(Stroke. 1995;26:74-80.)
© 1995 American Heart Association, Inc.
Articles |
From the Division of Medical Physics, Faculty of Medicine, University of Leicester, Leicester (R.B.P., D.H.E.), and the Neonatal Unit, Rosie Maternity Hospital, Cambridge (A.W.R.K., J.M.R.), UK.
Correspondence to Dr R.B. Panerai, Department of Medical Physics, Leicester Royal Infirmary, Leicester LE1 5WW, UK.
| Abstract |
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Methods Cerebral blood flow velocity was measured with Doppler ultrasonography in one middle cerebral artery for 5-minute periods in 33 babies of gestational age <33 weeks admitted to a neonatal intensive care unit. Two methods of evaluating autoregulation were developed. The first used linear regression analysis of blood flow velocity on blood pressure. Records were classified as showing loss of autoregulation if the regression slope was greater than a critical value. A minimum change in mean arterial blood pressure of 5 mm Hg and a critical slope of 1.5 %/mm Hg were found to be adequate criteria for the classification of records by the regression method. The second method used coherent averaging, a technique similar to that used in recording evoked potentials. Spontaneous transient increases in blood pressure were automatically detected, and the instant corresponding to its maximum rate of rise was used to synchronize averages of the blood pressure and blood velocity transients. The resulting coherent averages were classified into two groups based on the morphology of the cerebral blood flow velocity average.
Results Whereas the regression method allowed the classification of only 51 of 106 records, the coherent average method classified 101 of 106 (95.3%) of the records available. For 51 records that were classified by both methods, there was agreement in 42 cases (82.3%). The coherent average of all records classified as having an active autoregulation showed cerebral blood flow velocity returning to baseline much earlier than blood pressure, suggesting that autoregulation was taking place within 1 to 2 seconds. This pattern was absent in records in which autoregulation was classified as absent.
Conclusions Computerized coherent averaging of the cerebral blood flow velocity response to spontaneous blood pressure transients offers a promising new method for noninvasive bedside assessment of autoregulation in patients undergoing intensive care. The time course for autoregulation, when present, is in agreement with that reported in adults.
Key Words: autoregulation cerebral blood flow infants middle cerebral artery ultrasonics
| Introduction |
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A reliable, repeatable method to characterize autoregulation would allow further work in this important area. Previous studies have measured CBF with radioactive xenon3 6 or jugular occlusion plethysmography,4 but these methods are disruptive to the infant, cannot be repeated frequently, and are not suitable for study of the speed of response. Analysis of change in CBF velocity (CBFV) in response to change in mean arterial BP (MABP) occurring during clinical deterioration5 or tilting7 seemed promising, but it can only be carried out at irregular intervals, and the stimuli may initiate an autonomic nervous system response and shift the autoregulatory plateau.8 Ahmann et al9 obtained values for CBFV and BP from observations made many hours apart, and the duration of the recordings was not sufficient to ensure that the results were free from inaccuracies in CBFV estimation introduced by the presence of slow cycling.10 11
In adults, Aaslid et al12 developed an elegant method to study the dynamics of autoregulation, using a step change in arterial pressure produced by deflating leg cuffs in healthy volunteers. This approach allowed repeated measurements and provided valuable information about the dynamics of autoregulation. However, deflating a leg cuff does not produce a significant change in the BP of a newborn baby and might not be practical in an intensive care setting. We studied the feasibility of obtaining a measure of autoregulation using spontaneous small changes in BP. Concomitant changes in CBF were estimated by measurements of CBFV with Doppler ultrasonography in one middle cerebral artery. Because the changes in BP and CBFV were of small amplitude, we resorted to coherent averaging to improve the signal-to-noise ratio, a method analogous to that used in the detection of brain evoked potentials.
