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Dietary diversity and its determinants among children aged 6–23 months in Ethiopia: evidence from the 2016 Demographic and Health Survey

Published online by Cambridge University Press:  06 October 2022

Binyam Girma Sisay*
Affiliation:
Department of Nutrition and Dietetics, School of Public Health, Addis Ababa University, Addis Ababa, Ethiopia
Tsion Afework
Affiliation:
Department of Preventive Medicine, School of Public Health, Addis Ababa University, Addis Ababa, Ethiopia
Beshada Rago Jima
Affiliation:
Department of Nutrition and Dietetics, School of Public Health, Addis Ababa University, Addis Ababa, Ethiopia
Nardos Wondafrash Gebru
Affiliation:
Department of Nutrition and Dietetics, School of Public Health, Addis Ababa University, Addis Ababa, Ethiopia
Addisalem Zebene
Affiliation:
Department of Nutrition and Dietetics, School of Public Health, Addis Ababa University, Addis Ababa, Ethiopia
Hamid Y. Hassen
Affiliation:
Department of Primary and Interdisciplinary Care, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium
*
*Corresponding author: Binyam Girma Sisay, email [email protected]

Abstract

Dietary diversity in children may be influenced not only by individual circumstances but also by the features of the community in which they live. Our study aimed to assess community and individual-level determinants of minimum dietary diversity among children aged 6–23 months in Ethiopia. We included 2960 children aged 6–23 months from the recent Ethiopia Demographic and Health Survey. A minimum dietary diversity was defined as the consumption of at least five food groups out of the eight reference food groups within 24 h by children aged 6–23 months. Multilevel logistic regression was used to investigate the drivers of minimum dietary diversity in Ethiopian children aged 6–23 months. About 12⋅5 % of children met the bare minimum of dietary diversification. Age of the child (9–11 months AOR, 3⋅3 (95 % CI 1⋅8, 5⋅6), 12–17 months AOR, 4⋅0 (95 % CI 2⋅4, 6⋅7), 18–23 months AOR, 3⋅5 (95 % CI 2⋅0, 5⋅8)), caregiver listening radio at least once a week AOR, 1⋅6 (95 % CI 1⋅1, 2⋅4) and wealth quantiles (Second AOR, 1⋅8 (95 % CI 1⋅1, 3⋅1), Fourth AOR, 2⋅9 (95 % CI 1⋅6, 5⋅2) and Highest AOR, 2⋅2 (95 % CI 1⋅1, 4⋅2)) were individual characteristics associated with dietary diversity. Place of residence was the only community-level characteristic associated with children's dietary diversity (Rural AOR, 0⋅4 (95 % CI 0⋅2, 0⋅6)). The minimum dietary diversity among Ethiopian children is suboptimal. Nutrition programmes aimed at enhancing dietary diversity should be strengthened in this population, particularly for those from poor families and residing in rural areas.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s), 2022. Published by Cambridge University Press on behalf of The Nutrition Society

Introduction

Globally, childhood malnutrition poses a serious public health challenge(Reference Black, Victora and Walker1). Undernutrition is responsible for approximately 45 % of deaths among children under the age of five, particularly in low- and middle-income countries (LMICs)(2). Inappropriate infant and young child feeding (IYCF) practices contribute to more than half of under-five children's mortality(3). The first 2 years of life are recognised as a critical window in which children require more energy and nutrient-dense foods for optimal growth, physical and mental development(4). Furthermore, appropriate feeding practices for infants and young children reduce morbidity, mortality and risk of other chronic diseases. Thus, ensuring adequate nutrition during the period of 6–23 months of age is a major global health priority. However, meeting nutritional needs during this age interval is challenging(Reference Dewey5).

The World Health Organization (WHO) has developed a set of core indicators to assess IYCF practices among children aged 6–23 months considering both breast- and complementary feeding-related practices(6). Dietary diversity is one of the key indicators identified as a useful predictor of the nutrient adequacy of children's dietary patterns(Reference Nti7). It is a measure of the number of different food items/groups consumed over 24 h(6). The WHO identified eight food groups (breast milk, grains, roots and tubers; legumes and nuts; dairy products; flesh foods (meats/fish/poultry); eggs; vitamin A-rich fruits and vegetables; and other fruits and vegetables) which provide the required amount of macro and micronutrients for children aged 6–23 months. It is recommended that children aged 6–23 months consume at least five or more food groups daily(8).

Consumption of diversified food has been linked to the better nutritional status of children in LMICs(Reference Arimond and Ruel9,Reference Sawadogo, Martin-Prével and Savy10) . On the other hand, inadequate dietary diversity has been linked to stunting and being underweight among children. Children who do not meet the minimum dietary diversity requirements are more likely to be stunted, underweight and anaemic(Reference Rah, Akhter and Semba11Reference Belachew and Tewabe13). Furthermore, inadequately diversified diets predispose children to infection and severe illnesses(Reference Caulfield, de Onis and Blössner14).

