected to build the 3 models (model1-3). Then the analysis was performed in three steps: Model 1 (empty model or null model/ without explanatory variable); Model 2 (only individual-level factors) and Model 3 (both individual and contextual-level factors). The measures of association (fixed-effects) estimate the associations between the likelihood of women to take iron-folic acid and various explanatory variables were expressed as Adjusted Odds Ratio (AOR) with their 95% confidence level. A variable in which it’s a p-value < 0.05 was used to declare statistical significance. Intra-cluster Correlation coefficient (ICC), Median Odds Ratio (MOR), and proportional change in variance (PCV) were used to measure the variation between clusters. MOR is defined as the median value of the odds ratio between the area at highest risk and the area at the lowest risk when randomly picking out two areas. PCV measures the total variation attributed to individual-level factors and area-level factors in the multilevel model. The log-likelihood ratio test was used to estimate the goodness of fit of the adjusted final model in comparison to the preceding models.

Results

Socio-demographic characteristics of the respondents

The total numbers of pregnant women who gave birth within five years before the survey and included for analysis were 3,927. Out of this, 1,192 (30.37%) were founded in the age group 25–29 years. About 3,685 (93.84%) were currently married or living together. Of the total pregnant women, 2,014 (51.30%) had no education. Regarding household wealth, out of the total 825 (21.02%) lived in the poorest wealth quintile. Among responded mothers, 1,440 (36.69%) are orthodox in religion.

Regarding ANC visits, 1,013 (25.81%) of women had no ANC visits. Out of the total study participants, 2,900 (73.86%) resided in a rural area. About, 1,519 (38.69%) resided in Oromia region, and 839 (21.38%) resided in Amhara region. Concerning the total number of living children, about 1,539 (39.17%) women had 3–5 children (Table 1).

Table 1.

Characteristics of pregnant women in Ethiopia who gave birth within 5 years before the survey, mini-EDHS 2019

Variables Category Frequency Percentage
Age in years 15–19 227 5.79
20–24 768 19.58
25–29 1912 30.37
30–34 799 20.36
35–39 590 15.04
40–44 258 6.59
45–49 89 2.27
Marital status Single 241 6.16
Married 3684 93.84
Place of residence Urban 1026 26.14
Rural 2900 73.86
Educational status of a mother No education 2014 51.30
Primary 1414 36.03
Secondary 344 8.79
Higher 152 3.89
Wealth Poorest 2,843 63.34
Poorer 1,646 36.66
Middle 1,924 45.35
Richer 1,710 40.29
Richest 393 9.27
Religion Orthodox 1440 36.69
Muslim 1339 34.12
Protestant 1082 27.57
Others 63 1.62
ANC visit No 1013 25.81
Yes 2913 74.19
Total numbers of living child < 3 1583 40.33
3–5 1537 39.17
> 5 805 20.51
Region Tigray 286 7.3
Afar 51 1.3
Amhara 839 21.38
Oromia 1519 38.69
Somali 210 5.55
Benishangul 47 1.2
SNN 787 20
Gambela 19 0.49
Harari 11 0.28
Addis Ababa 126 3.22
Dire Dewa 21 0.54
Cluster ANC follow up Low 1818 46.31
High 2108 53.69
Cluster below middle wealth Low 1970 50.19
High 1955 49.81
Cluster secondary above education Low 2515 64.05
High 1411 35.95

Footnote: Cluster ANC follow up = Proportion of women who had ANC in a cluster, Cluster below middle wealth = Proportion of women blow the middle wealth quartile in a cluster, and Cluster above secondary = Proportion of women educated secondary and above in a cluster

Individual and contextual-level factors associated with iron-folic acid supplement intake (fixed-effects)

After adjusting for individual and contextual-level factors (model 3) education status of women, the total numbers of living children, ANC follow-up, region, and proportion of women who had ANC follow-up were found to have a statistically significant association with iron-folic acid intake among pregnant women in Ethiopia. Those primary educated pregnant women were 1.8 times more likely to take iron-folic acid as compared to those not educated [AOR = 1.83, 95% CI: (1.24, 2.74)]. Similarly, the odds of taking iron-folic acid were 2.75 times more in secondary educated pregnant women as compared to those not educated [AOR = 2.75, 95% CI: (1.57, 4.824)].

