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Search Results (344)

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15 pages, 890 KiB  
Article
Attitudes Toward General Vaccination Mediate the Association Between Influenza Vaccination History and Pneumococcal Vaccination Intention Among Older Adults in China
by Siwen Huang, Chi Ruan, Yan Jiang, Yudan Song, Yuhang Zhang, Zeying Qin, Xinyu Shi, Mengyue Zhang, Jingtao Zhou, Dingwan Chen, Yongkang Xiao, Liang Wang, Lili Tian, Rui Peng, Zongchao Peng and Sitong Luo
Vaccines 2025, 13(1), 20; https://doi.org/10.3390/vaccines13010020 - 29 Dec 2024
Viewed by 405
Abstract
Background: Influenza and pneumococcal vaccinations play a crucial role in disease prevention among older adults and are recommended to older adults aged 60 years and over in China, but the vaccination rates are suboptimal. Behavioral spillover indicates that a change in one behavior [...] Read more.
Background: Influenza and pneumococcal vaccinations play a crucial role in disease prevention among older adults and are recommended to older adults aged 60 years and over in China, but the vaccination rates are suboptimal. Behavioral spillover indicates that a change in one behavior may lead to changes in other related behaviors. Objective: Based on the Behavioral Spillover Theory, this study aimed to investigate the association between influenza vaccination history and pneumococcal vaccination intention, as well as the mediating role of negative attitudes toward general vaccination among older adults in China. Method: A multi-center cross-sectional survey was conducted among 1031 older adults, and 658 participants (median age: 65.0 ± 9.0 years) who had not received pneumococcal vaccination were included in the analysis. Correlation analysis and path analysis were performed. Results: A significant positive association was observed between influenza vaccination history and pneumococcal vaccination intention (r = 0.167, p < 0.001). In contrast, negative attitudes toward general vaccination, including mistrust of vaccine benefits (r = −0.253, p < 0.001), worries about unforeseen future effects (r = −0.180, p < 0.001), concerns about commercial profiteering (r = −0.360, p < 0.001), and a preference for natural immunity (r = −0.212, p < 0.001) were negatively associated with pneumococcal vaccination intention. Negative attitudes toward general vaccination mediated the association between influenza vaccination history and pneumococcal vaccination intention (total indirect effect = 0.119, p < 0.001, effect size = 50.0%). Conclusion: These findings demonstrated that influenza vaccination history may reduce negative attitudes toward general vaccination, which may further increase pneumococcal vaccination intention, indicating spillover effects of influenza vaccination history. To promote vaccination behavior among older adults, addressing negative attitudes toward general vaccination is crucial. Full article
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<p>Flowchart of participant selection for the analysis.</p>
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<p>The proposed mediation model with standard coefficients for the pneumococcal vaccination intention (N = 658). <span class="html-italic">Note:</span> * <span class="html-italic">p</span> &lt; 0.05, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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15 pages, 269 KiB  
Review
Vaccination After Haematopoietic Stem Cell Transplant: A Review of the Literature and Proposed Vaccination Protocol
by André Silva-Pinto, Isabel Abreu, António Martins, Juliana Bastos, Joana Araújo and Ricardo Pinto
Vaccines 2024, 12(12), 1449; https://doi.org/10.3390/vaccines12121449 - 23 Dec 2024
Viewed by 499
Abstract
Background/Objectives: Haematopoietic stem cell transplantation (HCT) induces profound immunosuppression, significantly increasing susceptibility to severe infections. This review examines vaccinations’ necessity, timing, and efficacy post-HCT to reduce infection-related morbidity and mortality. It aims to provide a structured protocol aligned with international and national recommendations. [...] Read more.
Background/Objectives: Haematopoietic stem cell transplantation (HCT) induces profound immunosuppression, significantly increasing susceptibility to severe infections. This review examines vaccinations’ necessity, timing, and efficacy post-HCT to reduce infection-related morbidity and mortality. It aims to provide a structured protocol aligned with international and national recommendations. Methods: A systematic review of current guidelines and studies was conducted to assess vaccination strategies in HCT recipients. The analysis included the timing of vaccine administration, factors influencing efficacy, and contraindications. Recommendations for pre- and post-transplant vaccination schedules were synthesised, specifically for graft-versus-host disease (GVHD), immunosuppressive therapy, and hypogammaglobulinemia. Results: Vaccination is essential as specific immunity is often lost after HCT. Inactivated vaccines are recommended to commence three months post-transplant, including influenza, COVID-19, and pneumococcal vaccines. Live attenuated vaccines remain contraindicated for at least two years post-transplant and in patients with ongoing GVHD or immunosuppressive therapy. Factors such as GVHD and immunosuppressive treatments significantly impact vaccine timing and efficacy. The review also underscores the importance of pre-transplant vaccinations and ensuring that patients’ close contacts are adequately immunised to reduce transmission risks. Conclusions: Implementing a structured vaccination protocol post-HCT is critical to improving patient outcomes. Timely and effective vaccination strategies can mitigate infection risks while addressing individual patient factors such as GVHD and immunosuppression. This review highlights the need for tailored vaccination approaches to optimize immune reconstitution in HCT recipients. Full article
(This article belongs to the Section Vaccination Optimization)
23 pages, 1261 KiB  
Systematic Review
Effectiveness of General Practitioners’ Involvement in Adult Vaccination Practices: A Systematic Review and Meta-Analysis of International Evidence
by Andrea Ceccarelli, Gabriele Munafò, Francesco Sintoni, Christian Cintori, Davide Gori and Marco Montalti
Vaccines 2024, 12(12), 1438; https://doi.org/10.3390/vaccines12121438 - 20 Dec 2024
Viewed by 383
Abstract
Background: General practitioners (GPs) and primary care units collaborate with Prevention Departments (PDs) to improve immunization by participating in vaccination campaigns, sharing tools, and implementing educational programs to raise patient awareness. This review aimed to identify effective strategies for involving GPs in PD [...] Read more.
