Risk of cytomegalovirus‐associated sequelae in relation to time of infection and findings on prenatal imaging
ABSTRACT Objective To determine the outcome of pregnancies with documented fetal cytomegalovirus (CMV) infection with and without abnormal findings on ultrasound examination and magnetic resonance imaging (MRI). Methods In this prospective cohort study of pregnant women with documented fetal CMV inf...
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Veröffentlicht in: | Ultrasound in obstetrics & gynecology 2013-05, Vol.41 (5), p.508-514 |
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creator | Lipitz, S. Yinon, Y. Malinger, G. Yagel, S. Levit, L. Hoffman, C. Rantzer, R. Weisz, B. |
description | ABSTRACT
Objective
To determine the outcome of pregnancies with documented fetal cytomegalovirus (CMV) infection with and without abnormal findings on ultrasound examination and magnetic resonance imaging (MRI).
Methods
In this prospective cohort study of pregnant women with documented fetal CMV infection, vertical CMV transmission occurred during the first and second trimesters following primary maternal infection. Patients underwent serial prenatal ultrasound scans and fetal MRI. All neonates underwent ocular fundus examination, ultrasound brain scan and hearing evaluation, and were then followed periodically by a pediatrician.
Results
Primary CMV infection occurred during the first and second trimesters of pregnancy in 71 and 74 patients, respectively. Seven patients (4.8%) decided to terminate pregnancy because of prenatal findings and one neonate died because of CMV complications. Patients with first‐trimester infection had infants with significantly more associated sequelae (either auditory damage or neurodevelopmental disabilities) than did patients with second‐trimester infection (19.7% vs 5.6%, respectively; P = 0.01). Abnormal prenatal findings on ultrasound examination were associated with increased risk of sequelae. When both ultrasound and MRI findings were normal, the rate of sequelae was decreased to 15.6% for first‐trimester infections and to 2.0% for second‐trimester infections, partial hearing loss being the sequela in most cases. In the presence of abnormal ultrasound and/or MRI findings the risk was 25% and 16%, respectively, and in most cases the sequelae were deafness and neurodevelopmental delay. The rate of intrauterine growth restriction (IUGR) in the study group was 11.7% and was not affected by the time of onset of maternal infection. Isolated IUGR was not associated with increased risk of sequelae.
Conclusion
The risk of sequelae is higher following first‐than second‐trimester CMV infection. However, the risk of severe sequelae is significantly reduced in the presence of normal prenatal ultrasound and MRI findings. Copyright © 2013 ISUOG. Published by John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/uog.12377 |
format | Article |
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Objective
To determine the outcome of pregnancies with documented fetal cytomegalovirus (CMV) infection with and without abnormal findings on ultrasound examination and magnetic resonance imaging (MRI).
Methods
In this prospective cohort study of pregnant women with documented fetal CMV infection, vertical CMV transmission occurred during the first and second trimesters following primary maternal infection. Patients underwent serial prenatal ultrasound scans and fetal MRI. All neonates underwent ocular fundus examination, ultrasound brain scan and hearing evaluation, and were then followed periodically by a pediatrician.
Results
Primary CMV infection occurred during the first and second trimesters of pregnancy in 71 and 74 patients, respectively. Seven patients (4.8%) decided to terminate pregnancy because of prenatal findings and one neonate died because of CMV complications. Patients with first‐trimester infection had infants with significantly more associated sequelae (either auditory damage or neurodevelopmental disabilities) than did patients with second‐trimester infection (19.7% vs 5.6%, respectively; P = 0.01). Abnormal prenatal findings on ultrasound examination were associated with increased risk of sequelae. When both ultrasound and MRI findings were normal, the rate of sequelae was decreased to 15.6% for first‐trimester infections and to 2.0% for second‐trimester infections, partial hearing loss being the sequela in most cases. In the presence of abnormal ultrasound and/or MRI findings the risk was 25% and 16%, respectively, and in most cases the sequelae were deafness and neurodevelopmental delay. The rate of intrauterine growth restriction (IUGR) in the study group was 11.7% and was not affected by the time of onset of maternal infection. Isolated IUGR was not associated with increased risk of sequelae.
