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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Clinical characteristics and intrauterine vertical transmission potential of COVID-19 infection in nine pregnant women: a retrospective review of medical records</title><author><name sortKey="Chen, Huijun" sort="Chen, Huijun" uniqKey="Chen H" first="Huijun" last="Chen">Huijun Chen</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Guo, Juanjuan" sort="Guo, Juanjuan" uniqKey="Guo J" first="Juanjuan" last="Guo">Juanjuan Guo</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Wang, Chen" sort="Wang, Chen" uniqKey="Wang C" first="Chen" last="Wang">Chen Wang</name><affiliation><nlm:aff id="aff5">Department of Obstetrics and Gynaecology, Peking University First Hospital, Beijing, China</nlm:aff></affiliation></author><author><name sortKey="Luo, Fan" sort="Luo, Fan" uniqKey="Luo F" first="Fan" last="Luo">Fan Luo</name><affiliation><nlm:aff id="aff4">State Key Laboratory of Virology/Institute of Medical Virology, School of Basic Medical Sciences, Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Yu, Xuechen" sort="Yu, Xuechen" uniqKey="Yu X" first="Xuechen" last="Yu">Xuechen Yu</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Zhang, Wei" sort="Zhang, Wei" uniqKey="Zhang W" first="Wei" last="Zhang">Wei Zhang</name><affiliation><nlm:aff id="aff6">Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA</nlm:aff></affiliation></author><author><name sortKey="Li, Jiafu" sort="Li, Jiafu" uniqKey="Li J" first="Jiafu" last="Li">Jiafu Li</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Zhao, Dongchi" sort="Zhao, Dongchi" uniqKey="Zhao D" first="Dongchi" last="Zhao">Dongchi Zhao</name><affiliation><nlm:aff id="aff2">Department of Paediatrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Xu, Dan" sort="Xu, Dan" uniqKey="Xu D" first="Dan" last="Xu">Dan Xu</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Gong, Qing" sort="Gong, Qing" uniqKey="Gong Q" first="Qing" last="Gong">Qing Gong</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Liao, Jing" sort="Liao, Jing" uniqKey="Liao J" first="Jing" last="Liao">Jing Liao</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Yang, Huixia" sort="Yang, Huixia" uniqKey="Yang H" first="Huixia" last="Yang">Huixia Yang</name><affiliation><nlm:aff id="aff5">Department of Obstetrics and Gynaecology, Peking University First Hospital, Beijing, China</nlm:aff></affiliation></author><author><name sortKey="Hou, Wei" sort="Hou, Wei" uniqKey="Hou W" first="Wei" last="Hou">Wei Hou</name><affiliation><nlm:aff id="aff4">State Key Laboratory of Virology/Institute of Medical Virology, School of Basic Medical Sciences, Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Zhang, Yuanzhen" sort="Zhang, Yuanzhen" uniqKey="Zhang Y" first="Yuanzhen" last="Zhang">Yuanzhen Zhang</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">32151335</idno><idno type="pmc">7159281</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7159281</idno><idno type="RBID">PMC:7159281</idno><idno type="doi">10.1016/S0140-6736(20)30360-3</idno><date when="2020">2020</date><idno type="wicri:Area/Pmc/Corpus">001262</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001262</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Clinical characteristics and intrauterine vertical transmission potential of COVID-19 infection in nine pregnant women: a retrospective review of medical records</title><author><name sortKey="Chen, Huijun" sort="Chen, Huijun" uniqKey="Chen H" first="Huijun" last="Chen">Huijun Chen</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Guo, Juanjuan" sort="Guo, Juanjuan" uniqKey="Guo J" first="Juanjuan" last="Guo">Juanjuan Guo</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Wang, Chen" sort="Wang, Chen" uniqKey="Wang C" first="Chen" last="Wang">Chen Wang</name><affiliation><nlm:aff id="aff5">Department of Obstetrics and Gynaecology, Peking University First Hospital, Beijing, China</nlm:aff></affiliation></author><author><name sortKey="Luo, Fan" sort="Luo, Fan" uniqKey="Luo F" first="Fan" last="Luo">Fan Luo</name><affiliation><nlm:aff id="aff4">State Key Laboratory of Virology/Institute of Medical Virology, School of Basic Medical Sciences, Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Yu, Xuechen" sort="Yu, Xuechen" uniqKey="Yu X" first="Xuechen" last="Yu">Xuechen Yu</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Zhang, Wei" sort="Zhang, Wei" uniqKey="Zhang W" first="Wei" last="Zhang">Wei Zhang</name><affiliation><nlm:aff id="aff6">Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA</nlm:aff></affiliation></author><author><name sortKey="Li, Jiafu" sort="Li, Jiafu" uniqKey="Li J" first="Jiafu" last="Li">Jiafu Li</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Zhao, Dongchi" sort="Zhao, Dongchi" uniqKey="Zhao D" first="Dongchi" last="Zhao">Dongchi Zhao</name><affiliation><nlm:aff id="aff2">Department of Paediatrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Xu, Dan" sort="Xu, Dan" uniqKey="Xu D" first="Dan" last="Xu">Dan Xu</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Gong, Qing" sort="Gong, Qing" uniqKey="Gong Q" first="Qing" last="Gong">Qing Gong</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Liao, Jing" sort="Liao, Jing" uniqKey="Liao J" first="Jing" last="Liao">Jing Liao</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Yang, Huixia" sort="Yang, Huixia" uniqKey="Yang H" first="Huixia" last="Yang">Huixia Yang</name><affiliation><nlm:aff id="aff5">Department of Obstetrics and Gynaecology, Peking University First Hospital, Beijing, China</nlm:aff></affiliation></author><author><name sortKey="Hou, Wei" sort="Hou, Wei" uniqKey="Hou W" first="Wei" last="Hou">Wei Hou</name><affiliation><nlm:aff id="aff4">State Key Laboratory of Virology/Institute of Medical Virology, School of Basic Medical Sciences, Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation></author><author><name sortKey="Zhang, Yuanzhen" sort="Zhang, Yuanzhen" uniqKey="Zhang Y" first="Yuanzhen" last="Zhang">Yuanzhen Zhang</name><affiliation><nlm:aff id="aff1">Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</nlm:aff></affiliation></author></analytic><series><title level="j">Lancet (London, England)</title><idno type="ISSN">0140-6736</idno><idno type="eISSN">1474-547X</idno><imprint><date when="2020">2020</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><title>Summary</title><sec><title>Background</title><p>Previous studies on the pneumonia outbreak caused by the 2019 novel coronavirus disease (COVID-19) were based on information from the general population. Limited data are available for pregnant women with COVID-19 pneumonia. This study aimed to evaluate the clinical characteristics of COVID-19 in pregnancy and the intrauterine vertical transmission potential of COVID-19 infection.</p></sec><sec><title>Methods</title><p>Clinical records, laboratory results, and chest CT scans were retrospectively reviewed for nine pregnant women with laboratory-confirmed COVID-19 pneumonia (ie, with maternal throat swab samples that were positive for severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2]) who were admitted to Zhongnan Hospital of Wuhan University, Wuhan, China, from Jan 20 to Jan 31, 2020. Evidence of intrauterine vertical transmission was assessed by testing for the presence of SARS-CoV-2 in amniotic fluid, cord blood, and neonatal throat swab samples. Breastmilk samples were also collected and tested from patients after the first lactation.