Twin-Star International ECS Instructions For Use Manual

Category
Measuring, testing & control
Type
Instructions For Use Manual

This manual is also suitable for

13-10006, Rev C Released 3/29/13 Page 1 of 36
Instructions for Use
ECS Monitoring System – PACS Study
Pressure Monitoring Module
Pressure Measurement Fluid Collection (PMFC) Catheter
Pressure Monitor Pressure Measurement Fluid
Collection (PMFC) Catheter
WARNING:
The personal safety of the patient may be involved. Disregarding
this information could result in injury to the patient.
CAUTION:
These instructions point out special service procedures or
precautions that must be followed to avoid damaging the device.
CAUTION:
Investigational device. Limited by Federal (or United States) Law to
Investigational Use
CAUTION - Investigational Device. Limited by Federal (or United States) Law to Investigational Use
13-10006, Rev C Released 3/29/13 Page 2 of 36
Classification
Type of protection against electric shock: Class 1.
Degree of protection against electric shock: Type BF applied part.
Equipment not suitable for use in the presence of flammable mixtures.
Mode of operation: Continuous:
Electromagnetic Interface
This equipment has been tested and found to comply with the limits for a Group 1
Class B device, pursuant to IEC/EN 60601-1-2. These limits are designed to
provide reasonable protection against harmful interference. This equipment, if
not installed and used in accordance with the instructions, may cause harmful
interference to other equipment. However, there is no guarantee that
interference will not occur in a particular installation. If this equipment does
cause harmful interference to other devices, which can be determined by turning
the equipment off and on, the user is encouraged to try to correct the interference
by one or more of the following measures:
Reorient or relocate the other equipment.
Increase the separation between the Twin Star Compartment
Monitoring System and the other equipment.
Connect the other equipment into an outlet on a circuit different
from that to which the Twin Star Compartment Monitoring System is
connected.
Consult Twin Star ECS Inc. for help.
Maintenance
Routine maintenance and operation to be performed by trained qualified
personnel only. Consult Twin Star ECS, Inc. for information on maintenance and
operation.
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Description
The Twin Star ECS Monitoring System consists of four major components, i.e.,
an Introducer, a Pressure Monitoring and Fluid Collection (PMFC) Catheter, and
a Pressure Monitor.
Indications
The Twin Star ECS Monitoring System is intended for the immediate or
continuous measurement of intracompartmental pressures and/or the withdrawal
of fluid for subsequent analysis. The measured compartmental pressures can be
used as an aid in the diagnosis of compartment syndrome.
CAUTION
As an interpretive tool, the Twin Star ECS Monitoring System should be
used along with other clinical indicators to aid the physician in the
diagnosis of compartment syndrome.
Patient Education
It is the responsibility of the physician to educate the patient and/or
representative(s) regarding compartment syndrome and the Twin Star ECS
Monitoring System. This should include a description of the complications
associated with the Twin Star ECS Monitoring System, and an explanation of
alternative treatments.
Warnings and Precautions
DANGER: Explosive Hazard. Do not use in the presence of flammable gas.
DANGER: Electrical Shock Hazard. Do not remove cover. Refer servicing to
qualified personnel.
WARNING: The Twin Star ECS Monitor measures a reference Blood Pressure
for the calculation of perfusion pressure in the muscle compartment. This blood
pressure measurement is for reference only, and should not be used for patient
monitoring.
CAUTION: Catheters are for SINGLE USE ONLY.
CAUTION: Twin Star catheters are supplied sterile. Inspect package and
contents for damage. If inner package seal is broken or the package has been
opened or is damaged, do not use product.
CAUTION: Only use accessories provided or recommended by Twin Star ECS.
Attention: RS-232 (DB9) port is for service use only.
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Attention: Use the Twin Star unit on battery if the grounding integrity is in doubt.
CAUTION: During monitoring period, the monitor must be located in close
proximity to the patient to avoid any accidental “pulling” on catheter. If patient
must be moved during monitoring period, secure monitor to patient bed during
transport. DO NOT leave monitor on IV pole while transporting patient. If unable
to secure the monitor to the patient bed, disconnect the catheter(s) from the
monitor while moving patient. DO NOT STOP ACQUISITION AT THIS TIME.
Reconnect catheter(s) to monitor after patient has been moved.
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Battery
The Twin Star ECS Monitor should be plugged into a wall socket during normal
use. The battery power is only to be used while transporting the system when
the patient is connected to from one location to another. The ECS Monitor can
be run on batteries for up to 2 hours without recharging. If the battery is
discharged completely or nearly completely, allow the unit to charge for 24 hours
to ensure the battery is fully charged. If the battery is only partially discharged,
the battery may take approximately 1-24 hours to charge depending on how
discharged the battery is at the time the system is plugged back into the wall.