Globally, only 28⋅2 % of children aged 6–23 months get the recommended level of dietary diversity. The situation is exacerbated in LMICs, particularly in South Asia, Eastern, West Southern and Central Africa(Reference White, Bégin and Kumapley15). Despite efforts to improve children's dietary diversity, Ethiopia remains the country with the lowest adequate dietary diversity among East African countries(Reference Kang, Chimanya and Matji16). In 2016, only 14 % of Ethiopian children had been given a sufficient number of food groups and were considered to have an adequately diverse diet(17).

Few studies in Ethiopia had attempted to assess the determinants of dietary diversity among children, particularly those aged 6–23 months(Reference Kuche, Moss and Eshetu18Reference Disha, Tharaney and Abebe21). However, available studies are restricted to certain areas and contexts, and comprehensive evidence-based nationally representative data are scarce. Hence, we investigated the community and individual-level determinants of minimum dietary diversity among children aged 6–23 months in Ethiopia, using an advanced statistical method, and considering the hierarchical nature of the Ethiopia Demographic and Health Survey (DHS) data.

Methods

Study setting

The study was carried out in Ethiopia, a country located in Northeastern Africa. The country has a total estimated population of 109⋅2 million people and covers about 1⋅1 million square kilometres of area and has great geographical diversity, ranging from 4550 m above sea level to 110 m below sea level. The data were collected based on the country's previous nine administrative regions and two administrative cities(17), but the country now has two additional regions (Sidama region and South West Ethiopia Region) that are separate from the Southern Nations, Nationalities and Peoples’ Region (SNNPR). The administrative region is divided into zones, districts, towns and kebeles (the smallest administrative units).

Study design

The present study used a cross-sectional, secondary data analysis design. We used the most recent and nationally representative 2016 Ethiopian Demographic Health Survey (EDHS) data(17). A stratified two-stage cluster sampling technique was applied. A total of 645 enumeration areas (EAs) were chosen in the first stage, using probabilities proportionate to EA size (202 in urban and 443 in rural) (based on the 2007 EPHC frame). A fixed number of twenty-eight households in each cluster were chosen using an equal probability systematic sampling technique in the second stage. For this study, Kids Record (KR) file containing information about women and children was used, and important variables related to inadequate dietary diversity were extracted from the dataset. In the present study, 2960 weighted data of children aged 6–23 months were used for analysis.

Measurement of outcome

Based on the updated WHO guideline(8), minimum dietary diversity was defined as the proportion of children aged 6–23 months who consumed at least five food groups out of the eight referenced food groups within 24 h. These food groups are (1) breast milk; (2) grains, roots, and tubers; (3) legumes and nuts; (4) dairy products; (5) flesh foods (meats/fish/poultry); (6) eggs; (7) vitamin A-rich fruits and vegetables; and (8) other fruits and vegetables. The total dietary diversity score ranges from 0 to 8, with 1 point given for each of the 8 food groups consumed. Children with dietary diversity scores ≥5 were classified as they attained the minimum dietary diversity, whereas those with scores <5 were classified as unmet MDD. The outcome variable was coded as 1 for adequate dietary diversity and 0 for inadequate dietary diversity.

Determinants

We selected possible determinants based on evidence from literature and the availability of variables in the EDHS-2016. We investigated the effect of explanatory factors on dietary diversity at both the individual and community levels.

The study included individual-level determinants such as child, maternal and paternal characteristics. The children's characteristics included sex, age (in months), birth order and episodes of cough or fever in the last 2 weeks. Maternal characteristics included: age (years), highest educational level, frequency of listening to the radio, frequency of watching television, attending Antenatal care (ANC) follow-up, place of delivery, postnatal care visit and maternal empowerment(Reference Choudhury, Headey and Masters22). Paternal characteristics included paternal characteristics including the highest educational level and occupation. Household characteristics include the household wealth index, the gender of the household head, the number of children under the age of five and the number of total household members. Parents’ occupations were classified as Not working (unemployed), Nonagricultural works (professional, technical, managerial, clerical, sales, services, skilled manual and unskilled manual), Agricultural works (agricultural – employee) and others.

The community-level determinants included contextual region (agrarian dominant, city dwellers dominant and pastoralist dominant), place of residence (either urban v. rural) and aggregate variables such as community poverty (higher v. lower), community distance to a health facility (distance a big problem v. distance, not a big problem) and remoteness of the location. Community poverties were created from mean values of wealth index categories of the individual mothers for each cluster. The two values for the community poverty level were higher poverty and lower poverty.

The EDHS did not capture data that can directly describe the characteristics of the community/clusters except the place of residence, mean rainfall, mean temperature and altitude. Hence, we created community variables by aggregating the individual-level characteristics within their clusters. The aggregates were computed using the average values of the proportions of women in each category of a given variable. Likewise, based on the national median values aggregate values were categorised into groups. These aggregate community-level determinants include contextual region, community distance to a health facility and remoteness of the location. We used GIS estimates of travel time to cities to construct a ‘living in a remote location’ dummy variable that equals 1 if the DHS cluster has more than a one-hour travel time to a town/city of 20 000 people or more(Reference Choudhury, Headey and Masters22).

