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Transcript
SYMPOSIUM
Cardiac Arrhythmias
(Part 6 )
Present Status of Electroversion in the Management
of Cardiac Dysrhythmias
By LEON RESNEKOV
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SUMMARY
The theoretical and practical considerations of electrical reversion of cardiac dysrhythmias are
reviewed and a comparison made between AC and DC defibrillation, indicating the superiority of DC under all circumstances. The indications for, immediate and late results of DC
shock for atrial and ventricular dysrhythmias are presented, the complication of such treatment
reviewed, and the need for anticoagulant cover, anesthesia, and drug therapy preceding and
following the electrical treatment discussed. Each patient requires individual assessment, particularly those with chronic rhythm disturbances, especially atrial fibrillation, in whom electrical
energy settings in excess of 300 joules are rarely indicated for the risk of complications becomes
progressively higher as the energy setting is increased and the length of time sinus rhythm persists in this group of patients may be short. Patients with acute rhythm disturbances, however,
with potentially serious hemodynamic consequences should be treated with maximum electric
energies if needed. Caution is also advised in patients with coronary heart disease, atrial fibrillation, and a slow ventricular rate, even in the absence of digoxin, patients with rapidly changing
rhythm disturbances, those who cannot maintain sinus rhythm for a significant period of time
despite drug therapy, patients with the "sick sinus syndrome," those with atrial fibrillation of
more than 5 years standing with a cardiothoracic ratio exceeding 55%, and patients in lone atrial
fibrillation. Heavily digitalized patients in general should have their electroversion postponed if
possible, but if not, they should be protected against serious ventricular rhythm disturbances immediately after the shock by an intravenous dose of lidocaine, phenylhydantoin, or procaine
amide immediately before and the initial energy setting should be reduced to 5 joules. Quinidine
or some other antidysrhythmic drug may be needed in an attempt to maintain sinus rhythm after
successful electroversion, but even when controlled with adequate blood levels, results are poor.
Additional Indexing Words:
AC defibrillation
Antidysrhythmic drugs
DC defibrillation
Digitalis
Sick sinus syndrome
Anticoagulants
regarding the choice of drug nor any standardized
dosage scheme applicable to all patients. Furthermore, the patient has to be kept under close
observation over several days while the dose given
and effect caused are titrated. Only a small margin
separates the therapeutic from toxic effects, and
many of the antidysrhythmic drugs also have
important negative inotropic and dromotropic
effects. Should toxic manifestations emerge, they
may be more serious than the original rhythm
disturbance for which the drug was given, and
DRUG therapy, often successful in treating
cardiac dysrhythmias, has many limitations
which cause serious disadvantages in its routine use.
There is, for example, no universal agreement
From the Department of Medicine, Section of Cardiology,
University of Chicago Pritzker School of Medicine, Chicago,
Illinois.
Supported in part by U. S. Public Health Service Contract
PH 68-13-34 (Myocardial Infaretion Research Unit),
National Heart and Lung Training Grants HL-05793, HL05673, and the Chicago Heart Association.
1356
C1tcuiation, Volume
XLVII, June 1973
ELECTROVERSION AND DYSRHYTHMIAS
paradoxically drug overdosage may well depress the
normal sinus mechanism, thereby inhibiting reversion to sinus rhythm.
In contrast, an electric shock across the chest and
myocardium causes momentary depolarization of
the majority of heart fibers, terminates the ectopic
rhythm, and allows the sinus node to be reestablished as the normal pacemaker.
Early History
In papers dealing with the effects of electric
current on the myocardium, Prevost and Battellil 2
noted almost as an afterthought that direct current
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shock across the heart would end ventricular
fibrillation in dogs. This important fact continued
generally unrecognized or seemed largely forgotten
until Kouwenhoven, Hooker, and Langworthy3 4
and Ferris, King, Spence, and Williams5 undertook
detailed studies on the effects of electricity on the
heart and reported the following important conclusions: (1) current rather than voltage is a proper
criterion for shock intensity, (2) the passage of
electrical current across the heart may precipitate
ventricular fibrillation even in the absence of any
recognizable myocardial damage, and (3) death
will follow unless this is successfully treated by
another shock within a few minutes.