The odds of taking iron-folic acid among pregnant women who had greater than 5 living children were two times higher than those who had less than or equal to two children [AOR = 2.02, 95% CI: (1.25, 3.27)].

Those pregnant women who had ANC visits were 21 times more likely to take iron-folic acid as compared to women who hadn’t [AOR = 21.26, 95% CI: (13.56, 33.32)]. Similarly, those pregnant women who lived in a cluster with a high proportion of women who had ANC visits were 1.72 times more likely to take iron-folic acid as compared to women who lived in a cluster with a low proportion of women who had ANC visits [AOR = 1.72, 95% CI: (1.17, 2.54)]. But, the odds of taking iron-folic acid among pregnant women who lived in Somali region were 56% less likely as compared to Dire Dawa [AOR = 0.44 0.73, 95% CI: (0.22, 0.87)] (Table 2).

Table 2.

Individual and contextual-level factors associated with iron-folic acid intake in Ethiopia, mini-EDHS 2019 dataset

Variables Category COR
(95% CI)
Null model Model 2
AOR (95% CI)
Model 3
AOR (95% CI)
Age of mother in years 15–19 1 1 1
20–24 1.71(3.10,8.46) 1.41 (0.73, 2.27) 1.34 (0.69, 2.59)
25–29 1.73(1.03,2.91) 1.30 (0.66, 2.55) 1.25 (0.64, 2.48)
30–34 1.40(0.84,2.33) 1.18 (0.59, 2.40) 1.08 (0.54, 2.21)
35–39 0.94(0.56,1.58) 0.80 (0.37, 1.72) 0.73 (0.34, 1.59)
40–44 1.07(0.55,2.08) 1.28 (0.48, 3.35) 1.12 (0.43, 2.93)
45–49 0.36(0.14,0.90) 0.37 (0.11, 1.25) 0.30 (0.09, 1.03)
Religion Orthodox 1 1 1
Muslim 0.54(0.34,0.84) 0.64 (0.42, 0.96) 1.08 (0.61, 1.923)
Protestant 0.65(0.40,1.02) 0.48 (0.30, 0.75) 0.72 (0.42, 1.27)
Other 0.64(0.4,1.73) 1.18 (0.50, 2.77) 1.76 (0.72, 4.35)
ANC visit No 1 1 1
Yes 27.14(17.25,42.71) 23.96 (15.32, 3746) 21.26 (13.56, 33.32)
Wealth Poorest 1 1 1
Poorer 1.90(1.33,2.72) 1.16 (0.75, 1.77) 1.05 (0.68, 1.63)
Middle 2.88(1.99,4.15) 1.66 (1.07, 2.57) 1.45 (0.93, 2.26)
Richer 2.84(1.88,4.29) 1.33 (0.82, 2.16) 1.10 (0.67, 1.82)
Richest 6.72(3.89,11.59) 1.70 (0.94, 3.07) 1.32 (0.5&, 3.12)
Marital status Single/not living together 1 1 1
Married/living together 1.36(0.73,2.50) 0.95 (0.50, 1.81) 0.95(0.5000–08121).
Number of living children  2 1 1 1
3–5 0.78(0.59,1.01) 1.26 (0.85, 1.86) 1.29 (0.88, 1.92)
> 5 0.63(0.47,0.85) 1.876 (1.15, 3.02) 2.02 (1.25, 3.27)
Education status of a mother No education 1 1 1
Primary 2.17 (1.62, 2.90) 1.87 (1.26, 2.78) 1.83 (1.24, 2.74)
Secondary 5.12(3.10,8.46 2.64 (1.51, 4.61) 2.75 (1.57, 4.82)
Higher 3.48(1.69,7.19) 1.69 (0.76, 0.38) 1.78 (0.81, 3.92)
Place of residence Rural 1 1
Urban 0.40(0.26,0.62) 0.01 (0.40, 1.65)
Region Dire Dewa 1 1
Tigray 2.44(1.35,4.420 2.00 (0.91, 4.39)
Afar 0.40(0.20,0.78) 1.05 (0.53, 2.0)
Amhara 1.27(0.69,2.31) 1.98 (0.89, 4.40)
Oromia 0.54(0.29,1.00) 0.91 (0.48, 1.75)
Somali 0.64(0.30,0.14) 0.44 (0.22, 0.87)
Benishangul 0.61(0.30,1.21) 0.74 (0.3, 1.46)
SNNP 0.47(0.26,0.86) 1.02 (0.46, 2.27)
Gambela 0.56(0.28,1.11) 0.53 (0.23, 1.22)
Harari 0.85(0.46,1.57) 0.86 (0.47, 1.56)
Addis Ababa 1.15(0.63,2.10) 0.49 (0.23, 1.03)
Cluster ANC follow up Low 1 1
High 7.06(5.2,9.6) 1.72 (1.17, 2.54)
Cluster below middle wealth Low 1 1
High 0.34(0.24,0.48) 0.81 (0.51, 1.28)
Cluster above secondary Low 1 1
High 2.84(1.97,4.09) 0.93 (0.58, 1.49)

