Effectiveness of the 10-valent pneumococcal conjugate vaccine on pediatric pneumonia confirmed by ultrasound: a matched case-control study.


Journal

Respiratory research
ISSN: 1465-993X
Titre abrégé: Respir Res
Pays: England
ID NLM: 101090633

Informations de publication

Date de publication:
01 Aug 2022
Historique:
received: 15 04 2022
accepted: 05 07 2022
entrez: 1 8 2022
pubmed: 2 8 2022
medline: 4 8 2022
Statut: epublish

Résumé

Bangladesh introduced the 10-valent pneumococcal conjugate vaccine (PCV10) for children aged < 1 year in March 2015. Previous vaccine effectiveness (VE) studies for pneumonia have used invasive pneumococcal disease or chest X-rays. None have used ultrasound. We sought to determine the VE of PCV10 against sonographically-confirmed pneumonia in three subdistrict health complexes in Bangladesh. We conducted a matched case-control study between July 2015 and September 2017 in three subdistricts of Sylhet, Bangladesh. Cases were vaccine-eligible children aged 3-35 months with sonographically-confirmed pneumonia, who were matched with two types of controls by age, sex, week of diagnosis, subdistrict health complex (clinic controls) or distance from subdistrict health complex (community controls) and had an illness unlikely due to Streptococcus pneumoniae (clinic controls) or were healthy (community controls). VE was measured using multivariable conditional logistic regression. We evaluated 8926 children (average age 13.3 months, 58% boys) with clinical pneumonia by ultrasound; 2470 had pneumonia with consolidations ≥ 1 cm; 1893 pneumonia cases were matched with 4238 clinic controls; and 1832 were matched with 3636 community controls. VE increased with the threshold used for consolidation size on ultrasound: the adjusted VE of ≥ 2 doses vs. non-recipients of PCV10 against pneumonia increased from 15.8% (95% CI 1.6-28.0%) for consolidations ≥ 1 cm to 29.6% (12.8-43.2%) for consolidations ≥ 1.5 cm using clinic controls and from 2.7% (- 14.2-17.2%) to 23.5% (4.4-38.8%) using community controls, respectively. PCV10 was effective at reducing sonographically-confirmed pneumonia in children aged 3-35 months of age when compared to unvaccinated children. VE increased with the threshold used for consolidation size on ultrasound in clinic and community controls alike. This study provides evidence that lung ultrasound is a useful alternative to chest X-ray for case-control studies evaluating the effectiveness of vaccines against pneumonia.

Sections du résumé

BACKGROUND BACKGROUND
Bangladesh introduced the 10-valent pneumococcal conjugate vaccine (PCV10) for children aged < 1 year in March 2015. Previous vaccine effectiveness (VE) studies for pneumonia have used invasive pneumococcal disease or chest X-rays. None have used ultrasound. We sought to determine the VE of PCV10 against sonographically-confirmed pneumonia in three subdistrict health complexes in Bangladesh.
METHODS METHODS
We conducted a matched case-control study between July 2015 and September 2017 in three subdistricts of Sylhet, Bangladesh. Cases were vaccine-eligible children aged 3-35 months with sonographically-confirmed pneumonia, who were matched with two types of controls by age, sex, week of diagnosis, subdistrict health complex (clinic controls) or distance from subdistrict health complex (community controls) and had an illness unlikely due to Streptococcus pneumoniae (clinic controls) or were healthy (community controls). VE was measured using multivariable conditional logistic regression.
RESULTS RESULTS
We evaluated 8926 children (average age 13.3 months, 58% boys) with clinical pneumonia by ultrasound; 2470 had pneumonia with consolidations ≥ 1 cm; 1893 pneumonia cases were matched with 4238 clinic controls; and 1832 were matched with 3636 community controls. VE increased with the threshold used for consolidation size on ultrasound: the adjusted VE of ≥ 2 doses vs. non-recipients of PCV10 against pneumonia increased from 15.8% (95% CI 1.6-28.0%) for consolidations ≥ 1 cm to 29.6% (12.8-43.2%) for consolidations ≥ 1.5 cm using clinic controls and from 2.7% (- 14.2-17.2%) to 23.5% (4.4-38.8%) using community controls, respectively.
CONCLUSIONS CONCLUSIONS
PCV10 was effective at reducing sonographically-confirmed pneumonia in children aged 3-35 months of age when compared to unvaccinated children. VE increased with the threshold used for consolidation size on ultrasound in clinic and community controls alike. This study provides evidence that lung ultrasound is a useful alternative to chest X-ray for case-control studies evaluating the effectiveness of vaccines against pneumonia.

Identifiants

pubmed: 35915495
doi: 10.1186/s12931-022-02115-5
pii: 10.1186/s12931-022-02115-5
pmc: PMC9341060
doi:

Substances chimiques

10-valent pneumococcal conjugate vaccine 0
Pneumococcal Vaccines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

198

Subventions

Organisme : Bill & Melinda Gates Foundation
ID : OPP1084286
Pays : United States
Organisme : Bill & Melinda Gates Foundation
ID : OPP1117483
Pays : United States
Organisme : GlaxoSmithKline
ID : 90063241

Informations de copyright

© 2022. The Author(s).

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Auteurs

William Checkley (W)

Division of Pulmonary and Critical Care, School of Medicine, Johns Hopkins University, 1830 E. Monument St, Room 555, Baltimore, MD, 21287, USA. wcheckl1@jhmi.edu.
Department of International Health, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, USA. wcheckl1@jhmi.edu.
Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, USA. wcheckl1@jhmi.edu.

Shakir Hossen (S)

Division of Pulmonary and Critical Care, School of Medicine, Johns Hopkins University, 1830 E. Monument St, Room 555, Baltimore, MD, 21287, USA.

Eric D McCollum (ED)

Department of International Health, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, USA.
Department of Pediatrics, School of Medicine, Johns Hopkins University, Baltimore, USA.

Farhan Pervaiz (F)

Division of Pulmonary and Critical Care, School of Medicine, Johns Hopkins University, 1830 E. Monument St, Room 555, Baltimore, MD, 21287, USA.

Catherine H Miele (CH)

Division of Pulmonary and Critical Care, School of Medicine, Johns Hopkins University, 1830 E. Monument St, Room 555, Baltimore, MD, 21287, USA.

Miguel A Chavez (MA)

Division of Pulmonary and Critical Care, School of Medicine, Johns Hopkins University, 1830 E. Monument St, Room 555, Baltimore, MD, 21287, USA.

Lawrence H Moulton (LH)

Department of International Health, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, USA.
Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, USA.

Nicole Simmons (N)

Department of International Health, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, USA.

Arunangshu D Roy (AD)

Johns Hopkins University -Bangladesh, Dhaka, Bangladesh.

Nabidul H Chowdhury (NH)

Johns Hopkins University -Bangladesh, Dhaka, Bangladesh.

Salahuddin Ahmed (S)

Johns Hopkins University -Bangladesh, Dhaka, Bangladesh.

Nazma Begum (N)

Johns Hopkins University -Bangladesh, Dhaka, Bangladesh.

Abdul Quaiyum (A)

Johns Hopkins University -Bangladesh, Dhaka, Bangladesh.

Mathuram Santosham (M)

Department of International Health, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, USA.
Department of Pediatrics, School of Medicine, Johns Hopkins University, Baltimore, USA.

Abdullah H Baqui (AH)

Department of International Health, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, USA.

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