American Association for
Thoracic Surgery
65TH ANNUAL MEETING
Scientific Program
MONDAY MORNING, April 29, 1985
8:30 a.m. Business Session (Limited to Members)
8:45 a.m. Scientific Session - Grand Ballroom
1. Experiences with the Carpentier Techniques of
Mitral Valve Reconstruction in 89 Patients
FRANK C. SPENCER, STEPHEN B. COLVIN*
And O. WAYNE ISOM
New York, New York
During the past 4 years (May 1980-August 1984) 89
patients have had some type of Carpentier reconstruction performed for mitral
insufficiency. There were two hospital deaths, unrelated to the operative
technique. No late deaths or major thromboembolic episodes occurred. All
patients are clinically well. Doppler studies in 71 found no insufficiency in
60 patients, a trace in 10, and moderate insufficiency in one. Catheterization
performed one to three years after operation in 15 patients found no signs of
insufficiency. Valve replacement was later necessary in two patients for
unrelated infections (heroin addiction).
The basic
disease was rheumatic in 9, prolapse in 27, ruptured chordae and prolapse in
45, endocarditis in 2, coronary disease in 6. Two patients had severe annular
calcification. Annuloplasty alone was adequate in only 16. Fifty-one had
resection of two or more cm of mitral leaflet combined with annuloplasty. In 22
aortic lesions, chordae transposition or shortening was used.
The absence of
recurrent insufficiency fully supports the durability of the reconstructive
techniques. Multiple abnormalities were present in most patients, explaining
the limited role of annuloplasty alone. With present techniques of myocardial
preservation, probably the vast majority of non-rheumatic, non-calcified valves
can be repaired. A much wider use of these techniques is indicated.
*By Invitation
2. Late Thrombosis of the Tricuspid
Bjork-Shiley Tilting Disc Valve: Thrombolytic Treatment with Streptokinase
DEJAN BOSKOVIC*, IVO ELEZOVIC*
and DARINKA
BOSKOVIC*
Beograd, Yugoslavia
Sponsored by: W.
DUDLEY JOHNSON
Milwaukee, Wisconsin
The main
complication after implantation of tricuspid Bjork-Shiley tilting disc valve is
late thrombotic obstruction. Of 28 patients with tricuspid valve replacement
(12 MVR + TVR and 16 MVR + AYR + TVR) (mean follow-up of 4.7 years), six
(21.4%) developed thrombosis of tricuspid prosthesis, an incidence of 4.6 valve
thromboses per 100 patient years. Thrombosis occurred 46, 43, 33, 35, 78 and 88
months after operation.
Clinical
deterioration presented with signs of congestive heart failure. In all
patients, the click of the tricuspid prosthesis was not heard and new systolic
or diastolic murmurs were audible. The diagnosis was confirmed with
bi-dimensional echocardiography (immobile disc, diminished opening angle of the
disc).
Thrombolytic
therapy with Streptokinase was used in all six patients. Treatment consisted of
Streptokinase (initial loading dose of 250,000 IU then 150,000 IU/h) for 12
hours in two patients and 24 hours in four patients. Thrombolytic therapy was
always monitored with thrombin time.
Complete
regression of clinical, echocardiographic and radiological signs of thrombosis
was seen in all six patients during the first 24 hours of thrombolytic
treatment. There were no bleeding complications. In one patient, clinical signs
of mild pulmonary embolism occurred and were confirmed with chest radiography.
Follow-up
extends between 4-24 months, mean 13 months. In four patients, long-term
results are excellent: There have been no clinical, radiological, or
echocardiographic signs of thrombosis of tricuspid prosthesis.
Rethrombosis of tricuspid
prosthesis was observed in two patients four and seven months after initial
treatment with Streptokinase. Repeat thrombolytic treatment with Streptokinase
was performed with success in both patients.
Summary: Fibrinolytic
treatment with steptokinase seems to be treatment of choice for thombosis of
tricuspid Bjork-Shiley valve and should always be tried before reoperation.