The battery is charging anytime the system is plugged into a wall socket
regardless if the system is on or off.
The battery should be replaced or serviced annually to ensure proper
performance and reliability. This should only be done by a qualified technician
approved by Twin Star ECS Inc.
Warning: Remove the batteries from the equipment if it is not likely to be used
for a long period of time. Removal of the battery should only be done by a
qualified technician.
Battery Pack Specifications:
Type: Li-ion Rechargeable Battery
Voltage: 7.4V
Amp Hour Rating: 9600mAh
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Introducer
The Introducer consists of a “tear-away” plastic Sheath placed over a stainless
steel Trocar as shown in Figure 1. The introducer size is 5 French (.070 inches
in diameter) by 11 cm in length. The sterile disposable Introducer provides an
access to the targeted muscle compartment to facilitate the placement of the
Pressure Monitoring and Fluid Collection (PMFC) Catheters. First, the sharp-
tipped Trocar and Sheath are inserted through the skin and into the targeted
muscle compartment. Once properly positioned, the Trocar is removed leaving
the hollow tear-away Sheath in place. The catheters can then be placed through
the hollow Sheath and into the muscle compartment. Once the catheters are
placed, the Sheath is designed to easily tear-away for removal.
Trocar
Tear-Away Sheath
Trocar Hub
Sheath Hub
Figure 1: Twin Star Introducer
The Introducer’s Trocar and tear-away Sheath design and materials are the
same as those used for standard cardiovascular or percutaneous access
devices. The tear-away Sheath is constructed of thin walled polyethylene tubing.
The Trocar is composed of stainless steel needle with a three-facet sharp tip
point.
Pressure Monitoring and Fluid Collection (PMFC)
Catheter
The PMFC Catheter is designed to monitor muscle compartment pressure as
well as remove interstitial fluid. The indwelling PMFC Catheter is provided as a
sterile disposable. The Catheter consists of a catheter body, a porous
membrane, a pressure sensor, a vacuum connector and pressure sensor
connectors, a catheter connection manifold, and a fluid sample chamber with
collection port as shown in Figure 2. The only section of the catheter that is
inserted into the patient is the distal 10 cm, which contains the pressure sensor,
porous membrane, and catheter body. The maximum diameter if the inserted
section of the catheter is .065 inches. The insertion depth will range from 5-10
centimeters, depending on which muscle compartment is being monitored.
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Figure 2: Pressure Monitoring and Fluid Collection (PMFC) Catheter
The PMFC Catheter (Figure 2) provides the following functions:
Measure compartment pressure
Remove interstitial fluid
Provide fluid analysis sample
Provide connections for additional fluid collection catheters
The catheter contains a pressure sensor at the distal tip that measures
compartment pressure throughout the treatment period. The sensor is
connected to the Pressure Monitor by fiber optic cable that extends through the
entire length of the catheter. A fiber optic connector is located at the proximal
end of the catheter that connects to the ECS Monitor.
Interstitial fluid is removed through the porous membranes located at the distal
section of the catheter. When vacuum is applied, fluid passes through the walls
of the micro-porous membranes, through the catheter body and into the 1 cc
Fluid Collection Chamber. The Pressure Monitor provides a low vacuum to the
catheter to draw fluid through the porous membranes. Fluid that is contained in
the Fluid Collection Chamber can be aspirated using a standard syringe through
the Fluid Sample Collection Port. The fluid can be transferred to a sterile vial and
saved for analysis.
Vacuum
Connector
Pressure Connector
Maximum
Insertion Length
Pressure
Sensor
Porous
Membrane
Catheter
Body
Fluid Sample
Collection Port
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The length of catheter from the patient to the monitor is approximately 2 meters
to allow the Pressure Monitor to be placed near the patient’s bed.
Pressure Monitor
NOTE – For the purposes of the PACS study, the ECS monitor has modified
as described below:
1.
The vacuum source has been disabled to prevent fluid
removal. Catheters should still be connected to the monitor
as described in the following instructions.
2.
The display has been modified to prevent users from seeing
real time pressures and the historical chart. Users will be
allowed two pressure readings during the monitoring
session.
The PMFC is designed to be used with the Twin Star ECS Monitor (Figure 3).
The ECS Monitor senses, displays and records compartment pressure as
measured by up to two PMFC catheters. In addition, the ECS Monitor measures
patient blood pressure, which is used for calculating the perfusion pressure of the
muscle compartment (Perfusion Pressure = Diastolic Pressure – Compartment
Pressure). The Twin Star ECS Monitor has been successfully tested to ensure
the delivery of the specified functional performance needed to reliably operate
the Twin Star Catheters. The Twin Star ECS Monitor has been tested and has
met current electrical safety standards established for clinical use.
