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Anemia and associated factors among 6 to 59 months age children attending health facilities in Kombolcha town, Northeast Ethiopia: a facility-based cross-sectional study



Childhood anemia is an important public health problem in Ethiopia. The northeast part of the country is among the areas affected by recurrent drought. Despite its significance, studies are scarce on childhood anemia particularly, in the study area. This study aimed to assess the proportion and factors associated with anemia among under-five children in Kombolcha town.


A facility-based cross-sectional study was conducted among 409 systematically selected 6 to 59 months aged children visited health institutions in Kombolcha town. Data were collected using structured questionnaires from mothers/caretakers. The data entry and analysis were done using EpiData version 3.1 and SPSS version 26 respectively. Binary logistic regression was fitted to identify factors associated with anemia. Statistical significance was declared at p-value ≤ 0.05. The effect size was reported using the adjusted odds ratio with its 95% confidence interval.


Of the participants, 213(53.9%) were males with a mean age of 26 months (SD ± 15.2). The proportion of anemia was 52.2% (95% CI, 46.8-57%). Being in the age of 6–11 months (AOR = 6.23, 95% CI: 2.44, 15.95), 12–23 months (AOR = 3.74, 95%CI: 1.63, 8.60), having low dietary diversity score (AOR = 2.61, 95% CI: 1.55, 4.38), having a history of diarrhea (AOR = 1.87, 95% CI: 1.12, 3.12) and having the lowest family monthly income (AOR = 16.97, 95% CI: 4.95, 58.20) were positively associated with anemia. Whereas, maternal age ≥ 30 years (AOR = 0.37 (0.18, 0.77) and exclusive breastfeeding until six months (AOR = 0.27, 95% CI: 0.16, 0.45) were negatively associated with anemia.


Childhood anemia was a public health problem in the study area. Child age, maternal age, exclusive breastfeeding, dietary diversity score, diarrhea, and family income were significantly associated with anemia.

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Anemia is a condition in which the hemoglobin concentration within the blood is lower than normal. The normal hemoglobin concentration varies by age, sex, elevation of residence, smoking habits and pregnancy status. Anemia among under-five children is defined as hemoglobin value less than 110 g/L [1]. The common causes of anemia in under-five children were found to be nutrient deficiencies, infectious diseases and genetic disorders [2, 3]. Iron deficiency is the most common cause of anemia and is estimated to contribute to approximately 42% of cases in children under 5 years of age worldwide [3].

Anemia is a major health problem throughout the world. The magnitude of the problem in developing countries is high since they are more exposed to various health and socioeconomic problems, which are directly or indirectly related to anemia. Though all age groups can develop anemia due to various factors, under-five children are among the most vulnerable age groups [4].

According to the 2019 estimation of the World Health Organization (WHO), 39.8% of under-five children in the world were anemic, of which 60.2% were in African region [5]. In East Africa, approximately 75% f under-five children have anemia with the prevalence ranging between 44% and 76% [6].As of the 2016 Ethiopian Demographic and Health Survey (EDHS), it was estimated that 57% of children under five years in Ethiopia had anemia with regional variation ranging from 42% in Amhara Region to 83% in Somali Region [7]. There are discrepancies in the prevalence of childhood anemia across studies conducted in different parts of the country. A study done in northeast Ethiopia (Guguftu) reported that 41.1% of under-five children were anemic [8]. Similarly, studies conducted in Gondar Town [9], North Shewa [10], Tigray [11], and Hawassa referral hospital [12] showed that the proportion of anemia among under-five children was 28.6%, 28.5%, 21.6% and 41.7% respectively.

The variation in the prevalence of anemia was attributed to multiplicity of factors. Childhood factors like age, residence, feeding practice, nutritional status, intestinal parasites, malaria, iron supplementation, vitamin A supplementation, deworming, eating raw foods, and dietary diversity were found to be associated with anemia. Moreover, familial and maternal factors including maternal age, educational status, marital status, family income, waste disposal practice, maternal anemia, household food insecurity, water source, family size, ante natal care, and maternal nutritional status were significantly associated with anemia [8,9,10,11,12,13,14,15,16,17].

