Hostname: page-component-cd9895bd7-jkksz Total loading time: 0 Render date: 2024-12-26T19:57:53.703Z Has data issue: false hasContentIssue false

Mothers’ feeding practices among infants (4–12 months) and associated factors: a cross-sectional study in Saudi Arabia

Published online by Cambridge University Press:  23 September 2022

Salwa Ali Albar*
Affiliation:
Food and Nutrition Department, King Abdulaziz University, Jeddah, Saudi Arabia
*
Corresponding author: Salwa Albar, email salbar1@kau.edu.sa

Abstract

A global target of increasing exclusive breast-feeding (EBF) to at least 50 % by the year 2025 was set by the WHO for infants under 6 months. The lowest prevalence in the world was found in the Eastern Mediterranean region in 2010–18 and little is known about the status of mothers’ feeding practices in Saudi Arabia. The present study aimed to assess mothers’ actual feeding and weaning practices used with their infants by the mothers’ different age groups. The present study was conducted among 247 mothers of infants aged 4–12 months who were attending public well-baby clinics. Quantitative data were obtained by nutritionists using an electronic semi-structured questionnaire about mothers’ feeding practices. Only 5·3 % of mothers engaged in EBF, 44·9 % breast-fed their infants after an hour of birth, while 92·7 % of infants had ever been breast-fed. The average intent/plan to continue breast-feeding was 4·9(±3·1) months. Younger mothers introduced weaning food around 4 weeks earlier than older mothers (mean differences were −0·4, 95 % CI −0·71, −0·13; P = 0·031). A total of 64·3 % of infants received complementary feeding before completing 17 weeks. Maternal age group and delivery mode were the only factors associated with the early introduction of complementary feeding. A total of 69·2 % of the mothers believed that ‘it is a good time’ and 61·1 % felt that ‘infants are hungry and need other sources of food’. Online sources and family advice were the top sources of information on mothers’ feeding practices. Provision of professional advice about EBF and optimal weaning practices are significant areas for improvement in terms of compliance with recommended infant feeding practices.

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

Introduction

Good infant feeding practices, in particular breast-feeding, are considered the most effective way to ensure a child's health and survival. The World Health Organization (WHO) and United Nations (UN) recommend that mothers in developing and developed countries should exclusively breast-feed (EBF) their infants for the first 6 months (24 weeks) of their lives(1), and then ensure that they receive adequately safe and nutritious solid foods about two to three times a day at age 6–8 months, increasing this to three to four times daily at age 9–11 months, with continuous breast-feeding until they reach 2 years old or older(Reference Qasem, Fenton and Friel2,3) . Additional healthy snacks should be offered one to two times/day by age 12–24 months(1). However, over the period 2015–2020, only 40 % of infants were exclusively breast-fed(4). Nearly two out of three infants are not exclusively breast-fed and this rate has not been enhanced in the last two decades(4). Current practices in the Middle East do not adhere to WHO recommendations. For instance, in Lebanon, United Arab Emirates, and Iraq, 53, 70 and 79 % of infants, respectively, are given complementary feeding between the ages of 4 and 6 months(Reference Nasreddine, Zeidan and Naja5). Available information indicates that feeding practices are not optimal among Saudi infants(Reference Azzeh6). The prevalence of EBF in Saudi was extremely low, at 1·7 % in 2010, and partial breast-feeding was the most common feeding style(Reference Al-Hreashy, Tamim and Al-Baz7). While in 2017, the rate of EBF was 31·4 % in North Saudi(Reference Alzaheb8), and the early intention of breast-feeding (EIBF) was fair in the Central, Western and Eastern regions in Saudi(Reference Ahmed and Osama9). One study has shown that 62·5 % of Saudi infants consume complementary feeding before reaching 4 months of age(Reference Alzaheb10).

The way in which infants are fed in their first year of life has important consequences in terms of the short- and long-term impact on an infant's health(Reference McAndrew, Thompson and Fellows11). A number of studies have shown that infants who are not breast-fed are more likely to develop certain health conditions and diseases, such as lower respiratory tract infection and gastrointestinal infection(Reference McAndrew, Thompson and Fellows11Reference Ip, Chung and Raman14).

The gradual introduction of complementary feeding or ‘weaning practice’ is very critical and essential to meet an infant's physiological stage (as their neurodevelopment, gastrointestinal systems and kidneys are still underdeveloped(Reference Rao, Swathi and Unnikrishnan15)) and nutritional requirements in their first year of life(Reference Calvo, Galindo and Aspres16). As recommended by the WHO, complementary feeding should be given in a timely and appropriate way, beginning at 6 months of age (after 5 months), and at appropriate amounts, frequency, consistency and using a good variety of foods(3,Reference Monte and Giugliani17) . An early introduction of solid food has been found to increase the incidence of respiratory infection and allergy(Reference Moroishi, Signes-Pastor and Li18). Also, it has been associated with an increased risk of eczema, allergies(Reference Armentia, Bañuelos and Arranz19,Reference Tarini, Carroll and Sox20) and the odds of obesity at 3 years of age(Reference Huh, Rifas-Shiman and Taveras21).

There is some evidence suggesting that weaning infants beyond the recommended time may increase the percentage of body fat in childhood(Reference Wilson, Forsyth and Greene22). One systematic review suggests that very early introduction (at 4 months) may increase the risk of being obese and overweight in childhood(Reference Pearce, Taylor and Langley-Evans23), and it may inversely affect dietary patterns and feeding behaviours(Reference Northstone, Emmett and Nethersole24,Reference Devine, Wolfe and Frongillo25) . It has also been found that food introduced in the first 24 months predicts young children's dietary intake(Reference Skinner, Carruth and Bounds26).

