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Review

Neonatal aortic stenosis

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Pages 831-843 | Published online: 10 Jan 2014

References

  • Sadler TW. Langman’s Medical Embryology. 9th Edition. Lippincott Williams & Wilkins, MD, USA, 223–274 (2004).
  • Collins P. Development of the heart. In: Gray’s Anatomy. The Anatomical Basis of Medicine and Surgery, 38th Edition PL Williams (Ed.). Churchill-Livingstone, London, UK, 305 (1995).
  • Rudic RD, Shesely EG, Maeda N, Smithies O, Segal SS, Sessa WC. Direct evidence for the importance of endothelium-derived nitric oxide in vascular remodeling. J. Clin. Invest.101, 731–736 (1998).
  • Lee TC, Zhao YD, Courtman DW, Stewart DJ. Abnormal aortic valve development in mice lacking endothelial nitric oxide synthase. Circulation101, 2345–2348 (2000).
  • Lakier JB, Lewis AB, Heymann MA, Stanger P, Hoffman JIE, Rudolph AM. Isolated aortic stenosis in the neonate: natural history and hemodynamic considerations. Circulation50, 801–808 (1974).
  • Hornberger LK, Sanders SP, Rein AJ, Spevak PJ, Parness IA, Colan SD. Left heart obstructive lesions and left ventricular growth in the midtrimester fetus. A longitudinal study. Circulation92, 1531–1538 (1995).
  • Shah P. Heart and great vessels. In: Gray’s Anatomy. The Anatomical Basis of Clinical Practice. 39th Edition. S Strandling (Ed.). Elsevier, Edinburgh, UK, 995–1027 (2005).
  • Sutton JP III, Ho SY, Anderson RH. The forgotten interleaflet triangles: a review of the surgical anatomy of the aortic valve. Ann. Thorac. Surg. 59, 419–427 (1995)
  • Roberts WC. The congenitally bicuspid aortic valve: a study of 58 autopsy cases. Am. J. Cardiol. 26, 72–83 (1970).
  • Angelini A, Ho SY, Anderson RH et al. The morphology of the normal aortic valve as compared with the aortic valve having two leaflets. J. Thorac. Cardiovasc. Surg. 98, 362–367 (1989).
  • Van Praagh R, Bano-Rodrigo A, Smolinsky A, Schuetz TJ, Fyler DC, Van Praagh S. Anatomic variations in congenital valvar, subvalvar and supravalvar aortic stenosis: a study of 64 postmortem cases. In: Challenges in the Treatment of Congenital Cardiac Anomalies. WJ Wells, EE Lindesmith (Eds). Futura Publishing Company, NY, USA, 13–41 (1986).
  • Cheitlin MD, Fenoglio JJ, McAllister HA, Davia JE, DeCastro CM. Congenital aortic stenosis secondary to dysplasia of congenital bicuspid aortic valves without commissural fusion. Am. J. Cardiol. 42, 102–107 (1978).
  • McKay R, Smith A, Leung MP, Arnold R, Anderson RH. Morphology of the ventriculoaortic junction in critical aortic stenosis. Implications for hemodynamic function and clinical management. J. Thorac. Cardiovasc. Surg. 104, 434–442 (1992)
  • Hastreiter AR, Oshima M, Miller RA, Lev M, Paul MM. Congenital aortic stenosis syndrome in infancy. Circulation28, 1084–1095 (1963).
  • Guyton AC, Hall JE. Textbook of Medical Physiology. 10th edition. WB Saunders, Philadelphia, PA, 103 (2000).
  • Rhodes LA, Colan SD, Perry SB, Jonas RA, Sanders SP. Predictors of survival in neonates with critical aortic stenosis. Circulation84, 2325–2335 (1991).
  • Rychik J, Rome JJ, Collins MH, DeCampli WM, Spray TL. The hypoplastic left heart syndrome with intact atrial septum: atrial morphology, pulmonary vascular histopathology and outcome. J. Am. Coll. Cardiol. 34, 554–560 (1999).
  • Baram S, McCrindle BW, Han RK, Benson LN, Freedom RM, Nykanen DG. Outcomes of uncomplicated aortic valve stenosis presenting in infants. Am. Heart J. 145, 1063–1070 (2003).
  • Lofland GK, McCrindle BW, Williams WG et al. Critical aortic stenosis in the neonate: a multi-institutional study of management, outcomes and risk factors. J. Thorac. Cardiovasc. Surg. 121, 10–27 (2001).
