American Association for Thoracic Surgery
67TH ANNUAL MEETING
Scientific Program
MONDAY MORNING,
April 6, 1987
8:30 a.m. Business Session (Limited to Members)
8:45 a.m. Scientific Session - Grand Ballroom
1. New
Approaches to the Management of Acute Ischemic Mitral Regurgitation
J. SCOTT
RANKIN*, MICHAEL P. FENELEY*,
RICHARD D.
FLOYD*, J. G. REYES*
and ROBERT M.
CALIFF*
Durham, North
Carolina
Sponsored by:
DAVID C. SABISTON, JR.
Durham, North
Carolina
Severe mitral regurgitation (MR) secondary to
acute myocardial infarction has been a particularly difficult management
problem with disappointing clinical results. Over a 20 month period, 15
patients were admitted with acute myocardial infarction and severe MR
associated with: acute pulmonary edema in 14, low cardiac output requiring
balloon pump placement in 10, and acute renal dysfunction in 7. The infarcts
were posterior in 14 patients and anterior in 1; 3 had ruptured papillary
muscles. Six patients underwent thrombolysis or angioplasty reperfusion within
6 hours of coronary occlusion, and the degree of MR then was monitored serially
with Doppler echo-cardiography. In 5 patients (Group I), reperfusion was
associated with resolution of MR to 1 + levels or less over 48-72 hours. Four
of these patients underwent conventional coronary revascularization, and 1
received percutaneous angioplasty, with 4 long-term survivors (>6 months).
In 10 patients (Group II), the MR persisted at severe levels, and all 10
underwent complete coronary revascularization, transventricular mitral
valvuloplasty through the infarcted area, and infarct exclusion/plication. The
valve repairs included posterior commissural annuloplasty in 8, papillary
muscle shortening procedures in 7, reimplantation of ruptured papillary muscles
in 3, and chorda! transfer in 1. Valve function was monitored intraoperatively
with transesophageal echocardiography. One acute failure of repair necessitated
transventricular mitral valve replacement, and 8 Group II patients have
survived long-term. All survivors are Class I for angina and heart failure.
Late postoperative color-flow Doppler studies of both groups revealed 0-1 + MR
in 9 and 2+ MR in 3. Thus, in severe acute ischemic MR, a policy of early
reperfusion when feasible, followed by 1) serial Doppler assessment of valve
competence, 2) subsequent coronary revascularization, and 3) a uniform
application of transventricular mitral valve repair when necessary resulted in
an 80% long-term survival. Late symptomatic status and valve function appear
satisfactory, and this approach offers the potential for improving therapeutic
results in this difficult clinical subgroup.
*By Invitation
2. Aortic
Valve Replacement with Cryopreserved Homograft Valves and with Antibiotic 4°C
Stored Valves: A Comparative Follow-Up Study
MARK F.
O'BRIEN*, E.G. STAFFORD*,
P.G. POHLNER*,
M.A.H. GARDNER*
and D.D.
McGIFFIN*
Chermsibe,
Brisbane, Australia
Sponsored by:
JOHN W. KIRKLIN
Birmingham,
Alabama
Aortic valve
replacement, with or without associated procedures, was performed in 304
patients with allograft (homograft) aortic valves; the allografts were
Cryopreserved between 1975 and August 1986 (n = 184) and antibiotic sterilized
and stored at 4°C between 1969 and 1975 (n = 120). All patients have follow-up,
with date of inquiry of August 1986. The 10 year actuarial survival, including
hospital deaths, of patients with the Cryopreserved valves and with the 4°C
stored valves was 70% (± 5% SD) and 67% (± 5% SD) respectively. With the 4°C
stored allografts, the 14 year survival was 51%.
Ten year
actuarial freedom from homograft valve reoperation in surviving patients with
Cryopreserved allografts and 4°C stored valves was 92% (± 3% SD) and 85% (± 4%
SD) respectively. The 14 year actuarial freedom in the case of 4°C stored
allografts was 62%. The longest follow-up in patients with Cryopreserved
allografts was 12 years and in those with 4°C stored allografts was 16 years.
Within these periods, no patients with Cryopreserved allografts (0% of 30 day
survivors) underwent reoperation for cusp perforation while 15 patients with
4°C stored allografts (14% of 30 day survivors) underwent reoperation for cusp
perforation (p for difference <.0001).