</p></sec><sec><title>Findings</title><p>All nine patients had a caesarean section in their third trimester. Seven patients presented with a fever. Other symptoms, including cough (in four of nine patients), myalgia (in three), sore throat (in two), and malaise (in two), were also observed. Fetal distress was monitored in two cases. Five of nine patients had lymphopenia (<1·0 × 10⁹ cells per L). Three patients had increased aminotransferase concentrations. None of the patients developed severe COVID-19 pneumonia or died, as of Feb 4, 2020. Nine livebirths were recorded. No neonatal asphyxia was observed in newborn babies. All nine livebirths had a 1-min Apgar score of 8–9 and a 5-min Apgar score of 9–10. Amniotic fluid, cord blood, neonatal throat swab, and breastmilk samples from six patients were tested for SARS-CoV-2, and all samples tested negative for the virus.</p></sec><sec><title>Interpretation</title><p>The clinical characteristics of COVID-19 pneumonia in pregnant women were similar to those reported for non-pregnant adult patients who developed COVID-19 pneumonia. Findings from this small group of cases suggest that there is currently no evidence for intrauterine infection caused by vertical transmission in women who develop COVID-19 pneumonia in late pregnancy.</p></sec><sec><title>Funding</title><p>Hubei Science and Technology Plan, Wuhan University Medical Development Plan.</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Zhu, N" uniqKey="Zhu N">N Zhu</name></author><author><name sortKey="Zhang, D" uniqKey="Zhang D">D Zhang</name></author><author><name sortKey="Wang, W" uniqKey="Wang W">W Wang</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Huang, C" uniqKey="Huang C">C Huang</name></author><author><name sortKey="Wang, Y" uniqKey="Wang Y">Y Wang</name></author><author><name sortKey="Li, X" uniqKey="Li X">X Li</name></author></analytic></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct><analytic><author><name sortKey="Corman, Vm" uniqKey="Corman V">VM Corman</name></author><author><name sortKey="Landt, O" uniqKey="Landt O">O Landt</name></author><author><name sortKey="Kaiser, M" uniqKey="Kaiser M">M Kaiser</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Gottfredsson, M" uniqKey="Gottfredsson M">M Gottfredsson</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Jamieson, Dj" uniqKey="Jamieson D">DJ Jamieson</name></author><author><name sortKey="Honein, Ma" uniqKey="Honein M">MA Honein</name></author><author><name sortKey="Rasmussen, Sa" uniqKey="Rasmussen S">SA Rasmussen</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Wong, Sf" uniqKey="Wong S">SF Wong</name></author><author><name sortKey="Chow, Km" uniqKey="Chow K">KM Chow</name></author><author><name sortKey="Leung, Tn" uniqKey="Leung T">TN Leung</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Schoeman, D" uniqKey="Schoeman D">D Schoeman</name></author><author><name sortKey="Fielding, Bc" uniqKey="Fielding B">BC Fielding</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zhang, Yz" uniqKey="Zhang Y">YZ Zhang</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="De Wit, E" uniqKey="De Wit E">E de Wit</name></author><author><name sortKey="Van Doremalen, N" uniqKey="Van Doremalen N">N van Doremalen</name></author><author><name sortKey="Falzarano, D" uniqKey="Falzarano D">D Falzarano</name></author><author><name sortKey="Munster, Vj" uniqKey="Munster V">VJ Munster</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zhou, P" uniqKey="Zhou P">P Zhou</name></author><author><name sortKey="Yang, Xl" uniqKey="Yang X">XL Yang</name></author><author><name sortKey="Wang, Xg" uniqKey="Wang X">XG Wang</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Li, Q" uniqKey="Li Q">Q Li</name></author><author><name sortKey="Guan, X" uniqKey="Guan X">X Guan</name></author><author><name sortKey="Wu, P" uniqKey="Wu P">P Wu</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Shek, Cc" uniqKey="Shek C">CC Shek</name></author><author><name sortKey="Ng, Pc" uniqKey="Ng P">PC Ng</name></author><author><name sortKey="Fung, Gp" uniqKey="Fung G">GP Fung</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Bouthry, E" uniqKey="Bouthry E">E Bouthry</name></author><author><name sortKey="Picone, O" uniqKey="Picone O">O Picone</name></author><author><name sortKey="Hamdi, G" uniqKey="Hamdi G">G Hamdi</name></author><author><name sortKey="Grangeot Keros, L" uniqKey="Grangeot Keros L">L Grangeot-Keros</name></author><author><name sortKey="Ayoubi, Jm" uniqKey="Ayoubi J">JM Ayoubi</name></author><author><name sortKey="Vauloup Fellous, C" uniqKey="Vauloup Fellous C">C Vauloup-Fellous</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Niu, Y" uniqKey="Niu Y">Y Niu</name></author><author><name sortKey="Yue, H" uniqKey="Yue H">H Yue</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zhang, Z" uniqKey="Zhang Z">Z Zhang</name></author><author><name sortKey="Wang, C" uniqKey="Wang C">C Wang</name></author><author><name sortKey="Gao, Cc" uniqKey="Gao C">CC Gao</name></author></analytic></biblStruct></listBibl></div1></back></TEI><pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Lancet</journal-id><journal-id journal-id-type="iso-abbrev">Lancet</journal-id><journal-title-group><journal-title>Lancet (London, England)</journal-title></journal-title-group><issn pub-type="ppub">0140-6736</issn><issn pub-type="epub">1474-547X</issn><publisher><publisher-name>Elsevier Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">32151335</article-id><article-id pub-id-type="pmc">7159281</article-id><article-id pub-id-type="publisher-id">S0140-6736(20)30360-3</article-id><article-id pub-id-type="doi">10.1016/S0140-6736(20)30360-3</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Clinical characteristics and intrauterine vertical transmission potential of COVID-19 infection in nine pregnant women: a retrospective review of medical records</article-title></title-group><contrib-group><contrib contrib-type="author" id="au10"><name><surname>Chen</surname><given-names>Huijun</given-names></name><degrees>PhD</degrees><xref rid="aff1" ref-type="aff">a</xref><xref rid="aff3" ref-type="aff">c</xref><xref rid="fn1" ref-type="fn">*</xref></contrib><contrib contrib-type="author" id="au20"><name><surname>Guo</surname><given-names>Juanjuan</given-names></name><degrees>MS</degrees><xref rid="aff1" ref-type="aff">a</xref><xref rid="aff3" ref-type="aff">c</xref><xref rid="fn1" ref-type="fn">*</xref></contrib><contrib contrib-type="author" id="au30"><name><surname>Wang</surname><given-names>Chen</given-names></name><degrees>PhD</degrees><xref rid="aff5" ref-type="aff">e</xref><xref rid="fn1" ref-type="fn">*</xref></contrib><contrib contrib-type="author" id="au40"><name><surname>Luo</surname><given-names>Fan</given-names></name><degrees>PhD</degrees><xref rid="aff4" ref-type="aff">d</xref></contrib><contrib contrib-type="author" id="au50"><name><surname>Yu</surname><given-names>Xuechen</given-names></name><degrees>MD</degrees><xref rid="aff1" ref-type="aff">a</xref><xref rid="aff3" ref-type="aff">c</xref></contrib><contrib contrib-type="author" id="au60"><name><surname>Zhang</surname><given-names>Wei</given-names></name><degrees>Prof</degrees><degrees>PhD</degrees><xref rid="aff6" ref-type="aff">f</xref></contrib><contrib contrib-type="author" id="au70"><name><surname>Li</surname><given-names>Jiafu</given-names></name><degrees>Prof</degrees><degrees>MS</degrees><xref rid="aff1" ref-type="aff">a</xref><xref