WEDNESDAY MORNING, MAY 13, 1981
8:30 A.M. Scientific Session - International
Ballroom
(Forum Papers)
27. Computerized
Fluoroscopy-A New Technique for the Noninvasive Evaluation of the Aorta,
Coronary Artery Bypass Graft Patency, and Left Ventricular Function
P. DAVID MYEROWITZ*,
ANDREW B. CRUMMY*,
DAVID L. ERGUN*,
CHORNG-GANG SHAW*,
PARAMJEET S. CHOPRA,
HERBERT A. BERKOFF*,
GEORGE M. KRONCKE*,
GEORGE G. ROWE*,
CHARLES A. MISTRETTA
* and WILLIAM D. TURNIPSEED*,
Madison, Wisconsin
A computerized fluoroscopy system (C.F.) has
been developed based on real time digital processing of x-ray transmission data
from traditional image-intensified fluoroscopy equipment. High quality
visualization of any part of the arterial system is obtained following
intravenous injection of 0.5 to 0.75 ml/kg of iodinated contrast materials.
Previous reports from this institution have outlined the usefulness of C.F. for
visualizing carotid, peripheral, and renal arteries following intravenous
contrast injections. This report describes the use of this technique to
evaluate the aortic arch, left ventricular function, and coronary artery bypass
graft patency. Fifty intravenous studies were performed in 25 patients. Among
20 patients with coronary artery bypass grafts, C.F. correctly identified 11 of
15 patent grafts and 11 of 11 occluded grafts as confirmed by standard coronary
arteriography in 11 of these patients. Unlike computerized tomography, our
technique gives a longitudinal view of the bypass graft much like direct
coronary angiography. Aortic arch studies included demonstration of a right
aortic arch with a small left subclavian artery, a coarctation, and a normal
aortic arch in a trauma patient with a wide mediastinum. Segmental wall motion
abnormalities have been clearly identified by a modification of the technique
which produces a negative outline on the ventriculogram in dyskinetic segments.
Ejection fractions may be calculated by analyzing the amount of iodine in the
ventricle in systole and diastole. This technique may also be used to evaluate
carotid disease in patients undergoing coronary artery bypass surgery. C.F.,
therefore, allows evaluation of the entire cardiovascular system by the
relatively noninvasive technique of intravenous angiography.
*By invitation
28. Establishment of Right Ventricle to
Hypoplastic Pulmonary Artery Continuity Without the Use of Extracorporeal
Circulation: A New Surgical Technique
FRANCISCO J. PUG A *
and GIDEON URETZKY*,
Rochester, Minnesota
Sponsored by: Dwight
C. McGoon, Rochester, Minnesota
A technique that allows establishment of continuity between the right
ventricle and hypoplastic pulmonary confluence without the use of
extracorporeal circulation in patients with pulmonary atresia and ventricular
septal defect has been applied successfully in the laboratory and in four
consecutive patients. Exposure is achieved by an anterolateral thoracotomy
through the left third intercostal space. A Dacron tubular graft of appropriate
size is anastomosed to the hypoplastic but confluent pulmonary artery
bifurcation. A fine, stranded, multifilament steel wire is passed through the
anterior wall of the outflow portion of the right ventricle so that a two to
three centimeter loop lies in the right ventricular cavity. The proximal end of
the nonvalved tubular graft is anastomosed to the epicardial surface of the
right ventricle around the exit points of the wire. The ventricular incision is
achieved by sawing through the right venricular wall with the wire in a manner
similar to a Gigli saw. No systemic heparinization is used. The characteristics
and adequacy of the right ventriculotomy were studied on the right ventricular
outflow tract of two dogs, while a third animal was remained alive and well up
to two months after undergoing the procedure in addition to interruption of its
main pulmonary artery. Four consecutive patients, ages 22, 12, 8 and 2 years,
have undergone this procedure. All had confluent but hypoplastic pulmonary
arteries measuring 6, 5, 5 and 3 mm. in diameter. There were no surgical deaths.
