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Trends of risk factors associated with childhood stunting and anaemia in Ghana: evidence from the Demographic Health Survey and Multiple Indicator Cluster Survey (2003–2017)

Published online by Cambridge University Press:  23 January 2024

Christian Sewor
Affiliation:
Department of Public Health and Community Medicine, Central University of Kerala, Kasaragod, KL 671316, India Public Health Research Group, Department of Biomedical Sciences, University of Cape Coast, Cape Coast, Ghana
Rajeev Jayalakshmi*
Affiliation:
Department of Public Health and Community Medicine, Central University of Kerala, Kasaragod, KL 671316, India
*
*Corresponding author: Email jayalakshmirajeev@cukerala.ac.in
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Abstract

Objective:

This study investigated the trend of effect estimates of the key risk factors of childhood stunting and anaemia between 2003 and 2017.

Design:

A secondary analysis of the Demographic Health Survey (DHS) and Multiple Indicator Cluster Survey (MICS) data for the Ghanaian population between 2003 and 2017. Associations of selected socio-demographic (child age and gender; maternal age and education), economic (household wealth), environmental, dietary (minimum dietary diversity and iodine use) and health system (place of delivery and vaccination) factors were explored using the Poisson regression model. Trend analysis was explored using a fitted linear regression line on a time series plot.

Setting:

Ghana

Participants:

Children under 5 years

Results:

The results showed a reduction in the prevalence of stunting and anaemia over the 15-year duration. These health outcomes were found to be negatively associated with a wide array of socio-demographic (child age and gender, maternal age and education, residency), economic (household wealth), dietary (iodised salt use) and health service (place of delivery and vaccination) factors; however, the most consistent statistically significant association was observed between child’s age and belonging to the poor wealth quintile.

Conclusion:

In order to prevent these indicators of child malnutrition, key consideration must be given to the early developmental stages of life. Child health policies must focus on addressing the key contextual factors of child malnutrition.

Type
Research Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of The Nutrition Society

Globally, child malnutrition resulting from macro and micronutrient deficiencies is a persisting public health challenge in many low- and middle-income countries. Recent evidence on adverse child health indicators such as stunting and anaemia demonstrates that these conditions remain endemic in many low- and middle-income countries. Childhood stunting as defined by the WHO is having a height-for-age z-score (HAZ) below −2 sd from the median HAZ of the reference population(1). Childhood anaemia amongst children under 5 years of age is given as a Hb concentration less than 110 g/l at sea level(1).

As of 2020, 22·0 % of under 5 years children which translates to about 149·2 million were reported to be stunted globally(2). The WHO report highlighted that although the proportion of stunted children in Africa has decreased over the years, it remains the only region where the absolute number of stunted children is increasing with about 61·4 million children being found stunted(2). Within the West African region, childhood stunting prevalence has been reported to be decreasing. Notwithstanding, the prevalence of stunting which stands at 30·9 % is higher than both Africa’s regional (30·7 %) and global estimates (22·0 %)(2,Reference Dwomoh, Sewor and Mohammed3) .

Similarly, the regional prevalence of anaemia which is 60·2 % is about one and a half times more than the global prevalence (39·8 %)(4). The prevalence estimate for West Africa which is 69·9 % is also higher than both global and regional estimates.

Recent estimates for Ghana, a West African country, indicate that the prevalence of stunting stood at 14·2 % in 2020(2), whereas that of anaemia was 59·5 %(4) making them the child malnutrition indicators, with the largest burden in the country. While both estimates are lower than the respective regional estimates in Africa, the prevalence of anaemia is higher than the global estimate. Over the years, there have been reductions in the prevalence of stunting and anaemia; however, this has occurred at fairly low and inconsistent rates(Reference Dwomoh, Sewor and Mohammed3,5,6) .

These adverse child health outcomes have been found to impair the developmental potential of children and contribute to long-term impairment in cognitive function and adult economic productivity(Reference de Onis and Branca7,Reference Ocansey, Adu-Afarwuah and Kumordzie8) . Findings from a meta-analysis of data from six African countries highlighted that the risk of death falls by 24 % for a 1 g/dl increase in Hb level(Reference Scott, Chen-Edinboro and Caulfield9).

The key reason underlying the continual existence of these adverse child health outcomes in Ghana and other African countries is the prevailing risk factors and the widening gap of the inequalities within the region. Various epidemiological studies reported that childhood stunting and anaemia are significantly associated with socio-economic (household wealth, dietary diversity and minimum acceptable diet), demographic (child age, gender and maternal education), environmental (type of cooking fuel use, sanitation and water source) and health system factors (place of delivery, micronutrient supplementation and child vaccination)(Reference Larsen, Grisham and Slawsky10,Reference Katoch11) . It is important to note that these factors often exert varying direct and indirect effects on child health outcomes as noted in the UNICEF framework for child undernutrition(12).

While recent child nutrition policies in Ghana have been reported to focus on improving nutrition, water and sanitation practices, social protection, and healthcare access(Reference Aryeetey, Atuobi-Yeboah and Billings13,Reference Yawson, Amoaful and Senaya14) , these policies are often hampered by endemic inequities, lack of multisectoral coordination, unavailability of funds and in some case a lack policy attention to health indicators(Reference Aryeetey, Atuobi-Yeboah and Billings13). This has in turn resulted in an uneven decline in the levels of child malnutrition indicators and the continual proliferation of some of these risk factors. In this regard, there is a need for a comprehensive, integrated, cost-effective and most importantly flexible health policy action to address the health challenges of children. In order to do this, it is crucial to understand the change in the effect estimates of the risk factors of child health outcomes over the years as it enables timely review of policy actions and subsequent modifications focusing on factors that will produce the greatest benefit.

