References

1.Backer CL, Mavroudis C. Vascular rings and pulmonary artery sling. In: Mavroudis C,Backer CL (eds) Pediatric Cardiac Surgery, 4thedn. Oxford, UK:Wiley-Blackwell, 2013, pp. 234–255.

2.Weinberg PM, Natarajan S, Rogers LS. Aortic arch and vascular anomalies. In: Allen HD, Driscoll DJ, Shaddy RE, Feltes TF (eds) Moss and Adams’ Heart Disease in Infants, Children, and Adolescents, including the Fetus and Young Adult, 8thedn. Phildelphia, PA:Lipincott, Williams, & Wilkins, 2013, pp. 758–98.

3.Backer CL, Mavroudis C. Congenital heart surgery nomenclature and database project: vascular rings, tracheal stenosis, pectus excavatum. Ann Thorac Surg 2000;69:S308–18.

4.Berdon WE. Rings, slings, and other things: vascular compression of the infant trachea updated from the mid-century to the millennium – the legacy of Robert E. Gross, MD, and Edward B. D. Neuhauser, MD. Radiology 2000;216:624–32.

5.Bakker DA, Berger RM, Witsenburg M, et al. Vascular rings: a rare cause of common respiratory symptoms. Acta Paediatr 1999;88:947–52.

6.Chun K, Colombani PM, Dudgeon DL, et al. Diagnosis and management of congenital vascular rings: a 22-year experience. Ann Thorac Surg 1992;53:597–603.

7.Alsenaidi K, Gurofsky R, Karamlou T, et al. Management and outcomes of double aortic arch in 81 patients. Am J Pediatr 2006;118:1336–41.

8.Backer CL, Hillman N, Mavroudis C, et al. Resection of Kommerell’s diverticulum and left subclavian artery transfer for recurrent symptoms after vascular ring division. Eur J Cardiothorac Surg 2002;22:64– 69.

9.Zani A, Morini F, Paolantonio P, et al. Not all symptoms disappear after vascular ring division. Pediatr Cardiol 2008;29:676–8.

10.Chiua PPL, Rusana M, Williams WG, et al. Long-term outcomes of clinically significant vascular rings associated with congenital tracheal stenosis. J Pediatr Surg 2006;41:335–41.

11.Burke RP, Chang AC. Video-assisted thoracoscopic division of a vascular ring in an infant: a new operative technique. J Card Surg 1993;8:537–40.

12.Backer CL, Kelle AM, Mavroudis C, et al. Tracheal reconstruction in children with unilateral lung agenesis or severe hypoplasia. Ann Thorac Surg 2009;88, 624–31.

13.Dodge-Khatami A, Mavroudis C, Backer CL. Congenital heart surgery nomenclature and database project: anomalies of the coronary arteries. Ann Thorac Surg 2000;69:S270–97.

14.Frapier JM, Leclercq F, Bodino M, et al. Malignant ventricular arrhythmias revealing anomalous origin of the left coronary artery in two adults. Eur J Cardiothorac Surg 1999;15:539–41.

15. Fierens C, Budts W, Denef B, et al. A 72 year old woman with ALCAPA. Heart 2000;83: E2.

16.Nielsen HB, Perko M, Aldershvile J, et al. Cardiac arrest during exercise: anomalous left coronary artery from the pulmonary trunk. Scand Cardiovasc J 1999;33:369–71.

17.Backer CL, Stout MJ, Zales VR, et al. Anomalous origin of the left coronary artery. A twenty-year review of surgical management. J Thorac Cardiovasc Surg 1992;103:1049–58.

18.Alsoufi A, SallehuddinA, Bulbul Z, et al. Surgical strategy to establish a dual-coronary system for the management of anomalous left coronary artery origin from the pulmonary artery. Ann Thorac Surg 2008;86:170–6.

19. Dodge-Khatami A, Mavroudis C, Backer CL. Anomalous origin of the left coronary artery from the pulmonary artery: collective review of surgical therapy. Ann Thorac Surg 2002;74:946–55.

20.Arciniegas E. Coronary artery anomalies. In: Arciniegas E (ed.) Pediatric Cardiac Surgery. Chicago: Year Book Medical Publishers, 1985, pp. 389–402.

21.Mavroudis C, Dodge-Khatami A, Backer CL, Lorber R. Coronary artery anomalies. In: Mavroudis C, Backer CL (eds) Pediatric Cardiac Surgery, 4thedn. Oxford, UK: Wiley-Blackwell,2013, pp. 714–43.

22.Takeuchi S, Imamura H, Katsumoto K, et al. New surgical method for repair of anomalous left coronary artery from pulmonary artery. J Thorac Cardiovasc Surg 1979;78:7–11.

