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Cambridge University Press
978-1-108-71663-5 — Infections in Pregnancy
Edited by Adel Elkady , Prabha Sinha , Soad Ali Zaki Hassan
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Infections in Pregnancy

© in this web service Cambridge University Press www.cambridge.org


Cambridge University Press
978-1-108-71663-5 — Infections in Pregnancy
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Cambridge University Press
978-1-108-71663-5 — Infections in Pregnancy
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Infections in Pregnancy
An Evidence-Based Approach
Edited by
Adel Elkady
Police Force Hospital, Cairo, Egypt

Prabha Sinha
College of Medical and Health Sciences, National University of Science and Technology, Oman

Soad Ali Zaki Hassan


Alexandria University, Alexandria Governorate, Egypt

© in this web service Cambridge University Press www.cambridge.org


Cambridge University Press
978-1-108-71663-5 — Infections in Pregnancy
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University Printing House, Cambridge CB2 8BS, United Kingdom


One Liberty Plaza, 20th Floor, New York, NY 10006, USA
477 Williamstown Road, Port Melbourne, VIC 3207, Australia
314–321, 3rd Floor, Plot 3, Splendor Forum, Jasola District Centre, New Delhi – 110025, India
79 Anson Road, #06–04/06, Singapore 079906

Cambridge University Press is part of the University of Cambridge.


It furthers the University’s mission by disseminating knowledge in the pursuit of
education, learning, and research at the highest international levels of excellence.

www.cambridge.org
Information on this title: www.cambridge.org/9781108716635
DOI: 10.1017/9781108650434
© Adel Elkady, Prabha Sinha and Soad Ali Zaki Hassan 2019
This publication is in copyright. Subject to statutory exception
and to the provisions of relevant collective licensing agreements,
no reproduction of any part may take place without the written
permission of Cambridge University Press.
First published 2019
Printed and bound in Great Britain by Clays Ltd, Elcograf S.p.A.
A catalogue record for this publication is available from the British Library.
Library of Congress Cataloging-in-Publication Data
Names: Elkady, Adel, editor. | Sinha, P. (Prabha), editor. | Hassan, Soad Ali Zaki, editor.
Title: Infections in pregnancy: an evidence-based approach / edited by Adel Elkady, Prabha Sinha,
Soad Ali Zaki Hassan.
Other titles: Infections in pregnancy (Elkady)
Description: Cambridge, United Kingdom ; New York, NY : Cambridge University Press, 2019. |
Includes bibliographical
references and index.
Identifiers: LCCN 2018042769 | ISBN 9781108716635 (pbk.)
Subjects: | MESH: Pregnancy Complications, Infectious
Classification: LCC RG571 | NLM WQ 256 | DDC 618.3–dc23
LC record available at https://lccn.loc.gov/2018042769
ISBN 978-1-108-71663-5 Paperback
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URLs for external or third-party internet websites referred to in this publication
and does not guarantee that any content on such websites is, or will remain,
accurate or appropriate.
................................................................................................................................
Every effort has been made in preparing this book to provide accurate and up-to-date
information that is in accord with accepted standards and practice at the time
of publication. Although case histories are drawn from actual cases, every effort has been
made to disguise the identities of the individuals involved. Nevertheless, the authors,
editors and publishers can make no warranties that the information contained herein is
totally free from error, not least because clinical standards are constantly changing through
research and regulation. The authors, editors and publishers therefore disclaim all liability
for direct or consequential damages resulting from the use of material contained in this
book. Readers are strongly advised to pay careful attention to information provided by the
manufacturer of any drugs or equipment that they plan to use.

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Cambridge University Press
978-1-108-71663-5 — Infections in Pregnancy
Edited by Adel Elkady , Prabha Sinha , Soad Ali Zaki Hassan
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Contents
List of Contributors vii
Foreword ix
Preface xi

