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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

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Chapter
Information
Congenital Cardiac Anesthesia
A Case-based Approach
, pp. 137 - 186
Publisher: Cambridge University Press
Print publication year: 2021

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References

Suggested Reading

Angeli, E., Raisky, O., Bonnet, D., et al. Late reoperations after neonatal arterial switch operation for transposition of the great arteries. Eur J Cardiothorac Surg 2008; 34: 32–6.
Cohen, M. S., Eidem, B. W., Cetta, F., et al. Multimodality imaging guidelines of patients with transposition of the great arteries from the American Society of Echocardiography developed in collaboration with the Society for Cardiovascular Magnetic Resonance and Society of Cardiovascular Computed Tomography. J Am Soc Echocardiogr 2016; 29: 571621.
Gottlieb, E. A. and Andropoulos, D. B. Anesthesia for the patient with congenital heart disease presenting for noncardiac surgery. Curr Opin Anesth 2013; 26: 318–26.
Latham, G. L., Joffe, D. C., Eisses, M. J., et al. Anesthestic considerations and management of transposition of the great arteries. Semin Cardiothorac Vasc Anesth 2015; 19: 233–43.
Morgan, C. T., Mertens, L., Grotenhuis, H., et al. Understanding the mechanism for branch pulmonary artery stenosis after the arterial switch operation for transposition of the great arteries. Eur Heart J Cardiovasc Imaging 2017; 18: 180–5.
Warnes, C. A., Williams, R. G., Bashore, T. M., et al. ACC/AHA 2008 Guidelines for the management of adults with congenital heart disease: a report of the American College of Cardiology/American Heart Association Task Force on practice guidelines (Writing Committee to develop guidelines on the management of adults with congenital heart disease). Circulation 2008; 118: 714833.

Suggested Reading

Cohen, M. S., Eidem, B. W., Cetta, F., et al. Multimodality imaging guidelines of patients with transposition of the great arteries: a report from the American Society of Echocardiography developed in collaboration with the Society for Cardiovascular Magnetic Resonance and the Society of Cardiovascular Computed Tomography. J Am Soc Echocardiogr 2016; 29: 571621.
Cuypers, J. A., Eindhoven, J. A., Slager, M. A., et al. The natural and unnatural history of the Mustard procedure: long-term outcome up to 40 years. Eur Heart J 2014; 35: 1666–74.
De Pasquale, G. High prevalence of baffle leaks in adults after atrial switch operations for transposition of the great arteries. Eur Heart J Cardiovasc Imaging 2017; 18: 531–5.
Dobson, R., Dantan, M., Nicola, W., et al. The natural and unnatural history of the systemic right ventricle in adult survivors. J Thorac Cardiovasc Surg 2013; 145: 1493–50.
Haeffele, C. and Lui, G. K. Dextro-transposition of the great arteries: long-term sequelae of atrial and arterial switch. Cardiol Clin 2015; 33: 543–58.
Joffe, D. C., Krishnan, S. K., Eisses, M., et al. The use of transesophageal echocardiography in the management of baffles leaks in a patient with transposition of the great arteries. AA Case Rep 2018; 13.
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Stout, K. K., Daniels, C. J., and Aboulhosn, J. A. 2018 AHA/ACC guideline for the management of adults with congenital heart disease: a report of the American College of Cardiology/American Heart Association task force on clinical practice guidelines. Circulation 2018; 139: e698800.
Warnes, C. A. Transposition of the great arteries. Circulation 2006; 114: 2699–709.

