1. Anatomy and pathophysiology of tetralogy of Fallot Yun Hee Chang Division of Pediatric Cardiac Surgery Department of Thoracic & Cardiovascular Surgery Seoul St. Mary’s Hospital Catholic University of Korea / Catholic Medical Center

2. History

3. 1671 1777 1785 1793 1797 1812 1814 1816 1846 1881 1888 Niels Stensen Eduard Sandifort Willam Hunter Pulteney 1784 Abernethy Bell Dorsey J.P.Farre Thaxter Thomas Bevil Peacock Widman Fallot: La maladie bleue 1924 Maude Abbott : “tetralogy of Fallot” 4 Anatomic features (1)Pulmonary (or RV) outflow stenosis (2)Ventricular septal defect (3)Aortic overriding (4)Right ventricular hypertrophy

4. Subtypes of TOF  Tetralogy of Fallot, Pulmonary stenosis  Tetralogy of Fallot, Absent pulmonary valve (3-6%)  Tetralogy of Fallot, Common atrioventricular canal (2%)  Tetralogy of Fallot, Pulmonary atresia (20%)

5. TOF with Pulmonary stenosis

6. Anatomic features Overriding of the aorta Subpulmonary stenosis Ventricular septal defect Right ventricular hypertrophy

7.  Van Praagh R et al. - Underdevelopment of the subpulmonary infundibulum Normal TOF Pathognomonic lesions

8.  Anderson RH et al. - Anterocephalad deviation of the outlet septum (relative to the limb of the septomarginal trabeculation) - Malformation of the septoparietal trabeculation Normal TOF A P

9. Deviated outlet septum Septal attachment of the muscular outlet septum Antero-cranial limb of TSM Hypertrophied Septoparietal trabeculation

10. Subvalvar stenosis  Infundibular stenosis - Essential part of tetralogy - Produced by the ‘Squeeze’ between the anterocephalad malalignment of the outlet septum and the abnormal situated septoparietal trabeculations Pulmonary outflow stenosis

11. Anterocephalad malalignment of the outlet septum without abnormal situated septoparietal trabeculations * vs. Eisenmenger type ventricular septal defect

12.  Additional muscular stenosis - By hypertrophy of the moderator band or by prominent apical trabeculations. - Often described as “two-chambered right ventricle”. Moderator band Apical trabeculations

13. -The pulmonary valve is stenotic in 75% cases : usually caused by hypoplasia and fusion of bicuspid leaflets, supravalvar tethering. -The valve is bicuspid in ½ to 2/3 of cases. - The pulmonary valve annulus is invariably smaller than the aorta; however, it is not necessarily significant obstructive. Valvar stenosis

14. -The main PA is usually somewhat diffusely small and is often short. - The narrowed portion of the main pulmonary artery is often at the sinotubular junction. - Branch PA abnormalities occurred in only 10 % of cases. Sinotubular junction Supravalvar stenosis

15. Outlet from left ventricle Interventricular plane Ventricular septal defect 3 important planes

16.  Perimembranous defect - In about 4/5 of Caucasian patients - VIF stops short of the postero-caudal limb of TSM, permitting fibrous continuity to exist between the leaflets of the aortic & tricuspid valves Muscular outlet septum Ventricular infundibular fold Remnant of the interventricular membranous septum AV node Right bundle branch Left bundle branch Postero-caudal limb of TSM Types of ventricular septal defect

17. Ventricular infundibular fold Septomarginal trabeculation Septoparietal trabeculation Aortic-tricuspid continuity

18.  Muscular defect - In about 1/5 of Caucasian patients - Postero-caudal limb of the TSM fuses with VIF, permitting muscular continuity throughout the right ventricular margin of the defect. Postero-caudal limb of TSM Ventricular infundibular fold Muscular outlet septum Hypertrophied septoparietal trabeculation Right bundle branch Left bundle branch AV node

