The Identification and
Management of Patients with a High Risk for Cardiac Arrhythmias During
Modified ECT
JOAN P GERRING. M.D. and HELEN M SHIELDS. M D
ABSTRACT
The authors describe the cardiovascular complications of ECT in 42 patients
undergoing this procedure during a one year period at a psychiatric referral
center. Twenty-eight percent of the entire group of patients developed
ischemic and/or arrhythmic complications following ECT. Seventy percent of the
patients who had a history, physical or EKG evidence of cardiac disease
developed cardiac complications. On the basis of this data, a high risk
category for ECT is defined more precisely than previously. Recommendations
are made for managing this high risk category of depressed patients In order
to treat them with maximum safety and effectiveness. (J Clin Psychiatry
43:140-143. 1982)
A mortality rate of less than 1% has been consistently reported for
patients undergoing electroconvulsive therapy (ECT), the most common side
effect being memory impairment. Fortunately this is usually a short term loss
which may be minimized with the use of unilateral ECT. With the addition of a
muscle relaxant to modify ECT, fractures are no longer the second most common
complication. Rather cardiovascular complications have taken this place. In
this study we define a psychiatric population with high medical risk to
develop cardiovascular complications of varying severity. We emphasize the
identification and special care of this group.
METHOD
The charts of the 42 patients who had undergone a course of
electroconvulsive therapy at Payne Whitney Clinic (PWC) during the period July
1, 1975 to July 1, 1976 were reviewed. Five patients had undergone two
separate courses of ECT during this time period.
During the year July 1975 to July 1976, 924 patients were admitted to PWC.
There were 347 males and 577 females: 42 patients or 4.5% received ECT. The
average age of the ten men receiving ECT was 51 years and the average age of
the 32 women receiving ECT was 54.7 years. Thirty-three patients (78%) of the
group were diagnosed as having an affective disorder. These patients had an
average age of 59.4 years and received an average of seven treatments. Seven
patients (16%) were diagnosed as schizophrenic. These patients were much
younger on the average than the preceding group (29.4 years) and had twice as
many treatments per patient.
Seventeen of our patients (40%) presented with cardiac disease. This group
included all patients with a history of angina, myocardial infarction,
congestive heart failure, abnormal electrocardiogram, hypertension. (Table l)
The standard preparation for ECT during the year July 1, 1975 to July 1,
1976 consisted of a physical examination, hematocrit, hemoglobin and white
count, urinalysis, chest x-ray, skull x-ray, lateral spine x-rays,
electrocardiogram and electroencephalogram. Medical clearance, if any value
was abnormal or the history revealed significant medical problems, was
obtained from an internist, cardiologist, or neurologist.
Psychotropic medications were discontinued on the day prior to the first
treatment and the patient was fasted overnight. One-half hour prior to a
treatment 0.6 mg atropine sulfate was injected intramuscularly. First and
second year psychiatric residents were in attendance in the ECT suite. After
application of electrodes, the patient was anesthetized with intravenous
thiopental, with a mean amount of 155 mg and a range of 100 to 500 mg.
Intravenous succinylcholine, with a mean of 44 mg and a range of 40 to 120 mg
was used for muscle relaxation. Mask ventilation with 100% oxygen was then
begun continuing until the point in treatment when the effects of the
succinylcholine were wearing off and the patient could resume breathing
without assistance. This usually occurred about five to ten minutes after the
dose. Patients with pulmonary disease were to have a baseline set of blood
gases, carbon dioxide retainers not being hyperventilated. The modified grand
mal convulsion was induced by an electric current that varied from l30 to 170
volts given over a period of 0.4 to 1 second (Medcraft Unit Model 324). In ten
of 17 patients with history, physical or EKG evidence of cardiovascular
disease, a cardiac monitor or twelve lead EKG machine was used to monitor
their rhythm immediately before, during and for a 10-15 minute period
following an ECT treatment.
The average systolic blood pressure on admission in the group who did not
experience cardiovascular complications was 129± 21 mm Hg. The average of the
highest systolic blood pressures recorded after the first ECT in this group
was 173 ± 40mm Hg. A multivariate analysis was performed on the baseline
blood pressure for each patient as recorded on his/her initial physical
examination, as well as the highest blood pressure noted after each of the
first four ECT treatments (unless the patient had less than four treatments).
