Vol. 281, Issue 2, H573-H580, August 2001
Assessment of LV systolic function in
atrial fibrillation using an index of preceding cardiac
cycles
Tomotsugu
Tabata1,
Richard A.
Grimm1,
Neil L.
Greenberg1,
Deborah A.
Agler1,
Kent A.
Mowrey2,
Don W.
Wallick2,
Youhua
Zhang2,
Shaowei
Zhuang2,
Todor N.
Mazgalev2, and
James D.
Thomas1
Sections of 1 Cardiovascular Imaging and
2 Electrophysiology, Department of Cardiology, Cleveland
Clinic Foundation, Cleveland, Ohio 44195
 |
ABSTRACT |
The clinical assessment
of left ventricular (LV) systolic function during atrial fibrillation
(AF) is unreliable and difficult because of beat-to-beat variability.
We evaluated an index for the estimation of LV systolic function in AF
that is based on the relationship between the preceding
(R-R1) and prepreceding (R-R2) R-R intervals.
LV Doppler stroke volume (SV), ejection fraction (EF), peak aortic flow
rate (AoF) and the maximum value of the first derivative of the LV
pressure curve (dP/dtmax) were evaluated in 13 healthy open-chest dogs during triggered AF. All parameters showed a
significantly strong positive linear relationship with the ratio of
R-R1/R-R2 (r = 0.65, 0.74, 0.75, and 0.70 for SV, EF, AoF, and dP/dtmax,
respectively). The calculated value of LV systolic parameters at
R-R1/R-R2 = 1 in the linear regression line showed a good relationship and an agreement with the measured average value of the parameter over all cardiac cycles (SV, 12.1 vs.
12.8 ml; EF, 49.6 vs. 51.2%; AoF, 1.37 vs. 1.48 l/min; and dP/dtmax, 2,323 vs. 2,454 mmHg/s). Using the LV
systolic parameters estimated at R-R1/R-R2 = 1 in the linear regression line allows the LV contractile function to
be accurately and reproducibly evaluated during AF and obviates the
less-reliable process of averaging multiple cardiac cycles.
preload; afterload; contractility; R-R interval; echocardiography; left ventricular
 |
INTRODUCTION |
ATRIAL FIBRILLATION
(AF) is a major health problem that affects 0.9% of the population and
is characterized classically by an irregularly irregular rhythm
(9). The resultant effect of this irregularity is the
absence of optimal left ventricular (LV) systolic function due to the
loss of atrial booster-pump function as well as beat-to-beat changes in
preload, afterload, and contractility (17). Yet another
hemodynamic consequence of AF is the rapid ventricular rate, which
further adversely affects LV function because preload and contractility
diminish due to decreased filling time.
The beat-to-beat variation, which is the signature of AF, can be
a detriment to the reliable and reproducible clinical assessment of LV
systolic function (see Fig. 1,
top). Owing to this variability, in clinical practice the
standard protocol for obtaining an accurate assessment of LV function
involves averaging a random number of consecutive cardiac cycles. In
addition to being cumbersome, this process is suboptimal, because the
averaged value is variable and dependent on a selected window of
cardiac cycles (5). It is well appreciated that LV
systolic function during AF varies depending on the preceding cardiac
cycle lengths (3, 7, 12-14, 16, 23, 24, 26, 27).
Nakamura and colleagues (22) reported a significant
positive linear relationship between the maximum value of the first
derivative of the LV pressure curve (dP/dtmax)
and the ratio of preceding (R-R1) to prepreceding
(R-R2) R-R intervals (R-R1/R-R2).
Recently Yamaguchi and co-workers (27) and Suzuki and
colleagues (26) reported that the value of end-systolic LV
maximum elastance (Emax) at
R-R1/R-R2 = 1 in the linear regression line could estimate stable LV systolic function. Clinically it would be
extremely valuable if LV systolic function could be accurately estimated using parameters that are noninvasively derived [such as
Doppler stroke volume (SV) and ejection fraction (EF) from echocardiography] and validated [using peak aortic flow rate (AoF) and dP/dtmax] and then the above index could be
applied to relate the preceding and prepreceding R-R intervals.

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Fig. 1.
