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Age-stratified burden of pneumococcal community acquired pneumonia in hospitalised Canadian adults from 2010 to 2015

BACKGROUND: In Canada, 13-valent pneumococcal conjugate vaccine (PCV13) is recommended in childhood, in individuals at high risk of invasive pneumococcal disease (IPD) and in healthy adults aged ≥65 years for protection against vaccine-type IPD and pneumococcal community-acquired pneumonia (pCAP). S...

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Autores principales: LeBlanc, Jason, ElSherif, May, Ye, Lingyun, MacKinnon-Cameron, Donna, Ambrose, Ardith, Hatchette, Todd F, Lang, Amanda LS, Gillis, Hayley D, Martin, Irene, Demczuk, Walter H, LaFerriere, Craig, Andrew, Melissa K, Boivin, Guy, Bowie, William, Green, Karen, Johnstone, Jennie, Loeb, Mark, McCarthy, Anne, McGeer, Allison, Semret, Makeda, Trottier, Sylvie, Valiquette, Louis, Webster, Duncan, McNeil, Shelly A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078693/
https://www.ncbi.nlm.nih.gov/pubmed/32188585
http://dx.doi.org/10.1136/bmjresp-2019-000550
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author LeBlanc, Jason
ElSherif, May
Ye, Lingyun
MacKinnon-Cameron, Donna
Ambrose, Ardith
Hatchette, Todd F
Lang, Amanda LS
Gillis, Hayley D
Martin, Irene
Demczuk, Walter H
LaFerriere, Craig
Andrew, Melissa K
Boivin, Guy
Bowie, William
Green, Karen
Johnstone, Jennie
Loeb, Mark
McCarthy, Anne
McGeer, Allison
Semret, Makeda
Trottier, Sylvie
Valiquette, Louis
Webster, Duncan
McNeil, Shelly A
author_facet LeBlanc, Jason
ElSherif, May
Ye, Lingyun
MacKinnon-Cameron, Donna
Ambrose, Ardith
Hatchette, Todd F
Lang, Amanda LS
Gillis, Hayley D
Martin, Irene
Demczuk, Walter H
LaFerriere, Craig
Andrew, Melissa K
Boivin, Guy
Bowie, William
Green, Karen
Johnstone, Jennie
Loeb, Mark
McCarthy, Anne
McGeer, Allison
Semret, Makeda
Trottier, Sylvie
Valiquette, Louis
Webster, Duncan
McNeil, Shelly A
author_sort LeBlanc, Jason
collection PubMed
description BACKGROUND: In Canada, 13-valent pneumococcal conjugate vaccine (PCV13) is recommended in childhood, in individuals at high risk of invasive pneumococcal disease (IPD) and in healthy adults aged ≥65 years for protection against vaccine-type IPD and pneumococcal community-acquired pneumonia (pCAP). Since vaccine recommendations in Canada include both age-based and risk-based guidance, this study aimed to describe the burden of vaccine-preventable pCAP in hospitalised adults by age. METHODS: Surveillance for community-acquired pneumonia (CAP) in hospitalised adults was performed prospectively from 2010 to 2015. CAP was radiologically confirmed, and pCAP was identified using blood and sputum culture and urine antigen testing. Patient demographics and outcomes were stratified by age (16–49, 50–64, ≥65 and ≥50 years). RESULTS: Of 6666/8802 CAP cases tested, 830 (12.5%) had pCAP, and 418 (6.3%) were attributed to a PCV13 serotype. Of PCV13 pCAP, 41% and 74% were in adults aged ≥65 and ≥50 years, respectively. Compared with non-pCAP controls, pCAP cases aged ≥50 years were more likely to be admitted to intensive care units (ICUs) and to require mechanical ventilation. Older adults with pCAP were less likely to be admitted to ICU or required mechanical ventilation, given their higher mortality and goals of care. Of pCAP deaths, 67% and 90% were in the ≥65 and ≥50 age cohorts, respectively. CONCLUSIONS: Adults hospitalised with pCAP in the age cohort of 50–64 years contribute significantly to the burden of illness, suggesting that an age-based recommendation for adults aged ≥50 years should be considered in order to optimise the impact of pneumococcal vaccination programmes in Canada.
