Tetralogy of Fallot

Tetralogy of Fallot is the most common form of cyanotic congenital heart disease. In this condition, episodic worsening of hypoxemia results from dynamic shifts in physiology, so-called “Tet spells.” The relative frequency of this lesion and the risks of exacerbating “Tet spells” make anesthetic management of this patient population challenging. The conduct of palliative and reparative cardiac surgery is determined in large part by the anatomic variations within the spectrum of this disorder, most notably the severity of right ventricular outflow tract obstruction. This review will address the impact that the anatomic substrate has on the perioperative management of this interesting patient population.

[1]  A. Redington,et al.  Tetralogy of Fallot , 2009, The Lancet.

[2]  H. Taussig,et al.  The Surgical Treatment of Malformations of the Heart: In Which There Is Pulmonary Stenosis or Pulmonary Atresia , 1945 .

[3]  J. Kirklin,et al.  Transannular outflow tract patching for tetralogy: indications and results. , 1990, Seminars in thoracic and cardiovascular surgery.

[4]  R. Califf,et al.  Clinical Outcomes of Palliative Surgery Including a Systemic-to-Pulmonary Artery Shunt in Infants With Cyanotic Congenital Heart Disease: Does Aspirin Make a Difference? , 2007, Circulation.

[5]  A. Cook,et al.  Problems with the right ventricular outflow tract: a review of morphologic features and current therapeutic options , 2004, Cardiology in the Young.

[6]  S. Kothari,et al.  Mechanism of cyanotic spells in tetralogy of Fallot--the missing link? , 1992, International journal of cardiology.

[7]  J. Christenson,et al.  Homografts and xenografts for right ventricular outflow tract reconstruction: long-term results. , 2010, The Annals of thoracic surgery.

[8]  A. Muster,et al.  Tetralogy of Fallot: underdevelopment of the pulmonary infundibulum and its sequelae. , 1970, The American journal of cardiology.

[9]  Robert H. Anderson,et al.  The anatomy of tetralogy of Fallot with pulmonary stenosis , 2008, Cardiology in the Young.

[10]  K. Dimopoulos,et al.  Structural abnormalities of the pulmonary trunk in tetralogy of Fallot and potential clinical implications: a morphological study. , 2009, Journal of the American College of Cardiology.

[11]  J. Edwards,et al.  Anatomic variations in the tetralogy of Fallot. , 1971, American heart journal.

[12]  D. De Wolf,et al.  Assessment of a right-ventricular infundibulum-sparing approach in transatrial-transpulmonary repair of tetralogy of Fallot. , 2011, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[13]  B. D. de Mol,et al.  Neonatal complete correction of tetralogy of Fallot versus shunting and deferred repair: is the future of the right ventriculo-arterial junction at stake, and what of it? , 2001, Cardiology in the Young.

[14]  R. Varco,et al.  Direct Vision Intracardiac Surgical Correction of the Tetralogv of Fallot, Pentalogy of Fallot, and Pulmonary Atresia Defects: Report of First Ten Cases , 1955, Annals of surgery.

[15]  C. Fraser,et al.  Tetralogy of Fallot: surgical management individualized to the patient. , 2001, The Annals of thoracic surgery.

[16]  E. Blackstone,et al.  Decision-making in repair of tetralogy of Fallot based on intraoperative measurements of pulmonary arterial outflow tract. , 1979, The Journal of thoracic and cardiovascular surgery.

[17]  R D Greenwood,et al.  Extracardiac abnormalities in infants with congenital heart disease. , 1975, Pediatrics.

[18]  Josep Girona Comas Congenital diseases of the heart: clinical-physiological considerations , 2001 .

[19]  C. Fraser,et al.  Tetralogy of Fallot repair: the Right Ventricle Infundibulum Sparing (RVIS) strategy. , 2009, Seminars in thoracic and cardiovascular surgery. Pediatric cardiac surgery annual.

[20]  F. Pigula,et al.  Repair of tetralogy of Fallot in neonates and young infants. , 1999, Circulation.

[21]  Joanne P. Starr,et al.  Tetralogy of Fallot: Yesterday and Today , 2010, World Journal of Surgery.

[22]  Robert H. Anderson,et al.  Surgical correction for patients with tetralogy of Fallot and common atrioventricular junction , 2008, Cardiology in the Young.

[23]  S. Siu,et al.  Risk factors for arrhythmia and sudden cardiac death late after repair of tetralogy of Fallot: a multicentre study , 2000, The Lancet.

[24]  E. Zackai,et al.  Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching. , 2001, Journal of the American College of Cardiology.

[25]  S. Ho,et al.  Surgical anatomy of tetralogy of Fallot. , 1981, The Journal of thoracic and cardiovascular surgery.

[26]  F. Pigula,et al.  Long-term results of right ventricular outflow tract reconstruction in neonatal cardiac surgery: options and outcomes. , 2009, The Journal of thoracic and cardiovascular surgery.

[27]  D. McElhinney,et al.  Routine primary repair of tetralogy of Fallot in neonates and infants less than three months of age. , 1995, The Annals of thoracic surgery.

[28]  G. V. van Arsdell,et al.  An apology for primary repair of tetralogy of Fallot. , 2005, Seminars in thoracic and cardiovascular surgery. Pediatric cardiac surgery annual.

[29]  P. D. del Nido,et al.  Coronary echocardiography in tetralogy of fallot: diagnostic accuracy, resource utilization and surgical implications over 13 years. , 2000, Journal of the American College of Cardiology.

[30]  J. Graham,et al.  Chromosome 22q1l Deletion Syndrome: An Update and Review for the Primary Pediatrician , 1997, Clinical pediatrics.

[31]  E. Zackai,et al.  Frequency of 22q11 deletions in patients with conotruncal defects. , 1998, Journal of the American College of Cardiology.

[32]  Y. Cheung,et al.  Meta-analysis of pulmonary valve replacement after operative repair of tetralogy of fallot. , 2010, The American journal of cardiology.

[33]  M. Silka,et al.  A population-based prospective evaluation of risk of sudden cardiac death after operation for common congenital heart defects. , 1998, Journal of the American College of Cardiology.