Top: simultaneous recording of left
ventricular (LV) outflow Doppler velocity profile (LVOF) and LV
pressure curve (LVP), which are showing beat-to-beat variation during
atrial fibrillation. Bottom: simultaneous recordings of the
surface electrocardiogram (ECG), LVP, the first derivative of LV
pressure curve (dP/dt), peak aortic flow rate (AoF), and
right ventricular ECG (RVe). R-R1 and R-R2 are
preceding and prepreceding cardiac cycle lengths of a given cardiac
beat (*), respectively.
|
|
The objectives of this study using an experimental canine AF
model were to evaluate: 1) the relationship between
hemodynamic parameters (SV, EF, AoF, and
dP/dtmax) and the R-R1 and
R-R2 intervals as well as the ratio of
R-R1/R-R2; and 2) whether the value
of these LV systolic parameters at
R-R1/R-R2 = 1 in the linear regression line could estimate LV systolic function despite the potential influence by preload and afterload.
 |
METHODS |
This study received institutional review and approval in
accordance with the American Association for Accreditation of
Laboratory Animal Care. A total of 13 healthy mongrel dogs weighing
25-35 kg were used in the present study. The dogs were placed in
the supine position and were initially anesthetized with thiopental (20 mg/kg iv). Anesthesia was maintained with an inhalation mixture of
oxygen and isoflurane (1.0-2.0%). The dogs were intubated with a
cuffed endotracheal tube and ventilated with room air and oxygen through a Dräger SAV respirator (North American Dräger;
Telford, PA), which was adjusted as needed to maintain normal arterial blood gases. Blood-gas values for the animals were maintained at a
PO2 of >80 mmHg, PCO2
of 35-45 mmHg, and pH 7.35-7.45 via infusion with bicarbonate
solutions and alteration of ventilation volume and rate. A median
sternotomy was performed to expose the heart.
Quadripolar electrodes for recording and pacing were sutured to the
right atrial (RA) appendage and the right ventricular (RV) apex. A
bipolar plate electrode was sutured to the epicardial sinus node fat
pad in the superior vena cava for delivery of vagal nerve stimulation
to initiate and maintain AF (11). The pacing protocol was
stored in a programmable stimulator Master-8. Surface electrocardiograms (ECGs; I, II, and III) and intracardiac ECGs (RV
apex and RA appendage) were displayed continuously on a monitor, amplified, and digitally recorded on our laboratory recording system
(EP Lab; Quinton Electrophysiology). AF was initiated by rapid-burst
stimulation of the RA through the electrode sutured to the sinus node
fat pad. Impulses were 1 ms in duration and were separated by a 50-ms
interimpulse interval; typical amplitude was 2-5 V. Once the AF
was initiated (usually after the first 5 s), the impulse was
reduced to 50 µs, which was sufficient to produce stimulation of
preganglionic vagal fibers to maintain AF.
A high-fidelity micromanometer catheter (Millar; Houston, TX) was
inserted into the carotid artery and advanced such that the tip was
near the LV apex for recording the LV pressure. Before the insertion,
the catheter was soaked in warm saline for 30 min and zeroed to air.
The LV dP/dtmax was obtained from the LV
pressure recording. The peak AoF was obtained by a transonic flow probe placed on the ascending aorta.
Epicardial echocardiography was performed using commercially available
equipment, specifically, a Sequoia C512 ultrasound system (Acuson;
Mountain View, CA) with a 3.5-MHz phased-array transducer. From the
four-chamber view, the LV volumes at end diastole (EDV) and end systole
(ESV) were calculated using the single-plane Simpson's rule. The LV EF
was calculated by the formula EF = (EDV
ESV)/EDV × 100 (percent). The LV outflow tract velocity was recorded from the
standard LV five-chamber view by placing the pulsed-wave Doppler sample
volume at the LV outflow tract ~1-2 cm below the aortic valve.
The diameter of the LV outflow tract during midsystole was measured
from the parasternal long-axis view. The Doppler SV was calculated as a
product of the velocity-time integral of the LV outflow Doppler
profile, and the LV outflow cross-sectional area was calculated from
the LV outflow tract diameter (assuming a circular geometry).
After preamplification with a universal amplifier (Gould; Valley View,
OH), the ECG data were digitized with 1-ms resolution using a 12-bit
analog-to-digital converter (National Instruments; Austin, TX)
interfaced with a Pentium 200-MHz computer running customized software
developed in the LabVIEW graphical programming environment
(National Instruments). All of the electrical and hemodynamic data
were recorded into data-acquisition boards simultaneously with an
echocardiogram during the baseline sinus rhythm and the triggered AF.
