User Manual Part 2

onset 3-33
rate sensing 3-3
rate threshold 3-4
reconfirmation/committed shock 4-23
redetection 3-11
stability 3-31
sustained rate duration (SRD) 3-34
tachyarrhythmia 3-1
tachyarrhythmia, safety mode 2-19
Vrate>Arate3-27
vector timing and correlation 3-26
ventricular, initial 3-6
window 3-13
Device
characteristics as shipped 1-22
descriptio n 1-4
mode 3-2
specification 1-19
storage 1-8
Diagnostic
battery status 6-2
histogram 7-11
lead test 6-6
patient triggered monitor 7-13
Disk
data 2-11
read 2-11
save 2-11
Disposal of pulse generator 10-8
DIVERT THERAPY 2-17
Duration 3-14
ATR (atrial tachy response) 5-21
post-shock 3-17
redetection 3-17
E
ECG (electrocardiogram)
display 2-7
EGM (electrogram)
display 2-7
Electrocautery
mode 3-3
Electrode, lead configu ration 5-31
Electromagnetic interference (EMI) 1-12
EMI (elec tromagnetic interference) 1-12
EndofATRepisode5-23
Energy
shock 4-21
Enhancement
detection 3-7, 3-22
Entry count 5-21
EP test (electrophysiologic test) 8-2
ATP, commanded 8-11
backup VVI pacing during atrial
stimulation 8-2
burst pacing, 50 Hz/manual 8-9
commanded therapy 8-10
fibrillation 8-5
induction 8-4
mode, temporary 8-2
programmed electrical stimulation
(PES) 8-7
shock on T 8-6
shock, commanded 8-10
VFib 8-5
Episode 3-19
end of ATR 5-23
nontreated 3-19, 7-11
treated 3-19, 7-11
ventricular 3-19
Event
adverse, potential 1-18
counter 7-11
icon 2-9
therapy history 7-2
Events
summary 7-6
Exit count 5-21
Explantation 10-8
- DRAFT -