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Chapter 24 - Total Anomalous Pulmonary Venous Return and Heterotaxy Syndrome

from Section 4 - Complex Mixing Lesions

Published online by Cambridge University Press:  09 September 2021

Laura K. Berenstain
Affiliation:
Cincinnati Children's Hospital Medical Center
James P. Spaeth
Affiliation:
Cincinnati Children's Hospital Medical Center
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Summary

Total anomalous pulmonary venous return is a rare disorder characterized by the lack of direct connection of the pulmonary veins to the left atrium; instead, the pulmonary veins connect either directly to the right atrium or indirectly via a vein connected to the right atrium. This results in oxygenated blood ultimately draining into the right atrium and mixing with deoxygenated blood, necessitating a right-to-left atrial shunt to survive. Although it can be an isolated defect, in approximately two-thirds of cases total anomalous pulmonary venous return is associated with complex cardiac defects and frequently with heterotaxy syndrome, an embryologic disruption of right and left laterality of the thoracic and abdominal organs. Children with heterotaxy and total anomalous pulmonary venous return have even higher rates of early and late morbidity and mortality. This chapter details the perioperative management of a patient with recurrent pulmonary venous stenosis and intestinal malrotation requiring urgent abdominal surgery and outlines the appropriate management strategies for high-risk patients with this physiology.

Type
Chapter
Information
Congenital Cardiac Anesthesia
A Case-based Approach
, pp. 169 - 177
Publisher: Cambridge University Press
Print publication year: 2021

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References

References

St. Louis, J. D., Harvey, B. A., Menk, J. S., et al. Repair of “simple” total anomalous pulmonary venous connection: a review from the Pediatric Cardiac Care Consortium. Ann Thorac Surg 2012; 94: 133–7.CrossRefGoogle ScholarPubMed
Oshima, Y., Yoshida, M., Maruo, A., et al. Modified primary sutureless repair of total anomalous pulmonary venous connection in heterotaxy. Ann Thorac Surg 2009; 888: 1348–50.Google Scholar
Sen, S., Duchon, J., Lampl, B., et al. Heterotaxy syndrome infants are at risk for early shunt failure after Ladd procedure. Ann Thorac Surg 2015; 99: 918–25.CrossRefGoogle ScholarPubMed

Suggested Reading

Khan, M. S., Bryant, R., Kim, S. H., et al. Contemporary outcomes of surgical repair of total anomalous pulmonary venous connection in patients with heterotaxy syndrome. Ann Thorac Surg 2015; 99: 2134–9.CrossRefGoogle ScholarPubMed
Loomba, R. S., Morales, D. L. S., and Redington, A. Heterotaxy. In Ungerleider, R. M., Meliones, J. N., Nelson McMillan, K. et al., eds. Critical Heart Disease in Infants and Children, 3rd ed. Philadelphia: Mosby Elsevier, 2019; 796803.CrossRefGoogle Scholar
Ryerson, L. M., Pharis, S., Pockett, C., et al. Heterotaxy syndrome and intestinal abnormalities. Pediatrics 2018; 142: e20174267.CrossRefGoogle Scholar
St. Louis, J., Molitor-Kirsch, E., Shah, S., et al. Total anomalous pulmonary venous return. In Ungerleider, R. M., Meliones, J. N., Nelson McMillan, K., et al., eds. Critical Heart Disease in Infants and Children, 3rd ed. Philadelphia: Mosby Elsevier; 2019; 587–96.Google Scholar

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