Anemia among under-five children has serious consequences including growth retardation, poor immune system, and increased susceptibility to diseases and death, and has severe socio-economic consequences for families and communities [18,19,20,21]. It creates long-term effects among female children resulting in low-birth-weight babies and postpartum hemorrhage especially young children from low-income families have a higher risk for developing iron deficiency anemia [22]. Anemia is an indicator of both poor nutrition and poor health [5].

Several studies have been conducted across different parts of Ethiopia related to childhood anemia [8, 9, 14, 23,24,25,26,27]. Especially important is the study conducted in south Wollo Zone (Guguftu) which is located near to Kombolcha. The Guguftu study was conducted at a single public health center. In addition, the agro-ecological condition of Kombolcha is different from that of Guguftu. Kombolcha is a lowland area compared to Guguftu which is a highland ranging 3000–4000 m above sea level. This results in differences in agricultural products and general living condition of the society. Despite these and other studies, evidence is still scarce on childhood anemia in the Northeastern part of the country where drought and food insecurity are rampant in the area. Therefore, this study was conducted to determine the proportion and factors associated with anemia among under-five children visiting health facilities in Kombolcha town.


Study design and population

This study employed a facility-based cross-sectional design in Kombolcha town, Northeast Ethiopia. The study population was all children 6 to 59 months and visited selected public and private health facilities for any services in the town during the study period.

Study area and period

The study was conducted in Kombolcha town located in Amhara Regional State, South Wollo zone at a distance of 378 km from the capital Addis Ababa to the Northeast. The town is an important commercial and industrial center in northeast Ethiopia. The area is known for recurrent drought and least productivity. The study was conducted from February 15 to May 14, 2020.

Eligibility criteria

All children aged 6 to 59 months who visited the selected health institutions were included in this study. Whereas, children with a known bleeding disorder, severe illness, mentally ill mothers or caretakers, and children who have taken blood and blood products (blood transfused) for the last 3 months were excluded from the study.

Sample size and sampling procedure

The sample size was determined based on the single population assumption taking the prevalence of anemia to be 41.1% with a 5% margin of error and 95% confidence level [8]. By considering a 10% non-response rate the final sample size was estimated to be 409. The list of health institutions (4 Public health centers & 14 private medium clinics) was obtained from the town administration health office and was stratified into public and private. Then, half of the public and one-third of the private institutions were selected using a simple random sampling technique (lottery method). The study subjects were selected using a systematic sampling method. The first child was selected by simple random sampling (lottery method) and then every 2 children was selected based on the order of their visit. Systematic random sampling can be applied in the absence of a frame for the population [28].

Operational definitions


In children under five years, anemia was defined as a hemoglobin level below 11 g/dl. In this study, the Hgb level was adjusted to the altitude. Since the study area is found 1842 m above sea level, 0.8 g/dl was added to the standard Hgb cut-off value. Therefore, children with an Hgb of 11.8 g/dl or more were considered normal while children who had an Hgb value < 11.8 g/dl were considered anemic [7]. This cut-off point works for both male and female children since there is no gender variation until 12 years of age [2, 29].

Dietary diversity score

this is determined by counting the number of food groups consumed in the last 24-hours. Consumption of 5 to 8 and 4 to 7 food groups were considered adequate dietary diversity for children 6 to 23 and 24 to 59 months respectively [30].


the person who is responsible for parenting the child. This person can be the biological parents (mother or father), any member of the family or anyone not a member of the family responsible for provision of care and support for the child.

Data collection tools and procedures

Pretested and structured questionnaires adapted from previous similar pieces of literature [8, 14, 26, 31,32,33,34,35,36] were used to collect relevant data for this study. The first part of the questionnaire included the socioeconomic and demographic characteristics of the child and the mother/caretaker. The average monthly family income was determined by asking the caretakers to recall the estimated monthly income in Ethiopian currency. The second part included common medical comorbidities pertaining to the child intended to recall the presence of history of malaria, TB, HIV, diarrhea and vitamin A supplementation in the last six months. The third part was a questionnaire on the individual dietary diversity score. The questionnaire was adopted from the FAO/FANTA guidelines for measuring household and individual dietary diversity [37] and WHO IYCF guideline [30] which are based on the 24-hour free recall approach. In addition, respondents were asked to indicate whether or not their child consumed any food over the previous 24 h from each of eight food groups for children 6 to 23 months and seven food groups for children 24 to 59 months. The questionnaire was prepared in English, translated into the local language, and then back to English by English language experts to ensure its consistency. Six trained nurses and six laboratory technicians conducted the data collection.

