Tetralogy of Fallot Associated with Pulmonary Atresia and Major Aortopulmonary Collateral Arteries: Comparison between the different surgical approaches.
- Author:
Jeong Ryul LEE
1
;
Jee Hyuck YANG
;
Yong Jin KIM
;
Joon Rhyang RHO
Author Information
1. Department of Thoracic and Cardiovascular Surgery, Seoul National University, Children's Hospital, Seoul National University College of Medicine, Seoul National University Medical Research Center, Heart Research Institute. jrl@plaza.snu.ac.kr
- Publication Type:Original Article
- Keywords:
Tetralogy of Fallot;
Pulmonary astresia;
Pulmonary artery, collateral
- MeSH:
Arteries*;
Cause of Death;
Follow-Up Studies;
Heart Ventricles;
Humans;
Mortality;
Paralysis;
Phrenic Nerve;
Pulmonary Artery;
Pulmonary Atresia*;
Survival Rate;
Tetralogy of Fallot*
- From:The Korean Journal of Thoracic and Cardiovascular Surgery
1999;32(5):471-479
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: Patients with tetralogy of Fallot(TOF), pulmonary atresia(PA) and major aortopulmonary collateral arteries(MAPCAs) have been managed by heterogenous surgical strategies. We have taken 5 different surgical approaches to this lesion. In this study, relative advantages and disadvantages of each strategy were discussed by analyzing our surgical results. MATERIAL AND METHOD: Between January 1986 and June 1998, 50 patients aged 1 to 177(39+/-31) months at a various morphologic spectrum of this lesion were treated at our institution. The groups, which were classified according to the initial approaches, consisted of one-stage unifocalization(A-1, n=9), staged unifocalization(A-2, n=11), right ventricle to pulmonary artery connection(RV-PA)(B-1, n=11), one-stage RV-PA plus unifocalization (B-2, n=11), and one-stage definitive repair(C, n=8). Morphologic charateristics, operative mortalities, and probabilities of definitive repair were compared between the groups and the causes of death, complications and the follow-up results were described. RESULT: Mean ages at the first operation were 57+/-18(A-1), 42+/-48(A-2), 18+/-14(B-1), 52+/-55(B-2), and 32+/-34(C) months (p<0.05). Mean numbers of MAPCAs were least in group C (A-1=4.3+/-1.0, A-2=4.5+/-1.3, B-1=4.1+/-1.9, B-2=4.1+/-1.6, C=3.4+/-1.8 : p<0.05). The ratios of the direct and the indirect MAPCAs in each group were not different between the grousps (A-1=91%/9%, A-2=78%/22%, B-1=80%/20%, B-2=80%/20%, C=81%/19% : p>0.05). Nineteen patients had more than 1 dependent MAPCAs. True pulmonary arteries were not present 13 patients and they were confluent in 29. A total of 101 operations were performed. Operative mortalities of initial procedures were 33%(3/9, A-1), 18%(2/11, A-2), 0%(0/11, B-1), 36%(5/11, B-2) and 13%(1/8, C) (p<0.05). Percentages of the definitive repair among the patients of each group were 22%(2/9, A-1), 18%(2/11, A-2). 45%(5/11, B-1), 27%(4/11, B-2), and 100%(8/8, C)(p<0.05). Hypoxic respiratory and cardiac failure(6), hypoxic encephalopathy(2) and sepsis(4) were the major causes of death. Phrenic nerve palsy occured in 5 patients. Thirty-one patients among the survivals have been followed up for a mean duration of 74+/-42(3-145) months. One and five year actuarial survival rates were 73% and 73 %. CONCLUSION: In conclusion, Right ventricle to pulmonary artery connection used in patients with TOF/PA/MAPCA as an inital procedure appeared to be highly successful in enhancing the chance of satisfactory definitive repair without the significant surgical risks. One-stage total repair at an ealier age group could be performed safely with the resonable outcomes. Unifocalization approach, whether it was performed in a single stage or in the multiple stages, resulted in the high operative mortality and the lowest chance of definitive repair, however more tailored selection of the patients and the long follow-up is mandatory to prove the usefulness of this approach.
