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Tuesday Afternoon, April 25,1995

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TUESDAY AFTERNOON, APRIL 25, 1995

1:45 am SIMULTANEOUS SCIENTIFIC SESSION A ADULT CARDIAC SURGERY

Auditorium, Hynes Convention Center

Moderators: Tirone E. David, M.D.

Bruce A. Reitz, M.D.

20. HOMOGRAFT MITRAL VALVE REPLACEMENT: MEASUREMENT TECHNIQUES FOR GRAFT SELECTION AND IMPLANTATION

Christophe Acar, M.D.*, Jullien Gaer, M.D.*, Alain Berrebi, M.D.*, Denis Tixier, M.D.*, Christian Brizard, M.D.*, Arnaud Farge, M.D.*, Alain Deloche, M.D.* and Alain F. Carpentier, M.D., Ph.D.

Paris, France and London, England

Homograft replacement of the mitral valve (HRMV) has experienced a renewal of interest since the introduction of improved methods of homograft preservation. However, the reliability of this technique remains a major concern due to the complexity and the frequent variations of the subvalvular apparatus. Our experience of 40 HRMV (19 total, 21 partial) carried out in the past 3 years made it possible to define precise measurement criteria which proved to be useful to achieve predictable results. The indications for HRMV were bacterial endocarditis in 16 patients and rheumatic valvular disease in 24 patients.

Measurement on the homograft were the following: 1) Circumference (assessed by prosthetic ring sizers), 2) Height of the anterior leaflet (average 23 ± 3 mm), 3) Distance from annulus to apex of the anterior papillary muscle (PM) (average 23 + 4 mm). In addition, the morphology of each papillary muscle was classified as follows: Type I, simple head (n=20); Type II, bifid head (n=52); Type III, complex PM (n=8).

Measurements on the recipient were obtained by transesophageal echocardiography (TEE): 1) Circumference of the annulus, 2) Distance from annulus to apex of the anterior PM which averaged 20 ± 3 mm in the bacterial endocarditis group and 8 ± 2 mm in the rheumatic valve group.

The homograft valve was selected to match as much as possible these measurements. Further adjustments were made by systematic use of a Carpentier-Edwards ring selected from the size of the anterior leaflet of the homograft and by side-to-side implantation of the graft PM to the recipient PM. Associated procedures comprised aortic valve repair (n=3), or replacement using homograft (n=2) and tricuspid valve repair (n=1), or replacement using homograft (n=1).

There has been 1 hospital death due to low cardiac output and 1 reopera-tion 10 days following the operation due to annulus dehiscence. The follow-up extended from 3 months to 34 months (average 8 months). There has been 1 late death due to lung cancer. All the remaining 37 patients were reviewed for this study and a TEE was performed. All patients were in NYHA class I (n=33) or II (n=4). TEE showed no mitral valve regurgitation (MVR) in 18 pts, trivial MVR in 15 and moderate MVR in 4. The valve surface area was 2.0 ± 0.3 cm2 for partial HRMV and 2.4 ± 0.2 cm2 for total HRMV with an average transvalvular gradient of 3 ± 2 mmHg.

This study shows that reliable results can be obtained with HRMV, a technique particularly useful for bacterial endocarditis in the adult and rheumatic valvular disease in children.


21. RECONSTRUCTION OF THE MITRAL ANNULUS - A TEN-YEAR EXPERIENCE

Christopher M. Feindel, M.D.*, Tirone E. David, M.D., Susan Armstrong, M.Sc.* and Zhao Sun, B.A.*

Toronto, Ontario, Canada

The mitral annulus (MA) may be damaged by extensive calcification, infective endocarditis or repeated mitral valve (MV) replacement making MV surgery hazardous. It is possible to reconstruct the MA with either autologous or bovine pericardium. All calcific or infected tissue is excised and a properly tailored pericardia! patch is sutured to the endocardium of the left ventricle posteriorly and to fibrous tissue underneath the aortic valve superiorly. If this fibrous tissue is also diseased, it can be replaced with pericardium, too. Thus, the MA can be repaired segmentally, circumferentially or along the entire base of the left ventricle.

Seventy-six pts have undergone reconstruction of the MA since 1984. There were 35 men and 41 women, ages 17 to 86 years, mean 58. The indications for reconstruction of the MA were: calcification in 19 pts (22%), MA abscess in 23 (30%), redo MV surgery in 30 (39%), and type I rupture of the left ventricle after MV replacement in 4 (5%). Three-fourths of the pts were in NYHA functional class IV and 18 were in septic and/or cardiogenic shock when operated on; 11 pts had coronary artery disease; and 48 pts had had at least one previous MV operation. The reconstruction of the MA was segmen-tal in 40 pts (52%), circumferential in 21 (27%), and involved both aortic and mitral annuli in 15 (20%). The MV was replaced in 70 pts and repaired in 6. There were 4 early reoperations in 3 pts: 1 for dehiscence of the patch, 1 for thrombosis of the valve, and 2 for new onset endocarditis. The operative mortality was 9% (7 pts). Pts have been followed up from 3 to 114 months, mean of 34. Every pt has had Doppler echocardiography annually. There has been no late patch dehiscence. Four pts have required reoperation: 2 for endocarditis, and 2 for failed bioprosthesis. There have been 13 late deaths, 8 cardiac and 3 valve-related. The actuarial survival at 5 years was 74% ± 4%.

Reconstruction of the MA with pericardium is an extremely useful operative technique in pts with damaged annulus, and provides excellent late results.

*By invitation


22. ATRIOVENTRICULAR VALVE REPAIR USING EXTERNALLY ADJUSTABLE FLEXIBLE RINGS

João Q. Melo, M.D.*, José S. Neves, M.D.*, Regina Ribeiras, M.D.*, Miguel Abecasis, M.D.*, Manuel Canada, M.D.*, Maria J. Rebocho, M.D.*, Narciso C. Andrade, M.D.* and Manuel M. Macedo, M.D.

Lisbon, Portugal

Mitral and tricuspid valve repair using annuloplasty rings have a significant incidence of residual regurgitation which leads either to suboptimal results or to the need of a reoperation. We have developed a new technique for partial annuloplasty using a flexible externally adjustable ring. If required, it is adjusted from outside the heart after hemodynamic stabilization is obtained following interruption of extracorporeal circulation. Adjustment of the ring is controlled using transesophageal echocardiography. Twenty patients (pts), with a mean age of 45 years, ranging from 7 to 70 years, had 25 rings implanted, 14 in mitral position and 11 in tricuspid position. Most pts (12) were rheumatic in origin. Eight pts had pure mitral insufficiency and the other mixed lesions. All tricuspid lesions were regurgitation. Eight pts had complex mitral repairs and 8 pts had associated procedures: aortic repair (1 pt), aortic replacement (3 pts), maze 3 operation (2 pts), left atrial isolation (2 pts), coronary artery bypass (1 pt). Mitral regurgitation before surgery was grade 4 in 5 pts, grade 3 in 6 pts and grade 2 in 3 pts. After surgery it reduced to grade 2 (1 pt), grade 1 (5 pts) or none (8 pts). Tricuspid regurgitation reduced from grade 4 (4 pts), grade 3 (3 pts) and grade 2 (3 pts) to grade 1 (3 pts) and no regurgitation (7 pts). Mean pulmonary artery pressure was reduced from 67 to 40 mmHg.