Saudi Vision 2030 has contributed to economic, social and cultural developments that have had a positive impact on women's participation in public spheres, improving women's status, empowering them and raising the level of their economic participation. As a result, the percentage of women in the labour force in Saudi Arabia (SA) rose from 24 to 27·5 % in the first quarter of 2020(Reference Rosenbauer, Herzig and Giani27). These social improvements may lead to a number of changes in mothers’ breast-feeding and general feeding practices among infants, especially young and first-time mothers. Furthermore, it is expected that the WHO's 2025 global targets in EBF will be disrupted due to the COVID-19 pandemic(Reference Mengistu28).

In SA, there has been a limited number of studies focusing on breast-feeding practice in general(Reference Al-Hreashy, Tamim and Al-Baz7,Reference Alzaheb10) , as well as on specific regions of SA. However, inadequate information is available in regards to EBF and mothers’ complementary feeding practice(Reference Alzaheb10). Furthermore, a review study in Saudi found that maternal age was an important factor associated with the prevalence of breast-feeding(Reference Al Juaid, Binns and Giglia29). Therefore, the present study aims to investigate Saudi mothers of different age groups and their actual feeding and weaning practices used with their infants (4–12 months), as well as to examine some factors that could influence the mother's decision.

Materials and methods

Study population

This is a cross-sectional survey conducted in Jeddah city, SA, between August and November 2021 among 247 mothers of fertility age (18–45 years old) and their infants. The estimated sample size for this research was calculated based on the findings from a previous study that found the prevalence of early introduction of complementary feeding at <17 weeks among infants was 62 %(Reference Alzaheb10), with a 95 % confidence level and a confidence limit of 5 %. The resulting sample size was 230 mothers, which was then approximated to 253 mothers, allowing for a 10 % attrition rate.

To gather data on the mothers’ feeding practices for their current infants aged between 4 and 12 months, the research team visited the pre-specified well-baby clinics (held at the largest public centre in Jeddah and serving a large number of people from different areas and from different socioeconomic statuses). In SA, all children under 5 years old have to visit a well-baby clinic for their infant vaccinations. The research team screened the mothers and their infants based on eligibility criteria, informed them of the objectives and invited them to participate in the study. The recruitment followed convenient sampling. Mothers and infants were chosen based on inclusion criteria. The Saudi mothers were aged between 18 and 45 years old and free of chronic disease. The infants had been of ≥37 weeks gestational age (full-term babies), aged 4–12 months and did not require specialised care. The exclusion criteria were mothers with chronic disease, preterm babies (<37 weeks of gestational age) and infants with congenital disease or a disease that could prevent breast-feeding.

All mothers who were willing to participate in the study were asked to sign a consent form. 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 Ethics Committee of King Abdulaziz University, Unit of Biomedical Ethics (reference: 443-21). Written informed consent was obtained from all subjects. A total of 97·6 % of the mothers approached agreed to participate in the study (recruitment rate).

Data collection

An electronic semi-structured questionnaire was developed using national and international questionnaires(Reference Al-Hreashy, Tamim and Al-Baz7,Reference Alzaheb10,Reference Al-Jassir, El-Bashir and Moizuddin30,31) . The questionnaire was content validated and culturally adapted by a panel of experts consisting of two neonatal physicians and a nutrition epidemiologist. Then the questionnaire was piloted among twenty-seven mothers prior to being administered among the final sample. The original version of the questionnaire was written in English and then translated into Arabic, since the questionnaire was planned to be administered to the study sample in their native Arabic language. The original and translated questionnaires were reviewed for consistency in terms of meaning. The questionnaire was administered by trained nutritionists through face-to-face interviews.

The questionnaire was semi-structured and consisted of three parts covering the mother's past/present breast-feeding and weaning feeding practices, the mother's demographical information, and the mother's general knowledge and sources of information.

Mother's feeding practices

Yes or no questions were asked regarding the mother's breast-feeding practice; for example, regarding EBF (whether their baby had only breast-milk from birth), EIBF, and the mother's intention to continue breast-feeding. The definition of EBF was in accordance with the WHO's definition, that the infant receives only breast-milk during the first 6 months of his/her life and no other solids or liquids are introduced(31); feeding of expressed breast-milk counts as being fed breast-milk. Also, mothers’ EIBF was defined as the percentage of infants who are breast-fed within an hour of birth. Furthermore, multiple choice questions were asked regarding the mother's knowledge of the WHO's EBF definition and the importance of breast-feeding infants within an hour of the infant's birth. Also, an open-ended question (based on the number of months) was included in the questionnaire regarding the mother's intention to continue breast-feeding her infant in general (duration), even if she had introduced different feeding practices. Also, a question about whether their baby had ever received breast-feeding (EvBF) was asked.

The early introduction of complementary feeding was defined in this study as the introduction of any food before the infant reaches 17 weeks. This was defined based on the European Society's guidance, that infants younger than 17 weeks should not be given any complementary foods(Reference Agostoni, Decsi and Fewtrell32), and has been used in many Western(Reference Scott, Binns and Graham33,Reference Castro, Layte and Kearney34) and Arab countries(Reference Alzaheb10,Reference Scott, Dashti and Al-Sughayer35) in studies with related objectives(Reference Alzaheb10). Complementary food was defined in this study based on the definition used by the Saudi Food and Drug Authority(36), which is in line with the European Food Safety Authority (EFSA)(Reference Turck, Castenmiller and De Henauw37). It includes all foods that are given to infants other than breast-milk, formula-milk, water or vitamins, and can be beverages, spoon-fed pureed foods, spoon-fed lumpy foods or finger foods, either prepared at home or produced commercially. Data on the early introduction of complementary feeding were generated from questions that asked mothers to state at which point in time they introduced complementary food to their infant.

Furthermore, open-ended questions were used to asked about the infant's age by month the first time a breast-milk substitute (formula, fresh or processed animal milk) was introduced, as well as beverages (other than milk and water), infant homemade food, infant ready-to-eat-food and regular family food.