Background: General practitioners (GPs) and primary care units collaborate with Prevention Departments (PDs) to improve immunization by participating in vaccination campaigns, sharing tools, and implementing educational programs to raise patient awareness. This review aimed to identify effective strategies for involving GPs in PD vaccination practices. Methods: A systematic review following PRISMA guidelines was conducted on MEDLINE, TripDatabase, ClinicalTrials, CINAHL, and Cochrane up to January 2024 to identify full-text studies in English evaluating the effectiveness of GP involvement. A meta-analysis was also performed. Results: Of 1018 records, 15 studies were included, with an intermediate quality assessment. Studies originated from the United States (n = 9), Europe (5), Singapore (1), and China (1). Eight studies investigated educational programs for GPs, while seven focused on organizational or technological interventions to enhance immunization practices. Twelve studies reported increased vaccine uptake after intervention. Vaccines addressed included influenza, SARS-CoV-2, pneumococcal, zoster, and trivalent (diphtheria, tetanus, pertussis). Interventions involving GPs in PD vaccination campaigns, focusing on organizational or technological strategies, demonstrated a significant increase in vaccine uptake (OR = 1.15; 95% CI: 1.03–1.27; p < 0.0001; I2 = 96%). Conclusions: GPs emerged as valuable allies for PDs due to their extensive territorial reach and trusted relationships with patients. Additionally, up-to-date organizational and technological tools could play a decisive role in increasing vaccine uptakes. This study, offering valuable insights into the effectiveness of GPs involvement, may be useful to implement similar intervention in different contexts. Full article
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<p>PRISMA flow diagram (PRISMA 2020 flow diagram for new systematic reviews which included searches of databases and registers only).</p>
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<p>Meta-analysis assessing vaccine uptake from interventions involving GP in vaccination educational program. Studies are presented in alphabetical order [<a href="#B26-vaccines-12-01438" class="html-bibr">26</a>,<a href="#B30-vaccines-12-01438" class="html-bibr">30</a>,<a href="#B34-vaccines-12-01438" class="html-bibr">34</a>,<a href="#B35-vaccines-12-01438" class="html-bibr">35</a>,<a href="#B36-vaccines-12-01438" class="html-bibr">36</a>].</p>
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<p>Meta-analysis assessing vaccine uptake from interventions involving GPs in organizational or technological implementations. Studies are presented in alphabetical order [<a href="#B27-vaccines-12-01438" class="html-bibr">27</a>,<a href="#B28-vaccines-12-01438" class="html-bibr">28</a>,<a href="#B32-vaccines-12-01438" class="html-bibr">32</a>,<a href="#B33-vaccines-12-01438" class="html-bibr">33</a>].</p>
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14 pages, 506 KiB  
Article
The Safety and Immunogenicity of a 13-Valent Pneumococcal Polysaccharide Conjugate Vaccine (CRM197/TT) in Infants: A Double-Blind, Randomized, Phase III Trial
by Zhiqiang Xie, Jiangjiao Li, Xue Wang, Lili Huang, Jinbo Gou, Wei Zhang, Haitao Huang, Wangyang You, Feiyu Wang, Xiaolong Li, Jinming Zhang, Qiang Han, Xiaomin Ma and Yanxia Wang
Vaccines 2024, 12(12), 1417; https://doi.org/10.3390/vaccines12121417 - 16 Dec 2024
Viewed by 608
Abstract
Objectives: This study aimed to evaluate the immunogenicity and safety of a 13-valent pneumococcal polysaccharide conjugate vaccine (CRM197/TT) (PCV13i) in infants. Methods: A total of 1200 infants were randomly assigned to either the experimental PCV13i group or the control PCV13 group in a [...] Read more.
Objectives: This study aimed to evaluate the immunogenicity and safety of a 13-valent pneumococcal polysaccharide conjugate vaccine (CRM197/TT) (PCV13i) in infants. Methods: A total of 1200 infants were randomly assigned to either the experimental PCV13i group or the control PCV13 group in a 1:1 ratio. Each group received a three-dose series of the vaccine at 2, 4, and 6 months of age, followed by a booster dose at 12–15 months. Blood samples were collected before and 30 days after both primary and booster vaccinations. The primary immunogenicity endpoints were the seropositive rate and the geometric mean concentration (GMC) of IgG antibodies against the 13 pneumococcal serotypes. The primary safety endpoint was the incidence of adverse reactions within 0–7 days and 0–30 days after vaccination. Results: Results showed that the experimental PCV13i was well tolerated, with a safety profile comparable to that of the control vaccine. Following primary vaccination, the GMCs of IgG responses against serotypes 1, 5, 6A, 6B, 14, and 18C in the experimental group were lower than those in the control group, while responses against serotypes 3, 4, 7F, 9V, 19A, 19F, and 23F were higher. The experimental group exhibited higher opsonophagocytic killing assay (OPA) geometric mean titers (GMTs) for serotypes 3, 7F, 19A, and 19F compared to the control group, while GMTs for serotypes 1, 5, 6A, and 18C were lower. Following booster vaccination, OPA GMTs of the experimental group remained higher than those of the control group for serotypes 3, 7F, and 19F, while GMTs for serotype 5 were lower. Both vaccines induced robust immune responses, with high seropositive rates and significant increases in antibody levels following vaccination. Conclusions: The experimental PCV13i demonstrated non-inferiority to the control PCV13 in terms of immunogenicity. Full article
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<p>Trial profile. Note: SS represents safety set. FAS represents full analysis set. PPS1 is a subset of per protocol set, which contains 2-month-old subjects who completed 3 vaccination doses and had pre- and post-3-dose IgG test results. PPS2 is also a subset of the per protocol set, which contains 2-month-old subjects completing the 4th vaccination with pre- and post-immunization IgG test results. PPS-O2 included the participants in PPS2 with post immunization opsonophagocytic killing assay results.</p>
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26 pages, 528 KiB  
Systematic Review
Cost-Effectiveness of the Pneumococcal Vaccine in the Adult Population: A Systematic Review
by Nam Xuan Vo, Huong Lai Pham, Uyen My Bui, Han Tue Ho and Tien Thuy Bui
Healthcare 2024, 12(23), 2490; https://doi.org/10.3390/healthcare12232490 - 9 Dec 2024
Viewed by 878
Abstract
Objectives: Pneumococcal disease (PD), caused by S. pneumoniae, is a serious global health issue, primarily for adults over 65, due to its high mortality and morbidity rates. Recently, broader-serotype vaccines have been introduced to cope with tremendous hospital costs and decreasing quality [...] Read more.
