140
Abstracts
blocking
drugs
negative
inotropic
NCE).
The
that
drugs
action
actions
have
blocked
which The
has
been
were done
By using ously The
isolated,
beating NIE
and NCE
dependent
of
Optical
isomers
and
achieved
(3)
fl-adrenergic
evident
even
or in which blocked
in hearts its release
while
from
some
chronotropic
effect
adrenergic
receptors
sympathetic
Cardiotoxicity specific chemical
at the
results
from
HIRSCH,
PH.D.
Chicago,
Ill. effect
single
pacing
ferent
when
atrium
(RA)
(RV).
PS,
cardiac ventricles,
of the
to
and
when
postextrasystolic hemodynamic pumping in A-V
transmission ventricular
to
the
(1) work
blood
of
Apparently of the responses
to
is difright
to the right ventricle a fall of
pressure,
of both atria.
evidence
rate
and
potentiation
ability.
compared
caused
of the pair in RA stimulation of paired
(PS) driving
SS,
stimulation
J.
and
Applied
in
both (2)
to the
to SS, is the opposite is used. occurs
In and
enhanced
atria1
lengthens so that
to
ventricular
demonstrated second
the RV, leads
delay impulse
minute
and
is
of total the
release
added
which
the
causes.
contribution
and
the in
obscure with
hemodynamic
effect,
due to the loss of presystolic
conduction
presence
the
or counteract
sinus rhythm
of
former. PS
when
the PS driving
this
the sinus
when
two
potentiation
sinus rate.
apt to occur
aberrant
These
rate is that of the pre-existing more
added
reduction
energy
has a detrimental
may
of the
of the
We found rate
in the
in
Aortic
dog was rapid. Late
Diastolic
Mitral
Regurgitation:
Its
Regurgitation
Relation
to the
Austin
Flint
SOMCHART LOCHAYA, M.D., MASAO IGA-
Murmur,
RASHI, M.D. and AARON B. SHAFFER, M.D., Chicago, Ill. The
Austin
Flint
mumur
has long been attributed diastole
of aortic
to vibrations
by impingement
regurgitation
produced
during
of both the aortic
regurgi-
tant jet and forward
mitral
valve flow on the anterior
leaflet
valve.
Left
of the mitral
exceeding
left
diastole
atria1
(reversed
recently aortic
been
pressure
mitral
premature mitral
valve
described
regurgitation.
latter
of the mitral
valve
flow
apical
late
during
this
pressure
latter
gradient)
in certain
This
closure
ventricular in the
part has
cases
valve,
of
more
of severe
finding
indicates
and forward
period
is thus
most
unlikely. variable aortic
length
diastolic
regurgitation
studies.
In
rumbling
was present who
underwent
all 3, a reversed
ventricular
pressure
gradient
the apical
murmur
coincided.
not adequate
to account
murmur
in
diastolic
mitral
aortic
this
normally
valve
wedge-left
was noted,
with which
Classic
concepts
A mild
was
but
are
of the Flint definite
in addition demonstrated
late
to severe cineangio-
in each of these patients.
It is concluded which
hemodynamic
for the genesis
setting.
of
with severe
pulmonary
regurgitation,
regurgitation,
graphically
murmur
in 3 patients
that the absence act
to appose
cusps at the onset of systole
regurgitation
as
the
Late
diastolic
basis
of the Austin
mitral
valve
valve Flint
of certain
perfectly
mitral
may permit
closes
some
prematurely.
regurgitation murmur
factors
the
may be the
in cases
such
as
these. Serial tricular
Hemodynamic Septal
Study
Defect,
in Infants
JOSHUA
with
LYNFIELD,
F.A.C.C. and JAMES S. TANG, M.D., F.A.c.c.,
the interval the second
per
to SS in RA,
ventricular
An Pacing
M.D., L.
output
in systemic
RA
the
M.D., F.A.c.c.,
is applied
the effect of PS, compared
of that
on
of Single Pacing
KATZ,
pacing
stimulus
stroke
to a nonspecific
of Paired
at the same
compared
to be action.
depends
S. LLUCH,
than when applied
output,
cardio-
appears
of any given drug.
N.
paired
(SS)
p-
where
blocking
to Those
a rise in mean pressure RV,
in conditions
Effects
L.
and of
the significant
Rate,
and
is
has been
blockade
which
constitution
Driving
drugs
inotropic
to be related action
Compared
Same
The
negative
Hemodynamic
in the Dog
NIE
agents.
of the
appears
on
endings
p-adrenergic
“quinidine-like”
Complex
nerve
is high)
from
effects (4) The
of this class of compounds
dissociated
be
of norepinephrine,
(especially
activity
toxic effects
can
of p-blocking
depleted
by pharmacologic
Thus,
differing
blockade
period.
(2)
the same
of “quinidine-like”
concentrations
was in-
while
SS in RV
in patients
(1)
potency.
drug,
and the refractory
of appropriate
drugs
blocking
given
that:
time
potentiation effects
i.e.,
use and
impulse
factors
or spontane-
still show essentially
independent
excitability
or
of any
NCE.
driven
recovery
compared
to cause
detrimental dominate,
oxygen
atria1 of
cardiotoxicity.
of 20 P-blocking
potency,
Therefore,
it was found
p-adrenergic
in p-blocking NIE
atria,
two
the
impulses
paired
the contributions
electrically
paired
NIE
of these
situated
Hence,
cardiac
a “quinidine-
however.
less favorably first.
diastolic
function.
to the observed
in producing
rabbit
to the fact
importance
assessed,
a
and
P-sympathetic
to have
to determine
each of these properties
(NIE
myocardial
contributes relative
not
the
moderating
both
effect
attributed
they are thought
NCE.
studies
of producing
are usually
normally
In addition, and
capable
and chronotropic
effects
these
influences like”
are
VenM.D.,
Brookyln,
N. Y. THE AMERICANJOURNAL OF CARDIOLOGY