Blood specimen collection and examination

After asking about the willingness of parents or caregivers, capillary blood samples were collected from children under strict aseptic precautions by trained laboratory technicians. The hemoglobin concentration was measured using HemoCue Hb 201 analyzer.

Stool specimen collection and examination

A clean plastic container marked with an identification number was used to collect about 2 mg of stool sample from each child. Then, a stool wet mount smear was prepared using saline and/or iodine solution for direct microscopic identification of intestinal parasites within 30 min of sample collection. The direct smear was examined first by 10x and then 40x objective for detection of helminth eggs, larvae, and protozoan parasites by experienced medical laboratory technicians.

Data quality control

The quality of data was assured through careful designing, translation, pre-testing of the questionnaire, and training of data collectors. Every day after data collection, the filled questionnaire was checked for completeness by the principal investigator, supervisors, and corrections were made accordingly for the next day. Standard operating procedures and manufacturers’ instruction was strictly followed for all laboratory activities. All laboratory reagents were checked for their expiry date. Samples were checked whether they are in the acceptable criteria like volume, consistency, and collection time. Microscopic slides and cover glasses were checked for cleanliness.

Data processing and analysis

The collected data were entered into a controlled data entry template using Epidata version 3.1 and exported to SPSS version 26.0 for analysis. Exploratory analysis was performed to check missing values, outliers and assumptions before the main analysis was carried out. Descriptive statistics like frequencies, proportions, and summary measures were computed. Binary logistic regression was employed to identify factors associated with anemia. First bivariate binary logistic regression was performed and variables found to be significant at P-value < 0.25 were imputed into multiple logistic regression. A p-value < 0.05 was used to indicate statistical significance in the multiple logistic regression model. Both the crude and adjusted Odds Ratios were reported as effect measures. The results were presented using tables, figures, and text narratives.


Characteristics of study participants

Out of 409 participants, 395 participants responded correctly making the response rate 96.6%. About 213(53.9%) children were males with a mean age of 26 months (SD ± 15.2). Of the total mothers interviewed, 211 (53.4%) attended secondary education and above; about 330 (83.5%) were from urban residences. Regarding the marital status of mothers, 357 (90.3%) were married (Table 1).

Table 1 Socio-demographic characteristics of children and mothers/caretakers attending health institutions of Kombolcha town, Northeast Ethiopia (n = 395)

Nutrition and disease morbidities

Out of 395 study subjects, 171 (43.3%) had diarrhea of which 102 (49.8%) were anemic. Most of the 256 (64.2%) children got adequate dietary diversity scores (four and more food groups) per 24 h out of them 104 (40.6) were anemic (Table 2).

Table 2 Characteristics related to nutrition and morbidity among children under-five years attending health facilities in Kombolcha town, Northeast Ethiopia (n = 395)

Anemia among children

The mean hemoglobin value of children was 11.4 g/dl (SD ± 18.3). Of all children, 206 (52.2%; 95% CI 46.8–57.0) were anemic, of which 114 (55.3%) were males (Fig. 1).

Fig. 1
figure 1

Proportion of anemia aggregated by child sex

Factors associated with anemia

Children in the age group of 6–11 months were six times more likely to have anemia as compared to 48–59 months (AOR: 6.23, 95% CI: 2.44, 15.95). Similarly, children 12–23 months of age were 3.74 times as likely to be anemic than 48–59 months children (AOR: 3.74, 95% CI: 1.63, 8.60). Children from mothers of at least 30 years old were 63% less likely to be anemic as compared to children from younger mothers (AOR: 0.37, 95% CI: 0.18, 0.77). Children who exclusively breastfed up to six months were 73% less likely to be anemic compared to children who were not exclusively breastfed (AOR: 0.27, 95% CI: 0.16, 0.45). Children having low dietary diversity scores were 2.6 times more likely to have anemia than those having adequate dietary diversity scores (AOR: 2.61, 95% CI: 1.55, 4.38). Children who have a history of diarrhea in the past 2 months before the data collection were nearly 2 times more likely to be anemic than children who do not have a history of diarrhea (AOR: 1.87, 95% CI: 1.12, 3.12). Children from households with a family monthly income of < 1,500 ETB were 17 times more likely to have anemia as compared to those who had a family income of > 4,500 ETB (AOR: 16.97, 95%CI: 4.95, 58.20) (Table 3).

