PneuMum: Impact from a randomised controlled trial of maternal 23-valent pneumococcal polysaccharide vaccination on middle ear disease amongst Indigenous infants, Northern Territory, Australia. Issue 48 (27th November 2015)

• Record Type: Journal Article
• Authors: Binks, Michael J.; Moberley, Sarah A.; Balloch, Anne; Leach, Amanda J.; Nelson, Sandra; Hare, Kim M.; Wilson, Cate; Morris, Peter S.; Nelson, Jane; Chatfield, Mark D.; Tang, Mimi L.K.; Torzillo, Paul; Carapetis, Jonathan R.; Mulholland, E. Kim; Andrews, Ross M.
• Is Part Of: Vaccine. Volume 33:Issue 48(2015)
• Page Start: 6579
• Page End: 6587
• Publication Date: 2015-11-27
• Subjects: 23-valent pneumococcal polysaccharide vaccine -- Pneumococcus -- Pregnancy -- Otitis media -- Australia -- Indigenous; Vaccines -- Periodicals; 615.372
• DOI: 10.1016/j.vaccine.2015.10.101
• Languages: English
• ISSNs: 0264-410X

Abstract

Highlights: We achieved our intended sample size of 210 participants. Rates of ear disease (71%) and 23vPPV-type carriage (26%) were lower than expected. We were unable to show maternal 23vPPV efficacy against infant ear disease or 23vPPV-type carriage. 23vPPV in pregnancy halved infant ear disease concurrent with 23vPPV-type carriage. 23vPPV in pregnancy may complement childhood pneumococcal vaccination programs. Abstract: Background: We assessed maternal 23-valent pneumococcal polysaccharide (23vPPV) vaccine efficacy (VE) against middle ear disease and pneumococcal carriage amongst Australian Indigenous infants. Methods: In an open label, allocation concealed, outcome-assessor blinded, community stratified, randomised controlled trial, healthy pregnant Indigenous women aged 17–39 years in the Northern Territory of Australia received the 23vPPV (1:1:1) at: 30–36 weeks gestation, birth, or were unvaccinated (ClinicalTrials.gov NCT00714064). Co-primary outcomes were the point prevalences of infant middle ear disease and 23vPPV-type carriage at age 7 months. Results: The consent rate was 50% (313/632). Among 227 eligible participants randomised, retention rates were 86% (66/77) controls; 89% (67/75) pregnancy vaccinees; 88% (66/75) birth vaccinees. At infant age 7 months, ear disease prevalence was: 71% (47/66) controls, 63% (42/67) pregnancy vaccinees, 76% (50/66) birth vaccinees; and 23vPPV-type carriage was: 26% (17/66) controls, 18% (12/67) pregnancy vaccinees, 18% (12/66) birth vaccinees. For pregnancy vaccinees, VE was 12% (95% CI −12% to 31%) against infant ear disease and 30% (95% CI −34% to 64%) against 23vPPV-type carriage. In a post-hoc analysis, VE against infant ear disease concurrent with carriage of 23vPPV or related types was 51% (95% CI −2% to 76%). There were no serious adverse effects following receipt of the 23vPPV in pregnancy or at birth. Conclusions: In a high risk population, our study was unable to demonstrate efficacy of 23vPPV in pregnancy against the co-primary outcomes of either all-cause infant ear disease or 23vPPV-type nasopharyngeal carriage at age 7 months. Efficacy against ear disease concurrent with carriage of vaccine-related serotypes (a more specific outcome) suggests 23vPPV in pregnancy may complement childhood pneumococcal vaccination programs.