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677
C L I N I C A L P R AC T I C E
Clinical Practice
This
Journal
feature begins with a case vignette highlighting
a common clinical problem. Evidence supporting various
strategies is then presented, followed by a review of formal
guidelines, when they exist. The article ends with the author’s
clinical recommendations.
A
ORTIC
S
TENOSIS
B
LASE
A. C
ARABELLO
, M.D.
From the Department of Medicine, Baylor College of Medicine, and the
Veterans Affairs Medical Center, Houston. Address reprint requests to Dr.
Carabello at the Veterans Affairs Medical Center Medical Service (111),
2002 Holcombe Blvd., Houston, TX 77030, or at blaseanthony.carabello@
med.va.gov.
A 60-year-old man is evaluated for a heart mur-
mur. He jogs 3 mi (5 km) per day and is asymp-
tomatic. Physical examination reveals a delayed
carotid upstroke, a 3/6 late-peaking systolic ejec-
tion murmur that radiates to the neck, and a sin-
gle S
2
. An echocardiogram shows normal systol-
ic function and a heavily calcified aortic valve.
The patient’s peak Doppler transvalvular gradient
is 64 mm Hg, with a mean gradient of 50 mm Hg.
His calculated valve area is 0.7 cm
2
. How should
this patient be treated?
THE CLINICAL PROBLEM
Aortic stenosis is the most common cardiac-valve
lesion in the United States. Two factors account for
its common occurrence: approximately 1 to 2 per-
cent of the population is born with a bicuspid aortic
valve, which is prone to stenosis; and aortic stenosis
develops with age, and the population is aging.
The clinician is usually first alerted to the presence
of aortic stenosis by the finding of a systolic ejection
murmur at the right upper sternal border that radiates
to the neck. Clues that the disease is at least moderate
in severity are peaking of the murmur late in systole,
palpable delay of the carotid upstroke, and a soft sin-
gle second heart sound, because the aortic component
of S
2
disappears when the valve no longer opens or
closes well.
Although once thought of as a degenerative lesion,
calcific aortic stenosis has many features in common
with coronary disease.
1
Both conditions are more com-
mon in men, older persons, and patients with hyper-
cholesterolemia, and both derive in part from an ac-
tive inflammatory process.
2
Aortic stenosis is distinguished from aortic sclero-
sis by the degree of valve impairment. In aortic scle-
rosis, the valve leaflets are abnormally thickened, but
obstruction to outflow is minimal, whereas in aortic
stenosis, the functional area of the valve has decreased
enough to cause measurable obstruction of outflow.
Little hemodynamic disturbance occurs as the valve
area is reduced from the normal 3 to 4 cm
2
to 1.5
to 2 cm
2
. However, as shown in Table 1, an addition-
al reduction in the valve area from half its normal
size to one quarter of its normal size produces severe
obstruction to flow and a progressive pressure over-
load on the left ventricle. The concentric hypertrophy
that develops in response to this overload is both adap-
tive and maladaptive. Whereas the increased muscle
mass allows the ventricle to generate the increased
force necessary to propel blood past the obstruction,
the hypertrophied myocardium has decreased coro-
nary blood flow reserve
3
(even in the presence of nor-
mal epicardial coronary arteries) and can also cause
both diastolic and systolic left ventricular dysfunction,
producing the symptoms of congestive heart failure.
4,5
The obvious question for the physician is when is the
optimal time for clinical intervention? Although aor-
*Data were derived with the Gorlin formula: aortic-valve
area =
cardiac output÷(systolic ejection period¬heart rate)
44.3
√
mean gradient
where the cardiac output was assumed to be 6 liters per min-
ute, the systolic ejection period was assumed to be 0.33 sec-
ond, and the heart rate was assumed to be 80 beats per minute.
T
ABLE
1.
R
ELATION
OF
THE
A
ORTIC
-V
ALVE
A
REA
TO
THE
M
EAN
G
RADIENT
.*
A
ORTIC
-V
ALVE
A
REA
M
EAN
G
RADIENT
cm
2
mm Hg
4
1.7
3
2.9
2
6.6
1
26
0.9
32
0.8
41
0.7
53
0.6
73
0.5
105
,
678
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Th e Ne w E n g l a nd Jo u r n a l o f Me d ic i ne
tic stenosis often coexists with other valvular diseases,
this review focuses on isolated aortic stenosis.
STRATEGIES AND EVIDENCE
There is no effective medical therapy for severe
aortic stenosis; aortic stenosis is a mechanical obstruc-
tion to blood flow that requires mechanical correction.
