1:30 p.m. SIMULTANEOUS SCIENTIFIC SESSION A
-ADULT CARDIAC SURGERY
Ballroom, Ernest N. Morial
Convention Center
Moderators: Floyd D. Loop, M.D.
Eric A. Rose, M.D.
7. Aortic Rupture after Aortic
Valve Surgery in Women
Monica L. McDonald*,
Nicholas G. Smedira*, Bruce W. Lytle and Delos M. Cosgrove, Cleveland, Ohio
Discussant: Robert J. Rizzo,
M.D., Boston, MA
OBJECTIVE: To examine
mortality in women after surgery for aortic regurgitarion (AR) and the
contribution of aortic rupture to that mortality.
METHODS: 109 women
underwent aortic valve replacement (AYR, n=92) or repair (n=17) for pure AR,
1985-96. In 59, concomitant aortic surgery (AOS) was performed by root
replacement (n=31) or interposition graft (n=28). Of 50 undergoing isolated
procedures, 31 had aortas >3.5 cm. The prevalence of larger aortas increased
with age (P=.02). Mean follow-up was 5.7±2.6 yrs.
RESULTS: At 5 and 10 yrs,
survival was 78% and 44%. 13 died of aortic rupture or sudden death and 3
underwent emergent operation for aortic rupture, 16 late aortic events (AE).
Freedom from AE was 86% and 75% at 5 and 10 yrs. Risk factors for AE were older
age (P=.07) and increasing ascending aorta diameter (P=.03) in women who had
not undergone AOS. Rupture location was ascending aorta in 71% without AOS, and
descending aorta in 56% with interposition grafts.
CONCLUSIONS: Late
mortality following surgery for AR in women is due in part to aortic rupture.
The figure depicts the risk of rupture according to AA size normalized to BSA
and age, offering guidance for management of high-risk patients.

*By Invitation
8. Aortic Valve Replacement: Is Valve
Size Important?
Benjamin Medalion*, Eugene H.
Blackstone, Bruce W. Lytle, Delos M. Cosgrove, and Jennifer White*, Cleveland,
Ohio
Discussant: Friedrich W Mohr,
Leipzig, Germany
OBJECTIVE: To determine if
patient-valve size mismatch affects long-term survival.
METHODS: We followed 892
patients (pts) up to 20 years (mean 5±3.9 years) after primary, isolated aortic
valve replacement who had received either 1) a mechanical prosthesis (St. Jude,
SJM, n=346); 2) a bovine pericardial valve (Carpentier-Edwards, CE, n=463); or
3) a cryopreserved allograft (ALLOG, n=83). Mean BSA was 1.86±0.23, range
1.15-2.57m2. 19mm prostheses were used in 19%. Multivariable analysis
was focused on the Z-value for valve size, defined as the patient-specific
number of standard deviations the internal prosthesis diameter departs from
predicted normal aortic annulus size based on that individual's body surface
area.
RESULTS: Internal Z-value
ranged from -4.4 to +6.8, with 25% <-2. SJM valves had the smallest Z-value
(-2.2±1.0), CE valves -0.5+0.99, and ALLOG the largest (0.2±1.4). Survival was
96%, 86%, 69%, and 49% at 1, 5, 10, and 15 years. Risk factors for death
included older age, emergency surgery, endocarditis, coronary artery disease,
and comorbidities, but no effect of valve size Z-value for any valve type
(P>.2), in early, constant, and late hazard phases.
CONCLUSIONS: Survival
after aortic valve replacement appears not to be adversely affected by mismatch
between prosthesis valve size and body size down to at least -4 SDs below
normal valve size.
*By Invitation
9. Minimally-Invasive Reoperative
Aortic Valve Replacement Reduces Blood Loss and Transfusion Requirements
John G. Byrne*, Sary F. Aranki,
Gregory S. Couper* and Lawrence H. Cohn, Boston, Massachusetts
Discussant: William A. Gay,
Jr., M.D., St Louis, MO
OBJECTIVE: We developed
techniques for minimally-invasive (min-inv) reoperative (reop) aortic
valve replacement (AVR), using an upper hemi-re-sternotomy, and compared
the results to reop AVR using conventional (conv) full re-sternotomy.
METHODS: We
retrospectively analysed 19 conv & 20 min-inv isolated elective reop AVRs,
performed between 11/96-9/98.
RESULTS: Age, sex, FC, EF,
previous operations, and Aprotinin® use were not different between
groups. Multivariate analysis determined that conv approach predicted greater
blood loss, transfusion needs and longer operative (op) duration (Table).
|
Table (multivariate analysis)
|
Conv, n=19
|
Min-inv, n=20
|
|
|
Deaths/Valve Morbidity
|
0/19 (0%)
|
0/20(0%)
|
|
|
Injury to Patent CABGs
|
1/19 (5%)
|
0/20 (0%)
|
|
|
Bypass Duration (min)
|
145±53
|
146±52
|
|
|
Aortic Clamping Duration
(min)
|
|
|
|
|
(3 full root replacements
in each group)
|
92±32
|
93±48
|
|
|
Total Operative Duration
(hours)
|
5.8±1.2
|
5.4±1.2*
|
*p=0.15
|
|
Blood Loss (ml) 1st 24
hours
|
1071±629
|
472±362
|
p=0.01
|
|
Transfusions (units) PRBC
|
5.2±2.4
|
3.013.0
|
p=0.10
|
|
Hospital Charges ($)
|
63K±15K
|
55K±20K
|
|
|
Length of Stay (days)
|
7.9±4.9
|
6.9±2.6
|
|
CONCLUSIONS: Min-inv reop
AVR avoids unnecessary lower mediastinal dissection, thereby reducing (1) blood
loss, (2) transfusion needs and (3) total op duration. Patent CABGs may be less
prone to injury. These beneficial effects, accomplished without compromising
the valve procedure, make min-inv upper hemi-re-sternotomy superior to conv
full re-sternotomy for reop AVR.
*By Invitation
10. Mitral Valve Repair and Replacement
for Rheumatic Disease
Terrence M. Yau*, Susan
Armstrong*, Joan Ivanov*, Yasser A. Farag El-ghoneimi* and Tirone E. David,
Toronto, Ontario, Canada
Discussant: Alain F.
Carpentier, M.D., Paris, France
OBJECTIVE: Repair of
rheumatic mitral valves (MVs) has generally been associated with poor long-term
results. We undertook this study to define the early and late results of
surgery for rheumatic MVs.
METHODS: From 1978 to
1995, 575 patients (pts) underwent surgery for rheumatic MVs. Demographics and
operative data were recorded prospectively. Followup was 97.7% complete (mean
67.5±45.7 mos). Survival and morbidity were evaluated univariately by
Kaplan-Meier analysis and multivariately by Cox regression.
RESULTS: Mean age was
53.7±14.2 years, 80.5% of pts were female, 54.7% had congestive failure, 23.6%
were undergoing redo MV surgery, and 9.7% also underwent coronary bypass.
Mitral stenosis was present in 52.5%, regurgitation in 15.4%, and both in
32.1%. Valve repair (REP) was performed in 24.4%, 27.5% had replacement with a
bioprosthesis (BIO) and 48.0% had a mechanical valve (MECH).
