Background Implantable cardioverter/defibrillators (ICDs) have convent
ionally been implanted in the operating room by surgeons. However, tec
hnological developments have reduced size and increased Simplicity, br
inging the procedure into the realm of the electrophysiologist. The pu
rpose of this study was to evaluate the safety and efficacy of implant
ation of the entire ICD system by electrophysiologists in an electroph
ysiology laboratory. Methods and Results Between July 1993 and Februar
y 1994, 23 patients (21 men; age, 64+/-11 years) underwent transvenous
ICD implantation by electrophysiologists working alone, entirely in t
he electrophysiology laboratory. Indications for ICD were sudden death
in 10 patients, uncontrolled life-threatening ventricular tachycardia
in 12, and syncope with cardiomyopathy and familial sudden death in 1
. Seventeen patients had coronary artery disease an a past history of
acute myocardial infarction. Four patients had idiopathic dilated card
iomyopathy, 1 had coronary ectasia and poor left ventricular function,
and another had poor left ventricular function related to valvular dy
sfunction. The mean left ventricular ejection fraction was 34+/-10% (r
ange, 20% to 50%). General anesthesia was administered in 22 cases, an
d deep sedation was used in 1 elderly patient. After positioning of tr
ansvenous leads and subcutaneous patch/array lead positioning, defibri
llation testing was performed. After transvenous and subcutaneous lead
tunneling, all generators were placed subcutaneously in an abdominal
pocket. The mean total time in the electrophysiology laboratory was 25
4+/-68 minutes (range, 150 to 375 minutes), with 104+/-42 minutes for
anesthetic and other preparation, 159+/-45 minutes for implantation, a
nd 8.7+/-5 minutes (range, 3 to 25 minutes) of fluoroscopy required fo
r positioning of transvenous and subcutaneous lead systems. Implant ti
mes showed a significant improvement when the first 10 cases (188+/-44
minutes) were compared with the last 10 in the series. (124+/-44 minu
tes, P<.01). The mean defibrillation threshold was 17+/-5 J (range, 5
to 25 J). There were 5 complications (22%): 1 patch-site hematoma, 1 p
neumothorax related to subclavian venous puncture, 1 pulmonary embolis
m, and 2 patients requiring overnight ventilation after hemodynamic de
terioration following defibrillation testing. There were no deaths, an
d there were no infections. The mean time to hospital discharge after
the implant was 5.1+/-3.5 days. After 11.6+/-9 weeks of follow-up, all
devices were functioning satisfactorily, all patients had successfull
y defibrillated at postimplant predischarge checkup with 29+/-5 J, and
there had been no late complications. Conclusions This is the first r
eport to show that nonthoracotomy ICD implantation may be successfully
carried out by electrophysiologists working alone in the electrophysi
ology laboratory, with a high rate of success and few complications, e
ven in high-risk patients. This high rate of success and safety probab
ly relates to the availability of high-quality fluoroscopy and familia
rity with electrophysiology laboratory equipment and personnel.