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. 2023 Sep 23;11(10):1515. doi: 10.3390/vaccines11101515

Predictors for Uptake of Vaccines Offered during the Second Year of Life: Second Dose of Measles-Containing Vaccine and Meningococcal Serogroup A-Containing Vaccine, Ghana, 2020

Pierre Muhoza 1,2,*, Monica P Shah 1, Hongjiang Gao 1, Kwame Amponsa-Achiano 3, Pamela Quaye 3, William Opare 3, Charlotte Okae 3, Philip-Neri Aboyinga 3, Kwadwo L Opare 4, Melissa T Wardle 1, Aaron S Wallace 1
Editor: S Louise Cosby
PMCID: PMC10611024  PMID: 37896919

Abstract

Background: Understanding the drivers of coverage for vaccines offered in the second year of life (2YL) is a critical focus area for Ghana’s life course approach to vaccination. This study characterizes the predictors of vaccine receipt for 2YL vaccines—meningococcal serogroup A conjugate vaccine (MACV) and the second dose of measles-containing vaccine (MCV2)—in Ghana. Methods: 1522 children aged 18–35 months were randomly sampled through household surveys in the Greater Accra Region (GAR), Northern Region (NR), and Volta Region (VR). The association between predictors and vaccination status was modeled using logistic regression with backwards elimination procedures. Predictors included child, caregiver, and household characteristics. Results: Coverage was high for infant vaccines (>85%) but lower for 2YL vaccines (ranging from 60.2% for MACV in GAR to 82.8% for MCV2 in VR). Predictors of vaccination status varied by region. Generally, older, first-born children, those living in rural settlements and those who received their recommended infant vaccines by their first birthday were the most likely to have received 2YL vaccines. Uptake was higher among those with older mothers and children whose caregivers were aware of the vaccination schedule. Conclusions: Improving infant immunization uptake through increased community awareness and targeted strategies, such as parental reminders about vaccination visits, may improve 2YL vaccination coverage.

Keywords: immunization, measles-containing vaccine dose, meningococcal serogroup a conjugate vaccine, life course, immunization schedule, immunization disparities

1. Introduction

Immunization prevents numerous childhood infectious diseases, including measles and meningitis, both of which are highly contagious and have the potential for serious sequelae. Although substantial progress in measles control has been achieved through routine immunization (RI) services and supplementary immunization activities (SIAs), measles continues to be a significant cause of mortality, particularly in sub-Saharan Africa, where an estimated 4.4 million cases and 66,000 deaths in 2021 were attributed to measles [1]. A coverage level of 95% or higher with two doses of measles-containing vaccine (MCV) is needed to create herd immunity to protect communities and advance toward measles elimination; at 41% coverage, the World Health Organization (WHO) African Region is currently short of the goal [1]. Likewise, bacterial meningitis remains an enormous strain on the public health system across the region with an estimated mean annual incidence of 216 cases per 100,000 inhabitants [2]. Before the introduction of meningococcal serogroup A conjugate vaccine (MACV) in 2010 through mass vaccination campaigns, Neisseria meningitidis serogroup A accounted for 80–85% of meningitis epidemics in the “African meningitis belt” stretching from Senegal to Ethiopia.

The WHO recommends the routine administration of MACV and the second dose of the measles-containing vaccine (MCV2) during the second year of life (2YL) [3,4]. Ghana completed an initial MACV mass campaign in 2012 and conducted a catch-up campaign for children aged 1–4 years in July 2016 [5]. In November 2016, Ghana was the second country in the meningitis belt, after Sudan, to introduce MACV into the routine Expanded Programme on Immunization (EPI) schedule. MCV2 was introduced in the Ghana EPI schedule as a measles–rubella combination vaccine in February 2012. MCV2 and MACV are scheduled to be administered at the 18-month well-child visit.

Although Ghana has sustained national coverage rates of at least 85% for all infant vaccinations (those given before 12 months of age) since 2008, challenges have hampered similar success for vaccinations offered during 2YL [6]. A 2016 study, estimating vaccination coverage levels in the first and second year of life across three regions in Ghana before MACV introduction, revealed that infant vaccination coverage levels, including the MCV1 dose, were high (≥87%). However, coverage for MCV2 ranged from 60% to 83% across the study regions with high dropout rates between MCV1 and MCV2 [7].

Previous studies have highlighted a range of factors that influence 2YL vaccine uptake. Such factors include child and caregiver socio-demographic characteristics, caregiver knowledge and attitudes towards 2YL vaccinations, utilization of maternal care services as well as practical constraints related to bringing older children for 2YL vaccination visits and other competing priorities for limited caregiver time [7,8,9,10,11]. Health system factors related to the availability and quality of immunization services including distance to health facilities, vaccine stockouts, and caregiver perception of quality of care during immunization visits have also been cited as important for 2YL vaccine uptake [8,10,11,12,13]. However, previous studies have either been qualitative or descriptive in nature [7,8,9,10], limited in geographic scope [9,12,14,15] and largely focused on MCV2.

To increase coverage for 2YL vaccines in Ghana and plan for improved health services utilization, decision makers need to have an updated understanding of the determinants of 2YL immunization status in the country. As a follow-up to the 2016 study which was descriptive and predated MACV introduction in Ghana, we assessed predictors of MCV2 and MACV vaccination among children aged 18–35 months across three regions of Ghana in 2020.

2. Methods

2.1. Study Sites and Survey Design

Study data were derived from a cross-sectional endline survey conducted in August 2020 to estimate vaccination coverage among children aged 12–35 months old as part of a broader project to strengthen the 2YL RI platform in Ghana [7]. We used a stratified multi-stage cluster sample design with sampling stratified by three regions (Greater Accra [GAR], Northern [NR], and Volta [VR] Regions shown in Figure 1). In the first stage, 141 enumeration areas (EA) (53 in GAR, 52 in NR, and 36 in VR) were selected by probability proportional to size (PPS). Within each selected EA, a household listing was conducted to determine the sampling frame of households with at least one child aged 12–35 months as of March 2020. The selection of the cutoff was intended to minimize potential confounding related to the disruptions caused by the COVID-19 pandemic [16]. In the second stage, households with at least one age-eligible child were selected by simple random sampling. If a household had more than one age-eligible child, one child was selected at random. A standardized questionnaire was administered by the survey teams to the selected child’s caregiver who was present at the household during the day of the survey. Survey questions included child, caregiver, household characteristics and demographics; caregiver’s immunization awareness, knowledge, attitudes, beliefs and perceptions regarding family, community, and healthcare worker support for immunizations; and childhood vaccination history assessed by home-based vaccination record (child health record booklet-CHRB) data, health facility records, or caregiver recall.

Figure 1.

Figure 1

Map of Ghana showing the location of the Greater Accra, Northern, and Volta regions based on administrative boundaries from 2018.

Sample sizes were calculated to measure a difference of 15% in MCV2 coverage among children 24–35 months of age from the baseline survey in 2016 to the post-intervention endline survey in 2020. We assumed 80% power at a significance level of alpha = 0.05 using a one-sided test and adjusted for a 10% non-response rate. The estimated proportions of households with eligible children were 7.3% in GAR, 18.0% in NR, and 9.4% in VR, respectively. The intra-class correlation coefficients were 0.18 in GAR, 0.50 in NR, and 0.30 in VR. Sample sizes were then calculated separately for each of the three regions, using results from the 2014 Ghana Demographic and Health Survey (GDHS) that provided region-level estimates for their indicators [17].

2.2. Study Population

Although data were collected for children aged between 12 and 35 months at the time of the endline survey, the present study was restricted to a subset of children aged 18–35 months, since this older age group was either due or had already passed the point of the recommended age at vaccination for MACV and MCV2 doses.

2.3. Variables

2.3.1. Measured Variables

MACV and MCV2 vaccination status at the time of the interview were analyzed as separate outcomes and dichotomized as single versus zero doses of MACV or two doses versus one or zero doses of MCV, respectively. Vaccination status was ascertained preferentially from either (1) the CHRB, (2) the child’s immunization record from health facility registers, or (3) based on caregiver recall. Vaccination coverage was defined as the proportion of children aged 18–35 months receiving the recommended vaccines. MCV1–MCV2 dropout was defined as the proportion of children aged 18–35 months having received MCV1, but not MCV2.

Variables examined as potential predictors of vaccine receipt were broadly classified into three categories (child, caregiver, and household) and analyzed at the child level. In addition to the child’s vaccination history, additional child-level characteristics included variables with known association to vaccination status: age, sex, birth order, and availability of RI services at the child’s school or daycare [18,19,20].

We considered caregiver variables that are known to be associated with their children’s immunization status, including maternal age at the time of the interview, highest educational level completed, occupation, and religion [21,22,23,24]. The survey included questions about caregivers’ awareness of vaccine schedules, attitudes toward vaccines in general (including attitudes about the importance, safety, and effectiveness of vaccines), 2YL vaccines specifically, vaccine-preventable infection and disease, source of vaccine-related information, perception of support for immunizations, and decision making on healthcare seeking and 2YL vaccination.

For household characteristics, we also included the settlement type (rural or urban residence). The full list of variables assessed as predictors in this study are shown in Supplementary Table S1.

