ZOLL ICY IC-3893AE/8700-0782-40 Mode D'emploi page 7

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Parameter
Condition
Maximum Whole Body
2-W/kg (Normal Operating Mode)
Averaged SAR
Whole body averaged SAR of 2-W/kg for
60 minutes of continuous RF exposure
Limits on Scan Duration
(i.e., per pulse sequence or back to back
sequences/series without breaks)
The presence of this implant produces an
imaging artifact. Therefore, carefully
MR Image Artifact
select pulse sequence parameters if the
implant is located in the area of interest.
The ZOLL Coolgard and Thermogard con-
soles are MR Unsafe and, thus, these con-
soles are not allowed in the MR system
t^okfkd
room. Therefore, the catheter must be
disconnected from the console prior to
moving the patient into the MR system
room.
dìáÇÉïáêÉ=fåëíêìÅíáçåë=Ñçê=rëÉ
kçíÉK=This information applies only to the use of guidewires in the
Seldinger technique of catheter placement in the vasculature.
t~êåáåÖë
The supplied guidewire is designed for single use only. Do not resterilize
or reuse. Do not reinsert, once removed from the patient.
Should resistance occur during insertion or withdrawal, do not continue
to move the guidewire. Determine the cause under fluoroscopy and
take action as needed.
Use extreme caution when moving a guidewire through a stent. Use of
a guidewire in stented vessels creates additional patient risk.
`~ìíáçåë
Avoid withdrawing the guidewire through metal needles; the guidewire
may shear.
Because of the delicate and fragile nature of guidewires, extra care in
handling must be taken. Avoid bending or kinking. Do not use dam-
aged guidewires.
During storage or procedures, avoid coiling the guidewire in less than 8
inch (20.32 cm) diameters, as smaller diameters place unnecessary
stress on the guidewire and may cause it to kink. The provided dis-
penser is the best means of storage and handling of the guidewire.
Sufficient guidewire length must remain exposed to maintain a firm
grip on the guidewire at all times.
aáëéÉåëÉê
Every guidewire is provided in a dispenser package. Remove the guide-
wire anti-migration clip before dispensing the guidewire. Remove the
guidewire protective cap immediately prior to guidewire use. Prepare
the guidewire prior to insertion. It is recommended that the dispenser
be filled with heparinized solutions (e.g. saline or dextrose) to bathe the
guidewire during insertion.
The preformed "J" guidewire will resume its shape when removed from
the product dispenser.
1.
Guidewire protector cap
2.
Guidewire anti-migration clip
fåëéÉÅíáçå
Inspect the guidewire prior to use and discard if any deformities are
present in the guidewire. Guidewire placement should be routinely
monitored by x-ray or fluoroscopic procedure.
qÉÅÜåáèìÉ
1.
Puncture the vessel.
2.
Insert the guidewire into the needle hub and gently advance
5-10 cm of the guidewire into the punctured vessel. Navigate the
guidewire to the desired position.
`~ìíáçåK=Avoid rough or overly vigorous manipulation of the
guidewire to prevent damage to the guide or the vessel.
3.
Remove the needle from the guidewire.
4.
Dilate the tissue and vessel with the dilator using a slight rotary
motion.
5.
Remove the dilator (the vessel dilator is intended for vascular
dilation only).
6.
Introduce the catheter by sliding it over the guidewire.
7.
Remove the guidewire.
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