Skip to main content
Download PDF

Spatial variation and determinants of childhood anemia among children aged 6 to 59 months in Ethiopia: further analysis of Ethiopian demographic and health survey 2016

BMC Pediatrics volume 21, Article number: 497 (2021) Cite this article

Abstract

Background

The magnitude of childhood anemia was increased from time to time. Thus, Even if the Ethiopian government applied tremendous efforts, anemia in children continues as a major public health problem. There is limited evidence on the spatial variation of and determinant factors of childhood anemia at the national level. Therefore, this study aimed to explore spatial distribution and determinants of anemia among children aged 6 to 59 months in Ethiopia.

Method

A stratified two-stage cluster sampling technique was used in Ethiopian Demographic Health Survey 2016 data. In this study 8602 children aged 6–59 months were included. Bernoulli model was used to explore the presence of purely spatial clusters of Anemia in children in age 6–59 months using Sat scan. ArcGIS version 10.3 was used to know the distribution of anemia cases across the country. A mixed-effects Logistic regression model was used to identify determinant factors of anemia.

Results

The finding indicates that the spatial distribution of childhood anemia was non-random in the country with Moran’s I: 0.65, p < 0.001. The SaT scan analysis identified a total of 180 significant primary clusters located in the Somali and Afar regions (LLR = 14.47, P-value< 0.001, RR = 1.47). Age of child 12–23 months (AOR = 0, 68, 95%CI: 0.55, 0.85), 24–35 months (AOR = 0.38, 95%CI: 0.31, 0.47), and36–47 months (AOR = 0.25, 95%CI, 0.20, 0.31), working mother (AOR = 0.87, 95%CI: 0.76, 0.99), anemic mother (AOR = 1.53, 95%CI, 1.35, 1.73), had fever in the last 2 weeks (AOR = 1.36,95%CI:1.13, 1.65), moderate stunting (AOR = 1.31,95%CI: 1.13, 1.50),Severely stunting (AOR = 1.82,95%CI: 1.54, 2.16), religion, wealth index, and number of under-five children in the household were statistically significant associated with childhood anemia.

Conclusion

Spatial variation of childhood anemia across the country was non-random. Age of the child, wealth index, stunting, religion, number of under-five children in the household, fever in the last 2 weeks, anemic mother, and working status of the mother were determinants of childhood anemia. Therefore, interventions should be a priority concern for high-risk (hot spot) areas regarding allocation of resources and improved access to health facilities, and to reduce the consequence of anemia among the generation policymakers and concerned bodies should be implemented these specific determinant factors.

Peer Review reports

Background

Anemia is a disease that is characterized by a decreased number of red blood cells or hemoglobin levels that result in the insufficient oxygen-carrying capacity of blood to meet the cellular metabolic demand of the body [1]. Iron deficiency is the major cause of anemia and there are also other causes of anemia like, nutritional deficiency, acute and chronic inflammations that affect the synthesis of hemoglobin and production [1, 2].

Globally, anemia affects more than 27% of the world’s population which is nearly 1.93 billion. However, there is a high burden of anemia cases in low and middle-income countries which is more than 89% [3]. Among the global burden of anemia two-third of under-five/ preschool children in Africa and southeast Asia were anemic [4]. On the other hand, according to World Health Organization (WHO) 2017 report, the global prevalence of anemia in under-five children was 41.7% whereas in the Africa region was 59% [5]. In sub-Saharan Africa including Ethiopia, the national prevalence of anemia among under five or preschool children was above 40% [6,7,8]. For example, in Ethiopia, the prevalence of anemia was persistently increased among 6–59 months of children from 44% in 2011 to 56% in 2016 within 5 years [6, 7].

World Health Organization defined as anemia is a major public health problem when prevalence is above 40% and Therefore, anemia is a worldwide public health problem that affects both developing and developed countries [4]. It increased mortality and morbidity of human health as well as poor social and economic development [4]. It occurs in all population groups of a human beings. However, children and pregnant women were the more risk age groups for anemia. The result of anemia in children is very severe and complicated like increasing child mortality, impaired cognitive and physical development [2, 4]. Previous various factors were associated with childhood anemia. For example, household wealth index [9,10,11,12,13], Family size [14,15,16], giving more diversified diet [12, 17, 18], stunting [7,8,9,10, 12, 14, 19], malaria infection [10, 11, 20], anemic mothers [13, 16, 19] history of diarrhea [12, 21], and history of fever [11, 13, 18] were determinant factors of childhood anemia.

Even though the Ethiopian government and different partners applied tremendous efforts to control the disease, anemia in under 5 years of children continues as a major public health problem [18]. As you know still anemia is a high burden of disease among under-five children and it varies from country to country, region to region. Identifying geographical variations of anemia among children is very important to prioritize and design targeted prevention and intervention programs to reduce the burden of anemia among children at the national level. Therefore, understanding the spatial variation and determinants of anemia among this group of children is important to design effective interventions and to manage program resources fairly.

