Skip to main content
The American Journal of Clinical Nutrition logoLink to The American Journal of Clinical Nutrition
. 2021 Jan 29;113(3):562–573. doi: 10.1093/ajcn/nqaa351

Formal maternal employment is associated with lower odds of exclusive breastfeeding by 14 weeks postpartum: a cross-sectional survey in Naivasha, Kenya

S B Ickes 1,2,3,, V M Oddo 4,5, H K Sanders 6, R Nduati 7, D M Denno 8,9,10,11, J A Myhre 12, J Kinyua 13, L L Iannotti 14, B Singa 15, C Farquhar 16,17,18, J L Walson 19,20,21,22,23
PMCID: PMC7948888  PMID: 33515015

ABSTRACT

Background

In many low- and middle-income countries, improvements in exclusive breastfeeding (EBF) have stalled, delaying reductions in child mortality. Maternal employment is a potential barrier to EBF.

Objectives

We evaluated associations between maternal employment and breastfeeding (BF) status. We compared formally and non–formally employed mothers in Naivasha, Kenya, where commercial floriculture and hospitality industries employ many women.

Methods

We conducted a cross-sectional survey among mothers (n = 1186) from September 2018 to October 2019 at 4 postpartum time points: at hospital discharge (n = 296) and at 6 wk (n = 298), 14 wk (n = 295), and 36 wk (to estimate BF at 24 wk; n = 297) postpartum. Mothers reported their BF status and reasons for EBF cessation. We used multivariable logistic regression models to test the association between formal maternal employment and 3 outcomes: early BF initiation (within 1 h of birth), EBF at each time point, and continued BF at 9 mo. Models were informed by a directed acyclic graph: a causal diagram used to characterize the relationship among variables that influence the independent (employment) and dependent (BF status) variables.

Results

EBF did not differ by employment status at hospital discharge or at 6 wk postpartum. However, formally employed mothers were less likely than those not formally employed to report EBF at 14 wk (59.0% compared with 95.4%, respectively; AOR: 0.19; 95% CI: 0.10, 0.34) and at 24 wk (19.0% compared with 49.6%, respectively; AOR: 0.25; 95% CI: 0.14, 0.44). The prevalence of continued BF at 36 wk did not differ by group (98.1% for formally employed compared with 98.5% for non–formally employed women; AOR: 0.80; 95% CI: 0.10, 6.08). The primary reasons reported for early EBF cessation were returning to work (46.5%), introducing other foods based on the child's age (33.5%), or perceived milk insufficiency (13.7%).

Conclusions

As more women engage in formal employment in low- and middle-income countries, additional supports to help prolong the period of EBF may be beneficial for formally employed mothers and their children.

Keywords: maternal employment, breastfeeding, diet quality, low- and middle-income countries, infant and young child feeding

Introduction

Exclusive breastfeeding (EBF) for the first 6 mo is among the most effective practices to promote survival during infancy (1–3). The universal scale-up of EBF could prevent over 800,000 deaths annually in children under 5 y (4). EBF reduces the risk of infections among infants, including diarrheal disease and pneumonia, and reduces the breast cancer risk among mothers (2, 4, 5).

In many low- and middle-income countries (LMICs), EBF coverage for the first 6 mo remains below international targets, and improvement has stalled in the most disadvantaged communities (4, 6). Despite nearly universal breastfeeding (BF) initiation in Kenya (62.2% within 1 h and 90.6% within 1 d of birth), only 42% of mothers maintain EBF through the recommended period of 6 mo (7). However, most Kenyan children (90.0%) continue BF for at 1 y (7). Following guidance on Infant and Young Child Feeding (IYCF) practices for HIV-infected women in 2010 (8), EBF promotion efforts have improved and the availability of antiretroviral therapy has increased, leading to improved EBF practices for the HIV-infected population (9).

Over the past 2 decades, there have been sharp increases in the proportion of women in the workforce and shifts from informal to more formalized work among women in LMICs (10, 11). These changes have been, in part, due to economic development strategies aimed at promoting women's employment to improve health and alleviate poverty (12). Approximately 50% of women in LMICs are employed (11).

Data on maternal employment and IYCF practices in LMICs are limited and inconclusive. A recent 49-country study found that formally employed mothers may breastfeed for shorter durations compared to informally employed mothers who work without legal and social protection (13). While maternal employment is the most frequently cited barrier to EBF in LMICs (14), there is conflicting evidence in single-country studies, which may be due to different employment classifications and the nature of the employment and EBF relationship (15, 16). Both behavioral interventions, such as IYCF education, and workplace accommodations, such as paid breaks, hygienic lactation spaces, on-site daycare, and national laws on maternity leave, may mitigate the adverse effects of employment on BF (17–20). In Kenya, current policies require employers to provide lactation breaks and suitable lactation facilities, including refrigerated storage for expressed milk and a paid 3-mo maternity leave (21–23). It is unclear how the type of employment influences BF. Commercial farms have led efforts to implement maternity and BF-support policies in Kenya.

Given the limited evidence and recent policy changes in Kenya, a better understanding of employment and the BF relationship is critical to better target interventions and supports for this population. The objective of this study was to evaluate the associations between formal work and the early initiation of BF, the duration of EBF, and continued BF practices among mothers in Naivasha, Kenya, and to describe factors related to these practices.

Methods

Overview

Between September 2018 and October 2019, we repeatedly conducted cross-sectional surveys at 4 postpartum time points to investigate the associations between maternal employment and BF practices in Naivasha, Kenya. We hypothesized that formal employment would be associated with a lower prevalence and reduced odds of BF at each time point and across each indicator (early initiation of BF at 0 wk; EBF at 0, 6, 14, and 24 wk; predominant BF at 0, 6, 14, and 24 wk; and continued BF at 36 wk).

Study setting

Naivasha is a peri-urban city in Nakuru County, located 100 km north of Nairobi, with a population of ∼355,000 (24). This area contains the largest concentration of commercial flower farms in the country, which are the primary sources of employment in this region. The majority of flower farm employees reside in several densely populated peri-urban informal settlements, with varying access to electricity and sanitation services. Employment within the floriculture industry is characterized by long commuting distances and separation from children, compared to employment in the informal sector (e.g., tailoring, subsistence farming, self-employment, trading), where women have more flexible schedules and BF opportunities (25).

Study participants and recruitment

Mothers were recruited 1–4 d postpartum and at routine infant immunization visits at 6, 14, and 36 wk postpartum at 2 public facilities (the Naivasha Sub-County Referral Hospital and the Karagita Dispensary) and a private facility subsidized by a local floriculture company that serves farmworkers (the South Lake Medical Center). All postpartum women with a live birth admitted to the maternity wards or presenting for immunizations to the health facilities on recruitment days were screened for eligibility. Mothers who were 1–4 d, 5–7 wk, 13–15 wk, or 9 mo (± 1 wk) postpartum were eligible, regardless of past or present child morbidity. Screening did not include evaluating mental health status. Health center staff introduced mothers to the research team. The research team explained the study purpose to all mothers present for immunizations and within the maternity wards through group announcements. Upon recruitment, we obtained written, informed consent from all participants. Surveys were administered verbally by a team of 5 trained research staff in Swahili, English, or another preferred language of the mother, using paper questionnaires. Mothers were eligible to participate once in the cross-sectional survey.