Footnote: 1 = Reference, Cluster ANC follow up = Proportion of women who had ANC in a cluster, Cluster below middle wealth = Proportion of women blow the middle wealth quartile in a cluster and Cluster above secondary = Proportion of women educated secondary and above in a cluster, COR = Crude Odds Ratio and AOR = Adjusted Odds Ratio

Random effect

The results of multilevel logistic regression for random effects showed that there was a significant variation in taking iron-folic acid across the clusters (Table 3). The Intra-cluster correlation coefficients showed that 32.04% of the variation in taking iron-folic acid was related to community-level factors. The full model also showed that there is a statistically significant variation in taking iron-folic acid across communities or clusters. About 64.52% of taking iron-folic acid in clusters was explained in the full model. Besides, the MOR confirmed that taking iron-folic acid was attributed to community-level factors. The MOR for taking iron-folic acid was 3.26 in the empty model which indicated that there was variation between communities (clustering) (3.26 times higher than the reference (MOR = 1)). The unexplained community variation in taking iron-folic acid decreased to MOR of 2.02 when all factors were added to the model. This showed that when all factors are considered, the effects of clustering are still statistically significant in the full models (Table 3).

Table 3.

Measure of variation on individual and contextual-level factors associated with iron-folic acid intake in Ethiopia, mini-EDHS 2019 dataset

Measure of variation Model 1 (Null model) Model 2 Model 3
Variance 1.55 0.68 0.55
Explained variance (PCV %) Reference 56.13 64.52
Median odds ratio (MOR) 3.26 2.18 2.02
The intra-cluster correlation coefficient (ICC) in % 32.04 17.14 14.33
Model fitness
Likelihood ratio test 0.0001 0.0085

Discussion

After adjusting for other variables and the effect of clustering, education status of women, the total numbers of living children, ANC follow-up, region, and living in a high proportion of women who had ANC follow-up were found to have a statistically significant association with iron-folic acid supplement intake among pregnant women in Ethiopia.

The result of this study indicated that as educational status increased, the odds of taking iron-folic acid supplementation among pregnant women also increased. The finding of this study is contrary to a study conducted in Ethiopia [21]. However, it is in line with a study conducted in Mecha district, Amhara, [25], and North Gondar, Ethiopia [26]. It is also in agreement with studies conducted in Addis Ababa [20, 27] and Southern Ethiopia [28] and a study conducted in India [29]. This may be due to the fact that education increases pregnant women’s knowledge, especially about the fates of micronutrient deficiency.

The odds of taking iron-folic acid supplementation among pregnant women who had greater than 5 living children were higher than those who had less than or equal to two children. This finding is consistent with a study conducted in North Gondar, Ethiopia [26]. It is also supported by the finding of a study conducted in Kenya [30]. This may be due to the presence of multiple exposures to its advantage and its risk as they have been exposed for medical care and counseling.

Those pregnant women who had ANC visits were more likely to take an iron-folic acid supplement as compared to women who hadn’t. This finding is supported by studies conducted in Ethiopia by using EDHS 2011 and 2016 respectively [21, 31]. Similarly, this finding is consistent with a study conducted in Tigray, Ethiopia [32], a systematic review and meta-analysis conducted in Ethiopia [33], and a study conducted in 22 countries [34]. The possible reason for the association may be due to the fact that women who had ANC visits may have the opportunity to know the benefits of iron-folic acid intake. In addition, the health care provider may provide counseling as to what will happen if they didn’t take it like postpartum anemia and neural tube defects [35, 36].

