Next Article in Journal
Oral Care Knowledge, Attitudes, and Practices of Black/African American Caregivers of Autistic Children and Non-Autistic Children
Next Article in Special Issue
Perceptions of Healthcare Providers and Caregivers Regarding Procedures for Early Detection of Developmental Delays in Infants and Toddlers in Saudi Arabia
Previous Article in Journal
Fatigue and Quality of Life in Children with Chronic Kidney Disease
Previous Article in Special Issue
Factors Affecting High-Risk for Diabetes among Korean Adolescents: An Analysis Using the Eighth Korea National Health and Nutrition Examination Survey (2020)
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Individual, Maternal, Household, and Community Level Variability in Determining Inequalities in Childhood Anaemia within Ethiopia: Four-Level Multilevel Analysis Approach

by
Kenenisa Abdisa Kuse
1,
Demie Seyoum Jima
1,
Teshita Uke Chikako
2,
John Elvis Hagan, Jr.
3,4,*,
Abdul-Aziz Seidu
5,6,
Richard Gyan Aboagye
7 and
Bright Opoku Ahinkorah
8
1
Department of Statistics, Bule Hora University, Bule Hora P.O.Box 144, Ethiopia
2
Wondo Genet College of Forestry and Natural Resource, Hawassa University, Hawassa P.O. Box 05, Ethiopia
3
Department of Health, Physical Education, and Recreation, University of Cape Coast, Cape Coast PMB TF0494, Ghana
4
Neurocognition and Action-Biomechanics-Research Group, Faculty of Psychology and Sport Sciences, Bielefeld University, Postfach 10 01 31, 33501 Bielefeld, Germany
5
College of Public Health, Medical and Veterinary Sciences, James Cook University, Townsville, QLD 4811, Australia
6
Centre for Gender, Takoradi Technical University, Takoradi P.O. Box 256, Ghana
7
Department of Family and Community Health, Fred N. Binka School of Public Health, University of Health and Allied Sciences, Ho PMB 31, Ghana
8
School of Public Health, Faculty of Health, University of Technology Sydney, Ultimo, NSW 2007, Australia
*
Author to whom correspondence should be addressed.
Children 2022, 9(9), 1415; https://doi.org/10.3390/children9091415
Submission received: 21 August 2022 / Revised: 8 September 2022 / Accepted: 9 September 2022 / Published: 19 September 2022

Abstract

:
Background: Childhood anaemia is a major public health issue necessitating rapid attention due to its debilitating consequences on the child, family, and society. Previous studies have assessed the prevalence and contributing factors to childhood anaemia in many developing countries. Yet, little is known about the factors that contribute to childhood anaemia in Ethiopia. The study examined the factors associated with inequalities of childhood anaemia in Ethiopia. Methods: Data for the study were extracted from the 2016 Demographic and Health Survey of Ethiopia. A total of 7960 children were considered in the final study. Bivariate and multilevel ordinal logistic regression analyses were used to estimate determinants of inequalities of childhood anaemia status. Results: Overall, the prevalence of mild, moderate, and severe anaemia among the children were 24.5%, 28.4%, and 2.2%, respectively. The child’s age (in months), sex of the child, preceding birth interval (in months), mother’s educational level, antenatal care visit, wealth index of mothers, source of drinking water, type of toilet facility, place of residence, and region were significantly associated with childhood anaemia. The multilevel random coefficient model found that there is a variation of childhood anaemia among women (intra-cluster correlation [ICC] = 15.06%), households (ICC = 15.6%), and communities (ICC = 14.22%) in Ethiopia. Conclusions: This study showed that anaemia is common among Ethiopian children. Factors found to be associated with childhood anaemia were the sociodemographic characteristics of the child and their mothers. We recommend that existing programs and interventions to prevent and reduce childhood anaemia be strengthened. Moreover, a targeted intervention includes deworming, intensified year-round behavior change communication campaigns and testing using digital methods, and point-of-care treatment.

1. Introduction

Anaemia, defined as a decrease in the concentration of circulating red blood cells or in the hemoglobin concentration and a concomitant impaired capacity to transport oxygen [1], is a major public health issue necessitating rapid attention due to the debilitating consequences it has on the individual, family, and their societies [2]. Among children under five, anemia is classified into mild (haemoglobin [Hb] =10.0–10.9 g/dL), moderate (Hb = 7.0–9.9 g/dL), severe (Hb < 7.0 g/dL), and normal (Hb ≥ 11.0 g/dL) Hb level concentration for children aged 6 to 59 months [2]. Signs and symptoms may include fatigue, skin pallor, shortness of breath, light-headedness, dizziness, or a fast heartbeat [3].
Anaemia is prevalent among pregnant women and children under five years of age, especially during their first two years of life. More than 1.62 billion people are anaemic worldwide, and approximately two-thirds of preschool children in Africa and South East Asia are anaemic [4]. The World Health Organization (WHO) listed iron deficiency, a major cause of anemia, as one of the top 10 risk factors in developing countries for “lost years of healthy life” [5,6]. Anaemia affects around 62.3% of sub-Saharan African children under five years of age [7]. Among preschool children in sub-Saharan Africa, anaemia is prevalent in 42% and 91% of children in Swaziland and Burkina Faso respectively [8].
Developing countries, particularly those in Africa and South-East Asia, account for over 89% of the global anaemia burden [9]. Aside from being disproportionately prevalent in these regions, anaemia prevalence varies by age group. Children under the age of five represent over 47% of the total burden [10], with Ethiopia having one of the highest rates [11].
Anaemia is a serious global public health problem affecting young children [4]. According to the WHO criteria, anaemia is a severe public health problem in Ethiopia, and 56.9% of Ethiopian under-five children are anemic, based on the Ethiopian Demographic and Health Survey (EDHS) [12]. This is a little lower than the average anaemia prevalence of 59.9% in under-five children from 27 Sub-Saharan African countries [13].
Low- and middle-income countries are more affected by the consequences of anaemia. For instance, a significant amount of human capital and economic resources are lost due to the premature morbidity and mortality of pregnant women and under-five children [14]. Anaemia impairs cognitive function during the early developmental stages of childhood, as previously reported in the literature [15], and affected children often suffer from other complications of iron and vitamin B12 deficiencies [15,16,17]. Long-term consequences include poor psychomotor skills, poor academic performance, and infection susceptibility [18,19]. Global food insecurity must therefore be addressed urgently as poor nutrition is the most common cause of anaemia [15,16,17].
Several interventions have been implemented in Ethiopia to address the high prevalence of anaemia among children, according to the EDHS 2011 report [20]. In the same report, more than four out of ten (44%) children in Ethiopia were anaemic. Thus, the prevalence of mild, moderate, and severe anaemia were 21%, 20%, and 3%, respectively. The prevalence of anaemia is highest in children aged 9–11 months (73%), and it decreases steadily from 12 to 59 months [20]. Children in rural areas have anaemia at a rate of 45 percent compared to children in urban areas, with a prevalence rate of 35 percent. Regional differences in anaemia in children range from 33% in Addis Ababa to 75% in Afar [20]. The national estimate of anaemia prevalence decreased by 19%, from 54% in 2005 to 44% in 2011 [20]. Evidence from the 2016 EDHS reports shows that more than half of children under five, around(57%), suffer from some degree of anaemia, 25% are mildly anaemic, 29% are moderately anaemic, and 3% are severely anaemic [12]. This increment of under-five child anaemic problems from year to year has received little research attention.
Studies have shown that socioeconomic, demographic, and environmental factors contribute to childhood anaemia [21,22,23,24]. Anaemia among children in Ethiopia has been associated with multiple risk factors in several studies [21,22,24,25]. However, these studies did not classify the severity of anaemia and its determinants. Therefore, this study examined socioeconomic, demographic, household, and environmental factors associated with inequality in childhood anaemia in Ethiopia.