  • Beekman RH, Rocchini AP, Gillon JH, Mancini GB. Hemodynamic determinants of the peak systolic left ventricular-aortic pressure gradient in children with valvar aortic stenosis. Am. J. Cardiol. 69, 813–815 (1992).
  • Lima VC, Zahn E, Houde C, Smallhorn J, Freedom RM, Benson LN. Non-invasive determination of the systolic peak-to-peak gradient in children with aortic stenosis: validation of a mathematical model. Cardiol. Young10, 115–119 (2000).
  • Marquis RM, Logan A. Congenital aortic stenosis and its surgical treatment. Br. Heart J. 17, 373–390 (1955).
  • Lewis FJ, Shumway NE, Niazi SA, Benjamin RB. Aortic valvulotomy under direct vision during hypothermia. J. Thorac. Surg. 32, 481–499 (1956).
  • Swan H, Kortz AB. Direct vision trans-aortic approach to the aortic valve during hypothermia: experimental observations and report of a successful clinical case. Ann. Surg. 144, 205–214 (1956).
  • Spencer FC, Neill CA, Bahnson HT. The treatment of congenital aortic stenosis with valvotomy during cardiopulmonary bypass. Surgery 44, 109–124 (1958).
  • Lababidi Z. Aortic balloon valvuloplasty. Am. Heart J. 106, 751–752 (1983).
  • Norwood WI, Kirklin JK, Sanders SP. Hypoplastic left heart syndrome: experience with palliative surgery. Am. J. Cardiol. 45, 87–91 (1980).
  • Norwood WI, Lang P, Castaneda AR, Campbell DN. Experience with operations for hypoplastic left heart syndrome. J. Thorac. Cardiovasc. Surg. 82, 511–519 (1981).
  • Norwood WI, Lang P, Hansen D. Physiologic repair of aortic atresia-hypoplastic left heart syndrome. N. Engl. J. Med. 308, 23–26 (1983).
  • Bailey LL, Nelsen-Cannarella SL, Doroshow RW et al. Cardiac allotransplantation in newborns as therapy for hypoplastic left heart syndrome. N. Engl. J. Med. 315, 949–951 (1985).
  • Calhoon J, Bolton J. Ross–Konno procedure for critical aortic stenosis in infancy. Ann. Thorac. Surg. 60, S597–S599 (1995).
  • Reddy VM, Rajasinghe HA, Teitel DF, Haas GS, Hanley FL. Aortoventriculoplasty with the pulmonary autograft: the ‘Ross–Konno’ procedure. J. Thorac. Cardiovasc. Surg. 111, 158–167 (1996).
  • Sudow G, Solymar L, Berggren H, Eriksson B, Holmgren D, Gilljam T. Aortic valve replacement with a pulmonary autograft in infants with critical aortic stenosis. J. Thorac. Cardiovasc. Surg. 112, 433–436 (1996).
  • Leung MP, McKay R, Smith A, Anderson RH, Arnold R. Critical aortic stenosis in early infancy. J. Thorac. Cardiovasc. Surg. 101, 526–535 (1991).
  • Parsons MK, Moreau GA, Graham TP, Johns JA, Boucek RJ. Echocardiographic estimation of critical left ventricular size in infants with isolated aortic valve stenosis. J. Am. Coll. Cardiol. 18, 1049–1055 (1991).
  • Kovalchin JP, Brook MM, Rosenthal GL, Suda K, Hoffman JIE, Silverman NH. Echocardiographic hemodynamic and morphometric predictors of survival after two-ventricle repair in infants with critical aortic stenosis. J. Am. Coll. Cardiol. 32, 237–244 (1998).
  • Corno AF. Borderline left ventricle. Eur. J. Cardiothorac. Surg. 27, 67–73 (2005).
  • Ashburn DA, McCrindle BW, Tchervenkov CI et al. Outcomes after the Norwood operation in neonates with critical aortic stenosis or aortic valve atresia. J. Thorac. Cardiovasc. Surg. 125, 1070–1082 (2003).
  • Alexiou C, Langley SM, Dalrymple-Hay MJR et al. Open commissurotomy for critical isolated aortic stenosis in neonates. Ann. Thorac. Surg. 71, 489–93 (2001).
  • Mosca RS, Iannettoni MD, Schwartz SM et al. Critical aortic stenosis in the neonate. A comparison of balloon valvuloplasty and transventricular dilation. J. Thorac. Cardiovasc. Surg. 109, 147–154 (1995).