23.Tashiro T, Todo K, Haruta Y, et al. Anomalous origin of the left coronary artery from the pulmonary artery: new operative technique. J Thorac Cardiovasc Surg 1993;106:718– 22.

24.del Nido PJ, Duncan BW, Mayer JE, et al. Left ventricular assist device improves survival in children with left ventricular dysfunction after repair of anomalous origin of the left coronary artery from the pulmonary artery. Ann Thorac Surg 1999;67:169–72.

25.Imamura M, Dossey AM, Jaquiss RD. Reoperation and mechanical circulatory support after repair of anomalous origin of the left coronary artery from the pulmonary artery: a twenty-year experience. Ann Thorac Surg 2011;92:167–72.

26.Isomatsu Y, Imai Y, Shin’oka T, et al. Surgical intervention for anomalous origin of the left coronary artery from the pulmonary artery: The Tokyo Experience. J Thorac Cardiovasc Surg 2001;121:792–7.

27.Kudumula V, Mehta C, Stumper O, et al. Twenty-year outcome of anomalous origin of left coronary artery from pulmonary artery: management of mitral regurgitation. Ann Thorac Surg 2014;97:938–44.

28.Callaghan MA, O'Hare B, Casey W. What other anomalies? Failure to wean post ventricular septal defect repair secondary to anomalous origin of the left coronary artery from the pulmonary artery. Paediatr Anaesth 2012;22:487–9.

29.Angelini P. Congenital heart disease for the adult cardiologist coronary artery anomalies an entity in search of an identity. Circulation 2007; 115:1296–305.

30.Poynter JA, Williams WG, McIntyre S, et al. Anomalous aortic origin of a coronary artery: a report from the Congenital Heart Surgeons Society Registry. World J Pediatr Congenit Heart Surg 2014;5:22–30.

31.Ata Y, Turk T, Bicer M, et al. Coronary arteriovenous fistulas in the adults: natural history and management strategies. J Cardiothorac Surg 2009;4:62.

32.Gupta P, Tobias JD, Goyal S, et al. Sudden cardiac death under anesthesia in pediatric patient with Williams syndrome: a case report and review of literature. Ann Card Anaesth 2010;13:44–8.

33.Burch TM, McGowan FX Jr, Kussman BD, et al. Congenital supravalvular aortic stenosis and sudden death associated with anesthesia: what's the mystery? Anesth Analg 2008;107:1848–54.

34.Spodick DH. Macrophysiology, microphysiology, and anatomy of the pericardium: a synopsis. Am Heart J 1992;124:1046–51.

35.Little WC, Freeman GL. Pericardial disease. Circulation 2006;113:1622–32.

36.Kuhn B, Peters J, Marx GR, et al. Etiology, management and outcome of pediatric pericardial effusions. Pediatr Cardiol 2008;29:90–4.

37.Bramlet MT, Hoyer MH. Single pediatric center experience with multiple device implantation for complex secundum atrial septal defects. Catheter Cardiovasc Interv 2008;72 :531–7.

38.Nowlen TT, Rosenthal GL, Johnson GL, et al. Pericardial effusion and tamponade in infants with central catheters. Pediatrics 2002;110:137–42.

39.Mott AR, Fraser CD, Kusnoor AV, et al. The effect of short-term prophylactic methylprednisolone on the incidence and severity ofpostpericardiotomy syndrome in children undergoing cardiac surgery with cardiopulmonary cypass. J Am CollCardiol 2001;37:1700–6.

40. Beck CS. Two cardiac compression triads. JAm Med Assoc 1935;104:714–6.

41.Tsang TS, El-Najdawi EK, Sewarg JB, et al. Percutaneous echocardiographically guided pericardiocentesis in pediatric patients: evaluation of safety and efficacy. J Am Soc Echocardiogr 1998;11:1072–77.

42.Zahn EM, Houde C, Benson L, et al. Percutaneous pericardial catheter drainage in childhood. Am J Cardiol 1992;70:678–80.

43.Mossad EB. Pericardial effusion – a life saver! J Cardiothorac Vasc Anesth 1998;12:673–5.

44.Mainwaring RD, Lamberti JJ. Congenital anomalies of the mitral valve. In:Mavroudis C, Backer CL (eds) Pediatric Cardiac Surgery, 4thedn. Oxford, UK:Wiley-Blackwell, 2013, pp. 640–58.

45.Ranganathan M, Lam JHC, Wigle ED, et al. Morphology of the human mitral valve. II: the valve leaflets. Circulation 1970;41:459–67.

46.Davachi F, Moller JH, Edwards JE. Diseases of the mitral valve in infancy: anatomic analysis of 55 cases. Circulation 1971;43:565–79.

