(Circulation. 2000;102:2365.)
© 2000 American Heart Association, Inc.
Clinical Investigation and Reports |
From the Cardiovascular Center (M.A.) and Division of Cardiology (H.T., H.Y., N.D.), Third Department of Internal Medicine, Teikyo University School of Medicine, Ichihara Hospital, Ichihara, Chiba, Japan.
Correspondence to Masayuki Abe, MD, Cardiovascular Center, Teikyo University School of Medicine, Ichihara Hospital, 3426-3 Anesaki, Ichihara, Chiba, Japan 299-0111. E-mail cao02110{at}pop02.odn.ne.jp
| Abstract |
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Methods and ResultsThe study population consisted of 46 consecutive patients with a moderate stenosis in the LAD in whom simultaneous measurements of aortic pressure, left ventricular pressure, and coronary pressure distal to the stenosis were obtained. Coronary flow velocity was successfully measured with a Doppler guidewire in 37 of the 46 patients. Values for FFR, d-FFR, and CFR in the noninvasive testpositive group were significantly lower than those in the negative group. With cutoff values of 0.75, 0.76, and 2.0 for FFR, d-FFR, and CFR, sensitivities were 83.3%, 95.8%, and 88.2% and specificities were 100%, 100%, and 95.0%, respectively.
ConclusionsThe close similarity of the sensitivity and specificity of FFR and d-FFR, around almost identical cutoff values (0.75 versus 0.76), confirms the physiological validity of FFR as a clinical standard. In clinical practice, FFR remains the index of choice for assessment of the functional severity of moderate coronary artery stenoses.
Key Words: ischemia coronary artery disease hemodynamics
| Introduction |
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| Methods |
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Noninvasive Tests
Symptom-limited bicycle exercise testing was performed at
an initial workload of 25 W and was increased by 25 W every 3 minutes.
A 12-lead ECG was continuously recorded. At peak exercise, 3 mCi
thallium chloride was administered intravenously. Exercise
was maintained for 1 additional minute. Within 10 minutes after the
termination of exercise, stress planar images were acquired in the
anterior, left lateral, and left anterior oblique views, followed by
the acquisition of cardiac SPECT images. After 3 to 4 hours,
redistribution planar and SPECT images were obtained. When chest pain
was accompanied by ST-segment depression of >-0.2 mV on bicycle
exercise testing or reversible ischemia was detected with SPECT
at baseline and after exercise, the noninvasive test was judged to be
positive.
Cardiovascular Catheterization
After the intravenous administration of 5000 IU
heparin, a 6F guiding catheter, without side holes, was advanced up to
the left coronary ostium through the right brachial artery.
Isosorbide dinitrate (5 mg) was administered through the inserted
catheter. Lesion severity was evaluated with an online analysis
system that operated on digital images (DLK-III; GE Medical Systems). A
4F pigtail catheter was placed in the left ventricle through the right
radial artery to measure left ventricular pressure.
A 2.6F intravascular ultrasound (IVUS) catheter (Discovery; Boston Scientific) was used to calculate the percent area stenosis of the lesion. Distal coronary flow velocity and pressure were obtained simultaneously with a 0.014-in Doppler guidewire (FloWire; Endosonics) and a 0.014-in pressure guidewire (WaveWire; Endosonics). Care was taken to position the 2 wire transducers at the same site.
Translesional Pressure Gradient Measurements
The pressure measurements with the WaveWire were
processed with the use of the WaveMap (Endosonics), and
mean aortic and mean distal coronary pressures were displayed
simultaneously on the analog display of the
WaveMap. The pressure signal was calibrated to the normal
atmosphere before insertion. When the sensor was in place close to the
tip of the guiding catheter and equal pressures were not observed at
that location, a normalization procedure was performed to superimpose
the 2 pressures at that point. All pressure measurements were completed
within 10 minutes, and after the final measurement, the
WaveWire was pulled back close to the tip of the guiding
catheter. If a pressure difference of >5 mm Hg was observed, the
coronary pressure distal to the stenosis was
recalculated, with this drift taken into account.