Table 3 Factors associated with anemia among children 6–59 months in Kombolcha town, Northeast Ethiopia (n = 395)


This study was conducted to determine the prevalence of anemia and associated factors among children 6 to 59 months in Kombolcha town, northeast Ethiopia. The proportion of children with anemia was found to be 52.2% (95%CI = 47.2%, 57.1%), which is considered a severe public health problem based on the WHO severity classification of anemia (> 40%) [38]. This finding is comparable with findings in Southern Ethiopia [39] and Brazil [40]. However, it is higher than findings from Guguftu (Northeast Ethiopia) [8], Gondar (Northwest Ethiopia) [9], and Hawassa (Southern Ethiopia) [27]. This discrepancy may be justified by the fact that the area, where this study was conducted, is frequently affected by drought and conflict incidents so there might be food insecurity [41]. According to the 2019 and 2020 analysis of the Integrated Food Security Phase Classification (IPC), the north eastern part of Ethiopia was classified in Phase 2 (stressed) and above food insecurity level [42, 43]. The seasonal variation of the studies may also explain the difference. However, this finding is lower than findings from Bedele Hospital (Southwest Ethiopia) [44], and Tanzania [45], The Bedele study was conducted among children admitted to the hospital. It seemed those children may have severe/complicated condition that made them to be admitted in the hospital. Even some of them may be admitted due to anemia and related conditions. These reasons may precipitate anemia and increase its proportion. The Tanzanian study was conducted in the community among rural children. Rural residence is one factor that increases the prevalence of anemia as evidenced by literatures [46]. In addition, the current prevalence of anemia is lower than the national anemia prevalence in children under five years of age. As Kombolcha is found in the Amhara region, the region had the lowest prevalence of anemia in the country [7].

Younger children were at a higher risk of anemia than older children. This finding is supported by studies in Guguftu (Northeast Ethiopia) [8], Gondar town (Northwest Ethiopia) [9], Adami Tullu (South Central Ethiopia) [47], Hawassa (Southern Ethiopia) [27] and Tanzania [45]. Infants began to eat complementary foods after six months old. From this time onwards up to 2 years there might be difficulty in ingesting such complementary feed and may result in a deficiency of nutrients leading to a higher probability of anemia. On contrary, children would have the ability to eat a variety of foods when they become older.

The age of the mother was significantly associated with anemia. Children born from older mothers were less likely to be anemic compared to children from younger mothers. This is in line with a study in Ghana [48]. As the maternal age increases, the mother probably will have more children so a better experience in child care and feeding. The better the care and feeding practice a child gets, the lesser risk of malnutrition.

Whether a child was exclusively breastfed or not also matters the occurrence of childhood anemia. Children who were exclusively breastfed until six months are less likely to be anemic than their counterparts. This finding contradicted a study in China [33]. This discrepancy may be explained by the socio-economic differences in the study participants and study design. Exclusive breastfeeding for the first six months is a highly recommended feeding practice by the WHO. It provides the optimal feeding option by preventing diarrheal diseases, respiratory tract infections, and chronic diseases [49]. This may help exclusively breastfed children to be at a lower risk of anemia.

The dietary diversity score of a child was associated with anemia. Children who had low dietary diversity scores were more likely to be anemic than children who had adequate dietary diversity scores. This finding is similar to a study done in Hohoe Municipality, Ghana [50]. However, there was no significant association between DDS and anemia among studies conducted in Menz Gera (Central Ethiopia) [10], and Kilte Awulaelo (Northern Ethiopia) [26]. Eating a variety of foods may provide all the necessary nutrients, prevent disease, and boost the immunity of the child. Hence, a child with an adequate dietary diversity score may have a low risk of anemia.