Average blood loss was 200 cc. and all patients showed an increase in
peripheral arterial oxygen saturation. All patients underwent postoperative
cardiac catheterization and angiography. All patients had patent conduits and
pulmonary arteries which had increased in diameter. Advantages of the procedure
are: avoidance of the median sternotomy which may simplify future closure of
the VSD; simplification of an effective technique which under extracorporeal
circulation is complicated by profuse collateral flow that tends to obscure the
operative field and distend the heart; minimal bleeding resulting from
avoidance of systemic heparinization which in these severely cyanotic patients
can lead to severe bleeding diathesis; and, hopefully, a decrease in the risk
of this type of reconstruction.
*By invitation
29. Successful Orthotopic Canine Heart
Transplantation After 24 Hour In Vitro Preservation
ALBERT J. GUERRATY*,
PETER A. ALIVIZATOS*,
MARK W. WARNER*,
MICHAEL L. HESS* and
RICHARD R. LOWER,
Richmond, Virginia
Prolonged in vitro preservation of
donor hearts may be of importance in the future expansion of clinical cardiac
transplantation to extend the distance over which donor hearts may be
transported and to allow for more extensive preoperative histocompatibility
testing.
A protocol was developed to provide continuous, hypothermic,
nonpulsatile perfustion with an oxygenated balanced electrolyte solution for
preservation of the isolated canine heart during 24 hours prior to orthotopic
transplantation. Important features of the cardiectomy technique include the
use of a calcium channel blocker, potassium arrest and rapid cooling of the
myocardium. The donor heart is then perfused at a pressure of 18-22 cm. of
water and at an average flow of 75 cc/mm/100/gm. of tissue. The septal
temperature is maintained at 5-7°C and the perfusate pH at 7.25-7.35.
Subcellular function after 24 hours of perfusion and transplantation, as
assessed by sarcoplasmic reticulum and myofibrilar ATPase activity were not
significantly different from control values.
Two groups of mongrel dogs were studied after
orthotopic transplantation: Group I (N= 15) received hearts perfused by the
above protocol for 24 hours and Group II (N = 9) received hearts removed by the
same cardiectomy technique, but transplanted immediately. All grafts functioned
well initially with support of the circulation after bypass. Eleven animals in
Group I survived 4 days to 2 months and six animals in Group II survived 4 days
to 3 weeks postoperatively. Measurements of heart rate, cardiac output,
pulmonary capillary wedge pressure, left ventricular pressure and peak
developed left ventricular pressure, before and after dobutamine infusion, were
normal in all animals and there were no statistical differences between Group I
and Group II animals.
Thus, a reliable and reproducible method for
24-hour in vitro perfusion of the canine heart has been obtained and
should be applicable in clinical cardiac transplantation, when periods of
preservation for longer than a few hours are required.
*By invitation
30. Prostacyclin Infusion During Cardiopulmonary
Bypass - Clinical Experiences
KJELL RADEGRAN* and
CHRISTOS
PAPACONSTANTINOU*, Gothenburg, Sweden
and Saloniki, Greece
Sponsored by: David
P. Hall, Chattanooga, Tennessee
Prostacyclin is an integral part of the body's
defence against platelet aggregation and intravascular coagulation. It has been
shown in experimental studies on dogs to preserve platelet number and function
during cardiopul-monary bypass (CPB). The present study reports our initial
experiences with prostacyclin infusion during CPB in man.
The study comprises 74 adult patients operated for acquired heart
disease during the period June 1979 - June 1980. CPB was by roller pump and
bubble oxygenator primed with a crystalloid solution. Moderate hypothermia was
used in all cases. Heparin was given in a dose of 3 mg/kg b.w. Anticoagulation
was checked by activated clotting time measurements (ACT). Twenty-eight
patients serving as controls did not receive prostacyclin. Ten patients were
infused with prostacyclin 2-20 ng/kg/min throughout the CPB period, while
twenty-two patients got 50 ng/kg/min for the first 30 min of CPB only and
fourteen patients got 100 ng/kg/min from start of CPB until 5-20 min before
termination of CPB.