Aortic and Left Ventricular Pressure
Measurements
Aortic pressure (guiding catheter) and left
ventricular pressure (pigtail catheter) were obtained with
2 separate fluid-filled pressure transducers (1290C; Hewlett Packard)
zeroed at mid chest level. All measurements, including aortic pressure,
left ventricular pressure, poststenotic
coronary pressure, and coronary flow velocity, were
obtained simultaneously, both at rest and during maximal
vasodilation, and were induced by the infusion of 150 µg ·
kg-1 · min-1 ATP
IV (Figure 1
).
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Translesional Coronary Flow Velocity
Measurements
The quadrature/Doppler signals were processed with the
FloMap (Endosonics). The Doppler transducer was
advanced distal to the stenosis by
5 artery diameter lengths,
to avoid placement in any side branches. The flow velocity measurements
distal to the stenosis were obtained under baseline conditions
and during hyperemia. CFR was computed as the ratio of the
average peak flow velocity (cm/s) during hyperemia to baseline
average peak flow velocity.7 8 9
Simultaneous Assessment of Aortic Pressure,
Poststenotic Coronary Pressure, Left
Ventricular Pressure, and Coronary Flow
Velocity Measurements
All measurements were continuously acquired with a personal
computer with a 12-bit analog-to-digital converter at a sampling
frequency of 250 Hz (MP100 systems and Acqknowledge; BIOPACK
Systems, Inc) (Figure 2
).
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Data Analysis
As shown in Figure 2
, we used the results obtained here
to calculate the dp-cor, which is the coronary distal pressure
minus left ventricular pressure during
diastole. With the difference in aortic pressure and left
ventricular pressure during diastole, we
calculated the driving pressure of the theoretically normal
coronary artery (dp-aor). The diastolic
intervals for analysis were defined manually from the peak
pressure point of the dp-cor to the sudden drop point of the dp-cor due
to myocardial contraction.
Calculation of FFR and d-FFR
FFR was calculated as the ratio of mean coronary distal
pressure, as measured with the WaveWire, to mean
arterial pressure, as measured with the guiding catheter,
at maximal hyperemia. The d-FFR was defined as the ratio of
dp-cor for a stenotic coronary artery to its dp-aor
value (Figure 3
); both intervals of the
dp-cor and dp-aor obtained at maximal hyperemia were integrated
(Figure 4
), and d-FFR was derived by
dividing dp-cor by the dp-aor (Figure 4
).
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Statistical Analysis
Results were expressed as mean±SD. Statistical analyses
were performed with the SPSS software package. All indexes derived from
pressure and velocity measurements and other continuous variables
were compared between the noninvasive testpositive and negative
groups with the 2-tailed Students unpaired t test. The
categorical variables were compared between the 2 groups by
2 test. To compare both sensitivities and
specificities of CFR, FFR, and d-FFR against the results of noninvasive
tests, the receiver operator characteristic (ROC) curves were used. The
best cutoff values were identified as the values with the highest sum
of sensitivity and specificity. To compare the sensitivity and
specificity of FFR, d-FFR, and CFR, the differences in the area under 3
respective ROC curves were compared.23
| Results |
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Patient Characteristics
As shown in Table 1
, of the total of 46 patients, 24 were
positive on the noninvasive test and 22 were negative. Of the 37
patients in whom flow velocity was also measured, 17 were positive and
20 were negative. For patient characteristics, age alone was
significantly higher in the noninvasive testpositive group than in
the negative group.
Percent Diameter Stenosis and Percent Area
Stenosis
As shown in Table 1
, quantitative coronary
angiography (QCA) revealed no significant difference in percent
diameter stenosis between the noninvasive testpositive
(56.8%) and negative (52.6%) groups. IVUS showed that percent area
stenosis was significantly higher in the noninvasive
testpositive group than in the negative group (60.0±15.7% versus
49.7±10.5%, P<0.05), which concurs with other
reports.24 The difference between QCA and IVUS may be
due to disease of the reference segment for measurement of percent
diameter stenosis that QCA fails to detect but IVUS does
detect.
FFR, d-FFR, and CFR
The values for FFR, d-FFR, and CFR for both noninvasive
testpositive and negative groups are shown in Table 1
. CFR,
FFR, and d-FFR were significantly lower in the noninvasive
testpositive group than in the negative group
(P<0.01).