Coherent averaging has been applied in many different areas to enhance the detection of waveform patterns buried in high-amplitude noise. In medicine, it has found important applications in the detection of visual and auditory evoked responses.13 In this case, a number of segments of an electroencephalogram are averaged in phase with the auditory or visual stimulus. In other applications, averaging can be synchronized by naturally occurring events such as the R wave of the electrocardiogram or by particular features of the signal. If the noise is random and uncorrelated with the signal of interest, it is possible to demonstrate that coherent averaging reduces the variance of the noise by a factor of n, which is exactly the number of transients used in the average.13 Coherent averaging has been previously applied to CBFV recordings from the posterior cerebral artery to detect the cortical blood flow response to visual stimulation.14
| Subjects and Methods |
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CBFV was measured using the semicontinuous system described by Evans et al.15 A small (0.5-cm diameter) continuous-wave Doppler ultrasound probe of power intensity <50mW · cm-2 was securely fixed to the skin overlying one middle cerebral artery using Dalzofoam (Seton). BP was measured continuously through an umbilical or peripheral arterial catheter using a P23 Spectromed transducer connected to a Simonsen and Weel Quadriscope monitor. Simultaneous recordings of CBFV (peak velocity envelope) and BP were obtained for at least 5 minutes and stored on a digital instrumentation tape recorder (PC-108M, Sony). Recordings were made at <6, 12, and 24 hours and on subsequent days if the infant had a functioning arterial catheter.
Recorded signals were low-pass-filtered at 30 Hz and converted to digital format at a rate of 200 samples per second on a microcomputer. Narrow spikes in the CBFV signal were detected and removed by linear interpolation. Both CBFV and BP signals were low-pass filtered with an eighth-order Butterworth zero-phase digital filter with a cutoff frequency of 20 Hz. The filtered BP signal was used to estimate the RR interval and to mark the beginning and the end of each cardiac cycle.
CBFV and BP data from individual transient BP peaks were averaged
together to produce a coherent average response.13 To
compute coherent averages, the mean values of CBFV and BP were
calculated for each cardiac cycle of the recording. The resulting
beat-to-beat sequences of mean CBFV and BP values were interpolated
with a third-order polynomial and resampled with an interval of 0.2
seconds to produce signals with a uniform time axis. The position of
peaks in the resampled BP signal was automatically detected, and the
foot of each peak was also detected by a foot-seeking
algorithm.16 Peaks were only accepted if they were at
least 6 seconds apart and if their relative amplitude (peak to foot)
was
2% of the baseline value. The largest peaks (up to a maximum
number of 25) were detected for each record. The position of the
maximum derivative of each BP peak was used as the point of synchronism
for coherent averaging. Although coherent averaging reduces the
influence of random noise on the estimated CBFV response to a transient
peak in BP, it is well known that CBFV recordings show low-frequency
oscillations and other large-amplitude artifacts that are not
random.10 11 17 To remove these interferences, signals
were accepted into the average only if CBFV and BP had a correlation
coefficient of r>.3 for the 3 seconds preceding the point
of synchronism. To test whether the results of averaging could be due
to artifact, averages were also obtained using random alignment between
the pressure peaks and the CBFV signal, using the same number of
waveforms.
Two distinct methods were used to classify each individual record with
respect to the presence or absence of autoregulation. In the first
method, the 5-minute recording was split into contiguous 8-second
intervals, and the mean values of CBFV and BP were calculated for each
interval. For recordings with mean BP changes greater than the minimum
pressure change (
Pmin), a linear regression of CBFV on
BP was performed using BP as the independent variable. Recordings were
classified as showing absence of autoregulation (group B) if the
regression had a slope significantly greater than the critical minimum
slope (SLmin). Otherwise, the recording was classified as
showing the presence of autoregulation (group A). This criterion
implies that regressions that are not statistically significant
(P<.05) will be classified as showing an active
autoregulation independent of the slope value. Reference values for
Pmin and SLmin are 5 mm Hg9
and 0.5 %/mm Hg,5 respectively. The effect of different
choices of
Pmin and SLmin on the
classification based on linear regression was studied by varying
Pmin between 3 and 7 mm Hg and SLmin
between 0 and 2%/mm Hg.
The second classification of individual records was based on the morphology of the CBFV coherent average. The total sample of records was randomly split into two groups, and the coherent average of each group was computed. Using the correlation coefficient between the CBFV average of each record and the group coherent average (for the 10-second period that follows the foot of the BP transient), individual records were reallocated to the group corresponding to the highest correlation. A new coherent average was computed for the two groups, and the process was repeated until there were no more transitions between the two groups.
