The wide variety of implantable defibrillators (ICDs) available from d
ifferent manufacturers and the lack of universal industry standards ha
s resulted in the frequent need for lead adapters at time of ICD impla
nt or change. We analyzed the performance of 81 consecutive ICD sensin
g/pacing lead adapters used between 1988 and 1993. A total of 66 adapt
ers was used for new epicardial systems, and 15 adapters served as lea
d connectors during ICD generator replacement. Pacing/sensing lead ada
pters used were: model LA-201 (n = 28; 34.5%); model 030-308 (n = 26;
32%); model 5866-24 (n = 15; 28.5%); and miscellaneous (n = 12; 15%).
After a mean follow-up of 21 +/- 16 months, nine pacing/sensing lead a
dapters had documented or strongly suspected failure. Most often pacin
g/sensing lead adapters presented clinically as frequent aborted shock
s. Actuarial probability of freedom from failure for model LA-201 was
83% at 1 year, and 72% at 2 and 3 years; this was poorer than for the
other sensing leads combined (P = 0.01; hazard ratio = 4.92; 95% confi
dence intervals = 1.2-20; log-rank test). in conclusion, pacing/sensin
g lead adapters are a potential source of ICD system complications. Pe
rformance is dissimilar among different models; specifically, model LA
-201 may not be safe in the long-term, and patients with this lead ada
pter need to be closely monitored.