Subsequently, pioneer work into the use of
capacitor discharge (direct current) for clinical
application was undertaken in the Soviet Union
between 1935 and 1950;6 these studies can be
regarded as an important inspiration to later
investigators, including Peleska of Czechoslovakia,
Tsukerman of the Soviet Union, and Lown and his
group7 in this country.
Alternating or Direct Current
Whether alternating or direct current is used,
electrical defibrillation requires a high-energy impulse of short duration to be passed across the
myocardium, either between two concave paddles
closely applied to the heart (internal defibrillation)
or through the chest wall using two flat paddles
(external defibrillation). The total electrical energy
delivered to the heart muscle depends not only on
the electrical current, but also on the resistance of
the heart, bony cage, and skin to its passage.
Much of the confusion in the earlier literature
comparing alternating with direct current defibrillation relates to the infinite wave forms obtainable
using direct current discharge. In contrast, the
alternating current wave form is constant and
determined at the power station as a sinusoidalCirculation, Volume XLVII, June 1973
1357
shaped impulse with a frequency of 60Hz but at a
variable voltage level. A minimal current of 1 amp
is needed to bring all the heart muscles instantaneously to the same refractory point. The required
voltage for internal defibrillation is 100 v and the
power 100 w. Electric energy (power X time) is not
synonymous with electrical current, and for internal
defibrillation the energy needed would be about 20
joules (wsec). In contrast, for external defibrillation
a sixfold current increase is used producing an
energy of 360 joules.
With direct current defibrillators, the duration of
the impulse is short (1.5-4 msec). The wave form is
shaped by adding varying amounts of inductance to
the circuit, thereby insuring minimal biologic damage to its passage across the tissues of the body,
particularly the heart. The important difference
between alternating and direct current defibrillation
is that DC develops many times the power of AC.
Direct current discharge, however, is much shorter
than alternating current (3 msec vs 200 msec).
The first successful human defibrillation was
reported by Beck, Pritchard, and Feil in 1947,8 and
thereafter the convenience of AC defibrillation
determined it as the standard method. Alternating
current, however, was subsequently found to fail on
many occasions when ventricular fibrillation was
due to myocardial infarction, and also the need for
electrically converting rhythm disturbances other
than ventricular fibrillation. These two factors
stimulated further work in the use of direct current.
Despite the fact that Lown and his colleagues
reported the first AC termination of an organized
rhythm disturbance," the experience of Zoll and
Linenthal'0 gave clear warning of the real risk of
precipitating ventricular fibrillation and even death
when alternating current was used in this way.
Furthermore, severe deterioration of ventricular
function follows transmyocardial AC shocks.'1 12 By
1966 Nachlas et al.13 were able to show conclusively
that DC was superior to AC in terminating
experimental ventricular fibrillation.
From all this evidence, therefore, it can be
concluded that alternating current is feasible for
treating ventricular fibrillation, but that direct
current is more effective; alternating current,
however, cannot be recommended for electively
treating atrial rhythm disturbances or ventricular
tachycardia.
Sy nchronization
For many years a vulnerable period of ventricular
excitability had been postulated in a wide variety of
1358
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animals and Wiggers and Wegria"4 were able to
show this to be 27 msec before end of systole in the
dog; a similar period of atrial vulnerability has also
been demonstrated.'5 Nonuniform recovery from
the refractory state occurs during the vulnerable
period of the ventricle, and reentry of the
depolarization wave and self-sustained activity are
thereby favored. The risk of ventricular fibrillation
following the shock should be reduced, therefore,
by synchronizing with the R or S wave, thereby
avoiding the apex of the T wave. It will be
appreciated that it is almost impossible to avoid this
phase when AC shocks are used because of their
long duration. The chance occurrence of ventricular
fibrillation following random unsynchronized DC
shocks is about 2% and Kreus, Salokannel, and
Waris'6 deliberately use no synchronization in
clinical practice without dire consequence. The
important point when no synchronizer is used,
however, is to insure that sufficient energy is
delivered so that a current of at least 1.5-2 amps
passes across the heart; smaller energies may well
be dangerous. Of course, when ventricular fibrillation is to be treated, the synchronizer must be
switched out of the circuit.