External adjustment was performed in 10 mitral rings and in 8 tricuspid rings, improving the regurgitation by 1 or 2 grades. There was no hospital or late mortality. At 6 months all pts are in functional Class I. One pt had a change of its residual mitral regurgitation from grade 1 to grade 2. The other had the same mitral or tricuspid evaluation as at hospital discharge.

We conclude that flexible, externally adjustable rings are safe and provide excellent early results. The external adjustment feature provides the possibility of a significant reduction of the incidence of residual regurgitation after mitral and/or tricuspid annuloplasty repair.

2:45 pm INTERMISSION - VISIT EXHIBITS

*By invitation


3:15 pm SIMULTANEOUS SCIENTIFIC SESSION A ADULT CARDIAC SURGERY

Auditorium, Hynes Convention Center

Moderators: Tirone E. David, M.D.

Bruce A. Reitz, M.D.

23. 1026 PATIENTS UNDERGOING COMBINED

CORONARY AND VALVULAR SURGERY: EARLY AND LATE PHASE EVENTS

Glenn W. Laub, M.D.*, Bridget M. Bailey, B.S.N.*, Chao L. Chen, Ph.D.*, Robert S. Clancy, B.S.N.*, Javier Fernandez, M.D., William A. Anderson, M.D.*, Joseph T. Costic, D.O.* and Lynn B. McGrath, M.D.

Browns Mills, New Jersey

Between January 1981 and December 1991, combined coronary and valve surgery was perfomed in 1,026 patients. Coronary revascularization was combined with aortic valve (AV) surgery in 551 (53.7%), mitral valve (MV) in 354 (34.5%), multiple valve in 119 (11.6%) and isolated pulmonic or tricuspid in 1 (0.2%) each, with valve repair being performed in 21% of procedures. Mean age was 66.7 years (range 31-90 yrs), 61% were male, and 56% were in CHF Class III and IV. There were 117 (11.4%) hospital deaths, with surgery on the MV being the most important risk factor, increasing mortality to 16% as compared to 7% without (p=0.001). CHF, cross clamp time, female gender, and previous surgery were also predictors of mortality, while extent of coronary disease, NYHA Class, and ejection fraction were not. Total follow-up was 5,021 pt-years (mean 5.5, range 1-13.3 yrs) and 99.9% complete. Actuarial survival at 5 and 10 yrs was 70 ± 2% and 42 ± 2% (70% CL), with survival of AV (74 and 48%) significantly longer than MV (67 and 32%, p=0.002). Risk factors for late death included MV surgery, preop NYHA and CHF Class, and liver disease. Survival with a mechanical valve was better than with a tissue valve at 10 yrs for AV (61 vs 34%, p=.0001), but not different for MV. The use of the internal mammary artery to the left anterior descending conferred a survival advantage at 10 yrs (59 vs 42%, p=0.02), while the number of vessels bypassed showed no effect. Of 415 late deaths, 33 (7.9%) were valve related: thromboembolic (TE) 10, prosthetic valve endocarditis 10, anticoagulant bleed (ACRH) 6, structural valve dysfunction (SVD) 6 and paravalvular leak (PVL) 1. Cardiac, non-valve related deaths (229) were comprised predominately of progressive heart failure or myocardial ischemia in 203 patients (89%). Postoperative angina occured in 85 (9.4%) and graft occlusion in 29 (3%) patients. Late survivors fared well as 453 (92%) were in CHF Class I and II. Overall actuarial freedom from complications at 10 years was 86.8% for TE, 84.2% from ACRH, 94.5% for PVL, 88.5% for SVD, 99.6% for valve thrombosis, and 84.1% for MI. Freedom for SVD at 8 yrs was far better with mechanical than tissue (98 v 71%, p=.01) as was freedom for re-operation at 10 yrs (AV:91 v 72%, p=.002; MV:79 v 64%, p=.04). Tissue valves had a superior freedom from ACRH at 5 yrs for AV (94 v 89%, p=.002) and MV (94 v 84%, p=.007), but TE rates were similar. Valve repair was not associated with a reduction in early or late phase events.

We conclude that although late survival was markedly lower than in an age, sex, race matched population (42 v 65%, 10 yr), the survivors' functional results are good. In addition, the use of the IMA and mechanical valve in the aortic position confer substantial long term survival advantages and freedom from reoperation in combined procedures.

*By invitation


24. REVASCULARIZATION OF THE CIRCUMFLEX ARTERY WITH THE PEDICLED RIGHT INTERNAL MAMMARY ARTERY: CLINICAL, FUNCTIONAL AND ANGIOGRAPHIC MIDTERM RESULTS

Michel Buche, M.D.*, Erwin Schroeder, M.D.*, Patrick Chenu, M.D.*, Olivier Gurne, M.D.*, Giulio Pompilio, M.D.* Baudouin Marchandise, M.D.*, Philippe Eucher, M.D.*, Yves Louagie, M.D.*, Robert Dion, M.D.* and Jean-Claude Schoevaerdts, M.D.*

Yvoir, Belgium

Sponsored by: Albert Starr, M.D., Portland, Oregon

Retroaortic crossing of the pedicled Right Internal Mammary Artery (RIMA) for revascularization of the Circumflex Artery (Cx) combined with a pedicled Left Internal Mammary Artery (LIMA) to the Left Anterior Descending Artery (LAD) and its branches is an attractive technique to achieve a complete arterial revascularization of the left ventricle. However there is a suspicion that pulling the RIMA through the transverse sinus could compromise its blood flow capacity and patency.

Material: Between January 1990 and July 1994, this technique was applied in 256 patients (202 male; 54 female; average age 62 years; range 31 to 80 years). 61 patients had a 2-vessel disease and 195 had a 3-vessel disease. 17 patients were undergoing a reoperation. 22 had a left ventricular ejection fraction <40%. 30 were diabetecs. The RIMA was directed to the Cx artery through the transverse sinus (259 anastomoses) and the LIMA was anastomosed to the LAD and its branches (375 anastomoses) in all patients. 195 patients with a 3-vessel disease received additional coronary artery bypasses to the Right Coronary Artery (93 Saphenous Vein grafts; 89 free Inferior Epigastric Artery; 12 pedicled Right Gastroepiploic Artery). In total, the patients received an average of 3.2 distal anastomoses (2.4 IMA anastomoses).

Clinical results: 3 patients died early and 8 had a nonfatal myocardial infarction (MI). 7 patients required postoperative intraaortic balloon pumping. 6 patients underwent early reoperation for excessive bleeding. Sternal wound complications occurred in 4 patients. One of these 4 patients died of the complication 10 months after the operation. No patient was lost for follow-up (average 28 months). During follow-up, one sudden death and 4 noncardiac deaths occurred. 2 patients experienced a nonfatal MI and 12 had recurrence of angina. There was no late reoperation.

