Abstract
Background: Periprosthetic femoral fractures following total hip
arthroplasty are becoming more prevalent. When a fracture occurs in a femur
with substantial proximal bone deficiency, the surgical options for revision
are limited. One option includes the use of a proximal femoral allograft.
Methods: We retrospectively assessed the results and complications
of the use of a proximal femoral allograft to treat twenty-five Vancouver
type-B3 periprosthetic fractures in twenty-four patients. The mean
duration of follow-up was 5.1 years. Clinical results were graded with use of
the Harris hip score. Radiographs were assessed for evidence of trochanteric
union, host-allograft union, allograft resorption, and component loosening or
fracture. Failure of the procedure was defined as the need for revision
surgery requiring graft removal.
Results: The mean postoperative Harris hip score was 70.8. At the
time of the final follow-up, twenty-one of the twenty-four patients reported
no or mild pain and twenty-three patients were able to walk; fifteen required
a walking aid. The greater trochanter united in seventeen of the twenty-five
hips, and osseous union of the allograft to the host femur occurred in twenty
hips. There was mild graft resorption in four hips and moderate graft
resorption in two. Four (16%) of the twenty-five hips required repeat
revision.
Conclusions: The use of a proximal femoral allograft for the
treatment of a Vancouver type-B3 periprosthetic femoral fracture
can provide a satisfactory result in terms of pain relief and function at five
years.
Level of Evidence: Therapeutic Level IV. See Instructions
to Authors for a complete description of levels of evidence.
Periprosthetic femoral fractures occur at a rate of 0.1% to 6% following
total hip
arthroplasty1-3.
Fracture comminution, bone deficiency, and femoral component loosening make
the treatment of these fractures particularly
challenging1,2,4,5,
and successful treatment strategies for fractures occurring around a loose
femoral component with inadequate bone stock remain
elusive6-13.
Duncan and Masri6
classified fractures into three patterns with use of the so-called Vancouver
classification system.
Current treatment options include traction, cast-bracing, open reduction
and internal fixation supplemented by cortical strut-grafting, and revision
arthroplasty14-19.
In instances of extreme bone deficiency, revision arthroplasty options are
limited to the use of a long-stemmed, uncemented femoral component or a
proximal femoral replacement with either a tumor-type megaprosthesis or an
allograft-prosthesis composite.
The present retrospective review describes the clinical and radiographic
results, at a mean of 5.1 years postoperatively, for a series of
periprosthetic fractures that were treated with a proximal femoral
allograft.
We retrieved, from our institution's joint registry, the records for a
consecutive series of thirty-four patients with thirty-five Vancouver
type-B3 fractures that had been treated between 1989 and 2001. All
patients had been managed with revision arthroplasty with use of a proximal
femoral allograft by the senior author (A.G.). At the time of the final
review, fifteen patients had died and two had been lost to follow-up, leaving
seventeen living patients (eighteen hips). Of the fifteen patients who died,
seven patients (seven hips) had been followed for at least two years and
therefore were included in the study. Thus, the study group consisted of
twenty-four patients (twenty-five hips) with a mean duration of follow-up of
5.1 years (range, two to 12.7 years).
The clinical record and radiographs of each patient were retrospectively
reviewed. The Harris hip score was calculated. All patients had initially been
seen as the result of an acute periprosthetic fracture; therefore, no
preoperative Harris hip scores had been obtained. The diagnosis at the time of
primary hip arthroplasty was osteoarthritis for nineteen hips, degenerative
hip dysplasia for two, rheumatoid arthritis for two, osteonecrosis for one,
and ankylosing spondylitis for one.
Radiographic assessment consisted of fracture classification with use of
the Vancouver
method6. All
fractures were classified as type B3 as they were located around or
just distal to a loose femoral component and were associated with inadequate
proximal femoral bone
stock6
(Figs. 1-A and 1-B).
Postoperative radiographs were assessed for evidence of trochanteric union,
host-allograft union, allograft resorption, and component loosening or
fracture. Union was defined as the presence of osseous trabeculae crossing the
trochanteric osteotomy site or the allograft-host junction. Radiolucent lines
were assessed according to the zones defined by Gruen et
al.20. Allograft
resorption was defined as mild if there was partial-thickness resorption of
one cortex measuring <1 cm in length, as moderate if there was
partial-thickness resorption of one cortex measuring >1 cm in length, and
as severe if there was any evidence of full-thickness cortical resorption. An
implant was defined as loose if there was evidence of migration into varus,
subsidence of >3 mm, or fracture of the cement mantle. Failure of the
procedure was defined as the need for revision surgery requiring graft
removal.
Operative Technique
The allograft used in these procedures was stored at -70°C after
irradiation with 2.5 Mrad in accordance with the American Association of
Tissue Banks
guidelines21. Graft
preparation was performed on a separate surgical table by a second surgical
team while fracture exposure was being performed by the operating surgeon.