2. Methodology

2.1. Data Source and Study Design

We performed a cross-sectional analysis of data from the EDHS. The survey was conducted from 18 January 2016, to 27 June 2016, based on a nationally representative sample that provides estimates at the national and regional levels for both urban and rural areas [8]. The EDHS utilized a descriptive cross-section design, relying on structured questionnaires to collect data from the respondents. EDHS employed a two-stage cluster sampling technique to recruit respondents for the survey. The detailed sampling procedure adopted for the EDHS can be found in the literature [12]. The dataset used is freely available to download at https://dhsprogram.com/data/dataset/Ethiopia_StandardDHS_2016.cfm?flag=1 (accessed on 8 January 2022).

2.2. Study Procedure

Blood specimens for testing anaemia were collected from all children aged 6–59 months for whom consent was obtained from their parents or other adults responsible for them. Blood samples were drawn from a drop of blood taken from a finger prick (or a heel prick in the case of children) and collected in a micro cuvette. Hemoglobin analysis was conducted on-site using a battery-operated portable HemoCue analyzer. The results were provided verbally and in writing. The parents or responsible adults of children whose Hb was below 7 g/dL were instructed to take the child to a health facility for follow-up care [12].

2.3. Study Variables

2.3.1. Dependent Variable

The dependent variable was the childhood anaemic status, measured as the altitude-adjusted Hb concentration (in g/L), and the severity of anaemia was categorized as [2].
Anaemic   status { 1 = m i l d ( 100 109 g L ) , 2 = m o d e r a t e   ( 70     99 g / L ) 3 = s e v e r e   ( < 70 g / L )

2.3.2. Independent Variables

Independent variables considered in this study were grouped by socioeconomic, demographic, household, and environmental factors.

2.3.3. Individual-Level Factors

Child’s age (in months) (0 = “<6”, 1 = “6–11”, 2 = “12–23”, 3 = “24–37”, 4 = “38–47”, 5 = “48–59”), Sex of child (0 = “Male”, 1 = “Female”), Preceding birth interval (in months) (0 = “<24”, 1 = “≥24”), Size of child at birth (0 = “Very Large”, 1 = “larger than Average”, 2 = “Medium”, 3 = “Smaller than Average”, 4 = “very Small”).

2.3.4. Maternal-Level Factors

Women’s Age (0 = “15–24”, 1 = “25–34”, 2 = “35–44”, 3 = “45 and above”), Mother’s educational level (0 = “No education”, 1 = “Primary”, 2 = “Secondary”, 3 = “Higher”), Antenatal care visit (0 = “None”, 1 = “1–7”, 2 = “≥8”), Mother’s occupational status (0 = “No”, 1 = “Yes”), Marital Status of mother (0 = “Never in union”, 1 = “Married/Living With Partner”, 2 = “Separated”), Wealth index of Mothers (0 = “Poorest”, 1 = “Poorer”, 2 = “Middle”, 3 = “Richer”, 4 = “Richest”).

2.3.5. Household-Level Factors

Source of drinking water (0 = “Improved Water”, 1 = “Un-Improved Water”), Type of toilet facility (0 = “Improved toilet/sanitation”, 1 = “Un-Improved toilet/Sanitation”), Type of Cooking fuel (0 = “Modern fuel”, 1 = “Traditional fuel”), Sex of household head (0 = “Male”, 1 = “Female”).

2.3.6. Community-Level Factors

Place of residence (0 = “Urban”, 1 = “Rural”), Region (0 = “Tigray”, 1 = “Afar”, 2 = “Amhara”, 3 = “Oromia”, 4 = “Somali”, 5 = “Benishangul-gumuz”, 6 = “SNNPR”, 7 = “Gambela”, 8 = “Harari”, 9 = “Addis Ababa”, 10 = “Dire Dawa”).

2.4. Statistical Model

2.4.1. Ordinal Logistic Regression

To identify the determining factors among the ordered response variable, the ordinal logistic regression was used and expressed as follows;
An alternative to least-squares regression that guarantees the fitted probabilities between 0 and 1 is the method of ordinal logistic regression. We arbitrarily designate the last group, group K, to serve as the baseline category. In the ordinal logit model;
f ( Y j ( X ) ) = log ( f ( y j ( X ) ) 1 f ( y j ( X ) ) ) = l o g ( p r ( Y j \ X ) p r ( Y > j \ X ) ) = α j + β X , j = 1 , 2 ,   ,   K 1
Y j ( X ) = e j + β X 1 + e j + β X , Where j indexes cut-off points for categories (K) of the response variables, the function f ( Y j ( X ) ) is the link function that connects the systematic components of the linear model, j represents a separate intercept for each cumulative probability and β represents the regression coefficient.
If multiple explanatory variables are applied to the ordinal regression model, βX is replaced by the linear combination of ( j + β 1 X j 1 + β 2 X j 2 + + β p X j p ).

Assumptions of the Ordinal Logistic Regression Model

Since the ordinal logistic regression model was fitted, the assumptions to ensure that it is a valid model were checked. The assumptions of the ordinal logistic regression are as follows and were tested in the following order:
1.
The dependent variable is ordered.
2.
One or more of the independent variables are either continuous, categorical or ordinal.
3.
No multicollinearity.
4.
Proportional odds.

The Proportional Odds Model (POM)

The proportional odds model assumes that the cumulative logits can be represented as parallel linear functions of independent variables. That is, for each cumulative logit, the parameters of the models should be the same, except for the intercept. Consequently, according to the proportional odds assumption, the odds ratio is the same for all categories of the response variable [26].
Given that the outcome categories of the dependent variable appear to be ordered in terms of the severity of anaemia, a typical approach is to use the standard ordered logit model called the proportional odds model.
The proportional odds model is the log odds of the first k −1 cumulative probabilities as:
l o g i t   [ p ( Y i ] =   log ( p [ ( Y i ) ] [ 1 p ( Y i ) ] ) = l o g [ π i j 1 π i j ]
And the relationship between the cumulative logits of Y is:
l o g [ π i j 1 π i j ] = l o g [ π i j π i j + 1 + + π k ] ; i = 1 ,   2 ,   , k 1

2.4.2. Bivariate Analysis

First, descriptive and bivariate analysis was performed. Bivariate analysis was used to select candidate variables with p-values less than 0.25 for multilevel ordinal regression models [27,28]. To analyze the bivariate analysis, the SPSS version 20 Statistical software and STATA version 12 were used for the multilevel analysis.

