Beehive Horizon Manual - Rev I
Beehive Horizon Manual - Rev I
Beehive Horizon
Long-term Monitoring
with AURA Amplifier System
USER &
SERVICE MANUAL
Release I
0086
© Copyright 2014 by Natus Neurology Incorporated
All rights reserved. This manual contains proprietary information, which is protected
by copyright and may not be copied in whole or in part except with the prior written
permission of Natus Neurology Incorporated. The copyright and the foregoing
restrictions on the copyright use extend to all media in which this information is
preserved.
This copy of the User Manual shall be used only in accordance with the conditions
of sale of Natus Neurology Incorporated or its distributors. Natus Neurology
Incorporated makes no representations or warranties of any kind whatsoever with
respect to this document. Natus Neurology Incorporated disclaims all liabilities for loss
or damage arising out of the possession, sale, or use of this document.
Trademarks
Other brand and product names are trademarks or registered trademarks of their
representative holders.
This manual is subject to periodic review, update, and revision. Customers are
cautioned to verify that the manual’s information applies to the software and hardware
present in the equipment.
This product performs as described in this manual, and in accompanying labels and/
or inserts, when assembled, operated, maintained, and repaired in accordance with the
instructions provided.
This product must be cleaned and checked periodically. Do not use a defective product.
Parts that are broken, missing, worn, or contaminated should be replaced immediately.
If repair or replacement becomes necessary, call or write to request service advice from
Grass.
This product must not be altered without the prior written approval of
Grass. The user of this product shall have the sole responsibility for any malfunction
that results from improper use, faulty maintenance, improper repair, unauthorized
service, or alteration by anyone other than Grass.
The safety, reliability, and performance of this device can only be assured under the
following conditions:
• If the device has been used according to the accompanying
operating instructions.
• If changes or repairs have been carried out by Grass.
• If it is used in buildings having ground equalization wiring that complies with
relevant UL, CSA, IEC or other local standards and regulations.
Regulatory Notices
This device has been designed and certified to comply with the requirements of the
international standard EN60601-1 and EN60601-2-26, EN60601-1-2, and EN60601-1-1
the United States standard UL2601-1, and the Canadian standard CAN/CSA22.2
No.601.1.
0086
The device is classified:
CLASS I, Type BF
100-250 VAC, 50/60 Hz, 80 VA
The above classification is based on the condition that this device is installed and
configured according to the instructions supplied. In order for the complete system to
maintain compliance with the relevant standards, the host computer must be approved
to the IEC950 standard.
Equipment Classifications
Explosion Hazard
Warning: Do not use this system in the presence of flammable anesthetics or
other flammable substances.
Patient Safety
Warning: The patient should be disconnected from the AURA system when high
frequency surgical equipment is used.
Warning: Do not connect or use the Battery Charger Power Supply in the
presence of the patient.
Warning: This system should not be used in place of electrocardiograph for vital
signs monitoring.
Warning: Use only by or on the order of medically-trained personnel.
Warning: MRI diagnostic imaging is not recommended with this
device in use.
Warning: Read manual before using.
Warning: Protect from exposure to liquids. If the Amplifier unit is exposed
to liquids during recording, discontinue use by disconnecting the
electrodes at the Pin Jack Adaptor and turning the Amplifier unit
power off. Resumption of recording is to be performed only by
qualified personnel.
Warning: AURA contains no user serviceable parts.
Intended Use
The AURA amplifier system is intended for recording routine EEG and EEG associated
with long term monitoring for epilepsy.
Caution
Use only accessories and electrodes identified for use with this device
(see instructions for the electrodes that are being used).
