Anesthetic management of tracheoesophageal fistula repair in a newborn with a double-outlet right ventricle

2011 ◽  
Vol 23 (8) ◽  
pp. 643-645
Author(s):  
Heather McClung ◽  
Rajeev Prasad ◽  
Roy Schwartz
Author(s):  
Catherine P. Seipel ◽  
Titilopemi A. O. Aina

Tracheoesophageal fistula (TEF) with esophageal atresia (EA) is a congenital malformation occurring in approximately 1:4,000 live births. TEF/EA is characterized by disrupted continuity of the esophagus. There are five distinct types, but the most common is EA with a distal TEF. Most cases are diagnosed postnatally after an inability to pass a nasogastric tube (NGT), with subsequent radiographic imaging finding the NGT coiled within the esophageal pouch. The anesthetic management of TEF/EA repair can be complicated by the presence of cardiac, renal, and vertebral anomalies. Additionally, ventilation can be challenging, and care must be taken to minimize insufflation of the stomach through the fistula. Postoperative analgesia should include consideration of intravenous opioids, nonopioid adjunct medications, and regional and neuraxial techniques.


2021 ◽  
Vol 9 (11) ◽  
pp. 2634-2640
Author(s):  
Ling-Can Tan ◽  
Wei-Yi Zhang ◽  
Yi-Ding Zuo ◽  
Hong-Yang Chen ◽  
Chun-Ling Jiang

2020 ◽  
Author(s):  
Lingcan Tan ◽  
Weiyi Zhang ◽  
Yiding Zuo ◽  
Hongyang Chen ◽  
Chunling Jiang

Abstract Background Acquired secondary polycythemia is common in patients with a double outlet right ventricle, and results from tissue hypoxia. Secondary erythrocytosis can cause coagulation deficiencies, and increases the risks of thrombosis and infarction. Perioperative management in double outlet right ventricle patients with severe erythrocytosis is intractable, and only a few cases have been reported. Case presentation: Herein, we report the anesthetic management of a 10-year-old female patient with a double outlet right ventricle. She lived in the low-oxygen Qinghai−Tibet Plateau, and presented with severe polycythemia (hemoglobin, 24.8 g/dL; hematocrit, 75%). She underwent a modified Fontan surgery, which was satisfactory and without any perioperative complications. Our anesthetic management highlights the importance of perioperative hemodilution to decrease the risk of thromboembolism, and correction of coagulopathy to prevent hemorrhage. Conclusions Anesthetic management is challenging in rare cyanotic congenital heart disease patients with severe polycythemia. For prevention of thrombosis and hemorrhage, it is important to adopt perioperative hemodilution and correction of coagulopathy.


Sign in / Sign up

Export Citation Format

Share Document