A contingency table was used to compare the results of the two
independent methods of classification, and the degree of agreement was
tested with Cohen's
.18 Differences between clinical
variables were assessed with the t test. A value of
P
.05 was adopted as the criterion for statistical
significance.
| Results |
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A record with large BP transients is plotted in Fig 1A
and 1B, with arrows indicating the points of
synchronism detected for coherent averaging. A record with smaller BP
transients but with a spontaneous large fall in mean BP followed by a
similar change in mean CBFV is presented in Fig 1C
and 1D
. This
record was classified as group B (absence of autoregulation) by the
linear regression method.
|
With a reference value of
Pmin=5 mm Hg, only 51 of the
106 records could be used for the classification based on linear
regression because 55 did not have a change in mean BP of >5 mm Hg.
With a reference value of SLmin=0.5 %/mm Hg, 18 records
from 16 infants were considered to show autoregulation because the
slope of the regression line was not significant (group A, Fig 2A
). Fig 2B
shows the regression lines for 33
records from 22 infants that had a significant slope greater than
SLmin (0.5 %/mm Hg) and were classified as showing an
absence of autoregulation. Eleven babies had recordings in both groups.
Increases in SLmin led to a reduction in the fraction of
records classified as showing an absence of autoregulation. Similarly,
changes in
Pmin determined the total number of records
that could be used for the classification based on linear regression.
The effects of changes in
Pmin and SLmin on
the linear regression classification are shown in Table 1
.
|
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Classification based on the morphology of the CBFV average made use of
101 of the 106 individual records available. One record did not have BP
transients with amplitude >2%, and four records did not have
transients satisfying the r>.3 condition (see
"Methods"). The final coherent averages for CBFV and BP for the
two groups separated by the algorithm described above are
represented in Fig 3
. The time course of the
change in BP was similar for the two groups, but there was a marked
difference in the temporal pattern of CBFV response. While the CBFV
waveform represented in Fig 3A
returned to baseline values before
the BP pulse, the group B average continued to increase after the BP
average returned to its baseline. We associate the waveform of Fig 3A
with the presence of autoregulation and the one in Fig 3B
with loss of
autoregulation. The first group included 60 records from 28 patients;
the second included 41 records from 24 patients. Nineteen patients had
records in both groups.
|
The number of records available for comparison of the two independent
methods of classification was restricted by the condition involving
Pmin (Table 1
). For the reference condition
(
Pmin=5 mm Hg, SLmin=0.5 %/mm Hg), there
was agreement between the two methods for 37 records of a total of 51,
with 18 in group A and 19 in group B. This leads to a coefficient of
agreement (Cohen's
) of 0.489, which is highly significant
(P<.001). The corresponding values of
for other values
of
Pmin and SLmin are given in Table 1
. All
these values are highly significant (P<.005). In Table 1
it
can be observed that for any value of
Pmin the highest
values of
are obtained for SLmin=1.5 %/mm Hg. In
particular, for
Pmin=5 mm Hg there are 42 correct
classifications for the 51 records (82.3 %) corresponding to a
of
0.649.
By adopting
Pmin=5 mm Hg and SLmin=1.5
%/mm Hg, the coherent averages of CBFV and BP can be calculated for
the group A and B records, as classified by the linear regression
method, and are plotted in Fig 4
. These waveforms
are strikingly similar to the ones depicted in Fig 3
, which resulted
from the coherent average classification. Furthermore, these patterns
of CBFV disappear when random alignment is adopted between the BP and
CBFV transients.
|
With values of
Pmin=5 and SLmin=1.5
%/mm Hg maintained for the classification based on linear regression,
analysis of the clinical variables recorded prospectively during
the study showed that mean BP was significantly lower in group B
(absence of autoregulation) when compared with the mean of group A
(P<.005, Table 2
). Gestational age
and PO2 were also significantly different in
the two groups (P=.04). Table 2
also shows that
P, the
maximum pressure change in the regression data, was significantly
greater in group A compared with group B. As expected from the decision
criteria adopted to separate the two groups, the mean normalized
regression slope of the group B records was much higher than the mean
of those from group A (3.26 versus 0.87 %/mm Hg).
|
| Discussion |
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Because of the uncertainty regarding the critical slope of the
CBFV-MABP linear regression, we conducted a sensitivity analysis,
also taking into consideration the minimum change in MABP
(
Pmin) that should be required to accept a certain
regression. Our results indicate that the classification of intact
versus impaired autoregulation is not affected for slopes ranging from
0.0 to 1.0 %/mm Hg (Table 1
). However, there is a marked change in
the number of records classified as showing absence of autoregulation
for slopes
1.5 %/mm Hg. This value seems to be in good agreement
with the studies mentioned above. In particular, the study of Menke et
al,19 which was based on a group of 16 neonates with
gestational ages similar to those of our population, would have
classified 4 of the 16 as having an impaired autoregulation if the
value of 1.5 %/mm Hg was used as a threshold. It should be emphasized
that slope values are meaningless for regressions that are not
significant. In this case, it is not possible to characterize the
absence of autoregulation, and the corresponding records are more
appropriately classified as showing an active autoregulation.
