This study evaluated the reliability of atrial sensing, expressed as A
V synchronous stimulation, in three VDD systems with the atrial sensit
ivity (AS) programmed to a conventional value with a 2:1 safety margin
compared to most-sensitive values. We studied 34 sex- and age-matched
patients with 3 VDD systems: 14 with Unity 292-07, 10 with Saphir 600
, and 10 with Thera VDD (5 model 8948 and 5 model 8968i). Two 24-hour
Holters were performed on consecutive days. The AS was programmed in a
randomized order to its most-sensitive value or to a 2:1 safety margi
n. All other parameters were programmed identically. The patients unde
rwent a myopotential oversensing test and a daily life activity protoc
ol. A beat-to-beat analysis of the Holters was performed to determine
AV synchrony. For the entire group AV synchrony with conventional AS w
as 98.63% +/- 2.57%, compared to 99.80% +/- 0.43% with most-sensitive
values (p = 0.002). There was no difference between the three systems
with conventional AS. With the most-sensitive AS, AV synchrony was: Un
ity 99.99% +/- 0.03 %, Saphir 99.42 % +/- 0.60 % (P = 0.002), Thera 99
.81% +/- 0.35% (ns). hn the Saphir system with an atrial blanking peri
od of 150 ms, ventricular far-field sensing could be demonstrated in 5
of 10 patients. This reduced the percentage of AV synchrony due to an
unwanted mode-switch to a nontracking mode. Myopotential oversensing
was not detected in any patient. Conclusion: The VDD systems tested un
der identical conditions showed reliable P wave sensing at the most-se
nsitive atrial sensing setting without myopotential oversensing. Ventr
icular far-field sensing reduced AV synchrony and must be avoided by a
ppropriate refractory periods.