2.2
Instructions for Use & Clinical Reference Manual (US)
2.2
Cardiopulmonary support (CPR) should be initiated immediately per hospital
protocol if indicated for any patient supported by the Impella
®
Catheter. When
initiating CPR, reduce the Impella
®
Catheter flow rate. When cardiac function has
been restored, return flow rate to the previous level and assess placement signals
on the controller.
During defibrillation, do
NOT
touch the Impella
®
Catheter, cables, or Automated
Impella
®
Controller.
Power the Automated Impella
®
Controller using its internal battery if the integrity of
the protective earth conductor is questionable.
Lithium-ion battery replacement by inadequately trained personnel could result in
excessive temperatures, fire, or explosion. Only technicians authorized by Abiomed
should remove or change the battery.
To avoid risk of electric shock, this equipment must only be connected to a supply
mains with protective earth.
No modification of this equipment is allowed.
Medical electrical equipment needs special precautions regarding EMC and needs
to be installed and put into service according to the electromagnetic compatibility
(EMC) information provided in section 9 of this manual.
During transport, the Automated Impella
®
Controller may be exposed to stronger
electromagnetic disturbance than during in-hospital use. Strong electromagnetic
disturbance may cause the Automated Impella
®
Controller to display soft button
menu selections that were not selected by the user. Operators should be aware
that, under these conditions, the operating parameters are not affected. No user
intervention is required. Monitor Impella
®
Catheter flow and patient hemodynamics
to confirm normal operation. The condition will resolve itself once the Automated
Impella
®
Controller is no longer exposed to the disturbance.
Portable and mobile RF communications equipment can affect medical electrical
equipment.
The equipment or system should not be used adjacent to or stacked with other
equipment. If adjacent or stacked use is necessary, the equipment or system should
be observed to verify normal operation in the configuration in which it will be used.
Use of cables, other than those sold by Abiomed, may result in increased emissions
or decreased immunity of the Automated Impella
®
Controller.
The Automated Impella
®
Controller uses RFID (radio frequency identification) to
identify and communicate with the purge cassette. Other equipment may interfere with
the Automated Impella
®
Controller even if that other equipment complies with CISPR
emission requirements.
Infusion through the sideport of the introducer can be done only after all air is
removed from the introducer. If performed, the infusion should be done for flushing
purposes only and
NOT
for delivering therapy or monitoring blood pressure.
Do
NOT
use the guidewire access port on the Impella CP
®
as an arterial line. The
stylet should remain in place until guidewire access is required through the Impella
®
Catheter.
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