2.3.2. Derived Variables

We derived variables to examine whether MACV and MCV2 coverage differed by timely receipt of infant vaccines scheduled at 6 weeks, 14 weeks, and 9 months of age. A dose was considered timely if the vaccine was provided within 4 weeks after the recommended age of administration according to Ghana’s EPI schedule (Table 1). Delayed vaccinations were defined as any vaccines received beyond this interval. In defining timely administration of recommended vaccines, doses were coded as missing if they were implausible (i.e., dose before a child’s date of birth), too early (i.e., dose received before the recommended age), or if the date of receipt could not be verified from the CHRB or the facility immunization register. For each scheduled age-based vaccination visit (i.e., 6 weeks, 14 weeks, and 9 months), timely receipt was coded as the timely receipt of all recommended vaccines versus untimely (i.e., early or delayed) receipt of one or more doses.

Table 1.

Ghana vaccine schedule, 2020, and antigen-specific vaccine coverage among children aged 18–35 months in Greater Accra Region (GAR), Northern Region (NR), and Volta Region (VR).

Recommended Age Vaccine Uptake % (95% CIs)
Vaccine GAR (N = 370) NR (N = 870) VR (N = 315)
BCG At birth or first contact 81.3 (76.4–86.3) 93.8 (91.7–95.8) 87.9 (82.4–93.4)
OPV1 6 weeks 82.8 (77.9–87.8) 96.0 (94.4–97.5) 96.9 (94.1–99.6)
PCV1 6 weeks 82.9 (78.0–87.9) 96.6 (95.3–98.0) 96.9 (94.1–99.6)
Pentavalent 1 6 weeks 82.9 (78.0–87.9) 96.6 (95.3–98.0) 96.9 (94.1–99.6)
Rotavirus 1 6 weeks 82.7 (77.8–87.6) 95.4 (93.9–96.8) 96.8 (94.0–99.6)
OPV2 10 weeks 82.4 (77.5–87.4) 92.3 (89.7–94.8) 96.6 (93.8–99.3)
PCV2 10 weeks 82.9 (78.0–87.9) 96.1 (94.4–97.8) 96.8 (94.0–99.6)
Pentavalent 2 10 weeks 82.9 (78.0–87.9) 96.3 (94.8–97.8) 96.8 (94.0–99.6)
Rotavirus 2 10 weeks 81.0 (76.0–86.0) 92.3 (89.9–94.7) 94.3 (91.5–97.0)
IPV * 14 weeks
OPV3 14 weeks 78.0 (72.8–83.2) 82.1 (78.0–86.2) 90.8 (84.9–96.7)
PCV3 14 weeks 82.1 (76.6–87.6) 93.9 (91.7–96.1) 95.7 (92.9–98.6)
Pentavalent 3 14 weeks 82.3 (76.8–87.8) 93.5 (91.3–95.6) 95.2 (92.3–98.0)
MCV1 9 months 81.0 (75.9–86.1) 91.7 (88.8–94.5) 94.7 (91.2–98.1)
Yellow Fever 9 months 81.2 (76.1–86.4) 88.2 (85.0–91.5) 93.6 (90.2–97.0)
MACV 18 months 60.2 (53.3–67.2) 62.2 (56.3–68.1) 77.7 (70.8–84.5)
MCV2 18 months 67.4 (62.1–72.6) 69.8 (63.3–76.3) 82.8 (76.6–88.9)
Fully immunized with infant vaccines ** 80.6 (75.3–85.9) 71.7 (66.6–76.8) 77.9 (70.9–84.8)
Fully immunized with infant vaccines plus MCV2 ** 67.1 (61.6–72.6) 56.4 (49.6–63.1) 67.1 (58.9–75.3)
Fully immunized with infant vaccines plus MCV2 & MACV ** 62.8 (56.5–69.2) 50.1 (44.2–56.0) 62.1 (53.0–71.2)
MCV1 to MCV2 dropout rate 16.9 (13.1–20.6) 23.8 (18.4–29.3) 12.6 (7.9–17.3)

BCG, bacillus Calmette–Guérin; MACV, meningitis serogroup A conjugate vaccine; MCV, measles-containing vaccine includes rubella vaccine, OPV, oral polio vaccine; pentavalent vaccines include diphtheria, pertussis, tetanus, Hemophilus influenzae type b, and hepatitis B vaccines; PCV, pneumococcal conjugate vaccine. * IPV, inactivated polio vaccine was introduced in Ghana in 2018 and was excluded from analyses in this study. ** Children with vaccination information from caregiver recall excluded from sub-analysis.

In univariate and multivariable analyses, we also examined whether the receipt of all infant vaccines by the age of one year was predictive of 2YL vaccine receipt. These sub-analyses excluded vaccination information derived from caregiver recall. Although the inactivated polio vaccine (IPV) was introduced to the national immunization schedule in June 2018 to be given to children aged 14 weeks, we excluded its receipt from analysis due to the potential time lag with scale-up and standardized recording of a newer vaccine.

2.4. Statistical Analysis

Design-based descriptive analyses were used to examine proportions, tabulations, and summary measures (i.e., median, range) for summarizing binary, categorical, and continuous variables, respectively. The Chi-square test was used to compare proportions for categorical variables. The univariate association between each predictor and either MCV2 or MACV receipt was modeled separately, using binomial logistic regression. We used multivariable logistic regression to model the adjusted association between multiple predictors and each outcome (MACV or MCV2) separately. Backward elimination was used to select the final (reduced) model containing statistically significant predictors of vaccination receipt. As a first step of model reduction, the statistical significance between each potential predictor and MCV2 and MACV receipt separately was estimated, using simple logistic regression. All potential predictors with p-values ≤ 0.2 in the univariate analysis were retained in the initial full multivariable logistic regression models. We then used a stepwise backward elimination approach to systematically remove predictors. Variables statistically associated with MCV2 or MACV receipt (p < 0.05) remained in the final model. Due to established associations based on literature, several demographic characteristics of the child (age, sex, birth order), mother (age, education, religion), and household (urban/rural residence) were specified as fixed predictors and were included in all models irrespective of statistical significance [11,22,25,26]. We also assessed multicollinearity between predictor variables, using variance inflation factors (VIF), and considered VIFs above 2.5 as indicative of multicollinearity [27]. For each outcome, we conducted model-building analyses separately for each region.

We considered the possibility of a child’s attendance at a school/daycare offering RI or caregiver awareness of the 18-month visit differentially affecting MCV2 or MACV immunization status depending on urban/rural residence and tested separately for significant interactions between these variables.

All analyses were performed, using the appropriate clustering and survey weighting statements to account for the complex survey design described above. The Taylor series linearization method was used to calculate the variance of the parameter estimates. We used Stata version 17 for all data analysis [28]. Unadjusted and adjusted odds ratios (ORs) and 95% confidence intervals (CIs) were estimated from model output parameters.

3. Results

3.1. Sample Characteristics

We collected data for 1990 children aged 12–35 months from 1712 households across the three regions and included data for 1522 children (76.5%) aged 18–35 months for the analysis of determinants of 2YL vaccination status. The median age of these children was 26 months (interquartile range [IQR]: 22–31 months), and 50.8% were males. The child’s mother was the primary respondent for 95.8% of the children in GAR, 92.8% in NR, and 90.7% in VR. The median maternal age was 30 years (IQR: 25–35 years). In GAR, 87.6% of the children lived in urban settlements whereas in NR and VR, 73.2% and 70.5%, respectively, lived in rural areas. Half of the children (51.2%) were third or higher in birth order. In NR, most mothers (70.5%) were Muslim, while in GAR and VR the majority (84.9%; 86.3%) were Christian. Most mothers in GAR (83.2%) and VR (63.9%) attained secondary education or higher compared to only 20.7% in NR. Nearly all children (96.9%) had their immunization history verified from CHRBs or health facility registers (Table 2 and Supplementary Figure S1).

Table 2.

Characteristics of children 18–35 months of age in Greater Accra (GAR), Northern (NR), and Volta (VR) regions, 2020 *.