Contextual region: For this study, the administrative regions were categorised into agrarian, pastoralist and city, based on their settings that may have a relationship with child dietary diversity. Since regions used for administrative purposes might not necessarily be related to the child feeding practice of the population. The regions of Tigray, Amhara, Oromia, SNNPR, Gambella and Benshangul-Gumuz were recorded as agrarian. The Somali and Afar regions were combined to form the pastoralist region and the city administrations – Addis Ababa, Dire Dawa and Harar – were combined as a city. Though Gambela and Benshangul-Gumuz have been considered pastoralists in recent times, their living settings approached the agrarian(Reference Yebyo, Alemayehu and Kahsay23).

Ecological level variables such as mean rainfall per year, 1985–2015 (mm), mean temperature, 1985–2015 (Celsius) and altitude (metres) were also included.

Data management and analysis

The data were analysed using STATA version 16 (StataCorp, College Station, TX, USA). In this analysis, households with children aged 6–23 months old with no missing information on dietary diversity were included. To adjust for the redistribution of samples to different regions and the possible variation in response rates, we used sampling weight in all the analyses. The ‘Svy’ command was used to allow for adjustments for the cluster sampling design. Categorical variables were reported using absolute and relative frequencies; whereas continuous variables were summarised using mean with standard deviation (sd) or median and interquartile range (IQR) for variables that deviate from normal distribution after visual examination using a histogram.

Due to the nature of the EDHS data, being a hierarchical structure, data are often correlated and thus cannot be assumed, independent. Hence, to identify individual and community-level determinants of dietary diversity, we performed a multilevel logistic regression. A multilevel approach adequately adjusts the unexplained variability of the nested structure and can estimate cluster-level effects on the outcome variable. Therefore, in the present study, a two-level mixed-effect logistic regression analysis was employed to estimate the independent (fixed) effects of the explanatory variables on dietary diversity adjusting for cluster and regional-level random effects. To investigate the community and individual-level determinants of minimum dietary diversity among children aged 6–23 months, any variable with a P-value of 0⋅25 on a univariable test was a candidate for the multivariable model, along with all variables of known clinical importance. Four models were fitted and compared. Model 1 was an empty model which was fitted without independent variables to test random variability using the Intraclass correlation coefficient (ICC); Model 2 include individual-level factors (age of the child, mother's educational level, frequency of listening a radio and wealth quintile of household); Model 3 include community-level factors (place of residence (either urban v. rural), mean annual rainfall of the cluster 1985–2015 (mm) and mean temperature 1985–2015 (Celsius)) and Model 4 include both individual and community-level factors. The relative fits of these models were then compared using the Akaike (AIC) and Bayesian Information Criterion (BIC), and the difference in model fit was compared using the χ 2 test. Finally, the adjusted odds ratios (AORs) with the 95 % confidence intervals (95 % CI) were reported.

Ethical considerations

We requested access to the datasets from the Demographic and Health Surveys (DHS) program/ICF International, and permission was granted by DHS program data archivists to download the dataset for this study. Before the authors could access the data, it was de-identified. The data were only used for the registered research topic and were not shared with anyone else.

Results

Participant's characteristics

Out of a total of 2960 children, the majorities (53⋅0 %) were girls, with 36⋅7 % aged 12–17 months. Nearly one-third (32 %) of children were second or third born for their families. The majority (52⋅0 %) of mothers were between the ages of 20 and 29 years, and 802 (60⋅9 %) had no formal education. More than half of the mothers (61⋅5 %) gave birth at home, and 1018 (34⋅0 %) did not seek ANC during their most recent pregnancy. The proportion of mothers who never watched television and never listened to the radio was 81⋅6 and 72⋅5 %, respectively. Two hundred and seven (7⋅4 %) of fathers and 1802 (57⋅5 %) of mothers were unemployed. Most children (87⋅8 %) resided in rural areas and agrarian dominant regions (91⋅8 %) (Table 1).

Table 1. Children's, parental, household, healthcare and community-level characteristics of living children aged 6–23 months, Ethiopia 2016

Dietary diversity

For children aged 6–23 months, the median dietary diversity score was 4 (IQR: 2–4), with only 12⋅5 % achieving the minimum dietary diversity (Fig. 1). The proportion of children who met the required minimum dietary diversity was higher among those who reside in urban (28⋅1 %) than rural (10⋅3 %). The percentage of children who achieved the minimum dietary diversity was lower among children belonging to households in the lower quantiles (7⋅4 %) compared to second, middle, fourth and highest households. Only 9⋅7 % of children whose mother has no education has achieved the minimum dietary diversity, which is much lower compared to children whose mothers have primary (13⋅3 %), secondary (20⋅6 %) and tertiary education (46⋅5 %) education (Table 2).

Fig. 1. Distribution of the dietary diversity score and prevalence of the minimum dietary diversity for 6–23 months children in Ethiopia 2016.