2.4.3. Multilevel Ordinal Logistic Regression Model

Four-Level Multilevel Model

To identify the variations across the individual, household, maternal, and community level factors, the multilevel logistic regressions were applied as follows;
For this study, the authors used the community as level 4, the household as level 3, mothers as level 2, and individuals (child characteristics) as level 1 variables, respectively.

Multilevel Empty Ordinal Logistic Regression Model

This model only contains random groups and random variation within groups and between groups.
η i j k l = β 0 + ε j k l + ε l
Whereas, ε j k l denote the random effect for the j t h level cluster, k t h cluster in the l t h level of cluster and ε l denote the random effect for the l t h fourth-level cluster.
For i = ,…, number of individuals, j = 1,…, number of mothers within each household in each community, k = 1,…, number of households in each community, and l = 1,…, number of community.

Random Intercept Multilevel Ordinal Logistic Regression Model

In this model, the covariates are included, and the intercept is the only random effect meaning that the groups differ with respect to the average value of the response variable.
η i j k l = β 0 + β 1 h h = 1 p X h i j k l + β 2 h h = 1 q X h j k l + β 3 h h = 1 l X h k l + β 4 h h = 1 m X h l ε j k l + ε j k l + ε l
Whereas, X h i j k l denote the vector of the first level variables, X h j k l denote the vector of the second level variables, X h k l denote the vector of 3rd level predictor variables, and X h l denote the vector of 4th level predictor variables. In addition, β 1 h denote the vector of regression parameters for the first-level variables, β 2 h denote the vector of regression parameters for second-level variables, β 3 h denote the vector of regression parameters for the third-level variables, and β 4 h denote the vector of regression parameters for fourth-level variables. ε j k l denote the random effect for the jth level cluster in the kth level cluster in the l t h level of cluster and ε l denote the random effect for the lth 4th level cluster.
For i = ,…, number of individuals, j = 1,…, number of mothers within each household in each community, k = 1,…, number of households in each community, and l = 1,…, number of community.

Random Coefficient Multilevel Ordinal Logistic Regression Model

In this model, the coefficients of the explanatory variables are considered as random.
η i j k l = β 0 + β 1 h h = 1 p X h i j k l + β 2 h h = 1 q X h j k l + β 3 h h = 1 l X h k l + β 4 h h = 1 m X h l ε j k l + ε j k l + ε l + ε o j l h = 1 p X h i j k l + ε l + ε o l h = 1 p X h i j k l
Whereas, X h i j k l denote the vector of the first level variables, X h j k l denote the vector of the second level variables, X h k l denote the vector of 3rd level predictor variables, and X h l denote the vector of 4th level predictor variables. In addition, β 1 h denote the vector of regression parameters for the first-level variables, β 2 h denote the vector of regression parameters for second-level variables, β 3 h denote the vector of regression parameters for the third-level variables, and β 4 h denote the vector of regression parameters for fourth-level variables. ε o j l and ε o l are the random slope. The part β 0 + β 1 h h = 1 p X h i j k l + β 2 h h = 1 q X h j k l + β 3 h h = 1 l X h k l + β 4 h h = 1 m X h l ε j k l are the fixed part of the model and ε j k l + ε l + ε o j l h = 1 p X h i j k l + ε l + ε o l h = 1 p X h i j k l are the random part of the model.
For i = ,…, number of individuals, j = 1,…, number of mothers within each household in each community, k = 1,…, number of households in each community, and l = 1,…, number of community.

2.5. Measures of Variation (Random Effects)

Intra Cluster Correlation
To understand the variation of childhood anaemia among the maternal, households, and communities, the researcher used intra-cluster correlation and determined as follows;
I C C m a t e r n a l = V m a t e r n a l V c o m m u n i t y + V h o u s e h o l d + V m a t e r n a l + π 2 3
I C C h o u s e h o l d = V h o u s e h o l d V c o m m u n i t y + V h o u s e h o l d + V m a t e r n a l + π 2 3
I C C c o m m u n i t y = V c o m m u n i t y V c o m m u n i t y + V h o u s e h o l d + V m a t e r n a l + π 2 3
where   V c o m m u n i t y , V h o u s e h o l d and V m a t e r n a l are the variances of childhood anaemia at the community, household, and maternal levels, respectively.

2.6. Proportional Change in Variance (PCV)

The proportional change in variance expresses the change in the area level variance between the intercept only model and the individual level model, and between the individual level model and the model further including the area level covariate and determined as follows;
P C V = τ ^ n u l l τ ^ f u l l τ ^ n u l l
where τ ^ f u l l   a n d   τ ^ n u l l denote the estimated variances of random-effects distributions for the full and null models, respectively.

2.7. Median Odds Ratio (MOR)

Measures of heterogeneity in logistic multilevel regression models can be determined as follows;
MOR = e x p ( 2 τ ^ 2 × Φ 1 ( 0.75 ) )
where τ ^ 2 is the estimated variance of the distribution of the random effects, and Φ denotes the cumulative distribution function of the standard normal distribution, while Φ 1 (0.75) = 0.6745 is the 75th percentile of a standard normal distribution.

2.8. Model Selection Criteria

Akaike Information Criterion (AIC)

Model suitability or fitting review is required prior to model fitting. Akaike Information Criterion (AIC) was used to select the best model. The model with the lowest AIC value is the best. The model with a small value of AIC is the optimal model, which means a model that is close to the actual one [23].
AIC is defined as:
A I C = 2 l n ( l i k e l i h o o d ) + 2 k
where k is the degrees of freedom of the model, computed as the rank of the variance-covariance matrix of the parameters. N is the number of observations used in the estimation, or more precisely, the number of independent terms in the probability. That means an intercept-only/null model (Model I), which did not include any covariate but includes outcome variables, individual-level factors (Model II), mothers-level factors(Model III), household-level factors (Model IV), and community-level factors (Model V).

3. Results

The data used for this analysis was obtained from EDHS 2016 on the factors related to childhood anemia in Ethiopia. Descriptive statistics and multilevel ordinal logistic regression were applied to analyze the data.
Assumption Checking
  • The dependent variable or childhood anaemic status was ordered. i.e., mild, moderate, and severe.
  • One or more of the independent variables are either continuous, categorical or ordinal, as shown in the table below.
  • No multicollinearity: as shown in the table below, the multicollinearity among the individual, household, maternal, and community-level explanatory variables was tested using the variance Inflation Factor (VIF). Table 1 shows that the VIF for each of the explanatory variables was less than five (5). It shows the absence of multicollinearity in the models, i.e., indicating no multicollinearity problem in the data.
  • Conducting the Brant test of the parallel regression (proportional odds) assumption for the status of children’s anaemic status. We identified no predictors found to violate the proportional odds assumption (Table 1).

3.1. Descriptive Statistics on Factors Associated with Childhood Anaemia Status

From the overall sample of 7960 under-five children, 1950 (24.5%) had mild anaemia, 2264 (28.4%) had moderate anaemia, and 179 (2.2%) were severe anaemia without including the child’s normal anaemic status. Among the overall sample of 7960 under-five children, 984 (24.39%) were mild, 1146 (28.41%) were moderate, and 95 (2.3%) were severe, while 966 (24.6%) females were mild anaemia, 1118 (28.5%) females were moderate anaemia, and 84(2.1%) females were severe anaemia without including child normal anaemic status. Similarly, among children who were mild, moderate, and severe anaemia, 430 (30%), 456 (31.8%), and 41 (2.87%) were those who resided in urban areas, respectively, but 1520 (23.3%), 1808 (27.7%), and 138 (2.1%), children were those who resided in rural areas, respectively without including child normal anaemic status.

