Below-Knee Polyethylene Semi-Rigid Dressing
Vein M. Swanson, CPO
ABSTRACT
This article will discuss an early postoperative patient management technique,
below-knee polyethylene semi-rigid
dressings. This approach is a contemporary alternative to the directly molded
removable rigid dressing. The polyethylene socket dressing is lightweight,
washable and flexible to enhance patient comfort and acceptance.
Introduction
Early postoperative fitting of below-knee (BK) amputations expedites the
rehabilitation process of lower-extremity patients. The goals of early postoperative fitting are to promote healing,
protect the wound from trauma, prevent edema, reduce pain and allow for
residual limb maturation and early ambulation (1).
Two postoperative patient management techniques are the immediate
postsurgical prosthesis and removable
rigid dressings (2-4).
The immediate postsurgical prosthesis is a technique wherein a nonremovable rigid plaster dressing is applied to
the residual limb immediately after BK
amputation. Usually a pylon is applied
at the first cast change so the patient
can begin partial weightbearing. One
disadvantage of immediate postsurgical fitting is surgeons are unable to inspect the amputation wound (5).
The second technique is the application of a BK removable rigid dressing
(RRD). The RRD is fabricated with
plaster or fiberglass bandage and is suspended by a stockinette and supracondylar plastic cuff. No pylon is attached.
The advantage of the RRD is it allows
frequent inspection of the wound after
amputation.
The purpose of this article is to describe a removable polyethylene semirigid dressing (PSRD) for postoperative patient management (see Figure
1
). This patient management technique
is a variant of the well-established directly molded RRD technique. The
PSRD differs from the RRD in that the
socket is flexible, and the patient also
wears a shrinker.
The combination of the BK shrinker
and the PSRD reduces edema and provides residual limb maturation. As
shrinkage occurs, the patient adds additional residual limb socks over the
shrinker to maintain the socket fit of
the PSRD.
In the author's experience, this combination is more effective than using
either a BK shrinker or an RRD by
itself. When a PSRD is used with a
shrinker, it provides additional volume
reduction and shaping of the residual
limb.
There is additional cost to provide
the PSRD for postoperative patient
management. However, in the author's
opinion, the PSRD will reduce costs to
patients and third-party payers over
time. Patients will have fewer problems with the fit of the preparatory
prosthesis due to the early shrinkage
that occurred while wearing the PSRD.
This result is particularly important
with diabetic patients who might develop abrasions due to excessive shrinkage during early ambulation.
PSRD Advantages
Two years of clinical experience fitting
the PSRD have shown several benefits
to the patient.
- The PSRD is a lighter-weight thermoplastic dressing, weighing six to seven ounces. No pylon or foot is attached
to minimize weight.
- The PSRD improves socket hygiene. Polyethylene is nonporous and
may be cleaned daily whereas a plaster
cast provides limited protection against
bacterial infection (5). In addition.
drainage from the wound may be absorbed into the cast.
- The PSRD improves patient comfort in donning and doffing due to the
polyethylene's flexible characteristics.
- The PSRD has partial weightbearing similar to an actual BK socket. Partial weightbearing helps the residual
limb become accustomed to tolerating
socket pressures.
- The PSRD helps patients become
involved in their own rehabilitation.
Patients learn about donning and doffing, adding residual limb socks for
shrinkage and keeping the socket
clean.
The PSRD is helpful to the prosthetist in patient management and clinical
evaluation since it helps the prosthetist
evaluate a patient as a candidate for a
prosthesis. Improved patient management reduces work stress.
Impression Method
The PSRD is applied five to seven days
postoperatively after the drain has
been removed. The staples are often
intact when the PSRD is applied (see
Figure 2
). In some cases the PSRD is
not applied until three to four weeks
postoperatively when the physician refers the patient to the prosthetist.
The only contraindication to fitting a
PSRD is the presence of a deep wound
infection that requires surgical intervention (4). To obtain an impression
for the PSRD:
- Measure the amputation (see Figure 3
) for a BK shrinker. A Juzo
shrinker is used for insensate amputations because it exerts 25 mm of Hg
pressure (6). For more sensitive amputations, use a Knit-Rite shrinker with
10 to 15 mm of Hg pressure or one
layer of Compressogrip sewn across
the distal end with 8 to 12 mm of Hg
pressure (7-10).
- Apply a one-ply cotton sock and
the medium compression BK shrinker
chosen in the previous step (see Figure
4
).
- Apply a one-ply wool sock over
the shrinker. Suspend the one-ply wool
sock with 25.4-mm (one-inch) elastic
and yates clamps (see Figure 5
).
- Apply another one-ply cotton sock
and mark the bony prominences.
- Take standard measurements over
all the socks to allow room in the socket for the shrinker and socks (see Figure 6
).
- The patient's knee should be in 10
degrees of flexion. Take the impression with one roll of elastic bandage
followed by one roll of regular fast-setting bandage. Lightly define the
sides of the patella tendon (see Figure
7
).
Model Modification- Extend the impression 50.8-mm
(2-inches) proximally before filling
with plaster to help the polyethylene
maintain a more uniform thickness on
the proximal walls.
- Check the measurements of the
positive model. These measurements
also represent the thickness of the
shrinker and the residual limb socks.