Most studies using linear regression to classify the status of
autoregulation do not specify the minimum value of
P that was
adopted to accept a certain segment of data into the regression
analysis. Ahmann et al9 adopted
Pmin=5
mm Hg, and we have looked into the effect of changes in
Pmin around this value. Menke et al19
introduced a similar condition, accepting only records with a
coefficient of variation of 5% or more for MABP. In studies involving
spontaneous changes in BP, the choice of
Pmin can have a
major influence: low values of this parameter lead to unreliable
estimates for the slope, while high values can drastically reduce the
number of records available for analysis. This trade-off is
reflected in our Table 1
. For a value of
Pmin=3 mm Hg,
77 records can be used in the regression analysis, but the
agreement with the coherent-average classification (
coefficient) is
the lowest, independent of SLmin. Increasing
Pmin increases
. With the exception of the case of
SLmin=1.5 %/mm Hg,
is maximum for
Pmin=5 mm Hg, and we suggest that this value be adopted
for any future similar work.
Application of coherent averaging of CBFV and BP to automatically
detected BP transients produced encouraging results, particularly as
some recordings yielded only a few spontaneous BP transients for
averaging. The method allowed the classification of individual
recordings as showing the presence or absence of autoregulation, and
the classification thus obtained was in good agreement with the
alternative method using linear regression of CBFV on BP. Furthermore,
coherent averaging allowed the time course of CBFV response to be
studied. Figs 3
and 4
suggest onset of autoregulation within 1 to 2
seconds in this group of preterm neonates. There are very few previous
reports of the dynamics of autoregulation in infants. Anthony et
al7 observed a biphasic CBFV response to tilt and
associated this with the presence of autoregulation. However, they have
not given an indication of the time course of the autoregulatory
response. Our observation of a relatively fast autoregulatory response
is in general agreement with the results obtained by Aaslid et
al12 in adults and from animal studies.20 21 22
Precise comparison of different studies is difficult; none of the
Doppler CBFV methods represents a "gold standard" for
comparison, although we chose linear regression because of the
existence of previously published work in the newborn. Aaslid et
al12 studied a negative step change in BP, whereas our
positive changes were not perfect steps. However, there is still very
good agreement between the results. Coherent averaging has several
potential advantages: the method seems likely to give a result on a
much larger number of recordings than linear regression, which requires
a relatively large change in BP before it can be applied, and coherent
averaging gives additional information about the time course.
Furthermore, the use of coherent averaging eliminates interference
produced by the background oscillations in CBFV, which we and others
have described.10 11 As a limitation, however, coherent
averaging cannot be used in recordings without spontaneous BP
transients.
The possibility that the results obtained were artifacts generated by
the averaging technique is unlikely. Similar distinct patterns could be
observed in single BP transients of large amplitude in recordings
without large background oscillations as shown in Fig 1A
and 1B
.
Unfortunately, direct analysis of single peaks could not be
generalized because the CBFV beat-to-beat signal presents
considerable variability, which frequently dominates the temporal
pattern and obscures the autoregulatory response to small BP
changes.10 11 17 To reject large oscillations of this
type, we computed the correlation coefficient between BP and CBFV in
the 3 seconds preceding the point of synchronism (t=0 in Fig 3
) and only accepted transients with r>.3 into the average.
This condition for r was particularly important when less
than 30 waveforms were available for the coherent average. Since slow
cycling of CBFV is not strictly random noise, it is possible that it
still affects the final CBFV coherent average. In Fig 3B
(and to a
minor extent Fig 4B
also), the CBFV average shows a secondary rise for
t >5 seconds despite the fact that the BP average is
returning to baseline. The reasons for this delayed increase in CBFV
are not clear, although they have also been observed in some individual
transients. One possibility could be the superposition of BP peaks
separated by a short interval (
6 seconds), but we recalculated the
coherent averages, rejecting all peaks separated by intervals of 12
seconds or less, and patterns very similar to those in Figs 3
and 4
are
still observed. Finally, the results obtained with random alignment
rather than those that used the position of the maximum derivative for
synchronization confirmed that the responses seen in Figs 3
and 4
are a
true reflection of the dynamic relationship between CBFV and BP.