3.2. Inferential Statistical Analysis on Factors Associated with Childhood Anaemia Status

Bivariate Analysis

Bivariate analyses were performed on all independent variables separately from the outcome variables prior to multilevel analysis. The variables associated with p-values < 0.25 for anaemic status were then selected and entered into multilevel analyses. From the result in Table 2, the size of the child at birth, the mother’s marital status, and the type of cooking fuel variables are not candidates for multilevel analysis on childhood anaemic because of their p-value greater than 0.25.

3.3. Multilevel Ordinal Logistic Regression Analysis of Childhood Anaemic Status among Maternal, Household, and Community Factors

3.3.1. Intercept Model Only

In this model, there is a parametric version of assessing heterogeneity of the childhood anaemic status among the maternal, household, and community factors.
From Table 3, the estimated variance for maternal, household, and community-level were σ o u 2 = 1.546, σ o u 2 = 1.698   and σ o u 2 = 1.425 , respectively, which was significantly different from zero, indicating variations of childhood anaemic across maternal, household, and community levels of Ethiopia. The result of ICC is 0.194, 0.213, and 0.179 for maternal, household, and community, respectively. This suggests that about 19.4%, 21.3%, and 17.9% of the variation in childhood anaemic were due to the variation across the maternal, household, and community level factors, respectively.

3.3.2. Model Comparison

Once the set of candidate models has been chosen, the statistical analysis allows us to select the best of these models. Good model selection is a balance between simplicity and goodness of fit. Choosing are levant multilevel model is therefore an important step and should be based on the need for model parsimony.
The smallest value of AIC indicates a better model. From the result of Table 4, the AIC for multilevel ordinal logistic regression of model VI is 12,368.45, which is small compared to the rest model. Therefore, it better fits the data to predict childhood anaemia status in Ethiopia. This suggests that the multilevel logistic regression of model VI with the fixed explanatory variables and random effects is a better model than the other. Thus, the interpretations of the parameter and conclusion of the finding were based on model VI.

3.4. Multilevel Ordinal Logistic Regression Model Result on Childhood Anaemia Status

It is possible to generalize the model so that the effect of the level one covariate is different in each mother, household, and community. This approach can be made by adding random coefficients in front of some of the individual-level covariates of the model. The following table presents some random coefficients and fixed explanatory variables with a significant effect on childhood anaemic in Ethiopia.
The child’s age (in months), sex of the child, preceding birth interval (in months), mother’s educational level, antenatal care visit, wealth index of mothers, source of drinking water, type of toilet facility, place of residence, and region were significant predictors of the childhood anaemic status at a 5% level of significance.
The odds of the status of child anaemia exposure to severe status were less likely in females(OR: 0.63) than males, and the odds of child anaemic status exposed to mild and moderate status were more likely in females(OR: 1.61), in comparison with the reference category relative to other anaemic status controlling for other variables in the model. The odds of child anaemic exposed to mild status were less likely in a child with age between 38 and 47 and between 48 and 59 months (OR: 0.81, OR: 0.79), respectively, in comparison with the reference category relative to the other anaemic status; The odds of child anaemic exposed to moderate status were less likely in a child with age between 38 and 47 and between 48 and 59 months (OR: 0.80, OR: 0.78), respectively, in comparison with the reference category relative to the other anaemic status; The odds of child anaemic exposed to sever status were less likely in a child with age between 38 and 47 and between 48 and 57 months (OR: 0.79, OR: 0.87), respectively, in comparison with the reference category relative to other anaemic status controlling for other variables in the model. The odds of child anaemic exposure to mild, moderate, and severe were more likely in mothers with primary education level (OR: 1.4, OR: 1.56, OR: 1.01), respectively, in comparison with the reference category relative to each other controlling for other variables in the model. The odds of child anaemic exposure to mild, moderate, and severe were less likely in 1–7 antenatal care visits(OR: 0.08, OR: 0.021, OR: 0.05), respectively, in comparison with the reference category relative to each other controlling for other variables in the model. The odds of child anaemic exposure to mild, moderate, and severe were more likely in the richest wealth index of the mother (OR: 1.44, OR: 1.36, OR: 1.4), respectively, in comparison with the reference category relative to each other controlling for other variables in the model. The odds of child anaemic exposure to mild, moderate, and severe were less likely in the un-improved water source of drinking water (OR: 0.57, OR: 0.49, OR: 0.62), respectively, in comparison with the reference category relative to each other controlling for other variables in the model. The odds of child anaemic exposure to mild, moderate, and severe were less likely in the un-improved toilet facility (OR: 0.66, OR: 0.64, OR: 0.65), respectively, in comparison with the reference category relative to each other controlling for other variables in the model. The odds of child anaemic exposure to mild, moderate, and severe were less likely in the rural residence (OR: 0.70, OR: 0.81, OR: 0.56), respectively, in comparison with the reference category relative to each other controlling for other variables in the model. The odds of child anaemic exposure to mild, moderate, and severe were less likely in the Affar region (OR: 0.68, OR: 0.72, OR: 0.0.70), Amhara region (OR: 0.57, OR: 0.42, OR: 0.56), respectively, and were more likely in the SNNPR (OR:1.12, OR:1.14, OR:1.15) and Addis Ababa (OR: 3.65, OR: 2.67, OR: 2.89), respectively, in comparison with the reference category relative to each other controlling for other variables in the model.
In the final model, the variation between women’s, household, and community on childhood anaemia concluded that there is a maternal variation of 15.06%, household variation of 15.6%, and community variation of 14.22% and close to half of the variance across the communities was explained by the child-, maternal-, household-, and community-level factors (PCV = 40.42%). Importantly, as determined by a proportional change in variance, 59.58% of the community-level variance of childhood anaemia was accounted for by the joint effects of maternal, household, and community-level factors.
Table 5 reveals that the addition of individual, maternal level, household level, and community level variables to the model at the same time leads to decreases in the ICC at all levels. This shows that about 15.06%, 15.6% and 14.2% variation in the prevalence of childhood anaemia is due to the difference in the maternal level, household level and community level, respectively.

