describes 28 years of experience in the surgical management of tetralogy of Fallot with subarterial VSD at Tenri Hospital in Japan.

Similar documents
Doubly committed or subarterial ventricular septal. Tetralogy of Fallot With Subarterial Ventricular Septal Defect

Perimembranous VSD: When Do We Ask For A Surgical Closure? LI Xin. Department of Cardiothoracic Surgery Queen Mary Hospital Hong Kong

Indication and Technique of Total Correction of Tetralogy of Fallot in 228 Patients

Surgical Management of TOF in Adults. Dr Flora Tsang Associate Consultant Department of Cardiothoracic Surgery Queen Mary Hospital

MRI (AND CT) FOR REPAIRED TETRALOGY OF FALLOT

Tetralogy of Fallot (TOF) with atrioventricular (AV)

Surgical Results in Patients With Double Outlet Right Ventricle: A 20-Year Experience

Surgical Treatment for Double Outlet Right Ventricle. Masakazu Nakao Consultant, Paediatric Cardiothoracic Surgery

Mid-term Result of One and One Half Ventricular Repair in a Patient with Pulmonary Atresia and Intact Ventricular Septum

In 1980, Bex and associates 1 first introduced the initial

Congenital Heart Defects

Complete atrioventricular septal defect with tetralogy

Since 1954, when Lillehei completed the first successful

Anatomically corrected malposition of the great arteries (ACMGA)

Atrioventricular valve repair: The limits of operability

The need for right ventricular outflow tract reconstruction

Perioperative Management of DORV Case

Giovanni Di Salvo MD, PhD, FESC Second University of Naples Monaldi Hospital

Fetal Tetralogy of Fallot

HISTORY. Question: What type of heart disease is suggested by this history? CHIEF COMPLAINT: Decreasing exercise tolerance.

The pulmonary valve is the most common heart valve

Anomalous muscle bundle of the right ventricle

Candice Silversides, MD Toronto Congenital Cardiac Centre for Adults University of Toronto Toronto, Canada

Adult Congenital Heart Disease: The New Reality. Disclosures

Double outlet right ventricle: navigation of surgeon to chose best treatment strategy

The background of the Cardiac Sonographer Network News masthead is a diagnostic image:

CARDIAC ANATOMY. David McGiffin Director of Cardiothoracic Surgery and Transplantation Alfred Health, Melbourne

CMR for Congenital Heart Disease

Cover Page. The handle holds various files of this Leiden University dissertation.

Complex Congenital Heart Disease in Adults

An anterior aortoventriculoplasty, known as the Konno-

"Giancarlo Rastelli Lecture"

Cover Page. The handle holds various files of this Leiden University dissertation.

Research Presentation June 23, Nimish Muni Resident Internal Medicine

Cardiac MRI in ACHD What We. ACHD Patients

Cardiac Catheterization Cases Primary Cardiac Diagnoses Facility 12 month period from to PRIMARY DIAGNOSES (one per patient)

Tetralogy of Fallot (TOF) with absent pulmonary valve

The Surgical Treatment of Tetralogy of Fallot

Congenital Heart Disease II: The Repaired Adult

LEFT VENTRICULAR OUTFLOW OBSTRUCTION WITH A VSD: OPTIONS FOR SURGICAL MANAGEMENT

The Double Switch Using Bidirectional Glenn and Hemi-Mustard. Frank Hanley

5.8 Congenital Heart Disease

A New Radiopaque Surgical Suture* Juro WADA, M.D. and Masahiro ENDO, M.D.

Late Results after Correction of Ventricular Septal Defect with Severe Pulmonary Hypertension

PULMONARY ARTERY STENTING AFfER TOTAL SURGICAL CORRECTION OF RIGHT VENTRICULAR OUTFLOW TRACT OBSTRUCTIVE LESIONS

IMAGES. in PAEDIATRIC CARDIOLOGY. Abstract. Case

Congenital Heart Disease An Approach for Simple and Complex Anomalies

HISTORY. Question: What category of heart disease is suggested by this history? CHIEF COMPLAINT: Heart murmur present since early infancy.

