Tactile Medical Actitouch, Руководство пользователя

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6
4 .2 Contraindications
The ACTitouch System is contraindicated if the patient has:
• An Ankle Brachial Pressure Index of less than 0.6 or ankle systolic pressure less
than 60 mmHg;
• Diagnosed or suspected acute Deep Vein Thrombosis (DVT) or pulmonary
embolism;
• Pulmonary edema;
• Leg gangrene;
• Acute thrombophlebitis;
• Decompensated/Congestive Cardiac Failure;
• Severe arteriosclerosis or other ischemic vascular disease;
• Diabetes in association with peripheral arterial disease;
• Acute infections of the skin such as cellulitis;
• Any lower limb malignancy.
Directions for Use
CHAPTER 5
• The ACTitouch System should be worn as recommended and prescribed by the
physician. The usual prescribed duration of use will range from 10 to 14 hours
per day, including both Sustained Compression and Intermittent Pneumatic
Compression Modes.
• The device should be applied immediately upon waking and worn throughout
the day. The ACTitouch System should be removed for bathing or showering,
and when driving or operating machinery. Reapply the device immediately
after these activities.
• The device should be removed just prior to going to bed and recharged (See
Section 5.3 Charging the Device) . Consult with your healthcare provider about
other compression options during sleep.
IMPORTANT: Failure to wear the device as recommended, even for short periods,
may delay ulcer healing or may negatively impact treatment outcomes .