Aims. Custom-made partial pelvis replacements (PPRs) are increasingly used in the reconstruction of large acetabular defects and have mainly been designed using a triflange approach, requiring extensive soft-tissue dissection. The monoflange design, where primary intramedullary fixation within the ilium combined with a monoflange for rotational stability, was anticipated to overcome this obstacle. The aim of this study was to evaluate the design with regard to functional outcome, complications, and acetabular reconstruction. Methods. Between 2014 and 2023, 79 patients with a mean follow-up of 33 months (SD 22; 9 to 103) were included. Functional outcome was measured using the Harris Hip Score and EuroQol five-dimension questionnaire (EQ-5D). PPR revisions were defined as an endpoint, and subgroups were analyzed to determine risk factors. Results. Implantation was possible in all cases with a 2D centre of rotation deviation of 10 mm (SD 5.8; 1 to 29). PPR revision was necessary in eight (10%) patients. HHS increased significantly from 33 to 72 postoperatively, with a mean increase of 39 points (p < 0.001). Postoperative EQ-5D score was 0.7 (SD 0.3; -0.3 to 1). Risk factor analysis showed significant revision rates for septic indications (p ≤ 0.001) as well as femoral defect size (p = 0.001). Conclusion. Since large acetabular defects are being treated surgically more often, custom-made PPR should be integrated as an option in treatment algorithms. Monoflange PPR, with primary iliac fixation, offers a viable treatment option for
Aims. The use of a porous metal shell supported by two augments with the ‘footing’ technique is one solution to manage
Aims. The advent of trabecular metal (TM) augments has revolutionized
the management of severe bone defects during acetabular reconstruction.
The purpose of this study was to evaluate patients undergoing revision
total hip arthroplasty (THA) with the use of TM augments for reconstruction
of
The management of severe acetabular bone defects poses a complex challenge in revision hip arthroplasty. Although biological fixation materials are currently dominant, cage has played an important role in complex acetabular revision in the past decades, especially when a biological prosthesis is not available. The purpose of this study is to report the long-term clinical and radiographic results of
Aims. The aim of this study was to examine the implant accuracy of custom-made partial pelvis replacements (PPRs) in revision total hip arthroplasty (rTHA). Custom-made implants offer an option to achieve a reconstruction in cases with severe acetabular bone loss. By analyzing implant deviation in CT and radiograph imaging and correlating early clinical complications, we aimed to optimize the usage of custom-made implants. Methods. A consecutive series of 45 (2014 to 2019) PPRs for
The use of trabecular metal (TM.) shells supported by two TM augments in the footing technique has been described as a potential option for the treatment of
Aims. The purpose of this retrospective study was to evaluate the minimum
five-year outcome of revision total hip arthroplasty (THA) using
the Kerboull acetabular reinforcement device (KARD) in patients
with
The advent of trabecular metal (TM) augments has revolutionized the management of severe bone defects during acetabular reconstruction. The purpose of this study was to evaluate patients undergoing revision total hip arthroplasty (THA) with the use of TM augments for reconstruction of
Introduction. Acetabular revision surgery remains a technically demanding procedure with higher failure rates than primary total hip arthroplasty (THA). An acetabular component with three dimensional porous titanium and anatomic screw holes (Figure 1) was designed to allow the cup to be positioned anatomically and provide reliable fixation. Methods. A prospective multicenter study of 193 cases (190 patients) was conducted to assess the midterm clinical outcomes of the revision titanium acetabular shell. Radiographs, demographics, Harris Hip Score (HHS), and Short Form 36 (SF-36) were collected preoperatively, at 6 weeks, 3 months, and annually thereafter to 5 years. The mean duration of follow-up was 3.36 years. The
We report the results of 62 hips in 62 patients
(17 males, 45 females) with mean age of 62.4 years (37 to 81), who underwent
revision of the acetabular component of a total hip replacement
due to aseptic loosening between May 2003 and November 2007. All
hips had a
Introduction. Different classification systems for acetabular deficiencies, including AAOS and
One of the many challenges in revision hip arthroplasty is massive bone loss. Subsidence of the collarless stem with impaction allografting has been reported by several authors. Impaction grafting has emerged as a useful technique in the armamentarium of the revision total hip arthroplasty surgeon. The original technique proposed by Ling has been associated with complications, including femoral shaft fractures, recurrent dislocations, and uncontrolled component subsidence. Modifications in that technique seem to be associated with a reduction in complications. The aim of this study was to assess the functional outcome of radial impaction grafting in femoral bone defects and the use of collared long stem prosthesis. A total of 107 patients underwent radial impaction allografting and collared long stem prosthesis during revision THA between 1997 and 2005. The patients with
As population grows older, and patients receive primary joint replacements at younger age, more and more patients receive a total hip prosthesis nowadays. Ten-year failure rates of revision hip replacements are estimated at 25.6%. The acetabular component is involved in over 58% of those failures. From the second revision on, the pelvic bone stock is significantly reduced and any standard device proves inadequate in the long term [Villanueva et al. 2008]. To deal with these challenges, a custom approach could prove valuable [Deboer et al. 2007]. A new and innovative CT-based methodology allows creating a biomechanically justified and defect-filling personalized implant for acetabular revision surgery [Figure 1]. Bone defects are filled with patient-specific porous structures, while thin porous layers at the implant-bone interface facilitate long-term fixation. Pre-operative planning of screw positions and lengths according to patient-specific bone quality allow for optimal fixation and accurate transfer to surgery using jigs. Implant cup orientation is anatomically analyzed for required inclination and anteversion angles. The implant is patient-specifically analyzed for mechanical integrity and interaction with the bone based upon fully individualized muscle modeling and finite element simulation.Introduction
Materials and methods
If a surgeon is faced with altered lesser trochanter
anatomy when revising the femoral component in revision total hip
replacement, a peri-prosthetic fracture, or
Aims. Revision total hip arthroplasty in patients with Vancouver type B3 fractures with
Acetabular bone loss is a challenging problem
facing the revision total hip replacement surgeon. Reconstruction
of the acetabulum depends on the presence of anterosuperior and
posteroinferior pelvic column support for component fixation and
stability. The
Acetabular distraction for the treatment of chronic pelvic discontinuity was first described by Sporer and
Revision of the failed femoral component can be challenging. Multiple reconstructive options are available and the procedure is technically difficult and thus meticulous pre-operative planning is required. The
Aims. Bone stock restoration of acetabular bone defects using impaction bone grafting (IBG) in total hip arthroplasty may facilitate future re-revision in the event of failure of the reconstruction. We hypothesized that the acetabular bone defect during re-revision surgery after IBG was smaller than during the previous revision surgery. The clinical and radiological results of re-revisions with repeated use of IBG were also analyzed. Methods. In a series of 382 acetabular revisions using IBG and a cemented component, 45 hips (45 patients) that had failed due to aseptic loosening were re-revised between 1992 and 2016. Acetabular bone defects graded according to
The treatment of severe acetabular bone loss is challenging, especially in the setting of an associated chronic pelvic discontinuity. There are several available treatment options for chronic pelvic discontinuity, each of which has its own disadvantages. One of the major difficulties with this entity, regardless of the reconstructive technique chosen, is the inability to obtain reproducible healing of the discontinuity. We evaluated the use of acetabular distraction, a technique which achieves peripheral or lateral distraction and central or medial compression across the discontinuity. We recommend acetabular distraction to allow for implantation of a stable construct, achieve biologic fixation and increase the likelihood of discontinuity healing. In this multi-center trial, 32 patients that underwent acetabular revision for a chronic pelvic discontinuity using acetabular distraction were radiographically evaluated at a minimum of 25 months (range, 25 to 160 months). The study cohort was categorized according to the
Previous reports on the outcomes of isolated head and liner exchange in revision total hip arthroplasty have found high rates of instability following these surgeries. Most reports have studied constructs using ≤28mm femoral heads. The purpose of this study was to determine if modern techniques with the use of larger head sizes can improve the rate of instability after head and liner exchange. We identified 138 hips in 132 patients who underwent isolated head and liner exchange for polyethylene wear/osteolysis (57%), acute infection (27%), metallosis (13%), or other (2%). All patients underwent revision with either 32mm (23%), 36mm (62%), or 40mm (15%) diameter heads. Crosslinked polyethylene was used in all revisions. Lipped and/or offset liners were used in 104 (75%) hips. Average follow up was 3.5 (1.0–9.1) years. Statistical analyses were performed with significance set at p<0.05. Revision-free survivorship for any cause was 94.6% and for aseptic causes was 98.2% at 5 years. 11 (8%) hips experienced a complication with 7 (5%) hips requiring additional revision surgery. Following revision, 4 (3%) hips experienced dislocation, 5 (4%) hips experienced infection, and 1 (1%) hip was revised for trunnionosis. No demographic or surgical factors significantly affected outcomes. Our study shows that isolated head and liner exchange using large femoral heads and modern liners provides for better stability than previous reports. The most common complication was infection. We did not identify specific patient, surgical or implant factors that reduced the risk of instability or other complication.
