(Circulation. 1999;100:171-177.)
© 1999 American Heart Association, Inc.
Clinical Investigation and Reports |
From the Mayo Clinic and Mayo Foundation (C.S.R., H.V.S., D.R.H.), Rochester, Minn; the University of Pittsburgh (K.S.-T., P.G.), Pittsburgh, Pa; New York Medical Center (N.M.K.), New York, NY; the Institute for Clinical and Experimental Medicine (R.J.), Prague, Czech Republic; and Duke Clinical Research Institute (M.A.S.), Durham, NC.
| Abstract |
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Methods and ResultsWe analyzed outcomes of 550 patients with PVD enrolled in the Bypass Angioplasty Revascularization Investigation randomized trial and registry. Compared with 1770 patients without PVD, those with PVD were older and had a greater prevalence of medical comorbid conditions. No significant differences in coronary anatomy or PTCA success rates were found. The risk of any major complication (death, myocardial infarction, stroke, coma, or emergency revascularization) after PTCA was significantly higher among patients with PVD (11.7% versus 7.8%, P=0.027). In multivariate analysis, this represented a 50% increase in the odds of having any major complication (multivariate odds ratio, 1.5; P=0.032). Among patients undergoing CABG, the risk of major complications was found to be markedly higher for patients with PVD (12%) than those without (6.1%, P=0.003) even after controlling for baseline differences (multivariate odds ratio, 1.8; P=0.018). Major differences between the PTCA and CABG groups were related primarily to a higher risk of neurological complications in PVD patients who had CABG (multivariate odds ratio, 2.8; P<0.001).
ConclusionsWe conclude that patients with PVD are at high risk for periprocedural complications after myocardial revascularization, in particular neurological events.
Key Words: angioplasty grafting coronary disease peripheral vascular disease revascularization
| Introduction |
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Patients with systemic coexisting disease, such as peripheral vascular disease (PVD), renal insufficiency, or cancer, are at increased risk for periprocedural complications and have poorer long-term outcomes than those without PVD.3 4 Few recent data are available describing periprocedural risks of myocardial revascularization among patients with vascular disease.5 6 7 The purpose of the present analysis was to examine periprocedural risks of CABG surgery and PTCA among patients with PVD enrolled in the Bypass Angioplasty Revascularization Investigation (BARI).
| Methods |
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This report is based on 1783 patients drawn from the randomized trial (56 of 1829 randomized patients either did not receive their assigned treatment or had missing PVD data) plus 1808 patients drawn from the registry who underwent nonrandomized PTCA or CABG within 3 months after enrollment. For the purpose of this analysis, PVD was defined as either atherosclerosis of the lower extremities or extracranial cerebrovascular disease. Atherosclerosis of the lower extremities was considered to be present if there was a history of lower-extremity vascular surgery, abdominal aortic aneurysm, or intermittent claudication. Extracranial cerebrovascular disease was considered to be present if there was a history of stroke, transient ischemic attacks, carotid endarterectomy, or carotid artery disease documented by the presence of bruits, duplex ultrasonography, or angiography.
Long-term follow-up (average, 5.4 years) has been performed, and
information relating to vital status, myocardial infarction, angina
pectoris, or repeat revascularization procedures
has been collected. Ascertainment of vital status is 98% complete.
Successful PTCA was defined as improvement in coronary artery
diameter stenosis of
20%, with a final residual
stenosis <50% and Thrombolysis in Myocardial
Infarction (TIMI) grade III flow, in the absence of a major
complication. Myocardial infarction was defined as the presence of new
pathological Q waves, in accordance with the Minnesota code, or
development of new left bundle-branch block, with abnormal cardiac
enzyme levels. ECG and coronary angiographic analyses
(except registry patients) were performed at core laboratories. Cause
of death and occurrence of myocardial infarction were adjudicated by
committee review. The University of Pittsburgh was the coordinating
center for the BARI study, including data management and statistical
analysis.
Statistical Methods
Demographic and baseline clinical characteristics were compared
for patients with and those without PVD by treatment strategy.
Student's t test or the Wilcoxon test was used to
compare continuous distributions.
2 tests were
used to compare proportions. Because of the small number of individual
in-hospital events in each patient group, Fisher's exact tests were
used to compare in-hospital complication rates. In addition, 3
composite variables were defined. These were "major events"
(death/myocardial infarction/stroke/coma), "major events including
emergency revascularization" (death/myocardial
infarction/stroke/coma/emergency
revascularization), and "neurological events"
(stroke/coma/transient ischemic attack/dementia).
