Safety of the recombinant cholera toxin B subunit, killed whole-cell (rBS-WC) oral cholera vaccine in pregnancy
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. Balancing this concern is the known higher risk of cholera and of complicat...
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Veröffentlicht in: | PLoS neglected tropical diseases 2012-07, Vol.6 (7), p.e1743 |
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creator | Hashim, Ramadhan Khatib, Ahmed M Enwere, Godwin Park, Jin Kyung Reyburn, Rita Ali, Mohammad Chang, Na Yoon Kim, Deok Ryun Ley, Benedikt Thriemer, Kamala Lopez, Anna Lena Clemens, John D Deen, Jacqueline L Shin, Sunheang Schaetti, Christian Hutubessy, Raymond Aguado, Maria Teresa Kieny, Marie Paule Sack, David Obaro, Stephen Shaame, Attiye J Ali, Said M Saleh, Abdul A von Seidlein, Lorenz Jiddawi, Mohamed S |
description | 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. 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.
From 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.
We 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.
ClinicalTrials.gov NCT00709410. |
doi_str_mv | 10.1371/journal.pntd.0001743 |
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From 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.
We 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.
ClinicalTrials.gov NCT00709410.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0001743</identifier><identifier>PMID: 22848772</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Abortion ; Adolescent ; Adult ; Age groups ; Child ; Child, Preschool ; Cholera ; Cholera toxin ; Cholera Toxin - administration & dosage ; Cholera Toxin - adverse effects ; Cholera Toxin - genetics ; Cholera Toxin - immunology ; Cholera Vaccines - administration & dosage ; Cholera Vaccines - adverse effects ; Cholera Vaccines - immunology ; Drug-Related Side Effects and Adverse Reactions - epidemiology ; Epidemics ; Female ; Health aspects ; Humans ; Immunization ; Infant, Newborn ; Male ; Medicine ; Middle Aged ; Pregnancy ; Pregnant women ; Prevention ; Recombinant molecules ; Risk factors ; Rural areas ; Tanzania ; Toxins ; Tropical diseases ; Vaccines ; Vaccines, Inactivated - administration & dosage ; Vaccines, Inactivated - adverse effects ; Vaccines, Inactivated - immunology ; Waterborne diseases ; Womens health ; Young Adult</subject><ispartof>PLoS neglected tropical diseases, 2012-07, Vol.6 (7), p.e1743</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 Hashim et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Hashim R, Khatib AM, Enwere G, Park JK, Reyburn R, et al. (2012) Safety of the Recombinant Cholera Toxin B Subunit, Killed Whole-Cell (rBS-WC) Oral Cholera Vaccine in Pregnancy. PLoS Negl Trop Dis 6(7): e1743. doi:10.1371/journal.pntd.0001743</rights><rights>Hashim et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c657t-27bc0e099e643b2c3337bc05b95a80e165ef197ca0416b5536bb6afeabb95e153</citedby><cites>FETCH-LOGICAL-c657t-27bc0e099e643b2c3337bc05b95a80e165ef197ca0416b5536bb6afeabb95e153</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3404114/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3404114/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2100,2926,23865,27923,27924,53790,53792,79371,79372</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22848772$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Ryan, Edward T.</contributor><creatorcontrib>Hashim, Ramadhan</creatorcontrib><creatorcontrib>Khatib, Ahmed M</creatorcontrib><creatorcontrib>Enwere, Godwin</creatorcontrib><creatorcontrib>Park, Jin Kyung</creatorcontrib><creatorcontrib>Reyburn, Rita</creatorcontrib><creatorcontrib>Ali, Mohammad</creatorcontrib><creatorcontrib>Chang, Na Yoon</creatorcontrib><creatorcontrib>Kim, Deok Ryun</creatorcontrib><creatorcontrib>Ley, Benedikt</creatorcontrib><creatorcontrib>Thriemer, Kamala</creatorcontrib><creatorcontrib>Lopez, Anna Lena</creatorcontrib><creatorcontrib>Clemens, John D</creatorcontrib><creatorcontrib>Deen, Jacqueline L</creatorcontrib><creatorcontrib>Shin, Sunheang</creatorcontrib><creatorcontrib>Schaetti, Christian</creatorcontrib><creatorcontrib>Hutubessy, Raymond</creatorcontrib><creatorcontrib>Aguado, Maria Teresa</creatorcontrib><creatorcontrib>Kieny, Marie Paule</creatorcontrib><creatorcontrib>Sack, David</creatorcontrib><creatorcontrib>Obaro, Stephen</creatorcontrib><creatorcontrib>Shaame, Attiye J</creatorcontrib><creatorcontrib>Ali, Said M</creatorcontrib><creatorcontrib>Saleh, Abdul A</creatorcontrib><creatorcontrib>von Seidlein, Lorenz</creatorcontrib><creatorcontrib>Jiddawi, Mohamed S</creatorcontrib><title>Safety of the recombinant cholera toxin B subunit, killed whole-cell (rBS-WC) oral cholera vaccine in pregnancy</title><title>PLoS neglected tropical diseases</title><addtitle>PLoS Negl Trop Dis</addtitle><description>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. 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.
