WEDNESDAY MORNING, APRIL 20, 1988
6:45 a.m. SIMULTANEOUS BREAKFAST SESSIONS**
(See page 5 for further
information)
C) CARDIAC ASSIST DEVICES AND STRATEGIES
Larry W. Stephenson, M.D.,
Philadelphia, Pennsylvania
D) PRE-OPERATIVE CARDIOPULMONARY EVALUATION
Joel D. Cooper, M.D., Toronto,
Ontario, Canada
8:30 a.m. SCIENTIFIC SESSION - Ballroom
29. Experience
with the Gore-Tex Surgical Membrane for Pericardia! Closure in Congenital Heart
Surgery
JOSEPH J. AMATO,
JOSEPH V. COTRONEO*,
RALPH J. GALDIERI*,
JOSE R. ANTILLON*,
R. LEE VOGEL* and
THOMAS M. CONNOR*
Newark, New Jersey
From 1984 through September 1987, pericardial
closure in 88 patients (pts.) who underwent repair of congenital heart defects,
was completed with placement of the Gore-Tex (polytetrafluoroethylene) surgical
membrane. Review of these cases shows increased use of the membrane over the 3½
year (yrs) period, with 6 cases in 1984, 19 in 1985, 27 in 1986 and 34 cases in
the first 9 months of 1987. The average age was 3.17 yrs. with a range of 3.0
to 44.6 kg. The pts. were divided into groups; Group I - 32 pts. with simple
repairs (ventricular septal defects, atrial septal defects, partial canal
defects, pulmonary stenosis, and uncomplicated tetralogy of Fallot); Group II -
16 pts., complex repairs with conduits; Group III - 40 pts. with complex
repairs (Mustard, Jatene, Fontan procedures, total anomalous pulmonary venous
drainage, aortic stenosis).
Early results show that there were no
infections in any group and also no complications secondary to the Gore-Tex
membrane. No increase in pericardial drainage was found in any group when
compared to similar groups without the membrane. There were a total of 16
deaths (17.7%). Group I 1/32 (3%), Group II 6/16 (37.5%, and Group III 9/40
(22.5%). None of these deaths could be attributed to the placement of the
Gore-Tex membrane.
There were two late reoperations which tested the
usefulness of the membrane and in both, the findings were the same. There were
no adhesions between the chest wall and the membrane which had basically become
transparent. It was loosely attached to epicardium and easily removed except at
the periphery where sutures had been placed. On the epicardium was a thin layer
of collagenous fibrous tissue which did not interfere with the visualization of
the heart anatomy including the coronary vessels.
In the postoperative follow-up, there was no
difficulty in the M - mode or 2 - D echocardiographic examination of the heart.
When the Gore-Tex membrane was placed externally on the chest wall and then the
echo probe placed on top of the membrane, there was moderate blurring of the
finer details of the cardiac architecture. Clinically this was evaluated by
reviewing the 2 - D echocardiogram of all the post operative Mustard pts. with
the Gore-Tex membrane and comparing these with Mustard pts. with no membrane.
There was no difference in the clarity of the studies between the groups.
Conclusions are:
1. The
Gore-Tex surgical membrane can be safely used for pericardial closure.
2. Reoperation
shows no adhesions to the chest wall or epicardium and visualization of the
cardiac surface, especially the coronary vessels, is not obscured.
3. No
difficulty was encountered in the echocardiographic examination of the pts.
with the Gore-Tex membrane.
*By Invitation
**Admission will be by ticket only and will be limited.
Tickets must be obtained in the Registration Area of the Century Plaza Hotel
prior to 2:00 p.m. on Monday, April 18. There are no provisions for
pre-registration. Breakfast will be served until 7:00 a.m. only.
30. Prevention of Reperfusion Injury in the
Neonatal Heart Using Leukocyte-Depleted Blood
MICHAEL A. BREDA *,
DAVIS C. DRINKWA TER*.
