Skip to content
View in the app

A better way to browse. Learn more.

Pediatric Surgery Club

A full-screen app on your home screen with push notifications, badges and more.

To install this app on iOS and iPadOS
  1. Tap the Share icon in Safari
  2. Scroll the menu and tap Add to Home Screen.
  3. Tap Add in the top-right corner.
To install this app on Android
  1. Tap the 3-dot menu (⋮) in the top-right corner of the browser.
  2. Tap Add to Home screen or Install app.
  3. Confirm by tapping Install.
Get your Pro Membership!

Featured Replies

[size=20px]A 38-week gestation, 2.9-kg infant is transferred to the NICU with the diagnosis of a left congenital diaphragmatic hernia (CDH). She is intubated and on 100% FiO2 with ventilator pressures of 28/6, IMV rate of 60/minute and a preductal ABG of pH 7.10, PaO2 75 and PaCO2 65. Head ultrasound is normal. However, her echocardiogram shows coarctation of the aorta with a large PDA and right to left flow to the aorta distal to the coarctation. The left ventricle does not appear small. Gentle ventilation is initiated, but the infant continues to deteriorate. Cardiology recommends prostaglandin E1 to maintain ductal flow. High frequency ventilation and nitric oxide are provided, but hypoxia and metabolic acidosis worsen.

 

The next best step in management of this patient with a CDH and aortic coarctation is

 

A emergent repair of the CDH.

 

B emergently repair the coarctation.

 

C continue medical management-not an ECMO candidate.

 

D VV ECMO.

 

E VA ECMO.[/size]

Edited by Admin

  • Author

correct answer

D VV ECMO.

​

Congenital diaphragmatic hernia (CDH) is frequently associated with congenital cardiac anomalies (30%), making treatment of these infants a major challenge. Aortic coarctation in the setting of CDH can be associated with left ventricular hypoplasia resulting in a nearly universally fatal condition. However, infants with CDH and isolated coarctation have survived.

 

CDH and coarctations can be difficult to diagnose. ECHO can demonstrate what appears to be a small arch due to the high pulmonary pressures and right to left flow. It may not be until the duct has closed to increase flow across the aorta that one can confidently rule out coarctation of the aorta.

 

If medical management can stabilize the infant (including PGE1), early repair of the CDH followed by repair of coarctation and PDA is feasible. However, if the infant continues to deteriorate then venovenous (VV) ECMO may be preferred to venoarterial (VA) cannulation. VA ECMO can improve preductal oxygen saturation, but would not effectively improve postductal oxygen delivery and metabolic acidosis may worsen. Furthermore, if VA ECMO proved helpful in managing pulmonary hypertension, ligation of the right carotid artery at the completion of ECMO creates limitations in the subsequent repair of the coarcation where clamping the aortic arch might be required. VV ECMO has the potential to improve oxygenation including postductal, postcoarctation flow.​

Account

Navigation

Search

Search

Configure browser push notifications

Chrome (Android)
  1. Tap the lock icon next to the address bar.
  2. Tap Permissions → Notifications.
  3. Adjust your preference.
Chrome (Desktop)
  1. Click the padlock icon in the address bar.
  2. Select Site settings.
  3. Find Notifications and adjust your preference.