Operative mortality was 4.1%. Ten-year survival was: REP
88.2±0.04%, BIO 70.2±0.04%, MECH 73.4±0.06% (p=0.0002). Mortality was predicted
by age, NYHA class, coronary disease, and reoperation.
Ten-year freedom from reoperation was: REP 72.0±0.05%,
BIO 69.0±0.05%, MECH 95.3±0.02% (p=0.005). Type of prosthesis predicted
reoperation after replacement. 23 pts underwent reoperation after initial
repair, with no operative deaths.
Ten-year freedom from thromboembolic complications was:
REP 92.5±0.02%, BIO 93.3±0.02%, MECH 71.6±0.07% (p<0.0001).
CONCLUSIONS: Mechanical
valves minimize reoperation but limit survival and are prone to
thromboembolism. Bioprostheses and repaired valves both have good freedom from
thromboembolism and poor freedom from reoperation, but patients selected for
valve repair had better late survival.
Patients with rheumatic MVs
should have repairs whenever technically feasible, accepting a risk of late
reoperation, to maximize survival and reduce morbidity.
*By Invitation
11. Influence of Size 19mm Aortic Valve
Replacement on Survival
David H. Adams*,
Raymond H. Chen*, Sary F. Aranki, Elizabeth N. Allied* and §Lawrence
H. Cohn, Boston, Massachusetts
Discussant: Donald B. Doty,
M.D., Salt Lake City, UT
OBJECTIVE: Does valve size
influence early and late clinical outcomes in patients ≥ 70 years of age
undergoing aortic valve replacement?
METHODS: Between 12/91 and
7/98 408 patients ≥ 70 years of age (median age 77, range 70-97,50% male)
underwent isolated AVR or AVR combined with CABG, utilizing either Carpentier-Edwards
bovine pericardium valves (n=300) or St. Jude mechanical valves (n=108).
Univariate methods were used to examine potential confounders (age ≥ 75,
sex distribution, body mass index, CABG, re-operation, hypertension, myocardial
infarction, renal failure, COPD, stroke, diabetes mellitus, congestive heart
failure, aortic stenosis, prolonged ischemia/ bypass times) among patients
receiving a small (19mm) or a large (≥ 21mm) aortic valve. Multivariate
logistic regression methods were used to predict operative mortality and
multivariate proportional hazards regression methods were used to predict late
death (median follow-up 22 months) related to 19mm valve replacement after
controlling for potential confounders.
RESULTS: Operative
mortality was 16% (18/111) for size 19mm valve replacement, 5.8% (8/138) for
21mm valve replacement, and 2.5% (4/159) for ≥ 23mm valve replacement (p
≤.0005). The unadjusted odds ratio for operative death for 19mm vs.
≥ 21mm valves was 4.6 (95% CI:2.1,9.9; p ≤.0005). In the final
multivariate model adjusted for potential confounders, small valve size
remained a significant predictor of operative death (OR 4.2, 95% CI:1.8,9.8;
p=.001). 19mm valve usage, however, did not predict late death in either the
univariate analysis (HR 0.96,95% CI:0.5,1.9;p=.92) or the multivariate analysis
(HR 0.6, 95% CI:0.3,1.4; p=.25).
CONCLUSIONS: Implantation of a 19mm aortic valve in a
patient ≥ 70 years of age appears to be an independejnt risk factor for
operative mortality, but does not impact on late death.
3:15 p.m. INTERMISSION - VISIT EXHIBITS
1992-94 AATS Research Scholar
§Authors have a relationship with St. Jude
Medical & Medtronic
*By Invitation
4:00 p.m. SIMULTANEOUS SCIENTIFIC SESSION A
-ADULT CARDIAC SURGERY
Ballroom, Ernest N. Morial
Convention Center
Moderators: Floyd D. Loop, M.D.
Eric A. Rose, M.D.
12. Hospital Readmission following
Cardiac Surgery: Prevalence, Patterns and Predisposing Factors
Richard S. D'Agostino*, Jerilynn
P. Jacobson*, Lars G. Svensson*, Christina Williamson* and David M. Shahian,
Burlington, Massachusetts
Discussant: Timothy J. Gardner,
M.D., Philadelphia, PA
OBJECTIVE: In this study,
we examine the incidence of readmission within the 30-day period following
hospital discharge after cardiac surgery, the reasons for readmission and
pre-discharge factors that predispose to readmission.
METHODS: Pre, intra and
postoperative clinical data were prosepctively collected for 1027 patients
undergoing coronary bypass, valve replacement or combined bypass/valve surgery
between 1/1/96 and 7/30/97. Thirty-day data was collected at the time of office
visit or by telephone and/or written survey.
RESULTS: 163 (15.8%)
patients were readmitted to a hospital within the 30-day period following
discharge. The clinical problems that prompted read-mission were as follows:
dysrhythmia=27 (16.5%), congestive heart failure/ dyspnea/pulmonary
edema/pleural effusions=34 (20.8%), chest pain/rule out myocardial
infarction=17 (10.4%), wound infection/problem=14 (8.5%), gastrointestinal
problem=7 (4.3%), stroke/TIA=2 (1.25%), pneumonia or other non-wound
infection=14 (8.5%), deep venous thrombosis or pulmonary embolus=8 (4.9%),
peripheral vascular problem=7 (4.2%), anemia/hypotension/transfusion=12 (7.4%)
and miscellaneous problems=22 (13.5%). Stepwise logistic regression analysis
(Hosemer and Lemeshow Goodness-of-Fit chi square= -5.85; df=8; p=0.6631) showed
that advancing age (p=0.04), increasing body mass index (p=0.0032), combined
valve/bypass surgery (p=0.0003), longer cardiopulmonary bypass (p=0.0013) and
crossclamp time (p=0.000), and longer postoperative length of stay (p=0.005) predispose
to readmission.
CONCLUSIONS: Readmission
within 30 days of discharge after cardiac surgery is a relatively common event.
Some patients appear to be at greater risk for readmission and future efforts
should focus on risk reduction strategies for these patients. Interestingly,
shorter hospital stays do not appear to impact adversely on the risk of
readmission.
*By Invitation
13. Mid-term Follow-up of Patients who had
LVAD Removal following Cardiac Recovery in End-stage Dilated Cardiomyopathy
Roland Hetzer, Johannes H.
Mueller*, Yu-guo Weng*, Thorsten Drews*, Matthias Loebe* and Gert Wallukat*,
Berlin, Germany
Discussant: Eric A. Rose, M.D., New York, NY
OBJECTIVE: Cardiac
recovery in end-stage dilated cardiomyopathy (DCM) was demonstrated after temporary
LVAD support. However, the durability of such recovery has remained a matter of
dispute. We report on our patients who had removal of LVAD up to 3-1/2 years
ago.
METHODS: Since 3/1995, 21
patients with end-stage DCM who had been supported by LVAD (19 Novacor, 2 TCI)
for periods of between 1 and 26 months (mean 6 months)had their LVAD removed
following complete or near complete cardiac recovery as documented by
echocardiography (LVEF, LVIDd) at time of pump-off trials.
RESULTS: Six patients
(group A) suffered recurrence of cardiac failure after between 4 and 24 months.