Data collection tools

The survey collected information on 5 domains: 1) household assets and demographics; 2) employment status and benefits; 3) IYCF practices; 4) access to reproductive and other health services; and 5) health status of the child and the mother.

Household assets and demographics

We queried participants about their household assets (house material composition, vehicle, television, mobile phone) and demographics (educational attainment, household income, marital status, household size, parity, religion, and tribe) using questions from the Demographic and Health Survey (7).

Employment status and benefits

We asked mothers about whether they were employed, the type of employment and responsibilities, the name of the employer, the availability of a formal contract, the hours worked, and the availability of maternity leave and other policies to support BF.

IYCF practices

IYCF practices were assessed using standardized questions from the Demographic Health Survey and WHO Indicators (7, 26). Using a 24-h list-based recall method, we recorded the types of liquid, semisolid, and solid foods given during the previous day and the number of BF and other feeding episodes.

Access to reproductive and other health services

Demographic Health Survey questions were used to assess antenatal care utilization, the delivery setting, the type of delivery, and the presence of a skilled attendant at childbirth (7).

Health status of the child and the mother

We assessed child morbidity in the prior 2 wk according to 5 common illnesses and symptoms: diarrhea, pneumonia, fever, malaria, and cough. The HIV status of the mother was self-reported.

The primary anticipated reason for EBF cessation was assessed using a single question with multiple response options (going to work, child refusal, uncomfortable/did not want to, perceived milk insufficiency, pregnant again, baby cries after being breastfed, child age, other). Upon cessation of EBF, we also queried mothers regarding actual reasons why they introduced mixed feeding, defined as the initiation of feeding other liquids and foods along with breastmilk (26). The same multiple response options were provided. The survey also assessed the availability of workplace supports for BF through questions on maternity leave benefits and the availability and use of employer-supported lactation rooms, childcare, and housing. The full survey is available in Supplementary Methods 1.

We examined missing data and replaced missing values by recontacting mothers by phone.

Sample size

To identify a 20% difference in EBF rates at each time point (1–4 d, 6 wk, 14 wk, and 24 wk postpartum), with 80% power and an alpha <0.05, we aimed to recruit a minimum of 124 mothers at each point. We successfully enrolled 296 women at 1–4 d postpartum, 298 women at 6 wk postpartum, 295 women at 14 wk postpartum, and 297 women at 36 wk postpartum who reported retrospectively to 24 wk postpartum. This higher sample size increased power to 96.4% for EBF, 96.4% for early initiation, and 99.9% for detecting a 20% difference in these outcomes between employment groups. Our initial recruitment approach did not use employment as a screening factor, which resulted in a higher proportion of non–formally employed mothers. Thus, we focused later recruitment on formally employed mothers at each time point, resulting in higher recruitment numbers than initially planned.

Primary independent variable

Maternal employment status was ascertained by self-report. We first asked women about their current employment or, if mothers were not working and were within 6 wk postpartum, about their recent employment status. Mothers were then asked about the type of occupation, the number of hours worked per week, and the existence of a contract to be further classified as formally, informally, or self-employed. We classified employment as formal if women worked for a registered employer (e.g., a commercial farm, business, company, school, health-care facility), worked ≥20 h/wk, and received regular compensation. For mothers currently on maternity leave (recruited at 0 and 6 wk postpartum), employment type was classified based on the type of work before delivery. Mothers were classified as not employed if they indicated that they reported no current employment. If mothers were employed during their pregnancies, but indicated that they did not intend to return to work and were not receiving maternity leave benefits, they were classified as not employed. In the study context, women usually work through 36 wk of pregnancy.

Primary dependent variables

Our dependent variables encompassed 3 BF indicators: 1) early initiation of BF; 2) EBF or predominant BF at 6, 14, and 24 wk postpartum (coded as separate variables in the analysis); and 3) continued BF at 9 mo postpartum. Early initiation of BF was defined as BF within 1 h of childbirth (26). EBF was defined as feeding breastmilk only with no other liquids or solids (26) from childbirth through the time point of data collection. EBF duration, defined as the number of weeks of reported EBF, was measured retrospectively by mothers who were recruited at 36 wk. These mothers were considered to have been EBF at 6 mo if only breastmilk was fed through 24 wk of age. To establish conservative estimates of BF status, we applied a modified approach to the WHO method to determine BF status. BF status was determined by the IYCF practices during the previous 24 h, as well as by assessing the last week when mothers gave breastmilk exclusively. Thus, a mother who was EBF during the previous day, but who fed infant formula in the previous week, was classified as not EBF. We classified children as predominantly breastfed if they were given breastmilk along with juice, water, or other liquids, including medicines and vitamins/minerals, but not milk or semisolid or other foods through the specified time (26). Continued BF at 9 mo was defined as any BF among children in this age group (26).

Minimizing bias

We attempted to minimize social desirability or recall bias in the assessment of BF outcomes by including multiple questions about BF duration and exclusivity. We assessed EBF duration, the week at which other foods and drinks were first consumed, and the child's diet in the 24 h preceding the survey, using the validated IYCF feeding practices tool (26). Vitamin or mineral supplements were not assessed. We sought to minimize temporal changes in BF practices by completing study recruitment over 13 mo. To reduce the likelihood of selection bias, we restricted our recruitment to 3 health facilities that represented 3 levels of the health-care system and we recruited women without prior knowledge of their socio-demographic factors. The research team received training on responsible conduct in research, survey procedures, and anthropometric assessments. Reporting bias related to maternal employment was minimized by describing the purpose of the study as seeking to identify opportunities to better support mothers by understanding the challenges they encounter in feeding their infants. The study was not promoted as an employment study. For questions related to reasons for cessation of EBF, self-reported answers were coded into categories. “Returning to work” was indicated if a participant responded that this was a reason for EBF cessation; it was not provided as an option before the respondent offered a response.

Statistical analysis

Confounders

To identify confounding variables, we constructed a directed acyclic graph (Supplemental Figure 1): a causal diagram used to characterize the relationships among variables that influence the primary independent variable (employment) and the dependent variable (BF status) and are not on the causal pathway (27). Informed by existing literature on the employment–BF relationship and influences of BF in the study context, the same set of confounders were used for all models (13, 16, 28). These include maternal age (years), marital status (married or not), maternal education (some secondary or higher versus less than secondary), tribal affiliation (Kikuyu, Luhya, Kiisi, or other), child morbidity (presence of diarrhea, fever, malaria, cough, or fever in the previous 2 wk), cesarean delivery (versus vaginal birth), and HIV status (positive or negative).

We assessed the linearity of continuous variables (maternal age, maternal education) with outcomes by specifying disjointed indicator variables. Household income was hypothesized as a mediator of the association a priori. Maternal employment would likely result in increased individual-level income, thus increasing household wealth and, subsequently, influencing BF practices. However, wealth prior to workforce entry could be a plausible confounder of the employment–EBF association (i.e., household wealth could influence whether a woman works or not). In these cross-sectional data, we cannot establish the temporality of wealth and workforce entry. Therefore, wealth was considered a mediator and was not included as a covariate in our models (29).

We employed separate multivariable logistic regression models to test the association between maternal employment (formally employed versus informally employed, self-employed, and not employed) and each BF variable (early initiation of BF and EBF, predominant BF, and continued BF at 9 mo).