HILLEL LAKS, ANTONIO
F. CORNO*,
HAKOB G. DAVTYAN*
and PAUL CHANG*
Los Angeles, California
Activated leukocytes release oxygen free
radicals and cause microvascular occlusion. This experiment tests the
hypothesis that reperfusion with leukocyte-depleted blood reduces injury
following extended ischemic preservation.
An in vitro model consisting of an
isolated, working neonatal piglet heart and an adult support pig was used.
Three groups were compared. Control hearts (n = 45), perfused with whole blood
without a period of preservation, developed a left ventricular stroke work
index (SWI) at a left atrial pressure of 9 mmHg of 1.29 ± 0.39 x 104
erg/g (Mean ± S.D.). In Groups 1 and 2, hearts were given crystalloid
cardioplegia, excised, and stored in 4°C saline for 12 hours. Group 1 (n = 8),
reperfused with whole blood, had a SWI of 0.031 ± 0.088 x 104 erg/g
(2.4% of control). Group 2 (n = 6), reperfused with blood rendered
leukocyte-depleted by a polyester filter, had a SWI of 1.16 ± 0.25 x 104
erg/g (89.9% of control). This difference was highly significant (p<0.0001).
Group 2 had normal ultrastructure on electron microscopy. Group 1 exhibited
severe injury with myofibrillar necrosis, mitochondria! disruption, nuclear
chromatin clumping, and moderate interstitial edema.
We conclude that reperfusion with
leukocyte-depleted blood prevents reperfusion injury and results in excellent
myocardial function after long-term heart preservation.
*By Invitation
31. End-To-Side and End-To-End Vascular
Anastomoses Using CO2 Laser
SEISUKE NAKA TA *,
CHARLES D. CAMPBELL,
RUTH PICK* and
ROBERT L. REPLOGLE
Chicago, Illinois
There are several theoretical advantages to
laser anastomoses. This study was designed to compare laser with conventional
suture anastomoses. 120 end-to-end (E-to-E) and 40 end-to-side (E-to-S) laser
anastomoses were performed on rabbit carotid arteries (2.0-3.0 mm). In each of
80 rabbits the divided left carotid artery was anastomosed using continuous
suture technique, and the right carotid was anastomosed using a CO2
laser. In each of other 40 rabbits both E-to-E laser and E-to-S laser
anastomosis were performed on a carotid artery. The laser technique involved
the placement of 3 stay sutures (E-to-E) or 4 stay sutures (E-to-S) of 7-0
polyplopylene and everting laser seal (65 mW, Ricoh Co. TC 3-C 100). The stay
sutures were placed slightly further from the vessel edges than the standard
suture technique. Examination of patency by angiography, tissue bonding
strength and scanning electron microscopy as well as standard histology of
laser anastomoses was carried out sequentially from one hour to one year.
The overall patency rate was 98% (78/80) in
E-to-E laser, 79% (63/80) in suture and 95% (38/40) in combined E-to-E and
E-to-S laser. No aneurysmal formation was observed in any group. Microscopic
findings in laser anastomoses demonstrated degeneration of collagen and protein
in the adventitia and media, but much less intimal injury as compared with
suture anastomoses. Reendothelialization began on day 3-7 and was completed by
day 14 in the laser groups in contrast to day 14 and 30, respectively, in the
suture group. The tissue bonding strength in laser was weaker at hour 1 as
compared with suture, but withstood the challenge of intraluminal pressure
loads of 350 mmHg.
Results indicate CO2 laser vascular
anastomosis results in substantially lesser intimal injury, allowing for rapid
early reendothelialization and excellent patency rate. Slight alterations of
laser technique produces consistent success of anastomosing this size of
vessels without aneurysmal formation. We will demonstrate the laser technique
for the anastomoses by videotape. This technique may improve healing and
patency in clinical aorto-coronary artery bypass operation.
*By Invitation
32. Metabolic Support of Remote Myocardium After
Acute Coronary Occlusion
FRIEDHELM
BEYERSDORF*, GERALD D. BUCK BERG,
and CHRISTOPHER
ACAR*
Los Angeles,
California
HYPOTHESIS: Metabolic support
of remote "non-ischemic" myocardium during acute infarction will reverse the
trend towards cardiogenic shock.
