User's Manual
Table Of Contents
- Introducing IntelliVue Telemetry
- Product Safety
- Transceiver Controls
- Basic Operation
- Alarms
- ECG Monitoring
- ST/AR Arrhythmia Monitoring
- SpO2 Monitoring
- Telemetry Functions at the Information Center & TeleMon
- Telemetry Functions at the Information Center
- Telemetry Controls in the Patient Window
- Locating the Transceiver (Find Device)
- Viewing Device Location in the Patient Window (optional)
- Viewing Device Location History (optional)
- Using the Device Location Client (optional)
- Patient Configurable Settings in Telemetry Setup
- Unit- Configurable Settings
- RF Auto Shutoff
- Transceiver Operation when Connected to TeleMon
- Telemetry Functions at the Information Center
- Pairing Monitoring Devices
- Maintenance, Cleaning & Troubleshooting
- Safety Standards & Specifications
- Accessories
- Sales and Support Offices
ECG Safety Information
6-2 ECG Monitoring
ECG Safety Information
WarningWarning
Always confirm Information Center observations with clinical observation
of the patient before administering interventions.
WarningWarning
Every lead must be secured to an electrode on the patient.
Conductive parts of electrodes must not contact earth or other conductive
parts.
Philips recommends that you change the lead label only to reflect the
physical placement of electrodes. This will ensure a match between the
monitored lead and the label, and prevent any possible confusion.
WarningWarning
When switching from EASI to standard monitoring, there is a loss of data
for 30 seconds.
WarningWarning
EASI derived 12-lead ECGs and their measurements are approximations
to conventional 12-lead ECGs. As the 12-lead ECG derived with EASI is
not exactly identical to the 12-lead conventional ECG obtained from an
electrocardiograph, it should not be used for diagnostic interpretations.
EASI lead placement is supported for adult patients only