Conclusion
The risk of sequelae is higher following first‐than second‐trimester CMV infection. However, the risk of severe sequelae is significantly reduced in the presence of normal prenatal ultrasound and MRI findings. Copyright © 2013 ISUOG. Published by John Wiley & Sons, Ltd.</description><identifier>ISSN: 0960-7692</identifier><identifier>EISSN: 1469-0705</identifier><identifier>DOI: 10.1002/uog.12377</identifier><identifier>PMID: 23288698</identifier><identifier>CODEN: UOGYFJ</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Abortion, Induced ; Brain ; Cytomegalovirus ; Cytomegalovirus Infections - diagnosis ; Cytomegalovirus Infections - transmission ; Developmental Disabilities - etiology ; Female ; Fetal Diseases - diagnosis ; Hearing Loss - embryology ; Humans ; Infectious Disease Transmission, Vertical ; Magnetic Resonance Imaging ; MRI ; Pregnancy ; Pregnancy Complications, Infectious - diagnosis ; Pregnancy Outcome ; Pregnancy Trimester, First ; Pregnancy Trimester, Second ; Prenatal Diagnosis - methods ; Prenatal Exposure Delayed Effects ; Prospective Studies ; Risk Factors ; Ultrasonography, Prenatal ; ultrasound</subject><ispartof>Ultrasound in obstetrics & gynecology, 2013-05, Vol.41 (5), p.508-514</ispartof><rights>Copyright © 2013 ISUOG. Published by John Wiley & Sons Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4877-535090a068cea08c81852b94f484cbe03174433e0fb2c0910932421dfed0881b3</citedby><cites>FETCH-LOGICAL-c4877-535090a068cea08c81852b94f484cbe03174433e0fb2c0910932421dfed0881b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fuog.12377$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fuog.12377$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23288698$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lipitz, S.</creatorcontrib><creatorcontrib>Yinon, Y.</creatorcontrib><creatorcontrib>Malinger, G.</creatorcontrib><creatorcontrib>Yagel, S.</creatorcontrib><creatorcontrib>Levit, L.</creatorcontrib><creatorcontrib>Hoffman, C.</creatorcontrib><creatorcontrib>Rantzer, R.</creatorcontrib><creatorcontrib>Weisz, B.</creatorcontrib><title>Risk of cytomegalovirus‐associated sequelae in relation to time of infection and findings on prenatal imaging</title><title>Ultrasound in obstetrics & gynecology</title><addtitle>Ultrasound Obstet Gynecol</addtitle><description>ABSTRACT
Objective
To determine the outcome of pregnancies with documented fetal cytomegalovirus (CMV) infection with and without abnormal findings on ultrasound examination and magnetic resonance imaging (MRI).
Methods
In this prospective cohort study of pregnant women with documented fetal CMV infection, vertical CMV transmission occurred during the first and second trimesters following primary maternal infection. Patients underwent serial prenatal ultrasound scans and fetal MRI. All neonates underwent ocular fundus examination, ultrasound brain scan and hearing evaluation, and were then followed periodically by a pediatrician.
Results
Primary CMV infection occurred during the first and second trimesters of pregnancy in 71 and 74 patients, respectively. Seven patients (4.8%) decided to terminate pregnancy because of prenatal findings and one neonate died because of CMV complications. Patients with first‐trimester infection had infants with significantly more associated sequelae (either auditory damage or neurodevelopmental disabilities) than did patients with second‐trimester infection (19.7% vs 5.6%, respectively; P = 0.01). Abnormal prenatal findings on ultrasound examination were associated with increased risk of sequelae. When both ultrasound and MRI findings were normal, the rate of sequelae was decreased to 15.6% for first‐trimester infections and to 2.0% for second‐trimester infections, partial hearing loss being the sequela in most cases. In the presence of abnormal ultrasound and/or MRI findings the risk was 25% and 16%, respectively, and in most cases the sequelae were deafness and neurodevelopmental delay. The rate of intrauterine growth restriction (IUGR) in the study group was 11.7% and was not affected by the time of onset of maternal infection. Isolated IUGR was not associated with increased risk of sequelae.