Mother's demographical information

The survey collected data on the mother's age, education, occupation status, family income, number of children, current contraceptive and infant delivery mode. The mother's current anthropometric information was self-reported while the infant's anthropometric data were collected from the infant's vaccination record. Mother's body mass index (BMI) was calculated (weight (kg)/height (m2)) and the value was interpreted based on WHO classifications, where BMI < 18·5 kg/m2 is underweight, 18·5–24·9 kg/m2 is normal, 25–29·9 kg/m2 is overweight and ≥30 kg/m2 is obese(38). Furthermore, the mother's sources of knowledge and reasons behind their practices were examined; the mothers could give more than one answer to ensure a better understanding of their practices.

Statistical analysis

The data gathered from the surveys were inputted and analysed using Stata statistical software release 12 (Stata Corporation)(39). Descriptive statistics were used to describe the general characteristics for the sample, for continuous variables such as height and weight the mean and ±sd were used, and for categorical variables like the mother's education level, occupation and family income, numbers and proportions were reported. An independent two-sample t-test and Pearson Chi-Square test were used to test the differences between younger mothers (18–29 years) and older mothers (30–45 years) in terms of their general characteristics.

Differences between younger mothers and older mothers in terms of their infant feeding practices were assessed using a regression model (with mother's feeding practice as a dependent variable and mother's age group as an independent variable) with adjustment made for the mother's education, occupation, family income, BMI, and the infant's gender and birth weight. In accordance with the literature, these variables were considered risk factors for early weaning practice(Reference Alzaheb10,Reference Tarrant, Younger and Sheridan-Pereira40Reference Bolling, Grant and Hamlyn42) . Furthermore, a binary logistic regression model, with the introduction of complementary feeding as a dependent variable, was then used to determine the variables that independently predicted early weaning among infants (mother's age group, education, occupation). Findings were assessed by the OR and 95 % CI. A statistical significance level of P < 0·05 was used.

Results

Sample characteristics

A total of 247 mothers aged between 18 and 45 years old participated in this study, and 59·9 % of them were of a younger age (24·9 ± 2·5). There were significant differences between the older mothers (30–45 years) and younger mothers (18–29 years) in terms of their BMI category. A total of 71 % of mothers had a bachelor's degree and 94·7 % of them did not smoke cigarettes. Most of the mothers came from second or third family income classes, at 48·6 and 23·9 % respectively, and there was no significant difference in this in relation to the mother's age group. A total of 55·5 % of the mothers were housewives and there was a significant difference between younger and older mothers in terms of their occupation status. Older mothers had a significantly greater number of children (2·9 ± 1·5) and family members (5 ± 1·5) compared to younger mothers. More than half of the infants who participated in this study were female (57 %) and there was no significant difference between mothers of different age groups in terms of their infant's weight (Table 1).

Table 1. General characteristics of study participants by total sample and mother's age group

a Differences were assessed by using independent sample t-test.

b Univariate analyses using cross-tabulation and χ 2 statistical tests to compare the differences between mothers’ different age groups.

Breast-feeding practice by mother's age group

Only 44·9 % of mothers had EIBF their infants after an hour of birth, and the average number of infants aged 4–12 months who had ever been breast-fed (EvBF) was 92·7 %. However, only 5·3 % of mothers adhered to the WHO definition of EBF of infants aged 6–12 months (this has been calculated by counting the number of infants aged 6–12 months EBF/total number of infants aged 6–12 months, n 152). Furthermore, none of the infants aged 4–5 months received EBF. Although mothers of an older age were found to be of a higher proportion than younger mothers in terms of EIBF, EvBF and EBF, there were no significant differences between mothers’ age groups.

Only 2·4 % of mothers believed in the importance of breast-feeding their infant in the first hour of their life, 14·9 % of mothers believed that it has no importance, and 82·6 % do not know about it; there were significant differences between mothers’ age groups (P = 0·040). Furthermore, only 10 % of mothers knew the WHO definition of EBF and there was no difference among mothers in the different age groups.

Complementary feeding practice by mother's age group

The mean of mothers’ intent/plan in the duration of continuing breast-feeding was 4·9 ± 3·1 months; younger aged mothers had less intent/plan in terms of duration of breast-feeding than older mothers (differences in mean −0·80, 95 % CI −1·58, −0·13; P = 0·046). Younger Saudi mothers generally introduced weaning food before older mothers by about 4 weeks (mean differences were −0·4, 95 % CI −0·71, −0·13; P = 0·031).

Regarding the introduction of different food types, the mean time for introducing a breast-milk substitute was at 3 ± 2·3 months; younger mothers introduced a breast-milk substitute earlier than older mothers and this difference was significant. This was followed by beverages other than milk at 3·3 ± 2·2 months, then ready-to-eat food, which was introduced at 5·6 ± 2·4 months. Furthermore, younger mothers introduced beverages other than milk and ready-to-eat food significantly earlier than older mothers, with differences in mean of −0·75; 95 % CI −1·33, −0·17; P = 0·011 and −0·85, 95 % CI −1·5, −0·22; P = 0·008, respectively. However, there were no significant differences between mothers’ age groups in terms of introducing homemade dishes and regular family food (Table 2).

Table 2. Complementary feeding practice by mother's age group

a Differences between mean younger mothers and older mothers in infant feeding practices were assessed by using a regression model with adjusting for occupation, mother education level, family income, mother BMI and infant gender.

b This has been asked for infants aged >6 months (n 152).

Factors associated with complementary feeding age

Mothers’ age was significantly associated with the early introduction of complementary feeding before 17 weeks. Mothers of younger age (18–29 years) were 45 % less likely to provide complementary feeding at ≥17 weeks (OR 0·55; 95 % CI 0·31, 0·98; P = 0·041). In addition, mothers who had a caesarean section were 47 % more likely to introduce complementary feeding at <17 weeks (OR 0·47; 95 % CI 0·25, 0·88; P = 0·019). Mothers’ education, occupation and family income were not associated with mothers’ decision to introduce complementary feeding. However, mother's belief regarding the time to introduce complementary feeding, the infant's hunger, and promoting the infant's weight and sleep were all significant factors influencing the mothers’ decision about the time to introduce complementary feeding (Table 3).