Region
GAR NR VR Total
No. % No. % No. % No. %
Child’s age group (months)
18–23 146 39.5 302 36.1 115 36.5 563 37.0
24–35 224 60.5 535 63.9 200 63.5 959 63.0
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Child’s sex
Female 184 49.7 396 47.3 177 56.2 757 49.7
Male 186 50.3 441 52.7 138 43.8 765 50.3
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Birth order
First 122 33.0 182 21.7 101 32.1 405 26.6
Second 100 27.0 175 20.9 62 19.7 337 22.1
Third or more 148 40.0 480 57.3 152 48.3 780 51.2
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Maternal age (years)
<25 42 11.4 108 12.9 71 22.5 221 14.5
25–34 184 49.7 215 25.7 134 42.5 533 35.0
≥35 144 38.9 514 61.4 110 34.9 768 50.5
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Maternal education
Never attended school 25 6.8 592 70.9 52 16.6 669 44.1
Primary 37 10.0 70 8.4 61 19.5 168 11.1
Secondary or higher 308 83.2 173 20.7 200 63.9 681 44.9
Total 370 100.0 835 100.0 313 100.0 1518 100.0
Paternal education
Never attended school 12 3.5 582 71.1 38 13.1 632 43.5
Primary 12 3.5 42 5.1 29 10.0 83 5.7
Secondary or higher 319 93.0 195 23.8 224 77.0 738 50.8
Total 343 100.0 819 100.0 291 100.0 1453 100.0
Maternal religion
Christian 314 84.9 178 21.3 272 86.3 764 50.2
Muslim 55 14.9 590 70.5 23 7.3 668 43.9
Traditionalist 0 0.0 55 6.6 6 1.9 61 4.0
None/Don’t know 1 0.3 14 1.7 14 4.4 29 1.9
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Maternal marital status
Single/Divorced/Separated/Widowed 48 13.0 16 1.9 39 12.4 103 6.8
Married/Cohabitating 322 87.0 821 98.1 276 87.6 1419 93.2
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Settlement type
Urban 324 87.6 224 26.8 93 29.5 641 42.1
Rural 46 12.4 613 73.2 222 70.5 881 57.9
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Attends school/daycare offering routine immunization (RI) **
No formal school/daycare attendance 179 48.4 737 88.1 221 70.2 1137 74.7
School/daycare does not offer RI 90 24.3 81 9.7 48 15.2 219 14.4
School/daycare offers RI 101 27.3 19 2.3 46 14.6 166 10.9
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Timely receipt of all 6-week infant vaccines
At least 1 recommended dose delayed 40 13.7 282 38.1 53 18.7 375 28.5
All recommended doses timely 251 86.3 458 61.9 230 81.3 939 71.5
Total 291 100.0 740 100.0 283 100.0 1314 100.0
Timely receipt of all 14-week infant vaccines
At least 1 recommended dose delayed 94 31.9 511 69.0 107 38.6 712 54.2
All recommended doses timely 201 68.1 230 31.0 170 61.4 601 45.8
Total 295 100.0 741 100.0 277 100.0 1313 100.0
Timely receipt of all 9 mos. infant vaccines
At least 1 recommended dose delayed 87 30.5 381 57.5 123 48.0 591 49.1
All recommended doses timely 198 69.5 282 42.5 133 52.0 613 50.9
Total 285 100.0 663 100.0 256 100.0 1204 100.0
Fully immunized child by 12 mos.
No 54 17.1 349 43.2 89 29.2 492 34.5
Yes 261 82.9 458 56.8 216 70.8 935 65.5
Total 315 100.0 807 100.0 305 100.0 1427 100.0
18 mos. well-child visit attendance
No 48 13.0 125 14.9 32 10.2 205 13.5
Yes 322 87.0 712 85.1 283 89.8 1317 86.5
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Caregiver aware of need for 18 mos. visit before 2nd birthday
No 163 44.1 452 54.0 151 47.9 766 50.3
Yes 207 55.9 385 46.0 164 52.1 756 49.7
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Caregiver knows MR dose should be given during 2YL
No 153 41.4 284 33.9 107 34.0 544 35.7
Yes 217 58.6 553 66.1 208 66.0 978 64.3
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Caregiver received phone reminder for 18 mos. visit
No access to phone 15 4.1 233 27.8 45 14.3 293 19.3
Access to phone but no reminder received 313 84.6 523 62.5 223 70.8 1059 69.6
Phone reminder received 42 11.4 81 9.7 47 14.9 170 11.2
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Caregiver believes healthcare provider provides enough information on 2YL vaccination
No 42 11.4 114 13.6 24 7.6 180 11.8
Yes 328 88.6 723 86.4 291 92.4 1342 88.2
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Caregiver believes 2YL vaccination is important for child
No 11 3.0 31 3.7 6 1.9 48 3.2
Yes 359 97.0 806 96.3 309 98.1 1474 96.8
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Caregiver believes 2YL vaccination is supported by spouse
No 22 5.9 29 3.5 21 6.7 72 4.7
Yes 348 94.1 808 96.5 294 93.3 1450 95.3
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Caregiver believes 2YL vaccination supported by other family members
No 34 9.2 53 6.3 17 5.4 104 6.8
Yes 336 90.8 784 93.7 298 94.6 1418 93.2
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Caregiver believes 2YL vaccination supported by friends
No 66 17.8 71 8.5 29 9.2 166 10.9
Yes 304 82.2 766 91.5 286 90.8 1356 89.1
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Caregiver believes 2YL vaccination supported by community
No 71 19.2 95 11.4 18 5.7 184 12.1
Yes 299 80.8 742 88.6 297 94.3 1338 87.9
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Most people caregiver knows bring child in for 2YL vaccination
No 42 11.4 118 14.1 21 6.7 181 11.9
Yes 328 88.6 719 85.9 294 93.3 1341 88.1
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Caregiver believes it is important for child to get missing doses
No 24 6.5 47 5.6 12 3.8 83 5.5
Yes 346 93.5 790 94.4 303 96.2 1439 94.5
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Caregiver informed of 18 mos. visit by healthcare provider
No 178 48.1 469 56.0 165 52.4 812 53.4
Yes 192 51.9 368 44.0 150 47.6 710 46.6
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Vaccination source for coverage estimates
Vaccination card 316 85.4 815 97.4 306 97.1 1437 94.4
Facility register 21 5.7 10 1.2 7 2.2 38 2.5
Caregiver recall 33 8.9 12 1.4 2 0.6 47 3.1
Total 370 100.0 837 100.0 315 100.0 1522 100.0
Same day receipt of MCV2 and MACV ***
No 34 15.1 70 13.4 23 9.6 127 12.9
Yes 191 84.9 452 86.6 216 90.4 859 87.1
Total 225 100.0 522 100.0 239 100.0 986 100.0

2YL, second year of life; MR, measles–rubella vaccine. * Results are unweighted. ** Information on school/daycare attendance refers to the pre-pandemic period. *** Among those having received both vaccines and with vaccination status for both verified using home-based immunization cards or facility records.

3.2. Vaccination Coverage

Across all regions, coverage was higher for infant vaccines compared to 2YL vaccines; and higher for MCV2 as compared with MACV (Table 1). Coverage generally decreased with each successive dose in the series as the recommended age of administration increased. Among those with documented vaccination dates, the proportion of children fully immunized with infant vaccines plus 2YL vaccines ranged from 50.1% (95% CI, 44.2–56.0) in NR to 62.3% (95% CI, 53.1–71.4) in VR. For all individual vaccine doses, coverage rates were lowest in GAR with MACV coverage at 60.2% (95% CI, 53.3–66.8) and MCV2 coverage at 67.4% (95% CI, 62.0–72.3). Coverage was highest for all doses in VR with MACV coverage at 77.7% (95% CI, 70.4–83.6) and MCV2 coverage at 82.8% (95% CI, 76.0–87.9). In NR, MACV coverage was 62.2% (95% CI, 56.3–67.7) whereas MCV2 coverage was 69.8% (95% CI, 63.2–75.8).

Among the 1475 children with documented immunization history, 986 (66.8%) had vaccination service dates available for both MACV and MCV2; 6 (0.4%) children lacked service date documentation for both 2YL vaccines, 129 (8.7%) received only one of the two vaccines, and 354 (24.0%) missed both. Among those (n = 986) who received both vaccines, 859 (87.1%) received them on the same date and 127 (12.9%) received them on different dates. Of the 129 who received only one of the 2YL vaccines, 118 (91.5%) were vaccinated for MCV2 only, and 74 (57.4%) of these instances occurred during 2019. The MCV1 to MCV2 dropout rate ranged from 12.6% (95% CI, 7.9–17.3) in VR to 23.8% (95% CI, 18.4–29.3) in NR.

MACV and MCV2 vaccination coverage by various characteristics are respectively shown in Table 3 (A and B) stratified by region. Across all regions, coverage for both vaccine doses was high among children attending the 18-month well-child visit, ranging from 67.7% (95% CI [59.8–74.6]) for MACV in GAR to 85.2% (95% CI [78.1–90.4]) for MCV2 in VR (Table 3 (A and B)). MACV and MCV2 coverage was higher among children who were fully immunized by 12 months of age, although the difference was not statistically significant for either dose in VR. Furthermore, children who received all vaccine doses recommended for the 9-month scheduled visit generally had higher MACV and MCV2 coverage rates as compared with children who had at least one delayed dose during the visit. The same trend did not hold for vaccine doses recommended during the 6 week and 14 week of age visits (Table 3 (A and B)).

Table 3.

(A): MACV coverage among children aged 18–35 months in Greater Accra Region (GAR), Northern Region (NR), and Volta Region (VR), Ghana, 2020 *. (B): MCV2 coverage among children aged 18–35 months children in Greater Accra Region (GAR), Northern Region (NR), and Volta Region (VR), Ghana, 2020 *.

