Integra Codman CereLink 826850 Guia De Inicio Rapido página 7

• Horizontal cylindrical bore MRI scanner
• Maximum MR system reported, whole body averaged specific absorption rate (SAR)
of 2.0 W/kg or head SAR of 3.2 W/kg
• MRI scan duration shall not exceed 15 minutes of continuous scanning
• Special positioning of the ICP Sensor is required to ensure patient safety during the
MRI procedure (see PREPARATION FOR THE MRI PROCEDURE below for specific
instructions)
• WARNING: Do not bring the monitor, cables or other accessories such as Tuohy
needles, trocar or stylet into the MRI suite
• WARNING: Do not use Transmit / Receive or Transmit-only RF Head coils; only use
Transmit / Receive RF Body coil or Transmit RF Body coil / Receive-only RF Head coil
• WARNING: Do not scan a patient with an elevated body temperature
MRI-Related Heating
Under the scanning conditions defined above, the ICP Sensor is expected to produce a
maximum temperature rise of less than 2°C after 15 minutes of continuous scanning. The
effects of scanning beyond 15 minutes are undetermined.
Artifact Information
In non-clinical testing, the maximum artifact size was seen on the gradient echo pulse
sequence at 3T and extends to a zone approximately 2 mm relative to the size and shape
of the ICP Sensor.
Preparation for the MRI Procedure:
1. Immediately prior to entering the MRI suite, verify that the ICP Sensor is
functioning properly. DO NOT perform an MRI procedure if the ICP Sensor is
damaged or otherwise not functioning properly.
2. Disconnect all cables and patient monitoring devices attached to the ICP Sensor
prior to transporting the patient into the MRI suite. DO NOT bring the monitors,
cables or other accessories into the MRI suite.
3. Special positioning of the ICP Sensor is required to ensure patient safety during the
MRI procedure. The ICP Sensor must be placed in a specific geometry to minimize
the potential for excessive heating of the ICP Sensor tip. Coil the tubing of the ICP
Sensor near the base of the electrical connector into 5 or 6 loops approximately 6 cm
in diameter and center on top of the patient's head (see Figure 7). Do not perform
MRI with the ICP Sensor in a "straight line" configuration (i.e., uncoiled). Failure to
follow this guideline can result in serious injury to the patient.
4. Insert a dry gauze pad at least 1 cm thick between the ICP Sensor electrical
connector with coiled tubing and the patient's scalp. Secure in place using tape
(see Figure 7). Use care when removing the tape to prevent damage to the ICP
Sensor.
5. Do not exceed the following MRI parameters during imaging:
a. Maximum spatial gradient magnetic field of 1,000 G/cm (10 T/m). The
highest SG magnetic field is commonly located off-axis, at a side wall,
and near the opening of the bore of the scanner. Please refer to MRI
manufacturers published value and location of the peak SG that is
accessible to the patient.
b. Maximum gradient field slew rate of 200 T/m/s.
c. Maximum MR system reported, whole body averaged specific absorption
rate (SAR) of 2.0 W/kg or head SAR of 3.2 W/kg.
Electrostatic Discharge (ESD) Information
CAUTION: Exposure to electrostatic discharge (ESD) energy could
damage this ICP Sensor. High levels of ESD could damage the electronic
components and cause the ICP Sensor to be rendered inaccurate or
inoperable. Take all precautions to reduce the buildup of electrostatic
charge during the use of this product.
• Provide patient grounding (e.g., grounding straps on gurneys).
• Avoid the use of materials that could generate ESD during patient movement and
transport; e.g., nylon transfer boards with bedding.
• Before touching the patient, caretakers should discharge ESD buildup by touching a
grounded metal surface, such as a bed rail.
It is recommended that all hospital personnel in contact with these devices receive an
explanation of the ESD symbol and training in ESD precautionary procedures. Training
should include, at a minimum, an introduction to electrostatic discharge, when and why it
occurs, the damage that can be done to electronic components if touched by a user who
is electrostatically charged, and precautionary measures.
Avoid touching the connector pins, which are identified with the ESD symbol, before
following ESD precautionary procedures. Avoid touching the ICP Sensor tip (sensing
element) at all times.
How Supplied
This device is intended for SINGLE USE ONLY; DO NOT RESTERILIZE.
Integra single use devices have not been designed to undergo or withstand any form
of alteration, such as disassembly, cleaning or resterilization, after a single patient use.
These devices are intended to come into contact with the central nervous system and the
ability does not currently exist to destroy possible contaminates such as those causing
Creutzfeldt-Jakob Disease. Reuse can also compromise device performance and any usage
beyond the design intent of this single-use device can result in unpredictable use hazards
or loss of functionality.
Integra will not be responsible for any product that is resterilized, nor accept for credit or
exchange any product that has been opened but not used.
As long as the individual package is not damaged or opened, the product is sterile.
All components have been tested and were determined to be nonpyrogenic, except for
the electrical connector of the ICP Sensor and the silicone tubing used for packaging,
which have not been tested.
The device is packaged using a combination of recyclable and non-recyclable materials.
Recycle or dispose of all packaging waste in accordance with hospital procedures and
regulations.
Connecting and Zeroing the ICP Sensor
CAUTION: The ICP Sensor must be zeroed at atmospheric pressure before implantation.
1. Connect the ICP Sensor to the ICP monitor using an appropriate Codman
Extension Cable. Refer to instructions for use provided with the Extension Cable
for sterilization information.
2. If applicable, connect the ICP monitor to an available pressure channel on an
external patient bedside monitor using a Patient Monitor Interface Cable.
CAUTION: Use Codman Patient Monitor Interface Cables only with the patient
bedside monitors for which they are specifically designed and designated.
3. If applicable, zero and calibrate the external patient bedside monitor according
to the instructions provided with the ICP monitor, as well as the external patient
bedside monitor manufacturer's instructions.
4. Prepare to zero the ICP Sensor by laying the tip of the ICP Sensor flat in a shallow
pool of sterile water or sterile saline. The accompanying sterile blister package
has a marked well that is suitable for this procedure. Pour sufficient sterile water
or sterile saline into the well, then lay at least a 5 cm section of the ICP Sensor
horizontally just under the surface of the sterile water or sterile saline.
CAUTION: Do not submerge the tip of the ICP Sensor vertically in a deep pool or
cup of sterile water or sterile saline. Doing so will impose a hydrostatic pressure
on the ICP Sensor diaphragm that is higher than atmospheric pressure, resulting
in an inaccurate zero reference.
EN – ENGLISH
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