Risks and safety of pandemic h1n1 influenza vaccine in pregnancy: Birth defects, spontaneous abortion, preterm delivery, and small for gestational age infants
•Information is needed on safety of pandemic H1N1 influenza vaccines in pregnancy.•1032 exposed pregnant women were followed to pregnancy outcome, 2009–2012.•No increases in birth defects, spontaneous abortion or growth restriction were seen.•Vaccinated women on average delivered 3 days earlier than...
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Published in | Vaccine Vol. 31; no. 44; pp. 5026 - 5032 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier Ltd
17.10.2013
Elsevier Elsevier Limited |
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Abstract | •Information is needed on safety of pandemic H1N1 influenza vaccines in pregnancy.•1032 exposed pregnant women were followed to pregnancy outcome, 2009–2012.•No increases in birth defects, spontaneous abortion or growth restriction were seen.•Vaccinated women on average delivered 3 days earlier than non-vaccinated.•This study adds to the reassuring literature about pH1N1 vaccines in pregnancy.
There is a need for additional information on the fetal risks and relative safety of the pandemic H1N1 monovalent or trivalent influenza (pH1N1)-containing vaccines in women exposed during pregnancy.
To assess risks and relative safety of the pH1N1-containing vaccines, we conducted a prospective cohort study of pH1N1-vaccine-exposed and unexposed comparison women residing in the U.S. or Canada who were recruited during pregnancy and followed to outcome between October 2009 and August 2012. For exposure to the pH1N1 vaccine, adjusted relative risks (RRs) and 95% confidence intervals (CIs) were estimated for major birth defects and infants small for gestational age. Adjusted hazard ratios (HRs) and 95% CIs were estimated for spontaneous abortion and preterm delivery for time-varying exposure.
There were 1032 subjects available for analysis; 841 women were exposed to a pH1N1-containing vaccine in pregnancy, and 191 women were unexposed to any influenza vaccine in pregnancy. Nine of 328 (2.7%) first-trimester-exposed pregnancies resulted in an infant with a major birth defect compared to 6/188 (3.2%) in the unexposed (adjusted RR 0.79, 95% CI 0.26–2.42). The HR for spontaneous abortion was not elevated (adjusted HR 0.92, 95% CI 0.31–2.72). Adjusted HRs for preterm delivery were elevated for exposure anytime in pregnancy (3.28, 95% CI 1.25–8.63), specifically with exposure in the 1st or 2nd trimester. However, the mean decrease in gestational age in the exposed pregnancies was approximately three days. Adjusted RRs for small for gestational age infants on weight and length approximated 1.0.
For the 2009–12 influenza seasons combined, we found no meaningful evidence of increased RR or HR for major birth defects, spontaneous abortion, or small for gestational age infants. There was some evidence of an increased HR for preterm delivery following pH1N1-influenza vaccine exposure; however the decrease in gestational age on average was approximately three days. |
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AbstractList | •Information is needed on safety of pandemic H1N1 influenza vaccines in pregnancy.•1032 exposed pregnant women were followed to pregnancy outcome, 2009–2012.•No increases in birth defects, spontaneous abortion or growth restriction were seen.•Vaccinated women on average delivered 3 days earlier than non-vaccinated.•This study adds to the reassuring literature about pH1N1 vaccines in pregnancy.
There is a need for additional information on the fetal risks and relative safety of the pandemic H1N1 monovalent or trivalent influenza (pH1N1)-containing vaccines in women exposed during pregnancy.
To assess risks and relative safety of the pH1N1-containing vaccines, we conducted a prospective cohort study of pH1N1-vaccine-exposed and unexposed comparison women residing in the U.S. or Canada who were recruited during pregnancy and followed to outcome between October 2009 and August 2012. For exposure to the pH1N1 vaccine, adjusted relative risks (RRs) and 95% confidence intervals (CIs) were estimated for major birth defects and infants small for gestational age. Adjusted hazard ratios (HRs) and 95% CIs were estimated for spontaneous abortion and preterm delivery for time-varying exposure.
There were 1032 subjects available for analysis; 841 women were exposed to a pH1N1-containing vaccine in pregnancy, and 191 women were unexposed to any influenza vaccine in pregnancy. Nine of 328 (2.7%) first-trimester-exposed pregnancies resulted in an infant with a major birth defect compared to 6/188 (3.2%) in the unexposed (adjusted RR 0.79, 95% CI 0.26–2.42). The HR for spontaneous abortion was not elevated (adjusted HR 0.92, 95% CI 0.31–2.72). Adjusted HRs for preterm delivery were elevated for exposure anytime in pregnancy (3.28, 95% CI 1.25–8.63), specifically with exposure in the 1st or 2nd trimester. However, the mean decrease in gestational age in the exposed pregnancies was approximately three days. Adjusted RRs for small for gestational age infants on weight and length approximated 1.0.