3. Installation........................................................................................... 3-23
Setting Up for Operation................................................................................ 3-23
Installation...................................................................................................... 3-24
Step 1: Installing Cabling. ....................................................................... 3-26
Step 2: Installing the Network Interface Card
for Associated Computers. ....................................................................... 3-26
Step 3: Setting up the RPSAS40 Regulated Power Supply.................... 3-26
Power Supply Line Voltage................................................................. 3-26
Step 4: Setting up the Base Station.......................................................... 3-26
Step 5: Connecting the Tether Cable...................................................... 3-27
Step 6: Connecting Amplifier Unit Inputs. ............................................. 3-28
Step 7: Connecting Other Equipment to the Base Station. .................. 3-28
Host Computer Setup....................................................................................... 3-29
AURA IP Address Setup. .......................................................................... 3-29
Subnet Mask Setup. ................................................................................... 3-30
AURA Version........................................................................................... 3-30
Network Interface Card (NIC) IP Address Setup........................................ 3-30
x Table of Contents
7. Maintenance. ........................................................................................ 7-57
Maintenance. ................................................................................................... 7-57
Calibration................................................................................................. 7-57
Cleaning..................................................................................................... 7-58
Electrodes............................................................................................ 7-58
Storage & Transportation. ...................................................................... 7-58
End-of-Life Disposal. ................................................................................ 7-58
A. Appendix A.............................................................................................A-61
Connector Pin-outs........................................................................................ A-61
Ethernet Cable, Cross-over.................................................................... A-61
Ethernet Cable, Patch............................................................................. A-61
Specifications
Amplifier ������������ Grass AURA system
32 referential EEG inputs (AC), 2 reference input,
2 patient ground (with PJAAD Pin Jack Adaptor)
8 DC inputs, non-isolated (not with BHHN-P)
AC Input
Signal Range ����� Referential AC channels: 4 mV peak to peak full-scale
Differential DC voltage tolerance: 500 mV maximum
DC Input
Signal Range ������ ±2.5 volts
Input
Characteristics ���� 12 Megohm impedance, all inputs including reference
All referential AC inputs electrically isolated from
earth ground
Frequency Response 0.5 Hz to 100 Hz, -3 dB
0.1 to 100 Hz recoverable with TWin software
Amplification (gain) � AC channels: 1000 ±2%
Vertical Resolution �� 16 bits (0.06 µV/bit)
Sampling Rate ������� 400 samples/second/channel
Data stored at 200 or 400 samples/sec, user definable
via host computer
CMMR �������������� >100 dB, all AC channels, at 50/60 Hz
Noise ��������������� <2 µV peak to peak referred to input
Impedance Test Mode Referential inputs only: 30 Hz square wave; range,
1 kohms to 100 kohms, 10%
Calibration Signal ��� Referential inputs only: 500 µV peak to peak ±2%;
10 Hz square wave
Patient Bias Current � Maximum: <4 nA
Typically: 300 pA
Event Input ��������� 2 pushbutton patient signaling inputs (1 on base
station, 1 on amplifier for use with 1 event pushbutton)
Direct Current
Courant Continu
Alternating Current
Courant Alternatif
Protective Earth
Terre de Protection
Type BF Equipment
Équipement de type BF
Dangerous Voltage
Tension Dangereuse
Equipotentiality
Equipotentialite’
Product Description
The Beehive Horizon is a 40-channel system designed specifically for recording
Long-term EEG. The system features a compact, wearable 32-channel AURA
Amplifier Unit and a Base Station that can be mounted in a variety of locations.
An 8-input DC module is also included with the system. With the optional
external battery, the AURA Amplifier can be used for 24 hours of ambulatory
recording. Options are available to upgrade the Beehive Horizon to 64 or
128 AC channels. The Beehive Horizon Portable has 32 channels.
The Amplifier unit is typically tethered to the Base Station, which streams data
to a host computer. However, the Amplifier unit is also capable of operating
untethered. When untethered, the Amplifier unit will run off an internal
battery and save data on a CompactFlash memory card. AURA is capable
of over 2 hours of untethered recording. If there is an immediate need to
download and review the data stored on the CompactFlash memory card, the
CF can be removed from AURA and the data can be downloaded quickly via
a USB CompactFlash Reader. With AURA, the patient can travel from their
patient room to a day room. When the patient arrives at the day room, AURA
simply needs to be plugged into any base station located in that room. Our
TWin recording software will recognize that the patient has switched to a new
base station, and tethered recording will resume again.
When tethered, the Amplifier unit connects to the Base Station via a single
cable that carries power and data through a proprietary serial interface. Battery
charging circuitry is built into the unit. Electrical isolation exists inside the
Amplifier unit and this cable meets patient isolation requirements.
The Amplifier Unit can also be used for 24-hour ambulatory monitoring when
connected to the optional external battery.
An intuitive user interface with LCD screen is present with the base station.