From 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.
We 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.
ClinicalTrials.gov NCT00709410.</description><subject>Abortion</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Age groups</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cholera</subject><subject>Cholera toxin</subject><subject>Cholera Toxin - administration & dosage</subject><subject>Cholera Toxin - adverse effects</subject><subject>Cholera Toxin - genetics</subject><subject>Cholera Toxin - immunology</subject><subject>Cholera Vaccines - administration & dosage</subject><subject>Cholera Vaccines - adverse effects</subject><subject>Cholera Vaccines - immunology</subject><subject>Drug-Related Side Effects and Adverse Reactions - epidemiology</subject><subject>Epidemics</subject><subject>Female</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Immunization</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Medicine</subject><subject>Middle Aged</subject><subject>Pregnancy</subject><subject>Pregnant women</subject><subject>Prevention</subject><subject>Recombinant molecules</subject><subject>Risk factors</subject><subject>Rural areas</subject><subject>Tanzania</subject><subject>Toxins</subject><subject>Tropical diseases</subject><subject>Vaccines</subject><subject>Vaccines, Inactivated - administration & dosage</subject><subject>Vaccines, Inactivated - adverse effects</subject><subject>Vaccines, Inactivated - immunology</subject><subject>Waterborne diseases</subject><subject>Womens health</subject><subject>Young 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Paule</au><au>Sack, David</au><au>Obaro, Stephen</au><au>Shaame, Attiye J</au><au>Ali, Said M</au><au>Saleh, Abdul A</au><au>von Seidlein, Lorenz</au><au>Jiddawi, Mohamed S</au><au>Ryan, Edward T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Safety of the recombinant cholera toxin B subunit, killed whole-cell (rBS-WC) oral cholera vaccine in pregnancy</atitle><jtitle>PLoS neglected tropical diseases</jtitle><addtitle>PLoS Negl Trop Dis</addtitle><date>2012-07-01</date><risdate>2012</risdate><volume>6</volume><issue>7</issue><spage>e1743</spage><pages>e1743-</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>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. 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.
From 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.
We 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.
ClinicalTrials.gov NCT00709410.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22848772</pmid><doi>10.1371/journal.pntd.0001743</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1935-2735 |
ispartof | PLoS neglected tropical diseases, 2012-07, Vol.6 (7), p.e1743 |
issn | 1935-2735 1935-2727 1935-2735 |
language | eng |
recordid | cdi_plos_journals_1288106718 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; Public Library of Science (PLoS); PubMed Central |
subjects | Abortion Adolescent Adult Age groups Child Child, Preschool Cholera Cholera toxin Cholera Toxin - administration & dosage Cholera Toxin - adverse effects Cholera Toxin - genetics Cholera Toxin - immunology Cholera Vaccines - administration & dosage Cholera Vaccines - adverse effects Cholera Vaccines - immunology Drug-Related Side Effects and Adverse Reactions - epidemiology Epidemics Female Health aspects Humans Immunization Infant, Newborn Male Medicine Middle Aged Pregnancy Pregnant women Prevention Recombinant molecules Risk factors Rural areas Tanzania Toxins Tropical diseases Vaccines Vaccines, Inactivated - administration & dosage Vaccines, Inactivated - adverse effects Vaccines, Inactivated - immunology Waterborne diseases Womens health Young Adult |
title | Safety of the recombinant cholera toxin B subunit, killed whole-cell (rBS-WC) oral cholera vaccine in pregnancy |
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