Sensitivity analyses

In sensitivity analyses, we compared BF outcomes by employment status when restricting formal employment to only mothers employed at flower farms or in other commercial agricultural farms (n = 398). In addition, we adjusted for multiple comparisons using the Holm-Bonferroni sequential correction, given that we assessed associations for multiple outcomes across 4 time points (30). First, results for both chi-square tests and linear regressions were ordered from the smallest P value to the largest P value. Second, the second-smallest P value was corrected with a Bonferroni approach [(number of tests − order of test + 1) × P value]. The correction procedure stops when the first nonsignificant test is obtained (30).

In our main analyses, the alpha was set to 0.05. STATA version 14.1 (StataCorp LP) was used to conduct all analyses. The study adhered to the Strengthening Research for Observational Studies in Epidemiology (STROBE) guidance (Supplementary Methods 2) (31). All study procedures were approved by the Kenya Medical Research Institute Scientific Ethical Review Unit (study number KEMRI/SERU/CCR/0112/3712) and the Wheaton College Institutional Review Board (study number 3712).

Results

Descriptive results

We approached 1198 mothers. There were 12 eligible mothers who refused participation; of these, 9 stated time constraints and the other 3 did not provide a reason. In total, 1186 mothers participated in the survey (n = 296 at 0 wk, n = 298 at 6 wk, n = 295 at 14 wk, and n = 297 at 36 wk).

Figure 1 illustrates the classification of maternal employment and the size of the final analytic sample. The final analytic sample included 2 groups: 1) formally employed mothers (n = 564); and 2) informally employed, nonemployed, and self-employed mothers (n = 622). BF practices were not statistically significantly different among informally employed, self-employed, and nonemployed women. Therefore, these women were aggregated into a single category of “non–formally employed” mothers (n = 622; Supplemental Table 1).

FIGURE 1.

FIGURE 1

Flowchart of final analytic sample selection and classification by maternal employment category.

Most participating mothers were married, and they had a mean of 2.2 children (Table 1). The mean age was 27.2 y. Approximately one-third (32.7%) of the mothers had at least some primary education, while nearly half (48.7%) had at least completed secondary education. The majority reported having electricity at their homes (91.2%), 42.8% reported a drinking water source at the household premises, and only 15.0% owned their home. Over half of employed mothers lived >5 km from their workplace. Most reported facility deliveries (97.8%), 4 or more antenatal care visits (64.3%), and receipt of BF counseling from a health-care worker (79.8%).

TABLE 1.

Descriptive characteristics of participants

All participants, n = 1186, n (%) Formally employed, n = 564, n (%) Not formally employed, n = 622, n (%) P value
Child age
 1–4 d 296 (25.0) 128 (22.7) 168 (27.0) 0.086
 6 wk 298 (25.1) 134 (23.8) 164 (26.4) 0.301
 14 wk 295 (24.9) 144 (25.5) 151 (24.3) 0.618
 36 wk/9 mo 297 (25.0) 158 (28.0) 139 (22.3) 0.0252
Child morbidity in the past 2 wk
 Any fever, diarrhea, cough, or lower respiratory symptoms1 369 (31.1) 176 (31.2) 193 (31.0) 0.945
Maternal age
 15–19 y 18 (1.5) 0 (0) 18 (2.9) <0.0012
 20–24 y 415 (35.0) 159 (28.2) 256 (41.2) <0.0012
 25–30 y 344 (29.0) 181 (32.1) 163 (26.2) 0.026
 >30 y 409 (34.5) 224 (39.7) 185 (29.7) <0.0012
Maternal education
 None 12 (1.0) 5 (0.9) 7 (1.1) 0.681
 Any primary to completed primary 388 (32.7) 167 (29.6) 221 (35.5) 0.0302
 Any secondary to completed secondary 578 (48.7) 261 (46.3) 317 (51.0) 0.107
 Above secondary (some university, diploma, completeduniversity) 208 (17.5) 131 (23.2) 77 (12.4) <0.0012
Tribe
 Kikuyu 595 (50.2) 206 (36.5) 389 (62.5) <0.0012
 Luyha 255 (21.5) 168 (29.8) 87 (14.0) <0.0012
 Kiisi 101 (8.5) 67 (11.9) 34 (5.5) <0.0012
 Luo 86 (7.3) 49 (8.7) 37 (5.9) 0.070
 Other: Kalenjin, Kamba, Maasai, Turkana, Meru, Pokot 149 (12.6) 74 (13.1) 75 (12.1) 0.521
Religion
 Christian 1170 (98.7) 559 (99.1) 611 (98.2) 0.189
Marital status
 Married/living with partner 974 (82.1) 476 (84.4) 498 (80.1) 0.052
 Single/divorced/separated/widowed 212 (17.9) 88 (15.6) 124 (19.9) 0.052
HIV status
 Know HIV status 1181 (99.6) 560 (99.3) 621 (99.8) 0.270
 HIV positive 100 (8.4) 51 (9.0) 49 (7.9) 0.453
Parity
 1 370 (31.2) 155 (27.5) 215 (34.6) 0.0092
 2–4 772 (65.1) 393 (69.7) 379 (60.9) 0.0022
 5 or more 44 (3.7) 16 (2.8) 28 (4.5) 0.130
Distance to drinking water
 On premises 509 (38.8) 221 (39.2) 288 (46.3) 0.0112
 <1 km 585 (49.3) 304 (53.9) 281 (45.2) 0.0032
 ≥1 km 92 (7.8) 39 (6.9) 53 (8.5) 0.302
Electricity access in household 1081 (91.2) 542 (96.1) 539 (86.7) <0.0012
Monthly household income
 ≤$50 259 (21.8) 80 (14.2) 179 (28.8) <0.0012
 $51 to $150 569 (48.0) 254 (45.0) 315 (50.6) 0.054
 $151 to $400 287 (24.2) 182 (32.3) 105 (16.9) <0.0012
 >$400 71 (6.0) 48 (8.5) 23 (3.7) <0.0012
Health service factors
 Facility-based delivery 1160 (97.8) 553 (98.0) 607 (97.6) 0.588
 Private facility delivery 219 (18.5) 148 (26.2) 71 (11.4) 0.028
 Attended 4 or more antenatal visits 763 (64.3) 389 (69.0) 374 (60.1) 0.0022
 Counseled on breastfeeding by a health worker afterdelivery 947 (79.8) 462 (81.9) 485 (78.0) 0.091
 Cesarean delivery 160 (13.5) 86 (15.3) 74 (11.9) 0.087
 Preterm birth: <37 weeks of gestation 50 (4.2) 28 (5.0) 22 (3.5) 0.222
1

Lower respiratory symptoms included wheezing, fast breathing, or chest in-drawing/retractions during inhalation.

2

P < 0.05, group differences are statistically significant.

Availability of workplace supports

Most formally employed mothers worked at commercial flower or other agricultural farms (70.6%). We examined workplace supports among all formally employed mothers (n = 564), as well as among a subgroup restricted to those who worked at commercial farms (n = 398). Among all formally employed mothers (n = 564), 16.9% had on-site housing provided by their workplace (Table 2). Few formally employed mothers (9.2%) reported the availability of a childcare facility at their workplace, including those employed at commercial farms (10.8%). Also, of those who reported access to such childcare facilities, few indicated visiting them during working hours to breastfeed (9.0% among all formally employed mothers and 5.3% among commercial farmworkers). Very few (2.3%) formally employed mothers (1.7% of farmworkers) reported the availability of private lactation rooms at their workplace (Table 2). Among all formally employed mothers, most (92.9%) reported that their employer provides maternity leave and 75.1% indicated that this leave was paid. The mean ± SE maternity leave lengths were 13.0 ± 1.0 and 13.2 ± 1.2 wk among formally employed and commercial farmworkers, respectively.

