Ormed Artromot-F, Руководство по эксплуатации

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The ARTROMOT ® -F is a motorized
motion device used for Continuous
Passive Motion (CPM) of the hand and
finger joints.
Its use is an important contribution to
medical-therapeutic treatment both in
clinics /doctors’ offices and in rental
services.
CPM therapy with the ARTROMOT ® -F
mainly serves to prevent the negative
impact of immobilization, regain painless
movement of the joints quickly, and
ensure a faster healing process with a
positive functional result.
Other objectives of the therapy include:
– Prevention of joint stiffness
(arthrofibrosis)
– Better joint metabolism
– Support for the healing of cartilage
areas and damaged ligaments
– Faster haematoma resorption
– Better lymph and blood circulation
– Prevention of thrombosis and
embolism
– Reduction of post-operative pain
The motion device is indicated in the
treatment of most injuries, postoperative
states, and diseases of the hand and
finger joints, for example:
– Capsulotomy, arthrolysis and tenolysis
for post-traumatic stiffness of MCP
and PIP joints
– Open reduction and rigid internal
fixation of intraarticular, diaphyseal
and metaphyseal fracture of the
phalanges and metacarpals
– Flexor and extensor tendon tenolysis
– Flexor and extensor tendon synovec-
tomies, following arthrotomy and
drainage of acute septic arthritis
– Prothetic replacement of MP and PIP
joints
– Stable fractures
– Crush injuries of hand without fractures
or dislocations
– Hand or digit reattachment
– Dupytren’s Contracture Release
– Burn injuries
– Reflex Sympathy Dystrophy (RSD)
The ARTROMOT ® -F should not be
used with:
– Untreated or uncontrolled infections
– Unstable fractures
– Hemorrhage
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English
1. How to use the motion device
1.1 Possible applications
1.2 Objectives of therapy
1.3 Indications
PRECAUTION!
NOTE: Upon using the device, if
signs of infection such as hyper-
thermia, fever, redness, irritation,
warmth, swelling, bleeding and /
or increased persistent pain are
present, discontinue operation
of the device and contact the pa-
tient’s physician. Do not proceed
with treatment until the physician
has approved continued use of
the device.