It is thus against this background, that this study sought to identify the key risk factors of childhood stunting and anaemia in Ghana between 2003 and 2017 and the trend of effect estimates associated with these risk factors over the years. By relying on two nationally representative surveys, the Demographic Health Survey (DHS) and the Multiple Indicator Cluster Survey (MICS), this study provides comprehensive evidence on the trend of the effect estimates of each risk factor.

Methods

Data source

The study was a quantitative study that involved the secondary analysis of two nationally representative surveys, namely DHS and the MICS conducted in Ghana between 2003 and 2017. For the DHS, datasets of 2003, 2008 and 2014 were analysed, whereas, for MICS, 2006, 2011 and 2017 datasets were used. Cross-sectional study designs which employ nationally representative sample sizes are adopted in both the DHS and MICS.

Study population and sampling size

The sample units for analysis were children. The analysis was restricted to children under 5 years (0–59 months) for stunting (data were available in DHS and MICS) and children between 6 and 59 months for anaemia (available in only DHS). The DHS programme employs a two-stage stratified sampling, whereas the MICS employs a two-stage cluster sampling design to sample the households before collecting information on women and men (aged 15–49 years) and their children (0–5 years).

Datasets

For the DHS datasets, the respective Children’s Recode file (KR) which provides information for every child of interviewed women born in the 5 years preceding the survey was used. These datasets contain information related to antenatal care, postnatal care, immunisation and the health of the selected children. The data for the mother of each of these children are included. For MICS datasets, the children’s under 5 years (ch) dataset was merged with the women (wm) and household (hh) datasets using the common identifiers (household line, cluster line and the women’s) in order to include other relevant household and maternal risk factors needed for the analysis as seen in the DHS datasets.

Research variables

The exposures of interests were socio-demographic (gender and age of the child, maternal age and education, history of illness, low birth weight), dietary (minimum dietary diversity (MDD) and iodised salt in the household), economic (household wealth status), environmental (sanitation, water source and household cooking fuel source) and health service factors (child vaccination, place of delivery and vitamin A supplementation). The outcomes of interest were child anaemia and stunting.

Data preparation

Since the MICS datasets were in spss format, they were converted into their respective Stata files in IBM SPSS version 26. The required sample weights as per the DHS and MICS guidelines were applied before undertaking the analysis. All missing values and flagged cases were removed before the analysis. Cases that gave unclear responses, such as ‘I don’t know’ and ‘other’ categories, were also dropped wherever applicable. Data available for children who were alive at the time of the survey only were used. The following variables were categorised as follows.

Water sources and sanitation in both the DHS and MICS datasets were classified into improved and unimproved sources based on the WHO/UNICEF criteria(15). Improved sanitation was defined as shared or non-shared facilities that flush/pour-flush to a piped sewer system, septic tank, or pit latrine; ventilated improved pit latrine, pit latrine with a slab, and composting toilet or flush elsewhere. Unimproved sanitation included pit latrines without slab/open pits, bucket toilets, hanging toilets/latrines and others. Improved water sources were the following: piped into dwelling, piped to yard/plot, public tap/standpipe, piped to a neighbour, tube well or borehole, protected well, protected spring, rainwater, tanker truck, cart with a small tank, bottled water, packaged or delivered water. Unimproved water sources were unprotected well, unprotected springs and surface water (river, dam, lake, pond, stream and canal/irrigation channel(15). Household cooking fuel type was categorised as being either clean or polluting. Clean fuels included electricity, liquid petroleum gas, natural gas, biogas and kerosene, whilst polluting fuels included coal/lignite, charcoal, wood, straw/shrubs/grass and animal dung.

MDD was defined by the proportion of children aged 6–23 months who consumed foods from at least four food groups out of the eight referenced food groups within 24 h (four out of eight food groups fed during the day or night preceding the survey). The eight food groups were the following: (1) breastmilk, (2) grains, roots, and tubers, (3) legumes and nuts, (4) dairy products, (5) flesh foods (meat, fish, poultry and liver/organ meats), (6) eggs, (7) vitamin A-rich fruits and vegetables, and (8) other fruits and vegetables(16).

The household wealth index which was initially in quintiles was recategorised into three categories, poor (poorest+poor), middle and rich (rich+richest).

Childhood stunting was defined as having a HAZ below −2 sd below the average on the WHO Child Growth Standards. Childhood anaemia amongst children 6–59 months is given as a Hb concentration less than 110 g/dl.

Statistical analysis

All statistical analyses were run on Stata version 16 (MP – Parallel Edition). The svy command was used in running all the analyses, controlling for both clustering and stratification. Univariate analysis was used to explore the report of the weighted proportions of the health outcomes and the risk factors within each survey year. Simple and multiple Poisson regression models were used to assess the association between the socio-demographic, economic, environmental, and health service factors and maternal and child health indicators across specific survey periods, with the respective prevalence ratios (PR) and 95 % CI generated. A Poisson regression model was used instead of a logistic model because of the high prevalence of both outcomes (stunting and anaemia) within the population. A fitted linear regression line was used to explore the trends of the effect estimates of the significant risk factors.

The risk factors included in the year-wise multiple Poisson regression (adjusted analysis) were selected based on the following criteria:

  • Only risk factors which were statistically significant in at least three time points for stunting and two time points for anaemia were included in the multivariate analysis.