4. Discussion

The study examined the inequalities and factors associated with childhood anaemia using a nationally representative EDHS dataset. We found that the prevalence of mild, moderate, and severe childhood anaemia was24.5%, 28.4%, and 2.2%, respectively.
The sex of the child was found to be significantly associated with anaemia. Specifically, females were more likely to be anaemic compared to their male counterparts in mild and moderate anaemia, but an inverse association was found regarding severe anaemia. Contrary to our findings, Venda [29] reported that male children were more likely to be anaemic. Previous studies conducted in Ethiopia to examine childhood anaemia found consistent findings [30,31]. The inconsistencies could be due to the sociocultural norms and differentials regarding the intake of iron-rich foods by gender and age. Also, household food security and other childhood infections could have played a key role in the observed association found in the study. Further studies are recommended to investigate the intrinsic association between the sex of a child and their anaemic status.
Further, the child’s age (in months) was a significant factor in childhood anaemia. A similar study conducted by Booth & Aukett and Lanzkowsky suggests that children aged 6–11 months had significantly higher odds of being anaemic. The study states that by 4 months of age, neonatal iron stores are usually reduced by half [5,32], and by 6 months, children have depleted the iron stores present at birth [4,33].
Maternal educational level has a significant effect on childhood anaemic in this study. The study conducted in Ethiopia by [19,34] confirmed this study and suggested that mothers are mostly caregivers for their children and that maternal education has always been linked to many child health outcomes. It may also affect health decision-making and thus influence the probability of a child meeting certain nutrition-related requirements [4,5]. In addition, in developing countries, there is a high prevalence of iron deficiency anaemia, which reduces cognitive performance, work performance, and endurance; it also causes learning difficulties and has a negative impact on the development of the infant population.
The wealth index is also the other significant factor in childhood anaemia in this study. Similar findings conducted in India and Maryland [35,36] suggest that the household wealth index directly influences broader socioeconomic conditions directly on hemoglobin levels among children and hence childhood anaemia. This condition has been attributed to generalized bone marrow failure resulting from malnutrition, other micronutrient deficiencies, contact with biofuel smoke, and mechanisms linked to lower-income and social statuses [6]. A similar finding from another study conducted in Ethiopia confirmed this study and suggested that households with a higher wealth quintile are more likely to provide balanced macronutrients and micronutrients to their children. Children from these households have more chances of accessing health care services [37]. Several studies confirm that children from a lower economic status are vulnerable to various nutritional disorders, including anaemia, and are at risk of easily preventable diseases [13].
The type of toilet facility has a significant effect on childhood anaemia in this study. Similar findings conducted in Lesotho [38] suggest that a better understanding of fuel usage in households can undeniably lead to the development of interventions and policies that can reinforce proper fuel usage and significantly reduce the prevalence of anaemia.

Limitations

The current study findings should be interpreted with caution. The cross-sectional nature of the data restricts causality from the observed findings. Moreover, the DHS data lacks detailed information on the other risk factors of anaemia, such as malaria, intestinal parasite, and dietary intake markers such as macro and micronutrients connected to anemia. We only used Hb concentration (in g/L) to determine childhood anaemia status; hence, we could not ascertain whether the anemia was caused by other factors such as iron deficiency.

5. Conclusions

The study has shown that anaemia is prevalent among children in Ethiopia with variation across maternal, household, and community characteristics. The result revealed that anaemia among the children was significantly associated with the age of the child, sex of the child, birth interval, the mother’s educational level, antenatal care attendance, wealth index, source of drinking water, type of toilet facility, place of residence, and region.Therefore, appropriate and tailored interventions are required to reduce the prevalence of childhood anaemia. These interventions include improving women’s access to education, providing health education on child feeding practices (e.g., complimentary feeding), and strengthening social support systems (e.g., free access to maternal healthcare). In light of the identified factors of childhood anaemia, a pragmatic approach is required from policymakers. Further research is needed to understand the risk factors and aetiologies of anaemia across different settings in Ethiopia.

Author Contributions

K.A.K. and T.U.C. developed the study concept and performed the analysis; K.A.K., T.U.C., D.S.J., J.E.H.J., A.-A.S., R.G.A. and B.O.A. drafted and revised the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

The authors sincerely thank Bielefeld University, Germany, for providing financial support through the Open Access Publication Fund for the article processing charge.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The dataset used is freely available to download at: https://dhsprogram.com/data/dataset/Ethiopia_Standard-DHS_2016.cfm?flag=1 (accessed on 8 January 2022).

Conflicts of Interest

The authors declare no competing interests.

Ethics Approval and Consent to Participate

Ethical clearance was obtained by the Institutional Review Board of ICF International. The authors requested and officially received approval from the DHS Program to use the dataset for this study. Supplementary information about the DHS data usage and ethical standards is available at http://goo.gl/ny8T6X (accessed on 8 January 2022).