Table 3. Factors associated with the introduction of complementary feeding by age (<17 weeks/≥17 weeks)

a Univariate analyses using cross-tabulation and χ 2 statistical tests to compare the differences in the proportion between mothers who complementary fed their infant <17 weeks and ≥17 weeks.

b Value is the odds ratio obtained from the logistic regression model. The model was adjusted for maternal education, occupation, family income, infant birth weight and gender.

Maternal weaning practice and sources of information

Fig. 1 shows fluids that mothers usually provide to their infants. Water was the most common fluid introduced to infants in total, then fresh fruit juice, and then date juice (84, 33 and 30 %, respectively). The proportion of infants introduced to date juice was higher among infants complementary fed at <17 weeks (34·6 %) compared to infants complementary fed ≥17 weeks (21·6 %); P = 0·033. Regarding foods that mothers initially introduced to their infants, cereal (ready to use or homemade) was the most common food item followed by mashed fruits and then mashed vegetables (65·2, 34·4 and 32·8 %, respectively). Pureed meat, poultry or fish was significantly different by infant complementary feeding age; 22 % of infants complementary fed at <17 weeks and 34 % of infants fed at ≥17 weeks; P = 0·015 (Fig. 2(a)). Furthermore, dates, salt, honey and sugar were the most common ingredients that Saudi mothers added to their infants’ weaning food, at 60, 28, 26 and 17·8 %, respectively. The proportion of mothers who added spices/condiments to their infants’ weaning food was significantly different by infant complementary feeding (28 % of infants complementary fed at <17 weeks and 15 % complementary fed at ≥17 weeks; P = 0·012) (Fig. 2(b)).

Fig. 1. Fluids mothers usually introduce to infants. *Significant differences between the proportion of infants complementary fed at <17 weeks and at ≥17 weeks, using χ 2 (significant at P = 0·033).

Fig. 2. Food and ingredients that mothers introduce to their infants by complementary feeding age.

There are many sources of information that Saudi mothers use to get information about infant feeding practices. Online sources, family advice, consultant doctors and previous experience were the most common sources, at 61·6, 57·1, 51·4 and 46·2 %, respectively. The proportion of mothers who introduced complementary feeding before 17 weeks was significantly higher than mothers who introduced complementary feeding after 17 weeks based on online sources and following family advice (67 %, 54 %, significant at P = 0·04 and 63 %, 47 %; P = 0·013, respectively).

Discussion

The present study demonstrates that there is a significant deviation from WHO recommendations among Saudi mothers in terms of infant feeding practices. Only 44·9 % of mothers breast-fed their infants after an hour of birth (EIBF) and 5·3 % of mothers with infants aged 6–12 months EBF. None of the infants aged 4–5 months received EBF. However, 92·7 % of mothers received EvBF. The average intent/plan of mothers to continue to breast-feed their infant was 4·9 (±3·1) months and younger mothers had significantly lower intent/plan than older mothers and provided a breast-milk substitute, beverages and ready-to-eat food at an earlier age than older mothers. A total of 64·3 % of infants were introduced to complementary feeding before completing 17 weeks. Maternal age group and mode of delivery were the only factors associated with the early introduction of complementary feeding. Most of the mothers attributed their feeding practices to their belief that ‘it is a good time’ and feeling that their infant was ‘hungry and in need of other sources of food’. Online sources and family advice were the top sources of information for the mothers in relation to infant feeding practices and there were significant differences between mothers’ age groups.

The WHO has set a global target of increasing EBF to at least 50 % for infants under 6 months by the year 2025(Reference Mengistu28). However, European countries, the Eastern Mediterranean region (EMR) and upper middle-income countries are facing the greatest challenges in meeting these WHO targets. EMR has the lowest prevalence of EBF and experiences a decline from 43·7 % between 2000 and 2008 to 38·4 % between 2010 and 2018(Reference Mengistu28). Recently, SA has witnessed a massive increase in women's participation in various work sectors, which may have led to changes in mothers’ feeding practices. Our findings confirm that there is a low rate of EBF practiced nationally, just as there is internationally. This study shows the lowest prevalence of EBF among infants below 6 months compared with 2018 when it was 16·3 %(Reference Alsulaimani43) and 27·3 % before 18 years(Reference Ogbeide, Siddiqui and Al Khalifa44). This is in line with the rate of EBF at 6 months in the UK, which remained at around 1 %(45); on average, 13 % of infants are EBF during the first 6 months in the European region(Reference Bagci Bosi, Eriksen and Sobko46).

In spite of the well-recognized benefit of breast-feeding, particularly in the first hour after childbirth, this study found that 44·9 % of mothers have EIBF. Similar to our finding, in 2019, the overall prevalence of EIBF in Saudi was 43·6 % and in Western regions, it was 45 %, which is considered fair(Reference Ahmed and Osama9). This might be due to a lack of knowledge about its importance, as 82·6 % of Saudi mothers do not know of its importance. Dukuzumuremyi et al. found that 47·9 % of mothers disagreed about the importance of colostrum(Reference Dukuzumuremyi, Acheampong and Abesig47). Another study found the rate of mothers’ intention to breast-feed in the first hour after childbirth was 13·9 %(Reference Alsulaimani43), as reflected in our study which found a lack of knowledge among Saudi mothers regarding the valuable effect of breast-feeding in the first hour of an infant's life.

