Treatment of fetal circular shunt with non-steroidal anti-inflammatory drugs.


Journal

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
ISSN: 1469-0705
Titre abrégé: Ultrasound Obstet Gynecol
Pays: England
ID NLM: 9108340

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 02 06 2018
revised: 24 08 2018
accepted: 19 10 2018
pubmed: 2 11 2018
medline: 7 1 2020
entrez: 2 11 2018
Statut: ppublish

Résumé

A circular shunt (CS) is a life-threatening condition involving massive shunting of systemic arterial blood via the ductus arteriosus to the left ventricle without traversing the lungs. In the prenatal setting, it occurs mainly in fetuses with severe forms of Ebstein's anomaly (EA) owing to unrestricted ductal flow and significant pulmonary and tricuspid regurgitation. We aimed to improve the fetal hemodynamics and chances of survival of affected fetuses by inducing ductal constriction using transplacental non-steroidal anti-inflammatory drugs (NSAIDs). Following initiation of treatment between 26 and 34 weeks' gestation, three (75%) of four fetuses with EA/CS responded with sustained ductal constriction and improved hemodynamic function, which allowed continuation of pregnancy for 3-7 weeks and elective delivery. All successfully treated cases underwent neonatal surgery immediately after birth to eliminate the CS and survived. This included two neonates that underwent single-ventricle palliation surgery that required postoperative extracorporeal membrane oxygenation and hemofiltration for transient respiratory and renal failure. The one case that did not respond to treatment with NSAIDs was delivered prematurely for progressive fetal compromise and died shortly after birth. Transplacental treatment with NSAIDs represents a novel approach to controlling fetal CS, avoiding in-utero death and prolonging the pregnancy to a more advanced gestational age, thereby potentially increasing the chances of neonatal survival. This treatment should be considered and initiated at an early stage of systemic steal to prevent brain injury due to hypoperfusion. Copyright © 2018 ISUOG. Published by John Wiley & Sons Ltd.

Identifiants

pubmed: 30381862
doi: 10.1002/uog.20169
doi:

Substances chimiques

Anti-Inflammatory Agents, Non-Steroidal 0
Indomethacin XXE1CET956

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

841-846

Subventions

Organisme : Niigata Prefectural Welfare Federation of Agricultural Cooperative, Japan

Informations de copyright

Copyright © 2018 ISUOG. Published by John Wiley & Sons Ltd.

Auteurs

T Torigoe (T)

Fetal Cardiac Program, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, Canada.

W Mawad (W)

Fetal Cardiac Program, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, Canada.
Diagnostic Imaging Program, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, Canada.

M Seed (M)

Fetal Cardiac Program, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, Canada.
Diagnostic Imaging Program, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, Canada.

G Ryan (G)

Fetal Medicine Unit, Department of Obstetrics & Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, Canada.

D Marini (D)

Diagnostic Imaging Program, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, Canada.

F Golding (F)

Fetal Cardiac Program, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, Canada.

T VAN Mieghem (T)

Fetal Medicine Unit, Department of Obstetrics & Gynecology, Mount Sinai Hospital, University of Toronto, Toronto, Canada.

E Jaeggi (E)

Fetal Cardiac Program, Labatt Family Heart Centre, Hospital for Sick Children, University of Toronto, Toronto, Canada.

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Classifications MeSH