Global Landscape Review of Serotype-Specific Invasive Pneumococcal Disease Surveillance among Countries Using PCV10/13: The Pneumococcal Serotype Replacement and Distribution Estimation (PSERENADE) Project.
Maria Deloria KnollJulia Catherine BennettMaria Garcia QuesadaEunice W KaguciaMeagan E PetersonDaniel R FeikinAdam L CohenMarissa K HetrichYangyupei YangJenna N SinkevitchKrow AmpofoLaurie AukesSabrina BacciGodfrey BigogoMaria Cristina de Cunto BrandileoneMichael G BruceRomina CamilliJesús CastillaGuanhao ChanGrettel Chanto ChacónPilar Ciruela NavasHeather CookMary CorcoranRon DaganKostas DanisSara de MiguelPhilippe De WalsStefanie DesmetYvonne GallowayTheano GeorgakopoulouLaura L HammittMarkus HiltyPak Leung HoSanjay JayasingheJames D KellnerJackie KleynhansMirjam J KnolJana KozakovaKarl Gústaf KristinssonShamez N LadhaniClaudia S LaraMaria Eugenia LeónTiia LeppGrant A MackenzieLucia Mad'arováAllison McGeerTuya MungunJason M MwendaJ Pekka NuortiNehemie NzoyikoreraKazunori OishiLucia Helena De OliveiraMetka ParagiTamara PilishviliRodrigo PuentesEric RafaiSamir K SahaLarisa SavrasovaCamelia SavulescuJ Anthony ScottKevin J ScottFatima SerhanLena Petrova SetchanovaNadja Sinkovec ZorkoAnna SkoczynskaTodd D SwarthoutPalle Valentiner-BranthMark van der LindenDidrik F VestrheimAnne von GottbergInci B YildirimKyla Hayfordnull nullPublished in: Microorganisms (2021)
Serotype-specific surveillance for invasive pneumococcal disease (IPD) is essential for assessing the impact of 10- and 13-valent pneumococcal conjugate vaccines (PCV10/13). The Pneumococcal Serotype Replacement and Distribution Estimation (PSERENADE) project aimed to evaluate the global evidence to estimate the impact of PCV10/13 by age, product, schedule, and syndrome. Here we systematically characterize and summarize the global landscape of routine serotype-specific IPD surveillance in PCV10/13-using countries and describe the subset that are included in PSERENADE. Of 138 countries using PCV10/13 as of 2018, we identified 109 with IPD surveillance systems, 76 of which met PSERENADE data collection eligibility criteria. PSERENADE received data from most (n = 63, 82.9%), yielding 240,639 post-PCV10/13 introduction IPD cases. Pediatric and adult surveillance was represented from all geographic regions but was limited from lower income and high-burden countries. In PSERENADE, 18 sites evaluated PCV10, 42 PCV13, and 17 both; 17 sites used a 3 + 0 schedule, 38 used 2 + 1, 13 used 3 + 1, and 9 used mixed schedules. With such a sizeable and generally representative dataset, PSERENADE will be able to conduct robust analyses to estimate PCV impact and inform policy at national and global levels regarding adult immunization, schedule, and product choice, including for higher valency PCVs on the horizon.