The LV volumes and EF were measured from the videotape off-line for 10 consecutive cardiac cycles. These data were expressed as an average
value ± SD. The differences in R-R intervals, LV volumes, and EF
values between the two conditions were analyzed using Student's paired
t-test.
Analysis of simultaneous electrical and hemodynamic data was performed
within the LabVIEW environment. The LV systolic function was evaluated
by pulsed-wave Doppler-derived SV and peak AoF in 11 of 13 dogs and the
dP/dtmax was used in all 13. We attempted to
obtain each LV systolic parameter for >100 consecutive cardiac cycles,
but the number of data points involving SV was <100 in 6 animals due
to intermittent suboptimal Doppler signal quality. The R-R intervals
were measured from the RV ECG. The R-R1 and R-R2 intervals for a given cardiac beat were measured with
all LV systolic parameters during AF (see Fig. 1, bottom).
The relationships between each LV systolic parameter at a given cardiac
beat and the R-R1 interval, as well as the
R-R1/R-R2 ratio, were evaluated. The
correlation coefficients were obtained by linear regression analysis.
The value of each LV systolic parameter at
R-R1/R-R2 = 1 was calculated from the
equation of linear regression line in the relationship between the
parameter and the R-R1/R-R2 ratio. Bland and
Altman analysis (2) was applied to evaluate the
relationship and agreement between the calculated values of each
parameter at R-R1/R-R2 = 1 in the linear
regression line and the measured average value of each systolic
parameter in all cardiac cycles. The difference in correlation
coefficients in the relationship between R-R1 or the
R-R1/R-R2 ratio and each parameter was
evaluated by a Fisher's Z transformation and a Student's
paired t-test. Estimation of the LV EF during AF was again
performed using the value at R-R1/R-R2 = 1 in the linear regression line with a smaller sample of consecutive
cardiac cycles (16-26 cycles) in 9 of 13 dogs. P < 0.05 was considered statistically significant.
 |
RESULTS |
Compared with sinus rhythm, triggered AF caused significant
shortening of the R-R interval (427 ± 81 vs. 341 ± 122 ms;
P < 0.0001) and decreases in average EF (61 ± 9 vs. 51 ± 8%; P < 0.01), LV EDV (22 ± 6 vs. 14 ± 4 ml; P < 0.0001), and peak systolic LV pressure (140 ± 58 vs. 80 ± 21 mmHg; P < 0.0001).
All LV systolic parameters during AF showed a significant positive
correlation with R-R1 intervals (r = 0.58, 0.58, 0.63, and 0.59 for SV, EF, AoF, and
dP/dtmax, respectively; see Fig. 2, left) and the
R-R1/R-R2 ratio (r = 0.65, 0.74, 0.75, and 0.70 for SV, EF, AoF, and
dP/dtmax, respectively; see Fig. 2,
right). However, the correlation coefficients were
significantly greater for the relationship between the systolic
parameters and the R-R1/R-R2 ratio than for
those between the parameters and the R-R1 interval alone
(P < 0.05, 0.01, 0.001, and 0.01 for SV, EF, AoF, and
dP/dtmax, respectively). Interestingly, even
when a relatively small number of cardiac cycles were used, LV EF and
SV also showed a significant positive correlation with the
R-R1/R-R2 ratio (see Fig.
3).

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Fig. 2.
Left: representative relationships between LV systolic
parameters and the R-R1 interval in one animal.
Right: representative relationships between LV systolic
parameters and the ratio of R-R1/R-R2 in one
animal. SV, stroke volume (A);
dP/dtmax, maximum value of dP/dt
(C). B: AoF.
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Fig. 3.
Representative relationships between LV ejection fraction
(EF) and SV and the ratio of R-R1/R-R2
evaluated by using a relatively small number of cardiac cycles in one
animal.
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Tables
1-4
show the average values during the baseline sinus rhythm,
the equation of the linear regression line (i.e., the relationship
between the LV systolic parameters and the
R-R1/R-R2 ratio), and the calculated values of
each parameter at R-R1/R-R2 = 1 in the
linear regression line, as well as the measured average value over all
cardiac cycles during AF in each of the studied dogs. The calculated
value of each LV systolic parameter at
R-R1/R-R2 = 1 in the linear regression
line was quite similar to the measured average value over all cardiac
cycles during AF (SV, 12.1 vs. 12.8 ml; AoF, 1.37 vs. 1.48 l/min;
dP/dtmax, 2,323 vs. 2,454 mmHg/s; EF, 49.6 vs.