TABLE 2.

Workplace data of cross-sectional survey sample among formally employed mothers

Number Percent
Distance to maternal workplace, among formally employed mothers,n = 564
 <1 km 100 17.7%
 1 to <5 km 96 17.0%
 5 to 10 km 286 50.7%
 >10 km 82 14.5%
On-site housing at workplace
 Formally employed, n = 564 95 16.9%
  Among commercial farmworkers,1  n = 398 69 17.3%
Use of childcare among formally employed mothers, n = 564 175 31.0%
 Among commercial farmworkers, n = 398 154 38.7%
Availability of childcare at workplace
 Formally employed, n = 564 52 9.2%
  Among commercial farmworkers, n = 398 43 10.8%
Visit on-site childcare during work
 Formally employed, n = 564 51 9.0%
  Among commercial farmworkers, n = 398 22 5.5%
Availability of private lactation rooms at workplace
 Formally employed, n = 564 13 2.3%
  Among commercial farmworkers, n = 398 7 1.7%

1Commercial farmworkers are a subset of formally employed mothers (n = 398).

Early initiation, EBF, and predominant BF

Two-thirds (65.6%) of formally employed mothers reported early initiation of BF, compared to 75.6% of non–formally employed mothers (Table 3). At 1–4 d postpartum, >96% of mothers in both groups reported practicing EBF. At 6 wk postpartum, the prevalence of EBF was 94.0% among formally employed mothers and 86.6% among those without formal employment.

TABLE 3.

Prevalence of early initiation, exclusive breastfeeding, and predominant breastfeeding by maternal employment status1

Formally employed,2n = 564 Not formally employed, n = 622 Formally employed in flower farm/commercial agriculture, n = 398
BF indicator Predominant BF or EBF3 BF indicator Predominant BF or EBF BF indicator Predominant BF or EBF
n Prevalence ± SE Prevalence ± SE n Prevalence ± SE Prevalence ± SE n Prevalence ± SE Prevalence ± SE Total n
Early initiation at 1–4 d4 128 65.6% ± 0.04% Not applicable 168 75.6% ± 0.03 Not applicable 85 72.9% ± 0.05 Not applicable 296
1–4 d, EBF 128 97.7% ± 0.01% 99.2% ± 0.01% 168 98.8% ± 0.01% 100 ± 0.00 85 96.4% ± 0.02% 98.8% ± 0.01% 296
6 wk, EBF 134 94.0% ± 0.02% 97.8% ± 0.01% 164 86.6% ± 0.03% 98.2 ± 0.01 82 91.4% ± 0.03% 96.3% ± 0.02% 295
14 wk, EBF 144 48.6% ± 0.04% 59.0% ± 0.04% 151 80.8% ± 0.04% 93.4 ± 0.02 106 37.7% ± 0.04% 48.1% ± 0.05% 297
24 wk,5 EBF 158 17.7% ± 0.03% 19.0% ± 0.01% 139 48.9% ± 0.03% 49.6 ± 0.04 128 16.8% ± 0.03% 18.4% ± 0.02%
Continued BF at 9 mo 158 98.1% ± 0.01% Not applicable 139 98.5% ± 0.01% Not applicable 128 97.6% ± 0.01% Not applicable 298
1

BF, breastfeeding; EBF, exclusive breastfeeding.

2Includes mothers employed at flower or other commercial farms.

3Predominant breastfeeding was defined as breastmilk along with juice, water, or other liquids, including medicines and vitamins/minerals, but not milk or semisolid or other foods in the 24 h preceding the survey (26).

4Early initiation was defined as BF within the first hour after delivery.

5EBF at 24 wk was estimated from retrospective recall from a 36-wk/9-mo immunization visit.

At 14 wk postpartum, formally employed mothers had a lower prevalence of EBF compared to non–formally employed mothers (48.6% versus 80.8%, respectively). Similarly, at 24 wk, we observed a lower prevalence among formally employed mothers (17.7%) compared to non–formally employed mothers (48.9%).

At 1–4 d postpartum, 99.2% of formally employed and 100% of non–formally employed mothers were practicing predominant BF, and over 96% of all mothers were predominantly BF at 6 wk postpartum (Table 3). However, by 14 wk postpartum, only 59.0% of formally employed mothers were predominantly BF, as compared to 93.4% of non–formally employed mothers. At 24 wk, 19.0% of formally employed mothers were predominantly or exclusively BF compared to 49.6% of non–formally employed mothers. The prevalence of predominant or EBF was lower among flower farm/agriculture workers, with the most substantial difference observed at 14 wk (48.1% of farm/agriculture workers compared to 95.4% of non–formally employed mothers; P < 0.001).

Continued BF at 9 mo

At 36 wk, the prevalence of continued BF was ≥98% in both groups.

Adjusted comparisons

Table 4 reports the unadjusted and adjusted comparisons of BF practices by employment status. Employment status was not associated with EBF at 1–4 d postpartum (OR: 0.62; 95% CI: 0.08, 4.70) nor at 6 wk postpartum (OR: 2.20; 95% CI: 0.87, 5.53). However, by 14 wk and 24 wk postpartum, formally employed mothers had 81% (OR: 0.19; 95% CI: 0.10, 0.34) and 75% (OR: 0.25; 95% CI: 0.14, 0.44) lower odds of EBF, respectively, compared to their non–formally employed counterparts. The odds of early initiation at 1–4 d (OR: 0.63; 95% CI: 0.35, 1.14) and continued BF at 36 wk (OR: 0.80; 95% CI: 0.10, 6.08) did not differ by group.

TABLE 4.

Unadjusted and multivariable models of early initiation, exclusive breastfeeding, and predominant breastfeeding by maternal employment status1

Unadjusted early initiation and EBF Early initiation and EBF2 Predominant or exclusive BF2,3
n OR 95% CI P value n AOR 95% CI P value n AOR 95% CI P value
1–4 d, early initiation 296 0.62 0.37, 1.02 0.061 2954 0.63 0.35, 1.14 0.13
1–4 d 296 0.50 0.08, 3.05 0.454 2675 0.62 0.08, 4.70 0.65 NA6 1.00 NA NA
6 wk 298 2.44 1.05, 5.70 <0.01 2974 2.20 0.87, 5.53 0.10 2377 0.71 0.12, 4.28 0.71
14 wk 295 0.22 0.13, 0.39 <0.01 2944 0.19 0.10, 0.34 <0.01 2944 0.09 0.04, 0.19 <0.01
24 wk8 297 0.22 0.13, 0.38 <0.01 2954 0.25 0.14, 0.44 <0.01 2954 0.26 0.15, 0.45 <0.01
Continued BF at 36 wk 297 0.75 0.12, 4.5 0.759 2399 0.80 0.10, 6.08 0.83
1

BF, breastfeeding; EBF, exclusive breastfeeding; NA, not applicable.

