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1436. Risk Factors for Invasive Pneumococcal Disease in Adults ≥65 Years Old Following Pneumococcal Conjugate Vaccine Recommendation
BACKGROUND: In 2014, pneumococcal conjugate (PCV13) and polysaccharide (PPSV23) vaccines were recommended in series for all US adults ≥65 years. We conducted a case–control study to evaluate risk factors for invasive pneumococcal disease (IPD) among adults ≥65 years old. METHODS: IPD cases (isolatio...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253797/ http://dx.doi.org/10.1093/ofid/ofy210.1267 |
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author | Almendares, Olivia M Xing, Wei Farley, Monica M Schaffner, William Thomas, Ann Reingold, Arthur Harrison, Lee H Holtzman, Corinne Rowlands, Jemma V Petit, Susan Barnes, Meghan Torres, Salina Beall, Bernard Whitney, Cynthia Pilishvili, Tamara |
author_facet | Almendares, Olivia M Xing, Wei Farley, Monica M Schaffner, William Thomas, Ann Reingold, Arthur Harrison, Lee H Holtzman, Corinne Rowlands, Jemma V Petit, Susan Barnes, Meghan Torres, Salina Beall, Bernard Whitney, Cynthia Pilishvili, Tamara |
author_sort | Almendares, Olivia M |
collection | PubMed |
description | BACKGROUND: In 2014, pneumococcal conjugate (PCV13) and polysaccharide (PPSV23) vaccines were recommended in series for all US adults ≥65 years. We conducted a case–control study to evaluate risk factors for invasive pneumococcal disease (IPD) among adults ≥65 years old. METHODS: IPD cases (isolation of pneumococcus from sterile sites) were identified through Active Bacterial Core surveillance during 2015–2018. Isolates were serotyped using whole genome sequencing. Four controls, identified through a commercial database, were matched per case by age and zip code. We obtained vaccination and medical histories from providers, vaccine registries and participant interviews. A functional status score was calculated based on participant interview. We calculated IPD odds ratios using multivariable conditional logistic regression. RESULTS: We enrolled 328 IPD cases and 1,280 matched controls. Fifty percent of case-patients and 55% of controls received a dose of PCV13. Case-patients were more likely than controls to have a chronic condition (heart, liver, or lung disease, diabetes, cochlear implant, alcohol abuse, smoking; 82% vs. 59%), immunosuppression (60% vs. 32%), poor functional status (score of ≥ 3; 71% vs. 50%), annual household income <$30,000 (38% vs. 25%) and education level of high school or less (36% vs. 25%). In a multivariable model, case-patients were more likely than controls to have a chronic condition (OR 2.48, 95% CI 1.72, 3.58), immunosuppression (OR 2.56, 95% CI 1.92,3.42), poor functional status (OR 3.66, 95% CI 2.42, 5.54), and primary or secondary smoking exposure (OR 3.09, 95% CI 1.32, 7.2). In analysis limited to PCV13-type cases and matched controls, adjusting for PCV13 receipt, measures of association were no longer significant for chronic conditions (OR 1.45, 95% 0.71, 2.95), immunosuppression (OR 1.51, 95% CI 0.83, 2.74), or poor functional status (OR 1.98, 95% CI 0.91, 4.3). CONCLUSION: Chronic and immunosuppressive conditions remain IPD risk factors for adults in the era of PCV13 use; poor functional status was also identified as a risk factor. Targeted evaluation of adults with poor functional status could inform IPD prevention strategies. PCV13 may reduce the risk of PCV13-type IPD associated with chronic conditions and poor functional status. DISCLOSURES: W. Schaffner, Merck: Member, Data Safety Monitoring Board, Consulting fee; Pfizer: Member, Data Safety Monitoring Board, Consulting fee Dynavax: Consultant, Consulting fee; Seqirus: Consultant, Consulting fee; SutroVax: Consultant, Consulting fee; Shionogi: Consultant, Consulting fee. |
format | Online Article Text |
