Contraindications
This neurostimulation system is contraindicated for
patients who are
▪
Unable to operate the system
▪
▪
Poor surgical risks
▪
Patients who failed to receive effective pain relief during
trial stimulation are contraindicated to proceed to the
permanent implant procedure.
MRI Safety Information
If you are using a trial system, you should not be
subjected to an MRI. The electromagnetic field
generated by an MRI may damage the device electronics
and induce voltage through the lead that could cause a
jolting or shocking sensation.
If you are using a permanent system, you may be
implanted with the parts that make up a Magnetic
Resonance (MR) Conditional system, which allows you
to receive an MRI scan if all the requirements for the
implanted parts and for scanning are met. Scanning
under different conditions may cause device
malfunction, severe injury, or death. Contact your
physician before receiving an MRI scan to find out if you
can undergo the procedure and to learn more about any
risks. Additionally, before receiving an MRI scan, inform
the healthcare professional that you are implanted with
a neurostimulation system. If you do not have an MR
Conditional system, you cannot receive an MRI.
8
Содержание NeuroSphere 3875
Страница 1: ...NeuroSphere Patient Controller Dorsal Root Ganglion Neurostimulation Systems Model 3875 User s Guide ...
Страница 56: ...If you only have one area you will see the following screen Figure 15 Strength screen One Area 52 ...
Страница 96: ...www abbott com 2022 08 ARTEN600266402 A 600266402 ...