<HashMap><database>biostudies-literature</database><scores/><additional><submitter>von Mollendorf C</submitter><funding>World Health Organization</funding><funding>Gavi</funding><funding>Wellcome Trust</funding><pagination>1137-1145</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7616686</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(8)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>Pneumococcal conjugate vaccines (PCVs) are effective in reducing pneumococcal disease. We measured 13-valent PCV (PCV13) effect on different pneumococcal outcomes using diverse studies in Lao People's Democratic Republic.&lt;h4>Methods&lt;/h4>Studies included: pre-PCV13 population-based record review of hospitalized childhood pneumonia cases; acute respiratory infection (ARI) study post-PCV13 to demonstrate effectiveness (VE) against hypoxic pneumonia; invasive pneumococcal disease (IPD) surveillance in all ages (2004-2018); carriage studies in children hospitalized with ARI (2013-2019); community carriage surveys pre- and post-PCV13.&lt;h4>Results&lt;/h4>Annual pneumonia incidence rate in children pre-PCV13 was 1,530 (95% confidence interval [CI] 1,477-1,584) per 100,000. Adjusted VE against hypoxic pneumonia was 37% (95% CI 6-57%). For IPD, 85% (11/13) of cases were due to vaccine-types pre-PCV13, and 43% (3/7) post-PCV13 in children aged &lt;5 years; for ≥5 years, 61% (27/44) and 42% (17/40), respectively. For ARI cases, adjusted VE for vaccine-type carriage was 39% (95% CI 4-60) in &lt;5 year olds; slightly higher than community surveys (23% [95% CI 4-39%] in 12-23 month olds).&lt;h4>Conclusions&lt;/h4>Despite limited baseline data, we found evidence of PCV13 impact on disease and carriage. Our approach could be used in similar settings to augment existing WHO PCV evaluation guidelines.</pubmed_abstract><journal>Expert review of vaccines</journal><pubmed_title>Evaluation strategies for measuring pneumococcal conjugate vaccine impact in low-resource settings.</pubmed_title><pmcid>PMC7616686</pmcid><funding_grant_id>001</funding_grant_id><funding_grant_id>219762</funding_grant_id><funding_grant_id>106698/Z/14/Z</funding_grant_id><pubmed_authors>Sychareun V</pubmed_authors><pubmed_authors>Ortika BD</pubmed_authors><pubmed_authors>von Mollendorf C</pubmed_authors><pubmed_authors>Lai JYR</pubmed_authors><pubmed_authors>Lim R</pubmed_authors><pubmed_authors>Mayxay M</pubmed_authors><pubmed_authors>Dance DAB</pubmed_authors><pubmed_authors>Choummanivong M</pubmed_authors><pubmed_authors>Chan J</pubmed_authors><pubmed_authors>Satzke C</pubmed_authors><pubmed_authors>Dunne EM</pubmed_authors><pubmed_authors>Datta SS</pubmed_authors><pubmed_authors>Weaver R</pubmed_authors><pubmed_authors>Phommachanh S</pubmed_authors><pubmed_authors>Nguyen CD</pubmed_authors><pubmed_authors>Fox K</pubmed_authors><pubmed_authors>Phetsouvanh R</pubmed_authors><pubmed_authors>Mulholland KE</pubmed_authors><pubmed_authors>Gray A</pubmed_authors><pubmed_authors>Russell FM</pubmed_authors><pubmed_authors>Moore KA</pubmed_authors><pubmed_authors>Vilivong K</pubmed_authors><pubmed_authors>Newton PN</pubmed_authors></additional><is_claimable>false</is_claimable><name>Evaluation strategies for measuring pneumococcal conjugate vaccine impact in low-resource settings.</name><description>&lt;h4>Objectives&lt;/h4>Pneumococcal conjugate vaccines (PCVs) are effective in reducing pneumococcal disease. We measured 13-valent PCV (PCV13) effect on different pneumococcal outcomes using diverse studies in Lao People's Democratic Republic.&lt;h4>Methods&lt;/h4>Studies included: pre-PCV13 population-based record review of hospitalized childhood pneumonia cases; acute respiratory infection (ARI) study post-PCV13 to demonstrate effectiveness (VE) against hypoxic pneumonia; invasive pneumococcal disease (IPD) surveillance in all ages (2004-2018); carriage studies in children hospitalized with ARI (2013-2019); community carriage surveys pre- and post-PCV13.&lt;h4>Results&lt;/h4>Annual pneumonia incidence rate in children pre-PCV13 was 1,530 (95% confidence interval [CI] 1,477-1,584) per 100,000. Adjusted VE against hypoxic pneumonia was 37% (95% CI 6-57%). For IPD, 85% (11/13) of cases were due to vaccine-types pre-PCV13, and 43% (3/7) post-PCV13 in children aged &lt;5 years; for ≥5 years, 61% (27/44) and 42% (17/40), respectively. For ARI cases, adjusted VE for vaccine-type carriage was 39% (95% CI 4-60) in &lt;5 year olds; slightly higher than community surveys (23% [95% CI 4-39%] in 12-23 month olds).&lt;h4>Conclusions&lt;/h4>Despite limited baseline data, we found evidence of PCV13 impact on disease and carriage. Our approach could be used in similar settings to augment existing WHO PCV evaluation guidelines.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-03T23:23:52.72Z</modification><creation>2025-04-03T23:23:52.72Z</creation></dates><accession>S-EPMC7616686</accession><cross_references><pubmed>34378467</pubmed><doi>10.1080/14760584.2021.1965474</doi></cross_references></HashMap>