The Twin Star ECS Monitor consists of a single housing that incorporates a
vacuum source, a muscle compartment pressure monitor, a blood pressure
monitor, and a user interface. The unit will be AC powered with battery back-up,
and sized to be fitted on a bedside pole and/or table top. The monitor measures
12 inches tall by 8 inches wide by 8 inches deep. An illustration of the ECS
Monitor is shown in Figure 3.
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Figure 3: Twin Star ECS Monitor
The vacuum source draws a constant vacuum of -150 mmHg to the interstitial
fluid collection line of the PMFC catheter. The pressure monitor works with
pressure sensors located in the PMFC catheter, to monitor the fluid pressure
within the muscle compartment.
The User Interface consists of a Touch Screen Display input to allow the user to
add a patient ID, start/stop the procedure and to save the data to a data storage
device. The Monitor will display the current compartment pressure and perfusion
pressure for each catheter, along with a historical chart of the pressure from the
start of the procedure.
How the
System
Works
Connect Catheters to Pressure Monitor
Before inserting the PMFC Catheter, connect the catheter to the ECS
Monitor
Insert Catheter into Muscle Compartment
To place the PMFC Catheter, an Introducer, consisting of a Polyethylene
Sheath placed over a stainless steel Trocar, is initially inserted into the
targeted muscle compartment. After the Introducer is positioned, the
Trocar is removed leaving the Sheath in place. The PMFC Catheter is
then inserted through the Sheath’s lumen. The tear-away Sheath is then
LCD Display
with
Touchscreen
Catheter
Pressure
Connection Port
Fluid Overflow
Reservoir
Blood Pressure
Cuff Connection
Catheter
Vacuum
Connection Port
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longitudinally split and separated for removal, allowing the PMFC
Catheter to remain in the muscle compartment. The PMFC Catheter is
designed to be indwelling for up to 24 hours. (refer to Figure 4 for Clinical
set-up).
Figure 4: Clinical Set-Up of the Twin Star ECS Catheter and Monitor
Monitor Compartment Pressure
The PMFC Catheter’s distal tip employs an integrated pressure sensor to
measure intra-muscular pressure. Both real time pressure and a
historical chart are displayed on the equipment module. Up to 2 catheters
can be accommodated by the ECS Monitor.
Integrated
Pressure
Sensor
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Obtaining an Interstitial Fluid Sample
NOTE: For purposes of the PACS study, the ECS monitor has
modified as described below:
1. The vacuum source has been disabled to prevent fluid removal.
Catheters should still be connected to the monitor as described in
the following instructions.
In addition to measuring pressure, the PMFC Catheter has a filtration fiber
located near its distal tip. A vacuum pressure of negative 150 mm Hg is
applied to remove interstitial fluid in the vicinity of the Catheter’s distal tip.
During the removal process, the fluid is collected into a 1cc Fluid
Collection Chamber located proximal to the catheter.
The Figure 5 illustrates the proper equipment set-up configuration for
intracompartment pressure monitoring using the Twin Star ECS Monitoring
System.
2 Catheters
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Figure 5: Proper Equipment Set-up Configuration
The anterior compartment is considered to be the “sentinel compartment” by
most physicians and is typically the primary compartment measured however,
multiple compartments can be measured using the Twin Star ECS Monitoring
System. If multiple compartments are measured in the same patient, each
pressure measurement should be considered individually. Individual pressure
measurements from multiple compartments should not be added together to form
a single measurement number. Importantly, it is imperative to never use
pressure measurements alone to make a compartment syndrome diagnosis.
Only in conjunction with other clinical signs and symptoms should pressure
measurements be used to make a diagnosis.
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Procedure Instructions
LCD Display
with
Touchscreen
Catheter
Pressure
Connection Port
Fluid Overflow
Reservoir
Blood Pressure
Cuff Connection
Catheter
Vacuum
Connection Port
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Equipment Set-Up
1
Attach
Fluid
Overflow
Container
Open package containing Fluid Overflow Container. Attach vacuum
hose to ECS Monitor and place container in ECS Monitor.
2
Power Up
Monitor
Plug ECS Monitor into AC outlet and power up ECS Monitor.
NOTE: Make sure monitor location is in close proximity to patient.
3
Enter
Patient ID
From the touch screen display, select “New Case”, and enter patient ID.
NOTE: The facility name will be displayed (i.e. “PACS-“), therefore it is
only necessary to enter the subject number (001, 002, etc.)
Selecting “Back Space” will move the cursor one space at a time.
Hitting “Clear Value” will clear the entire entry, requiring the user to
enter the complete patient ID.
