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Feeding practices of under-two children in Ethiopia: A systematic review and meta-analysis

  • Sisay Eshete Tadesse ,

    Roles Conceptualization, Data curation, Formal analysis, Methodology, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing

    sisliyu21@gmail.com

    Affiliations School of Public Health, College of Medicine and Health Sciences, Wollo University, Dessie, Ethiopia, Department of Nutrition and Dietetics, Faculty of Public Health, Institute of Health, Jimma University, Jimma, Ethiopia

  • Amare Tariku,

    Roles Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing

    Affiliation Department of Nutrition and Dietetics, Institute of Public Health, College of Medicine and Health Sciences, University of Gondar, Gondar, Ethiopia

  • Tefera Belachew

    Roles Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing

    Affiliation Department of Nutrition and Dietetics, Faculty of Public Health, Institute of Health, Jimma University, Jimma, Ethiopia

Abstract

Background

Globally, child feeding practices remain suboptimal and contribute substantially to a high burden of malnutrition. In Ethiopia, evidence on the overall status of feeding practices among children under two years of age is limited. This study therefore sought to estimate the pooled prevalence of timely initiation of breastfeeding, exclusive breastfeeding, timely initiation of complementary feeding, and minimum acceptable diet, as well as to identify the factors associated with these practices.

Method

This systematic review and meta-analysis was conducted following the Preferred Reporting Items for Systematic Review and Meta-Analysis guidelines. A comprehensive literature search was performed in Scopus, HINARI, the Cochrane Library, and PubMed/MEDLINE. Cross-sectional and case-control studies published in English were included. Study quality was assessed using the Joanna Briggs Institute critical appraisal checklist. Heterogeneity across studies was assessed using Cochran Q test and the I2 statistic. Data analysis was done using STATA/MP version 17.0. Adjusted odds ratios with 95% confidence intervals were used to identify factors. Publication bias was assessed using funnel plots, Egger weighted regression, and Begg rank correlation tests.

Results

A total of 107 articles were included in this study. The pooled prevalence of timely initiation of breastfeeding, exclusive breastfeeding, timely initiation of complementary feeding, and optimal feeding practice were 64% (95% CI: 50%, 78%), 58.6% (95% CI: 52.6%, 64.5%), 60.51% (95% CI: 54.2%, 66.9%), and 20.4% (95% CI: 13.6%, 27.0%), respectively. Antenatal care (AOR = 3.4; 95% CI: 1.5, 7.5), place of delivery (AOR = 2.3; 95% CI: 1.1, 4.9), and normal delivery (AOR = 3.3; 95% CI: 1.1, 10) were positively associated with timely initiation of breastfeeding. Exclusive breastfeeding was positively associated with infant age 0–1 (AOR = 4.4; 95% CI: 1.4, 13.6) and 2–3 months (AOR = 2.5; 95% CI: 1.2, 5.1), maternal age > 35 (AOR = 3.4; 95% CI: 1.3, 8.7), residence (AOR = 1.8; 95% CI: 1.1, 3.1), maternal occupation (AOR = 1.8; 95% CI: 1.2, 2.7), place of delivery (AOR = 2.1; 95% CI:1.2, 3.7), normal delivery (AOR = 1.7; 95 CI:1.2, 2.6), postnatal care (AOR = 2.3; 95% CI: 1.2, 4.3), counseling (AOR = 2.3; 95% CI:1.4, 3.9) and husband support (AOR = 2.9; 95% CI:1.9, 4.4) were positively associated with EBF. Antenatal care (AOR = 3.4; 95% CI:1.5, 7.5) and place of delivery (AOR = 2.3; 95% CI:1.1, 4.9) were positively associated with timely initiation of complementary feeding. Optimal infant feeding practice was positively associated with nutrition education through demonstrations (AOR = 2.1; 95% CI:1.3, 3.3) and age of child 18–23 months (AOR = 2.7; 95% CI:1.2, 6.1).

Conclusion

This study demonstrated that infant feeding practices were below both national and international recommendations, exposing children at higher risk of malnutrition, morbidity, and mortality. These suboptimal feeding practices also hinder progress toward achieving to achieving the Sustainable Development Goals. Several factors were identified as significant determinants of feeding practices, including antenatal care attendance, place and mode of delivery, postnatal care utilization, maternal occupation, maternal age, child’s age, breastfeeding counseling, husband’s support, place of residence, and participation in complementary food preparation demonstrations. Improving infant feeding practices therefore requires a comprehensive approach. Key strategies to improve infant feeding practices should include nutrition education through practical demonstrations, promoting full attendance of antenatal and postnatal care, increasing institutional deliveries, enhancing husband involvement, and tailoring interventions to the child’s age as well as the mother’s age and place of residence.

Introduction

Infant feeding practices are key determinants of child health and development. The World Health Organization (WHO) recommends exclusive breastfeeding for the first six months of life, followed by the introduction of complementary foods while continuing breastfeeding up to two years of age or beyond [1]. Globally, nearly half (49%) and 44% of the newborns-initiate breastfeeding within one hour of birth and exclusively breastfed for the first six months, respectively [2]. According to the 2020 global nutrition report, only 18.9% of children aged 6–23 months receive a nutritionally adequate diet [3]. In developing countries, 42% of infants are exclusively breastfed for six months of age, and 73% of children aged 6–8-months receive solid, semisolid, and soft foods [2].

Sub-optimal infant feeding practices are strongly linked to high morbidity and mortality among children. Most growth deficits occur between 6–12 months of age [4] and inappropriate feeding practices contribute up to a third of all cases of child malnutrition [5]. Current data suggest that over 1 million children die each year due to wasting [6]. Many children under-two-year experience delayed introduction of complementary foods, are fed infrequently, or receive foods of inadequate quality [79]. Such sub-optimal feeding practices contribute to feeding difficulties, increased risk of infection and allergies, early cessation of breastfeeding, undernutrition, obesity in childhood and adulthood, reduced breast milk intake, and long-term impacts on feeding performance [10,11].

Previous studies have shown that maternal education and age, antenatal care, postnatal care, place of delivery, household wealth, place of residence, maternal employment, household size, and father’s education all significantly influence feeding behaviors [1215].

Despite the well-established benefits of optimal infant feeding practices, suboptimal practices remain widespread in many regions, including Ethiopia. The 2019 Ethiopian Demographic and Health Survey (EDHS) reported that only 59% of infants under six months were exclusively breastfed, and merely 11.3% of children aged 6–23 months received a minimum acceptable diet [16]. World Bank estimates indicate that undernourished children may lose over 10% of their potential lifetime earnings, adversely affecting national productivity [17]. Although many studies were conducted on infant feeding practices, there were inconsistencies across studies, posing challenges for policymakers, practitioners, and stakeholders in making evidence-based decisions.

Previous systematic reviews and meta-analyses on child feeding practices in Ethiopia have several limitations. For instance, a systematic review and meta-analysis (SRMA) on timely initiation of breastfeeding (TIBF) included a retracted article and focused specifically on the effects of cesarean delivery and kangaroo mother care on preterm and low-birth-weight infants [13]. Similarly, a SRMA on exclusive breastfeeding (EBF) examined only a single influencing factor [14,15]. A SRMA on a minimum acceptable diet (MAD) included only nine studies and didn’t address the determinants [18]. Moreover, earlier SRMA predominantly included cross-sectional studies, limiting the comprehensiveness of the evidence.

The current study addresses the gaps identified in previous SRMA by incorporating a larger number of studies (107) including both case-control and cross-sectional designs, and examining the determinants of infant feeding practices. It also considers four core IYCF indicators: TIBF, EBF, TICF and MAD. This SRMA provides a comprehensive and rigorous synthesis of the available evidence on child feeding practices and will inform decision-making, guide resource allocation, and offer new insight for designing interventions to improve IYCF practices and reduce the burden of malnutrition in Ethiopia.

Materials and methods

Study setting

This systematic review and meta-analysis was conducted in Ethiopia, a country located in the northeastern part of Africa, also known as the Horn of Africa, and one of the most populous nations in the region. Traditional child feeding malpractices such as prelacteal feeding, discarding colostrum and inappropriate timing of complementary feeding remain a major concern, adversely affecting the health of many newborns and young children. Since 2000, efforts to reduce child malnutrition have been implemented through various intervention strategies, including the IYCF program, Seqota declaration, scaling up nutrition, multisectoral nutrition coordination, food and nutrition policy, and the National Nutrition Program, in collaboration with international partners. Similarly, one of the health packages that the country is working on is minimizing inappropriate child feeding and other maladaptive practices.

Search strategy

This systematic review and meta-analysis was performed according to the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) guidelines [19]. Three reviewers performed a comprehensive search of relevant articles across multiple databases, including MEDLINE (via PubMed), EMBASE, Cochrane Library, SCOPUS, HINARI, and Google Scholar. In addition, gray literature was identified through manual searches.