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, 444–454. [Google Scholar] [CrossRef] [PubMed]
  2. World Health Organization. Haemoglobin Concentrations for the Diagnosis of Anaemia and Assessment of Severity (No. WHO/NMH/NHD/MNM/11.1); World Health Organization: Geneva, Switzerland, 2011.
  3. MFMER. Mayo Foundation ForMeducation and Rsearch; Rockester, MI, USA. 2022. Available online: https://www.britannica.com/topic/Mayo-Foundation-for-Medical-Education-and-Research (accessed on 5 May 2022).
  4. Kawo, K.N.; Asfaw, Z.G.; Yohannes, N. Multilevel Analysis of Determinants of Anemia Prevalence among Children Aged 6–59 Months in Ethiopia: Classical and Bayesian Approaches. Anemia 2018, 2018, 3087354. [Google Scholar] [CrossRef] [PubMed]
  5. Sharma, H.; Singh, S.K.; Srivastava, S. Socio-economic inequality and spatial heterogeneity in anaemia among children in India: Evidence from NFHS-4 (2015–2016). Clin. Epidemiol. Glob. Health 2020, 8, 1158–1171. [Google Scholar] [CrossRef]
  6. Endris, B.S.; Dinant, G.-J.; Gebreyesus, S.H.; Spigt, M. Geospatial inequality of anaemia among children in Ethiopia. Geospat. Health 2021, 16, 1036. [Google Scholar] [CrossRef] [PubMed]
  7. Ogunsakin, R.E.; Babalola, B.T.; Akinyemi, O. Statistical Modeling of Determinants of Anemia Prevalence among Children Aged 6–59 Months in Nigeria: A Cross-Sectional Study. Anemia 2020, 2020, 4891965. [Google Scholar] [CrossRef] [PubMed]
  8. Magalhães, R.J.S.; Clements, A.C. Spatial heterogeneity of haemoglobin concentration in preschool-age children in sub-Saharan Africa. Bull. World Health Organ. 2011, 89, 459–468. [Google Scholar] [CrossRef]
  9. Kassebaum, N.J. The global burden of anemia. Hematol. Oncol. Clin. 2016, 30, 247–308. [Google Scholar] [CrossRef]
  10. Balarajan, Y.; Ramakrishnan, U.; Ozaltin, E.; Shankar, A.H.; Subramanian, S.V. Anaemia in low-income and middle-income countries. Lancet 2011, 378, 2123–2135. [Google Scholar] [CrossRef]
  11. World Health Organization (WHO). The Global Prevalence of Anaemia in 2011; World Health Organization: Geneva, Switzerland, 2015.
  12. Central Statistical Agency (CSA)[Ethiopia] and ICF. Ethiopia Demographic and Health Survey 2016; CSA: Addis Ababa, Ethiopia; ICF: Rockville, MD, USA, 2016. [Google Scholar]
  13. Moschovis, P.P.; O Wiens, M.; Arlington, L.; Antsygina, O.; Hayden, D.; Dzik, W.; Kiwanuka, J.P.; Christiani, D.C.; Hibberd, P.L. Individual, maternal and household risk factors for anaemia among young children in sub-Saharan Africa: A cross-sectional study. BMJ Open 2018, 8, e019654. [Google Scholar] [CrossRef]
  14. GBD 2016 Disease and Injury Incidence and Prevalence Collaborators. Global, regional, and national incidence, prevalence, and years lived with disability for 328 diseases and injuries for 195 countries, 1990–2016: A systematic analysis for the global burden of disease study 2016. Lancet 2017, 390, 1211–1259. [Google Scholar] [CrossRef] [Green Version]
  15. Magalhães, R.J.S.; Clements, A.C.A. Mapping the Risk of Anaemia in Preschool-Age Children: The Contribution of Malnutrition, Malaria, and Helminth Infections in West Africa. PLoS Med. 2011, 8, e1000438. [Google Scholar] [CrossRef] [PubMed]
  16. Simbauranga, R.H.; Kamugisha, E.; Hokororo, A.; Kidenya, B.R.; Makani, J. Prevalence and factors associated with severe anaemia amongst under-fve children hospitalized at Bugando medical centre, Mwanza, Tanzania. BMC Hematol. 2015, 15, 13. [Google Scholar] [CrossRef] [PubMed]
  17. Aguilar, R.; Moraleda, C.; Quinto, L.; Renom, M.; Mussacate, L.; Macete, E.; Menendez, C. Challenges in the diagnosis of iron defciency in children exposed to high prevalence of infections. PLoS ONE 2012, 7, e50584. [Google Scholar] [CrossRef] [PubMed]
  18. Melku, M.; Alene, K.A.; Terefe, B.; Enawgaw, B.; Biadgo, B.; Abebe, M.; Muchie, K.F.; Kebede, A.; Melak, T. Anemia severity among children aged 6–59 months in Gondar town, Ethiopia: A community based cross-sectional study. Ital. J. Pediatr. 2018, 44, 107. [Google Scholar] [CrossRef] [PubMed]
  19. Mohammed, S.H.; Habtewold, T.D.; Muhammad, F.; Esmaillzadeh, A. The contribution of dietary and non-dietary factors to socioeconomic inequality in childhood anemia in Ethiopia: A regression-based decomposition analysis. BMC Res. Notes 2019, 12, 646. [Google Scholar] [CrossRef] [PubMed]
  20. Central Statistical Agency [Ethiopia] and ICF International. Ethiopia Demographic and Health Survey 2011; Central Statistical Agency and ICF International: Addis Ababa, Ethiopia; Calverton, MD, USA, 2012.
  21. Gautam, S.; Min, H.; Kim, H.; Jeong, H.-S. Determining factors for the prevalence of anemia in women of reproductive age in Nepal: Evidence from recent national survey data. PLoS ONE 2019, 14, e0218288. [Google Scholar] [CrossRef]
  22. Harding, K.L.; Aguayo, V.M.; Namirembe, G.; Webb, P. Determinants of anemia among women and children in Nepal and Pakistan: An analysis of recent national survey data. Matern. Child Nutr. 2018, 14, e12478. [Google Scholar] [CrossRef]
  23. Sadeghian, M.; Fatourechi, A.; Lesanpezeshki, M.; Ahmadnezhad, E. Prevalence of Anemia and Correlated Factors in the Reproductive Age Women in Rural Areas of Tabas. J. Fam. Reprod. Health 2013, 7, 139–144. [Google Scholar]
  24. Kamruzzaman, M.; Rabbani, M.G.; Saw, A.; Sayem, M.A.; Hossain, M.G. Differentials in the prevalence of anemia among non-pregnant, ever-married women in Bangladesh: Multilevel logistic regression analysis of data from the 2011 Bangladesh Demographic and Health Survey. BMC Womens Health 2015, 15, 4–11. [Google Scholar] [CrossRef]
  25. Baig-Ansari, N.; Badruddin, S.H.; Karmaliani, R.; Harris, H.; Jehan, I.; Pasha, O.; Moss, N.; McClure, E.M.; Goldenberg, R.L. Anemia Prevalence and Risk Factors in Pregnant Women in an Urban Area of Pakistan. Food Nutr. Bull. 2008, 29, 132–139. [Google Scholar] [CrossRef]
  26. Agresti, A. Categorical Data Analysis, 2nd ed.; John Wiley & Sons: Hoboken, NJ, USA, 2002. [Google Scholar]
  27. Hayelom, G.; Hassan, V.; Cindy, F.; Pammla, P. Modeling the predictors of stunting in Ethiopia: Analysis of 2016 Ethiopian demographic health survey data (EDHS). BMC Nutr. 2020, 6, 52. [Google Scholar]
  28. Kasaye, H.K.; Bobo, F.; Yilma, M.T.; Woldie, M. Poor nutrition for under-five children from poor households in Ethiopia: Evidence from 2016 Demographic and Health Survey. PLoS ONE 2019, 14, e0225996. [Google Scholar] [CrossRef] [PubMed]
