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Review

Global Prevalence and Potential Influencing Factors of COVID-19 Vaccination Hesitancy: A Meta-Analysis

by
Jonny Karunia Fajar
1,
Malik Sallam
2,3,4,*,
Gatot Soegiarto
5,
Yani Jane Sugiri
6,
Muhammad Anshory
7,
Laksmi Wulandari
8,
Stephanie Astrid Puspitasari Kosasih
9,
Muhammad Ilmawan
10,
Kusnaeni Kusnaeni
11,
Muhammad Fikri
11,
Frilianty Putri
12,
Baitul Hamdi
13,
Izza Dinalhaque Pranatasari
14,
Lily Aina
15,
Lailatul Maghfiroh
16,
Fernanda Septi Ikhriandanti
17,
Wa Ode Endiaverni
18,
Krisna Wahyu Nugraha
18,
Ory Wiranudirja
18,
Sally Edinov
19,
Ujang Hamdani
18,
Lathifatul Rosyidah
18,
Hanny Lubaba
18,
Rinto Ariwibowo
18,
Riska Andistyani
18,
Ria Fitriani
20,
Miftahul Hasanah
21,
Fardha Ad Durrun Nafis
21,
Fredo Tamara
1,
Fitri Olga Latamu
1,
Hendrix Indra Kusuma
22,23,24,
Ali A. Rabaan
25,26,27,
Saad Alhumaid
28,
Abbas Al Mutair
29,30,31,32,
Mohammed Garout
33,
Muhammad A. Halwani
34,
Mubarak Alfaresi
35,36,
Reyouf Al Azmi
37,
Nada A. Alasiri
38,
Abeer N. Alshukairi
26,39,
Kuldeep Dhama
40 and
Harapan Harapan
22,41,42
add Show full author list remove Hide full author list
1
Brawijaya Internal Medicine Research Center, Department of Internal Medicine, Faculty of Medicine, Universitas Brawijaya, Malang 65145, Indonesia
2
Department of Pathology, Microbiology and Forensic Medicine, School of Medicine, The University of Jordan, Amman 11942, Jordan
3
Department of Clinical Laboratories and Forensic Medicine, Jordan University Hospital, Amman 11942, Jordan
4
Department of Translational Medicine, Faculty of Medicine, Lund University, 22184 Malmö, Sweden
5
Division of Allergy and Immunology, Department of Internal Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya 60286, Indonesia
6
Department of Pulmonology and Respiratory Medicine, Faculty of Medicine, Universitas Brawijaya, Malang 65145, Indonesia
7
Division of Allergy and Immunology, Department of Internal Medicine, Faculty of Medicine, Universitas Brawijaya, Malang 65145, Indonesia
8
Department of Pulmonology and Respiratory Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya 60286, Indonesia
9
Faculty of Medicine, Universitas Brawijaya, Malang 65145, Indonesia
10
Department of Urology, Faculty of Medicine, Universitas Brawijaya, Malang 65145, Indonesia
11
Faculty of Matematics and Sciences, Institut Pertanian Bogor, Bogor 16680, Indonesia
12
School of Veterinary Medicine and Biomedicine, Institut Pertanian Bogor, Bogor 16680, Indonesia
13
Faculty of Economy and Business, Universitas Airlangga, Surabaya 60286, Indonesia
14
Faculty of Public Health, Universitas Airlangga, Surabaya 60286, Indonesia
15
Faculty of Pharmacy, Universitas Airlangga, Surabaya 60286, Indonesia
16
Faculty of Veterinary Medicine, Universitas Airlangga, Surabaya 60286, Indonesia
17
Faculty of Medicine, Universitas Airlangga, Surabaya 60286, Indonesia
18
Faculty of Economy and Business, Universitas Brawijaya, Malang 65145, Indonesia
19
Faculty of Economics and Business, Riau University, Pekanbaru 28293, Indonesia
20
Faculty of Administrative Science, Universitas Brawijaya, Malang 65145, Indonesia
21
Faculty of Animal Science, Universitas Brawijaya, Malang 65145, Indonesia
22
Medical Research Unit, School of Medicine, Universitas Syiah Kuala, Banda Aceh 23111, Indonesia
23
Faculty of Mathematics and Natural Sciences, Universitas Syiah Kuala, Darussalam, Banda Aceh 23111, Indonesia
24
Faculty of Tarbiyah and Teacher Training, Universitas Islam Negeri Ar-Raniry, Banda Aceh 23111, Indonesia
25
Molecular Diagnostic Laboratory, Johns Hopkins Aramco Healthcare, Dhahran 31311, Saudi Arabia
26
College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia
27
Department of Public Health and Nutrition, The University of Haripur, Haripur 22610, Pakistan
28
Administration of Pharmaceutical Care, Al-Ahsa Health Cluster, Ministry of Health, Al-Ahsa 31982, Saudi Arabia
29
Research Center, Almoosa Specialist Hospital, Al Mubarrazs 36342, Saudi Arabia
30
College of Nursing, Princess Norah Bint Abdulrahman University, Riyadh 11564, Saudi Arabia
31
School of Nursing, Wollongong University, Wollongong, NSW 2522, Australia
32
Nursing Department, Prince Sultan Military College of Health Sciences, Dhahran 33048, Saudi Arabia
33
Department of Community Medicine and Health Care for Pilgrims, Faculty of Medicine, Umm Al-Qura University, Makkah 21955, Saudi Arabia
34
Department of Medical Microbiology, Faculty of Medicine, Al Baha University, Al Baha 4781, Saudi Arabia
35
Department of Pathology and Laboratory Medicine, Sheikh Khalifa General Hospital, Umm Al Quwain 499, United Arab Emirates
36
Department of Pathology, College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai 505055, United Arab Emirates
37
Infection Prevention and Control, Eastern Health Cluster, Dammam 32253, Saudi Arabia
38
Scientific Advisory Council, InsanCare Group for Scientific Studies and Specialized Business Solutions, Riyadh 13313, Saudi Arabia
39
Department of Medicine, King Faisal Specialist Hospital and Research Center, Jeddah 12713, Saudi Arabia
40
Division of Pathology, ICAR–Indian Veterinary Research Institute, Izatnagar, Bareilly 243122, India
41
Tropical Disease Centre, School of Medicine, Universitas Syiah Kuala, Banda Aceh 23111, Indonesia
42
Department of Microbiology, School of Medicine, Universitas Syiah Kuala, Banda Aceh 23111, Indonesia
*
Author to whom correspondence should be addressed.
Vaccines 2022, 10(8), 1356; https://doi.org/10.3390/vaccines10081356
Submission received: 16 June 2022 / Revised: 8 August 2022 / Accepted: 15 August 2022 / Published: 19 August 2022
(This article belongs to the Section Human Vaccines and Public Health)