  • Correlating independent variables were removed. For instance, all household environmental risk factors (sanitation, water source and cooking fuel) were excluded because these were incorporated in the composition of the household wealth(Reference Rutstein and Johnson17,Reference Martel18) .

In order to further strengthen the robustness of our findings, sensitivity analysis was carried out by pooling all the datasets after which a mixed effect Poisson regression with survey year as a random term was conducted to provide a composite estimate across all survey periods. For the adjusted analysis in the mixed effect Poisson regression, multiple nested models were run in order to ascertain whether the covariates removed in the year-wise adjusted analysis significantly impacted observed relationships. Seeing that the pseudo-R2 and likelihood ratio tests were inappropriate with the svy command(Reference Williams19), adjusted Wald test was used to explore the explanatory potential of variables in the regression model. Model fitness in the simple and multiple Poisson regression was explored using the Pearson goodness-of-fit, whereas for the mixed effect models the Akaike and Bayesian information criteria were used (AIC and BIC) to compare model. A P-value less than 0·05 was regarded as statistically significant. Percentages were rounded up to one decimal place, whilst PR and CI were reported in two decimal places.

Results

Descriptive Pattern of Selected Risk Factors and Child Health Outcomes

Table 1 provides descriptive information on the child outcomes under study and the selected risk factors. About 43–44 % of children interviewed in DHS were aged under 2 years, whereas 24–26 % of them were interviewed in the MICS. The majority of mothers recruited were within the age range of 25–34 years and had completed secondary education or higher.

Table 1 Descriptive pattern of selected risk factors and child health outcomes

Data for minimum dietary diversity and household iodised salt usage were unavailable in 2006 and 2008, respectively.

Most of the mothers and their children interviewed resided in poor households and rural areas. Concerning household environmental conditions, a majority of households across all the survey periods had improved water and sanitation sources and used polluting fuel.

The prevalence of low birth weight and history of illness amongst the children was observed to have shown an increasing trend. The proportion of children who were found to have met the MDD (6 and 23 months) was highest in 2008. An increasing number of households were observed to have been consuming iodised salt across the survey periods.

There was an increase in the proportion of hospital delivery across survey periods, and the highest prevalence of vitamin A supplementation was reported in 2006. Also, the highest proportion of children who reported to have received any vaccination was 93 % (in 2008)

The prevalence of stunting was observed to have decreased across the survey period with the highest estimate of 29·4 % recorded in 2003 and the lowest estimate of 17·5 % recorded in 2017. The prevalence of anaemia amongst children aged 6–59 months, on the other hand, was the highest at 78·4 % in 2008 and the lowest at 66·8 % recorded in 2014.

Association and trends of risk factors associated with child health outcomes

From the results, the key risk factors associated with stunting (Tables 2 and 4 ) were child age (above two years) and gender (male), maternal education (no education), household wealth (poor), low birth weight, and place of delivery (delivering at home or other places besides the hospital). Consistently, across the majority of the survey years, stunting was more likely amongst children above 2 years, low birth weight children, and children residing in poor households. On the contrary in 2017, we observed that children born to teenage mothers (15–19 years) were less likely to be stunted children than early adult mothers (20–34 years) (PR = 0·51, 95 % CI 0·28, 0·94). The PR of child age and gender, mothers with primary education, middle-income households, low birth weight, place of delivery (home) and use of iodised salt in homes showed an increasing trend, whereas the remaining showed a decreasing trend (Fig. 1).

Table 2 Crude prevalence ratios of risk factors associated with stunting

PR, prevalence ratio.

* P-value < 0·05.

** P-value < 0·01.

*** P-value < 0·001.

Model for 2003 failed to converge.

Table 3 Crude prevalence ratios of risk factors associated with anaemia

PR, prevalence ratio.

* P-value < 0·05.

** P-value < 0·01.

*** P-value < 0·001.

Fig. 1 Trend of prevalence ratio of the risk factors associated with childhood stunting

The key risk factors associated with anaemia (Tables 3 and 5) were child age (under 2 years), maternal education (no education), household wealth and place of delivery, history of illness, place of residence, and household iodised salt use. Consistently, across the majority of the survey years, childhood anaemia was more likely amongst children under 2 years, those born to mothers with no education, children residing in poor households and children with prior history of illness. The PR of all risk factors associated with anaemia showed an increasing trend in all risk factors except middle-income households and rural households (Fig. 2).

Table 4 Adjusted prevalence ratios of risk factors associated with stunting

PR, prevalence ratio.

* P-value < 0·05.

** P-value < 0·01.

*** P-value < 0·001.

Table 5 Adjusted prevalence ratios of risk factors associated with anaemia

PR, prevalence ratio.

* P-value < 0·05.

** P-value < 0·01.

*** P-value < 0·001.

Fig. 2 Trend of prevalence ratio of the risk factors associated with childhood anaemia

Sensitivity analysis

The results for the mixed model (Tables 6 and 7) that contained all the risk factors were found to have the smallest AIC. These results did not significantly differ from the main analysis, with the exception of MDD and childhood vaccination which were found as potential additional risk factors for stunting (Table 6) and anaemia (Table 7), respectively.

Table 6 Prevalence ratios of risk factors associated with stunting (mixed effect Poisson regression)

cPR, crude prevalence ratio; aPR, adjusted prevalence ratio; AIC, Akaike information criterion, BIC; Bayesian information criterion.

Model 1: Multiple regression model which included all risk factors.

Model 2: Multiple regression model which included all risk factors except household environmental conditions (cooking fuel, sanitation and water source).