51.2%). The Bland and Altman analysis showed a good relationship and
agreement between the calculated and measured values of each LV
systolic parameter (see Figs. 4 and
5).
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Table 1.
Average values of stroke volume during baseline sinus rhythm, equation
of the linear regression line, calculated value of stroke volume at
R-R1/R-R2 = 1 in the linear
regression line and measured average values of stroke volume over
all cardiac cycles during atrial fibrillation
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Table 2.
Average values of peak aortic flow rate during baseline sinus rhythm,
equation of the linear regression line, calculated values of aortic
flow rate at R-R1/R-R2 = 1 in
the linear regression line, and measured average values of aortic flow
rate over all cardiac cycles during atrial fibrillation
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Table 3.
Average values of dP/dtmax during baseline sinus rhythm,
equation of the linear regression line, calculated values of
dP/dtmax at R-R1/R-R2
= 1 in the linear regression line, and measured
average values of dP/dtmax over all cardiac cycles
during atrial fibrillation
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Table 4.
Average values of ejection fraction during baseline sinus rhythm,
equation of the linear regression line, calculated values of the
ejection fraction at R-R1/R-R2
= 1 in the linear regression line, and measured
average values of ejection fraction over all cardiac cycles during
atrial fibrillation
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Fig. 4.
Relationship and agreement between the measured average
value of all cardiac cycles (av) and the calculated value at
R-R1/R-R2 = 1 (x = 1) in
the linear regression line for SV and AoF in all animals.
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Fig. 5.
Relationship and agreement between the average value of
all cardiac cycles and the calculated value at
R-R1/R-R2 = 1 (x = 1) in
the linear regression line for dP/dtmax and LV
EF in all animals.
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For each of the LV systolic functional parameters, both the calculated
values at R-R1/R-R2 = 1 in the linear
regression line and the measured average values were significantly
smaller during triggered AF than during baseline sinus rhythm (see
Tables 1-4).
 |
DISCUSSION |
As a result of beat-to-beat variation, it has traditionally been
difficult to estimate LV systolic function in patients with AF. This
problem applies to all measures of ventricular contractile function
including noninvasively derived measures such as LV EF and SV as well
as invasively obtained parameters such as
dP/dtmax. It would be useful to have an accurate
and reproducible method available by which one could instantaneously
estimate LV systolic function during AF in patients undergoing routine
cardiac evaluations. In this study we demonstrated that impaired LV
systolic function during AF could be accurately assessed by invasively
derived peak AoF and dP/dtmax and echo
Doppler-derived SV and LV EF using the ratio of the preceding and
prepreceding R-R intervals.
A positive correlation between the R-R1 interval and
dP/dtmax, Doppler SV, and LV outflow peak
velocity was previously reported for AF (13, 16, 21). The
beat-to-beat variations in blood pressure that are also characteristic
of AF have been ascribed to time-dependent changes in ventricular
filling acting via the Frank-Starling mechanism (1, 3, 8).
Furthermore, Hardman and colleagues (13) reported that the
interval-force relationship (mechanical restitution) is a significant
determinant of the beat-to-beat variation that is typical of the LV
contractile state during AF. This mechanical restitution phenomenon is
a situation whereby a larger force development occurs after long
intervals and smaller force occurs after short intervals (4,
6).
A negative correlation between the R-R2 interval and
measures of systolic function has also been reported for AF (12,
14, 23). This inverse relationship between the prepreceding R-R interval and contractility (postextrasystolic potentiation) is a
phenomenon responsible for stronger contractions after a cardiac cycle
with a short coupling interval (14, 15, 20). Therefore, given the variability in cycle lengths, it is necessary to evaluate LV
systolic function during AF by taking into account both mechanical restitution (dependent on the R-R1 interval) and
postextrasystolic potentiation (dependent on the R-R2 interval).