In children with congenital aortic stenosis, the valve
leaflets are merely fused, and balloon valvotomy may
offer substantial benefit.
6
In adults with calcified
valves, however, balloon valvotomy only temporarily
relieves symptoms and does not prolong survival.
7
Thus, the intervention required in adults, other than
standard prophylactic antibiotics against infective en-
docarditis,
8
is the replacement of the valve. The risks
of replacing that valve must be weighed against the
risks of delaying the procedure. The procedure can
usually be delayed until symptoms develop.
9,10
Stud-
ies of aortic stenosis uniformly demonstrate that once
angina, syncope, dyspnea, or other symptoms of heart
failure develop and are found to be due to aortic ste-
nosis, the patient’s life span is drastically shortened un-
less the valve is replaced (Fig. 1). Of the 35 percent
of patients with aortic stenosis who present with an-
gina, half will die within five years in the absence of
aortic-valve replacement. Of the 15 percent of pa-
tients who present with syncope, half will die within
three years, and of the 50 percent of patients who
present with dyspnea, half will die within two years,
unless the aortic valve is replaced. In contrast, 10-year
age-corrected rates of survival among patients who
have undergone aortic-valve replacement approach the
rate in the normal population.
11,12
The striking contrast between the excellent prog-
nosis after aortic-valve replacement and the dismal
prognosis in the absence of replacement in sympto-
matic patients makes the presence or absence of symp-
toms the crucial factor with respect to management.
In general, the clinician can be confident that, in a giv-
en patient, the symptoms are due to aortic stenosis if
the mean aortic-valve gradient exceeds 50 mm Hg or
if the aortic-valve area is no larger than 1 cm
2
. I will
use these as criteria for severe disease, although there
is no universally accepted definition that relies on valve
area or gradient.
AREAS OF UNCERTAINTY
Management of Severe Asymptomatic Aortic Stenosis
There is overwhelming evidence that patients with
severe aortic stenosis who become symptomatic re-
quire prompt aortic-valve replacement. Conversely,
asymptomatic patients, even those with severe disease,
generally have an excellent prognosis without aortic-
valve replacement. Unfortunately, approximately 1 to
2 percent of asymptomatic patients die suddenly or
have a very rapid rate of progression to the sympto-
matic state and then to sudden death.
9,10,13,14
Thus, the
question arises whether patients with severe asymp-
tomatic aortic stenosis should undergo aortic-valve re-
placement to protect them from sudden death. Al-
though some experts advocate this approach, this
strategy exposes the entire group of asymptomatic pa-
tients with severe aortic stenosis to the risk of peri-
operative and valve-related complications and death.
Even in the best of circumstances, the surgical mor-
tality rate is approximately 1 percent and the risk of
a valve-related complication (including thromboem-
bolism; bleeding during therapy with anticoagulants;
deterioration of the prosthetic valve, requiring reoper-
ation; and infective endocarditis) is 1 percent per year.
15
Echocardiography and exercise testing may identify
asymptomatic patients who are likely to benefit from
surgery. Otto et al.
16
found that patients with asymp-
tomatic aortic stenosis whose peak transaortic blood
flow velocity exceeded 4 m per second (a peak gradi-
ent of 64 mm Hg) had a risk of becoming symptomat-
ic and requiring aortic-valve replacement of 70 percent
within two years. None of the patients in this mod-
erate-sized series died suddenly, and all underwent
exercise testing.
Although exercise testing is unwarranted and dan-
gerous in patients with symptomatic aortic stenosis, it
has proved safe in patients with moderate-to-severe
asymptomatic aortic stenosis.
16,17
A preliminary report
suggests that exercise testing may identify some pa-
tients with latent symptoms or exercise-induced he-
modynamic instability, facilitating timely aortic-valve
replacement. In a study of 58 asymptomatic patients,
18
21 had symptoms for the first time during the exer-
cise test. Most likely, these patients had failed to rec-
ognize the symptoms previously or had not engaged
in activities that would have precipitated symptoms.
Although patients with asymptomatic aortic stenosis
can exercise safely under a physician’s scrutiny, it seems
most unwise to permit patients with moderate-to-
severe aortic stenosis to engage in vigorous, unmon-
itored exercise in view of the limitations imposed by
left ventricular hypertrophy on coronary blood flow.