rid="aff3" ref-type="aff">c</xref></contrib><contrib contrib-type="author" id="au80"><name><surname>Zhao</surname><given-names>Dongchi</given-names></name><degrees>Prof</degrees><degrees>PhD</degrees><xref rid="aff2" ref-type="aff">b</xref></contrib><contrib contrib-type="author" id="au90"><name><surname>Xu</surname><given-names>Dan</given-names></name><degrees>MS</degrees><xref rid="aff1" ref-type="aff">a</xref><xref rid="aff3" ref-type="aff">c</xref></contrib><contrib contrib-type="author" id="au100"><name><surname>Gong</surname><given-names>Qing</given-names></name><degrees>MS</degrees><xref rid="aff1" ref-type="aff">a</xref><xref rid="aff3" ref-type="aff">c</xref></contrib><contrib contrib-type="author" id="au110"><name><surname>Liao</surname><given-names>Jing</given-names></name><degrees>PhD</degrees><xref rid="aff1" ref-type="aff">a</xref><xref rid="aff3" ref-type="aff">c</xref></contrib><contrib contrib-type="author" id="au120"><name><surname>Yang</surname><given-names>Huixia</given-names></name><degrees>Prof</degrees><degrees>MD</degrees><email>yanghuixia@bjmu.edu.cn</email><xref rid="aff5" ref-type="aff">e</xref><xref rid="cor3" ref-type="corresp">***</xref></contrib><contrib contrib-type="author" id="au130"><name><surname>Hou</surname><given-names>Wei</given-names></name><degrees>Prof</degrees><degrees>PhD</degrees><email>houwei@whu.edu.cn</email><xref rid="aff4" ref-type="aff">d</xref><xref rid="cor2" ref-type="corresp">**</xref></contrib><contrib contrib-type="author" id="au140"><name><surname>Zhang</surname><given-names>Yuanzhen</given-names></name><degrees>Prof</degrees><degrees>BS</degrees><email>zhangyuanzhen@whu.edu.cn</email><xref rid="aff1" ref-type="aff">a</xref><xref rid="aff3" ref-type="aff">c</xref><xref rid="cor1" ref-type="corresp">*</xref></contrib></contrib-group><aff id="aff1"><label>a</label>Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</aff><aff id="aff2"><label>b</label>Department of Paediatrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China</aff><aff id="aff3"><label>c</label>Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, China</aff><aff id="aff4"><label>d</label>State Key Laboratory of Virology/Institute of Medical Virology, School of Basic Medical Sciences, Wuhan University, Wuhan, Hubei, China</aff><aff id="aff5"><label>e</label>Department of Obstetrics and Gynaecology, Peking University First Hospital, Beijing, China</aff><aff id="aff6"><label>f</label>Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA</aff><author-notes><corresp id="cor1"><label>*</label>Correspondence to: Prof Yuanzhen Zhang, Department of Gynaecology and Obstetrics, Zhongnan Hospital of Wuhan University, Wuhan, Hubei 430071, China <email>zhangyuanzhen@whu.edu.cn</email></corresp><corresp id="cor2"><label>**</label>Prof Wei Hou, State Key Laboratory of Virology/Institute of Medical Virology, School of Basic Medical Sciences, Wuhan University, Wuhan, Hubei 430071, China <email>houwei@whu.edu.cn</email></corresp><corresp id="cor3"><label>***</label>Prof Huixia Yang, Department of Obstetrics and Gynaecology, Peking University First Hospital, Beijing 100034, China <email>yanghuixia@bjmu.edu.cn</email></corresp><fn id="fn1"><label>*</label><p id="cenpara20">Contributed equally</p></fn></author-notes><pub-date pub-type="pmc-release"><day>12</day><month>2</month><year>2020</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub" iso-8601-date="2020-03-13"><season>7-13 March</season><year>2020</year></pub-date><pub-date pub-type="epub"><day>12</day><month>2</month><year>2020</year></pub-date><volume>395</volume><issue>10226</issue><fpage>809</fpage><lpage>815</lpage><permissions><copyright-statement>© 2020 Elsevier Ltd. All rights reserved.</copyright-statement><copyright-year>2020</copyright-year><copyright-holder>Elsevier Ltd</copyright-holder><license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p></license></permissions><related-article related-article-type="article-reference" id="d32e351" ext-link-type="doi" xlink:href="10.1016/S0140-6736(20)30365-2"></related-article><abstract id="ceab10"><title>Summary</title><sec><title>Background</title><p>Previous studies on the pneumonia outbreak caused by the 2019 novel coronavirus disease (COVID-19) were based on information from the general population. Limited data are available for pregnant women with COVID-19 pneumonia. This study aimed to evaluate the clinical characteristics of COVID-19 in pregnancy and the intrauterine vertical transmission potential of COVID-19 infection.</p></sec><sec><title>Methods</title><p>Clinical records, laboratory results, and chest CT scans were retrospectively reviewed for nine pregnant women with laboratory-confirmed COVID-19 pneumonia (ie, with maternal throat swab samples that were positive for severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2]) who were admitted to Zhongnan Hospital of Wuhan University, Wuhan, China, from Jan 20 to Jan 31, 2020. Evidence of intrauterine vertical transmission was assessed by testing for the presence of SARS-CoV-2 in amniotic fluid, cord blood, and neonatal throat swab samples. Breastmilk samples were also collected and tested from patients after the first lactation.</p></sec><sec><title>Findings</title><p>All nine patients had a caesarean section in their third trimester. Seven patients presented with a fever. Other symptoms, including cough (in four of nine patients), myalgia (in three), sore throat (in two), and malaise (in two), were also observed. Fetal distress was monitored in two cases. Five of nine patients had lymphopenia (<1·0 × 10⁹ cells per L). Three patients had increased aminotransferase concentrations. None of the patients developed severe COVID-19 pneumonia or died, as of Feb 4, 2020. Nine livebirths were recorded. No neonatal asphyxia was observed in newborn babies. All nine livebirths had a 1-min Apgar score of 8–9 and a 5-min Apgar score of 9–10. Amniotic fluid, cord blood, neonatal throat swab, and breastmilk samples from six patients were tested for SARS-CoV-2, and all samples tested negative for the virus.</p></sec><sec><title>Interpretation</title><p>The clinical characteristics of COVID-19 pneumonia in pregnant women were similar to those reported for non-pregnant adult patients who developed COVID-19 pneumonia. Findings from this small group of cases suggest that there is currently no evidence for intrauterine infection caused by vertical transmission in women who develop COVID-19 pneumonia in late pregnancy.</p></sec><sec><title>Funding</title><p>Hubei Science and Technology Plan, Wuhan University Medical Development Plan.</p></sec></abstract></article-meta></front><body><sec id="cesec10"><title>Introduction</title><p id="para10">The type of pneumonia caused by the 2019 novel coronavirus disease (COVID-19) is a highly infectious disease, and the ongoing outbreak has been declared by WHO as a global public health emergency.<xref rid="bib1" ref-type="bibr">1</xref>, <xref rid="bib2" ref-type="bibr">2</xref> COVID-19 pneumonia was first reported in Wuhan, Hubei Province, China, in December, 2019, followed by an outbreak across Hubei Province and other parts of the country.