Suggested Reading

Atallah, J., Rutledge, J. M., and Dyck, J. D. Congenitally corrected transposition of the great arteries (atrioventricular and ventriculoarterial discordance). In Allen, H., Driscoll, D. J., Shaddy, R. E., et al., eds. Moss and Adams’ Heart Disease in Infants, Children and Adolescents, 8th ed. Philadelphia: Lippincott Williams & Wilkins; 2013, 1147–60.
Beauchesne, L. M., Warnes, C. A., Connolly, H. M., et al. Outcome of the unoperated adult who presents with congenitally corrected transposition of the great arteries. J Amer Coll Cardiol 2002; 40: 285–90.
Chu, D. I., Tan, J. M., Mattei, P., et al. Mortality and morbidity after laparoscopic surgery in children with and without congenital heart disease. J Pediatr 2017; 185: 8893.
Crossley, G. H., Poole, J. E., Rozner, M. A., et al. The Heart Rhythm Society (HRS)/American Society of Anesthesiologists (ASA) expert consensus statement on the perioperative management of patients with implantable defibrillators, pacemakers and arrhythmia monitors: facilities and patient management: this document was developed as a joint project with the American Society of Anesthesiologists (ASA), and in collaboration with the American Heart Association (AHA), and the Society of Thoracic Surgeons (STS). Heart Rhythm 2011; 8: 1114–54.
Graham, T. P., Bernard, Y. D., Mellen, B. G., et al. Long-term outcome in congenitally corrected transposition of the great arteries: a multi-institutional study. J Am Coll Cardiol 2000; 36: 255–61.
Hornung, T. S. and Calder, L. Congenitally corrected transposition of the great arteries. Heart 2010; 96: 1154–61.
McEwan, A. and Manolis, M. Anesthesia for transposition of the great arteries. In Andropoulos, D. B., Stayer, S., Mossad, E. B. et al., eds. Anesthesia for Congenital Heart Disease, 3rd ed. Hoboken, NJ: John Wiley & Sons; 2015; 542–66.
Nishimura, R. A., Otto, C. M., Bonow, R. O., et al. 2017 AHA/ACC focused update of the 2014 AHA/ACC guideline for the management of patients with valvular heart disease: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. J Am Coll Cardiol 2017; 70: 252–89.
Ross, R. D. The Ross classification for heart failure in children after 25 years: a review and an age-stratified revision. Pediatr Cardiol 2012; 33: 1295–300.
Warnes, C. A. Transposition of the great arteries. Circulation 2006; 114: 2699–709.

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.
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.
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.

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.
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.
Ryerson, L. M., Pharis, S., Pockett, C., et al. Heterotaxy syndrome and intestinal abnormalities. Pediatrics 2018; 142: e20174267.
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.

References

Collett, R. W. and Edwards, J. E.. Persistent truncus arteriosus: a classification according to anatomic types. Surg Clin North Am 1949; 29: 1245–70.
Van Praagh, R. and Van Praagh, S.. The anatomy of common aorticopulmonary trunk (truncus arteriosus communis) and its embryologic implications: a study of 57 necropsy cases. Am J Cardiol 1965; 16: 406–25.
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Carvalho, J. S., Mavrides, E., Shinebourne, E. A., et al. Improving the effectiveness of routine prenatal screening for major congenital heart defects. Heart 2002; 88: 387–91.
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Jacobs, M. L.. Congenital Heart Surgery Nomenclature and Database Project: truncus arteriosus. Ann Thorac Surg 2000; 69: 5055.
Parikh, R., Eisses, M., Latham, G. L., et al. Perioperative and anesthetic considerations in truncus arteriosus. Semin Cardiothorac Vasc Anesth 2018; 22: 285–93.
Momma, K.. Cardiovascular anomalies associated with chromosome 22q11.2 deletion syndrome. Am J Cardiol 2010; 105: 1617–24.
Buckley, J. R., Amula, V., Sassalos, P., et al. Multicenter analysis of early childhood outcomes after repair of truncus arteriosus. Ann Thorac Surg 2019; 107: 553–9.
Yotsui-Tsuchimochi, H., Higa, K., Matsunaga, M., et al. Anesthetic management of a child with chromosome 22q11 deletion syndrome. Pediatr Anesth 2006; 16: 454–7.
Wilson, W., Taubert, K. A., Gewitz, M., et al. Prevention of infective endocarditis. Circulation 2007; 116: 1736–54.
Chiono, J., Raux, O., Bringuier, S., et al. Bilateral suprazygomatic maxillary nerve block for cleft palate repair in children. Anesthesiology 2014; 120: 132–69.

Suggested Reading

Buckley, J. R., Amula, V., Sassalos, P., et al. Multicenter analysis of early childhood outcomes after repair of truncus arteriosus. Ann Thorac Surg 2019; 107: 553–59.
O’Byrne, M. L., Mercer-Rosa, L., Zhao, H., et al. Morbidity in children and adolescents after surgical correction of truncus arteriosus communis. Am Heart J 2013; 166: 512–18.
Parikh, R., Eisses, M., Latham, G. J., et al. Perioperative and anesthetic considerations in truncus arteriosus. Semin Cardiothorac Vasc Anesth 2018; 22: 285–93.
Yotsui-Tsuchimochi, H., Higa, K., Matsunaga, M., et al. Anesthetic management of a child with chromosome 22q11 deletion syndrome. Pediatr Anesth 2006; 16: 454–7.

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