Introduction. During revision total hip arthroplasty, successful treatment of acetabular bone loss with an associated chronic pelvic discontinuity is dependent upon the remaining bone stock, stability of the construct, potential for biologic fixation, and healing of the discontinuity. Several techniques have been described for the treatment of this clinical entity; the authors recommend the use of acetabular distraction technique in conjunction with a jumbo cup with or without augments. The authors recently evaluated the minimum two-year follow-up of acetabular distraction technique for the treatment of chronic pelvic discontinuity. In the process, a chronic pelvic discontinuity classification was created based on the type of reconstruction required. The purpose of this study is to introduce the initial observations of this novel classification system. Methods. Patients from two academic institutions undergoing acetabular distraction for chronic pelvic discontinuity were identified between January 2002 and December 2013 with minimum 2-year follow-up. Radiographs at latest follow-up were compared to serial radiographs from the index surgery. Data was collected by chart review in accordance with institutional IRB protocol from both institutions. Results. A cohort of 32 patients had minimum 2-year (range, 2.1–13.3 years) follow-up. Mean patient age was 67 years (range, 44–86) and 87% were female. All patients had a chronic pelvic discontinuity with the following bone loss patterns: 7 (22%) type IIC, 5 (15%) type IIIA and 20 (63%) type IIIB. At time of final follow-up, radiographs demonstrated 22 of 32 patients (69%) had evidence of a healed discontinuity. Chronic Pelvic Discontinuity Classification. The classification mirrors the
Aims. The aim of this modified Delphi process was to create a structured Revision Hip Complexity Classification (RHCC) which can be used as a tool to help direct multidisciplinary team (MDT) discussions of complex cases in local or regional revision networks. Methods. The RHCC was developed with the help of a steering group and an invitation through the British Hip Society (BHS) to members to apply, forming an expert panel of 35. We ran a mixed-method modified Delphi process (three rounds of questionnaires and one virtual meeting). Round 1 consisted of identifying the factors that govern the decision-making and complexities, with weighting given to factors considered most important by experts. Participants were asked to identify classification systems where relevant. Rounds 2 and 3 focused on grouping each factor into H1, H2, or H3, creating a hierarchy of complexity. This was followed by a virtual meeting in an attempt to achieve consensus on the factors which had not achieved consensus in preceding rounds. Results. The expert group achieved strong consensus in 32 out of 36 factors following the Delphi process. The RHCC used the existing
Aims. The aims of this study were to determine the success of a reconstruction algorithm used in major acetabular bone loss, and to further define the indications for custom-made implants in major acetabular bone loss. Methods. We reviewed a consecutive series of
Aims. The aim of this study was to compare the biomechanical models of two frequently used techniques for reconstructing severe acetabular defects with pelvic discontinuity in revision total hip arthroplasty (THA) – the Trabecular Metal Acetabular Revision System (TMARS) and custom triflange acetabular components (CTACs) – using virtual modelling. Methods. Pre- and postoperative CT scans from ten patients who underwent revision with the TMARS for a
Aims. Large bone defects resulting from osteolysis, fractures, osteomyelitis, or metastases pose significant challenges in acetabular reconstruction for total hip arthroplasty. This study aimed to evaluate the survival and radiological outcomes of an acetabular reconstruction technique in patients at high risk of reconstruction failure (i.e. periprosthetic joint infection (PJI), poor bone stock, immunosuppressed patients), referred to as Hip Reconstruction In Situ with Screws and Cement (HiRISC). This involves a polyethylene liner embedded in cement-filled bone defects reinforced with screws and/or plates for enhanced fixation. Methods. A retrospective chart review of 59 consecutive acetabular reconstructions was performed by four surgeons in a single institution from 18 October 2018 to 5 January 2023. Cases were classified based on the
Revision total hip arthroplasty (rTHA) in the presence of femoral defects can be technically challenging. Reconstruction with long stems is widely accepted as the standard. However long stems can be difficult to insert and can compromise distal bone stock for future revisions. The aims of this study were to identify whether there was a difference in survival and outcomes following rTHA using a long versus standard or short femoral stem. A comprehensive systematic review was performed according to PRISMA guidelines using the MEDLINE, EMBASE, Chochrane Library and Web of Science databases. Inclusion criteria were (i) adult patients >18 years; (ii) randomised controlled trials, joint registry, or cohort studies; (iii) single or staged rTHA for
The best treatment method of large acetabular bone defects at revision THR remains controversial. Some of the factors that need consideration are the amount of residual pelvic bone removed during revision; the contact area between the residual pelvic bone and the new implant; and the influence of the new acetabular construct on the centre of rotation of the hip. The purpose of this study was to compare these variables in two of the most used surgical techniques used to reconstruct severe acetabular defects: the trabecular metal acetabular revision system (TMARS) and a custom triflanged acetabular component (CTAC). Pre- and post-operative CT-scans were acquired from 11 patients who underwent revision THR with a TMARS construct for a
For over a decade, modular titanium fluted tapered (TFT) stems have demonstrated excellent clinical success for femoral revision total hip arthroplasty (THA) surgery. The aim of this study was to report the short-term outcomes of a novel modern monoblock TFT stem used for revision and complex primary THA with a minimum of 2 years follow-up. We identified 126 patients who received a single monoblock TFT stem - 26 patients for complex THA (failed fracture fixation) and 100 patients for revision THA. The reasons for revision THA included 40 for previous prosthetic joint infection (PJI), 42 for aseptic loosening, 9 for trunnionosis, 9 for periprosthetic fractures. The
Osteolysis, fractures, and bone destruction caused by osteomyelitis or metastasis can cause large bone defects and present major challenges during acetabular reconstruction in total hip arthroplasty. We sought to evaluate the survivorship and radiographic outcomes of an acetabular reconstruction consisting of a polyethylene liner (semi-constrained) embedded in cement filling bone defect(s) reinforced with screws and/or plates for enhanced fixation (HiRISC). Retrospective chart review of 59 consecutive acetabular reconstructions as described above performed by 4 surgeons in a single institution (10/18/2018-1/5/2023) was performed. After radiographs and operative reports were reviewed, cases were classified following the
As the number of patients who have undergone total hip arthroplasty rises, the number of patients who require surgery for a failed total hip arthroplasty is also increasing. It is estimated that 183,000 total hip replacements were performed in the United States in the year 2000 and that 31,000 of these (17%) were revision procedures. Reconstruction of the failed femoral component in revision total hip arthroplasty can be challenging from both a technical perspective and in preoperative planning. With multiple reconstructive options available, it is helpful to have a classification system which guides the surgeon in selecting the appropriate method of reconstruction. A classification of femoral deficiency has been developed and an algorithmic approach to femoral reconstruction is presented. An extensively coated, diaphyseal filling component reliably achieves successful fixation in the majority of revision femurs. The surgical technique is straightforward and we continue to use this type of device in the majority of our revision total hip arthroplasties. However, in the severely damaged femur (Type IIIB and Type IV), other reconstructive options may provide improved results. Based on our results, the following reconstructive algorithm is recommended for femoral reconstruction in revision total hip arthroplasty. Type I: In a Type I femur, there is minimal loss of cancellous bone with an intact diaphysis. Cemented or cementless fixation can be utilised. If cemented fixation is selected, great care must be taken in removing the neo-cortex often encountered to allow for appropriate cement intrusion into the remaining cancellous bone. Type II: In a Type II femur, there is extensive loss of the metaphyseal cancellous bone and thus, fixation with cement is unreliable. In this cohort of patients, successful fixation was achieved using a diaphyseal fitting, extensively porous coated implant. However, as the metaphysis is supportive, a cementless implant that achieves primary fixation in the metaphysis can be utilised. Type IIIA: In a Type IIIA femur, the metaphysis is non-supportive and an extensively coated stem of adequate length is utilised to ensure that more than 4cm of scratch fit is obtained in the diaphysis. Type IIIB: Based on the poor results obtained with a cylindrical, extensively porous coated implant (with 4 of 8 reconstructions failing), our present preference is a modular, cementless, tapered stem with flutes for obtaining rotational stability. Type IV: The isthmus is completely non-supportive and the femoral canal is widened. Cementless fixation cannot be reliably used in our experience, as it is difficult to obtain adequate initial implant stability that is required for osseointegration. Reconstruction can be performed with impaction grafting if the cortical tube of the proximal femur is intact. However, this technique can be technically difficult to perform, time consuming and costly given the amount of bone graft that is often required. Although implant subsidence and peri-prosthetic fractures have been associated with this technique, it can provide an excellent solution for the difficult revision femur where cementless fixation cannot be utilised. Alternatively, an allograft-prosthesis composite can be utilised for younger patients in an attempt to reconstitute bone stock and a proximal femoral replacing endoprosthesis used for more elderly patients.
