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Article

Vaccination Coverage of Greek Adults Aged ≥60 Years in a Primary Health Care Setting in Relation to Lifestyle Factors and Health Care Services Utilization

by
Nektaria Kossyva
1,
Marios Spanakis
1,*,†,
Lena Borboudaki
1,†,
Dimitrios Stylianakis
1,
Nikos Rikos
2,*,
Michael Rovithis
3,
Chryssoula Perdikogianni
4,
Manolis Linardakis
1 and
Emmanouil K. Symvoulakis
1
1
Department of Social Medicine, School of Medicine, University of Crete, 70013 Heraklion, Greece
2
Department of Nursing, School of Health Sciences, Hellenic Mediterranean University, 71410 Heraklion, Greece
3
Department of Business Administration & Tourism, School of Management and Economics Sciences, Hellenic Mediterranean University, 71410 Heraklion, Greece
4
Department of Pediatrics, School of Medicine, University of Crete, 70013 Heraklion, Greece
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Healthcare 2026, 14(9), 1167; https://doi.org/10.3390/healthcare14091167
Submission received: 31 March 2026 / Revised: 23 April 2026 / Accepted: 23 April 2026 / Published: 27 April 2026

Highlights

What are the main findings?
  • Influenza and COVID-19 vaccination coverage were high, whereas Tdap and RSV uptake remained low among adults aged ≥60 years.
  • Higher vaccination coverage was associated with greater health care utilization, higher education level, and increased comorbidity burden.
What are the implications of the main findings?
  • Strengthening Primary Health Care engagement and preventive service use may substantially improve adult vaccination uptake.
  • Targeted educational and access-focused strategies are needed to address gaps in Tdap and RSV vaccination among older adults.

Abstract

Background/Objectives: Vaccination represents a significant achievement of public health and should be regarded not only as a protective measure against infectious diseases but also an active preventive intervention and a component of health promotion. Methods: This cross-sectional study assessed vaccination coverage among adults aged ≥60 years who attended a Primary Health Care Center during a predefined period of at least two months (November–December 2025) in a rural area of Crete, Greece, and examined determinants of immunization, including demographic, clinical, psychosocial, and health service utilization factors. The sample comprised 366 participants who consented to complete a structured questionnaire, primarily via interview, followed by verification of vaccination status through medical records. Results: High vaccination coverage was observed for influenza (82.5%), moderate coverage for pneumococcal (68.3%) and herpes zoster (56.0%) vaccines, and very low coverage for tetanus–diphtheria–pertussis booster doses (≈13%) and RSV vaccination (5.2%). For SARS-CoV-2, 96.2% received the three doses which were mandatory during the pandemic years. The overall Vaccination Coverage Score (VCS) averaged 43.1/100, while only 10.1% of participants achieved high coverage. Regression analysis showed that higher educational level, multimorbidity, and extensive use of health services were independently associated with better vaccination coverage (p < 0.05). Conclusions: The findings reveal fragmented vaccination patterns and underscore the need for systematic assessment of adult vaccination status within routine Primary Health Care. Targeted counseling, promotion of health literacy, and preventive vaccination strategies are expected to reduce vaccine-preventable morbidity and support healthy aging.

1. Introduction

Vaccination represents one of the most significant achievements of public health. Technological advances have expanded vaccinology from prevention toward modulating applications and from infectious diseases to immune-mediated disorders [1]. Nevertheless, universal vaccination coverage among adults—particularly older and oldest-old populations—has not been effectively achieved and remains a major challenge for health systems and Primary Health Care (PHC) globally and nationally [2,3,4,5].
Vaccination programs have traditionally focused on infants and children whereas adult immunization has only recently become a priority [4,6,7]. One of the reasons is population aging, which represents a major societal challenge, intensifying research on older adults and healthcare systems [8,9]. Aging is characterized by the gradual accumulation of cellular damage that leads to loss of physiological integrity and decline in immune function, increasing susceptibility to infections and chronic diseases [10,11]. These processes contribute to multimorbidity and greater healthcare needs, highlighting the importance of preventive interventions [12,13]. As life expectancy rises globally, promoting healthy aging becomes essential for the sustainability of healthcare systems [14,15,16,17].
In recognition of these challenges, international recommendations and strategies have been developed to improve adult vaccination coverage. In 2009, a joint working group of the European Union Geriatric Medicine Society and the International Association of Gerontology and Geriatrics—European Region issued recommendations for vaccination in adults aged >60 years, outlining strategies to improve vaccination uptake in Europe [18,19,20]. Given that the burden of infectious diseases is greater at the extremes of age, the primary objective is healthy aging supported by lifelong immunization [7,21]. But since these initiatives, a complicating factor emerged regarding adult vaccination coverage, the COVID-19 pandemic [22,23]. Nevertheless, the Immunization Agenda 2030 (IA2030) initiative, led by international scientific bodies including the World Health Organization and UNICEF, aims to ensure that all individuals benefit from vaccination throughout the life course in conjunction with appropriate use of health services [24,25].
Vaccination protects older adults and vulnerable populations by increasing healthy life years, reducing infection transmission, lowering hospitalization rates, and mitigating the burden on healthcare systems [26,27,28]. Influenza, pneumococcal, herpes zoster, and COVID-19 vaccines are particularly important for older adults. Influenza vaccination reduces mortality, prevents co-infections, and mitigates healthcare utilization [27,29], while pneumococcal vaccination addresses a leading cause of morbidity and mortality [30,31,32]. Herpes zoster vaccination prevents painful reactivations, and COVID-19 vaccines have proven highly effective in preventing severe disease [33,34,35,36,37,38]. Other vaccines, including diphtheria, tetanus, pertussis, and respiratory syncytial virus (RSV), remain underutilized despite evidence of increased susceptibility among older adults [39,40,41,42,43].
However, despite the growing importance of adult immunization, evidence on vaccination coverage and its determinants among older adults in Primary Health Care settings remains limited, particularly in Mediterranean regions such as Greece. Vaccination should be regarded not only as a protective measure against infectious diseases but also as an active preventive intervention and a component of health promotion [17,44,45]. In rural areas with often limited healthcare facilities this can be crucial. Hence, understanding patterns of behavior—including healthcare service utilization, engagement with preventive care, and broader health-related behaviors—beyond simply recording vaccination coverage is important. Such insights can guide interventions that target behavioral health to enhance vaccination compliance, support preventive care, and ultimately improve quality of life.
Within this context, the present study aims to assess vaccination coverage for key vaccines recommended for adults aged ≥60 years who use Primary Health Care services in a rural area of Greece and to investigate associated demographic, clinical, and behavioral determinants. Findings are expected to inform targeted PHC interventions that strengthen preventive health strategies, promote active engagement in vaccination, and support healthy aging.

2. Materials and Methods

2.1. Study Design

This cross-sectional study was conducted at a Primary Health Care Center in Crete, Greece, under the supervision of the Department of Social Medicine, School of Medicine, University of Crete. The Primary Health Care Center is in the rural area of Kastelli Pediados, operating under the supervision of the 7th Health Region of Crete. The Primary Health Care Center currently actively serves a rural population of approximately 4000 residents in the district with approximately 25–30% of them being over 60 according to recent census data [46]. In this population for elderly people (≥60 years) the percentage distribution of the age groups 60–69, 70–79 and >80 is relatively homogeneous with an average percentage of around 30% for each group per area. Eligible participants were invited to enroll according to a predefined protocol including the collection of data on vaccination coverage, biometric and clinical characteristics, health behaviors, and health service utilization.

2.2. Ethical Approval and Informed Consent

The study protocol was approved by the 7th Health Region of Crete (Approval Number: 49520; Date: 10 November 2025). All participants were informed about the study objectives, procedures, and the voluntary nature of participation and provided written informed consent. The study was conducted in accordance with the Declaration of Helsinki and relevant national and institutional ethical guidelines. All data collected were anonymized prior to any analysis.

2.3. Setting and Participants

A total of n = 366 participants aged ≥60 years were recruited from routine outpatient visits at the Health Center during a predefined period of at least two months (November–December 2025). Participants were Greek-speaking residents of the area for at least 10 years. Exclusion criteria included cognitive or communication impairment, age < 60 years, and emergency clinical presentation. Recruitment occurred through consecutive routine appointments across three weekly clinical sessions. In total, 400 individuals were deemed eligible to participate, of whom 34 were excluded: 10 due to communication disorders and cognitive impairment, 18 due to refusal to participate or withdrawal of consent, and 6 due to acute illness. Overall, n = 366 participants were enrolled and provided complete data for analysis.

2.4. Data Collection Procedures

All interviews were conducted in a designated clinical office during routine visits. Participants were informed about the study objectives and data anonymity and provided written consent. Vaccination status was verified using medical records and used to calculate the VCS according to the national immunization program for influenza, tetanus, diphtheria, pertussis, herpes zoster, pneumococcal disease, SARS-CoV-2, and respiratory synRSV. Vaccination history was assessed in accordance with national adult immunization recommendations and standard booster schedules, in line with public health strategies aimed at improving vaccine uptake and ensuring consistent data retrieval from electronic medical records. The VCS (also expressed as a percentage) was defined based on vaccination status across these eight vaccines within the recommended timeframes. Each administered vaccine was assigned a value of 1 and non-vaccination a value of 0. If a participant has received an influenza vaccine in 2024 and 2025, they received a value of 1; if they had also received the tetanus vaccine, they also received a value of 1 and so forth with all the remaining 6 vaccines. The sum of the values received determines a score of 0–8 (0 no vaccine, 8 all vaccines), which was linearly transformed to a 0–100 scale [16]. High coverage was assessed as those with a score ≥ 66.7, a threshold that refers to the upper tertile or 2/3 of the distribution of the score 0–100.
Additional questionnaire included:
i.
Sociodemographic and clinical characteristics (gender, age, subjective age perception, family status, educational level, medication use in the past 6 months, and diagnosed chronic conditions; see results Section 3.1);
ii.
Health behaviors including body mass index (BMI), sleep duration, smoking, alcohol consumption, daily fruit or vegetable intake and physical activity, clustering of behavioral risk factors [47].
iii.
Health Care Services Utilization score (HCSUs) based on six questions (see Results Section 3.2). The HCSUs ranged from 0 to 100 and was calculated from coded responses (0–1) to six items (sum range 0–9) followed by linear transformation [9,16]. Similarly with the VCS, high usage was assessed as those with a score ≥ 66.7, a threshold that refers to the upper tertile or 2/3 of the 0–100 score distribution.
iv.
Alcohol consumption was assessed using the Greek version of the FAST-screening tool; high consumption was defined as ≥3 drinks for females and ≥4 drinks for males per occasion in the last year [47,48]. Behavioral risk factor clustering was defined as the presence of ≥3 of the following: BMI ≥ 25 kg/m2, smoking, high alcohol consumption, absence of daily fruit and vegetable intake (<7 days/week), and absence of daily physical activity (walking < 7 days/week) [47,48].
v.
Anxiety was measured using the Greek version of the Short Anxiety Screening Test—10 (SAST-10) (score range 10–40). Categories were defined as negative (<22), borderline (22–23), and positive (≥24) [49,50].