Results: Infusion of prostacyclin 50-100 ng/kg/min resulted in a consistent
protection of the platelet count. Even after 2 hours of bypass when in the
control group the platelets had decreased to 70 ± 14% (x ± S.D.) of
pre-CPB value, corrected for hemodilution, the platelet count was in the 50 and
100 ng groups resp. 93 ± 17 and 102 ± 20%. This difference remained also
one hour after CPB when protamine had been administered. The high dosages of
prostacyclin had pronounced effects also on arterial pressure and systemic
vascular resistance (SVR) during CPB. During hypothermia the arterial pressure
was in average around 20 mm Hg and the SVR was reduced to less than half of
that in the control group. Prostacyclin, 50-100 ng/kg/min also prolonged the
ACT to more than 1000 sec as compared with 544 ± 117 sec in the control group.
There were three deaths among the 28 control
patients and 2 deaths among the 46 patients infused with prostacyclin. There
was one instance of reversible hemiplegia in the control group and one among
the prostacyclin patients, both in patients with aortic valve replacement.
No difference in intraoperative blood loss was
observed between control and prostacyclin patients. In the postoperative period
prostacyclin patients bled on an average about 25% less than control patients,
i.e. 580 ± 250 versus 810 ± 450 ml.
*By invitation
31. Four Year Clinical Experience With the
Gelatine-Resorcine-Formol Biological Glue in Acute Aortic Dissection
JEAN E. BACHET*,
CLAUDE LAURIAN*,
OLIVIER BICAL*,
BERTRAND GOUDOT* and
DANIEL GUILMET*,
Suresnes, France
Sponsored by:
Charles DuBost, Paris, France
From Jan. 1977 to Sept. 1980, the Gelatine-Resorcine-Formol (G.R.F.)
biological glue was used for tissue reinforcement in 25 patients operated on
for acute dissection involving the ascending aorta.
The results of these patients (GRF group) were
compared to results of 25 patients operated on between 1970 and 1976 with
"classical techniques" (CT group). There were no significant differences
between the 2 groups regarding the age, the preoperative clinical and
anatomical data.
The ascending aorta was replaced in all
patients; the aortic valve was replaced twice (8%) in the GRF group and in 12
cases (48%) of the CT group the coronary arteries were by-passed or reimplanted
in 20% patients of each group. Average intra-operative blood transfusion volume
was 5800 ml in the CT group and 2100 in the GRF group (p 0.01). Four (16%)
preoperative deaths were registered in the CT group and none in the GRF group.
Postoperative renal failure, cerebral
ischemia, persisting peripheral ischemia and infection were more frequent in
the CT group. They were responsible for 8 hospital deaths in this group and for
two in the GRF group (p 0.01). Hospital mortality was therefore reduced from
48% (CT group to 8% (group GRF) (p 0.01) 2 late deaths were registered in the
CT group and none in the GRF group, all survivors being in good clinical
condition.
Sixteen patients of the GRF group underwent 19
control angiograms, 2 to 36 months following surgery, which documented 2
moderate aortic incompetence (8%), 3 persisting dissections of the descending
aorta, but good and stable repair in the other patients.
In conclusion, the use of the GRF glue
significantly reduce:
- the number of aortic valve replacements;
- the intra and postoperative bleeding;
- the frequency and severity of postoperative
complications.
Therefore, long-term (4 years) survival rate
has been raised from 40% to 92%.
*By invitation
32. In-Vitro Assessment of Anti-Neoplastic Therapy:
A New Indication for Thoracotomy
LARRY R. KAISER*, E. CARMACK HOLMES and
DAVID KERN*, Los
Angeles, California
Selection and determination of the efficacy of antineoplastic agents has
been dependent upon the trial and error method of observing measurable disease.