I Vaccination 12 Ebola 69
Adel Elkady, Prabha Sinha and Soad Ali
1 Vaccination in Pregnancy 1 Zaki Hassan
Akanksha Sood
13 Chikungunya 73
Shabnum Sibtain
II Infections in Pregnancy 14 Antibiotics during Pregnancy and Methicillin-
2 Viral Hepatitis 9 Resistant Staphylococcus aureus (MRSA) 76
Rashda Imran Adel Elkady, Prabha Sinha and Soad Ali
Zaki Hassan
3 HIV Infection 18
Maimoona Ahmed 15 Gonorrhoea, Syphilis and Lymphogranuloma
Venereum 83
4 Herpes Infections and Nutan Mishra
Measles 29
Rashda Imran 16 Mycoplasma, Ureaplasma, Chancroid,
Granuloma Inguinale (Donovanosis) 92
5 Zika Virus 42 Nutan Mishra
Youssef Abo Elwan
17 Genital Chlamydia trachomatis and Bacterial
6 Parvovirus 45 Vaginosis 100
Mohammed Hamed Adel Elkady, Prabha Sinha and Soad Ali
7 Influenza 50 Zaki Hassan
Adel Elkady, Prabha Sinha and Soad Ali 18 Streptococcal Infection 109
Zaki Hassan Rachana Dwivedi and Shabnum Sibtain
8 Cytomegalovirus 54 19 Enterococci and Bacterial
Tarek El Shamy Infections 115
9 Dengue Fever 60 Varsha S. Puranik
Adel Elkady, Prabha Sinha and Soad Ali 20 Listeriosis 121
Zaki Hassan Adel Elkady, Prabha Sinha and Soad Ali
10 Rubella 63 Zaki Hassan
Rania Hassan Mostafa Ahmed 21 Urinary Tract Infection 129
11 Molluscum Contagiosum 67 Ashok Kumar
Adel Elkady, Prabha Sinha and Soad Ali 22 Infections and Preterm Labour 134
Zaki Hassan Christine Helmy Samuel Azer

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Cambridge University Press
978-1-108-71663-5 — Infections in Pregnancy
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Contents

23 Appendicitis in Pregnancy 139 III Postpartum Infections


Christine Helmy Samuel Azer
29 Puerperal Sepsis 175
24 Complications Associated with Legal Christine Helmy Samuel Azer
Termination of Pregnancy 143
Christine Helmy Samuel Azer 30 Puerperal Endometritis 180
Christine Helmy Samuel Azer
25 Tuberculosis 146
Maimoona Ahmed 31 Puerperal Mastitis 183
Christine Helmy Samuel Azer
26 Vulvo Vaginitis, Candida (Yeast)
Infection 155 32 Breast Abscess 186
Adel Elkady, Prabha Sinha and Soad Ali Christine Helmy Samuel Azer
Zaki Hassan
33 Pelvic Inflammatory Disease 188
27 Malaria 159 Ahmed Khalil
Bhavya Balasubramanya
28 Parasitic Infestation: Protozoa 164
Mithila B. Prasad
Index 193

vi

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978-1-108-71663-5 — Infections in Pregnancy
Edited by Adel Elkady , Prabha Sinha , Soad Ali Zaki Hassan
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Contributors

Maimoona Ahmed MS-FNB (High-Risk Pregnancy Ahmed Khalil MSc MD MRCOG


& Perinatology) Department of Obstetrics & Gynaecology, Benha
Maternal–Fetal Medicine Department, Cloudnine University, Benha, Egypt and Department of
Hospital, Mumbai, India Obstetrics & Gynaecology, Medway Maritime
Hospital, Gillingham, UK
Rania Hassan Mostafa Ahmed MD
Department of Obstetrics & Gynaecology, Ain Shams Ashok Kumar FRCSI FRCS (Glas)
University, Cairo, Egypt Locum Consultant General Surgeon, UK
Christine Helmy Samuel Azer MRCOG FEOG- Nutan Mishra MD FRCOG
EBCOG Department of Obstetrics & Gynaecology,
Department of Obstetrics & Gynaecology, Dr Buckinghamshire Healthcare NHS Trust, Aylesbury,
Sulaiman Al Habib Medical Centre, Dubai, United UK
Arab Emirates
Mithila B. Prasad DGO MRCOG
Bhavya Balasubramanya MD (Community Department of Obstetrics & Gynaecology, North-
Medicine) West Deanery, Wythenshawe Hospital, Manchester,
Rural Unit for Health and Social Affairs, Department UK
of Community Health, Christian Medical College,
Vellore, Tamil Nadu, India Varsha S. Puranik MD Microbiology
Department of Microbiology, Cauvery Hospital &
Rachana Dwivedi FRCOG FICOG PGC (USS) College of Allied Health Sciences, Mysuru, Karnataka,
DFFP India
Department of Obstetrics & Gynaecology, Royal
Bournemouth & Christchurch Hospitals NHS Trust, Tarek El Shamy MSc MRCOG PGCert
Bournemouth, UK (Ultrasound)
Obstetrics and Gynaecology Department, West
Adel Elkady DGO FRCOG FICS Middlesex University Hospital, London, UK
Boulak El Dakror Hospital, Cairo, Egypt
Shabnum Sibtain FRCOG
Youssef Abo Elwan MD MRCOG Department of Obstetrics & Gynaecology, Azra
Department of Obstetrics & Gynaecology, Zagazig Naheed Medical College, Lahore, Pakistan
University, Zagazig City, Egypt
Prabha Sinha DGO FRCOG MRCPI
Mohammed Hamed Khedr MSc Department of Obstetrics and Gynaecology, Oman
Police Force Hospital, Giza, Egypt Medical College, Sultanate of Oman
Professor Soad Ali Zaki Hassan Akanksha Sood MS (ObGyn) DNB MRCOG
Professor of Microbiology, Alexandria University, Egypt FACOG
Rashda Imran FCPS MRCOG Department of Reproductive Medicine, St Mary’s
St Mary’s Hospital, Manchester, UK Hospital, Manchester, UK