Graft patency and functional assessment: 73 patients enrolled in a prospective angiographic study agreed to undergo a postoperative angiogram (average 12.6 months, range 6 to 24 months). 72/73 of the RIMA were patent. In comparison 73/73 of the LIMA (104/105 LIMA anastomoses) were patent. Stress Thallium Scintigraphy obtained in 25 of those patients did not reveal ischemia in the Cx area.

Conclusions: Complete arterial revascularization of the left ventricle by means of both pedicled IMA can be performed with acceptable mortality and morbidity.

The midterm patency rate of the pedicled RIMA passed through the transverse sinus and anastomosed to the Cx artery is excellent and does not differ of the patency rate of the LIMA anastomosed to the LAD.

*By invitation


25. RISK FACTORS FOR POSTOPERATIVE MORBIDITY

Victor A. Ferraris, M.D., Ph.D.* and Suellen P. Ferraris, Ph.D.*

Albany, New York

Sponsored by: L. Henry Edmunds, Jr., M.D., Philadelphia, Pennsylvania

Background: Analysis of outcomes after coronary artery bypass grafting (CABG) has focused on risk factors for operative motality. Non-fatal peri-operative morbidity is far more costly and more common after CABG and the factors that predispose to morbid events are not well documented. In order to identify the risk factors that lead to postoperative morbidity, we evaluated 938 patients undergoing CABG at our institution during 1993.

Methods: Univariate statistical analysis was performed on 46 patient variables in order to identify risk factors for either serious postoperative morbidity (stroke, perioperative Q-wave myocardial infarction, deep sternal infection, life-threatening postoperative hemorrhage) or increased hospital length-of-stay (LOS). Variables were considered both individually and in combination. For example, age was considered individually or in combination with other variables including parameters of blood volume (i.e., age divided by red blood cell volume or Age/RBCVOL), renal function, cardiac function, etc. Univariate analysis of these 46 variables revealed 16 that were significant risk factors for serious postoperative morbidity or increased LOS. These 16 variables were entered into multivariate analyses to determine independent risk factors for serious postoperative morbidity (logistic regression) or increased LOS (Cox proportional hazards regression). Similar multivariate analysis was performed to identify independent risk factors for hospital mortality (logistic regression).

Results: Hospital length-of-stay (LOS) was correlated with serious postoperative morbidity (Spearman rank correlation coefficient = -0.31, p<0.001) but not mortality (correlation coefficient = 0.03, p=0.38). In order of decreasing importance, the following patient variables were significantly associated with increased LOS by stepwise Cox proportional hazards analysis: Age/RBCVOL (p<0.001), history of CHF (p<0.001), CPB time (p<0.001), hypertension (p=0.004), chronic obstructive lung disease (p=0.002), and previous stroke (p=0.041). In order of decreasing importance the following patient variables were significantly associated with the occurrence of any serious postoperative morbidity by logistic regression: history of CHF (p<0.001), Age/RBCVOL: (p=0.001), hypertension (p=0.004), CPB time (p=0.003), and previous stroke (p=0.03). The ratio of age divided by the RBCVOL (blood volume multiplied by hematocrit) was an important risk factor for both increased LOS and serious postoperative morbidity. Interestingly, variables that were significant independent predictors of increased mortality such as, preoperative shock, previous open heart operation, renal failure, ejection fraction less than 20%, and MI within 6 hours of operation, were not risk factors for either serious morbidity or increased LOS. Using the variables and relative risk values identified in this analysis, it is possible to develop a scoring system that assigns morbidity risk scores to patients before operation.

Conclusions: We conclude that: 1) hospital length-of-stay is a continuous variable that correlates with postoperative morbidity but not with mortality, 2) advanced age and low red blood cell volume are very important risk factors for serious postoperative morbidity and increased LOS, and 3) risk factors for postoperative morbidity are different than those for postoperative mortality. These results suggest that older patients with preoperative anemia and low blood volume, who also have other co-morbidities (CHF, stroke, COPD or hypertension), are at increased risk for postoperative complications. These studies allow identification of a high-risk cohort of patients who are likely candidates for interventions to lessen postoperative morbidity.

*By invitation


26. IS BODY SIZE THE CAUSE FOR POOR OUTCOMES OF BYPASS SURGERY IN FEMALES?

George T. Christakis, M.D., Karen Buth, M.Sc.*, Richard D. Weisel, M.D., Vivek Rao, M.D.*, Kostas P. Panagiotopoulos, B.Sc.*, Joan Ivanov, R.N.* and Stephen E. Fremes, M.D.,

Toronto, Ontario, Canada

Females have a higher incidence of operative mortality (OM), low output syndrome (LOS), myocardial infarction (MI), postoperative bleeding (BLD), and infection (INF) than males (M) following CABG. The poor outcomes have been attributed to the smaller size of females and (by extension) to smaller coronary diameter. In order to assess risk factor differences between males and females, and the influence of body size on postoperative outcome, data were gathered prospectively on 7,025 patients (M=5,694, F=l,331) proceeding to isolated CABG between January 1990 and June 1994. Univariate and multivariate statistics were used to determine risk factors for CABG in M and F separately. Body size was assessed by both body mass index (BMI) and body surface area (BSA).

%

OM

%

LOS

%

MI

%

BLD

%

INF

BMI

(kg/m2)

"pts"

M

F

M

F

M

F

M

F

M

F

<20

125

3.5

7.5

13.0‡

20.0

3.5

5.1

3.5‡

2.5

2.3‡

15.0

20-25

1700

2.5

3.8

8.0

15.7*

3.2

5.8*

2.2

2.0

2.3

3.5

25-30

3169

1.8

3.9*

6.3

14.3*

2.8

5.5*

1.3

2.4*

3.5

5.1

>30

2031

1.6

3.1*

5.1

12.1*

2.8

5.3*

1.0

2.4

6.3

9.9*

*=M diff than F p<0.05 ‡=<20 diff than >30, p<0.05 for M

Small body size (BMI<20) resulted in increased morbidity postoperatively for both sexes. However, within each classification of body size females continued to have a higher morbidity and mortality. In patients with heights less than 164 cm, the incidence of OM (M=2.2%, F=3.7%) and LOS (M=7.9%, F=14.2%) was higher (p<0.05) for females. In patients with BSA<1.7 m2, the incidence of OM (M=3.8%, F=3.8%) and LOS (M=l 1.4%, F=15%) were similar for both sexes. BSA<1.7m2 accounted for 47% of F but only 8% of M. For patients with BSA>1.7m2, OM (M=1.7%, F=3.8%) and LOS (M=6.3%, F=14%) were higher (p<0.0001) in females. The multivariate risk factors (odds ratios) for OM in M were: age>70 (2.7), LVEF<40% (2.6), diabetes mellitus (DM) (1.6), peripheral vascular disease (PVD) (2.3), smoking (1.9), renal failure (2.5), preoperative MI (PMI) (2.0) and for F the predictors were: age>70 (2.0), urgent surgery (US) (2.5), LVEF<40% (3.2), PVD (2.8). The predictors of LOS in M were: age>70 (1.6), LVEF<40% (2.2), reoperative surgery (REDO) (5.6), left main stenosis (LMS) (1.3), endarterectomy (EA) (1.8), DM (1.6), congestive failure (2.1), PMI (2.0). LOS predictors for F were: US (1.6), LVEF<40% (2.5), LMS (1.7), REDO (4.2), EA (3.2).