Transplantation was successfully performed in five, one died on the waiting
list, four patients died from reasons unrelated to cardiac failure after
between 3 days and 29 months. Stable cardiac recovery has been enjoyed by 11
patients (group B) for between 6 and 41 months (mean 20±6). At time of LVAD
implant, there were no differences between groups A and B as to age, duration
of heart failure, invasive hemodynamic values, LVEF, LVIDd, amount of
apoptosis, TNF-u., b-receptor density, and level of autoanti-bodies. However,
the degree of cardiac recovery at the time of pump explan-tation was
significantly better in group B (A vs. B; LVEF 40±5 % vs. 48±4 % p < 0.01;
mean LVIDd 62±6 mm vs. 53±5 mm, p<0.01).
CONCLUSIONS: In a
selective group of patients with end-stage DCM complete and lasting cardiac
recovery may be achieved after ventricular unloading with LVAD. At present, no
reliable pre-LVAD-implant indices have been recognized that would allow
prediction of the degree of recovery after implant. However, lasting cardiac
recovery seems to be related to complete normalization of cardiac function
during the unloading period.
*By Invitation
14. Choice of Non-transplant Cardiac
Surgical Procedures for End-stage Cardiomyopathy
Hisayoshi Suma, Tadashi Isomura*,
Taiko Horii*, Toru Sato* and Norio Kikuchi*, Kamakura, Kanagawa, Japan
Discussant: Steven F. Bolling, M.D., Ann Arbor,
MI
OBJECTIVE: To treat
end-stage cardiomyopathy, endoventricular circular patch plasty (EVCPP),
partial left ventriculectomy (PLV) and solo-valvular reconstruction (VR) have
been proposed. To find a proper choice of those non-transplant cardiac
procedures, we evaluated our 2 years results of those procedures and introduce
echo-guided volume reduction test.
METHODS: From December
1996 to September 1998, 68 patients with end-stage cardiomyopathy (27 ischemic
and 41 non-ischemic) underwent EVCPP±CABG/VR, PLV1VR or Solo±VR. Preoperative
characteristics is shown in Table. For ischemic cardiomyopathy, EVCPP(Dor
procedure) was used for all patients. In non-ischemic group, Group I indicates
early 24 patients treated with PLV±VR (mostly replacement) and Group II
includes recent 17 patients treated with different types of procedures depends
on intraoperative volume reduction test which observes changes of LV size, wall
motion and thickness before and after CPB by echography. When the LV became
smaller and the wall increased thickness entirely with LV decompression,
solo-VR (mostly annuloplasty) was chosen and if akinetic thin wall remained,
PLV or EVCPP was added according to the site of akinesis.
RESULTS: Hospital
mortality was acceptably low in elective operations in each group whereas the
risk was high inongoing shock patients needed emergency operation (Table). With
colume reduction test, mortaily reduced from 12% to 0% in non-ischemic group.
|
Etiology
|
Ischemic
|
Non-ischemic
Group I
|
Non-ischemic
Group II
|
No. of Patients
|
27
|
24
|
17
|
|
Male/Female (Age)
|
21/6(63±7)
|
19/5(48±15)
|
15/2(51±13)
|
|
NYHA class (Pre-»Post)
|
3.3→1.3
|
3.6→1.7
|
3.3→1.2
|
|
EF (%) (Pre-»Post)
|
23→38
|
18→31
|
23→38
|
|
EDVI (mi/m2)
(Pre->Post
|
160→103
|
203→99
|
162→119
|
|
ESVI (mi/m2)
(Pre-»Post)
|
118→72
|
164→70
|
121→82
|
|
Hospital Death
|
|
|
|
|
elective op.
|
1/22(5%)
|
2/17(12%)
|
0/15(0%)
|
|
emergency op.
|
3/5(60%)
|
6/7(86%)
|
1/2(50%)
|
|
Late Death
|
3/27(11%)
|
4/24(17%)
|
1/17(6%)
|
|
IABP/LVAD
|
0/0
|
6/0
|
0/1
|
CONCLUSIONS: EVCPP is
favorable for ischemic cardiomyopathy because septal exclusion is effective.
Volume redution test is useful to choose an optimal procedure for non-ischemic
cardiomyopathy to avoid excessive LV excision.
*By Invitation
15. Passive Ventricular Constraint With
the Acorn Prosthetic Jacket Prevents Progressive Left Ventricular Remodeling
and Functional Mitral Regurgitation in Dogs With Moderate Heart Failure
Pervaiz A. Chaudhry*, Gaetano
Paone*, Victor G. Sharov*, Takayuki Mishima*, James Hawkins*, §Clif
Alferness* and §Hani N. Sabbah*, Detroit, Michigan
Sponsored By: Norman A.
Sttverman, Detroit, Michigan
Discussant: Gerald D. Buckberg,
M.D., Los Angeles, CA
OBJECTIVE: The purpose of
this study was to determine if passive mechanical constraint of the cardiac
ventricles with a surgically placed prosthetic jacket prevents progressive left
ventricular (LV) remodeling and attenuates functional mitral regurgitation (MR)
in dogs with moderate heart failure (HP).
METHODS: HF (LV ejection
fraction 30-40%) was produced in 12 dogs by multiple sequential intracoronary
microembolizations. Six dogs underwent mid-sternotomy and pericardiotomy
followed by placement of the prosthetic jacket (a preformed-knitted polyester
mesh, Acorn Cardiovascular, Inc.) snugly around the ventricles and anchored at
the AV groove. Six untreated HF dogs served as controls (CON). LV end-diastolic
(EDV) and end-systolic (ESV) volumes and the presence and severity of
functional MR were determined angiographically before (PRE) and 3 months after
(POST) treatment. Cardiomyocyte cross-sectional area (CCSA), a measure of
myocyte hypertrophy, was assessed histomorphometrically.
RESULTS: In CON dogs, EDV
increased 15±5 ml between PRE and POST but decreased 7±1 ml in dogs treated
with the Acorn prosthetic jacket (P=0.002). Similarly, ESV increased 17±5 ml in
CON dogs but decreased 9±1 ml in dogs treated with the jacket (P=0.001). In CON
dogs, 4 of 6 had 1+ to 2+ MR that persisted and/or increased after 3 months of
follow-up. In contrast, 4 of 6 surgically treated dogs had 1+ to 2+ MR that was
completely abolished after 3 months. In dogs treated with the prosthetic
jacket, the average CCSA area was smaller than in CON (791+51 vs. 987±37 mm2,
p=0.011).
CONCLUSIONS: Passive
ventricular constraint with the Acorn prosthetic jacket prevents progressive LV
remodeling and abolishes functional MR in dogs with moderate HF.
§Authors have a relationship with Acor
Cardiovascular, Inc.
*By Invitation
1:45 p.m. SIMULTANEOUS SCIENTIFIC SESSION B
-
GENERAL THORACIC SURGERY
Room 211-213, Ernest N. Morial
Convention Center
Moderators: Thomas R. J. Todd, M.D.
Steven J. Mentzer, M.D.
16. Secondary Pulmonary Hypertension Does
Not Adversely Affect Outcome After Single Lung Transplant.
Scott Huerd*, Frederick L. Grover,
James R. Mault*, Max B. Mitchell*, David N. Campbell, Fernando Torres*, Paul
Chetham*, Tony Hodges* and Martin Zamora*, Denver, Colorado
Discussant: Vaughn A. Starnes, M.D.,
Los Angeles, CA
OBJECTIVE(s): Elevated
pulmonary artery pressures (PAP) have been associated with poor outcomes in
patients undergoing SLT. Some groups advocate double lung transplant or the
routine use of cardiopulmonary bypass (CBP) for SLT in this population. These
recommendations remain controversial. The goal of our study was to determine
whether secondary PHTN requires CPB and adversely affects outcomes following
SLT.