  • Pass RH, Hellenbrand WE. Catheter intervention for critical aortic stenosis in the neonate. Catheter. Cardiovasc. Interv. 55, 88–92 (2002).
  • De Giovanni JV, Edgar RA, Cranston A. Adenosine induced transient cardiac standstill in catheter interventional procedures for congenital heart disease. Heart 80, 330–333 (1998).
  • Daehnert I, Rotzsch C, Wiener M, Schneider P. Rapid right ventricular pacing is an alternative to adenosine in catheter interventional procedures for congenital heart disease. Heart 90, 1047–1050 (2004).
  • Beekman RH, Rocchini AP, Andes A. Balloon valvuloplasty for critical aortic stenosis in the newborn: influence of new catheter technology. J. Am. Coll. Cardiol. 17, 1172–1176 (1991).
  • Fischer DR, Ettedgui JA, Park SC, Siewers RD, del Nido PJ. Carotid artery approach for balloon dilation of aortic valve stenosis in the neonate: a preliminary report. J. Am. Coll. Cardiol. 15, 1633–1666 (1990).
  • Carminati M, Giusti S, Spadoni I et al. Balloon aortic valvuloplasty in the first year of life. J. Interv. Cardiol. 8(Suppl. 6), 759–766 (1995).
  • Maeno Y, Akagi T, Hashino K et al. Carotid artery approach to balloon aortic valvuloplasty in infants with critical aortic valve stenosis. Pediatr. Cardiol. 18, 288–291 (1997).
  • Tometzki AJ, Gibbs JL, Weil J. Balloon valvoplasty of critical aortic and pulmonary stenosis in the premature neonate. Int. J. Cardiol. 30, 248–249 (1991).
  • Benito Bartolome F, Jimenez Casso S, Sanchez Fernandez-Bernal C. Aortic balloon valvuloplasty in critical aortic stenosis in the newborn and infants. Rev. Esp. Cardiol. 49, 277–280 (1996).
  • Egito EST, Moore P, O’Sullivan et al. Transventricular balloon dilation for neonatal critical aortic stenosis: early and midterm results. J. Am. Coll. Cardiol. 29, 442–447 (1997).
  • Reich O, Tax P, Marek J et al. Long-term results of percutaneous balloon valvoplasty of congenital aortic stenosis: independent predictors of outcome. Heart 90, 70–76 (2004).
  • McElhinney DB, Lock JE, Keane JF, Moran AM, Colan SD. Left heart growth, function and reintervention after balloon aortic valvuloplasty for neonatal aortic stenosis. Circulation111, 451–458 (2005).
  • Cowley CG, Dietrich M, Mosca RS, Bove EL, Rocchini AP, Lloyd TR. Balloon valvuloplasty versus transventricular dilation for neonatal critical aortic stenosis. Am. J. Cardiol. 87, 1125–1127 (2001).
  • McCrindle BW, Blackstone EH, Williams WG et al. Are outcomes of surgical versus transcatheter balloon valvotomy equivalent in neonatal critical aortic stenosis? Circulation104(Suppl. I), I-152–I-158 (2001).
  • Balmer C, Beghetti M, Fasnacht M, Friedli B, Arbenz U. Balloon aortic valvoplasty in paediatric patients: progressive aortic regurgitation is common. Heart 90, 77–81 (2004).
  • Magee AG, Nykanen D, McCrindle BW, Wax D, Freedom RM, Benson LN. Balloon dilation of severe aortic stenosis in the neonate: comparison of anterograde and retrograde catheter approaches. J. Am. Coll. Cardiol. 30, 1061–1066 (1997).
  • Sandor GG, Olley PM, Trusler GA, Williams WG, Rowe RD, Morch JE. Long-term follow-up of patients after valvotomy for congenital valvular aortic stenosis in children. J. Thorac. Cardiovasc. Surg. 80, 171–176 (1980).
  • Pelech AN, Dyck JD, Trusler GA et al. Critical aortic stenosis: survival and management. J. Thorac. Cardiovasc. Surg. 94, 510–517 (1987).
  • Ettedgui JA, Tallman-Eddy T, Neches WH et al. Long-term results of survivors of surgical valvotomy for severe aortic stenosis in infancy. J. Thorac. Cardiovasc. Surg. 104, 1714–1720 (1992).
  • Turley K, Bove EL, Amato JJ et al. Neonatal aortic stenosis. J. Thorac. Cardiovasc. Surg. 99, 679–684 (1990).
