Reference Manual
244 Pages
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Avance CS² User's Reference Manual Software Revision 12
User responsibility Datex-Ohmeda, Inc. a General Electric Company, doing business as GE Healthcare. This product will perform in conformity with the description thereof contained in this User’s Reference manual and accompanying labels and/or inserts, when assembled, operated, maintained, and repaired in accordance with the instruction provided. This Product must be checked periodically. A defective Product should not be used. Parts that are broken, missing, plainly worn, distorted, or contaminated should be replaced immediately. Should repair or replacement become necessary, Datex-Ohmeda recommends that a telephonic or written request for service advice be made to the nearest DatexOhmeda Customer Service Center. This Product or any of its parts should not be repaired other than in accordance with written instructions provided by Datex-Ohmeda and by Datex-Ohmeda trained personnel. The Product must not be altered without the prior written approval of Datex-Ohmeda. The user of this Product shall have the sole responsibility for any malfunction which results from improper use, faulty maintenance, improper repair, damage, or alteration by anyone other than Datex-Ohmeda.
CAUTION
U.S. Federal law restricts this device to sale by or on the order of a licensed medical practitioner.Outside the U.S.A., check the local laws for any restriction that may apply.
Table of Contents 1 Introduction Intended use... 1-2 Indications for use... 1-2 General information... 1-2 Serial numbers...1-4 Trademarks... 1-5 Symbols used in the manual or on the equipment... 1-6 Symbols used on the equipment...1-6 Symbols used on the user interface... 1-9 Typeface conventions used...1-10 Abbreviations... 1-11 System information... 1-14 System classification... 1-14 Device standards IEC 60601-1:2005... 1-14 Device standards IEC 60601-1:1988... 1-14 Integral system components... 1-15 Not integral system components...1-15 System accessories...1-15 System safety... 1-16 Preparing for use... 1-16 Inspecting the system... 1-17 Electrical safety... 1-18
2 System controls and menus System overview... 2-2 Using the brake... 2-4 Using the O2 flush button... 2-4 Positioning the display...2-4 Advanced breathing system components... 2-6 Using the bag support arm... 2-7
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Avance CS² Vaporizer controls... 2-8 Display controls... 2-9 Touch points...2-10 Measured value touch points... 2-10 Active alarm touch points... 2-11 Anesthesia system display... 2-12 Digit fields... 2-13 Waveform fields... 2-13 Split screen field... 2-13 Display navigation... 2-15 Using menus... 2-15 Using the ComWheel... 2-16 Using quick keys... 2-16
3 Operation System operation safety... 3-2 Turning on the system... 3-3 Start a case... 3-4 Minimum Alveolar Concentration... 3-4 Starting a case using default settings... 3-5 Starting a case using custom settings... 3-5 End a case...3-6 Turning off the system... 3-7 Ventilator setup... 3-8 Changing ventilator mode... 3-8 Changing ventilator settings... 3-8 Optional ventilator procedures... 3-8 Gas setup... 3-9 Changing gas settings...3-9 Changing balance gas...3-9 Changing circuit type... 3-9 System setup... 3-11 Patient demographics... 3-11
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Table of Contents Screen setup menu... 3-11 Fresh gas usage... 3-14 Alarm setup... 3-15 Setting CO2 alarms... 3-15 Setting MV/TV alarms... 3-16 Setting alarm limits... 3-16 Viewing alarm history... 3-17 Setting alarm volume...3-17 Setting apnea delay...3-17 Silencing leak audio alarms... 3-17 Setting auto MV limits... 3-18 Setting to default limits... 3-18 Next page... 3-19 Trends... 3-20 Setting trends... 3-20 Spirometry... 3-21 Setting loop type... 3-21 Setting loop graph scaling... 3-22 Setting patient and sensor type...3-22 Setting the data source... 3-22 Setting spirometry volume type...3-23 Saving, viewing, and deleting spirometry loops... 3-23 Procedures... 3-24 Pause gas flow... 3-24 Cardiac bypass... 3-24 Vital capacity... 3-25 Cycling... 3-26 Timer function... 3-28 Using the timer... 3-28 ecoFLOW...3-29 Using ecoFLOW... 3-30 Alternate O2 control...3-31 Using Alternate O2 control... 3-31 EZchange canister mode... 3-32
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Avance CS² Using EZchange canister mode... 3-33 Condenser... 3-34 Draining the condenser... 3-34 Auxiliary Common Gas Outlet...3-35 Using the ACGO... 3-35
