End-tidal carbon dioxide (etco, General information, Product description – ZOLL E Series Monitor Defibrillator Rev E ETCO2 User Manual

Page 3: How to use this manual

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9650-1212-01 Rev. E

1

END-TIDAL CARBON DIOXIDE (EtCO

2

)

General Information

Product Description

E Series

®

units equipped with software revision 2.00.000 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 E Series unit and may be used interchangeably.

The first option uses a unique, mainstream, solid-state, infrared sensor called the CAPNOSTAT

®

5 Mainstream CO

2

Sensor. The CAPNOSTAT 5 CO

2

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™ 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 patients who cannot tolerate the 50ml/min removal of the sample gases from their breathing circuit. The sidestream
module uses specially designed cannulas 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 cannulas 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

2

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 sample cell,

absorbs some of this infrared energy. The E 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 E 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. This capnogram 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 E Series End Tidal Carbon Dioxide option. Important safety
information relating to general use of the E Series End Tidal Carbon Dioxide monitor appears in the “Safety
Considerations” section of this manual.

The E Series Operator’s Guide provides information operators need for the safe and effective use and care of the
E Series unit. It is important that persons using this device read and understand all the information contained therein.

Please read both safety considerations and warnings sections thoroughly before operating your E Series unit.

All CAPNOSTAT 5 sensor, LoFlo module, 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

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