A
GAR NR VR
n % 95% CI n % 95% CI n % 95% CI
Child’s age group (months)
18–23 146 48.9 (39.9–57.9) 302 48.7 (41.8–55.7) 115 57.8 (45.0–69.6)
24–35 224 67.8 (59.5–75.1) 535 70.1 (63.4–76.1) 200 90.0 (84.0–94.0)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Child’s sex
Female 184 61.3 (52.0–69.8) 396 66.6 (60.5–72.2) 177 73.6 (62.7–82.2)
Male 186 59.2 (49.1–68.6) 441 58.3 (50.6–65.6) 138 83.5 (74.3–89.8)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Birth order
First 122 63.9 (53.1–73.4) 182 65.7 (55.7–74.5) 101 83.4 (74.4–89.7)
Second 100 58.5 (43.7–71.8) 175 60.9 (51.3–69.8) 62 83.3 (66.4–92.6)
Third or more 148 58.1 (48.8–66.8) 480 61.2 (55.3–66.8) 152 70.7 (59.7–79.7)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Maternal age (years)
<25 42 50.2 (32.2–68.2) 108 51.0 (40.2–61.7) 71 81.0 (66.3–90.2)
25–34 184 63.3 (54.0–71.8) 215 68.3 (61.0–74.9) 134 77.9 (70.2–84.1)
≥35 144 59.2 (49.2–68.5) 514 62.1 (56.1–67.8) 110 75.1 (64.4–83.5)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Maternal education
Never attended school 25 63.8 (45.2–79.1) 592 64.5 (58.8–69.8) 52 74.7 (64.5–82.8)
Primary 37 55.0 (37.8–71.1) 70 46.2 (29.5–63.8) 61 76.7 (61.7–87.1)
Secondary or higher 308 60.5 (52.8–67.6) 173 61.4 (51.6–70.3) 200 79.1 (69.4–86.4)
Total 370 60.2 (53.3–66.8) 835 62.1 (56.3–67.6) 313 78.0 (71.1–83.6)
Paternal education
Never attended school 12 77.1 (56.0–89.9) 582 63.8 (57.3–69.8) 38 77.5 (60.2–88.7)
Primary 12 60.2 (28.2–85.3) 42 62.3 (40.7–79.9) 29 73.7 (51.9–87.9)
Secondary or higher 319 60.5 (53.4–67.1) 195 58.2 (49.6–66.3) 224 79.2 (70.1–86.0)
Total 343 60.8 (53.9–67.3) 819 62.3 (56.4–67.8) 291 78.5 (71.3–84.2)
Maternal religion
Christian 314 60.9 (52.7–68.5) 178 76.1 (67.1–83.3) 272 78.4 (70.3–84.8)
Muslim 55 54.5 (40.2–68.1) 590 58.1 (51.6–64.4) 23 72.1 (56.1–83.9)
Traditionalist 0 0.0 55 70.7 (59.0–80.2) 6 76.7 (32.2–95.8)
None/Don’t know 1 0.0 14 55.8 (34.3–75.3) 14 72.0 (35.2–92.4)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Maternal marital status
Single/Divorced/Separated/Widowed 48 50.5 (34.0–66.9) 16 65.1 (44.5–81.3) 39 74.9 (50.6–89.7)
Married/Cohabitating 322 61.8 (54.8–68.3) 821 62.1 (56.2–67.7) 276 78.0 (71.6–83.4)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Settlement type
Urban 324 59.0 (51.8–65.8) 224 52.5 (44.5–60.3) 93 77.1 (63.2–86.8)
Rural 46 71.7 (59.8–81.2) 613 66.2 (59.0–72.6) 222 77.9 (68.9–84.9)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Attends school/daycare offering routine immunization (RI)
No formal school/daycare attendance 179 51.6 (42.4–60.7) 737 61.5 (55.0–67.5) 221 73.5 (64.8–80.7)
School/daycare does not offer RI 90 62.6 (52.2–72.0) 81 66.5 (55.4–76.0) 48 95.6 (86.5–98.7)
School/daycare offers RI 101 72.9 (65.1–79.4) 19 72.7 (50.9–87.3) 46 81.0 (65.5–90.5)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Timely receipt of all 6-week infant vaccines
At least 1 recommended dose delayed 40 82.7 (68.5–91.3) 282 62.9 (56.2–69.2) 53 83.5 (64.7–93.3)
All recommended doses timely 251 70.3 (63.8–76.0) 458 64.4 (57.7–70.6) 230 79.7 (73.0–85.0)
Total 291 71.9 (65.8–77.3) 740 63.9 (58.0–69.4) 283 80.3 (74.0–85.4)
Timely receipt of all 14-week infant vaccines
At least 1 recommended dose delayed 94 73.4 (63.1–81.6) 511 64.2 (57.9–70.1) 107 81.8 (72.7–88.4)
All recommended doses timely 201 74.0 (66.6–80.3) 230 68.1 (61.2–74.2) 170 80.1 (72.4–86.0)
Total 295 73.8 (67.7–79.2) 741 65.5 (60.2–70.4) 277 80.7 (74.3–85.8)
Timely receipt of all 9 mos. infant vaccines
At least 1 recommended dose delayed 87 72.2 (59.3–82.2) 381 66.3 (59.6–72.4) 123 80.9 (70.5–88.2)
All recommended doses timely 198 74.8 (66.8–81.5) 282 71.7 (64.7–77.9) 133 80.5 (73.3–86.1)
Total 285 74.1 (67.5–79.7) 663 68.7 (63.7–73.3) 256 80.7 (75.0–85.3)
Fully immunized child by 12 mos.
No 54 59.1 (44.3–72.4) 349 54.3 (46.9–61.6) 89 77.9 (62.7–88.1)
Yes 261 75.1 (68.8–80.4) 458 71.8 (66.6–76.4) 216 80.8 (74.8–85.7)
Total 315 72.5 (66.4–77.8) 807 64.3 (58.6–69.6) 305 80.0 (74.0–84.9)
18 mos. well-child visit attendance
No 48 14.1 (5.4–32.0) 125 24.8 (14.4–39.3) 32 50.3 (29.2–71.3)
Yes 322 67.7 (59.8–74.6) 712 69.8 (65.0–74.2) 283 80.3 (72.6–86.2)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Caregiver aware of need for 18 mos. visit before 2nd birthday
No 163 56.2 (46.7–65.3) 452 55.1 (47.9–62.1) 151 68.5 (59.0–76.7)
Yes 207 62.8 (52.6–72.1) 385 70.9 (64.0–76.9) 164 85.8 (78.9–90.7)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Caregiver knows MACV dose should be given during 2YL
No 153 56.2 (47.1–65.0) 284 59.4 (50.2–68.1) 107 73.7 (65.1–80.8)
Yes 217 63.4 (54.2–71.7) 553 63.7 (57.9–69.2) 208 80.3 (71.7–86.8)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Phone reminder for 18 mos. visit
No access to phone 15 30.6 (12.0–58.8) 233 66.0 (59.1–72.2) 45 65.7 (46.6–80.8)
Access to phone but no reminder received 313 60.2 (51.3–68.4) 523 59.8 (52.7–66.5) 223 78.5 (70.4–84.9)
Phone reminder received 42 69.5 (50.7–83.5) 81 70.1 (57.3–80.4) 47 84.6 (71.3–92.3)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Gets enough 2YL vaccination info from provider
No 42 62.3 (47.9–74.7) 114 54.7 (41.3–67.4) 24 78.1 (53.9–91.5)
Yes 328 60.0 (52.5–67.0) 723 63.3 (57.7–68.5) 291 77.6 (70.1–83.7)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Caregiver believes 2YL vaccine important for child
No 11 68.1 (43.4–85.5) 31 43.5 (28.7–59.5) 6 91.4 (54.0–99.0)
Yes 359 60.0 (52.9–66.8) 806 63.1 (57.4–68.4) 309 77.4 (69.9–83.5)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Caregiver believes 2YL vaccination supported by spouse
No 22 60.5 (38.1–79.3) 29 40.5 (19.9–65.1) 21 82.5 (65.0–92.3)
Yes 348 60.2 (53.2–66.9) 808 63.1 (57.5–68.3) 294 77.3 (69.6–83.5)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Caregiver believes 2YL vaccination supported by other family members
No 34 57.2 (41.9–71.3) 53 40.3 (22.6–61.0) 17 89.2 (67.3–97.0)
Yes 336 60.5 (53.5–67.2) 784 63.7 (58.4–68.8) 298 76.9 (69.1–83.2)
Total 370 60.2 (53. –-66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Caregiver believes 2YL vaccination supported by friends
No 66 54.8 (39.5–69.3) 71 55.3 (43.7–66.3) 29 90.0 (64.8–97.8)
Yes 304 61.4 (54.4–68.0) 766 62.9 (57.0–68.5) 286 76.2 (68.1–82.8)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Caregiver believes 2YL vaccination supported by community
No 71 59.7 (47.1–71.1) 95 57.0 (42.3–70.5) 18 77.4 (41.6–94.3)
Yes 299 60.4 (53.2–67.2) 742 62.8 (57.1–68.2) 297 77.7 (69.9–84.0)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Most people caregiver knows bring child in for 2YL vaccination
No 42 53.9 (38.3–68.8) 118 55.3 (42.4–67.6) 21 86.0 (66.1–95.1)
Yes 328 61.1 (53.5–68.2) 719 63.3 (57.4–68.8) 294 77.0 (69.3–83.2)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Caregiver believes it is important for child to get missing doses
No 24 51.2 (27.7–74.1) 47 46.0 (29.6–63.3) 12 89.6 (62.2–97.8)
Yes 346 60.8 (53.4–67.7) 790 63.2 (57.7–68.4) 303 77.2 (69.6–83.3)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
Caregiver informed of 18 mos. visit by healthcare provider
No 178 56.9 (47.9–65.4) 469 55.6 (48.8–62.2) 165 70.5 (60.7–78.7)
Yes 192 62.8 (52.4–72.1) 368 71.1 (63.8–77.5) 150 85.4 (79.0–90.1)
Total 370 60.2 (53.3–66.8) 837 62.2 (56.3–67.7) 315 77.7 (70.4–83.6)
B