Table 2. The distribution of children 6–23 months who achieve the minimum dietary diversity in Ethiopia 2016

Food groups consumed

Grain, roots and tubers (63⋅6 %) were the most consumed food items 24 h preceding the survey. However, only 8⋅7 and 17⋅2 % of children, respectively, have consumed flesh foods and eggs in the past 24 h preceding the survey. In addition, only 2⋅8 % of children aged 6–8 months consumed flesh foods such as meat and poultry (Table 3).

Table 3. The distribution of intake of eight food groups for children 6–23 months of age, in Ethiopia 2016

Determinants of minimum dietary diversity

Compared to those mothers who had no exposure to listening to a radio, those who had listened to the radio at least once a week (AOR 1⋅6; 95 % CI 1⋅1, 2⋅4) or less than once a week (AOR 1⋅6; 95 % CI 1⋅1, 2⋅4) are nearly twice more likely to meet the minimum dietary diversity. Furthermore, compared to the children from the lowest wealth quintile household, those who were from the second wealth quintile household were nearly two times more likely (AOR 1⋅8; 95 % CI 1⋅1, 3⋅0), from the fourth wealth quintile household were nearly three times more likely (AOR 2⋅8; 95 % CI 1⋅6, 4⋅9) and from the highest wealth quintile household were two times more likely (AOR 2⋅1; 95 % CI 1⋅1, 4⋅0) to meet the minimum dietary diversity (Table 4).

Table 4. Determinants of minimum dietary diversity in children aged 6–23 months in Ethiopia 2016

COR, crude odds ratio; AOR, adjusted odds ratio; CI, confidence interval.

Discussion

The present study aimed to assess the determinants of dietary diversity using nationally representative 2016 EDHS data. We found that only 12⋅5 % of children aged 6–23 months have adequate minimum dietary diversity, indicating a suboptimal level of dietary diversity score. In addition, we observed that only a small proportion of children consumed animal-source foods. Furthermore, the child's age, caregivers’ frequency of radio listening, residence and household wealth index were all significantly associated with children's minimum dietary diversity.

The prevalence of minimum dietary diversity was found to be lower in this study than in the 2016 EDHS report(17). This could be due to the disparity in cut-off points and the number of food groups used to calculate the dietary diversity score. The previous dietary diversity score was constructed based on seven food groups and a child consuming at least four food groups is considered to have achieved the minimum dietary diversity; however, according to the most recent WHO guidelines, the dietary diversity is based on eight food groups, and a child consuming at least five of the food groups is considered to have achieved the minimum dietary diversity(6,8) . Furthermore, the low level of dietary diversity in the study indicates that the majority of children consume a monotonous diet that focuses on a limited number of food groups. Similarly, a systematic review of Ethiopian studies found a low suboptimal level of dietary diversity (23⋅25 %) among children aged 6–23 months(Reference Temesgen, Negesse and Woyraw24). According to studies conducted in India, Rwanda and Burundi, only a small proportion of children receive the required minimum dietary diversity(Reference Beckerman-Hsu, Kim and Sharma25,Reference Custodio, Herrador and Nkunzimana26) . This low dietary diversity may indicate an insufficient intake of micronutrients(Reference Kennedy, Pedro and Seghieri27). Therefore, National Nutrition Program in collaboration with other sectors needs to put an effort to improve the accessibility and utilisation of diversified food types to improve the dietary diversity of children.

Our study showed that grains, roots and tubers were the most consumed food items. Another study conducted in southern Ethiopia found that grains, roots and tubers are the primary staples of children aged 6–23 months(Reference Temesgen28). Meanwhile, animal-source foods such as meat, dairy products and eggs are consumed only by a small proportion of children in the present study, which is consistent with studies conducted in other parts of Ethiopia(Reference Feyisa, Tefera and Endris29,Reference Tessema, Belachew and Ersino30Reference Beyene, Worku and Wassie32) . Similarly, animal-source food consumption is lower in sub-Saharan African countries than in other parts of the world(Reference Choudhury, Headey and Masters22). Animal-source foods contain a variety of vitamins and minerals, including calcium, iron, vitamin B-12, vitamin A, riboflavin and zinc, which are difficult to obtain in sufficient quantities from plant-based foods alone(Reference Neumann, Harris and Rogers33). Hence, inadequate intake of animal-source foods may lead to inadequate intake of these micronutrients(Reference Dror and Allen34). One reason for the low consumption could be that most animal-source foods were intended for market and a profitable income rather than consumption by family members. Another reason could be a lack of knowledge about the nutritional benefits of these foods(Reference Haileselassie, Redae and Berhe35). A study conducted on Ethiopian mothers showed that mothers are afraid of feeding their children animal-source foods because they believe their children are incapable of digesting them(36). As a result, we recommend that public health practitioners should increase parental and caregiver awareness of the importance of animal-source foods for child growth and development.

