Assessment of immunity to polio among Rohingya children in Cox's Bazar, Bangladesh, 2018: A cross-sectional survey.


Journal

PLoS medicine
ISSN: 1549-1676
Titre abrégé: PLoS Med
Pays: United States
ID NLM: 101231360

Informations de publication

Date de publication:
03 2020
Historique:
received: 27 09 2019
accepted: 27 02 2020
entrez: 2 4 2020
pubmed: 2 4 2020
medline: 25 6 2020
Statut: epublish

Résumé

We performed a cross-sectional survey in April-May 2018 among Rohingya in Cox's Bazar, Bangladesh, to assess polio immunity and inform vaccination strategies. Rohingya children aged 1-6 years (younger group) and 7-14 years (older group) were selected using multi-stage cluster sampling in makeshift settlements and simple random sampling in Nayapara registered camp. Surveyors asked parents/caregivers if the child received any oral poliovirus vaccine (OPV) in Myanmar and, for younger children, if the child received vaccine in any of the 5 campaigns delivering bivalent OPV (serotypes 1 and 3) conducted during September 2017-April 2018 in Cox's Bazar. Dried blood spot (DBS) specimens were tested for neutralizing antibodies to poliovirus types 1, 2, and 3 in 580 younger and 297 older children. Titers ≥ 1:8 were considered protective. Among 632 children (335 aged 1-6 years, 297 aged 7-14 years) enrolled in the study in makeshift settlements, 51% were male and 89% had arrived after August 9, 2017. Among 245 children (all aged 1-6 years) enrolled in the study in Nayapara, 54% were male and 10% had arrived after August 9, 2017. Among younger children, 74% in makeshift settlements and 92% in Nayapara received >3 bivalent OPV doses in campaigns. Type 1 seroprevalence was 85% (95% CI 80%-89%) among younger children and 91% (95% CI 86%-95%) among older children in makeshift settlements, and 92% (88%-95%) among younger children in Nayapara. Type 2 seroprevalence was lower among younger children than older children in makeshift settlements (74% [95% CI 68%-79%] versus 97% [95% CI 94%-99%], p < 0.001), and was 69% (95% CI 63%-74%) among younger children in Nayapara. Type 3 seroprevalence was below 75% for both age groups and areas. The limitations of this study are unknown routine immunization history and poor retention of vaccination cards. Younger Rohingya children had immunity gaps to all 3 polio serotypes and should be targeted by future campaigns and catch-up routine immunization. DBS collection can enhance the reliability of assessments of outbreak risk and vaccination strategy impact in emergency settings.

Sections du résumé

BACKGROUND
We performed a cross-sectional survey in April-May 2018 among Rohingya in Cox's Bazar, Bangladesh, to assess polio immunity and inform vaccination strategies.
METHODS AND FINDINGS
Rohingya children aged 1-6 years (younger group) and 7-14 years (older group) were selected using multi-stage cluster sampling in makeshift settlements and simple random sampling in Nayapara registered camp. Surveyors asked parents/caregivers if the child received any oral poliovirus vaccine (OPV) in Myanmar and, for younger children, if the child received vaccine in any of the 5 campaigns delivering bivalent OPV (serotypes 1 and 3) conducted during September 2017-April 2018 in Cox's Bazar. Dried blood spot (DBS) specimens were tested for neutralizing antibodies to poliovirus types 1, 2, and 3 in 580 younger and 297 older children. Titers ≥ 1:8 were considered protective. Among 632 children (335 aged 1-6 years, 297 aged 7-14 years) enrolled in the study in makeshift settlements, 51% were male and 89% had arrived after August 9, 2017. Among 245 children (all aged 1-6 years) enrolled in the study in Nayapara, 54% were male and 10% had arrived after August 9, 2017. Among younger children, 74% in makeshift settlements and 92% in Nayapara received >3 bivalent OPV doses in campaigns. Type 1 seroprevalence was 85% (95% CI 80%-89%) among younger children and 91% (95% CI 86%-95%) among older children in makeshift settlements, and 92% (88%-95%) among younger children in Nayapara. Type 2 seroprevalence was lower among younger children than older children in makeshift settlements (74% [95% CI 68%-79%] versus 97% [95% CI 94%-99%], p < 0.001), and was 69% (95% CI 63%-74%) among younger children in Nayapara. Type 3 seroprevalence was below 75% for both age groups and areas. The limitations of this study are unknown routine immunization history and poor retention of vaccination cards.
CONCLUSIONS
Younger Rohingya children had immunity gaps to all 3 polio serotypes and should be targeted by future campaigns and catch-up routine immunization. DBS collection can enhance the reliability of assessments of outbreak risk and vaccination strategy impact in emergency settings.

Identifiants

pubmed: 32231366
doi: 10.1371/journal.pmed.1003070
pii: PMEDICINE-D-19-03533
pmc: PMC7108688
doi:

Substances chimiques

Poliovirus Vaccine, Oral 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1003070

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Déclaration de conflit d'intérêts

I have read the journal's policy and the authors of this manuscript have the following competing interests: JMA is a Health Specialist at UNICEF Bangladesh. MH is a Health Specialist at UNICEF Bangladesh.

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Auteurs

Concepcion F Estivariz (CF)

Global Immunization Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Sarah D Bennett (SD)

Global Immunization Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Jacquelyn S Lickness (JS)

Global Immunization Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Leora R Feldstein (LR)

Global Immunization Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
Epidemic Intelligence Service, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

William C Weldon (WC)

Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Eva Leidman (E)

Division of Global Health Protection, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Daniel C Ehlman (DC)

Global Immunization Division, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Muhammad F H Khan (MFH)

World Health Organization, Dhaka, Bangladesh.

Jucy M Adhikari (JM)

United Nations Children's Fund, Dhaka, Bangladesh.

Mainul Hasan (M)

United Nations Children's Fund, Dhaka, Bangladesh.

Mallick M Billah (MM)

Institute of Epidemiology, Disease Control and Research, Dhaka, Bangladesh.

M Steven Oberste (MS)

Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

A S M Alamgir (ASM)

Institute of Epidemiology, Disease Control and Research, Dhaka, Bangladesh.

Meerjady D Flora (MD)

Institute of Epidemiology, Disease Control and Research, Dhaka, Bangladesh.

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Classifications MeSH