Abstract

:
Countries worldwide have deployed mass COVID-19 vaccination drives, but there are people who are hesitant to receive the vaccine. Studies assessing the factors associated with COVID-19 vaccination hesitancy are inconclusive. This study aimed to assess the global prevalence of COVID-19 vaccination hesitancy and determine the potential factors associated with such hesitancy. We performed an organized search for relevant articles in PubMed, Scopus, and Web of Science. Extraction of the required information was performed for each study. A single-arm meta-analysis was performed to determine the global prevalence of COVID-19 vaccination hesitancy; the potential factors related to vaccine hesitancy were analyzed using a Z-test. A total of 56 articles were included in our analysis. We found that the global prevalence of COVID-19 vaccination hesitancy was 25%. Being a woman, being a 50-year-old or younger, being single, being unemployed, living in a household with five or more individuals, having an educational attainment lower than an undergraduate degree, having a non-healthcare-related job and considering COVID-19 vaccines to be unsafe were associated with a higher risk of vaccination hesitancy. In contrast, living with children at home, maintaining physical distancing norms, having ever tested for COVID-19, and having a history of influenza vaccination in the past few years were associated with a lower risk of hesitancy to COVID-19 vaccination. Our study provides valuable information on COVID-19 vaccination hesitancy, and we recommend special interventions in the sub-populations with increased risk to reduce COVID-19 vaccine hesitancy.

1. Introduction

Coronavirus disease 2019 (COVID-19) vaccination has been progressing globally since the beginning of 2021. Several types of vaccines, including inactivated, vector-based, messenger ribonucleic acid (mRNA), and protein subunit vaccines, are being administered to recipients [1]. Since the vaccines became available, there have been expectations of the COVID-19 pandemic ending, considering that previous vaccination programs have been effective in managing several infectious diseases such as rubella, mumps, measles, and polio. These vaccination programs have been proven to improve global health and the economy [2,3]. However, the probability of failure of any vaccination program should be assessed. A study reported that the barriers to effective vaccination programs include inconvenient and limited clinic hours for immunization, inadequate access to healthcare, high vaccine administration fees, and vaccine hesitancy [4]. Of these factors, vaccine hesitancy is considered one of the most critical [5]. Individuals who are hesitant to be immunized have a tendency to spread incorrect information about vaccination, which may influence people close to them to reject vaccines as well [6].
Vaccine hesitancy is commonly observed in the case of new vaccines or vaccine candidates [7,8]. This phenomenon was reported in the case of malaria [9], dengue [10], and Ebola [11]. The factors contributing to vaccine hesitancy are complex and may include a lack of awareness regarding disease prevention and socioeconomic status [12,13]. This phenomenon poses a dilemma to vaccine coverage. Moreover, governments—as the highest regulatory authority of any nation—seemingly do not provide special interventions to reduce hesitancy toward vaccination programs. It is observed in the guidelines on COVID-19 vaccination, that the primary recommendation only focused on dose allocation, outreach, delivery, and monitoring; there was no information on how to reduce COVID-19 vaccination hesitancy [14].
Regarding COVID-19 vaccination, several studies have been conducted to assess the prevalence of COVID-19 vaccine hesitancy and its associated predictors [7,8,15]. However, the findings were inconclusive with variability regarding the correlation between COVID-19 vaccine acceptance and the following: sociodemographic factors, vaccine confidence and trust regarding vaccine safety, complacency towards the disease, conspiracy beliefs towards COVID-19 vaccination and willingness to pay for the vaccine [7,16,17,18,19,20,21]. Therefore, a meta-analysis is necessary to determine the potential factors influencing COVID-19 vaccination hesitancy.

2. Materials and Methods

2.1. Study Design

During the period May–June 2022, we conducted a meta-analysis that followed the protocols of the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) [22,23]. In line with the purpose of our study, we first performed an organized search of PubMed, Scopus, and Web of Science and, subsequently, collected the required information to calculate the global prevalence of vaccine hesitancy and effect estimates of the potential influencing factors. The PRISMA checklist for this review is provided in (Supplementary Materials). Additionally, data used in this review are available in Figshare (https://doi.org/10.6084/m9.figshare.20055539.v3, accessed on 6 December 2022) [23].

2.2. Eligibility Criteria

We determined the eligibility criteria before conducting the organized search. An article was included in the analysis if the following inclusion criteria were met: (1) whether it assessed the prevalence of COVID-19 vaccination hesitancy or (2) identified potential factors influencing COVID-19 vaccination hesitancy. Reviews, commentaries, letters to the editor, grey literature, and double publications were excluded.

2.3. Search Strategy and Data Extraction

As of 25 May 2022, we performed an organized search of PubMed, Scopus, and Web of Science. Prior to the search for the main outcomes, the potential factors associated with COVID-19 vaccination hesitancy were determined. We used keywords from the following medical subject headings: “vaccine”, “vaccination”, or “immunization”; “COVID-19” or “coronavirus disease 2019”; “hesitancy” or “acceptance”. We limited the organized search to the English language. If we found any duplication, we included the studies with larger sample sizes. Furthermore, we also conducted an organized search of the reference lists of the relevant articles to obtain additional papers. Thereupon, the following information was collected from the selected articles: (1) first author name, (2) year of publication, (3) study design, (4) study period, (5) Newcastle–Ottawa scale (NOS), (6) the prevalence of COVID-19 vaccination hesitancy, and (7) event rate of potential factors associated with COVID-19 vaccination hesitancy. Two independent teams, led by JKF and SAPK, conducted the article search and data extraction. Prior to the systematic search, the kappa statistic was used to measure the agreement between the two investigators. If the kappa statistic was greater than the p-value, agreement was established.

