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Tetralogy of Fallot

Tetralogy of Fallot is a congenital cardiac malformation that consists of an interventricular communication, also known as a ventricular septal defect, obstruction of the right ventricular outflow tract, override of the ventricular septum by the aortic root, and right ventricular hypertrophy.

Hypertension

The presence of chronic increased pressure in the systemic arterial system.

Total: 22

(per page)

PMID (PMCID)
29455823	MALE	Infant, Newborn
	Sequential Melody Valve Insertion After Repair of Tetralogy of Fallot Atrioventricular Septal Defect.
	Kenny D, Prendiville T, Walsh KP, McGuinness J. Ann Thorac Surg. 2018;105(3):e119-e121.
	Repair of tetralogy of Fallot with atrioventricular septal defect may be associated with hemodynamic challenges in the postoperative period particularly as left atrial hypertension secondary to left atrioventricular valve dysfunction may exacerbate pulmonary regurgitation and augment low cardiac output.
25063464	FEMALE	Adult
	Pheochromocytoma and tetralogy of Fallot: Coincidence or a rare association?
	Singh GD, Anuradha S, Sethi P, Singla S, Saran RK, Dewan R. Asian Cardiovasc Thorac Ann. 2016;24(1):75-7.
	We report the case of a 25-year-old woman with tetralogy of Fallot who presented with chest pain and hypertension, and on further investigation, was diagnosed with a pheochromocytoma in the right adrenal gland.
26354665	FEMALE	Adult
	Aortic Coarctation Diagnosed During Pregnancy in a Woman With Repaired Tetralogy of Fallot.
	Jalal Z, Iriart X, Thambo JB. Ann Thorac Surg. 2015;100(3):e45-7.
	We report the case of a 26 year old woman presenting with systemic hypertension at 17 weeks of pregnancy after repair of tetralogy of Fallot in childhood.
24702799	MALE
	Aspergillus endocarditis in a paediatric patient after a cardiac surgery, associated with septic pulmonary embolism and pulmonary hypertension.
	Miranda JO, de Sousa AR, Monterroso J. Cardiol Young. 2015;25(3):563-5.
	We report a rare case of pulmonary prosthetic valve endocarditis due to Aspergillus fumigatus, associated with septic pulmonary embolism and secondary pulmonary hypertension, in a 4-year-old boy with surgically corrected tetralogy of Fallot.
25190952 (4152684)	OTHER
	Spinal anesthetic for emergency cesarean section in a parturient with uncorrected tetralogy of Fallot, presenting with abruptio placentae and gestational hypertension.
	Adinarayanan S, Parida S, Kavitha J, Balachander H. J Anaesthesiol Clin Pharmacol. 2014;30(3):400-2.
	Spinal anesthetic for emergency cesarean section in a parturient with uncorrected tetralogy of Fallot, presenting with abruptio placentae and gestational hypertension.
23970921 (3746948)	OTHER
	A case report of truncus arteriosus communis and genetic counseling.
	Nourzad G, Baghershiroodi M. ARYA Atheroscler. 2013;9(4):254-9.
	In addition, various disorders are reported like ventricular septal defect (VSD), mitral and tricuspid valves defects, aortic septal defect (ASD), reduction of lung and lung vessels' resistance, pulmonary hypertension, increase in heart rate, high perspiration, bad digestion, and tetralogy of Fallot.
22923029	FEMALE
	Atherosclerosis causing recurrent catastrophic aortopulmonary shunt dehiscence in a patient with Alagille syndrome.
	May L, Hanley FL, Connolly AJ, Reddy S. Pediatr Cardiol. 2013;34(8):1945-8.
	This report describes a 3 year-old girl with Alagille syndrome, hepatic cholestasis, systemic hypertension, hypercholesterolemia, hypertriglyceridemia, and tetralogy of Fallot, pulmonary atresia, and major aortopulmonary collaterals (TOF/PA/MAPCAs).
23149090	MALE	Infant
	Systemic hypertension in an infant with unrepaired tetralogy of Fallot: case report.
	Khoury M, Kallile M, May J, Punn R. Cardiol Young. 2013;23(5):746-8.
	Here we present the case of an infant with tetralogy of Fallot and severe pulmonary valve stenosis, complicated by systemic hypertension, the presence of which altered flow dynamics and possibly prevented cyanosis.
23149090	MALE	Infant
	Systemic hypertension in an infant with unrepaired tetralogy of Fallot: case report.
	Khoury M, Kallile M, May J, Punn R. Cardiol Young. 2013;23(5):746-8.
	Systemic hypertension in an infant with unrepaired tetralogy of Fallot: case report.
22034598 (3198627)	OTHER
	Severe pulmonary artery hypertension following intracardiac repair of tetralogy of Fallot: An unusual finding.
	Kumar B, Puri GD, Manoj R, Gupta K, Shyam KS. Pulm Circ. 2011;1(1):115-8.
	Severe pulmonary artery hypertension following intracardiac repair of tetralogy of Fallot: An unusual finding.
