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Note: The paced and sensed event counters do not count all events recorded by the device.
For example, a ventricular safety pace is considered to be a pace, and the preceding
ventricular sense is not counted. Due to rounding, percentages may not add up to 100%.
Arrhythmia episode information – This section shows the number of treated and
monitored arrhythmia episodes that have occurred since the last patient session. It also
shows the number of shocks that were delivered since the last session. In addition, it shows
the number of episodes for which ventricular oversensing (VOS) was detected by the
TWave Discrimination feature or the RV Lead Noise Discrimination feature.
Select the [>>] button to review details of all arrhythmia episodes. For information about the
Arrhythmia Episodes Data screen, see Section 6.8, “Viewing Arrhythmia Episodes data and
setting data collection preferences”, page 166.
6.2.2.3 Quick Look II observations
Observations are based on an analysis of programmed parameters and data collected since
the last session. The following types of observations may occur:
●
Device status observations inform you when the device is approaching RRT or End of
Service (EOS). An observation is also reported if a charge circuit irregularity or device
reset has occurred.
●
Lead status observations report any potential issues with the sensing integrity of the
leads, possible lead dislodgments, and abnormal capture management results. You
may also be warned about possible inconsistencies in the programming of lead polarity.
●
Parameter observations warn of any inconsistencies in the programming of detection
and therapy parameters. One example is if certain parameter settings result in a therapy
being disabled.
●
Diagnostic data observations report noteworthy arrhythmia episodes. Examples
include arrhythmias of different types occurring together, or episodes for which
therapies were unsuccessful. Conditions that prevent diagnostic data from being
collected effectively are also reported.
●
Medtronic CareAlert observations can report system or device performance conditions
and certain heart rhythm conditions. For more information, see Section 6.3, “Automatic
alerts and notification of clinical management and system performance events”,
●
Clinical status observations alert you to abnormal patient conditions, such as low activity
rates, unexpectedly high heart rates, high arrhythmia burden, or fluid accumulation.
If you select one of the displayed observations and more information about the selected
observation is available, the [>>] button becomes active. You can use the [>>] button to look
at relevant details.
Medtronic
PROTECTA™ XT DR D314DRG
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Clinician Manual
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