The occurrence of anemia was not the same among children who had diarrhea and no diarrhea. The odds of anemia among children who had diarrhea for the last two months before the date of the interview were almost two times higher than their counterparts. This finding contradicted a study in the University of Gondar specialized hospital (Northwest Ethiopia) [14]. This contradiction can be explained by the difference in the study participants. The current study was conducted among ambulatory patients while the study in the University of Gondar specialized hospital was conducted among admitted pediatric patients. On the other hand, the University of Gondar hospital study considered acute diarrhea so that there might be a decrease in body fluid and mask the low level of hemoglobin value. Chronic diarrhea results the depletion of important nutrients including iron due to its poor absorption in the gastrointestinal tract. But diarrhea had no association with anemia among studies conducted in Gondar (Northwest Ethiopia) [9] and Tigray (Northern Ethiopia) [11].

As family monthly income increased, the prevalence of anemia decreased markedly similar to the findings in the Tigray region (Northern Ethiopia) [51], Bedele Hospital (Southwest Ethiopia) [44], Guguftu Health Center (Northeast Ethiopia) [8] and Sudan [36]. The relationship between socioeconomic status and malnutrition is well established. Low socioeconomic status may result in food scarcity, poor hygiene, and poor child care in general. This in turn may precipitate the occurrence of malnutrition including iron deficiency anemia.

The result of this study indicated that anemia is a major public health problem among children under-five years attending health institutions in Northeast Ethiopia. According to the WHO classification for persistent anemia in a population (40%) and above, this finding confirmed that anemia among under-five children was a severe public health problem. Such a high magnitude of anemia among under-five children corroborates the finding of EDHS affirming the fact that despite the implementation of micronutrient deficiency prevention and control guidelines for several years. Endorsement and implementation of the national nutrition strategy and the greater emphasis given to anemia in the newly endorsed food and nutrition policy, there remains much to be done to cure the problem of anemia. The findings call for a galvanizing community-level intervention that addresses key behaviors such as breastfeeding and dietary behaviors.

Limitations of the study

Anemia was measured based on only hemoglobin concentration parameters, the inclusion of other measures such as serum ferritin could lead to a better differentiation of cases. Being an institution-based study, the result cannot be extrapolated to the larger community. The presence of comorbidities like malaria, TB, HIV and diarrhea were not confirmed by objective methods. We only asked the caretakers to respond whether their child was encountered with these conditions in the last six months. The certainty of this response would be affected by the recall and literacy of respondents. Moreover, the study was done only in one season and may not represent the magnitude year-round.


The burden of anemia among children aged 6–59 months in the study site was high and it has severe public health problems according to the WHO cut-off points. The age of the child, the age of the mother, family monthly income, exclusive breastfeeding status, and having a low dietary diversity score are significantly associated with anemia. The healthcare workers are advised to educate the pregnant and lactating mothers, and the whole community about good dietary practices, the benefit of exclusive breastfeeding, and income-generating activities by collaborating with the finance and economy development sectors. Researchers are recommended to use additional biomarkers to differentiate the cause of anemia and its seasonality using longitudinal designs. Moreover, studies aimed at measuring the effect of the covid-19 and the conflict on childhood anemia are recommended so as to produce evidences to achieve resilient health system.

Data Availability

All data generated or analyzed during this study are included in this published article and its supplementary information files.



Ante Natal Care


Adjusted Odds Ratio


Confidence Interval


Crude Odds Ratio


Dietary Diversity Scores


Exclusive Breastfeeding


Ethiopian Demographic and Health Survey


Ethiopian Birr


Gram per deciliter


Health center






Human Immunodeficiency Virus




Odds Ratio


Standard Deviation


Statistical Product and Service Solutions




United Nation


World Health Organization


  1. World Health Organization. Health topics: Anaemia. Accessed 19 Feb 2023.

  2. Fairman JE, Wang M. Iron Deficiency and other types of Anemia in Infants and Children. Am Fam Physician. 2016;93:270–8.