Those pregnant women who lived in a cluster with a high proportion of women who had ANC visits were more likely to take an iron-folic acid supplement as compared to women who lived in a cluster with a low proportion of women who had ANC visits. The possible association may be due to observational learning or as the women were living in a cluster with a high proportion of ANC visits, most of her intimate friends may be knowledgeable regarding it and there may be peer pressure even if she may not have the interest to take it.

Whereas, the odds of taking iron-folic acid supplementation among pregnant women who lived in Somali region were less likely as compared to Dire Dawa. This may be due to the fact that Somali region was one of the developing regions and there may be short access to media as compared to Dire Dawa. Despite different strengths: considering the clustering effect, and using a large sample size for analysis, it is not without limitations. Since this study takes secondary data, only small numbers of individual and contextual-level variables were included in the analysis as potential determinant factors for iron-folic acid intake. Furthermore, the finding of the study may also be prone to recall bias since the data was collected from women who gave birth five years before the survey.

Conclusions

After adjusting for other variables and the effect of clustering, both individual and contextual factors were significantly associated with iron-folic acid intake during pregnancy. From individual-level factors: education status of women, the total numbers of living children, and ANC follow-up are significant and from contextual factors: region and living in a high proportion of women who had ANC follow-up were found to have a statistically significant association with iron-folic acid intake among pregnant women in Ethiopia. Promoting women’s education and maternal health services like ANC and intervention targeting Somali region would be the recalled area of the government.

Acknowledgements

Our special thanks go to DHS program for helping us to access the dataset for conducting the research.

Authors’ Contribution

MY, MGA, GWB, WM, MA, TB, SDA and KM: Analyzed the data and wrote the result, MY, HH, BA, BK, YD, EA, FT and AB: Drafted the manuscript, MY, RD, TFW, AH, KM, LD, SET, TCM, NC, ZT, MT, TDT, YW, GTB, BW, SZ, AM, BB, AAZ, FYA, MB, BKA, MKT and SG: Edited and revised the manuscript. All the authors read and approved the final manuscript.

Funding

No specific fund was received.