Regardless of EBF, the present study found that the average duration of ‘mother's intention’ to continue breast-feeding was also low (4·9 ± 3·1 months); the minimum was 1 month and the maximum was 12 months. This seems to suggest that the mean duration of breast-feeding has continued to decline in SA over time, especially these days due to the various developments that the kingdom is witnessing. It stood at 13·4 months in 1987 and declined to 8·5 months in 2010(Reference Al Juaid, Binns and Giglia29). Lactation duration also dropped to 50 % at 6 months of an infant's age(Reference Al-Hreashy, Tamim and Al-Baz7). This is in line with a cohort study in Spain where it was found that the duration of breast-feeding was shorter among mothers who were younger(Reference Lechosa-Muñiz, Paz-Zulueta and Sota48). Similarly, only 58·3 % of US infants were breast-fed at 6 months and mixed feeding practice in the first 2 days of life increased from 16·9 % in 2016 to 19·2 % in 2017(49).

Although there is consensus on the WHO recommendations and other organisations such as the European Society for Paediatric Gastroenterology Hepatology and Nutrition(Reference Agostoni, Decsi and Fewtrell32,50) agree that the earliest introduction of complementary feeding should not be done before 4 months or 17 weeks, 64 % of our sample introduced complementary feeding when the infant was <17 weeks and this was influenced significantly by the mother's age, with 45 % of younger mothers more likely to wean their infants at <17 weeks than older mothers. Higher rates (62·5 %) of early weaning practice have also been found in Tabouk city in SA and similar findings have been made in other Middle East countries. For example, in the United Arab Emirates, 65 % of infants were reported to have been introduced to solid foods at age 3 months(Reference Gardner, Green and Gardner51). In China, the median age for starting complementary feeding was found to be 4·5 months (95 % CI 4·4–4·6 months). Early weaning remains a concern not just in the Middle East but also internationally, as data from England and New Zealand show that 22·6 % of infants are prematurely introduced to solid foods at ≤ 12 weeks(Reference Tarrant, Younger and Sheridan-Pereira40).

Similar to the present study's findings, it has been found that increasing maternal age is associated with a high prevalence of breast-feeding and longer duration(Reference Al Juaid, Binns and Giglia29,Reference Doub, Moding and Stifter52) , and younger aged mothers are more likely to practice early complementary feeding(Reference Alzaheb10,Reference Wijndaele, Lakshman and Landsbaugh53) . One cohort study found that an increase in mothers’ age added 2 % more breast-feeding time per year(Reference Lechosa-Muñiz, Paz-Zulueta and Sota48). However, in 2015 studies based on Kuwait(Reference Scott, Dashti and Al-Sughayer35) and the United Arab Emirates(Reference Gardner, Green and Gardner51), it was found that there was no positive association between mothers’ age and early complementary feeding. Factors associated with the early introduction of solid foods have been found to vary between different studies. For example, family income, occupation and mothers’ education have been found to be important factors linked with mothers’ early complementary feeding practices(Reference Lechosa-Muñiz, Paz-Zulueta and Sota48,Reference Alzaheb54) . In a study among 1791 Saudi mothers in Riyadh, it was found that breast-feeding was higher among non-working mothers, those with lower family income, and those less educated(55). Another study found that lower education, employment within 6 months post-birth, and low family income were factors associated with the early introduction of solid foods(Reference Alzaheb10). In line with our findings, a longitudinal study among 695 mothers found no association between the early introduction of food and family income(Reference Tang, Lee and Binns56). Regarding mothers’ education level, our findings were consistent with previous findings for SA(Reference Al-Hreashy, Tamim and Al-Baz7), Kuwait(Reference Scott, Dashti and Al-Sughayer35) and Turkey(Reference Camurdan, Ilhan and Beyazova57). Furthermore, a 2019 Saudi study identified an enormous gap between EBF knowledge (95 % got more than 50 % of the questions right) and mothers’ feeding practices(Reference Alsulaimani43).

In this research, 69·2 and 61 % of mothers changed their feeding practice as they thought it was ‘a good time to start’ and that the ‘infant is hungry and needs sources other than milk’. This was significantly different based on time of complementary feeding. Many studies have come to the same conclusion. In SA, one study found that 51·4 % of mothers believed that their infant was hungry and 26·6 % said that their child was old enough to be fed solid food(Reference Alzaheb8). In the MENA region, the common reasons given were ‘breastmilk is not naturally sufficient to feed three to four months old infants’ and the ‘child is old enough to have solid food’(Reference Nasreddine, Zeidan and Naja5). Similarly, Tarrant et al. found that later complementary feeding during the first 6 months was associated with later prediction of weaning time(Reference Tarrant, Younger and Sheridan-Pereira40).

Although the present study did not collect information on the amount and frequency of consumption of specific foods or fluids, fruit juice, date juice, baby cereal and pureed fruits were the most common foods and drinks provided to infants. Dates, honey and salt were the most common ingredients that mothers added to infant foods. Condiments were introduced significantly more among infants weaning at ≥17 weeks. This finding is in agreement with that of Tarrant et al., which also found that with early weaning a high frequency of consumption of non-recommended weaning foods was provided to infants, drinking of sugary supplementary fluids and frequent addition of condiments to weaning food(Reference Tarrant, Younger and Sheridan-Pereira40). According to the Committee on Medical Aspects of Food Policy, unsweetened foods should be encouraged in preference to sugary food or drink among this age group(58), as regular consumption of non-recommended foods during weaning practice increases the palatability of these foods and may affect long-term compliance with health eating guidelines(50,58) . Also, it has been suggested that it might lead to risk factors for being overweight and obese later in life(Reference Baughcum, Burklow and Deeks59). The obesity rate among Saudi children and adolescents has doubled over a 10-year period compared with the WHO national prevalence(Reference Al-Hussaini, Bashir and Khormi60). Furthermore, consumption of diets rich in salt during infancy encourages a taste for salted foods and may contribute to an increased risk of blood pressure in later life(Reference Zinner, McGarvey and Lipsitt61,Reference Bernstein62) .