<xref rid="bib1" ref-type="bibr">1</xref>, <xref rid="bib2" ref-type="bibr">2</xref> A study in <italic>The Lancet</italic> by Huang and colleagues<xref rid="bib2" ref-type="bibr"><sup>2</sup></xref> reported the epidemiological, clinical, laboratory, and radiological characteristics, as well as treatment and clinical outcomes, of patients with laboratory-confirmed COVID-19 pneumonia. However, Huang and colleagues’ report mainly focused on non-pregnant adults. The clinical characteristics and vertical transmission potential of COVID-19 pneumonia in pregnant women is unknown. Urgent questions that need to be addressed promptly include whether pregnant women with COVID-19 pneumonia will develop distinct symptoms from non-pregnant adults, whether pregnant women who have confirmed COVID-19 pneumonia are more likely to die of the infection or to undergo preterm labour, and whether COVID-19 could spread vertically and pose risks to the fetus and neonate. Answers to these questions are essential for formulating the principles of obstetric treatment for pregnant women with COVID-19 infection. Therefore, to facilitate efforts, both in China and globally, to prevent and control COVID-19 pneumonia in children and pregnant women,<xref rid="bib3" ref-type="bibr"><sup>3</sup></xref> we retrospectively collected and analysed detailed clinical data from pregnant women with laboratory-confirmed COVID-19 infection at Zhongnan Hospital of Wuhan University, Wuhan, China. In this study we present clinical features of pregnant women with confirmed COVID-19 pneumonia and examine the vertical transmission potential of COVID-19.</p><p id="para20"><boxed-text id="cetextbox10"><caption><title>Research in context</title></caption><p id="para30"><bold>Evidence before this study</bold></p><p id="para40">We searched PubMed and the China National Knowledge Infrastructure database for articles published up to Feb 6, 2020, using the keywords “novel coronavirus”, “2019 novel coronavirus”, “2019-nCoV”, “pneumonia”, “coronavirus”, “Wuhan”, AND “novel” ,“pregnancy”, “maternal infection”, AND “fetal infection” for articles published in both Chinese and English. We found two articles: one titled <italic>Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China</italic>, published in <italic>The Lancet</italic>, and another titled <italic>Early transmission dynamics in Wuhan, China, of novel coronavirus-infected pneumonia</italic>, published in the <italic>New England Journal of Medicine</italic>. We identified no published studies on pregnant women with the 2019 novel coronavirus disease (COVID-19) infection.</p><p id="para50"><bold>Added value of this study</bold></p><p id="para60">We retrospectively reviewed clinical records, laboratory findings, and chest CT scans for nine pregnant women with laboratory-confirmed COVID-19 pneumonia. Evidence of vertical transmission was assessed by testing for the presence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in amniotic fluid, cord blood, breastmilk, and neonatal throat swab samples from six of nine patients. All nine women were in the third trimester. Seven presented with fever without chill. Other symptoms included cough (in four of nine patients), myalgia (in three), sore throat (in two), and malaise (in two). Fetal distress occurred in two cases. Five of the nine patients had lymphopenia (<1·0 × 10⁹ cells per L). Three patients had increased aminotransferase concentrations. None of the patients developed severe COVID-19 pneumonia or died. Nine livebirths were recorded. No severe neonatal asphyxia was observed. All nine livebirths had a 1-min Apgar score of 8–10 and 5-min Apgar score of 9–10. Amniotic fluid, cord blood, neonatal throat swab, and breastmilk samples from six of the nine patients were tested for SARS-CoV-2, and all results were negative.</p><p id="para70"><bold>Implications of all the available evidence</bold></p><p id="para80">The clinical characteristics of COVID-19 pneumonia in pregnant women were similar to those of non-pregnant adult patients with COVID-19 pneumonia. Based on data from this small group of patients, there is currently no evidence of vertical transmission in pregnant women who develop COVID-19 pneumonia in the third trimester.</p></boxed-text></p></sec><sec id="cesec20"><title>Methods</title><sec id="cesec30"><title>Study design and patients</title><p id="para90">We did a retrospective review of medical records from nine pregnant women with COVID-19 pneumonia admitted to Zhongnan Hospital of Wuhan University from Jan 20 to Jan 31, 2020. Diagnosis of COVID-19 pneumonia was based on the New Coronavirus Pneumonia Prevention and Control Program (4th edition) published by the National Health Commission of China.<xref rid="bib4" ref-type="bibr"><sup>4</sup></xref> All nine pregnant women with COVID-19 pneumonia tested positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by use of quantitative RT-PCR (qRT-PCR) on samples from the respiratory tract.</p><p id="para100">This study was reviewed and approved by the Medical Ethical Committee of Zhongnan Hospital of Wuhan University (approval number 2020004). Written informed consent was obtained from each enrolled patient.</p></sec><sec id="cesec40"><title>Data collection</title><p id="para110">We reviewed clinical records, laboratory findings, and chest CT scans for all nine pregnant women. All information was obtained and curated with a customised data collection form. Two study investigators (JG and XY) independently reviewed the data collection forms to verify data accuracy.</p><p id="para120">Maternal throat swab samples were collected and tested for SARS-CoV-2 with the Chinese Center for Disease Control and Prevention (CDC) recommended Kit (BioGerm, Shanghai, China), following WHO guidelines for qRT-PCR.<xref rid="bib5" ref-type="bibr">5</xref>, <xref rid="bib6" ref-type="bibr">6</xref>, <xref rid="bib7" ref-type="bibr">7</xref> All samples were processed simultaneously at the Department of Clinical Laboratory of Zhongnan Hospital and State Key Laboratory of Virology/Institute of Medical Virology, School of Basic Medical Sciences, Wuhan University. Positive confirmatory cases of COVID-19 infection were defined as those with a positive test result from either laboratory.</p><p id="para130">Amniotic fluid samples from patients with COVID-19 pneumonia were obtained via direct syringe aspiration at the time of delivery. Cord blood and neonatal throat swab samples were collected immediately after delivery in the operating room. Additionally, breastmilk samples from patients with COVID-19 pneumonia were collected after their first lactation. Evidence of vertical transmission was evaluated by testing for the presence of SARS-CoV-2 in these clinical samples. Sample collection was successful in six cases (patients 2, 4–6, 8, and 9). Among the three patients from whom sample collection was not successful, patient 1 was diagnosed after caesarean section, thus no sample was obtained. Patients 3 and 7 underwent caesarean section at night, thus immediate sample collection was not possible. All samples were processed at the State Key Laboratory of Virology/Institute of Medical Virology, School of Basic Medical Sciences, Wuhan University, for further testing. Sample collection, processing, and laboratory testing complied with WHO guidance.<xref rid="bib6" ref-type="bibr"><sup>6</sup></xref> All samples, as described above, were tested for SARS-CoV-2 by use of qRT-PCR with the CDC recommended Kit. The test results were confirmed by nested RT-PCR with designed primers. For the nested RT-PCR assay, total RNA was extracted from samples by use of the TRIzol LS reagent (Invitrogen, Carlsbad, CA, USA), followed by reverse transcription by use of the one-step RT-PCR Kit (TaKaRa, Dalian, China). Primers were designed on the basis of the sequence of Wuhan-Hu-1 (MN908947). Partial S segment sequences (nt 21730-22458) were amplified with primers: 5′-CTCAGGACTTGTTCTTACCTT-3′ and 5′-CAAGTGCACAGTCTAC-AGC-3′.