
6 Lumax Technical Manual
The following leads were evaluated in a retrospective study with
BIOTRONIK’s ICDs/CRT-Ds:
•
Medtronic Sprint 6932
•
Medtronic Sprint 6943
•
Medtronic Sprint Quattro 6944
•
Medtronic Transvene RV 6936
•
St. Jude (Ventritex) TVL- ADX 1559
•
St. Jude SPL SP02
•
Guidant Endotak DSP
•
Guidant Endotak Endurance EZ, Endotak Reliance
•
Guidant (Intermedics) 497-24.
The following leads were bench tested for compatibility with
BIOTRONIK’s ICDs/CRT-Ds:
•
Guidant Endotak Endurance “CPI 0125”
•
Guidant Endotak Reliance 0148
•
Medtronic Sprint 6932
•
Medtronic Sprint 6942
•
Medtronic Sprint 6943
•
Medtronic Sprint 6945
•
Medtronic Sprint Quattro 6944
•
St. Jude Riata 1571/65
•
St. Jude SPL SPO1
Resuscitation Availability
- Do not perform induction testing
unless an alternate source of patient defibrillation such as an
external defibrillator is readily available. In order to implant the
ICD/CRT-D system, it is necessary to induce and convert the
patient’s ventricular tachyarrhythmias.
Unwanted Shocks
– Always program ICD Therapy to OFF prior
to handling the device to prevent the delivery of serious shocks to
the patient or the person handling the device during the implant
procedure.
Rate-Adaptive Pacing
– Use rate-adaptive pacing with care in
patients unable to tolerate increased pacing rates.
Summary of Contents for Lumax DR ICD Series
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