METHODS: Of 34 dogs undergoing LAD ligation
and 50% stenosis of the circumflex artery (Cx) (allowing 70 - 100% reactive
hyperemia), 20 developed irreversible ventricular fibrillation. The 14
survivors were followed for 6 hours measuring global and regional left
ventricular function (CI, SWI, ultrasonic crystals) and regional blood flow
(radioactive microspheres). After 2 hours 8 dogs received an intravenous
infusion of glutamate/aspartate, glucose, insulin, potassium and Coenzyme Q10
for 4 hours. Data are expressed as mean ± SEM; differences were considered
significant at the p < 0.05 level.
RESULTS: The substrate infusion for 4 hours caused
no change in regional or global cardiac function or coronary blood flow in 5
control dogs. The 6 untreated dogs developed cardiogenic shock (40% decrease in
CI, 50% decrease in SWI)* due to persistent dyskinesis in the LAD region (- 40%
systolic shortening [SS])* and hypocontractility in the Cx region (48% SS)*
despite normal transmural blood flow in the posterior wall of the left
ventricle (76 ml/100 g/min). In contrast, treated dogs recovered
hypercontractility in the circumflex segment (138% SS)* and raised SWI to
control levels (91%) without changing regional blood flow.
CONCLUSIONS: Cardiogenic shock after
myocardial infarction is due to impaired ability of "non-ischemic" myocardium to
maintain hypercontractility. This limitation can be prevented by metabolic
support of viable muscle with intravenous substrate infusion before the
definite treatment (e.g. CABG) is started. *p < 0.05)
9:10 a.m. Basic Science Lecturer
PHYSIOLOGY AND PATHOPHYSIOLOGY
OF ESOPHAGEAL PERISTALSIS
Raj K. Goyal, M.D., Boston,
Massachusetts
9:55 a.m. Intermission - Visit Exhibits
*By Invitation
10:25 a.m. Scientific Session - Ballroom
33. Coronary Angioplasty vs Coronary Bypass: Three
Year Follow-up of a Matched Series of 250 Patients
MARK S. HOCHBERG,
ISAAC GIELCHINSKY,
VICTOR PARSONNET,
SYED M. HUSSAIN*,
ERIC MIRSKY* and
DANIEL A. FISCH*
Newark, New Jersey
Two hundred fifty consecutive patients treated
for one or two vessel coronary artery disease with either balloon angioplasty
or surgical bypass were followed for three years to determine the comparative
long term effectiveness of each treatment. The 125 angioplasty patients were
matched with the 125 bypass patients so that both groups had a similar number
of patients with single or double vessel disease. The two groups did not
significantly differ in age, male:female ratio, NYHA Class, risk factors or
ejection fraction. The LVEDP was 11 ± 7 mmHg in the angioplasty group and 14 ±
9 mmHg in the surgical patients (p = 0.0046).
Angioplasty was deemed initially successful in 88%
(110/125), it failed in 10% (12/125) and in 2% (3/125) the lesion could not be
crossed. Emergency bypass was performed in 10% (12/125). Four of these 125
angioplasty patients (3%) died within 30 days. Coronary artery bypass grafting
was successfully performed on the matched set of surgical patients with 99%
(124/125) discharged well. There was one (1%, 1/125) surgical death. The
average hospital stay per patient was 4.8 ± 3.1 days for angioplasty and 12.1 ±
4.2 days for bypass.
Three year post procedure follow-up was
obtained on 96% (236) of the 245 patients discharged alive. A second
angioplasty was required in 18% and 11 angioplasty patients subsequently
required surgical bypass. Overall, 19% (23/121) of the angioplasty patients
ultimately required bypass. Four late deaths occurred in the angioplasty group,
bringing the early and late mortality to 7% (8/121). There were two late
surgical deaths bringing the combined surgical mortality to 2.5% (3/120), p =
0.1263.
The evaluation of symptoms revealed that 62%
(75/121) of the angioplasty patients are alive and in NYHA Class I or II three
years following one or two angioplasty procedures. This compares to 92%
(110/120) of surgical patients alive and in the same two NYHA Classes, (p =
0.0000).