2.4. Assessment of the Methodological Quality

All potential articles for inclusion in the study were assessed for quality using NOS [24]. The quality was considered high, moderate, or low if the score was 7–9, 4–6, or 0–3, respectively. Low-quality articles were excluded from the analysis. Using a pilot form, the two independent teams, led by JKF and SAPK, conducted the NOS assessment, and any discrepancies were resolved through discussion.

2.5. Outcome Measures

The major outcomes were global prevalence and potential influencing factors of COVID-19 vaccination hesitancy. To identify the potential factors associated with vaccine hesitancy, we performed an initial organized search in PubMed, Scopus, and Web of Science. We identified the following potential factors: age group, gender, marital status, educational attainment, religion, employment status, healthcare-related job, socioeconomic status, urbanity, presence of children and elderly people at home, household size, and presence of family members with a medical background. Additionally, wearing masks, hand hygiene, compliance with physical distancing norms, smoking, history of chronic disease, personal history of COVID-19 diagnosis, COVID-19 diagnosis of a family member/friend, hospitalization due to COVID-19 among people in the same social circle, death owing to COVID-19 among people in the same social circle, safety conceptions about COVID-19 vaccines, and history of influenza vaccination in the past few years were also factors of interest.

2.6. Statistical Analysis

Before calculating the global prevalence of COVID-19 vaccination hesitancy and effect estimates of potential predictors of such hesitancy, we conducted an analysis of potential publication bias and heterogeneity among the studies. We analyzed the risk of publication bias using the Egger’s test, with a p-value of <0.05 suggesting the existence of publication bias. Furthermore, we performed an analysis of heterogeneity among studies using the Q test, with a p-value of <0.10 indicating heterogeneity; thus, a random effects model was applied for data analysis—in cases where there was no heterogeneity, a fixed-effects model was used. A single-arm meta-analysis was performed using the dichotomous covariate method to calculate the event rate from each study to discern the global prevalence of COVID-19 vaccination hesitancy. The effect estimate was presented as the event rate. The analysis was performed using the R package (RStudio version 4.1.1, R Studio, Boston, MA, USA). The effect estimates of potential factors associated with COVID-19 vaccination hesitancy were outlined in a forest plot as a pooled odds ratio and 95% confidence interval (OR, 95% CI).

3. Results

3.1. Selection of Studies

We retrieved 4299 potential papers from the databases mentioned and 18 from the reference lists of related articles. Of these, 23 papers were excluded owing to duplication and 4219 papers with irrelevant subjects. Thus, 75 articles were included in the full-text review. Subsequently, six reviews and thirteen articles were excluded because of insufficient data. Eventually, a total of 56 articles were included in the final analysis to calculate the global prevalence and potential influencing factors in COVID-19 vaccination hesitancy [19,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79]. The plotting of article selection in our study is presented in (Figure 1), and the characteristics of the included articles are listed in (Table 1).

3.2. Global Prevalence of COVID-19 Vaccination Hesitancy

To calculate the global prevalence of COVID-19 vaccination hesitancy, we included a total of 56 articles. Data analysis using the random effects model revealed that the global prevalence was 25% (event rate: 0.25; 95% CI: 0.19, 0.32; p Egger’s: 1.2710; p heterogeneity: <0.0001; p < 0.0001). The global prevalence of COVID-19 vaccination hesitancy is presented in (Figure 2A). In sub-group analysis, we found that the prevalence of COVID-19 vaccination hesitancy in the general population (Figure 2B), healthcare workers (Figure 2C), and students (Figure 2D) was 25%, 26%, and 25%, respectively.

3.3. Potential Factors Associated with COVID-19 Vaccination Hesitancy

The potential factors associated with COVID-19 vaccination hesitancy are summarized in (Table 2) and presented in (Figure 3, Figure 4, Figure 5 and Figure 6). Our analysis revealed that out of 25 factors, 12 of them were associated with COVID-19 vaccine hesitancy. The following factors were associated with a higher risk of vaccination hesitancy: being a woman (compared to man) (Figure 3A), being ≤50 years old (compared to those older than 50 years (Figure 3B), being single (compared to married individuals) (Figure 3C), being unemployed (compared to employed) (Figure 4A), living in a household with five or more individuals (compared to living in smaller households) (Figure 4B), having an educational attainment lower than an undergraduate degree (compared to those with an undergraduate degree or higher) (Figure 5A), having a non-healthcare-related job (compared to having a healthcare-related job) (Figure 5B), and considering COVID-19 vaccines to be unsafe (compared to those who consider COVID-19 vaccines to be safe) (Figure 5C).
In contrast, living with children at home (compared to having no child at home) (Figure 6A), maintaining physical distancing norms (compared to not following such norms) (Figure 6B), having ever tested for COVID-19 (compared to having never tested for COVID-19) (Figure 6C), and having a history of influenza vaccination in the past few years (compared to not having been vaccinated for influenza in the past few years) (Figure 6D) were associated with a lower risk of hesitancy to COVID-19 vaccination.

3.4. Source of Heterogeneity and Potential Publication Bias

Heterogeneity was not found for six variables (Christian religion, household size ≥ 5 individuals, family members with a medical background, smoking, hospitalization due to COVID-19 among people in the same social circle, and death owing to COVID-19 among people in the same social circle). Therefore, we used a fixed-effects model. Conversely, other variables were assessed using a random effects model. The Egger’s test was used to assess potential bias among the studies. Our pooled analyses revealed a risk of publication bias for the following covariates: the Christian religion, family members with a medical background, hospitalization due to COVID-19 among people in the same social circle, and death owing to COVID-19 among people in the same social circle (Table 2).

