IN OFFICIAL RELATIONS WITH THE WHO

WORLD HEALTH ORGANIZATION

Lower limb orthosis with polypropylene articulation

Jean Claude Vesan, Orthotist-Prosthetist
This article is a modification of a report from Handicap International and the Hô Chi Minh Ville Rehabilitation Centre for
Disabled Children contributed by Jean Claude Vesan, Orthotist-Prosthetist

Handicap International, like many non-governmental organizations involved in orthopaedic devices, used to focus on prostheses supply, the first priority in post-conflict times. Our actions in low-income countries (often in the framework of community-based programs), where poliomyelitis or cerebral palsy are the major causes of disabilities, has now led us to develop our expertise in the field of orthotics, destined for a more varied and numerous target population.

Traditionally, the most commonly used technology in developing countries has been the metal orthosis (aluminium, steel, etc.), which simply requires basic equipment. On the other hand, this kind of device is heavy and unaesthetic and also obliges one to wear a closed or half-closed shoe, which is hardly supported by children in tropical climates. In addition, the identification and purchasing of good quality sidebars and joints is often a problem.

Thanks to socio-economical progress in some of these countries, a new type of orthosis could be fabricated by different agencies: the "mixed" orthosis. This orthosis uses thermoplastics, which are more comfortable and more precise, and which do not require any special footwear. The purchasing of sidebars and joints for this orthosis, however, is still a problem. This "transitory" technology was already an important step for our beneficiaries. However, in Vietnam, the motivation and the technical level reached by Handicap International's partners allowed us to progress further. In the Hô Chi Minh Ville Rehabilitation Centre for Disabled Children, the polypropylene knee joint for lower-limb orthoses was created, showing new properties:

· Fabricated solely of polypropylene, with the exception of the articulating screws, the straps, and the locks1
· Weight: For a 50 kg user, for example, the knee-ankle-foot orthosis is only 550 g. This is an improvement of approximately 30% in comparison to a mixed orthosis, and a 40% improvement compared to an aluminium orthosis
· Independence from steel joint and sidebar supply
· Improved function of the device, due to the improved stiffness of the knee, maintaining both joints in the proper alignment
· Easy repairs of the lock and the joints
· Wider distribution of the posterior knee pressures, allowing more comfort, particularly in case of genu (knee) recurvatum
· Cost of the device, decrease for the joints and sidebars
· No particular knowledge or material needed

Fabrication
This technical description will only be related to the specific process, not the general principles of any orthotic device. In addition to the basic material used for mixed orthoses, a polypropylene joint requires:
· One alignment guide, composed of a threaded rod with an 8 mm diameter, and two aluminium cylindrical pieces of 35 mm diameter

· One 6 mm drill, to be used for rounding off the joints' heads
· One hinge, used for the making extension stop
· One circular saw with a 100 mm blade, to be adapted on a drill for the manufacturing of the extension block stops

Required Materials

Casting & measurements
The patient is standing in a corrected position, the hip joint in 6o of external rotation, knee straight, and ankle at 90o. Particular attention must be paid to the following measurements:
· Diameter above the condyles
· Knee joint axis diameter
· Ankle malleolus diameter

Positive Mold

Positive mold plaster correction
Taking these measurements into account, rectifications are performed on the anterior of the leg cast in order to make the donning of the orthosis easier.

Joints guide positioning
Thanks to a round "surform" file, the positive mould is carved to make room for the alignment guide. To increase the security of the lock, the alignment guide should be placed in a more posterior position than normally placed. A minimum distance of 1cm behind the joint's physiological axis is appropriate. The alignment guide protrudes on each side (medially and laterally) of the positive mold, by 3 mm.

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