22034598 (3198627)	OTHER
	Severe pulmonary artery hypertension following intracardiac repair of tetralogy of Fallot: An unusual finding.
	Kumar B, Puri GD, Manoj R, Gupta K, Shyam KS. Pulm Circ. 2011;1(1):115-8.
	We report a child with tetralogy of Fallot and Down's syndrome, who developed severe pulmonary hypertension and low cardiac output syndrome following an intracardiac repair, which was resistant to specific pulmonary vasodilators and increasing ionotropes.
18006164	MIXED_SAMPLE	Adult
	Sildenafil therapy in complex pulmonary atresia with pulmonary arterial hypertension.
	Lim ZS, Vettukattill JJ, Salmon AP, Veldtman GR. Int J Cardiol. 2008;129(3):339-43.
	A cross-sectional retrospective review of patients >16 years with CPA or Tetralogy of Fallot with MAPCAs and PA hypertension treated with sildenafil was conducted.
18006164	MIXED_SAMPLE	Adult
	Sildenafil therapy in complex pulmonary atresia with pulmonary arterial hypertension.
	Lim ZS, Vettukattill JJ, Salmon AP, Veldtman GR. Int J Cardiol. 2008;129(3):339-43.
	pulmonary atresia with ventricular septal defect and major aorto-pulmonary collaterals (MAPCAs) or Tetralogy of Fallot with MAPCAs frequently have a clinical course complicated by development of pulmonary arterial (PA) hypertension.
16945829	MALE	Middle Aged
	Closure of patent Potts shunt with aortic endoluminal stent graft.
	Ahmar W, Aggarwal A, Skillington P, Atkinson N. Cardiovasc Revasc Med. 2006;7(3):192-4.
	A 59-year-old male with a history of tetralogy of Fallot was noted, on a full heart study, to have persistent pulmonary hypertension, normal left ventricular function, severe aortic regurgitation, and a residual Potts shunt.
17057907	FEMALE	Infant
	Complete repair in total atrioventricular canal defect with cyanosis.
	Tanamati C, Suguimoto RL, Atik E, Copolla SG, Galles FR, Aiello VD, Barbero-Marcial ML. Arq Bras Cardiol. 2006;87(3):e1-3.
	Cyanosis is rarely found in infants and suggests irreversible pulmonary hypertension or associated cardiac defects as tetralogy of Fallot, double outlet right ventricle, Ebstein anomaly, persistent left superior vena cava draining in the left atrium (Barbero Marcial, personal communication).
16004342	FEMALE
	[Repair of tetralogy of Fallot with obstruction of right pulmonary artery; report of a case].
	Sugiura J, Akita T, Sakurai H, Kato N, Hasegawa H, Sawaki S, Sakurai H. Kyobu Geka. 2005;58(7):577-80.
	Patients with tetralogy of Fallot showing unilateral obstruction of a pulmonary artery, especially the right pulmonary artery, are a high-risk group for pulmonary hypertension after repair.
15587179	FEMALE	Middle Aged
	[Anesthetic management for removal of pheochromocytoma in a patient after repair of tetralogy of Fallot].
	Yano T, Maruta T, Kawano T, Hamakawa T, Suzuki N, Takasaki M. Masui. 2004;53(11):1273-5.
	A 45-year-old woman after repair of tetralogy of Fallot at the age of 19, was admitted to the hospital for treatment of paroxysmal hypertension.
14661574	MALE	Adult
	[Postoperative pulmonary bleeding and reperfusion pulmonary edema in an adult patient after repair of tetralogy of Fallot with pulmonary atresia--percutaneous cardiopulmonary support (PCPS) and lung protective ventilatory strategy].
	Takauchi Y, Imanaka H, Takeuchi M, Tachibana K. Masui. 2003;52(11):1227-32.
	After total correction of tetralogy of Fallot, pulmonary atresia and major aorto-pulmonary collateral arteries, a 31-year-old man developed life-threatening pulmonary hypertension and reperfusion pulmonary edema, leading to pulmonary hemorrhage, right heart failure and hypoxia.
2395242	MIXED_SAMPLE	Infant, Newborn
	[Digital subtraction angiography for congenital heart disease].
	Kawai T, Wada Y, Okumura S, Ito M, Hashimoto S, Nishiyama K, Ohga K, Oka T. Kyobu Geka. 1990;43(7):522-6.
	The diagnoses of the patients include total anomalous pulmonary venous return (TAPVR), transposition of great arteries, patent ductus arteriosus with pulmonary hypertension, giant hemangioma of the left leg, asplenia (two cases), tetralogy of Fallot (two), and tricuspid atresia (two).
2426677	FEMALE
	Septal origin of sustained ventricular tachycardia in a patient with right ventricular outflow tract obstruction after correction of tetralogy of Fallot.
	Swerdlow CD, Oyer PE, Pitlick PT. Pacing Clin Electrophysiol. 1986;9(4):584-8.
	Right ventricular hypertension and ventricular arrhythmias are risk factors for sudden death after correction of tetralogy of Fallot, but sustained ventricular tachycardia has been reported only in patients without residual hemodynamic abnormalities.