    Google Scholar 

  3. World Health Organization. Nutritional anaemias: tools for effective prevention and control. Geneva; 2017.

  4. William Gardner, Nicholas Kassebaum. Global, Regional, and National Prevalence of Anemia and its causes in 204 countries and Territories, 1990–2019. Curr Dev Nutr. 2020;4.

  5. World Health Organization. Global anaemia estimates in women of reproductive age, by pregnancy status, and in children aged 6–59 months. 2021. Accessed 19 Feb 2023.

  6. McLean E, Cogswell M, Egli I, Wojdyla D, De Benoist B. Worldwide prevalence of anaemia, WHO vitamin and Mineral Nutrition Information System, 1993–2005. Public Health Nutr. 2009;12:444–54.

    Article  PubMed  Google Scholar 

  7. Central Statistical Agency (CSA) [Ethiopia], ICF. Ethiopia Demographic and Health Survey 2016. Addis Ababa, Ethiopia; 2017.

  8. Gebreweld A, Ali N, Ali R, Fisha T. Prevalence of anemia and its associated factors among children under five years of age attending at Guguftu health center, South Wollo, Northeast Ethiopia. PLoS One. 2019;14:1–13.

    Article  Google Scholar 

  9. Melku M, Alene KA, Terefe B, Enawgaw B, Biadgo B, Abebe M, et al. Anemia severity among children aged 6–59 months in Gondar town, Ethiopia: a community-based cross-sectional study. Ital J Pediatr. 2018;44:1–12.

    Article  Google Scholar 

  10. Engidaye G, Melku M, Yalew A, Getaneh Z, Asrie F. Under nutrition, maternal anemia and household food insecurity are risk factors of anemia among preschool aged children in Menz Gera Midir district, Eastern Amhara, Ethiopia: a community based cross-sectional study. BMC Public Health. 2019; 19:968.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Wasihun AG, Teferi M, Negash L, Marugán J, Yemane D, McGuigan KG, et al. Intestinal parasitosis, anaemia and risk factors among pre-school children in Tigray region, northern Ethiopia. BMC Infect Dis. 2020; 20:1–11.

    Article  Google Scholar 

  12. Gebereselassie Y, Birhanselassie M, Menjetta T, Alemu J, Tsegaye A. Magnitude, Severity, and Associated factors of Anemia among under-five children attending Hawassa University Teaching and Referral Hospital, Hawassa, Southern Ethiopia, 2016. Anemia. 2020;2020.

  13. Molla A, Egata G, Mesfin F, Arega M, Getacher L. Prevalence of Anemia and Associated Factors among Infants and Young Children Aged 6–23 Months in Debre Berhan Town, North Shewa, Ethiopia. J Nutr Metab. 2020;2020.

  14. 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. The Journal of the International Federation of Clinical Chemistry and Laboratory Medicine. 2019; 30:35–47.

    PubMed  Google Scholar 

  15. Wasihun AG, Teferi M, Negash L, Marugán J, Yemane D, McGuigan KG, et al. Intestinal parasitosis, anaemia and risk factors among pre-school children in Tigray Region, Northern Ethiopia. bioRxiv. 2019;1–29.

  16. Gari T, Loha E, Deressa W, Solomon T, Atsbeha H, Assegid M, et al. Anaemia among children in a drought affected community in south-central Ethiopia. PLoS One. 2017;12.

  17. Jembere M, Kabthymer RH, Deribew A. Determinants of Anemia among Children aged 6 to 59 months in Dilla Town, Southern Ethiopia: a facility based Case Control Study. Glob Pediatr Health. 2020;7.

  18. Haas JD, Brownlie IV T. Iron deficiency and reduced work capacity: a critical review of the research to determine a causal relationship. Journal of Nutrition. 2001;131 2 SUPPL. 2:676–90.

    Article  Google Scholar 

  19. Lozoff B. Iron deficiency and child development. Food Nutr Bull. 2007;28 4 SUPPL.:560–71.

    Article  Google Scholar 

  20. Oppenheimer SJ. Iron-deficiency anemia: reexamining the nature and magnitude of the public health problem. J Nutr. 2001; 131:616–35.

    Article  Google Scholar 

  21. Grantham-Mcgregor S, Baker-Henningham H. Iron deficiency in childhood: causes and consequences for child development. Annales Nestle. 2010; 68:105–19.