Objectives: Pneumococcal disease (PD), caused by S. pneumoniae, is a serious global health issue, primarily for adults over 65, due to its high mortality and morbidity rates. Recently, broader-serotype vaccines have been introduced to cope with tremendous hospital costs and decreasing quality of life. Our study aims to systematically review the cost-effectiveness of current PCVs (pneumococcal conjugate vaccines) and PPVs (pneumococcal polysaccharide vaccine) from 2018 to April 2024. Methods: Articles were identified through PubMed, Embase, and Cochrane. Key outcomes include an improved incremental cost-effectiveness ratio (ICER) and quality-adjusted life-years (QALY), with the article’s quality assessed via the Consolidated Health Economic Evaluation Reporting Standards 2022 (CHEERS 2022). In total, 23 studies were included, with 22 studies of high quality and 1 of moderate quality. Results: These articles showed that PCV20 was the most cost-effective option compared with other vaccines, including PPV23, PCV13, PCV15, and PCV15/PPV23, for both young and older adults, regardless of risk factors. PCV20, when used alone, saved greater costs than PCV20, followed by PPV23. Conclusions: For countries applying lower-valency vaccines, switching to PCV20 as a single regimen would be the most beneficial for averting pneumococcal cases and reducing costs in adults aged 18–64 and over 65. Full article
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<p>PRISMA flow diagram of the article selection process.</p>
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10 pages, 228 KiB  
Article
Vaccination Coverage for Medically Indicated Vaccines in a Convenience Sample of Severely Immunocompromised Patients with COVID-19: An Observational Cohort Study
by Elsemieke te Linde, Marjolein P. M. Hensgens, Albert M. Vollaard, Annelies Verbon and Anke H. W. Bruns
Vaccines 2024, 12(12), 1383; https://doi.org/10.3390/vaccines12121383 - 9 Dec 2024
Viewed by 707
Abstract
Background: In recent decades, the number of immunocompromised patients (ICPs) has increased significantly. ICPs have an impaired immune system, making them susceptible to complicated infections. To protect them from infections, ICPs are eligible to receive several medically indicated vaccines. To obtain insight into [...] Read more.
Background: In recent decades, the number of immunocompromised patients (ICPs) has increased significantly. ICPs have an impaired immune system, making them susceptible to complicated infections. To protect them from infections, ICPs are eligible to receive several medically indicated vaccines. To obtain insight into the uptake of these medically indicated vaccines, we determined the coverage of these vaccines in ICPs. Methods: This observational cohort study was conducted at the University Medical Centre Utrecht, the Netherlands, from September 2021 to April 2022. All adult ICPs admitted for COVID-19 were asked to complete a questionnaire on their vaccination history (pneumococcal, herpes zoster, human papillomavirus vaccination, influenza, and COVID-19 vaccines) and history of vaccine-preventable infections. In addition, patients’ vaccination history was reviewed in medical files. Results: A total of 115 patients completed the questionnaire and were included. Although all patients had an indication for pneumococcal vaccination, only 22 received it (19%). Coverage for herpes zoster was low (1%, 1/106 eligible patients). Coverage for human papillomavirus vaccination (HPV) was also low (40%, two out of five eligible patients). In contrast, 92% of patients received vaccination against SARS-CoV-2, and 77% of patients received seasonal influenza vaccination. Conclusions: Although coverage for influenza and COVID-19 vaccination was high in ICPs, coverage for other medically indicated vaccines was low. Identifying which factors contributed to high COVID-19 and influenza vaccine uptake can help to improve vaccination rates for the other recommended vaccines. Clear guidelines for clinicians and the removal of organizational obstacles are needed to improve vaccination coverage. Full article
28 pages, 3325 KiB  
Systematic Review
Clozapine and Pneumonia: Synthesizing the Link by Reviewing Existing Reports—A Systematic Review and Meta-Analysis
by Victor Zhao, Yiting Gong, Naveen Thomas and Soumitra Das
Medicina 2024, 60(12), 2016; https://doi.org/10.3390/medicina60122016 - 6 Dec 2024
Viewed by 742
Abstract
Background and Objectives: Clozapine is a highly effective antipsychotic used for treating treatment-refractory psychotic and mood disorders. However, clozapine also has a serious risk of side effects leading to mortality, particularly its potentiated risk of leading to pneumonia. This review aims to overview [...] Read more.