METHODS: We
retrospectively reviewed 76 consecutive SLT performed from 1992-98. Patients
with primary PHTN and Eisenmenger's syndrome were excluded. Recipients were
stratified according to preoperative PAP (PA systolic pressure > 40mm Hg);
58 had low PAP and 18 high PAP (13 with COPD or A1AT deficiency, 5 with
idiopathic pulmonary fibrosis).
RESULTS: No patient in the
high PAP group required CPB or inhaled nitric oxide (iNO) intraoperatively.
Postoperatively, no significant differences were seen in length of stay (LOS,
14.6 ±.9 vs.ll.9±1.5 days), 30 day survival (95 vs 89%) or lung injury as
measured by CXR score or PaO2/FiO2 or the need for iNO (5(8.6%) in the low and
2(11.1%) in the high group) in the low versus high groups respectively (p=NS).
There were also no differences in FEV1 or six minute walk at 1 and 2 yrs or in
the incidence of acute rejection, infection or BOS>grade 2. Survival at 1,
2, and 4 yrs posttransplant was 85,79, and 71% in the low group and 78, 78, and
67% in the high group (p=NS).
CONCLUSIONS: Our data
demonstrate that secondary PHTN is not associatied with significantly increased
morbidity, mortality, or LOS after SLT and that double lung transplant or the
routine use of CPB are not necessary for patients with pulmonary parenchymal
disease and secondary PHTN.
*By Invitation
17. Hyperthermic Pleural Perfusion with
Cisplatinum -Preliminary and Midterm Results
Yael Refaely*, David A. Simansky*,
Michael Paley* and Alon Yellin*, Tel Hashomer, Israel
Sponsored By: John R. Benfield,
Los Angeles, California
Discussant: TBA
OBJECTIVE: Intrapleural
chemotherapy and hyperthermia have been investigated separately for the
treatment of pleural tumors or rumors with pleural extension . The aim of this
study is to conduct a phase I and n study of operation, chemotherapy and
hyperthermia in one session for the treatment of pleural cancers.
METHODS: Since 1994, 26
pts with the following underlying conditions had intraoperative HPF:Thymoma-11,
Mesothelioma-8, others-6. Technique of per-fusion was: Use extracorporal
circuit and heat exchanger, circulating the pleural space with 1000-2500 ml/min
of Ringer lactate. Cisplatinum (60mg-2 pts, 100mg-2,120mg-1,150mg-18,200mg-3
pts) was added when the inrrapleural temperature stabilized (mean- 40.8ºc). The
associated operations were: extended extrapleural pneumonectomy-8, resection of
rumor with pleurectomy -10, resection of rumor without pleurectomy -4,
exploration and HPF only -4( Thora-cotomy-2, VATS-2).
RESULTS: There were no
technical problems during the perfusion period. The maximal systemic
temperature reached 38ºc. There were no renal or hematological toxicity except
one case of thrombocytopenia. One pt died from complications developing after
herniation of the stomach through the sutured diaphragm. Additional
complications were: bleeding which required re-thoracotomy-1 pt;empyema-3(early-2,
late-1); prolonged air leak -2; atrial fibrillation -1. Median postoperative
stay was 7 days (range 2-50). four pts died 6-15 months following HPF from
systemic disease progression. Two of them had contralateral or peritoneal
spread without local reccurence. 20 are alive 1-47 months after surgery. 1-year
survival is 81%. 2 and 3-years survival is 70%.
CONCLUSIONS: Intraoperative
HPF including cisplatinum was adequately safe. Finding to date show that this
method offers excellent local control for pleural cancers.
*By Invitation
18. Surgical Treatment of Lung Cancer with
Synchronous Brain Metastasis
Peter S. Billing*, Daniel L.
Miller*, Mark S. Allen, Claude Deschamps, Victor F. Trastek, and Peter C.
Pairolero, Rochester, Minnesota
Discussant: Joseph I. Miller, Jr., M.D., Atlanta,
GA
OBJECTIVE: Although
resection of primary lung cancer and metachronous brain metastasis is superior
to other treatment modalities in prolonging survival, resection of primary lung
cancer and synchronous brain metastasis is controversial.
METHODS: From January 1975
to December 1997, 220 patients received treatment at our institution for
synchronous brain metastasis and primary non-small cell lung cancer.
Twenty-seven of these patients (12.3%) underwent staged surgical resection of
solitary synchronous brain metastasis and primary non-small cell lung cancer.
RESULTS: There were 18 men
and 9 women. Median age was 56 years (range, 35-71). Twenty-four patients
(88.9%) presented with neurological symptoms. Craniotomy was performed first in
all 27 patients. Median time between craniotomy and thoracotomy was 13 days
(range, 4-67 days). Lobectomy was performed in 21 patients, bilobectomy in 3,
and pneumonectomy in 3. There were no operative deaths. Cell type was adenocarcinoma
in 11 patients, squamous cell in 8, and large cell in 8. At the time of the
pulmonary resection, 14 patients had no evidence of lymph node metastases, 6
had hilar metastases and 7 had mediastinal metastases. Twenty-two patients
(81.5%) received adjuvant therapy: whole brain radiation (WBR) alone in 15;
WBR/systemic chemotherapy in 4; and WBR, chest radiation and systemic
chemotherapy in 3. Follow-up was complete in all patients for a median of 22
months (range, 2-104 months). Median survival was 18.5 months (range, 2-104).
Actuarial survival at 1, 2 and 5 years was 60%, 36% and 20%, respectively.
CONCLUSIONS: The survival
for patients who present with brain metastasis from lung cancer is poor.
However, a therapeutic plan including staged resection of synchronous solitary
brain metastasis followed by pulmonary resection can be beneficial in a select
group of patients.
*By Invitation
19. Chest Wall Resection for Recurrent
Breast Carcinoma
Robert J. Downey*, Valerie Rusch,
F. Ida Hsu*, David Linehan*, Manjit S. Bains, and Robert J. Ginsberg, New York,
New York
Discussant: Mark S. Allen,
M.D., Rochester, MN
OBJECTIVE: To define
safety and efficacy of resection of bony thorax for recurrent breast carcinoma
METHODS: Retrospective
chart review. Survival by Kaplan-Meier, prognostic factors by log rank/Cox
regression, p significant if ≤0.05
RESULTS: During
10/87-4/97, 41 women (med age 56yrs) underwent resection of sternum
(2), ribs (17), or sternum/ribs (22). Operative mortality 0%, resection rate
80%. Skeletal reconstruction: MMMM(35), MM(2), Gore-tex (1), other/no material(3).