Model 3: Multiple regression model which includes all risk factors except household wealth.

Model 4: Multiple regression model which includes only significant risk factors.

Model 5: Multiple regression model which includes only significant risk factors in unadjusted analysis and household environmental conditions.

Model 6: Multiple regression model which includes only significant risk factors in unadjusted analysis and household wealth.

* P-value < 0·05.

** P-value < 0·01.

*** P-value < 0·001.

Table 7 Prevalence ratios of risk factors associated with anaemia (mixed effect Poisson regression)

cPR, crude prevalence ratio; aPR, adjusted prevalence ratio; AIC, Akaike information criterion; BIC, Bayesian information criterion.

1 Model 1: Multiple regression model which includes all risk factors.

2 Model 2: Multiple regression model which includes all risk factors except household environmental conditions (cooking fuel, sanitation and water source).

3 Model 3: Multiple regression model which includes all risk factors except household wealth.

4 Model 4: Multiple regression model which includes only significant risk factors.

5 Model 5: Multiple regression model which includes only significant risk factors in unadjusted analysis and household environmental conditions.

6 Model 6: Multiple regression model which includes only significant risk factors in unadjusted analysis and household wealth.

* P-value < 0·05.

** P-value < 0·01.

*** P-value < 0·001.

Discussion

We observed that childhood stunting and anaemia were significantly negatively associated with various socio-demographic (child-level age and gender, maternal age and education, residence), economic (household wealth), nutrition (iodised salt use) and health service (place of delivery and vaccination) factors. The most consistent among these across all survey periods were the child’s age and living in a poor household.

Risk factors of stunting

Epidemiological studies conducted have provided indicative evidence that corroborates the risk factors of stunting noted in this study. For instance, concerning child-level factors such as age and gender, other epidemiological studies have reported similar findings. Jonah et al. (Reference Jonah, Sambu and May20) and Keino et al. (Reference Keino, Plasqui and Ettyang21) reported that childhood stunting in Africa seems to be higher amongst male children as was observed in this present study. A possible reason was highlighted by Thompson(Reference Thompson22), who noted that gender differences in growth trajectories which start during the early developmental stages of life predispose boys to a greater risk of infection and undernutrition.

Maternal risk factors such as maternal age and education were identified as key risk factors. Generally, educated women are more likely to have a direct influence on the dietary choices of their children, thereby reducing the risk of undernutrition. Concerning maternal age, younger mothers are more likely to give birth to children with low birth weight who are likely to grow to be undernourished(Reference Yu, Mason and Crum23). Reviews by Akombi et al. (Reference Akombi, Agho and Hall24) and Obasohan et al. (Reference Obasohan, Walters and Jacques25) on SSA have all reported that maternal age is associated with childhood stunting status.

Furthermore, adverse birth outcomes such as low birth weight have been identified to be associated with child stunting status. As was reported in a review by Quamme and Iversen(Reference Quamme and Iversen26), childhood stunting in SSA is common amongst children born with low birth weight.

Seeing that household wealth has been reported to be a significant predictor of health status, with poor households being reported to have poor nutritional, economic, environmental and health status(Reference Siddiqui, Salam and Lassi27). It thus comes as no surprise that it was a significant risk factor for stunting as has been reported(Reference Obasohan, Walters and Jacques25,Reference Christian and Dake28) .

Risk factors associated with anaemia

In a study by Shenton et al. (Reference Shenton, Jones and Wilson29), various child factors (age and fever) household level (water source, toilet and wealth) maternal factors (age, education and anaemia status), family-related factors (number of wives and children) religion and ethnicity were noted to be significantly associated with anaemia between 2003 and 2014 in Ghana. The study found child age, history of illness (fever) and maternal anaemia status to be the most consistent risk factors for childhood anaemia in Ghana. Also, a review by Obasohan et al. (Reference Obasohan, Walters and Jacques30) reported anaemia in SSA to be significantly associated with child age and gender, birth order, maternal education, age, and anaemia, the occurrence of co-morbidities (such as fever, diarrhoea and acute respiratory infection), malnutrition, household wealth and place of residence. From these sets identified, five of the risk factors were identified in this study.

Childhood anaemia seems to disproportionately affect younger children with a relatively high prevalence reported amongst children below 2 years(Reference Silveira, Carvalho and Viola31). A plausible reason underlying this observation could be the fact that the period from prenatal life to the first 24 months after birth is a critical susceptibility window of the development(Reference Black, Walker and Fernald32). Aside from this, children under 2 years have been reported to be at a high risk of Fe deficiency, which is a key risk factor for anaemia(Reference Silveira, Carvalho and Viola31). Additionally, most mothers, particularly the poor, may regard children under 2 years as being too young, thereby failing to initiate complementary feeding early enough in order to ensure that children receive the necessary micronutrients and reduce the risk of anaemia(Reference Shenton, Jones and Wilson29).

In relation to micronutrient supplement consumption, iodised salt use was found to be associated with anaemia status. This iodine supplementation has been reported to improve Hb levels amongst children(Reference Ramirez-Luzuriaga, Larson and Mannar33). Just as was observed in stunting, children born to young mothers and non-educated mothers were found to be more probable of being anaemic(Reference Moschovis, Wiens and Arlington34).

Place of residence and household wealth were found to be key risk factors for anaemia. Studies have confirmed that childhood anaemia is disproportionately concentrated in low socio-economic groups and rural areas(Reference Silveira, Carvalho and Viola31,Reference Tezera, Sahile and Yilma35) . Poor and rural households often have poor nutritional status and as were reported by Wegmuller et al. (Reference Wegmuller, Bentil and Wirth36), anaemia and various micronutrient deficiencies (vitamin A, folate and Fe) seem to be more endemic in rural areas and poor households in Ghana.