Multivariate analysis demonstrated the
dominant effect of the homograft valve preservation technique on the prevalence
of reoperation for cusp rupture. Earlier studies showed fibroblast viability in
Cryopreserved allografts and lack of fibroblast viability in antibiotic
sterilized 4 °C stored allografts. These considerations, plus the low
prevalence of thromboembolism (2% of 30 day survivors) and valve endocarditis
(3% of 30 day survivors) in the patients receiving Cryopreserved allograft
aortic valves, indicate the superiority of this method of storage.
*By Invitation
3. The
Carpentier-Edwards Supra-Annular Porcine Bioprosthesis - A New Generation
Tissue Valve with Excellent Clinical Performance
W.R. ERIC
JAMIESON, ALFRED N. GEREIN*,
A. IAN MUNROE*,
ROBERT T. MIYAGISHIMA*,
MICHAEL T.
JANUSZ* and G. FRANK O. TYERS
Vancouver,
British Columbia
This investigational valve was implanted in
1176 patients (1185 operations, 1270 valves) November 1981-December 1985 (age
13-85 years, mean 61 years). Early mortality was 7.0% (with concomitant
procedures 10.6%, without 4.7%); (previous operation 10.2%, without 6.4%). Late
mortality was 4.5%/patient year (AYR 4.0%, MVR 4.8%, MR 0.4%). Total cumulative
follow-up was 2288 years. Thromboembolism (TE) 2.6%/patient year (fatal
0.3%/patient year), (major 1.4%, minor 1.2%). Anticoagulant hemorrhage (ACH)
0.7% (fatal 0.04%). Hemolyses 0.04%. Prosthetic valve endocarditis (PVE) 0.3%
(fatal 0.1%) Periprosthetic leak (PPL) 0.3% (fatal 0.04%). Structural failure
(SF) (primary tissue failure/structural failure) 0.09%/patient year.
Hemodynamic valve dysfunction (HVD) 1£ (0.7). Re-operation 0.6%/patient year
(TE 0.09%, hemolysis 0.04%, PVE 0.04%, PPL 0.3%, SF 0.09%). TE incidence
reduced after 2 years, ACH throughout observation, PVE early, PPL throughout,
SF late. Survival 79.2 ± 3.3% (5 years). Freedom from (5 years) TE 91.8 ± 2.5%
ACH 96.5 ± 2.4% (4 years), PVE 95.7 ± 6.1%, PPL 88.5 ± 8.2%, SF 98.8 ± 1.6%,
reoperation 97.6 ± 1.8%. Freedom from all complications (5 years) 85.5 ± 3.7%,
complication mortality 98.8 ± 0.8% and valve failure (mortality and
reoperation) 96.7 ± 1.6%. This investigational Carpentier-Edwards,
supra-annular porcine bioprosthetic valve has provided excellent clinical
performance and remains our overall prosthesis of choice.
*By Invitation
4. Do
Heart Valve Bioprostheses "Degenerate" Metabolically? Or Just "Wear and Tear"
(Forum)
SHLOMO GABBAY*,
PANKESH KADAM*,
STEPHEN FACTOR*
and TAK KE CHEUNG*
Newark and
Piscataway, New Jersey and Bronx, New York
Sponsored by:
WILLIAM E. NEVILLE
Newark, New
Jersey
The ideal
substitute for diseased cardiac valves has yet to be found, dissatisfaction
exist with currently available valvular prostheses, due to the still high rate
of thromboembolic complications of mechanical valves, and the limited
durability of bioprostheses. Failure of bioprostheses is defined as "degeneration,"
which is a broad term, and considered as metabolic consequences, while most of
the valves just' wear and tear.'' (Except the calcification in children). We
have tested a large number of heart valves, porcine and pericardial
bioprostheses, using a Fatigue Test System with a high degree of reproducible
test conditions. The results have allowed us to define causes of "wear and
tear," previously insufficiently stressed, in each type of valve tested. There
is a clear difference in factors influencing tissue disruption between porcine
and pericardia! valves. We have compared these in vitro results with in vivo
clinical findings. The main conclusions are: 1) Bioprostheses rupture and fail
in the same fashion in vitro as in vivo, 2) Mechanical and design factors are
involved in tissue failure, 3) The ratio in vivo/vitro in durability is not
1:1. The ratio depends on the test conditions, 4) Pericardial valves fail by
damage at time of closure, while porcine valves wear and tear in both opening
and closing (mostly opening sequence) because of design features, 5) There is a
wide variability in durability of similar valve types. Design improvement can
minimize the variability. (Valves can fail as early as 2-3 million cycles or
more than 100 million cycles). Similarly bioprostheses can be explanted in few
months or last 10-13 years in patients, 6) "Domino effect" exist in tissue
disruption: once one cusp fail and prolapse, the other cusps will fail in an
accelerated fashion, 7) Most valves that last less than 40 to 50 x 106
cycles under our test conditions, probably will not last in patients for a
period of 10 years. Durability of 100 x 106 cycles can be considered
excellent. Very few bioprostheses reach this record, 8) Fatigue Testing is an
excellent and valuable tool in developing heart valves. This study definitely
shows that design improvement can prolong the durability of bioprostheses.