    Google Scholar 

  22. E. RB, Kliegman RM, Jenson HB. Nelson Textbook of Pediatrics. 17th edition. Judith Fletcher; 2004.

  23. Reithinger R, Ngondi JM, Graves PM, Hwang J, Getachew A, Jima D. Risk factors for anemia in children under 6 years of age in Ethiopia: analysis of the data from the cross-sectional Malaria Indicator Survey, 2007. Trans R Soc Trop Med Hyg. 2013; 107:769–76.

    Article  CAS  PubMed  Google Scholar 

  24. Gebremeskel MG, Mulugeta A, Bekele A, Lemma L, Gebremichael M, Gebremedhin H, et al. Individual and community level factors associated with anemia among children 6–59 months of age in Ethiopia: a further analysis of 2016 Ethiopia demographic and health survey. PLoS One. 2020; 15:1–17.

    Article  Google Scholar 

  25. Gebreegziabher T, Regassa N, Wakefield M, Pritchett K, Hawk S. Disparities in the prevalence and risk factors of anaemia among children aged 6–24 months and 25–59 months in Ethiopia. J Nutr Sci. 2020;9.

  26. Gebreegziabiher G, Etana B, Niggusie D. Determinants of Anemia among children aged 6–59 months living in Kilte Awulaelo Woreda, Northern Ethiopia. Anemia. 2014;2014.

  27. Gebereselassie Y, Birhanselassie M, Menjetta T, Alemu J, Tsegaye A. Magnitude, Severity, and Associated factors of Anemia among under-five children attending Hawassa University Teaching and Referral Hospital, Hawassa, Southern Ethiopia, 2016. Anemia. 2020;2020.

  28. Elfil M, Negida A. Sampling methods in Clinical Research; an Educational Review. Emergency YYYY; NN (I)`. 2016; pp-pp.

  29. Janus J, Moerschel SK. Evaluation of Anemia in Children. Am Fam Physician. 2010; 81:1462–71.

    PubMed  Google Scholar 

  30. World Health Organization (WHO). Indicators for assessing infant and young child feeding practices: part 2 measurement. Geneva; 2010.

  31. Birhanu M, Gedefaw L, Asres Y. Anemia among School-Age Children: Magnitude, Severity and Associated factors in Pawe Town, Benishangul-Gumuz Region, Northwest Ethiopia. Ethiop J Health. 2017; 28:256.

    Google Scholar 

  32. FerreiraI AA, Santos RV, Souza JAM de, Welch JR, Jr CEAC. Anemia and hemoglobin levels among indigenous Xavante children, Central Brazil. Rev BRas epidemiol. 2017; 20:102–14.

    Article  Google Scholar 

  33. Li H, Xiao J, Liao M, Huang G, Zheng J, Wang H, et al. Anemia prevalence, severity and associated factors among children aged 6–71 months in rural Hunan Province, China: a community-based cross-sectional study. BMC Public Health. 2020; 20:989.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. ChowdhuryID MRK, Khan MdMH, Khan HTA, Rahman MdS, Islam MR, Islam MM, et al. Prevalence and risk factors of childhood anemia in Nepal: a multilevel analysis. PLoS One. 2020;15.

  35. Mesfin F, Berhane Y, Worku A. Anemia among primary School children in Eastern Ethiopia. PLoS One. 2015; 10:1–10.

    Article  Google Scholar 

  36. Elmardi KA, Adam I, Malik EM, Ibrahim AA, Elhassan AH, Kafy HT, et al. Anaemia prevalence and determinants in under 5 years children: findings of a cross-sectional population-based study in Sudan. BMC Pediatr. 2020; 20:1–14.

    Article  Google Scholar 

  37. Food and Agriculture Organization (FAO). Guidelines for measuring household and individual dietary diversity. 2013.

  38. Ali Salami, Ghassan Ghssein, Lamis Salloum HF. Prevalence of anemia among lebanese hospitalized children. PLOS. 2018;13.

  39. Malako BG, Asamoah BO, Tadesse M, Hussen R, Gebre MT. Stunting and anemia among children 6–23 months old in Damot Sore district, Southern Ethiopia. BMC Nutr. 2019; 5:1–11.