Women who deliver at home are likely to have little access to pregnancy-related health services which include receiving essential services such as nutrition education and micronutrient supplementation which are crucial in improving the health status of their children(Reference Crawley37).

Exploring the trend of risk factors of childhood stunting and anaemia

The overarching reason underlying the continual existence of childhood stunting and anaemia, in Ghana can be attributed to the pervading presence of the risk factors associated with these health outcomes.

For instance, the consistent association noted with respect to child’s age and gender in stunting and anaemia may be attributed to the fact that most nutritional policies implemented amongst children pay little attention and gender and age distributions of child malnutrition indicators. For instance, concerning age disparities, it has been reported that routine childhood growth monitoring, which is instrumental in the early identification of childhood malnutrition and provides the opportunity for the administration of micronutrient supplements such as vitamin A, has been reported to be significantly low amongst children between 2 and 5 years in Ghana(Reference Ghartey38). Ghartey(Reference Ghartey38) reported that most caregivers often consider the 0–2 years age interval as the critical period to attend growth monitoring sessions and immunisation. Sadly after this age interval, caregivers begin to pay little attention to these sessions, as they would rather prefer to engage in income generation ventures to help support their family(Reference Ghartey38).

In Ghana, over the years, public health policies, strategies, and programmes have been initiated and implemented to address childhood stunting and anaemia; however, the majority of these initiatives focus on improving access to maternal and child health services such as hospital-based delivery, antenatal and postnatal visit, immunisation, vaccination, micronutrient supplementation (Fe and vitamin A supplementation), and diet fortification (iodised salt)(Reference Aryeetey, Atuobi-Yeboah and Billings13,39,40) . Although these policies provide an excellent framework for improving access and utilisation of health services as well as addressing dietary-related factors, endemic challenges owing to socio-demographic inequalities often derail their impact. For instance, policies such as micronutrient supplementation (vitamin A, Fe and Iodine fortification) which were implemented within the later end of the 20th century are in urgent need of review and improved government funding(Reference Ghartey38). These pitfalls have led to a widening of inequalities in the implementation of the policies, thereby resulting in the weakening of the desired effect expected by some of these policies. The resultant effect has been the increased risk observed amongst the risk groups as noted in the case of the effect of iodine status on anaemia.

Furthermore, to reduce the risk and occurrence of adverse birth outcomes such as low birth weight and childhood illnesses amongst children, policies such as the National Health Insurance Scheme (NHIS) have been rolled out to improve maternal healthcare services(Reference Anarwat, Salifu and Akuriba41). However, whilst this scheme was mandated to also help decrease socio-economic inequalities in healthcare utilisation within the country, studies have highlighted the existence of inequalities(Reference Fenny, Asuman and Crentsil42,Reference Asamoah and Agardh43) . Fenny et al. (Reference Fenny, Asuman and Crentsil42) and Asamoah and Agardh(Reference Asamoah and Agardh43) have reported that these inequalities in maternal health services occur along the lines of the urban and rural divide and wealth and education statuses. These endemic inequalities might be a key factor in the continual occurrence of home deliveries in Ghana, which was observed to be significantly associated with either increased risk in both outcomes (stunting and anaemi) albeit with somewhat inconsistent trends.

In the case of low birth weight and childhood history of illness which were observed to be showing an increasing trend in relation to stunting and anaemia, respectively, improving maternal and child healthcare services may not be enough to address them properly. For instance, policies such as sleeping insecticide and vaccination which are crucial in preventing childhood infections seem to experience some setbacks in implementation. Aryeetey et al. (Reference Aryeetey, Atuobi-Yeboah and Billings13) observed that although there was an increase in the ownership of insecticide-treated bed nets, between 2008 (42 %) and 2014 (68 %), only about a third of young children slept under these treated nets in 2014. Similarly, only about a third of young children received deworming medication in the past 6 months in 2014(Reference Aryeetey, Atuobi-Yeboah and Billings13). This situation could be a probable reason why effect estimates of child illness showed an increasing trend.

Child feeding indicators in Ghana have remained largely inconsistent, thus explaining the inconsistency in the effect estimates observed in this present study. According to Aryeetey et al. (Reference Aryeetey, Atuobi-Yeboah and Billings13), there was no clear improvement in exclusive breast-feeding practice which is a key part of MDD between 2009 and 2018. While improvements were reported in 2008 (63 % 2008), there was however a drastic decline to about 43 % in 2017. Aryeetey et al. (Reference Aryeetey, Atuobi-Yeboah and Billings13) again noted there has been a consistent decline in complementary feeding performance amongst children between 2009 and 2017 with the decline observed in both MDD and minimum acceptable diet rates in the last decade.

Maternal factors such as age and education are critical factors affecting both maternal and child health outcomes. As was observed in the study, younger mothers are more likely to have children who are malnourished. In Ghana, adolescent pregnancy has remained rife with very few changes observed in its prevalence(Reference Ahinkorah, Hagan and Seidu44). Concerning maternal education, as highlighted in a multi-country study by Smith et al. (Reference Smith, Ramakrishnan and Ndiaye45), women of higher education status are more likely to have children with better nutritional status seeing that they have better nutritional status themselves and provide higher quality care to their children. In recent years, there has been progressive improvement in women’s education in Ghana(46). Despite this progress, it must be highlighted there are still some key disparities based on various intersecting axes. Whilst at early-life and youthful ages, both males and females are almost parred in relation to educational attainment, the gap widens as one progresses into the adult and elderly populations(47). As observed in this study, whilst stunting and anaemia were probable to occur amongst children of mothers with no education, the trends of the effect estimate differed for conditions. Although it is unclear why this differing trend was observed, it can be suggested that the inherent disparities in maternal education distribution across regions and wealth status could be a contributing factor(47). Also, a large majority of the policies seem to focus on improving only basic education, which although helpful may not fully equip mothers with the requisite knowledge needed to strongly impact the nutritional status of their children.