Such methods not only subject the patient to loss of precious time, but to
needless toxicity if the drug is ineffective. The clonogenic assay, a technique
for evaluating the patient's response to neoplastic agents, has been developed
which has the potential for individualizing therapy. In this assay, tumor cells
exposed to various drugs are cloned into colonies. Of the 14 primary and 17
metastatic pulmonary tumors tested with this technique, a growth rate of 80-85%
was achieved. Fifty percent of the primary tumors and 60% of the metastatic
lesions responded in vitro to one or more of the test drugs. The correlation
between in vitro and in vivo response was 60%. No drug that was inactive in
vitro had activity in vivo. Prior knowledge of in vitro sensitivity may dictate
a more aggressive surgical approach to pulmonary metastatic disease, whereas in
vitro resistance would call for more conservative treatment. Just as with
estrogen receptor status in breast cancer, data derived from the clonogenic assay
may ultimately be of such import that thoracotomy would be warranted solely for
the purpose of obtaining tissue for the assay.
*By invitation
33. An Endobronchial Blocker for One-Lung
Anaesthesia
ROBERT JASON
GINSBERG, Toronto, Ontario, Canada
One-lung anaesthesia is a valuable adjunct in the conduct of pulmonary
and esophageal anaesthesia. The standard technique for one-lung anaesthesia
employs a double-lumen endotracheal tube (Robertshaw, Carlens). These tubes
have many disadvantages. A simpler method has been developed. All that is
required is an 8-14 Fogarty occlusion catheter, a fiberoptic bronchoscope and a
standard cuffed endotracheal tube.
After induction of the anaesthetic, the
Fogarty catheter is passed through the larynx into the lower trachea and, then,
the endotracheal tube is inserted. Using the fiberoptic bronchoscope, the tip
of the Fogarty catheter is positioned in either main-stem bronchus under direct
vision. The cuff of the endotracheal tube is then inflated, fixing the catheter
in position. One-lung anaesthesia can then be accomplished simply by inflating
the balloon of the Fogarty catheter.
This method has been used in over 150
thoracotomies. It has always been successful with no complications except in
right posterolateral thoracotomies where occasional dislodgement of the
catheter can occur. The advantages of this method over the double-lumen tube
include:
- Simple
(no need for anaesthetic experise for insertion of a double-lumen tube).
- Applicable
in small patients.
- More
reliable and faster.
- Does
not interfere with bronchial closure at the carina.
- It
can be repositioned under direct vision any time during the operation,
(although rarely necessary in our experience).
- It
allows for large-bore endotracheal and endobronchial suctioning.
Because of its simplicity, this method has
also been used as an adjunct to anterior mediastinoscopy, pleuroscopy and talc
poudrage. It allows for total visualization of the pleural space during these
diagnostic and therapeutic procedures.
34. The Relationship of a Hiatal Hernia to the
Function of the Body of the Esophagus and Gastroesophageal Reflux
TOM R. DeMEESTER,
LAWRENCE F. JOHNSON*,
EDWIN LaFONTAINE*
and DAVID B. SKINNER,
Chicago, Illinois
and Washington, D.C.
Sixty-nine patients referred to our esophageal function laboratory
without endoscopic esophagitis were divided into two groups based on the
presence or absence of a hiatal hernia on both a radiographic study and
endoscopic examination. Fifty-one patients had a hiatal hernia and 18 patients
did not have a hiatal hernia. Both groups had esophageal manometry, 24-hour
esophageal pH monitoring and esophageal mucosal biopsy to evaluate the effect
of a hiatal hernia on esophageal function. There was no difference in the
length of esophagus exposed to the positive pressure environment of the abdomen
between the two groups. Patients with a hiatal hernia had a statistically lower
distal esophageal sphincter pressure (p<001), and calculated closing force
of the cardia (length x pressure x 1.33 assuming a standard breadth of
esophagus) (p<.01). The body of the esophagus in the presence of a hiatal
hernia was less effective in clearing refluxed acid back into the stomach
(p<.025). This occurred only in the supine position and not while upright,
when gravity assisted clearance. These functional impairments were reflected by
abnormal epithelial change (Pope's criteria), indicating mucosal damage by
refluxed acid, and prolonged acid mucosal contact time in patients with a
hiatal hernia (p<.025).
