Clinical Presentations and Outcomes of Children in Canada With Recurrent Invasive Pneumococcal Disease From the IMPACT Surveillance Network.


Journal

The Pediatric infectious disease journal
ISSN: 1532-0987
Titre abrégé: Pediatr Infect Dis J
Pays: United States
ID NLM: 8701858

Informations de publication

Date de publication:
01 04 2022
Historique:
pubmed: 31 1 2022
medline: 20 4 2022
entrez: 30 1 2022
Statut: ppublish

Résumé

Invasive pneumococcal disease due to Streptococcus pneumoniae can cause mortality and severe morbidity due to sepsis, meningitis and pneumonia, particularly in young children and the elderly. Recurrent invasive pneumococcal disease is rare yet serious sequelae of invasive pneumococcal disease that is associated with the immunocompromised and leads to a high mortality rate. This retrospective study reviewed recurrent invasive pneumococcal disease cases from the Canadian Immunization Monitoring Program, ACTive (IMPACT) between 1991 and 2019, an active network for surveillance of vaccine-preventable diseases and adverse events following immunization for children ages 0-16 years. Data were collected from 12 pediatric tertiary care hospitals across all 3 eras of public pneumococcal conjugate vaccine implementation in Canada. The survival rate within our cohort of 180 recurrent invasive pneumococcal disease cases was 98.3%. A decrease of 26.4% in recurrent invasive pneumococcal disease due to vaccine serotypes was observed with pneumococcal vaccine introduction. There was also a 69.0% increase in the rate of vaccination in children with preexisting medical conditions compared with their healthy peers. The decrease in recurrent invasive pneumococcal disease due to vaccine-covered serotypes has been offset by an increase of non-vaccine serotypes in this sample of Canadian children.

Sections du résumé

BACKGROUND
Invasive pneumococcal disease due to Streptococcus pneumoniae can cause mortality and severe morbidity due to sepsis, meningitis and pneumonia, particularly in young children and the elderly. Recurrent invasive pneumococcal disease is rare yet serious sequelae of invasive pneumococcal disease that is associated with the immunocompromised and leads to a high mortality rate.
METHOD
This retrospective study reviewed recurrent invasive pneumococcal disease cases from the Canadian Immunization Monitoring Program, ACTive (IMPACT) between 1991 and 2019, an active network for surveillance of vaccine-preventable diseases and adverse events following immunization for children ages 0-16 years. Data were collected from 12 pediatric tertiary care hospitals across all 3 eras of public pneumococcal conjugate vaccine implementation in Canada.
RESULTS
The survival rate within our cohort of 180 recurrent invasive pneumococcal disease cases was 98.3%. A decrease of 26.4% in recurrent invasive pneumococcal disease due to vaccine serotypes was observed with pneumococcal vaccine introduction. There was also a 69.0% increase in the rate of vaccination in children with preexisting medical conditions compared with their healthy peers.
CONCLUSION
The decrease in recurrent invasive pneumococcal disease due to vaccine-covered serotypes has been offset by an increase of non-vaccine serotypes in this sample of Canadian children.

Identifiants

pubmed: 35093996
doi: 10.1097/INF.0000000000003454
pii: 00006454-202204000-00028
pmc: PMC8920017
doi:

Substances chimiques

Pneumococcal Vaccines 0
Vaccines, Conjugate 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e166-e171

Informations de copyright

Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc.

Références

Gaschignard J, Levy C, Chrabieh M, et al. Invasive pneumococcal disease in children can reveal a primary immunodeficiency. Clin Infect Dis. 2014;59:244–251.
Alsina L, Basteiro MG, de Paz HD, et al. Recurrent invasive pneumococcal disease in children: underlying clinical conditions, and immunological and microbiological characteristics. PLoS One. 2015;10:e0118848.
Mason EO Jr, Wald ER, Tan TQ, et al. Recurrent systemic pneumococcal disease in children. Pediatr Infect Dis J. 2007;26:480–484.
Einarsdöttir HM, Erlendsdóttir H, Kristinsson KGG, et al. Nationwide study of recurrent invasive pneumococcal infections in a population with a low prevalence of human immunodeficiency virus infection. Clin Microbiol Infect. 2005;11:744–749.
Ingels H, Schejbel L, Lundstedt AC, et al. Immunodeficiency among children with recurrent invasive pneumococcal disease. Pediatr Infect Dis J. 2015;34:644–651.
Picard C, Bobby Gaspar H, Al-Herz W, et al. International union of immunological societies: 2017 primary immunodeficiency diseases committee report on inborn errors of immunity. J Clin Immunol. 2018;38:96–128.
Scheifele D. IMPACT after 17 years: lessons learned about successful networking. Can J Infect Dis Med Microbiol. 2009;20:12–14.
Scheifele DW, Halperin SA; CPS/Health Canada, Immunization Monitoring Program, Active (IMPACT). Immunization Monitoring Program, Active: a model of active surveillance of vaccine safety. Semin Pediatr Infect Dis. 2003;14:213–219.
Austrian R. The quellung reaction, a neglected microbiologic technique. Mt Sinai J Med. 1976;43:699–709.
National Advisory Committee on Immunization. Update on pediatric invasive pneumococcal disease and recommended use of conjugate pneumococcal vaccines. Canada Commun Dis Rep. 2010;36:1–30.
Wu S, Guo X, Xu Z, et al. Early clinical predictors for the prognosis of invasive pneumococcal disease. BMC Infect Dis. 2020;20:1–7.
King MD, Whitney CG, Parekh F, et al.; Active Bacterial Core Surveillance Team/Emerging Infections Program Network. Recurrent invasive pneumococcal disease: a population-based assessment. Clin Infect Dis. 2003;37:1029–1036.
Ingels H, Lambertsen L, Harboe ZB, et al. Recurrent invasive pneumococcal disease in children: epidemiological, microbiological, and clinical aspects from a Danish 33-year nationwide survey (1980–2013). Scand J Infect Dis. 2014;46:265–271.
Malo JA, Ware RS, Lambert SB. Estimating the risk of recurrent invasive pneumococcal disease in Australia, 1991–2016. Vaccine. 2021;39:5748–5756.
Mufson MA, Hao JB, Stanek RJ, et al. Clinical features of patients with recurrent invasive Streptococcus pneumoniae disease. Am J Med Sci. 2012;343:303–309.
Butters C, Phuong LK, Cole T, et al. Prevalence of immunodeficiency in children with invasive pneumococcal disease in the pneumococcal vaccine era: a systematic review. JAMA Pediatr. 2019;173:1084–1094.
Bettinger JA, Scheifele DW, Kellner JD, et al. The effect of routine vaccination on invasive pneumococcal infections in Canadian children, Immunization Monitoring Program, Active 2000–2007. Vaccine. 2010;28:2130–2136.
Sanz JC, Rodríguez-Avial I, Ríos E, et al. Recurrent pneumococcal invasive disease in the region of Madrid during a five-year period. Infection. 2014;42:475–483.

