Electrophysiology(EP) Study When an arrhythmia is
seen or strongly suspected from symptoms reported, an EP study may be recommended to
clarify the problem. The EP study is a procedure during which electrical recordings
are gathered both from the inside of the heart and from the body surface. ECG
electrodes are placed on the body surface and are recorded throughout the study.
Wires called electrode catheters mounted small metal bands are guided into the heart
from veins in the leg and/or the neck using X-ray. The catheters are positioned at various locations in
the heart so that electrical signals can be recorded from each of the locations
simultaneously. The catheters can also serve as pacemakers that allow the physician
to stimulate the heart and start the arrhythmia. The study therefore allows the
physician to observe what part of the heart is involved in the production of the
arrhythmia and, in some cases, to map the location and attempt to destroy it so that
the arrhythmia cannot recur. The external (ECG) signals allow the physician to match
the arrhythmia with arrhythmias which have already been observed in the other
recordings (ECG or other monitors) made by the patient.
The EP study is
performed in a specially equipped laboratory which is very similar to a typical heart
catheterization laboratory. Since X-ray equipment is used, women are not allowed in
the laboratory while they are pregnant. The studies vary in length but usually last
approximately 2 hours. The catheters are sometimes inserted into an artery in the leg
as well if access to the left atrium or ventricle is required. Local anesthesia and
IV tranquilizers and sedatives are used to make the study as comfortable as possible
for the patient. At the end of the study, bed rest of 4-8 hours duration is necessary
while the catheter insertion sites seal. Recovery time from the EP study is minimal.
Strenuous activity is prohibited for 4 days after the study, but routine activities
of daily living can resume the day after the study.
Like any invasive procedure, there are some risks associated with EP studies. The
main risks are bleeding at the site of catheter insertion or damage to the blood
vessel or vessels entered during the study. Infection can also occur at the sites of
catheter insertion, although the procedure is performed using strict sterile
technique. If veins in the neck or chest are used for access, it is possible,
although rare, to puncture the lung and cause an air leak into the space in which the
lung resides. If the leak is persistent, air may need to be drained from the space by
insertion of a tube through the chest wall. The catheters are stiff wires which can
actually perforate the thin walls of the right ventricle and cause bleeding into the
pericardial space around the heart. Most of the time these perforations seal
themselves and no therapy of any kind is necessary. Rarely, however, the blood must
be drained from the pericardial space with a needle or with surgery. Death has been
reported during EP studies, but the incidence is less than one one-hundredth of one
percent.
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When an arrhythmia is
seen or strongly suspected from symptoms reported, an EP study may be recommended to
clarify the problem. The EP study is a procedure during which electrical recordings
are gathered both from the inside of the heart and from the body surface. ECG
electrodes are placed on the body surface and are recorded throughout the study.
Wires called electrode catheters mounted small metal bands are guided into the heart
from veins in the leg and/or the neck using X-ray.
The catheters are positioned at various locations in
the heart so that electrical signals can be recorded from each of the locations
simultaneously. The catheters can also serve as pacemakers that allow the physician
to stimulate the heart and start the arrhythmia. The study therefore allows the
physician to observe what part of the heart is involved in the production of the
arrhythmia and, in some cases, to map the location and attempt to destroy it so that
the arrhythmia cannot recur. The external (ECG) signals allow the physician to match
the arrhythmia with arrhythmias which have already been observed in the other
recordings (ECG or other monitors) made by the patient.
The EP study is
performed in a specially equipped laboratory which is very similar to a typical heart
catheterization laboratory. Since X-ray equipment is used, women are not allowed in
the laboratory while they are pregnant. The studies vary in length but usually last
approximately 2 hours. The catheters are sometimes inserted into an artery in the leg
as well if access to the left atrium or ventricle is required. Local anesthesia and
IV tranquilizers and sedatives are used to make the study as comfortable as possible
for the patient. At the end of the study, bed rest of 4-8 hours duration is necessary
while the catheter insertion sites seal. Recovery time from the EP study is minimal.
Strenuous activity is prohibited for 4 days after the study, but routine activities
of daily living can resume the day after the study.