Corrective Repair of Complete Atrioventricular

Double Outlet Right Ventricle with Anterior and Left-Sided Aorta and Subpulmonary Ventricular Septal Defect

Long-Term Results After the Rastelli Repair for Transposition of the Great Arteries

Surgical options for tetralogy of Fallot

RVOTO adult and post-op

Clinical material and methods. Fukui Cardiovascular Center, Fukui, Japan

Debanding and repair of ventricular septal defect: a new technique for older patients

The Rastelli procedure has been traditionally used for repair

BIVENTRICULAR REPAIR FOR AORTIC ATRESIA OR HYPOPLASIA AND VENTRICULAR SEPTAL DEFECT

Adult Congenital Heart Disease: What All Echocardiographers Should Know Sharon L. Roble, MD, FACC Echo Hawaii 2016

Indications for the Brock operation in current

The role of intraoperative TOE in congenital cardiac surgery

CONGENITAL HEART DISEASE (CHD)

ABSTRACT In general, it has been thought that

Accessory mitral valve tissue causing left ventricular outflow tract obstruction

14 Valvular Stenosis

Pulmonary Artery Debanding

Journal of the American College of Cardiology Vol. 36, No. 7, by the American College of Cardiology ISSN /00/$20.

Assessing Cardiac Anatomy With Digital Subtraction Angiography

Yuichi Shiokawa, MD Anton E. Becker, MD, PhD

CONGENITAL HEART DEFECTS IN ADULTS

Adult Congenital Heart Disease T S U N ` A M I!

Anomalous Systemic Venous Connection Systemic venous anomaly

Pulmonary Valve Replacement

SURGICAL TREATMENT AND OUTCOME OF CONGENITAL HEART DISEASE

A teenager with tetralogy of fallot becomes a soccer player

Heart and Lungs. LUNG Coronal section demonstrates relationship of pulmonary parenchyma to heart and chest wall.

가천의대길병원소아심장과최덕영 PA C IVS THE EVALUATION AND PRINCIPLES OF TREATMENT STRATEGY

Double outlet right ventricle with L-position pulmonary stenosis

Echocardiographic assessment in Adult Patients with Congenital Heart Diseases

42yr Old Male with Severe AR Mild LV dysfunction s/p TOF -AV Replacement(tissue valve) or AoV plasty- Kyung-Hwan Kim

3/14/2011 MANAGEMENT OF NEWBORNS CARDIAC INTENSIVE CARE CONFERENCE FOR HEALTH PROFESSIONALS IRVINE, CA. MARCH 7, 2011 WITH HEART DEFECTS

Clinicians and Facilities: RESOURCES WHEN CARING FOR WOMEN WITH ADULT CONGENITAL HEART DISEASE OR OTHER FORMS OF CARDIOVASCULAR DISEASE!!

The modified Konno procedure, or subaortic ventriculoplasty,

Hemodynamic Assessment After Complete Repair of Pulmonary Atresia With Major Aortopulmonary Collaterals

Case 47 Clinical Presentation

Pulmonary Valve Replacement Late After Repair of Tetralogy of Fallot

Surgical treatment of ventricular septal defect

T ventricle and the pulmonary artery has allowed repair. Extracardiac Valved Conduits in the Pulmonary Circuit

Adults With Congenital Heart. Disease. An Expanding Population. In this article:

Notes by Sandra Dankwa 2009 HF- Heart Failure DS- Down Syndrome IE- Infective Endocarditis ET- Exercise Tolerance. Small VSD Symptoms -asymptomatic

Outcomes of Mitral Valve Repair for Mitral Regurgitation Due to Degenerative Disease

List of Videos. Video 1.1

Anatomy & Physiology

Conduit Reconstruction of Right Ventricular Outflow Tract

ADULT CONGENITAL HEART DISEASE. Stuart Lilley

Surgical Repair of Ventricular Septal Defect; Contemporary Results and Risk Factors for a Complicated Course

Pulmonarv Arterv Plication: with Type I Trunms Arteriosus. A New S&gical Procedure for Small Infants

ECHOCARDIOGRAPHIC APPROACH TO CONGENITAL HEART DISEASE: THE UNOPERATED ADULT

For Personal Use. Copyright HMP 2013

Management of a Patient after the Bidirectional Glenn

Stenosis of Pulmonary Veins

Transcription:

