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Cardiac Compass Report – The Cardiac Compass Report provides a picture of the
patient’s condition during the last 14 months. The report includes graphs that show trends
in the frequency of arrhythmias, the amount of physical activity, heart rates, and device
therapies. Dates and event annotations allow you to correlate trends from different graphs.
The report can also help you to assess whether device therapies or drug therapies are
effective. For more information, see Section 6.5, “Viewing long-term clinical trends with the
Cardiac Compass Report”, page 148.
6.1.2 Reviewing the presenting rhythm
The presenting rhythm may indicate the presence of undersensing, far-field oversensing,
or loss of capture. These are basic pacing issues that can affect the delivery of therapy.
These issues can often be resolved by making basic programming changes.
Review the presenting rhythm by viewing the Live Rhythm Monitor and by printing the EGM
and Marker Channel traces. If you identify issues with the patient’s presenting rhythm,
review the device settings and reprogram the device to values that are appropriate for the
patient.
6.1.3 Verifying the status of the implanted system
To verify that the device and leads are functioning correctly, review the device and lead
status information, lead trends data, and Observations available from the Quick Look II
screen.
For detailed information about viewing and interpreting all of the information available from
the Quick Look II screen, see Section 6.2, “Viewing a summary of recently stored data”,
6.1.3.1 How to review the battery voltage and device status indicators
Warning: Replace the device immediately if the programmer displays an EOS indicator.
The device may lose the ability to pace, sense, and deliver therapy adequately after the
EOS indicator appears.
1. Review the displayed battery voltage and compare it to the Recommended
Replacement Time (RRT). For more information, see Section A.2, “Replacement
indicators”, page 448.
Note: You may see a temporary drop in the displayed battery voltage if high-voltage
charging has occurred within the past 24 hours.
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PROTECTA™ XT DR D314DRG
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Clinician Manual
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