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spelling pubmed-70786932020-03-23 Age-stratified burden of pneumococcal community acquired pneumonia in hospitalised Canadian adults from 2010 to 2015 LeBlanc, Jason ElSherif, May Ye, Lingyun MacKinnon-Cameron, Donna Ambrose, Ardith Hatchette, Todd F Lang, Amanda LS Gillis, Hayley D Martin, Irene Demczuk, Walter H LaFerriere, Craig Andrew, Melissa K Boivin, Guy Bowie, William Green, Karen Johnstone, Jennie Loeb, Mark McCarthy, Anne McGeer, Allison Semret, Makeda Trottier, Sylvie Valiquette, Louis Webster, Duncan McNeil, Shelly A BMJ Open Respir Res Respiratory Epidemiology BACKGROUND: In Canada, 13-valent pneumococcal conjugate vaccine (PCV13) is recommended in childhood, in individuals at high risk of invasive pneumococcal disease (IPD) and in healthy adults aged ≥65 years for protection against vaccine-type IPD and pneumococcal community-acquired pneumonia (pCAP). Since vaccine recommendations in Canada include both age-based and risk-based guidance, this study aimed to describe the burden of vaccine-preventable pCAP in hospitalised adults by age. METHODS: Surveillance for community-acquired pneumonia (CAP) in hospitalised adults was performed prospectively from 2010 to 2015. CAP was radiologically confirmed, and pCAP was identified using blood and sputum culture and urine antigen testing. Patient demographics and outcomes were stratified by age (16–49, 50–64, ≥65 and ≥50 years). RESULTS: Of 6666/8802 CAP cases tested, 830 (12.5%) had pCAP, and 418 (6.3%) were attributed to a PCV13 serotype. Of PCV13 pCAP, 41% and 74% were in adults aged ≥65 and ≥50 years, respectively. Compared with non-pCAP controls, pCAP cases aged ≥50 years were more likely to be admitted to intensive care units (ICUs) and to require mechanical ventilation. Older adults with pCAP were less likely to be admitted to ICU or required mechanical ventilation, given their higher mortality and goals of care. Of pCAP deaths, 67% and 90% were in the ≥65 and ≥50 age cohorts, respectively. CONCLUSIONS: Adults hospitalised with pCAP in the age cohort of 50–64 years contribute significantly to the burden of illness, suggesting that an age-based recommendation for adults aged ≥50 years should be considered in order to optimise the impact of pneumococcal vaccination programmes in Canada. BMJ Publishing Group 2020-03-17 /pmc/articles/PMC7078693/ /pubmed/32188585 http://dx.doi.org/10.1136/bmjresp-2019-000550 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Respiratory Epidemiology
LeBlanc, Jason
ElSherif, May
Ye, Lingyun
MacKinnon-Cameron, Donna
Ambrose, Ardith
Hatchette, Todd F
Lang, Amanda LS
Gillis, Hayley D
Martin, Irene
Demczuk, Walter H
LaFerriere, Craig
Andrew, Melissa K
Boivin, Guy
Bowie, William
Green, Karen
Johnstone, Jennie
Loeb, Mark
McCarthy, Anne
McGeer, Allison
Semret, Makeda
Trottier, Sylvie
Valiquette, Louis
Webster, Duncan
McNeil, Shelly A
Age-stratified burden of pneumococcal community acquired pneumonia in hospitalised Canadian adults from 2010 to 2015
title Age-stratified burden of pneumococcal community acquired pneumonia in hospitalised Canadian adults from 2010 to 2015
title_full Age-stratified burden of pneumococcal community acquired pneumonia in hospitalised Canadian adults from 2010 to 2015
title_fullStr Age-stratified burden of pneumococcal community acquired pneumonia in hospitalised Canadian adults from 2010 to 2015
title_full_unstemmed Age-stratified burden of pneumococcal community acquired pneumonia in hospitalised Canadian adults from 2010 to 2015
title_short Age-stratified burden of pneumococcal community acquired pneumonia in hospitalised Canadian adults from 2010 to 2015
title_sort age-stratified burden of pneumococcal community acquired pneumonia in hospitalised canadian adults from 2010 to 2015
topic Respiratory Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078693/
https://www.ncbi.nlm.nih.gov/pubmed/32188585
http://dx.doi.org/10.1136/bmjresp-2019-000550
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