4 Preoperative checkout Every day before your first patient... 4-2 Before every patient... 4-3
5 Preoperative tests Vaporizer installation... 5-2 Vaporizer installation procedure... 5-2 Flow and pressure calibration... 5-3 Circuit compliance compensation... 5-4 Checkout menu... 5-5 Full test... 5-6 Vent and gas... 5-6 Circuit leak... 5-6 Circuit O2 cell... 5-6 External gas monitor... 5-7 Individual tests... 5-8 Vent and gas... 5-8 Circuit leak... 5-8 Circuit O2 cell... 5-8 Low P leak... 5-8 Low P leak (machines with ACGO)...5-9 Positive low pressure leak test (ACGO systems only)... 5-10 Vaporizer back pressure test... 5-11
6 Airway modules Airway modules... 6-2
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Table of Contents E and M series airway modules... 6-3 CARESCAPE airway modules... 6-4 Connecting the airway module... 6-5 Parameters setup... 6-6 Data source... 6-6 Automatic agent identification... 6-7 Calibrating the airway module...6-8
7 Alarms and troubleshooting Alarms... 7-2 Alarm priorities...7-2 Pausing alarms... 7-2 Cancelling audio pause... 7-3 Display changes during alarms... 7-3 De-escalating alarms...7-3 Battery indicator...7-3 Internal failure... 7-4 Informational tones... 7-4 List of alarms... 7-5 Sustained pressure threshold... 7-11 Alarm ranges... 7-13 Alarm tests...7-15 Breathing system problems...7-17 Electrical problems... 7-18 Pneumatic problems... 7-19
8 Setup and connections Setup safety...8-2 Moving and transporting the system... 8-4 Setting up the absorber canister... 8-5 When to change the absorbent... 8-6 Removing a canister... 8-7 Removing an EZchange canister... 8-7
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Avance CS² Filling the Reusable Multi Absorber canister... 8-8 Electrical connections... 8-10 Mains inlet... 8-10 Equipotential stud... 8-10 Outlets... 8-10 Serial port... 8-10 Pneumatic connections... 8-12 Pipeline inlets... 8-12 Scavenging... 8-12 Sample gas return port... 8-14 Vacuum suction regulator (optional)... 8-14 Venturi suction regulator (optional)... 8-15 Auxiliary O2 flowmeter... 8-16 Installing gas cylinders... 8-18 Installing cylinders with pin indexed yokes... 8-18 Installing cylinders with DIN connections... 8-18 Performing a high-pressure leak test... 8-18 Attaching equipment to the top of the machine... 8-20 Passive AGSS... 8-21 Connecting passive AGSS... 8-21 Active AGSS... 8-22 Connecting active AGSS with a flow indicator... 8-22 Connecting active adjustable AGSS... 8-23 Cable management arm (optional)... 8-25
9 User maintenance Maintenance safety... 9-2 Repair policy... 9-3 Maintenance summary and schedule... 9-4 Circuit O2 cell replacement... 9-6 Calibration menu... 9-7 Flow and pressure calibration... 9-7 Circuit O2 cell... 9-7
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Table of Contents Airway gas calibration... 9-8 Water buildup...9-8
10 Parts Flow sensor module... 10-2 Breathing circuit module... 10-3 Bellows... 10-4 Complete advanced breathing system... 10-5 Absorber canister... 10-6 Exhalation valve assembly... 10-7 AGSS... 10-8 EZchange canister system... 10-10 Condenser... 10-11 Test tools and system parts...10-12
11 Specifications and theory of operation System pneumatic circuit...11-2 Gas supplies... 11-3 O2 flow... 11-4 Air and N2O... 11-4 Mixed gas...11-4 EZchange canister...11-5 Condenser... 11-5 Pneumatic specifications... 11-6 Gas supplies... 11-6 ACGO port relief... 11-6 Non-circle circuit relief... 11-6 Electrical block diagram...11-7 Electrical power... 11-9 Power cord...11-9 Battery information...11-9 Flow specifications...11-11 Breathing system specifications... 11-12
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Avance CS² Gas scavenging... 11-13 Physical specifications...11-15 Lower dovetail loading...11-15 Upper dovetail loading...11-16 Top shelf rail loading... 11-16 Environmental requirements... 11-17 Airway module specifications... 11-18 Gas specifications for E-, M-series modules...11-18 Gas specifications for CARESCAPE modules... 11-19 Typical performance... 11-20 Suction regulators (optional)... 11-21 Ventilator theory...11-22 O2 monitoring theory of operation...11-22 ecoFLOW theory of operation... 11-23 Ventilation modes... 11-23 Ventilation modes factory default settings...11-33 Ventilation mode transition... 11-34 Ventilator operating specifications...11-36 Pneumatics... 11-36 Fresh gas compensation... 11-36 Pressure...11-36 Volume... 11-36 Oxygen...11-37 Ventilator accuracy data... 11-38 Electromagnetic compatibility (EMC)... 11-39 Essential performance...11-39 Cables... 11-39 Guidance and manufacturer’s declaration electromagnetic emissions... 11-40 Guidance and manufacturer’s declaration electromagnetic immunity... 11-41 Recommended separation distances... 11-42