Treatment of the Patient with a Low Gradient
and Reduced Ejection Fraction
In patients with left ventricular dysfunction who
have a substantial transvalvular gradient (a mean gra-
dient of more than 40 mm Hg), the outcome of sur-
gery is excellent despite the presence of a reduced ejec-
tion fraction preoperatively.
19
In these patients, the
excessive afterload generated by the obstructing valve
is a prime contributor to the left ventricular dysfunc-
tion. Once the obstruction is removed and the after-
load is reduced, left ventricular function returns to or
approaches normal.
Patients with a reduced ejection fraction and a small
C L I N I C A L P R AC T I C E
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679
transvalvular gradient (less than 30 mm Hg)
19,20
have
a high operative risk, and only half such patients are
alive three to four years after surgery.
21
The poor out-
come in these patients is related to the presence of
both severely depressed myocardial contractility and
the excessive afterload.
19
Although the overall prognosis for this group of pa-
tients is poor, some patients in this category, pre-
sumably those with severe valve obstruction, benefit
from surgery.
21,22
In other patients, the calculated valve
area may be severely reduced because cardiomyopathy
inhibits the left ventricle from completely opening a
mildly but not a severely stenotic valve. The presence
of low output may lead clinicians to the false conclu-
sion that the valve is severely stenotic (aortic pseudo-
stenosis).
23-25
The best method for distinguishing these
two conditions is to increase cardiac output during
Doppler echocardiography or cardiac catheterization
Figure 1.
Survival among Patients with Severe Symptomatic Aortic Stenosis Who Underwent Valve
Replacement and Similar Patients Who Declined to Undergo Surgery.
The overall and individual P values are shown, as is the overall chi-square value. Reprinted from
Schwarz et al.
11
with the permission of the publisher.
0
100
0
5
20
40
60
80
1
2
3
4
Year
Valve replacement
Chi-square=23.5
P<0.001
No surgery
P<0.001
P<0.05
Survival (%)
N
O. AT
R
ISK
Valve replacement
No surgery
125
0
19
87
0
8
51
0
2
35
0
1
9
0
0
0
680
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Th e Ne w E n g l a nd Jo u r n a l o f Me d ic i ne
and to use the new data to recalculate the valve area.
In the case of pseudostenosis, increased output causes
a large increase in the calculated valve area, often to
more than 1 cm
2
. In this group of patients, valve re-
placement is unlikely to be beneficial. Conversely, pa-
tients in whom increased cardiac output produces a
substantial increase in gradient have a true outflow
obstruction and may benefit from surgery. Patients
with a low gradient who have no response to ino-
tropic stimulation have a poor outcome, presumably
because the myocardial damage is so far advanced.
26
Safety of Cardiac Surgery in Patients
with Mild-to-Moderate Aortic Stenosis
Controversy also exists regarding the optimal ap-
proach to patients with mild-to-moderate aortic steno-
sis (as indicated by a transvalvular gradient in the range
of 10 to 30 mm Hg and a valve area of more than
1 cm
2
) who require cardiac surgery for some other
cause, usually coronary revascularization. Concomitant
aortic-valve replacement increases the risk of both per-
ioperative death and complications related to the pros-
thetic valve. However, if the native valve is left in place,
aortic stenosis may progress so rapidly that another
cardiac surgery is required despite the fact that the
bypass grafts are functioning normally.
27
Unfortunate-
ly, there is wide individual variability in the rate of dis-
ease progression,
27-29
virtually precluding prognosti-
cation of the course of a given patient. Concomitant
aortic-valve replacement is considered unwise if it is
likely to increase the gradient even further.
Safety of Noncardiac Surgery in Patients
with Severe Asymptomatic Aortic Stenosis
On the basis of a small number of adverse events,
one study indicated that noncardiac surgery posed an
increased risk among patients with aortic stenosis.
30
However, O’Keefe et al. examined the course of 48
patients with severe aortic stenosis who underwent
noncardiac surgery
31
and found that there were no
complications in the 25 patients who had local anes-
thesia and only one complication in the 23 patients
who received general anesthesia. Thus, although intra-
operative hemodynamics must be closely monitored
during noncardiac surgery in patients with asympto-
matic aortic stenosis, there is no apparent need for
concomitant aortic-valve intervention.
Ability to Slow or Halt Progression of the Valve Lesion
As noted above, the lesion of aortic stenosis shares
many features with coronary disease. Although recent
data suggest that hydroxymethylglutaryl coenzyme A
reductase inhibitors (referred to as “statins”) can retard
the progression of aortic stenosis,
32
in my opinion it
is a bit too early to begin prescribing statins for this
purpose.
