WARNING
Patient injury and inaccurate measurement risk.
Do not use tape to secure the sensor to the patient. This can
restrict blood flow, damage the patient's skin, cause
inaccurate readings, and damage the sensor.
WARNING
Patient injury risk. Exercise caution whe applying
a sensor to a patient with compromised skin integrity.
Applying tape or pressure to compromised sites can reduce
circulation and cause additional skin damage.
Note
If a sterile sensor is required, select a sensor that has been
validated for sterilization, and follow the sensor
manufacturer's directions for sterilizing the sensor.
Place the sensor and the NIBP cuff on different limbs to reduce unnecessary alarms
when you monitor these parameters at the same time.
Note
A range of sensors is available for different patient sizes and
measurement sites. Consult the sensor manufacturer's
instructions for selecting the correct sensor.
5. Confirm that the monitor displays SpHb or SpHbv data after connection to the
patient.
WARNING
Patient injury risk. Incorrect sensor application or
excessive duration of sensor use can cause tissue damage.
Inspect the sensor site periodically as directed in the sensor
manufacturer's instructions.
While SpHb is being measured, the displayed SpO2 and pulse rate are derived from the
same sensor. If SpO2 is not available, the pulse rate is derived from NIBP.
Detaching the sensor during a measurement triggers an alarm.
If SpHb is being measured continuously on a patient for an extended period, change the
sensor location at least every three hours or as indicated by the sensor manufacturer's
instructions.
Pulse rate frame
The Pulse rate frame displays data, information, and controls used in reading pulse rates.
Pulse rate is derived from one of three sensors based on your configuration: the SpO2
sensor, the NIBP sensor, or the EarlySense sensor. The source of Pulse rate
measurements appears in the lower left corner of the frame.
WARNING
Inaccurate measurement risk. Pulse rate measurements
generated through the blood pressure cuff or through SpO2 are subject to
artifact and might not be as accurate as heart rate measurements
generated through ECG or through manual palpation.
Note
You can specify pulse tone volume in the Pulse rate vertical tab (located in
the
Settings
>
Setup
tab).
Directions for use
Patient monitoring 173
Summary of Contents for Connex IWS
Page 1: ...Welch Allyn Connex Devices Directions for use Software version 2 3X...
Page 10: ...4 Introduction Welch Allyn Connex Devices...
Page 14: ...8 Symbols Welch Allyn Connex Devices...
Page 20: ...14 Screen elements Welch Allyn Connex Devices...
Page 28: ...22 About warnings and cautions Welch Allyn Connex Devices...
Page 72: ...66 Navigation Welch Allyn Connex Devices...
Page 96: ...90 Profiles Welch Allyn Connex Devices...
Page 106: ...100 Patient data management Welch Allyn Connex Devices...
Page 120: ...114 Alarms Welch Allyn Connex Devices...
Page 184: ...178 Patient monitoring Welch Allyn Connex Devices...
Page 212: ...206 Advanced settings Welch Allyn Connex Devices...
Page 244: ...238 Specifications Welch Allyn Connex Devices...
Page 250: ...244 Standards and compliance Welch Allyn Connex Devices...
Page 252: ...246 Guidance and manufacturer s declaration Welch Allyn Connex Devices...
Page 266: ......