Median skin defect 110 cm2 (range 0-448). Soft tissue closure:
primary(10), pedicled flap(26), microvascular flap(4), combination(l). At last
FU, 24 patients were without local recurrence, 14 with local recurrence, and 3
status unknown. Synch mets, + margins, + lymph nodes, size largest nodule, #
nodules, or bony invasion did not correlate with local recurrence. Synch mets,
+ margins, + lymph nodes, (but not size largest nodule, no. nodules, or bony
invasion) correlated with survival.
|
Survival after chest wall
resection for recurrent breast cancer
|
|
|
1 YEAR
|
3 YEAR
|
5 YEAR
|
OVERALL
|
97%
|
97%
|
67%
|
|
SYNCHRONOUS METASTASES
|
94%
|
94%
|
50%
|
|
NO SYNCHRONOUS METASTASES
|
100%
|
100%
|
77%
|
CONCLUSIONS:
1. Resection/reconstruction of
the bony thorax for recurrent breast carcinoma is safe
2. Survival and local control
following resection are favorable, even if distant metastases present
3:05 p.m. INTERMISSION - VISIT EXHIBITS
*By Invitation
3:50 p.m. SIMULTANEOUS SCIENTIFIC SESSION B
-
GENERAL THORACIC SURGERY
Room 211-213, Ernest N. Morial
Convention Center
Moderators: Thomas R. J. Todd, M.D.
Steven J. Mentzer, M.D.
20. The Current Role of Mediastinoscopy in
the Evaluation of Thoracic Diseases
Zane T. Hammoud*, Bryan F.
Meyers*, Tracey J. Guthrie*, Joel D. Cooper, Charles L. Roper and G. Alexander
Patterson, St. Louis, Missouri
Discussant: Douglas E. Wood,
M.D., Seattle, WA
OBJECTIVE:
Mediastinoscopy(med) is a commonly employed procedure utilized for the
diagnosis of thoracic disease and the staging of lung cancer. We sought to
re-evaluate the safety and efficacy of med in an academic thoracic surgical
program.
METHODS: We conducted a
retrospective review of all patients undergoing med on our service between 1/88
and 8/98.
RESULTS: We performed med
on 2069 patients during the study period, including 1909 cervical meds, 62
anterior mediastinotomies, and 98 combined procedures. A total of 1668 patients
underwent med for known or suspected lung cancer. In 427(26%) of these, N2 or
N3 disease was identified; only 29(7%) of these patients underwent resection,
with a 5 yr. survival of 25%. In 1241(74%) of patients with suspected lung
cancer, med was negative; all of these patients underwent exploration. In these
patients, 954(77%) had lung cancer. Only 74(8%) of the lung cancer patients
were found to have N2 disease at exploration; the 5 yr. survival in this group
was 24%. Among the 1241 patients with a negative med, 71(6%) had a
non-bronchogenic malignancy and 216(17%) had resection of what proved to be a
benign lesion. In 156 patients, the med proved positive for a non-bronchogenic
malignancy. Evaluation of mediastinal aden-opathy in the absence of any
identifiable intrathoracic tumor in 245 patients led to a definitive diagnosis
in 218(89%). In the entire group of 2069 patients, we observed 4(0.2%)
perioperative deaths and 10(0.5%) complications. Only one death was attributed
to med(tumor invading the aorta). No deaths or complications occurred in
patients undergoing med for benign disease.
CONCLUSIONS:
Mediastinoscopy is a highly effective and safe procedure. We believe that
mediastinoscopy should currently be used routinely in the diagnosis and staging
of thoracic diseases.
*By Invitation
21. Bronchoplastic Procedures in Malignant
and Non-Malignant Disease - Results of 144 Cases
Adelheid End*, Peter Hollaus*,
Andreas Pentsch*, Michael Mueller*, Ernst Wolner and Franz Eckersberger*,
Vienna, Austria
Discussant: Thomas R. J. Todd, MD., Toronto,
Ontario, Canada
OBJECTIVE(s): We present
our experience with bronchoplastic procedures in a seven year period.
METHODS: Data from 144
patients who underwent bronchoplastic surgery between 1991 and 1997 were
collected retrospectively. There were 110 men and 34 women, mean age was 59±9
years (range, 26 - 79 years). Indication for surgery was primary lung cancer
(n=130), metastases (n=4) and carcinoid tumors (n=10). Full bronchial sleeve
resections were performed in 108 cases, bronchial wedge resections in 28 and
sleeve pneumonectomies in 8 cases; 103 procedures were done on the right (72 %)
and 41 on the left side (28%). In 15% (n=21) an angioplasty and in 3, 5% (n=5)
resection of the thoracic wall was performed. In 3 extended resections
cardiopulmonary bypass was used. 61% of patients presented with cardiovascular
risk factors, 62% were smokers and 64% had chronic pulmonary obstruction.
RESULTS: 30-day mortality
was 8 %. Causes of death were cardiac failure and myocardial infarction (n=3),
pulmonary embolism (n=2), hepatorenal failure (n=1), stroke (n=1), pneumonia
(n=3), gastrointestinal bleeding (n=1) and mesenteric infarction (n=1). Major
complications consisted of anastomotic dehiscence in 5 cases beyond the 30th
postoperative day, 4 of them died, rethoracotomy for bleeding (n=3) and empyema
(n=3). The presence of cardiac risk factors, chronic obstructive disease,
N2-disease, R1-resection and performance of sleeve pneumonectomy had an adverse
influence on survival (p<0.05).
CONCLUSIONS:
Bronchoplastic procedures have evolved as an alternative to pneumonectomy in
high-risk patients with centrally located tumors or in non-malignant disease.
However, our mortality rate of 8 % demonstrates that patients should be
selected carefully assessing their preoperative risk profile.
*By Invitation
22. M1a/M1b Esophageal Carcinoma: Surgical
Relevance
Neil A. Christie*, Thomas W. Rice,
Malcolm M. DeCamp *, John R. Goldblum*, David J. Adelstein*, Lisa A. Rybicki*
and Eugene H. Blackstone, Cleveland, Ohio
Discussant: Mark J. Krasna,
M.D., Baltimore, MD
OBJECTIVE: The 1997
staging system for esophageal carcinoma subdivides distant metastatic disease
(M1) into M1a (non-regional lymph node metastases) and M1b (visceral
metastases). This study evaluates the clinical relevance of this
classification.
METHODS: From our
prospective esophageal database, 141 patients (pts) were identified with M1
disease, 37 (26%) with M1a and 104 (74%) with M1b. Histology was adenocarcinoma
in 119 (84%) pts, squamous cell in 18 (13%) and adenosquamous in 4 (3%), with a
similar distribution for Mia and M1b (P=.3). Forty-seven pts underwent surgery.
Of these, 29 (78%) were M1a and 18 (17%) M1b (P<.001). Medical therapy
(chemotherapy and/or radiation therapy) was given to 99 (70%) pts; 31 (84%) Mia
and 68 (65%) M1b (P=.04).
RESULTS: Median and 5-year
survival were 11 months and 6% for Mia pts, and 5 months and 2% for M1b pts
(P=.002). Surgery provided no evident advantage in M1b and a small benefit
after 12 months in Mia. Multivariable analysis demonstrated that M1b pts had
1.7 times the risk of death of M1a pts (CI 1.1-2.5, P=.009), and pts without
medical therapy had 2.2 times the risk of those with medical therapy (CI
1.5-3.2, P<.001). Despite the high prevalence of surgery for M1a disease,
the analysis suggests that M1a and use of medical therapy, rather than surgery per
se, account for the small and clinically unimportant differences in
survival.
CONCLUSIONS: We conclude
that: 1) although there are statistically significant survival differences
between M1a and M1b pts, these differences are not clinically important; 2)
medical therapy is associated with a modest survival benefit; and 3) surgery
offers no advantage in the treatment of these pts.
