H. Migaud et al., CUSTOM TEMPORARY ANTIBIOTIC-LOADED CEMENT PROSTHESIS FOR 2-STAGE SEPTIC HIP REVISION ARTHROPLASTY, Revue de chirurgie orthopedique et reparatrice de l'appareil moteur, 84(5), 1997, pp. 466-468
Purpose of the study During the excision period of a two-stage revisio
n arthroplasty, the hip has a low function and an unacceptable leg len
gth discrepancy. The goal of this study was to expose technical detail
s in order to perform a simple articulated cement spacer which could b
e implanted during this period to improve hip function, to authorize p
artial weight bearing and to avoid leg length discrepancy. Material Th
is method was applied in three two-stage procedures justified because
of particular immunodeficiency conditions: a 43 years old man who had
bone marrow allograft and immunosuppressive therapy because of leukemi
a suffering of subacute septic hip arthritis; a 58 years old man suffe
ring of diabetes and active C-hepatitis who had a septic loosening of
a total hip arthroplasty (THA); a 76 years old woman suffering of diab
etes who had a third septic loosening of THA. Method The prosthesis wa
s made of antibiotic-impregnated cement according to organisms antibio
tic resistance. The prosthetic junction between head and diaphysis was
reinforced with a tibial plate. Prosthetic shape was identical to the
one of femoral broaches inserted in the femur after prosthetic and ce
ment removal. The broach size was chosen when mechanical stability in
the femur was obtained, and avoided leg length discrepancy after trial
s with cups. The tibial plate was bent in order to reinforce the junct
ion with regard to the shape of the determined broach. Two doses of an
tibiotic-impregnated cement were mixed and molded with hands, then the
plate was incorporated at the appropriate location, finaly the broach
was applied on this composite and cement in excess was removed before
polymerisation. For prosthetic head, two options were available: to m
old the cephalic zone of the cement at the patient acetabulum diameter
with a soft aluminium cup previously molded in the acetabulum; to mol
d the cement cephalic zone with a trial cup in order to obtain a 22 or
28 ball. For this last option, a third dose of antibiotic-impregnated
cement was prepared and placed in the acetabulum, a trial femoral hea
d was applied in it to mold the location for the 22 or 28 prosthetic h
ead. Before insertion, a collar was applied on the stem to prevent mig
ration. Active mobilization was encouraged, and partial weight-bearing
authorized. Results The mean range of hip flexion during period was 6
0 degrees. The patients were discharged approximatively 12 days after
the first stage. Two patients had effective painless partial weight-be
aring. The second stage was performed six weeks later on the average.
The second procedure was easier than the second stage of a conventiona
l two-stage procedure because of: easy and low hemoragic dissection au
thorized by the prosthesis; low difficulties with soft tissue tension
as the prosthesis prevents leg length discrepancy; preservation of the
articular space which prevents soft tissue sacrifice during the secon
d stage. Conclusion This simple technique is effective to prevent comp
lications related to the excision period of a two-stage hip revision a
rthroplasty. Likewise, the economical aspect (short delay of hospitali
sation, quick functional recovery) should be considered when compared
with the excision period of a conventional two-stage procedure.