From the base station itself, the technologist is able to implement such features
as electrode impedance checking, amplifier calibration, and photic stimulator
control. Also from the LCD display it is possible to obtain information such
as connection status to the host computer. Menu selections can be made for
configuring the unit and communicating with the host computer.
Power is supplied to the Base Station through a rear side connector that
attaches to the RPSAS40 Medical-grade Power Supply (+12 VDC).
A 36-pin connector is also located on the rear side and allows for the connection
of the CAB-21648-10 patient pushbutton and CAB-21617 pushbutton adaptor
cable. Two Auxiliary DC inputs are available for recording external voltage
sources. All other connections (Ethernet, oximeter, photic stimulation control,
etc.) are also located on the rear side of the Base Station.
Functional Components
The Beehive Horizon system consists of the following main functional
components:
• AURA Amplifier unit with CompactFlash card and reader
• PJAAD Pin Jack Adaptor
• Base Station
• RPSAS40 Medical-grade Power Supply
• Isolated Medical-grade Power System
• Auxiliary DCM8 DC Input Module (not in BHHN-P)
• Optional External Battery
• Software including: TWin LTM, SzAC automatic
seizure/spike analysis, Panorama digital video
• Latest high-performance PC-based acquisition
system, network ready
Black Button
3 7
Grass® DCM8
4 8
SINGLE ENDED DIFFERENTIAL
Made in USA
For more information regarding the compatibility of a device with the Horizon
system, please contact Grass Technical Support Department.
The Amplifier unit is worn by the patient and is typically tethered to the Base
Station. However, the Amplifier unit is also capable of operating un-tethered.
When un-tethered, the Amplifier unit will run off an internal battery and save
data on a CompactFlash® memory card.
The Base Station itself, and the associated power supply, can be attached to a
cart or stand for routine EEG studies, Long-term Monitoring and Video EEG
with optional mounting brackets. Grass provides a full line of mobile carts and
mounting brackets. Please consult Grass Customer Support for further details.
Take care to locate these components away from dirt, dust, high temperatures,
and liquid spill hazards. Avoid locating the unit where the power switches or
controls or cables could be bumped inadvertently.
Tether Cable
CAB-22255 Amplifier Unit Event Pushbutton
CAB-21778-02
Event Button
CAB-21648-10
Tether Cable
CAB-22256
Base Station
AUXILIARY DC INPUT MODULE
1 5
EVENT
2 6
DCM8
DC Input 3 7
CON-20486 To PC
Networking Ethernet
Cable Connector Card
Event Pushbutton
CAB-21648-10 or
CAB-21617
CAB-20576-03
Ethernet Cross-over
Cable
CAB-21064 or
Ethernet Patch
Cable
To Ethernet Hub or Switch
Tether Cable
CAB-22255 Amplifier Unit Event Pushbutton
CAB-21778-02
Tablet PC
Power Switch Video
Camera
Tether Cable
CAB-22256
Base Station
RPSAS40 Regulated
Power Supply AC Power
Line In
USB Ports
CAB-20576-1
Null Ethernet
Base Station Cable
Grass recommends that all network, video, or intercom cabling, and any other
cabling for auxiliary instrumentation be run by qualified personnel under
hospital supervision and according to local standards and regulations.
The Beehive Horizon system may be supplied with a network interface card for
computers associated with the Beehive Horizon system. Follow the instructions
that are supplied with this card to install and test the interface card before
connecting to the Beehive Horizon system.
Select an appropriate location that will allow for ventilation around the unit
and the outlet to be within safe reach of the Base Station. The power cable
should be run so as it will be out of the way and not be a tripping hazard.
(The Beehive Horizon Portable has the power supply already installed in the
carry case. )
The Base Station can be located remotely from or locally to the host computer.
Depending on the setup, the network cable required will be either a Cross-over
or Patch 10BaseT, category 5, Ethernet cable. (The Beehive Horizon Portable
has the Base Station already installed in the carry case.)
A tether cable is used to connect the Amplifier unit to the Base Station. Connect
one end of the tether cable to the Base Station by inserting the connector into
place. See Figure 3-2. Connect the other end of the tether cable to the Amplifier
unit. To disconnect the tether cable, pull on the outer sleeve of the connector to
unlock it from the unit.