2.5. Statistical Analysis

Data was analyzed using SPSS (IBM SPSS Statistics for Windows, version 25.0; IBM Corp., Armonk, NY, USA). Descriptive statistics were calculated for participant characteristics and prevalence of chronic conditions, multimorbidity, health behaviors, mental status, HCSUs, and VCSs. Percentage frequency of vaccination coverage was also reported using the corresponding 95% confidence intervals (95%CI). Cluster analysis was performed using Ward’s method and Euclidean distance for binary data for the eight vaccines, followed by dendrogram visualization. The distribution normality of HCSUs and VCs was assessed using Blom’s method (Q–Q plot). Due to slight skewness (abnormality), associations between VCs and participant characteristics, health behaviors, anxiety levels, and HCSUs were examined using Spearman’s correlation. Hierarchical multiple logistic regression analysis was also performed to assess the high VCS (≥66.7). The acceptable level of significance was set at 0.05.

3. Results

3.1. Participant Characteristics

Table 1 presents the characteristics of the 366 adults aged ≥60 years who participated in the study. Females comprised 50.8% (n = 186) of the sample. Participants aged ≥80 years were 30.3% (n = 111) of the study sample while the mean age of all was 74.6 years (SD = 8.0) and the mean subjective age was 64.1 years (SD = 19.4).
Regarding socioeconomic and health characteristics, 51.9% (n = 190) of participants had no or low educational attainment and 93.2% (n = 341) reported medication use during the previous six months. The most prevalent chronic condition was hypertension (69.9%, n = 242), followed by dyslipidemia (63.3%, n = 219) and diabetes mellitus (28.6%, n = 99). Multimorbidity, defined as the presence of ≥3 chronic conditions, was observed in 54.9% (n = 201) of participants.

3.2. Health Habits, Mental Status, and Health Care Services Utilization

Health-related behaviors and anxiety levels are summarized in Table 2. The mean BMI was 27.9 kg/m2 (SD = 4.7), with 74.3% of participants classified as overweight or obese. Participants reported a mean nightly sleep duration of 6.7 h (SD = 1.5).
Current smoking was reported by 15.9% of participants, with a mean consumption of 18.7 cigarettes per day (SD = 10.9) and a mean smoking duration of 43.3 years (SD = 11.8). High alcohol consumption during the previous year was reported by 11.2% (n = 41) of participants. The majority (58.5%, n = 214) did not consume fruits and vegetables daily, and 23.2% (n = 85) reported no daily physical activity. Multiple behavioral risk factors were present in 24.0% (n = 24) of participants.
The mean SAST score was 16.2 (SD = 4.8). Most participants were classified as negative for anxiety disorder (82.2%, n = 301), while 8.8% (n = 32) were classified as borderline and 9.0% (n = 33) as positive for anxiety disorder.
Health care utilization patterns are presented in Table 3. More than half of the participants (52.5%, n = 192) reported visiting a primary care provider up to twice annually, while 32.5% (n = 119) reported 3–4 visits and 15.0% (n = 55) reported more than four visits per year. Hospitalization within the previous three years was reported by 25.7% (n = 94) of participants. Nearly all participants (94.0%, n = 344) reported monthly out-of-pocket medication expenses, with a mean cost of €35.4.
Preventive service use was limited: 54.9% (n = 201) had never undergone colonoscopy screening, 10.2% (n = 19) of women had never undergone mammography, and 45.6% (n = 167) had never undergone a cardiac stress test. The mean HCSUs was 37.8 (SD = 18.0). Most participants (90.7%, n = 332) demonstrated low-to-moderate utilization levels, while 9.3% (n = 34) demonstrated high utilization.

3.3. Vaccination Status

Vaccination coverage levels are presented in Table 4. Influenza vaccination coverage was 82.5% (n = 302) for 2025 and 80.6% (n = 295) for 2024. Vaccination coverage for tetanus, diphtheria, and pertussis between 2017 and 2025 was low [13.1% (n = 48), 12.8% (n = 47), and 12.3% (n = 45), respectively]. Coverage for herpes zoster vaccination was 56.0% (n = 205), with 22.4% (n = 46) having received the second dose. Pneumococcal vaccination coverage was 68.3% (n = 250), and SARS-CoV-2 vaccination coverage reached 96.6% (n = 340) of vaccinated individuals having received three doses but none reported the updated subsequent doses. RSV vaccination coverage during 2024–2025 was 5.2% (n = 19).
The mean VCS was 43.1 (SD = 20.2). Most participants (89.9%, n = 329) demonstrated low-to-moderate vaccination coverage, whereas 10.1% (n = 37) achieved high coverage. Eight participants (2.2%) had received none of the assessed vaccines, whereas five participants (1.4%) had received all eight. Given that the VCS reflects the proportion of the 8 assessed vaccines received, the threshold for high coverage (VCS ≥ 66.7) corresponds approximately to receipt of at least 5–6 of the vaccines assessed in the current study.
Hierarchical cluster analysis identified two main vaccine groupings which are combined with each other and within the groups (Figure 1):
(i)
Tetanus, diphtheria, pertussis, and RSV vaccines;
(ii)
Influenza, herpes zoster, pneumococcal, and SARS-CoV-2 vaccines.

3.4. Correlates of Vaccination Coverage and Predictors of High VCS

Associations between vaccination coverage and participant characteristics, health service utilization, health behaviors, and anxiety levels are presented in Table 5. Higher VCS values were significantly associated with male gender (rho = −0.141, p = 0.007), younger age (rho = −0.119, p = 0.023), younger subjective age perception (rho = −0.163, p = 0.002), higher educational level (rho = 0.203, p < 0.001), and multimorbidity (rho = 0.123, p = 0.018). Higher VCS was also associated with having undergone colonoscopy (rho = 0.133, p = 0.011), having undergone a cardiac stress test (rho = 0.180, p = 0.001), and higher HCSUs (rho = 0.129, p = 0.013).
Regarding health behaviors, higher VCs values were associated with daily fruit and vegetable consumption (rho = 0.104, p = 0.048), daily physical activity (rho = 0.120, p = 0.022), and lower anxiety scores (rho = −0.105, p = 0.045). No significant associations were observed for BMI, smoking status, alcohol consumption, sleep duration, or clustering of behavioral risk factors.
Results of hierarchical multiple logistic regression analysis are presented in Table 6. In Model 1, higher educational level (OR = 1.42, p = 0.008) and multimorbidity (OR = 3.52, p = 0.004) were independently associated with high vaccination coverage (VCS ≥ 66.7). In Model 2, with each level of increase in educational level, the odds of high vaccination coverage significantly increase (OR = 1.37, p = 0.022) as does the presence of multimorbidity (OR = 3.53, p = 0.006). Also, each unit increase in HCSUs appears to significantly increase the odds of high vaccination coverage (OR = 1.03, p = 0.012). Lifestyle behaviors and anxiety levels were not independently associated with VCS (p > 0.05).