Additionally, low consumption of animal-source foods may be due to a lack of access caused by economic constraints(Reference Gebremedhin, Baye and Bekele37). The high price of animal-source foods does not encourage consumption by poor households. This can further be explained by the observed association between household economic status – as measured by wealth quantile and inadequate dietary diversity in this study. Children from the highest wealth quintile of households were more likely to achieve the minimum dietary diversity than children from the lowest wealth quintile of households. This finding is in line with several studies conducted in different parts of Ethiopia and other parts of the world(Reference Beyene, Worku and Wassie32,Reference Joshi, Agho and Dibley38Reference Belew, Ali and Abebe40) . This association could be explained by the fact that second, middle, fourth and highest households are more likely to be food secure and can purchase a variety of foods(Reference Dafursa and Gebremedhin41).

In our study, older children had a higher odds of achieving minimum dietary diversity than younger children, indicating that infants receive inadequately diversified food when compared to older children. This might be due to the delayed introduction of complementary foods or to the use of only milk and cereals as complementary foods. Another possible explanation is that mothers believe that certain foods, such as bananas, eggs, pumpkin, carrots, green vegetables and meat, are difficult for young children to digest(Reference Tassew, Tekle and Belachew42). This finding is supported by similar studies conducted in Ethiopia among children aged 6–23 months(Reference Beyene, Worku and Wassie32,Reference Belew, Ali and Abebe40,Reference Tegegne, Sileshi and Benti43,Reference Patel, Pusdekar and Badhoniya44) .

The present study showed that mothers who listen to the radio at least once a week are more likely to feed their children a diverse diet than those who do not. Consistently, a study done in India found that listening to the radio was a significant factor in children's dietary diversity(Reference Patel, Pusdekar and Badhoniya44). Similar studies conducted in Northwest Ethiopia and Bangladesh found that a mother's exposure to mass media was a significant predictor of her children's dietary diversity(Reference Beyene, Worku and Wassie32,Reference Blackstone and Sanghvi45) . This suggests that disseminating information about IYCF through the media may have a positive impact on their children's dietary diversity(Reference Bedada Damtie, Benti Tefera and Tegegne Haile46).

Even though studies conducted in Ethiopia and Asia have found a positive association between maternal education and children's dietary diversity(Reference Tegegne, Sileshi and Benti43,Reference Gautam, Adhikari and Khatri47Reference Khan, Kayina and Agrawal49) , we did not find a statistically significant association between mother's educational status and children's minimum dietary diversity. This suggests that, regardless of the mother's educational attainment, there may be difficulties in translating education into improved dietary practices and subsequent improvements in nutritional status(Reference Khan, Kayina and Agrawal49). The other reason might be due to the presence of a very low number of mothers with the highest educational level.

The study's findings should be interpreted considering the following strengths and limitations. First, the use of nationally representative survey data from Demographic Health Surveys enhances the generalizability of our findings. Second, the application of multilevel analysis to account for individual and community-level contributors to children's dietary diversity. In Ethiopia due to religious or societal reasons, animal-source foods are commonly consumed during feast days, holidays and on special occasions or avoided during the fasting period(Reference Haileselassie, Redae and Berhe35). We do not know whether the data were collected on a representative day, and the data collection period could have resulted in misclassification bias. The data collection period coincided with the longest religious fasting period, which may have resulted in an underestimation of animal-source food consumption, and as a result, a low dietary diversity score.

In conclusion, a suboptimal level of dietary diversity has been observed among Ethiopian children aged 6–23 months. This low dietary diversity is more prevalent in rural children and children from low-income families. The present study also found that individual and community-level factors such as a child's age, frequency of radio listening, residence and household wealth status influence children's dietary diversity. Nutrition programmes promoting dietary diversity should be implemented throughout the country, particularly for those from low-income families living in rural areas, in collaboration with health workers and/or the media. Furthermore, reinforcing optimal feeding practices through nutrition education provided by the healthcare providers will assist parents and other caregivers in providing a more diverse diet for their children. Further studies should assess community and individual-level determinants of adequate minimum dietary diversity using representative data.

Acknowledgements

We would like to show gratitude to the DHS program for making the data freely available.

The authors’ roles were as follows: B. G. S., T. A., B. R. J. and N. W. were conceptualised and designed the study. B. G. S. and H. Y. H. were checked the data and performed the analysis; and all authors wrote and corrected the paper, as well as read and approved the final manuscript.

The authors declare that there is no conflict of interest.

Data that support the findings of this study are available from the DHS program.