Data Availability

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Declarations

Ethics approval and consent to participate

An authorization letter of permission for downloading 2019 mini-EDHS dataset was obtained from DHS program, by requesting the website: www.measuredhs.com. The data was used only for this study. It was not passed to other researchers without the consent of DHS. All data were treated as confidential and no need to identify any household or individual respondent interviewed in the survey. In this study, all of the methods were carried out in accordance with the relevant institutional guidelines and regulations. Again, all methods were conducted in accordance with the ethical standards of the declaration of Helsinki.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.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(4):444–54. doi: 10.1017/S1368980008002401. [DOI] [PubMed] [Google Scholar]
  • 2.Badham J, Zimmermann MB, Kraemer K. The guidebook nutritional anemia. Task Force Sight and Life; 2007.
  • 3.ICF CSACEa. Ethiopia Demographic and Health Survey 2016.Addis Ababa, Ethiopia, and Rockville, Maryland, USA: CSA and ICF.
  • 4.Macro O. Central Statistical Agency. Ethiopia demographic and health survey. 2005.
  • 5.World Health Organization. The global prevalence of anaemia in 2011. World Health Organization; 2015.
  • 6.Chaparro CM, Suchdev PS. Anemia epidemiology, pathophysiology, and etiology in low-and middle‐income countries. Ann N Y Acad Sci. 2019;1450(1):15–31. doi: 10.1111/nyas.14092. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Handelman GJ, Levin NW. Iron and anemia in human biology: a review of mechanisms. Heart Fail Rev. 2008;13(4):393–404. doi: 10.1007/s10741-008-9086-x. [DOI] [PubMed] [Google Scholar]
  • 8.Green R. Vitamin B12 deficiency from the perspective of a practicing hematologist. Blood The Journal of the American Society of Hematology. 2017;129(19):2603–11. doi: 10.1182/blood-2016-10-569186. [DOI] [PubMed] [Google Scholar]
  • 9.Begum S. Factors associated with adherence to iron folic acid supplementations during pregnancy in Uttar Pradesh. Indian J Maternal Child Health. 2012;14(2):8. [Google Scholar]
  • 10.Zakia M, El-Hamid S, Mikhail H, Maged S. Assessment of adherence to Iron and folic acid supplementation and prevalence of Anemia in pregnant women Ismailia governorate. Egypt Med J Cairo Univ. 2011;79(2):115–21. [Google Scholar]
  • 11.Ogundipe O, Hoyo C, Østbye T, Oneko O, Manongi R, Lie RT, et al. Factors associated with prenatal folic acid and iron supplementation among 21,889 pregnant women in Northern Tanzania: a cross-sectional hospital-based study. BMC Public Health. 2012;12(1):1–10. doi: 10.1186/1471-2458-12-481. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Sengpiel V, Bacelis J, Myhre R, Myking S, Pay ASD, Haugen M, et al. Folic acid supplementation, dietary folate intake during pregnancy and risk for spontaneous preterm delivery: a prospective observational cohort study. BMC Pregnancy Childbirth. 2014;14(1):1–12. doi: 10.1186/s12884-014-0375-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Allen LH. Anemia and iron deficiency: effects on pregnancy outcome. Am J Clin Nutr. 2000;71(5):1280S–4S. doi: 10.1093/ajcn/71.5.1280s. [DOI] [PubMed] [Google Scholar]
  • 14.Gebremichael TG, Welesamuel TG. Adherence to iron-folic acid supplement and associated factors among antenatal care attending pregnant mothers in governmental health institutions of Adwa town, Tigray, Ethiopia: cross-sectional study. PLoS ONE. 2020;15(1):e0227090. doi: 10.1371/journal.pone.0227090. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Gebremariam AD, Tiruneh SA, Abate BA, Engidaw MT, Asnakew DT. Adherence to iron with folic acid supplementation and its associated factors among pregnant women attending antenatal care follow up at Debre Tabor General Hospital, Ethiopia, 2017. PLoS ONE. 2019;14(1):e0210086. doi: 10.1371/journal.pone.0210086. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Birhanu TM, Birarra MK, Mekonnen FA. Compliance to iron and folic acid supplementation in pregnancy, Northwest Ethiopia. BMC Res Notes. 2018;11(1):1–5. doi: 10.1186/s13104-018-3433-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Dessie MA, Zeleke EG, Workie SB, Berihun AW. Folic acid usage and associated factors in the prevention of neural tube defects among pregnant women in Ethiopia: cross-sectional study. BMC Pregnancy Childbirth. 2017;17(1):1–8. doi: 10.1186/s12884-017-1506-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Kassa ZY, Awraris T, Daba AK, Tenaw Z. Compliance with iron folic acid and associated factors among pregnant women through pill count in Hawassa city, South Ethiopia: a community based cross-sectional study. Reproductive health. 2019;16(1):1–8. doi: 10.1186/s12978-019-0679-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Demis A, Geda B, Alemayehu T, Abebe H. Iron and folic acid supplementation adherence among pregnant women attending antenatal care in North Wollo Zone northern ethiopia: institution based cross-sectional study. BMC Res Notes. 