</p></sec><sec id="cesec50"><title>Statistical analysis</title><p id="para140">Statistical analysis was done with SPSS, version 20.0. Continuous variables were directly expressed as a range. Categorical variables were expressed as number (%).</p></sec><sec id="cesec60"><title>Role of the funding source</title><p id="para150">The funding agencies did not participate in study design, data collection, data analysis, or writing of the report. The corresponding authors were responsible for all aspects of the study to ensure that issues related to the accuracy or integrity of any part of the work were properly investigated and resolved. The final version was approved by all authors.</p></sec></sec><sec id="cesec70"><title>Results</title><p id="para160">The nine pregnant women were all in their third trimester, and all underwent caesarean section. All patients had a history of epidemiological exposure to COVID-19. The age range of the patients was 26–40 years, and the range of gestational weeks at admission was 36 weeks to 39 weeks plus 4 days. None of the patients had underlying diseases such as diabetes, chronic hypertension, or cardiovascular disease. One patient, however, had gestational hypertension since 27 gestational weeks, while another developed pre-eclampsia at 31 gestational weeks. Both of these patients were in a stable condition during pregnancy. Additionally, one patient was found to have influenza virus infection upon admission to hospital (<xref rid="tbl1" ref-type="table">table 1</xref>; <xref rid="sec1" ref-type="sec">appendix</xref>).<table-wrap position="float" id="tbl1"><label>Table 1</label><caption><p>Maternal clinical and laboratory characteristics</p></caption><table frame="hsides" rules="groups"><thead><tr><th></th><th></th><th align="left"><bold>Patient 1</bold></th><th align="left"><bold>Patient 2</bold></th><th align="left"><bold>Patient 3</bold></th><th align="left"><bold>Patient 4</bold></th><th align="left"><bold>Patient 5</bold></th><th align="left"><bold>Patient 6</bold></th><th align="left"><bold>Patient 7</bold></th><th align="left"><bold>Patient 8</bold></th><th align="left"><bold>Patient 9</bold></th><th align="left"><bold>n (%)</bold></th></tr></thead><tbody><tr><td colspan="12" align="left"><bold>Clinical characteristics</bold></td></tr><tr><td colspan="2" align="left">Date of admission</td><td align="left">Jan 20</td><td align="left">Jan 25</td><td align="left">Jan 27</td><td align="left">Jan 26</td><td align="left">Jan 27</td><td align="left">Jan 27</td><td align="left">Jan 28</td><td align="left">Jan 29</td><td align="left">Jan 30</td><td align="left">··</td></tr><tr><td colspan="2" align="left">Age (years)</td><td align="left">33</td><td align="left">27</td><td align="left">40</td><td align="left">26</td><td align="left">26</td><td align="left">26</td><td align="left">29</td><td align="left">28</td><td align="left">34</td><td align="left">··</td></tr><tr><td colspan="2" align="left">Gestational age on admission</td><td align="left">37 weeks, 2 days</td><td align="left">38 weeks, 2 day</td><td align="left">36 weeks</td><td align="left">36 weeks, 2 days</td><td align="left">38 weeks,1 day</td><td align="left">36 weeks, 3 days</td><td align="left">36 weeks, 2 days</td><td align="left">38 weeks</td><td align="left">39 weeks, 4 days</td><td align="left">··</td></tr><tr><td colspan="2" align="left">Epidemiological history</td><td align="left">Yes (exposure to relevant environment)<xref rid="tbl1fn1" ref-type="table-fn">*</xref></td><td align="left">Yes (contact with infected person)</td><td align="left">Yes (contact with infected person)</td><td align="left">Yes (exposure to relevant environment)<xref rid="tbl1fn1" ref-type="table-fn">*</xref></td><td align="left">Yes (exposure to relevant environment)<xref rid="tbl1fn1" ref-type="table-fn">*</xref></td><td align="left">Yes (contact with infected person)</td><td align="left">Yes (contact with infected person)</td><td align="left">Yes (contact with infected person)</td><td align="left">Yes (exposure to relevant environment)<xref rid="tbl1fn2" ref-type="table-fn">†</xref></td><td align="left">9 (100%)</td></tr><tr><td colspan="2" align="left">Other family members affected</td><td align="left">No</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">Yes</td><td align="left">No</td><td align="left">Yes</td><td align="left">No</td><td align="left">4 (44%)</td></tr><tr><td colspan="2" align="left">Onset to delivery (days)</td><td align="left">1</td><td align="left">6</td><td align="left">4</td><td align="left">3</td><td align="left">1</td><td align="left">4</td><td align="left">2</td><td align="left">2</td><td align="left">7</td><td align="left">··</td></tr><tr><td colspan="2" align="left">Complications</td><td align="left">Influenza</td><td align="left">None</td><td align="left">Gestational hypertension</td><td align="left">Pre-eclampsia</td><td align="left">Fetal distress</td><td align="left">None</td><td align="left">PROM</td><td align="left">Fetal distress</td><td align="left">PROM</td><td align="left">··</td></tr><tr><td colspan="12" align="left">Signs and symptoms</td></tr><tr><td></td><td align="left">Fever on admission</td><td align="left">No</td><td align="left">Yes</td><td align="left">No</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">7 (78%)</td></tr><tr><td></td><td align="left">Post-partum fever</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">Yes</td><td align="left">6 (67%)</td></tr><tr><td></td><td align="left">Myalgia</td><td align="left">No</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">3 (33%)</td></tr><tr><td></td><td align="left">Malaise</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">2 (22%)</td></tr><tr><td></td><td align="left">Rigor</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">0</td></tr><tr><td></td><td align="left">Cough</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">4 (44%)</td></tr><tr><td></td><td align="left">Dyspnoea</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">1 (11%)</td></tr><tr><td></td><td align="left">Sore throat</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">2 (22%)</td></tr><tr><td></td><td align="left">Diarrhoea</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">1 (11%)</td></tr><tr><td></td><td align="left">Chest pain</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">0</td></tr><tr><td colspan="12" align="left"><bold>Laboratory characteristics</bold></td></tr><tr><td colspan="2" align="left">White blood cell count (×10<sup>9</sup> cells per L)</td><td align="left">6·15</td><td align="left">5·07</td><td align="left">8·78</td><td align="left">7·63</td><td align="left">9·34</td><td align="left">5·57</td><td align="left">10·61</td><td align="left">9·96</td><td align="left">7·08</td><td align="left">··</td></tr><tr><td colspan="2" align="left">Low or normal leukocyte count (<9·5×10<sup>9</sup> cells per L)</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">Yes</td><td align="left">7 (78%)</td></tr><tr><td colspan="2" align="left">Lymphocyte count (×10<sup>9</sup> cells per L)</td><td align="left">1·59</td><td align="left">0·56</td><td align="left">0·46</td><td align="left">2·83</td><td align="left">0·69</td><td align="left">0·66</td><td align="left">0·87</td><td align="left">1·53</td><td align="left">1·47</td><td align="left">··</td></tr><tr><td