References

Black, RE, Victora, CG, Walker, SP, et al. (2013) Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet 382, 427451. doi:10.1016/S0140-6736(13)60937-X, Epub 2013 Jun 6. Erratum in: Lancet 2013;382(9890):396. PMID: 23746772.CrossRefGoogle ScholarPubMed
WHO (2020) Malnutrition. https://www.who.int/news-room/fact-sheets/detail/malnutrition (accessed 5 January 2021).Google Scholar
Nutrition IC (2013) The Achievable Imperative for Global Progress. New York, NY: UNICEF.Google Scholar
World Health Organization (2009) Guiding Principles for Feeding Non-breastfed Children 6–24 Months of Age. 2005. Geneva: WHO.Google Scholar
Dewey, KG (2013) The challenge of meeting nutrient needs of infants and young children during the period of complementary feeding: an evolutionary perspective. J Nutr 143, 20502054. doi:10.3945/jn.113.182527, Epub 2013 Oct 16. PMID: 24132575; PMCID: PMC3827643.CrossRefGoogle Scholar
World Health Organization (2010) Indicators for Assessing Infant and Young Child Feeding Practices Part 3: Country Profiles. Geneva, Switzerland: World Health Organization.Google Scholar
Nti, CA (2011) Dietary diversity is associated with nutrient intakes and nutritional status of children in Ghana. Asian J Med Sci 2, 105109.CrossRefGoogle Scholar
World Health Organization (2017) Global Nutrition Monitoring Framework: operational guidance for tracking progress. Geneva, Switzerland: World Health Organization.Google Scholar
Arimond, M & Ruel, MT (2004) Dietary diversity is associated with child nutritional status: evidence from 11 Demographic and Health Surveys. J Nutr 134, 25792585. doi:10.1093/jn/134.10.2579, PMID: 15465751.CrossRefGoogle ScholarPubMed
Sawadogo, PS, Martin-Prével, Y, Savy, M, et al. (2006) An infant and child feeding index is associated with the nutritional status of 6- to 23-month-old children in rural Burkina Faso. J Nutr 136, 656663. doi:10.1093/jn/136.3.656, PMID: 16484539.CrossRefGoogle ScholarPubMed
Rah, JH, Akhter, N, Semba, RD, et al. (2010) Low dietary diversity is a predictor of child stunting in rural Bangladesh. Eur J Clin Nutr 64, 13931398. doi:10.1038/ejcn.2010.171, Epub 2010 Sep 15. PMID: 20842167.CrossRefGoogle ScholarPubMed
Khamis, AG, Mwanri, AW, Ntwenya, JE, et al. (2019) The influence of dietary diversity on the nutritional status of children between 6 and 23 months of age in Tanzania. BMC Pediatr 19, 518. doi:10.1186/s12887-019-1897-5, PMID: 31881999; PMCID: PMC6935228.CrossRefGoogle ScholarPubMed
Belachew, A & Tewabe, T (2020) Under-five anemia and its associated factors with dietary diversity, food security, stunted, and deworming in Ethiopia: systematic review and meta-analysis. Syst Rev 9, 31. doi:10.1186/s13643-020-01289-7, PMID: 32051034; PMCID: PMC7017616.CrossRefGoogle ScholarPubMed
Caulfield, LE, de Onis, M, Blössner, M, et al. (2004) Undernutrition as an underlying cause of child deaths associated with diarrhea, pneumonia, malaria, and measles. Am J Clin Nutr 80, 193198. doi:10.1093/ajcn/80.1.193, PMID: 15213048.CrossRefGoogle Scholar
White, JM, Bégin, F, Kumapley, R, et al. (2017) Complementary feeding practices: current global and regional estimates. Matern Child Nutr 13, e12505. doi:10.1111/mcn.12505, PMID: 29032623; PMCID: PMC6865887.CrossRefGoogle ScholarPubMed
Kang, Y, Chimanya, K, Matji, J, et al. (2019) Determinants of minimum dietary diversity among children aged 6–23 months in 7 countries in East and Southern Africa (P10-035-19). Curr Dev Nutr 3, nzz034-P10.CrossRefGoogle Scholar
Ethiopian Public Health Institute (EPHI), ICF (2017) Ethiopia Demographic and Health Survey 2016: Final Report. Rockville, Maryland, USA.Google Scholar
Kuche, D, Moss, C, Eshetu, S, et al. (2020) Factors associated with dietary diversity and length-for-age z-score in rural Ethiopian children aged 6–23 months: a novel approach to the analysis of baseline data from the Sustainable Undernutrition Reduction in Ethiopia evaluation. Matern Child Nutr 16, e12852. doi:10.1111/mcn.12852, Epub 2019 Jul 13. PMID: 31124274; PMCID: PMC7038872.CrossRefGoogle Scholar
Gatahun, EA & Abyu, DM (2015) Dietary diversity feeding practice and determinants among children aged 6–23 months in Kemba Woreda, southern Ethiopia implication for public health intervention. J Nutr Food Sci 13, S13003.Google Scholar