For the 2009–12 influenza seasons combined, we found no meaningful evidence of increased RR or HR for major birth defects, spontaneous abortion, or small for gestational age infants. There was some evidence of an increased HR for preterm delivery following pH1N1-influenza vaccine exposure; however the decrease in gestational age on average was approximately three days. There is a need for additional information on the fetal risks and relative safety of the pandemic H1N1 monovalent or trivalent influenza (pH1N1)-containing vaccines in women exposed during pregnancy.INTRODUCTIONThere is a need for additional information on the fetal risks and relative safety of the pandemic H1N1 monovalent or trivalent influenza (pH1N1)-containing vaccines in women exposed during pregnancy.To assess risks and relative safety of the pH1N1-containing vaccines, we conducted a prospective cohort study of pH1N1-vaccine-exposed and unexposed comparison women residing in the U.S. or Canada who were recruited during pregnancy and followed to outcome between October 2009 and August 2012. For exposure to the pH1N1 vaccine, adjusted relative risks (RRs) and 95% confidence intervals (CIs) were estimated for major birth defects and infants small for gestational age. Adjusted hazard ratios (HRs) and 95% CIs were estimated for spontaneous abortion and preterm delivery for time-varying exposure.METHODSTo assess risks and relative safety of the pH1N1-containing vaccines, we conducted a prospective cohort study of pH1N1-vaccine-exposed and unexposed comparison women residing in the U.S. or Canada who were recruited during pregnancy and followed to outcome between October 2009 and August 2012. For exposure to the pH1N1 vaccine, adjusted relative risks (RRs) and 95% confidence intervals (CIs) were estimated for major birth defects and infants small for gestational age. Adjusted hazard ratios (HRs) and 95% CIs were estimated for spontaneous abortion and preterm delivery for time-varying exposure.There were 1032 subjects available for analysis; 841 women were exposed to a pH1N1-containing vaccine in pregnancy, and 191 women were unexposed to any influenza vaccine in pregnancy. Nine of 328 (2.7%) first-trimester-exposed pregnancies resulted in an infant with a major birth defect compared to 6/188 (3.2%) in the unexposed (adjusted RR 0.79, 95% CI 0.26-2.42). The HR for spontaneous abortion was not elevated (adjusted HR 0.92, 95% CI 0.31-2.72). Adjusted HRs for preterm delivery were elevated for exposure anytime in pregnancy (3.28, 95% CI 1.25-8.63), specifically with exposure in the 1st or 2nd trimester. However, the mean decrease in gestational age in the exposed pregnancies was approximately three days. Adjusted RRs for small for gestational age infants on weight and length approximated 1.0.RESULTSThere were 1032 subjects available for analysis; 841 women were exposed to a pH1N1-containing vaccine in pregnancy, and 191 women were unexposed to any influenza vaccine in pregnancy. Nine of 328 (2.7%) first-trimester-exposed pregnancies resulted in an infant with a major birth defect compared to 6/188 (3.2%) in the unexposed (adjusted RR 0.79, 95% CI 0.26-2.42). The HR for spontaneous abortion was not elevated (adjusted HR 0.92, 95% CI 0.31-2.72). Adjusted HRs for preterm delivery were elevated for exposure anytime in pregnancy (3.28, 95% CI 1.25-8.63), specifically with exposure in the 1st or 2nd trimester. However, the mean decrease in gestational age in the exposed pregnancies was approximately three days. Adjusted RRs for small for gestational age infants on weight and length approximated 1.0.For the 2009-12 influenza seasons combined, we found no meaningful evidence of increased RR or HR for major birth defects, spontaneous abortion, or small for gestational age infants. There was some evidence of an increased HR for preterm delivery following pH1N1-influenza vaccine exposure; however the decrease in gestational age on average was approximately three days.CONCLUSIONSFor the 2009-12 influenza seasons combined, we found no meaningful evidence of increased RR or HR for major birth defects, spontaneous abortion, or small for gestational age infants. There was some evidence of an increased HR for preterm delivery following pH1N1-influenza vaccine exposure; however the decrease in gestational age on average was approximately three days. There is a need for additional information on the fetal risks and relative safety of the pandemic H1N1 monovalent or trivalent influenza (pH1N1)-containing vaccines in women exposed during pregnancy. To assess risks and relative safety of the pH1N1-containing vaccines, we conducted a prospective cohort study of pH1N1-vaccine-exposed and unexposed comparison women residing in the U.S. or Canada who were recruited during pregnancy and followed to outcome between October 2009 and August 2012. For exposure to the pH1N1 vaccine, adjusted relative risks (RRs) and 95% confidence intervals (CIs) were estimated for major birth defects and infants small for gestational age. Adjusted hazard ratios (HRs) and 95% CIs were estimated for spontaneous abortion and preterm delivery for time-varying