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nocturnal arrhythmias
Patients requiring arrhythmia evaluation for etiology of stroke or
transient cerebral ischemia, possibly secondary to Atrial
Fibrillation
To use the ACT monitoring system, the user or primary care provider
must be able to perform all of the following:
Understand the principle of operation and system messages
described in this manual
Place the sensor and electrodes on the chest
Operate a handheld device (cell phone monitor)
Operate simple push-buttons
The ACT monitoring system is safe for use by patients wearing an
oxygen mask for breathing.
The ACT monitoring system is not water resistant and must not get
wet. Do not use or store the ACT monitoring system where liquids of
any nature may come into contact with it. Raindrops, water spray,
juice, coffee, steam, perspiration, perfume, deodorant, etc. may also
affect the performance of the monitoring system and cause a possible
malfunction. While bathing or showering, the system should be placed
in a dry environment, outside of the bathroom. The electrode patches
may be worn in the shower or bath as long as they are disconnected
from the sensor.
The function of the ACT monitoring system is dependent on cellular
phone service and Bluetooth technology. Limitations in data
transmission may occur if there is limited cellular service in the area.
A landline modem can be provided for locations with limited cellular
service coverage and/or if interference with the wireless Bluetooth
connection is experienced.