2Models compare being formally employed with not being formally employed in women and control for maternal age, maternal education, HIV status, delivery type, child morbidity, parity, delivery setting, marital status, and tribal affiliation.

3Predominant breastfeeding was defined as breastmilk along with juice, water, or other liquids, including medicines and vitamins/minerals, but not milk or semisolid or other foods in the 24 h preceding the survey (26).

4Missing data due to unknown HIV status (1 at 1–4 d, 1 at 6 wk, 1 at 14 wk, 2 at 24 wk/36 wk).

5The 29 observations dropped because of HIV status, delivery setting, and morbidity predict success perfectly.

6Model at 1–4 d could not be calculated because of a lack of variation in the outcome.

7The 60 observations dropped because of HIV status (n = 36) and delivery type (n = 24) predict the outcome perfectly.

8EBF at 24 wk estimated from retrospective recall from a 36-wk immunization visit.

9The 56 observations dropped because of marital status predict the outcome perfectly.

At 6 wk postpartum, the odds of predominant or exclusive BF were the same among formally employed versus non–formally employed mothers (OR: 0.71; 95% CI: 0.12, 4.28). At 14 wk and 24 wk postpartum, formally employed mothers had 91% (OR: 0.09; 95% CI: 0.04, 0.19) and 74% (OR: 0.26; 95% CI: 0.15, 0.45) lower odds, respectively, of predominant or exclusive BF, compared to their non–formally employed counterparts.

Sensitivity analysis

Supplemental Table 2 reports the adjusted comparisons of BF practices in an analysis restricted to mothers formally employed at flower farms or in other commercial agricultural farms and compared to those who are not formally employed. There were no meaningful differences in outcomes in this analysis compared to the main analysis of all formally employed women.

The results did not change after adjustment for multiple comparisons.

Reasons for EBF cessation

The most common reported reason for discontinuing EBF was returning to work (46.5%), followed by the belief that it is appropriate to introduce other foods based on the child's age (33.5%) and perceived milk insufficiency (13.7%; Figure 2 ). Mothers of 14-wk-old children were more likely to report returning to work as the primary reason for EBF cessation than mothers surveyed at 9 mo (60.6% ± 0.05 compared with 38.9% ± 0.03, respectively; P < 0.001). Among the 746 women who were still practicing EBF, mothers were asked what would cause them to eventually introduce other foods or liquids to their child's diet. The main expected reasons were child age (i.e., when the child turned 6 mo; 53.2%) and returning to work (39.7%; Figure 3).

FIGURE 2.

FIGURE 2

Reported reasons for introducing mixed feeding (n = 440).

FIGURE 3.

FIGURE 3

Reported reasons for anticipated mixed feeding among mothers still practicing EBF (n = 746). EBF, exclusive breastfeeding.

Discussion

Results from this study indicate that most mothers had initiated BF within 1 h of birth and were practicing EBF at the time of discharge after childbirth, irrespective of employment status. The prevalence of EBF declined somewhat by 6 wk, regardless of employment status. However, the prevalence of EBF (and predominant BF) among formally employed mothers dropped in half by 14 wk, coinciding with the end of the federally protected 3-mo maternity leave. There were still lower odds of EBF among formally compared to non–formally employed mothers at 24 wk, at which point less than one-fifth of formally employed mothers were EBF compared to almost half among those who were not formally employed. It was noteworthy that mothers described returning to work after maternity leave as the primary reason for introducing liquids and foods, ahead of perceived milk insufficiency, which is a leading barrier to EBF in other contexts (32).

These findings from a semi-urban region of Kenya where many women work for commercial flower farms are consistent with other data throughout LMIC contexts, where similarly high rates of early initiation of BF and lower odds of EBF after 3 mo are practiced among formally employed mothers (13). A recent study in Ethiopia that compared the EBF prevalence by maternal employment status and included mothers working for government and nongovernmental agencies found a lower prevalence of EBF among employed mothers after 3 mo. The delivery setting and receipt of BF education did not explain differences in the odds of EBF between 3 and 5 mo (33). The prevalence estimates of EBF in our study are consistent with those in national surveys in Kenya that report the median duration of EBF to be 3.3 mo and show a 42% prevalence of EBF between 4 and 5 mo (7).

Our study also demonstrated that most formal employment settings, including commercial farms, lacked private lactation rooms. Also, there is a lack of availability of childcare facilities at workplaces; among mothers who do have access to such facilities, very few report visiting these facilities to breastfeed during working hours. Notably, our study was conducted soon after the Health Act in Kenya that mandated private lactation spaces and flexible work schedules to support BF (23). This act was approved in March 2017, 6 mo before data collection began for this survey. Most commercial farms that employed mothers in our study had not yet complied with this policy, based on the low percentage of mothers reporting the availability of on-site lactation rooms.

Improving BF practices requires multilevel supports, including legislation, BF promotion, peer or health worker BF counseling, workplace support policies and services, and addressing social norms (9, 34–37). Maternal employment is considered to be a component of mothers’ “resources” for the provision of nutrition and health behaviors that contributes to and reflects women's autonomy (38–40). Formal employment is associated with improved complementary practices in the first 2 y, especially related to dietary diversity and meal frequency (13). When modeled through autonomy, the employment and dietary association is also positive and significant, as demonstrated in a recent study in Bangladesh and Vietnam (38). Notably, a study in Indonesia that included a multidimensional measure of women's empowerment, with labor force participation as 1 component, only found significant associations of reduced EBF with employment status, but not with other empowerment variables (41). However, greater autonomy has also been linked with poorer BF outcomes (42). While strengthened autonomy enables mothers to make favorable decisions for children and to spend more on nutrition (43), it may also create unintended adverse nutrition effects through reduced time with children and using childcare that is unsupportive of EBF or healthful complementary feeding (44). Given that many countries do not yet substantially align with the International Code of Marketing of Breastmilk Substitutes in their legal measures (45), it is possible that the autonomy and increased income associated with employment may unintentionally increase the purchasing of breastmilk substitutes. Female empowerment through formal employment should continue without neglecting improved structural support for EBF.

Breastfeeding promotion efforts and the establishment of policies to achieve global targets should take into account the workplace setting, particularly within industries where lactation support is not yet normative. It is noteworthy that in this population of formally employed mothers, the availability of BF education and health-seeking behaviors did not attenuate the barriers to EBF that result from formal employment. As fewer than half of nonemployed and informally employed mothers practice EBF at the recommended period of 24 wk, this group is also in need of further BF supports, especially given the potentially lower access to health insurance and health services in this population (46).

Kenya has undertaken several national BF strategies, in addition to recent maternity leave and workplace lactation support legislation. The Baby-Friendly Hospital Initiative (BFHI) was successful in promoting BFHI certifications between 1994 and 2008, with 69% of targeted facilities designated as baby friendly in 2008. By 2010, only 11% of facilities qualified for this designation (47). In 2012, Kenya passed the Breast Milk Substitutes Act and implemented the Maternal and Infant and Young Child Nutrition Strategy, which guided facility-based BF promotion through 2017. To complement these facility-based efforts, Kenya also championed the Baby-Friendly Community Initiative (BFCI) in 2016, which trained and deployed community health workers as BF promoters. Despite these efforts, continued support for the BFHI has proven challenging, and linkages between facility and community BF promotion strategies have been weak (47). Health worker training and the provision of small incentives to motivate community health workers have been suggested to improve the implementation of BFHI and BFCI in Kenya (48). While BF counseling—through facilities and communities—can effectively increase the duration of EBF, the impact of this strategy depends on the counseling quality and the relationship between the counselor and mother (49). A lack of training and misconceptions about optimal BF practices among health workers can diminish counseling quality through inconsistent messaging and may increase mothers’ distrust of counselors (50). Furthermore, one-off exposures to BF counseling may be insufficient; 4 to 8 sessions are optimally needed across the antenatal and postnatal periods (49, 51).