The systolic and diastolic pressure rise after each of the treatments were
separately compared to the baseline blood pressure.
The treatment course for depression consisted of from five to 12 treatments
given as three treatments per week. For the treatment of schizophrenic
illness, the treatment plan consisted of five treatments per week to a total
of 15 to 20 treatments. RESULTS
During July 1, 1975 to July 1, 1976. 12 of the 42 patients (28%) who
underwent modified ECT at the New York Hospital developed an arrhythmia or
ischemia following the procedure. In patients with known cardiac disease, the
complication rate rose to 70%. This rate may have been even higher had all 17
cardiac patients been monitored. The four cardiac patients with no
complications were not monitored so arrhythmias could easily have been missed.
The 12 patients who developed cardiac complications of ECT came entirely front
this group of 17 cardiac patients (Table 1) with known cardiovascular disease
prior to ECT. Six of the cardiac patients had a history of hypertension, four
had rheumatic heart disease, four had ischemic heart disease and three had
arrhythmias or a history of arrhythmias. Sixteen of the 17 patients had an
abnormal electrocardiogram prior to ECT: these included three who had a
definite old myocardial infarction, two who had a possible old myocardial
infarction, three other patients who had a bundle branch block, four patients
with arrhythmias and four others with either left ventricular hypertrophy,
left atrial abnormality or first degree heart block. Thirteen of the 17
patients were on a digitalis preparation, six were on diuretics and six were
on an antiarrhythmic spent.
Four of the complications in this series were life threatening events while
the rest were largely asymptomatic arrhythmias. These latter included
ventricular begeminy (two patients), ventricular trigeminy (one patient),
coupled premature ventricular contractions (one patient), premature
ventricular contractions (four patients), atrial flutter (two patients), and
atrial bigeminy (one patient) (Table 1). The complications were scattered
throughout the entire treatment course and were not localized to the initial
one or two treatments. Not included as a complication is the hypertensive
response immediately following ECT which occurred in the majority of patients.
The group of 12 patients with cardiovascular problems who developed
cardiovascular complications did not have a significantly greater increase in
systolic or diastolic blood pressure after any of the first four treatments as
compared to all the other patients.
Arrhythmias were the most common cardiac complication. Of the nine patients
who developed an arrhythmia, six had a previous history or EKG evidence of
arrhythmia. Four patients developed severe complications following an ECT
treatment. Patient E.S. sustained a cardiopulmonary arrest 45 minutes after
her fifth treatment. She expired despite an intensive resuscitative effort.
Autopsy did not reveal evidence of a recent infarction, but only evidence of
an old infarct that had occurred clinically seven months previously. Patient
D.S, with a history of infarction seven years prior to admission, showed
electrocardiographic evidence of a subendocardial infarction after his first
ECT. After transfer and treatment on the medical service, DS. completed a
course of seven ECT. A.B. developed hypotension, chest pain, and premature
ventricular contractions after his first treatment. In the patient M.O. rapid
atrial fibrillation following the second treatment led to severe heart
failure. The latter two patients were also transferred to the medical service
before resumption of their ECT treatment courses.
Twenty-eight (67%) of the patients in this series were age 50 or older.
Although the non-cardiac complications were evenly distributed between the
younger and older patients. 100% of the cardiac complications occurred in the
age group over 50 with 11 of 12 occurring over age 60. No cardiac
complications occurred in the schizophrenic group all of whom were less than
50 years of age, despite the higher number of treatment courses in this group
(Table 2).
Fourteen (33%) of the patients had other medical complications temporally
related to ECT. The most common non-cardiac complication was a rash seen in
six patients. described as urticarial or maculopapular. In two instances
patients developed transient laryngospasm following ECT. None of the other
non-cardiac complications would be classified as serious. Only one of the 42
patients had both a medical and cardiac complication.
DISCUSSION
Using our review of 42 patients who underwent ECT during one year at a
psychiatric referral hospital. we have identified more precisely than
previously a group of patients at high risk for the development of
cardiovascular complications. This group is comprised of those patients with a
known history of angina, myocardial infarction, congestive heart failure,
arrhythmias, rheumatic heart disease, hypertension or a baseline abnormal
electrocardiogram. It is interesting that all the severe or life threatening
complications occurred in patients who had previous myocardial infarctions or
congestive heart failure: they appear to be a special subset of the high risk
category. Since all the patients in this series with heart disease were over
50 years of age, it is impossible to say whether patients under 50 years of
age with heart disease will have the same complication rate.