  29. Heckman, J.; Samie, A.; Bessong, P.; Hamandi, H.; Ntsieni, M.; Kohler, M.; Milam, B.; Scriver, J.; Dillingham, R. Anaemia among clinically well under-fives attending a community health centre in Venda, Limpopo Province. S. Afr. Med. J. 2010, 100, 445–448. [Google Scholar] [CrossRef] [PubMed]
  30. 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. [Google Scholar] [CrossRef] [PubMed]
  31. Guled, R.A.; Mamat, N.M.; Balachew, T.; Bakar, M.A.; Azdie, W.; Assefa, N. Predictors and prevalence of anemia, among children aged 6 to 59 months in shebelle zone, somali region, eastern Ethiopia: A cross sectional study. Int. J. Dev. Res. 2017, 7, 11189–11196. [Google Scholar]
  32. Booth, I.W.; AAukett, M. Iron deficiency anaemia in infancy and early childhood Commentary. Arch. Dis. Child. 1997, 76, 549–554. [Google Scholar] [CrossRef]
  33. Lanzkowsky, P.; Lipton, J.; Fish, J.D. Lanzkowsky’s Manual of Pediatric Hematology and Oncology, 6th ed.; Elsevier: Amsterdam, The Netherlands, 2016. [Google Scholar]
  34. Enawgaw, B.; Workineh, Y.; Tadesse, S.; Mekuria, E.; Addisu, A.; Genetu, M. Prevalence of Anemia and Associated Factors Among Hospitalized Children Attending the University of Gondar Hospital, Northwest Ethiopia. EJIFCC 2019, 30, 35–47. [Google Scholar]
  35. Skalicky, A.; Meyers, A.F.; Adams, W.G.; Yang, Z.; Cook, J.T.; Frank, D.A. Child food insecurity and iron deficiency anemia in low-income infants and toddlers in the United States. Matern Child Health J. 2006, 10, 177–185. [Google Scholar] [CrossRef]
  36. Rutstein, S.O.; Kiersten, J. The DHS Wealth Index; DHS Comparative Reports No. 6; ORC Macro: Calverton, MD, USA, 2004. [Google Scholar]
  37. Ekholuenetale, M.; Tudeme, G.; Onikan, A.; Ekholuenetale, C.E. Socioeconomic inequalities in hidden hunger, undernutrition, and overweight among under-five children in 35 sub-Saharan Africa countries. J. Egypt. Public Health Assoc. 2020, 95, 9. [Google Scholar] [CrossRef]
  38. Letuka, T.; Frade, S. Household and individual risk factors of anaemia among under-5 children in Lesotho. Afri. Health Sci. 2020, 20, 1478–1486. [Google Scholar] [CrossRef]
Table 1. Proportional odds assumption checking.
Table 1. Proportional odds assumption checking.
Co-VariableRegression CoefficientVIFBrant Test (p-Value)95% Confidence Interval
Lower BoundUpper Bound
[Mothers occupational status = No]−0.0891.0630.090−0.1910.014
[Mothers occupational status = Yes]0 a
[Sex of child = Male]0.0102.6650.814−0.0760.097
[Sex of child = Female]0 a
[Current marital status = Never in Union]−0.3541.5710.584−1.6220.913
[Current marital status = Married/living with partner]−0.2530.203−0.6430.137
[Current marital status = separated]0 a
[Age of Mothers = 15–24]−5.4841.0690.300−6.213−4.754
[Age of Mothers = 25–34]−2.3010.089−3.036−1.566
[Age of Mothers = 35–44]−4.0380.063−4.764−3.312
[Age of Mothers = 45 and above]0 a
[Wealth index of mothers = Poorest]−0.2251.9230.078−0.437−0.013
[Wealth index of mothers = Poorer]−0.1860.085−0.3990.026
[Wealth index of mothers = Middle]−0.2520.091−0.467−0.037
[Wealth index of mothers = Richer ]−0.1100.879−0.3220.102
[Wealth index of mothers = Richest ]0 a
[Child Age (in Months) = <6]0.0031.0270.967−0.1570.163
[Child Age (in Months = 6–11]−0.0160.853−0.1810.150
[Child Age (in Months = 12–23]−0.035 0.632−0.1770.107
[Child Age (in Months = 24–37]0.0200.775−0.1160.156
[Child Age (in Months = 38–47]0.0550.773−0.0960.206
[Child Age (in Months = 48–59]0 a
[Region = Tigray]−0.1011.1860.921−0.3480.146
[Region = Afar]0.0990.749−0.157
[Region = Amhara]−0.2670.941−0.523−0.011
[Region = Oromia]−0.3970.801−0.640−0.154
[Region = Somalia]0.4160.0610.1780.654
[Region = Benishangul-gumuz]−0.3230.717−0.588−0.058
[Region = SNNPR]−0.0340.787−0.2800.212
[Region = Gambela]−0.3060.630−0.582−0.030
[Region = Harari]0.1320.650−0.1450.409
[Region = Addis Ababa]−0.0790.627−0.3950.238
[Region = Dire dawa]0 a
[Place of residence = Urban]−0.2393.1400.816−0.433−0.045
[Place of residence = Rural]0 a
[Mothers Educational level = No education]0.1761.8750.654−0.1260.477
[Mothers Educational level = primary]0.2460.902−0.0490.541
[Mothers Educational level = secondary]0.1240.618−0.1760.425
[Mothers Educational level = higher]0 a
[Sex of household head = Male]−0.0121.1340.845−0.1300.107
[Sex of household head = Female]0 a
[Size of child at birth = Very large]−0.2211.0450.615−0.373−0.068
[Size of child at birth = larger than Average]−0.0880.778−0.2470.071
[Size of child at birth = Medium]−0.0720.663−0.1990.054
[Size of child at birth = Smaller than average]−0.0480.691−0.2220.126
[Size of child at birth = Very Small]0 a
[Preceding birth interval (months) = <24]−0.0431.0290.803−0.1450.058
[Preceding birth interval (months = ≥24]0 a
[Antenatal care visit = None]0.6041.4640.5010.2430.964
[Antenatal care visit = 1–7]0.2540.558−0.0550.563
[Antenatal care visit = ≥8]0 a
[Type of cooking fuels = Modern fuel]−0.0851.3500.664−0.3140.143
[Type of cooking fuels = Traditional fuel]0 a
[Type of toilet facility = Improved toilet facility]−0.0341.5220.656−0.1840.116
[Type of toilet facility = Un-improved toilet facility]0 a
[Source of drinking water = Improved water]0.0971.2010.056−0.0020.197
[Source of drinking water = Un-improved water]0 a
a = reference category. Overall Brant test of parallel regression assumption: Chi-square = 48.66, p-value = 0.025. Goodness-of-fit test of overall model (Likelihood Ratio): Chi-square = 756.21, p-value = 0.000.
Table 2. Summaries of the descriptive statistics and bivariate analysis on factors associated with childhood anaemia status.
Table 2. Summaries of the descriptive statistics and bivariate analysis on factors associated with childhood anaemia status.
VariablesCategoriesAnaemic Status
MildModerateSevere x 2 p-Value
Place of residenceUrban43045641p < 0.000 *
Rural15201808138
Mothers Educational levelNo education1209146693p < 0.000 *
Primary49755259
Secondary16014620
Higher841007
Sex of household headMale15421771141p < 0.000 *
Female40849338
Wealth index of mothersPoorest66083562p < 0.000 *
Poorer36334234p < 0.000 *
Middle25329921
Richer22630610
Richest44848252
Age of Mothers15–2410102383p < 0.000 *
25–34193986768
35–4413678
45 and above0720
Current marital statusNever in Union321
Married/living with partner187121861760.987
Separated76762
RegionTigray21522624p < 0.000 *
Afar1472505
Amhara1791995
Oromia29826713
Somalia
Benishangul-gumuz27935959