The present study found that ‘online sources’ and ‘family advice’ were the main sources of information about feeding practices among mothers. Another study found that younger mothers who introduced sub-optimal weaning practices used their maternal grandmother as their primary source of advice on infant feeding(Reference Tarrant, Younger and Sheridan-Pereira40). One study found that 65·3 % of mothers scored over 75 % when asked questions regarding the benefits of breast-feeding(Reference Alsulaimani43). However, another study found that parents are not aware of the predicted harmful effects of early weaning and may perceive it to be helpful for their infant's health(Reference Forsyth, Ogston and Clark63).

Therefore, to address the high prevalence of sub-optimal feeding practices, public health initiatives are required that aim to improve the quality and quantity of infant feeding practices and strategies are needed to ensure compliance with weaning recommendations in Saudi Arabia, in particular among younger aged and first time mothers.

There may be a number of limitations related to this study. Firstly, the length of breast-feeding and feeding practice was reported by mothers and there may have been some recall bias due to the mother's social expectations, leading to over- or under-estimating of feeding practices(Reference Livingstone, Robson and Wallace64). Secondly, this was a cross-sectional study and so by its nature it prevented the determination of the direction of association. Also, no information regarding infant dietary intake portion size and frequency was collected; such information would advance our awareness of mothers’ feeding practices and sub-optimal weaning. On the other hand, results of this study shed light on many different aspects of mothers’ feeding practices. It has covered EBF, EIBF, EvBF and mothers’ practices in terms of introducing complementary food, as well as influencing factors, reasons and sources of information used for feeding practice. All of this information has the potential to provide policymakers in the public health sphere with a comprehensive understanding of Saudi mothers’ different feeding practices, particularly at this time after the COVID-19 pandemic and during the enormous developments that the kingdom is witnessing nowadays.

Conclusion

The present study has shown that there is still a big gap between WHO feeding recommendations and what is actually occurring in SA, as EBF and duration of breast-feeding were poor and EIBF was fair. There is a high prevalence of sub-optimal weaning practices among Saudi mothers. Mothers’ age and mode of delivery was found to be an important factor influencing mothers’ feeding practice. Online sources and family advice were the most common sources of information for mothers regarding infant feeding. There is a need to conduct a cohort study at the country level to gain a broader understanding of mothers’ feeding practices and risk factors associated with them. The findings of this study can serve as baseline information for upcoming cohort/longitudinal studies. This study also highly emphasises the importance of initiating breast-feeding counselling and weaning advice for parents during the first year of an infant's life in order to increase EBF and compliance with healthy weaning guidelines.

Acknowledgements

The author would like to thank the nutritionist Asmaa D. Alshehri and Kholoud A. Aleriani for their invaluable help in carrying the interviews in this study. Also, I thank the mothers who participated in this project.

The Deanship of Scientific Research (DSR) at King Abdulaziz University (KAU), Jeddah, Saudi Arabia, has funded this Project Under grant no (G: 683-253-3443).

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 Ethics Committee of King Abdulaziz University, Unit of Biomedical Ethics (reference: 443-21). Written informed consent was obtained from all subjects/patients.

