Severe Acute Respiratory Syndrome Coronavirus 2 Placental Infection and Inflammation Leading to Fetal Distress and Neonatal Multi-Organ Failure in an Asymptomatic Woman.


Journal

Journal of the Pediatric Infectious Diseases Society
ISSN: 2048-7207
Titre abrégé: J Pediatric Infect Dis Soc
Pays: England
ID NLM: 101586049

Informations de publication

Date de publication:
28 May 2021
Historique:
received: 22 07 2020
accepted: 23 11 2020
pubmed: 29 12 2020
medline: 4 6 2021
entrez: 28 12 2020
Statut: ppublish

Résumé

In general, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection during pregnancy is not considered to be an increased risk for severe maternal outcomes but has been associated with an increased risk for fetal distress. Maternal-fetal transmission of SARS-CoV-2 was initially deemed uncertain; however, recently a few cases of vertical transmission have been reported. The intrauterine mechanisms, besides direct vertical transmission, leading to the perinatal adverse outcomes are not well understood. Multiple maternal, placental, and neonatal swabs were collected for the detection of SARS-CoV-2 using real-time quantitative polymerase chain reaction (RT-qPCR). Serology of immunoglobulins against SARS-CoV-2 was tested in maternal, umbilical cord, and neonatal blood. Placental examination included immunohistochemical investigation against SARS-CoV-2 antigen expression, with SARS-CoV-2 ribonucleic acid (RNA) in situ hybridization and transmission electron microscopy. RT-qPCRs of the oropharynx, maternal blood, vagina, placenta, and urine were all positive over a period of 6 days, while breast milk, feces, and all neonatal samples tested negative. Placental findings showed the presence of SARS-CoV-2 particles with generalized inflammation characterized by histiocytic intervillositis with diffuse perivillous fibrin depositions with damage to the syncytiotrophoblasts. Placental infection by SARS-CoV-2 leads to fibrin depositions hampering fetal-maternal gas exchange with resulting fetal distress necessitating a premature emergency cesarean section. Postpartum, the neonate showed a fetal or pediatric inflammatory multisystem-like syndrome with coronary artery ectasia temporarily associated with SARS-CoV-2 for which admittance and care on the neonatal intensive care unit (NICU) were required, despite being negative for SARS-CoV-2. This highlights the need for awareness of adverse fetal and neonatal outcomes during the current coronavirus disease 2019 pandemic, especially considering that the majority of pregnant women appear asymptomatic.

Sections du résumé

BACKGROUND BACKGROUND
In general, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection during pregnancy is not considered to be an increased risk for severe maternal outcomes but has been associated with an increased risk for fetal distress. Maternal-fetal transmission of SARS-CoV-2 was initially deemed uncertain; however, recently a few cases of vertical transmission have been reported. The intrauterine mechanisms, besides direct vertical transmission, leading to the perinatal adverse outcomes are not well understood.
METHODS METHODS
Multiple maternal, placental, and neonatal swabs were collected for the detection of SARS-CoV-2 using real-time quantitative polymerase chain reaction (RT-qPCR). Serology of immunoglobulins against SARS-CoV-2 was tested in maternal, umbilical cord, and neonatal blood. Placental examination included immunohistochemical investigation against SARS-CoV-2 antigen expression, with SARS-CoV-2 ribonucleic acid (RNA) in situ hybridization and transmission electron microscopy.
RESULTS RESULTS
RT-qPCRs of the oropharynx, maternal blood, vagina, placenta, and urine were all positive over a period of 6 days, while breast milk, feces, and all neonatal samples tested negative. Placental findings showed the presence of SARS-CoV-2 particles with generalized inflammation characterized by histiocytic intervillositis with diffuse perivillous fibrin depositions with damage to the syncytiotrophoblasts.
CONCLUSIONS CONCLUSIONS
Placental infection by SARS-CoV-2 leads to fibrin depositions hampering fetal-maternal gas exchange with resulting fetal distress necessitating a premature emergency cesarean section. Postpartum, the neonate showed a fetal or pediatric inflammatory multisystem-like syndrome with coronary artery ectasia temporarily associated with SARS-CoV-2 for which admittance and care on the neonatal intensive care unit (NICU) were required, despite being negative for SARS-CoV-2. This highlights the need for awareness of adverse fetal and neonatal outcomes during the current coronavirus disease 2019 pandemic, especially considering that the majority of pregnant women appear asymptomatic.

Identifiants

pubmed: 33367801
pii: 6053141
doi: 10.1093/jpids/piaa153
pmc: PMC7798999
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

556-561

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of The Journal of the Pediatric Infectious Diseases Society.

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Auteurs

Sam Schoenmakers (S)

Department of Obstetrics and Gynaecology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Pauline Snijder (P)

Department of Neonatology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Robert M Verdijk (RM)

Department of Pathology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Thijs Kuiken (T)

Department of Viroscience, Erasmus University Medical Center, Rotterdam, The Netherlands.

Sylvia S M Kamphuis (SSM)

Department of Pediatric Infectiology, Immunology and Rheumatology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Laurens P Koopman (LP)

Department of Pediatric Cardiology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Thomas B Krasemann (TB)

Department of Pediatric Cardiology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Melek Rousian (M)

Department of Obstetrics and Gynaecology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Michelle Broekhuizen (M)

Department of Neonatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Department of Pharmacology and Vascular Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands.

Eric A P Steegers (EAP)

Department of Obstetrics and Gynaecology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Marion P G Koopmans (MPG)

Department of Viroscience, Erasmus University Medical Center, Rotterdam, The Netherlands.

Pieter L A Fraaij (PLA)

Department of Viroscience, Erasmus University Medical Center, Rotterdam, The Netherlands.
Department of Pediatric Infectiology, Immunology and Rheumatology, Erasmus University Medical Center, Rotterdam, The Netherlands.

Irwin K M Reiss (IKM)

Department of Neonatology, Erasmus University Medical Center, Rotterdam, The Netherlands.

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