Conclusion
The risk of sequelae is higher following first‐than second‐trimester CMV infection. However, the risk of severe sequelae is significantly reduced in the presence of normal prenatal ultrasound and MRI findings. Copyright © 2013 ISUOG. Published by John Wiley & Sons, Ltd.</description><subject>Abortion, Induced</subject><subject>Brain</subject><subject>Cytomegalovirus</subject><subject>Cytomegalovirus Infections - diagnosis</subject><subject>Cytomegalovirus Infections - transmission</subject><subject>Developmental Disabilities - etiology</subject><subject>Female</subject><subject>Fetal Diseases - diagnosis</subject><subject>Hearing Loss - embryology</subject><subject>Humans</subject><subject>Infectious Disease Transmission, Vertical</subject><subject>Magnetic Resonance Imaging</subject><subject>MRI</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Infectious - diagnosis</subject><subject>Pregnancy Outcome</subject><subject>Pregnancy Trimester, First</subject><subject>Pregnancy Trimester, Second</subject><subject>Prenatal Diagnosis - methods</subject><subject>Prenatal Exposure Delayed Effects</subject><subject>Prospective Studies</subject><subject>Risk Factors</subject><subject>Ultrasonography, Prenatal</subject><subject>ultrasound</subject><issn>0960-7692</issn><issn>1469-0705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAQxy1URJfCoS-ALPUCh7Tjr8Q-VhUUpEqVED1HjjNZuU3sxU5a7Y1H4Bl5ErzdwgEJ9TQf-s1fM_Mn5JjBKQPgZ0tcnzIumuYFWTFZmwoaUAdkBaaGqqkNPySvc74FgFqK-hU55IJrXRu9IvGrz3c0DtRt5zjh2o7x3qcl__rx0-Ycnbcz9jTj9wVHi9QHmkoy-xjoHOnsJ9wN-zCge2za0NPBh96Hdaal3iQMdrYj9ZNdl-Yb8nKwY8a3T_GI3Hz6-O3ic3V1ffnl4vyqclI3TaWEAgMWau3QgnaaacU7IweppesQBGukFAJh6LgDw8AILjnrB-xBa9aJI_J-r7tJseye53by2eE42oBxyS2TQsLuCfp5VEilWGNUXdCTf9DbuKRQDimUkEYorVihPuwpl2LOCYd2k8r5adsyaHeGtcWw9tGwwr57Uly6Cfu_5B-HCnC2Bx78iNv_K7U315d7yd9VtZ--</recordid><startdate>201305</startdate><enddate>201305</enddate><creator>Lipitz, S.</creator><creator>Yinon, Y.</creator><creator>Malinger, G.</creator><creator>Yagel, S.</creator><creator>Levit, L.</creator><creator>Hoffman, C.</creator><creator>Rantzer, R.</creator><creator>Weisz, B.</creator><general>John Wiley & Sons, Ltd</general><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>201305</creationdate><title>Risk of cytomegalovirus‐associated sequelae in relation to time of infection and findings on prenatal imaging</title><author>Lipitz, S. ; Yinon, Y. ; Malinger, G. ; Yagel, S. ; Levit, L. ; Hoffman, C. ; Rantzer, R. ; Weisz, B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4877-535090a068cea08c81852b94f484cbe03174433e0fb2c0910932421dfed0881b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Abortion, Induced</topic><topic>Brain</topic><topic>Cytomegalovirus</topic><topic>Cytomegalovirus Infections - diagnosis</topic><topic>Cytomegalovirus Infections - transmission</topic><topic>Developmental Disabilities - etiology</topic><topic>Female</topic><topic>Fetal Diseases - diagnosis</topic><topic>Hearing Loss - embryology</topic><topic>Humans</topic><topic>Infectious Disease Transmission, Vertical</topic><topic>Magnetic Resonance Imaging</topic><topic>MRI</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Infectious - diagnosis</topic><topic>Pregnancy Outcome</topic><topic>Pregnancy Trimester, First</topic><topic>Pregnancy Trimester, Second</topic><topic>Prenatal Diagnosis - methods</topic><topic>Prenatal Exposure Delayed Effects</topic><topic>Prospective Studies</topic><topic>Risk Factors</topic><topic>Ultrasonography, Prenatal</topic><topic>ultrasound</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lipitz, S.</creatorcontrib><creatorcontrib>Yinon, Y.</creatorcontrib><creatorcontrib>Malinger, G.</creatorcontrib><creatorcontrib>Yagel, S.</creatorcontrib><creatorcontrib>Levit, L.</creatorcontrib><creatorcontrib>Hoffman, C.