4. Discussion

4.1. Main Findings in the Context of Existing Literature

Population aging represents a major societal challenge that has increased attention on the health needs of older adults and the sustainability of healthcare systems [8,9]. The gradual accumulation of cellular senescence due to aging mechanisms that also impact the immune system increases the vulnerability to infections and contributes to multimorbidity [10,11,12]. Promoting healthy aging becomes increasingly important, and vaccination constitutes a key preventive intervention for reducing the burden of vaccine-preventable diseases and their complications among older adults [6,14,20]. Vaccination should be seen as a prospective measure for an individual to achieve healthy aging [51]. Therefore, addressing existing gaps and barriers that hinder the advancement of a life course approach to vaccination is essential to guide approaches for strengthening vaccination compliance [14,17,35,44,52,53].
The present study evaluated vaccination coverage among individuals aged over 60 years according to the Greek national adult vaccination program. The study population was characterized by a considerable clinical burden, with a high prevalence of multimorbidity and frequent pharmaceutical treatment, suggesting a population that could benefit substantially from preventive measures. Despite this profile, overall vaccination coverage remained moderate, with only a small proportion of participants achieving high vaccination coverage. This finding suggests that vaccination among older adults is often implemented selectively rather than as part of a comprehensive preventive strategy. All assessed vaccines are provided free of charge to eligible adults under the national immunization program in Greece. Therefore, financial barriers were unlikely to significantly influence vaccination uptake in our study population.
Influenza vaccination coverage was particularly high, exceeding 80%, a finding consistent with previous studies in Greece [33,42,54]. This may reflect the long-standing implementation of national vaccination campaigns and the active involvement of community pharmacies in vaccine administration [33,55,56]. Influenza infection is associated with increased healthcare utilization, complications, and hospitalizations among older adults, highlighting the importance of vaccination in reducing disease burden and healthcare system pressure [57,58,59,60,61,62,63].
SARS-CoV-2 vaccination coverage was deemed high regarding the mandatory doses, with 96.6% of the sample having received a third dose. As for later updated doses, negligence and aversion to continuing receiving it was reported. Widespread use of COVID-19 vaccines was necessary for controlling the COVID-19 pandemic. Randomized trials for COVID-19 vaccines demonstrated approximately 95% efficacy and protection against severe disease [36,37,38]. Among the elderly, the benefits of vaccination far outweigh potential risks [64]. Generally, the results of this work are comparable with previously published data as to the vaccine coverage for SARS-CoV-2, the mandatory three dosages and the subsequent updated ones [54,65,66,67]. The annual immunization for high-risk groups indicates the need of a stable acceptance of the vaccine in the elderly despite any vaccination fatigue. One strategy to enhance uptake is to promote the fact that COVID-19 vaccination is part of a routine, annual immunization schedule for vulnerable groups—like influenza vaccines—rather than a single, isolated dose. Cultivating this understanding is critical, as it may positively influence vaccination compliance and support broader efforts to increase coverage in the community [24,68,69,70,71].
In contrast, vaccination coverage for diphtheria, tetanus, and pertussis was low. Previous studies have shown that protective antibody levels for these infections decline with age, increasing vulnerability among older populations [39,40,41,42]. Similarly, tetanus cases are disproportionately reported among individuals over 65 years of age, while pertussis has also been associated with increased mortality in older adults [72,73,74].
Pneumococcal vaccination coverage in the present study was relatively high compared with previous Greek studies [33,42,54]. Considering that respiratory infections remain a major cause of morbidity and mortality worldwide, pneumococcal vaccination represents an important preventive intervention for older adults [31,32,75,76]. Herpes zoster vaccination coverage was also higher than previously reported in Greek populations, which may reflect increased preventive awareness or local characteristics of the healthcare system and population [33,34,77].
Conversely, vaccination coverage for RSV was very low, likely due to the recent introduction of this vaccine into adult immunization programs and limited public awareness [43,78]. Nevertheless, RSV is increasingly recognized as an important cause of respiratory infection among older adults and is associated with significant morbidity, hospitalization, and mortality [79,80,81,82]. Emerging evidence indicates substantial vaccine effectiveness in preventing severe outcomes [83,84,85].
Overall, the clustering of influenza and COVID-19 vaccination coverage and the subsequent findings regarding the rest of the vaccine compliance as observed in this study suggests that vaccination behavior may be influenced by perceived disease risk and the intensity of public health communication [68,77,86,87]. Vaccines associated with widely discussed or urgent health threats appear to achieve higher coverage, whereas vaccines linked to long-term complications or less visible diseases may receive lower priority [69,88,89].
Several demographic and clinical factors were associated with vaccination coverage. Gender differences were observed, with men demonstrating higher vaccination rates than women, a pattern previously reported in other studies for influenza and COVID-19 vaccines [90,91,92,93]. Educational level was positively associated with vaccination coverage, supporting the importance of health literacy in preventive decision-making [94,95,96]. Multimorbidity was also associated with higher vaccination coverage, possibly because individuals with multiple chronic conditions have more frequent interactions with healthcare services and greater perceived vulnerability to infectious diseases [54,97,98].
Healthcare service utilization was generally low in the study population, although higher utilization was associated with higher vaccination coverage. Preventive examinations such as colonoscopy and cardiac stress testing were also linked to higher vaccination rates, suggesting that vaccination may be part of a broader pattern of preventive healthcare behaviors. These findings highlight the important role of Primary Health Care in promoting vaccination among older adults, as regular contact with healthcare providers creates opportunities for vaccination recommendations and patient education [71,86,99,100].
Vaccination coverage among older adults has important implications for healthcare system sustainability and population health outcomes. As aging populations increase the burden of vaccine-preventable diseases, vaccination remains a cost-effective strategy to reduce complications, healthcare utilization, and mortality [4,17,20,28]. However, vaccination coverage often remains suboptimal despite free vaccination programs, indicating that psychological, educational, and social barriers also influence vaccine uptake [7,28,88,90,101]. Factors such as vaccine confidence, perceived risk, digital literacy, and sociocultural influences may shape vaccination decisions [26,27,102,103,104,105]. Strengthening vaccination strategies within Primary Health Care and promoting a life course approach to immunization may therefore contribute to improving vaccination coverage and supporting healthy aging.

4.2. Strengths, Limitations, and Directions for Future Research

This study provides a comprehensive assessment of vaccination coverage across multiple vaccines in a community-dwelling older population, while simultaneously examining sociodemographic, behavioral, psychological, and health system factors. The inclusion of a composite VCS and health care utilization index strengthens the analytical framework.
However, several limitations should be acknowledged. The cross-sectional design does not permit causal inference. Self-reported data may introduce recall bias. The use of factors, mainly personal characteristics, was assessed as marginally non-significant in their relationship with vaccination coverage, while overall a low coefficient of determination (R2) was attributed to the parameters evaluated. The study population also represents a specific geographic region, which may limit generalizability. Also, a potential selection bias related to recruitment during routine outpatient visits should be considered, as individuals with higher healthcare utilization may be more likely to be included. However, the study was conducted in the only major Primary Health Care facility in the area, which serves the entire local population through both regular and unscheduled visits, thereby reducing, but not eliminating, the risk of systematic selection bias. In addition, although the mean VCS suggests moderate coverage, its skewed distribution indicates substantial heterogeneity, with few participants at the extremes. Under the current protocol, this pattern was not explored in depth and warrants further investigation, ideally in larger cohorts to better understand selective vaccination behaviors.
Future research should move beyond cross-sectional designs by adopting longitudinal and mixed methods approaches to better capture changes in vaccination behavior over time. The use of objective data sources, such as electronic health records or immunization registries, would improve validity and reduce recall bias. Studies should also identify distinct vaccination profiles and test targeted interventions, including reminder systems and primary care–based or pharmacist-led strategies. Greater emphasis on psychosocial determinants—such as risk perception, vaccine confidence, and cognitive biases—may further clarify drivers of vaccine uptake, particularly among vulnerable subgroups, including the oldest-old, socially isolated individuals, and those with low health literacy.

4.3. Implications for Practice and Policy

Findings highlight the importance of strengthening Primary Health Care engagement, promoting participation in preventive screenings, and implementing targeted communication strategies [47,106,107]. Policies should prioritize systematic vaccination reminders for older adults, the integration of vaccination with chronic disease management, targeted outreach to socially isolated individuals, expansion of health literacy programs, and improved accessibility and convenience of vaccination services. Community pharmacists, who actively perform adult vaccinations such as influenza, represent an essential resource for increasing vaccination coverage, improving adherence, and enhancing preventive care in older adults [56,108]. Life course immunization strategies should be embedded within broader healthy aging policies to ensure sustained protection against vaccine-preventable diseases and to support the overall health and well-being of the aging population [109]. Educational strategies should extend beyond information provision to address misconceptions, fear, and cognitive biases. Techniques derived from cognitive-behavioral approaches may help reduce overestimation of vaccine-related risks and improve decision-making [110]. Tailored interventions could be particularly relevant for individuals with low health literacy or high uncertainty. A unified prevention concept may overcome health decision fragmentation or service inertia in the future.

5. Conclusions

Vaccination coverage among adults aged ≥60 years in Greece is high for influenza, moderate for pneumococcal and herpes zoster, and low for diphtheria-tetanus-pertussis and RSV. Factors associated with higher coverage include male sex, higher educational level, multimorbidity, preventive health behaviors, and greater use of healthcare services. Increasing age was associated with lower vaccination uptake in this study, although the underlying mechanisms were not directly assessed. These findings underscore the importance of life course vaccination strategies, targeted education, and accessibility improvements, particularly for adults with low healthcare utilization or limited preventive care engagement. Strengthening adult vaccination in primary care can improve healthy aging, reduce infectious disease burden, and enhance the sustainability of healthcare systems.

Author Contributions

Conceptualization, N.K., E.K.S. and C.P.; Methodology, N.K., E.K.S. and C.P.; Software, M.L.; Validation, N.K. and M.L.; Formal Analysis, M.L.; Investigation, N.K., E.K.S. and C.P.; Resources, E.K.S. and C.P.; Data Curation, M.L.; Writing—Original Draft Preparation, M.S., L.B., N.K., C.P., D.S., M.R., M.L., N.R. and E.K.S.; Writing—Review and Editing, M.S., L.B., M.L. and E.K.S.; Visualization, M.L.; Supervision, E.K.S. and C.P.; Project Administration, E.K.S. and C.P.; Funding Acquisition, NONE. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by the 7th Health Region of Crete (Approval Number: 49520; Date: 10 November 2025).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data presented in this study are available on request from the corresponding authors due to confidentiality requirements related to the use of individual-level medical records and electronic health data.