CONCLUSION: Risk factors for OM and LOS were similar for males and females. Small body size increases morbidity following isolated CABG. Independent of body size, females still have a higher operative mortality and morbidity. Increased risk of surgery for F may be due to differences in atherogenesis.

4:35 pm EXECUTIVE SESSION (Limited to Members)

Republic Ballroom, Sheraton Boston Hotel

6:30 pm MEMBER RECEPTION

Museum of Fine Arts

*By invitation


1:45 pm SIMULTANEOUS SCIENTIFIC SESSION B GENERAL THORACIC SURGERY

Republic Ballroom, Sheraton Boston Hotel

Moderators: J. Kent Trinkle, M.D.

Valerie W. Rusch, M.D.

27. MUTATION IN THE P53 TUMOR SUPPRESSOR GENE IN BARRETT'S ESOPHAGUS IS A MARKER FOR DEVELOPMENT OF ADENOCARCINOMA: RESULTS OF AN INTERNATIONAL MULTI-INSTITUTIONAL PROSPECTIVE STUDY

Paul M. Schneider, M.D.*, Alan G. Casson, M.D.*, Harinder S. Garewal, M.D.*, Bernard Levin, M.D.*, A.H. Hoelscher, M.D.*, J. Rudinger Stewart, M.D.* and Jack A. Roth, M.D.

Munich, Germany, Toronto, Ontario, Canada,

Houston, Texas and Tucson, Arizona

Current histologic criteria are not adequate to predict which patients with Barrett's esophagus (BE) are at high risk of developing invasive cancer and thus are candidates for esophagectomy. The purpose of this study was to determine the value of p53 mutation in BE as a marker for the development of adenocarcinoma. The p53 gene, a tumor suppressor gene whose function is critical to cell cycle control and DNA repair, is the most commonly mutated gene in human cancers. We had previously identified p53 mutations in BE and therefore began a multi-institutional study to determine their significance as a marker for malignancy. Ninety-seven patients from four institutions were studied. Forty-seven (37 males and 10 females, mean age 55) had BE with metaplasia or dysplasia but no evidence of malignancy at a mean follow-up of 2.2 ± 0.2 years. The BE was classified as metaplasia in 30, low-grade dysplasia in 12, and high-grade dysplasia in 5. The other 50 patients (46 males and four females, mean age 63) had adenocarcinoma arising in BE (BC). Tissue for DNA analysis, including normal stomach or esophagus, tumor, and BE, was obtained by endoscopic biopsy in patients with BE or BC or during surgery in some patients with BC. Exons 5-9 of the p53 gene were studied for mutations by single-strand conformational polymorphism analysis (SSCP) after polymerase chain reactions. Mutations detected by SSCP were confirmed by direct DNA sequencing. None of the tissue samples from patients with BE alone with metaplasia or low-grade dysplasia had a p53 mutation, and only one of five patients with high-grade dysplasia but no evidence of invasive malignancy had a p53 mutation. However, 23 of the BC patients (46%) had a p53 mutation in Barrett's epithelium, tumor, or both. Twenty of these had a p53 mutation in the tumor only (N=16) or in both (N=4), suggesting a direct role for the mutation in carcinogenesis. In the other three, a mutation was present in the Barrett's epithelium but not the tumor, suggesting that p53 mutation may be a marker for genetic instability predisposing to tumor formation. Biopsies of BE were classified as metaplasia or low-grade dysplasia for 16 patients with a p53 mutation and cancer, indicating that p53 mutation is associated with cancer regardless of the degree of clinically detectable dysplasia. We conclude that mutation in the p53 gene identifies a subset of BE patients at increased risk for developing cancer.

*By invitation


28. ERYTHROMYCIN STIMULATES GASTRIC EMPTYING STATUS POST-ESOPHAGECTOMY: A RANDOMIZED CLINICAL TRIAL

Michael Burt, M.D., Ph.D., William Williard, M.D.*, Andrew Scott, M.D.*, Samuel Yeh, M.D.*, Manjit Bains, M.D., Allan Turnbull, M.D.*, Joseph Former, M.D.*, Patricia McCormack, M.D. and Robert Ginsberg, M.D.

New York, New York

Delayed gastric emptying following esophagogastrectomy can pose a significant early post-operative problem. Since erythromycin, which stimulates the gastric antral and duodenal motilin receptor, has been demonstrated to significantly increase gastric emptying in patients with diabetic gastroparesis, we decided to evaluate its effect on gastric emptying after esophagogastrectomy.

Methods: 24 patients (age: 41-79 yr, median 66; 18 men/6 women) were randomized to receive either erythromycin lactobionate (200 mg in 50ml NSIV, n=13) or placebo (50 ml NS IV, n=11) eleven days after esophagogastrectomy (with pyloric drainage procedure). After infusing erythromycin or placebo over 15 min, patients ate a solid meal (scrambled egg with bread) labelled with [99mTc] sulfur colloid (500 |aCi) over approximately 15 min. Dynamic images of the post-surgical stomach were then acquired over 90 min in the supine position by gamma counter. Results were expressed as percentage of counts retained in the stomach (% gastric retention) over time.

Results: There were no side effects of eryhromycin. The figure displays the gastric emptying over time for both groups.

Analysis of covariance demonstrated that the rate of gastric emptying (slope of the line) was significantly greater in the erythromycin treated group compared to the placebo group (p<0.0001).

Conclusion: Early satiety following esophagogastrectomy is secondary to decreased gastric motility and not secondary to a decrease in the gastric reservoir. Intravenous erythromycin significantly improves gastric emptying in patients following esophagogastrectomy by stimulating gastric motility.

*By invitation


29. THE ROLE OF FUNDOPLICATION IN THE TREATMENT OF TYPE II PARAESOPHAGEAL HERNIA

Clark B. Fuller, M.D.*, Jeffrey H. Peters, M.D.*, Manfred Ritter, M.D.*, Cedric G. Bremner, M.D.* and Tom R. DeMeester, M.D.

Los Angeles, California

The role of fundoplication in patients with pure Type II paraesophageal hiatal hernia remains controversial. Conventional thinking suggests that because the lower esophageal sphincter (LES) is located within the abdomen, it is competent, and fundoplication unnecessary. Few studies have used objective evaluation to guide the addition of an antireflux procedure.

Patients and Methods: Sixteen consecutive patients with Type II paraesophageal hernia were treated from May 1991 to July 1994. All demonstrated radiographic criteria of pure Type II hernias. Evaluation before surgery included upper endoscopy, esophageal manometry, and 24-hour ambulatory pH monitoring. The lower esophageal sphincter was considered incompetent if any of the following criteria were present; a resting pressure <6 mmHg, abdominal length <1 cm or total length <2 cm. Primary symptoms responsible for surgery were related to the hernia in 81% of patients postprandial pain (n=7), abdominal distension (n=5), vomiting (n=1), and anemia (n=0). Symptoms typical of gastroesophageal reflux disease were noted in 3 patients heartburn in 2 and regurgitation in 1.