Figure 5
shows a comparison of the
3 ROC curves for d-FFR, FFR, and CFR used to discriminate the
noninvasive test positive from the negative. d-FFR seemed to be both
more sensitive and more specific than FFR and CFR, but the difference
in the area under 3 respective ROC curves was not statistically
significant. The cutoff values for d-FFR, FFR, and CFR were taken as
0.76, 0.75, and 2.0, respectively. The sensitivities of d-FFR, FFR, and
CFR were 95.8%, 83.3%, and 88.2%, respectively, and the
specificities of d-FFR, FFR, and CFR were 100%, 100%, and 95.0%,
respectively (Table 2
).
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| Discussion |
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Pijls et al22 pointed out that the specificity and sensitivity of FFR for myocardial ischemia detected with noninvasive tests were 100% and 85% to 95%, respectively, and in the present study, the specificity of FFR was 100% and sensitivity was 83.3%, around the 0.75 cutoff. It is encouraging that the cutoff value for d-FFR was 0.76, whereas the cutoff point for conventional FFR has been claimed to be 0.75 in a number of previous studies. The simple fact that the cutoff points are so similar is a strong confirmation of the physiological soundness of the principles that underlies the concept of FFR. FFR is generally considered to be independent of changes in heart rate, aortic pressure, and myocardial contractility. In the present study, we used d-FFR to identify the influences in left ventricular diastolic pressure and dp-cor and to predict the results of noninvasive testing. The diagnostic value of d-FFR is similar to that of classic FFR, because of the similar cutoff values and diagnostic accuracy; that is, FFR is also independent of those influences.
Study Limitations
We divided all patients into binary positive or negative groups
according to the results of noninvasive testing. However, it is well
known that 201Tl SPECT with symptom-limited
exercise bicycle testing has limited accuracy, with a sensitivity of no
greater than 85% and specificity of
90%. Therefore, discrepancies
between the invasive parameters and the thallium testing
could also be due to false-positive or false-negative thallium tests.
The only way to know whether an abnormal perfusion scintigram is truly
abnormal is to repeat the test after
revascularization. In this case, the positive case
that becomes negative can be considered truly positive, and the
negative test that was negative before
revascularization can be considered truly negative.
Because noninvasive tests after revascularization
were not available for all patients, we were unable to resolve this
question in the present study.
Another limitation of the present study is that the acquisition of d-FFR is complex and therefore more vulnerable to measurement errors, although in here, all measurements were performed at least twice without difficulties. This can be important because the applicability of a parameter is also determined by the ease with which it can be obtained.
Signal acquisition with the Doppler FloWire can sometimes be unstable, especially because the elevation of basal flow velocity during hyperemia may cause an abnormal CFR value.
In some patients, effort-induced vasospasm may occur during exercise testing. The influence of effort-induced vasospasm cannot be excluded during noninvasive testing, because all cardiac medications except aspirin were stopped for 24 hours before the tests. In addition, the administration of nitroglycerin during the measurement of flow velocity and pressure could eliminate the vasospastic mechanism. These 2 sets of diverse effects may modify the interpretation of our results.
We compared FFR and d-FFR with the results of noninvasive tests, but the latter obviously reflect the influence of epicardial coronary stenosis as well as of microvascular disease, which was difficult to exclude entirely from our results. Reference vessel CFR would confirm microvascular disease but that was not determined in the present study. One final limitation is that we investigated FFR and d-FFR only in the LAD.
Conclusion
We evaluated the functional impact of moderate coronary
stenosis on myocardial perfusion by simultaneously
measuring aortic pressure, distal coronary pressure, left
ventricular pressure, and coronary flow velocity,
and we compared the results of noninvasive testing with FFR, d-FFR, and
CFR. The close similarity of the sensitivity and specificity of both
FFR and d-FFR, around almost identical cutoff values, confirms the
physiological soundness of the principles that
underlie the concept of FFR. We believe that in clinical practice, FFR
remains the index of choice for assessment of the functional severity
of moderate coronary artery stenoses.
| Acknowledgments |
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Received May 4, 2000; revision received June 16, 2000; accepted June 26, 2000.
| References |
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