Identifying and handling factors of childhood anemia is very important to reduce the prevalence of childhood anemia and allocate resources fairy and give more emphasis for regions that had a high distribution of childhood anemia for a better outcome. Thus, this study is designed to assess spatial distribution and determinants of anemia among children aged 6 to 59 months in Ethiopia. The conceptual frame work is described in detail (Fig. 1).

Fig. 1
figure 1

Conceptual framework of the study adopted from kinds of literature [9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25]

Full size image

Method

Study area and data source

The Ethiopian Demographic and Health Survey (EDHS) is a community-based cross-sectional study conducted from 18 January to 27 June 2016. The study was conducted in Ethiopia (3o-14o N and 33o - 48°E), situated at the eastern horn of Africa (Fig. 2). The country covers 1.1 million square kilometers and has a great geographical diversity, which ranges 4550 m above sea level down to the Afar depression to 110 m below sea level [26]. There are nine regional states and two city administrations subdivided into 68 zones, 817 districts, and 16,253 kebeles (lowest local administrative units of the country in the administrative structure of the country) [7]. The source of the data for this study was the Ethiopian Demographic and Health Survey (EDHS) 2016 (N = 7794) and used to assess the spatial variation and determinants of childhood anemia among children age 6–59 months in Ethiopia.

Fig. 2
figure 2

Map of Study Area

Full size image

Sample size determination and sampling procedure

EDHS used a two-stage cluster sampling technique. Since Ethiopia has 9 regional states and 2 administrative cities. Administratively, regions in Ethiopia are divided into zones, and zones, into administrative units called woreda. Each woreda is further subdivided into the lowest administrative unit, called kebeles. During the 2007 census, each kebele was subdivided into census enumeration areas (EA), which were convenient for the implementation of the census [7].

A stratified two-stage cluster sampling procedure was employed where EA is the sampling unit for the first stage and households for the second stage. In 2016 EDHS, a total of 645 EAs (202 in urban areas and 443 in rural areas) were selected with probability proportional to EA size (based on the 2007 housing and population census) and with independent selection in each sampling stratum. Of this 18,008 households were included. A total of 8602 children were interviewed. But in the present study, a total of 7794 children the age of 6–59 months were included in the analysis. The source population was all births from reproductive-age women within 5 years before the survey in Ethiopia and all births from reproductive-age women in the selected enumeration areas within 5 years before the survey were the study population. Birth’s from reproductive age women within 5 years before the survey within enumeration areas with missed global positioning system (GPS) cells were excluded for spatial analysis.

Outcome variable

The outcome variable for this study was anemia, which was dichotomized as anemic and not anemic. Individuals are considered to be not anemic was defined as Adjusted concentration of blood hemoglobin greater than or equal to 11 mg/dl and those individuals with less than 11 mg/dl were anemic [1]. Anemia status was determined based on hemoglobin concentration in blood adjusted to the altitude.

Independent variables

The independent variables were classified as: socio-demographic factors, nutritional factors, clinical factors, and service-related factors.

The socio-demographic factors were the sex of a child, age of child, residence, educational status of the mother, maternal age, husband’s educational status, the religion of mother, wealth index, working status of the mother, and a number of children in the household. The nutritional factors were stunting status of a child, wasting status of child, and size of child at birth. The clinical factors were also maternal anemic status, diarrhea in a child in the last 2 weeks, fever in a child in the last 2 weeks, and cough in a child in the last 2 weeks and the service-related factors were taking of vitamin A in the last 6 months, taking of iron pills or sprinkles or syrup and taking of drugs for intestinal parasites in the last 6 months.

Data management and statistical analysis

Descriptive and summary statistics were done using STATA version 14 after extraction and edition of data from EDHS 2016 child data set. Since EDHS data had hierarchical and clustering nature, the assumption of independence among observations was violated. This implies a need to consider the between-cluster variability by using advanced models. The goodness of fit test was checked using Intraclass correlation (ICC) and deviance [27]. So logistic regression (non-anemic child = 0, anemic child = 1), and GLMM (generalized linear mixed model) were fitted. Then the GLMM was selected based on the result of Akaikie Information Criteria (AIC) and Bayesian information criteria (BIC). The model with the smallest AIC value was chosen. Variables having a p-value up to 0.2 in the bi-variable analysis were selected to fit the model in the multi-variable analysis. Finally, a p-value less than 0.05 in the multivariable model of mixed-effects logistic regression was used to select variables that had a statistically significant association with anemia.

Spatial autocorrelation

ArcGIS version 10.3 was used for Moran’s I analysis. The Global Moran’s I spatial statistic measures were used to measure spatial autocorrelation by taking the total data set and producing a single output value that ranges from − 1 to+ 1. Global Moran’s I value closes to − 1 which indicates dispersed childhood anemia, whereas Moran’s I value closest to + 1 indicted clustered childhood anemia and the Moran’s I value is 0 which indicates randomly distributed childhood anemia. Moran’s I (P-value < 0.05) indicates the presence of spatial autocorrelation.