In relation to household economic status, as per the Ghana Living Standards Report, poverty trends in Ghana between 1992 and 2013 reduced by more than half (from 56·5 % to 24·2 %), thus explaining the increase in the rich category as observed in the present study(Reference Cooke, Hague and McKay48). Cooke et al. (Reference Cooke, Hague and McKay48) also noted that child poverty, which could be a key indicator of child health status, has also reduced significantly across the years. Afful et al. (Reference Afful, Nunoo and Arthur-Biney49) noted that despite improvements in the economic growth rate between 1992 and 2013, this has not been complemented by a decline in inequality. This inequality has been reported to occur across various social stratification(Reference Afful, Nunoo and Arthur-Biney49), consequently leading to an increasing number of people living in extreme poverty. For instance, Cooke et al. (Reference Cooke, Hague and McKay48) noted that the inequity in the ratio of children to adults living in poverty had risen substantially from the 1990s with about 15 % more children being likely to live in extreme poverty than adults(Reference Cooke, Hague and McKay48). This could explain the consistency in the effect estimates associated with poor households for both anaemia and stunting.

Strengths and limitations

The present study provides evidence on the trend of the effect estimates of the risk factors associated with childhood stunting and anaemia. To the best of the authors’ knowledge, only one similar study has been conducted(Reference Shenton, Jones and Wilson29). The aforementioned study only explored the risk factors of stunting and used only DHS datasets (2003, 2008 and 2014). This study, however, examined both stunting and anaemia and used secondary data from both the DHS and MICS which helps bridge the missing year gaps. Both surveys use nationally representative sample sizes and have high response rates, thus making the present study findings generalisable. Also as relates to regression model choice, the use of Poisson regression to generate PR offers some key advantages. As noted by Barros and Hirakata(Reference Barros and Hirakata50), Poisson regression in cross-sectional studies provides more correct and consistent estimates than logistic regression, which is traditionally used in case–control studies. Besides this, it has been reported that when the outcome is interest is rare (less than 10 %) OR are similar to PR; however, when the outcome prevalence is not rare (greater than 10 %) as can be observed in this study, the OR often overestimates the PR(Reference Thompson, Myers and Kriebel51).

Despite these strengths, it must be noted that because the study relies on cross-sectional data, temporarity cannot be established. Aside from this whilst many risk factors could have been explored, however, to prevent overburdening of the regression model, such risk factors were logically dropped. To prevent multicollinearity between household environmental conditions (sanitation, water source and cooking fuel type) and household wealth, the former was dropped for the multivariate model. We, however, tried to address this by undertaking a mixed effect Poisson regression with the multiple adjusted models being considered to account for the dropped covariates.

Conclusion

From this study, childhood stunting and anaemia were found to be significantly negatively associated with a wide array of socio-demographic (child age and gender, maternal age and education, place of residence, and household use of iodised salt) economic (household wealth) and health service (place of delivery and vaccination) factors. The trend of PR of the risk factors of the health outcomes reported was generally inconsistent. However, the most consistent risk factors associated with stunting and anaemia were child age and household wealth. To address these child malnutrition indicators, key consideration must be given to the early developmental stages of life. Also, child health policies must focus on addressing the key contextual factors of child malnutrition.

Acknowledgement

The authors are grateful to the operators of MICS and DHS who have made the data readily available.

Financial support

The authors received no financial support for this research.

Conflict of interest

The authors declare no conflicts of interest.

Authorship

C.S. and J.R. conceptualised the study and applied for the dataset; C.S. conducted the data analysis and wrote the draft of the manuscript. J.R. critically revised the manuscript.

Ethics of human subject participation

This study was conducted according to the guidelines laid down in the Declaration of Helsinki, and all procedures involving research study participants were approved by the Technical Advisory Committee of the Department of Public Health and Community Medicine and the Institutional Human Ethics Committee of the Central University of Kerala (approval number: ref no: IHEC /CUK/2022/22). The IRB-approved procedures were used in DHS and MICS. In both surveys, all adults interviewed gave verbal consent before data were collected. For children, parental verbal consent, as well as assent, was obtained from the children. Before the use of the dataset, approval was obtained from the programme directors.