Acknowledgments

The authors would like to thank the participants in the study.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Mettens, P.; Monteyne, P. Life-Style Vaccines. Br. Med. Bull. 2002, 62, 175–186. [Google Scholar] [CrossRef][Green Version]
  2. Wu, L.A.; Kanitz, E.; Crumly, J.; D’Ancona, F.; Strikas, R.A. Adult Immunization Policies in Advanced Economies: Vaccination Recommendations, Financing, and Vaccination Coverage. Int. J. Public Health 2013, 58, 865–874. [Google Scholar] [CrossRef]
  3. Esposito, S.; Franco, E.; Gavazzi, G.; de Miguel, A.G.; Hardt, R.; Kassianos, G.; Bertrand, I.; Levant, M.C.; Soubeyrand, B.; López Trigo, J.A. The Public Health Value of Vaccination for Seniors in Europe. Vaccine 2018, 36, 2523–2528. [Google Scholar] [CrossRef]
  4. Bonanni, P.; Bonaccorsi, G.; Lorini, C.; Santomauro, F.; Tiscione, E.; Boccalini, S.; Bechini, A. Focusing on the Implementation of 21st Century Vaccines for Adults. Vaccine 2018, 36, 5358–5365. [Google Scholar] [CrossRef]
  5. Esposito, S.; Durando, P.; Bosis, S.; Ansaldi, F.; Tagliabue, C.; Icardi, G. Vaccine-Preventable Diseases: From Paediatric to Adult Targets. Eur. J. Intern. Med. 2014, 25, 203–212. [Google Scholar] [CrossRef] [PubMed]
  6. Gellin, B.G.; Shen, A.K.; Fish, R.; Zettle, M.A.; Uscher-Pines, L.; Ringel, J.S. The National Adult Immunization Plan: Strengthening Adult Immunization Through Coordinated Action. Am. J. Prev. Med. 2016, 51, 1079–1083. [Google Scholar] [CrossRef]
  7. de Gomensoro, E.; Del Giudice, G.; Doherty, T.M. Challenges in Adult Vaccination. Ann. Med. 2018, 50, 181–192. [Google Scholar] [CrossRef]
  8. Dominguez, L.J.; Galioto, A.; Ferlisi, A.; Pineo, A.; Putignano, E.; Belvedere, M.; Costanza, G.; Barbagallo, M. Ageing, Lifestyle Modifications, and Cardiovascular Disease in Developing Countries. J. Nutr. Health Aging 2006, 10, 143–149. [Google Scholar] [PubMed]
  9. Borboudaki, L.; Linardakis, M.; Markaki, A.M.; Papadaki, A.; Trichopoulou, A.; Philalithis, A. Health Service Utilization among Adults Aged 50+ across Eleven European Countries (the SHARE Study 2004/5). J. Public Health 2020, 29, 671–681. [Google Scholar] [CrossRef]
  10. Mogilenko, D.A.; Shchukina, I.; Artyomov, M.N. Immune Ageing at Single-Cell Resolution. Nat. Rev. Immunol. 2022, 22, 484–498. [Google Scholar] [CrossRef]
  11. López-Otín, C.; Blasco, M.A.; Partridge, L.; Serrano, M.; Kroemer, G. Hallmarks of Aging: An Expanding Universe. Cell 2023, 186, 243–278. [Google Scholar] [CrossRef]
  12. Partridge, L.; Deelen, J.; Slagboom, P.E. Facing up to the Global Challenges of Ageing. Nature 2018, 561, 45–56. [Google Scholar] [CrossRef]
  13. Srakar, A.; Hren, R.; Rupel, V.P. Health Services Utilization in Older Europeans: An Empirical Study. Organizacija 2016, 49, 127–136. [Google Scholar] [CrossRef]
  14. Beard, J.R.; Officer, A.; De Carvalho, I.A.; Sadana, R.; Pot, A.M.; Michel, J.P.; Lloyd-Sherlock, P.; Epping-Jordan, J.E.; Peeters, G.M.E.E.; Mahanani, W.R.; et al. The World Report on Ageing and Health: A Policy Framework for Healthy Ageing. Lancet 2016, 387, 2145–2154. [Google Scholar] [CrossRef]
  15. He, W.; Goodkind, D.; Kowal, P. An Aging World: 2015; U.S. Census Bureau: Washington, DC, USA, 2016.
  16. Borboudaki, L.; Linardakis, M.; Tsiligianni, I.; Philalithis, A. Utilization of Health Care Services and Accessibility Challenges among Adults Aged 50+ before and after Austerity Measures across 27 European Countries: Secular Trends in the SHARE Study from 2004/05 to 2019/20. Healthcare 2024, 12, 928. [Google Scholar] [CrossRef]
  17. Doherty, T.M.; Del Giudice, G.; Maggi, S. Adult Vaccination as Part of a Healthy Lifestyle: Moving from Medical Intervention to Health Promotion. Ann. Med. 2019, 51, 128–140. [Google Scholar] [CrossRef] [PubMed]
  18. Michel, J.P.; Chidiac, C.; Grubeck-Loebenstein, B.; Johnson, R.W.; Lambert, P.H.; Maggi, S.; Moulias, R.; Nicholson, K.; Werner, H. Advocating Vaccination of Adults Aged 60 Years and Older in Western Europe: Statement by the Joint Vaccine Working Group of the European Union Geriatric Medicine Society and the International Association of Gerontology and Geriatrics-European Region. Rejuvenation Res. 2009, 12, 127–135. [Google Scholar] [CrossRef]
  19. Michel, J.P.; Chidiac, C.; Grubeck-Loebenstein, B.; Johnson, R.W.; Lambert, P.H.; Maggi, S.; Moulias, R.; Nicholson, K.; Werner, H. Coalition of Advocates to Vaccinate of Western European Citizens Aged 60 Years and Older. Aging Clin. Exp. Res. 2009, 21, 254–257. [Google Scholar] [CrossRef][Green Version]
  20. Michel, J.P.; Gusmano, M.; Blank, P.R.; Philp, I. Vaccination and Healthy Ageing: How to Make Life-Course Vaccination a Successful Public Health Strategy. Eur. Geriatr. Med. 2010, 1, 155–165. [Google Scholar] [CrossRef]
  21. Simon, A.K.; Hollander, G.A.; McMichael, A. Evolution of the Immune System in Humans from Infancy to Old Age. Proc. Biol. Sci. 2015, 282, 20143085. [Google Scholar] [CrossRef]
  22. Bonanni, P.; Angelillo, I.F.; Villani, A.; Biasci, P.; Scotti, S.; Russo, R.; Maio, T.; Vitali Rosati, G.; Barretta, M.; Bozzola, E.; et al. Maintain and Increase Vaccination Coverage in Children, Adolescents, Adults and Elderly People: Let’s Avoid Adding Epidemics to the Pandemic: Appeal from the Board of the Vaccination Calendar for Life in Italy: Maintain and Increase Coverage Also by Re-Organizing Vaccination Services and Reassuring the Population. Vaccine 2021, 39, 1187–1189. [Google Scholar] [CrossRef]
  23. Basu, S.; Ashok, G.; Debroy, R.; Ramaiah, S.; Livingstone, P.; Anbarasu, A. Impact of the COVID-19 Pandemic on Routine Vaccine Landscape: A Global Perspective. Hum. Vaccin. Immunother. 2023, 19, 2199656. [Google Scholar] [CrossRef] [PubMed]
  24. World Health Organization (WHO). Immunization Agenda 2030: Leveraging the Global Response to COVID-19 to Strengthen Health Systems and Build Back Better|Knowledge Action Portal on NCDs. Available online: https://knowledge-action-portal.com/en/content/immunization-agenda-2030-leveraging-global-response-covid-19-strengthen-health-systems-and (accessed on 11 March 2026).
  25. World Health Organization (WHO). Working Together: An Integration Resource Guide for Planning and Strengthening Immunization Services Throughout the Life Course. Available online: https://www.who.int/publications/i/item/9789241514736 (accessed on 11 March 2026).
  26. Gao, S.; Li, Y.; Wang, X.; Li, S.; Chen, M.; Yue, B. Vaccine Literacy, Vaccination Intention, and Their Correlation among Adults in Mainland China: A Cross-Sectional Study. J. Health Popul. Nutr. 2024, 43, 122. [Google Scholar] [CrossRef] [PubMed]
  27. Collini, F.; Bonaccorsi, G.; Del Riccio, M.; Bruschi, M.; Forni, S.; Galletti, G.; Gemmi, F.; Ierardi, F.; Lorini, C. Does Vaccine Confidence Mediate the Relationship between Vaccine Literacy and Influenza Vaccination? Exploring Determinants of Vaccination among Staff Members of Nursing Homes in Tuscany, Italy, during the COVID-19 Pandemic. Vaccines 2023, 11, 1375. [Google Scholar] [CrossRef] [PubMed]
  28. Teresa Aguado, M.; Barratt, J.; Beard, J.R.; Blomberg, B.B.; Chen, W.H.; Hickling, J.; Hyde, T.B.; Jit, M.; Jones, R.; Poland, G.A.; et al. Report on WHO Meeting on Immunization in Older Adults: Geneva, Switzerland, 22–23 March 2017. Vaccine 2018, 36, 921–931. [Google Scholar] [CrossRef]
  29. World Health Organization (WHO). Influenza (Seasonal). Available online: https://www.who.int/news-room/fact-sheets/detail/influenza-(seasonal) (accessed on 11 March 2026).
  30. World Health Organization (WHO). The Top 10 Causes of Death. Available online: https://www.who.int/news-room/fact-sheets/detail/the-top-10-causes-of-death (accessed on 11 March 2026).
  31. Yamada, N.; Nakatsuka, K.; Tezuka, M.; Murata, F.; Maeda, M.; Akisue, T.; Fukuda, H.; Ono, R. Pneumococcal Vaccination Coverage and Vaccination-Related Factors among Older Adults in Japan: LIFE Study. Vaccine 2024, 42, 239–245. [Google Scholar] [CrossRef]
  32. World Health Organization (WHO). Pneumococcus: Vaccine Preventable Diseases Surveillance Standards. Available online: https://www.who.int/publications/m/item/vaccine-preventable-diseases-surveillance-standards-pneumococcus (accessed on 11 March 2026).
  33. Tsiligianni, I.; Bouloukaki, I.; Papazisis, G.; Paganas, A.; Chatzimanolis, E.; Kalatharas, M.; Platakis, I.; Tirodimos, I.; Dardavesis, T.; Tsimtsiou, Z. Vaccination Coverage and Predictors of Influenza, Pneumococcal, Herpes Zoster, Tetanus, Measles, and Hepatitis B Vaccine Uptake among Adults in Greece. Public Health 2023, 224, 195–202. [Google Scholar] [CrossRef]
  34. Kefalogianni, M.; Dimitriou, H.; Bertsias, A.; Marinos, G.; Kofteridis, D.; Symvoulakis, E.K. Latest Vaccination Trends against Herpes Zoster within Two Primary Care Settings in Crete, Greece: Rates and Perception Driven Determinants. Semergen 2025, 51, 102394. [Google Scholar] [CrossRef]
  35. Lu, P.J.; Hung, M.C.; Srivastav, A.; Grohskopf, L.A.; Kobayashi, M.; Harris, A.M.; Dooling, K.L.; Markowitz, L.E.; Rodriguez-Lainz, A.; Williams, W.W. Surveillance of Vaccination Coverage Among Adult Populations—United States, 2018. MMWR Surveill. Summ. 2021, 70, 1–26. [Google Scholar] [CrossRef]
  36. Polack, F.P.; Thomas, S.J.; Kitchin, N.; Absalon, J.; Gurtman, A.; Lockhart, S.; Perez, J.L.; Pérez Marc, G.; Moreira, E.D.; Zerbini, C.; et al. Safety and Efficacy of the BNT162b2 MRNA COVID-19 Vaccine. N. Engl. J. Med. 2020, 383, 2603–2615. [Google Scholar] [CrossRef]
  37. Baden, L.R.; El Sahly, H.M.; Essink, B.; Kotloff, K.; Frey, S.; Novak, R.; Diemert, D.; Spector, S.A.; Rouphael, N.; Creech, C.B.; et al. Efficacy and Safety of the MRNA-1273 SARS-CoV-2 Vaccine. N. Engl. J. Med. 2021, 384, 403–416. [Google Scholar] [CrossRef]
  38. Cai, M.; Xie, Y.; Al-Aly, Z. Association of 2024–2025 COVID-19 Vaccine with COVID-19 Outcomes in U.S. Veterans. N. Engl. J. Med. 2025, 393, 1612–1623. [Google Scholar] [CrossRef]