Hot spot analysis (Getis-OrdGi* statistic)

Getis-OrdGi* statistics were computed to measure how spatial autocorrelation varies over the study location by calculating GI* statistics for each area. Z-score is computed to determine the statistical significance of clustering, and the p-value is computed for the significance [28]. Statistical output with high GI* indicates “hotspot” whereas low GI* means a “cold spot [29,30,31].

Spatial interpolation

It is very difficult and expensive in terms of resources and time to collect reliable data in all areas of the country to know the burden of a certain event. Therefore, part of a certain area can be predicted by using observed data using a method called interpolation. The spatial interpolation technique is used to predict childhood anemia in the un-sampled areas in the country based on sampled EAs. There are different deterministic and geostatistical interpolation methods. Among those methods, ordinary Kriging and empirical Bayesian Kriging are considered the best method since it incorporates the spatial autocorrelation and it statistically optimizes the weight [32]. The ordinary Kriging spatial interpolation method was used for this study for predictions of childhood anemia in unobserved areas of Ethiopia.

Disease cluster detection and spatial scan statistical analysis

Spatial scan statistical analysis was employed to test for the presence of statistically significant spatial hotspots/clusters of childhood anemia using Kuldorff’s SaT Scan version 9.6 software. The spatial scan statistic uses a scanning window that moves across the study area. Children with anemia were taken as cases and without it as controls to fit the Bernoulli model. The numbers of cases in each location had Bernoulli distribution and the model required data for cases, controls, and geographic coordinates. The default maximum spatial cluster size of < 50% of the population was used, as an upper limit, which allowed both small and large clusters to be detected and ignored clusters that contained more than the maximum limit.

For each potential cluster, a likelihood ratio test statistic and p-value were used to determine if the number of observed childhood anemia within the potential cluster was significantly higher than expected or not. The primary and secondary clusters are identified and assigned p-values and ranked based on their likelihood ratio test, based on 999 Monte Carlo replications.

Result

Socio-demographic characteristics

The EDHS of 2016 includes 8602 children aged 6 to 59 months in the survey. Among these children, 7815(90.8%) were granted the consent statement for hemoglobin. Of the total of 7815 children whose consent statement is granted, the hemoglobin level was determined for 7794 children which gives a 90.6% response rate of the study. Their mean age was found to be 32 months (SD ± 0.18 months). Almost half, 48.6%, of the children were females. The Majority of study participants, 83%, had rural residency. Regarding the educational status of their mothers, two-third (65%) of mothers had no formal education (Table 1).

Table 1 A Socio-demographic characteristic of the children aged 6 to 59 months and their parents in Ethiopia from January 18 to June 27 in 2016 (N = 7794)
Full size table

Spatial distribution of childhood anemia in Ethiopia

A total of 622 clusters were considered for spatial analysis of childhood anemia. The red color indicates a high proportion of childhood anemia whereas the green color indicates a low proportion of childhood anemia. A high proportion of childhood anemia occurred in southwest Somali, the eastern and southern part of Oromia, south Afar, Hareri Northern part of Gambella, and Dire Dawa whereas a low proportion of childhood anemia were aggregated in Amhara, Addis Ababa, west of SNNP, and east of Benshangul (Fig. 3).

Fig. 3
figure 3

Spatial distribution of childhood anemia in Ethiopia, 2016

Full size image

Spatial autocorrelation

The analysis of spatial autocorrelation indicated that the spatial distribution of childhood anemia was non-random in Ethiopia. The Global Moran’s I value 0.14 (p-value < 0.0001) indicated that there was significant clustering of childhood anemia in the study area (Fig. 4).

Fig. 4
figure 4

Spatial autocorrelation of childhood anemia in Ethiopia, 2016

Full size image

Hot and cold spot analysis of childhood anemia in Ethiopia

In the Getis OrdGi statistical analysis, significant hotspot areas (high risk of childhood anemia) were aggregated in North and south Eastern part of Somali, Northwest and Sothern part of Afar, Northern part of Gambella, Dire Dawa, and Hareri, while the cold spot areas (low-risk childhood anemia) were found southwest Amhara, Addis Ababa, North West SNNPR and North and South part of Beneshangul Gumuz (Fig. 5).

Fig. 5
figure 5

Hot and cold spot analysis of childhood anemia in Ethiopia, 2016

Full size image

The spatial interpolation analysis result

The spatial ordinary kriging interpolation analysis predicted high-risk regions for childhood anemia. Predication of high-risk areas was indicated by red predictions. West and eastern part of Somali, the eastern part of Amhara, South East Tigray, Eastern and Southern afar, Harari, and Dire Dawa regions were predicted as more risky areas compared to other regions. To the opposite of this North West Amhara, Addis Ababa, South West Oromia, and Benshangul Gumuz regions were predicated as having the least risk for anemia (Fig. 6).