*By Invitation
34. Late Results After Intracoronary Thrombolysis
and Early Bypass Surgery for Acute Myocardial Infarction
BRUNO J. MESSMER,
RAINER UEBIS*,
CHRISTOPH RIEGER*,
CARMINE MINALE*,
FERDINAND HOFSTADTER* and SVEN EFFERT*
Aachen, Federal
Republic of Germany
Treatment of acute myocardial infarct has
undergone major changes ever since thrombolytic therapy has proved to reduce
significantly early mortality in comparison to conventional therapy. Thrombolysis
results in reperfusion but does not alter the underlying arteriosclerotic
stenosis. Additional and more definite treatment is necessary. Between April
1980 and the end of 1985 we performed early (1-10 days) bypass surgery in 70
patients. Hospital mortality was 1.4%. During a follow-up period from two to
seven years (average 56 months) two cardiac and four non-cardiac deaths
occurred. Actuarial survival was 90% at seven years. Reoperation was necessary
in one patient. Postoperative angiocardiography was done in 50 patients (72%)
to assess left ventricular wall motion in the formerly ischemic area. Normal or
near normal wall motion was more often (68%) present when ischemia had been
below three hours. In patients with reperfusion after three hours more
persistent damage was recorded but complete recovery was still found in 45%.
Correlation between ischemic time interval and late wall motion score was only
0.35.
In 24 patients transmural needle biopsies for
electron microscopy studies had been taken from the formerly ischemic area at
the time of surgery. Similar to late wall motion the extent of necrosis did not
correlate with the ischemic time interval (r = 0.17) nor did the peak enzyme
level or total enzyme activity. A clear correlation was, however, present
between enzyme levels and the amount of necrosis within the biopsies (r = 0.76)
as well as between the amount of necrosis and late wall motion (r = 0.69) in
those patients who had intraoperative biopsy and late angiography.
It is concluded that early surgery after
successful thrombolysis yields excellent long-term results but more reliable
criteria for optimal aptient selection are mandatory.
*By Invitation
35. Six Months Postoperative Clinical and
Angiographic Assessment of 163 Consecutive Sequential Mammary Grafts
ROBERT DION*, ROBERT
VERHELST*,
MICHEL ROUSSEAU*,
MARTIN GOENEN*,
ROBERT PONLOT* and
CHARLES CHALANT*
Brussels, Belgium
Sponsored by: MARK
BRAIMBRIDGE, London, England
Between October 1985 and
March 1987, 163 consecutive sequential mammary grafts (SMG) were performed in
155 patients. Age averaged 61 years; 78% had a triple vessel disease; 69% had a
history of myocardial infarction (MI); ejection fraction was below 0.4 in 25%;
33% had unstable angina. There were 16 (9.7%) reoperations. The length of the
internal mammary artery (IMA) pedicle was the only limitation imponed on its
use, and complex IMA grafting was confronted to the whole spectrum of grafting
circumstances. No account was taken of the IMA free cut end flow. There were 8
free SMG, 16 triple SMG. Of the 340 sequential mammary anastomoses, 319 were
built with the left IMA; 83 (24.4%) were diamond-shaped anastomoses. The right
IMA was brought 27 times through the transverse sinus, 7 times for sequential
grafting of circumflex branches. Taking in account the adjunctive venous
anastomoses, and the single IMA anastomoses, there were 4.5 distal anastomoses
per patient, 2.4 being mammary anastomoses, 2.2 being sequential mammary
anastomoses. Extensive coronary endarterectomy could not be avoided in 22 cases
(14%): in 17 cases, the left IMA was implanted into a venous patch primarily
used to close the long arteriotomy. Additional procedures were valvular
replacements or repairs (2 aortic, 3 mitral), right coronary ostium patch
plastics (2), left main trunk plasty (1) and carotid endarterectomies (2).
Hospital mortality rate was 1.3%. Perioperative significant MI rate was 3.3%.