Details of the surgical technique are shown in
Figures 2-A through 2-F. The
fracture was approached with use of a sliding trochanteric
osteotomy22. The
deficient femoral shaft was osteotomized in the coronal plane. Care was taken
to minimize soft-tissue stripping from the femur. To maximize stability at the
graft-host junction, a step or oblique cut was made in the host femur. An
allograft was chosen that best matched the host bone size radiographically but
that would also allow at least a 2-mm-thick implant-bone cement mantle after
reaming and broaching. A femoral component length was chosen to allow at least
four cortical diameters of implant beyond the anticipated host-allograft
junction. The femoral component (Johnson and Johnson, Raynham, Massachusetts)
had a matte finish. Seventeen 254-cm, eight 270-cm, and ten 300-cm stems were
implanted. The mean length of the proximal femoral allograft was 14.5 cm
(range, 9 to 25 cm).
The femoral component was cemented into the allograft, and the cement was
allowed to polymerize on a separate table; this ensured that no cement would
enter the graft-host junction. The allograft-prosthesis composite was then
impacted without cement into the host femur. The residual osteotomized host
bone was fixed around the junction of the graft and the distal part of the
host femur with its soft-tissue attachments intact with use of cerclage wires
and the addition of autograft bone that had been obtained from the femur
during the process of extracting and débriding the loose implant. The
greater trochanter was reattached by passing cerclage wires around the lesser
trochanter of the allograft and the greater trochanter of the host.
Postoperatively, patients were managed with intravenous antibiotics for
five days and were mobilized without weight-bearing until there was
radiographic evidence of allograft-host union, usually at three to six
months.
Clinical Results
Eight patients had died and two had been lost to follow-up less than two
years postoperatively. The mean Harris hip score for the eight patients who
had died was 62.5 (range, 25 to 98) after a mean duration of follow-up of 1.1
years (range, 0.1 to 1.9 years). Three of these patients had reported no pain,
four had reported mild pain, and one had reported severe pain. Clinical data
were available at six months postoperatively for the two patients who had been
lost to follow-up. At that time, both patients had been able to walk with
crutches. The Harris hip scores for these two patients were 62 and 29.
The study group included twenty-five hips in twenty-four patients (thirteen
men and eleven women) who had had a mean age of 70.2 years (range, sixty to
eighty-one years) at the time of surgery. The mean duration of follow-up was
5.1 years (range, two to 12.7 years). The mean postoperative Harris hip score
at a minimum of two years of follow-up was 70.8 (range, 18.2 to 95.5). At the
time of the final follow-up, twenty-one of twenty-four patients reported no or
mild pain. Twenty-three of the twenty-four patients were able to walk; fifteen
required a walking aid. Walking distance was limited for all twenty-three
patients: two were able to walk in the house only, thirteen were able to walk
one to four blocks, and eight were able to walk five to six blocks.
Eighteen patients had a mild abductor lurch, and six patients had a severe
lurch. Seventeen hips (in sixteen patients) had a positive Trendelenburg
sign.
Radiographic Results
The greater trochanter united in seventeen of the twenty-five hips, and
osseous union of the allograft to the host femur occurred in twenty hips.
Trochanteric nonunion with >1 cm of migration of the greater trochanter
occurred in six hips (24%). The host bone and the proximal femoral allograft
failed to unite in four hips (16%). Allograft resorption occurred in six hips
(24%). Resorption was seen in Gruen zones 2 and 7 in four hips, Gruen zones 2
and 3 in one hip, and Gruen zones 6 and 7 in one hip. Resorption was mild in
four hips and moderate in two. There were no instances of severe resorption
necessitating revision surgery.
Three femora had loosening of the proximal femoral allograft as defined by
composite subsidence in excess of 3 mm (range, 4 to 8 mm) or progressive varus
angulation of the construct. These femora were treated with another proximal
femoral allograft; all of these revision allografts have been successful to
date.
Of the four hips in which the host bone-allograft junction failed to unite,
two hips were treated with observation as they were not painful, one went on
to achieve union following internal fixation and bone-grafting of the
host-graft junction, and one was revised with a second proximal femoral
allograft. There were no deep infections.
Other Complications
Two patients sustained a postoperative hip dislocation and were managed
with closed reduction. The dislocation occurred at fourteen months
postoperatively in one hip and at twenty months postoperatively in the other,
and neither recurred. There were six medical complications in the
perioperative period, including two instances of deep venous thrombosis, two
myocardial infarctions, one cerebrovascular accident, and one episode of renal
failure resulting in death at one month after surgery.
Overall Results
Four (16%) of the twenty-five hips that had been treated with a proximal
femoral allograft because of Vancouver type-B3 periprosthetic
fracture had a failure and required repeat revision after a mean duration of
follow-up of 5.1 years (range, two to 12.7 years).