Fig. 6
figure 6

Spatial interpolation of childhood anemia in Ethiopia, 2016

Full size image

Spatial SaT scan analysis of childhood anemia (Bernoulli based model)

A total of 6 clusters with 70 significant enumeration areas were identified and there are two most likely primary clusters and 4 secondary clusters. The primary clusters spatial window encompasses North West of part Oromia, Harari, Dire Dawa, North West Somali, and entire and North West Afar regions. It was centered at .775278 N, 37.939392 E) / 0 km radius and 11.195383 N, 39.269363 E) / 9.21 km, with a relative risk (RR) of 1.67 and Log-Likelihood ratio (LLR) of 16.36 and 13.29, at p-value < 0.001. The RR of 1.67 for clusters spatial window means children within the spatial window had a 67% increased risk of anemia than children outside the window (Fig. 7) (Table 2).

Fig. 7
figure 7

Spatial SaT Scan analysis of childhood anemia in Ethiopia, 2016

Full size image
Table 2 Sat Scan analysis of significant clusters of childhood anemia in Ethiopia among children aged 6 to 59 months, 2016
Full size table

Factors associated with childhood anemia

The null model, variance component analysis was performed to decompose the total variance of childhood anemia. The cluster-level variance which shows the total variance of childhood anemia that can be attributed to the context of the community (cluster) in which the child was living was estimated. The applicability of the multi-level mixed-effects logistic regression model in the analysis was justified by the significance of the community-level variance [community variance = 1.24; standard error (SE) =0.089; P-value = 0.001], indicating the existence of significant differences between communities (clusters) regarding the childhood anemia. This was supported by the ICC value (ICC = 0.12) which revealed that 12% of the total variance of childhood anemia in Ethiopia can be attributed to the context of the communities. Since it was above the cut of point.

According to mixed-effects logistic regression analysis age of child, religion, wealth index, mother’s current working status, maternal anemic status, number of under-five children in the household, fever in the last 2 weeks, and stunting remained statistically significant variables for anemia in children aged 6 to 59 months.

The odds of developing anemia in children whose age was between 12 and 23, 24–35, 36–47 and 48–59 months is lower by 32% (AOR =0.68, 95%CI = 0.55–0.85), 62% (AOR = 0.38, 95%CI = 0.31–0.47), 75% (AOR = 0.25, 95%CI = 0.2–0.31) and 84% (AOR = 0.16, 95%CI = 0.13–0.20) respectively as compared with those whose age was between 6 and 11 months.

The odds of developing anemia in children having Muslim mother is 2.07 times (AOR = 2.07, 95%CI = 1.75–2.46) that of children having Orthodox mother. Regarding the wealth index, The odds of developing anemia in children with family wealth index of poor, middle, richer and richest is lower by 26% (AOR =0.74, 95%CI = 0.63–0.88), 40% (AOR =0.60, 95%CI = 0.50–0.72), 35% (AOR = 0.65, 95%CI = 0.53–0.79) and 43% (AOR = 0.57, 95%CI = 0.43–0.74) as compared with those with family wealth index of poorest.

Children whose mother was currently working are lower by 13% (AOR =0.87(95%CI = 0.76–0.99) developing childhood anemia than their counterparts. Regarding maternal anemia status, children whose mother was anemic is 1.53 times (AOR =1.53, 95%CI = 1.35–1.73) more likely to develop anemia as compared to children whose mother is free from an anemic.

The odds of developing anemia in children whose household had three or more under-five children is 1.19 times (AOR = 1.19, 95%CI = 1.03–1.38) that of children whose household had one or two under-five children.

Children who had a fever within the last 2 weeks preceding the interview are 1.36 times (AOR =1.36, 95%CI = 1.13–1.65) more likely to develop childhood anemia as compared to those who had no fever within the last 2 weeks.

The odds of developing anemia in a child who had moderate and severe stunting is 1.30 (AOR = 1.30, 95%CI = 1.13–1.50) and 1.82 (AOR = 1.82, 95%CI = 1.54–2.16) times that of those who had no stunting (Table 3).

Table 3 i-variable and multi-variable mixed-effects logistic regression analysis for determinants of anemia among children aged 6 to 59 months in Ethiopia from January 18 to June 27 in 2016 (N = 7794)
Full size table

Discussion

The purpose of this study is to investigate spatial variation and determinants of childhood anemia aged 6 to 59 months in Ethiopia by using 2016 EDHS data. The spatial variation of childhood anemia was non-random across the country with Global Moran’s I 0.65 (p-value < 0.0001). This indicated that there was significant clustering of childhood anemia in Ethiopia. The Purely Spatial Sat Scan analysis identified primary and secondary significant clusters of childhood anemia.