Results: Objective evidence of gastroesophageal reflux disease was present in the majority of patients. Five patients (31%) had evidence of esophageal mucosal injury: esophagitis in 3, stricture and esophageal ulceration in 1 patient each. Eleven of 15 patients (69%) were found to have pathologic esophageal acid exposure on 24-hour pH monitoring. Twelve (75%) patients had a defective LES usually secondary to an inadequate intra-abdominal length (8/12, 66%). Hernia reduction, crural closure and Nissen fundoplication was performed in 14/16 patients (2 patients await definitive surgery). Symptomatic relief has been excellent/good in all patients. No patients has developed hernia recurrence at an average follow-up of 8.8 months (range 2-28 months).

Conclusion: Objective evaluation reveals that gastroesophageal reflux accompanies type II paraesophageal hernia in a high proportion of patients, usually secondary to an incompetent LES. Appropriate treatment includes reduction of the hernia, crural closure and fundoplication in most if not all patients.

2:45 pm INTERMISSION - VISIT EXHIBITS

*By invitation


3:15 pm SIMULTANEOUS SCIENTIFIC SESSION B GENERAL THORACIC SURGERY

Republic Ballroom, Sheraton Boston Hotel

Moderators: J. Kent Trinkle, M.D.

Valerie W. Rusch, M.D.

30. OBJECTIVE ASSESSMENT OF GASTROESOPHAGEAL REFLUX AFTER SHORT ESOPHAGOMYOTOMY FOR ACHALASIA USING MANOMETRY AND PH MONITORING

John M. Streitz, Jr., M.D.*, F. Henry Ellis, Jr., M.D., Ph.D., Warren A. Williamson, M.D.*, Michael E. Glick, M.D.*, Johannes A. Aas, M.D.* and Robert L. Tilden, Dr.P.H.*

Duluth, Minnesota and Burlington, Massachusetts

The role of an antireflux procedure as an adjunct to esophagomyotomy for achalasia remains controversial. In our experience, a short myotomy alone is followed by a low incidence of severe reflux symptoms (4-5%). However, little objective documentation exists of this operation's effect upon sphincteric competence and the degree of postoperative gastroesophageal reflux. This report provides such documentation.

We performed esophageal manometry and 24 hour pH monitoring on 14 patients with esophageal achalasia who had previously undergone a short esophagomyotomy without antireflux procedure by us. Eight of the 14 were tested to evaluate the postoperative symptom of heartburn, and the remaining six asymptomatic patients were studied to assess postoperative sphincteric function.

Esophagomyotomy reduced lower esophageal sphincter (LES) pressure by 12 to 71% (mean 41%) from a preoperative mean of 27 mmHg to 14 mmHg postoperatively. The number of postoperative acid reflux episodes per patient in 24 hours was below 29 (normal <47) in 12 patients, with a median of 12 episodes for the entire group. Esophageal acid exposure, measured as % total time with pH <4.0 (normal <4.5%), was below 4.5% in 9 patients, 6 of whom had values less than 1%. Of the five patients with values greater than 4.5%, a temporal correlation of symptoms with an episode of acid reflux occurred in only one. Multivariate analysis showed that esophageal acid exposure time correlated only with the level of residual LES pressure during the relaxation phase of deglutition. A pressure less than 8 mmHg was predictive of normal acid contact time (p<.018). Age greater than 42 was a covariant and predictive of normal acid exposure by predicting low residual pressure (p<.001), irrespective of follow-up duration. Mean LES pressure, percent reduction in LES amplitude, postoperative vector volume and length of the LES did not significantly correlate with amount of esophageal acid exposure.

We conclude that a short esophagomyotomy without an antireflux procedure results in a competent LES in most patients, and that symptomatic gastro-esophageal reflux is unusual. Increased esophageal acid exposure, when it occurs, is due to slow esophageal acid clearance of relatively few reflux episodes, not from too extensive a myotomy, and is more likely to occur when the myotomy results in a high residual pressure during deglutition, a finding more common in young patients. In view of these findings, the addition of an antireflux procedure to a short esophagomyotomy would not be expected to improve results.

*By invitation


31. COMBINED THORACOSCOPIC AND LAPAROSCOPIC LYMPH NODE STAGING IN ESOPHAGEAL CANCER: THE UNIVERSITY OF MARYLAND EXPERIENCE

Mark J. Krasna, M.D.*, John L. Flowers, M.D.*, Safuh Attar, M.D. and Joseph S. McLaughlin, M.D.

Baltimore, Maryland

Unlike mediastinoscopy in lung cancer, there exists no standard minimally invasive test to stage esophageal cancer. If it were possible to obtain exact preoperative staging in esophageal cancer, patients could be separated prospectively to receive adjuvant therapy appropriately. We studied the feasibility and efficacy of thoracoscopic lymph node staging (TSLN) and laparoscopic lymph node staging (LSLN) in esophageal cancer. TSLN was performed in 45 patients with biopsy proven carcinoma of the esophagus. LSLN was done in the last 19 pts (after missing celiac LN in 3 pts). TSLN was aborted in 3 pts due to adhesions. LN stage was NO in 39 pts, N1 in 3 and N3 (celiac LN) in 6 patients. Esophageal resection was performed in 30 patients after TSLN; 17 of these underwent LSLN. These patients form the basis for subsequent data analysis.

TSLN staging showed NO lymph node status in 28 patients and N1 in 2 patients. Two of the 28 NO patients (7%) were found at resection to have para-esophageal lymph node involvement (N1) and were thus understaged by TSLN. One patient with Nl disease at thoracoscopy had no lymph node involvement (NO) after esophagectomy. The other patient remained N1 at the time of resection. Thus TSLN was accurate in detecting the presence of thoracic LN in 28/30 cases (93% accuracy).

LSLN staging found NO disease in 12 pts and N3 in 5 pts. After esophagectomy, final pathology of the 12 NO patients was NO in 11 and N3 in one patient. LSLN missed one pt with N3 disease. Final pathologic staging of the 5 N3 patients revealed N3 status in 2 patients and NO status in 3 patients. Thus, LSLN was accurate in detecting lymph node metastases in 16/17 patients (94%).

TSLN/LSLN staging are more accurate than existing staging methods. 6/18 LSLN pts had unsuspected celiac axis LN involvement missed by standard noninvasive techniques. 3% of thoracic LN and 17% of celiac LN were downstaged after preoperative chemo/radiotherapy. LN near the diagphragmatic hiatus may be difficult to sample without extensive dissection. The role of TSLN/LSLN in staging esophageal cancer should be further evaluated in a multi-institutional trial.

*By invitation


32. CATASTROPHIC COMPLICATIONS ASSOCIATED WITH CERVICAL ESOPHAGOGASTRIC ANASTOMOSIS

Mark D. Iannettoni, M.D.*, Richard I. Whyte, M.D.* and Mark B. Orringer, M.D.