Limitations and strengths

The strengths of the study include a large sample size, robust examination of confounding factors, and recruitment of a representative sample across multiple time points. However, there were several limitations. First, because of the cross-sectional study design, we cannot make any causal inferences. However, we hypothesize that employment is a durable social and economic characteristic that precedes BF practices. Moreover, while a cohort study offers the advantages of longitudinal trajectories of BF status according to employment type, the high degree of migration out of the study catchment area meant that maintaining contact with mothers over 6 or more months was not feasible in this setting. Since many mothers seek perinatal and postnatal care at a variety of health-care settings within the district, maintaining contact with the same mothers over 6 mo would pose considerable challenges. Second, BF practices at 24 wk were estimated using retrospective recall at 36 wk. In the study context, mothers do present to maternal and child health clinics at 24 wk, but do so for anthropometric check-ups and not immunizations, representing a sample of mothers who are either more motivated in caregiving or whose children are more likely to be unhealthy. While mothers may have inaccurately recalled BF practices from 12 wk prior, we recruited mothers at 36 wk because this visit was part of the regular immunization sequence, increasing the likelihood that mothers at each time point represented the same source population. The use of multiple questions (week of last exclusive BF, week of introducing complementary foods and other liquids) to estimate the BF status at 24 wk attempted to mitigate this potential recall bias. Additionally, due to some missing demographic data, the adjusted models omit some observations. The pattern of missing data was random, and therefore would not be expected to introduce selection bias in the analysis.

We cannot rule out the possibility of recall and social desirability bias, given the self-reported assessments of BF practices. Our study used a different method for assessing BF than most national surveys; we included the last week when mothers gave breastmilk exclusively, along with the feeding practices from the previous 24 h, to determine BF status. However, the low prevalence of EBF at 6 mo is similar to the prevalence rates reported in national surveys. We included the category “predominant or exclusive BF” in an adjusted analysis to help demonstrate that more children in both groups are BF predominantly or exclusively when we broaden the criteria. Use of this definition also demonstrates that the trend of lower odds of predominant or exclusive BF among formally employed mothers at 14 and 24 wk still stands.

Some of the findings may be specific to the study setting, which should be considered when interpreting the external validity. The study sample included mothers who presented with their children for immunizations, mainly from government or company-subsidized health facilities. Employed mothers commuted a relatively long distance to work, as the median distance between home and work was between 5 and 10 km. Many women commuted via company buses that do not generally provide opportunities to return home for nursing breaks in the middle of shifts. The 2017 Health Act makes provision for a lactation room where mothers can express breastmilk and mandates refrigeration to store expressed milk (23). However, mothers in this study had limited access to these benefits. The women included in this study reported high rates of maternal health services utilization and exposure to ≥1 postpartum BF counseling session with a health worker. It is noteworthy that despite these opportunities, 83.3% of formally employed and 51.1% of non–formally employed mothers do not practice EBF for the recommended duration. Finally, the primary type of employment in the study sample—commercial agriculture—may pose an additional challenge to EBF that does not apply to other forms of work, as mothers may be concerned about transmitting pesticides through milk expressed during work (52, 53).

In conclusion, formally employed mothers in Naivasha, Kenya, experience shorter durations of EBF by 14 wk postpartum as compared to mothers who are not formally employed, and this association continues at 24 wk. Additional supports for formally employed mothers to help prolong the period of EBF may be beneficial to improve child health. A follow-up evaluation is needed to understand whether recent legislation in Kenya will help to address employment-related BF disparities.

Supplementary Material

nqaa351_Supplemental_File

ACKNOWLEDGEMENTS

We wish to thank Ange Hellen Sankaine Lemein for leading the data collection and translation, Dana Brody for assisting in data collection and cleaning, and Dr. Angeline Ithondeka, Medical Superintendent of Naivasha District Hospital, for study oversight and support.

The authors’ responsibilities were as follows—SBI, RN, DMD, CF, JAM, BS, LLI, JK, VMO, JLW: designed the research; SBI: conducted the research, analyzed the data, wrote the paper, and had primary responsibility for the final content; HKS: supported data collection, cleaning and analysis; and all authors: assisted in interpretation of the analysis, provided critical feedback on the manuscript, and read and approved the final manuscript.

The authors report no conflicts of interest.

Notes

This study was supported by the National Institutes of Health Fogarty International Center (grant number K01TW010827).

Supplemental Tables 1 and 2 and Supplemental Figure 1 are available from the “Supplementary data” link in the online posting of the article and from the same link in the online table of contents at https://academic.oup.com/ajcn/.

Abbreviations used: BF, breastfeeding; BFCI, Baby-Friendly Community Initiative; BFHI, Baby-Friendly Hospital Initiative; EBF, exclusive breastfeeding; IYCF, Infant and Young Child Feeding; LMIC, low- and middle-income country.

Contributor Information

S B Ickes, Wheaton College Department of Applied Health Science, Wheaton, IL, USA; University of Washington Department of Health Services, Seattle, WA, USA; University of Washington Department of Global Health, Seattle, WA, USA.

V M Oddo, University of Washington Department of Health Services, Seattle, WA, USA; University of Illinois Chicago, Department of Kinesiology and Nutrition, Chicago, IL, USA.

H K Sanders, Wheaton College Department of Applied Health Science, Wheaton, IL, USA.

R Nduati, University of Nairobi Department of Pediatrics and Child Health, Nairobi, Kenya.

D M Denno, University of Washington Department of Health Services, Seattle, WA, USA; University of Washington Department of Global Health, Seattle, WA, USA; University of Washington Department of Pediatrics, Seattle, WA, USA; Childhood Acute Illnesses Network (CHAIN), Nairobi, Kenya.

J A Myhre, Naivasha Sub-County Referral Hospital and Serge East Africa, Naivasha, Kenya.

J Kinyua, Kenya Medical Research Institute, Nairobi, Kenya.

L L Iannotti, Washington University in St. Louis Brown School, St. Louis, MO, USA.

B Singa, Kenya Medical Research Institute, Nairobi, Kenya.

C Farquhar, University of Washington Department of Global Health, Seattle, WA, USA; University of Washington Department of Medicine (Allergy and Infectious Disease), Seattle, WA, USA; University of Washington Department of Epidemiology, Seattle, WA, USA.

J L Walson, University of Washington Department of Global Health, Seattle, WA, USA; University of Washington Department of Pediatrics, Seattle, WA, USA; Childhood Acute Illnesses Network (CHAIN), Nairobi, Kenya; University of Washington Department of Medicine (Allergy and Infectious Disease), Seattle, WA, USA; University of Washington Department of Epidemiology, Seattle, WA, USA.