Searching terms

Search strategies for each database were developed based on the CoCoPop framework:

Condition: studies documenting infant feeding practices

Context: studies conducted in Ethiopia

Population: Studies targeting children under two years of age were included

Relevant articles were searched using the following searching terms: (prevalence) OR (magnitude) AND (determinants) OR (“associated factors”) OR (“risk factors”) AND (“infant feeding practices”) AND (“exclusive breastfeeding”) OR (complementary feeding*) OR (“minimum acceptable diet”) OR (optimum nutrition) AND (Ethiopia). Since no eligible studies were found prior to 2011, only articles published from 2011 onwards were included. This SRMA was registered in PROSPERO with a CRD number of 42023489496. No separate study protocol was prepared.

Eligibility criteria

All studies conducted in Ethiopia that reported prevalence, determinants and factors associated with infant feeding practices, which were published in English were included. Both cross-sectional and case-control study designs were considered. Studies were excluded if the full text was unavailable after attempting to contact the primary investigator for three months, systematic reviews of interventions, review articles, conference abstracts, and editorials.

Data extraction

After obtaining the full texts, duplicates were identified and removed using EndNote. Data extraction was conducted independently by three reviewers (SE, TB, and AT), who screened titles, abstracts, and full articles. The study selection procedure is presented using a PRISMA flow diagram [19]. Studies that met the inclusion criteria were retained, while those “included” and “undecided” studies underwent further full-text assessment. To minimize bias, reviewers independently ranked articles without knowing each other’s decisions, and any discrepancies were resolved through discussion and consensus. Data were then extracted using a Microsoft Excel 2021 extraction sheet, capturing study characteristics (author, year of publication, region, target population, sample size, study design, and response rate), infant feeding practices, subject recruitment procedures, adjusted odds ratios, and population characteristics.

Quality assessment and risk of bias

The quality of included studies was assessed independently by three investigators using the Joanna Briggs Institute (JBI) critical appraisal checklist, and the quality scores were averaged. Any disagreement was resolved through discussion and consensus. During data extraction data quality was ensured by selecting reliable and relevant data sources, removing duplicates and cross-checking extracted data against the original article. Finally, studies with a score of 50% and above were included in this systematic review and meta-analysis.

Data synthesis and analysis

Data were analyzed using STATA/MP version 17.0. The prevalence of infant feeding practices was reported by the forest plots. To estimate the determinants of feeding practices, adjusted odds ratio with a 95% confidence interval (CI) was pooled. Heterogeneity between studies was assessed using the Cochrane Q statistic (significant if the P-value was < 0.05) and quantified with the I² statistic (at least 50%, was considered suggestive of statistically significant heterogeneity) [20].

A Der Simonian and Laird random-effects model was used for studies with high heterogeneity, and a fixed effects model with inverse variance methods was used for similar studies. Heterogeneity was further explored using the Galbraith plot and Forest plot. The source of heterogeneity was tested by running meta-regression, subgroup analysis by sex, age and region), and sensitivity analysis. Publication bias was assessed by funnel plots, Egger weighted regression, and Begg rank correlation tests at p-values < 0.05.

Results

Study characteristics

A total of 975 articles were retrieved from databases by a literature search (Fig 1).

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Fig 1. Preferred Reporting Items for Systematic Review and Meta-Analysis for literature screening and selection process, June 2020.

https://doi.org/10.1371/journal.pone.0342932.g001

After screening the title and abstract, 189 articles were identified as having information relevant to infant feeding practices. Following full text review, 107 articles were evaluated to have better quality data that met the criteria for abstraction. Of these, 18 studies involving 16,405 participants were included for TIBF [2133]; 39 papers with 19,987 participants addressed EBF [3463]; 26 papers involving 15,855 participants assessed TIBF [6479]; and 24 papers including 15, 495 infants aged 6–23 months were included for assessing MAD [64,75, 8099]. All included articles were full-text articles employing cross-sectional and case-control designs and were published between 2011 and 2024 (Table 1).

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Table 1. Summary of Extracted Studies on Infant Feeding Practices among Under-two Children in Ethiopia.

https://doi.org/10.1371/journal.pone.0342932.t001

Pooled prevalence of infant feeding practices

The pooled prevalence of TIBF was 64% (95% CI: 50, 78%). There was substantial heterogeneity among the included studies (χ² = 1404.11; p < 0.0001; I2 = 99.7%) (Fig 2).

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Fig 2. Forest plot showing the pooled prevalence of timely initiation of breastfeeding among infants in Ethiopia, 2024.

https://doi.org/10.1371/journal.pone.0342932.g002

Based on the subgroup analysis, the highest (77.8%) and lowest (47.4%) prevalence of TIBF was reported from Afar and Somali regions, respectively.

The pooled prevalence of EBF among under-two children was 59.6% (95% CI: 52.6, 64.5%). Significant heterogeneity was observed across studies (χ² = 3561.76; p < 0.0001; I2 = 98.9%, p = 0.0001) (Fig 3).

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Fig 3. Forest plot showing the pooled prevalence of exclusive breastfeeding among children in Ethiopia, 2024.

https://doi.org/10.1371/journal.pone.0342932.g003

Based on the subgroup analysis, the highest (79%) and lowest (23.9%) prevalence was reported from the Amhara region. The subgroup analysis was done by region and study setting, and still, there is high heterogeneity.

The pooled prevalence of TICF was 60.5% (95% CI: 54.2, 66.9%) with high heterogeneity between studies (chi-squared = 6066.37, I-squared = 99.6%%, p < 0.001) (Fig 4).

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Fig 4. Forest plot showing the pooled prevalence of timely initiation of complementary feeding among infants in Ethiopia, 2024.

https://doi.org/10.1371/journal.pone.0342932.g004

The pooled prevalence of MAD among children aged 6–23 months was 19.8% (95% CI: 15.6, 23. 9%) (Fig 5).

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Fig 5. Forest plot showing the pooled prevalence of minimum acceptable diet among children aged 6-23 months, 2024.

https://doi.org/10.1371/journal.pone.0342932.g005

The subgroup analysis demonstrated that studies conducted in the Amhara region and those conducted at the national level were major contributors for the observed heterogeneity.

Sensitivity analysis

The sensitivity analysis demonstrated that the quality score didn’t affect the outcome of the meta-analysis and there was no significant difference in the overall pooled prevalence.

Publication bias

Publication bias was assessed both subjectively using a funnel plot and objectively using Begg’s and Egger’s tests. For TIBF, the funnel plot and Egger’s test (p = 0.011) suggested the presence of publication bias, whereas Begg’s test indicated no evidence of publication bias (p = 0.289) (Fig 6).

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Fig 6. Funnel plot for timely initiation of breastfeeding among infants in Ethiopia, 2024.

https://doi.org/10.1371/journal.pone.0342932.g006

Consequently, a trim and fill analysis was done for TIBF (Fig 7).

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Fig 7. Funnel plots based on trim and fill analysis for the timely initiation of breastfeeding in children aged 6-23 months in Ethiopia, 2024.

https://doi.org/10.1371/journal.pone.0342932.g007

The funnel plot for EBF visually suggested the presence of publication bias, however, both Begg’s (p = 0.556) and Egger’s (p = 0.433) tests didn’t indicate statistically significant publication bias (Fig 8).

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Fig 8. Funnel plot for exclusive breastfeeding of infants in Ethiopia, 2024.

https://doi.org/10.1371/journal.pone.0342932.g008

Regarding TICF, neither the funnel plot nor Begg’s (p = 0.056) and Egger’s (p = 0.060) tests showed evidence of publication bias (Fig 9).

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Fig 9. Funnel Plot for the timely initiation of complementary feeding among children aged 6-23 months in Ethiopia, 2024.

https://doi.org/10.1371/journal.pone.0342932.g009

Similarly, the funnel plot for MAD practices showed the presence of possible publication bias; but Begg’s (p = 0.89) and Egger’s (p = 0.934) tests revealed no statistically significant publication bias (Fig 10).

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Fig 10. Funnel plot for minimum acceptable diet among children aged 6–23 months in Ethiopia, 2024).

https://doi.org/10.1371/journal.pone.0342932.g010

Factors associated with feeding practices of under-two children

Mothers who had antenatal care follow-up were almost three times more likely to initiate breastfeeding early compared with those without antenatal care (AOR = 3.4%; 95% CI: 1.5, 7.5). Mothers who delivered by cesarean section were 70% less likely to initiate breastfeeding timely than those who had vaginal delivery (AOR = 0.3; 95% CI: 0.1, 0.9). Similarly, facility-based delivery was associated with higher odds of timely initiation of breastfeeding compared with home delivery (AOR = 2.3; 95% CI: 1.1, 4.9) (Table 2).

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Table 2. Determinants of feeding practices among under-two children in Ethiopia, 2024.

https://doi.org/10.1371/journal.pone.0342932.t002

Infants aged 0–1 and 2–3 months were over four times and three times more likely to be exclusively breastfed compared with infants aged 4–6 months (AOR = 4.4; 95% CI: 1.4, 13.6) and (AOR = 2.5; 95% CI: 1.2, 5.1), respectively. Mothers aged 35 years and above were about three times more likely to exclusively breastfeed their children compared with younger mothers (AOR = 3.4; 95% CI: 1.3, 8.7). Rural mothers had significantly higher odds of practicing exclusive breastfeeding compared with their urban counterparts (AOR = 1.8; 95% CI: 1.1, 3.1). Unemployed mothers were also 80% more likely to exclusively breastfeed than employed mothers (AOR = 1.8; 95% CI: 1.2, 2.7). Mothers who delivered in health facilities were twice as the likelihood of exclusively breastfeed compared with those who delivered at home (AOR = 2.1; 95% CI:1.2, 3.7).