Aims. There is a paucity of long-term studies analyzing risk factors for failure after single-stage revision for periprosthetic joint infection (PJI) following total hip arthroplasty (THA). We report the mid- to long-term septic and non-septic failure rate of single-stage revision for PJI after THA. Methods. We retrospectively reviewed 88 cases which met the Musculoskeletal Infection Society (MSIS) criteria for PJI. Mean follow-up was seven years (1 to 14). Septic failure was diagnosed with a Delphi-based consensus definition. Any reoperation for mechanical causes in the absence of evidence of infection was considered as non-septic failure. A competing risk regression model was used to evaluate factors associated with septic and non-septic failures. A Kaplan-Meier estimate was used to analyze mortality. Results. The cumulative incidence of septic failure was 8% (95% confidence interval (CI) 3.5 to 15) at one year, 13.8% (95% CI 7.6 to 22) at two years, and 19.7% (95% CI 12 to 28.6) at five and ten years of follow-up. A femoral bone defect worse than
While THA is associated with positive results and long-term improvement in patient quality of life, outcomes are nonetheless associated with adverse events and post-procedural deficits related to discrepancies in leg length (LLD), offset and cup placement. Post-THA errors in these parameters are associated with gait alteration, low back pain and patient dissatisfaction. Such discrepancies often necessitate revision and increasingly lead to medical malpractice litigation. Maintaining accuracy in post-surgical leg length, offset and cup placement during THA is difficult and subject to error. The sensitivity of these factors is highlighted in studies that have shown that a change of as little as 5 degrees of flexion or abduction can induce alterations in leg length of up to several millimeters. Similarly, positioning of implants can alter global and femoral offset, affecting abductor strength, range of motion and overall physical function. Compounding the biochemical issues associated with inaccurate leg length are the costs associated with these deficits. Traditional freehand techniques of managing intra-operative parameters rely on surgeon experience and tissue tensioning to manually place components accurately. These methods, however, are only able to assess leg length and are subject to inaccuracies associated with patient movement or orientation changes during surgery. Mechanical methods of minimizing post-surgical discrepancies have been developed, such as outrigger or caliper devices, although these methods also address leg length only and provide poor feedback regarding offset and center of rotation, therefore providing insufficient data to accurately achieve appropriate post-surgical leg length. Computer-assisted navigation methods provide more data regarding leg length, offset and center of rotation, but are limited by their cumbersome nature and the large capital costs associated with the systems. The Intellijoint HIP® surgical smart tool (Intellijoint Surgical, Inc., Waterloo, ON) is an intra-operative guidance tool that provides surgeons with real time data on leg length, offset and center of rotation, thereby allowing for confident selection of the correct implant in order to ensure appropriate post-surgical biomechanics. The early clinical results from an initial cohort of patients indicate that Intellijoint HIP® is safe and effective. No adverse events were reported in the initial cohort, and the smart tool was able to measure surgical parameters to within 1mm when compared to radiographic measurements. With training cases removed, 100% of cases had a post-procedure leg length discrepancy of less than 5mm. This paper describes the indications, procedural technique and early clinical results of the Intellijoint HIP® smart tool, which offers a safe, accurate and easy-to-use option for hip surgeons to manage leg length, offset and cup position intra-operatively.Introduction
The unacceptable failure rate of cemented femoral revisions led to many different cementless femoral designs employing fixation in the damaged proximal femur with biological coatings limited to this area. The results of these devices were uniformly poor and were abandoned for the most part by the mid-1990's. Fully porous coated devices employing distal fixation in the diaphysis emerged as the gold standard for revisions with several authors reporting greater than 90% success rate 8–10 years of follow-up. Surgical techniques and ease of insertion improved with the introduction of the extended trochanteric osteotomy as well as curved, long, fully porous coated stems with diameters up to 23mm. The limits of these stems were stretched to include any stem diameter in which even 1–2cm of diaphyseal contact could be achieved. When diaphyseal fixation was not possible (Type IV), the alternatives were either impaction grafting or allograft prosthetic composite (APC). As the results of fully porous coated stems were very carefully scrutinised, it became apparent that certain types of bone loss did not yield the most satisfactory results both clinically and radiographically. When less than 4cm of diaphyseal press fit (Type IIIB) was achieved, the mechanical failure rate (MFR) was over 25%. It also became apparent that even when there was 4–6cm diaphyseal contact (Type IIIA), and the stem diameter was 18mm or greater, post-operative pain and function scores were significantly less than those with smaller diameter stems. This was probably due to poorer quality bone. Many of these Type IIIA and Type IIIB femurs had severe proximal torsional remodeling leading to marked distortion of anteversion. This made judging the amount of anteversion to apply to the stem at the time of insertion very difficult, leading to higher rates of dislocation. These distortions were not present in Type I and Type II femurs. This chain of events which was a combination of minimal diaphyseal fixation, excessively stiff stems and higher dislocation rates led to the conversion to modular type stems when these conditions existed. For the past 13 years, low modulus taper stems of the Wagner design have been used for almost all Type IIIA and Type IIIB bone defects. The taper design with fluted splines allows for fixation when there is less than 2cm of diaphysis. The results in these femurs even with diameters of up to 26mm have led to very low MFRs and significantly less thigh pain. Independent anteversion adjustment is also a huge advantage in these modular stems. Similar success rates, albeit with less follow-up, have been noted in Type IV femurs.
Bone is a dynamic organ with remarkable regenerative properties seen only otherwise in the liver. However, bone healing requires vascularity, stability, growth factors, a matrix for growth, and viable cells to obtain effective osteosynthesis. We rely on these principles not only to heal fractures, but also achieve healing of benign bone defects. Unfortunately we are regularly confronted with situations where the local environment and tissue is insufficient and we must rely on our “biologic tool box.” When the process of bone repair requires additional assistance, we often look to bone grafting to provide an osteoconductive, osteoinductive, and/or osteogenic environment to promote bone healing and repair. The primary workhorses of bone grafting include autogenous bone, cadaver allograft, and bone graft substitutes. Among the first types of bone graft used and still used in large quantities today include autogenous and cadaver allograft bone. Allografts are useful because it is present in multiple forms that conform to the desired situation. But autogenous bone graft is considered the gold standard because it possesses all the fundamental properties to heal bone. However, it has been associated with high rates of donor site morbidity and typically requires an inpatient hospitalization following the procedure only adding to the associated costs. The first bone graft substitute use was calcium sulfate in 1892, and over the past 122 years advancements have achieved improved material properties of calcium sulfate and helped usher in additional bioceramics for bone grafting. Today there are predominantly four types of bioceramics available, which include calcium sulfate, calcium phosphate, tricalcium phosphate, and coralline hydroxyapatite. They come in multiple forms ranging from pellets and solid blocks to injectable and moldable putty. In comparison to autogenous bone graft, the primary limitation of bioceramics are the lack of osteogenic and osteoinductive properties. Bioceramics work by creating an osteoconductive scaffold to promote osteosynthesis. The options of bone graft substitutes don't end with these four types of bioceramics. Composite bioceramics take advantage of the differing biomechanical properties of these four basis types of bioceramics to develop improved materials. To overcome the lack of osteoinductive and osteogenic properties growth factors or bone marrow aspirate can be added to the bioceramic. As a result, the list of combinations available in our “biologic tool box” continues to expand. More than 20 BMPs have been identified, but only BMP-2 and BMP-7 have FDA approval. As we look forward to areas of future research and need within orthobiologics, some will likely come in the near future while others are much further in the future. We will continue to strive for the ideal bone graft substitute, which will have similar osteoinductive properties as autograft. The ultimate bone graft substitute will likely involve stem cells because it will allow an alternative to autogenous bone with the same osteogenic potential.
The extended proximal femoral osteotomy has been used primarily in conjunction with cementless fixation, but has been described for use with cemented stems as well. The extended proximal femoral osteotomy is indicated for the removal of well-fixed cemented and cementless implants, as well as removal of cement in patients with a loose femoral component in a well-fixed cement mantle. Although the osteotomy is not required for many femoral revisions, it is an absolute indication in patients with femoral component loosening and subsequent varus remodeling of the proximal femur. The osteotomy diminishes the risk of an inadvertent fracture of the often compromised greater trochanter especially upon removal of a failed femoral component from its subsided or migrated position. The osteotomy enhances the exposure of the acetabulum which may be difficult in the revision setting due to multiple surgeries, severe migration of the acetabular component or the heterotopic ossification. The extended proximal femoral osteotomy can also be used in the primary setting when a proximal femoral deformity interferes with straight reaming of the femoral canal, such as in patients with various dysplasias, previous corrective osteotomies or malunions.
As the number of patients who have undergone total hip arthroplasty rises, the number of patients who require surgery for a failed total hip arthroplasty is also increasing. It is estimated that 183,000 total hip replacements were performed in the United States in the year 2000 and that 31,000 of these (17%) were revision procedures. Reconstruction of the failed femoral component in revision total hip arthroplasty can be challenging from a technical perspective and in pre-operative planning. With multiple reconstructive options available, it is helpful to have a classification system which guides the surgeon in selecting the appropriate method of reconstruction. A classification of femoral deficiency has been developed and an algorithmic approach to femoral reconstruction is presented.
