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Heart rate (HR; top),
mean arterial pressure (MAP; middle), and thoracic impedance (bottom)
of a representative fainting patient during head-up tilt (HUT) to 70°.
All patients were characterized by similar physiological events that occur
at discrete times denoted "fiducial points". The fiducial points
shown are “baseline,” “1 min” HUT, “early” onset of the
gradual decrease in BP, “mid” decrease in BP, “late” decrease in
BP, and “faint” are indicated. After a gradual decrease in BP, marked
hypotension and bradycardia occurred.
Thoracic impedance gives an inverse measure of thoracic or central
blood volume since, as blood within the heart and lungs decreases by
upright positioning, the impedance (electrical resistance) increases
substantially. |
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Heart rate, HR (top), mean arterial
pressure, MAP (middle), and cardiac index (CI; bottom) in
fainters and healthy control subjects during 10 min of upright tilt at
70° are shown. Fainters had significant tachycardia and decreased CI
until fainting supervened. MAP decreased throughout tilt, only reaching
significance at faint. #P < 0.05 compared with baseline.
*P < 0.05, between-group comparison.
Thus, peripheral resistance is higher in
young fainters than in comparable healthy volunteers as is heart rate
while the cardiac output is reduced. The extent of tachycardia in these
syncopal youngsters may fulfill the "excessive tachycardia"
criteria of POTS and the presyncopal symptoms are common to all forms of
orthostatic intolerance. However, distinguishing these patients who faint
from POTS patients is the episodic nature fainting separated by long
periods of orthostatic well-being in the former (fainters) and the general
absence of fainting in real life of POTS patients who generally have
day-to-day symptoms of OI.
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Table 1. Demographic
and resting hemodynamics in fainters
and healthy control
subjects
Parameters
Fainters
Controls
n
11
7
Age,
yr
15.6±0.9
18±1.2
Sex, %
female
58.3
57.14
Resting SBP,
mmHg
121±3
121±6
Resting DBP,
mmHg
64±2
66±4
Resting MAP,
mmHg
84±2
88±5
Resting HR,
beats/min
67±2
65±5
Resting RR,
min1
19±1
19±2
Values are means ± SE; n = no. of
subjects. SBP, systolic blood pressure; DBP, diastolic blood pressure; MAP, mean
arterial pressure; HR, heart rate; RR, respiratory rate.
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Regional changes
in blood flow (%change) during HUT in fainters and healthy
controls.Splanchnic blood flow (top)
increased throughout tilt in fainters but was slightly reduced in
healthy control subjects. Pelvic (bottom
left) and leg blood flow (bottom
right) decreased in fainters and
controls, although there was a single significant increase in leg blood
flow late during tilt in fainters. Changes in thoracic blood flow are
represented as changes in CI in the last figure. #P
< 0.05
compared with baseline(bsl). *P <
0.05, between-group comparison. |
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Segmental volume changes
(%change) in fainters and healthy control subjects during upright tilt.
Thoracic blood volume is shown top left, splanchnic blood volume at top
right, pelvic blood volume at bottom left, and leg blood volume at bottom
right. Tilt results in thoracic emptying and splanchnic filling that are
markedly enhanced in fainting subjects. Pelvic and leg filling are similar
in fainters and control subjects. #P < 0.05 compared with baseline. *P
<0.05, between-group comparison.
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Arterial resistance in
fainters and healthy control subjects during upright tilt. Total
peripheral resistance (TPR) is shown at top left, splanchnic resistance at
top right, pelvic resistance at bottom left, and leg resistance at bottom
right. Fainters demonstrated biphasic change in TPR, pelvic, and leg
resistances in which an initial increase in TPR was followed by a decrease
in resistance until faint occurred. This was not observed in healthy
control subjects. Splanchnic resistance never increased in fainters. #P
< 0.05 compared with baseline. $P < 0.05 compared with 1 min. *P
< 0.05, between group comparison.
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In this panel we
assessed blood pressure (top panel) and blood pressure variability using a
wavelet analysis to separate systolic, diastolic and mean arterial
pressure during HUT in fainters and controls. Bottom from top down:
systolic, mean, and diastolic pressure low-frequency (low freq.) power.
■, Fainters; , healthy controls. Systolic pressure initially
increases above control and then gradually decreases until syncope when it
abruptly falls. Diastolic pressure changes are less marked. With the
exception of 1 min posttilt, LF systolic, mean, and diastolic power are
significantly lower in fainters than in controls (P 0.05). The difference
in power widens as HUT progresses. Bsl, baseline; ERec, early recovery;
LRec, late recovery. Pgroup, probability of group differences; Ptime,
probability of time differences.
Differences are
particularly noted during late tilt as fainting approaches. The blood
pressure variability at 0.1 Hz corresponds to the intrinsic frequency of
the sympathetic baroreflex and suggests that sympathetic baroreflex
failure may account for loss of TPR and vascular compensation during late
tilt.
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Changes in respiratory
parameters during HUT70 in fainters and healthy control subjects.
Respiratory rate (Resp) is shown at top left, relative tidal volume (TV)
at top right, relative minute volume ventilation (MVV) at bottom left, and
end-tidal partial pressure of carbon dioxide (PETCO2, or ETCO2) at bottom
right. Respiratory rate decreased while TV increased, reaching a maximum
just before faint. MVV increased and ETCO2 decreased monotonically in
fainters.#P < 0.05 compared with baseline. *P < 0.05, between
group comparison.
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Maximum tidal volume occurred
just before fainting. The increase in minute ventilation was inversely
proportionate to the decrease in ETCO2. Our data suggest that excessive
splanchnic pooling and thoracic
hypovolemia result in initially increased peripheral resistance and hyperpnea in simple
postural faint. Tachycardia in the presyncope period may emulate POTS. Hyperpnea
and pulmonary stretch may contribute to the sympathoinhibition, sympathetic
baroreflex failure, and abrupt
decreases in peripheral resistance that occurs at the time of faint and
characterizes the classic vasovagal faint in the young.
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