Mothers who had normal (vaginal) deliveries were 70% more likely to exclusively breastfeed than those who delivered by cesarean section (AOR = 1.7; 95 CI:1.2, 1.2, 2.6). Postnatal care attendance was also positively associated with exclusive breastfeeding (AOR = 2.3; 95% CI: 1.2, 4.3). Additionally, mothers who received breastfeeding counseling were more likely to practice exclusive breastfeeding compared to those who didn’t (AOR = 2.3; 95% CI:1.4, 3.9) and mothers who received husband support were nearly three times more likely to exclusively breastfeed their infants (AOR = 2.9; 95% CI:1.9, 4.4) (Table 2).

Mothers who attended antenatal care were almost three times more likely to initiate complementary feeding at the recommended time compared with those who did not attend ANC (AOR = 3.4; 95% CI:1.5, 7.5). Likewise, mothers who delivered in health facilities had twice the likelihood of initiating complementary feeding on time compared with mothers who delivered at home (AOR = 2.3; 95% CI:1.1, 4.9) (Table 2).

Receiving nutrition education through practical demonstrations on complementary food preparation was also associated with better feeding practices; mothers exposed to such demonstrations were twice as likely to practice optimal feeding compared with their counterparts (AOR = 2.06; 95% CI:1.28, 3.31). Additionally, children aged 18–23 months were almost three times more likely to receive optimal feeding practices than those aged 6–11 months (AOR = 2.68; 95% CI:1.18, 6.13) (Table 2).

Discussion

The aim of this study was to assess the pooled prevalence of feeding practices and the factors associated with them among children under two years of age in Ethiopia. The pooled prevalence of TIBF, EBF, TICF, and MAD were 64%, 59.56%, 59%, and 19.77%, respectively. A range of determinants were identified, including antenatal care, place and mode of delivery, postnatal care, maternal age and occupation, counseling, husband’s support, place of residence, maternal education, involvement in complementary food preparation demonstrations, and the child’s age.

The pooled prevalence of TIBF was 64%, which is in line with a SRMA done in Ethiopia (61.4%) [15], Sub-Saharan Africa (50.5%) [100] and Bangladesh [101]. According to WHO IYCF standards, it is considered good [102]. However, it was lower than the national and WHO IYCF recommendations [102,103]. But it was higher than the pooled prevalence reported among cesarean delivered mothers in Ethiopia (40.1%) and the recent estimate from 53 WHO European Region member countries (43%) [12,104]. These differences might be attributed to variations in study setting, methodological approaches, socio-demographic and economic characteristics, and health service utilization.

This study demonstrated that the pooled prevalence of EBF in Ethiopia was 59.56%. It is rated good according to the WHO IYCF standards (50%–89%). This result aligns with previous SRMA conducted in Ethiopia and Iran [14,15], the 2019 mini-EDHS report (59%), and a study in Southern Africa (56.57%) [15,105,106]. However, it is higher than the global EBF prevalence of exclusive breastfeeding (44%), SRMAs conducted in Ghana and Iran [107,108], and studies from Sub-Saharan Africa (36%), and Central Africa (53.48%) [105]. Conversely, the prevalence reported in this study is lower than findings from several regions of India and the Nepal DHS [109111]. Such may be attributed to differences in socio-demographic and economic contexts, access to information, study periods, and methodological approaches.

This study also showed that more than half (59%) of infants received complementary feeding timely. According to WHO standards, it is rated as ‘fair’ (60–79%). This finding is consistent with a SRMA conducted in Ethiopia and a study conducted in South Asia [112,113], and it is congruent with the recent global estimate of 64.5% [114]. However, it is higher than a study conducted in five European Union countries (47%) [115]. These differences might be due to the differences in the study settings.

The pooled prevalence of minimum acceptable diet was 19.77%. This finding is consistent with a SRMA conducted in Ethiopia [18], as well as studies from South Asia [113] and Bangladesh [101], underscoring that many Ethiopian children continue to consume diets of inadequate quality [16]. However, the prevalence observed in this study is higher than the 2019 mini-EDHS report (11.3%), and the Ghana DHS [116], east Africa (11.58%) [117] and Sub-Saharan Africa (9.98%) [118]. In contrast, it was lower than reports from the Democratic Republic of Congo (33%) [119], and a study conducted in Indonesia (29%) [120]. These may reflect differences in the study methodologies, socio-demographic and economic contexts, access to diverse foods, and the time periods during which the studies were conducted.

Antenatal follow-up was identified as a predictor of TIBF. Mothers who attended ANC were three times more likely to initiate breastfeeding timely. This finding is consistent with evidence from a study done in Sub-Saharan African countries [121]. This might be because the nutrition education given during ANC visits which encourages skilled delivery and supports mothers in initiating breastfeeding soon after birth. However, this finding contrasts with studies done in Ethiopia and Namibia, where mothers who attended antenatal care were reported to be less likely to initiate breastfeeding on time [122,123]. This discrepancy may be due to variation in the interaction of health care providers during visits, as well as lack of coordinated responsibility, which could hinder the delivery of consistent messages to mothers.

This study identified place of delivery as a determinant of TIBF. Mothers delivered in a health facility were twice as likely to initiate breastfeeding on time compared with those who delivered at home. This finding is similar with evidence from a global systematic review and meta-analysis, as well as studies conducted in Iran, Namibia, and Nepal [108,123125]. This might be because mothers who gave birth in a health facility were encouraged by health care providers through counseling and support on colostrum feeding, which enables them to initiate breastfeeding within the recommended time. Additionally, mothers delivering in health facilities are less likely to give prelacteal foods before initiating breastfeeding. On the other hand, studies from Ireland and the UK, and Canada revealed that home delivery was associated with higher odds of timely initiation of breastfeeding [126,127].

There was also a significant association between mode of delivery and TIBF. Mothers who delivered by cesarean section were 70% less likely to initiate breastfeeding timely as compared to vaginal delivery. This finding is consistent with studies conducted in Ghana and Kenya [128,129]. This may be due to post-operative care needs, pain, and fatigue, which can interfere with early skin-to-skin contact and immediate newborn care, both essential for timely initiation of breastfeeding. In contrast, a study from Central America reported a significant association between mode of delivery and timely initiation of breastfeeding [130]. This inconsistency may be due to the difference in socio-economic conditions and the quality and accessibility of health care services.

Younger children were more likely to be exclusively breastfed than older ones, with the likelihood of exclusive breastfeeding declining as age increases. This pattern is consistent with findings from several West African countries [131133]. A possible explanation is that many mothers perceive breast milk alone as inadequate to meet the growing nutritional needs of older infants, prompting earlier introduction of complementary foods.

Maternal age was emerged as a significant predictor of exclusive breastfeeding. Mothers aged 35 years and older were three times more likely to exclusively breastfeed compared with those aged 15–24 years. This finding is in line with evidence from systematic reviews conducted in Brazil and Ghana [107,134]. One possible explanation is that younger mothers may perceive prolonged exclusive breastfeeding as affecting breast size or physical appearance, which could lead to earlier introduction of supplementary foods [135,136]. Furthermore, younger mothers may have limited awareness on the benefits of EBF, insufficient breastfeeding skills, or more frequent experiences of breastfeeding-related discomfort, all of which may contribute to lower exclusive breastfeeding practices. [137139].

Maternal employment was a significant negative predictor of EBF. Employed mothers were 43% less likely to exclusively breastfeed their children compared with employed mothers. This finding is consistent with studies conducted across 19 developing countries [140], low and middle-income countries [141], and a SRMA from Ethiopia [14]. This could be because employed mothers return to work too early after birth due to short maternity leave, which can limit their ability to establish and sustain regular exclusive breastfeeding practices.

Conversely mothers from rural areas were 82% more likely to EBF their infants than urban residents. A similar result was reported by a previous SRMA conducted in Asia, Europe, and Africa [142]. This may be because rural mothers are predominantly housewives, are less likely to be engaged in formal employment, and tend to view breastfeeding as a natural maternal norm, unlike many of their urban counterpart. In addition, mothers living in rural areas are less exposed to and less familiar with breast milk substitutes promoted through media marketing compared with those in urban areas [143].

Mothers who delivered in a health facility were twice as likely to EBF their infants than home delivered mothers. This result was in line with studies done in Ethiopia, Tanzania and a systematic review and meta-analysis from Asia, Europe, and Africa [15,142,144]. This might be because women who delivered in a health facility could have a golden opportunity for nutrition education on the importance of EBF. In contrast, this finding contradicts with studies reported from Canada, Ireland and the UK, and Canada, which reported higher EBF rates among mothers who delivered at home [145]. This controversy could be explained by cultural differences among study participants and variations in awareness and understanding of exclusive breastfeeding practices [126,127].

Mothers who had normal delivery were twice as likely to EBF than those who delivered by cesarean section. This finding is consistent with a SRMA conducted in Iran [108]. This could be because of the nutrition counseling and breastfeeding support provided during labor and the immediate postpartum period, which encourage exclusive breastfeeding practices.