Attach the electrodes, via Electrode Board/Pin Jack Adaptor, and Patient Event
Pushbutton to the Amplifier unit.
Attach any additional equipment such as the Event Button, DC Input Module,
or optional Photic Stimulator, or Nonin Xpod™ Pulse Oximeter.
Note that waveforms from AUX 1 and AUX 2 DC input ports, the Nonin Xpod™
Pulse Oximeter, and Photic Stimulator marker, are only recorded when the
Amplifier unit is tethered to the Base Station.
If Grass TWin software is used on the host computer, refer to the TWin
software manual for details on the operation of the system. A system
calibration and test recording should be preformed following the instructions
supplied in the TWin manual.
Note: If the MENU button is pressed while changing the IP address, the
modifications will not be saved.
This section will provide instructions on programming the Subnet Mask of the
Beehive Horizon system.
AURA Version
1. From the Windows task bar, select Start > Settings > Control Panel.
2. Double-click on the Network and Dial up Connections icon.
3. In the Network and Dial up Connections window, double-click on the icon
that represents your NIC. This may be listed as Local Area Connection.
4. In the Status window, click on the Properties button.
5. Highlight Internet TCP/ICP protocol by clicking on it once, then click
Properties. The Internet Protocol (TCP/IP) Properties window will appear.
Base Station
The controls available on the Base Station include the DC power switch on the
rear and eight keys associated with the LCD.
There are eight push buttons, or keys, for interacting with the Base Station
and the host computer. Some of the selections in the menu require the host
computer to be connected to the Base Station.
The following list describes each key on the Base Station and a brief description
of its use.
A power indicator is located above the LCD and is green when the Base
Station power is on. The LCD displays the menus, electrode impedance results,
connection status, and any error messages that may occur.
Additionally, two indicator lights are used by the Ethernet connection on the
back of the Base Station. The green light indicates the Base Station is attached to
an active node, and the yellow light indicates communication activity over the
connection.
Amplifier Unit
The controls on the Amplifier unit are
used to turn the power on and off.
Power Buttons
Green LED
Steady Amplifier unit is functioning.
Flashing Slow
(about 1/sec) Amplifier unit is functioning and writing to a
CompactFlash card.
Yellow LEDs
#4 Flashing Battery is fully charged.
#2 or #3 Flashing Battery is moderately charged.
#1 Flashing Battery is very low.
All Off Battery is discharged or missing.
All Flashing Memory Warning: CompactFlash card is missing (after
power on), or full (after write).
Three Flashing
(#1, #2, #3 ) Memory Warning: The CompactFlash card is not ready
for writing data. This could be caused by Patient/
Record ID not matching the previously stored values
(often caused by inserting a card from a different
patient), an incorrect format, or a faulty card. Correct
this by entering (or re-entering) the correct patient
information or by inserting the correct CompactFlash
card. Note that entering patient information may
overwrite the patient information currently stored
on either the CompactFlash card, or the memory in
CompactFlash Card
Bottom View
The CompactFlash card slides into the drive of the Amplifier unit. The top of
the card must face the top of the Amplifier unit to be oriented properly for
insertion. To remove the card, simply pull it out of the drive.
Note: Do not pull the CompactFlash card out of the Amplifier unit if the
green LED is flashing (at any speed). The flashing greeen LED indicates
that Amplifier unit is still writing to a CompactFlash card or updating
the CompactFlash file system. Wait for the green LED to glow steadly
before removing the CompactFlash card.
Calibration
The Beehive Horizon system includes a built-in calibration signal generator
and the means to connect this generator to the amplifier inputs at the first stage
preamplifier. The generator outputs a 5 Hz, 500 µV peak-to-peak square wave.
Gain calibration and correction is critical to the accurate creation of montages
from the referentially recorded data.
Refer to the instructions for calibrating the amplifier hardware in the TWin
software manual for more details. Typically calibration involves starting
the recorder software, putting the Beehive Horizon into calibration mode,
recording a segment of the calibration signal then confirming the peak-to-peak
value of the AC calibration signal. This data is then used to automatically
generate a list of correction values for both offset and gain.
Event Pushbutton
An Event Pushbutton can be used to signal the recording software for event
marking or to start a recording session. The state of this pushbutton is reported
in every scan of data in one of the status bits.