Follow-up averaged 15 months. 4 patients (2.5%) still experienced moderate
angina pectoris and 4 other patients complained of residual dyspnea. 93
patients (60%) underwent a maximal stress test combined to a thallium
scintigraphy at an average of 6 months post-operatively, with abnormal results
in respectively 6/3% and 5.8% of the cases. 108 patients (70%) consented to a
repeat catheterization at an average of 6 months after operation: 323 (95%)
sequential mammary anastomoses were still patent. The patency rate of the
diamond-shaped mammary anastomoses was 97%, that of the anastomoses
corresponding to the right IMA's brought through the transverse sinus was 95%.
As the attrition rate of the IMA grafts beyond 6 months postoperatively has
proved to be minimal, gratifying long-term results with systematic use of SMG
can be anticipated.
*By Invitation
36. Prospective Study of Adjuvant Surgery After
Chemotherapy for Limited Small Cell Lung Cancer
ROBERT J. GINSBERG,
FRANCES A. SHEPHERD*,
G. ALEXANDER
PATTERSON*, RONALD FELD* and
MARTIN E.
BLACKSTEIN*
Toronto, Ontario,
Canada
Seventy-two patients with central L-SCLC were
identified as candidates for adjuvant surgical resection (ASR) after remission
induction with chemothrapy (CT). There were 47 male and 25 female patients,
median age 61 yrs (range 39-77). Pre-treatment clinical staging revealed 21
stage I, (T1-2 NO), 16 stage II (T1-2N1), and 35 stage III (MO). Pre-operative
CT included cyclophosphamide, adriamycin, and vincristine (CAV) for 62, CAV and
etoposide for 7, and cisplatin and etoposide for 3 patients. Twenty-six
patients achieved complete remission, 29 partial remission, 15 less than
partial remission, and there were 2 early deaths. Thirty-four patients did not
undergo ASR for the following reasons: randomized to radiation in another study
protocol (10), patient refusal (9), inadequate response to CT (4), medically
unfit for thoracotomy (3), early death (2). The remaining 38 patients underwent
thoracotomy (8 pneumonectomy, 25 lobectomy). Five patients were not resected at
thoracotomy (4 unresectable, 1 no tumor identified). Post-operative
pathological stage for the 38 ASR patients revealed 7 stage I, 10 stage II, and
21 stage III. N1 disease was not identified pre-operatively for 2 patients, N2
disease for 6, and M1 (pleural) for 1. Postoperative pathology showed no tumor
for 3, SCLC only for 29, non-SCLC for 4, and mixed histology for 2.
Post-operative treatment included mediastinal irradiation (27) and cranial
irradiation (24), but no further CT. Twenty-eight of 72 patients were alive
without disease (18 of 38 ASR and 10 of 34 non-ASR). Seven patients died without
recurrent SCLC and 37 died in relapse. Median survival for the ASR group is 91
wks versus 47 wks for the non-ASR group (p =0.001). Within the ASR group,
patients with stage I (NO) disease had significantly (p = 0.037) longer
survival (median not reached) than stage II or III patients (median 69 and 52
wks, respectively). Their survival was also significantly longer than that of
the 10 stage I non-ASR patients (p = 0.001). No survival advantage was seen for
stage II and III ASR patients (p = 0.086). The median survival (51 wks) of the
19 patients who were eligible but did not undergo ASR (10 randomized, 9
refused) was significantly less than that of the ASR patients (p = 0.049), and
only 1 of 6 stage I patients is alive in this group.
In summary, ASR for responding patients after
chemotherapy results in long-term survival and perhaps cure for a significant
number of stage I patients. Because a survival advantage cannot be demonstrated
for patients with stages II and III, intensive pre-treatment and pre-operative
investigation including mediastinoscopy is essential to exclude patients who
would not benefit from such combined modality therapy. At this time, surgery
cannot be recommended outside the clinical trial setting.