References

  • 1. Jones  G, Steketee  RW, Black  RE, Bhutta  ZA, Morris  S; Bellagio Child Survival Study Group . How many child deaths can we prevent this year?  Lancet. 2003;362:65–71. [DOI] [PubMed] [Google Scholar]
  • 2. Liu  L, Oza  S, Hogan  D, Chu  Y, Perin  J, Zhu  J, Lawn  JE, Cousens  S, Mathers  C, Black  RE. Global, regional, and national causes of under-5 mortality in 2000–15: An updated systematic analysis with implications for the Sustainable Development Goals. Lancet. 2016;388(10063):3027–35. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Ogbo  F, Agho  K, Ogeleka  P, Woolfenden  S, Page  A, Eastwood  J; Global Child Health Research Interest Group . Infant feeding practices and diarrhea in sub-Saharan African countries with high diarrhoea mortality. PLOS One. 2017;12;e0171792. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Victora  CG, Bahl  R, Barros  AJD, França  GVA, Horton  S, Krasevec  J, Murch  S, Sankar  MJ, Walker  N, Rollins  NC; Lancet Breastfeeding Series Group . Breastfeeding in the 21st century: Epidemiology, mechanisms, and lifelong effect. Lancet North Am Ed. 2016;387(10017):475–90.. doi:10.1016/S0140-6736(15)01024-7. [DOI] [PubMed] [Google Scholar]
  • 5. Bhutta  ZA, Das  JK, Rizvi  A, Gaffey  MF, Walker  N, Horton  S, Webb  P, Lartey  A, Black  RE; Lancet Nutrition Interventions Review Group, the Maternal and Child Nutrition Study Group . Evidence-based interventions for improvement of maternal and child nutrition: What can be done and at what cost?  Lancet North Am Ed. 2013;382(9890):452–77.. doi:10.1016/S0140-6736(13)60996-4. [DOI] [PubMed] [Google Scholar]
  • 6. World Health Organization . Global nutrition targets 2025: Policy brief series (WHO/NMH/NHD/14.2). Geneva, Switzerland: World Health Organization; 2014. [Google Scholar]
  • 7. Kenya National Bureau of Statistics (KNBS) and IRC Macro . 2014 Kenya demographic and health survey: Final report. Rockville, MD; 2015. [Google Scholar]
  • 8. World Health Organization . Guidelines on HIV and infant feeding. Geneva, Switzerland: World Health Organization; 2010. [Google Scholar]
  • 9. Bosire  R, Betz  B, Aluiso  A, Hughes  JP, Nduati  R, Kiari  J, Chohan  BH, Merkel  M, Lohman-Paynem John-Stewart  G, Farquahr  C. High rates of exclusive breastfeeding in both arms of a peer counseling study promoting EBF among HIV-infected Kenyan women. Breastfeeding Med. 2016;11:53–63. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Adair  L, Guilkey  D, Bisgrove  E, Gultiano  S. Effect of childbearing on Filipino women's work hours and earnings. J Popul Econ. 2002;15:625–45. [Google Scholar]
  • 11. Head  S, Zweimueller  S, Marchena  C, Hoel  E. Women's lives and challenges: Equality and empowerment since 2000. Rockville, MD: ICF International; 2014. [Google Scholar]
  • 12. World Bank . Adolescent girls initiative, the economic empowerment of adolescent girls and young women: Status of pilot implementation. [Internet]. 2014. Available at: http://www.worldbank.org/en/programs/adolescent-girls-initiative. [Google Scholar]
  • 13. Oddo  VM, Ickes  SB. Maternal employment in low- and middle-income countries is associated with improved infant and young child feeding. Am J Clin Nutr. 2018;107(3);335–44. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Balogun  OO, Dagvadorj  A, Anigo  KM, Ota  E, Sasaki  S. Factors influencing breastfeeding exclusivity during the first 6 months of life in developing countries: A quantitative and qualitative systematic review. Matern Child Nutr. 2015;11(4);433–51., doi: 10.1111/mcn.12180. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Lesorogol  C, Bond  C, Dulience  SJL, Iannotti  L  Economic determinants of breastfeeding in Haiti: The effects of poverty, food insecurity, and employment on exclusive breastfeeding in an urban population. Matern Child Nutr. 2018;14(2), doi: 10.1111/mcn.12524. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Ahmed  KY, Page  A, Arora  A, Ogbo  FA. Trends and determinants of early initiation of breastfeeding and exclusive breastfeeding in Ethiopia from 2000 to 2016. Int Breastfeed J. 2019;14:40. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Heyman  J, Raub  A, Earle  A. Breastfeeding policy: A globally comparative analysis. Bull World Health Organ. 2013;91:398–406. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18. Steurer  LM. Maternity leave length and workplace policies’ impact on the sustainment of breastfeeding: Global perspectives. Public Health Nurs. 2017;34(3):286–94. [DOI] [PubMed] [Google Scholar]
  • 19. Kimani-Murage  EW, Wekesah  F, Wanjohi  M, Kyobutungi  C, Ezeh  AC, Musoke  RN, Norris  SA, Madise  NJ, Griffiths  P.  Factors affecting actualisation of the WHO breastfeeding recommendations in urban poor settings in Kenya. Matern Child Nutr. 2015;11(3):314–32., doi: 10.1111/mcn.12161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. Kavle  JA, LaCroix  E, Dau  H, Engmann  C. Addressing barriers to exclusive breast-feeding in low- and middle-income countries: A systematic review and programmatic implications. Public Health Nutr. 2017;20(17):3120–34. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. National Council for Law Reporting . Laws of Kenya: Employment act. 2012, The National Council for Lawe Reporting. Chapter 226, [Internet], Available at: http://kenyalaw.org/kl/fileadmin/pdfdownloads/Acts/EmploymentAct_Cap226-No11of2007_01.pdf. [Google Scholar]
  • 22. Republic of Kenya Parliament . The health bill, 2015. Kenya Gazette Supplement. 2015;44, 222–273.. [Internet], Available at: http://kenyalaw.org/kl/fileadmin/pdfdownloads/bills/2015/HealthBill2015.pdf. [Google Scholar]
  • 23. Government of Kenya . Government of Kenya health act 2017. Kenya Gazette Supplement.  2017;101(21), 415–483.. [Internet]. Available at: http://kenyalaw.org/kl/fileadmin/pdfdownloads/Acts/HealthActNo.21of2017.pdf. [Google Scholar]
  • 24. Kenya National Bureau of Statistics . 2019 Kenya population and housing census. Volume 1: Population by county and sub-county, Kenya National Bureau of Statistics. Nairobi, Kenya; 2019. [Google Scholar]
  • 25. Nkrumah  J. Maternal work and exclusive breastfeeding practice: A community based cross-sectional study in Efutu Municipal, Ghana. Int Breastfeed J. 2016;12:10. doi:10.1186/s13006-017-0100-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. World Health Organization . World Health Organization indicators for assessing infant and young child feeding practices: Part 1: Definitions. Geneva, Switzerland: World Health Organization; 2008. [Google Scholar]
  • 27. Textor  J, Hardt  J, Knuppel  S. DAGitty: A graphical tool for analyzing causal diagrams. Epidemiology. 2011;22:745. [DOI] [PubMed] [Google Scholar]
  • 28. Kimani-Murage  EW, Madise  NJ, Fotso  JC, Kyobutungi  C, Mutua  MK, Gitau  TM, Yatich  N. Patterns and determinants of breastfeeding and complementary feeding practices in urban informal settlements, Nairobi Kenya. BMC Public Health. 2011;11:396. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. VanderWeele  TJ. Principles of confounder selection. Eur J Epidemiol. 2019;34(3):211–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Holms  S. A simple sequential rejective multiple test procedure. Scan J Statist. 1979;6(2):65–70. [Google Scholar]