Clinical Use of Direct Current Capacitor
Discharge for the Management
of Cardiac Dysrhythmias
The overall success rate for the DC termination
of atrial and ventricular rhythm disturbances
approaches 90%.17-20 Even when determined efforts
at conversian with drugs fail, direct current may
often succeed.21 The correct choice of patient,
meticulous attention to detail, correction of electrolyte imbalance, postponement of treatment
in the presence of overdigitalization, proper
synchronization, and choice of antidysrhythmic
agent immediately prior to and following treatment
insure both immediate success and an absence of a
high incidence of complications. The importance of
ineticulous attention to detail, however, cannot be
overemphasized. Monthly checks of the apparatus
should be made for overall electrical safety,
including inspection of the wave form and measurement of the actual electrical energy following
discharge across a 50-ohm load in the laboratory.
Most apparatus provides a moving coil meter
calibrated in joules (wsec). Models, however, are
still in use, in which the desired energies are
obtained by depressing a labeled switch, a highly
undesirable feature. During actual patient treatment, the assisting personnel should not touch the
RESNEKOV
patient, his bed, or any of the apparatus, for the
large electrical field created at the moment of
discharge may result in shocking any person in
contact. The synchronizer should always be tested
just before undertaking patient treatment by
carefully examining the superimposed artifact on the
ECG signal, or if this welcome refinement is not
available, by discharging the capacitor away from
the patient with the two paddles in close contact
and their leads in apposition to the patient's
electrocardiogram leads. In this way an artifact is
superimposed on the electrocardiogram tracing and
can be examined for correct timing.
Paddles used should always be of adequate size,
for if they are too small the electric current density
is extremely high and the possibility of myocardial
damage very real.22 It has been reported that the
anterior and posterior paddle position for external
defibrillation significantly lowers the electric energy
needed for electroversion;23 others, however, could
not confirm this.20 Indeed, experimental work13 has
shown that anterior positioning of both paddles in
the longitudinal plane delivers more current to the
heart. The failure to note more striking clinical
differences with changes in paddle positioning is
probably due to the excess electrical energies which
are consistently used to achieve electroversion. The
added safety of a flat posterior paddle supported
only by the weight of the patient and untouched by
the operator is advantageous, however, and the
anteroposterior position is therefore recommended.
Digoxin or other digitalis preparations should be
withheld for 24-28 hours before treatment if at all
possible. If the treatment cannot be postponed but
has to be undertaken in the presence of heavy
digitalization, the initial energy setting should be
markedly reduced to 5 joules for an adult, and an
intravenous injection of 50 mg lidocaine, 50-100 mg
phenylhydantoin, or 50-100 mg of procaine amide
should always precede the shock. Many use
quinidine or some other antidysrhythmic agent
routinely before administering the shock, but their
efficacy in reducing energy requirements or in
helping to maintain sinus rhythm thereafter is
questionable.20 General anesthesia is not mandatory, and amnesia produced by diazepam 5-10 mg
i.v., can now be recommended.24
Treatment should be undertaken in an area fully
equipped for cardiac monitoring and resuscitation,
including emergency pacemaking. The heart rate
should be displayed on a tachometer, and the
electrocardiogram constantly on an oscilloscope,
and preferably recorded as a direct tracing as well.
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ELECTROVERSION AND DYSRHYTHMIAS
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A short strip of V, before administering the shock is
advantageous for subsequent comparison, as immediately after the shock P waves can be difficult to
detect in the standard limb leads, even when sinus
rhythm is present. The skin should be prepared by a
liberal application of ECG paste rubbed well in to
reduce electrical resistance, and thereby prevent
painful skin burns. Great care must be taken to
insure that no part of the patient's skin is in direct
contact with the metal of the trolley or the metal of
the bed on which he is lying.
With either two anterior, or preferably an
anterior and a posterior paddle, small energies
should be administered first, and if unavailing,
shocks are repeated at increased energy level
settings. For an adult, an initial setting of 25-50
joules is satisfactory, increasing in 25-50-joule steps
as needed. If heavy digitalization is present, an initial shock of 5 joules is appropriate. Should ectopic
beats follow the first shock, 50 mg lidocaine should
be given intravenously and as a routine before any
patient known to be heavily digitalized.