Minimal loss of metaphyseal cancellous bone with an intact diaphysis. Often seen when conversion of a cementless femoral component without biological ingrowth surface requires revision. Type II: Extensive loss of metaphyseal cancellous bone with an intact diaphysis. Often encountered after the removal of a cemented femoral component. Type IIIA: The metaphysis is severely damaged and non-supportive with more than 4cm of intact diaphyseal bone for distal fixation. This type of defect is commonly seen after removal of grossly loose femoral components inserted with first generation cementing techniques. Type IIIB: The metaphysis is severely damaged and non-supportive with less than 4cm of diaphyseal bone available for distal fixation. This type of defect is often seen following failure of a cemented femoral component that was inserted with a cement restrictor and cementless femoral components associated with significant distal osteolysis. Type IV: Extensive meta-diaphyseal damage in conjunction with a widened femoral canal. The isthmus is non-supportive. An extensively coated, diaphyseal filling component reliable achieves successful fixation in the majority of revision femurs. The surgical technique is straightforward and we continue to use this type of device in the majority of our revision total hip arthroplasties. However, in the severely damaged femur (Type IIIB and Type IV), other reconstructive options may provide improved results. Based on the poor results obtained with a cylindrical, extensively porous coated implant (with 4 of 8 reconstructions failing), our preference is a modular, cementless, tapered stem with flutes for obtaining rotational stability. Excellent results have been reported with this type of implant and by virtue of its tapered design, excellent initial axial stability can be obtained even in femurs with a very short isthmus. Subsidence has been reported as a potential problem with this type of implant and they can be difficult to insert. However, with the addition of modularity to many systems that employ this concept of fixation, improved stability can be obtained by impaction of the femoral component as far distally as needed while then building up the proximal segment to restore appropriate leg length. The isthmus is completely non-supportive and the femoral canal is widened. Cementless fixation cannot be reliably used in our experience, as it is difficult to obtain adequate initial implant stability that is required for osseointegration. Reconstruction can be performed with impaction grafting if the cortical tube of the proximal femur is intact. However, this technique can be technically difficult to perform, time consuming and costly given the amount of bone graft that is often required. Although implant subsidence and peri-prosthetic fractures (both intra-operatively and post-operatively) have been associated with this technique, it can provide an excellent solution for the difficult revision femur where cementless fixation cannot be utilised. Alternatively, an allograft-prosthesis composite can be utilised for younger patients in an attempt to reconstitute bone stock and a proximal femoral replacing endoprosthesis used for more elderly patients.
As the number of patients who have undergone total hip arthroplasty rises, the number of patients who require surgery for a failed total hip arthroplasty is also increasing. Reconstruction of the failed femoral component in revision total hip arthroplasty can be challenging from both a technical perspective and in pre-operative planning. With multiple reconstructive options available, it is helpful to have a classification system which guides the surgeon in selecting the appropriate method of reconstruction. Type I: Minimal loss of metaphyseal cancellous bone with an intact diaphysis. Often seen when conversion of a cementless femoral component without biological ingrowth surface requires revision. Type II: Extensive loss of metaphyseal cancellous bone with an intact diaphysis. Often encountered after the removal of a cemented femoral component. Type IIIA: The metaphysis is severely damaged and non-supportive with more than 4 cm of intact diaphyseal bone for distal fixation. This type of defect is commonly seen after removal of grossly loose femoral components inserted with first generation cementing techniques. Type IIIB: The metaphysis is severely damaged and non-supportive with less than 4 cm of diaphyseal bone available for distal fixation. This type of defect is often seen following failure of a cemented femoral component that was inserted with a cement restrictor and cementless femoral components associated with significant distal osteolysis. Type IV: Extensive meta-diaphyseal damage in conjunction with a widened femoral canal. The isthmus is non-supportive. Based on our results, the following reconstructive algorithm is recommended for femoral reconstruction in revision total hip arthroplasty. An extensively coated, diaphyseal filling component reliably achieves successful fixation in the majority of revision femurs and the surgical technique is straightforward. However, in the severely damaged femur (Type IIIB and Type IV), other reconstructive options may provide improved results. Type I: Cemented or cementless fixation can be utilised. If cemented fixation is selected, great care must be taken in removing the neo-cortex often encountered to allow for appropriate cement intrusion into the remaining cancellous bone. Type II: In this cohort of patients, successful fixation was achieved using a diaphyseal fitting, extensively porous coated implant. However, as the metaphysis is supportive, a cementless implant that achieves primary fixation in the metaphysis can be utilised. Type IIIA: An extensively coated stem of adequate length is utilised to ensure that more than 4 cm of scratch fit is obtained in the diaphysis. Type IIIB: Our present preference is a modular, cementless, tapered stem with flutes for obtaining rotational stability. Type IV: Cementless fixation cannot be reliably used in our experience, as it is difficult to obtain adequate initial implant stability that is required for osseointegration. Reconstruction can be performed with impaction grafting if the cortical tube of the proximal femur is intact. However, this technique can be technically difficult to perform, time consuming and costly given the amount of bone graft that is often required. Although implant subsidence and peri-prosthetic fractures (both intra-operatively and post-operatively) have been associated with this technique, it can provide an excellent solution for the difficult revision femur where cementless fixation cannot be utilised. Alternatively, an allograft-prosthesis composite can be utilised for younger patients in an attempt to reconstitute bone stock and a proximal femoral replacing endoprosthesis used for more elderly patients.
Introduction. Biological repair of acetabular bone defects after impaction bone grafting (IBG) in total hip arthroplasty could facilitate future re-revisions in case of failure of the reconstruction again using the same technique. Few studies have analysed the outcome of these acetabular re-revisions. Patients and Methods. We analysed 34 consecutive acetabular re-revisions that repeated IBG and a cemented cup in a cohort of 330 acetabular IBG revisions. Fresh-frozen femoral head allografts were morselized manually. All data were prospectively collected. Kaplan-Meier survivorship analysis was performed. The mean follow-up after re-revision was 7.2 years (2–17). Intraoperative bone defect had lessened after the first failed revision. At the first revision there were 14 hips with
The management of femoral bone loss is challenging during revision hip arthroplasty. In patients with
As the number of patients who have undergone total hip arthroplasty rises, the number of patients who require surgery for a failed total hip arthroplasty is also increasing. Reconstruction of the failed femoral component in revision total hip arthroplasty can be challenging from both a technical perspective and in preoperative planning. With multiple reconstructive options available, it is helpful to have a classification system which guides the surgeon in selecting the appropriate method of reconstruction. We have developed a classification of femoral deficiency and an algorithmic approach to femoral reconstruction is presented. Type I: Minimal loss of metaphyseal cancellous bone with an intact diaphysis. Often seen when conversion of a cementless femoral component without biological ingrowth surface requires revision. Type II: Extensive loss of metaphyseal cancellous bone with an intact diaphysis. Often encountered after the removal of a cemented femoral component. Type IIIA: The metaphysis is severely damaged and non-supportive with more than four centimeters of intact diaphyseal bone for distal fixation. This type of defect is commonly seen after removal of grossly loose femoral components inserted with first generation cementing techniques. Type IIIB: The metaphysis is severely damaged and non-supportive with less than four centimeters of diaphyseal bone available for distal fixation. This type of defect is often seen following failure of a cemented femoral component that was inserted with a cement restrictor and cementless femoral components associated with significant distal osteolysis. Type IV: Extensive meta-diaphyseal damage in conjunction with a widened femoral canal. The isthmus is non-supportive.
Patella fracture after total knee arthroplasty has a variety of etiologies and has been reported to occur with an incidence ranging from 3% to 21%. Heavy patients with full flexion are at greatest risk for sustaining patella fracture. Overstuffing the patellofemoral joint with an oversized femoral component, an anteriorised femoral component or a femoral component placed in excessive extension can also overload the underlying patella. A similar phenomenon may be seen with underrsection of the patella or use of a thick button. Excessive patellar resection can predispose to patellar fracture as well. It has been demonstrated that a residual patella thickness of less than 15 mm can substantially increase anterior patellar strain. Asymmetric patellar resection can also critically alter the mechanical strength of the patella making it vulnerable to failure. Elevation of the tibiofemoral joint line, from excessive femoral resection and hastened by posterior cruciate ligament release, will result in a relative patella baja. This can cause early patellofemoral articulation, which may result in patellar impingement on the tibial insert in late flexion and ultimately predispose the patella to fracture. Surgical approach and soft tissue dissection should be as atraumatic to the patellar blood supply as possible to preserve the superolateral geniculate artery when performing a lateral retinacular release. The classification used by Goldberg, et al is helpful for planning appropriate intervention: Type I fractures: Avulsion type fractures generally involving the periphery of the patella without involving the implant. Type II fractures: Disrupt the cement-prosthesis interfaces of the quadriceps mechanism. Type IIIA fractures: Involve the pole of the patella with disruption of the patella ligament. Type IV fractures: Fracture dislocations of the patella. Non-operative treatment is preferred when fractures are non-displaced.