Ann Arbor, Michigan

Recent enthusiasm for the cervical esophagogastric anastomosis (CEGA) has arisen because of its perceived low morbidity. While catastrophic complications of a CEGA are unusual, they can and do occur, and prevention is possible if the potential for them is recognized. In 866 patients undergoing a CEGA after transhiatal esophagectomy, catastrophic complications associated with anastomotic disruption have occured in 12 patients (1.4%): vertebral body osteomyelitis (1); epidural abscess with neurologic impairment (2); pulmonary microabscesses from internal jugular vein abscess (1); tracheogastric fistula (1); and major dehiscence requiring anastomotic takedown (7). These complications became manifest from 8 to 85 days after the esophageal resection and reconstruction (mean 23 days). Leakage from a suspension stitch placed in the anterior spinal ligament over the vertebral bodies resulted in a posterior gastric leak and either osteomyelitis or an epidural abscess in three patients, none of whom had evidence of extravasation on their routine 10 day postoperative barium swallow. Cervical exploration for a presumed anastomotic leak lead to the unexpected discovery of an abscess formed by the stomach and the adjacent wall of the internal jugular vein which was ligated and resected. One asymptomatic patient who was discharged with a contained anastomotic leak on his postoperative barium swallow was readmitted 7 days later with a cervical tracheogastric fistula from which he ultimately died. In 7 patients, 9% of all who have experienced anastomotic leaks, there was sufficient gastric ischemia and/or necrosis to require takedown of the anastomosis and intrathoracic stomach with a plan for later reconstruction. As a result of this experience, it is recommended that cervical gastric suspension sutures either be omitted entirely or placed in the fascia over the longus coli muscles anterior to the spine but not directly into the prevertebral fascia overlying the vertebral bodies or cervival discs. All cervical anastomotic leaks, even if apparently contained, are best drained rather then treated expectantly. Patients who remain febrile and ill after bedside drainage of a leak should undergo cervical reexploration in the operating room; major gastric ischemia and/or necrosis may warrant takedown of the anastomosis and intrathoracic stomach. Refinement of any operation frequently evolves from complications associated with previous experience. With an awareness of their possibility and with minor technical modifications, the incidence of these catastrophic complications and their morbidity can be reduced.

*By invitation


33. DELAYED PRIMARY REPAIR OF ESOPHAGEAL PERFORATION: IS IT SAFE?

Nan Wang, M.D.*, Ali Safavi, M.D.*, Anees J. Razzouk, M.D.*, Karen Gan, M.D.*, Arthur C. Hill, M.D.*, Bryan Fandrich, M.D.*, Michael J. Wood, M.D.*, Edwin E. Vyhmeister, M.D.*, Changwoo Ahn, M.D.* and Steven R. Gundry, M.D.

Loma Linda and Fontana, California

The management of esophageal perforation with delayed diagnosis (>24 hrs) is controversial. Because of the obvious advantages of primary repair as a simple single-stage operation, this technique was preferentially used to treat 17 of 21 consecutive esophageal perforations. Patients were stratified into three groups according to the time elapsed between perforation and operation:

n

Age

Delay

Iatrogenic

Preop

(yrs)

(hrs)

Perforation

Sepsis

Grp A - <6 hrs

5

77 ± 12

5.2 ± 0.8

4 (80%)

0 (0%)

Grp B - <24 hrs

6

59 ± 12

13.8 ± 2.9

2 (33%)

2 (33%)

Grp C - >24 hrs

6

62 ± 12

46.0 ± 12.8

3 (50%)

3 (50%)

In addition to primary repair in these pts, additional coverage of the sutured site was performed using a fundic wrap in 7 pts (41%), pericardial fat in 2 pts (12%), diaphragmatic flap in 2 pts (12%), pleural patch in 1 pt (6%), and intercostal pedicle in 1 pt (6%). Results:

n

Leaks

Sepsis

MOF

Mortality

Grp A

5

0 (0%)*

2 (40%)

0 (0%)

1 (20%)

Grp B

6

4 (67%)

4 (67%)

1 (17%)

1 (17%)

Grp C

6

4 (67%)

5 (83%)

2 (33%)

1 (17%)

*p<0.03

In Group C, the only death occurred in a profoundly septic pt whose diagnosis was delayed by more than 2 weeks. Esophageal continuity was maintained in all of the 14 (82%) survivors. We conclude that in the era of advanced intensive-care capabilities, delayed primary repair of esophageal perforation in the properly selected pt can lead to a satisfactory outcome. Although an esophageal leak is common unless immediate repair of the perforation is performed, the leak does not necessarily lead to an adverse outcome.

4:35 pm EXECUTIVE SESSION (Limited to Members)

Republic Ballroom, Sheraton Boston Hotel

6:30 pm MEMBER RECEPTION

Museum of Fine Arts

*By invitation


1:45 pm SIMULTANEOUS SCIENTIFIC SESSION C CONGENITAL HEART DISEASE

Independence Ballroom, Sheraton Boston Hotel

Moderators: Richard A. Hopkins, M.D.

Richard A. Jonas, M.D.

34. APPLICATION OF COMPUTATIONAL FLUID

DYNAMICS TO THE STUDY OF COMPETITIVE FLOWS IN CAVOPULMONARY CONNECTIONS

‡Marc Roger de Leval, M.D., FRCS, Gabriele Dubini, Ph.D.*, Francesco Migliavacca, Ph.D.*, Homayoun Jalali, M.D.*, Riccardo Pietrabissa, Ph.D.* and Andrew Redington, M.D.*

London, England

Computational fluid dynamics (CFD) based on a finite element method were applied to the study of (i) competition of inferior (IVC) and superior vena caval flows (SVC) in the total cavopulmonary connection (TCPC) and (ii) competition between SVC flow and forward flow from a stenosed pulmonary artery (PA) in the bidirectional cavopulmonary anastomosis (BCPA). 3-D parametric models of the connections were created from angiocardiograms and the fluid dynamics (pressure and velocity) were computed by a fluid dynamic computational code.

1. TCPC: 12 models corresponding to various degrees of offsetting and shape of the IVC-PA anastomosis were simulated to evaluate energy dissipation and flow distribution between the two lungs. A minimal energy loss was found with an offset value close to zero and the enlargement of the IVC anastomosis towards the right PA was shown to divert more IVC flow to the right lung, thus distributing more caval flow to the bigger lung (QLPA/QRPA = 0.75).

2. BCPA: The wisdom of leaving forward flow from a stenosed PA while constructing a BCPA remains controversial. 98 such operations were performed between January 1988 and September 1994. Nine patients (9%) had postoperative SVC hypertension (18 mmHg or more), of whom five were reoperated. A computational model of the operation was developed in an attempt to predict postoperative haemodynamics. In tight PA stenosis (75% or more) the non-pulsatile forward QP is primarily directed to the LPA with little influence on the SVC pressure. A pulsatile forward flow through the PA corresponding to 15, 30, 50 and 75% of the systemic cardiac output increases the mean PA and SVC pressure respectively by 1.0, 1.7, 2.4 and 3.6 mmHg.

Inferences:

1. CFD has been applied clinically to refine the design of the TCPC. A small triangular patch is now placed on the right lateral aspect of the IVC pathway to reduce energy loss and achieve a more physiological distribution of flow between the two lungs.

