Published online by Cambridge University Press: 06 July 2010
Introduction
Pregnancy is a vulnerable period for the acquisition of infections and infectious diseases. Not only can the pregnant woman herself become infected, but fetal and/or neonatal transmission may also occur. Although pregnancy does not usually affect the incidence and severity of infections, some physiological adaptations of pregnancy can result in increased risk for some infections particularly urinary tract infections, pneumonia and chorioamnionitis. In addition to maternal sequelae, the developing fetus is often placed at risk secondary to hyperpyrexia, hypoxia, preterm labour and congenital infection. The number of maternal infections known to be associated with adverse pregnancy outcomes continues to increase. Adverse pregnancy outcomes can be a direct consequence of fetal or neonatal infection or an indirect effect secondary to vaginal, cervical or intrauterine infections. Specific fetal risks are highly dependent on the causal organism, potential for transplacental passage, timing of exposure and maternal/ fetal immune status. Adverse outcomes associated with maternal infection during pregnancy are varied and include infertility, ectopic pregnancy, miscarriage, congenital anomalies, stillbirth, intrauterine growth retardation, preterm delivery, neonatal death, and long-term disability of the infant.
Maternal infection and pregnancy
Infections are common during pregnancy, but the risks associated with infections vary by pathogen and disease site (Alexander, 1984). Infections such as acute cystitis, upper respiratory viral infections and trichomoniasis are generally of concern for maternal health but pose less risk to the fetus. In contrast, infections such as cytomegalovirus (CMV), genital herpes simplex virus (HSV), parvovirus, and rubella can lead to significant fetal morbidity/mortality but have little or no maternal sequelae. Similarly, relatively innocuous constituents of the genital and rectal flora, such as group B streptococcus (Streptococcus agalactica) and Escherichia coli, may represent benign maternal colonization.
To save this book to your Kindle, first ensure no-reply@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
Find out more about the Kindle Personal Document Service.
To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.
To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.