It was observed that mothers who received breastfeeding counseling were twice as likely to exclusively breastfeed their children compared with those who did not receive counseling, which was in accord with a SRMA performed by McFadden A et al. [146] and Ethiopia [147]. This may be due to the interactions with individual mothers during counselling, which enhance their knowledge, confidence, and decision-making regarding exclusive breastfeeding.

This study demonstrated that mothers who received support from their husband were almost three times more likely to exclusively breastfeed. This finding was corroborated by a SRMA conducted in Ghana and China [148,149]. This may be attributed to the emotional, physical, and practical support provided by husbands, which can strengthen maternal confidence, reduce stress, and ultimately enhance both the success and duration of exclusive breastfeeding. However, this finding contrasts with evidence from a systematic review and meta-analysis conducted by Sinha B. et a [150].

Mothers who attended postnatal care were more likely to EBF than their counterparts. This finding was in congruence with SRMA conducted in Ethiopia [151,152]. This may be because of the nutrition education and counseling received during the postnatal period, can help address breastfeeding difficulties, increase maternal confidence, and encourage social and family support, ultimately enabling mothers to maintain exclusive breastfeeding for six months.

Mothers who had antenatal care follow-up were more likely to initiate complementary feeding on time. This finding was consistent with a SRMA conducted in Ethiopia [112]. This could be because antenatal care visits provide an opportunity for mothers to receive information and counseling on appropriate complementary feeding practices from healthcare providers, thereby improving infant and young child feeding behaviors.

This study also showed that mothers who delivered at a health facility were more likely to initiate complementary feeding than home delivered mothers, which is in line with a SRMA in Ethiopia [153]. This could be attributed to the fact that mothers who gave birth in health institutions are more likely to receive counseling guidance from health professionals on appropriate child feeding practices.

It was also observed that children aged 18–23 months were more likely to receive a diet of good quality as per the recommendation compared to children aged 6–11 months. This finding was in line with studies done in Ethiopia, Ghana, and Uganda [154157]. This may be because of the introduction of complementary feeding with a limited food item. Additionally, mothers may perceive that younger children have less developed digestive capacity for foods such as fruits, green leafy vegetables, and meat.

Mothers who received nutrition education through demonstration of complementary food preparation were more likely to achieve MAD as compared to their counterparts. This might be because such demonstration provides practical knowledge and skills on how to select, clean, and cook nutritious food preparation that meet the child’s nutritional needs. By observing and practicing food preparation during demonstrations, caregivers are more likely to adopt positive feeding behaviors, which enhances their confidence, promotes appropriate feeding practices, and supports the overall health and well-being of infants and young children.

This systematic review and meta-analysis have several limitations, including the exclusion of studies published in languages other than English. Furthermore, the high level of heterogeneity observed across the included studies may affect the reliability of the findings by introducing variability that can obscure true effects and potentially lead to misleading conclusions

Conclusions

The pooled prevalence of child feeding practices in Ethiopia remains below both national and global infant and young child feeding recommendations. These suboptimal feeding practice act as an early warning signal, indicating heightened risks of malnutrition, morbidity, and mortality. Under such conditions, achieving the Sustainable Development Goals and the national aspiration of becoming a lower-middle-income country becomes increasingly challenging.

Key determinants influencing infant feeding practices include the child’s age, maternal age, maternal employment status, place of residence, antenatal care attendance, place of delivery, postnatal care utilization, and exposure to complementary food preparation demonstrations.

Strengthening infant feeding practices therefore requires a multifaceted approach. Priority actions should include enhancing nutrition education through practical demonstrations, extending maternity leave to six months or establishing workplace breastfeeding and feeding corners, promoting consistent attendance of antenatal and postnatal care services, increasing facility-based deliveries, and tailoring interventions to maternal age and residential context. Equal emphasis should be placed on promoting age-appropriate feeding practices to ensure optimal growth and development.

Acknowledgments

We would like to acknowledge PROSPERO for registering this systematic review and meta-analysis.