*By Invitation
23. The Role of Positron Emission
Tomography in Evaluating the Mediastinum in Patients with Non-Small Cell Lung
Cancer
Tracey L. Weigel*, Carolyn C.
Meltzer*, David Friedman*, Robert J. Keenan, Peter F. Person* and James D.
Luketich*, Pittsburgh, Pennsylvania
Discussant: Kemp H. Kernstine,
M.D., Iowa City, IA
OBJECTIVE: Currently,
mediastinoscopy with histologic nodal examination is the gold standard for
preoperative assessment of the mediastinum. Positron Emission Tomography (PET)
is a new, noninvasive tool that differentiates malignant from benign processes
based upon metabolic status rather than anatomic structure. This study compares
the accuracy of PET and CT scanning, as compared to histology, in staging the
mediastinum in patients with NSCLC.
METHODS: Histologic
examination of mediastinal lymph nodes (MLNs) was performed on 34 patients with
NSCLC by multi-station lymph node sampling at mediastinoscopy and/or
mediastinal lymph node dissection at surgical resection. PET scans were read by
a single radiologist, blinded to histologic assessment, using CT scans for
anatomic localization. CT scans were independently assessed for mediastinal
lymphadenopathy.
RESULTS: The overall
accuracy, sensitivity, and specificity for PET in the determination of
metastases to the mediastinum was better than CT when compared to histologic
findings (see table). PET scan staging, however, correlated poorly with
histologic MLN staging; R=0.553, (p=0.001).
|
Scan
|
Accuracy
|
Sensitivity
|
Specificity
|
|
PET
|
85.3%
(29/34)
|
80% (4/5)
|
86.2%
(25/29)
|
|
CT
|
58.8%
(20/34)
|
60% (3/5)
|
58.6%
(17/29)
|
CONCLUSIONS: PET scanning
appears to be more accurate than CT for staging the mediastinum in patients
with NSCLC. However, PET imaging still fails to identify 20% of
histologically-proven MLN metastases. At present, mediastinoscopy should remain
the standard of care for pre-operative staging of the mediastinum in patients
with NSCLC.
*By Invitation
24. Primary Mediastinal Nonseminomatous
Germ Cell Tumors: The Influence of Postchemotherapy Pathology On Long-Term
Survival After Surgery
Kenneth A. Kesler*, Karen
M. Rieger*, Kristen N. Ganjoo*, Matt Sharma*, Naomi S. Fineberg*, Lawrence H.
Einhorn* and John W. Brown, Indianapolis, Indiana
Discussant: Scott J. Swanson,
M.D., Boston, MA
OBJECTIVE(s): Treatment of
nonseminomatous germ cell tumors (NSGCT) with cisplatin based chemotherapy (CT)
followed by surgical resection of residual disease, represents a successful
model for multimodaliry cancer therapy. We reviewed 104 Pts from 1981 to 1997
with primary mediastinal NSGCT to evaluate variables which may influence
survival following surgery.
METHODS: 27 (26%) Pts did
not undergo post-CT resection due to progression during CT (n=25) or had a
complete response after CT (n=2). 77 Pts (74%) underwent 80 resections and were
further analyzed with respect to multiple variables including pre and post CT
pathology and serum tumor markers (STM). All were male between 12 and 49 yrs
(mean=28). The majority (95%, 69/73) had elevated STM, 44 of which (64%)
demonstrated normalization after primary or secondary CT. 21 Pts (27%) had
extra-mediastinal disease at presentation.
RESULTS: The finding of
tumor necrosis in the resected specimen (n=16) predicted excellent survival
which was significant compared to teratoma (n=26), sarcomatous degeneration
(n=6) or persistant NSGCT pathologies (n=44). The finding of teratoma predicted
significantly better survival than persistent NSGCT. No other variable was
significantly predictive.
CONCLUSIONS: Primary NSGCT
of the mediastinum can be cured with a multimodality approach. Post-CT
pathologic findings of tumor necrosis and teratoma predict excellent and
intermediate long-term survival respectively. Survival is poor but possible in
patients suspected of unfavorable pathology following CT, justifying an
aggressive surgical approach.

ADJOURN
*By Invitation
1:45 p.m. SIMULTANEOUS SCIENTIFIC SESSION C
- CONGENITAL HEART DISEASE
Room 208-210, Ernest N. Mortal
Convention Center
Moderators: John J. Lamberti, M.D.
John A. Waldhausen, M.D.
25. Revision of Previous Fontan
Connections to Total Extracardiac Cavopulmonary Anastomosis: a Multicenter
Study
Carlo F. Marcelletti, Frank L.
Hanley, Constantine Mavroudis, Mohan V. Reddy*, Raul F. Abella*, Stefano M.
Marianeschi*, Francesco Seddio*, Marco Meli*, Fiore S. lorio* and Francis
Fontan, Bordeaux, France, Chicago, Illinois, Modena, Italy and San Francisco, California
Discussant: John E. Mayer,
M.D., Boston, MA
OBJECTIVE: Conversion of
modified Fontan procedure to a total extracardiaccavopulmonary connection
(TECPC)has been proposed as an alternative surgical treatment of pts who showed
manifestation of surgical failure. The aim of the present multicenter study is
to evaluate the midterm outcome after conversion.
METHODS: Between Oct'92
and Sept'98, 24 pts (mean age 21, 1 yrs; range 10-39) underwent revision of the
atriopulmonary connection to TECPC in 4 different Institutions. In these pts
who have received previously an atriopulmonary connection, complications due to
right atrial enlargement were: Fontan pathway obstruction(10), progressive
CHF(16), atrial dysrhythmias(19), RA thrombus(2),obstruction of right pulmonary
veins(6), subAo stenosis(1), protein losing enteropathy(PLE)(2)and
effusions(6). Conversion to a TECPC was carried out with a non-valved conduit
from the IVC to RPA.PTFE tube graft was used in 18 pts, homograft conduit in 3
pts and Dacron tube in 3 pts.
RESULTS: Three deaths
occurred: 1 pt with severe cachexia, in whom transplantation was
controindicated for social reasons, died in the early postoperative period of
massive effusions. The second patient died for irreversible heart failure
during the operation and the third pt died at home 8 months postop for
arrhythmia. All surviving pts have improved to NYHA class I (16 pts)or II (4
pts) except 1 pt in NYHA class IV who underwent OHTX. Postop arrhythmias
occurred in 10 pts:4 pts underwent PMK implantation and in 6 pts medical
therapy was sufficient to manage the symptoms. Two pts with PLE improved within
30 days.
CONCLUSIONS: Conversion of
failing previous Fontan procedure to TECPC can be accomplished with a low
mortality and it appears to be a viable option. However the revision should be
undertaken early in symptomatic pts before irreversible ventricular failure
ensues.
*By Invitation
26. Repair of the Truncal Valve and
Associated Interrupted Arch in Neonates with Truncus Arteriosus
Marjan Jahangiri*, David
Zurakowski*, Pedro J. Del Nido, John E. Mayer and Richard A. Jonas, Boston,
Massachusetts
Discussant: Edward L. Bove, M.D.,
Ann Arbor, MI
OBJECTIVE: Truncal valve
regurgitation and interrupted aortic arch have frequently been identified as risk
factors in the repair of truncus asteriosus. We wished to examine these factors
in the current era including the impact of truncal valve repair.