Emax is an index for evaluating LV
systolic function that is considered to be relatively load independent
(25-27). Yamaguchi and co-workers (27)
reported that the Emax at
R-R1/R-R2 = 1 in the linear regression
line of the relationship between Emax and the
R-R1/R-R2 ratio during AF could estimate
resting LV systolic function. Unfortunately,
Emax is not a parameter that is clinically available and can be readily measured in a simple, routine, and noninvasive manner (18). Furthermore, there is a critical
limitation for the use of this method in patients with AF due to the
beat-to-beat variability observed in pressure-volume loops. Yamaguchi
and colleagues (27) determined Emax
during irregular heart beats as the slope of the line connecting the
left-upper corner of the pressure-volume loop of each cardiac cycle and
a "predetermined" LV volume at which the peak isovolumic LV
pressure was zero (V0). This was derived during
regular pacing in an experimental canine model with the assumption that
V0 is constant during AF. Therefore, not only is
this assumption flawed, but we cannot apply this methodology to the
clinical setting where determination of V0 is
not feasible.
Conversely, the LV EF and Doppler SV obtained by echocardiography are
widely available as noninvasive measures of LV function and
dP/dtmax, and peak AoF can be readily obtained
in the catheterization laboratory and operating room. It would be
clinically useful if the values of these LV systolic parameters at
R-R1/ R-R2 = 1 in the linear regression
line could also estimate resting LV systolic function similar to the
findings using Emax.
In our study, >100 consecutive cardiac cycles were evaluated to
obtain a reliable estimate of LV systolic function. This suggests that
the calculated values obtained with
R-R1/R-R2 = 1 in the linear regression
line, which showed a good agreement with the averaged values over all
cardiac cycles, can be expected to reliably estimate LV systolic
function during AF. Recently it was reported (5) that the
optimal number of beats necessary for estimating LV systolic function
during AF is at least 13. Notably, we have also observed a high
correlation coefficient when a smaller number of cardiac cycles were
evaluated for an estimation using the parameters (EF and Doppler SV) at
R-R1/R-R2 = 1 (see Fig. 3). We conclude therefore that it is possible to obtain an accurate and reliable estimated value at R-R1/R-R2 = 1 in the
linear regression line for the average LV systolic function during AF
using a relatively small number of consecutive cardiac cycles.
Suzuki and colleagues (26) have recently presented a
computer-simulation study in which they used equations proposed by Yue
and co-workers (28) to describe ventricular contractility (measured as Emax) during AF as a result of the
combined action of mechanical restitution and postextrasystolic
potentiation. These authors found that ventricular contractility of any
given irregular beat could be reasonably predicted by the value of the R-R1/R-R2 ratio for that beat. Moreover, it has
been demonstrated that the value when the intervals are equal
(R-R1 = R-R2; hence R-R1/R-R2 = 1) in the regression line
closely estimates the average value of ventricular contractility.
In general, our results confirm the findings of Suzuki and colleagues
(26) and extend that work by demonstrating that
R-R1/R-R2 = 1 can be used with the
regression line to determine the average values for a number of
important echocardiographic (EF and SV) and hemodynamic
(dP/dtmax and peak AoF) parameters. However, it should be noted that our results suggest the need for a cautious extrapolation of the computer-simulation results. The linear
combination of the two mechanisms [as in the model of Suzuki and
colleagues (24)] may not be true for a wide range of
irregular R-R1 and R-R2 intervals. As shown in
Figs. 2 and 3, there was a substantial scattering of data points for
each of the measured physiological parameters when
R-R1/R-R2 = 1. This precludes the use of
just any given pair of equal subsequent intervals.
The possible reason for the above restriction can be understood in the
context of combined effects of restitution and potentiation. The
potential potentiation and the time required for mechanical restitution
might be variable in different individuals depending on
pathophysiological conditions. The smallest degree of LV contractility (i.e., the minimum potentiation) can be realized when the longest duration of the prepreceding R-R interval and the shortest restitution time are combined. Furthermore, the greatest degree of contractility (i.e., maximum potentiation) could be produced when the shortest duration of the prepreceding R-R interval and the longest restitution time are combined. The correct estimation of the average physiological parameter principally requires substitution of
R-R1/ R-R2 = 1 in the regression line
that is obtained on the basis of a large number of fibrillatory
intervals. We have demonstrated, however, that in some cases the total
number of observed fibrillatory intervals can be relatively small (see
Fig. 3). Furthermore, the linear regression line could be determined by
the maximum and minimum potential LV contractility in relation to the
ratio of R-R1/R-R2 because the value at
R-R1/ R-R2 = 1 in the linear regression
line can be regarded as a mean LV contractility. In the clinical
scenario, we speculate that the LV systolic value at x = 1 in the equation of the linear regression line (which could be drawn
by connecting only extreme values at which the
R-R1/R-R2 ratio are maximum and minimum) may
provide a reliable estimate of LV systolic function during AF.