*By Invitation
3. Experience with 110 Consecutive Patients
Undergoing Surgery for the Wolff-Parkinson-White Syndrome
JAMES L. COX, JOHN J. GALLAGHER*
and MICHAEL E. CAIN*
St. Louis, Missouri
and Charlotte, North Carolina
Between July 1,
1980 and October 1, 1984, 110 patients underwent surgery for correction of the
Wolff-Parkinson-White (WPW) syndrome by the senior author. There were 67 males
and 43 females with ages ranging from 9 months to 70 years (mean, 28 ± 6 yrs).
The major indications for surgery were medical refractoriness or drug
intolerance (79%) and previous cardiac arrest (13%). Associated abnormalities
included Ebstein's anomaly (8%), other arrhythmias (36%), coronary artery
disease (5%), cardiomyopathy (6%), and other congenital heart disease (24%).
Two patients had undergone WPW surgery previously at other institutions. Twenty
percent of patients had multiple (2-4) accessory pathways, a total of 138
pathways being present in the 110 patients. Distribution of the accessory
pathways was: 56% left free-wall, 24% posterior septal, 14% right free-wall,
and 6% anterior septal. The surgical technique employed previously for the WPW
syndrome was modified in August, 1981 to include: 1) 2.5 power optical
magnification, 2) exclusive use of the endocardia! approach under cardioplegic
arrest, 3) wider margins of surgical excision, 4) sharp dissection of the involved
valve annulus,
5) division of
only the ventricular insertion of the accessory pathway, and
6) internal
identification of the ventricular epicardial peel in all regions of dissection.
Using these modifications, 137 of 138 accessory pathways were divided
successfully in the 110 patients. In comparison to our initial 200 patients
previously reported, the modified surgical technique resulted in an increase in
the success rate from 86% to 99.3%, a decrease in the reoperation rate from
19.5% to 0%, and a decrease in the incidence of heart block from 10.5% to 0.9%.
The mortality rate was 5.5% in the entire series but only one death occurred
following elective surgery in the absence of associated cardiac anomalies. The
present surgical technique and attendant results suggest that surgery is the
conservative alternative to a lifetime of medical therapy in young, otherwise
healthy patients suffering from the WPW syndrome.
*By Invitation
4. Twelve Year Experience with Internal
Mammary Artery for Coronary Artery Bypass
HENDRICK B. BARNER,
JOHN W. STANDEVEN*
and JEFFRY REESE*
St. Louis, Missouri
From January
1972 to January 1984 1000 patients have had primary coronary reconstruction
with one or two (100 patients operated between 6/72 and 6/74) internal mammary
arteries (IMA). Patients having associated procedures such as valve replacement
or aneurysmectomy were excluded. Prior to 6/74, patients were not selected and
subsequently they were. Overall operative mortality was 1.3% but eight deaths
occurred in the 100 patients having bilateral IMA bypass and all but one death
occurred in the first 500 patients. Survival at five years is 89% and at 10
years 76%.
One or more
postoperative cardiac catheterizations have been done in 485 patients; 345 of
these were operated from 1972 through 1975 and 30% of them have had three
postoperative studies. Patency for IMA grafts at one year is 94%, at five years
90% and at 10 years 88%. Patency for saphenous vein grafts in these same
patients is 92% at one year, 81% at five years and 67% at 10 years. We have not
recognized progressive graft atherosclerosis leading to IMA closure.
Although the
durability of the IMA has been established this has not been firmly translated
into enhanced survival. The right IMA was usually placed to the right coronary
artery at the acute margin and did not bypass all disease so that follow up
angiograms frequently revealed a patient IMA into a distally diseased or
occluded vessel. More appropriate use of the right IMA is to the obtuse
marginal artery, usually as an in situ graft, or to the posterior descending
artery, usually as a free graft. It is hoped that use of bilateral IMA grafts,
with sequential grafting when appropriate, will be associated with enhanced
survival and a reduced need for reoperation.
10:00 a.m. Intermission - Visit Exhibits - Grand Salon
Complimentary Coffee
*By Invitation
10:45 a.m. Scientific
Session - Grand Ballroom
5. Electron
Microscopy in Selection of Patients with Small Cell Carcinoma of the Lung for
Medical Versus Surgical Therapy
J. DIRK IGLEHART*, WALTER G. WOLFE,
WALTER B. VERNON*, ROBIN T. VOLLMER*,
JOHN D. SHELBURNE* and DAVID C. SABISTON, JR.
