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 EtCO

2

 - 1

 

END-TIDAL CARBON DIOXIDE (EtCO

2

)

General Information

Product Description

M Series

™ 

units, equipped with software revision 38.25 or higher, and M Series CCT units, equipped with software 

revision 57.50 or higher, support two End Tidal Carbon Dioxide (EtCO

2

) monitoring options for the continuous 

measurement of respiratory carbon dioxide (CO

2

) and respiration rate. These options use the same connector on the 

M Series unit and may be used interchangeably.
The first option uses a unique mainstream, solid-state infrared sensor called the CAPNOSTAT® 3 Mainstream CO

2

 

sensor. The CAPNOSTAT 3 sensor is attached to an airway adapter that connects to an endotracheal (ET) tube or 
other airway and measures gases flowing through these breathing circuit components. A disposable mouthpiece may 
be connected to the adapter for monitoring non-intubated patients. A Capno

2

mask is also available for use with non-

intubated patients. This option provides for O

2

 delivery while monitoring expired CO

2

.

The second option is a sidestream sampling system called the LoFlo™ Sidestream CO

2

 Module. The LoFlo module 

contains a gas sampling pump, which draws small samples of gas from the patient’s airway via a nasal/oral cannula or 
airway adapter, and passes these gases through a solid state infrared sensor (located away from the patient’s airway) 
that measures CO

2

. While the sidestream system is typically used on non-intubated patients, it can also be used for 

EtCO

2

 measurement on intubated infant, pediatric, and adult patients. The sidestream system should not be used, 

however, on intubated patients who cannot tolerate the 50ml/min removal of the sample gases from their breathing 
circuit. The sidestream module uses specially designed sampling cannulae and airway adapters for sampling airway 
gases and passing them through an integrated sample cell, which connects to the LoFlo Module’s CO

2

 sensor. These 

cannulae incorporate a filter and sample cell, providing maximum filtration of fluids and contaminants, and protecting 
the system from aspiration of these fluids.
In both systems, the CO

sensor generates infrared light and beams it through the airway adapter or sample cell to a 

detector on the opposite side. CO

2

 from the patient, flowing through the mainstream airway adapter or aspirated into 

the sample cell, absorbs some of this infrared energy. The M Series

 

unit determines CO

2

 concentration in the breathing 

gases by measuring the amount of light absorbed by gases flowing through the airway or sample cell. 
The M Series

 

unit displays EtCO

2

 (

the concentration of carbon dioxide detected at the end of each exhalation) as a 

numerical value in millimeters of mercury (mmHg), percent (%), or kilopascals (kPa). In addition, the unit can display a 
capnogram waveform. This waveform is a valuable clinical tool that can be used to assess patient airway integrity and 
proper endotracheal (ET) tube placement. The unit calculates respiration rate by measuring the time interval between 
detected peaks of the CO

2

 waveform. The technology differentiates between waveforms caused by breathing and 

those caused by cardiogenic oscillations and artifact.

How to Use This Manual

This section explains how to set up and use the M Series

 

End-Tidal Carbon Dioxide option. Important safety 

information relating to general use of the M Series

 

End Tidal Carbon Dioxide monitor appears in the “Safety 

Considerations” section of this manual.
The 

M Series Operator’s Guide

 provides information operators need for the safe and effective use and care of the 

M Series

 

unit. It is important that persons using this device read and understand all the information contained therein.

Please thoroughly read both safety considerations and warnings sections before operating your M Series unit.
All CAPNOSTAT 3, LoFlo, airway adapter and cannula questions with regards to the Declaration of Conformity with 
European Union Directives should be directed to the authorized representative for Respironics Novametrix LLC:

Respironics Novametrix LLC

Authorized European Contact

Respironics Deutschland

Gewerbestrasse 17

82211 Herrsching

Germany

+49 8152 93060

Summary of Contents for Capnostat 3

Page 1: ...9650 0223 01 Rev D TM End Tidal Carbon Dioxide EtCO2...

Page 2: ...l Corporation CAPNOSTAT is a registered trademark and LoFlo is a trademark of Respironics Novametrix LLC Cidex is a registered trademark of Advanced Sterilization Products a Johnson and Johnson Compan...

Page 3: ...mum filtration of fluids and contaminants and protecting the system from aspiration of these fluids In both systems the CO2 sensor generates infrared light and beams it through the airway adapter or s...