colspan="2" align="left">Lymphopenia (<10<sup>9</sup> cells per L)</td><td align="left">No</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">5 (56%)</td></tr><tr><td colspan="2" align="left">C-reactive protein concentration (mg/L)</td><td align="left">20·3</td><td align="left">14·4</td><td align="left">33·4</td><td align="left">3·3</td><td align="left">28·2</td><td align="left">18·2</td><td align="left">NA</td><td align="left">6·2</td><td align="left">24·9</td><td align="left">··</td></tr><tr><td colspan="2" align="left">Elevated C-reactive protein (>10 mg/L)</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">NA</td><td align="left">No</td><td align="left">Yes</td><td align="left">6 (75%)<xref rid="tbl1fn3" ref-type="table-fn">‡</xref></td></tr><tr><td colspan="2" align="left">Elevated ALT (>45 U/L) or AST (>35 U/L)</td><td align="left">Yes</td><td align="left">No</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">3 (33%)</td></tr><tr><td colspan="2" align="left">ALT (U/L)</td><td align="left">2093</td><td align="left">9</td><td align="left">62</td><td align="left">54</td><td align="left">18</td><td align="left">14</td><td align="left">6</td><td align="left">16</td><td align="left">12</td><td align="left">··</td></tr><tr><td colspan="2" align="left">AST (U/L)</td><td align="left">1263</td><td align="left">24</td><td align="left">71</td><td align="left">67</td><td align="left">24</td><td align="left">23</td><td align="left">15</td><td align="left">22</td><td align="left">21</td><td align="left">··</td></tr><tr><td colspan="2" align="left">Confirmatory test done (SARS-CoV-2 quantitative RT-PCR)</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">9 (100%)</td></tr><tr><td colspan="12" align="left"><bold>CT evidence of pneumonia</bold></td></tr><tr><td colspan="2" align="left">Typical signs of viral infection</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">8 (89%)</td></tr><tr><td colspan="12" align="left"><bold>Delivery</bold></td></tr><tr><td colspan="2" align="left">Method of delivery</td><td align="left">C-section</td><td align="left">C-section</td><td align="left">C-section</td><td align="left">C-section</td><td align="left">C-section</td><td align="left">C-section</td><td align="left">C-section</td><td align="left">C-section</td><td align="left">C-section</td><td align="left">··</td></tr><tr><td colspan="2" align="left">Indication for C-section</td><td align="left">Severely elevated ALT or AST; COVID-19 pneumonia</td><td align="left">Mature; COVID-19 pneumonia</td><td align="left">History of C-section (×2); COVID-19 pneumonia</td><td align="left">Pre-eclampsia; COVID-19 pneumonia</td><td align="left">Fetal distress; COVID-19 pneumonia</td><td align="left">History of stillbirth (×2); COVID-19 pneumonia</td><td align="left">PROM; COVID-19 pneumonia</td><td align="left">Fetal distress; COVID-19 pneumonia</td><td align="left">PROM; COVID-19 pneumonia</td><td align="left">··</td></tr><tr><td colspan="12" align="left">Treatment after delivery</td></tr><tr><td></td><td align="left">Oxygen support (nasal cannula)</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">9 (100%)</td></tr><tr><td></td><td align="left">Antiviral therapy</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">6 (67%)</td></tr><tr><td></td><td align="left">Antibiotic therapy</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">9 (100%)</td></tr><tr><td></td><td align="left">Use of corticosteroid</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">0</td></tr></tbody></table><table-wrap-foot><fn><p>PROM=premature rupture of membrane. NA=not applicable. ALT=alanine transaminase. AST=aspartate transaminase. COVID-19=2019 novel coronavirus disease. C-section=caesarean section. SARS-CoV-2=severe acute respiratory syndrome coronavirus 2.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tbl1fn1"><label>*</label><p id="cenpara30">Exposure to Hankou, the area in Wuhan where the epidemic was first detected.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tbl1fn2"><label>†</label><p id="cenpara40">A university where the patient works, and a gathering of people.</p></fn></table-wrap-foot><table-wrap-foot><fn id="tbl1fn3"><label>‡</label><p id="cenpara50">Data missing for one patient.</p></fn></table-wrap-foot></table-wrap></p><p id="para170">Seven of the nine patients presented with a fever without chills, but none had a high fever (body temperature >39°C). Patients’ body temperatures fluctuated within a range of 36·5–38·8°C. The two patients with a normal body temperature before caesarean section both had post-partum fever (range 37·8–39·3°C). Other symptoms of an upper respiratory tract infection were also observed: four patients had a cough, three had myalgia, two reported a sore throat, and two indicated malaise. Additionally, one patient showed obvious gastrointestinal symptoms. Another patient had shortness of breath and pre-eclampsia. However, none of the nine patients developed severe pneumonia, requiring mechanical ventilation, or died of COVID-19 pneumonia, as of Feb 4, 2020. Pregnancy complications that appeared after the onset of COVID-19 infection included fetal distress (in two of nine patients) and premature rupture of the membrane (in two of nine; <xref rid="tbl1" ref-type="table">table 1</xref>).</p><p id="para180">All patients were given oxygen support (nasal cannula) and empirical antibiotic treatment. Six patients were administered antiviral therapy (<xref rid="tbl1" ref-type="table">table 1</xref>).</p><p id="para190">Data from laboratory tests showed that five of the nine pregnant women with COVID-19 pneumonia had lymphopenia (<1·0 × 10⁹ cells per L). Six patients had elevated concentrations of C-reactive protein (>10 mg/L). Three had increased concentrations of alanine aminotransferase (ALT) and aspartate aminotransferase (AST), one of whom had ALT reaching 2093 U/L and AST reaching 1263 U/L. Additionally, seven patients had a normal white cell count, with none of the patients having a white cell count below the normal range (<xref rid="tbl1" ref-type="table">table 1</xref>).</p><p id="para200">All nine patients had a chest CT scan. Eight patients showed typical findings of chest CT images—multiple patchy ground-glass shadows in lungs<xref rid="bib2" ref-type="bibr"><sup>2</sup></xref> (<xref rid="fig1" ref-type="fig">figure</xref>).<fig id="fig1"><label>Figure</label><caption><p>Chest CT scans (transverse plane) of nine patients</p><p>(A) Patient 1: left-sided patchy consolidation and multiple bilateral ground-glass opacities. (B) Patient 2: subpleural patchy consolidation in the right lung and slightly infiltrated shadows around left bronchus. (C) Patient 3: bilateral multiple ground-glass opacities, prominent on the left. (D) Patient 4: left-sided patchy ground-glass opacity. (E) Patient 5: multiple ground-glass opacities bilaterally. (F) Patient 6: bilateral clear lung fields with no obvious ground-glass opacities. (G) Patient 7: right-sided subpleural patchy consolidation. (H) Patient 8: multiple bilateral ground-glass opacities, prominent on the right. (I) Patient 9: multiple bilateral ground-glass opacities.