Background and Objectives: Clozapine is a highly effective antipsychotic used for treating treatment-refractory psychotic and mood disorders. However, clozapine also has a serious risk of side effects leading to mortality, particularly its potentiated risk of leading to pneumonia. This review aims to overview the demographic and health-related risk factors leading to pneumonia to better inform risk assessment for clozapine users and to summarise current theories on the mechanisms for clozapine-associated pneumonia. This paper will highlight the need to prioritise pneumococcal vaccination in this population group. Materials and Method: We conducted a literary search of five online databases conforming to PRISMA. Our review includes all peer-reviewed papers with original data that discuss clozapine and pneumonia and excludes case reports. Baseline information of participants, pneumonia-related information and information regarding risk factors and mechanisms causing pneumonia were also extracted. Results: Clozapine was found to have an increased risk of pneumonia compared to other antipsychotic medications. Factors included comorbidities, higher clozapine dosages, and concurrent use of other antipsychotic medications. Key mechanisms for clozapine-associated pneumonia include clozapine-induced hyper sedation, sialorrhea and neutropoenia. Conclusions: While clozapine improves overall mortality for patients, our review confirms clozapine has the highest risk of pneumonia of all antipsychotics. The review also highlights the prevalent underuse of pneumococcal vaccines among clozapine users and the urgent need to increase uptake. Full article
(This article belongs to the Special Issue Mental Health Care: Pandemic and Beyond)
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<p>PRISMA 2020 Flowchart Diagram.</p>
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<p>Forest plot for clozapine vs. SGAs [<a href="#B12-medicina-60-02016" class="html-bibr">12</a>,<a href="#B14-medicina-60-02016" class="html-bibr">14</a>,<a href="#B18-medicina-60-02016" class="html-bibr">18</a>,<a href="#B19-medicina-60-02016" class="html-bibr">19</a>,<a href="#B20-medicina-60-02016" class="html-bibr">20</a>,<a href="#B31-medicina-60-02016" class="html-bibr">31</a>,<a href="#B33-medicina-60-02016" class="html-bibr">33</a>,<a href="#B34-medicina-60-02016" class="html-bibr">34</a>,<a href="#B35-medicina-60-02016" class="html-bibr">35</a>].</p>
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<p>Forest plot for clozapine vs. FGAs [<a href="#B19-medicina-60-02016" class="html-bibr">19</a>,<a href="#B20-medicina-60-02016" class="html-bibr">20</a>,<a href="#B31-medicina-60-02016" class="html-bibr">31</a>,<a href="#B34-medicina-60-02016" class="html-bibr">34</a>].</p>
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<p>Funnel plot for clozapine vs. SGAs [<a href="#B12-medicina-60-02016" class="html-bibr">12</a>,<a href="#B14-medicina-60-02016" class="html-bibr">14</a>,<a href="#B18-medicina-60-02016" class="html-bibr">18</a>,<a href="#B19-medicina-60-02016" class="html-bibr">19</a>,<a href="#B20-medicina-60-02016" class="html-bibr">20</a>,<a href="#B31-medicina-60-02016" class="html-bibr">31</a>,<a href="#B33-medicina-60-02016" class="html-bibr">33</a>,<a href="#B34-medicina-60-02016" class="html-bibr">34</a>,<a href="#B35-medicina-60-02016" class="html-bibr">35</a>].</p>
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<p>Funnel plot for clozapine vs. FGAs [<a href="#B19-medicina-60-02016" class="html-bibr">19</a>,<a href="#B20-medicina-60-02016" class="html-bibr">20</a>,<a href="#B31-medicina-60-02016" class="html-bibr">31</a>,<a href="#B34-medicina-60-02016" class="html-bibr">34</a>].</p>
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<p>Figure of bidirectional relationship of clozapine and pneumonia.</p>
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<p>Infection pneumonia mechanism for clozapine.</p>
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<p>Infection pneumonia mechanism for clozapine use.</p>
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17 pages, 526 KiB  
Article
Evaluation of Integrated Child Health Days as a Catch-Up Strategy for Immunization in Three Districts in Uganda
by Mansoor Farahani, Tonny Tindyebwa, Nandita Sugandhi, Kirsten Ward, Youngjoo Park, Pamela Bakkabulindi, Shibani Kulkarni, Aaron Wallace, Samuel Biraro, Yvette Wibabara, Hannah Chung, Giles A. Reid, Driwale Alfred, Rita Atugonza, Elaine J. Abrams and Ledor S. Igboh
Vaccines 2024, 12(12), 1353; https://doi.org/10.3390/vaccines12121353 - 29 Nov 2024
Viewed by 737
Abstract
Background: Uganda’s Integrated Child Health Day (ICHD) initiative aims to improve children’s access to vaccinations. Although widely used as a catch-up vaccination strategy, the effectiveness of the ICHD program in increasing immunization coverage, especially among vulnerable populations, has not been recently evaluated. This [...] Read more.