INTRODUCTION: As the number of patients who have undergone total hip arthroplasty rises, the number of patients who require surgery for a failed total hip arthroplasty is also increasing. It is estimated that 183,000 total hip replacements were performed in the United States in the year 2000 and that 31,000 of these (17%) were revision procedures. Reconstruction of the failed femoral component in revision total hip arthroplasty can be challenging from both a technical perspective and in pre-operative planning. With multiple reconstructive options available, it is helpful to have a classification system which guides the surgeon in selecting the appropriate method of reconstruction. DISCUSSION: An extensively coated, diaphyseal filling component reliably achieves successful fixation in the majority of revision femurs. The surgical technique is straightforward and we continue to use this type of device in the majority of our revision total hip arthroplasties. However, in the severely damaged femur (Type IIIB and Type IV), other reconstructive options may provide improved results. Based on our results, the following reconstructive algorithm is recommended for femoral reconstruction in revision total hip arthroplasty: TYPE I: In a Type I femur, there is minimal loss of cancellous bone with an intact diaphysis. Cemented or cementless fixation can be utilised. If cemented fixation is selected, great care must be taken in removing the neo-cortex often encountered to allow for appropriate cement intrusion into the remaining cancellous bone. TYPE II: In a Type II femur, there is extensive loss of the metaphyseal cancellous bone and thus fixation with cement is unreliable. In this cohort of patients, successful fixation was achieved using a diaphyseal fitting, extensively porous coated implant in 26 of 29 cases (90%) However, as the metaphysis is supportive, a cementless implant that achieves primary fixation in the metaphysis can be utilized. TYPE III A: In a Type IIIA femur, the metaphysis is non-supportive and an extensively coated stem of adequate length is utilised to ensure that more than 4 cm of scratch fit is obtained in the diaphysis. TYPE III B: Based on the poor results obtained with a cylindrical, extensively porous coated implant, our present preference is a modular, cementless, tapered stem with flutes for obtaining rotational stability. Excellent results have been reported with this type of implant and by virtue of its tapered design, excellent initial axial stability can be obtained even in femurs with a very short isthmus. Subsidence has been reported as a potential problem with this type of implant and they can be difficult to insert. However, with the addition of modularity to many systems that employ this concept of fixation, improved stability can be obtained by impacting the femoral component as far distally as needed while then building up the proximal segment to restore appropriate leg length. TYPE IV: In a Type IV femur, the isthmus is completely non-supportive and the femoral canal is widened. Cementless fixation cannot be reliably used in our experience, as it is difficult to obtain adequate initial implant stability that is required for osseointegration. Reconstruction can be performed with impaction grafting if the cortical tube of the proximal femur is intact. However, this technique can be technically difficult to perform, time consuming and costly given the amount of bone graft that is often required. Although implant subsidence and peri-prosthetic fractures have been associated with this technique, it can provide an excellent solution for the difficult revision femur where cementless fixation cannot be utilised. Alternatively, an allograft-prosthesis composite can be utilised for younger patients in an attempt to reconstitute bone stock and a proximal femoral replacing endoprosthesis used for more elderly patients.
The extended proximal femoral osteotomy has been used primarily in conjunction with cementless fixation, but has been described for use with cemented stems as well. The extended proximal femoral osteotomy is indicated for the removal of well-fixed cemented and cementless implants, as well as removal of cement in patients with a loose femoral component in a well-fixed cement mantle. Although the osteotomy is not required for many femoral revisions, it is an absolute indication in patients with femoral component loosening and subsequent varus remodeling of the proximal femur. The osteotomy diminishes the risk of an inadvertent fracture of the often compromised greater trochanter especially upon removal of a failed femoral component from its subsided or migrated position. The osteotomy enhances the exposure of the acetabulum which may be difficult in the revision setting due to multiple surgeries, severe migration of the acetabular component or heterotopic ossification. The extended proximal femoral osteotomy can also be used in the primary setting when a proximal femoral deformity interferes with straight reaming of the femoral canal, such as in patients with various dysplasias, previous corrective osteotomies or malunions.
Cup-cage constructs are one of several methods commonly used to treat severe acetabular bone loss during contemporary revision total hip arthroplasty. The purpose of this study was to provide a long-term results of the technique with emphasis on implant survivorship, radiographic results, and clinical outcomes for both full and half cup-cage reconstructions. We identified 57 patients treated with a cup-cage reconstruction for major acetabular bone loss between 2002–2012. All patients had
Chronic pelvic discontinuity (CPD) during revision hip arthroplasty is a challenging entity to address. The aim of this study was to evaluate the clinical and radiologic outcomes, and complications of the “acetabular distraction technique” for the management of CPD during revision hip arthroplasty. Patients with CPD, who underwent acetabular revision between 2014 and 2022 at two tertiary care centres, using an identical distraction technique, were evaluated. Demographic parameters, pre-operative acetabular bone loss, duration of follow-up, clinical and radiologic outcomes, and survivorship were evaluated. In all, 46 patients with a mean follow-up of 34.4 (SD=19.6, range: 24–120) months were available for evaluation. There were 25 (54.3%) male, and 21 (45.7%) female patients, with a mean age of 58.1 (SD=10.5, range: 40–81) years at the time of revision surgery. Based on the
Aim. Aim of this monocentric, prospective study was to evaluate the safety, efficacy, clinical and radiographical results at 24-month follow-up (N = 6 patients) undergoing hip revision surgery with severe acetabular bone defects (Paprosky 2C-3A-3B) using a combination of a novel phase-pure betatricalciumphosphate - collagen 3D matrix with allograft bone chips. Method. Prospective follow-up of 6 consecutive patients, who underwent revision surgery of the acetabular component in presence of massive bone defects between April 2018 and July 2019. Indications for revision included mechanical loosening in 4 cases and history of hip infection in 2 cases. Acetabular deficiencies were evaluated radiographically and CT and classified according to the
Stem loosening can be associated with a wide spectrum of bone loss and deformity that represent key factors for choosing the most appropriate revision implant. The aim of this study was to evaluate the clinical outcomes and the survivorship of a consecutive series of THA revisions using a taper rectangular cementless stem for primary implants (Alloclassic® Zweymuller®, Zimmer Warsaw US) at medium-term follow-up. We retrospectively evaluated 113 patients (115 revisions) who underwent femoral revision with Zweymuller stem with a preoperative
First-time revision acetabular components have a 36% re-revision rate at 10 years in Australia, with subsequent revisions known to have even worse results. Acetabular component migration >1mm at two years following revision THA is a surrogate for long term loosening. This study aimed to measure the migration of porous tantalum components used at revision surgery and investigate the effect of achieving press-fit and/or three-point fixation within acetabular bone. Between May 2011 and March 2018, 55 patients (56 hips; 30 female, 25 male) underwent acetabular revision THR with a porous tantalum component, with a post-operative CT scan to assess implant to host bone contact achieved and Radiostereometric Analysis (RSA) examinations on day 2, 3 months, 1 and 2 years. A porous tantalum component was used because the defects treated (Paprosky IIa:IIb:IIc:IIIa:IIIb; 2:6:8:22:18; 13 with pelvic discontinuity) were either deemed too large or in a position preventing screw fixation of an implant with low coefficient of friction. Press-fit and three-point fixation of the implant was assessed intra-operatively and on postoperative imaging. Three-point acetabular fixation was achieved in 51 hips (92%), 34 (62%) of which were press-fit. The mean implant to host bone contact achieved was 36% (range 9-71%). The majority (52/56, 93%) of components demonstrated acceptable early stability. Four components migrated >1mm proximally at two years (1.1, 3.2, 3.6 and 16.4mm). Three of these were in hips with
Subsidence remains a concern when utilizing modern tapered fluted titanium (TFT) femoral stems and may lead to leg length discrepancy, impingement, instability and failure to obtain stem osseointegration. This study aims to compare stem subsidence across three modern TFT stems. Our secondary aim was to investigate the influence of bicortical contact or ‘scratch fit’ on subsidence, as well as the role of intraoperative imaging in maximizing this bicortical contact and preventing stem subsidence. A retrospective review of 271 hip arthroplasties utilizing modern TFT stems in a single institution was performed. Three stem designs were included in the analysis: one monoblock TFT stem (n=91) and two modular TFT stems (Modular A [n=90]; Modular B [n=90]). Patient demographics,
The
Revision total hip arthroplasty (THA) is projected
to increase by 137% from the years 2005 to 2030. Reconstruction of
the femur with massive bone loss can be a formidable undertaking.
The goals of revision surgery are to create a stable construct,
preserve bone and soft tissues, augment deficient host bone, improve
function, provide a foundation for future surgery, and create a
biomechanically restored hip. Options for treatment of the compromised femur
include: resection arthroplasty, allograft prosthetic composite
(APC), proximal femoral replacement, cementless fixation with a
modular tapered fluted stem, and impaction grafting. The purpose
of this article is to review the treatment options along with their
associated outcomes in the more severe femoral defects (Paprosky types
IIIb and IV) in revision THA.