GAR NR VR
n % 95% CI n % 95% CI n % 95% CI
Child’s age group (months)
18–23 146 61.0 (54.3–67.3) 302 58.7 (50.1–66.7) 115 69.2 (59.6–77.3)
24–35 224 71.6 (64.4–77.8) 535 76.4 (69.5–82.1) 200 91.2 (83.2–95.6)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Child’s sex
Female 184 69.4 (61.9–76.0) 396 74.2 (68.4–79.2) 177 81.3 (70.3–88.9)
Male 186 65.3 (56.9–72.8) 441 66.0 (56.6–74.2) 138 84.8 (76.9–90.3)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Birth order
First 122 73.0 (64.2–80.3) 182 71.4 (61.8–79.4) 101 86.1 (76.8–92.0)
Second 100 66.7 (54.8–76.8) 175 68.1 (57.3–77.3) 62 90.1 (81.2–95.1)
Third or more 148 62.5 (54.2–70.0) 480 69.8 (63.2–75.8) 152 76.8 (66.2–84.8)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Maternal age (years)
<25 42 61.3 (44.6–75.8) 108 57.4 (46.8–67.4) 71 85.1 (74.0–92.0)
25–34 184 72.1 (63.0–79.6) 215 72.6 (65.5–78.8) 134 82.1 (72.7–88.8)
≥35 144 63.0 (52.9–72.1) 514 71.4 (63.8–78.0) 110 81.9 (71.9–88.9)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Maternal education
Never attended school 25 63.8 (45.2–79.1) 592 72.3 (65.9–78.0) 52 79.9 (65.6–89.3)
Primary 37 59.4 (41.9–74.8) 70 58.0 (37.2–76.4) 61 78.6 (62.8–88.8)
Secondary or higher 308 68.3 (62.3–73.8) 173 66.8 (56.6–75.6) 200 84.4 (76.3–90.1)
Total 370 67.4 (62.0–72.3) 835 69.8 (63.1–75.7) 313 82.7 (75.9–87.8)
Paternal education
Never attended school 12 73.8 (56.5–86.0) 582 71.9 (65.1–77.8) 38 75.5 (63.8–84.4)
Primary 12 60.2 (28.2–85.3) 42 68.8 (44.7–85.8) 29 84.9 (64.5–94.6)
Secondary or higher 319 68.8 (63.3–73.8) 195 65.6 (55.1–74.9) 224 85.1 (76.2–91.1)
Total 343 68.6 (63.5–73.2) 819 70.1 (63.5–76.0) 291 84.0 (76.6–89.4)
Maternal religion
Christian 314 67.9 (61.7–73.6) 178 81.8 (71.2–89.0) 272 83.7 (76.4–89.0)
Muslim 55 62.2 (49.6–73.3) 590 65.8 (58.2–72.6) 23 75.4 (55.3–88.3)
Traditionalist 0 55 89.2 (75.6–95.7) 6 76.7 (32.2–95.8)
None/Don’t know 1 100.0 14 59.9 (30.4–83.6) 14 77.7 (45.4–93.6)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Maternal marital status
Single/Divorced/Separated/Widowed 48 64.2 (48.9–77.2) 16 69.3 (52.7–82.0) 39 85.7 (65.7–95.0)
Married/Cohabitating 322 67.8 (61.9–73.3) 821 69.8 (63.1–75.9) 276 82.4 (75.4–87.7)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Settlement type
Urban 324 66.8 (61.1–72.0) 224 57.4 (49.2–65.1) 93 77.7 (64.7–86.9)
Rural 46 72.9 (63.2–80.8) 613 74.9 (67.0–81.4) 222 84.8 (76.1–90.7)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Attends school/daycare offering routine immunization
No formal school/daycare attendance 179 62.4 (55.2–69.0) 737 69.7 (62.4–76.2) 221 79.1 (70.8–85.4)
School/daycare does not offer RI 90 67.2 (56.5–76.4) 81 67.5 (56.2–77.0) 48 99.4 (95.8–99.9)
School/daycare offers RI 101 75.9 (67.6–82.7) 19 85.7 (65.3–95.0) 46 85.2 (68.9–93.7)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Timely receipt of all 6–week infant vaccines
At least 1 recommended dose delayed 40 86.0 (72.3–93.5) 282 72.0 (63.6–79.2) 53 88.3 (72.9–95.5)
All recommended doses timely 251 78.9 (74.0–83.1) 458 71.6 (64.5–77.8) 230 85.7 (80.2–89.9)
Total 291 79.9 (75.1–83.9) 740 71.8 (65.1–77.6) 283 86.1 (81.1–90.0)
Timely receipt of all 14–week infant vaccines
At least 1 recommended dose delayed 94 80.0 (71.6–86.4) 511 73.5 (66.3–79.6) 107 85.9 (76.2–92.1)
All recommended doses timely 201 82.0 (76.6–86.3) 230 74.4 (66.5–81.0) 170 84.9 (77.6–90.1)
Total 295 81.3 (77.1–85.0) 741 73.8 (67.7–79.1) 277 85.3 (79.4–89.7)
Timely receipt of all 9 mos. infant vaccines
At least 1 recommended dose delayed 87 79.1 (66.0–88.1) 381 74.8 (68.2–80.5) 123 81.4 (71.1–88.6)
All recommended doses timely 198 85.5 (80.5–89.5) 282 80.6 (73.7–86.0) 133 91.5 (86.4–94.8)
Total 285 83.7 (79.4–87.1) 663 77.4 (72.1–81.9) 256 87.0 (81.0–91.2)
Fully immunized child by 12 mos.
No 54 65.4 (50.1–78.1) 349 62.0 (54.3–69.1) 89 81.0 (67.9–89.5)
Yes 261 84.0 (80.1–87.3) 458 79.9 (73.8–84.9) 216 86.9 (81.3–91.0)
Total 315 81.0 (76.7–84.7) 807 72.2 (65.8–77.9) 305 85.2 (79.7–89.4)
18 mos. well–child visit attendance
No 48 14.8 (5.9–32.4) 125 31.3 (19.7–45.9) 32 56.3 (36.2–74.5)
Yes 322 75.8 (69.9–80.9) 712 77.6 (72.6–82.0) 283 85.2 (78.1–90.4)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Caregiver aware of need for 18 mos. visit before 2nd birthday
No 163 64.4 (54.2–73.5) 452 64.2 (54.5–72.8) 151 74.4 (64.6–82.3)
Yes 207 69.2 (59.3–77.6) 385 76.7 (71.3–81.5) 164 90.1 (84.7–93.8)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Caregiver knows MCV dose should be given during 2YL
No 153 60.0 (51.6–67.9) 284 62.6 (52.4–71.8) 107 81.4 (72.4–88.0)
Yes 217 73.1 (65.9–79.3) 553 73.9 (67.9–79.1) 208 83.6 (75.9–89.2)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Caregiver received phone reminder for 18 mos. visit
No access to phone 15 39.9 (16.4–69.2) 233 78.2 (69.7–84.8) 45 72.5 (57.7–83.6)
Access to phone but no reminder received 313 67.0 (59.9–73.4) 523 65.9 (58.5–72.6) 223 83.6 (76.1–89.1)
Phone reminder received 42 78.2 (59.3–89.9) 81 77.3 (65.1–86.1) 47 88.1 (74.0–95.1)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Caregiver believes they get enough 2YL vaccination info from provider
No 42 68.2 (54.6–79.3) 114 58.0 (45.1–70.0) 24 78.1 (53.9–91.5)
Yes 328 67.2 (61.1–72.8) 723 71.5 (65.0–77.2) 291 83.3 (75.8–88.8)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Caregiver believes 2YL vaccine is important for child
No 11 68.1 (43.4–85.5) 31 46.3 (28.6–65.1) 6 91.4 (54.0–99.0)
Yes 359 67.3 (62.0–72.3) 806 71.0 (64.8–76.5) 309 82.6 (75.8–87.8)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Caregiver believes 2YL vaccination supported by spouse
No 22 62.3 (39.5–80.7) 29 40.5 (19.9–65.1) 21 85.4 (67.3–94.3)
Yes 348 67.6 (62.2–72.6) 808 71.0 (64.8–76.5) 294 82.5 (75.3–88.0)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Caregiver believes 2YL vaccination supported by other family members
No 34 61.3 (45.6–74.9) 53 46.2 (25.1–68.9) 17 93.5 (75.3–98.5)
Yes 336 67.9 (62.7–72.8) 784 71.5 (65.7–76.6) 298 82.1 (75.2–87.3)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Caregiver believes 2YL vaccination supported by friends
No 66 68.7 (56.8–78.5) 71 63.1 (47.2–76.5) 29 90.0 (64.8–97.8)
Yes 304 67.1 (60.6–72.9) 766 70.5 (64.1–76.3) 286 81.9 (74.8–87.4)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Caregiver believes 2YL vaccination supported by community
No 71 72.9 (63.2–80.8) 95 62.2 (45.9–76.2) 18 81.3 (44.3–96.0)
Yes 299 66.0 (59.4–72.0) 742 70.7 (64.5–76.3) 297 82.8 (76.0–88.0)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Most people caregiver knows bring child in for 2YL vaccination
No 42 69.6 (51.6–83.1) 118 58.0 (45.0–70.0) 21 86.0 (66.1–95.1)
Yes 328 67.0 (61.1–72.5) 719 71.6 (65.3–77.2) 294 82.5 (75.5–87.8)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Caregiver believes it is important for child to get missing doses
No 24 62.7 (38.9–81.7) 47 47.2 (30.1–64.9) 12 100.0
Yes 346 67.6 (62.0–72.7) 790 71.3 (65.2–76.6) 303 82.0 (75.2–87.2)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)
Caregiver informed of 18 mos. visit by healthcare provider
No 178 64.8 (55.6–73.0) 469 64.7 (55.5–72.9) 165 75.9 (66.1–83.5)
Yes 192 69.3 (59.3–77.8) 368 76.8 (71.1–81.6) 150 90.1 (84.1–94.0)
Total 370 67.4 (62.0–72.3) 837 69.8 (63.2–75.8) 315 82.8 (76.0–87.9)