Durham, North Carolina
Although most
patients with small cell carcinoma of the lung (SCCL) are currently managed by
a combination of chemotherapy and radiotherapy, controversy continues
concerning indications for surgical treatment. A study was conducted to
determine the role of electron microscopic sections (EM) in establishing a
pathological diagnosis in patients with SCCL. The EM findings were correlated
with the clinical pathological state and the prognosis. Forty-five patients
with a pulmonary lesion demonstrated on chest film were evaluated. Twenty
underwent thoracotomy and 12 had biopsy of a metastatic lesion. Light microscopy
(LM) of the tissue in each of these patients was reviewed independently. All EM
preparations were examined for features of squamous epithelial differentiation,
for features of adenocarcinoma, and for those which were classic for SCCL. A
postoperative "TNM" state was established and actuarial survival determined for
each group. When examined by EM, 26 (59%)of the neoplasms appeared to
be classical SCCL, whereas 19 (41%) displayed features of squamous
differentiation (15) or of adenocarcinoma (4). There was no relationship
between LM and EM characteristics. While the majority of patients with classic
SCCL by EM presented with inoperable disease and underwent biopsy of a
metastatic lesion, 14 of 19 patients with electron microscopic features of
squamous differentiation presented with operable disease and a curative
resection was possible in 9. The actuarial survival in patients with EM
features of squamous differentiation exceeded 25% at 5 years and was comparable
to figures for bona fide squamous carcinoma. In contrast, only one patient with
classic SCCL survived longer than 22 months. This study has identified a
special and sizable group of patients with SCCL who have a quite favorable
prognosis and cannot be distinguished by LM alone. In view of the markedly
improved results with surgical therapy in this group, preoperative anatomic
staging and selective surgical resection followed by EM examination is
recommended.
*By Invitation
6. Treatment of Bronchopleural Fistula After
Pneumonectomy
JOHN C. BALDWIN* and
JAMES B.D. MARK
Stanford, California
Disruption of the closure
of a mainstem bronchus after pneumonectomy is frequently a catastrophic
complication; those patients who survive frequently develop empyema and
bronchopleural fistula. Management of these fistulae remains a formidable
therapeutic challenge, which has been approached with a variety of surgical
techniques. We report our experience with anterior transpericardial closure of
bronchopleural fistulae, emphasizing the possibility of approaching either
mainstem bronchus and the efficacy of in-continuity ligation of the bronchus.
Three patients are presented, who developed
bronchopleural fistulae after pneumonectomy. The first patient had left
pneumonectomy for complicated tuberculosis; the second had right pneumonectomy
for neoplasm; and the third had right pneumonectomy for trauma. All patients
were approached surgically using median sternotomy and transpericardial
approach to the distal trachea, dividing the posterior pericardium between the
superior vena cava and aorta. Simple in-continuity staple closure of the
proximal mainstem bronchus was employed in all cases. All patients are
clinically well at 16, 12, and 2 months after surgery.
In
post-pneumonectomy bronchopleural fistula, the technique of anterior
transpericardial approach to bronchial ligation carries the advantages of the
well-tolerated median sternotomy incision, the avoidance of dealing directly
with a devascularized bronchial stump and areas of post-surgical scarring, the
avoidance of areas of chronic sepsis, and the avoidance of surgical deformity
of the chest wall with associated compromise in pulmonary function. Our
experience also indicates that either mainstem bronchus is accessbile using an
approach between the superior vena cava and aorta without division of either
pulmonary artery. In addition, since closure of a divided distal bronchial
stump would increase the risk of mediastinal sepsis and still leave a blind
stump, we propose that the procedure of in-continuity staple ligation is safer
and no less satisfactory from the theoretical viewpoint.
11:30 a.m. Presidential Address - Grand Ballroom
Observations On The Coronary Circulation
DAVID C. SABISTON
12:15 p.m. Adjourn for lunch
*By Invitation