Custom acetabular components have become an established method of treating massive acetabular bone defects in hip arthroplasty. Complication rates, however, remain high and migration of the cup is still reported. Ischial screw fixation (IF) has been demonstrated to improve mechanical stability for non-custom, revision arthroplasty cup fixation. We hypothesise that ischial fixation through the flange of a custom acetabular component aids in anti-rotational stability and prevention of cup migration. Electronic patient records were used to identify a consecutive series of 49 custom implants in 46 patients from 2016 to 2022 in a unit specializing in complex joint reconstruction. IF was defined as a minimum of one screw inserted into the ischium passing through a hole in a flange on the custom cup. The mean follow-up time was 30 months. IF was used in 36 cups. There was no IF in 13 cups. No difference was found between groups in age (68.9 vs. 66.3, P = 0.48), BMI (32.3 vs. 28.2, P = 0.11) or number of consecutively implanted cups (3.2 vs. 3.6, P = 0.43). Aseptic loosening with massive bone loss was the primary indication for revision. There existed no difference in
Different techniques have been described to address massive bone loss of the acetabulum in revision hip surgery. aMace has gained popularity as it provides customization aiming to restore hip centre and provide good initial stability in cases of large non-contained defects. It takes into account quality of host bone. Its porous defect filling scaffold provides an excellent surface for osteointegration. Our aim was to assess the short and mid-term outcomes of patients who underwent revision surgery using aMace system. Ethical approval was obtained. A retrospective study included all patients who had aMace between June 2013 and October 2022 allowing for a minimum of 12-months follow-up. Patients’ demographics, indication, bone-loss severity, reconstruction details, re-operation, complications, mortality, pain and function were assessed. 52 cases were performed by 13 surgeons with median 51 months follow-up. Median age was 72.7 years. 86.5% were female. Average BMI was 25.3. Average ASA grade was 3. 65% were classified as
Contemporary acetabular reconstruction in major acetabular bone loss often involves the use of porous metal augments, a cup-cage construct or custom implant. The aims of this study were: To determine the reproducibility of a reconstruction algorithm in major acetabular bone loss. To determine the subsequent success of reconstruction performed in terms of re-operation, all-cause revision and Oxford Hip Score (OHS) and to further define the indications for custom implants in major acetabular bone loss. Consecutive series of
We evaluated the accuracy with which a custom-made
acetabular component could be positioned at revision arthroplasty
of the hip in patients with a
Acetabular components used to treat large defects are at greater risk of loosening. Porous tantalum acetabular components have reported the most promising early to midterm revision rates. Early stability of acetabular components used at revision THR was shown to be a good predictor of later loosening. The primary aim was to assess the migration of porous acetabular component used to reconstruct severe acetabular defects. Secondarily, we investigated the effect of acetabular defect severity and type of component fixation on migration. Radiosterometric analysis was used to measure migration at a mean follow-up of four years, (range 2–10) in 59 reconstructions of severe acetabular defects with porous tantalum components. Acetabular component fixation was classified as superior if augmented with screws through cup, augments or cage in the ilium only. Fixation was classified as combined, superior and inferior, if flanges and/or screws were also placed in the ischium and or pubis. Acceptable limits of proximal migration were defined as ≤1mm within 2 years and ≤2.5mm at any time point. Eight hips had reconstruction of
Over a four year period of time, 142 consecutive hip revisions were performed with the use of an extended proximal femoral osteotomy. Twenty patients had insufficient follow-up or were followed elsewhere and were excluded from the review. The remaining 122 revisions included 83 women and 39 men. Average age at time of revision was 63.8 (26–84) years. Indications for revision were aseptic loosening (114), component failure (4), recurrent dislocation (2), femoral fracture (1) and second stage re-implantation for infection (1). The extended proximal femoral osteotomy gave easy access to the distal bone-cement or bone prosthesis interface in all cases. It allowed neutral reaming of the femoral canal and implantation of the revision component in proper alignment. Varus remodeling of the proximal femur secondary to loosening was handled with relative ease implementing the osteotomy. Average time from the beginning of the osteotomy procedure to the complete removal of prosthesis and cement was 35 minutes. There were no non-unions of the osteotomised fragments at an average post-operative follow-up of 2.6 years with no cases of proximal migration of the greater trochanteric fragment greater than 2 mm, there was evidence of radiographic union of the osteotomy site in all cases by 3 months. Stem fixation with bone ingrowth was noted in 112 (92%) of 122 hips, stable fibrous fixation was seen in 9 (7%) and 1 stem was unstable and was subsequently revised. However, there was an incidence of 7% perforation rate of the femoral canal distal to the osteotomy site during cement removal. This was most prevalent where there was greater than 2 cm of cement plug present which was well bonded. When OSCAR was used instead of hand tools or power reamers, there were no perforations in 51 cases. There has been no failure of fixation with fully porous coated stems inserted in the canals where OSCAR had removed cement. Also, the use of OSCAR has allowed us to shorten the osteotomy, thus allowing a longer, intact isthmus to remain so that shorter stems can be used. We highly recommend the use of OSCAR in conjunction with the extended osteotomy for removal of well-fixed distal cement beyond the extended osteotomy site.
Recurrent dislocation following total hip arthroplasty (THA) is a complex, multifactorial problem that has been shown to be the most common indication for revision THA. The purpose of this study was to classify causes of instability and evaluate outcomes based on an algorithmic approach to treatment. Two surgeons performed 77 consecutive revisions for instability. Patients had a mean of 2 (range, 0 to 6) prior operative attempts to resolve their instability. Subjects were divided into 6 types based on the etiology of instability: I) malposition of the acetabular component, II) malposition of the femoral component, III) abductor deficiency, IV) impingement, V) late wear, or VI) unclear etiology. Types I /II were treated with revision of the malpositioned component, Type III/VI with a constrained liner, Type IV by removing sources of impingement and Type V with a liner change. Large (>36 mm) femoral heads were used routinely.Introduction
Methods
To resurface or not to resurface the patella… that is the question. It all comes down to where you practice. It is controversial in that there is a risk of possible complications from resurfacing versus the potential for simply having complaints of pain which may supposedly arise from the anterior knee stemming from the unresurfaced patella. The evolution of more favorable anatomic femoral component designs which are very friendly to the patellofemoral articulation have resulted in lower patella resurfacing complications. The insertion of appropriately externally rotated tibial and femoral components, if not reducing anterior knee pain, have certainly minimised the risk of resurfaced patella complications. Also, with current surgical techniques of component insertion, the lateral release rate is extremely low, thus avoiding the possibility of avascularity developing in the resurfaced patella. This complication will almost completely be eliminated if the patella thickness is kept greater than 13 mm after patella resection. In my experience, patella complications from the resurfaced patella are extremely rare. Many unicompartmental knees require re-operation because of the development of progressive patellofemoral arthritis. Re-operation from anterior knee pain from progressive arthritis from the unresurfaced patella has given inferior results. Overall, meta-analysis data demonstrates decreased satisfaction, increased anterior knee pain and higher early revision rates in the unresurfaced group. National joint registries, especially the Australian registry support routine resurfacing; complications are low and outcomes are improved. Even though there exists controversy as to whether the patella should be resurfaced or not, there is an overwhelming consensus in the U.S. that there is little downfall nowadays with respect to resurfacing the patella.
Aims. Although good clinical outcomes have been reported for monolithic tapered, fluted, titanium stems (TFTS), early results showed high rates of subsidence. Advances in stem design may mitigate these concerns. This study reports on the use of a current monolithic TFTS for a variety of indications. Methods. A multi-institutional retrospective study of all consecutive total hip arthroplasty (THA) and revision total hip arthroplasty (rTHA) patients who received the monolithic TFTS was conducted. Surgery was performed by eight fellowship-trained arthroplasty surgeons at four institutions. A total of 157 hips in 153 patients at a mean follow-up of 11.6 months (SD7.8) were included. Mean patient age at the time of surgery was 67.4 years (SD 13.3) and mean body mass index (BMI) was 28.9 kg/m. 2. (SD 6.5). Outcomes included intraoperative complications, one-year all-cause re-revisions, and subsidence at postoperative time intervals (two weeks, six weeks, six months, nine months, and one year). Results. There were eight intraoperative complications (4.9%), six of which were intraoperative fractures; none occurred during stem insertion. Six hips (3.7%) underwent re-revision within one year; only one procedure involved removal of the prosthesis due to infection. Mean total subsidence at latest follow-up was 1.64 mm (SD 2.47). Overall, 17 of 144 stems (11.8%) on which measurements could be performed had >5 mm of subsidence, and 3/144 (2.1%) had >10 mm of subsidence within one year. A univariate regression analysis found that additional subsidence after three months was minimal. A multivariate regression analysis found that subsidence was not significantly associated with periprosthetic fracture as an indication for surgery, the presence of an extended trochanteric osteotomy (ETO),
Total knee arthroplasty in the setting of osseous defects has multiple management options. However, the optimal treatment strategy remains controversial. The purpose of this study is to report the clinical and radiographic results of trabecular metal cones in managing osseous defects in the setting of complex primary and revision total knee arthroplasty. There were 129 consecutive total knee arthroplasty procedures performed utilising trabecular metal cones reviewed for clinical and radiographic outcomes. Twenty-five had less than 2 years of follow-up and seven died, leaving 96 patients for evaluation. This cohort included a total of eighty-six (86) tibias with eleven (11) having Type 1 defects, twenty-five (25) having Type 2A defects, forty-three (43) with Type 2B defects and seven (7) with Type 3 defects. There were twenty-seven (27) femurs with one (1) Type 1 defect, nine (9) Type 2A defects, sixteen (16) with Type 2B defects and one (1) Type 3 defect based on the AORI classification. There were 28 male patients and 68 female patients, with an average age of 68 years and an average BMI of 35.0. There were six primary procedures and ninety revision procedures. Continuous variables were evaluated using a t-test. Twelve patients required revision leaving 84 knees (87.5%) with the cones in place at an average of 31 months of follow-up (range, 24–77.3 months). The mean KSS score increased from 51.0 preoperatively to 80.2 postoperatively (p<0.0001). The mean KSS functional score increased from 32.9 preoperatively to 47.8 postoperatively (p=0.0002). Including the twelve revisions, there were twenty-two knees requiring re-operation (22.9%) with another seventeen requiring manipulation under anesthesia and there were four additional non-operative complications (1 foot drop, 1 stress fracture, 2 superficial infections).