Other factors that could have influenced the results described in the
previous section, particularly the agreement between the two
independent methods of classification, could not be identified by the
analysis of the sample studied (Table 2
). The lower MABP and
gestational age observed for the group B records support the view that
prematurity might be a primary cause of loss of
autoregulation.5 7 MABP is known to increase with birth
weight,23 and for the 51 recordings of Table 2
there is a
very significant correlation between MABP and gestational age
(r=.425, P=.002). Furthermore, a plot of MABP
versus gestational age (not shown here) indicates clustering of group B
records for low values of MABP and gestational age, partly explaining
the differences expressed in Table 2
. For MABP <40 mm Hg, there are
10 records in group B and only 2 in group A
(
2=6.6, P=.01). It is possible that
the lower limit of autoregulation is closer to 40 mm Hg for these
patients than to the value of 30 mm Hg as previously estimated by De
Bor and Walther.1 The difference observed for
PO2 in Table 2
, however, is more difficult to
explain. We believe it results from the occurrence of an outlying value
of 150 mm Hg, which is more than 3 SD above the mean of group B. If
this value is removed, the t test result changes from
P=.045 to P=.09, and the difference observed for
PO2 ceases to be significant. Finally, the
observation that
P is higher in group A compared with group B (Table 2
) suggests that the regression method might have a bias toward
classifying records with smaller values of
P as having a loss of
autoregulation. However, the results in Table 1
show that this is not
the case because values of
Pmin of 3 mm Hg give a
relative frequency of classification for group B that is lower or
approximately the same as those given by
Pmin of 7
mm Hg.
In summary, there are no "gold standards" for classification of
cerebral autoregulation. The approach most commonly seen in the
literature is an assessment of the CBF and CBFV changes that follow
changes in MABP. This "static" method intrinsically assumes that
if autoregulation is active then the CBF-MABP relation is described by
the classic autoregulation curve with a plateau of CBF for a wide range
of MABP. This method has been used with very wide criteria and, to our
knowledge, we are the first group to carry out a thorough sensitivity
analysis of the influence of
Pmin and
SLmin. On the other hand, Aaslid et al12 have
shown that in normal subjects a step change in MABP leads to a CBFV
transient followed by fast recovery to baseline value. They have
assumed that this pattern characterizes the dynamics of autoregulation,
and we have extended this concept to the neonatal circulation using
coherent averaging of spontaneous transients of MABP. Because of
multiple problems associated with the practicality and reproducibility
of classification of autoregulation based on steady-state changes in
MABP (static method), it is more likely that in the future a standard
method of classification of autoregulation will be found with the
dynamic approach, as proposed by Aaslid and ourselves, than with the
less controllable static method.
The fact that Doppler ultrasonography does not give a direct
measurement of absolute flow but gives the mean spatial velocity (which
is equal to flow divided by cross-sectional area) has to be considered
in any situation where changes in cross-sectional area might affect the
conclusions of a study. Aaslid et al12 have addressed this
problem by analyzing the instantaneous spectral power of the reflected
Doppler signal, which is proportional to the number of red cells
scattering ultrasound and, consequently, proportional to the
cross-sectional area. Their conclusion is that the adult middle
cerebral artery cross-sectional area does not change significantly
during a step decrease of 20 mm Hg in MABP. No similar investigation
has been performed in the case of neonates. For the hypothetical
situation in which the diameter of the middle cerebral artery is
changing in response to BP changes, the speed of such changes has to be
considered. If the cross-sectional area were to change with the same
speed as the coherent averages in Figs 3
and 4
, it is unlikely that
these changes would be such as to exactly cancel the observed
differences between parts A and B of those figures. On the other hand,
for slower changes in diameter, the observed patterns of CBFV would be
expected to remain unchanged. In this case, the regression method would
be likely to lead to the wrong classification, since mean CBFV and MABP
measurements are taken during a 5-minute recording, and changes in
diameter throughout the recording period could influence the regression
significance and slope value.