vii

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978-1-108-71663-5 — Infections in Pregnancy
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Foreword

This book is particularly welcome, as pregnant women over 40 years. He has marshalled an international
are exceptionally vulnerable to infection, due to an group of obstetricians and gynaecologists who are
increased immune tolerance which is a protective familiar with diseases that many of us will have
mechanism for the fetus; physiological changes in the never come across, but with our increasing immigrant
mother which make them more susceptible to infec- and nomadic populations we need to be aware of
tion; and the addition of a placenta which can house them as their incidence in the UK and globally is
pathogens. Therefore as an obstetrician, infection is a rising.
problem that we all find challenging at some stage. To This book should be read by every obstetrician,
date we have not had access to a book such as this. from trainee to senior consultant, to understand
This book gives a comprehensive coverage of infec- about infections in pregnancy, both how they present
tion in pregnancy, from simple everyday infections to and how they are managed, and then it will serve as a
severe life-threatening infections. The authors com- valuable reference book on the shelf for any challen-
mence by addressing vaccination in pregnancy, and ging infection problems one might come across in
then provide extensive coverage of a diverse range of one’s everyday future clinical practice.
infections not only during pregnancy but postpartum.
The book has been directed by an internationally Janice Rymer, Professor of Obstetrics and Gynaecology,
renowned obstetrician who has been practising for King’s College London

ix

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Preface

We the editors, Adel, Prabha and Souad, are pleased We felt the medical literature was lacking an up-
and honoured to offer this book to our dear readers. to-date book to help and guide health care providers
Infections during pregnancy are major causes and health authorities in the diagnosis, management
of maternal and fetal morbidity and mortality. and prevention of these serious conditions.
Infections can be transmitted to the fetus transpla- We have aimed to present the latest information,
centally and during birth, which becomes apparent knowledge and different national and international
during the early days of life. Postnatal infection can guidelines to offer our readers a useful, comprehen-
occur through breastfeeding or direct contact. sive and handy guide. We have tried to cover all
The clinical manifestations of fetal/neonatal infec- possible infections.
tions vary depending on the infective agent and gesta- We welcome any contact or criticisms from our
tional age at exposure. The risk of infection is higher readers.
during earlier gestation age at exposure, resulting in a
severe congenital malformation syndrome. Adel Elkady
Infections in pregnancy can have serious maternal Prabha Sinha
and fetal implications; even death can result if infec- Soad Hassan
tion is severe and is not immediately diagnosed and
properly managed, particularly during epidemics.

xi

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Section 1 Vaccination
Chapter
Vaccination in Pregnancy