</creatorcontrib><creatorcontrib>Rantzer, R.</creatorcontrib><creatorcontrib>Weisz, B.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Ultrasound in obstetrics & gynecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lipitz, S.</au><au>Yinon, Y.</au><au>Malinger, G.</au><au>Yagel, S.</au><au>Levit, L.</au><au>Hoffman, C.</au><au>Rantzer, R.</au><au>Weisz, B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk of cytomegalovirus‐associated sequelae in relation to time of infection and findings on prenatal imaging</atitle><jtitle>Ultrasound in obstetrics & gynecology</jtitle><addtitle>Ultrasound Obstet Gynecol</addtitle><date>2013-05</date><risdate>2013</risdate><volume>41</volume><issue>5</issue><spage>508</spage><epage>514</epage><pages>508-514</pages><issn>0960-7692</issn><eissn>1469-0705</eissn><coden>UOGYFJ</coden><abstract>ABSTRACT
Objective
To determine the outcome of pregnancies with documented fetal cytomegalovirus (CMV) infection with and without abnormal findings on ultrasound examination and magnetic resonance imaging (MRI).
Methods
In this prospective cohort study of pregnant women with documented fetal CMV infection, vertical CMV transmission occurred during the first and second trimesters following primary maternal infection. Patients underwent serial prenatal ultrasound scans and fetal MRI. All neonates underwent ocular fundus examination, ultrasound brain scan and hearing evaluation, and were then followed periodically by a pediatrician.
Results
Primary CMV infection occurred during the first and second trimesters of pregnancy in 71 and 74 patients, respectively. Seven patients (4.8%) decided to terminate pregnancy because of prenatal findings and one neonate died because of CMV complications. Patients with first‐trimester infection had infants with significantly more associated sequelae (either auditory damage or neurodevelopmental disabilities) than did patients with second‐trimester infection (19.7% vs 5.6%, respectively; P = 0.01). Abnormal prenatal findings on ultrasound examination were associated with increased risk of sequelae. When both ultrasound and MRI findings were normal, the rate of sequelae was decreased to 15.6% for first‐trimester infections and to 2.0% for second‐trimester infections, partial hearing loss being the sequela in most cases. In the presence of abnormal ultrasound and/or MRI findings the risk was 25% and 16%, respectively, and in most cases the sequelae were deafness and neurodevelopmental delay. The rate of intrauterine growth restriction (IUGR) in the study group was 11.7% and was not affected by the time of onset of maternal infection. Isolated IUGR was not associated with increased risk of sequelae.
Conclusion
The risk of sequelae is higher following first‐than second‐trimester CMV infection. However, the risk of severe sequelae is significantly reduced in the presence of normal prenatal ultrasound and MRI findings. Copyright © 2013 ISUOG. Published by John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>23288698</pmid><doi>10.1002/uog.12377</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abortion, Induced Brain Cytomegalovirus Cytomegalovirus Infections - diagnosis Cytomegalovirus Infections - transmission Developmental Disabilities - etiology Female Fetal Diseases - diagnosis Hearing Loss - embryology Humans Infectious Disease Transmission, Vertical Magnetic Resonance Imaging MRI Pregnancy Pregnancy Complications, Infectious - diagnosis Pregnancy Outcome Pregnancy Trimester, First Pregnancy Trimester, Second Prenatal Diagnosis - methods Prenatal Exposure Delayed Effects Prospective Studies Risk Factors Ultrasonography, Prenatal ultrasound |
title | Risk of cytomegalovirus‐associated sequelae in relation to time of infection and findings on prenatal imaging |
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