* Sample sizes are unweighted, percentages and 95% CIs are weighted. MACV, meningococcal serogroup A conjugate vaccine. MCV2, second dose of measles–containing vaccine. Bold values denote statistical significance of the design-based Chi-square test at the p < 0.05 level.

3.3. Predictors of MACV and MCV2 Vaccine Receipt

The unadjusted and adjusted (final, reduced model) associations between child, caregiver, and household factors and MACV and MCV2 receipt are shown in Table 4, respectively.

Table 4.

(A): Univariable and multivariable analysis of predictors of MACV receipt among children aged 18–35 months in Greater Accra Region (GAR), Northern Region (NR), and Volta Region (VR), Ghana, 2020. (B): Univariable and multivariable analysis of predictors of MCV2 receipt among children aged 18–35 months in Greater Accra Region (GAR), Northern Region (NR), and Volta Region (VR), Ghana, 2020.

A
GAR (N = 370) NR (N = 870) VR (N = 315)
Unadjusted Adjusted Unadjusted Adjusted Unadjusted Adjusted
OR 95% CI OR 95% CI OR 95% CI OR 95% CI OR 95% CI OR 95% CI
Child’s age (months)
18–23 REF REF REF REF REF REF
24–35 2.2 (1.4–3.4) *** 4.0 (2.2–7.0) *** 2.4 (1.9–3.2) *** 3.0 (2.2–4.2) *** 6.6 (3.0–14.3) *** 7.2 (3.3–15.7) ***
Child’s sex
Female REF REF REF REF REF REF
Male 0.9 (0.5–1.6) REF7 (0.5–1.9) 0.7 (0.5–0.9) 0.7 (0.5–1.0) 1.8 (0.8–3.9) 1.6 (0.6–3.9)
Birth order
First REF REF REF REF REF REF
Second 0.8 (0.3–1.6) 0.7 (0.2–2.0) 0.8 (0.5–1.2) 0.8 (0.4–1.4) 0.9 (0.3–2.8) 1.2 (0.4–3.4)
Third or more 0.7 (0.4–1.3) 0.5 (0.2–1.2) 0.8 (0.5–1.2) 0.5 (0.3–1.0) 0.5 (0.2–0.8) ** 0.3 (0.2–0.7) **
Maternal education
Never attended school REF REF REF REF REF REF
Primary 0.6 (0.2–2.1) 1.0 (0.3–3.6) 0.5 (0.2–0.9) 0.5 (0.2–1.1) 1.1 (0.4–2.7) 2.0 (0.6–6.5)
Secondary or higher 0.8 (0.3–1.9) 1.1 (0.5–2.4) 0.9 (0.6–1.2) 0.9 (0.6–1.4) 1.3 (0.6–2.4) 1.4 (0.5–4.0)
Maternal age (years)
<25 REF REF REF REF REF REF
25–34 1.7 (0.7–3.8) 1.8 (0.7–4.3) 2.1 (1.2–3.3) ** 2.2 (1.4–3.4) 0.8 (0.3–1.8) 1.0 (0.4–2.3)
≥35 1.4 (0.6–3.0) 2.7 (1.1–6.4) * 1.6 (1.1–2.2) * 1.8 (1.2–2.7) ** 0.7 (0.3–1.5) 1.1 (0.4–2.9)
Maternal religion
Other REF REF REF REF REF REF
Christian 1.2 (0.6–2.5) 1.0 (0.4–2.8) 2.2 (1.3–3.7) ** 1.9 (1.1–3.5) * 1.3 (0.6–3.0) 0.8 (0.2–2.8)
Settlement type
Urban REF REF REF REF REF REF
Rural 1.7 (0.9–3.2) 2.7 (1.2–5.9) ** 1.8 (1.1–2.8) 1.9 (1.2–3.0) *** 1.0 (0.4–2.4) 1.0 (0.4–2.6)
Fully immunized child by 12 mos. of age
No REF REF REF REF
Yes 2.0 (1.1–4.0) * 3.1 (1.4–7.1) ** 2.1 (1.6–2.8) *** 2.4 (1.7–3.4) ***
Caregiver knows MACV dose should be given during 2YL
No REF REF
Yes 1.7 (1.1–2.5) * 1.8 (0.8–3.9)
Caregiver aware of need for 18 mos. visit before 2nd birthday
No REF REF REF REF
Yes 2.0 (1.4–2.8) *** 1.9 (1.3–2.6) *** 2.8 (1.6–4.6) *** 2.8 (1.7–4.5) ***
Child attends school/daycare offering routine immunization
No REF
Yes 2.2 (1.4–3.4) **
Caregiver believes 2YL vaccine is important for their child
No REF REF
Yes 2.2 (1.1–4.2) * 1.9 (1.1–3.3) *
Caregiver believes it is important for child to get missing doses
No REF
Yes 2.0 (1.0–3.9) *
Caregiver agrees that 2YL vaccination is supported by spouse
No REF
Yes 2.5 (0.9–6.8)
Caregiver believes that 2YL vaccination supported by other family members
No REF
Yes 2.6 (1.1–5.7) *
Most people caregiver knows bring child in for 2YL vaccination
No REF
Yes 1.3 (0.8–2.2)
Caregiver believes healthcare provider provides enough information on 2YL vaccination
No REF
Yes 1.4 (0.8–2.3)
Maternal occupation
Unemployed/Housewife REF
Farmer/Laborer/Fisherwoman 0.9 (0.5–1.6)
Civil servant 0.7 (0.2–2.5)
Other occupation 0.5 (0.3–1.1)
Trader/Merchant 0.5 (0.2–1.1)
Caregiver received phone reminder for 18 mos. visit
No REF
Yes 1.4 (0.8–2.6)
B
GAR (N = 370) NR (N = 870) VR (N = 315)
Unadjusted Adjusted Unadjusted Adjusted Unadjusted Adjusted
OR 95% CI OR 95% CI OR 95% CI OR 95% CI OR 95% CI OR 95% CI
Child’s age (months)
18–23 REF REF REF REF REF REF
24–35 1.6 (1.0–2.4) * 3.2 (1.7–6.2) *** 2.2 (1.6–3.0) *** 2.9 (2.1–4.1) *** 4.6 (2.1–9.9) *** 4.6 (2.1–10.5) ***
Child’s sex
Female REF REF REF REF REF REF
Male 0.8 (0.4–1.3) 0.9 (0.5–1.9) 0.6 (0.4–0.9) * 0.7 (0.4–1.1) 1.2 (0.5–3.0) 1.2 (0.5–2.7)
Birth order
First REF REF REF REF REF REF
Second 0.7 (0.3–1.4) 0.6 (0.2–2.0) 0.8 (0.5–1.4) 0.8 (0.4–1.4) 1.4 (0.5–4.2) 1.5 (0.4–4.7)
Third or more 0.6 (0.3–1.1) 0.3 (0.1–0.8) * 0.9 (0.6–1.4) 0.6 (0.3–1.1) 0.5 (0.3–0.9) * 0.4 (0.2–0.8) **
Maternal education
Never attended school REF REF REF REF REF REF
Primary 0.8 (0.2–2.5) 1.4 (0.4–4.9) 0.5 (0.2–1.2) 0.7 (0.3–1.9) 0.9 (0.2–2.9) 1.2 (0.4–3.8)
Secondary or higher 1.2 (0.5–2.8) 1.9 (0.8–4.2) 0.7 (0.4–1.2) 1.0 (0.6–1.6) 1.3 (0.6–3.0) 1.3 (0.5–3.4)
Maternal age (years)
<25 REF REF REF REF REF REF
25–34 1.6 (0.6–3.9) 1.8 (0.4–8.2) 2.0 (1.2–3.2) ** 2.1 (1.3–3.4) ** 0.8 (0.3–1.7 1.0 (0.4–2.1)
≥35 1.0 (0.5–2.0) 2.2 (0.7–7.2) 1.9 (1.2–2.7) ** 2.2 (1.4–3.3) *** 0.7 (0.2–2.2) 1.1 (0.4–2.8)
Maternal religion
Other REF REF REF REF REF REF
Christian 1.2 (0.6–2.2) 1.1 (0.4–2.4) 2.2 (1.1–4.2) * 1.9 (0.9–3.7) 1.6 (0.7–3.5) 1.1 (0.4–2.6)
Settlement type
Urban REF REF REF REF REF REF
Rural 1.3 (0.7–2.2) 1.8 (0.8–4.0) 2.2 (1.3–3.7) ** 2.6 (1.5–4.3) *** 1.5 (0.6–3.8) 1.7 (0.6–4.4)
Fully immunized child by 12 mos. of age
No REF REF REF REF
Yes 2.7 (1.4–5.5) ** 3.8 (1.6–8.5) ** 2.4 (1.7–3.3) *** 2.9 (1.9–4.3) ***
Caregiver knows MCV dose should be given during 2YL
No REF REF REF
Yes 1.8 (1.1–2.9) * 2.4 (1.2–4.9) * 1.7 (1.1–2.5) **
Caregiver aware of need for 18 mos. visit before 2nd birthday
No REF REF REF REF
Yes 1.8 (1.2–2.7) *** 1.7 (1.1–2.5) ** 3.1 (1.9–5.3) *** 2.7 (1.7–4.3) ***
Child attends school/daycare offering routine immunization
No REF REF
Yes 1.8 (1.1–2.9) *** 2.6 (0.7–9.1)
Caregiver believes 2YL vaccine is important for their child
No REF REF
Yes 2.8 (1.3–5.9) ** 2.8 (1.4–5.6) **
Caregiver believes it is important for child to get missing doses
No REF
Yes 2.7 (1.4–5.3) **
Caregiver agrees that 2YL vaccination is supported by spouse
No REF
Yes 3.6 (1.3–9.6) *
Caregiver believes that 2YL vaccination supported by other family members
No REF REF
Yes 2.9 (1.2–6.9) * 0.3 (0.0–1.5)
Most people caregiver knows bring child in for 2YL vaccination
No REF
Yes 1.8 (1.1–3.0) *
Caregiver believes healthcare provider provides enough information on 2YL vaccination
No REF
Yes 1.8 (1.1–2.9) *
Paternal education
Never attended school REF REF
Primary 0.8 (0.3–2.1) 1.8 (0.4–7.4)
Secondary or higher 0.7 (0.4–1.2) 1.8 (0.8–4.1)