  39. Kaml, M.; Weiskirchner, I.; Keller, M.; Luft, T.; Hoster, E.; Hasford, J.; Young, L.; Bartlett, B.; Neuner, C.; Fischer, K.H.; et al. Booster Vaccination in the Elderly: Their Success Depends on the Vaccine Type Applied Earlier in Life as Well as on Pre-Vaccination Antibody Titers. Vaccine 2006, 24, 6808–6811. [Google Scholar] [CrossRef]
  40. Weinberger, B.; Schirmer, M.; Gothe, R.M.; Siebert, U.; Fuchs, D.; Grubeck-Loebenstein, B. Recall Responses to Tetanus and Diphtheria Vaccination Are Frequently Insufficient in Elderly Persons. PLoS ONE 2013, 8, e82967. [Google Scholar] [CrossRef]
  41. Grasse, M.; Meryk, A.; Schirmer, M.; Grubeck-Loebenstein, B.; Weinberger, B. Booster Vaccination against Tetanus and Diphtheria: Insufficient Protection against Diphtheria in Young and Elderly Adults. Immun. Ageing 2016, 13, 26. [Google Scholar] [CrossRef] [PubMed]
  42. Papagiannis, D.; Rachiotis, G.; Mariolis, A.; Zafiriou, E.; Gourgoulianis, K.I. Vaccination Coverage of the Elderly in Greece: A Cross-Sectional Nationwide Study. Can. J. Infect. Dis. Med. Microbiol. 2020, 2020, 5459793. [Google Scholar] [CrossRef] [PubMed]
  43. Surie, D.; Self, W.H.; Yuengling, K.A.; Lauring, A.S.; Zhu, Y.; Safdar, B.; Ginde, A.A.; Simon, S.J.; Peltan, I.D.; Brown, S.M.; et al. RSV Vaccine Effectiveness Against Hospitalization Among US Adults Aged 60 Years or Older During 2 Seasons. JAMA 2025, 334, 1442–1451. [Google Scholar] [CrossRef] [PubMed]
  44. Arghittu, A.; Deiana, G.; Dettori, M.; Castiglia, P. Vaccination, Public Health and Health Communication: A Network of Connections to Tackle Global Challenges. Vaccines 2025, 13, 245. [Google Scholar] [CrossRef]
  45. Laupèze, B.; Del Giudice, G.; Doherty, M.T.; Van der Most, R. Vaccination as a Preventative Measure Contributing to Immune Fitness. npj Vaccines 2021, 6, 93. [Google Scholar] [CrossRef]
  46. Hellenic Statistical Authority (ELSTAT) 2021 Census Results (Provisional Data on Resident Population) of Population and Housing. Available online: https://www.statistics.gr/2021-census-res-pop-results (accessed on 11 March 2026).
  47. Symvoulakis, E.K.; Stachteas, P.; Smyrnakis, E.; Volkos, P.; Mantadaki, A.E.; Karelis, A.; Petraki, C.; Nioti, K.; Mastronikolis, S.; Antoniou, A.M.; et al. Multiple Behavioral Risk Factors As Assets for Chronic Disease Prevention: Observations From Urban Primary Care Settings in Crete, Greece. Cureus 2024, 16, e56711. [Google Scholar] [CrossRef]
  48. John, B.; Newstead, S.; Heirene, R.; Hodgson, R.; Roderique-Davies, G. Does the Fast Alcohol Screening Test Accurately Distinguish between Harmful and Severely Dependent Tiers of Alcohol Misuse? Alcohol Alcohol. 2021, 56, 737–745. [Google Scholar] [CrossRef] [PubMed]
  49. Sinoff, G.; Liora, O.; Zlotogorsky, D.; Tamir, A. Short Anxiety Screening Test—A Brief Instrument for Detecting Anxiety in the Elderly. Int. J. Geriatr. Psychiatry 1999, 14, 1062–1071. [Google Scholar] [CrossRef]
  50. Grammatikopoulos, I.A.; Sinoff, G.; Alegakis, A.; Kounalakis, D.; Antonopoulou, M.; Lionis, C. The Short Anxiety Screening Test in Greek: Translation and Validation. Ann. Gen. Psychiatry 2010, 9, 1. [Google Scholar] [CrossRef]
  51. Del Riccio, M.; Maggi, S.; Wieczorowska-Tobis, K.; Newell, K.; Czech, M.; Botelho-Nevers, E.; Michel, J.-P.; Hummers, E.; Duque, S.; Lundgren, J.; et al. Advancing Vaccination Strategies for Older Adults: Insights of the Adult Immunization Board Meeting. Drugs Aging 2026, 43, 223–237. [Google Scholar] [CrossRef]
  52. Wallace, A.S.; Ryman, T.K.; Privor-Dumm, L.; Morgan, C.; Fields, R.; Garcia, C.; Sodha, S.V.; Lindstrand, A.; Nic Lochlainn, L.M. Leaving No One behind: Defining and Implementing an Integrated Life Course Approach to Vaccination across the next Decade as Part of the Immunization Agenda 2030. Vaccine 2024, 42, S54–S63. [Google Scholar] [CrossRef]
  53. Roses, M.; Bonhevi, P.E. Vaccines in Adults. Medicina 2019, 79, 552–558. [Google Scholar] [PubMed]
  54. Dafnou, P.; Elefsiniotis, I.; Adamakidou, T.; Margari, N.; Parissopoulos, S.; Kourkouta, L.; Giakoumidakis, K.; Dokoutsidou, E. Examining Vaccination Coverage in Patients with Diagnosis of Chronic Liver Disease and Cirrhosis: A Cross-Sectional Study in Greece. Livers 2025, 5, 68. [Google Scholar] [CrossRef]
  55. Dedoukou, X.; Nikolopoulos, G.; Maragos, A.; Giannoulidou, S.; Maltezou, H.C. Attitudes towards Vaccination against Seasonal Influenza of Health-Care Workers in Primary Health-Care Settings in Greece. Vaccine 2010, 28, 5931–5933. [Google Scholar] [CrossRef]
  56. Haems, M.; Lanzilotto, M.; Mandelli, A.; Mota-Filipe, H.; Paulino, E.; Plewka, B.; Rozaire, O.; Zeiger, J. European Community Pharmacists Practice in Tackling Influenza. Explor. Res. Clin. Soc. Pharm. 2024, 14, 100447. [Google Scholar] [CrossRef]
  57. Thompson, W.W.; Shay, D.K.; Weintraub, E.; Cox, N.; Anderson, L.J.; Fukuda, K. Mortality Associated with Influenza and Respiratory Syncytial Virus in the United States. JAMA 2003, 289, 179–186. [Google Scholar] [CrossRef] [PubMed]
  58. Goodwin, K.; Viboud, C.; Simonsen, L. Antibody Response to Influenza Vaccination in the Elderly: A Quantitative Review. Vaccine 2006, 24, 1159–1169. [Google Scholar] [CrossRef]
  59. Somes, M.P.; Turner, R.M.; Dwyer, L.J.; Newall, A.T. Estimating the Annual Attack Rate of Seasonal Influenza among Unvaccinated Individuals: A Systematic Review and Meta-Analysis. Vaccine 2018, 36, 3199–3207. [Google Scholar] [CrossRef] [PubMed]
  60. Smetana, J.; Chlibek, R.; Shaw, J.; Splino, M.; Prymula, R. Influenza Vaccination in the Elderly. Hum. Vaccin. Immunother. 2018, 14, 540–549. [Google Scholar] [CrossRef] [PubMed]
  61. Athanassoglou, V.; Wilson, L.A.; Liu, J.; Poeran, J.; Zhong, H.; Memtsoudis, S.G. The Impact of Immunization and Use of Oseltamivir on Influenza-Related Hospitalizations: A Population-Based Study. J. Prim. Care Community Health 2021, 12, 21501327211005904. [Google Scholar] [CrossRef] [PubMed]
  62. Van Ranst, M.; Zöllner, Y.; Schelling, J.; Palache, B. The Burden of Seasonal Influenza: Improving Vaccination Coverage to Mitigate Morbidity and Its Impact on Healthcare Systems. Expert Rev. Vaccines 2023, 22, 518–519. [Google Scholar] [CrossRef]
  63. Presa, J.; Arranz-Herrero, J.; Alvarez-Losa, L.; Rius-Rocabert, S.; Pozuelo, M.J.; Lalueza, A.; Ochando, J.; Eiros, J.M.; Sanz-Muñoz, I.; Nistal-Villan, E. Influenza Vaccine Outcomes: A Meta-Analysis Revealing Morbidity Benefits amid Low Infection Prevention. Eur. Respir. Rev. 2025, 34, 240144. [Google Scholar] [CrossRef]
  64. Xu, K.; Wang, Z.; Qin, M.; Gao, Y.; Luo, N.; Xie, W.; Zou, Y.; Wang, J.; Ma, X. A Systematic Review and Meta-Analysis of the Effectiveness and Safety of COVID-19 Vaccination in Older Adults. Front. Immunol. 2023, 14, 1113156. [Google Scholar] [CrossRef]
  65. Bouloukaki, I.; Christoforaki, A.; Christodoulakis, A.; Krasanakis, T.; Lambraki, E.; Pateli, R.; Markakis, M.; Tsiligianni, I. Vaccination Coverage and Associated Factors of COVID-19 Uptake in Adult Primary Health Care Users in Greece. Healthcare 2023, 11, 341. [Google Scholar] [CrossRef]
  66. European Centre for Disease Prevention and Control. COVID-19 Vaccination Coverage in the EU/EEA During the 2023–24 Season Campaigns, 1 September 2023–31 July 2024; European Centre for Disease Prevention and Control: Solna, Sweden, 2025. [Google Scholar]
  67. European Centre for Disease Prevention and Control. COVID-19 Vaccination Coverage in the EU/EEA During the 2024–25 Season Campaigns; European Centre for Disease Prevention and Control: Solna, Sweden, 2024. [Google Scholar]
  68. Kiiza, D.; Semanda, J.N.; Kawere, B.B.; Ajore, C.; Wasswa, C.K.; Kwiringira, A.; Tumukugize, E.; Sserubidde, J.; Namyalo, N.; Wadria, R.B.; et al. Strategies to Enhance COVID-19 Vaccine Uptake among Prioritized Groups, Uganda-Lessons Learned and Recommendations for Future Pandemics. Emerg. Infect. Dis. 2024, 30, 1326–1327. [Google Scholar] [CrossRef]
  69. Breznik, J.A.; Miller, M.S.; Bowdish, D.M.E. Rationalizing Recommendations for Influenza and COVID-19 Vaccines. Vaccine 2025, 65, 127775. [Google Scholar] [CrossRef]
  70. Robinson, E.; Jones, A.; Lesser, I.; Daly, M. International Estimates of Intended Uptake and Refusal of COVID-19 Vaccines: A Rapid Systematic Review and Meta-Analysis of Large Nationally Representative Samples. Vaccine 2021, 39, 2024–2034. [Google Scholar] [CrossRef]
  71. Arsenault, C.; Lewis, T.P.; Kapoor, N.R.; Okiro, E.A.; Leslie, H.H.; Armeni, P.; Jarhyan, P.; Doubova, S.V.; Wright, K.D.; Aryal, A.; et al. Health System Quality and COVID-19 Vaccination: A Cross-Sectional Analysis in 14 Countries. Lancet Glob. Health 2024, 12, e156–e165. [Google Scholar] [CrossRef]
  72. Filia, A.; Bella, A.; von Hunolstein, C.; Pinto, A.; Alfarone, G.; Declich, S.; Rota, M.C. Tetanus in Italy 2001–2010: A Continuing Threat in Older Adults. Vaccine 2014, 32, 639–644. [Google Scholar] [CrossRef] [PubMed]
  73. Ridda, I.; Yin, J.K.; King, C.; Raina MacIntyre, C.; McIntyre, P. The Importance of Pertussis in Older Adults: A Growing Case for Reviewing Vaccination Strategy in the Elderly. Vaccine 2012, 30, 6745–6752. [Google Scholar] [CrossRef] [PubMed]
  74. Gil, A.; Oyagüez, I.; Carrasco, P.; González, A. Hospital Admissions for Pertussis in Spain, 1995–1998. Vaccine 2001, 19, 4791–4794. [Google Scholar] [CrossRef] [PubMed]
  75. Bulkhi, A.; Khadawardi, H.A.; Dairi, M.S.; Alwafi, H.; Alim, H.M.; Turkistani, Y.A.; Almoallim, H.M.; Alghamdi, I.A.; Alqashqri, H.S.; Obaid, M.S.; et al. Effectiveness of Pneumococcal Vaccination in Reducing Hospitalization and Mortality among the Elderly: A Systematic Review and Meta-Analysis. Hum. Vaccin. Immunother. 2025, 21, 2561315. [Google Scholar] [CrossRef]
  76. Gravenstein, S.; Ozisik, L. The New Era of Pneumococcal Vaccination in Adults: What Is Next? Vaccines 2025, 13, 498. [Google Scholar] [CrossRef]
  77. Prieto-Campo, Á.; García-Álvarez, R.M.; López-Durán, A.; Roque, F.; Herdeiro, M.T.; Figueiras, A.; Zapata-Cachafeiro, M. Understanding Primary Care Physician Vaccination Behaviour: A Systematic Review. Int. J. Environ. Res. Public Health 2022, 19, 13872. [Google Scholar] [CrossRef]