Dangura, D & Gebremedhin, S (2017) Dietary diversity and associated factors among children 6-23 months of age in Gorche district, Southern Ethiopia: cross-sectional study. BMC Pediatr 17, 6. doi:10.1186/s12887-016-0764-x, PMID: 28068965; PMCID: PMC5223415.CrossRefGoogle ScholarPubMed
Disha, A, Tharaney, M, Abebe, Y, et al. (2015) Factors Associated with Infant and Young Child Feeding Practices in Amhara Region and Nationally in Ethiopia: Analysis of the 2005 and 2011 Demographic and Health Surveys, vol. 2, pp. 659, Washington, DC: Alive and Thrive.Google Scholar
Choudhury, S, Headey, DD & Masters, WA (2019) First foods: diet quality among infants aged 6–23 months in 42 countries. Food Policy 88, 101762. doi:10.1016/j.foodpol.2019.101762, PMID: 31853163; PMCID: PMC6894322.CrossRefGoogle Scholar
Yebyo, H, Alemayehu, M & Kahsay, A (2015) Why do women deliver at home? Multilevel modeling of Ethiopian National Demographic and Health Survey data. PLoS One 10, e0124718. doi:10.1371/journal.pone.0124718, PMID: 25874886; PMCID: PMC4398378.CrossRefGoogle ScholarPubMed
Temesgen, H, Negesse, A, Woyraw, W, et al. (2018) Dietary diversity feeding practice and its associated factors among children age 6-23 months in Ethiopia from 2011 up to 2018: a systematic review and meta-analysis. Ital J Pediatr 44, 109. doi:10.1186/s13052-018-0567-9, PMID: 30223854; PMCID: PMC6142683.CrossRefGoogle ScholarPubMed
Beckerman-Hsu, JP, Kim, R, Sharma, S, et al. (2020) Dietary variation among children meeting and not meeting minimum dietary diversity: an empirical investigation of food group consumption patterns among 73,036 children in India. J Nutr 150, 28182824. doi:10.1093/jn/nxaa223, PMID: 32805040; PMCID: PMC7762760.CrossRefGoogle Scholar
Custodio, E, Herrador, Z, Nkunzimana, T, et al. (2019) Children's dietary diversity and related factors in Rwanda and Burundi: a multilevel analysis using 2010 Demographic and Health Surveys. PLoS One 14, e0223237. doi:10.1371/journal.pone.0223237, PMID: 31596868; PMCID: PMC6785172.CrossRefGoogle ScholarPubMed
Kennedy, GL, Pedro, MR, Seghieri, C, et al. (2007) Dietary diversity score is a useful indicator of micronutrient intake in non-breast-feeding Filipino children. J Nutr 137, 472477. doi:10.1093/jn/137.2.472, PMID: 17237329.CrossRefGoogle ScholarPubMed
Temesgen, M (2013) Nutritional status of Ethiopian weaning and complementary foods: a review. Open Access Sci Rep 2, 19.Google Scholar
Feyisa, BB, Tefera, GM, Endris, BS, et al. (2020) Feeding practice, energy, and nutrient intake adequacy among children aged 6–23 months in southern Ethiopia: a community based cross-sectional study. Food Sci Nutr 8, 66806690. doi:10.1002/fsn3.1962, PMID: 33312551; PMCID: PMC7723221.CrossRefGoogle ScholarPubMed
Tessema, M, Belachew, T & Ersino, G (2013) Feeding patterns and stunting during early childhood in rural communities of Sidama, South Ethiopia. Pan Afr Med J 14, 75. doi:10.11604/pamj.2013.14.75.1630, PMID: 23646211; PMCID: PMC3641921.Google ScholarPubMed
Temesgen, H, Yeneabat, T & Teshome, M (2018) Dietary diversity and associated factors among children aged 6–23 months in Sinan Woreda, Northwest Ethiopia: a cross-sectional study. BMC Nutr 4, 5. doi:10.1186/s40795-018-0214-2, PMID: 32153869; PMCID: PMC7050891.CrossRefGoogle ScholarPubMed
Beyene, M, Worku, AG & Wassie, MM (2015) Dietary diversity, meal frequency and associated factors among infant and young children in Northwest Ethiopia: a cross-sectional study. BMC Public Health 15, 1007. doi:10.1186/s12889-015-2333-x, PMID: 26433689; PMCID: PMC4592571.CrossRefGoogle Scholar
Neumann, C, Harris, DM & Rogers, LM (2002) Contribution of animal source foods in improving diet quality and function in children in the developing world. Nutr Res 22, 193220.CrossRefGoogle Scholar
Dror, DK & Allen, LH (2011) The importance of milk and other animal-source foods for children in low-income countries. Food Nutr Bull 32, 227243. doi:10.1177/156482651103200307, PMID: 22073797.CrossRefGoogle ScholarPubMed
Haileselassie, M, Redae, G, Berhe, G, et al. (2020) Why are animal source foods rarely consumed by 6–23 months old children in rural communities of Northern Ethiopia? A qualitative study. PLoS One 15, e0225707. doi:10.1371/journal.pone.0225707. Erratum in: PLoS One 2020;15(3):e0230527. PMID: 31914130; PMCID: PMC6948827.CrossRefGoogle ScholarPubMed
Alive & Thrive (2010) IYCF practices, beliefs and influences in Tigray region, Ethiopia. Addis Ababa, Ethiopia: Alive & Thrive.Google Scholar