METHODS: Between 1992 and
August 1998, 50 patients underwent surgical repair of truncus asteriosus. Their
ages ranged from 2 days to 6 months (median, 2 weeks). Nine patients had
associated interrupted aortic arch. Of the 14 patients (28%) who were diagnosed
to have truncal valve regurgitation pre-operatively, five underwent truncal
valve repaid and one underwent homograft replacement of the truncal valve with
coronary reimplantation.
RESULTS: The acturial
survival was 96% at 30 days, 1 year and 3 years. There were no deaths in
patients with associated interrupted aortic arch. The two deaths in the series
occurred in patients with truncal valve regurgitation, neither of whom
underwent repair. Postoperative transthoracic echocardiography in patients who
underwent valve repair showed minimal residual valvar regurgitation. None of
the patients have required reoperation for truncal valve problems or aortic
arch stenosis at a mean follow-up of 22 months. Conduit replacement has been
performed in 17 patients (34%) after a mean duration of 2 years. The freedom
from reoperation for those who had an aortic homograft was 4 years and for
those who had pulmonary homograft was 3 years.
CONCLUSIONS: Despite the
magnitude of surgery, excellent results can be achieved in complex forms of
truncus arteriosus. In the current era interrupted aortic arch is no longer a
risk factor for repair of truncus. Aggressive application of truncal
valvuloplasty methods neutralize the traditional risk factors of truncal valve
regurgitation.
*By Invitation
27. Five To Fifteen Year Follow-Up of
Fresh Autologous Pericardial Valved Conduits
Andres J. Schlichter*, Christian
Kreutzer, Rita C. Mayorquim*, Jorge L. Simon*, Maria I. Roman*, Haydee
Vazquez*, Eduardo A. Kreutzer* and Guillermo O. Kreutzer*, Buenos Aires,
Argentina
Sponsored by: Richard A Jonas,
Boston, Massachustts
Discussant: William G.
Williams, M.D., Toronto, Ontario, Canada
OBJECTIVE: To evaluate the
long term results of an autologous pericardial valved conduit (APVC) in the
venous ventricle outflow tract.
METHODS: Between 1983 and
1993, 82 conduits were placed in the subpulmonary position. Patients receiving
homografts(n=2), heterografts(n=3) or valveless conduits(n=19) and dying within
90 days were excluded. Thus, 54 late survivors of venous ventricle outflow
reconstruction with a fresh bicuspid APVC were followed from 5 to 15 years with
a median of 7 years. Yearly evaluations by two dimensional echo Doppler were
made and 9 patients had cardiac catheterization. Diagnosis include
D-transposition of the great arteries (n=16), L-transposition of the great
arteries(n=14), Tetralogy of Fallot(n=11), Truncus arteriousus(n=10) and double
outlet right ventricle(n=3). Mean age at implantation was 2.9 ± 6.3 years(2
months to 24 years). Cath or surgical intervention was indicated when the
gradient exceed 50 mm Hg.
RESULTS: In 27 patients
the APVC increased its diameter (1 to 7 mm), in 20 it remained unchanged and a
reduction of 1 mm was noted in 4. Median conduit diameter at implantation was
16 mm and was 17.5 mm at last evaluation.(p=0.0001) Freedom from reintervention
at 5, and 10, years was 89% and 80%. Freedom from reintervention was 100% at 10
years for conduits larger than 16 mm at the time of implantation and it was 85%
at 5 years and 72% at 10 years for those 16 mm or less. The valve had good
function in the first six months but late failure without obstruction. Conduit
related reoperation was required only in 6 cases between 4.5 and 10 years after
implantation and 2 patients underwent balloon dilation of APVC. There were 3
late deaths caused by arrhythmia, sepsis and brain tumor.
CONCLUSIONS: Pericardial
valved conduits show excellent results and compare favorably to those of other
conduits.
2:45 p.m. INTERMISSION - VISIT EXHIBITS
1998-99
AATS Graham Fellow
*By Invitation
3:30 p.m. SIMULTANEOUS SCIENTIFIC SESSION C
-
CONGENITAL HEART DISEASE
Room 208-210, Ernest N. Morial
Convention Center
Moderators: John J. Lamberti, M.D.
John A. Waldhausen, M.D.
28. Pre-Surgical Risk-of-Death Prediction
Model in Neonatal Repair of Congenital Heart Disease
Robert R. Clancy*, Susan A.
McGaurn*, James E. Coin*, Gil Wernovsky*, Thomas L. Spray, William I. Norwood,
Marshall L. Jacobs*, John D. Murphy*, Deboral G. Hirtz* and J. William Gaynor*,
Bethesda, Maryland, Browns Mills, New Jersey, Media, Pennsylvania,
Philadelphia, Pennsylvania and Wilmington, Delaware
Discussant: Marc R. de Leval,
M.D., London, U.K.
OBJECTIVE: To generate a
pre-surgical risk-of-death prediction model in a population of neonates with
congenital heart disease (CHD) undergoing surgery with deep hypothermic
circulatory arrest (DHCA).
METHODS: We completed a
single-center, prospective, randomized, double-blind, placebo-controlled
neuroprotection trial in a population of neonates with CHD requiring surgical
repair or palliation utilizing DHCA. An extensive 5,500 item database was generated
and included pre-surgical, intra- and post-operative variables. Stepwise
logistic regression evaluated 49 presurgical variables (delivery, maternal
& infant related factors) producing a risk prediction model.
RESULTS: Between 7/92 and
9/97, 350 of 481 eligible infants were enrolled of whom 317 were deemed
evaluable cases. The overall mortality was 52 of 317 (16.4%), unaffected by the
investigational drug. The resulting model contained information on 4
presurgical categories: (i) cardiac anatomical classification (two vs single
ventricle, with/without arch obstruction), (ii) 1 min. Apgar score (≤5 vs
>5), (iii) presence of named genetic syndrome or chromosomal abnormality and
(iv) age at hospital admission for surgery (≤5 or >5 days). Mortality
for two ventricle repair was 4 of 129 (3.1%). Mortality for single ventricle
palliation was 48 of 188 (25.5%) but this rate was significantly increased by
the presence of low Apgar score, genetic diagnosis and older age at admission.
The logistic regression model based on the 4 categories resulted in a
prediction accuracy of 81%.
CONCLUSIONS: In this
population, much of the force of mortality is determined by conditions that
exist pre-operatively. The identification of high risk subgroups may impact
family counseling, therapeutic intervention and risk stratification for future
study designs, (funded by NIH contract NS-NO1-2315)
*By Invitation
29. Simplified Single Patch Technique for
the Repair of Atrioventricular Septal Defect
Ian A. Nicholson*, Graham R.
Nunn*, Gary F. Sholler*, Richard E. Hawker*, Stephen G. Cooper* and Kai C.
Lau*, Westmead, Australia
Sponsored By: Lawrence H. Cohn,
M.D., Boston, Massachusetts
Discussant: John W. Brown,
M.D., Indianapolis, IN
OBJECTIVE: Due to the
complexity of traditional one and two patch techniques for the repair of
complete atrioventricular septal defect we modified our repair technique to
avoid the use of any ventricular septal patch material. We report our
prospective experience with this simplified one patch technique.