exposure. There were 1032 subjects available for analysis; 841 women were exposed to a pH1N1-containing vaccine in pregnancy, and 191 women were unexposed to any influenza vaccine in pregnancy. Nine of 328 (2.7%) first-trimester-exposed pregnancies resulted in an infant with a major birth defect compared to 6/188 (3.2%) in the unexposed (adjusted RR 0.79, 95% CI 0.26-2.42). The HR for spontaneous abortion was not elevated (adjusted HR 0.92, 95% CI 0.31-2.72). Adjusted HRs for preterm delivery were elevated for exposure anytime in pregnancy (3.28, 95% CI 1.25-8.63), specifically with exposure in the 1st or 2nd trimester. However, the mean decrease in gestational age in the exposed pregnancies was approximately three days. Adjusted RRs for small for gestational age infants on weight and length approximated 1.0. For the 2009-12 influenza seasons combined, we found no meaningful evidence of increased RR or HR for major birth defects, spontaneous abortion, or small for gestational age infants. There was some evidence of an increased HR for preterm delivery following pH1N1-influenza vaccine exposure; however the decrease in gestational age on average was approximately three days. Highlights•Information is needed on safety of pandemic H1N1 influenza vaccines in pregnancy. •1032 exposed pregnant women were followed to pregnancy outcome, 2009–2012. •No increases in birth defects, spontaneous abortion or growth restriction were seen. •Vaccinated women on average delivered 3 days earlier than non-vaccinated. •This study adds to the reassuring literature about pH1N1 vaccines in pregnancy. Introduction There is a need for additional information on the fetal risks and relative safety of the pandemic H1N1 monovalent or trivalent influenza (pH1N1)-containing vaccines in women exposed during pregnancy. Methods To assess risks and relative safety of the pH1N1-containing vaccines, we conducted a prospective cohort study of pH1N1-vaccine-exposed and unexposed comparison women residing in the U.S. or Canada who were recruited during pregnancy and followed to outcome between October 2009 and August 2012. For exposure to the pH1N1 vaccine, adjusted relative risks (RRs) and 95% confidence intervals (CIs) were estimated for major birth defects and infants small for gestational age. Adjusted hazard ratios (HRs) and 95% CIs were estimated for spontaneous abortion and preterm delivery for time-varying exposure. Results There were 1032 subjects available for analysis; 841 women were exposed to a pH1N1-containing vaccine in pregnancy, and 191 women were unexposed to any influenza vaccine in pregnancy. Nine of 328 (2.7%) first-trimester-exposed pregnancies resulted in an infant with a major birth defect compared to 6/188 (3.2%) in the unexposed (adjusted RR 0.79, 95% CI 0.26-2.42). The HR for spontaneous abortion was not elevated (adjusted HR 0.92, 95% CI 0.31-2.72). Adjusted HRs for preterm delivery were elevated for exposure anytime in pregnancy (3.28, 95% CI 1.25-8.63), specifically with exposure in the 1st or 2nd trimester. However, the mean decrease in gestational age in the exposed pregnancies was approximately three days. Adjusted RRs for small for gestational age infants on weight and length approximated 1.0. Conclusions For the 2009-12 influenza seasons combined, we found no meaningful evidence of increased RR or HR for major birth defects, spontaneous abortion, or small for gestational age infants. There was some evidence of an increased HR for preterm delivery following pH1N1-influenza vaccine exposure; however the decrease in gestational age on average was approximately three days. There is a need for additional information on the fetal risks and relative safety of the pandemic H1N1 monovalent or trivalent influenza (pH1N1)-containing vaccines in women exposed during pregnancy.To assess risks and relative safety of the pH1N1-containing vaccines, we conducted a prospective cohort study of pH1N1-vaccine-exposed and unexposed comparison women residing in the U.S. or Canada who were recruited during pregnancy and followed to outcome between October 2009 and August 2012. For exposure to the pH1N1 vaccine, adjusted relative risks (RRs) and 95% confidence intervals (CIs) were estimated for major birth defects and infants small for gestational age. Adjusted hazard ratios (HRs) and 95% CIs were estimated for spontaneous abortion and preterm delivery for time-varying exposure.There were 1032 subjects available for analysis; 841 women were exposed to a pH1N1-containing vaccine in pregnancy, and 191 women were unexposed to any influenza vaccine in pregnancy. Nine of 328 (2.7%) first-trimester-exposed pregnancies resulted in an infant with a major birth defect compared to 6/188 (3.2%) in the unexposed (adjusted RR 0.79, 95% CI 0.26–2.42). The HR for spontaneous abortion was not elevated (adjusted HR 0.92, 95% CI 0.31–2.72). Adjusted HRs for preterm delivery were elevated for exposure anytime in pregnancy (3.28, 95% CI 1.25–8.63), specifically with exposure in the 1st or 2nd trimester. However, the mean decrease in gestational age in the exposed pregnancies was approximately three days. Adjusted RRs for small for gestational age infants on weight and length approximated 1.0.For the 2009–12 influenza seasons combined, we found no meaningful evidence of increased RR or HR for major birth defects, spontaneous abortion, or small for gestational age infants. There was some evidence of an increased HR for preterm delivery following pH1N1-influenza vaccine exposure; however the decrease in gestational age on average was approximately three days. |