Different methods of spatial analysis most consistently demonstrate anemia high risk and low-risk regions. The hotspot areas (high risk of childhood anemia) were aggregated in the North and southeastern part of Somali, North West and Sothern part of Afar, Northern part of Gambella, Dire Dawa, and Hareri. Whereas the most significant clusters were North West of part Oromia, Harari, and Dire Dawa, North West Somali, and entire and North West Afar regions. Regional differences in feeding habits, the distribution of infectious diseases, and the availability and access to use maternal and child health care services could be the most important reasons for the result of regional variability of childhood anemia in our country [33]. Geographic variation is the risk of anemia and dynamics of the soil content of minerals since the identified high-risk regions were categorized to Eastern and South-Eastern parts of the country. Meaning high-risk regions share similar environmental conditions as evidenced by boundary formation to each other. In addition, epidemiological factors such as fever and stunting which are identified as determinants of anemia in different studies including our studies were more common in some regions. Similarly, the finding from Nigeria showed a distinct North-South divide in the Hemoglobin concentration of the children and that states in the Northern part possess a higher risk of anemia [11]. Furthermore, our finding is also supported by the study conducted in sub-Saharan Africa which concludes that the distribution of anemia is driven by large-scale environmental factors [8]. These all imply that the dynamics of the mineral content of the soil is the most probable explanation for observed geographical variation in the risk of anemia.

According to mixed-effect logistic regression, age of the child, the religion of mother, wealth index, mother’s current working status, maternal anemic status, number of under-five children in the household, fever in the last 2 weeks, and stunting were statistically significant factors childhood anemia in Ethiopia.

Age is one of the most important predictors of childhood anemia. The odds of developing childhood anemia in children whose age was between 12 and 23, 24–35, 36–47 and 48–59 months is lower by 32, 62, 75, and 84% respectively as compared with those whose age was between 6 and 11 months. This finding is consistent with several studies around the world [9, 10, 12,13,14,15,16,17, 19,20,21,22,23]. This is due to a wide gap between high iron demand for fast growth [4] and low iron supply because of inappropriate initiation of complementary feeding [12, 34] and the highest depletion of the prenatal iron store starting at 6 months of age [35]. Furthermore, children’s age more than 12 months commonly consume a variety of foods that contain iron contents like meat, fish, poultry, and cereals [36]. In addition, different infectious diseases like intestinal helminths are very common in younger children because they might ingest contaminated things into their mouths compared to older ones, particularly children living in an unsanitary environment [37, 38]. All these reasons in turn younger age which is less than 12 months more prone to anemia.

Wealth index was a determinant factor of childhood anemia in Ethiopia The odds of developing anemia in a child with family wealth index of poor, middle, richer, and richest was lower by 25.8, 40.4, 35.2, and 43.3% compared with those with family wealth index of poorest, respectively. The finding is supported by studies conducted in Brazil [9, 13], Nigeria [11], and Ethiopia [10, 12]. Evidence suggested that children from lower socioeconomic status are susceptible to various nutritional disorders like anemia, as well as prone to easily preventable diseases [39,40,41]. That is why children from the poorest families are less likely to provide a balanced diet because no capability to afford and utilized diversified foods and they are prone to poor health conditions that cause anemia like parasitic infections [4, 42].

The odds of developing anemia in a child whose mother was currently working is lower by 13.3% as compared with those whose mother was currently not working. This finding was consistent with the previous study conducting Ethiopia [16]. The possible reason could be increased empowerment of working mothers to care for their children and other health-related actions [43, 44]. Therefore, working mothers are exposed to different health education regarding child caring and they know the impact of disease very well.

Maternal anemia is also another important factor of childhood anemia. The odds of having anemia in children whose mother was anemic is 1.53 times as compared to their counterparts. The result is in line with findings in Cuba [19], Burma [13], and Ethiopia [16]. This is the fact that maternal anemia can be a risk factor for the development of childhood anemia [45]. It is explained by the influence of poor maternal iron reserve during pregnancy and breastfeeding on the iron store of their child [46, 47]. Besides, maternal anemia increases the risk of maternal death, preterm birth, and low birth weight [48, 49]. This leads to children being more prone to develop anemia.

The odds of developing anemia in children whose household had three or more under-five children is 1.19 times that of children whose household had one or two under-five children. This result was concordant with previous studies conducted in Brazil [14], Lao People’s Democratic Republic [15], and Ethiopia [16]. The possible reason could be when the number of under-five children increases has an impact on health problems due to competition for foods, getting appropriate health care services this also leads to infections and cross contaminations [50]. This might worsen the quality of care for children, and increase the risk of anemia.

Fever is also one of the determinants of childhood anemia. The odds of developing anemia in children who had a fever within the last 2 weeks preceding the interview is 1.36 times that of children who had no fever within the last 2 weeks. This finding is consistent with studies conducted in Burma [13], Nigeria [11], and Southern Ethiopia [18]. This could be a fever in children that can be caused by different infectious diseases like malaria, septicemia, tuberculosis, and kalazar that cause anemia by infecting and destructing red blood cells or by different mechanisms [51].

Children with moderate or severe stunting were 1.30 and 1.82 times more likely to have anemia than children who were not stunted. This result is in agreement with previous studies conducted in Burma [13], Kenya [20], and Ethiopia [10, 12, 16,17,18, 24]. Pathophysiological explanation implies reverse causation between stunting and anemia. In malnourished children, gastrointestinal epithelium disturbance leads to the development of anemia by impairing the absorption of nutrients [51]. on the other hand, anemia during the period of rapid growth leads to irreversible growth retardation [4, 46], coexist with other micronutrient deficiencies, and stunting may increase the development of anemia by a synergism association. The problem of anemia continues to be a public health challenge in these countries, particularly in Africa, with serious consequences for the most vulnerable populations such as children and pregnant women. Therefore, to reduce childhood anemia in different settings policies and programs for anemia control should account for the spatial heterogeneity of anemia.