  78. Britton, A.; Roper, L.E.; Kotton, C.N.; Hutton, D.W.; Fleming-Dutra, K.E.; Godfrey, M.; Ortega-Sanchez, I.R.; Broder, K.R.; Talbot, H.K.; Long, S.S.; et al. Use of Respiratory Syncytial Virus Vaccines in Adults Aged ≥60 Years: Updated Recommendations of the Advisory Committee on Immunization Practices—United States, 2024. MMWR Morb. Mortal. Wkly. Rep. 2024, 73, 696–702. [Google Scholar] [CrossRef]
  79. Falsey, A.R.; Hennessey, P.A.; Formica, M.A.; Cox, C.; Walsh, E.E. Respiratory Syncytial Virus Infection in Elderly and High-Risk Adults. N. Engl. J. Med. 2005, 352, 77. [Google Scholar] [CrossRef]
  80. Falsey, A.R.; Walsh, E.E.; House, S.; Vandenijck, Y.; Ren, X.; Keim, S.; Kang, D.; Peeters, P.; Witek, J.; Ispas, G. Risk Factors and Medical Resource Utilization of Respiratory Syncytial Virus, Human Metapneumovirus, and Influenza-Related Hospitalizations in Adults—A Global Study During the 2017–2019 Epidemic Seasons (Hospitalized Acute Respiratory Tract Infection [HARTI] Study). Open Forum Infect. Dis. 2021, 8, ofab491. [Google Scholar] [CrossRef]
  81. Falsey, A.R.; Williams, K.; Gymnopoulou, E.; Bart, S.; Ervin, J.; Bastian, A.R.; Menten, J.; De Paepe, E.; Vandenberghe, S.; Chan, E.K.H.; et al. Efficacy and Safety of an Ad26.RSV.PreF-RSV PreF Protein Vaccine in Older Adults. N. Engl. J. Med. 2023, 388, 609–620. [Google Scholar] [CrossRef]
  82. Belongia, E.A.; King, J.P.; Kieke, B.A.; Pluta, J.; Al-Hilli, A.; Meece, J.K.; Shinde, V. Clinical Features, Severity, and Incidence of RSV Illness During 12 Consecutive Seasons in a Community Cohort of Adults ≥60 Years Old. Open Forum Infect. Dis. 2018, 5, ofy316. [Google Scholar] [CrossRef] [PubMed]
  83. Payne, A.B.; Watts, J.A.; Mitchell, P.K.; Dascomb, K.; Irving, S.A.; Klein, N.P.; Grannis, S.J.; Ong, T.C.; Ball, S.W.; DeSilva, M.B.; et al. Respiratory Syncytial Virus (RSV) Vaccine Effectiveness against RSV-Associated Hospitalisations and Emergency Department Encounters among Adults Aged 60 Years and Older in the USA, October, 2023, to March, 2024: A Test-Negative Design Analysis. Lancet 2024, 404, 1547–1559. [Google Scholar] [CrossRef] [PubMed]
  84. Surie, D.; Yuengling, K.A.; Decuir, J.; Zhu, Y.; Lauring, A.S.; Gaglani, M.; Ghamande, S.; Peltan, I.D.; Brown, S.M.; Ginde, A.A.; et al. Severity of Respiratory Syncytial Virus vs. COVID-19 and Influenza Among Hospitalized US Adults. JAMA Netw. Open 2024, 7, e244954. [Google Scholar] [CrossRef] [PubMed]
  85. Prasad, N.; Walker, T.A.; Waite, B.; Wood, T.; Trenholme, A.A.; Baker, M.G.; McArthur, C.; Wong, C.A.; Grant, C.C.; Huang, Q.S.; et al. Respiratory Syncytial Virus-Associated Hospitalizations Among Adults with Chronic Medical Conditions. Clin. Infect. Dis. 2021, 73, E158–E163. [Google Scholar] [CrossRef]
  86. Arsenault, C.; Ravishankar, S.; Lewis, T.; Armeni, P.; Croke, K.; Doubova, S.V.; McKee, M.; Tarricone, R.; Kruk, M.E. The Role of Health Systems in Shaping Vaccine Decisions: Insights from Italy, Mexico, the United Kingdom, and the United States. Vaccine 2025, 54, 127134. [Google Scholar] [CrossRef]
  87. Arlt, J.; Flaegel, K.; Goetz, K.; Steinhaeuser, J. Regional Differences in General Practitioners’ Behaviours Regarding Influenza Vaccination: A Cross-Sectional Study. BMC Health Serv. Res. 2021, 21, 197. [Google Scholar] [CrossRef]
  88. Bish, A.; Yardley, L.; Nicoll, A.; Michie, S. Factors Associated with Uptake of Vaccination against Pandemic Influenza: A Systematic Review. Vaccine 2011, 29, 6472–6484. [Google Scholar] [CrossRef]
  89. Pulcini, C.; Massin, S.; Launay, O.; Verger, P. Factors Associated with Vaccination for Hepatitis B, Pertussis, Seasonal and Pandemic Influenza among French General Practitioners: A 2010 Survey. Vaccine 2013, 31, 3943–3949. [Google Scholar] [CrossRef]
  90. Galanis, P.; Vraka, I.; Fragkou, D.; Bilali, A.; Kaitelidou, D. Intention of Healthcare Workers to Accept COVID-19 Vaccination and Related Factors: A Systematic Review and Meta-Analysis. Asian Pac. J. Trop. Med. 2021, 14, 543–554. [Google Scholar] [CrossRef]
  91. Jiménez-García, R.; Hernández-Barrera, V.; de Andres, A.L.; Jimenez-Trujillo, I.; Esteban-Hernández, J.; Carrasco-Garrido, P. Gender Influence in Influenza Vaccine Uptake in Spain: Time Trends Analysis (1995–2006). Vaccine 2010, 28, 6169–6175. [Google Scholar] [CrossRef] [PubMed]
  92. Lin, C.; Tu, P.; Beitsch, L.M. Confidence and Receptivity for COVID-19 Vaccines: A Rapid Systematic Review. Vaccines 2020, 9, 16. [Google Scholar] [CrossRef] [PubMed]
  93. Zintel, S.; Flock, C.; Arbogast, A.L.; Forster, A.; von Wagner, C.; Sieverding, M. Gender Differences in the Intention to Get Vaccinated against COVID-19: A Systematic Review and Meta-Analysis. J. Public Health 2022, 31, 1303–1327. [Google Scholar] [CrossRef]
  94. Klüwer, B.; Margrethe Rydland, K.; Nybru Gleditsch, R.; Mamelund, S.E.; Laake, I. Social and Demographic Patterns of Influenza Vaccination Coverage in Norway, Influenza Seasons 2014/15 to 2020/21. Vaccine 2023, 41, 1239–1246. [Google Scholar] [CrossRef]
  95. Meier, C.; Uwitonze, J.P.; Wieczorek, M. Digital Exclusion, Functional Health Literacy, and COVID-19 Vaccination in Later Life: Evidence from 30,801 Older Adults across Europe. Public Health 2026, 253, 106174. [Google Scholar] [CrossRef]
  96. Chen, X.; Xia, S.; Zhu, Z.; Hui, Z.; Wu, J.; Sun, C.; Zhou, C.; Ceng, L. Influenza Vaccine Hesitancy in Older Adults in China: A Latent Profile Analysis. Hum. Vaccin. Immunother. 2026, 22, 2616943. [Google Scholar] [CrossRef]
  97. Harrison, S.M.; Wei, M.Y.; Lamerato, L.E.; Petrie, J.G.; Toth Martin, E. Multimorbidity Is Associated with Uptake of Influenza Vaccination. Vaccine 2018, 36, 3635. [Google Scholar] [CrossRef]
  98. Liu, D.; Zhang, Y.; Lei, J.; Li, J.; Xiang, C.; Peng, Y.; Hu, Y.; Fang, L.; Feng, L.; Shan, G.; et al. Influenza, Pneumococcal, COVID-19 Vaccine Willingness and Uptake with Influencing Factors in 38,184 Chinese Older Adults in 2022: A Nationwide Cross-Sectional Study. Vaccine 2025, 68, 127961. [Google Scholar] [CrossRef]
  99. Schmid, P.; Rauber, D.; Betsch, C.; Lidolt, G.; Denker, M.L. Barriers of Influenza Vaccination Intention and Behavior—A Systematic Review of Influenza Vaccine Hesitancy, 2005–2016. PLoS ONE 2017, 12, e0170550. [Google Scholar] [CrossRef]
  100. Cavaliere, A.F.; Zaami, S.; Pallottini, M.; Perelli, F.; Vidiri, A.; Marinelli, E.; Straface, G.; Signore, F.; Scambia, G.; Marchi, L. Flu and Tdap Maternal Immunization Hesitancy in Times of COVID-19: An Italian Survey on Multiethnic Sample. Vaccines 2021, 9, 1107. [Google Scholar] [CrossRef]
  101. Telford, R.; Rogers, A. What Influences Elderly Peoples’ Decisions about Whether to Accept the Influenza Vaccination? A Qualitative Study. Health Educ. Res. 2003, 18, 743–753. [Google Scholar] [CrossRef]
  102. Dodd, R.H.; Pickles, K.; Nickel, B.; Cvejic, E.; Ayre, J.; Batcup, C.; Bonner, C.; Copp, T.; Cornell, S.; Dakin, T.; et al. Concerns and Motivations about COVID-19 Vaccination. Lancet Infect. Dis. 2021, 21, 161–163. [Google Scholar] [CrossRef]
  103. Dib, F.; Mayaud, P.; Chauvin, P.; Launay, O. Online Mis/Disinformation and Vaccine Hesitancy in the Era of COVID-19: Why We Need an EHealth Literacy Revolution. Hum. Vaccin. Immunother. 2022, 18, 1–3. [Google Scholar] [CrossRef]
  104. Nath, R.; Imtiaz, A.; Nath, S.D.; Hasan, E. Role of Vaccine Hesitancy, EHealth Literacy, and Vaccine Literacy in Young Adults’ COVID-19 Vaccine Uptake Intention in a Lower-Middle-Income Country. Vaccines 2021, 9, 1405. [Google Scholar] [CrossRef]
  105. MacDonald, N.E.; Eskola, J.; Liang, X.; Chaudhuri, M.; Dube, E.; Gellin, B.; Goldstein, S.; Larson, H.; Manzo, M.L.; Reingold, A.; et al. Vaccine Hesitancy: Definition, Scope and Determinants. Vaccine 2015, 33, 4161–4164. [Google Scholar] [CrossRef]
  106. Frantzeskakis, N.; Tziraki, M.; Spanakis, M.; Katsarou, S.D.; Papadopoulos, N.; Linardakis, M.; Vova-Chatzi, C.; Kamekis, A.; Pitsoulis, G.; Papadakis, A.; et al. Implementing a Mixed Health Service Model as an Informed Modality to Enhance Prevention and Promote Workplace Health in the Greek Regional Public Sector: A Pilot Study in Crete. Healthcare 2025, 13, 2337. [Google Scholar] [CrossRef] [PubMed]
  107. Lionis, C.; Symvoulakis, E.K.; Markaki, A.; Petelos, E.; Papadakis, S.; Sifaki-Pistolla, D.; Papadakakis, M.; Souliotis, K.; Tziraki, C. Integrated People-Centred Primary Health Care in Greece: Unravelling Ariadne’s Thread. Prim. Health Care Res. Dev. 2019, 20, e113. [Google Scholar] [CrossRef]
  108. Murray, E.; Bieniek, K.; del Aguila, M.; Egodage, S.; Litzinger, S.; Mazouz, A.; Mills, H.; Liska, J. Impact of Pharmacy Intervention on Influenza Vaccination Acceptance: A Systematic Literature Review and Meta-Analysis. Int. J. Clin. Pharm. 2021, 43, 1163–1172. [Google Scholar] [CrossRef] [PubMed]
  109. Gomez Rial, J.; Redondo, E.; Rivero-Calle, I.; Mascarós, E.; Ocaña, D.; Jimeno, I.; Gil, Á.; Linares, M.; Onieva-García, M.Á.; González-Romo, F.; et al. Immunofitness in the Elderly: The Role of Vaccination in Promoting Healthy Aging. Hum. Vaccin. Immunother. 2026, 22, 2624234. [Google Scholar] [CrossRef] [PubMed]
  110. Gangemi, A.; Gragnani, A.; Dahò, M.; Buonanno, C. Reducing Probability Overestimation of Threatening Events: An Italian Study on the Efficacy of Cognitive Techniques in Non-Clinical Subjects. Clin. Neuropsychiatry 2019, 16, 149. [Google Scholar] [PubMed]
Figure 1. Cluster analysis dendrogram of the 8 types of vaccines on 366 participants. Colors (blue and brown) denote the two main clusters identified through hierarchical clustering, indicating vaccines with similar uptake patterns.
Figure 1. Cluster analysis dendrogram of the 8 types of vaccines on 366 participants. Colors (blue and brown) denote the two main clusters identified through hierarchical clustering, indicating vaccines with similar uptake patterns.