Author | Johnson, Diana Jones, Kenneth L. Chambers, Christina D. Louik, Carol Schatz, Michael Xu, Ronghui Luo, Yunjun Mitchell, Allen A. |
Author_xml | – sequence: 1 givenname: Christina D. surname: Chambers fullname: Chambers, Christina D. email: chchambers@ucsd.edu organization: Department of Pediatrics, University of California San Diego, La Jolla, CA, United States – sequence: 2 givenname: Diana surname: Johnson fullname: Johnson, Diana organization: Department of Pediatrics, University of California San Diego, La Jolla, CA, United States – sequence: 3 givenname: Ronghui surname: Xu fullname: Xu, Ronghui organization: Department of Family and Preventive Medicine, University of California San Diego, La Jolla, CA, United States – sequence: 4 givenname: Yunjun surname: Luo fullname: Luo, Yunjun organization: Department of Pediatrics, University of California San Diego, La Jolla, CA, United States – sequence: 5 givenname: Carol surname: Louik fullname: Louik, Carol organization: Slone Epidemiology Center at Boston University, Boston, MA, United States – sequence: 6 givenname: Allen A. surname: Mitchell fullname: Mitchell, Allen A. organization: Slone Epidemiology Center at Boston University, Boston, MA, United States – sequence: 7 givenname: Michael surname: Schatz fullname: Schatz, Michael organization: American Academy of Allergy Asthma and Immunology, Milwaukee, WI, United States – sequence: 8 givenname: Kenneth L. surname: Jones fullname: Jones, Kenneth L. organization: Department of Pediatrics, University of California San Diego, La Jolla, CA, United States |
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ContentType | Journal Article |
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Copyright | 2013 Elsevier Ltd Elsevier Ltd 2015 INIST-CNRS Copyright © 2013 Elsevier Ltd. All rights reserved. Copyright Elsevier Limited Oct 17, 2013 |
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DOI | 10.1016/j.vaccine.2013.08.097 |
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Keywords | Pregnancy Birth defects Pandemic H1N1 influenza vaccination Small for gestational age Spontaneous abortion Preterm delivery Human Intrauterine growth retardation Pregnancy disorders Vaccination Premature delivery Orthomyxoviridae Infant Vaccine Abortion Virus Fetal diseases Influenzavirus A Prematurity Influenza A virus |
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Asthma medication use in pregnancy and fetal growth publication-title: J Allergy Clin Immunol doi: 10.1016/j.jaci.2005.05.027 |
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Snippet | •Information is needed on safety of pandemic H1N1 influenza vaccines in pregnancy.•1032 exposed pregnant women were followed to pregnancy outcome,... Highlights•Information is needed on safety of pandemic H1N1 influenza vaccines in pregnancy. •1032 exposed pregnant women were followed to pregnancy outcome,... There is a need for additional information on the fetal risks and relative safety of the pandemic H1N1 monovalent or trivalent influenza (pH1N1)-containing... Introduction There is a need for additional information on the fetal risks and relative safety of the pandemic H1N1 monovalent or trivalent influenza... Introduction: There is a need for additional information on the fetal risks and relative safety of the pandemic H1N1 monovalent or trivalent influenza... |
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SubjectTerms | Abortion abortion (animals) Abortion, Spontaneous - epidemiology Adult Allergy and Immunology Applied microbiology Biological and medical sciences Birth defects Canada cohort studies confidence interval congenital abnormalities Congenital Abnormalities - epidemiology Epidemiological Monitoring Exposure Female Fetuses Fundamental and applied biological sciences. Psychology gestational age Humans Immunization Infant, Newborn Infant, Small for Gestational Age Infants influenza Influenza A Virus, H1N1 Subtype Influenza Vaccines - administration & dosage Influenza Vaccines - adverse effects Influenza, Human - prevention & control Interviews Microbiology Miscellaneous pandemic Pandemic H1N1 influenza vaccination Pandemics Pregnancy Premature Birth - epidemiology Preterm delivery Prospective Studies Risk Risk assessment Safety Small for gestational age Spontaneous abortion Studies Swine flu United States Vaccines Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) Virology women |
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Title | Risks and safety of pandemic h1n1 influenza vaccine in pregnancy: Birth defects, spontaneous abortion, preterm delivery, and small for gestational age infants |
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