References

  1. 1. Organization WH. Infant and young child feeding: model chapter for textbooks for medical students and allied health professionals. World Health Organization. 2009.
  2. 2. UNICEF. UNICEF advocacy strategy guidance for the prevention of overweight and obesity in children and adolescents. New York: UNICEF. 2020. https://www.unicef.org/media/92331/file/Advocacy-Guidance-Overweight-Prevention.pdf
  3. 3. Micha R, Mannar V, Afshin A, Allemandi L, Baker P, Battersby J. 2020 global nutrition report: action on equity to end malnutrition. 2020. https://repository.mdx.ac.uk/item/89022
  4. 4. Bhutta ZA, Das JK, Rizvi A, Gaffey MF, Walker N, Horton S, et al. Evidence-based interventions for improvement of maternal and child nutrition: what can be done and at what cost?. Lancet. 2013;382(9890):452–77. pmid:23746776
  5. 5. Black R, Victora C, Walker S, Bhutta Z, Christian P, de Onis M. Global nutrition report 2016: from promise to impact ending malnutrition by 2030. Washington DC: International Food Policy Research Institute. 2016. http://dx.doi.org/102499/9780896295841
  6. 6. Ssentongo P, Ssentongo AE, Ba DM, Ericson JE, Na M, Gao X. Global, regional and national epidemiology and prevalence of child stunting, wasting and underweight in low-and middle-income countries, 2006–2018. Scientific Reports. 2021;11(1):5204.
  7. 7. Organization WH. Exclusive breastfeeding for six months best for babies everywhere. Geneva, Switzerland. 2011. https://pubmed.ncbi.nlm.nih.gov/25164443
  8. 8. Fewtrell MS, Morgan JB, Duggan C, Gunnlaugsson G, Hibberd PL, Lucas A, et al. Optimal duration of exclusive breastfeeding: what is the evidence to support current recommendations?. Am J Clin Nutr. 2007;85(2):635S-638S. pmid:17284769
  9. 9. UNICEF. WHO - The World Bank: Joint child malnutrition estimates - Levels and trends. Geneva: World Health Organization. 2012. https://data.unicef.org/resources/jme/
  10. 10. Rollins NC, Bhandari N, Hajeebhoy N, Horton S, Lutter CK, Martines JC, et al. Why invest, and what it will take to improve breastfeeding practices?. Lancet. 2016;387(10017):491–504. pmid:26869576
  11. 11. Dey SK, Chisti MJ, Das SK, Shaha CK, Ferdous F, Farzana FD, et al. Characteristics of diarrheal illnesses in non-breast fed infants attending a large urban diarrheal disease hospital in Bangladesh. PLoS One. 2013;8(3):e58228. pmid:23520496
  12. 12. Getaneh T, Negesse A, Dessie G, Desta M, Temesgen H, Getu T, et al. Impact of cesarean section on timely initiation of breastfeeding in Ethiopia: a systematic review and meta-analysis. Int Breastfeed J. 2021;16(1):51. pmid:34225731
  13. 13. Mekonnen AG, Yehualashet SS, Bayleyegn AD. The effects of kangaroo mother care on the time to breastfeeding initiation among preterm and LBW infants: a meta-analysis of published studies. Int Breastfeed J. 2019;14:12. pmid:30820239
  14. 14. Wake GE, Mittiku YM. Prevalence of exclusive breastfeeding practice and its association with maternal employment in Ethiopia: a systematic review and meta-analysis. Int Breastfeed J. 2021;16(1):86. pmid:34717673
  15. 15. Alebel A, Tesma C, Temesgen B, Ferede A, Kibret GD. Exclusive breastfeeding practice in Ethiopia and its association with antenatal care and institutional delivery: a systematic review and meta-analysis. Int Breastfeed J. 2018;13:31. pmid:30026786
  16. 16. Indicators K. Mini demographic and health survey. EPHI and ICF. 2019. https://www.dhsprogram.com/pubs/pdf/FR363/FR363.pdf
  17. 17. Consensus C. Expert panel findings. 2012. https://copenhagenconsensus.com/publication/third-copenhagen-consensus-outcome-document
  18. 18. Kassie GA, Gebrekidan AY, Enaro EY, Asgedom YS. Minimum acceptable dietary intake among children aged 6-23 months in Ethiopia: A systematic review and meta-analysis. PLoS One. 2023;18(6):e0287247. pmid:37384754
  19. 19. Moher D, Shamseer L, Clarke M, Ghersi D, Liberati A, Petticrew M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement. Syst Rev. 2015;4(1):1. pmid:25554246
  20. 20. Higgins JP, Green S. Cochrane handbook for systematic reviews of interventions. London, UK: The Cochrane Collaboration. 2011.
  21. 21. Ayalew T, Tewabe T, Ayalew Y. Timely initiation of breastfeeding among first time mothers in Bahir Dar city, North West, Ethiopia, 2016. Pediatr Res. 2019;85(5):612–6. pmid:30661083
  22. 22. Gebremeskel SG, Gebru TT, Gebrehiwot BG, Meles HN, Tafere BB, Gebreslassie GW, et al. Early initiation of breastfeeding and associated factors among mothers of aged less than 12 months children in rural eastern zone, Tigray, Ethiopia: cross-sectional study. BMC research notes. 2019; 12:1–6.
  23. 23. Gebretsadik GG, Tkuwab H, Berhe K, Mulugeta A, Mohammed H, Gebremariam A. Early initiation of breastfeeding, colostrum avoidance, and their associated factors among mothers with under one year old children in rural pastoralist communities of Afar, Northeast Ethiopia: a cross sectional study. BMC Pregnancy Childbirth. 2020;20(1):448. pmid:32758166
  24. 24. Mengistu GT, Mengistu BK. Early initiation of breast feeding and associated factors among mother-baby dyads with immediate skin-to-skin contact: cross-sectional study based on the 2016 Ethiopian Demographic and Health Survey data. BMJ Open. 2023;13(3):e063258. pmid:36990497
  25. 25. Liben ML, Yesuf EM. Determinants of early initiation of breastfeeding in Amibara district, Northeastern Ethiopia: a community based cross-sectional study. Int Breastfeed J. 2016;11:7. pmid:27064535
  26. 26. Setegn T, Gerbaba M, Belachew T. Determinants of timely initiation of breastfeeding among mothers in Goba Woreda, South East Ethiopia: a cross sectional study. BMC Public Health. 2011;11:217. pmid:21473791
  27. 27. Alemayehu M. Factors Associated with Timely Initiation and Exclusive Breast Feeding among Mothers of Axum Town, Northern Ethiopia. SJPH. 2014;2(5):394.
  28. 28. Gargamo DB, Hidoto KT, Abiso TL. The prevalence and associated factors on timely initiation of breastfeeding among mothers of children age less than 12 months in Wolaita Sodo City, Wolaita, Ethiopia. 2020.
  29. 29. Shiferaw R, Tadesse SE, Mekonnen TC, Zerga AA. Timely Initiation of Breast Feeding and Associated Factors among Caesarian Section Delivered Mothers in Health Facilities of Dessie City Administration, North Eastern Ethiopia. Pediatr Rep. 2020;13(1):1–8. pmid:33374654
  30. 30. Gedefaw G, Goedert MH, Abebe E, Demis A. Effect of cesarean section on initiation of breast feeding: Findings from 2016 Ethiopian Demographic and Health Survey. PLoS One. 2020;15(12):e0244229. pmid:33338080
  31. 31. Tilahun G, Degu G, Azale T, Tigabu A. Prevalence and associated factors of timely initiation of breastfeeding among mothers at Debre Berhan town, Ethiopia: a cross-sectional study. Int Breastfeed J. 2016;11:27. pmid:27729937
  32. 32. Tariku A, Biks GA, Wassie MM, Worku AG, Yenit MK. Only half of the mothers practiced early initiation of breastfeeding in Northwest Ethiopia, 2015. BMC Research Notes. 2017;10:1–7.
  33. 33. Gebretsadik GG, Berhe K, Gebregziabher H. Determinants of early initiation of breast feeding during COVID-19 pandemic among urban-dwelling mothers from Tigray, Northern Ethiopia: a community-based cross-sectional study. BMJ Open. 2023;13(7):e070518. pmid:37429688
  34. 34. Belachew A, Tewabe T, Asmare A, Hirpo D, Zeleke B, Muche D. Prevalence of exclusive breastfeeding practice and associated factors among mothers having infants less than 6 months old, in Bahir Dar, Northwest, Ethiopia: a community based cross sectional study. BMC Research Notes. 2018;11:1–6.
  35. 35. Seid AM, Yesuf ME, Koye DN. Prevalence of Exclusive Breastfeeding Practices and associated factors among mothers in Bahir Dar city, Northwest Ethiopia: a community based cross-sectional study. Int Breastfeed J. 2013;8(1):14. pmid:24152996
  36. 36. Sonko A, Worku A. Prevalence and predictors of exclusive breastfeeding for the first six months of life among women in Halaba special woreda, Southern Nations, Nationalities and Peoples’ Region/SNNPR/, Ethiopia: a community based cross-sectional study. Archives of Public Health. 2015;73:1–11.
  37. 37. Hagos D, Tadesse AW. Prevalence and factors associated with exclusive breastfeeding among rural mothers of infants less than six months of age in Southern Nations, Nationalities, Peoples (SNNP) and Tigray regions, Ethiopia: a cross-sectional study. Int Breastfeed J. 2020;15(1):25. pmid:32276666
  38. 38. Teka B, Assefa H, Haileslassie K. Prevalence and determinant factors of exclusive breastfeeding practices among mothers in Enderta woreda, Tigray, North Ethiopia: a cross-sectional study. Int Breastfeed J. 2015;10(1):2. pmid:25621000
  39. 39. Egata G, Berhane Y, Worku A. Predictors of non-exclusive breastfeeding at 6 months among rural mothers in east Ethiopia: a community-based analytical cross-sectional study. Int Breastfeed J. 2013;8(1):8. pmid:23919800
  40. 40. Tadesse T, Mesfin F, Chane T. Prevalence and associated factors of non-exclusive breastfeeding of infants during the first six months in rural area of Sorro District, Southern Ethiopia: a cross-sectional study. Int Breastfeed J. 2016;11:25. pmid:27660644