1 Akanksha Sood

Introduction pathogenicity by repeated culturing. They do not


cause illness, but retain their ability to replicate and
Vaccination is one of the most cost-effective success-
stimulate production of antibodies. The immune
ful public health interventions. Maternal vaccination
response is virtually identical to the naturally pro-
protects both mother and baby from the morbidity of
duced long-term immunity with one dose, except
certain preventable diseases.
oral vaccines which need repeating.6
Side effects of live vaccines are:
Basics of Immunology • The organisms might revert to a virulent
Immune response is the ability of the body to identify, form resulting in infection although of milder
recognise and defend against harmful toxins, infec- form
tions or disease by making specific antibodies or sen- • Contraindicated in pregnancy as they have the
sitised white blood cells.1,2 potential to infect the fetus
The different antibodies produced by plasma cells
• In immunocompromised individuals they cause
as classified by isotype are five major isotypes (IgA,
uncontrolled replication of organisms, which may
IgD, IgE, IgG and IgM).3
cause fatal reaction
Immunity is produced by one of two body reactions:
• Vaccine can become ineffective by heat, light,
1. Active immunity is the ability to produce presence of antibodies from other sources
immunity either by exposure to the disease, (transplacental or blood transfusion)6
infection, organism or by vaccination (killed or
Examples of a live attenuated vaccine are measles–
weakened form of organism).4 The protection is
mumps–rubella vaccine (MMR combined vaccine),
provided by a person’s own immune system, is
varicella, measles, rotavirus, smallpox, chickenpox,
natural and often lasts for life.
yellow fever or the antibacterial vaccines, Bacillus
2. Passive immunity involves administration of
Calmette-Guérin (BCG) vaccine and oral polio
immunoglobulins which provides a quick but
vaccine.
short-term immunity that wanes with time. These
include varicella zoster hepatitis
B immunoglobulin or transplacental transfer of 2 Live Inactivated Vaccines
antibodies from the mother. These vaccines are produced by growing bacteria or
the virus in culture media and then inactivating it
with heat or chemicals. They are not alive and cannot
Vaccination replicate, and are therefore unable to cause disease
Vaccination stimulates immune response against even in an immune-deficient person.
a specific antigen and provides protection from con- Unlike live vaccines, these are not affected by
tracting the disease by forming antibodies.5 circulating antibodies and hence can be given when
antibodies are present in the blood, e.g. in infancy or
Types of Vaccines following receipt of antibody-containing blood pro-
ducts. They require multiple doses. The first dose
1 Live Attenuated Vaccines only primes the immune system. A protective
These vaccines contain pathogens, which have immune response develops after the second or
been weakened to diminish their infectivity and third dose.
1
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Section 1: Vaccination

Antibody titres diminish with time and, as a result, 2. Vaccinations specially recommended during
may require to be boosted with periodic supplemental pregnancy, e.g. the trivalent inactivated influenza
doses. vaccine during the influenza season.
Examples of inactivated vaccines: hepatitis A, flu, 3. Vaccinations recommended for women at risk of
polio, rabies. exposure (hepatitis B).8

3 Recombinant Vaccines
Recombinant vaccines are produced by genetic engi- Rubella
neering technology. Currently eight such vaccines are Vaccine against rubella is routinely given to all as part
available: of childhood immunisation, and 97 per cent of
1. Hepatitis B vaccine women in the UK are immune.
2. HPV (human papillomavirus) vaccine Rubella vaccine is contraindicated during preg-
nancy as it is presumed to cause fetal anomalies;
3. Live typhoid vaccine
however, if the vaccine is inadvertently administered
4. Live attenuated influenza vaccine (LAIV)
to a pregnant woman, or pregnancy occurs within 28
5. Whooping cough (part of the diphtheria, tetanus
days of vaccination, it should not be the reason for
and pertussis (DTaP) combined vaccine)
termination of pregnancy. She should be counselled
6. Pneumococcal vaccine about the theoretical risks to the fetus and the need for
7. Meningococcal vaccine close follow-up.9
8. Shingles vaccine At the preconception counselling, a non-immune
woman (immunoglobin (IgG) levels <10 IU/mL) should
4 Toxoid Vaccines be offered MMR vaccine as a single dose and counselled
Toxoid vaccines implies administration of the toxin to avoid pregnancy for 28 days after vaccination.
produced by certain bacteria (tetanus or diphtheria) A pregnant non-immune woman should be
after making them harmless. offered vaccination during the postpartum period
even if she is breastfeeding. Rubella virus is secreted
Vaccination in Pregnancy in breastmilk; seroconversion without serious infec-
Vaccination during pregnancy is not a routine event, tion is reported in breastfed infants.
and attenuated live virus vaccinations are generally
contraindicated. A woman should be up to date with Varicella Zoster (VZV)
her routine immunisation before pregnancy against Approximately 90 per cent of women are immune
preventable diseases. because of childhood vaccination or exposure.
Vaccination during pregnancy is warranted when: Universal screening to check immune status is not
1. The risk of exposure is high recommended; however, in certain situations the
2. Infection poses risk to mother/fetus immune status should be checked.10
3. Vaccine is unlikely to be harmful 1. Women with an uncertain or no previous
The benefits to mother and fetus should outweigh chickenpox infection
the risk of vaccination. It is preferable to delay 2. Those who come from tropical or subtropical
immunisation until the second trimester to avoid countries
the period of organogenesis unless medically 3. Those who had an exposure to the infection
indicated; however, no evidence exists of risk to Varicella vaccine contains live attenuated virus
fetus from inactivated vaccines or toxoids.7,8 derived from the Oka strain of VZV and is contra-
[evidence levels EL 2 & 3] indicated in pregnancy due to theoretical risks of fetal
In the clinical context, vaccines can be broadly infection.
divided into three groups. If a woman is sero-negative, she should be offered
1. Vaccines contraindicated during pregnancy: live postpartum immunisation of two separate doses four
attenuated vaccines could cross the placenta and to eight weeks apart and advised to avoid pregnancy
result in viral infection of the fetus, e.g. MMR and for four weeks after the second dose. She should be
the varicella vaccines. reassured about its safety during breastfeeding.