Further studies are needed, however, to determine if a representative
regression line can be produced with a limited number of observations.
There are some limitations in the present study. In measuring the
beat-to-beat variability of each LV systolic parameter, it was
necessary to include all values, even those approaching zero. Had we
omitted those values, an R-R interval might have been misrepresented as
being longer than it actually was. We only excluded beats appearing
during the mechanical refractory period; otherwise, it would be
impossible to obtain a reasonable correlation between LV systolic
parameters and the R-R1/R-R2 ratio. Another limitation was the use of healthy mongrel dogs in this experiment. We
did not evaluate whether these relationships could also be observed in
the pathological heart. However, other investigators have shown that LV
SV variability during AF was not influenced by impaired LV systolic
function (19), and interval-dependent potentiation of
contractility was preserved in patients with depressed LV function
(21). A validation study would be necessary to determine whether this index could be applied to depressed or failing hearts. In
the present study, AF was acutely induced by burst stimulation of the
right atrium and was perpetuated by vagal nerve stimulation in
anesthetized open-chest dogs. The resultant ventricular response rate
and depolarization sequence might be different in patients with chronic
AF. An advantage of this model is that the cycle-length variability was
random and not controlled. Clinical study may be necessary to determine
whether these relationships are valid for naturally occurring AF.
Finally, we evaluated relatively short R-R intervals in this study as
was dictated by our AF model. This is because most animals in this
triggered AF model manifested a rapid ventricular rate. If the R-R
interval exceeded 600 ms, the curve might plateau with complete
mechanical restitution, and the relation could be exponential
(10). However, the relation was mostly linear when R-R
intervals were short. Furthermore, the relationship between LV systolic
function and the R-R1/R-R2 ratio was more
likely linear, and the correlation coefficient obtained by
monoexponential fitting might not be significantly different from that
by linear regression analysis (27). Therefore, the
evaluation of LV systolic function using a linear regression line seems
reasonable. Further study is needed to evaluate whether this index
would remain true even with very slow ventricular rates.
The pulsed-wave Doppler SV and EF are used clinically and are more
practical than the complex invasive method that is required to measure
Emax, AoF, and dP/dtmax.
Furthermore, both of these parameters have shown a significantly
positive correlation with the R-R1/R-R2 ratio
even when a relatively small number of cardiac cycles was sampled. The
typical practice of averaging LV systolic parameters is hindered in
that it is time consuming and variable depending on the cardiac cycles
selected. By contrast, obtaining a value of the LV systolic parameter
at R-R1/R-R2 = 1 in the linear regression
line may provide a more accurate method for estimating resting LV
systolic function during AF. Finally, although clinically useful and
readily available parameters were tested, the implementation of this
index, which relates preceding cardiac cycles, will require automated
methods of sampling several cardiac cycles for it to become a
clinically useful and practical tool. Methods currently commercially
available on ultrasound equipment, such as on-line and real-time
automated endocardial border-detection algorithms for determination of
EF as well as automated Doppler signal envelope-detection methods,
would allow data acquisition and output of a long consecutive series of
cardiac cycles.
We conclude that measured parameters of LV systolic function during AF
closely correlate with the ratio of the preceding and prepreceding R-R
intervals. Using the LV systolic parameters calculated at
R-R1/R-R2 = 1 in the linear regression
line allows LV contractile function to be accurately and reproducibly
evaluated in AF, which obviates the less-reliable and cumbersome
process of averaging multiple cardiac cycles.
 |
ACKNOWLEDGEMENTS |
This work is supported in part by American Heart Assoication Grant
AHA-9808489A (T. N. Mazgalev) and National Institutes of Health
Grant RO1-HL-60833-01A1.
 |
FOOTNOTES |
Address for reprint requests and other correspondence: R. A. Grimm, Cardiovascular Imaging Center, Dept. of Cardiology, Desk F-15, Cleveland Clinic Foundation, 9500 Euclid Ave., Cleveland, OH
44195 (E-mail: grimmr{at}ccf.org).
The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement"
in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
Received 13 November 2000; accepted in final form 9 February 2001.
 |
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