Auteurs

Yousif Murad (Y)

From the Faculty of Medicine, University of British Columbia, Vancouver, Canada.
Vaccine Evaluation Center, BC Children's Hospital Research Institute, Vancouver, Canada.

Te-Yu Hung (TY)

Vaccine Evaluation Center, BC Children's Hospital Research Institute, Vancouver, Canada.
Royal Darwin Hospital, Top End Health Service, Northern Territory, Australia.
Royal Melbourne Hospital, Doherty Institute for Infection Immunity, Victoria, Australia.

Manish Sadarangani (M)

Vaccine Evaluation Center, BC Children's Hospital Research Institute, Vancouver, Canada.
Department of Pediatrics, University of British Columbia, Vancouver, Canada.

Shaun K Morris (SK)

Division of Infectious Diseases, Hospital for Sick Children, Toronto, Canada.
Department of Pediatrics, Temerty Faculty of Medicine, University of Toronto, Toronto, Canada.

Nicole Le Saux (N)

Children's Hospital of Eastern Ontario, Paediatric Infectious Disease, Ottawa, ON, Canada.

Otto G Vanderkooi (OG)

Departments of Microbiology, Immunology and Infectious Diseases, Pathology & Laboratory Medicine and Community Health Sciences, Alberta Children's Hospital, Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Department of Pediatrics, University of Calgary, Calgary, AB, Canada.

James D Kellner (JD)

Department of Pediatrics, University of Calgary, Calgary, AB, Canada.

Gregory J Tyrrell (GJ)

Division of Diagnostic and Applied Microbiology, Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Canada.
Alberta Precision Laboratories-Public Health, Edmonton, Canada.

Irene Martin (I)

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

Walter Demczuk (W)

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

Scott A Halperin (SA)

Canadian Center for Vaccinology, Dalhousie University, IWK Health, and Nova Scotia Health, Halifax, Canada.

Julie A Bettinger (JA)

Vaccine Evaluation Center, BC Children's Hospital Research Institute, Vancouver, Canada.
Department of Pediatrics, University of British Columbia, Vancouver, Canada.

N Bridger (N)

Janeway Children's Health & Rehabilitation Centre, St. John's, NL.

Cheryl Foo (C)

Janeway Children's Health & Rehabilitation Centre, St. John's, NL.

S A Halperin (SA)

IWK Health Centre, Halifax, NS.

K A Top (KA)

IWK Health Centre, Halifax, NS.

R Thibeault (R)

Centre Mère-Enfant de Québec, CHUL, Quebec City, PQ.

D Moore (D)

The Montreal Children's Hospital, Montreal, PQ.

J Papenburg (J)

The Montreal Children's Hospital, Montreal, PQ.

M Lebel (M)

CHU Ste-Justine, Montreal, PQ.

N Le Saux (N)

Children's Hospital of Eastern Ontario, Ottawa, ON.

S Morris (S)

The Hospital for Sick Children, Toronto, ON.

J Embree (J)

Winnipeg Children's Hospital, Winnipeg, MB.

B Tan (B)

Jim Pattison Children's Hospital, Saskatoon, SK.

Athena McConnell (A)

Jim Pattison Children's Hospital, Saskatoon, SK.

T Jadavji (T)

Alberta Children's Hospital, Calgary, AB.

C Constantinescu (C)

Alberta Children's Hospital, Calgary, AB.

W Vaudry (W)

Stollery Children's Hospital, Edmonton, AB.

D Scheifele (D)

BC Children's Hospital, Vancouver, BC.

M Sadarangani (M)

BC Children's Hospital, Vancouver, BC.

J Bettinger (J)

BC Children's Hospital, Vancouver, BC.

L Sauvé (L)

BC Children's Hospital, Vancouver, BC.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH