Thoracoamniotic shunt placement for a right-sided congenital diaphragmatic hernia complicated by hydrops

S. Christopher Derderian; Corey W. Iqbal; Juan M. Ganzalez; Tippi C. MacKenzie; Doug Miniati; Shinjiro Hirose

doi:10.1016/j.epsc.2013.08.002

Thoracoamniotic shunt placement for a right-sided congenital diaphragmatic hernia complicated by hydrops

S. Christopher Derderian, Corey W. Iqbal, Juan M. Ganzalez, Tippi C. MacKenzie, Doug Miniati, Shinjiro Hirose

Surgery

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

Abstract

Mortality associated with congenital diaphragmatic hernia (CDH) is high, and the role of prenatal management continues to evolve. We report a case of a right-sided CDH complicated by fetal hydrops successfully managed with thoracoamniotic shunt placement. Subsequent ultrasounds indicated resolution of hydrops. Despite preterm premature rupture of membrane and preterm delivery at 32 3/7 weeks gestation, the infant survived to hospital discharge at 2.5 months of life. This is the first case of a hydropic right-sided CDH successfully treated with a thoracoamniotic shunt.

Original language	English (US)
Pages (from-to)	281-283
Number of pages	3
Journal	Journal of Pediatric Surgery Case Reports
Volume	1
Issue number	9
DOIs	https://doi.org/10.1016/j.epsc.2013.08.002
State	Published - Jan 1 2013

Keywords

Fetal hydrops
Right-sided congenital diaphragmatic hernia
Thoracoamniotic shunt

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Surgery

Access to Document

10.1016/j.epsc.2013.08.002

Cite this

Thoracoamniotic shunt placement for a right-sided congenital diaphragmatic hernia complicated by hydrops. / Derderian, S. Christopher; Iqbal, Corey W.; Ganzalez, Juan M.; MacKenzie, Tippi C.; Miniati, Doug; Hirose, Shinjiro.

In: Journal of Pediatric Surgery Case Reports, Vol. 1, No. 9, 01.01.2013, p. 281-283.

Research output: Contribution to journal › Article › peer-review

@article{338067ca54fd4fdb93294b1436cb0cac,

title = "Thoracoamniotic shunt placement for a right-sided congenital diaphragmatic hernia complicated by hydrops",

abstract = "Mortality associated with congenital diaphragmatic hernia (CDH) is high, and the role of prenatal management continues to evolve. We report a case of a right-sided CDH complicated by fetal hydrops successfully managed with thoracoamniotic shunt placement. Subsequent ultrasounds indicated resolution of hydrops. Despite preterm premature rupture of membrane and preterm delivery at 32 3/7 weeks gestation, the infant survived to hospital discharge at 2.5 months of life. This is the first case of a hydropic right-sided CDH successfully treated with a thoracoamniotic shunt.",

keywords = "Fetal hydrops, Right-sided congenital diaphragmatic hernia, Thoracoamniotic shunt",

author = "Derderian, {S. Christopher} and Iqbal, {Corey W.} and Ganzalez, {Juan M.} and MacKenzie, {Tippi C.} and Doug Miniati and Shinjiro Hirose",

year = "2013",

month = jan,

day = "1",

doi = "10.1016/j.epsc.2013.08.002",

language = "English (US)",

volume = "1",

pages = "281--283",

journal = "Journal of Pediatric Surgery Case Reports",

issn = "2213-5766",

publisher = "Elsevier BV",

number = "9",

}

TY - JOUR

T1 - Thoracoamniotic shunt placement for a right-sided congenital diaphragmatic hernia complicated by hydrops

AU - Derderian, S. Christopher

AU - Iqbal, Corey W.

AU - Ganzalez, Juan M.

AU - MacKenzie, Tippi C.

AU - Miniati, Doug

AU - Hirose, Shinjiro

PY - 2013/1/1

Y1 - 2013/1/1

N2 - Mortality associated with congenital diaphragmatic hernia (CDH) is high, and the role of prenatal management continues to evolve. We report a case of a right-sided CDH complicated by fetal hydrops successfully managed with thoracoamniotic shunt placement. Subsequent ultrasounds indicated resolution of hydrops. Despite preterm premature rupture of membrane and preterm delivery at 32 3/7 weeks gestation, the infant survived to hospital discharge at 2.5 months of life. This is the first case of a hydropic right-sided CDH successfully treated with a thoracoamniotic shunt.

AB - Mortality associated with congenital diaphragmatic hernia (CDH) is high, and the role of prenatal management continues to evolve. We report a case of a right-sided CDH complicated by fetal hydrops successfully managed with thoracoamniotic shunt placement. Subsequent ultrasounds indicated resolution of hydrops. Despite preterm premature rupture of membrane and preterm delivery at 32 3/7 weeks gestation, the infant survived to hospital discharge at 2.5 months of life. This is the first case of a hydropic right-sided CDH successfully treated with a thoracoamniotic shunt.

KW - Fetal hydrops

KW - Right-sided congenital diaphragmatic hernia

KW - Thoracoamniotic shunt

UR - http://www.scopus.com/inward/record.url?scp=84893041205&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84893041205&partnerID=8YFLogxK

U2 - 10.1016/j.epsc.2013.08.002

DO - 10.1016/j.epsc.2013.08.002

M3 - Article

AN - SCOPUS:84893041205

VL - 1

SP - 281

EP - 283

JO - Journal of Pediatric Surgery Case Reports

JF - Journal of Pediatric Surgery Case Reports

SN - 2213-5766

IS - 9

ER -

Thoracoamniotic shunt placement for a right-sided congenital diaphragmatic hernia complicated by hydrops

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this