Background: Uganda’s Integrated Child Health Day (ICHD) initiative aims to improve children’s access to vaccinations. Although widely used as a catch-up vaccination strategy, the effectiveness of the ICHD program in increasing immunization coverage, especially among vulnerable populations, has not been recently evaluated. This study assessed the reach and uptake of ICHD for immunizations in Uganda. Methods: A mixed-methods evaluation was conducted in three districts (Rakai, Kayunga, and Bukedea) where ICHDs occurred. The data collection included a cross-sectional household survey using validated WHO-adapted questionnaires of 1432 caregivers of children under five years old, key informant interviews with 42 health managers and workers, and nine focus group discussions with caregivers between October and December 2022. The vaccines assessed were Bacillus Calmette–Guerin, oral polio, Pentavalent, pneumococcal conjugate, rotavirus (RV), and measles-rubella (MR). Results: The immunization coverage based on child health cards was over 90% for all vaccines except for the second dose of RV (88.3%) and MR (16.2%). Among the children, 2.3% had received no Pentavalent vaccine, and 69.4% were fully vaccinated for their age. Of the 631 children who attended ICHDs, 79.4% received at least one vaccine during the event. Village Health Teams (49%), health workers (18.3%), and megaphone outreach (17.9%) were the primary information sources. Key informants cited challenges with coordination, vaccine delivery, and mobilization. Conclusions: Despite operational challenges, ICHDs appear to have contributed to routine childhood vaccinations. Further research is needed to assess the sustainability and cost-effectiveness of the program. Full article
(This article belongs to the Section Human Vaccines and Public Health)
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<p>Vaccination by vaccine type and ICHD attendance among children under five years of age, Uganda, 2022 (based on household survey and Child Health Card Records). Attended 558, not attend = 111 = total 669; Bacillus Calmette–Guerin (BCG); oral polio vaccine (OPV); diphtheria–tetanus–pertussis–hepatitis B–<span class="html-italic">Haemophilus influenza</span> type b (Penta); Pneumococcal Conjugate Vaccine (PCV); rotavirus vaccine (Rota); measles-rubella vaccine (MR). The numbers indicate 1st, 2nd, and 3rd doses.</p>
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12 pages, 300 KiB  
Review
The Impact of Vaccinations Against Respiratory Infections on the Prognosis in Heart Failure Patients
by Berenika Jankowiak, Marta Wleklik and Marta Rosiek-Biegus
Vaccines 2024, 12(12), 1321; https://doi.org/10.3390/vaccines12121321 - 26 Nov 2024
Viewed by 552
Abstract
Heart failure (HF) affects 64 million people worldwide and is one of the most prevalent causes of hospitalization in adults. Infection is believed to be one of the potential triggers that may facilitate HF decompensation and the need for hospitalization. Therefore, it seems [...] Read more.
Heart failure (HF) affects 64 million people worldwide and is one of the most prevalent causes of hospitalization in adults. Infection is believed to be one of the potential triggers that may facilitate HF decompensation and the need for hospitalization. Therefore, it seems crucial to safeguard against such a situation. Vaccinations seem to be a very reasonable option. However, this remains an underutilized solution among HF patients. This review investigates the impact of available vaccinations, including influenza, COVID-19, pneumococcal, and RSV, on prognosis in specific HF populations only, as there are pathophysiological reasons to believe that this population of patients may benefit the most from the intervention. It will provide information about the safety profile of these vaccines and summarize the available evidence on their impact on hard clinical outcomes. In summary, this article will discuss the impact of preventive vaccinations against seasonal infections in the HF population. Full article
(This article belongs to the Collection Vaccines against Infectious Diseases)
19 pages, 340 KiB  
Review
Impact of Immunosenescence on Vaccine Immune Responses and Countermeasures
by Li Chen, Chengwei Shao, Jingxin Li and Fengcai Zhu
Vaccines 2024, 12(11), 1289; https://doi.org/10.3390/vaccines12111289 - 19 Nov 2024
Viewed by 1027
Abstract
The biological progression of aging encompasses complex physiological processes. As individuals grow older, their physiological functions gradually decline, including compromised immune responses, leading to immunosenescence. Immunosenescence significantly elevates disease susceptibility and severity in older populations while concurrently compromising vaccine-induced immune responses. This comprehensive [...] Read more.
The biological progression of aging encompasses complex physiological processes. As individuals grow older, their physiological functions gradually decline, including compromised immune responses, leading to immunosenescence. Immunosenescence significantly elevates disease susceptibility and severity in older populations while concurrently compromising vaccine-induced immune responses. This comprehensive review aims to elucidate the implications of immunosenescence for vaccine-induced immunity and facilitate the development of optimized vaccination strategies for geriatric populations, with specific focus on COVID-19, influenza, pneumococcal, herpes zoster, and respiratory syncytial virus (RSV) vaccines. This review further elucidates the relationship between immunosenescence and vaccine-induced immunity. This review presents a systematic evaluation of intervention strategies designed to enhance vaccine responses in older populations, encompassing adjuvant utilization, antigen doses, vaccination frequency modification, inflammatory response modulation, and lifestyle interventions, including physical activity and nutritional modifications. These strategies are explored for their potential to improve current vaccine efficacy and inform the development of next-generation vaccines for geriatric populations. Full article
11 pages, 991 KiB  
Article
The Health and Economic Effects of PCV15 and PCV20 During the First Year of Life in the US
by Aleksandar Ilic, Maria J. Tort, Alejandro Cane, Raymond A. Farkouh and Mark H. Rozenbaum
Vaccines 2024, 12(11), 1279; https://doi.org/10.3390/vaccines12111279 - 14 Nov 2024
Viewed by 883
Abstract
(1) Background/Objectives: Two pneumococcal conjugate vaccines, 15-(PCV15) and 20-(PCV20) valent formulations, are routinely recommended for US children in a 3+1 schedule. The first three doses are administered during the first year of life at 2, 4, and 6 months, while a booster dose [...] Read more.