References

WHO (2010) Nutrition Landscape Information System (NLIS) Country Profile Indicators: Interpretation Guide. Geneva: World Health Organization.Google Scholar
WHO & UNICEF Bank W (2021) Levels and Trends in Child Malnutrition: UNICEF/WHO/The World Bank Group Joint Child Malnutrition Estimates: Key Findings of the 2021 Edition. Geneva: World Health Organization.Google Scholar
Dwomoh, D, Sewor, C, Mohammed, SA et al. (2022) Secular trends in low birth weight and child undernutrition in West Africa: evidence from complex nationwide surveys, 1985–2019. Public Health Nutr 25, 113.Google ScholarPubMed
NDPC (2019) GHANA: Voluntary National Review Report on the Implementation of the 2030 Agenda for Sustainable Development. National Development Planning Commission. Accra: National Development Planning Commission.Google Scholar
GSS, GHS & ICF (2015) Ghana Demographic and Health Survey 2014. Rockville, MD: GSS, GHS, and ICF International.Google Scholar
de Onis, M & Branca, F (2016) Childhood stunting: a global perspective. Matern Child Nutr 12, 1226.CrossRefGoogle ScholarPubMed
Ocansey, ME, Adu-Afarwuah, S, Kumordzie, SM et al. (2019) The association of early linear growth and haemoglobin concentration with later cognitive, motor, and social-emotional development at preschool age in Ghana. Matern Child Nutr 15, e12834.CrossRefGoogle ScholarPubMed
Scott, SP, Chen-Edinboro, LP, Caulfield, LE et al. (2014) The impact of anemia on child mortality: an updated review. Nutrients 6, 59155932.CrossRefGoogle ScholarPubMed
Larsen, DA, Grisham, T, Slawsky, E et al. (2017) An individual-level meta-analysis assessing the impact of community-level sanitation access on child stunting, anemia, and diarrhea: evidence from DHS and MICS surveys. PLoS Negl Trop Dis 11, e0005591.CrossRefGoogle ScholarPubMed
Katoch, OR (2022) Determinants of malnutrition among children: a systematic review. Nutrition (Burbank, Los Angeles County, Calif) 96, 111565.CrossRefGoogle ScholarPubMed
UNICEF (2013) Improving Child Nutrition: the Achievable Imperative for Global Progress. New York: UNICEF.Google Scholar
Aryeetey, R, Atuobi-Yeboah, A, Billings, L et al. (2021) Stories of change in nutrition in Ghana: a focus on stunting and anemia among children under-five years (2009–2018). Food Secur 14, 355379.CrossRefGoogle Scholar
Yawson, AE, Amoaful, EO, Senaya, LK et al. (2017) The lancet series nutritional interventions in Ghana: a determinants analysis approach to inform nutrition strategic planning. BMC Nutr 3, 27.CrossRefGoogle Scholar
WHO & UNICEF (2017) Progress on Drinking Water, Sanitation and Hygiene: 2017 Update and SDG Baseline. Geneva: World Health Organization. pp. 6666.Google Scholar
WHO & UNICEF (2021) Indicators for Assessing Infant and Young Child Feeding Practices Definitions and Measurement Methods. Geneva: World Health Organization (WHO) and the United Nations Children’s Fund (UNICEF).Google Scholar
Rutstein, SO & Johnson, K (2004) The DHS Wealth Index. DHS Comparative Report no. 6. Calverton, MD: ORC Macro.Google Scholar
Martel, P (2016) Review of Options for Reporting Water, Sanitation and Hygiene Coverage by Wealth Quintile. DoD Data and Analytics Section, Research and Policy. MICS Methodological Papers. New York: UNICEF.Google Scholar
Williams, R (2021) Analyzing Complex Survey Data: Some Key Issues to be Aware of University of Notre Dame. https://www3.nd.edu/~rwilliam/stats2/SvyCautions.pdf. Accessed June, 2022.Google Scholar
Jonah, CMP, Sambu, WC & May, JD (2018) A comparative analysis of socioeconomic inequities in stunting: a case of three middle-income African countries. Arch Public Health 76, 77.CrossRefGoogle ScholarPubMed
Keino, S, Plasqui, G, Ettyang, G et al. (2014) Determinants of stunting and overweight among young children and adolescents in sub-Saharan Africa. Food Nutr Bull 35, 167178.CrossRefGoogle ScholarPubMed
Thompson, AL (2021) Greater male vulnerability to stunting? Evaluating sex differences in growth, pathways and biocultural mechanisms. Ann Hum Biol 48, 466473.CrossRefGoogle ScholarPubMed
Yu, SH, Mason, J, Crum, J et al. (2016) Differential effects of young maternal age on child growth. Glob Health Action 9, 31171.CrossRefGoogle ScholarPubMed
Akombi, BJ, Agho, KE, Hall, JJ et al. (2017) Stunting, wasting and underweight in Sub-Saharan Africa: a systematic review. Int J Environ Res Public Health 14, 863.CrossRefGoogle ScholarPubMed
Obasohan, PE, Walters, SJ, Jacques, R et al. (2020) Risk factors associated with malnutrition among children under-five years in Sub-Saharan African countries: a scoping review. Int J Environ Res Public Health 17, 8782.CrossRefGoogle ScholarPubMed
Quamme, SH & Iversen, PO (2022) Prevalence of child stunting in Sub-Saharan Africa and its risk factors. Clin Nutr Open Sci 42, 4961.CrossRefGoogle Scholar
Siddiqui, F, Salam, RA, Lassi, ZS et al. (2020) The intertwined relationship between malnutrition and poverty. Front Public Health 8, 453.CrossRefGoogle ScholarPubMed
Christian, AK & Dake, FA (2021) Profiling household double and triple burden of malnutrition in sub-Saharan Africa: prevalence and influencing household factors. Public Health Nutr 25, 114.Google ScholarPubMed