SNNPR1321708
Gambela26128731
Harari1351251
Addis Ababa1211357
Dire dawa9213323
Mothers occupational statusNo14251617128p < 0.000 *
Yes52564751
Sex of childMale984114695p < 0.000 *
Female966111884
Preceding birth interval (months)<2453559348p < 0.000 *
≥2414151671131
Size of the child at birthVery large321364190.581
larger than Average28831033
Medium82996882
Smaller than average18521613
Very Small32740632
Child Age (in Months)<627128422p < 0.000 *
6–1123525518
12–2337344231
24–3746551254
38–4727536228
48–5933140926
Antenatal care visitNone1168940p < 0.000 *
1–717282063131
≥81061128
Source of drinking waterImproved water12031450116p < 0.000 *
Un-improved water11681463
Type of toilet facilityImproved toilet facility36342653p < 0.000 *
Un-improved toilet facility15871838126
Type of cooking fuelsModern fuel147159200.615
Traditional fuel18032105159
* Chi-square was significant at (p < 0.25).
Table 3. Results of multilevel logistic regression of intercept-only model.
Table 3. Results of multilevel logistic regression of intercept-only model.
ModelCoefficientStandard ErrorZ-Valuep-Value
Fixed intercept (β0)−0.7810.099−7.880.000
Random effect
Variance (community)1.4250.213
Variance (household)1.6980.254
Variance (maternal)1.5460.651
Icc (community)0.179
Icc (household)0.213
Icc (maternal)0.194
Table 4. Model comparisons among multilevel multinomial models.
Table 4. Model comparisons among multilevel multinomial models.
Model Comparison CriteriaNull Model (Model I)Individual-Level Factors (Model II)Maternal Level Factors (Model III)Households Level Factors (Model IV)Community-Level Factors (Model V)Individual, Maternal, Household, and Community-Level Factors (Model VI)
AIC19,059.3421,025.6914,191.2115,124.8715,001.5412,368.45
AIC: Akaike Information Criteria.
Table 5. Results of multilevel logistic regression model on childhood anaemia status.
Table 5. Results of multilevel logistic regression model on childhood anaemia status.
VariableMildModerateSevere
Fixed PartOR[95% C.I]p-ValueOR[95% C.I]p-ValueOR[95% C.I]p-Value
Constant2.8[2.0–3.9]0.0002.58[2.24–2.96]0.0003.09[2.03–4.70]0.000
Individual-level factors
Child Age (in Months) (ref. < 6)
6–110.96[0.73–1.10]0.3290.91[0.75–1.11]0.3970.91[0.75–1.12]0.406
12–230.86[0.72–1.03]0.1200.87[0.73–1.04]0.1300.82[0.72–1.03]0.115
24–370.83[0.70–0.98]0.0350.86[0.70–0.99]0.0000.84[0.71–1.0]0.057
38–470.81[0.67–0.97]0.0290.80[0.65–0.94]0.0000.79[0.66–0.94]0.011
48–590.79[0.66–0.95]0.0120.78[0.65–0.93]0.0000.87[0.71–0.98]0.000
Sex of child (ref. Male)
Female1.54[1.04–1.99]0.0001.61[1.24–1.89]0.0000.63[0.31–0.99]0.000
Preceding birth interval (months) (ref. < 24)
≥240.51[0.33–0.87]0.0040.89[0.80–0.99]0.0480.40[0.14–0.81]0.001
Maternal level factors
Mother’s age (ref. 15–24)
25–341.1[0.97–1.31]0.0931.01[0.95–1.19]0.2290.73[0.58–1.79]0.681
35–441.06[0.91–1.25]0.4060.64[0.40–1.68]0.1290.41[0.29–1.44]0.149
45 and above1.14[0.97–1.35]0.1010.51[0.42–1.58]0.4090.26[0.15–1.05]0.331
Mother’s educational level (ref. No education)
Primary1.4[0.86–1.99]0.0001.56[0.74–1.48]0.5471.01[0.91–1.1]0.628
Secondary1.27[0.97–1.34]0.0001.27[0.56–1.74]0.2411.8[1.45–2.3]0.000
Higher1.2[0.73–1.48]0.0001.32[1.09–1.9]0.0003.3[2.22–4.96]0.000
Antenatal care visit (ref. None)
1–70.03[0.008–0.14]0.0000.06[0.009–0.15]0.0000.01[0.009–0.20]0.000
≥80.08[0.019–0.16]0.0000.021[0.01–0.12]0.0000.05[0.010–0.14]0.000
Mother’s occupational status (ref. No)
Yes0.98[0.88–1.10]0.7810.92[0.83–1.03]0.1910.96[0.86–1.07]0.495
Wealth index (ref. poorest)
Poorer1.01[0.90–1.1]0.7631.01[0.88–1.17]0.7781.02[0.89–1.1]0.718
Middle1.78[1.40–2.2]0.0000.94[0.81–1.09]0.4620.95[0.82–1.103]0.535
Richer3.11[2.0–4.6]0.0000.98[0.84–1.14]0.8291.01[0.86–1.1]0.870
Richest1.44[1.15–2.1]0.0001.36[1.15–1.59]0.0001.4[1.11–1.75]0.003
Household-level factors
Sex of household head (ref. Male)
Female0.53[0.28–1.34]0.0650.65[0.41–1.42]0.3340.25[0.18–1.39]0.091
Source of drinking water (ref. Improved Water)
Unimproved Water0.57[0.18–0.88]0.0010.49[0.29–0.79]0.0380.62[0.43–0.91]0.022
Type of toilet facility (ref. Improved toilet)
Unimproved toilet0.66[0.57–0.78]0.0000.64[0.55–0.75]0.0000.65[0.55–0.76]0.000
Community level factors
Place of residence (ref. urban)
Rural0.70[0.60–0.82]0.0000.81[0.65–0.99]0.0000.56[0.48–0.64]0.000
Region (ref. Tigray)
Afar0.68[0.55–0.85]0.0010.72[0.57–0.89]0.0030.70[0.56–0.87]0.001
Amhara0.57[0.46–0.71]0.0000.42[0.19–0.82]0.0000.56[0.41–0.75]0.000
Oromia0.45[0.37–0.55]0.0000.47[0.39–0.57]0.0000.47[0.39–0.57]0.000
Somali0.98[0.79–1.20]0.8601.01[0.82–1.25]0.8540.96[0.78–1.19]0.772
Benishangul-gumuz0.70[0.56–0.88]0.0030.72[0.58–0.91]0.0060.72[0.57–0.91]0.005
SNNPR1.12[0.91–1.39]0.2681.14[0.92–1.41]0.2181.15[0.93–1.42]0.194
Gambela0.84[0.66–1.07]0.1740.76[0.59–0.97]0.0000.81[0.64–1.04]0.114
Harari0.87[0.67–1.14]0.3380.83[0.64–1.09]0.1900.84[0.64–1.09]0.201
Addis Ababa3.65[2.4–5.4]0.0002.67[1.75–4.05]0.0002.89[1.8–4.44]0.000
Diredawa0.56[0.43–0.72]0.0000.54[0.42–0.71]0.0000.53[0.39–0.67]0.000
Random-effect
Var (Cons.) Community0.849
ICC for Community (%)14.22%PCV for Community (%)40.42%
Var (Cons.) Household0.931
ICC for Household(%)15.6%PCV for Household (%)45.17%
Var (Cons.) Mothers0.899
ICC for Mothers(%)15.06%PCV for Maternal (%)41.85%
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Kuse, K.A.; Jima, D.S.; Chikako, T.U.; Hagan, J.E., Jr.; Seidu, A.-A.; Aboagye, R.G.; Ahinkorah, B.O. Individual, Maternal, Household, and Community Level Variability in Determining Inequalities in Childhood Anaemia within Ethiopia: Four-Level Multilevel Analysis Approach. Children 2022, 9, 1415. https://doi.org/10.3390/children9091415

AMA Style

Kuse KA, Jima DS, Chikako TU, Hagan JE Jr., Seidu A-A, Aboagye RG, Ahinkorah BO. Individual, Maternal, Household, and Community Level Variability in Determining Inequalities in Childhood Anaemia within Ethiopia: Four-Level Multilevel Analysis Approach. Children. 2022; 9(9):1415. https://doi.org/10.3390/children9091415

Chicago/Turabian Style

Kuse, Kenenisa Abdisa, Demie Seyoum Jima, Teshita Uke Chikako, John Elvis Hagan, Jr., Abdul-Aziz Seidu, Richard Gyan Aboagye, and Bright Opoku Ahinkorah. 2022. "Individual, Maternal, Household, and Community Level Variability in Determining Inequalities in Childhood Anaemia within Ethiopia: Four-Level Multilevel Analysis Approach" Children 9, no. 9: 1415. https://doi.org/10.3390/children9091415

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop