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ACC/AHA
Guideline Update for Perioperative Cardiovascular Evaluation
for Noncardiac Surgery
A
Report of the American College of Cardiology/American
Heart Association Task Force on Practice Guidelines
(Committee to Update the 1996 Guidelines on Perioperative
Cardiovascular Evaluation for Noncardiac Surgery)
X.
Postoperative and Long-Term Management
It
has been recognized since the early 1980s that cardiac
events are a frequent outcome in postoperative vascular
surgery patients (358).
Over the course of the last decade, advances
in preoperative, intraoperative, and postoperative management
have resulted in better patient outcomes in noncardiac
(especially vascular) surgery (359,360).
This is due to a number of factors that involve better
detection of underlying CAD in preoperative patients,
as well as greater skill and experience in the perioperative
care of such patients. The combination of improved medical
therapy, which typically includes beta blockers, aspirin,
and lipid-lowering agents, and coronary revascularization
in appropriate cases should result in improved event-free
survival.
Despite
optimal perioperative management, some patients will
experience perioperative MI, which is associated with
a 40% to 70% mortality (361).
The reason for the high mortality is undoubtedly multifactorial
and related in part to significant comorbidity in such
patients. However, the inability to administer reperfusion
therapy undoubtedly contributes to the high mortality
associated with MI early after noncardiac surgery.
Many
perioperative MIs are a result of a sudden thrombotic
coronary occlusion, as is the case with MI that occurs
in the nonoperative setting (362,363).
Among eligible patients, rapid reperfusion therapy is
the cornerstone of therapy (364).
Thrombolytic therapy markedly reduces mortality when
administered to patients who have MI unrelated to a
surgical procedure. However, because of the substantial
risk of bleeding at the surgical site, patients who
have recently undergone surgery have been excluded from
all trials of thrombolytic therapy, and recent surgery
is generally considered a strong contraindication to
thrombolytic therapy. Although thrombolytic therapy
has been administered to patients for life-threatening
pulmonary embolus shortly after noncardiac surgery,
the thrombolytic dosage has generally been less and
has been administered over a longer time interval than
is standard for the treatment of acute MI (365,366).
Immediate coronary angioplasty has been favorably compared
with thrombolytic therapy in the treatment of acute
MI (367),
but of greater importance is that the risk of bleeding
at the surgical site is believed to be less with direct
angioplasty than with thrombolytic therapy. Only a single
small study (368)
has evaluated the role of immediate angiography and
angioplasty among 48 patients who were believed able
to take aspirin and intravenous heparin, and to undergo
immediate angiography and PCI. This study suggested
that such a strategy is feasible and may be beneficial.
However, time to reperfusion is a critical determinant
of outcome in acute MI, and any hope of benefiting patients
who have a perioperative acute MI due to an acute coronary
occlusion requires that angiography and revascularization
be rapidly performed (i.e., within 12 hours of symptom
onset) (368,369).
In addition, these reperfusion procedures should not
be performed routinely on an emergency basis in postoperative
patients in whom MI is not related to an acute coronary
occlusion. For instance, in cases of increased myocardial
demand in a patient with postoperative tachycardia or
hypertension, lowering the heart rate or blood pressure
is likely to be of greater benefit, and certainly less
risk. There is also no evidence to support immediate
angiography in patients found to have an elevated cardiac
marker, such as CK-MB band or cardiac troponin, who
are otherwise clinically stable.
Although
reperfusion therapy is an important therapy in acute
ST-segment-elevation MI, the emphasis on reperfusion
therapy should not detract from pharmacological therapy,
which is also very important and has been shown to reduce
adverse events in such patients, as well as in patients
with non-ST-elevation acute coronary syndromes. Therapy
with aspirin, a beta blocker, and an ACE inhibitor,
particularly for patients with low ejection fractions
or anterior infarctions, may be beneficial, whether
or not the patients are rapidly taken to the catheterization
laboratory (370).
An extensive evidence-based review of therapy for acute
MI can be found in the ACC/AHA guidelines for the management
of patients with acute MI (370).
Although not intended specifically for patients who
have a postoperative MI, they are nonetheless appropriate
for these high-risk patients. Similarly, the ACC/AHA
guidelines for unstable angina represent an important
template for management of this condition in the postoperative
setting (371).
In
the approach to the long-term postoperative management
of noncardiac surgery patients, one should first appreciate
that the occurrence of an intraoperative nonfatal MI
carries a high risk for future cardiac events that are
often dominated by cardiovascular death
(214,372).
Therefore, patients who sustain acute myocardial injury
in the perioperative or postoperative period should
receive careful medical evaluation for residual ischemia
and overall left ventricular function. The ACC/AHA guidelines
for post-MI evaluation in these types of patients should
be followed as soon as possible after surgical recovery.
The use of pharmacological stress (26)
or dynamic exercise (if feasible)
for risk stratification should also be a priority in
patients to help determine who would benefit from coronary
revascularization. In all cases, the appropriate evaluation
and management of complications and risk factors such
as angina, HF, hypertension, hyperlipidemia, cigarette
smoking, diabetes (hyperglycemia), and other cardiac
abnormalities should commence before hospital discharge.