The initial setting for a child is 5-10 joules
delivered across appropriately sized pediatric paddles and increasing by 5-10-joule increments.
There should be great reluctance to exceed an
energy setting level of 300 joules in an adult being
treated for a chronic rhythm disturbance, although
the situation is quite different when an acute
rhythm disturbance producing serious hemodynamic effects is present; maximal energies (400 joules)
should now be used if needed.
The initial setting for treating ventricular fibrillation (no synchronizer in circuit) in an adult is 200
joules, increasing by 100-joule steps to a maximum
of 400 joules.
Appropriate settings for internal defibrillation
(special paddles) are 20-100 joules in 20-joule
increments for an adult, and 5-50 joules in 5-joule
increments for a child.
Immediately after the shock with the development of sinus rhythm or failure to achieve sinus
rhythm after optimal energy, the amnesic drug is
discontinued and a 12-lead electrocardiogram recorded. The electrocardiogram should be monitored
for the next 24 hours or longer if need be, and
records of blood pressure should be taken every
half hour if hypotension occurs.
Individual Rhythm Disturbances
Atrial Fibrillation
Atrial fibrillation is the most common
rhythm
disturbance to be treated, but lone atrial fibrillation
Circulation, Volume XLVII, June 1973
1359
deserves special mention, for the success rate of its
electroversion is low, the incidence of complications
high, and the length of time during which sinus
rhythm persists is often disappointingly short.25
Initial success rates for atrial fibrillation are in
general around 90%, irrespective of the underlying
cause; for lone atrial fibrillation it is only 79%.
Successful electroversion is not related to age or sex,
type of heart disease (lone atrial fibrillation
accepted), overall body size, nor to the size of the f
waves in lead V1 of the electrocardiogram,18 but
does depend on the duration of the rhythm
disturbance, being less than 50% when atrial
fibrillation has been present for 5 years or longer.
Similarly, a cardiothoracic ratio of 50% or more and
selective enlargement of the left atrium lessen the
chance of success.'7' 20
Every patient, therefore, with chronic atrial
fibrillation requires individual assessment to determine whether treatment is worthwhile. Nevertheleiss, hemodynamic benefit maybe achieved in sinus
rhythm,26 27 especially when patients are studied at
progressive exercise loads.28 Certain groups of
patients, particularly those with severe mitral
regurgitation, may only be maintained free of
cardiac failure by repeated electric terminations of
episodes of atrial fibrillation.
Unless sinus rhythm is needed to maintain the
circulation or the mechanical efficiency of prosthetic
heart valves, electroversion should be postponed
until patients are convalescing following open- or
closed-heart surgery.29 Reversion to atrial fibrillation in the immediate postoperative phase is almost
universal if open-chest electroversion is undertaken
at the time of surgery, and atrial fibrillation with a
ventricular rate controlled by digoxin is often to be
preferred to rapidly changing rhythms in the
postoperative phase.
The following groups of patients are not suitable
for the electroversion of atrial fibrillation, which
should be attempted only under unusual circumstances: (1) Coronary heart disease with atrial
fibrillation in which the basic ventricular rate is
slow, even in the absence of digoxin; (2) patients
not able to maintain sinus rhythm for more than a
brief period, even when maintained on an adequate
dose of an antidysrhythmic drug; (3) patients
presenting with variable atrial rhythm disturbances
in rapid succession; (4) patients with the "sick
sinus syndrome".30 If electroversion is done during
the rapid atrial phase of the syndrome, a transvenous pacemaker should first be positioned in the
RESNEKOV
1360
right ventricle, for there is a serious risk of severe
bradyeardia or complete asystole following the
shock; (5) patients with chronic valvar heart
disease and long-standing atrial fibrillation (more
than 5 years), considerable enlargement of the
heart (cardiothoracic ratio more than 55%), and in
whom cardiac surgery is not contemplated; and
(6) patients with lone atrial fibrillation.