* p-value < 0.05; ** p-value < 0.01; *** p-value < 0.001.

3.3.1. Child-Level Predictors

In all regions, children aged 24–35 months were more likely to be vaccinated with 2YL vaccines compared with those aged 18–23 months with aORs ranging from 3.0 (95% CI, 2.1–4.2) for MCV2 in NR to 7.2 (95% CI, 3.3–15.8) for MACV in VR. Higher birth order (third or higher) was significantly associated with lower odds of vaccination for MCV2 compared to being born first in both GAR (aOR: 0.4; 95% CI, 0.2–0.9) and VR (aOR: 0.5; 95% CI, 0.3–0.8), and for MACV in VR only (aOR: 0.4; 95% CI, 0.2–0.7). Being fully immunized with all infant vaccine doses by 12 months of age was positively associated with both MACV and MCV2 receipt in GAR and NR, but not VR.

3.3.2. Caregiver-Level Predictors

Children of older mothers were more likely to be vaccinated with either MACV or MCV2; this association was significant in GAR and NR but not in VR. In NR only, children of Christian mothers were twice as likely to receive MACV (aOR: 1.9, 95% CI [1.1–3.5]). There was no statistically significant association between caregiver education and occupation and MCV2 or MACV in any region.

Factors related to caregiver knowledge, attitudes, and beliefs around 2YL vaccination were found to exert some influence on 2YL vaccination status. In GAR, children of caregivers who were aware that MCV was recommended during the second year of life were almost twice as likely to receive MCV2 compared to those who were unaware (aOR:1.8; 95% CI, 1.1–2.9). In both NR and VR, children of caregivers who were aware of the 18-month child well-child visit were more likely to receive either 2YL vaccine with aORs ranging from 1.7 (95% CI, 1.16–2.6) for MCV2 in NR to 2.8 (95% CI, 1.7–4.5) for MACV in VR. In NR only, children of caregivers who believed in the importance of vaccination during the second year of life were more likely to be vaccinated with either MACV (aOR: 1.9; 95% CI, 1.1–3.4) or MCV2 (aOR: 2.9; 95% CI, 1.4–5.7).

3.3.3. Household-Level Predictors

Compared to urban areas, children living in rural areas were more likely to be vaccinated for MCV2 and MACV; however, the association was statistically significant only in GAR for MACV (aOR: 2.7; 95% CI, 1.2–5.9) and in NR for MACV (aOR:1.9; 95% CI, 1.2–3.0) and MCV2 (aOR: 2.6; 95% CI, 1.6–4.4).

3.3.4. Interaction Analysis

Although initial interaction analysis suggested that the effect of urban/rural residence in GAR depended on the availability of RI services at the child’s school (interaction term p value = 0.03), further assessment suggested that strata-specific effects were not statistically significant (Supplementary Tables S2 and S3). Therefore, the interaction term was dropped from the final model for GAR. Nonetheless, among children in urban areas of GAR, the proportion of children vaccinated with MCV2 among those attending schools with RI services was 76.9% (95% CI, 67.5–84.3) compared to 62.6% (95% CI, 55.9–68.9]) among those attending schools without the services (Chi-square p value = 0.01). In rural areas of GAR, however, the MCV2 coverage was not significantly different among children attending schools with and without RI services (Supplementary Table S4).

4. Discussion

The present study found low uptake of MACV and MCV2 among children aged 18–35 months living in three regions of Ghana in 2020 and identified several predictors of vaccine receipt during the second year of life. Vaccination coverage for 2YL vaccines was lower than the infant vaccination coverage levels and below the goal of “95% coverage for all antigens by 2019” set forth by the Ghanaian Government [29]. MCV1 to MCV2 dropout rates were substantial (12.6% to 23.8%) suggesting further opportunity to strengthen the 2YL vaccination platform. Our results indicate that predictors of 2YL vaccination include characteristics for the child (age, birth order, and immunization history), caregiver (awareness of the RI schedule, attitudes about the importance of 2YL vaccination, and maternal age) and the household (urban–rural residence).

Consistent with prior literature on childhood immunization, older children across all regions were more likely to be vaccinated with either dose compared to younger children. Although older children have a comparatively longer window of opportunity to receive the vaccine, it is also possible that the finding could reflect delays in vaccination, as studies from other low-and middle-income countries have suggested [30,31]. Further research on the timing or age of 2YL vaccine receipt could provide a better understanding of the latter hypothesis.

Increasing birth order generally reduced the likelihood of being vaccinated with 2YL vaccines. This was in line with previous research on infant immunizations in Ghana and elsewhere in Africa [22,32]. Caring for multiple children places competing demands on caregivers, with the time and resources required to meet an individual child’s healthcare needs decreasing with each additional child. Furthermore, given the importance of family support for childhood vaccination [33], those without it may experience even greater barriers. In NR, factors related to caregiver perception of spousal and other family support for 2YL immunization were significant in univariate analysis but were dropped in the final model. Possibly, the effect of these factors may be masked by other more influential factors identified in the multivariable analysis. Additional research is needed to better understand how household decision-making processes and social support for immunizations influence 2YL vaccination, particularly among large families. Nonetheless, it is concerning that younger children from larger families are less likely to receive the protection of MACV and MCV2 since these children are also more likely to be exposed to meningitis and measles by older siblings and other household members [34,35]. Leveraging health visits by caregivers from large families and home visits by healthcare workers to such families to provide tailored public health messaging on the importance of all vaccinations, including 2YL doses for younger children should be considered.

Receipt of all recommended infant vaccines prior to one year of age was strongly predictive of 2YL vaccine receipt in both GAR and NR. This finding highlights that early immunization adherence can lead to continued immunization uptake throughout childhood; 2YL vaccine coverage could be promoted by leveraging health visits during the first year of life, which are crucial opportunities to educate caregivers about the benefits of vaccination and the need to complete their child’s vaccination schedule. We found that 2YL vaccine coverage was higher among children receiving timely 9-month visit vaccinations, but not for children receiving timely 6- or 14-week visit vaccinations, which suggests that sustained vaccine schedule compliance during the first year of life may improve 2YL vaccination uptake. Possible interventions to improve 2YL vaccine uptake include strengthening the tracking of children who receive vaccinations in the first year of life, but fail to receive vaccinations in the second year of life (i.e., defaulters), improving the health system’s ability to consistently reach caregivers of under-vaccinated children, and employing simple-to-use reminder systems to improve caregiver adherence to the immunization schedule.

Caregivers’ awareness of the RI schedule was an important determinant of childhood vaccination uptake in our study. Children of caregivers who were aware of the 18-month well-child visit were significantly more likely to be vaccinated with 2YL vaccines in NR and VR. Similarly, in GAR, children of caregivers who knew that an MCV dose is needed before the second birthday were more than twice as likely to receive MCV2. These findings are consistent with a recent qualitative assessment of behavioral drivers of MACV and MCV2 vaccination among caregivers in Burkina Faso, which also concluded that knowledge gaps about the 2YL vaccination visit were a key barrier to vaccine uptake [8]. Improving awareness of the 18-month vaccination visit may increase attendance at these visits and improve 2YL vaccine coverage. Across all regions in our study, at least three-quarters of the children attending the 18-month visit received MCV2 and at least two-thirds received MACV. Altogether, these findings emphasize the need to promote the 18-month visit which can be accomplished by providing reminders to caregivers and targeted communication to communities. Ensuring that healthcare providers and community health workers receive adequate training and support in interpersonal communication regarding vaccination schedules, particularly during the second year of life, may also improve uptake. The interpersonal communication training will also need to emphasize respectful treatment of clients given previous reports that caregivers who have missed scheduled visits or bring older children for 2YL vaccinations sometimes experience rude or condescending treatment from healthcare providers [8,10].