To determine if the inability of the body of
the esophagus to clear acid in the presence of a hernia was due to the lack of
anchoring the esophagus at its distal end to the lumbar spine as occurs
normally, the pre and postoperative studies of 13 hiatal hernia patients who
had a posterior abdominal gastropexy without imbrication of the cardia were
reviewed. A significant improvement in esophageal clearance and amount of
mucosal acid exposure over pre-operative levels was noted, indicating that
anchoring the distal esophagus improved the ability of the body of the
esophagus to clear its luminal contents (p<.05).
Conclusions: (1) The presence of a hiatal
hernia was associated with poor esophageal clearance in the supine position, a
reduced distal esophageal sphincter pressure, and a normal length of abdominal
esophagus. (2) Patients with a hiatal hernia had more acid reflux into the
esophagus than those without a hernia. (3) Reduction of the hernia and
anchoring the distal esophagus corrected the clearance abnormality and reduced
esophageal acid exposure. (4) The presence of a hiatal hernia with its
detrimental effect on clearance by the body of the esophagus contributes to the
pathologic effects of gastro esophageal reflux from an incompetent cardia.
*By invitation
35. Use of the Silastic Tracheal "T" Tube for the
Management of Complex Tracheal Injuries
JOEL DAVID COOPER,
THOMAS R. J. TODD*,
RIIVO ILVES* and
FREDERICK GRIFFITH PEARSON,
Toronto, Ontario,
Canada
This paper reports on the use of the silastic
Montgomery "T" tube as a useful adjunct in 18 patients with complex problems
requiring tracheal resection and reconstruction.
In five cases, the "T" tube was used to
maintain a patent airway at a time when the general condition of the patient,
or of the tracheal lesion itself, would not permit resection and
reconstruction. In these five patients, the tube was in place for an average of
13 months before resection and primary anastomosis were undertaken.
In three cases with complicated subglottic
strictures, the mucosa at the proximal resection line was unhealthy and the
upper limb of the "T" tube was used to stent the subglottic airway
postoperatively. The average duration of stenting in these cases was 13 months,
and all were successfully ex-tubated. In an additional five cases, the "T" tube
was inserted postoperatively when it was determined that a primary anastomosis
was failing. Two of these five were subsequently successfully extubated, two
died of unrelated disease, and one is still under treatment.
In the remaining five patients the tracheal
pathology was considered unsuitable for resection and reconstruction and the
"T" tube was used to maintain an airway. Following an average of 12 months of
such stenting, four of the five were extubated and required no further
treatment.
It is concluded that the Montgomery "T" tube
is a valuable adjunct in the management of selected complex tracheal problems.
In subglottic lesions the upper limb of the tube may be positioned between the
vocal cords, and yet these patients maintain a functional voice and aspiration
has not been a problem. Furthermore, cord function was normal upon extubation.
Since humidification is through the normal route, crusting and obstruction of
the tube does not occur and the tubes can be left in place for long periods
without the need for change.
INTERMISSION - VISIT EXHIBITS
*By invitation
MYOCARDIAL
PRESERVATION SYMPOSIUM
Moderator: Quentin
R. Stiles
Discussor: John
W. Kirklin
36. Myocardial Damage Caused by Keeping pH 7.4
During Systemic Deep Hypothermia
HEINZ BECKER*, JAKOB
VINTEN-JOHANSEN*,
GERALD D. BUCKBERG,
JOHN M. ROBERTSON* and
JERRY D. LEAF*, Los
Angeles, California
With rare exception, hypothermia is routine during cardiac operations
and pH (measured at 37°C) is kept at 7.4. This clinical constraint does not
occur in nature where poikilotherms vary blood pH in concordance with a
temperature dependent neutrality point of water. This study tests the
hypothesis that keeping pH 7.4 during hypothermia produces a degree of
myocardial damage and limitation of effectiveness of cardioplegic protection
which is avoidable by appropriate pH management.
Methods: In 14 puppies, body temperature was lowered to 22°C with surface
hypothermia, then to 17°C with extracorporeal circulation. During 60 minutes of
circulatory arrest all hearts were protected with the same miltidose K +
cardioplegic solution. In 7 dogs, pH was kept at 7.4 and in 7 others pH was
varied as in poikilotherms (i.e. 7.9 at 17°C) principally by adjusting pCO2
during cooling and rewarming.