9:55 a.m. Intermission -
Visit Exhibits - Wacker Hall
Complimentary coffee available
*By Invitation
10:40 a.m. Scientific Session - Grand Ballroom
5. Cerebral
Microembolism During Cardiopulmonary Bypass: Retinal Microvascular Studies In
Vivo Using Fluorescein Angiography
CHRISTOPHER I.
BLAUTH*, JOHN V. ARNOLD*
EDWARD W.
SCHULENBURG*,
ALISON C.
MCCARTNEY*,
and KENNETH M.
TAYLOR* London, England
Sponsored by:
FLOYD D. LOOP
Cleveland, Ohio
We have
recently reported the use of retinal fluorescein angiography to demonstrate the
occurrence of occlusions in the cerebrovascular micro-circulation during
cardiopulmonary bypass (CPB). In the present study, 21 patients undergoing
elective coronary artery surgery had retinal fluorescein angiography 5 minutes
before the end of CPB. Patients with diabetes or known cerebro vascular disease
were excluded. Anaesthetic and perfusion protocols were standardised in all
cases, with non-pulsatile flow and a bubble oxygenator (Harvey H1700). After
31-167 minutes of CPB, 21/21 (100%) of patients had retinal microvascular
occlusions consistent with microembolism. Control fluorescein angiograms
obtained in 5 patients immediately before CPB but after heparinisation
and aortic cannulation showed normal retinal perfusion. During CPB there were a
mean of 3·5 (range 1-7) blocked arteries of less than 50mm caliber, and a mean of 6·3 (range
1-10) focal areas of capillary non-perfusion per 30° field of retina centered
on the macula per patient. The microembolic count did not correlate with bypass
time (r = 0-14). Repeat studies 30 minutes after discontinuation of CPB showed
partial resolution with occlusions in 4/5 (80%) of patients. In later studies
at a median of 8 days (range 5-11) postoperatively, only 2/16 (12·5%)
patients had persistently occluded retinal vessels, in both cases single areas
of capillary non-perfusion. Psychometric testing with 4 standardised tests was
performed in 18 patients. The mean total microembolic count in patients with
psychometric deficit was 11*1 occlusions per field (n = 7), compared to
8·6 occlusions per field in patients with no deficit (n = 11). In a
parallel study of 15 dogs, 8/9 (88·9%) had retinal microvascular
occlusions during CPB after 10-90 minutes of perfusion, and retinal histology
revealed platelet-fibrin microemboli 20-70 mm diameter in 7 of the 8 dogs (87·5%) with
angiographic occlusions. 6 dogs undergoing sham CPB with heparinisation and
aortic cannulation had normal retinal perfusion. This study demonstrates a very
high incidence of microvascular occlusions in the territory of the internal
carotid artery during CPB consistent with microembolism.
*By Invitation
6. Reconstruction
of Left Ventricular Wall with Autologous Pericardium
TIRONE E. DAVID,
CHRISTOPHER M. FEINDEL*
and GLORIANNE
ROPCHAN*
Toronto,
Ontario
Autologous
pericardium has been used to reconstruct different areas of the left ventricle
in 24 patients (pts). Fifteen pts had active infective endocarditis with
abscess formation in an infarcted myocardium (3 pts), in the aortic root (5
pts), in the central fibrous body and mitral annulus (3 pts), in the central
fibrous body and tricuspid annulus (1 pt) and in the mitral annulus alone (3
pts). The remaining patients had acute ventricular septal defect (5 pts), acute
rupture of the posterior wall of the left ventricle following mitral valve
replacement (1 pt) or excessive calcification of the mitral annulus to properly
secure a prosthesis (3 pts).