47.Mc Enany MT, English TA, Ross DN. The congenitally cleft posterior mitral valve leaflet. An antecedent to mitral regurgitation. Ann Thorac Surg 1973;16:281.

48.Mitruka SN, Lamberti JL. Congenital heart surgery nomenclature and database project: mitral valve disease. Ann Thorac Surg 2000;69:S132–46.

49.Oppido G, Davies B, McMullan DM, et al. Surgical treatment of congenital mitral valve disease: midterm results of a repair-oriented policy. J Thorac Cardiovasc Surg 2008;135:1313–21.

50.Henaine R, Roubertie F, Vergnat M, Ninet J. Valve replacement in children: a challenge for a whole life. Arch Cardiovasc Dis 2012;105:517–28.

51.Lee HR, Montenegro LM, Nicolson SC, et al. Usefulness of intraoperative transesophageal echocardiography in predicting the degree of mitral regurgitation secondary to atrioventricular defect in children. Am J Cardiol 1999;83:750–3.

52.Uzun O, Wilson DG, Vujanic GM, et al. Cardiac tumours in children. Orphanet J Rare Dis. 2007;2:11.

53.Lange R, Guther T. Cardiac tumors. In: Mavroudis C, Backer CL (eds) Pediatric Cardiac Surgery, 4thedn. Oxford, UK: Wiley-Blackwell, 2013, pp. 744–57.

54.Demir HA, Ekici F, Erdem AY,et al. Everolimus: a challenging drug in the treatment of multifocal inoperable cardiac Rhabdomyoma. Pediatrics 2012; 130: e243 –7.

55.Jain D, Dietz HC, Oswald GL, et al. Causes and histopathology of ascending aortic disease in children and young adults. Cardiovasc Pathol 2011;20:15–25.

56.Bolar N, Van Laer L, Loeys BL. Marfan syndrome: from gene to therapy.CurrOpin Pediatr 2012;24:498–504.

57.Loeys BL, Dietz HC, Braverman AC, et al. The revised Ghent nosology for the Marfan syndrome. J Med Genet 2010;47:476–85.

58.Dietz HC, Pyeritz RE. Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders. Hum Mol Genet 1995;4:1799–809.

59.Caglayan AO, Dundar M. Inherited diseases and syndromes leading to aortic aneurysms and dissections. Eur J Cardiothorac Surg 2009; 35:931–40.

60.Williams A, Davies S, Stuart AG, et al. Medical treatment of Marfan syndrome: a time for change. Heart 2008;94:414–21.

61.Ring WS. Congenital heart surgery nomenclature and database project: aortic aneurysm, sinus of Valsalva aneurysm, and aortic dissection. Ann Thorac Surg 2000;69:S147–63.

62.Zanjani KS, Niwa K. Aortic dilatation and aortopathy in congenital heart diseases. J Cardiol 2013;61:16 –21.

63.Gillinov AM, Zehr KJ, Redmond JM, et al. Cardiac operations in children with Marfan’s Syndrome: indications and results. Ann Thorac Surg 1997;64:1140–45.

64.Shimizu H, Yozu R. Valve-sparing aortic root replacement. Ann ThoracCardiovasc Surg 2011;17:330–6.

65.Patel ND, Arnaoutakis GJ, George TJ, et al. Valve-sparing aortic root replacement in children: intermediate-term results. CardiovascThorac Surg 2011;12:415–9.

66.Van Dyck MJ, Watremez, C, Boodhwani M, et al. Transesophagealechocardiographic evaluation during aortic valve repair surgery. Anesth Analg 2010;111:59–70.

67.Simpson I, Campbell PE. Mediastinal masses in childhood: a review from a paediatric pathologist's point of view. ProgPediatr Surg 1991;27:92–126.

68.Shamberger RC, MD Robert S. Holzman RS, et al. Prospective evaluation by computed tomography and pulmonary function tests of children with mediastinal masses. Surgery 1995;118:468–71.

69.Perger L, Lee EY, Shamberger RC. Management of children and adolescents with a critical airway due to compression by an anterior mediastinal mass. J Pediatr Surg 2008; 43:1990–97.

70.Anghelescu DL, Burgoyne LL, Liu T, et al. Clinical and diagnostic imaging findings predict anesthetic complications in children presenting with malignant mediastinal masses PaediatrAnaesth 2007 17:1090–98 .

71.Latham GJ. Anesthesia for the child with cancer.AnesthesiolClin 2014;32:185–213.

72.Hammer GB. Anaesthetic management for the child with a mediastinal mass. Paediatr Anaesth 2004;14:95–7.