Results: During surface cooling, keeping pH at 7.4 caused inadequate cardiac
output (hypotension, systemic lactic acidosis, 11 ± 5%production).
Conversely, pH adjustment allowed 25%* higher cardiac output with normal
systemic lactate metabolism. Cerebral blood flow at 22°C, pH of 7.4, pCO2
40 mmHg fell 75%* (from 26 ± 6 to 10 ± 3 cc/100/min); raising pH to 7.75 by
lowering pCO2 below 10 mmHg allowed twice as much cerebral flow (20
± 6 cc/100gm/min*). Despite optimum myocardial protection with blood cardioplegia
during circulatory arrest, postischemic myocardial performance was depressed
50% by keeping pH 7.4. In contrast, postischemic performance was normal when pH
was varied appropriately during cooling and rewarming (stroke work index 0.62
vs 1.27 at 25 mmHg LAP)*.
Conclusion: Constraining pH to 7.4 during hypothermia causes a degree of myocardial
damage and limitation of cardioplegic protection which is avoidable by
adjusting pH the way poikilotherms do. These findings have major implication in
the routine management of hypothermia during all cardiac operations.
*p .05
*By invitation
37. Does Topical Hypothermia Prevent Sublethal
Intraoperative Injury During Coronary Artery Bypass Surgery
RODERICK W.
LANDYMORE*, DAVID TICE,
NARESH TREHAN* and
FRANK C. SPENCER,
New York, New York
Recent reports have suggested that myocardial
protection is inadequate during coronary artery bypass surgery for severely
diseased coronary arteries. Since methods of myocardial preservation vary
considerably between cardiac centers, this study was designed to determine
whether or not topical hypothermia is a necessary adjunct to systemic
hypothermia and potassium cardioplegia during myocardial revascularization, in
patients (pts) with diffuse coronary artery disease. Twenty-two pts ages 47-68
yrs were included in the study. Pts were placed on bypass and cooled to 28°
centigrade (c). Temperature (temp) was measured over the right and left
coronary distributions. The aorta was then cross-clamped and 1000cc of
potassium blood cardioplegia 5.7-11°c (X 8.7) was infused into the aortic root
at a pressure of 100-120 mm hg. Temp was measured and then 6 liters of cold
plasmalyte 2.3-5.1°c (X 3.5) was poured over the heart into the pericardial
well. Temp was again measured. In addition cold plasmalyte was continuously
dripped over the heart during the cross-clamp.
|
Anatomical Region
|
Myocardial Temperature Effect of Systemic Hypothermia
28 °c
|
Degrees Centigrade Temp after 1000cc Blood
Cardioplegia
|
Temp after cold Topical
|
|
RCA
|
Normal
|
30.4 ± 0.33*
|
14.3 ± 0.87
|
12.3 ± 0.65
|
|
|
Stenotic
|
31.8 ± 0.39
|
20.7 ± 1.10
|
13.9 ± 0.37**
|
|
|
Occluded
|
31.5 ± 0.22
|
23.3 ± 0.52
|
13.7 ± 0.53**
|
|
LAD
|
Stenotic
|
31.2 ± 0.21
|
19.1 ± 0.38
|
12.8 ± 0.44**
|
|
|
Occluded
|
30.6 ±0.61
|
24.6 ± 1.25
|
13.3 ± 0.87**
|
|
OM
|
Normal
|
30.6 ± 0.26
|
14.5 ± 0.43
|
10.6 ± 0.31
|
|
|
Stenotic
|
30.4 ± 0.45
|
17.7 ±1.17
|
11.6 ± 0.89**
|
|
|
Occluded
|
31.2 ± 0.00
|
23.8 ± 0.00
|
13.8 ± 0.00
|
*SEM + -Standard
Error of The Mean
**Students T-Test
P<0.01
Systemic hypothermia and potassium (K + )
cardioplegia uniformally failed to protect the myocardium in regions supplied
by severely Stenotic or occluded arteries. The addition of cold topical reduced
myocardial temperature to the safe operative range. This data demonstrates that
combined systemic hypothermia and K+ cardioplegia alone do not provide adequate
protection in pts with diffuse coronary disease. We conclude that the addition
of topical hypothermia ensures adequate protection during coronary bypass
surgery and recommend the routine use of intra-operative myocardial temp monitoring.