Strength and limitations of the study

The strengths of this study, first, the study was based on nationally representative weighted data and can be generalized at the national level. Second, the use of spatial analysis to explore the spatial variation and significant hotspot areas of childhood anemia and using the mixed-effect advanced model to get a real estimate. The limitation of this study is some variables there is retrospective nature so mothers were asked to remember events that happen in the past which leads to recall bias and it is secondary data collected at appoint in time so doesn’t show temporal relationship.

Conclusion

This study found that childhood anemia was not random in Ethiopia. High-risk areas for childhood anemia were found in West of part Oromia, Harari, Dire Dawa, North West Somali, and entire and North West Afar regions of the country. Anemia is a major public health problem in Ethiopia in under-five children. In general, age of child, wealth index, mother’s current working status, maternal anemic status, number of under-five children in the household, fever in the last 2 weeks, and stunting were variables that had achieved statically significant association for childhood anemia. Therefore, high-risk areas for childhood anemia needs to be given priority and targeted with interventions to reduce the burden of childhood anemia in under-five children.

Availability of data and materials

All relevant data are publically available and here is the link to the Ethiopian Demographic and Health Survey 2016 data and you can access the data by clicking the following link https://dhsprogram.com/data/dataset/Ethiopia_Standard-DHS_2016.cfm?flag=0

Abbreviations

AIC:

Akaikie Information Critreia

AOR:

Adjusted Odds Ratio

BIC:

Bayesian Information Criteria

COR:

Crude Odds Ratio

EDHS:

Ethiopian Demographic and Health Survey

ICC:

Intra Class Correlation

LLR:

Log Likelihood Ratio test

References

  1. WHO V. Haemoglobin concentrations for the diagnosis of anaemia and assessment of severity. Geneva: Vitamin and Mineral Nutrition Information System, WHO; 2011.

    Google Scholar 

  2. Organization WH. Assessing the iron status of populations: report of a joint World Health Organization/Centers for Disease Control and Prevention technical consultation on the assessment of iron status at the population level. Geneva: World Health Organization; 2007.

    Google Scholar 

  3. Kassebaum NJ, Collaborators GA. The global burden of anemia. Hematol Oncol Clin North Am. 2016;30(2):247–308.

    Article  PubMed  Google Scholar 

  4. Benoist Bd, McLean E, Egll I, Cogswell M. Worldwide prevalence of anaemia 1993-2005: WHO global database on anaemia. 2008. p. 4–7.

  5. Organization WH. Global Health Observatory data repository: prevalence of anaemia in women Accessed 2 May 2018 http://apps.who.int/gho/data/viewmainGSWCAH28REG; 2016.

  6. Agency C. Ethiopia Demographic and Health Survey Addis Ababa. USA: Ethiopia ICF International Calverton; 2011.

  7. Agency CS. Ethiopian demographic and health survey 2016. Addis Ababa, Ethiopia, and Rockville, Maryland, USA CSA and ICF: Key Indicators Report; 2016.

    Google Scholar 

  8. Magalhães RJS, Clements AC. Spatial heterogeneity of haemoglobin concentration in preschool-age children in sub-Saharan Africa. Bull World Health Organ. 2011;89(6):459–68.

    Article  Google Scholar 

  9. Cardoso MA, Scopel KK, Muniz PT, Villamor E, Ferreira MU. Underlying factors associated with anemia in Amazonian children: a population-based, cross-sectional study. PLoS One. 2012;7(5):e36341.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Gari T, Loha E, Deressa W, Solomon T, Atsbeha H, Assegid M, et al. Anaemia among children in a drought affected community in south-Central Ethiopia. PLoS One. 2017;12(3):e0170898.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Gayawan E, Arogundade ED, Adebayo SB. Possible determinants and spatial patterns of anaemia among young children in Nigeria: a Bayesian semi-parametric modelling. Int Health. 2014;6(1):35–45.

    Article  PubMed  Google Scholar 

  12. 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;2015:928632.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Zhao A, Zhang Y, Peng Y, Li J, Yang T, Liu Z, et al. Prevalence of anemia and its risk factors among children 6–36 months old in Burma. Am J Trop Med Hyg. 2012;87(2):306–11.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Gondim SSR, Diniz AS, RAd S, RGdS B, ECd A, AdA P. Magnitude, time trends and factors associate with anemia in children in the state of Paraíba, Brazil. Rev Saude Pub. 2012;46(4):649–56.