2. In BCPA it is safe to maintain forward flow so as to have an overall systemic to pulmonary flow ratio of 1, thus improving the systemic arterial saturation without excessive SVC hypertension.

‡1973-74 Graham Fellow

*By invitation


35. ATRIAL FLUTTER INDUCED BY LATERAL TUNNEL CONSTRUCTION IN THE MODIFIED FONT AN OPERATION

Mark D. Rodefeld, M.D.*, Hurt I. Bromberg, M.D.*, Charles B. Huddleston, M.D.*, Richard B. Schuessler, Ph.D.*, John P. Boineau, M.D.* and James L. Cox, M.D.

St. Louis, Missouri

The cavopulmonary connection, or modified Fontan operation, utilizes a lateral tunnel through the right atrium. Intra-atrial reentry or atrial flutter (AFL) is a relatively common post-operative problem. We postulate that the lateral tunnel suture line establishes the anatomic substrate for AFL in these patients. The purposes of this study were 1) to determine if the lateral tunnel suture line alone is sufficient to permit initiation of AFL and 2) to map any resultant arrhythmias.

After induction of general anesthesia, 30-35 kg canines (n=6) underwent median sternotomy, cradling of the pericardium, and placement of a pacing electrode on the right atrial appendage. Normothermic cardiopulmonary bypass was initiated. Through a right atriotomy, a sham modified Fontan operation was performed. A suture line (no baffle) was placed beginning at the fossa ovalis, around the IVC, up the crista terminalis, around the SVC, and back to the fossa ovalis, simulating lateral tunnel construction. After closure of the atriotomy, bi-atrial 256 point form-fitting endocardia! electrodes were transannularly positioned in the atria via bilateral ventriculotomies. Atrial burst pacing and programmed extrastimulation were performed before and after placement of the lateral tunnel suture line.

AFL was non-inducible in 6/6 dogs prior to suture line placement. After suture line placement, sustained AFL was repeatedly inducible in all cases (100%), although in one case isoproterenol was required. The mean flutter cycle length was 196±77 msec. Activation sequence mapping revealed that the suture line was integral to the AFL pathway in all cases (100%). In each case, the AFL circuit revolved in the right atrium where slow conduction and unidirectional block occurred at the suture line. In no instance did the flutter pathway revolve around the atriotomy site alone.

We conclude that the baffle suture line used in the modified Fontan operation, without any alteration in circulatory physiology, is sufficient to create the substrate for AFL. A more complete understanding of the reentrant circuit may permit use of prophylactic measures such as incisional modification or placement of cryolesions that create bi-directional block, thereby inhibiting AFL in patients undergoing the modified Fontan operation.

*By invitation


36. STAGED OPERATION TO FONT AN INCREASES THE INCIDENCE OF SINO-ATRIAL NODE DYSFUNCTION

Peter B. Manning, M.D.*, John E. Mayer, Jr., M.D., Gil Wernovsky, M.D.*, Steven B. Fishberger, M.D.* and Edward P. Walsh, M.D.*

Kansas City, Missouri and Boston, Massachusetts

Morbidity and mortality of total cavo-pulmonary connection (modified Fontan procedure) is decreased in many high-risk single ventricle patients by performing the operations in a staged fashion. Some have advocated routine use of the bidirectional Glenn or "hemi-Fontan" procedure in all patients with single ventricle physiology. Each operative intervention, however, exposes the sino-atrial (SA) node region to risk of injury. A multi-stage approach may increase the risk of SA node dysfunction in patients that may not tolerate such a dysrhythmia or atrio-ventricular dysynchrony.

All patients completing a Fontan procedure between January 1988 and December 1992 were reviewed. Of 324 total patients, 227 completed the Fontan in a single operation, and 97 followed a two-stage approach. The mean age at Fontan completion was not different between groups (5.3 vs 4.6 yrs, p=.21). Overall survival was the same for both groups (91%).

The incidence of transient and fixed SA node dysfunction was similar for both groups following the first operative intervention despite a heterogeneous patient population (1 stage: 14%/7%, 2 stage: 12%/3%, p=28). Second operative intervention resulted in a higher incidence of dysrhythmia (transient: 29%, fixed: 23%), and more frequent SA node dysfunction on follow-up (1 stage: 11%, 2 stage: 46%, p<.002). In the two-stage group, 49% of patients without arrhythmia following first intervention experienced an arrhythmia after the second intervention, while of those with an arrhythmia following first operation, 67% experienced one at second intervention (p<.01). Despite these findings, most patients with SA node dysfunction tolerated it well clinically, with few patients requiring permanent pacing for atrial arrhythmias (1 stage: 3%, 2 stage: 7%, p=18).

In conclusion, a multi-staged operative pathway to Fontan reconstruction is associated with a higher early risk of SA node dysfunction. Longer follow-up is needed to assess the full impact of this finding. The possibility of this complication must be weighed carefully against factors increasing the risk of a single-staged approach.

2:45 pm INTERMISSION - VISIT EXHIBITS

*By invitation


3:15 pm SIMULTANEOUS SCIENTIFIC SESSION C CONGENITAL HEART DISEASE

Independence Ballroom, Sheraton Boston Hotel

Moderators: Richard A. Hopkins, M.D.

Richard A. Jonas, M.D.

37. CLINICAL EXPERIENCE WITH REPAIR OF

CONGENITAL HEART DEFECTS USING ADJUNCTIVE ENDOVASCULAR DEVICES

John G. Coles, M.D., Jeanne M. Lukanich, M.D.*, Jean Perron, M.D.*, Greg J. Wilson, M.D.*, Marlene Rabinovitch, M.D.*, David G. Nykanen, M.D.*, Lee N. Benson, M.D.*, Ivan M. Rebeyka, M.D.*, George A. Trusler, M.D., Robert M. Freedom, M.D.* and William G. Williams, M.D.

Toronto, Ontario, Canada

The use of intravascular devices as an adjunct in the repair of congenital heart anomalies represents a novel but unproven therapeutic approach. Intra-operative occlusion of an apical muscular ventricular septal defect (VSD) using a clamshell device from the right atrial approach was accomplished in 4 patients. One patient died following associated aortic arch reconstruction as a result of a hypoplastic left ventricle (LV). The results in the remaining 3 patients were favourable based on absence of late residual shunting, LV dysfunction or arrhythmia. Intraoperative implantation of pulmonary arterial stent (5-15 mm expanded diameter) was performed in 15 patients (unilateral 8; bilateral 7) during repair of neonatal pulmonary atresia VSD (n=4), obstructed pulmonary arterial confluence following truncus repair (n=3), bidirectional cavopulmonary shunt (n=2), Fontan procedure (n=2), and miscellaneous pulmonary arterial stenoses (n=5). The endovascular stents were effective at achieving immediate patency in all patients. There were 2 early deaths. Early reoperation was required in each of the 3 survivors of neonatal stent implantation due to bilateral, obstructive neointimal hyperplasia at 3, 10 and 11 months postoperatively. Intraoperative stent implantation was used at the site of obstructed pulmonary venous drainage in 4 patients. Lethal recurrent intraluminal obstruction occurred in all 4 patients, evident histologically as smooth muscle cell proliferation and extracellular matrix deposition. This initial experience supports continued application of intraoperative deployment of endovascular devices for closure of muscular VSD's otherwise inaccessible from the right atrial approach, and for cases of pulmonary arterial obstruction within larger calibre pulmonary arteries. Recurrent obstruction due to a pro-liferative healing response appears to be an eventual certainty in currently designed small diameter endovascular stents.