  • Gildein HP, Kleinert S, Weintraub RG, Wilkinson JL, Karl TR, Mee RBB. Surgical commissurotomy of the aortic valve: outcome of open valvotomy in neonates with critical aortic stenosis. Am. Heart J. 131, 754–759 (1996).
  • Hawkins JA, Minich LL, Tani LY et al. Late results and reintervention after aortic valvotomy for critical aortic stenosis in neonates and infants. Ann. Thorac. Surg. 65, 1758–1763 (1998).
  • Bhabra MS, Dhillon R, Bhudia S et al. Surgical aortic valvotomy in infancy: impact of leaflet morphology on long-term outcomes. Ann. Thorac. Surg. 76, 1412–1416 (2003).
  • Alexiou C, Chen Q, Langley SM et al. Is there still a place for open surgical valvotomy in the management of aortic stenosis in children? The view from Southampton. Eur. J. Cardiothorac. Surg. 20, 239–246 (2001).
  • Dittrich H, Bührer C, Grimmer I, Dittrich S, Abdul-Khaliq, Lange PE. Neurodevelopment at 1 year of age in infants with congenital heart disease. Heart 89, 436–441 (2003).
  • Lacour-Gayet F, Sauer H, Ntalakoura K et al. Ross–Konno procedure in neonates: report of three patients. Ann. Thorac. Surg. 77, 2223–2225 (2004).
  • Ohye RG, Gomez CA, Ohye BJ, Goldberg CS, Bove EL. The Ross/Konno procedure in neonates and infants: intermediate-term survival and autograft function. Ann. Thorac. Surg. 72, 823–830 (2001).
  • Elkins RC, Lane MM, McCue C. Ross operation in children: late results. J. Heart Valve Dis. 10, 736–741 (2001).
  • Hraska V, Krajci M, Haun Ch et al. Ross and Ross-Konno procedure in children and adolescents: mid-term results. Eur. J. Cardiothorac. Surg. 25, 742–747 (2004).
  • Elkins RC, Knott-Craig CJ, Ward KE, McCue C, Lane MM. Pulmonary autograft in children: realized growth potential. Ann. Thorac. Surg. 57, 1387–1394 (1994).
  • Solowiejczyk DE, Bourlon F, Apfel HD et al. Serial echocardiographic measurements of the pulmonary autograft in the aortic valve position after the Ross operation in a pediatric population using normal pulmonary artery dimensions as the reference standard. Am. J. Cardiol. 85, 119–123 (2000).
  • Hanley FL. Discussion of: Lofland GK, McCrindle BW, Williams WG et al. Critical aortic stenosis in the neonate: a multi-institutional study of management, outcomes and risk factors. J. Thorac. Cardiovasc. Surg. 121, 25–26 (2001).
  • Serraf A, Roux D, Lacour-Gayet F et al. Reoperation after the arterial switch operation for transposition of the great arteries. J. Thorac. Cardiovasc. Surg. 110, 892–899 (1995).
  • Haas F, Wottke M, Poppert H, Meisner H. Long-term survival and functional follow-up in patients after the arterial switch operation. Ann. Thorac. Surg. 68, 1692–1697 (1999).
  • Tworetzky W, Marshall AC. Fetal interventions for cardiac defects. Pediatr. Clin. N. Am. 51, 1503–1513 (2004).
  • Sharland GK, Chita SK, Fagg NL et al. Left ventricular dysfunction in the fetus: relation to aortic valve anomalies and endocardial fibroelastosis. Br. Heart J. 66, 419–424 (1991).
  • McCaffrey FM, Sherman FS. Prenatal diagnosis of severe aortic stenosis. Pediatr. Cardiol. 18, 276–281 (1997).
  • Kohl T, Sharland G, Allan LD et al. World experience of percutaneous ultrasound-guided balloon valvuloplasty in human fetuses with severe aortic valve obstruction. Am. J. Cardiol. 85, 1230–1233 (2000).
  • Tworetzky W, Wilkins-Haug L, Jennings RW et al. Balloon dilation of severe aortic stenosis in the fetus. Potential for prevention of hypoplastic left heart syndrome: candidate selection, technique and results of successful intervention. Circulation110, 2125–2131 (2004).

Website

  • Congential Heart Surgeons’ Society www.chssdc.org (Accessed August 2005)

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