Atrial Flutter
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The success rate is more than 90%, and the
average energy level setting required for electroversion is only 50 joules. Unlike lone atrial fibrillation,
patients with idiopathic atrial flutter may still be
successfully reverted by direct-current shock at low
energy level settings, even when the rhythm
disturbance is known to have been present for
several years; furthermore, sinus rhythm is frequently maintained for a significant period of
time.25
Paroxysmal Atrial Tachycardia
Simple vagal stimulation and drug therapy
remain the initial treatment of choice and when
used for resistant PAT, electroversion succeeds in
about 80% of cases. It should only be used for
digitalis-induced supraventricular or junctional
tachycardias under the most exceptional circumstances, for the risk of ventricular fibrillation being
precipitated is high.3'
Ventricular Tachycardia
This is a particularly gratifying dysrhythmia to
treat; the initial success rate is 97% and electric
energies needed are low, the average setting being
50 joules. There should therefore be no hesitation in
recommending electroversion for any ventricular
tachycardia which fails to respond quickly to
emergency drug therapy. Caution has to be
advised, however, when ventricular tachycardia is
digitalis-induced; electroversion can now only be
recommended under the most exceptional circumstances and drug therapy is the treatment of
choice.
Ventricular Fibrillation
Controlled clinical trials of direct current (unsynchronized) vs alternating current for defibrillation
are difficult to design, but there is good animal
experimental work to indicate the superiority of
DC,13 and in clinical practice successful resuscitation (patient leaving hospital) has been reported in
more than 50% of patients treated by DC shock and
well conducted principles of resuscitation.32 The ini-
tial energy setting should be 200 joules, increasing
by 100-joule increments if needed.
Complications
Complications occur more frequently than initially predicted, and do not only relate to drugs given
to maintain sinus rhythm. Indeed, an incidence of
14.5% among 220 consecutive patients has been
reported;33 these did not include minor complications such as superficial skin burns due to poor
preparation of the skin or transient rhythm
disturbances after the shock. Included, however,
were the following.
Raised Levels of the Serum Enzymes LDH and CPK (10%)
Their origin, however, is still uncertain
Mandecki et al.34 consider skeletal muscle damage
as the cause, but as other signs of myocardial
damage frequently coexist when the serum enzyme
levels are raised, the matter awaits definitive
study.
Hypotension (3%)
Hypotension is more common when higher electric energies are used, and may persist for several
hours, frequently requiring no particular intervention, but the patient should be carefully observed.
ECG Evidence of Myocardial Damage (3%)
Patterns of myocardial infarction may follow the
shock and persist for many months; they are most
common following electroversion at high energy
settings.
Pulmonary and Systemic Emboli (1.4%)
The incidence is similar to that following quinidine conversion of rhythm disturbances but does
indicate the need for anticoagulant cover (see
below).
Ventricular Rhythm Disturbances
Ventricular premature beats and tachycardia are
common at low energy settings when the patient is
heavily digitalized, and at high energy level settings even in the absence of any digitalis preparation. Should a ventricular dysrhythmia follow the
first shock, an intravenous antidysrhythmic drug, as
previously recommended, should be given before
increasing to high energy settings.
Pulmonary Edema and Increase in Heart Size
These may occur in -3% of patients coming on
within 1-3 hours of treatment.35 Unlike other major
complications, they occur only in patients actually
reverted to sinus rhythm. While Lown considers
Circulation, Volume XLVII, June 1973
ELECTROVERSION AND DYSRHYTHMIAS
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pulmonary emboli as a possible cause, others
believe that following electroversion there is
considerable depression of the mechanical function
of the left atrium.36 Any additional obstruction to
flow across the mitral valve, any lessening of left
ventricular wall compliance or left ventricular
dysfunction will aggravate the situation and may
result in pulmonary edema.
The incidence of complications relates to the
energy level setting, being 6% at 150 joules but rising to exceed 30% at a setting of 400 joules. One can
conclude, therefore, that there is rarely an indication for exceeding a 300-joules setting in patients
presenting with long-standing rhythm disturbances,
particularly atrial fibrillation of more than 5 years'
duration.