Two types of Event Pushbuttons are supplied with the Beehive Horizon.
The pushbutton and cabling can be unplugged and removed without affecting
the normal operation of the system.
With the optional rechargeable, external Battery Pack, the Amplifier unit can be
used for 24-hour, out-of-lab epilepsy monitoring.
There are four indicator lights on the optional external Battery Pack.
A 24-volt power supply (RPS-21794) is provided with the external Battery Pack.
This power supply is used to charge the battery. A fully charged battery will
provide approximately 24 hours of ambulatory recording time.
Warning: Do not connect or use the Battery Charger Power Supply in the
presence of the patient.
External Battery
CH
AR
FA G
CHG USE
E
TR ST
IC
KL
E
FAULT
POWER
RPS-21794
To Grounded AC Power Power Supply
Wall Outlet Line In
Supply power to the battery for four hours. While the external Battery Pack
is charging, the indicators will light to provide status information. These
indicators are only used during the charging process.
Event Pushbutton
CAB-21778-02
Electrode Board/
Pin Jack Adaptor
Switch - Side View PJAAD
CHG USE
External Amplifier
Battery Unit
Switch - USE Selected
CH
AR
FA G
TR ST E
IC
KL
E
FAULT
POWER
Move the switch on the external Battery Pack to the USE position. Then
connect the external Battery Pack to the Amplifier Unit.
Switch - Side View
Note: The USE/CHG switch must be in the USE position to
perform 24-hour ambulatory recordings. CHG USE
The Electrode Board/Pin Jack Adaptor and Event Pushbutton are also used
during ambulatory recording. Switch - USE Selected
CH
AR
FA G
E
TR ST
IC
KL
E
FAULT
POWER
When the Amplifier unit is connected to the optional external Battery Pack, the
internal battery in the Amplifier unit will constantly be charged by the external
Battery Pack. During this process, yellow LED indicators on the Amplifier unit
will flash in continuous order.
Connection Interruptions
The design of the optional external Battery Pack and Amplifier unit allows
temporary disconnection of the external Battery Pack without interruption
of recording.
If the external Battery Pack and Amplifier unit become disconnected during
ambulatory recording, the battery in the Amplifier unit will become the
primary power source and recording will continue.
The Amplifier unit internal battery is constantly charged while the external
Battery Pack is connected. Therefore, if the external Battery Pack is
disconnected, the Amplifier unit battery will typically contain a full charge. The
charge level of the Amplifier unit while not connected to the external Battery
Pack is indicated by the yellow LEDs. When fully charged, the Amplifier unit
battery will provide approximately two hours of power.
When the external Battery Pack is reconnected to the Amplifier unit, the
external Battery Pack will become the primary power source. It will also charge
the battery contained in the Amplifier unit. The yellow LEDs on the
Amplifier unit will flash in continuous order to indicate that the Amplifier unit
battery is charging.
During Ambulatory recording, use caution to avoid contact with the Amplifier
unit Off button. If the Off button is held for more than 10 seconds and the
Amplifier is writing to the CompactFlash card, the Amplifier will stop taking
in data and begin closing the file (as evidenced by the fast flashing of the green
LED). It will shut down when it is finished. Writing to the CF will resume when
the Amplifier unit is turned back on.
To stop ambulatory recording press and hold the Off button on the
Amplifier Unit until the green LED begins flashing rapidly. The LED will
continue flashing for about 30 seconds and then the Amplifier will turn off.
If the Amplifier unit will not respond properly, holding the Off button for at
least 45 seconds will force the unit to power off.
Grass TWin software can be used on the host computer to read the file and
process the data. TWin software is powerful and easy to use, providing data
acquisition, recording, and review capabilities in one flexible package.
Remove the CompactFlash card from the Amplifier unit. See Chapter 4,
CompactFlash Card, Figure 4-3. Then insert it into the CompactFlash card
reader on the computer. Although TWin software can read directly from the
CompactFlash card, it is recommended that data files be copied to a different
medium such as the computer’s hard disk for further review and analysis.