  41. 41. Feleke DG, Kassahun CW, Tassaw SF, Chanie ES. Non-exclusive breast feeding and its factors in the first 6-month life of infants among mother-infant pairs of 6–12 months in Debre Tabor town, Northwest Ethiopia, 2019: community-based cross-sectional study. Heliyon. 2021;7(4).
  42. 42. Mekebo GG, Argawu AS, Likassa HT, Ayele W, Wake SK, Bedada D, et al. Factors influencing exclusive breastfeeding practice among under-six months infants in Ethiopia. BMC Pregnancy Childbirth. 2022;22(1):630. pmid:35941576
  43. 43. Setegn T, Belachew T, Gerbaba M, Deribe K, Deribew A, Biadgilign S. Factors associated with exclusive breastfeeding practices among mothers in Goba district, south east Ethiopia: a cross-sectional study. Int Breastfeed J. 2012;7(1):17. pmid:23186223
  44. 44. Liben ML, Gemechu YB, Adugnew M, Asrade A, Adamie B, Gebremedin E, et al. Factors associated with exclusive breastfeeding practices among mothers in dubti town, afar regional state, northeast Ethiopia: a community based cross-sectional study. Int Breastfeed J. 2016;11:4. pmid:26997971
  45. 45. Yimer DS, Adem OS, Arefayene M, Chanie T, Endalifer ML. Exclusive breastfeeding practice and its associated factors among children aged 6-23 months in Woldia Town, Northwest Ethiopia. Afr Health Sci. 2021;21(4):1877–86. pmid:35283943
  46. 46. Shitie A, Tilahun A, Olijira L. Exclusive breastfeeding practice and associated factors among mothers of infants age 6 to 12 months in Somali region of Ethiopia. Scientific Reports. 2022;12(1):19102.
  47. 47. Tewabe T, Mandesh A, Gualu T, Alem G, Mekuria G, Zeleke H. Exclusive breastfeeding practice and associated factors among mothers in Motta town, East Gojjam zone, Amhara Regional State, Ethiopia, 2015: a cross-sectional study. Int Breastfeed J. 2017;12:12. pmid:28261318
  48. 48. Mebratu L, Mengesha S, Tegene Y, Alano A, Toma A. Exclusive Breast-Feeding Practice and Associated Factors among HIV-Positive Mothers in Governmental Health Facilities, Southern Ethiopia. J Nutr Metab. 2020;2020:7962054. pmid:33014458
  49. 49. Jama A, Gebreyesus H, Wubayehu T, Gebregyorgis T, Teweldemedhin M, Berhe T, et al. Exclusive breastfeeding for the first six months of life and its associated factors among children age 6-24 months in Burao district, Somaliland. Int Breastfeed J. 2020;15(1):5. pmid:32000821
  50. 50. Gebrekidan K, Plummer V, Fooladi E, Hall H. Attitudes and experiences of employed women when combining exclusive breastfeeding and work: A qualitative study among office workers in Northern Ethiopia. Matern Child Nutr. 2021;17(4):e13190. pmid:33830656
  51. 51. Kebede T, Woldemichael K, Jarso H, Bekele BB. Exclusive breastfeeding cessation and associated factors among employed mothers in Dukem town, Central Ethiopia. Int Breastfeed J. 2020;15(1):6. pmid:32019563
  52. 52. Chekol DA, Biks GA, Gelaw YA, Melsew YA. Exclusive breastfeeding and mothers’ employment status in Gondar town, Northwest Ethiopia: a comparative cross-sectional study. Int Breastfeed J. 2017;12:27. pmid:28638435
  53. 53. Tadesse F, Alemayehu Y, Shine S, Asresahegn H, Tadesse T. Exclusive breastfeeding and maternal employment among mothers of infants from three to five months old in the Fafan zone, Somali regional state of Ethiopia: a comparative cross-sectional study. BMC Public Health. 2019;19(1):1015. pmid:31357979
  54. 54. Hunegnaw MT, Gezie LD, Teferra AS. Exclusive breastfeeding and associated factors among mothers in Gozamin district, northwest Ethiopia: a community based cross-sectional study. Int Breastfeed J. 2017;12:30. pmid:28702071
  55. 55. Mekuria G, Edris M. Exclusive breastfeeding and associated factors among mothers in Debre Markos, Northwest Ethiopia: a cross-sectional study. Int Breastfeed J. 2015;10(1):1. pmid:25635183
  56. 56. Zewdie A, Taye T, Kasahun AW, Oumer A. Effect of maternal employment on exclusive breastfeeding practice among mothers of infants 6–12 months old in Wolkite town, Ethiopia: a comparative cross-sectional study. BMC women’s health. 2022;22(1):222.
  57. 57. Asemahagn MA. Determinants of exclusive breastfeeding practices among mothers in azezo district, northwest Ethiopia. Int Breastfeed J. 2016;11:22. pmid:27489561
  58. 58. Lenja A, Demissie T, Yohannes B, Yohannis M. Determinants of exclusive breastfeeding practice to infants aged less than six months in Offa district, Southern Ethiopia: a cross-sectional study. Int Breastfeed J. 2016;11:32. pmid:27990174
  59. 59. Awoke S, Mulatu B. Determinants of exclusive breastfeeding practice among mothers in Sheka Zone, Southwest Ethiopia: A cross-sectional study. Public Health Pract (Oxf). 2021;2:100108. pmid:36101636
  60. 60. Tiruye G, Mesfin F, Geda B, Shiferaw K. Breastfeeding technique and associated factors among breastfeeding mothers in Harar city, Eastern Ethiopia. Int Breastfeed J. 2018;13:5. pmid:29434650
  61. 61. Jebena DD, Tenagashaw MW. Breastfeeding practice and factors associated with exclusive breastfeeding among mothers in Horro District, Ethiopia: A community-based cross-sectional study. PLoS One. 2022;17(4):e0267269. pmid:35476799
  62. 62. Mamo K, Dengia T, Abubeker A, Girmaye E. Assessment of Exclusive Breastfeeding Practice and Associated Factors among Mothers in West Shoa Zone, Oromia, Ethiopia. Obstet Gynecol Int. 2020;2020:3965873. pmid:32849875
  63. 63. Bewket Zeleke L, Welday Gebremichael M, Mehretie Adinew Y, Abebe Gelaw K. Appropriate Weaning Practice and Associated Factors among Infants and Young Children in Northwest Ethiopia. J Nutr Metab. 2017;2017:9608315. pmid:28808588
  64. 64. Kassa T, Meshesha B, Haji Y, Ebrahim J. Appropriate complementary feeding practices and associated factors among mothers of children age 6–23 months in Southern Ethiopia, 2015. BMC Pediatrics. 2016;16:1–10.
  65. 65. Wondimu SME, Tariku A. Determinants of timely initiation of complementary feeding among mothers with children aged 6–23 months in Lalibela District, Northeast Ethiopia, 2015. 2016.
  66. 66. Gilano G, Sako S, Gilano K. Determinants of timely initiation of complementary feeding among children aged 6–23 months in Ethiopia. Scientific Reports. 2022;12(1):19069.
  67. 67. Ayana D, Tariku A, Feleke A, Woldie H. Complementary feeding practices among children in Benishangul Gumuz Region, Ethiopia. BMC Res Notes. 2017;10(1):335. pmid:28750674
  68. 68. Semahegn A, Tesfaye G, Bogale A. Complementary feeding practice of mothers and associated factors in Hiwot Fana Specialized Hospital, Eastern Ethiopia. Pan Afr Med J. 2014;18:143. pmid:25419281
  69. 69. Yeshaneh A, Zebene M, Gashu M, Abebe H, Abate H. Complementary feeding practice and associated factors among internally displaced mothers of children aged 6-23 months in Amhara region, Northwest Ethiopia: a cross-sectional study. BMC Pediatr. 2021;21(1):583. pmid:34930219
  70. 70. Ahmed JA, Sadeta KK, Lenbo KH. Magnitude and factors associated with appropriate complementary feeding practice among mothers of children 6-23 months age in Shashemene town, Oromia- Ethiopia: Community based cross sectional study. PLoS One. 2022;17(3):e0265716. pmid:35349586
  71. 71. Toma YT, Emebet BE, Manaye YM, Yinager YW. Timely initiation of complementary feeding and associated factors among children aged 6 to 12 months in Addis Ababa Ethiopia. Ethiopian Journal of Health Sciences. 2016;26(1):1–10.
  72. 72. Agedew E, Demissie M, Misker D, Haftu D. Early initiation of complementary feeding and associated factors among 6 months to 2 years young children. J Nutr Food Sci. 2014;4(6):314.
  73. 73. Gessese D, Bolka H, Alemu Abajobir A, Tegabu D. The practice of complementary feeding and associated factors among mothers of children 6-23 months of age in Enemay district, Northwest Ethiopia. Nutrition & Food Science. 2014;44(3):230–40.
  74. 74. Neme K, Olika E. Knowledge and practices of complementary feeding among mothers/caregivers of children age 6 to 23 months in Horo Woreda, Horo Guduru Wollega Zone, Oromia Region, Ethiopia. Journal of Biomedical Research and Reviews. 2017;1(1):1–10.
  75. 75. Mekbib E. Magnitude and Factors Associated with Appropriate Complementary Feeding among Mothers Having Children 6-23 Months-of-Age in Northern Ethiopia; A Community-Based Cross-Sectional Study. JFNS. 2014;2(2):36.
  76. 76. Chane T, Bitew S, Mekonnen T, Fekadu W. Initiation of complementary feeding and associated factors among children of age 6-23 months in Sodo town, Southern Ethiopia: Cross-sectional study. Pediatr Rep. 2018;9(4):7240. pmid:29383219
  77. 77. Yemane S. Timely Initiation of Complementary Feeding Practice and Associated Factors among Mothers of Children Aged from 6 to 24 Months in Axum Town, North Ethiopia. IJNFS. 2014;3(5):438.
  78. 78. Tafesse T, Badacho AS, Kuma DM. Timely Introduction of Complementary Feeding among Caregivers of Children 6-12 Month Sodo Town, Ethiopia. Health Sci J. 2018;12(1).
  79. 79. Akalu E. Assessment of timely initiation of complementary feeding and associated factors among mothers/care givers with children aged six to twenty-three months at kolfe keranyo subcity of Addis Ababa, Ethiopia. 2020.
  80. 80. Mulat E, Alem G, Woyraw W, Temesgen H. Uptake of minimum acceptable diet among children aged 6–23 months in orthodox religion followers during fasting season in rural area, DEMBECHA, north West Ethiopia. BMC nutrition. 2019; 5:1–10.