  • 31. von Elm  E, Altman  DG, Egger  M, Pocock  SJ, Gøtzsche  PC, Vandenbroucke  JP; Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Initiative . The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: Guidelines for reporting observational studies. Lancet. 2007;370(9596):1453–7. [DOI] [PubMed] [Google Scholar]
  • 32. Desai  A, Mbuya  MNN, Chigumira  A, Chasekwa  B, Humphrey  JH, Moulton  LH, Pelto  G, Gerema  G, Stoltzfus  RJ. Traditional oral remedies and perceived breast milk insufficiency are major barriers to exclusive breastfeeding in rural Zimbabwe. J Nutr. 2014;144(7):1113–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. Tadesse  F, Alemayehu  Y, Shine  S, Asresahegn  H, Tadesse  T. Exclusive breastfeeding and maternal employment among mothers of infants from three to five months old in the Fafan zone, Somali regional state of Ethiopia: A comparative cross-sectional study. BMC Public Health. 2019;19(1):1015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Bhandari  N, Kabir  AK, Salam  MA. Mainstreaming nutrition into maternal and child health programmes: Scaling up of exclusive breastfeeding. Matern Child Nutr. 2008;4(Suppl 1):5–23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35. Chapman  DJ, Morel  K, Anderson  AK, Damio  G, Perez-Escamilla  R. Breastfeeding peer counseling: From efficacy through scale-up. J Hum Lact. 2010;26:314–26. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36. Rollins  NC, Bhandari  N, Hajeebhoy  N, Horton  S, Lutter  CK, Martines  JC, Piwoz  EG, Richter  LM, Victora  CG; Lancet Breastfeeding Series Group . Why invest, and what it will take to improve breastfeeding practices?. Lancet North Am Ed. 2016;387(10017):491–504. [DOI] [PubMed] [Google Scholar]
  • 37. Tylleskär  T, Jackson  D, Meda  N, Engebretston  I, Chopra  M, Diallo  A, Doherty  T, Ekström  EC, Fadnes  LT, Goga  A, PROMISE-EBF Study Group  et al. , Exclusive breastfeeding promotion by peer counsellors in sub-Saharan Africa (PROMISE-EBF): A cluster-randomised trial. Lancet North Am Ed. 2011;378:420–7. [DOI] [PubMed] [Google Scholar]
  • 38. Basnet  S, Frongillo  EA, Nguyen  PH, Moore  S, Arabi  M. Associations of maternal resources with care behaviours differ by resource and behaviour. Matern Child Nutr, 2020, 16(3):e12977. doi:10.1111/mcn.12977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39. Carlson  GJ, Kordas  K, Murray-Kolb  LE. Associations between women's autonomy and child nutritional status: A review of the literature. Matern Child Nutr. 2015;11(4):452–82.. doi:10.1111/mcn.12113. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40. Engle  PL, Menon  P, Haddad  L. Care and nutrition: Concepts and measurement. World Dev. 1999;27(8):1309–37.. doi:10.1016/S0305-750X(99)00059-5. [Google Scholar]
  • 41. Sebayang  SK, Dibley  MJ, Astutik  E, Efendi  F, Kelly  PJ, Li  M. Determinants of age-appropriate breastfeeding, dietary diversity, and consumption of animal source foods among Indonesian children. Matern Child Nutr. 2020;16(1):e12889. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42. Ziaei  S, Contreras  M, Blandón  EZ, Persson  LÅ, Hjern  A, Ekström  EC. Women's autonomy and social support and their associations with infant and young child feeding and nutritional status: Community‐based survey in rural Nicaragua. Public Health Nutr. 2015;18(11):1979–90. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43. Quisumbing  AR, Maluccio  JA. Intrahousehold allocation and gender relations: New empirical evidence from four developing countries. Washington, DC: International Food Policy Research Institute; 2000. [Google Scholar]
  • 44. Cunningham  K, Ploubidis  GB, Menon  P, Ruel  M, Kadiyala  S, Uauy  R, Ferguson  E. Women's empowerment in agriculture and child nutritional status in rural Nepal. Public Health Nutr. 2015;18:3134–45. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45. World Health Organization, UNICEF, and the International Baby Foods Action Network . Marketing of breast-milk substitutes: National implementation of the international code, status report 2020. [License: CC BY-NC-SA239;3.0;IGO]. Geneva, Switzerland: World Health Organization; 2020. [Google Scholar]
  • 46. Horwood  C, Haskins  L, Engebretsen  I, Connolly  C, Coutsoudis  A, Spies  L. Are we doing enough? Improved breastfeeding practices at 14 weeks but challenges of non-initiation and early cessation of breastfeeding remain: Findings of two consecutive cross-sectional surveys in KwaZulu-Natal, South Africa. BMC Public Health. 2020;20(1):440. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47. United Nationals Children's Fund . Country experiences with the baby-friendly hospital initiative: Compendium of case studies from around the world. 2017; [Internet]. Available at: https://www.unicef.org/nutrition/files/BFHI_Case_Studies_FINAL.pdf. [Google Scholar]
  • 48. Kavle  JA, Ahoya  B, Kiige  L, Mwando  R, Olwenyi  F, Straubinger  S, Gathi  CM. Baby-friendly community initiative–From national guidelines to implementation: A multisectoral platform for improving infant and young child feeding practices and integrated health services. Matern Child Nutr. 2019;15(Suppl 1):e12747. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49. McFadden  A, Siebelt  L, Marshall  JL, Gavine  A, Girard  L-C, Symon  A, MacGillivray  S. Counselling interventions to enable women to initiate and continue breastfeeding: A systematic review and meta-analysis. Int Breastfeed J. 2019;14, 1–19., doi: 10.1186/s13006-019-0235-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50. Nyoni  S, Sweet  L, Clark  J, Ward  P. A realist review of infant feeding counselling to increase exclusive breastfeeding by HIV-positive women in sub Saharan-Africa: What works for whom and in what contexts. BMC Public Health. 2019;19(1):570. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51. Olufunlayo  TF, Roberts  AA, MacArthur  C, Thomas  N, Odeyemi  KA, Price  M, Jolly  K. Improving exclusive breastfeeding in low and middle-income countries: A systematic review. Matern Child Nutr. 2019;15(3):e12788. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52. Müller  MHB, Polder  A, Brynildsrud  OB, Karimi  M, Lie  E, Manyilizu  WB, Mdegela  RH, Mokiti  F, Murtadha  M, Nonga  HE  et al.  Organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) in human breast milk and associated health risks to nursing infants in Northern Tanzania. Environ Res. 2017;154:425–34. [DOI] [PubMed] [Google Scholar]
  • 53. Ntow  WJ, Tagoe  LM, Drechsel  P, Kelderman  P, Gijzen  HJ, Nyarko  E. Accumulation of persistent organochlorine contaminants in milk and serum of farmers from Ghana. Environ Res. 2008;106(1):17–26. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

nqaa351_Supplemental_File

Articles from The American Journal of Clinical Nutrition are provided here courtesy of American Society for Nutrition

RESOURCES