SynthesisFrontiers in public health2025
Serotype distribution of invasive and non-invasive pneumococcal disease in adults ≥65 years of age following the introduction of 10- and 13-valent pneumococcal conjugate vaccines in infant national immunization programs: a systematic literature review.
Synthesis in Frontiers in public health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Serotype distribution of invasive and non-invasive pneumococcal disease in children ≤5 years of age following the introduction of 10- and 13-valent pneumococcal conjugate vaccines in infant national immunization programs: a systematic literature review.Frontiers in public health · 2025Pooled it
- Erratum: Pneumococcal Vaccination of Adults in Italy: What Strategies?Journal of preventive medicine and hygiene · 2025Article
- Pneumococcal Vaccination of Adults in Italy: What Strategies?Journal of preventive medicine and hygiene · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Despite the widespread implementation of 10- and 13-valent pneumococcal conjugate vaccines (PCVs) in infant national immunization programs and anticipated herd effects, pneumococcal disease incidence remains relatively high among older adults. In this vulnerable population, this includes not only invasive pneumococcal disease (IPD), but, more notably, non-invasive community-acquired pneumonia (CAP). A comprehensive understanding of adult pneumococcal epidemiology, particularly that of non-invasive CAP, is essential to guide future vaccination strategies for this population. Methods: We systematically reviewed observational studies (2006-2020) on pneumococcal serotype distribution in IPD and non-invasive CAP among adults aged ≥65 years after PCV implementation in children, focusing on the period post-implementation of the 10-valent pneumococcal non-typeable Results: Our analysis of 17 IPD and 17 CAP studies indicates the persistence of several vaccine serotypes, particularly serotypes 3 and 19A, in both clinical manifestations. Also serotype 7F remained frequently reported. The predominant non-PCV13 serotypes identified in both manifestations were serotypes 8, 12F, 15A, and 22F. Conclusion: The persistence of certain PCV13-serotypes in pneumococcal disease among adults aged ≥65 years suggests that herd immunity by infant PCV immunization may be insufficient to provide optimal protection in this population. This, coupled with emerging non-PCV13 serotypes due to serotype replacement and other limitations of current vaccines, supports the need for new vaccination technologies and strategies to improve protection of older adults.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.