*By invitation
38. Myocardial Protection During Aortic Valve
Replacement. Comparison of Different Methods by Intraoperative Coronary Sinus
Blood Sampling and Postoperative Serial Serum Enzyme Determinations.
CHRISTIAN L. OLIN*,
VOLLMER BOMFIM*,
LENNART KAIJSER*,
CHRISTER SYLYEN* and
STELLAN STROM*,
Stockholm, Sweden
Sponsored by: Viking
J. Bjork, Stockholm, Sweden
Ninety-seven patients undergoing isolated
aortic valve replacement were studied during operation by simultaneous blood
sampling from the coronary sinus and brachial artery and after operation by
serial determinations of myocardium specific serum enzymes. Myocardial
protection was accomplished by selective coronary perfusion in 26 patients,
hypothermic potassium cardioplegia in 38, single dose blood cardioplegia in 15
and continuous blood cardioplegia in 18 patients. The continuous blood
cardioplegia method consisted of a slow pulsatile infusion of 15°C cold
oxygenated blood from the heart-lung machine (with 20 mekv K+ and 16 mekv Mg + +
per liter added) selectively into the left coronary artery during aortic
cross-clamping. The intraoperative blood samples were analysed for PO2,
O2-saturation, O2-content, PcO2, pH, lactate,
pyruvate, glucose, potassium and myoglobin, the postoperative blood samples for
creatine kinase (CK) its isoenzyme (CK-MB), and aspartate aminotransferase
(ASAT, equivalent to S-GOT). Myocardial biopsies were taken from the left
ventricle on commencement and termination of cardioplegia in the blood
cardioplegia groups and analysed for adenosine triphosphate (ATP), creatine (C)
and creatinephosphate (CP).
In the coronary perfusion group, one patient
(4%) died of left ventricular failure due to ischemic myocardial damage and
three (12%) needed vasopressor support postoperatively. In the three
cardioplegia groups (71 patients), there was no mortality and none of the
patients needed vasopressor support.
The metabolic studies showed that selective
coronary perfusion failed to protect the myocardium completely in spite of high
coronary flow. Ten minutes after bypass there was still a production of lactate
by the heart. The metabolic pattern was similar in the three cardioplegia
groups and was characterized by an early washout of lactate and other metabolic
products, decreased oxygen extraction, increased potassium and myoglobin
release. The CK-MB activity peaked between 3 and 4 hours after reperfusion. If
the three cardioplegia methods were compared, the continuous blood cardioplegia
method was the best. The metabolic changes were significantly smaller and
normalized more quickly during reperfusion. Blood samples from the coronary
sinus during cardioplegia showed that the heart extracted oxygen in spite of
its relaxed state. The myocardial biopsies also showed significantly less ATP
and CP decrease in the continuous blood cardioplegia patients.
*By invitation
39. The First American Clinical Trial of
Nifedipine in Cardioplegic Solution for Myocardial Preservation: A Preliminary
Report
RICHARD E. CLARK,
IGNACIO Y. CHRISTLIEB*,
THOMAS B. FERGUSON,
CLARENCE S. WELDON,
JOHN P. MARBARGER*,
PHILLIP N. WEST*,
BUR TON E. SOBEL*,
ROBER T ROBERTS*,
DANIEL R. BIELLO*
and BARBARA K. CLARK*,
St. Louis, Missouri
A continuing prospective, FDA approved,
clinical trial of high risk cardiac patients was begun in May, 1980 after five
years of extensive evaluation in dogs of the efficacy of the addition of
nifedipine, a calcium antagonist, to cold hyperkalemic cardioplegic solutions.