There are many situations other than neonatal intensive care in which a bedside technique for assessing autoregulatory capacity would be useful, such as in the care of adults and children with head injury and patients suffering from meningitis, intracranial hemorrhage, and stroke. As yet, we have not applied the method to enough newborns to realize its full potential, but these preliminary results demonstrated that more of the recordings classified as showing absence of autoregulation came from less mature infants and from those with lower MABP. In several babies, the ability to autoregulate came and went at different times; further research may reveal the reasons for this. Possibilities include drug therapy such as morphine or pancuronium, changes in the baseline cerebral perfusion pressure, and recent hypoxia or hypothermia, all of which have been shown to disturb autoregulation in animals. We feel that computerized coherent averaging of CBFV in response to BP transients offers clear advantages over alternative methods for the study of cerebral autoregulation, the most exciting being the ability to characterize the dynamics of autoregulation repeatedly in individual patients.
| Acknowledgments |
|---|
Received May 9, 1994; revision received September 12, 1994; accepted September 12, 1994.
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C. Limperopoulos, H. Bassan, L. A. Kalish, S. A. Ringer, E. C. Eichenwald, G. Walter, M. Moore, M. Vanasse, D. N. DiSalvo, J. S. Soul, et al. Current Definitions of Hypotension Do Not Predict Abnormal Cranial Ultrasound Findings in Preterm Infants Pediatrics, November 1, 2007; 120(5): 966 - 977. [Abstract] [Full Text] [PDF] |
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D. W. Brown, D. Lee, V. S. Kumaran, and T.-Y. Lee Age-dependent cerebral hemodynamic effects of indomethacin in the newborn piglet J Appl Physiol, November 1, 2004; 97(5): 1880 - 1887. [Abstract] [Full Text] [PDF] |
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M. Hayashida, N. Kin, T. Tomioka, R. Orii, H. Sekiyama, H. Usui, M. Chinzei, and K. Hanaoka Cerebral ischaemia during cardiac surgery in children detected by combined monitoring of BIS and near-infrared spectroscopy Br. J. Anaesth., May 1, 2004; 92(5): 662 - 669. [Abstract] [Full Text] [PDF] |
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M.-P. Bonnet, E. Larousse, K. Asehnoune, and D. Benhamou Spinal Anesthesia with Bupivacaine Decreases Cerebral Blood Flow in Former Preterm Infants Anesth. Analg., May 1, 2004; 98(5): 1280 - 1283. [Abstract] [Full Text] [PDF] |
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S J Dasgupta and A B Gill Hypotension in the very low birthweight infant: the old, the new, and the uncertain Arch. Dis. Child. Fetal Neonatal Ed., November 1, 2003; 88(6): F450 - 454. [Abstract] [Full Text] [PDF] |
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R. B. Panerai, S. L. Dawson, P. J. Eames, and J. F. Potter Cerebral blood flow velocity response to induced and spontaneous sudden changes in arterial blood pressure Am J Physiol Heart Circ Physiol, May 1, 2001; 280(5): H2162 - H2174. [Abstract] [Full Text] [PDF] |
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B. Meyer, C. Schaller, C. Frenkel, B. Ebeling, and J. Schramm Distributions of Local Oxygen Saturation and Its Response to Changes of Mean Arterial Blood Pressure in the Cerebral Cortex Adjacent to Arteriovenous Malformations Stroke, December 1, 1999; 30(12): 2623 - 2630. [Abstract] [Full Text] [PDF] |
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R. B. Panerai, S. L. Dawson, and J. F. Potter Linear and nonlinear analysis of human dynamic cerebral autoregulation Am J Physiol Heart Circ Physiol, September 1, 1999; 277(3): H1089 - H1099. [Abstract] [Full Text] [PDF] |
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J Zhang, D J Penny, N S Kim, V Y H Yu, and J J Smolich Mechanisms of blood pressure increase induced by dopamine in hypotensive preterm neonates Arch. Dis. Child. Fetal Neonatal Ed., September 1, 1999; 81(2): 99F - 104. [Abstract] [Full Text] |
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R. B. Panerai, R. P. White, H. S. Markus, and D. H. Evans Grading of Cerebral Dynamic Autoregulation From Spontaneous Fluctuations in Arterial Blood Pressure Stroke, November 1, 1998; 29(11): 2341 - 2346. [Abstract] [Full Text] [PDF] |
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