The cardiovascular complications in this series and in others are probably
attributable to the physiological changes that accompany ECT. Autonomic
nervous system activity is triggered by the electric shock. During the early
phase of the seizure, parasympathetic activity predominates with a fall in
pulse rate and blood pressure. This is followed by a sympathetically induced
rise in pulse and blood pressure. Pulse rates of between 130 and 190 and
systolic blood pressures of 200 or over are common following electric shock
even in modified ECT. Atropine has been recommended for all patients
undergoing ECT in order to block the excess secretions and reduce the impact
of the initial parasympathetic discharge. Unfortunately. there is still a
significant rate of arrhythmias subsequent to atropine as shown in our study
and in others. Some of these probably result from inadequate vagal blockage
and others from unblocked sympathetic stimulation. In addition.
succinylcholine has a cholingeric action which may be increasingly severe with
successive doses and has been shown to cause hyperkalemia.
Methohexital has been associated with fewer arrhythmias than thiopental
which was the short acting barbiturate used in our patient group. Although it
is not clear why arrhythmias are fewer with methohexital its use is
recommended rather than thiopental for all patients undergoing ECT.
Arrhythmias were the most common complication in our series accounting for
ten of the 13 complications. Except for the patient M.O. who developed severe
congestive failure secondary to rapid atrial fibrillation, the arrhythmias
noted after ECT in this series were benign, terminating within minutes without
symptoms or signs of hypotension. congestive heart failure or ischemia. It is
possible however that an arrhythmia contributed to the death of E.S.
In a recent study by Troup et al on the incidence of arrhythmias in a group
of 15 patients undergoing ECT who were monitored by 24 hour Holter recordings
before, during and after ECT, there was no significant difference between the
number of premature atrial or ventricular contractions prior to ECT and that
noted during or after ECT. The discrepancy between their findings and other
reports including the present series may he accounted for by the younger age
in their group of patients. The majority were in their twenties with only one
patient being over 50. Of equal or greater importance may be the fact that
only the one patient over 50 (age 51) had historical, physical and EKG
evidence of cardiovascular disease.
In this series two patients developed ischemic complications. Other
investigators have previously reported ischemic changes on the EKG during and
immediately after the convulsive period. ECT induced ischemic damage is
presumably mediated by the marked sympathetic stimulation as evidenced by the
rise in pulse and blood pressure. The mild hypoxia, hypercapnia and
respiratory acidosis which can complicate ECT may also contribute. There was
no statistical correlation between the height of the systolic or diastolic
blood pressure rise after ECT and the occurrence of ischemic complications.
However, different susceptibilities to the rise in blood pressure may play a
role in complications in a given individual.
A recent report of the task force on ECT protocol emphasized the careful
tailoring of both the anesthetic agent and muscle relaxant to the individual
patient based on body weight and other medications. It also stressed the use
of 100% oxygen via the anesthetic mask for 2-3 minutes before injecting the
anesthetic agent in patients with higher risk. On the basis of our data
showing that arrhythmias and ischemic events occur more frequently in patients
in the high risk category, we suggest that other precautions be taken for ECT
in this group to minimize the morbidity and mortality of ECT. The additional
precautions should include: 1) medical clearance from an internist or
cardiologist familiar with the complications of ECT. 2) cardiac monitoring
immediately preceding during and for at least a ten to 15 minute period
following ECT. 3) the presence at ECT of personnel trained in cardiopulmonary
resuscitation and the emergency management of arrhythmias. 4) an EKG reading
before each successive treatment to establish no significant interval change
and 5) frequent electrolytes particularly in patients on a diuretic or
digitalis therapy throughout the ECT course.
Both suicidal and non-suicidal deaths are higher in the depressed
population and ECT is effective in reducing the incidence of both types of
deaths. Studies indicate that ECT is superior to tricyclics in rapidity of
response and in the percentage of positive responses. ECT exposes the patient
to a very short period of risk during which time he is under the direct
supervision of trained personnel. In addition tricyclic use has been
associated with a variety of cardiotoxicities.
Although the rate of complications for ECT is very low, those that occur
most often are cardiovascular in nature. It is hoped that through early
identification and management of the group of patients at high risk for these
complications that the morbidity and mortality of this extremely effective
treatment for severe depression will be lowered even further.
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