Shenton, LM, Jones, AD & Wilson, ML (2020) Factors associated with anemia status among children aged 6–59 months in Ghana, 2003–2014. Matern Child Health J 24, 483502.CrossRefGoogle ScholarPubMed
Obasohan, PE, Walters, SJ, Jacques, R et al. (2020) A scoping review of the risk factors associated with anaemia among children under five years in Sub-Saharan African Countries. Int J Environ Res Public Health 17, 8829.CrossRefGoogle ScholarPubMed
Silveira, VNC, Carvalho, CA, Viola, P et al. (2021) Prevalence of iron-deficiency anaemia in Brazilian children under 5 years of age: a systematic review and meta-analysis. Br J Nutr 126, 12571269.CrossRefGoogle ScholarPubMed
Black, MM, Walker, SP, Fernald, LCH et al. (2017) Early childhood development coming of age: science through the life course. Lancet 389, 7790.CrossRefGoogle ScholarPubMed
Ramirez-Luzuriaga, MJ, Larson, LM, Mannar, V et al. (2018) Impact of double-fortified salt with iron and iodine on hemoglobin, anemia, and iron deficiency anemia: a systematic review and meta-analysis. Adv Nutr 9, 207218.CrossRefGoogle ScholarPubMed
Moschovis, PP, Wiens, MO, Arlington, L et al. (2018) Individual, maternal and household risk factors for anaemia among young children in sub-Saharan Africa: a cross-sectional study. BMJ Open 8, e019654.CrossRefGoogle ScholarPubMed
Tezera, R, Sahile, Z, Yilma, D et al. (2018) Prevalence of anemia among school-age children in Ethiopia: a systematic review and meta-analysis. Syst Rev 7, 80.CrossRefGoogle Scholar
Wegmuller, R, Bentil, H, Wirth, JP et al. (2020) Anemia, micronutrient deficiencies, malaria, hemoglobinopathies and malnutrition in young children and non-pregnant women in Ghana: findings from a national survey. PLoS One 15, e0228258.CrossRefGoogle ScholarPubMed
Crawley, J (2004) Reducing the burden of anemia in infants and young children in malaria-endemic countries of Africa: from evidence to action. Am J Trop Med Hyg 71, 2534.CrossRefGoogle ScholarPubMed
Ghartey, AB (2010) Nutrition Policy and Programs in Ghana: The Limitation of a Single Sector Approach. Washington, DC: World Bank.CrossRefGoogle Scholar
GHS (2007) Infant and Young Child Feeding Strategy for Ghana. Accra, Ghana: Ghana Health Service.Google Scholar
MOH (2007) Under Five’s Child Health Policy: 2007–2015. Accra, Ghana: Ministry of Health.Google Scholar
Anarwat, SG, Salifu, M & Akuriba, MA (2021) Equity and access to maternal and child health services in Ghana a cross-sectional study. BMC Health Serv Res 21, 864.CrossRefGoogle ScholarPubMed
Fenny, AP, Asuman, D, Crentsil, AO et al. (2019) Trends and causes of socioeconomic inequalities in maternal healthcare in Ghana, 2003–2014. Int J Social Econ 46, 288308.CrossRefGoogle Scholar
Asamoah, BO & Agardh, A (2017) Inequality trends in maternal health services for young Ghanaian women with childbirth history between 2003 and 2014. BMJ Open 7, e011663.CrossRefGoogle ScholarPubMed
Ahinkorah, BO, Hagan, JE Jr, Seidu, AA et al. (2019) Access to adolescent pregnancy prevention information and services in Ghana: a community-based case-control study. Front Public Health 7, 382.CrossRefGoogle Scholar
Smith, LC, Ramakrishnan, U, Ndiaye, A et al. (2003) The importance of Women’s status for child nutrition in developing countries: International Food Policy Research Institute (IFPRI) research report abstract 131. Food Nutr Bull 24, 287288.CrossRefGoogle Scholar
UNESCO (2015) Education for All 2000–2015: Achievements and Challenges no. 9231000853. UNESCO.Google Scholar
GSS, GHS & ICF (2015) Education in Ghana: Data from the 2014 Ghana Demographic and Health Survey (DHS). Rockville, MD: GSS, GHS, and ICF International.Google Scholar
Cooke, E, Hague, S & McKay, A (2016) The Ghana Poverty and Inequality Report: Using the 6th Ghana Living Standards Survey. Brighton: University of Sussex. pp. 143.Google Scholar
Afful, JB, Nunoo, J & Arthur-Biney, A (2019) Income and wealth in Ghana: issues of distribution and determinants. UDS Int J Dev 6, 4278.Google Scholar
Barros, AJ & Hirakata, VN (2003) Alternatives for logistic regression in cross-sectional studies: an empirical comparison of models that directly estimate the prevalence ratio. BMC Med Res Methodol 3, 21.CrossRefGoogle ScholarPubMed
Thompson, ML, Myers, JE & Kriebel, D (1998) Prevalence odds ratio or prevalence ratio in the analysis of cross sectional data: what is to be done? Occup Environ Med 55, 272277.CrossRefGoogle ScholarPubMed
Figure 0

Table 1 Descriptive pattern of selected risk factors and child health outcomes

Figure 1

Table 2 Crude prevalence ratios of risk factors associated with stunting

Figure 2

Table 3 Crude prevalence ratios of risk factors associated with anaemia

Figure 3

Fig. 1 Trend of prevalence ratio of the risk factors associated with childhood stunting

Figure 4

Table 4 Adjusted prevalence ratios of risk factors associated with stunting

Figure 5

Table 5 Adjusted prevalence ratios of risk factors associated with anaemia

Figure 6

Fig. 2 Trend of prevalence ratio of the risk factors associated with childhood anaemia

Figure 7

Table 6 Prevalence ratios of risk factors associated with stunting (mixed effect Poisson regression)

Figure 8

Table 7 Prevalence ratios of risk factors associated with anaemia (mixed effect Poisson regression)