Autofit 2008 Hun



 
 
 
 
 
 
 

Autofit 2008 Hun

Each year the AUTOFIT® newsletter highlights the newest enhancements in the AUTOFIT® equipment with live demonstrations of their automated features. The wide variety of features in the AUTOFIT® equipment has made them a leader in the field of Digital Automatic Camera Control.

The AUTOFIT® page also displays past issues of the company’s newsletter. Furthermore, the AUTOFIT® website gives an in-depth look at all the AUTOFIT® products including current NEWS, DEMO VIDEOS and VIDEOS that give insight into the AUTOFIT® manufacturing process and other AUTOFIT® features.

The TrueColor Display on the Autofit Control System lets you select, store, and retrieve most any color from the images you have captured. A large touch screen allows you to readjust parameters quickly and easily. The System also has the ability to store up to five custom settings for each camera. The custom settings can be stored in memory, on the SD card, or both. Simply select the SD card if you plan to store an image at a later time. Selecting the memory makes more sense for storing settings that you plan to change when the camera is not in use.

Features

  • Robust hardware and user-friendly interface
  • No-nonsense operation
  • Easy to use and flexible
  • Quick, accurate camera fits
  • Continuously available, up-to-date system information and tutorials
  • Customizable profile settings and feedback options

autofit 2008 hun

Micro USB (USB 2.0) interface provides fast access to the AUTOFIT settings, control functions, and content via a single cable connection. The AUTOFIT Control System’s intuitive user interface makes it easy to navigate and operate.

Methods: Thirty-four women with BRCL were consecutively enrolled and randomized (D0) for 1 month in 1:1 ratio either in night-use group: with MOBIDERM Autofit (on top of a daytime compression hosiery), or in no night-use group: without MOBIDERM Autofit (daytime hosiery alone). From Day 31 to Day 90, all patients were fitted with MOBIDERM Autofit. Primary endpoint was lymphedema volume variation between Day 0 and Day 30. Secondary endpoints were compliance, quality of life (LYMQOL arm questionnaire), functional symptoms (heaviness, limb use limitation, pain), sleep quality, and safety.
Methods: Fourty-nine women with BRCL were consecutively enrolled and randomized (D0) for 1 month in 1:1 ratio either in night-use group: with MOBIDERM Autofit (on top of a daytime compression hosiery), or in no night-use group: without MOBIDERM Autofit (daytime hosiery alone). From Day 31 to Day 90, all patients were fitted with MOBIDERM Autofit. Primary endpoint was lymphedema volume variation between Day 0 and Day 30. Secondary endpoints were compliance, quality of life (LYMQOL arm questionnaire), functional symptoms (heaviness, limb use limitation, pain), sleep quality, and safety.
Methods: Forty-three women with BRCL were consecutively enrolled and randomized (D0) for 1 month in 1:1 ratio either in night-use group: with MOBIDERM Autofit (on top of a daytime compression hosiery), or in no night-use group: without MOBIDERM Autofit (daytime hosiery alone). From Day 31 to Day 90, all patients were fitted with MOBIDERM Autofit.
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