Invasive pneumococcal disease surveillance in Canada, 2020.

Canada IPD PCV13 Streptococcus pneumoniae antimicrobial resistance invasive pneumococcal disease pneumococcus serotype surveillance

Journal

Canada communicable disease report = Releve des maladies transmissibles au Canada
ISSN: 1188-4169
Titre abrégé: Can Commun Dis Rep
Pays: Canada
ID NLM: 9303729

Informations de publication

Date de publication:
01 Sep 2022
Historique:
medline: 1 9 2022
pubmed: 1 9 2022
entrez: 21 12 2023
Statut: epublish

Résumé

Invasive pneumococcal disease (IPD), which is caused by The Public Health Agency of Canada's National Microbiology Laboratory (Winnipeg, Manitoba) collaborates with provincial and territorial public health laboratories to conduct national surveillance of IPD. A total of 2,108 IPD isolates were reported in 2020. Serotyping was performed by Quellung reaction and antimicrobial susceptibilities were determined in collaboration with the University of Manitoba/Canadian Antimicrobial Resistance Alliance. Population-based IPD incidence rates were obtained through the Canadian Notifiable Disease Surveillance System. Overall incidence of IPD in Canada decreased significantly from 11.5 (95% confidence interval [CI]: 10.1-13.1) to 6.0 (95% CI: 5.0-7.2), and from 10.0 (95% CI: 9.7-10.3) to 5.9 (95% CI: 5.7-6.2) cases per 100,000 from 2019 to 2020; in those younger than five years and those five years and older, respectively. The most common serotypes overall were 4 (11.2%, n=237), 3 (10.9%, n=229) and 8 (7.2%, n=151). From 2016 to 2020, serotypes with increasing trends ( Though the incidence of IPD decreased in 2020 in comparison to previous years across all age groups, disease due to PCV13 serotypes 3 and 4, as well as non-PCV13 serotypes such as 8 and 12F, increased in prevalence. Continued surveillance of IPD is imperative to monitor shifts in serotype distribution and antimicrobial resistance.

Sections du résumé

Background UNASSIGNED
Invasive pneumococcal disease (IPD), which is caused by
Methods UNASSIGNED
The Public Health Agency of Canada's National Microbiology Laboratory (Winnipeg, Manitoba) collaborates with provincial and territorial public health laboratories to conduct national surveillance of IPD. A total of 2,108 IPD isolates were reported in 2020. Serotyping was performed by Quellung reaction and antimicrobial susceptibilities were determined in collaboration with the University of Manitoba/Canadian Antimicrobial Resistance Alliance. Population-based IPD incidence rates were obtained through the Canadian Notifiable Disease Surveillance System.
Results UNASSIGNED
Overall incidence of IPD in Canada decreased significantly from 11.5 (95% confidence interval [CI]: 10.1-13.1) to 6.0 (95% CI: 5.0-7.2), and from 10.0 (95% CI: 9.7-10.3) to 5.9 (95% CI: 5.7-6.2) cases per 100,000 from 2019 to 2020; in those younger than five years and those five years and older, respectively. The most common serotypes overall were 4 (11.2%, n=237), 3 (10.9%, n=229) and 8 (7.2%, n=151). From 2016 to 2020, serotypes with increasing trends (
Conclusion UNASSIGNED
Though the incidence of IPD decreased in 2020 in comparison to previous years across all age groups, disease due to PCV13 serotypes 3 and 4, as well as non-PCV13 serotypes such as 8 and 12F, increased in prevalence. Continued surveillance of IPD is imperative to monitor shifts in serotype distribution and antimicrobial resistance.

Identifiants

pubmed: 38124782
pii: 480904
pmc: PMC10732480

Types de publication

Journal Article

Langues

eng

Pagination

396-406

Déclaration de conflit d'intérêts

Competing interests None.

Auteurs

Alyssa Golden (A)

National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB.

Averil Griffith (A)

National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB.

Walter Demczuk (W)

National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB.

Brigitte Lefebvre (B)

Laboratoire de santé publique du Québec, Sainte-Anne-de- Bellevue, QC.

Allison McGeer (A)

Toronto Invasive Bacterial Diseases Network (TIBDN), Department of Microbiology, Mount Sinai Hospital, Toronto, ON.

Gregory Tyrrell (G)

Provincial Laboratory for Public Health (Microbiology), Edmonton, AB.

George Zhanel (G)

Department of Medical Microbiology and Infectious Diseases, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB.

Julianne Kus (J)

Public Health Ontario, Toronto, ON.
Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON.

Linda Hoang (L)

British Columbia Centre for Disease Control, Vancouver, BC.

Jessica Minion (J)

Roy Romanow Provincial Laboratory, Regina, SK.

Paul Van Caeseele (P)

Cadham Provincial Laboratory, Winnipeg, MB.

Hanan Smadi (H)

New Brunswick Department of Health, Fredericton, NB.

David Haldane (D)

Queen Elizabeth II Health Science Centre, Halifax, NS.

George Zahariadis (G)

Newfoundland and Labrador Public Health Laboratory, St. John's, NL.

Kristen Mead (K)

Queen Elizabeth Hospital, Charlottetown, PE.

Laura Steven (L)

Stanton Territorial Hospital Laboratory, Yellowknife, NT.

Lori Strudwick (L)

Yukon Communicable Disease Control, Whitehorse, YT.

Anita Li (A)

Centre for Immunization & Respiratory Infectious Diseases, Public Health Agency of Canada, Ottawa, ON.

Michael Mulvey (M)

National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB.
Department of Medical Microbiology and Infectious Diseases, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB.

Irene Martin (I)

National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB.

Classifications MeSH