Recurrent dislocation following total hip arthroplasty (THA) is a complex, multifactorial problem that has been shown to be the most common indication for revision THA. The purpose of this study was to classify causes of instability and evaluate outcomes based on an algorithmic approach to treatment. Two surgeons performed 77 consecutive revisions for instability. Patients had a mean of 2 years (range, 0 to 6) prior operative attempts to resolve their instability. Subjects were divided into 6 types based on the etiology of instability: I) malposition of the acetabular component, II) malposition of the femoral component, III) abductor deficiency, IV) impingement, V) late wear, or VI) unclear etiology. Types I /II were treated with revision of the malpositioned component, Type III/VI with a constrained liner, Type IV by removing sources of impingement and Type V with a liner change. Large (>36mm) femoral heads were used routinely.Introduction:
Methods:
The aim of this study was to examine the results of the acetabular
distraction technique in achieving implantation of a stable construct,
obtaining biological fixation, and producing healing of chronic
pelvic discontinuity at revision total hip arthroplasty. We identified 32 patients treated between 2006 and 2013 who underwent
acetabular revision for a chronic pelvic discontinuity using acetabular
distraction, and who were radiographically evaluated at a mean of
62 months (25 to 160). Of these patients, 28 (87.5%) were female.
The mean age at the time of revision was 67 years (44 to 86). The patients
represented a continuous series drawn from two institutions that
adhered to an identical operative technique.Aims
Patients and Methods
Total joint arthroplasty rates have increased dramatically in recent decades. However, a comprehensive analysis of trends in revision total hip arthroplasty has not been performed recently to address the changing volume, costs, and location of these complex cases. We sought to identify trends in volume of these procedures, geographic distribution changes, and cost trends using a national sample. The National Inpatient Sample, a representative sample of all hospital discharges within the United States, was used to determine the volume of revision total hip arthroplasty (THA) from 1993 to 2014. Procedures were identified by ICD-9 codes corresponding to revision THA. Annual incidence of revision THA was compared to annual incidence of primary THA to determine whether relative growth of revisions differed proportionally from the primary procedure. State-specific data was analyzed where available to develop geographic trend maps in the incidence of revision THA procedures using the estimated state population for years under review. Trends were also reviewed for hospital location (urban versus rural; teaching versus non-teaching) and total hospital charges. Analysis of trends was performed using linear regression models.Introduction
Materials and methods
Over a four year period of time, 142 consecutive hip revisions were performed with the use of an extended proximal femoral osteotomy. Twenty patients had insufficient follow up or were followed elsewhere and were excluded from the review. The remaining 122 revisions included 83 women and 39 men. Average age at time of revision was 63.8 (26–84) years. Indications for revision were aseptic loosening (114), component failure (4), recurrent dislocation (2), femoral fracture (1) and second stage re-implantation for infection (1). The extended proximal femoral osteotomy gave easy access to the distal bone-cement or bone prosthesis interface in all cases. It allowed neutral reaming of the femoral canal and implantation of the revision component in proper alignment. Varus remodeling of the proximal femur secondary to loosening was handled with relative ease implementing the osteotomy. Average time from the beginning of the osteotomy procedure to the complete removal of prosthesis and cement was thirty-five minutes. There were no non-unions of the osteotomised fragments at an average post-op follow up of 2.6 years with no cases of proximal migration of the greater trochanteric fragment greater than 2mm, there was evidence of radiographic union of the osteotomy site in all cases by 3 months. Stem fixation with bone ingrowth was noted in 112 (92%) of 122 hips, stable fibrous fixation was seen in 9 (7%) and 1 stem was unstable and was subsequently revised. However, there was an incidence of 7% perforation rate of the femoral canal distal to the osteotomy site during cement removal. This was most prevalent where there was greater than 2cm of cement plug present which was well bonded. When OSCAR was used instead of hand tools or power reamers, there were no perforations in 51 cases. There has been no failure of fixation with fully porous coated stems inserted in the canals where OSCAR had removed cement. Also, the use of OSCAR has allowed us to shorten the osteotomy, thus allowing a longer, intact isthmus to remain so that shorter stems can be used. We highly recommend the use of OSCAR in conjunction with the extended osteotomy for removal of well-fixed distal cement beyond the extended osteotomy site.
Stabilisation of a chronic pelvic discontinuity with a posterior column plate with or without an associated acetabular cage sometimes results in persistent micromotion across the discontinuity with late fatigue failure and component loosening. We believe that these chronic discontinuities are really chronic fracture non-unions incapable of healing. Acetabular distraction offers an alternative technique for reconstruction in cases of severe bone loss with an associated pelvic discontinuity. We describe the technique of acetabular distraction with porous tantalum components and evaluate its survival, function and complication rate in patients undergoing revision surgery for chronic pelvic discontinuity. Between 2002 and 2006, we treated 28 patients with a chronic pelvic discontinuity acetabular reconstruction using acetabular distraction. A porous tantalum elliptical acetabular component was used alone or with an associated modular porous tantalum augment in all patients. Three patients died and five patients were lost to follow up before two years. The remaining twenty patients were followed semiannually for a minimum of two years (average, 5.5 years; range, 2–9 years) with clinical pain and walking scores as well as radiographic evaluation for loosening, migration or failure. In the remaining twenty patients available for follow up, one patient did require re-revision for aseptic loosening. Fifteen patients remained radiographically stable at last follow up. Four patients had early migration of their acetabular component but thereafter remained radiographically stable and clinically asymptomatic. The average improvement using the modified Merle d'Aubigne – Postel pain and ambulation score was 6.6 (range, 3.3–9.6). There were no post-operative dislocations; however, we did encounter one infection, one vascular injury and one bowel injury. In this series, the use of acetabular distraction with porous tantalum components provides a biologic alternative to cage constructs with more predictable clinical results (average follow up 5.5 years) for reconstruction of severe acetabular defects with associated pelvic discontinuity.
The goals of revision arthroplasty of the hip are to restore the anatomy and achieve stable fixation for new acetabular and femoral components. It is important to restore bone stock, thereby creating an environment for stable fixation for the new components. The bone defects encountered in revision arthroplasty of the hip can be classified either as contained (cavitary) or uncontained (segmental). Contained defects on both the acetabular and femoral sides can be addressed by morselised bone graft that is compacted into the defect. Severe uncontained defects are more of a problem particularly on the acetabular side where bypass fixation such as distal fixation on the femoral side is not really an alternative. Most authors agree that the use of morselised allograft bone for contained defects is the treatment of choice as long as stable fixation of the acetabular component can be achieved and there is a reasonable amount of contact with bleeding host bone for eventual ingrowth and stabilisation of the cup. On the femoral side, contained defects can be addressed with impaction grafting for very young patients or bypass fixation in the diaphysis of the femur using more extensively coated femoral components or taper devices. Segmental defects on the acetabular side have been addressed with structural allografts for the past 15 to 20 years. These are indicated in younger individuals with Type 3A defects. Structural grafts are unsuccessful in Type 3B defects. Alternatives to the structural allografts are now being utilised with shorter but encouraging results in most multiply operated hips with bone loss. New porous metals such as trabecular metal (tantalum), which has a high porosity similar to trabecular bone and also has a high coefficient of friction, provide excellent initial stability. The porosity provides a very favorable environment for bone ingrowth and bone graft remodeling. Porous metal acetabular components are now more commonly used when there is limited contact with bleeding host bone. Porous metal augments of all sizes are being used instead of structural allografts in most situations. On the femoral side, metaphyseal bone loss, whether contained or uncontained, is most often addressed by diaphyseal fixation with long porous or tapered implants, modular if necessary. Distal fixation requires at least 4 centimeters of diaphyseal bone and in Type IV femurs, a choice must be made between a mega prosthesis or a proximal femoral allograft. The proximal femoral allograft can restore bone stock for future surgery in younger patients. The mega prosthesis which is more appropriate in the older population may require total femoral replacement if there is not enough diaphyseal bone for distal fixation with cement. Cortical struts are used for circumferential diaphyseal bone defects to stabilise proximal femoral allografts, to bypass stress risers and to serve as a biological plate for stabilising peri-prosthetic fractures.
