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Pertussis immunisation strategies to optimise infant pertussis control: A narrative systematic review
Elise Tessier1, Daniel Newport2, Anh Tran1
1UK Health Security Agency, London, UK.
Insights
Choosing the best infant immunization schedule for acellular pertussis vaccine is challenging. Current evidence is insufficient to declare one schedule superior, emphasizing the need for high vaccine coverage to protect infants.
Area of Science:
- Immunology
- Public Health
- Vaccinology
Background:
- Countries face challenges in optimizing acellular pertussis vaccine schedules due to waning long-term protection.
- Infant pertussis disease, hospitalizations, and deaths remain significant public health concerns.
Approach:
- A narrative systematic review synthesized findings from 98 studies on primary, booster, and maternal pertussis vaccination series.
- Studies were categorized based on accelerated (early) versus extended (later) vaccination schedules.
- Risk of bias was assessed using the Risk of Bias in Non-randomised Studies of Intervention tool.
Key Points:
- Recurring themes included vaccination timing, coverage, waning immunity, and vaccine effectiveness.
- Direct and indirect effectiveness of different schedules were analyzed.
- The impact of changes in diagnostic testing on pertussis surveillance was also considered.
Conclusions:
- Insufficient evidence exists to definitively recommend one pertussis vaccination schedule over another.
- Selecting a schedule that ensures high vaccine coverage and timely infant protection is crucial.
- Further research is needed to establish optimal pertussis immunization strategies.
Objective:
Countries routinely offering acellular pertussis vaccine, where long-term protection is not sustained, have the challenge of selecting an optimal schedule to minimise disease among young infants. We conducted a narrative systematic review and synthesis of information to evaluate different pertussis immunisation strategies at controlling pertussis disease, hospitalisation, deaths, and vaccine effectiveness among young infants.
Methods:
We conducted a review of the literature on studies about the primary, booster, and/or maternal vaccination series and synthesised findings narratively. Countries offering the first three doses of vaccine within six-months of life and a booster on or before the second year or life were defined as accelerated primary and booster schedules, respectively. Countries offering primary and booster doses later were defined as extended primary and booster schedules. All search results were screened, and articles reviewed and reconciled, by two authors. The Risk of Bias in Non-randomised Studies of Intervention tool was used to evaluate the risk of bias.
Findings:
A total of 98 studies were included in the analyses and the following recurring themes were described: timing of vaccination, vaccine coverage, waning immunity/vaccine effectiveness, direct and indirect effectiveness, switching from an accelerated to extended schedule, impact of changes in testing. The risk of bias was generally low to moderate for most studies.
Conclusion:
Comparing schedules is challenging and there was insufficient evidence to that one schedule was superior to another. Countries must select a schedule that maintains high vaccine coverage and reduced the risk of delaying the delivery vaccines to protect infants.
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