Logistic regression was used to assess the likelihood of an in-hospital complication associated with treatment strategy, adjusting for other risk factors. Multivariate models were developed for the combined population of randomized and registry patients as well as for randomized patients alone. For both models, covariates included age, sex, treated diabetes mellitus at baseline, history of congestive heart failure, and blood pressure. To control for possible treatment selection bias among registry patients, a variable created by logistic regression and indicating the likelihood of undergoing CABG on the basis of baseline characteristics was also included in the model ("propensity score").
| Results |
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Baseline coronary anatomic characteristics are tabulated in
Table 2
. There were few differences
between patients with PVD and those without PVD. Mean ejection fraction
was 56.7% to 58.3% in all groups, and 16% to 21% had an ejection
fraction <50%. The distribution of 1-, 2-, and 3-vessel
coronary artery disease was not different, nor were the mean
numbers of lesions per patient or the numbers of chronic total
occlusions. In the PTCA group, the myocardial jeopardy index was
slightly lower for those without PVD than for those with PVD (58.3
versus 60.6, P=0.030). No difference in the distribution of
American College of Cardiology/American Heart
Association class A, B, or C lesions was found between groups.
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Patients Undergoing PTCA
PTCA success rates were only slightly lower for patients with PVD:
567 of 663 (85.5%) target lesions in patients with PVD were dilated
successfully. In comparison, 3220 of 3671 (87.7%) target lesions in
patients without PVD were dilated successfully (P=0.117).
Abrupt closure of the dilated vessel occurred in 4.8% of lesions in
patients with PVD and in 4.0% of lesions in patients without PVD.
Specific reasons for PTCA were identifiable in 228 lesions (46%
failure to cross, 52% failure to dilate, 2% not attempted for
clinical reasons).
In-hospital procedural complication rates are tabulated in Table 3
. In comparison with 1770 patients
without PVD, the 316 patients with PVD who had PTCA had a greater
incidence of death (2.2% versus 0.6%, P=0.012) but not of
Q-wave myocardial infarction (2.5% versus 2.5%). Sixteen of 18 deaths
were cardiac in nature. The incidence of major neurological
complications was low, regardless of the presence or absence of PVD.
Nonetheless, the incidence of any major complication (death, myocardial
infarction, stroke, coma, or emergency
revascularization) was significantly higher among
patients with PVD than those without PVD (11.7% versus 7.8%,
respectively, P=0.027). Because patients with PVD had higher
baseline risk profiles, age, sex, diabetes mellitus, congestive heart
failure, and blood pressure were controlled for with
multivariate analysis. In
multivariate analysis, the odds of having any
major complication after PTCA were >50% greater for patients with PVD
(multivariate odds ratio, 1.5; P=0.032) than
for those without PVD.
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Patients Undergoing CABG
Two hundred thirty-four patients with PVD and 1271 without
PVD underwent CABG. The incidence of death or Q-wave myocardial
infarction (9.4% versus 5.5%, P=0.036) was significantly
higher in the presence of PVD. Similarly, the risk of major
neurological complications (stroke, coma, transient ischemic
attack, or dementia) was significantly higher in the presence of PVD
(4.7% versus 1.2%, P=0.001), even after controlling for
baseline patient differences (multivariate odds ratio,
2.8; P<0.001). Among patients with PVD, the risk of
neurological complications after CABG was especially high in the
presence of carotid atherosclerosis (6.2% versus 1.3%
with lower-extremity vascular disease, P<0.001).
Neurological complications after CABG occurred both with and without
previous neurological symptoms (incidence, 2.1% and 1.7%,
respectively). The overall risk of any major complication (death,
myocardial infarction, stroke, coma) after CABG was markedly higher for
patients with PVD (12% versus 6.1% [P=0.003];
multivariate odds ratio, 1.8
[P=0.019]).
Multivariate Logistic Regression Analysis
in Patients With PVD
Results of multivariate regression of predictors
of periprocedural complications among patients with PVD are
presented in Table 4
. Congestive
heart failure and renal dysfunction (serum creatinine
>1.5) were particularly powerful correlates of complications,
especially procedural mortality. Multivariate odds
ratios of death were 5.30 (95% CI, 1.26 to 22.29) if there was a
history of congestive heart failure and 13.45 (95% CI, 3.07 to 58.90)
in the presence of an increased creatinine level.
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Among all patients with PVD, the risk of major complications, including death, myocardial infarction, stroke, coma, or emergency revascularization, was similar whether patients had PTCA or CABG (11.7% versus 12.0%; multivariate odds ratio, 1.0; 95% CI, 0.6 to 1.7). Excluding emergency revascularization, however, patients treated with CABG were at greater risk (12% CABG versus 4.4% PTCA; multivariate odds ratio, 3.32; 95% CI, 1.58 to 6.95). The major differences were higher observed rates of periprocedural myocardial infarction (7.3% CABG versus 2.5% PTCA) and neurological complications (stroke, coma, transient ischemic attack, dementia) after CABG in comparison with PTCA (4.7% versus 0.3%; multivariate odds ratio, 13.99; 95% CI, 1.76 to 111.05). These differences were not seen among the randomized trial subset, however, and should be interpreted with caution. Wide CIs associated with the multivariate odds ratios were found and were due primarily to the relatively low number of observed events.
