User Manual Part 4

onset 3-34
rate sensing 3-3
rate th reshold 3-4
reconfirmation/committed shock 4-23
redetection 3-11
stability 3 -32
sustained rate duration (SRD) 3-35
tachyarrhythmia 3-1
tachyarrhythmia, safety mode 2-19
Vrate>Arate3-28
vector timing and correlation 3-27
ventricular, initial 3-6
window 3-13
Device
characteristics as shipped 1-23
description 1-4
mode 3-2
programming recommendation 5-2
specification 1-21
storage 1-8
Diagnostic
battery status 6-2
heart r a te variability (HRV) 7-12
histogram 7-11
lead test 6-6
patient triggered monitor 7-17
Disk
data 2-11
read 2-11
save 2-11
Disposal of pulse generator 10-8
DIVERT THER APY 2-16
Duration 3-15
ATR (atrial tachy response) 5-29
post-shock 3-18
redetection 3-18
E
ECG (electrocardiogram)
display 2-7
EGM (electrogram)
display 2-7
Electrocautery
mode 3-3
Electrode, lead configuration 5-42
Electromagnetic interference (EMI) 1-12
EMI (electromagnetic interference) 1-12
EndofATRepisode5-32
Energy
shock 4-21
Enhancement
detection 3-7, 3-23
Entry count 5-29
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 3-20
end of ATR 5-32
nontreated 3-20, 7-15
treated 3-20, 7-15
ventricular 3-20
Event
adverse, potential 1-19
counter 7-15
icon 2-9
therapy history 7-2
Events
summary 7-7
Exit count 5-30
Explantation 10-8
- DRAFT -