id | pubmed-6253797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62537972018-11-28 1436. Risk Factors for Invasive Pneumococcal Disease in Adults ≥65 Years Old Following Pneumococcal Conjugate Vaccine Recommendation Almendares, Olivia M Xing, Wei Farley, Monica M Schaffner, William Thomas, Ann Reingold, Arthur Harrison, Lee H Holtzman, Corinne Rowlands, Jemma V Petit, Susan Barnes, Meghan Torres, Salina Beall, Bernard Whitney, Cynthia Pilishvili, Tamara Open Forum Infect Dis Abstracts BACKGROUND: In 2014, pneumococcal conjugate (PCV13) and polysaccharide (PPSV23) vaccines were recommended in series for all US adults ≥65 years. We conducted a case–control study to evaluate risk factors for invasive pneumococcal disease (IPD) among adults ≥65 years old. METHODS: IPD cases (isolation of pneumococcus from sterile sites) were identified through Active Bacterial Core surveillance during 2015–2018. Isolates were serotyped using whole genome sequencing. Four controls, identified through a commercial database, were matched per case by age and zip code. We obtained vaccination and medical histories from providers, vaccine registries and participant interviews. A functional status score was calculated based on participant interview. We calculated IPD odds ratios using multivariable conditional logistic regression. RESULTS: We enrolled 328 IPD cases and 1,280 matched controls. Fifty percent of case-patients and 55% of controls received a dose of PCV13. Case-patients were more likely than controls to have a chronic condition (heart, liver, or lung disease, diabetes, cochlear implant, alcohol abuse, smoking; 82% vs. 59%), immunosuppression (60% vs. 32%), poor functional status (score of ≥ 3; 71% vs. 50%), annual household income <$30,000 (38% vs. 25%) and education level of high school or less (36% vs. 25%). In a multivariable model, case-patients were more likely than controls to have a chronic condition (OR 2.48, 95% CI 1.72, 3.58), immunosuppression (OR 2.56, 95% CI 1.92,3.42), poor functional status (OR 3.66, 95% CI 2.42, 5.54), and primary or secondary smoking exposure (OR 3.09, 95% CI 1.32, 7.2). In analysis limited to PCV13-type cases and matched controls, adjusting for PCV13 receipt, measures of association were no longer significant for chronic conditions (OR 1.45, 95% 0.71, 2.95), immunosuppression (OR 1.51, 95% CI 0.83, 2.74), or poor functional status (OR 1.98, 95% CI 0.91, 4.3). CONCLUSION: Chronic and immunosuppressive conditions remain IPD risk factors for adults in the era of PCV13 use; poor functional status was also identified as a risk factor. Targeted evaluation of adults with poor functional status could inform IPD prevention strategies. PCV13 may reduce the risk of PCV13-type IPD associated with chronic conditions and poor functional status. DISCLOSURES: W. Schaffner, Merck: Member, Data Safety Monitoring Board, Consulting fee; Pfizer: Member, Data Safety Monitoring Board, Consulting fee Dynavax: Consultant, Consulting fee; Seqirus: Consultant, Consulting fee; SutroVax: Consultant, Consulting fee; Shionogi: Consultant, Consulting fee. Oxford University Press 2018-11-26 /pmc/articles/PMC6253797/ http://dx.doi.org/10.1093/ofid/ofy210.1267 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Almendares, Olivia M Xing, Wei Farley, Monica M Schaffner, William Thomas, Ann Reingold, Arthur Harrison, Lee H Holtzman, Corinne Rowlands, Jemma V Petit, Susan Barnes, Meghan Torres, Salina Beall, Bernard Whitney, Cynthia Pilishvili, Tamara 1436. Risk Factors for Invasive Pneumococcal Disease in Adults ≥65 Years Old Following Pneumococcal Conjugate Vaccine Recommendation |
title | 1436. Risk Factors for Invasive Pneumococcal Disease in Adults ≥65 Years Old Following Pneumococcal Conjugate Vaccine Recommendation |
title_full | 1436. Risk Factors for Invasive Pneumococcal Disease in Adults ≥65 Years Old Following Pneumococcal Conjugate Vaccine Recommendation |
title_fullStr | 1436. Risk Factors for Invasive Pneumococcal Disease in Adults ≥65 Years Old Following Pneumococcal Conjugate Vaccine Recommendation |
title_full_unstemmed | 1436. Risk Factors for Invasive Pneumococcal Disease in Adults ≥65 Years Old Following Pneumococcal Conjugate Vaccine Recommendation |
title_short | 1436. Risk Factors for Invasive Pneumococcal Disease in Adults ≥65 Years Old Following Pneumococcal Conjugate Vaccine Recommendation |
title_sort | 1436. risk factors for invasive pneumococcal disease in adults ≥65 years old following pneumococcal conjugate vaccine recommendation |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253797/ http://dx.doi.org/10.1093/ofid/ofy210.1267 |
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