When finished select “Done”. Place monitor near sterile tray for catheter
connections.
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Operating Instructions
Connect Catheter To Monitor
NOTE: The vacuum source has been disabled to prevent fluid removal.
Catheters should be connected to the monitor as described in the following
instruction.
1
Connect
Catheter to
Monitor
Remove protective cap from Fiber Optic Pressure Connector and
connect to the ECS Monitor’s Catheter Connection Port.
2
Connect
Vacuum
Line
(Pressure
Monitoring)
Pressure Monitoring and Fluid Removal (PMFC) Catheter
Connect the vacuum connector on the proximal end of the Catheter
to a 2-way stopcock (not supplied), and attach the stopcock to one of
the luer fittings on the ECS Monitor Fluid Overflow Reservoir. NOTE:
Be sure the stopcock valve is in the “Closed” position.
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Place Catheter Using Introducer
1
Open Sterile
Package
In sterile environment, open contents of Catheters onto sterile tray.
For each muscle compartment, up to 2 PMFC Catheters can be
used.
2
Insert
Introducer
into Muscle
Compartment
Prepare the skin surface of the targeted insertion site using standard
aseptic methods.
Remove the Introducer’s protective cover and insert the Introducer
into the targeted site of injury. Avoid excessive bending or
manipulation of Introducer during insertion to minimize distortion of
Sheath when Trocar is removed.
Figure 6: Insert Introducer
Warning: Care should be taken when inserting introducer to
avoid any nerves or large blood vessels in vicinity of treatment
site.
3
Remove
Trocar
Gently grasp the Trocar Hub and pull back to disengage from the
Sheath Hub and then gently remove the Trocar and dispose of
according to normal Sharps procedure.
Figure 7: Remove Trocar
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4
Insert Twin
Star Catheter
Remove and dispose of the protective cover from the Catheter.
Carefully insert the Catheter’s tip into the tear-away Sheath’s Hub.
Care should be taken during insertion to ensure that the slit tubing at
the Catheter’s tip is not damaged or distorted. Continue inserting
the Catheter into the Sheath until the clear tubing on the Catheter
touches the Sheath hub. This will place the distal tip of the Catheter
approximately 2 to 3 mm from the distal end of the Sheath.
Figure 8: Insert Catheter into Sheath Hub
Caution: Tubing tip and hollow fiber bundle are fragile. Care
should be taken when inserting Catheter into Sheath. Damage
to tip may lead to false pressure readings.
5
Remove
Tear-Away
Sheath
With the Catheter in a desired position, tear the Sheath in two by
first splitting the Sheath’s hub. As the Sheath is being removed,
continue to tear apart the Sheath while holding the Catheter in
place. Two people may be necessary to ensure a steady Catheter
position during Sheath removal. Dispose of the separated Sheath.
Caution: Immediately secure the catheters to the patient’s leg
with adhesive tape to prevent catheters from migrating out of
insertion site.
Figure 9: Tear Sheath Away from Catheter
Caution: If Catheter is not located in desired location, remove
Catheter and insert a new Introducer to reposition catheter at
new location.
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6
Maintain
Indwelling
Catheter
Use standard of care for indwelling catheters at the Catheter
entrance/exit site. Stabilize Catheter shaft with adhesive tape to
prevent excessive bending and kinking of the Catheter. Make sure
collection chamber and collection port are exposed outside of tape.
7
Position
Catheter
Tubing
After visually confirming the Catheter has been properly placed,
position the extension tubing to avoid kinking. Affix Catheter to the
leg using tape.
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Blood Pressure
1
Chose BP
Method
To take blood pressure readings using the ECS Monitor, select “Cuff
BP”.
If the patient’s blood pressure is being monitored with another device,
the blood pressure values can be manually entered by selecting
“Manual BP”.
CMS Cuff BP
Place blood pressure cuff around arm of patent and connect to ECS
Monitor.
NOTE: To ensure consistent readings during the treatment period, it
is recommended that the same cuff be used throughout the 24 hour
period.
When completed to initiate a BP reading select “Begin Measure”.
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If the reading is successful, the blood pressure will be displayed.
Select OK to continue.
NOTE: If the value displayed seems incorrect (loose cuff, incorrect
placement, etc.), select “Measure Again” to take a new measurement.
If the monitor fails to obtain a reading, “Measurement Failed” will be
temporarily displayed (see below). Select “Measure Again” to take a
new measurement, or “Stop/PrevScr” to return to the main Blood
Pressure screen to select “Manual BP”.
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Twin-Star International ECS Instructions For Use Manual

Category
Measuring, testing & control
Type
Instructions For Use Manual
This manual is also suitable for

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