    Article  Google Scholar 

  15. Kounnavong S, Sunahara T, Hashizume M, Okumura J, Moji K, Boupha B, et al. Anemia and related factors in preschool children in the southern rural Lao People’s Democratic Republic. Trop Med Health. 2011;39(4):95–103.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Muchie KF. Determinants of severity levels of anemia among children aged 6–59 months in Ethiopia: further analysis of the 2011 Ethiopian demographic and health survey. BMC Nutrition. 2016;2(1):51.

    Article  Google Scholar 

  17. Gebreegziabiher G, Etana B, Niggusie D. Determinants of anemia among children aged 6–59 months living in Kilte Awulaelo Woreda, Northern Ethiopia. Hindawi J Anemia. 2014:1–6.

  18. Tiku YS, Mekonnen TC, Workie SB, Amare E. Does Anaemia have major public health importance in children aged 6–59 months in the Duggina Fanigo District of Wolaita zone, southern Ethiopia? Ann Nutr Metab. 2018;72(1):3–11.

    Article  PubMed  Google Scholar 

  19. 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(1):16–23.

    Article  PubMed  Google Scholar 

  20. Foote EM, Sullivan KM, Ruth LJ, Oremo J, Sadumah I, Williams TN, et al. Determinants of anemia among preschool children in rural, western Kenya. Am J Trop Med Hyg. 2013;88(4):757–64.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Semedo RM, Santos MM, Baião MR, Luiz RR, da Veiga GV. Prevalence of anaemia and associated factors among children below five years of age in Cape Verde, West Africa. J Health Popul Nutr. 2014;32(4):646.

    PubMed  PubMed Central  Google Scholar 

  22. Dey S, Goswami S, Dey T. Identifying predictors of childhood anaemia in North-East India. J Health Popul Nutr. 2013;31(4):462.

    PubMed  PubMed Central  Google Scholar 

  23. Konstantyner T, Roma Oliveira TC, de Aguiar Carrazedo Taddei JA. Risk factors for anemia among Brazilian infants from the 2006 National Demographic Health Survey. Anemia. 2012;2012.

  24. Roba KT, O’Connor TP, Belachew T, O’Brien NM. Anemia and undernutrition among children aged 6–23 months in two agroecological zones of rural Ethiopia. Pediatric Health Med Ther. 2016;7:131.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Tengco LW, Rayco-Solon P, Solon JA, Sarol JN Jr, Solon FS. Determinants of anemia among preschool children in the Philippines. J Am Coll Nutr. 2008;27(2):229–43.

    Article  PubMed  Google Scholar 

  26. Ababa A, Calverton E. Central statistical agency (Ethiopia) and ICF international. Ethiopia Demographic and Health Survey: Ethiopia and Calverton; 2011.

    Google Scholar 

  27. Rodriguez G, Elo I. Intra-class correlation in random-effects models for binary data. Stata J. 2003;3(1):32–46.

    Article  Google Scholar 

  28. Zulu LC, Kalipeni E, Johannes E. Analyzing spatial clustering and the spatiotemporal nature and trends of HIV/AIDS prevalence using GIS: the case of Malawi, 1994-2010. BMC Infect Dis. 2014;14(1):285.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Anselin L, Sridharan S, Gholston S. Using exploratory spatial data analysis to leverage social indicator databases: the discovery of interesting patterns. Soc Indic Res. 2007;82(2):287–309.

    Article  Google Scholar 

  30. Krivoruchko K. Empirical bayesian kriging. ArcUser Fall. 2012:6–10.

  31. Naish S, Tong S. Hot spot detection and spatio-temporal dynamics of dengue in Queensland, Australia. Int Arch Photogrammetry Remote Sensing Spatial Inf Sci. 2014;40(8):197.

    Article  Google Scholar 

  32. Bhunia GS, Shit PK, Maiti R. Comparison of GIS-based interpolation methods for spatial distribution of soil organic carbon (SOC). J Saudi Soc Agric Sci. 2018;17(2):114–26.

    Google Scholar 

  33. Woldemichael A, Takian A, Sari AA, Olyaeemanesh A. Inequalities in healthcare resources and outcomes threatening sustainable health development in Ethiopia: panel data analysis. BMJ Open. 2019;9(1):e022923.

    Article  PubMed  PubMed Central  Google Scholar 

  34. Disha A, Tharaney M, Abebe Y, Alayon S, Winnard K. Factors associated with infant and young child feeding practices in Amhara region and nationally in Ethiopia: analysis of Ethiopia demographic and health surveys 2005 and 2011; 2015.

    Google Scholar 

  35. Black MM, Quigg AM, Hurley KM, Pepper MR. Iron deficiency and iron-deficiency anemia in the first two years of life: strategies to prevent loss of developmental potential. Nutr Rev. 2011;69(s1).

  36. Weatherhead JE, Hotez PJ. Worm Infections in Children. Pediatr Rev. 2015;36(8):341–52.

    Article  PubMed  Google Scholar 

  37. Organization WH. Deworming in children 2017.

    Google Scholar 

  38. Moschovis PP, Wiens MO, Arlington L, Antsygina O, Hayden D, Dzik W, et al. Individual, maternal and household risk factors for anaemia among young children in sub-Saharan Africa. BMJ Open. 2018;8(5):1–2.

