Programmatic Effectiveness of a Pediatric Typhoid Conjugate Vaccine Campaign in Navi Mumbai, India.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
05 07 2023
Historique:
received: 22 10 2022
medline: 6 7 2023
pubmed: 23 3 2023
entrez: 22 3 2023
Statut: ppublish

Résumé

The World Health Organization recommends vaccines for prevention and control of typhoid fever, especially where antimicrobial-resistant typhoid circulates. In 2018, the Navi Mumbai Municipal Corporation (NMMC) implemented a typhoid conjugate vaccine (TCV) campaign. The campaign targeted all children aged 9 months through 14 years within NMMC boundaries (approximately 320 000 children) over 2 vaccination phases. The phase 1 campaign occurred from 14 July 2018 through 25 August 2018 (71% coverage, approximately 113 420 children). We evaluated the phase 1 campaign's programmatic effectiveness in reducing typhoid cases at the community level. We established prospective, blood culture-based surveillance at 6 hospitals in Navi Mumbai and offered blood cultures to children who presented with fever ≥3 days. We used a cluster-randomized (by administrative boundary) test-negative design to estimate the effectiveness of the vaccination campaign on pediatric typhoid cases. We matched test-positive, culture-confirmed typhoid cases with up to 3 test-negative, culture-negative controls by age and date of blood culture and assessed community vaccine campaign phase as an exposure using conditional logistic regression. Between 1 September 2018 and 31 March 2021, we identified 81 typhoid cases and matched these with 238 controls. Cases were 0.44 times as likely to live in vaccine campaign communities (programmatic effectiveness, 56%; 95% confidence interval [CI], 25% to 74%; P = .002). Cases aged ≥5 years were 0.37 times as likely (95% CI, .19 to .70; P = .002) and cases during the first year of surveillance were 0.30 times as likely (95% CI, .14 to .64; P = .002) to live in vaccine campaign communities. Our findings support the use of TCV mass vaccination campaigns as effective population-based tools to combat typhoid fever.

Sections du résumé

BACKGROUND
The World Health Organization recommends vaccines for prevention and control of typhoid fever, especially where antimicrobial-resistant typhoid circulates. In 2018, the Navi Mumbai Municipal Corporation (NMMC) implemented a typhoid conjugate vaccine (TCV) campaign. The campaign targeted all children aged 9 months through 14 years within NMMC boundaries (approximately 320 000 children) over 2 vaccination phases. The phase 1 campaign occurred from 14 July 2018 through 25 August 2018 (71% coverage, approximately 113 420 children). We evaluated the phase 1 campaign's programmatic effectiveness in reducing typhoid cases at the community level.
METHODS
We established prospective, blood culture-based surveillance at 6 hospitals in Navi Mumbai and offered blood cultures to children who presented with fever ≥3 days. We used a cluster-randomized (by administrative boundary) test-negative design to estimate the effectiveness of the vaccination campaign on pediatric typhoid cases. We matched test-positive, culture-confirmed typhoid cases with up to 3 test-negative, culture-negative controls by age and date of blood culture and assessed community vaccine campaign phase as an exposure using conditional logistic regression.
RESULTS
Between 1 September 2018 and 31 March 2021, we identified 81 typhoid cases and matched these with 238 controls. Cases were 0.44 times as likely to live in vaccine campaign communities (programmatic effectiveness, 56%; 95% confidence interval [CI], 25% to 74%; P = .002). Cases aged ≥5 years were 0.37 times as likely (95% CI, .19 to .70; P = .002) and cases during the first year of surveillance were 0.30 times as likely (95% CI, .14 to .64; P = .002) to live in vaccine campaign communities.
CONCLUSIONS
Our findings support the use of TCV mass vaccination campaigns as effective population-based tools to combat typhoid fever.

Identifiants

pubmed: 36947143
pii: 7083728
doi: 10.1093/cid/ciad132
pmc: PMC10320126
doi:

Substances chimiques

Typhoid-Paratyphoid Vaccines 0
Vaccines, Attenuated 0
Vaccines, Conjugate 0

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

138-144

Subventions

Organisme : World Health Organization
ID : 001
Pays : International
Organisme : NIAID NIH HHS
ID : T32 AI007502
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Déclaration de conflit d'intérêts

Potential conflicts of interest. K. D. reports support for attending meetings and/or travel by their employer (the CDC). S. P. L. reports support for attending meetings and/or travel from the Bill & Melinda Gates Foundation (conferences where some of the work from this project were reported). All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

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Auteurs

Seth A Hoffman (SA)

Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.

Christopher LeBoa (C)

Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.

Kashmira Date (K)

Global Immunization Division, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Pradeep Haldar (P)

Ministry of Health & Family Welfare, Government of India, New Delhi, India.

Pauline Harvey (P)

World Health Organization-Country Office for India, National Public Health Surveillance Project, New Delhi, India.

Rahul Shimpi (R)

World Health Organization-Country Office for India, National Public Health Surveillance Project, New Delhi, India.

Qian An (Q)

Global Immunization Division, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Chenhua Zhang (C)

Global Immunization Division, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Niniya Jayaprasad (N)

World Health Organization-Country Office for India, National Public Health Surveillance Project, New Delhi, India.

Lily Horng (L)

Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.

Kirsten Fagerli (K)

Global Immunization Division, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Priyanka Borhade (P)

World Health Organization-Country Office for India, National Public Health Surveillance Project, New Delhi, India.

Savita Daruwalla (S)

Department of Pediatrics, NMMC General Hospital, Navi Mumbai, India.

Dhanya Dharmapalan (D)

Dr. Yewale Multispecialty Hospital for Children, Navi Mumbai, India.

Jeetendra Gavhane (J)

Department of Pediatrics, MGM New Bombay Hospital, MGM Medical College, Navi Mumbai, India.

Shrikrishna Joshi (S)

Dr. Joshi's Central Clinical Microbiology Laboratory, Navi Mumbai, India.

Rajesh Rai (R)

Department of Pediatrics & Neonatology, Dr. D.Y. Patil Medical College and Hospital, Navi Mumbai, India.

Varsha Rathod (V)

Rajmata Jijau Hospital, Airoli (NMMC), Navi Mumbai, India.

Keertana Shetty (K)

Department of Microbiology, Dr. D.Y. Patil Medical College and Hospital, Navi Mumbai, India.

Divyalatha S Warrier (DS)

Department of Pediatrics, Mathadi Trust Hospital, Navi Mumbai, India.

Shalini Yadav (S)

Department of Microbiology, MGM New Bombay Hospital, Navi Mumbai, India.

Debjit Chakraborty (D)

National Institute of Cholera and Enteric Diseases, Indian Council of Medical Research, Kolkata, India.

Sunil Bahl (S)

World Health Organization South-East Asia Regional Office, New Delhi, India.

Arun Katkar (A)

World Health Organization-Country Office for India, National Public Health Surveillance Project, New Delhi, India.

Abhishek Kunwar (A)

World Health Organization-Country Office for India, National Public Health Surveillance Project, New Delhi, India.

Vijay Yewale (V)

Dr. Yewale Multispecialty Hospital for Children, Navi Mumbai, India.

Jason R Andrews (JR)

Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.

Pankaj Bhatnagar (P)

World Health Organization-Country Office for India, National Public Health Surveillance Project, New Delhi, India.

Shanta Dutta (S)

National Institute of Cholera and Enteric Diseases, Indian Council of Medical Research, Kolkata, India.

Stephen P Luby (SP)

Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.

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