EARLY AND LATE RESULTS OF REPAIR OF TETRALOGY OF FALLOT WITH SUBARTERIAL VENTRICULAR SEPTAL DEFECT A comparative evaluation of tetralogy with perimembranous ventricular septal defect Between November 1966 and December 1990, 511 pediatric patients with tetralogy of Fallot underwent corrective operation at Tenri Hospital. There were 78 patients with subarterial ventricular septal defect. Mean age at repair was 5.6 +- 3.3 years. The method of right ventricular outflow tract reconstruction was simple infundibulectomy in 14 patients, right ventricular outflow patch in 36, and transannular patch in 28. There were 7 (9.0%) early deaths as a result of low cardiac output syndrome and acute renal failure. The pressure ratio of the right ventricle to the left ventricle was 0.62-0.18 during the early postoperative catheterization. Follow-up was achieved for 442.6 patient-years and ranged from 0.5 to 27 years, with an average of 8.5-6.7 years. There were three late deaths (2 cardiac and 1 noncardiac). Actuarial survival was 94.8% -+ 4.0% at 20 years. Catheterization during late follow-up (6.8 -+ 4.7 years after repair) was done in 53 patients and the pressure ratio of the right ventricle to the left ventricle was 0.48-0.21. Fifteen patients underwent subsequent operation because of residual lesions, including ventricular septal defect in four patients, pulmonary stenosis in nine, combined ventricular septal defect and pulmonary stenosis in one, and pulmonary regurgitation in one, with no mortality. Actuarial rate of freedom from reoperation was 71.1% -+ 8.0% at 10 years and 58.8% -+ 16.8% at 20 years. Patients with tetralogy and subarterial ventricular septa defect were more likely to have the development of residual obstruction at the level of the pulmonary valve anulus after repair than were those with tetralogy and perimembranous ventricular septal defect. (J THORAC CARDIOVASC SURG 1995;110:180-5) Yutaka Okita, MD, a* Shigehito Mild, MD, a Yuichi Ueda, MD, a Takafumi Tahata, MD, a Tetsuro Sakai, MD, a Katsuhiko Matsuyama, MD, a Masahiko Matsumura, MD, b and Tokio Tamura, MD, b Tend, Nara, Japan etralogy of Fallot with doubly committed subar- T terial ventricular septal defect (VSD) is relatively more common among Orientals than among whites and has special features of surgical importance. 1 Despite the benign natural course, mild cyanosis, and large pulmonary arteries, a considerable prevalence of residual pulmonary stenosis after repair of this anomaly has been reported. 2'3 This report From the Departments of a and Pediatric Cardiology, b Tenri Hospital, Tenri, Nara, Japan. Received for publication May 26, 1994. Accepted for publication Nov. 28, 1994. Address for reprints: Yutaka Okita, MD, Department of Cardiovascular Surgery, National Cardiovascular Center, Fujishirodai 5-7-1, Suita, Osaka, Japan 565. *Present address: Department of, Natio.nal Cardiovascular Center, Osaka, Japan. Copyright 9 1995 by Mosby-Year Book, Inc. 0022-5223/95 $3.00 + 0 12/1/62465 describes 28 years of experience in the surgical management of tetralogy of Fallot with subarterial VSD at Tenri Hospital in Japan. Patients and methods Between November 1966 and December 1990, 547 patients with tetralogy of Fallot underwent corrective operation at Tenri Hospital. With the exclusion of patients older than 16 years and of those with VSD and pulmonary atresia, 511 patients remained. The study population included 78 patients with subarterial VSD, including 41 patients with a VSD that extended from the pulmonary anulus to the membranous septum, the socalled total conal defect. The control group included 433 patients with tetralogy and perimembranous VSD who underwent repair during the same period (Table I). Before operation, patients with subarterial VSD had less frequent anoxic spells, better arterial oxygen saturation. greater pulmonary blood flow, and well-developed pulmonary arterial trees compared with respective findings in patients with perimembranous VSD. All patients underwent operation with the use of cardiopulmonary bypass with moderate hypothermia. 180

