User's Manual
Table Of Contents
- About this Manual
- Product Description, Indications for Use, Contraindications, and Features
- Safety Information, Warnings, and Cautions
- Chapter 1: Technology Overview
- Signal Extraction Technology (SET)
- rainbow Pulse CO-Oximetry Technology
- Pulse CO-Oximetry vs. Drawn Whole Blood Measurements
- General Description for Total Hemoglobin (SpHb)
- General Description for Total Arterial Oxygen Content (CaO2)
- General Description for Carboxyhemoglobin (SpCO)
- General Description for Methemoglobin (SpMet)
- SpCO, SpMet, and SpHb Measurements During Patient Motion
- rainbow Acoustic Monitoring (RAM) Technology
- Chapter 2: Radical-7 Descriptions
- Chapter 3: Setup
- Chapter 4: Operation
- Using the Touchscreen and Buttons
- Using Screen Lock
- Using the Home Button
- Navigating the Radical-7
- About the Display View
- Sensitivity Modes Overview
- Changing Sensitivity Modes
- Accessing the Main Menu
- Navigating the Main Menu
- Parameter Settings
- Sounds
- Device Settings
- Trends
- About
- Chapter 5: Profiles
- Chapter 6: Alarms and Messages
- About Alarms
- Silencing the Alarms
- Adaptive Threshold Alarm (ATA) Feature
- 3D Alarms
- Messages
- Replace Sensor Message
- Replace Cable Message
- Replace Adhesive Sensor Message
- Incompatible Sensor Message
- Incompatible Adhesive Sensor Message
- No Adhesive Sensor Connected Message
- Interference Detected Message
- SpO2 Only Mode Message
- Low Battery Message
- Low Perfusion Index Message
- Low Signal IQ Message
- Low SpCO SIQ Message
- Low SpMet SIQ Message
- Low SpHb SIQ Message
- Speaker Failure Message
- No Cable Connected Message
- No Sensor Connected Message
- Pulse Search Message
- Sensor Initializing Message
- Sensor Off Patient Message
- Incompatible Cable Message
- Chapter 7: Troubleshooting
- Chapter 8: Specifications
- Measurement Range
- Accuracy
- Resolution
- Electrical
- Environmental
- Physical Characteristics
- Trending
- Alarms
- Display Indicators
- Compliance
- Output Interface
- Wireless Radio (If Installed)
- Serial Interface Specifications
- Serial Interface Setup
- Analog Output and Nurse Call Specifications
- Symbols
- Country Codes (FCC and EU)
- Citations
- Chapter 9: Service and Maintenance
- Appendix: Best Practices for Comparisons to Reference Measurements
- Index
www.masimo.com 111 Masimo
Chapter 7: Troubleshooting
The following chapter contains information about troubleshooting the Radical-7 system.
Troubleshooting Measurements
See Parameter Related Safety Information, Warnings, and Cautions on page 11.
Signal IQ (SIQ)
The Signal IQ provides an indicator of the assessment of the confidence in the displayed
SpO2 value. The SpO2 SIQ can be also used to identify the occurrence of a patient’s pulse.
With motion, the plethysmographic waveform is often distorted and may be obscured by
artifact. Shown as a vertical line, the SpO2 SIQ coincides with the peak of an arterial
pulsation. Even with a plethysmographic waveform obscured by artifact, the Signal IQ
identifies the timing that the algorithms have determined for the arterial pulsation. The
pulse tone (when enabled) coincides with the vertical line of the SpO2 SIQ.
The height of the vertical line of the SpO2 SIQ provides an assessment of the confidence in
the measurement displayed. A high vertical bar indicates higher confidence in the
measurement. A small vertical bar indicates lower confidence in the displayed
measurement. When the Signal IQ is very low, this suggests that the accuracy of the
displayed measurement may be compromised. See About the Status Bar on page 49.
When parameters are dimly lit, proceed with caution and do the following:
• Assess the patient.
• Check the sensor and ensure proper sensor application. The sensor must be well
secured to the site for the Radical-7 Pulse CO-Oximeter to maintain accurate
readings. Misalignment of the sensor’s emitter and detector can result in smaller
signals and cause erroneous readings.
• Determine if an extreme change in the patient’s physiology and blood flow at the
monitoring site occurred, (e.g. an inflated blood pressure cuff, a squeezing motion,
sampling of an arterial blood specimen from the hand containing the pulse
oximetry sensor, severe hypotension, peripheral vasoconstriction in response to
hypothermia, medications, or an episode of Raynaud’s syndrome.)
• With neonates or infants, check that the peripheral blood flow to the sensor site is
not interrupted. Interruption, for example, may occur while lifting or crossing their
legs during a diaper change.
• After performing the above, if the parameter remains dimly lit frequently or
continuously, obtaining an arterial blood specimen for CO-Oximetry analysis may
be considered to verify the oxygen saturation value.
See Parameter Related Safety Information, Warnings, and Cautions on page 11.