(1) Background/Objectives: Two pneumococcal conjugate vaccines, 15-(PCV15) and 20-(PCV20) valent formulations, are routinely recommended for US children in a 3+1 schedule. The first three doses are administered during the first year of life at 2, 4, and 6 months, while a booster dose is given at 12 to 15 months. This study evaluated the health and economic effects of the PCV20 infant series within the first year of life compared to PCV15. (2) Methods: Using a decision-analytic model, we calculated the health and economic effects of introducing PCV15 or PCV20 for five subsequent birth cohorts. Epidemiological data were drawn from peer-reviewed studies and estimates for vaccine effectiveness were extrapolated from established PCV13 effectiveness and PCV7 efficacy studies. Direct medical costs related to the disease treatment were extracted from the literature and inflated to 2024 dollars. (3) Results: Over the course of five years, the implementation of PCV20 vaccination for newborns in the United States, compared to PCV15, is projected to prevent an additional 220 cases of invasive pneumococcal disease, 6542 cases of community-acquired pneumonia, and 112,095 cases of otitis media within the first year of life across five subsequent birth cohorts. This strategy could prevent 66 infant deaths linked to these illnesses and confer extra health gains, amounting to 5058 years of life and 5037 quality-adjusted life years. These prevented cases are estimated to save approximately USD 147 million over 5 years. (4) Conclusions: This study demonstrated that vaccinating with PCV20 during the first 12 months of life compared to PCV15 in the US would yield a substantially greater health and economic return due to the five additional serotypes covered by PCV20. Full article
(This article belongs to the Special Issue The Effectiveness of Pneumococcal Conjugate Vaccines)
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<p>Model schematic.</p>
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<p>Results of the Deterministic Sensitivity Analysis (DSA)–PCV20 vs. PCV15 costs averted.</p>
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<p>Results of the Deterministic Sensitivity Analysis (DSA)–PCV20 vs. PCV15 QALYs gained.</p>
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14 pages, 1558 KiB  
Article
Sequential Vaccination Against Streptococcus pneumoniae Appears as Immunologically Safe in Clinically Stable Kidney Transplant Recipients
by Monika Lindemann, Lukas van de Sand, Nils Mülling, Kim L. Völk, Ulrich W. Aufderhorst, Benjamin Wilde, Peter A. Horn, Andreas Kribben, Adalbert Krawczyk, Oliver Witzke and Falko M. Heinemann
Vaccines 2024, 12(11), 1244; https://doi.org/10.3390/vaccines12111244 - 31 Oct 2024
Viewed by 894
Abstract
Background: Vaccination against Streptococcus pneumoniae is advised for transplant recipients to reduce morbidity and mortality associated with invasive pneumococcal disease. However, data on alloantibodies after sequential vaccination (with a pneumococcal conjugate vaccine followed by a polysaccharide vaccine) are still lacking. Methods: In the [...] Read more.
Background: Vaccination against Streptococcus pneumoniae is advised for transplant recipients to reduce morbidity and mortality associated with invasive pneumococcal disease. However, data on alloantibodies after sequential vaccination (with a pneumococcal conjugate vaccine followed by a polysaccharide vaccine) are still lacking. Methods: In the current study, we determined HLA class I and II and major histocompatibility class I-related chain A (MICA) antibodies in 41 clinically stable kidney transplant recipients. These antibodies were measured prior to and post sequential pneumococcal vaccination over a period of 12 months. Alloantibodies were measured by Luminex bead-based assays, and pneumococcal IgG antibodies were measured by ELISA. Results: Over a 12-month period, the sequential analysis revealed no significant change in alloantibodies. One patient developed de novo donor-specific antibodies (DSA) 1.5 months after the first vaccination, with mean fluorescence intensities of up to 2300. These DSA became undetectable in the follow-up, and the patient showed no signs of allograft rejection. Another patient experienced a biopsy-proven borderline rejection 7 months after the first vaccination but did not develop de novo DSA. Both maintained stable kidney function. As expected, the pneumococcal antibodies increased significantly after vaccination (p < 0.0001). Conclusions: Given the overall risk of alloimmune responses in transplant recipients, we would not attribute the two noticeable patient courses to vaccination. Thus, we consider sequential vaccination immunologically safe. Full article
(This article belongs to the Special Issue Vaccine Efficacy and Safety in Transplant Recipients)
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<p>Study design. Sequential pneumococcal vaccination and blood collection in 41 kidney transplant recipients. The blood droplets indicate the time points of blood collection. The first vaccination was performed with a 13-valent conjugated vaccine (PCV13), the second with a 23-valent polysaccharide vaccine (PPSV23). Month 0 indicates baseline (pre-vaccination) and months 1–12 follow-up after the first vaccination. For example, month 7 means 7 months after the first vaccination and 1 month after the second vaccination.</p>
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<p>Time-course of antibodies determined in 41 kidney transplant recipients prior to vaccination (month 0, M0) and after vaccination against pneumococci (months 1 to 12, M1–M12). The first vaccination was performed at month 0 (directly after blood collection) with a 13-valent pneumococcal conjugate vaccine and the second vaccination at month 6 with a 23-valent pneumococcal polysaccharide vaccine. The time points of vaccination are indicated by arrows. The left panels show antibodies against human leukocyte antigen (HLA) class I and II and major histocompatibility class I-related chain A (MICA), which were expressed either as cumulative (cum.) antibody scores as detailed in the Methods section (<b>a</b>) or as cumulative mean fluorescence intensity (MFI) (<b>b</b>). Panel (<b>c</b>) indicates IgG antibodies against <span class="html-italic">S. pneumoniae</span>. Antibodies against HLA and MICA are presented as mean and standard error of the mean (SEM), pneumococcal antibodies as geometric mean and 95% confidence interval. To compare the results at the various time points, we used a 1-way ANOVA, the Friedman test with Dunn’s multiple comparisons test (** <span class="html-italic">p</span> &lt; 0.01; **** <span class="html-italic">p</span> &lt; 0.0001).</p>
