Abstract

ABSTRACT We previously reported 10-valent pneumococcal non-typeable Haemophilus influenzae (NTHi) protein D conjugate vaccine (PHiD-CV) efficacy in a double-blind randomized trial (ClinicalTrials.gov: NCT00466947) against various diseases, including acute otitis media (AOM). Here, we provide further analyses. In the Panamanian subset, 7,359 children were randomized (1:1) to receive PHiD-CV or control vaccine at age 2/4/6 and 15–18 months. Of these, 2,000 had nasopharyngeal swabs collected. AOM cases were captured when parents sought medical attention for children with AOM symptoms; surveillance was enhanced approximately 2 y into the study through regular telephone calls or home visits by study personnel, who advised parents to visit the clinic if their child had AOM symptoms. Mean follow-up was 31.4 months. Clinical AOM (C-AOM) cases were assessed by physicians and confirmed by otorhinolaryngologists. Middle ear fluid samples, taken from children with C-AOM after specific informed consent, and nasopharyngeal samples were cultured for pathogen identification. For 7,359 children, 2,574 suspected AOM cases were assessed by a primary healthcare physician; 649 cases were C-AOM cases as per protocol definition. From the 503 MEF samples collected, 158 resulted in a positive culture. In the intent-to-treat cohort (7,214 children), PHiD-CV showed VE against first C-AOM (24.0% [95% CI: 8.7, 36.7]) and bacterial (B-AOM) episodes (48.0% [20.3, 66.1]) in children <24 months, which declined thereafter with age. Pre-booster VE against C-AOM was 30.7% [12.9, 44.9]; post-booster, −6.7% [−36.4, 16.6]. PHiD-CV VE was 17.7% [−6.1, 36.2] against moderate and 32.7% [−20.5, 62.4] against severe C-AOM. VE against vaccine-serotype pneumococcal NPC was 31.2% [5.3, 50.3] 3 months post-booster, and 25.6% [12.7, 36.7] across all visits. NTHi colonization rates were low and no significant reduction was observed. PHiD-CV showed efficacy against C-AOM and B-AOM in children younger than 24 months, and reduced vaccine-serotype NPC.

Highlights

  • Acute otitis media (AOM) is one of the most common bacterial diseases in young children, with a peak of incidence at the age of 6–18 months.[1]

  • In Panama, we have reported a clinically-confirmed AOM (C-AOM) incidence rate of 0.036 episodes per child-year in the control group of the Clinical Otitis Media and Pneumonia Study (COMPAS).[6]

  • Samples have shown that Streptococcus pneumoniae and nontypeable Haemophilus influenzae (NTHi) are the main bacterial pathogens responsible for pediatric AOM in Argentina, Colombia, Mexico, Venezuela, Costa Rica and Chile, in line with observations from other regions worldwide.[7,8,9,10,11,12]

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Summary

Introduction

Acute otitis media (AOM) is one of the most common bacterial diseases in young children, with a peak of incidence at the age of 6–18 months.[1] In many countries, AOM remains the main reason for antimicrobial prescriptions in children, contributing to the development of antibiotic resistance, and resulting in a major burden on healthcare systems.[2,3,4] In Latin America, limited data on AOM incidence have shown a range of 0.01–0.36 episodes per person-year in children younger than 5 y.5. Samples have shown that Streptococcus pneumoniae and nontypeable Haemophilus influenzae (NTHi) are the main bacterial pathogens responsible for pediatric AOM in Argentina, Colombia, Mexico, Venezuela, Costa Rica and Chile, in line with observations from other regions worldwide.[7,8,9,10,11,12]. Efficacy/effectiveness against AOM was evaluated in double-blind randomized studies for only one of the 3 licensed pneumococcal conjugate vaccines (PCVs), the 7-valent CRM197-conjugate vaccine (7vCRM; Prevenar/PrevnarTM, Pfizer Inc., NY)..[13,14] For the 10-valent pneumococcal NTHi protein D conjugate vaccine (PHiD-CV; SynflorixTM, GSK Vaccines, Rixensart, Belgium), a recently published randomized controlled trial (RCT) in Finland reported a trend towards

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