4. Discussion

Our study estimated the global prevalence of COVID-19 vaccination hesitancy at 25%. The current findings are consistent with those of previous meta-analyses, which estimated the prevalence of vaccine hesitancy in the general population at 26–42% [15,80,81,82,83]. In special populations, previous meta-analyses revealed that the hesitancy for COVID-19 vaccination was estimated at 24%, 27%, and 26% in multiple sclerosis patients, older people, and healthcare students, respectively [84,85,86]. Furthermore, hesitancy to receive a COVID-19 booster was reported at 21% in the general population [87]. Moreover, high rates of COVID-19 vaccine hesitancy were reported among the ethnic minorities in the UK [88]. Our estimate was in the range of extant literature. However, our study had a larger sample size, which might have provided a more accurate calculation. Moreover, in sub-group analysis, we also identified that the prevalence of COVID-19 vaccination hesitancy was 25%, 26%, and 25% in the general population, healthcare workers, and students, respectively. This study also identified the potential predictors of COVID-19 vaccine hesitancy, thereby providing more comprehensive evidence on this phenomenon.
The current study noted that the potential factors associated with COVID-19 vaccination hesitancy can be contextualized in terms of awareness, knowledge, and socioeconomic status. In the context of awareness of COVID-19 vaccination, we found that older people (>50 years), those living with children at home, individuals who have ever tested for COVID-19, and those with a history of influenza vaccination had a lower risk of COVID-19 vaccination hesitancy. In contrast, several factors, such as single marital status and unemployment, were associated with an increased risk of hesitancy toward COVID-19 vaccination.
The precise underlying factors contributing to COVID-19 vaccination hesitancy could not be defined clearly. However, some presumptions may explain these findings. Older individuals are more likely to suffer from one or more chronic diseases compared to younger people. In our previous investigation, we found that advanced age and comorbidity were associated with an increased risk of severity in COVID-19 patients [89]. Therefore, the possibility of an increased risk of severe COVID-19 might influence the awareness of such individuals and contribute to a lower risk of COVID-19 vaccination hesitancy in this group due to low levels of complacency [90].
Similarly, individuals living with children at home might be afraid of transmitting the virus to their children should they be infected with COVID-19. Therefore, it is reasonable that this group is less hesitant to receive COVID-19 vaccination. Interestingly, a similar impact was not observed in individuals living with elderly people at home. This ironic finding is supported by previous studies, which found that living with children was a crucial determinant of health-related behavior [91], whereas this was not the case for individuals living with elderly people [92].
Furthermore, individuals who have ever tested for COVID-19 and had a history of influenza vaccination might have had good practice in disease prevention. Disease screening and vaccination history have been shown to affect health behavior, which can possibly explain why this group is less averse to COVID-19 vaccination. Moreover, married individuals might engage in protective behavior toward their spouse; couples have mutual concern and might have a better life expectancy than single individuals. A previous study found that married individuals had better health behavior and a lower risk of mortality than single individuals [93]. Thus, single individuals might be more averse than married individuals to COVID-19 vaccination. This reason, in the context of poor health behavior, might also explain vaccine hesitancy in unemployed individuals.
Our study also found that individuals with lower educational levels and those who consider COVID-19 vaccines to be unsafe had a higher risk of COVID-19 vaccination hesitancy. In contrast, individuals with healthcare-related jobs had a lower risk of COVID-19 vaccination hesitancy. The association between higher educational levels, knowledge of disease prevention, and vaccine acceptance or hesitancy has been widely investigated [16,94,95,96]. Individuals with higher educational levels and healthcare-related jobs might have adequate information on the global pandemic and consider vaccination to be a great step toward ending the pandemic, which can explain why this group had a lower risk of vaccine hesitancy. Our current findings are supported by previous studies in the context of dengue, Ebola, and monkeypox vaccines. Those studies also showed that knowledge of disease prevention and good health practices had a significant impact on the acceptance of vaccine candidates [97,98,99,100,101].
Although we could not elucidate the role of socioeconomic status in COVID-19 vaccination hesitancy in this study, we found that some factors related to socioeconomic status, such as unemployment and household size (≥5 individuals), were associated with COVID-19 vaccination hesitancy. Socioeconomic status has been proven to affect health-related behavior [102]. Individuals with a low socioeconomic status might lack knowledge of the pandemic and the role of vaccination in the pandemic. Moreover, individuals with a low socioeconomic status might also lack social interaction; therefore, they might lack adequate knowledge concerning disease prevention, which could contribute to COVID-19 vaccination hesitancy. Previous meta-analyses in this context did not assess the role of socioeconomic status in COVID-19 vaccination hesitancy. However, in other settings, such as in the case of dengue vaccines, socioeconomic status was found to affect vaccination acceptance [100].
To the best of our knowledge, this meta-analysis is the first comprehensive study to assess COVID-19 vaccination hesitancy worldwide. In sub-group analysis, our study identified similar prevalence rates of hesitancy to COVID-19 vaccination in the general population, healthcare workers, and students; suggesting that interventions to reduce the risk of COVID-19 vaccination hesitancy in those populations do not need to be differentiated. In addition to reporting the global prevalence, we also identified the potential factors associated with hesitancy to receive COVID-19 vaccination. Although the COVID-19 vaccination program targets the global population, some people have been hesitant to receive the vaccine. Our study identified the factors associated with such hesitancy, thereby shedding light on the populations that require special attention in order for the vaccination program to be successful. We recommend customized interventions and education for these special populations. A study suggested that customized effective, ethical, and evidence-based communication may be able to increase the acceptance of the COVID-19 vaccination [103]. This customized intervention was suggested to provide by community leaders and healthcare practitioners to establish the trust of COVID-19 vaccination [88]. Moreover, a recent study also reported that providing the population with reliable information regarding the COVID-19 pandemic and the COVID-19 vaccination was associated with the increased rate of vaccination acceptance among the Israeli parents [104]. On the other hand, while we have provided the valuable information on the factors associated with the risk COVID-19 vaccine hesitancy, it should be realized that the main factor driving individuals to be able to receive the vaccinations is the proven effectiveness and safety of vaccines in well-documented long-term studies. However, among those exhibiting COVID-19 vaccination hesitancy, there are people who outright refuse vaccination. Therefore, further studies should be performed with a focus on this group.
There are some potential limitations of our study. First, a meta-analysis is a methodological approach conducted by calculating the crude effect of the related factors to determine the evidence. However, the impact of potential confounding factors is difficult to evaluate. In the current study, potential confounding factors such as the types of COVID-19 vaccine, government regulations, source of information regarding COVID-19 vaccination, and environmental factors were not included; therefore, our findings should be interpreted carefully. We reported that considering the COVID-19 vaccine to be unsafe was one of the factors associated with increased risk of COVID-19 vaccination hesitancy. Considering that the different types of COVID-19 vaccine have different side effects; the factors of the type of vaccine might also govern the final findings. Moreover, the government regulations in several countries have implemented COVID-19 vaccination as a condition of administration, and the regulations in each country may have differences; thereby, this circumstance may also affect the final findings of this study. Therefore, we reiterate the importance of the basic tenet in studying the phenomenon of vaccine hesitancy, which is the time, context, place, and type specificity. All these peculiarities need to be considered in the efforts aiming to fathom the determinants of vaccine hesitancy [105]. Second, our study involved a multi-national population, and the knowledge of disease prevention among people with similar socioeconomic status and educational level might vary in each region. Third, all the papers included in our study had an observational research design. Therefore, further studies including randomized controlled trials are required in order to obtain better levels of evidence.