The Journal of Thoracic and Volume 11 O, Number 1 Okita et al. 18 1 Table I. Preoperative variables Subarterial VSD Perimembranous VSD p Value Age (yr) 5.6 _+ 3.3 4.5 + 2.7 NS Anoxic spells 2 (15.3%) 141 (32.6%) <0.01 Preceding palliation 3 (3.8%) 35 (8.1%) NS Sao2 (%) 85.1 z 9.3 77.7 z 11.5 <0.01 Qp/Qs 1.08 _+ 0.67 0.79 : 0.53 <0.05 0Ao/0PA 0.67 z 0.20 0.53 z 0.19 <0.05 PA branch abnormalities 9 (11.5%) 19 (4.4%) <0.01 CTR 0.56 -'- 0.05 0.52 z 0.03 NS NS. not significant; Sa% arterial oxygen saturation ratio; Qp/Qs, ratio of pulmonary blood flow to systemic blood flow: OAo/OPA. ratio of the diameter of the ascending aorta to that of the main pulmonary artery; PA, pulmonary artery; CTR. cardiothoracic ratio. Table II. Reconstruction of the RVOT Subarterial VSD Perirnembranous VSD Simple infundibulectomy 14 (17.9%) 142 (32.8%) Outflow patch limited in RV 36 (46.2%) 227 (52.4%) Transannular patch 28 (35.8%) p < 0.05 64 (14.7%) Total No. ~ 43~ Table III. Operative result Subarterial VSD Perimembranous VSD p Value Death 7/78 (9.0%) 52/433 (12.1%) NS Catheterization (n) 42 199 Early postop. (1-2 too) P (RV/LV) 0.62 z 0.18 0.52 z 0.20 <0.05 P (RV-PA) 33.3 z 17.4 24.0 z 19.2 <0.05 Residual VSD 10 (23.8%) 24 (12.1%) <0.05 Residual PS* 16 (38.1%) 38 (19.1%) <0.01 NS, Not significant; P (RV-PA), pressure gradient between the RV and right pulmonary artery. *Criteria for residual PS; P(RV-PA) > 50 mm Hg or P(RV/LV) > 0.70. Myocardial protection with topical cooling and cardioplegic solution has been done since 1979. The majority of patients underwent operation through a right ventriculotomy; however, a combined right atrial and pulmonary approach has been preferred in recent years. The VSD was closed with a Dacron fabric or xenopericardial patch. Pulmonary valvotomy or pulmonary annular enlargement was done when the minimal requirement for annular size, according tothe study of Rowlatt, Rimoldi, and Lev 4 was not fulfilled. In the subarterial VSD group, there was a greater prevalence of the use of a transannular patch to increase the size of the outflow tract of the right ventricle (RV) to the main pulmonary artery (Table II). Postoperative catheterization was done 1 to 2 months after repair in 241 patients in whom residual lesions were suspected and in 318 patients 6.8 + 3.8 years after operation. Residual pulmonary stenosis (PS) was defined as a pressure gradient between the RV and the right pulmonary artery of more than 50 mm Hg or a pressure ratio of the RV to the left ventricle of more than 0.70. Severity of pulmonary regurgitation and aneurysm of the fight ventricular outflow tract (RVOT) was graded in four degrees ranging from none to severe. Survival data and the event-free curve were analyzed by actuarial methods. Statistical analysis was done with Student's t test, Welch t test, Wilcoxon test, and Fisher test. Multivariate analysis (stepwise logistic regression) was done to detect preoperative and intraoperative clinical predictors of postoperative residual PS. The preoperative and intraoperative variables were age at operation, VSD site, arterial oxygen saturation, ratio of pulmonary blood flow to systemic blood flow, ratio of the diameter of the main pulmonary artery to that of the ascending aorta, cardiothoracic ratio, history of palliation, abnormality of the peripheral pulmonary artery, and the mode of reconstruction of the RVOT. Results There was no significant difference detected regarding early postoperative mortality in 7 patients (9.0%) in the subarterial VSD group and 52 patients (12.1%) in the perimembranous VSD group. The