  81. 81. Ahmed KY, Page A, Arora A, Ogbo FA. Trends and factors associated with complementary feeding practices in Ethiopia from 2005 to 2016. Matern Child Nutr. 2020;16(2):e12926. pmid:31833239
  82. 82. Teshome F, Tadele A. Trends and determinants of minimum acceptable diet intake among infant and young children aged 6-23 months in Ethiopia: a multilevel analysis of Ethiopian demographic and health survey. BMC Nutr. 2022;8(1):44. pmid:35513888
  83. 83. Molla A, Egata G, Getacher L, Kebede B, Sayih A, Arega M, et al. Minimum acceptable diet and associated factors among infants and young children aged 6-23 months in Amhara region, Central Ethiopia: community-based cross-sectional study. BMJ Open. 2021;11(5):e044284. pmid:33972337
  84. 84. Yisak H, Ambaw B, Walle Z, Alebachew B, Ewunetei A. Minimum acceptable diet and associated factors among HIV-exposed children aged 6–24 months in Debre Tabor Town, Ethiopia. HIV/AIDS-Research and Palliative Care. 2020;:639–45.
  85. 85. Abebe H, Gashu M, Kebede A, Abata H, Yeshaneh A, Workye H, et al. Minimum acceptable diet and associated factors among children aged 6-23 months in Ethiopia. Ital J Pediatr. 2021;47(1):215. pmid:34717712
  86. 86. Birhanu H, Gonete KA, Hunegnaw MT, Aragaw FM. Minimum acceptable diet and associated factors among children aged 6–23 months during fasting days of orthodox Christian mothers in Gondar city, North West Ethiopia. BMC nutrition. 2022;8(1):76.
  87. 87. Birie B, Kassa A, Kebede E, Terefe B. Minimum acceptable diet practice and its associated factors among children aged 6-23 months in rural communities of Goncha district, north West Ethiopia. BMC Nutr. 2021;7(1):40. pmid:34281613
  88. 88. Dejene Y, Mezgebu GS, Tadesse SE. Minimum acceptable diet and its associated factors among children aged 6-23 months in Lalibela, northeast Ethiopia: a community-based cross-sectional study. J Nutr Sci. 2023;12:e41. pmid:37123396
  89. 89. Farah S, Derese T, Abera L. Minimum acceptable diet and associated factors among children aged 6-23 months in Jig-Jiga, Somali region, eastern Ethiopia, 2022. BMC Nutr. 2024;10(1):11. pmid:38212859
  90. 90. Belete S, Kebede N, Chane T, Melese W, Tadesse SE. Optimal complementary feeding practices and associated factors among mothers having children 6 to 23 months, south WOLLO zone, Dessie ZURIA, Ethiopia. J Pediatr Nurs. 2022;67:e106–12. pmid:36115754
  91. 91. Gebretsadik MT, Adugna DT, Aliyu AD, Belachew T. Optimal complementary feeding practices of children aged 6-23 months in three agro-ecological rural districts of Jimma zones of southwest Ethiopia. J Nutr Sci. 2023;12:e40. pmid:37008415
  92. 92. Birhanu M, Abegaz T, Fikre R. Magnitude and Factors Associated with Optimal Complementary Feeding Practices among Children Aged 6-23 Months in Bensa District, Sidama Zone, South Ethiopia. Ethiop J Health Sci. 2019;29(2):153–64. pmid:31011263
  93. 93. Fanta M, Cherie HA. Magnitude and determinants of appropriate complementary feeding practice among mothers of children age 6-23 months in Western Ethiopia. PLoS One. 2020;15(12):e0244277. pmid:33382749
  94. 94. Areja A, Yohannes D, Yohannis M. Determinants of appropriate complementary feeding practice among mothers having children 6–23 months of age in rural Damot sore district, Southern Ethiopia; a community based cross sectional study. BMC nutrition. 2017; 3:1–8.
  95. 95. Epheson B, Birhanu Z, Tamiru D, Feyissa GT. Complementary feeding practices and associated factors in Damot Weydie District, Welayta zone, South Ethiopia. BMC Public Health. 2018;18(1):419. pmid:29587689
  96. 96. Dagne AH, Zewude SB, Semahegn AM. Appropriate Complementary Feeding Practice and Its Associated Factors among Mothers Who Have Children Aged between 6 and 24 Months in Ethiopia: Systematic Review and Meta-Analysis. J Nutr Metab. 2022;2022:1548390. pmid:36245817
  97. 97. Demilew YM, Tafere TE, Abitew DB. Infant and young child feeding practice among mothers with 0–24 months old children in Slum areas of Bahir Dar City, Ethiopia. International breastfeeding journal. 2017; 12:1–9.
  98. 98. Isse AA, Tafese Z, Mohamed A, Hassan SM, Ahmed Z. Minimum Acceptable Diet and Associated Factors Among Infants and Young Children Aged 6-23 Months in Jigjiga, Ethiopia. Journal of Agriculture, Food and Natural Resources. 2023;1(2):1–11.
  99. 99. Gizaw G, Tesfaye G. Minimum Acceptable Diet and Factor Associated with It Among Infant and Young Children Age 6-23 Months in North Shoa, Oromia Region, Ethiopia. IJHNM. 2019;5(1):1.
  100. 100. Gebremedhin S. Core and optional infant and young child feeding indicators in Sub-Saharan Africa: a cross-sectional study. BMJ Open. 2019;9(2):e023238. pmid:30782876
  101. 101. Jubayer A, Nowar A, Islam S, Islam MH, Nayan MM. Complementary feeding practices and their determinants among children aged 6-23 months in rural Bangladesh: evidence from Bangladesh Integrated Household Survey (BIHS) 2018-2019 evaluated against WHO/UNICEF guideline -2021. Archives of public health = Archives belges de sante publique. 2023;81(1):114.
  102. 102. Organization WH. Infant and young child feeding: a tool for assessing national practices, policies and programmes. 2003. https://www.who.int/publications/i/item/9241562544
  103. 103. Federal Ministry of Health FHDE. National strategy for infant and young child feeding. Addis Ababa: Federal Ministry of Health, Family Health Department Ethiopia. 2004. https://leap.unep.org/en/countries/et/national-legislation/national-strategy-infant-and-young-child-feeding
  104. 104. Bagci Bosi AT, Eriksen KG, Sobko T, Wijnhoven TMA, Breda J. Breastfeeding practices and policies in WHO European Region Member States. Public Health Nutr. 2016;19(4):753–64. pmid:26096540
  105. 105. Issaka AI, Agho KE, Renzaho AM. Prevalence of key breastfeeding indicators in 29 sub-Saharan African countries: a meta-analysis of demographic and health surveys (2010-2015). BMJ Open. 2017;7(10):e014145. pmid:29070635
  106. 106. Gebeyehu NA, Tegegne KD, Shewangashaw NE, Biset G, Abebaw N, Tilahun L. Knowledge, attitude, practice and determinants of exclusive breastfeeding among women in Ethiopia: Systematic review and meta-analysis. Public Health Pract (Oxf). 2023;5:100373. pmid:36941951
  107. 107. Mohammed S, Yakubu I, Fuseini A-G, Abdulai A-M, Yakubu YH. Systematic review and meta-analysis of the prevalence and determinants of exclusive breastfeeding in the first six months of life in Ghana. BMC Public Health. 2023;23(1):920.
  108. 108. Behzadifar M, Saki M, Behzadifar M, Mardani M, Yari F, Ebrahimzadeh F, et al. Prevalence of exclusive breastfeeding practice in the first six months of life and its determinants in Iran: a systematic review and meta-analysis. BMC Pediatr. 2019;19(1):384. pmid:31656169
  109. 109. UNICEF. The extension of the 2025 maternal, infant and young child nutrition targets to 2030. 2021. https://www.bing.com/search?q=UNICEF.±The±extension±of±the±2025±maternal%2C±infant±and±young±child±nutrition±targets±to±2030%3A±WHO.±2021
  110. 110. Khanal V, Sauer K, Zhao Y. Exclusive breastfeeding practices in relation to social and health determinants: a comparison of the 2006 and 2011 Nepal Demographic and Health Surveys. BMC Public Health. 2013;13:1–13.
  111. 111. Ogbo FA, Dhami MV, Awosemo AO, Olusanya BO, Olusanya J, Osuagwu UL, et al. Regional prevalence and determinants of exclusive breastfeeding in India. Int Breastfeed J. 2019;14:20. pmid:31131015
  112. 112. Abdurahman AA, Chaka EE, Bule MH, Niaz K. Magnitude and determinants of complementary feeding practices in Ethiopia: A systematic review and meta-analysis. Heliyon. 2019;5(7):e01865. pmid:31317077
  113. 113. Aguayo VM. Complementary feeding practices for infants and young children in South Asia. A review of evidence for action post-2015. Matern Child Nutr. 2017;13 Suppl 2(Suppl 2):e12439. pmid:29032627
  114. 114. White JM, Bégin F, Kumapley R, Murray C, Krasevec J. Complementary feeding practices: Current global and regional estimates. Matern Child Nutr. 2017;13 Suppl 2(Suppl 2):e12505. pmid:29032623
  115. 115. Hirvonen K, Wolle A, Laillou A, Vinci V, Chitekwe S, Baye K. Understanding delays in the introduction of complementary foods in rural Ethiopia. Matern Child Nutr. 2024;20 Suppl 5(Suppl 5):e13247. pmid:34523796
  116. 116. Wegmüller R, Bentil H, Wirth JP, Petry N, Tanumihardjo SA, Allen L, et al. Anemia, micronutrient deficiencies, malaria, hemoglobinopathies and malnutrition in young children and non-pregnant women in Ghana: Findings from a national survey. PLoS One. 2020;15(1):e0228258. pmid:31999737
  117. 117. Worku MG, Alamneh TS, Tesema GA, Alem AZ, Tessema ZT, Liyew AM, et al. Minimum acceptable diet feeding practice and associated factors among children aged 6–23 months in east Africa: a multilevel binary logistic regression analysis of 2008–2018 demographic health survey data. Archives of public health. 2022;80(1):127.
  118. 118. Belay DG, Taddese AA, Gelaye KA. Minimum acceptable diet intake and its associated factors among children age at 6-23 months in sub-Saharan Africa: a multilevel analysis of the sub-Saharan Africa demographic and health survey. BMC Public Health. 2022;22(1):684. pmid:35392871