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Table of Contents
12 Super user mode Super user mode... 12-2 Gas usage... 12-3 Resetting cumulative gas usage... 12-3 Setting ecoFLOW... 12-3 Setting agent costs... 12-3 System configuration...12-5 Display settings... 12-5 Ventilator settings... 12-5 Alarm settings... 12-6 Parameter settings... 12-6 Trends setup... 12-7 Page setup...12-8 Case defaults...12-10 Configuring case defaults... 12-10 Setting case name...12-10 Setting volume apnea defaults... 12-10 Default case type settings... 12-11 Gas controls...12-15 Setting gas preset values... 12-15 Setting fresh gas controls... 12-15 Procedures setup... 12-16 Setting vital capacity defaults... 12-16 Setting cycling controls and settings...12-16
Index
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Avance CS²
x
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1 Introduction
Introduction
In this section
Intended use... 1-2 Symbols used in the manual or on the equipment...1-6 Typeface conventions used... 1-10 Abbreviations...1-11 System information... 1-14 System safety... 1-16
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Avance CS²
Intended use The Avance CS2 anesthesia system combines our highly advanced anesthesia delivery, patient monitoring, and care information management. The contemporary, compact design addresses many ergonomic considerations including an efficient cable management solution and storage system and an extra large work surface area. Optional, integrated features include three position vaporizer manifold, auxiliary common gas outlet, and suction control. This anesthesia system provides integration of ventilation, gas delivery and gas monitoring, on a 15-inch color touchscreen interface. This system also features electronic gas mixing of up to three gases. This anesthesia system is designed for mixing and delivering inhalation anesthetics, Air, O2, and N2O. This anesthesia system uses SmartVent ventilation technology offering Volume Control Ventilation with tidal volume compensation and electronic PEEP. The proven SmartVent technology also features optional Pressure Control Ventilation, Pressure Support Ventilation with an Apnea Backup (PSVPro) that is used for spontaneously breathing patients, Synchronized Intermittent Mandatory Ventilation (SIMV) modes, Pressure Control VentilationVolume Guarantee (PCV-VG), Continuous Positive Airway Pressure + Pressure Support Ventilation (CPAP + PSV), and VCV Cardiac Bypass. In Volume Control Ventilation, a patient can be ventilated using a minimal tidal volume of 20 ml. In Pressure Control Ventilation, volumes as low as 5 ml can be measured. These advanced features allow for the ventilation of a broad patient range.
WARNING
MR unsafe. This system is not suitable for use in a magnetic resonance imaging (MRI) environment.
Indications for use The system is intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (neonate, pediatric, and adult). The device is intended for volume or pressure control ventilation.
General information This anesthesia system uses the Advanced Breathing System (ABS). This integrated breathing system is easy to remove and disassemble and is autoclavable. Its fully integrated design enhances the system’s elegance while minimizing tube connections, minimizing circuit volume, and increasing the work surface area. This anesthesia system is designed for expansion and upgrades, so it is easy to add new technologies and ventilation capabilities without investing in a new system.
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1 Introduction The anesthesia system is suitable for use in a patient environment, such as hospitals, surgical centers, or clinics. The system must only be operated by personnel trained and qualified in the administration of general anesthesia. The User’s Reference manual is intended to provide training on the operation of the system. Operate the system from the front with a clear view of the display. It must be operated according to the instructions in this User’s Reference manual. Make sure that all user documents are obtained from the manufacturer. Refer to the Technical Reference manual for service information including: special installation instructions, installation checklist, means of isolating the supply mains, and replacement of fuses, supply cord, and other parts.