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<p>Patterns of antibodies in 41 kidney transplant recipients prior to vaccination (month 0, M0) and after vaccination against pneumococci (months 1 to 12, M1–M12). The time points of vaccination are indicated by arrows. Panel (<b>a</b>,<b>b</b>) indicate the number of patients with positive or negative antibody responses against human leukocyte antigen (HLA) class I and II and major histocompatibility class I-related chain A (MICA), setting the cutoff for positive responses at a ratio of 3.0 (<b>a</b>) or 4.5 (<b>b</b>), respectively. Panel (<b>c</b>) shows changes in the cumulative antibody score, determined pre-vaccination (month 0) and at month 12, i.e., after two vaccinations. Red symbols/numbers indicate patients with an increase (the score in month 12 was at least 1 higher than in month 0), black with constant values, and green with a decrease.</p>
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<p>Comparison of antibody patterns in female and male kidney transplant recipients prior to vaccination (month 0, M0) and after vaccination against pneumococci (months 1 to 12, M1–M12). The time points of vaccination are indicated by arrows. Panel (<b>a</b>) indicates cumulative antibody scores for antibodies against human leukocyte antigen (HLA) class I and II and major histocompatibility class I-related chain A (MICA); panel (<b>b</b>) indicates IgG antibodies against pneumococci and kidney function (estimated glomerular filtration rate, eGFR). Data on alloantibodies and kidney function are presented as mean and standard error of the mean (SEM), and data on pneumococcal antibodies as geometric mean and 95% confidence interval.</p>
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15 pages, 1783 KiB  
Article
Cost-Effectiveness of Bivalent Respiratory Syncytial Virus Prefusion F Vaccine for Prevention of Respiratory Syncytial Virus Among Older Adults in Greece
by George Gourzoulidis, Charalampos Tzanetakos, Argyro Solakidi, Eleftherios Markatis, Marios Detsis, Diana Mendes and Myrto Barmpouni
Vaccines 2024, 12(11), 1232; https://doi.org/10.3390/vaccines12111232 - 29 Oct 2024
Viewed by 1055
Abstract
Background/Objectives: To evaluate the health benefits, costs, and cost-effectiveness of vaccination with bivalent respiratory syncytial virus stabilized prefusion F vaccine (RSVpreF) for the prevention of lower respiratory tract disease caused by respiratory syncytial virus (RSV) in Greek adults 60 years of age and [...] Read more.
Background/Objectives: To evaluate the health benefits, costs, and cost-effectiveness of vaccination with bivalent respiratory syncytial virus stabilized prefusion F vaccine (RSVpreF) for the prevention of lower respiratory tract disease caused by respiratory syncytial virus (RSV) in Greek adults 60 years of age and older. Methods: A Markov model was adapted to simulate lifetime risk of health and economic outcomes from the public payer’s perspective over a lifetime horizon. Epidemiology, vaccine effectiveness, utilities, and direct medical costs (EUR, 2024) were obtained from published studies, official sources, and local experts. Model outcomes included the number of medically attended RSV cases, stratified by care setting (i.e., hospital, emergency department [ED], outpatient visits [OV]), and attributable RSV-related deaths, costs, life years (LY), quality-adjusted life-years (QALY), and incremental cost-effectiveness ratios (ICERs) of RSVpreF vaccination compared with no vaccination. Results: The model projected 258,170 hospitalizations, 112,248 ED encounters, 1,201,604 OV, and 25,463 deaths related to RSV in Greek older adults resulting in direct medical costs of EUR 1.6 billion over the lifetime horizon. Assuming RSV vaccination would reach the same coverage rates as pneumococcal and influenza programmes, 18,118 hospitalizations, 7874 ED encounters, 48,079 OV, and 1706 deaths could be prevented over the modelled time horizon. The health benefits associated with RSVpreF contributed to an incremental gain of 10,976 LYs and 7230 QALYs compared with no vaccination. The incremental analysis reported that vaccination with RSVpreF was estimated to be a cost-effective strategy resulting in ICERs of EUR 12,991 per LY gained, EUR 19,723 per QALY gained, and EUR 7870 per hospitalized RSV case avoided compared with no vaccination. Conclusions: Vaccination with RSVpreF was a cost-effective strategy for the prevention of RSV disease in Greek adults over 60 years of age. The introduction of RSV vaccination can improve public health by averting RSV cases and deaths and has the potential to fulfil an unmet medical need. Full article
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<p>Model schematic.</p>
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<p>Distribution of RSV cases by calendar month. Source: local clinical experts.</p>
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<p>Tornado diagram of RSVpreF vaccination strategy versus no vaccination strategy. RSV: respiratory syncytial virus, OV: outpatient visit, ED: emergency department, VE: vaccine effectiveness.</p>
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<p>Scatterplot from probabilistic sensitivity analyses results of RSVpreF vaccination strategy versus no vaccination strategy.</p>
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13 pages, 3980 KiB  
Article
Invasive Pneumococcal Diseases in People over 65 in Veneto Region Surveillance
by Silvia Cocchio, Claudia Cozzolino, Andrea Cozza, Patrizia Furlan, Irene Amoruso, Francesca Zanella, Filippo Da Re, Debora Ballarin, Gloria Pagin, Davide Gentili, Michele Tonon, Francesca Russo, Tatjana Baldovin and Vincenzo Baldo
Vaccines 2024, 12(11), 1202; https://doi.org/10.3390/vaccines12111202 - 23 Oct 2024
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Abstract
Background: Elderly individuals over 65, along with children under 5, are the most affected by invasive pneumococcal diseases (IPDs). Monitoring vaccination coverage and conducting surveillance are essential for guiding evidence-based prevention campaigns and public health measures. Methods: Since 2007, the Veneto Region has [...] Read more.