Cables/Adaptors
Part Number Description
CAB-21615-5 DCM8 to Base Station patch cable, 5-foot (1.5 m) cable
CAB-21610-10 Auxiliary DC, 3.5 mm to 3.5 mm, 10-foot (3 m) cable
CAB-21612-20 Auxiliary DC, dual 3.5 mm to dual 3.5 mm,
20-foot (6 m) cable
CAB-21616-10 Phono to 3.5 mm 10-foot (3 m) cable. Used to connect
the CAB-21648 event button to the DCM8 (included with
CAB-21648)
CAB-21617 Event button to Base Station adaptor, used to connect an
event button directly to the AS40 when an optional
DCM8 DC Input Module is not available,
1-foot (0.3 m) cable length
MCB-21678-03 AC Cordset IEC320, 3-foot (0.9 m) cable
MCB-20018 Hospital-grade AC cordset, USA, 6-foot (1.8 m) cable
26832000 Booster cable. Used to connect optional External Battery to
Amplifier unit.
CAB-20576-1 Null Ethernet cable, 1-foot (0.3 m) cable
NET-CKIT Network Cabling Kit includes:
CAB-21064-010 Ethernet cable, patch. Used to connect Base Station to Host
via a hub/switch, 10-foot (3 m) cable
CAB-21064-025 Ethernet cable, patch. Used to connect Base Station to Host
via a hub/switch, 25-foot (7.5 m) cable
CAB-20576-03 Ethernet cable, cross-over. Used to directly connect Base
Station to Host, 3-foot (0.9 m) cable
CON-20486 Ethernet cable connector. Used to daisy chain two Ethernet
cables (RJ45 connectors) together.
Oximeter (optional)
Part Number Description
XPOD Nonin Xpod™ Pulse Oximeter, 80” (2 m) length cable
8000J Adult Flex Sensor, straight, 3’ (1 m) length cable, includes
a package of 25 8000JFW FlexiWrap® Sensor Wraps
8000JFW FlexiWrap® Sensor Wraps, package of 25
8008J Infant Flex Sensor, straight, 40” (1 m) length cable, includes a
package of 25 8008JFW FlexiWrap® Sensor Wraps
8008JFW Infant FlexiWrap® Sensor Wraps, package of 25
7000A Adult Finger Flexi-form Disposable Sensors,
40” (1 m) length cable, package of 10
7000P Pediatric Finger Flexi-form Disposable Sensors,
40” (1 m) length cable, package of 10
Maintenance
There is no routine maintenance required for the Grass Beehive Horizon/
AURA systems and accessories other than normal periodic checks for unusual
wear, cable abrasion, and routine cleaning.
Calibration
Cautions
• Do not autoclave or pressure sterilize the BHHN/AURA system.
• Do not soak or immerse the BHHN/AURA system in any liquid.
• Do not gas sterilize the BHHN/AURA system.
• Do not use petroleum based or acetone solutions, or other harsh
solvents to clean the BHHN/AURA system.
To clean the BHHN/AURA system, use a soft cloth dampened with mild soap
and water solution. To disinfect the Amplifier unit use 70% isopropyl alcohol.
Be sure that the components are unplugged before cleaning and that the
components are completely dry before use.
Electrodes
Refer to the cleaning instructions supplied with the electrodes for details on
cleaning, disinfection, and/or sterilization.
For storage and transportation, it is recommended that the system and its
accessories be within the temperature range of -40 to 70° C, 500 to 1060 hPa,
and 10 to 100% RH, including condensation. When returning from temperature
extremes, allow the system to stabilize to room temperature before use.
End-of-Life Disposal
Base Station power light Base Station Power Turn on Base Station
not on switch off
No patient signals Amplifier unit not Check Amplifier unit is seated properly
present plugged in fully
No pulse or oximeter Oximeter not plugged Check cable connections of the XPOD
readings from the XPOD into Base Station or at both the Base Station and sensor.
or incorrect readings sensor not plugged in
AUX inputs 1 & 2 on Cables are not plugged Verify cabling connections
Base Station are not in fully
present in recording
software
Photic unit not Photic flash unit not Verify photic cabling for both power and
functioning plugged in or photic not the flash unit
powered up
Pin Jack Adaptor unit Check Pin Jack Adaptor unit is seated
not plugged in properly
Poor signal quality Poor electrode Check electrode application and reapply
application if needed
Pin Jack Adaptor not Check Pin Jack Adaptor unit is seated
plugged in properly
Connector Pin-outs
Ethernet Cable, Cross-over
Used to connect Base Station directly to the Host computer.