Gebremedhin, S, Baye, K, Bekele, T, et al. (2017) Predictors of dietary diversity in children ages 6 to 23 mo in largely food-insecure area of South Wollo, Ethiopia. Nutrition 33, 163168. doi:10.1016/j.nut.2016.06.002, Epub 2016 Jun 16. PMID: 27499206.CrossRefGoogle Scholar
Joshi, N, Agho, KE, Dibley, MJ, et al. (2012) Determinants of inappropriate complementary feeding practices in young children in Nepal: secondary data analysis of Demographic and Health Survey 2006. Matern Child Nutr 8, 4559. doi:10.1111/j.1740-8709.2011.00384.x, PMID: 22168518; PMCID: PMC6860874.CrossRefGoogle ScholarPubMed
Solomon, D, Aderaw, Z & Tegegne, TK (2017) Minimum dietary diversity and associated factors among children aged 6-23 months in Addis Ababa, Ethiopia. Int J Equity Health 16, 181. doi:10.1186/s12939-017-0680-1, PMID: 29025434; PMCID: PMC5639776.CrossRefGoogle ScholarPubMed
Belew, AK, Ali, BM, Abebe, Z, et al. (2017) Dietary diversity and meal frequency among infant and young children: a community based study. Ital J Pediatr 43, 73. doi:10.1186/s13052-017-0384-6, PMID: 28810887; PMCID: PMC5558775.CrossRefGoogle Scholar
Dafursa, K & Gebremedhin, S (2019) Dietary diversity among children aged 6–23 months in Aleta Wondo District, Southern Ethiopia. J Nutr Metab 2019, 2869424. doi:10.1155/2019/2869424, PMID: 31815015; PMCID: PMC6878804.CrossRefGoogle ScholarPubMed
Tassew, AA, Tekle, DY, Belachew, AB, et al. (2019) Factors affecting feeding 6-23 months age children according to minimum acceptable diet in Ethiopia: a multilevel analysis of the Ethiopian Demographic Health Survey. PLoS One 14, e0203098. doi:10.1371/journal.pone.0203098, PMID: 30789922; PMCID: PMC6383941.CrossRefGoogle ScholarPubMed
Tegegne, M, Sileshi, S, Benti, T, et al. (2017) Factors associated with minimal meal frequency and dietary diversity practices among infants and young children in the predominantly agrarian society of Bale zone, Southeast Ethiopia: a community based cross sectional study. Arch Public Health 75, 53. doi:10.1186/s13690-017-0216-6, PMID: 29158896; PMCID: PMC5682638.CrossRefGoogle ScholarPubMed
Patel, A, Pusdekar, Y, Badhoniya, N, et al. (2012) Determinants of inappropriate complementary feeding practices in young children in India: secondary analysis of National Family Health Survey 2005–2006. Matern Child Nutr 8, 2844. doi:10.1111/j.1740-8709.2011.00385.x, PMID: 22168517; PMCID: PMC6860525.CrossRefGoogle ScholarPubMed
Blackstone, S & Sanghvi, T (2018) A comparison of minimum dietary diversity in Bangladesh in 2011 and 2014. Matern Child Nutr 14, e12609. doi:10.1111/mcn.12609, Epub 2018 Apr 16. PMID: 29663657; PMCID: PMC6866105.CrossRefGoogle ScholarPubMed
Bedada Damtie, S, Benti Tefera, T & Tegegne Haile, M (2020) Dietary diversity practice and associated factors among children aged 6–23 months in Robe Town, Bale zone, Ethiopia. J Nutr Metab 2020, 9190458. doi:10.1155/2020/9190458, PMID: 32685209; PMCID: PMC7350076.CrossRefGoogle ScholarPubMed
Gautam, KP, Adhikari, M, Khatri, RB, et al. (2016) Determinants of infant and young child feeding practices in Rupandehi, Nepal. BMC Res Notes 9, 135. doi:10.1186/s13104-016-1956-z, PMID: 26936368; PMCID: PMC4776375.CrossRefGoogle Scholar
Kabir, I, Khanam, M, Agho, KE, et al. (2012) Determinants of inappropriate complementary feeding practices in infant and young children in Bangladesh: secondary data analysis of Demographic Health Survey 2007. Matern Child Nutr 8, 1127. doi:10.1111/j.1740-8709.2011.00379.x, PMID: 22168516; PMCID: PMC6860519.CrossRefGoogle Scholar
Khan, AM, Kayina, P, Agrawal, P, et al. (2012) A study on infant and young child feeding practices among mothers attending an urban health center in East Delhi. Indian J Public Health 56, 301304. doi:10.4103/0019-557X.106420, PMID: 23354143.CrossRefGoogle Scholar
Figure 0

Table 1. Children's, parental, household, healthcare and community-level characteristics of living children aged 6–23 months, Ethiopia 2016

Figure 1

Fig. 1. Distribution of the dietary diversity score and prevalence of the minimum dietary diversity for 6–23 months children in Ethiopia 2016.

Figure 2

Table 2. The distribution of children 6–23 months who achieve the minimum dietary diversity in Ethiopia 2016

Figure 3

Table 3. The distribution of intake of eight food groups for children 6–23 months of age, in Ethiopia 2016

Figure 4

Table 4. Determinants of minimum dietary diversity in children aged 6–23 months in Ethiopia 2016