Follow-up Studies
While the initial success rate is remarkably good,
direct current shock is disappointing in long-term
follow-up studies, particularly when atrial fibrillation is treated.17, 20, 37 Reversion to atrial fibrillation
is most likely by the end of the first month of
electroversion, and not infrequently occurs within
the first day. Those in whom atrial fibrillation has
persisted for more than 3 years, those with
significant underlying heart disease, or with considerable overall enlargement of the heart are
particularly liable to revert to atrial fibrillation.
Those with lone atrial fibrillation are exceptional;
they do not remain in sinus rhythm even in the
absence of these unfavorable circumstances.25
Quinidine and Other Antidysrhythmic Drugs
Rossi and Lown38 reported that quinidine preceeding direct current shock improves the chances
of persistent sinus rhythm, diminishes the electric
energy needed for the conversion, and reduces the
incidence of postconversion rhythm disturbances.
Studies such as these are difficult to control, and
other groups have been unable to confirm their
conclusion.37'39 Several groups, however, have
investigated the use of drugs alone or in combination to maintain sinus rhythm.39' 40 After transmyocardial DC shock, acetylcholine and catecholamines
are liberated,4' and their combined effects may
precipitate ectopic rhythms, permit their continuance, and either prevent the emergence of sinus
rhythm or curtail its duration. Szekely42 reported
that quinidine, procaine amide, and propranolol do
not necessarily reduce the instance of DC shockinduced rhythm disturbances, except for those
directly related to digitalis. Furthermore, their
Circulation, Volume XLVII, June 1973
1361
clinical and experimental observations suggest that
the toxic cardiac effects of these drugs may even be
enhanced by high energy electric current; they
therefore advise caution in their routine use. More
recently, quinidine bisulfate as a long-acting
preparation has been extensively investigated in an
attempt to maintain sinus rhythm following DC
shock.43 Even when a long-acting preparation is
controlled with adequate blood levels, sinus rhythm
persists only for a slightly longer period of time,
and furthermore, the incidence of complications
with quinidine may still be high.
It can be concluded, nevertheless, that quinidine
or some other antidysrhythmic drug should be
considered for any patient who has reverted to his
original rhythm disturbance, and in whom sinus
rhythm is important. The chances of sinus rhythm
persisting, however, are not good, even when
adequate blood levels are maintained.
Digitalis and Electroversion
Lown, Kleiger, and Williams44 reported that in
experimental animals the DC threshold for the
emergence of ventricular tachycardia fell to 0.2
joules in the presence of heavy digitalization.
In man, the counterpart of these observations is
demonstrated by ventricular premature beats,
tachycardia, or even fibrillation being precipitated by the DC shock in heavily digitalized
patients.17' 20, 31 In the presence of a known
digitalis-induced rhythm disturbance, electroversion
should therefore rarely be used, for despite the very
occasional record of a successful outcome, fatal
ventricular fibrillation may follow the shock, even
when properly synchronized.45
Anticoagulants and Electroversion
The need for and efficiency of anticoagulant
protection has been the subject of much debate, in
the absence of any well-controlled study. Such a
study has now been reported46 demonstrating a
statistical benefit in a group of patients who had
electroversion under anticoagulant control. Unless a
contraindication to its use is present, all patients
going forward to electroversion should be protected
by anticoagulant therapy, particularly patients with
recent cardiac infarction, chronic coronary heart
disease, mitral valvar disease, cardiomyopathy, and
prosthetic heart valves when a coumadin derivative
should be given or heparin used if the indication for
DC shock is urgent. As the risk of reversion to the
original rhythm disturbance is highest within the
first month of treatment, it is wise to maintain oral
RESNEKOV
1362
anticoagulant therapy for at least 4 weeks after
successful DC shock when it may be discontinued
unless the underlying heart disease requires its
continuance.
Electric defibrillation of the heart, particularly
synchronized DC shock, is an exciting advance but
further effort is needed to uncover the basic
mechanisms of rhythm disturbances, thereby encouraging the development of more physiologic
approaches to their treatment and particularly to
the maintenance of sinus rhythm thereafter.
References
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Present Status of Electroversion in the Management of Cardiac Dysrhythmias
LEON RESNEKOV
Circulation. 1973;47:1356-1363
doi: 10.1161/01.CIR.47.6.1356
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