  119. 119. Kambale RM, Ngaboyeka GA, Kasengi JB, Niyitegeka S, Cinkenye BR, Baruti A, et al. Minimum acceptable diet among children aged 6-23 months in South Kivu, Democratic Republic of Congo: a community-based cross-sectional study. BMC Pediatr. 2021;21(1):239. pmid:34011304
  120. 120. Zebadia E, Mahmudiono T, Atmaka DR, Dewi M, Helmyati S, Yuniar CT. Factors Associated with Minimum Acceptable Diet in 6–11-Month-Old Indonesian Children Using the 2017 IDHS. Open Access Maced J Med Sci. 2021;9(E):1403–12.
  121. 121. Ogbo FA, Eastwood J, Page A, Efe-Aluta O, Anago-Amanze C, Kadiri EA, et al. The impact of sociodemographic and health-service factors on breast-feeding in sub-Saharan African countries with high diarrhoea mortality. Public Health Nutr. 2017;20(17):3109–19. pmid:28980521
  122. 122. Ahmed KY, Page A, Arora A, Ogbo FA. Trends and determinants of early initiation of breastfeeding and exclusive breastfeeding in Ethiopia from 2000 to 2016. Int Breastfeed J. 2019;14:40. pmid:31528197
  123. 123. Ndirangu MN, Gatimu SM, Mwinyi HM, Kibiwott DC. Trends and factors associated with early initiation of breastfeeding in Namibia: analysis of the Demographic and Health Surveys 2000-2013. BMC Pregnancy Childbirth. 2018;18(1):171. pmid:29769063
  124. 124. Adhikari M, Khanal V, Karkee R, Gavidia T. Factors associated with early initiation of breastfeeding among Nepalese mothers: further analysis of Nepal Demographic and Health Survey, 2011. International Breastfeeding Journal. 2014;9:1–9.
  125. 125. Prior E, Santhakumaran S, Gale C, Philipps LH, Modi N, Hyde MJ. Breastfeeding after cesarean delivery: a systematic review and meta-analysis of world literature. Am J Clin Nutr. 2012;95(5):1113–35. pmid:22456657
  126. 126. Quigley C, Taut C, Zigman T, Gallagher L, Campbell H, Zgaga L. Association between home birth and breast feeding outcomes: a cross-sectional study in 28 125 mother-infant pairs from Ireland and the UK. BMJ Open. 2016;6(8):e010551. pmid:27503858
  127. 127. Norris S, Collin SM, Ingram J. Breastfeeding practices among the Old Order Mennonites in Ontario, Canada: a multiple methods study. J Hum Lact. 2013;29(4):605–10. pmid:23942391
  128. 128. Duodu PA, Duah HO, Dzomeku VM, Boamah Mensah AB, Aboagye Mensah J, Darkwah E, et al. Consistency of the determinants of early initiation of breastfeeding in Ghana: insights from four Demographic and Health Survey datasets. Int Health. 2021;13(1):39–48. pmid:32300776
  129. 129. Matanda DJ, Mittelmark MB, Urke HB, Amugsi DA. Reliability of demographic and socioeconomic variables in predicting early initiation of breastfeeding: a replication analysis using the Kenya Demographic and Health Survey data. BMJ Open. 2014;4(6):e005194. pmid:24939811
  130. 130. Kiani SN, Rich KM, Herkert D, Safon C, Pérez-Escamilla R. Delivery mode and breastfeeding outcomes among new mothers in Nicaragua. Matern Child Nutr. 2018;14(1):e12474. pmid:28621054
  131. 131. Onah S, Osuorah DIC, Ebenebe J, Ezechukwu C, Ekwochi U, Ndukwu I. Infant feeding practices and maternal socio-demographic factors that influence practice of exclusive breastfeeding among mothers in Nnewi South-East Nigeria: a cross-sectional and analytical study. Int Breastfeed J. 2014;9:6. pmid:24860612
  132. 132. Mogre V, Dery M, Gaa PK. Knowledge, attitudes and determinants of exclusive breastfeeding practice among Ghanaian rural lactating mothers. Int Breastfeed J. 2016;11:12. pmid:27190546
  133. 133. de Gusmão AM, Béria JU, Gigante LP, Leal AF, Schermann LB. The prevalence of exclusive breastfeeding and associated factors: a cross-sectional study of teenage mothers between 14 and 16 years of age in the city of Porto Alegre in the State of Rio Grande do Sul, Brazil. Cien Saude Colet. 2013;18(11):3357–68. pmid:24196900
  134. 134. Pereira-Santos M, Santana M de S, Oliveira DS, Nepomuceno Filho RA, Lisboa CS, Almeida LMR, et al. Prevalence and associated factors for early interruption of exclusive breastfeeding: meta-analysis on Brazilian epidemiological studies. Rev Bras Saude Mater Infant. 2017;17(1):59–67.
  135. 135. Otoo GE, Lartey AA, Pérez-Escamilla R. Perceived incentives and barriers to exclusive breastfeeding among periurban Ghanaian women. J Hum Lact. 2009;25(1):34–41. pmid:18971507
  136. 136. Acheampong AK. Promoting exclusive breastfeeding among teenage-mothers in Ghana: towards a behavioural conceptual model. SIGNATURE. 2018. https://ir.unisa.ac.za/handle/10500/25293
  137. 137. Nuampa S, Chanprapaph P, Tilokskulchai F, Sudphet M. Breastfeeding challenges among Thai adolescent mothers: hidden breastfeeding discontinuation experiences. JHR. 2020;36(1):12–22.
  138. 138. Patil DS, Pundir P, Dhyani VS, Krishnan JB, Parsekar SS, D’Souza SM, et al. A mixed-methods systematic review on barriers to exclusive breastfeeding. Nutr Health. 2020;26(4):323–46. pmid:33000699
  139. 139. Mundagowa PT, Chadambuka EM, Chimberengwa PT, Mukora-Mutseyekwa F. Determinants of exclusive breastfeeding among mothers of infants aged 6 to 12 months in Gwanda District, Zimbabwe. Int Breastfeed J. 2019;14:30. pmid:31333755
  140. 140. Balogun OO, Dagvadorj A, Anigo KM, Ota E, Sasaki S. Factors influencing breastfeeding exclusivity during the first 6 months of life in developing countries: a quantitative and qualitative systematic review. Matern Child Nutr. 2015;11(4):433–51. pmid:25857205
  141. 141. Oddo VM, Ickes SB. Maternal employment in low- and middle-income countries is associated with improved infant and young child feeding. Am J Clin Nutr. 2018;107(3):335–44. pmid:29566201
  142. 142. Amallia A, Pamungkasari EP, Adriani RB. Meta Analysis the Effects of Maternal Education, Residence, and Birth Delivery Place, on Exclusive Breastfeeding. J Matern Child Health. 2023;8(2):154–68.
  143. 143. Pries AM, Huffman SL, Mengkheang K, Kroeun H, Champeny M, Roberts M, et al. Pervasive promotion of breastmilk substitutes in Phnom Penh, Cambodia, and high usage by mothers for infant and young child feeding. Matern Child Nutr. 2016;12 Suppl 2(Suppl 2):38–51. pmid:27061955
  144. 144. Nkala TE, Msuya SE. Prevalence and predictors of exclusive breastfeeding among women in Kigoma region, Western Tanzania: a community based cross-sectional study. Int Breastfeed J. 2011;6(1):17. pmid:22070861
  145. 145. Chudasama RK, Amin CD, Parikh YN. Prevalence of exclusive breastfeeding and its determinants in first 6 months of life: A prospective study. Online J Health Allied Scs. 2009;8(1):3.
  146. 146. McFadden A, Siebelt L, Marshall JL, Gavine A, Girard L-C, Symon A, et al. Counselling interventions to enable women to initiate and continue breastfeeding: a systematic review and meta-analysis. Int Breastfeed J. 2019;14:42. pmid:31649743
  147. 147. Habtewold TD, Mohammed SH, Endalamaw A, Akibu M, Sharew NT, Alemu YM, et al. Breast and complementary feeding in Ethiopia: new national evidence from systematic review and meta-analyses of studies in the past 10 years. European journal of nutrition. 2019; 58:2565–95.
  148. 148. Normann AK, Bakiewicz A, Kjerulff Madsen F, Khan KS, Rasch V, Linde DS. Intimate partner violence and breastfeeding: a systematic review. BMJ Open. 2020;10(10):e034153. pmid:33130559
  149. 149. Su M, Ouyang Y-Q. Father’s Role in Breastfeeding Promotion: Lessons from a Quasi-Experimental Trial in China. Breastfeed Med. 2016;11:144–9. pmid:26836960
  150. 150. Sinha B, Chowdhury R, Sankar MJ, Martines J, Taneja S, Mazumder S, et al. Interventions to improve breastfeeding outcomes: a systematic review and meta-analysis. Acta Paediatr. 2015;104(467):114–34. pmid:26183031
  151. 151. Habte MH, Seid SJ, Alemu A, Hailemariam HA, Wudneh BA, Kasa RN, et al. The effect of unemployment and post-natal care on the exclusive breast-feeding practice of women in Ethiopia: a systematic review and meta-analysis. Reprod Health. 2022;19(1):94. pmid:35428313
  152. 152. Habtewold TD, Sharew NT, Alemu SM. Effect of gender of new-born, antenatal care and postnatal care on breastfeeding practices in Ethiopia: evidence from systematic review and meta-analysis of national studies. bioRxiv. 2018.
  153. 153. Muche A, Fentaw Z, Dewau R, Chanie MG, Melaku MS, Tsega Y. Timely initiation of complementary feeding and its associated factors among children 6-23 months in Ethiopia: A systematic review and meta-analysis. Abyssinia Journal of Science and Technology. 2021;6(2):1–14.
  154. 154. Tassew AA, Tekle DY, Belachew AB, Adhena BM. 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. 2019;14(2):e0203098. pmid:30789922
  155. 155. Worku MG, Alamneh TS, Tesema GA, Alem AZ, Tessema ZT, Liyew AM, et al. Minimum acceptable diet feeding practice and associated factors among children aged 6-23 months in east Africa: a multilevel binary logistic regression analysis of 2008-2018 demographic health survey data. Archives of public health = Archives belges de sante publique. 2022;80(1):127.
  156. 156. Issaka AI, Agho KE, Burns P, Page A, Dibley MJ. Determinants of inadequate complementary feeding practices among children aged 6-23 months in Ghana. Public Health Nutr. 2015;18(4):669–78. pmid:24844532
  157. 157. Mokori A, Schonfeldt H, Hendriks SL. Child factors associated with complementary feeding practices in Uganda. South African Journal of Clinical Nutrition. 2016;30(1):7–14.