182 Okita et al The Journal of Thoracic and July 1995 % 100-95- T 98.7........... : T = ; : 6 90-.?. g 85- n No significance 9 Doubly committed subarterial VSD "~ Perimembranous VSD 10 5- n 61 57 48 35 25 15 11 6 5 5 3 314 282 229 177 138 103 72 54 27 17 10 4 6 8 1'0 12 14 16 18 20 22 Postoperative years Fig. 1. Actuarial survival after repair of tetralogy of Fallot. 1 2'4 Table IV. Late results Death Cardiac death Noncardiac death Catheterization (n) After repair (yr) P(RV/LV) P(RV-PA) Residual VSD Residual PS PR None Mild Moderate Severe RV aneurysm None Mild Moderate Severe TR CTR ECG Normal RBBB RBBB + LAH / CAVB, Digitalization Subarterial VSD Perimembranous VSD p Value 3 (4.2%) 2 1 53 6.8 + 4.7 0A8 _+ 0.21 29.7 _+ 24.1 6 (11.3%) 10 (18.9%) 4 (7.6%) 10 (18.9%) "23 (43.4%) 16 (30.2%) 10 (18.9%) 9 (17.0%) 26 (49.0%) 8 (15.1%) 2 (3.8%) 0.57 + 0.06 19 (36.5%) 42 (16.1%) 31 (56.3%) 205 (78.8%) 1 (1.9%) 10 (3.8%) 1 (1.9%) 3 (1.2%) 2 (2.6%) 12 (0.9%) 10 (2.6%) NS 7 3 NS 265 6.7-4- 3.1 NS 0.43 -+ 0.18 NS 20.9 _+ 19.7 <0.05 19 (0.7%) NS 33 (12.5%) NS 31 (11.7%) 84 (31.7%) 91 (34.3%) 49 (18.4%) <0.05 48 (18.1%) 96 (36.2%) 89 (33.6% 32 (12.1%) <0.05 2 (0.8%) NS 0.54 -+ 0.08 NS NS, Not significant; P(RV-PA), pressure gradient between the RV and right pulmonary artery; TR, tricuspid regurgitation; ECG, electrocardiogram; RBBB, right bundle branch block; LAH, left anterior h~miblock; CAVB, complete atrioventricular block. <0.01 NS

The Journal of Thoracic and Volume 110, Number 1 Okita et al. 183 C 0 % 100" 90-80" 70- O. o 60- "~ 50- ~- 40- o 30-20- 10-9 ~ P<0.05 9 ~ P<0,01 ', 9 Doubly committed subarterial VSD Perimembranous VSD 59 55 46 30 20 13 8 4 4 4 2 314 280 225 164 126 92 65 47 23 14 7 Postoperative years 2'4 Fig. 2. Actuarial freedom from reoperation after repair of tetralogy of Fallot. Table V. Subsequent operation Subarterial VSD Perimembranous VSD Residual VSD 4 4 Residual PS 9 15 Residual PS + VSD 1 8 PR 1 ' 0 Total No. 15/71 (21.1%) 27/381 (7.1%) p < 0.01 cause of death in the subarterial VSD group was low cardiac output syndrome in five patients and acute renal failure in two. Early postoperative catheterization showed a significantly higher prevalence of residual VSD and PS in the subarterial VSD group (Table III). Follow-up was maintained in 410 patients (80.4%) in the overall series. Follow-up ranged from 3 months to 27 years, averaged 8.3 _+ 5.5 years, and totaled 3401.6 patient-years. There were 3 late deaths, 2 of cardiac causes and 1 of noncardiac causes, in the subarterial VSD group and 10 deaths, 7 of cardiac causes and 3 of noncardiac causes, in the perimembranous VSD group (Table IV). Actuarial survival was 94.8% _ 4.0% at 20 years in the subarterial VSD group, which was comparable to 91.6% at 20 years in the perimembranous VSD group (Fig. 1). Late catheterization revealed a significantly greater prevalence of residual PS and a greater degree of pulmonary regurgitation (PR) or bulging RV in the subarterial VSD group. However, postoperative conduction disturbance was less severe in the subarterial VSD group than that in the perimembranous VSD group. Residual lesions necessitated subsequent operation in 15 patients (21.1%) (VSD in 5 patients, PS in 10, and PR in 1), but there were no reoperation-related mortalities (Table V). The prevalence of reoperation was higher in the subarterial VSD group. On actuarial study, the incidence of subsequent operation was significantly lower at 10, 15, and 20 years in the subarterial VSD group than that in the perimembranous VSD group (Fig. 2). Stepwise logistic regression analysis of nine variables in the overall series demonstrated that two of the variables, subarterial VSD and smaller ratio of pulmonary blood flow to systemic blood flow, were significant predictors of a higher pressure ratio of RV to left ventricle (P[RV/LV]) on early postoper-