Healthcare 14 01167 g001
Table 1. Demographic and health characteristics of 366 participants (60+ years) in the study.
Table 1. Demographic and health characteristics of 366 participants (60+ years) in the study.
n%
Gendermales/females180/18649.2/50.8
Age, (years)mean ± stand. dev. (median, IQR)74.6 ± 8.0 (74.5, 14.4)
60–6912534.2
70–7913035.5
≥8011130.3
Subjective sense of Age, (years)mean ± stand. dev. (median, IQR)64.1 ± 19.4 (65.0, 30.0)
Family statusmarried, in relationship26472.1
unmarried, divorced, widows10227.9
Educational levelminimum/no education19051.9
Secondary5515.0
High school5414.8
Technical School349.3
University339.0
Taking medication during the last 6 monthsyes34193.2
Chronic conditions (most frequent) ahypertension24269.9
dyslipidemia21963.3
diabetes mellitus9928.6
thyroid disease8123.4
coronary heart disease7421.4
Multimorbidity≥3 chronic conditions20154.9
IQR, interquartile range; a 21 chronic conditions such as hypertension, dyslipidemia, diabetes mellitus (I, II), thyroid disease, coronary heart disease, osteoarthritis, chronic obstructive pulmonary disease, atrial fibrillation, osteoporosis, heart failure, rheumatoid arthritis, cancer, allergy, asthma, chronic kidney failure, acute myocardial infarction, stroke, dementia, peripheral angiopathy, hepatitis and Parkinson’s disease.
Table 2. Health habits and anxiety levels of 366 participants in the study.
Table 2. Health habits and anxiety levels of 366 participants in the study.
n%
Body Mass Index, (kg/m2)mean ± stand. dev. (median, IQR)27.9 ± 4.7 (27.7, 5.6)
underweight (<18.5)51.4
normal (18.5–24.9)8924.3
Overweight, obese (≥25.0)27274.3
Night-time sleep hoursmean ± stand. dev. (median, IQR)6.7 ± 1.5 (7.0, 2.0)
Smokingcurrently smoking5815.9
non-smoker18650.8
ex-smoker12233.3
cigarettes/daymean ± stand. dev. (median, IQR)18.7 ± 10.9 (20.0, 10.0)
years of smokingmean ± stand. dev. (median, IQR)43.3 ± 11.8 (45.0, 10.0)
High alcohol consumption
[≥3 drinks (♀) or ≥4 (♂) per occasion during the last year or FAST score ≥ 3]
4111.2
Daily consumption of fruits & vegetablesno21458.5
yes15241.5
Daily physical activity (walking for ≥10 min/day)no8523.2
yes28176.8
Multiple behavioral risk factors (MBRFs) a0–227876.0
≥3 or multiple presence2424.0
Short Anxiety Screening Test—SAST scale bmean ± stand. dev. (median, IQR)16.2 ± 4.8 (15.0, 7.0)
negative for anxiety disorder (<22)30182.2
borderline (22–23)328.8
positive (≥24)339.0
IQR, interquartile range; a behavioral risk factors for chronic diseases are referred to the unhealthy habits as: high body weight (BMI ≥ 25.0 kg/m2), smoking habit, alcohol consumption (FAST score ≥3/4 per gender), absence of daily consumption of fruits and vegetables (<7 days/week) and absence of daily physical activity (walking < 7 days/week). The clustering of multiple behavioral risk factors is based on the multiple presence of 3 or more factors. b Score was extracted by summing up the responses of 10 items, ranging from 10 to 40. The higher the score, the higher the anxiety.
Table 3. Components (questions) of HCSUs in participants in the study.
Table 3. Components (questions) of HCSUs in participants in the study.
Relevant QuestionsScoringn%
How often do you visit a health center, regional clinic, or private clinic for medical reasons within a year?0: 0–2 times19252.5
1: 3–411932.5
2: >45515.0
Have you been hospitalized in the last 3 years?0: never27274.3
1: 1 time6718.3
2: 2 times143.8
3: 3 or more133.6
How much do you spend on co-payments for medications each month?mean ± stand. dev. (median, IQR)35.4 ± 26.5 (30.0, 30.0)
0: 0 euros226.0
1: at least 1 euro34494.0
Have you ever had a preventive colonoscopy?0: no20154.9
1: yes16545.1
Have you ever had a preventive mammogram?
(♀, n = 186)
0: no1910.2
1: yes16789.8
Have you ever taken a cardio-stress test?0: no16745.6
1: yes19954.4
Health Care Services Utilization score (HCSUs)mean ± stand. dev. (median, IQR)37.8 ± 18.0 (33.3, 22.2)
low to moderate (0–66.6 or 2/3)33290.7
high (≥66.7)349.3
IQR, interquartile range; score ranges from 0 to 100, with a higher score indicating greater use of health services. The assessment was based on the coded responses (scoring 0 and 1) to the six questions. After they were added up with a possible range of 0–9, a linear transformation was performed on a scale of 0–100.
Table 4. Frequency of VCs and assessment of relative score in 366 adults aged 60+ years, participants in the current study.
Table 4. Frequency of VCs and assessment of relative score in 366 adults aged 60+ years, participants in the current study.
Types of VaccinesYear and Doses of Vaccinationn%95%CIs
Influenza202530282.578.4, 86.1
202429580.676.3, 84.4
2024 & 2025 (1) a29580.676.3, 84.4
Tetanusfrom 2017 to 2025 (1)4813.110.0, 16.9
Corynebacterium diphtheriaefrom 2017 to 2025 (1)4712.89.7, 16.6
Bordetella pertussisfrom 2017 to 2025 (1)4512.39.2, 16.0
Herpes Zosterfrom 2017 to 2025 (1)20556.050.9, 61.0
1 dose15977.671.5, 82.9
2 doses4622.417.1, 28.5
Streptococcus pneumoniaefrom 2014 to 2025 (1)25068.363.4, 72.9
SARS-CoV-2from 2021 to 2025 (1)35296.293.8, 97.8
1 dose10.3
2 doses113.1
3 doses34096.6
RSV (Respiratory Syncytial Virus)2024 & 2025 (1)195.23.3, 7.8
Vaccination Coverage Score (VCS)mean ± stand. dev. (median, IQR)43.1 ± 20.2 (50.0, 25.0)
low-to-moderate (0–66.6 or 2/3)32989.986.5, 92.7
high (≥66.7)3710.17.3, 16.5
IQR, interquartile range; the VCS (also expressed as a percentage) was defined based on the administration of the above eight vaccines, for the periods of time, either in combination or individually, to which they relate. For each vaccine administered, a value of 1 was given (a respectively in parentheses) and for non-vaccination a value of 0. After adding them up with a possible range of 0–8, a linear transformation was performed on a scale of 0–100. It is noticed that without any vaccine were found n = 8 participants (2.2%) as with eight vaccines were found n = 5 participants (1.4%).
Table 5. VCS for 366 participants as to their demographic characteristics, the components (questions) HCSUs, health habits and anxiety levels.
Table 5. VCS for 366 participants as to their demographic characteristics, the components (questions) HCSUs, health habits and anxiety levels.
VCS (0–100)
Rho-Spearmanp-Value
Demographic
Characteristics
Gender (1: males, 2: females)−0.1410.007
Age (1: 60–69 years, 2: 70–79, 3: ≥80)−0.1190.023
Subjective sense of age (years)−0.1630.002
Family status (1: married, in relationship, 2: unmarried, divorced, widows)−0.1680.001
Educational level (1: minimum/no education, 2: Secondary, 3: High school, 4: Technical School, 5: University)0.203<0.001
Taking medication during the last 6 months (1: no, 2: yes)0.0190.718
Multimorbidity (1: 0–2 chronic conditions, 2: ≥3)0.1230.018
Components (questions) & HCSUsHow often do you visit a health center, regional clinic, or private clinic for medical reasons within a year? (0: 0–2 times, 1: 3–4, 2: >4)0.0850.105
Have you been hospitalized in the last 3 years? (0: never, 1: 1 time, 2: 2 times, 3: 3 or more)0.0600.122
How much do you spend on co-payments for medications each month? (euros)0.0090.288
Have you ever had a preventive colonoscopy? (0: no, 1: yes)0.1330.011
Have you ever had a preventive mammogram? (♀, n = 186) (0: no, 1: yes)0.0090.900
Have you ever taken a cardio-stress test? (0: no, 1: yes)0.1800.001
Health Care Services Utilization score—HCSUs (0–100)0.1290.013
Health habits and anxiety levelsBody Mass Index (kg/m2)0.0700.200
Night-time sleep hours0.0080.639
Smoking (1: non, ex-smokers, 2: currently smokers)0.0280.591
High alcohol consumption (FAST score as 1: up to 2 & 2: ≥3) −0.0330.530
Daily consumption of fruits & vegetables (1: no, 2: yes)0.1040.048
Daily physical activity (1: inactivity or walking for less than 10 min/day, 2: walking for ≥10 min/day)0.1200.022
Multiple behavioral risk factors (MBRFs) (with none up to 5)−0.0570.303
Short Anxiety Screening Test—SAST scale (score)−0.1050.045
Table 6. Hierarchical multiple logistic regression analysis of 366 participants with high VCS (≥66.7) in relation to those with low-to-moderate and their characteristics, the HCSUs, the health habits and anxiety levels.
Table 6. Hierarchical multiple logistic regression analysis of 366 participants with high VCS (≥66.7) in relation to those with low-to-moderate and their characteristics, the HCSUs, the health habits and anxiety levels.
VCS
(High Versus Low-to-Moderate)
1st Model2nd Model
Prognostic FactorsOdds Ratio (95%CI)p-ValueOdds Ratio (95%CI)p-Value
Gender (females vs. males)0.48
(0.20, 1.06)
0.0670.47
(0.19, 1.03)
0.080
Age (per decade change or 1: 60–69 yrs, 2: 70–79 and 3: ≥80)0.75
(0.43, 1.23)
0.2890.75
(0.43, 1.31)
0.319
Family status (unmarried, divorced or widows vs. married or in relationship)0.23
(0.05, 1.01)
0.0520.25
(0.06, 1.17)
0.073
Educational level (per level change or 1: minimum/no education, 2: Secondary, 3: High school, 4: Technical School, 5: University)1.42
(1.15, 1.93)
0.0081.37
(1.10, 1.89)
0.022
Multimorbidity (≥3 chronic conditions vs. 0–2)3.52
(1.77, 9.30)
0.0043.53
(1.52, 8.78)
0.006
Health Care Services Utilization score—HCSUs (per unit change in the scale of 0–100) 1.03
(1.01, 1.04)
0.012
Daily consumption of fruits & vegetables (yes versus no) 1.90
(0.93, 4.22)
0.098
Daily physical activity (walking for ≥10 min/day versus inactivity or walking for less than 10 min/day) 2.24
(0.66, 8.68)
0.224
Short Anxiety Screening Test—SAST scale (per unit change in the scale of 1–40) 0.96
(0.31, 1.69)
0.392
R2 Nagelkerke0.200.26
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Kossyva, N.; Spanakis, M.; Borboudaki, L.; Stylianakis, D.; Rikos, N.; Rovithis, M.; Perdikogianni, C.; Linardakis, M.; Symvoulakis, E.K. Vaccination Coverage of Greek Adults Aged ≥60 Years in a Primary Health Care Setting in Relation to Lifestyle Factors and Health Care Services Utilization. Healthcare 2026, 14, 1167. https://doi.org/10.3390/healthcare14091167