5. Conclusions

Our study estimated the global prevalence of COVID-19 vaccination hesitancy at 25%. It also recommended special interventions to minimize COVID-19 vaccination hesitancy among unmarried individuals, women, people with low educational levels, the unemployed, people living in households with five or more individuals, and those who believe COVID-19 vaccines to be unsafe.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/vaccines10081356/s1, Supplementary S1: PRISMA 2020 Checklist.

Author Contributions

Conceptualization, J.K.F. and G.S.; methodology, J.K.F., Y.J.S., M.A. (Muhammad Anshory), L.W., S.A.P.K., M.I., K.K., M.F., F.P., B.H., I.D.P., L.A., L.M., F.S.I., W.O.E., K.W.N., O.W., S.E., U.H., L.R., H.L., R.A. (Rinto Ariwibowo), R.A. (Riska Andistyani), R.F., M.H., F.A.D.N., F.T. and F.O.L.; software, J.K.F.; validation, J.K.F., M.S., G.S., Y.J.S., M.A. (Muhammad Anshory), L.W., S.A.P.K., M.I., K.K., M.F., F.P., B.H., I.D.P., L.A., L.M., F.S.I., W.O.E., K.W.N., O.W., S.E., U.H., L.R., H.L., R.A. (Rinto Ariwibowo), R.A. (Riska Andistyani), R.F., M.H., F.A.D.N., F.T., F.O.L., H.I.K., A.A.R., S.A., A.A.M., M.G., M.A.H., M.A. (Mubarak Alfaresi), R.A.A., N.A.A., A.N.A., K.D. and H.H.; formal analysis, J.K.F.; investigation, J.K.F., Y.J.S., M.A. (Mubarak Alfaresi), L.W., S.A.P.K., M.I., K.K., M.F., F.P., B.H., I.D.P., L.A., L.M., F.S.I., W.O.E., K.W.N., O.W., S.E., U.H., L.R., H.L., R.A. (Rinto Ariwibowo), R.A. (Riska Andistyani), R.F., M.H., F.A.D.N., F.T. and F.O.L.; re-sources, M.S., H.I.K., A.A.R., S.A., A.A.M., M.G., M.A.H., M.A. (Mubarak Alfaresi), R.A.A., N.A.A., A.N.A., K.D. and H.H.; data curation, J.K.F., Y.J.S., M.A. (Muhammad Anshory), L.W., S.A.P.K., M.I., K.K., M.F., F.P., B.H., I.D.P., L.A., L.M., F.S.I., W.O.E., K.W.N., O.W., S.E., U.H., L.R., H.L., R.A. (Rinto Ariwibowo), R.A. (Riska Andistyani), R.F., M.H., F.A.D.N., F.T. and F.O.L.; writing—original draft preparation, J.K.F., Y.J.S., M.A. (Muhammad Anshory), L.W., S.A.P.K., M.I., K.K., M.F., F.P., B.H., I.D.P., L.A., L.M., F.S.I., W.O.E., K.W.N., O.W., S.E., U.H., L.R., H.L., R.A. (Rinto Ariwibowo), R.A. (Riska Andistyani), R.F., M.H., F.A.D.N., F.T. and F.O.L.; writing—review and editing, J.K.F., M.S., G.S., A.A.R., S.A., A.A.M., M.G., M.A.H., M.A. (Mubarak Alfaresi), R.A.A., N.A.A., A.N.A., K.D. and H.H.; visualization, J.K.F.; supervision, G.S., A.A.R., S.A., A.A.M., M.G., M.A.H., M.A. (Muhammad Anshory), R.A.A., N.A.A., A.N.A., K.D. and H.H.; project administration, J.K.F. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All data underlying the results are available at the Supplementary Files (https://doi.org/10.6084/m9.figshare.20055539.v3). Accessed on 11 June 2022.

Acknowledgments

We thank Lembaga Pengelola Dana Pendidikan (LPDP) Republic of Indonesia for supporting this project.

Conflicts of Interest

The authors declare no conflict of interest.