Periprosthetic fractures about a well-fixed stem (Vancouver
type-B1 fractures) can be treated with internal fixation, and
fractures about a loose implant in a femur with adequate bone stock (Vancouver
type-B2 fractures) can be treated with revision hip
arthroplasty6.
However, in the case of a periprosthetic fracture about a loose stem with
inadequate bone stock (Vancouver type-B3 fractures), the challenge
is to simultaneously achieve implant and fracture stability. The surgical
options include proximal femoral replacement with either a megaprosthesis or
an allograft-prosthesis
composite23 or the
use of a long uncemented bypass femoral stem with distal
fixation24.
The use of a megaprosthesis was described by Springer et al. in a report
involving a limited number of
patients23. The
technique has the advantage of initial construct stability that allows
immediate patient mobilization. However, Duncan and
Masri6 reported a
higher dislocation rate in comparison with that associated with the use of a
proximal femoral allograft and recommended the use of either a bipolar
prosthesis or a constrained acetabular liner in conjunction with a
megaprosthesis. Additionally, the fixation of a megaprosthesis with or without
cement requires the presence of at least 6 cm of diaphyseal bone, which we
believe may not be possible in the case of severe bone stock deficiency. Other
disadvantages of megaprostheses include the lack of viable soft tissues for
reattachment and very limited treatment options should additional revision
surgery become necessary. A megaprosthesis therefore may be indicated for
patients with a limited life expectancy in whom early mobilization with
unrestricted weight-bearing is paramount and who have at least 6 cm of intact
diaphyseal bone to achieve adequate fixation.
Berry reported good early results in a study of eight patients with
Vancouver type-B3 fractures that were treated with a long,
uncemented, fluted
stem24. Although
the follow-up period in that report was short (mean, 1.5 years; range, one to
two years), the same technique was used successfully in two other reports on
revision surgery in the absence of femoral
fracture25,26.
This type of stem relies on fixation in the femoral diaphysis for initial
stability. Its utility is therefore limited if bone stock deficiency extends
beyond the femoral isthmus as distal fixation may be tenuous.
The allograft-prosthesis composite described here offers the advantages of
bone stock reconstitution, reattachment of soft tissues to the construct, and
the possibility of osseous union of the host greater trochanter. Furthermore,
it also can be used in situations in which bone deficiency extends beyond the
femoral isthmus. However, absolute construct stability is not conferred until
the host-graft junction unites, which usually necessitates a three to
six-month period of non-weight-bearing. We are not aware of any other study on
the use of proximal femoral allograft to treat Vancouver type-B3
fractures. However, we are encouraged because one of us (A.G.) and colleagues
used the same technique for revision arthroplasty in the absence of femoral
fracture and reported satisfactory results after nine to fifteen years of
follow-up27.
Although the numbers were smaller and the duration of follow-up was shorter in
the current report than in the previous report, the functional results and
success rates to date are similar.
Certain steps of the technique are essential. First, the cementing
technique should include pressurized cementing of the prosthesis into a clean
and dry allograft to gain a cement mantle of at least 2 mm; however, a
consequence of using a stem that allows a 2-mm cement mantle is that it will
not be readily possible to gain a press-fit between the distal part of the
stem and the host femoral canal because of the size mismatch of the narrow
stem and the large host diaphysis. Second, the femoral stem must be long
enough to bypass the host-allograft junction by four cortical diameters.
Third, adjunctive screws or plates should be avoided because they may weaken
the graft. Fourth, rigid stabilization of the graft-host junction with strut
grafts and cerclage wires should be achieved. Fifth, femoral autograft
(obtained during the process of extracting and débriding the loose
implant) should be placed at the graft-host junction. Sixth, using the host,
osteotomized vascularized bone to wrap around the junction can provide a
vascular bed for osseous union.
Unfortunately, we were not able to identify any risk factors associated
with the occurrence of periprosthetic fracture such as stem design, the
presence of stress-shielding, or osteoporosis. Nor were we able to identify
any predictors of failure of the proximal femoral allograft in terms of the
nature of the cut (step or oblique) at the graft-host junction, the cement
mantle thickness, or the prosthesis or allograft length. Two of the composites
that subsided were in younger active patients with ages of sixty and sixty-two
years, but no loosening of the prosthesis within the allograft had
occurred.
Why allograft resorption occurred predominantly in Gruen zones 2 and 7 is
unclear. These two zones represent the most proximal part of the graft, and
stress-shielding could only occur in the presence of vascularized bone. The
only sources of vascularity are a united graft-host junction and the
osteotomized proximal part of the host femur that was wrapped around the
construct.
In conclusion, treatment of a Vancouver type-B3 periprosthetic
fracture is particularly challenging, and, while no single technique is ideal,
the present study demonstrated that the use of a proximal femoral allograft
offers a reliable option to obtain a stable construct and can provide a
satisfactory result at five years. However, patients should be cautioned that
their postoperative functional goals should be limited. ?
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