METHODS: Forty seven
consecutive patients between September 1995 and August 1998 underwent repair
using this technique without modification. All patients were repaired by direct
suturing of the common atrioventricular valve leaflets to the crest of the
ventricular septum . No division of valve leaflets was necessary. A single
pericardial patch was used to close the defect in the atrial septal component.
Follow-up included electrocardiography and echocardiographic assessment of
ventricular function, AV valve function and the adequacy the left ventricular
outflow tract.
RESULTS: There were two
deaths (4%), only one cardiac related, in the series. There were 17 males and
30 females. Mean age at repair was 5.6 months (median 3.4 months). Associated
lesions were repaired in 19 patients (40%). Mean follow-up was 1.85 years (
median 1.9 years). There was no heart block. There were no significant residual
ventricular septal defects detected and no left ventricular outflow tract
obstruction seen on echocardiography in any patient to date. Mitral valve
status post-operatively was assessed as no incompetence in 13 (28%) patients ,
minimal in 19 (40%), mild in 12 (26%) and moderate in 3 (6%).
CONCLUSIONS: Therepair
of complete atrioventricular septal defect by direct suturing of the
atrioventricular valve leaflets to the crest of the ventricular septum using a
single patch technique greatly simplifies the repair and does not lead to left
ventricular outflow tract obstruction nor interfere with valve function.
*By Invitation
30. Lung Transplantation in Very Young
Infants
Charles Burford Huddleston, George
B. Mallory*, Stuart C. Sweet*, Aaron Hamvas* and Eric N. Mendeloff*, St. Louis,
Missouri
Discussant: Thomas L, Spray,
M.D., Philadelphia, PA
OBJECTIVE(s): There are
rare congenital pulmonary parenchymal and pulmonary vascular diseases that
occur in infants resulting in the death of these otherwise normal infants even
with aggressive medical therapy. In these circumstances, lung transplantation
(LTX) offers the only effective treatment.
METHODS: We reviewed our
experience with LTX in infants presenting at less than 6 months of age with
either end-stage pulmonary parenchymal or pulmonary vascular disease. 25
infants were listed for LTX at an average age of 67 ± 52 days (range = 8-169
days). All were mechanically ventilated and 18 had been so since birth; 12
infants required ECMO and 5 others required high frequency oscillating
ventilator prior to transplantation. 7 patients died while awaiting donor
organs and thus 18 were transplanted, forming the basis for this review.
RESULTS: The average age
at transplant was 104 ± 44 days; the average weight was 4.9 ± 1.6 kg. There
were 6 early deaths. The 12 surviving hospitalization were ventilated 24 ± 21
days and had an average post-LTX hospital stay of 58 ± 33 days. The followup
for these survivors is 2.6 ±1.8 years (range = 0.5-5 years). Transbronchial
biopsies as part of a surveillance protocol or due to clinical indications
revealed only 2 episodes of acute rejection (A2 or greater) and only one
patient out of the 12 early survivors (8%) has developed bronchiolitis
obliterans over an average followup of 2.6 ± 1.8 years. One required
re-transplantation for severe respiratory failure following sepsis. Somatic
growth has been at eh 20th percentile for length and 25th percentile for
weight. There have been 2 late deaths for an overall survival of 56%.
CONCLUSIONS: Although high
risk, LTX for infants with end-stage pulmonary parenchymal and pulmonary
vascular disease is feasible. Acute rejection and bronchiolitis obliterans have
not posed significant problems in early followup.
*By Invitation
31. Improved Results with Selective
Management in Pulmonary Atresia with Intact Ventricular Septum
Marjan Jahangiri*, David
Zurakowski*, David P. Bichell*, John E. Mayer, Pedro J. Del Nido and Richard A.
Jonas, Boston, Massachusetts
Discussant: Frank L. Hartley, M.D.,
San Francisco, CA
OBJECTIVE: Late outcome of
neonatal pulmonary atresia with intact ventricular septum remains poor in most
reported series. We have followed a selective approach towards either single
ventricle repair versus complete or partial biventricular repair based on the
presence of right ventricular dependent coronary circulation (RVDCC) and growth
of the RV.
METHODS: Forty seven
patients underwent surgery between January 1991 and September 1998.
RESULTS: Sixteen (34%)
patients had RVDCC with a tricuspid valve Z score of -3.0+.66 versus -2.0+.95
(p=0.002) for those without RVDCC. A systemic to pulmonary artery shunt only
was performed in all patients with RVDCC with one death. Thirteen of the
sixteen patients with RVDCC underwent a bidirectional Glenn at a median time of
9 months after their first operation, nine of whom have had a Fontan procedure
(no death). One patient has had a 1.5-ventricle repair. In the 31 (66%)
patients without RVDCC, 6 patients underwent a systemic to pulmonary artery
shunt only, 23 had a shunt and right ventricular decompression and 2 had only a
transannular patch. In this group, 10 patients received a 2-ventricle repair, 6
a 1.5-ventricle repair and 8 patients had a Fontan procedure. The overall
actuarial survival was 97.7% at 1 month, 1 year, 5 years and 7 years.
CONCLUSIONS: If stratified
well, excellent survival can be achieved in the treatment of pulmonary atresia
with intact ventricular septum. This may be at the price of achieving a
1-ventricle as opposed to a 2-ventricle repair.
*By Invitation
32. Repair of Ebstein's Anomaly Associated
with Bidirectional Cavopulmonary Shunt in High Risk Patients
Sylvain Chauvaud*, Jean Francois
Fuzellier*, Alain Berrebi* and Alain Carpentier, Paris, France
Discussant: Jan M. Quaegebeur, M.D.,
New York, NY
OBJECTIVE: Patients
suffering from Ebstein's anomaly and severely impaired right ventricular (RV)
function often present with difficult postoperative course. The aim of this
study is to report the use of bidirectional Cavopulmonary shunt (BCPS)
associated with intracardiac repair in this high risk group.
METHODS: Since 1980, 125
patients (pts) have been operated on for Ebstein's anomaly. Only 3 pts had a
tricuspid valve (TV) replacement and 122 had an intracardiac repair (ICR) using
Carpenrier's technique. Among the later group, 67 pts were classified as high
risk because of severe RV dysfunction and/or severe arrhythmia. This cohort was
divided into 2 groups: GI (45 pts) had isolated ICR and Gil (22 pts) had ICR
associated with BCPS. All pts had the same preoperative clinical pattern and
age (mean 22y). The ICR was identical in all patients (TV repair and RV plication).
The a trial septal defect when present was closed.
RESULTS: Operative
mortality was 9.8% in the whole group, 24.4% in GI (CL 95%: 13-43) and 0% in
Gil (CL 95%: 0-18) p<0.05. The main cause of mortality in GI was RV failure
(5/11 deaths). Significant residual or recurrent TV insufficiency was present
in 12% of both groups. However, the need for a reoperation was more frequent in
GI: 11% (5/45) than in Gil: 0%, due to RV preload reduction. No deleterious
effect of the BCPS was observed.
CONCLUSIONS: Bidirectional
Cavopulmonary shunt associated with intracardiac repair decreased the operative
mortality in high risk patients suffering from Ebstein's anomaly. It improved
clinical tolerance of occasional residual TV insufficiency.
*By Invitation