Pin 1 = Pin 3
Pin 2 = Pin 6
Pin 3 = Pin 1
Pin 4 = Pin 4
Pin 5 = Pin 5
Pin 6 = Pin 2
Pin 7 = Pin 7
Pin 8 = Pin 8
Pin 1 = Pin 1
Pin 2 = Pin 2
Pin 3 = Pin 3
Pin 4 = Pin 4
Pin 5 = Pin 5
Pin 6 = Pin 6
Pin 7 = Pin 7
Pin 8 = Pin 8
The external Battery Pack enables approximately 24-hour continuous recording in an ambulatory setting, removing the need for the patient to be confined to a hospital. This flexibility enhances patient comfort and compliance, improves the ability to monitor conditions such as epilepsy in natural environments, and increases diagnostic yield . The extended recording capability is vital for capturing accurate clinical data unobtainable in a limited or laboratory setting.
Using incompatible power supplies can lead to device malfunctions, power failures, or even electrical hazards. The external Battery Pack and Base Station power supplies are deliberately designed with different connectors to prevent misuse . Precautions include rigorously training personnel to recognize and use only the designated power supplies for each component and strictly following the setup guidelines provided. This ensures system safety and reliability.
To configure the subnet mask, ensure the Base Station is powered on, press the MENU button five times to display 'Set Subnet Mask', then press ENTER. Adjust the numeric values with the up and down buttons and confirm with ENTER . Proper subnet mask configuration is significant as it defines network boundaries and ensures effective communication between devices, reducing data collision and enhancing network performance.
To configure the IP address for the Beehive Horizon Base Station, ensure the Base Station is powered on. Press the MENU button four times to display 'Set IP Address', then press ENTER. Use the left and right buttons to toggle numeric entry and up and down buttons to change the value. Confirm the entry by pressing ENTER . Each step is crucial to ensure the device is correctly networked, facilitating communication with the host computer and preventing system mismatches that may disrupt data flow.
Setting up the RPSAS40 regulated power supply correctly ensures sufficient ventilation and safety, as improper setup might pose a tripping hazard or electrical accident risk. It also supports proper system function by accepting line voltage from 100 to 250 volts without manual adjustment, hence accommodating varied hospital-grade power standards . Proper setup is crucial for system reliability and uninterrupted operation.
LED indicators on the external Battery Pack are crucial for monitoring the charging and operational status of the battery. FAST and TRICKLE LEDs indicate different charging stages, while the FAULT LED warns of potential errors needing technical support. The POWER LED confirms charging power availability . These indicators offer real-time feedback essential for managing battery health and ensuring uninterrupted recording, directly impacting data integrity and patient monitoring efficacy.
The Tether Cable connects the Amplifier unit to the Base Station, forming a crucial link that allows for the transmission of electrical signals and data between these components. Improper connection can lead to data loss or corruption, affecting the system's ability to capture and process accurate readings . It is vital for maintaining the integrity of medical monitoring and ensuring precise data capture required in clinical assessments.
An isolation transformer enhances safety by reducing the leakage current to the level of the transformer itself when multiple pieces of equipment are interconnected. This aligns with appropriate standards (EN60601-1) and mitigates the risk of electrical hazards that may arise from current summation . It ensures patient and operator safety, especially critical in medical environments.
Critical factors include ensuring a distinct IP address within the hospital’s networking range, configuring TCP/IP properties accurately, and matching the Subnet mask . These settings affect system operation by dictating data flow efficiency, minimizing communication errors, and ensuring secure, reliable integration with other hospital information systems. Misconfigurations can lead to connectivity issues, disrupting the monitoring process and data collection.
To start ambulatory recording, insert a CompactFlash card into the Amplifier unit, connect patient electrodes via the Electrode Board/Pin Jack Adaptor, configure the Amplifier via the Base Station and TWin software, initiate recording, disconnect from the Base Station, and connect to a fully-charged external Battery Pack ensuring it is set to USE mode . Each step ensures the system is ready, the patient signals are recorded accurately, and power is sustained throughout the ambulatory session, vital for long-duration monitoring.