References

World Health Organization (WHO) (2020) Infant and young child feeding. Available at https://www.who.int/en/news-room/fact-sheets/detail/infant-and-young-child-feeding.Google Scholar
Qasem, W, Fenton, T & Friel, J (2015) Age of introduction of first complementary feeding for infants: a systematic review. BMC Pediatr 15, 111.CrossRefGoogle ScholarPubMed
Fund WHOUNCs (2003) Global strategy for infant and young child feeding Geneva. Available at http://www.who.int/nutrition/publications/gs_infant_feeding_text_eng.pdfGoogle Scholar
World Health Organization (WHO) (2022) Health topic: breastfeeding, recommendations. Available at https://www.who.int/health-topics/breastfeeding#tab=tab_1.Google Scholar
Nasreddine, L, Zeidan, M, Naja, F, et al. (2012) Complementary feeding in the MENA region: practices and challenges. Nutr Metab Cardiovasc Dis 22, 793798.CrossRefGoogle ScholarPubMed
Azzeh, FS (2017) Determinants of exclusive breastfeeding and patterns of complementary feeding practices in Mecca city, Saudi Arabia. Int J Child Health Nutr 6, 8089.CrossRefGoogle Scholar
Al-Hreashy, FA, Tamim, HM, Al-Baz, N, et al. (2008) Patterns of breastfeeding practice during the first 6 months of life in Saudi Arabia. Saudi Med J 29, 427.Google ScholarPubMed
Alzaheb, RA (2017) Factors influencing exclusive breastfeeding in Tabuk, Saudi Arabia. Clin Med Insights Pediatr 11, 1179556517698136, doi: 10.1177/1179556517698136.CrossRefGoogle ScholarPubMed
Ahmed, AES & Osama, A (2019) Determinants of the early initiation of breastfeeding in the Kingdom of Saudi Arabia. Int Breastfeed J 14, 13.CrossRefGoogle ScholarPubMed
Alzaheb, RA (2016) Factors associated with the early introduction of complementary feeding in Saudi Arabia. Int J Environ Res Public Health 13, 702.CrossRefGoogle ScholarPubMed
McAndrew, F, Thompson, J, Fellows, L, et al. (2012) Infant feeding survey 2010. Leeds: Health Social Care Inf Centre 2.3-15.Google Scholar
Horta, BL, Bahl, R, Martinés, JC, et al. (2007) Evidence on the long-term effects of breastfeeding : systematic review and meta-analyses. World Health Organization.Geneva 9789241595230.Google Scholar
Quigley, MA, Kelly, YJ & Sacker, A (2007) Breastfeeding and hospitalization for diarrheal and respiratory infection in the United Kingdom Millennium Cohort Study. Pediatrics 119, e837e842.CrossRefGoogle ScholarPubMed
Ip, S, Chung, M, Raman, G, et al. (2007) Breastfeeding and maternal and infant health outcomes in developed countries. Evid Rep Technol Assess 153, 1186.Google Scholar
Rao, S, Swathi, P, Unnikrishnan, B, et al. (2011) Study of complementary feeding practices among mothers of children aged six months to two years - a study from coastal South India. Aust Med J 4, 252257.CrossRefGoogle Scholar
Calvo, EB, Galindo, AC & Aspres, NB (1992) Iron status in exclusively breast-fed infants. Pediatrics 90, 375379.CrossRefGoogle ScholarPubMed
Monte, CM & Giugliani, ER (2004) Recommendations for the complementary feeding of the breastfed child. J Pediatr 80, s131ss41.CrossRefGoogle ScholarPubMed
Moroishi, Y, Signes-Pastor, AJ, Li, Z, et al. (2022) Infant infections, respiratory symptoms, and allergy in relation to timing of rice cereal introduction in a United States cohort. Sci Rep 12, 4450.CrossRefGoogle Scholar
Armentia, A, Bañuelos, C, Arranz, ML, et al. (2001) Early introduction of cereals into children's diets as a risk-factor for grass pollen asthma. Clin Exp Allergy 31, 12501255.CrossRefGoogle ScholarPubMed
Tarini, BA, Carroll, AE, Sox, CM, et al. (2006) Systematic review of the relationship between early introduction of solid foods to infants and the development of allergic disease. Arch Pediatr Adolesc Med 160, 502507.Google ScholarPubMed
Huh, SY, Rifas-Shiman, SL, Taveras, EM, et al. (2011) Timing of solid food introduction and risk of obesity in preschool-aged children. Pediatrics 127, e544e551.CrossRefGoogle ScholarPubMed
Wilson, AC, Forsyth, JS, Greene, SA, et al. (1998) Relation of infant diet to childhood health: seven year follow up of cohort of children in Dundee infant feeding study. Br Med J 316, 2125.CrossRefGoogle ScholarPubMed
Pearce, J, Taylor, M & Langley-Evans, S (2013) Timing of the introduction of complementary feeding and risk of childhood obesity: a systematic review. Int J Obes 37, 12951306.CrossRefGoogle ScholarPubMed
Northstone, K, Emmett, P & Nethersole, F (2001) The effect of age of introduction to lumpy solids on foods eaten and reported feeding difficulties at 6 and 15 months. J Hum Nutr Diet 14, 4354.CrossRefGoogle ScholarPubMed
Devine, CM, Wolfe, WS, Frongillo, EA Jr, et al. (1999) Life-course events and experiences: association with fruit and vegetable consumption in 3 ethnic groups. J Am Diet Assoc 99, 309314.CrossRefGoogle ScholarPubMed
Skinner, JD, Carruth, BR, Bounds, W, et al. (2002) Do food-related experiences in the first 2 years of life predict dietary variety in school-aged children? J Nutr Educ Behav 34, 310315.CrossRefGoogle ScholarPubMed
Rosenbauer, J, Herzig, P & Giani, G (2008) Early infant feeding and risk of type 1 diabetes mellitus—a nationwide population-based case–control study in pre-school children. Diabetes Metab Res Rev 24, 211222.CrossRefGoogle ScholarPubMed
Mengistu, AK (2021) Predictors of Early Initiation of Breast Feeding; Evidence from 2019 Ethiopian Mini Demographic and Health Survey Europe PMC plus. doi: 10.21203/rs.3.rs-1039172/v1.Google Scholar
Al Juaid, DA, Binns, CW & Giglia, RC (2014) Breastfeeding in Saudi Arabia: a review. Int Breastfeed J 9, 19.CrossRefGoogle ScholarPubMed
Al-Jassir, MS, El-Bashir, BM & Moizuddin, SK (2004) Surveillance of infant feeding practices in Riyadh city. Ann Saudi Med 24, 136140.CrossRefGoogle ScholarPubMed
World Health Organization W (1991) Indicators for Assessing Breastfeeding Practices, Division of Child Health and Development. Geneva: WHO: Google Scholar.Google Scholar
Agostoni, C, Decsi, T, Fewtrell, M, et al. (2008) Complementary feeding: a commentary by the ESPGHAN committee on nutrition. J Pediatr Gastroenterol Nutr 46, 99110.CrossRefGoogle ScholarPubMed
Scott, JA, Binns, CW, Graham, KI, et al. (2009) Predictors of the early introduction of solid foods in infants: results of a cohort study. BMC Pediatr 9, 19.CrossRefGoogle ScholarPubMed