19. Ventricular infundibular fold Septomarginal trabeculation Septoparietal trabeculation

20.  Doubly committed & juxta-arterial defect - Commoner in the Far East and South America - Consequence of failure of formation of a complete muscular subpulmonary infundibulum Ventricular infundibular fold Fibrous continuity between the leaflets of the arterial valves Postero-caudal limb of TSM

21. Unobstructed but relatively high- resistance systemic vascular bed Obstructed pulmonary outflow tract Anatomic route of balance between the two circulatory beds RV hypertension Normal or low PA pressure Pathophysiology

22. Hypercyanotic spell Catecholamine State of low intravascular volume state Crying /feeding, etc

23. TOF with Pulmonary atresia

24. Anatomic features

26. - Confluent or non-confluent. - Confluent in about 2/3 of the cases - The caliber of the central PAs varies : When the ductus or collateral arteries connect proximally to the central PAs or their lobar branches, the central vessels may be only mildly hypoplastic or even normal in size. Atretic arterial segment - Can be recognized as a solid elastic cord in about ¾ - Rarely only the PV is imperforate. The central right & left PAs

27. “Entirely from the systemic circulation”. - Ductus arteriosus - Systemic-to - pulmonary collateral arteries - Coronary artery - Plexus of bronchial or pleural arteries The blood supply to the lungs

28. Systemic-to-pulmonary collateral arteries Pulmonary arteries Pulmonary atreisia Patent ductus arteriosus * Ductal & collateral sources may coexist in the same patients but only rarely coexist in the same lung segment.

29.  Ductus arteriosus - Usually is a unilateral structure - Associated with confluent PAs in > 80% of cases - Rarely, bilateral ductus may occur with non-confluent arteries - Because the ductus is widely patent during fetal life, the PAs may be a normal size at birth. - Normal postnatal ductal narrowing usually occurs and produce distal stenosis in 35-50% of cases. Patent ductus arteriosus Pulmonary coarctation

30.  Collateral arteries - Most commonly from the descending thoracic aorta - Less commonly the subclavian arteries - Rarely from the abdominal aorta - Their number varies from 1 to 6 - Their diameter ranges from 1 to 20mm - More stable source of pulmonary blood flow

31. - Anastomoses between the central PAs (or their branches) and the collateral arteries : About 40% of subjects : May occur at the hilum or within the lung : In the remaining 60%, the collateral arteries enter the pulmonary hilum, travel with the bronchi as PAs

32. - Stenosis : nearly 60% of collateral arteries : tend to occur near the aortic or intrapulmonary anastomosis : may be discrete or segmental : may be congenital or acquired

33. - Ductus supplies confluent central PAs : Intra-PAs of both lungs are normal - Ductus supplies one of the non-confluent central PAs : Contra-lateral lung usually has arborization abnormalities - Ductus is absent : Both lungs have arborization abnormalities  Intrapulmonary artery distribution

34. Classification - There is no standard classification system for PAVSD, but several have been proposed. - Most classification schemes focus on the patterns of pulmonary blood flow. Congenital Heart Surgery Nomenclature and Database Project

35. Boston group IIIa. Central pulmonary artery Z – score > -2.5 IIIb. Central pulmonary artery Z – score < -2.5

36. Pathophysiology One of Three  Marked heart failure because of lung overflow  Cyanotic because of reduced lung flow  Fairly well balanced with systemic oxygen saturation in the high 70s to low 80s Extrapulmonary collateral Obstruction Collateral stenosis Intrapulmonary collateral has thin- walled elastic media

37. TOF with Absent Pulmonary Valve

38. Absence of ductus arteriosus Pulmonary annular hypoplasia Anatomic features Dilated pulmonary arterial trees Deviated muscular outlet septum Rudimentary leaflets of PV

39. Pathophysiology  Free pulmonary regurgitation throughout fetal life - Transmission of chronic volume load of the RV to PAs Proximal PA : aneurismal dilatation PA NormalTOF with APV Airway compression

40. Common atrioventricular canal

41. Anatomic features Septoparietal trabeculations Outlet septum Pulmonary trunk Aorta Anterior papillary muscle Common atrioventricular valve