AMA Style

Kossyva N, Spanakis M, Borboudaki L, Stylianakis D, Rikos N, Rovithis M, Perdikogianni C, Linardakis M, Symvoulakis EK. Vaccination Coverage of Greek Adults Aged ≥60 Years in a Primary Health Care Setting in Relation to Lifestyle Factors and Health Care Services Utilization. Healthcare. 2026; 14(9):1167. https://doi.org/10.3390/healthcare14091167

Chicago/Turabian Style

Kossyva, Nektaria, Marios Spanakis, Lena Borboudaki, Dimitrios Stylianakis, Nikos Rikos, Michael Rovithis, Chryssoula Perdikogianni, Manolis Linardakis, and Emmanouil K. Symvoulakis. 2026. "Vaccination Coverage of Greek Adults Aged ≥60 Years in a Primary Health Care Setting in Relation to Lifestyle Factors and Health Care Services Utilization" Healthcare 14, no. 9: 1167. https://doi.org/10.3390/healthcare14091167

APA Style

Kossyva, N., Spanakis, M., Borboudaki, L., Stylianakis, D., Rikos, N., Rovithis, M., Perdikogianni, C., Linardakis, M., & Symvoulakis, E. K. (2026). Vaccination Coverage of Greek Adults Aged ≥60 Years in a Primary Health Care Setting in Relation to Lifestyle Factors and Health Care Services Utilization. Healthcare, 14(9), 1167. https://doi.org/10.3390/healthcare14091167

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