    Article  Google Scholar 

  40. Ferreira R. Prevalence of anemia in under five-year-old children in a children’s hospital in. 2010;100–4.

  41. FEWS NET. Ethiopia Food Security Outlook: Food aid remains insufficient amid very high levels of hunger and malnutrition. 2022.

  42. Integrated Food Insecurity Phase Classification (IPC). Ethiopia: Acute Food Insecurity Situation July - September 2019 and Projections for October 2019 - January 2020 and February - June 2020. 2019.

  43. Integrated Food Insecurity Phase Classification (IPC). Ethiopia: Acute Food Insecurity Situation: October - December 2020 and Projections for January - June 2021 and July - September 2021. 2020.

  44. Abdisa Boka and Dessalegn Nigatu. Prevalence of anemia and association factors among under five children in Bedele hospital, Iluababora zone, Oromia regional state south west Ethiopia, 2017. IJDR. 2018; 08:24284–90.

    Google Scholar 

  45. Kejo D, Petrucka P, Martin H, Kimanya M, Mosha T. Prevalence and predictors of anemia among children under 5 years of age in Arusha District, Tanzania. Pediatric Health Med Ther. 2018; Volume 9:9–15.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Gebreegziabher T, Regassa N, Wakefield M, Pritchett K, Hawk S. Disparities in the prevalence and risk factors of anaemia among children aged 6–24 months and 25–59 months in Ethiopia. J Nutr Sci. 2020;9.

  47. Gari T, Loha E, Deressa W, Solomon T, Atsbeha H, Assegid M, et al. Anaemia among children in a drought affected community in south-central Ethiopia. PLoS One. 2017; 12:1–16.

    Article  Google Scholar 

  48. Parbey PA, Tarkang E, Manu E, Amu H, Ayanore MA, Aku FY, et al. Risk Factors of Anaemia among Children under Five Years in the Hohoe Municipality, Ghana: A Case Control Study. Anemia. 2019;2019.

  49. WHO/UNICEF. Global Nutrition Target 2025: Breastfeeding Policy Brief (WHO/NMH/NHD/14.7). 2014;8.

  50. Parbey PA, Tarkang E, Manu E, Amu H, Ayanore MA, Aku FY, et al. Risk Factors of Anaemia among Children under Five Years in the Hohoe Municipality, Ghana: A Case Control Study. 2019;2019.

  51. Araya Gebreyesus Wasihun*1, Mekonen Teferi2, Letemichal Negash1, Javier Marugán3, Dejen Yemane4, Kevin G. McGuigan5, Ronan M. Conroy6, Haftu Temesgen Abebe 7 TAD. Intestinal parasitosis, anaemia and risk factors among pre-school children Affiliations: 2019;1–29.

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We highly acknowledge the study participants and data collectors for their keen cooperation in getting quality data.


There was no any funding received to carry out this study.

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WF contributed in the conception, design, analysis and draft write up of this study. TB and AA contributed in the design, analysis and revision of this study. All authors read and approved the final manuscript.

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Correspondence to Assefa Andargie.

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Ethics approval and consent to participate

Ethical clearance was obtained from the ethical approval committee of the Wollo University College of medicine and health science on the date of February 4, 2020 (the date is written as 26/5/2012 on the ethical approval letter which is according to the Ethiopian calendar) with approval number cmhs1178/13/12. After ethics approval, permissions were obtained from the South Wollo Health Department and the authorities of the health facilities. Since the participants were minors, the parents or guardians of the children were informed about the risks and benefits of participation and written informed consent was obtained. The participants were addressed while they were visiting the health facilities for a routine healthcare and hence the data were collected as part of the routine check-up. All the procedures were carried out in accordance with the standard operating procedures of the health facilities and WHO guidelines. To ensure confidentiality, the data were linked to a code number anonymously. Abnormal test results of participants were linked to the health center for the provision of treatment.

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Not applicable.

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Fentaw, W., Belachew, T. & Andargie, A. Anemia and associated factors among 6 to 59 months age children attending health facilities in Kombolcha town, Northeast Ethiopia: a facility-based cross-sectional study. BMC Pediatr 23, 209 (2023).

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