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WARNING
Explosion Hazard. Do not use this system with flammable anesthetic agents.
Note
Configurations available for this product depend on local market and standards requirements. Illustrations in this manual may not represent all configurations of the product. This manual does not cover the operation of every accessory. Refer to the accessory documentation for further information.
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Avance CS²
Figure 1-1 • Front view
Serial numbers Datex-Ohmeda products have unit serial numbers with coded logic which indicates a product group code, the year of manufacture, and a sequential unit number for identification. The serial number can be in one of two formats.
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AAAX11111
AAAXX111111AA
The X represents an alpha character The XX represents a number indicating the year the product was indicating the year the product was manufactured; H = 2004, J = 2005, manufactured; 04 = 2004, 05 = 2005, etc. I and O are not used. etc.
Trademarks Avance, Carestation, Advanced Breathing System, ComWheel, D-fend, EZchange, Disposable Multi Absorber, Reusable Multi Absorber, PSVPro, SmartVent, Tec 6 Plus, and Tec 7 are registered trademarks of Datex-Ohmeda, Inc. Other brand names or product names used in this manual are trademarks or registered trademarks of their respective holders.
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Symbols used in the manual or on the equipment Symbols replace words on the equipment, on the display, or in product manuals. Warnings and Cautions tell you about dangerous conditions that can occur if you do not follow all instructions in this manual. Warnings tell about a condition that can cause injury to the operator or the patient. Cautions tell about a condition that can cause damage to the equipment. Read and follow all warnings and cautions.
Symbols used on the equipment .
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O2 Flush button
O2 cell connection
Air
Air
APL settings are approximate
Anesthetic Gas Scavenging System
Maximum
Vacuum
Serial number
Stock number
Exhaust
Bellows volumes are approximate
Plus, positive polarity
Minus, negative polarity
Maximum mass of configured mobile equipment
Caution: federal law prohibits dispensing without prescription.
Autoclavable
Selectatec Series Vaporizers Tec 6 Plus or greater
On (power)
Off (power)
Standby
Non-ionizing electromagnetic radiation
Type BF equipment
Type B equipment
Dangerous voltage
Frame or chassis ground
Protective earth ground
Earth ground
Direct current
Alternating current
Caution
Refer to instruction manual or booklet (blue background)
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Operating instructions
General warning (yellow background)
Electrical input/output
Sample gas inlet to scavenging
Pneumatic inlet
Pneumatic outlet
Equipotential
Lamp, lighting, illumination
Variability
Variability in steps
Suction bottle outlet
Vacuum inlet
Bag position/manual ventilation
Mechanical ventilation
Inspiratory flow
Expiratory flow
Movement in one direction
Movement in two directions
Lock
Unlock
Open drain (remove liquid)
Low pressure leak test
This way up
Not autoclavable
Read to center of float
EZchange canister (CO2 bypass)
Systems with this mark agree with the European Council Directive (93/42/ EEC) for Medical Devices when they are used as specified in their User’s Reference manuals. The xxxx is the certification number of the Notified Body used by Datex-Ohmeda’s Quality Systems.
Authorized representative in the European Community
Date of manufacture
Manufacturer
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Indicates that the waste of electrical and electronic equipment must not be disposed as unsorted municipal waste and must be collected separately. Please contact an authorized representative of the manufacturer for information concerning the decommissioning of equipment.
GOST R Russian certification
Stepping prohibited
When moving or transporting anesthesia machine, place the display arm and shelf in the transport position as shown.
Device contains phthalates XXXX indicates phthalate Possible phthalates include: DBP: Di-n-butyl phthalate DNPP: 1,2-Benzenedicarboxylic acid, dipentylester, branched and linear; Npentyl-isopentylphthalate; Di-n-pentyl phthalate; Diisopentylphthalate BBP: Benzyl butyl phthalate DEHP: Bis(2-ethylhexyl) phthalate; Di(2-ethylhexyl) phthalate DMEP: Bis(2-methoxyethyl) phthalate DIBP: Dissobutyl phthalate
Single use device
Union made
Stacking limit by mass
Keep dry
Do not stack
Temperature limitation
Fragile, handle with care
Protect from heat and radioactive sources
Recyclable material
Humidity limitation
Electrical test certification
USB port
Network
Not a USB port
VGA connection
Serial connection
Pinch hazard
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