Often the circumference of the bulbous
distal end will be larger than the proximal circumference (see Figure 8
). This
is the advantage of using polyethylene.
Its flexible characteristics will allow the
proximal socket to expand for donning
and doffing.
- Modify the positive model for partial weightbearing. Remove only two
mm of plaster in the pretibial areas.
Remove only four mm of plaster on the
patella tendon bar. Remove plaster
proximally to blend in the 50.8-mm
(two-inch) extension (see Figure 9
).
- Do not reduce the ML dimension.
The goal for the ML dimension is to
equal the measured ML over the
shrinker and the socks plus 6 mm (1/4
inch). The goal for the AP dimension is
to equal the measured AP over the
shrinker and the socks plus 6 mm.
- The posterior trimline should be 6
mm (1/4-inch) below MTP level.
- Apply buildups over the bony
prominences. Apply a one-mm buildup
on the crest of the tibia, two mm on the
fibula head, three mm on the distal fibula and four mm on the distal tibia (see
Figure 10
).
Fabrication of the PSRD- Apply two layers of nylon, twisted
and reflected back over the model.
Powder the nylons with cornstarch.
- Heat 10 mm (3/8-inch) modified
polyethylene in the oven at 204°C
(400°F) for about 15 minutes supported
by a frame (11,12). Let the plastic
- droop or bubble about half the length
of the model (see Figure 11
).
- Invert the plastic on the model and
let it fall slowly. Use cups to keep the
frame from falling too low, which
would thin out the plastic. Pull from
the corners of the polyethylene to create a seal around the vacuum table.
- The vacuum should be applied
slowly to ensure no webbing occurs,
then apply full vacuum (see Figure 12
).
- Let PSRD sit overnight to help
prevent shrinkage (see Figure 13
). The
next day cure the PSRD in the oven for
20 minutes at 93°C (200°F) to relieve
stress in the plastic and help prevent
shrinkage.
- After curing, let the PSRD cool
for about three minutes. Cut the trimlines 50.8 mm above MTP, and pull the
PSRD off while it's still warm. Sand
and buff the proximal trimlines.
Patient Instructions
Usually the patient receives the PSRD
two to three days after the impression
is taken. Instruct the patient to apply
the medium compression shrinker. Initially, if the amputation is too sensitive,
substitute a one-ply wool for the
shrinker until the amputation desensitizes.
Have the patient apply the appropriate number of socks over the shrinker
(generally a one- or two-ply wool sock
will do) then show the patient how to
apply the PSRD (see Figure 14
). Show
the patient how to don and doff the
Juzo suspension sleeve (see Figure 15
)
(13).
Tell the patient to wear the PSRD
during the day. The patient can remove
the PSRD at bedtime but should keep
the shrinker on. The patient should
then redon the PSRD in the morning.
The patient should apply clean socks
daily and add additional socks if the
socket fit becomes loose. The patient
should also clean the PSRD daily with
rubbing alcohol and a washcloth.
The patient should stop wearing the
PSRD if it causes irritation.
Instruct the patient to apply 4.55 kg minutes under the supervision of a
to 9.1 kg (10 to 20 pounds) of weight on physical therapist (see Figure 16
). Give
the PSRD twice a day for one to two the patient a copy of these instructions.
Patient Follow-Up
Check the patient's progress with the
PSRD in one week (see Figure 17
). Is
the patient following instructions?
Wearing the socket regularly? Tolerating socket pressure? Reinstruct the patient if necessary.
Evaluate the patient's progress again
in another week. Take the impression
for the BK preparatory prosthesis at
this appointment if the patient has followed directions, tolerated wearing the
socket and the residual limb is ready.
The BK preparatory prosthesis is fitted in one week. In the meantime, the
patient continues to wear the PSRD.
The BK preparatory is delivered two
to three days after the fitting (see Figure 18
). The patient is instructed to
start wearing the preparatory three
hours per day and to don the PSRD
when he or she doffs the preparatory.
If the patient is not following the instructions or has poor tolerance to
wearing the PSRD, the preparatory
prosthesis should not be started until
there is improvement. Instead, encourage the patient to follow the instructions and get involved in his or her own
rehabilitation. If this approach doesn't
work, consult with the patient's physician. In this way, the PSRD assists the
prosthetist in evaluating a patient as a
prosthesis candidate.
Conclusion
During the past two years the PSRD
assisted in the rehabilitation and evaluation of 43 BK patients (see Figure 19
, and Figure 20
).
Forty patients successfully tolerated
the PSRD and were subsequently fit
with BK preparatory prostheses. Two
patients were not fit with preparatory
prostheses due to poor tolerance of the
PSRD and were evaluated to be nonprosthetic candidates. One patient
died due to congestive heart failure be
fore being fit with the preparator
prosthesis.
The PSRD offers improvements in
weight, hygiene and socket design. It
also encourages patient participation
and assists the prosthetist in patient
evaluation and management.
Future improvements to the PSRI
could include the use of CAD/CAM to
expedite the procedure and collect
data about residual limb shrinkage.
The data could be used to study the
effects of different postoperative management techniques and to justify medical necessity.
Vern M. Swanson, CP, is manager of Swanson Orthotic and Prosthetic Center Inc., 3102 Sylvania Ave., Toledo, OH 43613. He is past president of the Ohio Chapter of the American Academy of Orthotists and Prosthetists Inc.
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