184 Okita et al The Journal of Thoracic and July 1995 Table VI. Preoperative and intraoperative risk factors predicting a higher postoperative P(RV/LV) ratio on early postoperative catheterization Variable Coefficient p Value Age at repair 1.235 0.403 Preceding palliation 11.118 0.188 CTR 0.629 0.800 VSD site 7.192 0.0tl Sao a 0.167 0.149 Qp/Qs -5.669 0.029 0Ao/PA 0.026 0.745 PA branch abnormalities 0.607 0.932 RVOT reconstruction 0.824 0.074 Constant 0.177 -- CTtL Cardiothoracic ratio: Saoz arterial oxygen saturation ratio; Qp/Qs, ratio of pulmonary blood flow to systemic blood flow: OAo/OPA. ratio of the diameter of the ascending aorta to that of the main pulmonary artery; PA, pulmonary artery. Table VII. Preoperative and intraoperative risk factors predicting a higher postoperative P(RV/LV) ratio on late postoperative catheterization Variable Coeficient p Value Age at repair 1.107 0.471 Preceding palliation 7.388 0.169 CTR 0.632 0.120 VSD site 1.341 0.037 Sao 2-0.033 0.735 Qp/Qs 1.991 0.426 0Ao/PA -0.030 0.603 PA branch abiaormalities 2.653 0.608 RVOT reconstruction 1.329 0.147 Constant 0.471 CTR, Cardiothoracic ratio: Sao2, arterial oxygen saturation ratio; Qp/Qs, ratio of pulmonary blood flow to systemic blood flow; OAo/OPA, ratio of the diameter of the ascending aorta to that of the main pulmonary artery; PA, pulmonary artery. ative catheterization (Table VI). On analysis of the variables against late PS, only subarterial VSD was a significant predictor of greater P(RV/LV) and residual gradient in the outflow tract (Tables VII and VIII). Discussion Similar to the simple type of doubly committed subarterial VSD, tetralogy of Fallot with doubly committed subarterial VSD is much more common in Oriental than Occidental countries. Although these cases account for approximately 10% to 30% of all tetralogy cases in Japan, 1'5 in the United States and western Europe the incidence of tetralogy with doubly committed subarterial VSD is only 6% to 8%. 2, 3, 6 In strict morphologic terms, these Table VIII. Preoperative and intraoperative risk factors predictive of postoperative higher pressure gradient between the RV and the right pulmonary artery at late postoperative catheterization Variable Coefficient p Value Age at repair 0.744 0.767 Preceding palliation 8.121 0.606 CTR 0.446 0.108 VSD site 1.616 0.039 Sao 2-0,140 0.198 Qp/Qs 2.206 0.438 0Ao/0PA 0.004 0.952 PA branch abnormalities 2.996 0.606 RVOT reconstruction 0.496 0.096 Constant 0.320 -- CTR, Cardiothoracic ratio; Sao9 arterial oxygen saturation ratio; Qp/Qs, ratio of pulmonary blood flow to systemic blood flow; OAo/OpA, ratio of the diameter of the ascending aorta to the main pulmonary artery; PA, pulmonary artery. cases should not be classified as tetralogy because they lack the anteriorly deviated infundibular septurn of tetralogy that produces the malalignment VSD with aortic overriding and PS. 7 In most cases, the pulmonary arteries are of adequate size, usually with a sound pulmonary valve anulus, and patients show less severe cyanosis than.patients with tetralogy combined with perimembranous VSD. 8' 9 This is presumed to be related to the absence or deficiency of part of the anteriorly displaced infundibular septum, Which prevents development of a fixed obstruction in the RVOT. The severity of the RV obstruction depends on the severity of pulmonary valvular stenosis, the development of the septal or anterior muscle of the RVOT, or hypoplasia of the pulmonary arterial tree. Despite the benign natural course and less severe anatomy, the prevalence of unrelieved PS and resultant poor outcome is quite high if the RVOT is not properly enlarged. 1' 2 The VSD patch extends up to the RVOT and causes a narrowing beneath the pulmonic ring, for which patch enlargement is required in the majority of cases. The patch does not always need to extend across the pulmonary anulus. There is further risk of surgical damage to the aortic valve that may produce aortic regurgitation during ventriculotomy and during closure of the VSD. Neirotti and associates 2 stressed that the closure of the subarterial VSD increased the apparent severity of PS and necessitated a transannular patch in patients whose RVOT before repair did not appear to need such patching, de Leval and associates 3