Page 4: ...es EtCO2 option Activate oxygen compensation if O2 levels in excess of 60 are introduced Activate N2O compensation if nitrous oxide is introduced into the airway circuit The presence of Desflurane bey...

Page 5: ...h windows in a vertical NOT a horizontal position This helps keep patient secretions from pooling on the windows Do NOT insert any object other than the sample cell into the sample cell receptacle on...

Page 6: ...t and property even if ZOLL has been advised of the possibility of such damages THE WARRANTY SET FORTH HEREIN IS EXCLUSIVE AND ZOLL MEDICAL CORPORATION EXPRESSLY DISCLAIMS ALL OTHER WARRANTIES WHETHER...

Page 7: ...EtCO2 setup as follows Attaching the CAPNOSTAT 3 sensor cable Selecting a mainstream airway adapter Attaching the airway adapter to the CAPNOSTAT 3 sensor Zeroing the mainstream sensor airway adapter...

Page 8: ...ximately 15 seconds The unit displays the message ZERO DONE upon completion of the zeroing Note Do not attempt zeroing for 20 seconds after removing the adapter from the patient s airway This time all...

Page 9: ...ow steps a through c else go to step 4 a Verify proper connection of the adapter to the sensor b Verify that the airway adapter windows are clean and dry c If the adapter is properly connected and the...

Page 10: ...after its use When the previously used module is reconnected to the M Series unit module zeroing does not have to be repeated as long as no other LoFlo module has been connected and zeroed during the...

Page 11: ...lo module and ensure that it clicks into place 2 If the unit displays either of the following messages take the appropriate action 3 Place the airway adapter assembly at the proximal end of the airway...

Page 12: ...o module and rubber protective covering can be cleaned and disinfected by wiping with one or more of the following solutions 70 isopropyl alcohol 2 gluteraldehyde 10 bleach solution Use a soft cloth d...

Page 13: ...ftkey from the physiological monitoring menu cycles the display from the capnogram waveform to the plethysmograph waveform if SpO2 is installed to no second waveform displayed Use the Zoom softkey fro...

Page 14: ...airway circuit If the concentration of oxygen in the breathing circuit exceeds 60 and nitrous oxide is in use both O2 and N2O should be activated When the Comp softkey is pressed the unit displays the...

Page 15: ...alarm functions are disabled Background ECG analysis functions continue to operate as described in the AED section of the M Series Operator s Guide The ALARM SUSPEND button can be used to activate dea...

Page 16: ...ature unit displays WARM UP message 4 Perform a zero procedure if necessary see Zeroing the LoFlo CO2 Module on page 8 5 Breath normally into the adapter 6 Verify that the unit displays EtCO2 readings...

Page 17: ...3 kPa 0 95 mmHg OFF 0 12 5 OFF 0 12 6 kPa OFF High Respiration Rate Alarm Limit 120 respirations per min 5 150 respirations per min OFF Low Respiration Rate Alarm Limit 5 respirations per min 0 100 re...

Page 18: ...PU Oral Nasal CO2 sampling only pediatric Nasal CO2 Sampling with O2 Delivery Cannula Adult 8000 0356 SPU Nasal CO2 sampling with O2 delivery adult Nasal CO2 Sampling with O2 Delivery Cannula Pediatri...

Page 19: ...problem persists return for service CO2 DEVICE NOT READY The zero operation cannot be initiated because The sensor or module is still warming up No sensor or module is attached to the unit Wait for se...

Page 20: ...g the adapter type Clean airway adapter and reattach it If the problem persists or the adapter type was changed perform a mainstream airway adapter zero as described in Zeroing the Mainstream Sensor A...

Page 21: ...line is set below 0 mmHg Perform a sidestream module zero as described in Zeroing the LoFlo CO2 Module on page 8 CHECK CO2 LINE Sample line blockage Verify that the sample line is plugged into the mod...

Page 22: ...han 5 minutes Replace module ZERO CO2 MODULE Module cable connected to M Series unit for the first time Probe drift error detected or negative CO2 detected Perform module zero as described in Zeroing...

Page 23: ...lt pediatric adapters 50 ms Neonatal adapters 200 ms Respiration Rate Range 0 150 breaths per minute Respiration Rate Accuracy 1 breath per minute Sample Flow Rate N A 50 ml min Compensations Barometr...

Page 24: ...at maximum energy 360J or 1 5 hours minimum of continuous ECG monitoring or 1 0 hour of continuous ECG monitoring pacing at 60 mA 70 beats min For a new fully charged XL battery pack at 20 C 60 defibr...

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