*By Invitation
37. The Effect of Vertebral Column Invasion on
the Surgical Treatment of Lung Cancer
CLAUDIO BOTTI*. TOM
R. DeMEESTER
and PETER J. DAWSON*
Omaha, Nebraska
The New International TNM Staging System, as
proposed by Mountain, characterizes all tumors invading the vertebral column as
having a sufficiently poor prognosis to discourage resection. This is contrary
to our experience with 12 patients treated between 1976 and 1987 whose tumors
clinically extended into the vertebral column. All received 3000 rads of
preoperative radiation followed by en bloc resection of the lung and
costovertebral angle including a portion of the vertebral body. A complete
mediastinal lymphadenectomy was also performed. In two patients the lowest
trunk of the brachial plexus was resected, including the subclavian vessels in
one. Preoperatively, three patients had a true Pancoast syndrome and in eight
the tumor was located in the apex of the lung. All patients were free of
mediastinal node involvement as assessed by pre-radiation mediastinoscopy.
Resectability was based on the absence of tumor invasion as assessed by
tomograms or CT scans into the triangle formed by the rib and the transverse
process and pedicle of the vertebra (costo-transverse foramen) (Figure 1). The
first two structures were transected posteriorly and pushed inward, allowing
the vertebral body to be resected with a tangentially oriented osteotome
(Figure 2). There were eight adenocarcinoma, three squamous carcinoma and one
large cell carcinoma. All were T3NO. Follow-up ranged from five months to 11
years with an average of 36 months. Five patients died within 12 months from
recurrent disease (one local, two distant and two local and distant). One
patient died at five months disease free. Six patients are alive at five months
to 11 years (three beyond five years) without evidence of tumor recurrence and
arthritic pain. The overall five and ten year survival rate (Kaplan-Meier
method) was 42 percent, which is similar to other resected T3NO tumors.
Vertebral involvement does not always preclude resection. In proper patient
selection, the removal of the involved portion of the vertebral body as
described is associated with long term survival without sequelae.

*By Invitation
38. Primary Isolated Aortic Valve Replacement:
Early and Late Results
BRUCE W. LYTLE,
DELOS M. COSGROVE,
PAUL C. TAYLOR*,
FLOYD D. LOOP,
LEONARD A.R.
GOLDING*, ROBERT W. STEWART*,
CARL C. GILL* and
MARLENE GOORMASTIC*
Cleveland, Ohio
One thousand three hundred eighty-two
consecutive patients underwent primary isolated aortic valve replacement (AYR)
from 1972 through 1983. There were 52 (3.8%) in-hospital deaths. Multivariate
analysis identified advanced age (p<0.0001), preoperative shock or cardiac
arrest (p = 0.0002) and preoperative BUN >25 mg/100 ml (p = 0.006) as independent
variables increasing in-hospital mortality, and the use of cardioplegia for
myocardial protection (p = 0.006) as a factor decreasing mortality.
Follow-up (mean postoperative interval 103
months, range 39-187 months for late survivors, total of 10,125 patient years
of follow-up) documented survival of 85% and 66% and event-free survival of 71%
and 43% at 5 and 10 postoperative years, respectively. Mutivariate models were
used to examine the impact of variables over a 10-year follow-up and advanced age,
moderate or severe impairment of left ventricular function, coronary artery
disease and preoperative BUN of >25 mg/100 ml were identified as factors
decreasing late survival and event-free survival (all p<0.05). Patients with
bioprostheses had better survival (p = 0.0001) and event-free survival (p =
0.0007) than patients with mechanical valves. Patients with bioprostheses had
superior results only if not taking warfarin, and experienced more reoperations
and endocarditis; those with mechanical prostheses suffered more strokes,
myocardial infarctions, bleeding complications and thromboembolic events.
Survival and event-free survival curves for patients grouped according to
prosthesis type converged late in the follow-up. At 5 postoperative years
univariate comparisons showed a significant advantage for bioprostheses while
at 10 postoperative years they did not.
Analysis of patients grouped according to age
at operation showed that bioprostheses were associated with improved survival
and event-free survival for patients >60 years, improved survival but not
improved event-free survival for patients in the 40-59 year range and did not
influence either survival or event-free survival for patients <40 years.
We conclude the 10-year results after isolated
AYR are influenced by both patient-related and management-related factors and
the impact of those factors is different for patients of different ages.
12:30 p.m. ADJOURN
*By Invitation