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Vaccines for preventing pneumococcal infection in adultsMoberley S, Holden J, Tatham DP, Andrews RM SummaryVaccination for preventing pneumococcal infection in adultsStreptococcus pneumoniae is responsible for illness and death in adults worldwide, usually from pneumonia and less often from invasive pneumococcal disease (IPD). Vaccination (using pneumococcal polysaccharide vaccine (PPV)) in different populations might reduce this illness and death. This review found 15 randomised controlled trials (RCTs) and seven non-RCTs (contributing outcomes for culture-confirmed IPD only). Both RCTs and non-RCTs provided strong and consistent evidence of the effectiveness of PPV against IPD. In these studies, vaccination might not afford as much protection in adults with chronic illness as it does for healthy adults.
This is a Cochrane review abstract and plain language summary, prepared and maintained by The Cochrane Collaboration, currently published in The Cochrane Database of Systematic Reviews 2010 Issue 1, Copyright © 2010 The Cochrane Collaboration. Published by John Wiley and Sons, Ltd.. The full text of the review is available in The Cochrane Library (ISSN 1464-780X).
This version first published online:
October 20. 2003 AbstractBackgroundDiseases caused by Streptococcus pneumoniae (S. pneumoniae) continue to cause substantial morbidity and mortality globally. Whilst pneumococcal polysaccharide vaccines (PPV) have the potential to prevent disease and death, the degree of protection afforded against various clinical endpoints and within different populations is uncertain. ObjectivesTo assess the effectiveness of PPV in preventing disease or death in adults. Adverse events were not assessed. Search strategyWe searched the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library 2007, issue 2); MEDLINE (January 1966 to June 2007); and EMBASE (1974 to June 2007). Selection criteriaA) Randomised controlled trials (RCTs) comparing PPV with placebo, control vaccines, or no intervention. Data collection and analysisA) RCTs: trial quality assessment was conducted by two review authors and data extracted by three authors; odds ratios (OR) and 95% confidence intervals (CI) were estimated using a random-effects model. Main resultsTwenty-two studies met our inclusion criteria (15 RCTs involving 48,656 participants and 7 non-RCTs involving 62,294 participants). Meta-analysis of the RCTs found strong evidence of PPV efficacy against IPD with no statistical heterogeneity (OR 0.26, 95% CI 0.15 to 0.46; random-effects model, I-squared (I2) = 0%). Efficacy against all cause pneumonia was inconclusive with substantial statistical heterogeneity (OR 0.71, 95% CI 0.52 to 0.97; random-effects model, I2 = 87.3%). PPV was not associated with substantial reductions in all-cause mortality (OR 0.87, 95% CI 0.69 to 1.10; random-effects model, I2 = 75.3%). Vaccine efficacy against primary outcomes appeared poorer in adults with chronic illness but the difference was not statistically significant. Non-RCTs provided evidence for protection against IPD in populations for whom the vaccine is currently utilised (OR 0.48, 95% CI 0.37 to 0.61; random-effects model, I2 = 31.4%). Authors' conclusionsThis meta-analysis provides evidence supporting the recommendation for PPV to prevent IPD in adults. The evidence from RCTs is less clear with respect to adults with chronic illness. This might be because of lack of effect or lack of power in the studies. The meta-analysis does not provide compelling evidence to support the routine use of PPV to prevent all-cause pneumonia or mortality. |