References

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Figure 1. A flowchart of article selection in this review.
Figure 1. A flowchart of article selection in this review.
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Figure 2. The global prevalence of hesitancy to COVID-19 vaccination (event rate: 0.25; 95% CI: 0.20, 0.32; p Egger: 1.2580; p heterogeneity: <0.0001; p: <0.0001) (A). The prevalence of hesitancy to COVID-19 vaccination among general population (event rate: 0.25; 95% CI: 0.18, 0.34; p Egger: 1.3090; p heterogeneity: <0.0001; p: <0.0001) (B). The prevalence of hesitancy to COVID-19 vaccination among healthcare workers (event rate: 0.26; 95% CI: 0.18, 0.37; p Egger: 0.7670; p heterogeneity: <0.0001; p: <0.0001) (C). The prevalence of hesitancy to COVID-19 vaccination among students (event rate: 0.25; 95% CI: 0.14, 0.40; p Egger: 1.2090; p heterogeneity: <0.0001; p: 0.0030) (D). The studies included are provided in the reference list [19,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79].
Figure 2. The global prevalence of hesitancy to COVID-19 vaccination (event rate: 0.25; 95% CI: 0.20, 0.32; p Egger: 1.2580; p heterogeneity: <0.0001; p: <0.0001) (A). The prevalence of hesitancy to COVID-19 vaccination among general population (event rate: 0.25; 95% CI: 0.18, 0.34; p Egger: 1.3090; p heterogeneity: <0.0001; p: <0.0001) (B). The prevalence of hesitancy to COVID-19 vaccination among healthcare workers (event rate: 0.26; 95% CI: 0.18, 0.37; p Egger: 0.7670; p heterogeneity: <0.0001; p: <0.0001) (C). The prevalence of hesitancy to COVID-19 vaccination among students (event rate: 0.25; 95% CI: 0.14, 0.40; p Egger: 1.2090; p heterogeneity: <0.0001; p: 0.0030) (D). The studies included are provided in the reference list [19,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79].
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Figure 3. Female was associated with increased risk of hesitancy to COVID-19 vaccination compared to male (OR: 1.32; 95% CI: 1.17, 1.49; p Egger: 0.2840; p heterogeneity: <0.0001; p: <0.0001) (A). Individuals with age > 50 years was associated with lower risk of hesitancy to COVID-19 vaccination compared to individuals with age ≤ 50 years (OR: 0.79; 95% CI: 0.64, 0.98; p Egger: 0.2980; p Het: <0.0001; p: 0.0290) (B). Single individuals had higher risk of hesitancy to COVID-19 vaccination than married individuals (OR: 1.19; 95% CI: 1.06, 1.34; p Egger: 0.1950; p heterogeneity: <0.0001; p: 0.0040) (C). The studies included are provided in the reference list [19,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79].
Figure 3. Female was associated with increased risk of hesitancy to COVID-19 vaccination compared to male (OR: 1.32; 95% CI: 1.17, 1.49; p Egger: 0.2840; p heterogeneity: <0.0001; p: <0.0001) (A). Individuals with age > 50 years was associated with lower risk of hesitancy to COVID-19 vaccination compared to individuals with age ≤ 50 years (OR: 0.79; 95% CI: 0.64, 0.98; p Egger: 0.2980; p Het: <0.0001; p: 0.0290) (B). Single individuals had higher risk of hesitancy to COVID-19 vaccination than married individuals (OR: 1.19; 95% CI: 1.06, 1.34; p Egger: 0.1950; p heterogeneity: <0.0001; p: 0.0040) (C). The studies included are provided in the reference list [19,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79].
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Figure 4. Unemployed individuals were associated with increased risk of hesitancy to COVID-19 vaccination compared to working individuals (OR: 1.20; 95% CI: 1.02, 1.42; p Egger: 0.1790; p heterogeneity: 0.0090; p: 0.0300) (A); individuals with household number ≥ 5 individuals had higher risk of hesitancy to COVID-19 vaccination (OR: 1.36; 95% CI: 1.13, 1.63; p Egger: 0.1680; p heterogeneity: 0.1620; p: 0.0010) (B). The studies included are provided in the reference list [19,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79].
Figure 4. Unemployed individuals were associated with increased risk of hesitancy to COVID-19 vaccination compared to working individuals (OR: 1.20; 95% CI: 1.02, 1.42; p Egger: 0.1790; p heterogeneity: 0.0090; p: 0.0300) (A); individuals with household number ≥ 5 individuals had higher risk of hesitancy to COVID-19 vaccination (OR: 1.36; 95% CI: 1.13, 1.63; p Egger: 0.1680; p heterogeneity: 0.1620; p: 0.0010) (B). The studies included are provided in the reference list [19,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79].
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Figure 5. Individuals with the education levels < BSC had higher risk of hesitancy to COVID-19 vaccination than ≥ BSC (OR: 1.30; 95% CI: 1.03, 1.65; p Egger: 0.5260; p heterogeneity: <0.0001; p: 0.0300) (A); individuals having the healthcare-related job had lower risk of hesitancy to COVID-19 vaccination (OR: 0.68; 95% CI: 0.52, 0.89; p Egger: 0.3340; p heterogeneity: <0.0001; p: 0.0040) (B); Individuals considering that COVID-19 vaccines are not safe had higher risk of hesitancy to COVID-19 vaccination (OR: 2.24; 95% CI: 1.21, 4.14; p Egger: 0.7000; p heterogeneity: <0.0001; p: 0.0100) (C). The studies included are provided in the reference list [19,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79].
Figure 5. Individuals with the education levels < BSC had higher risk of hesitancy to COVID-19 vaccination than ≥ BSC (OR: 1.30; 95% CI: 1.03, 1.65; p Egger: 0.5260; p heterogeneity: <0.0001; p: 0.0300) (A); individuals having the healthcare-related job had lower risk of hesitancy to COVID-19 vaccination (OR: 0.68; 95% CI: 0.52, 0.89; p Egger: 0.3340; p heterogeneity: <0.0001; p: 0.0040) (B); Individuals considering that COVID-19 vaccines are not safe had higher risk of hesitancy to COVID-19 vaccination (OR: 2.24; 95% CI: 1.21, 4.14; p Egger: 0.7000; p heterogeneity: <0.0001; p: 0.0100) (C). The studies included are provided in the reference list [19,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79].