Among the 550 patients with PVD, 12 major neurological events (stroke, coma, transient ischemic attack, dementia) occurred, 10 of which occurred in patients with identifiable extracranial cerebrovascular disease. In contrast, for patients without PVD, no difference in the incidence of neurological complications was observed whether patients were treated with CABG or PTCA (1.2% versus 0.6%, P=NS), indicating that the risk is attributable almost entirely to the presence of PVD.
| Discussion |
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That the risks of coronary
revascularization are significantly higher among
patients with PVD is not unexpected. These patients tend to be older,
more frequently are smokers, and have
1 major medical coexisting
conditions. However, even after multivariate
analysis controlling for age and coexisting medical conditions,
the presence of PVD remained an independent marker of periprocedural
risk. Interestingly, coronary angiographic findings did not
differ significantly by presence or absence of PVD (at least for the
qualitative variables that could be described). Coronary
angiography may have been insensitive in disclosing abnormalities of
the vessel wall that may have predisposed to complications such
as acute myocardial infarction or abrupt closure. The presence of
systemic atherosclerosis may indicate more advanced,
aggressive, and high-risk vascular disease, including that of the
coronary arterial bed, but this hypothesis remains
unproved.
The present study extends previous observations of neuropsychiatric morbidity after CABG.12 13 Among patients receiving CABG, the presence of PVD correlated with an extraordinarily high risk of stroke. Such patients frequently have atherosclerosis of the ascending aorta and extracranial cerebral vessels, which correlates with a high prevalence of demonstrable systemic atheroembolism at autopsy.14 The increased incidence of neurological complications after cardiopulmonary bypass and CABG most likely represents a combination of factors, including inherent risk in aortic cannulation in these patients, relatively poor intracranial cerebral perfusion pressure, and atheroembolism.
The present study also has implications for the subset of patients with coronary artery disease undergoing noncardiac procedures. Patients scheduled for peripheral vascular surgery, in particular, are frequently referred for coronary angiography with selective coronary revascularization in an attempt to reduce the risks of subsequent noncardiac surgery.15 16 17 Decision analyses have suggested that coronary angiography before vascular surgery only be performed when the risk of vascular surgery is relatively high (>5%) and the anticipated risk of coronary angiography plus selective revascularization is relatively low (<3%).18 19 Our data would suggest that recommendations to proceed with coronary angiography before noncardiac surgery be made cautiously and not be carried out as a matter of routine clinical practice, but a prospective, randomized trial is needed to address this issue definitively.
Since the BARI study was performed, new revascularization techniques such as rotational atherectomy, intracoronary stents, or minimally invasive surgical approaches to CABG, in which cannulation of the ascending aorta is not required, have been introduced. Whether these newer percutaneous and surgical techniques will result in a lower risk of periprocedural complications among patients with PVD remains to be determined.
Strengths and Limitations
Conclusions drawn on the basis of these data are strengthened by
the detailed and careful prospective enrollment of patients as well as
the prospective surveillance for complications patients had as part of
the main study. Several limitations to these data exist. First, because
nonrandomized registry patients were included and baseline
randomization (in the trial) was not stratified according to the
presence of vascular disease, conclusions pertaining to comparisons
between PTCA and CABG treatments should be drawn with caution. Second,
patients with single-vessel disease were excluded from enrollment.
Thus, these data may not be generalizable to those patients, who may
have a lower intrinsic risk of procedural complications. Third, as
mentioned above, although this was a relatively recent cohort, advances
in both CABG and PTCA techniques have not only continued but even
accelerated. Fourth, although no gross coronary anatomic
differences between patients with and those without PVD were
documented, angiography is limited by the ability to visualize only the
lumen of vessels, and it is possible that more severe mural disease of
the coronary arteries or diffuse mural disease was not
appreciated. Despite some inherent limitations, our data
represent the largest recent series of relatively unselected
patients with PVD undergoing myocardial
revascularization. The presence of PVD was
prospectively searched for and identified, minimizing
misclassification, selection bias, and major problems with post hoc
analyses.
Conclusions and Recommendations
In multivariate analysis, patients with
PVD had a significantly higher risk of major periprocedural
complications after either CABG or PTCA than patients without PVD.
These risks should specifically be taken into account before treatment
recommendations are made. In counseling of individual patients, these
data aid in the assessment of cumulative risk-benefit ratios. Among
patients with PVD, myocardial revascularization may
remain indicated if the higher short-term risks are outweighed by
future anticipated benefits. Additional clinical research is needed to
further define such risks and benefits.
| Footnotes |
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Received May 28, 1998; revision received April 7, 1999; accepted April 22, 1999.
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PTCA was higher among 316 patients with peripheral vascular
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patients with PVD are at high risk for periprocedural complications
after myocardial revascularization.
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