Castro, PD, Layte, R & Kearney, J (2014) Ethnic variation in breastfeeding and complimentary feeding in the republic of Ireland. Nutrients 6, 18321849.CrossRefGoogle ScholarPubMed
Scott, JA, Dashti, M, Al-Sughayer, M, et al. (2015) Timing and determinants of the introduction of complementary foods in Kuwait: results of a prospective cohort study. J Hum Lact 31, 467473.CrossRefGoogle ScholarPubMed
Saudi Food and Drug Authority (SFDA) (2020) Complementary feeding guide for infants and young children: a healthy start for your baby: SFDA. Available at https://sfda.gov.sa/sites/default/files/2021-02/Food17222021th.pdf.Google Scholar
Turck, D, Castenmiller, J, De Henauw, S, EFSA NDA Panel (EFSA Panel on Nutrition, Novel Foods and Food Allergens) (2019) Scientific Opinion on the safety of phenylcapsaicin as a novel food pursuant to Regulation (EU), p. 2283.Google Scholar
World Health Organization (2006) Global Database on Body Mass Index: BMI Classification. Geneva, Switzerland: World Health Organization.Google Scholar
StataCorp (2009) Statistical Software Release 11. College Station, TX: Stata Corporation.Google Scholar
Tarrant, RC, Younger, KM, Sheridan-Pereira, M, et al. (2010) Factors associated with weaning practices in term infants: a prospective observational study in Ireland. Br J Nutr 104, 15441554.CrossRefGoogle ScholarPubMed
Alder, EM, Williams, FL, Anderson, AS, et al. (2004) What influences the timing of the introduction of solid food to infants? Br J Nutr 92, 527531.CrossRefGoogle ScholarPubMed
Bolling, K, Grant, C, Hamlyn, B, et al. (2007) Infant Feeding Survey 2005. London: The Information Centre for Health and Social Care.Google Scholar
Alsulaimani, NA (2019) Exclusive breastfeeding among Saudi mothers: exposing the substantial gap between knowledge and practice. J Family Med Prim Care 8, 28032809.CrossRefGoogle ScholarPubMed
Ogbeide, DO, Siddiqui, S, Al Khalifa, IM, et al. (2004) Breast feeding in a Saudi Arabian community. Profile of parents and influencing factors. Saudi Med J 25, 580584.Google Scholar
UNICEF UK (2018) Find Out About Breastfeeding Rates in the UK and Our Work to Improve Them. The Baby Friendly Initiative. (accessed 20 September 2021).Google Scholar
Bagci Bosi, T A, Eriksen, G K, Sobko, , et al. (2016 ) Breastfeeding practices and policies in WHO European Region Member States. Public Health Nutr 19, 753764, doi: 10.1017/S1368980015001767.CrossRefGoogle ScholarPubMed
Dukuzumuremyi, JPC, Acheampong, K, Abesig, J, et al. (2020) Knowledge, attitude, and practice of exclusive breastfeeding among mothers in East Africa: a systematic review. Int Breastfeed J 15, 70.CrossRefGoogle ScholarPubMed
Lechosa-Muñiz, C, Paz-Zulueta, M, Sota, SM, et al. (2020) Factors associated with duration of breastfeeding in Spain: a cohort study. Int Breastfeed J 15, 79.CrossRefGoogle ScholarPubMed
CDC (2017) National Immunization Survey (NIS) 2018–2019, among 2017 births. Breastfeeding rate indicators are the percentage of infants breastfeeding at the specified time points, calculated among all infants.Google Scholar
Food Safety Authority of Ireland (1999) Recommendations for a National Infant Feeding Policy: Food Safety Authority of Ireland Dublin.Google Scholar
Gardner, H, Green, K & Gardner, A (2015) Infant feeding practices of Emirati women in the rapidly developing city of Abu Dhabi, United Arab Emirates. Int J Environ Res Public Health 12, 1092310940.CrossRefGoogle ScholarPubMed
Doub, AE, Moding, KJ & Stifter, CA (2015) Infant and maternal predictors of early life feeding decisions. The timing of solid food introduction. Appetite 92, 261268.CrossRefGoogle ScholarPubMed
Wijndaele, K, Lakshman, R, Landsbaugh, JR, et al. (2009) Determinants of early weaning and use of unmodified cow's milk in infants: a systematic review. J Am Diet Assoc 109, 20172028.CrossRefGoogle ScholarPubMed
Alzaheb, RA (2017) A review of the factors associated with the timely initiation of breastfeeding and exclusive breastfeeding in the Middle East. Clin Med Insights Pediatr 11, 1179556517748912.CrossRefGoogle ScholarPubMed
General Authority for Statistics, Kingdom of Saudi Arabia (2019).Google Scholar
Tang, L, Lee, AH & Binns, CW (2015) Predictors of early introduction of complementary feeding: longitudinal study. Pediatr Int 57, 126130.CrossRefGoogle ScholarPubMed
Camurdan, AD, Ilhan, MN, Beyazova, U, et al. (2008) How to achieve long-term breast-feeding: factors associated with early discontinuation. Public Health Nutr 11, 11731179.CrossRefGoogle ScholarPubMed
Committee on Medical Aspects of Food Policy (1994) Weaning and the weaning diet. Report of the working group on the weaning diet of the committee on medical aspects of food policy. Rep Health Soc Subj 45, 1113.Google Scholar
Baughcum, AE, Burklow, KA, Deeks, CM, et al. (1998) Maternal feeding practices and childhood obesity: a focus group study of low-income mothers. Arch Pediatr Adolesc Med 152, 10101014.CrossRefGoogle ScholarPubMed
Al-Hussaini, A, Bashir, MS, Khormi, M, et al. (2019) Overweight and obesity among Saudi children and adolescents: where do we stand today? Saudi J Gastroenterol 25, 229235.Google ScholarPubMed
Zinner, SH, McGarvey, ST, Lipsitt, LP, et al. (2002) Neonatal blood pressure and salt taste responsiveness. Hypertension 40, 280285.CrossRefGoogle ScholarPubMed
Bernstein, IL (1990) Salt preference and development. Dev Psychol 26, 552.CrossRefGoogle Scholar
Forsyth, JS, Ogston, SA, Clark, A, et al. (1993) Relation between early introduction of solid food to infants and their weight and illnesses during the first two years of life. Br Med J 306, 15721576.CrossRefGoogle ScholarPubMed
Livingstone, MBE, Robson, PJ & Wallace, JMW (2004) Issues in dietary intake assessment of children and adolescents. Br J Nutr 92, S213SS22.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. General characteristics of study participants by total sample and mother's age group

Figure 1

Table 2. Complementary feeding practice by mother's age group

Figure 2

Table 3. Factors associated with the introduction of complementary feeding by age (<17 weeks/≥17 weeks)

Figure 3

Fig. 1. Fluids mothers usually introduce to infants. *Significant differences between the proportion of infants complementary fed at <17 weeks and at ≥17 weeks, using χ2 (significant at P = 0·033).

Figure 4

Fig. 2. Food and ingredients that mothers introduce to their infants by complementary feeding age.