It is also important to communicate these new observations
and determinations of cardiac status and risk to the
physician who will be responsible for arranging subsequent
medical care and follow-up.
It
is also appropriate to recommend secondary risk reduction
in the relatively large number of elective-surgery patients
in whom cardiovascular abnormalities are detected during
preoperative evaluations. Although the occasion of surgery
is often taken as a specifically high-risk time, most
of the patients who have known or newly detected CAD
during their preoperative evaluations will not have
any events during elective noncardiac surgery. A recent
review
(261)
of a national Medicare population
sample identified a cohort of patients (n=6895) who
underwent elective vascular surgery during a 17-month
period in 1991 and 1992. The authors noted a relatively
high mortality rate (15%) at 1 year of follow-up among
patients who did not undergo preoperative stress testing.
However, in those patients (19%) undergoing preoperative
stress testing with or without coronary bypass surgery,
the mortality rate was lower (less than 6%). In other
follow-up studies (372,373)
of vascular surgery patients who
were followed up for a mean of 40 to 48 months, cardiac
events were significantly more frequent in those who
had a reduced LVEF of less than 35% or 40% and who demonstrated
ischemia of at least moderate size on dipyridamole-thallium
imaging. Therefore, it is important to consider which
preoperative clinical risk factors and noninvasive testing
parameters can be used to help predict long-term cardiac
risk.
Most
of the long-term follow-up studies in postoperative
patients involve vascular surgery. Figure
3 summarizes some large follow-up studies in patients
undergoing major vascular surgery who were followed
up over the next 2 to 5 years for subsequent cardiac
death or MI. It is clear that preoperative clinical
risk assessment as determined by the Goldman criteria,
LVEF, coronary angiography, dipyridamole-thallium imaging,
and dobutamine echocardiography can also be used to
evaluate long-term cardiac risk. Cardiac mortality in
the postoperative period increases with higher clinical
risk, lower LVEF (less than 35%), multivessel CAD, abnormal
thallium scans, or multiple ischemic segments on dobutamine
echocardiography studies. Other studies (374-376)
also confirm the value of semiquantitative
analysis of myocardial perfusion imaging when using
these types of perioperative tests to predict future
cardiac events. All these studies have the ability to
combine an assessment of myocardial ischemia and left
ventricular function into a more useful clinical index.
It
is clear from these and other imaging studies
(377-379)
that the extent of ischemia or
reduced ventricular function achieves the best level
of prognostic utility for future cardiac events. Overall,
a normal or near-normal stress imaging study suggests
a relatively small risk, but the positive predictive
accuracy of abnormal studies is greatly enhanced by
the establishment of a progressive gradient for that
abnormality.
Although
the perioperative cardiac event rate for renal and liver
transplantation is fairly low, the long-term risk for
MI or cardiovascular death associated with such transplants
often results in referrals for preoperative cardiac
consultation and testing. Compared with the data for
long-term follow-up in vascular surgery patients, the
results in renal and liver transplants are somewhat
less compelling. Not all publications support the routine
use of cardiac screening to help stratify renal patients
according to risk
(380),
but more recent publications (262,381)
have shown significant prognostic
value for preoperative stress testing in these patients.
This is especially true if there are cardiac risk factors
and for patients with diabetes (382).
There are only a few reports (264,383)
dealing with the evaluation of
cardiac risk in liver transplant patients, and the data
are not compelling for routine testing. This is most
likely because of the very low incidence of cardiac
events in these studies. However, until more data are
available, it may be prudent to consider preoperative
testing in those liver transplant patients who have
clinical cardiac risk factors.
These
types of observations should encourage us to pay closer
attention to the medical outcome of patients seen for
perioperative evaluations, especially in the context
of vascular surgery. After the preoperative cardiac
risk has been determined by clinical or noninvasive
testing, most patients will benefit from pharmacological
agents to lower low-density lipoprotein cholesterol
levels, increase high-density lipoprotein levels, or
both. On the basis of expert opinion, the goal should
be to lower the low-density lipoprotein level to less
than 100 mg per deciliter (2.6 mmol per deciliter)
(229,384,385).
In
general, the indications for additional screening or
testing in postoperative patients depend on individual
patient characteristics. A recent decision-tree model
(244)
was constructed to compare cost-effectiveness of various
preoperative screening protocols in postoperative vascular
surgery patients for up to 5 years after discharge.
The best event-free survival and cost-effectiveness
ratio were noted for selective preoperative stress testing
(using dipyridamole-thallium imaging) in patients with
intermediate clinical risk, whereas high-risk patients
were referred to coronary angiography and low-risk patients
were sent to elective surgery without further workup.
This is the general approach suggested in these guidelines.
In addition, another recent report (386)
showed that the clinical risk factors used in
these guidelines were more sensitive than surgical factors
for predicting perioperative cardiac events. These recent
studies confirm the importance of clinical evaluations
for both the perioperative and long-term follow-up periods.
The performance of prospective clinical trials would
be an important addition to this overall clinical analysis.
Finally, as noted for patients having a perioperative
MI, it is important that the physician(s) responsible
for the long-term care of the patient be provided with
complete information about any cardiovascular abnormalities
or risk factors for CAD identified during the perioperative
period.
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