The diseased
portion of the myocardium and or fibrous skeleton of the heart was excised when
indicated, and reconstruction was accomplished by suturing an appropriately
tailored autologous pericardial patch directly to the endocardium. A double
patch was used in pts with acute ventricular septal defect (one on each side of
the septum). All other pts had a single patch sutured directly to the
endocardium with running polypropelene suture. In cases of valvular disease, a
prosthetic valve was secured to the patch in those areas where the pericardium
replaced the fibrous skeleton.
There were 3
hospital deaths (one pt had acute VSD and 2 pts had annular abscesses) but none
were related to the technique or patch material. All survivors have been
followed from 3 to 61 months, mean of 32. There has been no late death and
every patient has had at least one non-invasive assessment test of the
pericardial patch. No patient has had patch or valve dehiscence or pericardial
patch aneurysm.
Autologous
pericardium can be safely used to reconstruct left ventricular wall. It handles
very well and problems with suture line bleeding is practically non-existent.
Autologous pericardial patch is particularly useful in pts with myocardial and
or annular abscess secondary to infective endocarditis.
*By Invitation
7. Identification
of Free Radicals Produced During Myocardial Ischemia and Reperfusion Using
Electron Paramagnetic Resonance Spectroscopy and High Precision Liquid
Chromatography (Forum)
JOHN M. LUBER*,
PARINAM S. RAO*
and MARK S.
CROWDER*
New Hyde Park,
New York and Danbury, Connecicut
Sponsored by:
DENIS H. TYRAS
New Hyde Park,
New York
The presence of
free radicals (FR) were assessed in left ventricular myocardium (LV) of 1 month
old swine (N = 5) during cardiopulmonary bypass pre crossclamp (C), with 30
minutes of normothermic ischemia (I) and after 10 minutes of reperfusion (R).
LV biopsies were quick frozen in liquid N2 and examined by EPR at
10°K and by high precision liquid chromatography (HPLC) using electrochemical
(EC) and UV detectors. The EPR difference spectra between C and I revealed a 3
line spectrum (g = 2.015, 2.005, 1.988) with splitting between lines of 2.25 m
Tesla. Power saturation studies revealed g = 2 signal saturation at lower
microwave powers than the 3 line EPR signal. This suggests a nitrogen triplet
or an organic biradical. EPR signals with I were irreversibly lost at 200°K.
With R the 3 line spectrum was present but diminished.
HPLC verification of FR was accomplished by
incubating the LV homogenate (50 mg) with a spin trap
(5.5-dimethyl-l-pyrroline-n-oxide [DMPO]); 50 ul, 10mM at pH = 7.8 in 50 mM
phosphate buffer using a 5 u resolve C18 column and EC. A DMPO
adduct signal was noted. This could not be modified by superoxide dismutase
(SOD), or dimethylthiourea indicating that it is not an oxy derived species.
Lipid peroxidation measured by tissue malondialdehyde (MDA) with UV absorbance
at 254 nm and catechol levels using EC revealed the following:
|
MDA (nm/mg protein)
|
Catechols (ng/mg protein)
|
|
|
|
Norepinephrine
|
Epinephrine
|
Dopamine
|
|
C
|
0.52 ± .01
|
3.3 ± .38
|
.04 ± .01
|
.017 ± .008
|
|
I
|
0.63 ± .05
|
1.7 ± .98
|
.02 + .01
|
.01 ± .005
|
|
R
|
0.58 ± .02
|
3.0 ± .56
|
.04 ± .01
|
.018 ± .008
|
These
data indicate that (1) with 30 minutes of normothermic ischemia there are
directly measurable FR by EPR and HPLC (2) these FR do not seem to be oxygen
derived species and, therefore, cannot be effected by SOD or catalase (3) lipid
peroxidation and catechol oxidation may play a role in cellular damage during I
but not R. (4) The FR concentration does not increase with R and, therefore,
efforts at free radical scavenging emphasizing the reperfusion period may be in
error.
11:30 a.m. Presidential Address - Grand Ballroom
"Some Thoughts From The Other Side
of The Table, or The Last Presidential Address"
Norman E. Shumway, M.D., Stanford,
California
12:15 p.m. Adjourn for Lunch
Luncheon Service available in
Exhibit Area - Wacker Hall
*By
Invitation