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Chapter 1: Vaccination in Pregnancy

Women are advised to avoid contact with chick- Argentina currently recommend vaccination against
enpox or shingles and to inform a health care worker whooping cough in pregnancy.
in case of significant contact. Contact with pregnant Pregnant women need to be vaccinated even if
women should be avoided if a post-vaccination rash they have been vaccinated in childhood or in
occurs. [EL 2] a previous pregnancy. Both randomised clinical trials
If the pregnant woman is not immune to VZV and and cohort studies support its safety (no increase in
she has had a significant exposure, she should be pregnancy complications, preterm birth, low birth-
offered varicella zoster immunoglobulin (VZIG) as weight, congenital anomalies, spontaneous abortion,
soon as possible.10 or stillbirth).13 [EL 1]
Inadvertent exposure to vaccine in pregnancy is Vaccination of the close contacts of the neonate
not an indication for termination as there has been no (mother’s partner) is recommended as a strategy for
increase in the risk of fetal abnormality above the newborn prevention, when the mother has not been
background risk. timely vaccinated.13
A review of the Pregnancy Registry for VARIVAX
following 362 pregnancies inadvertently exposed to Tetanus
varicella vaccine showed there was no case of conge-
Worldwide, each year, tetanus kills an estimated
nital varicella syndrome and no abnormal features or
180 000 neonates (about 5 per cent of all neonatal
birth defects in the infants. [EL 2]
deaths, 2002 data) and up to 30 000 women (about
5 per cent of all maternal deaths).
Whooping Cough (Pertussis) Tetanus vaccine is a toxoid vaccine and protects
This is an acute bacterial infection. It is highly con- against both maternal and neonatal tetanus.
tagious, caused by Bordetella pertussis spreading All pregnant women should receive a tetanus tox-
through droplets (coughing and sneezing). oid vaccine during each pregnancy, irrespective of any
Vaccinating pregnant women against whooping previous history of immunisation.
cough has been highly effective in protecting newborn The optimum time for passive antibody transfer is
babies. It offers immediate protection to cover the from the 27th until the 36th week. A booster dose is
newborn until they can have their first vaccination at indicated if a pregnant woman is exposed to the risk of
two months of age. tetanus infection during or immediately after delivery.
Babies born to women vaccinated at least a week
before birth had a 91 per cent reduced risk of becom- Diphtheria
ing ill with whooping cough in their first weeks of life,
Diphtheria can lead to breathing problems, heart fail-
compared with babies whose mothers were not
ure, paralysis and death. The Tdap vaccine has a dose
vaccinated.11
of tetanus toxoid, reduced diphtheria toxoid and acel-
In 2012, the UK experienced a nationwide epi-
lular pertussis.
demic of pertussis, resulting in serious complications
All pregnant women should get a Tdap vaccina-
(pneumonia, encephalitis, seizures, brain damage)
tion in each pregnancy.
including death, especially in young babies.
A programme for the vaccination of pregnant
women between 28 and 32 weeks against pertussis Influenza
was introduced in October 2012.11 ‘The flu’, as is it commonly known, is a highly con-
However, it can be given at any time until the start tagious disease caused by an influenza virus which
of labour, although after 38 weeks the fetus is less occurs in all parts of the world. It spreads by coughing
likely to be protected by maternal immunity. and sneezing of an infected person.
The Joint Committee on Vaccination and There are three types of Influenza virus, type
Immunisation (JCVI) of the Royal College of A (H1N1), type B (H3N2) and type C.
Obstetricians and Gynaecologists (RCOG) recom- Type C generally causes mild respiratory illness
mended that from April 2016 the vaccination should and does not usually cause epidemics.14
be offered from 20 weeks (after the anomaly scan).12 Influenza A and B viruses cause outbreaks or epi-
Many countries including the United States, demics and therefore should be included in seasonal
Spain, Australia, New Zealand, Belgium and influenza vaccine.