The Journal of Thoracic and Volume 110, Number 1 Okita et al 185 reported that 10 (76%) of 13 patients with tetralogy and subarterial VSD needed transannular patch enlargement. However, Vargas and associates 1~ reported that patients with tetralogy with subarterial VSD had a nonrestrictive pulmonary ring more often than previously thought and that the prevalence of transannular patching had decreased to 20% in their recent series. The prevalence of transannular patching in our series was 36% and the prevalence of resultant PR and bulging RV was higher than that in patients with perimembranous VSD~ Although a high postrepair P(RV/LV) ratio is a well-known determinant for early and late death in tetralogy,11.12 severe PR caused by an excessively large transannular patch is likely to cause RV dysfunction after repair. 13, 14 Presently, our standard minimal requirement for pulmonary annular size, measured by direct Hegar's dilator immediately after right ventriculotomy or pulmonary arteriotomy, to preserve the pulmonary annular ring is a Z value 4 of -3 for tetralogy with perimembranous VSD n or a Z value of 0 for tetralogy with subarterial VSD. Liberal use of outflow patch, transannular if necessary, and extensive infundibulectomy were essential to relieve PS in this anomaly. However, postoperative conduction disturbance in patients with tetralogy and subarterial VSD was less frequent in our series. Thirty-seven (47.4%) patients had subarterial VSD, which did not extend to the membranous portion of the interventricular septum. The fusion of the posterior limb of the trabecula septomarginalis with the ventriculoinfundibular fold produced a protective muscular bundle for the conduction systems at the posteroinferior angle of the VSD. 7 Conclusion. Seventy-eight pediatric patients who had tetralogy of Fallot with subarterial VSD underwent corrective operation. There were 7 (9.0%) early deaths and three late deaths. Although the late survival was satisfactory, actuarial study revealed that 71% of patients remained free from subsequent operation necessitated by residual PS and VSD at 10 years and this rate dropped to 59% at 20 years. More radical management in the relief of RV obstruction in this group of patients is justified. REFERENCES 1. Ando M. Subpulmonary ventricular septal defect with pulmonary stenosis. Circulation 1974;50:412. 2. Neirotti R, Galindez E, Kreutzer G, Coronel AR, Pedrini M, Becu L. Tetralogy of Fallot with subpulmonary ventricular septal defect. Ann Thorac Surg 1978;25:51-6. 3. de Leval MR, Pozzi M, Starnes V, et al. Surgical management of doubly committed subarterial ventricular septal defect. Circulation 1988;78(suppl):III40-6). 4. Rowlatt UF, Rimoldi HJA, Lev M. The quantitate anatomy of the normal child's heart. Pediatr Clin North Am 1963;10:499-519. 5. Matsuda H, Ihara K, Mori T, Kitamura S, Kawashima Y. Tetralogy of Fallot associated with aortic insufficiency. Ann Thorac Surg 1979;29:529-33. 6. Warden HE, DeWall RA, Cohen M, Varco RL, Lillehei CW. A surgical-pathologic classification for isolated ventricular septal defects and for those in Fallot's tetralogy based on observations made on 120 patients during repair under direct vision. J TnORAC SURG 1957;33:21-44. 7. Satyanarayana, Rao BN, Edwards JE. Conditions simulating the tetralogy of Fallot. Circulation 1974; 49:173-8. 8. Anderson RH, Allwork SP, Ho SY, Lenox CC, Zuberbuhler JR. Surgical anatomy of tetralogy of Fallot. J THORAC CARDIOVASC SURG 1981;81:887-96. 9. Capeili H, Somerville J. Atypical Fallot's tetralogy with doubly committed subarterial ventricular septal defect. Am J Cardiol 1983;51:282-5. 10. Vargas FJ, Kreutzer GO, Pedrini M, Capelli H, Coronel AR. Tetralogy of Fallot with subarterial ventricular septal defect. J THORAC CARDIOVASC SURG 1986;92:908-12. 11. Kirklin JW, Blackstone EH, Jonas RA, et al. Morphologic and surgical determinants of outcome events after repair of tetralogy of Fallot and pulmonary stenosis. J "IkqOe, AC CAROIOVASC SURG 1992;103:706-23. 12. Poirier RA, McGoon DC, Danielson GK, et al. Late results after repair of tetralogy of Fallot. J THOgAC CARDIOVASC SURG i977;73:900-8. 13. Ilbawi MN, Idriss FS, DeLeon SY, et al. Factors that exaggerate the deleterious effects of pulmonary insufficiency on the right ventricle after tetralogy repair. J THORAC CARDIOVASC SURG 1987;93:36-44. 14. Ebert PA. Second operation for pulmonary stenosis or insufficiency after repair of tetralogy of Fallot. Am J Cardiol 1982;50:637-40.