Protocol patients received preoperative and postoperative (0-72 hrs., 1 and 6
wks) determinations of ejection fraction and wall motion by radionuclide
ventriculography (4/pt), MB-CK isoenzyme (33/pt), myocardial pyrophosphate
scans (≥2/pt) for evidence of biochemical and morphologic changes and
extensive and frequent intra and postoperative hemodynamic measurements to
assess functional status and six 24 hr. ECG recordings. Thirty-six patients
have received nifedipine in cardioplegic solution, 21 within the protocol and
15 outside the protocol for emergent reasons. 28 of the 36 had Class III or IV
severe left ventricular dysfunction and required single, multiple and/or
re-placement valvular surgery (10), CABG (9) or a combination of both (9).
During the same calendar interval, 37 patients with equally poor ventricular dysfunction
and similar distribution of operations (5 within the protocol) have had
cardioplegic solution (CPS) without nifedipine. The results to date are:
|
|
CPS ONLY
|
NIFEDIPINE
|
|
|
|
%
|
|
%
|
|
No. of High Risk
Patients
|
37
|
|
36
|
|
|
Low Output Deaths
|
5
|
(14)
|
0
|
(0)
|
|
IABP
|
11
|
(30)
|
4
|
(11)
|
These preliminary results are reported because of
the reduction in mortality, threefold decrease in use of IABP, and concordant
data of functional, biochemical and morphologic improvement in nifedipine
treated patients which will be reported. It is concluded that high risk
patients with severe ventricular dysfunction who have been treated with
nifedipine in cold cardioplegic solution have superior clinical outcomes in
comparison to those treated with cold cardioplegic solution alone.
*By invitation
40. Preservation of Myocardial Ultrastructure and
High Energy Phosphates in Humans
SAMUEL C.
BALDERMAN*, JOGINDER N. BHAYANA*,
PAUL BINETTE*,
ARTHUR CHAN* and
ANDREW A. GAGE*,
Buffalo, New York
Sponsored by:
Richard H. Adler, Buffalo, New York
To establish whether multidose crystalloid
potassium hypothermia car-dioplegia provides adequate preservation of
myocardial ultrastructure and high energy phosphates, 25 patients with EF of
≥50%, undergoing cardiac surgery were studied. Eight patients had three
biopsies taken for ATP and CP determination from the left ventricular apex.
Biopsies were taken immediately prior to aortic cross clamping immediately
after the release of the aortic cross clamp and 30 minutes after the release of
the cross clamp. Seventeen patients had six biopsies taken from the left
ventricular apex at the above stated time. Three for ATP and CP determination
and three additional biopsies for electron microscopy. One patient sustained a
small perioperative infarction and another patient died on the 5th
postoperative day from an aortic dissection. The mitochondria on the electron
microscopic specimens were graded on a scale from 0 - 4 (4 = severe changes).
|
|
|
Pre clamp
|
Post clamp
|
30 minutes Post clamp
|
|
ATP
|
N = 25
|
4.19 ± 1.52
|
3.31 ± 1.12
|
3.332 ± 1.44
|
|
CP
|
N = 25
|
2.5 ± 1.7
|
.813 ± .96
|
1.664 ± 1.22
|
|
MITOCONDRIAL SCORE
|
N = 17
|
1.23 ± .53
|
1.36 ± .45
|
1.50 ± .59
|
|
1p≤.01
|
2p≤.025
|
3p≤.005
|
4p≤.05
|
|
There was no significant difference in the
mitochondial scores. The preservation of high energy phosphates was less
complete. ATP was reduced to 78% of control and CP was reduced in the immediate
post clamp period to 32% of control.
The differences are particularly significant
if one looks at patients whose aortic cross clamp time was ≥90 minutes
(12 patients). In this group, ATP and CP preservation was 71% (3.33/4.60 m
moles/kg, wet weight) and 53% (1.48/2.81) respectively 30 min. after clamp
removal. (p≤.01)
Conclusion: Hypothermic potassium cardioplegia
gives excellent preservation of the myocardial ultrastructure in humans.
However, the preservation of high energy phosphates with this technique is
imperfect.
*By invitation