*By invitation


38. MANAGEMENT OF TETRALOGY OF FALLOT WITH PULMONARY ATRESIA AND DIMINUTIVE PULMONARY ARTERIES

Francis D. Pagani, M.D, Ph.D.*, John P. Cheatham, M.D.*, Robert H. Beekman, III, M.D.*, Thomas R. Lloyd, M.D.*, Ralph S. Mosca, M.D.* and Edward L. Bove, M.D.

Ann Arbor, Michigan and Omaha, Nebraska

Since September 1991, 14 consecutive patients with tetralogy of Fallot, pulmonary atresia, and diminutive pulmonary arteries (PA) have undergone staged repair. All patients had multiple aortopulmonary collateral arteries and the ductus arteriosus was absent in 12. Mean size of the right and left PA's was 2.3±1.0 mm and 2.0±0.8 mm, respectively (range, 1-3 mm). Six patients (42%) have gone on to complete repair (CR). Age at initial procedure (BT shunt [1], direct aorta-PA anastomosis or conduit [3], RV-PA conduit [2]) was 6.0±7.7 months. The number of operative procedures to achieve CR was 3.3±1.6 per patient (range, 2-6). Post bypass RV/LV was 0.5±0.1. Most patients required one or more interventional catheterizations for balloon dilatation of peripheral stenoses and/or stents in addition to collateral embolization. Mean follow-up in this group was 7.4±8.4 months (range, 0.5 to 20.3 months) and was 100% complete. There were 2 late deaths secondary to neurological complications in one and following reoperation for RV to PA conduit stenosis in the other. Eight patients are awaiting further surgery. Age at initial procedure was 22.2±57.2 months and follow-up was 8.5±8.0 months. Initial palliative procedures included unifocalization (1), direct ascending aorta-PA anastomosis (3), RV to PA conduit (3), and transannular RV outflow patch (1). One patient has had 2 additional procedures (RV to PA conduit and unifocalization). Operative mortality was 25% (2 of 8 patients). Six of 8 patients are alive and awaiting further intervention or repair.

Of the total of 4 deaths in this series, 3 occurred in patients undergoing shunts or unifocalization as the initial procedure (3/5, 60%). Among these 5 patients, only 1 is alive with a CR. There was only 1 death among 9 patients (11%) receiving RV to PA conduits (5) or direct ascending aorto-PA anastomosis (4) as the intial operative procedure. Three of these 9 patients have gone on to complete repair with no deaths.

This experience suggests that CR is feasible even in patients with extremely diminutive PA's (<3 mm) and may be achieved by early (3-6 month) establishment of central PA flow by RV to PA conduit (PA's > 1.5 mm) or direct ascending aorta-PA anastomosis (PA's < 1.5 mm). Subsequent interventional catheterization and additional operative procedures as required for further PA stenoses and collateral embolization allow continued recruitment of central PA's and may obviate or minimize the need for unifocalization procedures.

*By invitation


39. PH-STAT COOLING IMPROVES CEREBRAL METABOLIC RECOVERY AFTER CIRCULATORY ARREST IN INFANTS WITH AORTOPULMONARY COLLATERALS

Paul M. Kirshbom, M.D.*, Lynne A. Skaryak, M.D.*, Louis R. DiBernardo, M.D.*, Frank H. Kern, M.D.*, William J. Greeley, M.D.*, J. William Gaynor, M.D.* and Ross M. Ungerleider, M.D.

Durham, North Carolina

The presence of aortopulmonary collateral arteries (APCA's) in infants with congenital heart disease has been associated with an increased incidence of neurologic injury following deep hypothermic circulatory arrest (DHCA). This may be due to a "steal" phenomenon resulting in inadequate cooling of the brain. This study was designed to examine the effects of different blood gas management strategies during cooling on cerebral blood flow (CBF) and metabolic recovery following DHCA in the presence of APCA's. PTFE shunts (4mm) were placed between the left subclavian and pulmonary arteries in twenty 1-month old piglets. Animals were randomized as follows:

Alpha-State (α -S)

pH-Stat (pH-S)

Control (shunts ligated)

C- α (n=5)

C-pH (n=5)

Shunt (shunts open)

S- α (n=5)

S-pH (n=5)

All animals were placed on CPB, cooled to a nasopharyngeal temperature of 18°C with either α-S or pH-S blood gas strategy, arrested for 90 minutes, and then rewarmed to 37°C. Global CBF (radioactive microspheres) and cerebral metabolic rate of oxygen consumption (CMRC>2) were measured: I) Warm on CPB, II) Cold on CPB before DHCA, and III) Warm on CPB post-DHCA.

CBF (ml/100gm/min±S.E.)

CMROj (ml O2/100gm/min±S.E.)

C-α

C-pH

S-α

S-pH

C-α

C-pH

S-α

S-pH

I

68 ± 6

65 ± 3

46 ± 4†

47 ± 2†

3.2 ± 0.2

3.2 ± 0.5

2.5 ± 0.2†

2.8 ± 0.4

II

22 ± 4

45 ± 12

12 ± 2†

16 ± 1

0.5 ± 0.1

0.6 ± 0.2

0.4 ± 0.1

0.4 ± 0.01

III

50 ± 5

41 ± 6

23 ± 4†

37 ± 4*

2.3 ± 0.2

2.0 ± 0.3

1.2 ± 0.2†

2.1 ± 0.2*

†p<0.05 vs C-α, * p<0.05 vs S-α

Conclusions: In the absence of APCA's (C-α and C-pH), a-stat and pH-stat cooling strategies provide equivalent cerebral protection. In the presence of APCA's (S-α and S-pH), CBF and CMRO2 recovery following DHCA are significantly decreased when compared to controls if a-stat cooling is employed. This effect is eliminated through the use of pH-stat cooling. In infants with APCA's which are not amenable to pre-operative embolization or intra-operative ligation, pH-stat cooling may reduce the likelihood of neurologic injury.

*By invitation


40. BYPASS EFFECTS OF DELAYED REWARMING ON CEREBRAL BLOOD FLOW IN INFANTS FOLLOWING TOTAL CIRCULATORY ARREST

Erie H. Austin, III, M.D.*, Rosendo A. Rodriguez, M.D.* and Steve M. Audenaert, M.D.*

Louisville, Kentucky

Sponsored by: Laman A. Gray, Jr., M.D., Louisville, Kentucky

Purpose: A possible mechanism of brain injury after TCA may be cerebral hypoperfusion, which results in an unbalanced flow/metabolism ratio. A single report (Astudillo et al. 1993) that a delay in rewarming modified the flow pattern of recovery suggested that cold reperfusion could improve this unbalanced ratio. Our purpose was to detect any possible beneficial effect.

Methods:Transcranial Doppler son