    Article  Google Scholar 

  39. 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(1):1–12.

    Article  Google Scholar 

  40. Moschovis PP, Wiens MO, Arlington L, Antsygina O, Hayden D, Dzik W, et al. Individual, maternal and household risk factors for anaemia among young children in sub-Saharan Africa: a cross-sectional study. BMJ Open. 2018;8(5):e019654.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Habyarimana F, Zewotir T, Ramroop S. Structured additive quantile regression for assessing the determinants of childhood anemia in Rwanda. Int J Environ Res Public Health. 2017;14(6):652.

    Article  PubMed Central  Google Scholar 

  42. Allen L, Dary O, de Benoist B, Hurrel R. WHO guidelines on food fortification with micronutrients; WHO: Geneva, Switzerland, 2006; 2010.

    Google Scholar 

  43. Datta PB, Gailey R. Empowering women through social entrepreneurship: case study of a women's cooperative in India. Entrepreneurship Theory aPract. 2012;36(3):569–87.

    Article  Google Scholar 

  44. Presser H, Sen G. Women's empowerment and demographic processes: moving beyond Cairo: Oxford University press; 2000.

    Google Scholar 

  45. Shukla AK, Srivastava S, Verma G. Effect of maternal anemia on the status of iron stores in infants: a cohort study. J Fam Community Med. 2019;26(2):118.

    Google Scholar 

  46. Kotecha PV. Nutritional anemia in young children with focus on Asia and India. Indian J Commun Med. 2011;36(1):8.

    Article  Google Scholar 

  47. Pasricha S-R, Black J, Muthayya S, Shet A, Bhat V, Nagaraj S, et al. Determinants of anemia among young children in rural India. Pediatrics. 2010;126(1):e140–e9.

    Article  PubMed  Google Scholar 

  48. Menon KC, Ferguson EL, Thomson CD, Gray AR, Zodpey S, Saraf A, et al. Effects of anemia at different stages of gestation on infant outcomes. Nutrition. 2016;32(1):61–5.

    Article  PubMed  Google Scholar 

  49. Allen LH. Anemia and iron deficiency: effects on pregnancy outcome. Am J Clin Nutr. 2000;71(5):1280S–4S.

    Article  CAS  PubMed  Google Scholar 

  50. Feleke BE. Nutritional status and intestinal parasite in school age children: a comparative cross-sectional study. Int J Pediatr. 2016;2016.

  51. Organization WH. Pocket book of hospital care for children: guidelines for the management of common childhood illnesses: World Health Organization; 2013.

    Google Scholar 

Download references

Acknowledgments

We would like to acknowledge the Ethiopian demographic and health survey staff and major DHS programs for permitting data access.

Funding

The authors received no specific funding for this work.

Author information

Authors and Affiliations

  1. Department of Epidemiology and Biostatistics, Institute of Public Health, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia

    Tiruneh Ayele Jember, Destaw Fetene Teshome & Lemma Derseh Gezie

  2. School of Nursing, College of Medicine and Health Sciences and Comprehensive specialized hospital, University of Gondar, Gondar, Ethiopia

    Chilot Desta Agegnehu

Authors
  1. Tiruneh Ayele Jember
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Destaw Fetene Teshome
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Lemma Derseh Gezie
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Chilot Desta Agegnehu
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

Data curation, formal analysis, resources, software, validation, visualization: Tiruneh Ayele, Destaw Fetene Teshome, Lemma Derseh Gezie, Chilot Desta Agegnehu,

The investigation, Methodology, supervision, conceptualization, analysis, and interpretation writing a detailed review, editing, and preparing manuscript: Tiruneh Ayele, Destaw Fetene Teshome, Lemma Derseh Gezie, Chilot Desta Agegnehu. Finally all the authors approved the final manuscript.

Corresponding author

Correspondence to Chilot Desta Agegnehu.

Ethics declarations

Ethics approval and consent to participate

Our study was based on secondary data from Ethiopian Demographic and Health survey and we have secured the permission letter from major Demographic Health and Survey.

Written consent was obtained from the Measure DHS International Program which authorized the data sets. Permission for data access was obtained from major demographic and health surveys through the online request form http://www.dhsprogram.com. All the data used in this study are publicly available, aggregated secondary data with not having any personal identifying information that can be linked to particular individuals, communities, or study participants.

Consent for publication

It is not applicable.

Competing interests

All authors declare that they have no competing interest final content of the manuscript.

Additional information

Publisher’s Note

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

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Jember, T.A., Teshome, D.F., Gezie, L.D. et al. Spatial variation and determinants of childhood anemia among children aged 6 to 59 months in Ethiopia: further analysis of Ethiopian demographic and health survey 2016. BMC Pediatr 21, 497 (2021). https://doi.org/10.1186/s12887-021-02901-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12887-021-02901-y

Keywords

BMC Pediatrics

ISSN: 1471-2431

Contact us