2019;12(1):1–7. doi: 10.1186/s13104-019-4142-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Gebreamlak B, Dadi AF, Atnafu A. High adherence to iron/folic acid supplementation during pregnancy time among antenatal and postnatal care attendant mothers in Governmental Health Centers in Akaki Kality sub City, Addis Ababa, Ethiopia: hierarchical negative binomial poisson regression. PLoS ONE. 2017;12(1):e0169415. doi: 10.1371/journal.pone.0169415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Tadesse AW, Aychiluhm SB, Mare KU. Individual and community-level determinants of Iron-folic acid intake for the recommended period among pregnant women in Ethiopia: a multilevel analysis. Heliyon. 2021;7(7):e07521. doi: 10.1016/j.heliyon.2021.e07521. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Barrere B, Fishel J, McInturff S, Pullum T, Reinis K, Rutstein S et al. The Demographic and Health Surveys (DHS) program. 2014.
  • 23.Adane B, Fisseha G, Walle G, Yalew M. Factors associated with postnatal care utilization among postpartum women in Ethiopia: a multi-level analysis of the 2016 Ethiopia demographic and health survey. Archives of Public Health. 2020;78(1):1–10. doi: 10.1186/s13690-020-00415-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Yalew M, Adane B, Kefale B, Damtie Y. Individual and community-level factors associated with unmet need for contraception among reproductive-age women in Ethiopia; a multi-level analysis of 2016 Ethiopia demographic and Health Survey. BMC Public Health. 2020;20(1):1–9. doi: 10.1186/s12889-020-08653-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Taye B, Abeje G, Mekonen A. Factors associated with compliance of prenatal iron folate supplementation among women in Mecha district, Western Amhara: a cross-sectional study. Pan Afr. Med. J. 2015;20(1). [DOI] [PMC free article] [PubMed]
  • 26.Agegnehu G, Atenafu A, Dagne H, Dagnew B. Adherence to iron and folic acid supplement and its associated factors among antenatal care attendant mothers in Lay Armachiho health centers, Northwest, Ethiopia, 2017. Int J Reprod Med.. 2019;2019. [DOI] [PMC free article] [PubMed]
  • 27.Nasir BB, Fentie AM, Adisu MK. Adherence to iron and folic acid supplementation and prevalence of anemia among pregnant women attending antenatal care clinic at Tikur Anbessa Specialized Hospital, Ethiopia. PLoS ONE. 2020;15(5):e0232625. doi: 10.1371/journal.pone.0232625. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Boti N, Bekele T, Godana W, Getahun E, Gebremeskel F, Tsegaye B et al. Adherence to Iron-Folate supplementation and associated factors among Pastoralist’s pregnant women in Burji districts, Segen area People’s zone, southern Ethiopia: community-based cross-sectional study. Int J Reprod Med. 2018;2018. [DOI] [PMC free article] [PubMed]
  • 29.Mithra P, Unnikrishnan B, Rekha T, Nithin K, Mohan K, Kulkarni V, et al. Compliance with iron-folic acid (IFA) therapy among pregnant women in an urban area of south India. Afr Health Sci. 2014;14(1):255–60. doi: 10.4314/ahs.v14i1.39. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Dinga LA. Factors associated with adherence to iron/folate supplementation among pregnant women attending antenatal clinic at Thika District Hospital in Kiambu County. Kenya: University of Nairobi; 2013. [Google Scholar]
  • 31.Gebremedhin S, Samuel A, Mamo G, Moges T, Assefa T. Coverage, compliance and factors associated with utilization of iron supplementation during pregnancy in eight rural districts of Ethiopia: a cross-sectional study. BMC Public Health. 2014;14(1):1–8. doi: 10.1186/1471-2458-14-607. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Gebre A, Mulugeta A, Etana B. Assessment of factors associated with adherence to iron-folic acid supplementation among urban and rural pregnant women in North Western Zone of Tigray, Ethiopia: comparative study. Int J Nutr Food Sci. 2015;4(2):161. doi: 10.11648/j.ijnfs.20150402.16. [DOI] [Google Scholar]
  • 33.Workineh Y, Semachew A, Ayalew E, Temesgen WA. Compliance to Iron-Folic Acid Supplementation and Its Association with the Number of ANC Visits in Ethiopia: Systematic Review and Meta-Analysis. Adv Prev Med. 2019;2019. [DOI] [PMC free article] [PubMed]
  • 34.Sununtnasuk C, Fiedler J, D’Agostino A. Iron-folic Acid Distribution and Consumption through Antenatal Care: Identifying Barriers across Countries. European J. Nutr. Food Saf. 2015:524–5. [DOI] [PMC free article] [PubMed]
  • 35.Grieger JA, Clifton VL. A review of the impact of dietary intakes in human pregnancy on infant birthweight. Nutrients. 2015;7(1):153–78. doi: 10.3390/nu7010153. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Sendeku FW, Azeze GG, Fenta SL. Adherence to iron-folic acid supplementation among pregnant women in Ethiopia: a systematic review and meta-analysis. BMC Pregnancy Childbirth. 2020;20(1):1–9. doi: 10.1186/s12884-020-2835-0. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.


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