3
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Section 1: Vaccination

Pregnant women are particularly vulnerable to The vaccine offered is given as intramuscular
influenza. Strong evidence shows that pregnant and injection; it takes up to two weeks after vaccination
postpartum women are at higher risk of severe illness to give protection and is 50 per cent effective.
and complications than women who are not pregnant.
Due to reduced immunity during pregnancy, Human Papillomavirus (HPV)
influenza increases the risk for both mother and Human papillomavirus (HPV) infection during preg-
fetus with resulting preterm and low birthweight nancy is not well studied. There has not been any
babies. association with an increased risk of birth defects.
Influenza vaccine is an integral element of pre- A link between HPV infection and preterm birth
conception, prenatal and postpartum care. was shown in a case control study.18
Studies have shown that vaccination reduces the Currently there are two inactive recombinant
risk of serious maternal medical complications and HPV vaccines, the quadrivalent vaccine, which pro-
provides passive protection to the neonate from influ- tects against HPV types 6, 11, 16 and 18, and
enza in the first six months before the baby is eligible a bivalent vaccine, which provides protection against
for vaccination. HPV types 16 and 18.
Recent systematic review has confirmed that The Centers for Disease Control and Prevention
decreased risk of laboratory-confirmed influenza (CDC) do not recommend HPV vaccination during
infection in infants is associated with uptake of influ- pregnancy, nor do they recommend testing for preg-
enza vaccine during pregnancy.15 [EL 1] nancy before the routine HPV vaccination.19,20
There are two types of vaccine: the inactivated If the vaccine has been inadvertently given to
(injection) and the live attenuated (intra-nasal spray). a pregnant woman, there is no need for termination
The live attenuated nasal spray is not recom- of pregnancy, but the second dose should be post-
mended for pregnant women. poned until after the pregnancy. If a woman has
Pregnant women should be counselled about the received an HPV vaccine and then plans to become
benefits of the single influenza vaccine for them- pregnant, there is no need to delay pregnancy, as the
selves and their unborn child. According to the HPV vaccines are inactive.
Mothers and Babies Reducing Risk through Audits In a recent retrospective observational cohort
and Confidential Enquiries, UK (MBRRACE-UK) study, quadrivalent HPV vaccine inadvertently admi-
report 2010–12, 1 in 11 pregnant women died from nistered in pregnancy or during the periconceptional
flu, and more than half of these deaths could have period was not associated with adverse pregnancy or
been prevented by a flu vaccination.16 Increasing birth outcomes [EL 1].
immunisation rates in pregnancy therefore remain
important. Hepatitis A
Increasing immunisation rates in pregnancy
This is a formalin inactivated vaccine. The theoretical
against seasonal influenza must remain a public
risk to the developing fetus is expected to be low.
health priority.
The safety during pregnancy has not been deter-
It is recommended that all pregnant women have
mined. The risk associated with vaccination should be
influenza vaccine at whatever stage of pregnancy
weighed against the risk of hepatitis A in pregnant
when the pandemic starts. The vaccine protects
women. It is recommended for pregnant women who
against three of the most likely strains. It is important
are at high risk due to travel or pre-existing high-risk
to have the vaccine every year as flu virus is very
condition, e.g.
variable and strains change over time.
It is strongly recommended by RCOG that flu • Long-term liver disease
vaccine be offered17 • Haemophilia
• Intravenous drug users
• To all pregnant women
• Occupational risk – working with or near sewage,
• In each pregnancy
working in institutions where levels of personal
• At any stage of pregnancy (first, second or third
hygiene may be poor
trimester)
• Working with primates (monkeys, apes, gorillas
• To have the vaccine in autumn before the outbreak
etc.)20
of flu starts

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