Additionally, our findings highlight the critical role of caregiver attitudes in improving childhood vaccination [36,37,38]. Of the behavioral factors we examined, belief in the importance of 2YL vaccination emerged as an important predictor of a child’s vaccination status with both MACV and MCV2 among caregivers in NR. This finding is consistent with a previous assessment that found caregiver perception of the combined benefits and risks of vaccination was the strongest predictor of vaccine compliance relative to the other factors evaluated in this context [36]. Accordingly, public health messaging in northern Ghana could be further tailored to address the concerns about vaccine safety and to communicate the benefits of timely vaccination, particularly during the second year of life. More broadly, demand generation activities should be tailored to address caregiver demographic and cultural differences across regions. For instance, different communication approaches could be considered in NR where most caregivers are Muslim and with low literacy levels compared with those in GAR who are mostly Christian and with higher education levels. In areas such as NR where religious affiliation appears to influence 2YL vaccination, it is possible that greater involvement of religious leaders and faith-based organizations in vaccine promotion may be an effective strategy for building community trust and increasing vaccine confidence which in turn may increase uptake [39,40,41].

Children of mothers aged 25 years or older were more likely to be vaccinated with either MACV or MCV2 as compared to children of younger mothers. Although the associations were not significant across all regions, the directionality of estimates was consistent across models. Previous research assessing the effect of maternal age on child immunization status in Ghana has focused on infant vaccines with some studies finding positive, negative, or inconclusive associations [26,32,42]. Consistent with our study, a recent secondary analysis from eight sub-Saharan African countries with publicly available MCV2 data found that older maternal age was associated with a higher likelihood of vaccination with MCV2 [11]. Compared with younger mothers, older mothers may have more resources at their disposal and more bargaining power with other family members in intra-household decision-making processes related to their child’s health [43,44]. It is also possible that older mothers have higher levels of immunization-related knowledge than younger mothers [45,46].

Similar to previous studies focused on infant vaccination in Ghana, we noted urban–rural disparities with children from rural areas being more likely to be vaccinated with 2YL vaccines [25,32]. This was particularly evident for both MACV and MCV2 in NR, and for MCV2 only in GAR where residence in rural settlements was highly predictive of vaccine receipt. The rural advantage has been observed for infant vaccines since at least 2014 and is likely explained by a combination of the unequal success of Ghana’s Community-based Health Planning and Service (CHPS) initiative that had implementation challenges in urban areas, and the challenges with primary healthcare service delivery in rapidly growing informal settlements in urban areas [25,32,47]. Future immunization program planning will need to focus on underserved urban communities to address the persistent immunization inequities, particularly in GAR, which had the lowest 2YL vaccine coverage rates and highest urban population. Our findings also suggested that service delivery in urban areas of GAR could be augmented by school-based vaccination programs to increase access and close coverage gaps. Nonetheless, additional research is needed to further clarify the effectiveness of intensifying the integration of 2YL vaccination into school-based health services and daycares in urban areas.

Across all regions, coverage with MACV was lower than MCV2 coverage. This could be due to the lag effects of the more recently introduced MACV on coverage or national-level MACV stockouts for two months in 2019 due to funding delays [48]. This is consistent with our observation that nearly half of the vaccination visits MACV and MCV2 were not co-administered occurred in 2019, ultimately resulting in missed opportunities for MACV vaccination. Although children in both age groups in our study were impacted by the MACV stockouts, it is difficult to determine to what extent the stockouts impacted the observed associations. Of note, Ghana experienced disruptions to immunization services during 2020 due to the COVID-19 pandemic [49]. Since we only analyzed immunizations received prior to the beginning of the pandemic, we are unable to examine the extent to which 2YL vaccine coverage was affected by the disruptions.

5. Strengths and limitations

Our study has several strengths. First, it provides important insights into the predictors of vaccination during 2YL in Ghana, which was among the first countries in the African region to introduce 2YL vaccines [5,13]. Second, the data used for these analyses come from a household vaccination coverage survey specifically tailored to assess barriers to 2YL vaccine uptake. Third, survey methodology was used to account for the survey sampling design which minimized bias in the calculated estimates. Finally, vaccination status was verified using CHRBs and facility registers for 96.9% of the children in the study, thereby reducing the possibility of outcome misclassification bias.

This study is also subject to some limitations. First, we were unable to distinguish routine MCV doses from supplemental doses delivered through the MCV SIA campaign in Ghana during 2018 [50]. Since the survey was conducted more than a year after completion of the SIA campaign and because supplemental doses given are typically not designated as such on the CHRB, there could have been recall bias in ascertainment of MCV vaccination status. Additionally, many variables were measured based on respondent self-report, which may be subject to recall bias. Furthermore, this survey is cross-sectional so we cannot establish a temporal relationship between the examined predictors and 2YL vaccine receipt. We can only make claims on statistical associations; hence no causal inference can be made. Finally, there may be important predictors of vaccination receipt that were unmeasured in this study. For instance, place of delivery, socioeconomic status, accessibility, and convenience of vaccination services are known to influence immunization outcomes, but these data were not collected as part of the household survey. Wherever possible, we used proxy variables that could capture the effect of the omitted variable. For instance, the inclusion in our models of caregiver occupation and education levels may also capture caregiver socioeconomic status in Ghana as previously done [25]. We also did not assess the impact on 2YL vaccine uptake for health facility factors such as healthcare worker knowledge and attitudes towards immunization, adherence to EPI guidelines, workload, or vaccination supply stock practices. Future research should incorporate these aspects as they likely influence 2YL vaccine uptake.

6. Conclusions

Using data from three regions of Ghana, we found that MACV and MCV2 vaccination uptake remains lower than the infant vaccination uptake. Thus, there is room for improvement in reaching the Ghana government’s vaccination targets. Predictors of vaccination during 2YL varied across regions and included sociodemographic characteristics, as well as caregiver knowledge, attitudes, and beliefs toward vaccination. Disparities persist with children in urban areas being less likely to be vaccinated. Effective interventions will require multifaceted and context-specific approaches to improve immunization compliance overall while specifically promoting the 18-month well-child visit. Robust tracking of defaulters, targeted communication to communities, and reminders to caregivers may improve 2YL vaccine coverage. Caregivers, particularly younger mothers, with multiple children likely experience practical barriers to bringing their children for 2YL vaccination. Leveraging every health facility or home visit contacts with such caregivers to emphasize the importance of immunizations and schedule adherence should be a key consideration to increase 2YL vaccine uptake.

Acknowledgments

The efforts of the staff of the Ghana Expanded Program on Immunization and the Centers for Disease and Control, Global Immunization Division, who were involved in survey instrument design and data collection are deeply appreciated.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/vaccines11101515/s1, Figure S1: Flowchart for selection of analytic samples. Table S1. Variables assessed as predictors of 2YL vaccine receipt. Table S2. Model output for the predictors of MCV2 receipt in Greater Accra Region with interaction term for school availability of RI services and settlement type. Table S3. Joint effects of settlement type and school RI service availability on MCV2 receipt among children aged 18–35 months in Greater Accra Region. Table S4: MCV2 coverage among children aged 18–35 months by availability of RI services at school and settlement type in Greater Accra region, Ghana, 2020.

Author Contributions

Conceptualization, P.M., M.T.W., K.A.-A., P.Q., M.P.S., H.G., C.O., P.-N.A., K.L.O., W.O. and A.S.W.; methodology, P.M., M.P.S., H.G. and A.S.W.; software, P.M.; validation, H.G. and M.P.S.; formal analysis, P.M. and M.P.S.; investigation, A.S.W.; resources, M.T.W.; writing—original draft preparation, P.M.; writing—review and editing, M.T.W., K.A.-A., P.Q., M.P.S., H.G., C.O., P.-N.A., K.L.O., W.O. and A.S.W.; supervision, M.T.W., P.Q., K.A.-A., K.L.O., W.O. and A.S.W.; project administration, M.T.W., P.Q., K.A.-A., K.L.O., W.O. and A.S.W. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

The protocol was approved by the Ethical Review Board at the Ghana Health Service. The Human Subjects Office at the U.S. Centers for Disease Control and Prevention (CDC) deemed this activity as an assessment of public health practice and determined it as non-research.

Informed Consent Statement

Informed consent was obtained from all persons involved in the household survey.

Data Availability Statement

The datasets used and/or analyzed during the current project may be available upon reasonable request.

Conflicts of Interest

The authors declare no conflict of interest.

Funding Statement

This study was funded by the United States Centers for Disease Control and Prevention.

Footnotes

Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

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Associated Data

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

Supplementary Materials

Data Availability Statement

The datasets used and/or analyzed during the current project may be available upon reasonable request.


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