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Article: Thoracoscopic removal of a displaced thoracoamniotic shunt in a newborn with antenatal pleural effusion—a case report

TitleThoracoscopic removal of a displaced thoracoamniotic shunt in a newborn with antenatal pleural effusion—a case report
Authors
KeywordsThoracoamniotic shunt displacement
congenital chylothorax
thoracoscopy
case report
Issue Date2020
PublisherAME Publishing Company. The Journal's web site is located at https://tp.amegroups.com/
Citation
Translational Pediatrics, 2020, v. 9 n. 5, p. 702-706 How to Cite?
AbstractThoracoamniotic shunt has been considered as a treatment for antenatal pleural effusion and complication is rare. In majority of cases, the shunt can be removed uneventfully. In this article, we reported a rare complication of shunt migration resulting in the need of thoracoscopic removal at newborn period. The patient born at 39+3 weeks of gestation suffered from antenatal chylothorax detected at 28 weeks and was managed by intrauterine thoracoamniotic shunt insertion. This was complicated by shunt displacement, which caused respiratory distress after birth requiring ventilatory support and progressive pleural effusion in this patient. To prevent further neonatal compromise, thoracoscopic removal of the retained shunt was done on day 7 of life followed by post-op chest drain insertion. Post-op condition was stable with resolution of respiratory distress, and the patient was discharge on post-op day 16. We would like to remind clinicians about this potential complication of thoracoamniotic shunt, which can pose a potential risk of severe neonatal compromise, and that it can be managed by minimal invasive surgery even in the newborn period.
Descriptioneid_2-s2.0-85096463576
Persistent Identifierhttp://hdl.handle.net/10722/295268
ISSN
2021 Impact Factor: 4.047
2020 SCImago Journal Rankings: 0.702
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorSham, GTW-
dc.contributor.authorChung, PHY-
dc.contributor.authorChan, IMC-
dc.contributor.authorLeung, WC-
dc.contributor.authorWong, KKY-
dc.date.accessioned2021-01-11T13:57:43Z-
dc.date.available2021-01-11T13:57:43Z-
dc.date.issued2020-
dc.identifier.citationTranslational Pediatrics, 2020, v. 9 n. 5, p. 702-706-
dc.identifier.issn2224-4336-
dc.identifier.urihttp://hdl.handle.net/10722/295268-
dc.descriptioneid_2-s2.0-85096463576-
dc.description.abstractThoracoamniotic shunt has been considered as a treatment for antenatal pleural effusion and complication is rare. In majority of cases, the shunt can be removed uneventfully. In this article, we reported a rare complication of shunt migration resulting in the need of thoracoscopic removal at newborn period. The patient born at 39+3 weeks of gestation suffered from antenatal chylothorax detected at 28 weeks and was managed by intrauterine thoracoamniotic shunt insertion. This was complicated by shunt displacement, which caused respiratory distress after birth requiring ventilatory support and progressive pleural effusion in this patient. To prevent further neonatal compromise, thoracoscopic removal of the retained shunt was done on day 7 of life followed by post-op chest drain insertion. Post-op condition was stable with resolution of respiratory distress, and the patient was discharge on post-op day 16. We would like to remind clinicians about this potential complication of thoracoamniotic shunt, which can pose a potential risk of severe neonatal compromise, and that it can be managed by minimal invasive surgery even in the newborn period.-
dc.languageeng-
dc.publisherAME Publishing Company. The Journal's web site is located at https://tp.amegroups.com/-
dc.relation.ispartofTranslational Pediatrics-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectThoracoamniotic shunt displacement-
dc.subjectcongenital chylothorax-
dc.subjectthoracoscopy-
dc.subjectcase report-
dc.titleThoracoscopic removal of a displaced thoracoamniotic shunt in a newborn with antenatal pleural effusion—a case report-
dc.typeArticle-
dc.identifier.emailChung, PHY: chungphy@hku.hk-
dc.identifier.emailLeung, WC: leungwc6@hkucc.hku.hk-
dc.identifier.emailWong, KKY: kkywong@hku.hk-
dc.identifier.authorityChung, PHY=rp02002-
dc.identifier.authorityWong, KKY=rp01392-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.21037/tp-20-74-
dc.identifier.pmid33209734-
dc.identifier.pmcidPMC7658768-
dc.identifier.scopuseid_2-s2.0-85096463576-
dc.identifier.hkuros320792-
dc.identifier.volume9-
dc.identifier.issue5-
dc.identifier.spage702-
dc.identifier.epage706-
dc.identifier.isiWOS:000583840400016-
dc.publisher.placeHong Kong-

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