</p></caption><graphic xlink:href="gr1_lrg"></graphic></fig></p><p id="para210">Nine livebirths were recorded. No fetal death, neonatal death, or neonatal asphyxia was observed. Four patients had preterm labour, but all beyond 36 gestational weeks. Two of the four premature neonates at 36 gestational weeks plus 2 days had a birthweight lower than 2500 g (<xref rid="tbl2" ref-type="table">table 2</xref>). Neonate 4 had a birthweight of 1880 g and the pregnancy was complicated by pre-eclampsia. Neonate 7 had a birthweight of 2460 g. All nine livebirths had a 1-min Apgar score of 8–9 and a 5-min Apgar score of 9–10 (<xref rid="tbl2" ref-type="table">table 2</xref>). Neonate 1 had a mild increase in myocardial enzymes on the day of birth (myoglobin 170·8 ng/mL and creatine kinase-myocardial band 8·5 ng/mL), but without any clinical symptoms.<table-wrap position="float" id="tbl2"><label>Table 2</label><caption><p>Neonatal outcomes</p></caption><table frame="hsides" rules="groups"><thead><tr><th></th><th align="left"><bold>Patient 1</bold></th><th align="left"><bold>Patient 2</bold></th><th align="left"><bold>Patient 3</bold></th><th align="left"><bold>Patient 4</bold></th><th align="left"><bold>Patient 5</bold></th><th align="left"><bold>Patient 6</bold></th><th align="left"><bold>Patient 7</bold></th><th align="left"><bold>Patient 8</bold></th><th align="left"><bold>Patient 9</bold></th><th align="left"><bold>n (%)</bold></th></tr></thead><tbody><tr><td align="left">Gestational age at delivery</td><td align="left">37 weeks, 2 days</td><td align="left">38 weeks, 3 days</td><td align="left">36 weeks</td><td align="left">36 weeks, 2 days</td><td align="left">38 weeks, 1 day</td><td align="left">36 weeks, 3 days</td><td align="left">36 weeks, 2 days</td><td align="left">38 weeks</td><td align="left">39 weeks, 4 days</td><td align="left">··</td></tr><tr><td align="left">Birthweight (g)</td><td align="left">2870</td><td align="left">3730</td><td align="left">3820</td><td align="left">1880</td><td align="left">2970</td><td align="left">3040</td><td align="left">2460</td><td align="left">2800</td><td align="left">3530</td><td align="left">··</td></tr><tr><td align="left">Low birthweight (<2500 g)</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">2 (22%)</td></tr><tr><td align="left">Premature delivery</td><td align="left">No</td><td align="left">No</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">Yes</td><td align="left">Yes</td><td align="left">No</td><td align="left">No</td><td align="left">4 (44%)</td></tr><tr><td align="left">Apgar score (1 min, 5 min)</td><td align="left">8, 9</td><td align="left">9, 10</td><td align="left">9, 10</td><td align="left">8, 9</td><td align="left">9, 10</td><td align="left">9, 10</td><td align="left">9, 10</td><td align="left">9, 10</td><td align="left">8, 10</td><td align="left">··</td></tr><tr><td align="left">Severe neonatal asphyxia</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">0</td></tr><tr><td align="left">Neonatal death</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">0</td></tr><tr><td align="left">Fetal death or stillbirth</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">No</td><td align="left">0</td></tr></tbody></table></table-wrap></p><p id="para220">The presence of SARS-CoV-2 was tested in amniotic fluid, cord blood, neonatal throat swab, and breastmilk samples collected from six patients. Neither the Kit recommended by CDC nor our in-house nested RT-PCR assays detected SARS-CoV-2 in these samples.</p></sec><sec id="cesec80"><title>Discussion</title><p id="para230">We report clinical data from nine pregnant women with laboratory-confirmed COVID-19 pneumonia. The clinical characteristics of these patients with COVID-19 infection during pregnancy were similar to those of non-pregnant adults with COVID-19 infection, as previously reported.<xref rid="bib2" ref-type="bibr"><sup>2</sup></xref> None of the nine patients developed severe pneumonia or died, as of Feb 4, 2020. Notably, based on our findings in these nine patients, there is currently no evidence to suggest that development of COVID-19 pneumonia in the third trimester of pregnancy could lead to the occurrence of severe adverse outcomes in neonates and fetal infection that might be caused by intrauterine vertical transmission.</p><p id="para240">Pregnant women are particularly susceptible to respiratory pathogens and severe pneumonia, because they are at an immunosuppressive state, and physiological adaptive changes during pregnancy (eg, diaphragm elevation, increased oxygen consumption, and oedema of respiratory tract mucosa) can render them intolerant to hypoxia. For example, the 1918 influenza pandemic caused a mortality rate of 2·6% in the overall population, but 37% among pregnant women.<xref rid="bib8" ref-type="bibr"><sup>8</sup></xref> Pregnant women were reported to be at an increased risk of complications from the pandemic H1N1 2009 influenza virus infection, and were more than four times more likely to be admitted to hospital than the general population (relative risk 4·3 [95% CI 2·3–7·8]).<xref rid="bib9" ref-type="bibr"><sup>9</sup></xref> Wong and colleagues<xref rid="bib10" ref-type="bibr"><sup>10</sup></xref> also reported that around 50% of pregnant women who developed SARS were admitted to the intensive care unit, around 33% of pregnant women with SARS required mechanical ventilation, and the mortality rate was as high as 25% for these women. In the current study, we treated nine pregnant women with COVID-19 pneumonia in 11 days from Jan 20 to Jan 31, 2020. Considering that SARS-CoV-2 has up to 85% sequence similarity with SARS,<xref rid="bib11" ref-type="bibr">11</xref>, <xref rid="bib12" ref-type="bibr">12</xref>, <xref rid="bib13" ref-type="bibr">13</xref>, <xref rid="bib14" ref-type="bibr">14</xref> although none of our patients developed severe pneumonia or died of COVID-19 infection, we should be alert to the possibility that the disease course and prognosis of COVID-19 pneumonia could follow the same trend as SARS in pregnant women. However, our observations are based on a small number of cases and the time between illness onset and delivery was short.</p><p id="para250">According to our study, pregnant women with COVID-19 pneumonia showed a similar pattern of clinical characteristics to non-pregnant adult patients, as recently reported.<xref rid="bib2" ref-type="bibr">2</xref>, <xref rid="bib15" ref-type="bibr">15</xref> Common symptoms at the onset of COVID-19 pneumonia for these women included a fever and cough, whereas less common symptoms were myalgia, malaise, sore throat, diarrhoea, and shortness of breath. Laboratory tests indicated that lymphopenia is also likely to occur. Additionally, increased concentrations of ALT or AST might be one of the clinical manifestations. However, none of these symptoms was present in every patient, nor were the symptoms specific to pregnant women with COVID-19 pneumonia. By contrast, chest CT might have a high diagnostic value because of its typical images of virus infection, high accuracy with a low false negative rate, and time efficiency. Therefore, we recommend that, in addition to using nucleic acid tests as the gold standard for the diagnosis of COVID-19 pneumonia, relevant clinical examinations are done, including blood counts and chest CT and a comprehensive evaluation of a patient's medical history, epidemiological exposure, and symptoms.