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Summary of Contents for Dynasplint Type II
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00131.455 231 303 fax www.dynasplint.com Dislocations Fractures, e.g., Colles, distal radius, etc. Head trauma Hemophilia Rheumatoid arthritis Spinal cord injuries Tendon and ligament repairs DYNASPLINT® and Dynasplint® Systems are registered trademarks of Dynasplint Systems, Inc. Stretch Beyond Your Expectations. ®...
FITTING INSTRUCTIONS IMPORTANT: Movement and rattling of spacer in the tension window is normal. This will subside when more tension is applied to the tension screw. STANDARD FITTING INSTRUCTIONS: STEP 1: Completely open top-of-forearm cuff and strap. Loosen the bottom-of- forearm cuff.
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STEP 16: Make a reference line with a marker on the top-of-forearm cuff and counter- force strap so that the patient knows where to close them. STEP 17: Have the patient practice applying and removing the unit. Give the patient the Patient Instruction Booklet to take home with the Dynasplint® Wrist Extension System.
Patients should wear the unit at the lowest tolerable tension setting for the longest time possible. Optimally, the patient will wear the Dynasplint® System for six to eight continuous hours, usually overnight. The tension should be set to produce as much as, but not more than, one hour of post-wear stiffness beyond normal discomfort.
NEUROLOGICAL PROTOCOL: Neurological patients being fit in a standard unit that is neurologically dressed should follow the NEUROLOGICAL protocol. Please see the Neurological Wrist Extension Clini- cian Booklet for detailed instructions. nOTE: Tension settings are different for the standard and neurological systems. If patient is transferring from a NEUROLOGICAL unit to a STANDARD unit that is neuro- logically dressed, please see the tension scale below to adjust tension properly.
TROUBLESHOOTING Instruct patient to remove the Dynasplint® System immediately if pain or numbness occurs. A hand pan can be substituted for the palmar bar and is available through the Dynasplint® Systems representative. See options in Figure 2. PrOBlEM: Metal joints are pressing into the wrist.
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The product described in the enclosed literature is intended for the specific purpose as per the instructions attached. Any use of this product outside of its intended purpose on any body part or in a manner outside the protocol established by Dynasplint Systems, Inc., is a use of the product for which it, its divisions and employees cannot be held responsible.
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Do you have a question about the Type II and is the answer not in the manual?
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