Background: Elderly individuals over 65, along with children under 5, are the most affected by invasive pneumococcal diseases (IPDs). Monitoring vaccination coverage and conducting surveillance are essential for guiding evidence-based prevention campaigns and public health measures. Methods: Since 2007, the Veneto Region has relied on three sources for surveillance of invasive bacterial infections, contributing to an increase in reported IPD cases. This study analyzed notifications related to individuals aged ≥65 years from 2007 to 2023. Results: A total of 1527 cases of IPDs in elderly individuals were reported between 2007 and 2023. The notification rate significantly increased from 5.61 to 14.63 per 100,000 inhabitants, despite underreporting during the COVID-19 pandemic. Cases associated with sepsis increased from 3.89 to 9.58 per 100,000, while notifications of meningitis and case fatality rates remained stable at 1.5 per 100,000 and 11.8%, respectively. Serotyping was not performed in 52% of the notifications. The most common serotypes were 3 (21.6%), 8 (11.1%), and 19A (5.0%), with fluctuations over time. There was a significant decline in serotypes covered by PCV7 and PCV13 and an increase in non-vaccine serotypes. Conclusions: The regional surveillance system allows for an increasingly comprehensive profile of the epidemiological landscape of IPDs in Veneto. However, the surveillance of pneumococcal infections still presents challenges. The currently available data are likely to be underestimated, mainly referring to the most severe cases, and the serotyping necessary to identify the etiological agent is still not often performed. Full article
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<p>Notification rates of invasive pneumococcal disease (per 100,000 inhabitants) trends with average annual percentage change (AAPC) and 95% confidence intervals: (<b>a</b>) by age group and (<b>b</b>) by invasive bacterial diseases.</p>
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<p><span class="html-italic">Streptococcus pneumoniae</span> serotype distribution over the study years excluding untyped cases (<b>a</b>) and notification rates of invasive pneumococcal disease (per 100,000 inhabitants) trends with average annual percentage change (AAPC) and 95% confidence intervals by vaccine group (<b>b</b>).</p>
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<p>Trends of (<b>a</b>) invasive pneumococcal disease case fatality rate (CFR) and (<b>b</b>) pneumococcal vaccination coverage percentage with average annual percentage change (AAPC) and 95% confidence intervals.</p>
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<p>Absolute (<b>a</b>) and relative distribution of <span class="html-italic">Streptococcus pneumoniae</span> serotypes including untyped/untypable samples (<b>b</b>) over the study years.</p>
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13 pages, 392 KiB  
Article
Burden of Pneumococcal Disease in Young Children Due to Serotypes Contained in Different Pneumococcal Conjugate Vaccines in Eight Asian Countries and Territories
by Liping Huang, Xiuyan Li, Ng Eugenia, Johnnie Leung, Sheng-Tzu (Alice) Hung, Ervin Zhi Bin Cheong, Ricardo Avila, Winniefer Nua, Kornvipa Choowanich, Ritika Rampal, Namrata Kulkarni, Derek Daigle and Bulent Nuri Taysi
Vaccines 2024, 12(10), 1197; https://doi.org/10.3390/vaccines12101197 - 19 Oct 2024
Viewed by 1386
Abstract
Background: Pneumococcal disease (PD) is a major cause of morbidity and mortality in young children in Asia and globally. Pneumococcal conjugate vaccines (PCVs) have significantly reduced the burden of PD when included in pediatric national immunization programs (NIPs). This study estimates the clinical [...] Read more.
Background: Pneumococcal disease (PD) is a major cause of morbidity and mortality in young children in Asia and globally. Pneumococcal conjugate vaccines (PCVs) have significantly reduced the burden of PD when included in pediatric national immunization programs (NIPs). This study estimates the clinical and economic burden of PD due to serotypes contained in different PCVs in children aged < 5 years in eight Asian countries/territories. Methods: Based on published data, a cohort-based decision analytic model was used to estimate annual PD cases, deaths, and direct medical costs associated with serotypes contained in PCV10, PCV13, PCV15, and PCV20. Results: PD incidence rates were lower in regions with PCV13 in their NIP than those without. Serotypes contained in higher but not lower valency PCVs resulted in a significant incremental clinical and economic burden, although the difference between PCV13 and PCV15 serotypes was generally small. Moving from PCV13 to PCV20 was estimated to result in greater clinical and economic burden reductions. Conclusions: This study demonstrates the remaining and incremental burden of PD from PCV10 to PCV20 serotypes in young children in selected Asian regions. Extending NIP access to higher-valency PCVs with broader serotype coverage and improving vaccine uptake will help prevent morbidity and deaths and save healthcare costs. Full article
(This article belongs to the Special Issue Pneumococcal vaccines: Current Status and Future Prospects)
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<p>Derivation of clinical and cost outcomes in the model. CFR, case fatality rate; IPD, invasive pneumococcal disease; OM, otitis media; PCV, pneumococcal conjugate vaccine; <span class="html-italic">SPn</span>, <span class="html-italic">Streptococcus pneumoniae</span>. cases*cost, cases multiplied by cost per case.</p>
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