GUIDELINES
Guidelines for the use of valve replacement in pa-
tients with aortic stenosis are provided in Table 2. In
1998 the American Heart Association and American
College of Cardiology issued guidelines for the treat-
ment of valvular heart disease (available at http://
www.americanheart.org).
8
These guidelines recom-
mend the use of standard antibiotic prophylaxis against
infective endocarditis. Doppler echocardiography is
recommended for the initial diagnosis and assessment
of the severity of aortic stenosis and the function and
hemodynamics of the left ventricle, as well as for the
reevaluation of patients whose symptoms and signs
are changing and of patients known to have severe
asymptomatic aortic stenosis.
CONCLUSIONS AND RECOMMENDATIONS
Doppler echocardiography is indicated for the ini-
tial evaluation in all patients suspected of having aortic
stenosis, as well as in patients with established disease
if symptoms develop or physical signs change. The de-
velopment of angina, syncope, or dyspnea in a patient
with severe aortic stenosis constitutes a grave medical
condition, requiring prompt aortic-valve replacement.
For patients with severe asymptomatic disease, such
as the patient described in the clinical vignette, the
presence of an aortic-jet velocity of at least 4 m per
second on Doppler echocardiography indicates the
need for close scrutiny. I routinely recommend ex-
ercise testing in this group (but never in symptomat-
ic patients), since it may help identify which of these
patients are at high enough risk to warrant undergo-
ing surgery (Fig. 2).
The postoperative prognosis of patients with a re-
duced ejection fraction is good if the mean transval-
vular pressure gradient exceeds 40 mm Hg. Thus, a
low ejection fraction alone should never be an abso-
*Aortic-valve replacement is not indicated to prevent sudden death in
asymptomatic patients who have none of the findings listed.
T
ABLE
2.
R
ECOMMENDATIONS
FOR
THE
U
SE
OF
A
ORTIC
-V
ALVE
R
EPLACEMENT
IN
P
ATIENTS
WITH
A
ORTIC
S
TENOSIS
.
Aortic-valve replacement indicated
Patients with severe aortic stenosis and any of its classic symptoms (angina,
syncope, or dyspnea)
Patients with severe aortic stenosis who are undergoing coronary-artery by-
pass surgery
Patients with severe aortic stenosis who are undergoing surgery on the aor-
ta or other heart valves
Aortic-valve replacement possibly indicated
Patients with only moderate aortic stenosis who require coronary-artery by-
pass surgery or surgery on the aorta or other heart valves
Asymptomatic patients with severe aortic stenosis and at least one of the
following: an ejection fraction of no more than 0.50, hemodynamic in-
stability during exercise (e.g., hypotension), or ventricular tachycardia*
C L I N I C A L P R AC T I C E
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681
lute contraindication to surgery. However, the prog-
nosis of patients with a low gradient and a low ejec-
tion fraction is worse. For such patients I recommend
hemodynamic manipulation in the catheterization or
echocardiographic laboratory to help determine which
patients are more likely to benefit from surgery.
Preliminary evidence indicates that patients who
have moderate aortic stenosis (as indicated by a gra-
dient of more than 20 mm Hg and a valve area of less
than 1.2 cm
2
) but who require heart surgery for oth-
er diseases should probably undergo concomitant aor-
tic-valve replacement. Further study of this approach
is required.
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Figure 2.
Algorithm for the Management of Aortic Stenosis.
Aortic stenosis without
symptoms present on
physical examination
Severe
aortic stenosis
and symptoms
present on
physical
examination
Perform Doppler
echocardiography
If echocardiography shows
mild-to-moderate aortic
stenosis, monitor patient
for the development
of symptoms
If echocardiography
shows severe
aortic stenosis,
perform exercise
testing
If results
are
normal,
monitor
patient
closely
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develop,
repeat
echocardi-
ography
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stenosis
becomes
severe,
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coronary
arteriography
and aortic-
valve
replacement
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remains
asymptomatic
but findings
on examination
change, repeat
echocardi-
ography
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stenosis
remains mild
to moderate,
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follow-up
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are abnormal,
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arteriography
and aortic-valve
replacement
Mild-to-moderate
aortic stenosis
and symptoms
present on physical
examination
Search for other
causes of symptoms
Perform
coronary
arteriography
and aortic-valve
replacement
682
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·
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Th e Ne w E n g l a nd Jo u r n a l o f Me d ic i ne
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Copyright © 2002 Massachusetts Medical Society.
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