</p><p id="para260">All nine pregnant women in this study underwent a caesarean section. Indications for a caesarean section included severe pre-eclampsia, a history of caesarean sections, and fetal distress. Importantly, uncertainty about the risk of intrapartum mother-to-child transmission by vaginal delivery was another reason for carrying out caesarean sections. Four of the nine patients had preterm labour. However, the causes of premature birth were not related to COVID-19 pneumonia: one patient had severe pre-eclampsia, one had a history of two stillbirths, one had a history of two caesarean sections and irregular contractions; and one had premature rupture of the membrane for about 12 h and suspected intrauterine infection. Moreover, one neonate in our study had a birthweight of 1880 g at 36 gestational weeks plus 2 days, and this case was complicated by pre-eclampsia. Furthermore, the time period from onset of COVID-19 pneumonia to admission was only 3 days for this patient; therefore we reasoned that the fetal intrauterine growth restriction was more likely to be a symptom associated with pre-eclampsia. Importantly, all nine livebirths had a 1-min Apgar score of 8–9 and 5-min Apgar score of 9–10. One infant had a mild increase in myocardial enzymes on the day of birth, but without any clinical symptoms. None of the neonates needed special paediatric treatment.</p><p id="para270">The main focus of this study was to investigate the possibility of intrauterine transmission of COVID-19 infection. We chose to test amniotic fluid, cord blood, and neonatal throat swab samples at birth to ascertain the possibility of intrauterine fetal infection. Notably, all the samples tested in our study were collected in the operating room at the time of the caesarean section, thus guaranteeing that the samples were not contaminated and best represented fetal intrauterine conditions. Our results show that SARS-CoV-2 was negative in all of the above samples, suggesting that no intrauterine fetal infections occurred as a result of COVID-19 infection during a late stage of pregnancy. Our findings are in accordance with what was observed in SARS, which has a similar sequence to SARS-CoV-2.<xref rid="bib14" ref-type="bibr"><sup>14</sup></xref> Previous studies have already shown no evidence of perinatal SARS infection among infants born to mothers who developed SARS infection during pregnancy.<xref rid="bib10" ref-type="bibr">10</xref>, <xref rid="bib16" ref-type="bibr">16</xref></p><p id="para280">However, our observation of no fetal infection caused by intrauterine vertical transmission could be affected by our small sample size and the stage of pregnancy at the onset of COVID-19 infection. All patients in the study were recruited in their third trimester, so we were unable to ascertain the possibility of intrauterine vertical transmission during the first or second trimester. For example, rubella infection in the first trimester can affect more than 50% of fetuses via intrauterine infection, whereas by the end of the second trimester the incidence rate is reduced by half.<xref rid="bib17" ref-type="bibr"><sup>17</sup></xref></p><p id="para290">We did not collect samples of vaginal mucosa or shedding in birth canals, which prevented us from analysing whether COVID-19 could be transmitted during vaginal delivery. Notably, however, our results showed that breastmilk samples from mothers with COVID-19 infection appeared to be free from SARS-CoV-2.</p><p id="para300">On Feb 6, 2020, a neonate born to a pregnant woman with COVID-19 pneumonia tested positive for SARS-CoV-2 infection 36 h after birth.<xref rid="bib18" ref-type="bibr">18</xref>, <xref rid="bib19" ref-type="bibr">19</xref> Although many important clinical details of this single case were not available at the time of writing this report, there are reasonable concerns that COVID-19 could be contracted in the womb. Reportedly, the pregnant woman had developed fever for 8 h and was suspected to have COVID-19 pneumonia on the basis of her typical chest CT image before admission; an emergency caesarean section was subsequently done, which was followed by confirmation of COVID-19 pneumonia. Moreover, the neonate's throat swab sample was collected approximately 30 h after birth, thus providing no direct evidence for intrauterine infection. Additionally, no direct testing of intrauterine tissue samples such as amniotic fluid, cord blood, or placenta was done to confirm that the COVID-19 infection in the neonate was due to intrauterine transmission. Therefore, we cannot conclude whether or not intrauterine COVID-19 infection occurred in this particular case. Nonetheless, this single case of an infected neonate suggests that we should pay special attention to prevent infections in newborn babies born to mothers with COVID-19 pneumonia.</p><p id="para310">This study is limited by the small sample size and retrospective method. Several considerations should be taken into account when interpreting the findings. First, all enrolled patients were in the third trimester. The effect of COVID-19 infection on the fetus in the first or second trimester of pregnancy remains to be clarified. Second, whether vaginal delivery increases the risk of mother-to-child intrapartum transmission, and whether uterine contraction could increase the possibility of the virus ascending, needs to be further investigated. Third, the risk of infection in pregnant women and the effects of the time or mode of delivery on pregnancy outcomes were not evaluated. Fourth, whether COVID-19 could damage the placenta, which represents an important link in vertical transmission, also needs to be further investigated. Future investigations of these issues and follow-up studies of pregnant women with COVID-19 infection, as well as neonates, will be necessary to ascertain the safety and health of mothers and babies exposed to SARS-CoV-2.</p><p id="para320">In summary, the symptoms of pregnant women with COVID-19 pneumonia were diverse, with the main symptoms being fever and cough. We found no evidence for vertical transmission in late pregnancy. Considering the significance of this ongoing global public health emergency, although our conclusions are limited by the small sample size, we believe that the findings reported here are important for understanding the clinical characteristics and vertical transmission potential of COVID-19 infection in pregnant women.</p></sec><sec sec-type="data-availability" id="cesec90"><title>Data sharing</title><p>With the permission of the corresponding authors, we can provide participant data without names and identifiers, but not the study protocol, statistical analysis plan, or informed consent form. Data can be provided after the Article is published. Once the data can be made public, the research team will provide an email address for communication. 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substantial contributions to the study concept and design. HC was in charge of the manuscript draft. JG took responsibility for obtaining written consent from patients, obtaining ethical approval, collecting samples, and confirming data accuracy. CW participated in drafting the manuscript, and revising it on the basis of reviewers’ comments. XY made substantial contributions to data acquisition, analysis, and interpretation. DZ was the paediatrician in charge of treatment of the newborn babies. DX, QG, JL, and JL were the obstetricians of the pregnant women, and were responsible for data collection and confirmation. WH and FL were in charge of the laboratory tasks, including sample processing and detection. WZ made substantial revisions to the manuscript.</p></ack><ack><title>Declaration of interests</title><p>We declare no competing interests.</p></ack></back></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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