Abstract

IntroductionMass vaccinations are a main strategy in the deployment of oral cholera vaccines. Campaigns avoid giving vaccine to pregnant women because of the absence of safety data of the killed whole-cell oral cholera (rBS-WC) vaccine. Balancing this concern is the known higher risk of cholera and of complications of pregnancy should cholera occur in these women, as well as the lack of expected adverse events from a killed oral bacterial vaccine.Methodology/Principal FindingsFrom January to February 2009, a mass rBS-WC vaccination campaign of persons over two years of age was conducted in an urban and a rural area (population 51,151) in Zanzibar. Pregnant women were advised not to participate in the campaign. More than nine months after the last dose of the vaccine was administered, we visited all women between 15 and 50 years of age living in the study area. The outcome of pregnancies that were inadvertently exposed to at least one oral cholera vaccine dose and those that were not exposed was evaluated. 13,736 (94%) of the target women in the study site were interviewed. 1,151 (79%) of the 1,453 deliveries in 2009 occurred during the period when foetal exposure to the vaccine could have occurred. 955 (83%) out of these 1,151 mothers had not been vaccinated; the remaining 196 (17%) mothers had received at least one dose of the oral cholera vaccine. There were no statistically significant differences in the odds ratios for birth outcomes among the exposed and unexposed pregnancies.Conclusions/SignificanceWe found no statistically significant evidence of a harmful effect of gestational exposure to the rBS-WC vaccine. These findings, along with the absence of a rational basis for expecting a risk from this killed oral bacterial vaccine, are reassuring but the study had insufficient power to detect infrequent events.Trial RegistrationClinicalTrials.gov NCT00709410

Highlights

  • Mass vaccinations are a main strategy in the deployment of oral cholera vaccines

  • A more affordable oral cholera vaccine which could be used more widely in endemic settings has recently been developed, licensed, and prequalified for purchase by UN agencies [6]. This second generation killed oral cholera vaccine (Shanchol) is composed of a different set of V.cholerae strains than the rBS-WC vaccine, includes O1 and an O139 strain, does not include the recombinant B subunit, does not require buffer for administration, and has afforded 66% protection during a 3 year trial in Kolkata, India [7]

  • We found no significant differences in birth outcomes among pregnancies exposed and unexposed to the rBS-WC oral cholera vaccine

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Summary

Introduction

Mass vaccinations are a main strategy in the deployment of oral cholera vaccines. Campaigns avoid giving vaccine to pregnant women because of the absence of safety data of the killed whole-cell oral cholera (rBS-WC) vaccine. The recombinant cholera toxin B subunit, killed whole-cell oral cholera (rBS-WC, Dukoral) vaccine, has been found to be safe and protective in a range of settings over the last 30 years [1,2,3] This vaccine is mainly used by tourists visiting endemic areas [4] where the control of cholera has traditionally been based on safe water supply, sanitation and health education [5]. A more affordable oral cholera vaccine which could be used more widely in endemic settings has recently been developed, licensed, and prequalified for purchase by UN agencies [6] This second generation killed oral cholera vaccine (Shanchol) is composed of a different set of V.cholerae strains than the rBS-WC vaccine, includes O1 and an O139 strain, does not include the recombinant B subunit (rBS), does not require buffer for administration, and has afforded 66% protection during a 3 year trial in Kolkata, India [7]. In early 2010, the Strategic Advisory group of the World Health Organization (WHO) recommended that oral cholera vaccines be used preventively as well as reactively in the management of cholera outbreaks [8].

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