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Figure 6. Individuals living with children in the home had lower risk of hesitancy to COVID-19 vaccination (OR: 0.37; 95% CI: 0.14, 0.99; p Egger: 1.4040; p heterogeneity: <0.0001; p: 0.0490) (A); individuals keeping physical distancing had lower risk of hesitancy to COVID-19 vaccination (OR: 0.23; 95% CI: 0.08, 0.65; p Egger: 0.8370; p heterogeneity: 0.0010; p: 0.0050 (B); individuals with history of COVID-19 test were associated with lower risk of hesitancy to COVID-19 vaccination (OR: 0.46; 95% CI: 0.31, 0.68; p Egger: 0.4340; p heterogeneity: <0.0001; p: <0.0001) (C); individuals with history of influenza vaccination in the past few years had lower risk of hesitancy to COVID-19 vaccination (OR: 0.46; 95% CI: 0.36, 0.58; p Egger: 0.3460; p heterogeneity: <0.0001; p: <0.0001) (D). The studies included are provided in the reference list [19,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79].
Figure 6. Individuals living with children in the home had lower risk of hesitancy to COVID-19 vaccination (OR: 0.37; 95% CI: 0.14, 0.99; p Egger: 1.4040; p heterogeneity: <0.0001; p: 0.0490) (A); individuals keeping physical distancing had lower risk of hesitancy to COVID-19 vaccination (OR: 0.23; 95% CI: 0.08, 0.65; p Egger: 0.8370; p heterogeneity: 0.0010; p: 0.0050 (B); individuals with history of COVID-19 test were associated with lower risk of hesitancy to COVID-19 vaccination (OR: 0.46; 95% CI: 0.31, 0.68; p Egger: 0.4340; p heterogeneity: <0.0001; p: <0.0001) (C); individuals with history of influenza vaccination in the past few years had lower risk of hesitancy to COVID-19 vaccination (OR: 0.46; 95% CI: 0.36, 0.58; p Egger: 0.3460; p heterogeneity: <0.0001; p: <0.0001) (D). The studies included are provided in the reference list [19,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79].
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Table 1. Baseline characteristics of articles included in our analysis [19,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79].
Table 1. Baseline characteristics of articles included in our analysis [19,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79].
Author and YearCountrySample SizeStudy PeriodPopulationFundingNOS 1
Aemro et al., 2021 [25]Ethiopia418May–June 2021Healthcare workersNo funding5
Ali et al., 2021 [26]Bangladesh1134January 2021General populationNo funding6
Barry et al., 2021 [27]Saudi Arabia1512November 2020Healthcare workersNo funding6
Bell et al., 2020 [28]England1252April–May 2020General populationLondon School of Hygiene and Tropical Medicine6
Chen et al., 2021 [29]China2531January 2021General populationNA7
Chudasama et al., 2022 [30]Multinational275April–July 2021Healthcare workersNA6
Detoc et al., 2020 [31]France3259March–April 2020General populationNA5
Dong et al., 2020 [32]China1236June–July 2020General populationChinese University of Hong Kong6
Dror et al., 2020 [33]Israel16612020–2022Healthcare workersNA5
Faasse et al., 2020 [34]Australia2232March 2020General populationUNSW Science Goldstar (2020)5
Fisher et al., 2020 [35]US991April 2020General populationAgency for Healthcare Research and Quality 7
Goodwin et al., 2022 [36]Multinational3059December 2020–January 2021General populationAriel University, JSPS KAKENSHI, Hungaria National Excellence Program6
Habib et al., 2022 [37]Saudi Arabia1445August–October 2021StudentsKing Saud University7
Bou Hamdan et al., 2021 [38]Lebanon758May–June 2021StudentsNo funding7
Harapan et al., 2020 [39]Indonesia1359March–April 2020General populationNo funding6
Horiuchi et al., 2021 [40]Japan1200May–June 2021General populationNo funding7
Hossain et al., 2021 [41]Bangladesh1497February 2021General populationNo funding6
Huang et al., 2022 [42]China4227January–March 2021General populationNational Health Commission of the People’s Republic of China7
Ikiisik et al., 2021 [43]Turkey384December 2020General populationNA7
Jabessa et al., 2022 [44]Ethiopia350August–September 2021General populationNo funding6
Jain et al., 2021 [45]India1068February–March 2021StudentsNo funding6
Kelekar et al., 2021 [46]US408September–December 2020StudentsNA6
Khubchandani et al., 2021 [47]US1878June 2020General populationNo funding8
Koh et al., 2022 [48]Singapore528May–June 2021Healthcare workersNo funding6
Kumar et al., 2021 [49]Qatar1414October–November 2020Healthcare workersQatar National Library5
Lazarus et al., 2020 [50]Multinational13,426June 2020General populationCity University of New York6
Lee et al., 2022 [51]South Korea1016January 2021General populationNo funding6
Li et al., 2022 [52]China721June 2021StudentsXuzhou Medical University7
Liddell et al., 2021 [53]Australia437June 2021General populationUNSW Sydney/Australian Red Cross6
Lucia et al., 2021 [54]US167NAStudentsNo funding5
Malik et al., 2020 [55]US672May 2020General populationYale Institute for Global Health8
Marzo et al., 2022 [56]Multinational5260February–May 2021General populationNo funding7
Mascarenhas et al., 2021 [57]US2452020StudentsNo funding6
Mohammed et al., 2021 [58]Ethiopia614March–July 2021Healthcare workersNo funding7
Mose et al., 2022 [59]Ethiopia420March 2021StudentsNo funding6
Nery et al., 2022 [60]Brazil2537November 2020–January 2021General populationBrazilian Ministry of Health8
Neumann-Böhme et al., 2020 [61]Multinational7664April 2020General populationEuropean Union’s Horizon 2020 research and innovation programme6
Ousseine et al., 2022 [62]France15,427February–April 2021General populationNational Agency for Research on AIDS and Viral Hepatitis (ANRS)6
Patwary et al., 2021 [19]Bangladesh543July–August 2021General populationNo funding6
Qunaibi et al., 2021 [63]Multinational36,220January 2021General populationNo funding7
Raja et al., 2022 [64]Sudan217June–July 2021StudentsNo funding5
Reiter et al., 2020 [65]US2006May 2020General populationNational Center for Advancing Translational Sciences7
Rodríguez-Blanco et al., 2021 [66]Spain2494November–December 2020General populationNo funding6
Saied et al., 2021 [67]Egypt2133January 2021StudentsNA7
Salali et al., 2020 [68]Multinational5024May 2020General populationNo funding6
Schwarzinger et al., 2021 [69]France1942July 2020General populationFrench Public Health Agency 7
Shah et al., 2021 [70]India274February 2021StudentsNA7
Singh et al., 2021 [71]Hong Kong245May 2021General populationTung Foundation7
Tao et al., 2021 [72]China1392November 2020General populationNational Key Research and Development Project of China7
Tlale et al., 2022 [73]Botswana4952February 2021General populationNo funding6
Wang et al., 2020 [74]Hong Kong806February–March 2020Healthcare workersNo funding6
Ward et al., 2020 [75]France5018April 2020General populationAgence Nationale de la Recheche and the CNRS8
Wong et al., 2020 [76]Malaysia1159April 2020General populationMinistry of Education Malaysia8
Wu et al., 2021 [77]China29,925August 2021General populationNational Social Science Fund of China7
Xu et al., 2021 [78]China5247January 2021Healthcare workersHealth Commission of Chongqing municipal, China6
Yassin et al., 2022 [79]Sudan365April 2021Healthcare workersNA6
1 NOS: Newcastle–Ottawa scale; all selected studies were based on a cross-sectional design.
Table 2. The potential factors associated with the hesitancy to COVID-19 vaccination.
Table 2. The potential factors associated with the hesitancy to COVID-19 vaccination.
CovariatesHesitancy/Total (n [%])NSp Eggerp HetOR95% CIp
Age group (years)
≤306568/14,356 [45.8]160.2320<0.00011.140.98–1.320.0870
31–405097/11,335 [45.0]160.2360<0.00011.090.94–1.260.2630
41–503034/6536 [46.4]150.2730<0.00010.880.74–1.060.1760
>502034/4677 [43.5]130.2980<0.00010.790.64–0.980.0290
Sex
Male8934/22,362 [40.0]310.2840<0.00010.760.67–0.85<0.0001
Female11,170/28,707 [38.9]310.2840<0.00011.321.17–1.49<0.0001
Marital status
Married6888/20,496 [33.6]170.1950<0.00010.840.75–0.950.0040
Single7173/18,764 [38.2]170.1950<0.00011.191.06–1.340.0040
Educational attainment
<BSC12,130/22,950 [52.9]220.5260<0.00011.301.03–1.650.0300
≥BSC17,532/41,182 [42.6]220.5260<0.00010.770.61–0.970.0300
Religion
Christian1053/2124 [49.6]5<0.00010.43801.171.01–1.350.0340
Muslim1265/3961 [31.9]60.5110<0.00011.390.85–2.260.1860
Hindu16/129 [12.4]21.57000.07100.280.02–3.400.3150
Employment
Not working1704/4455 [38.2]100.17900.00901.201.02–1.420.0300
Working5883/16,413 [35.8]100.17900.00900.830.71–0.980.0300
Healthcare-related job2886/8313 [34.7]100.3340<0.00010.680.52–0.890.0040
Socioeconomic status
Low income1320/2939 [44.9]70.4840<0.00011.310.88–1.940.1790
Middle income1217/3220 [37.8]71.2050<0.00010.610.25–1.520.2900
High income1427/2515 [56.7]71.2860<0.00011.280.49–3.380.6140
Urbanicity
Urban9192/28,583 [32.2]150.4500<0.00010.920.72–1.180.5070
Rural3128/8338 [37.5]150.4500<0.00011.090.85–1.390.5070
Children at home1207/4595 [26.3]81.4040<0.00010.370.14–0.990.0490
Aged people at home456/1542 [29.6]50.27600.01401.070.78–1.450.6920
Household number (n)
≤2930/3192 [29.1]50.3900<0.00010.940.64–1.360.7270
3–4564/2067 [27.3]50.22900.01100.890.69–1.140.3510
≥5278/712 [39.0]40.16800.16201.361.13–1.630.0010
Family members with medical backgrounds464/1382 [33.6]20.04100.31700.920.78–1.070.2770
Wearing masks all the time1523/6606 [23.1]60.5570<0.00010.610.36–1.050.0720
Constantly washing hands1209/4974 [24.3]40.8900<0.00010.450.18–1.160.0980
Keep physical distancing213/745 [28.6]30.83700.00100.230.08–0.650.0050
Smoker665/2236 [29.7]50.05900.33601.130.99–1.290.0610
History of chronic disease(s)3828/8197 [46.7]170.1840<0.00010.910.80–1.030.1420
Ever tested for COVID-19670/4430 [15.1]60.4340<0.00010.460.31–0.68<0.0001
Personal history of COVID-19 diagnosis4114/7733 [53.2]150.6090<0.00010.940.66–1.330.7150
Family member/friend ever diagnosed with COVID-191192/3759 [31.7]70.2960<0.00010.830.63–1.090.1730
Hospitalization due to COVID-19 among people in the same social circle69/621 [11.1]2<0.00010.97700.570.37–0.880.0110
Death due to COVID-19 among people in the same social circle63/537 [11.7]3<0.00010.94500.730.49–1.080.1160
COVID-19 vaccines are not safe628/1595 [39.4]60.7000<0.00012.241.21–4.140.0100
Influenza vaccination in the past few years3481/10,687 [32.6]110.3460<0.00010.460.36–0.58<0.0001
OR: odds ratio; CI: confidence interval; NS: number of studies; p Het: p heterogeneity; BSC: Bachelor of Science.
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Fajar, J.K.; Sallam, M.; Soegiarto, G.; Sugiri, Y.J.; Anshory, M.; Wulandari, L.; Kosasih, S.A.P.; Ilmawan, M.; Kusnaeni, K.; Fikri, M.; et al. Global Prevalence and Potential Influencing Factors of COVID-19 Vaccination Hesitancy: A Meta-Analysis. Vaccines 2022, 10, 1356. https://doi.org/10.3390/vaccines10081356

AMA Style

Fajar JK, Sallam M, Soegiarto G, Sugiri YJ, Anshory M, Wulandari L, Kosasih SAP, Ilmawan M, Kusnaeni K, Fikri M, et al. Global Prevalence and Potential Influencing Factors of COVID-19 Vaccination Hesitancy: A Meta-Analysis. Vaccines. 2022; 10(8):1356. https://doi.org/10.3390/vaccines10081356

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Fajar, Jonny Karunia, Malik Sallam, Gatot Soegiarto, Yani Jane Sugiri, Muhammad Anshory, Laksmi Wulandari, Stephanie Astrid Puspitasari Kosasih, Muhammad Ilmawan, Kusnaeni Kusnaeni, Muhammad Fikri, and et al. 2022. "Global Prevalence and Potential Influencing Factors of COVID-19 Vaccination Hesitancy: A Meta-Analysis" Vaccines 10, no. 8: 1356. https://doi.org/10.3390/vaccines10081356

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