Aims. The use of trabecular metal (TM) shells supported by augments has provided good mid-term results after revision total hip arthroplasty (THA) in patients with a bony defect of the acetabulum. The aim of this study was to assess the long-term implant survivorship and radiological and clinical outcomes after acetabular revision using this technique. Patients and Methods. Between 2006 and 2010, 60 patients (62 hips) underwent acetabular revision using a combination of a TM shell and augment. A total of 51 patients (53 hips) had complete follow-up at a minimum of seven years and were included in the study. Of these patients, 15 were men (29.4%) and 36 were women (70.6%). Their mean age at the time of revision THA was 64.6 years (28 to 85). Three patients (5.2%) had a
Recurrent dislocation following total hip arthroplasty (THA) is a complex, multifactorial problem that has been shown to be the most common indication for revision THA. The purpose of this study was to classify causes of instability and evaluate outcomes based on an algorithmic approach to treatment. Two surgeons performed 77 consecutive revisions for instability. Patients had a mean of 2 (range, 0 to 6) prior operative attempts to resolve their instability. Subjects were divided into 6 types based on the etiology of instability: I) malposition of the acetabular component, II) malposition of the femoral component, III) abductor deficiency, IV) impingement, V) late wear, or VI) unclear etiology. Types I/II were treated with revision of the malpositioned component, Type III/VI with a constrained liner, Type IV by removing sources of impingement and Type V with a liner change. Large (>36mm) femoral heads were used routinely.Introduction
Methods
Stabilisation of a pelvic discontinuity with a posterior column plate with or without an associated acetabular cage sometimes results in persistent micromotion across the discontinuity with late fatigue failure and component loosening. Acetabular distraction offers an alternative technique for reconstruction in cases of severe bone loss with an associated pelvic discontinuity. We describe the technique of acetabular distraction with porous tantalum components and evaluate its survival, function and complication rate in patients undergoing revision surgery for chronic pelvic discontinuity. Between 2002 and 2006, we treated 28 patients with a chronic pelvic discontinuity acetabular reconstruction using acetabular distraction. A porous tantalum elliptical acetabular component was used alone or with an associated modular porous tantalum augment in all patients. Three patients died and five patients were lost to follow-up before two years. The remaining twenty patients were followed semiannually for a minimum of two years (average, 4.5 years; range, 2–7 years) with clinical pain and walking scores as well as radiographic evaluation for loosening, migration or failure. In the remaining twenty patients available for follow-up, one patient did require re-revision for aseptic loosening. Fifteen patients remained radiographically stable at last follow-up. Four patients had early migration of their acetabular component but thereafter remained radiographically stable and clinically asymptomatic. The average improvement using the modified Merle d'Aubigne – Postel pain and ambulation score was 6.6 (range, 3.3–9.6). There were no postoperative dislocations; however, we did encounter one infection, one vascular injury and one bowel injury. In this series, the use of acetabular distraction with porous tantalum components provides a biologic alternative to cage constructs with more predictable clinical results (average follow-up 4.5 years) for reconstruction of severe acetabular defects with associated pelvic discontinuity.
Over a four year period of time, 142 consecutive hip revisions were performed with the use of an extended proximal femoral osteotomy. Twenty patients had insufficient follow-up or were followed elsewhere and were excluded from the review. The remaining 122 revisions included 83 women and 39 men. Average age at time of revision was 63.8 (26–84) years. Indications for revision were aseptic loosening (114), component failure (4), recurrent dislocation (2), femoral fracture (1) and second stage re-implantation for infection (1). The extended proximal femoral osteotomy gave easy access to the distal bone-cement or bone prosthesis interface in all cases. It allowed neutral reaming of the femoral canal and implantation of the revision component in proper alignment. Varus remodeling of the proximal femur secondary to loosening was handled with relative ease implementing the osteotomy. Average time from the beginning of the osteotomy procedure to the complete removal of prosthesis and cement was thirty-five minutes. There were no non-unions of the osteotomised fragments at an average post-op follow-up of 2.6 years with no cases of proximal migration of the greater trochanteric fragment greater than 2mm, there was evidence of radiographic union of the osteotomy site in all cases by 3 months. Stem fixation with bone ingrowth was noted in 112 (92%) of 122 hips, stable fibrous fixation was seen in 9 (7%) and 1 stem was unstable and was subsequently revised. However, there was an incidence of 7% perforation rate of the femoral canal distal to the osteotomy site during cement removal. This was most prevalent where there was greater than 2cm of cement plug present which was well bonded. When OSCAR was used instead of hand tools or power reamers, there were no perforations in 51 cases. There has been no failure of fixation with fully porous coated stems inserted in the canals where OSCAR had removed cement. Also, the use of OSCAR has allowed us to shorten the osteotomy, thus allowing a longer, intact isthmus to remain so that shorter stems can be used. We highly recommend the use of OSCAR in conjunction with the extended osteotomy for removal of well-fixed distal cement beyond the extended osteotomy site.
The unacceptable failure rate of cemented femoral revisions led to many different cementless femoral designs employing fixation in the damaged proximal femur with biological coatings limited to this area. The results of these devices were uniformly poor and were abandoned for the most part by the mid 1990's. Fully porous coated devices employing distal fixation in the diaphysis emerged as the gold standard for revisions with several authors reporting greater than 90% success rate at 8–10 years of follow-up. Surgical techniques and ease of insertion improved with the introduction of the extended trochanteric osteotomy as well as curved, long, fully porous coated stems with diameters up to 23 mm. The limits of these stems were stretched to include any stem diameter in which even 1–2 cm of diaphyseal contact could be achieved. When diaphyseal fixation was not possible (Type IV), the alternatives were either impaction grafting or allograft prosthetic composite (APC). As the results of fully porous coated stems were very carefully scrutinised, it became apparent that certain types of bone loss did not yield the most satisfactory results both clinically and radiographically. When less than 4 cm of diaphyseal press fit (Type IIIB) was achieved, mechanical failure rate (MFR) was over 25%. It also became apparent that even when there was 4–6 cm. diaphyseal contact (Type IIIA), and the stem diameter was 18 mm or greater, post-op pain and function scores were significantly less than those with smaller diameter stems. This was probably due to poorer quality bone. Many of these Type IIIA and Type IIIB femurs had severe proximal torsional remodeling leading to marked distortion of anteversion. This made judging the amount of anteversion to apply to the stem at the time of insertion very difficult, leading to higher rates of dislocation. These distortions were not present in Type I and Type II femurs. This chain of events which was a combination of minimal diaphyseal fixation, excessively stiff stems and higher dislocation rates led to the conversion to modular type stems when these conditions existed. For the past 8 years, low modulus taper stems of the Wagner design have been used for almost all Type IIIA and Type IIIB bone defects. The taper design with fluted splines allows for fixation when there is less than 2 cm of diaphysis. The results in these femurs even with diameters of up to 26 mm have led to very low M.F.R.'s and significantly less thigh pain. Independent anteversion adjustment is also a hug advantage in these modular stems. Similar success rates, albeit with less follow-up, have been noted in Type IV femurs.
We investigated the early results of modular porous metal components used in 23 acetabular reconstructions associated with major bone loss. The series included seven men and 15 women with a mean age of 67 years (38 to 81), who had undergone a mean of two previous revisions (1 to 7). Based on
Given the increasing number of total hip arthroplasty
procedures being performed annually, it is imperative that orthopaedic
surgeons understand factors responsible for instability. In order
to treat this potentially complex problem, we recommend correctly
classifying the type of instability present based on component position, abductor
function, impingement, and polyethylene wear. Correct classification
allows the treating surgeon to choose the appropriate revision option
that ultimately will allow for the best potential outcome. Cite this article:
Re-revision due to instability and dislocation can occur in up to 1 in 4 cases following revision total hip arthroplasty (THA). Optimal placement of components during revision surgery is thus critical in avoiding re-revision. Computer-assisted navigation has been shown to improve the accuracy and precision of component placement in primary THA; however, its role in revision surgery is less well documented. The purpose of our study was to evaluate the effect of computer-assisted navigation on component placement in revision total hip arthroplasty, as compared with conventional surgery. To examine the effect of navigation on acetabular component placement in revision THA, we retrospectively reviewed data from a multi-centre cohort of 128 patients having undergone revision THA between March 2017 and January 2019. An imageless computer navigation device (Intellijoint HIP®, Intellijoint Surgical, Kitchener, ON, Canada) was utilized in 69 surgeries and conventional methods were used in 59 surgeries. Acetabular component placement (anteversion, inclination) and the proportion of acetabular components placed in a functional safe zone (40° inclination/20° anteversion) were compared between navigation assisted and conventional THA groups.Introduction
Methods
Abstract. Objectives. Stem malalignment in total hip arthroplasty (THA) has been associated with poor long-term outcomes and increased complications (e.g. periprosthetic femoral fractures). Our understanding of the biomechanical impact of stem alignment in cemented and uncemented THA is still limited. This study aimed to investigate the effect of stem fixation method, stem positioning, and compromised bone stock in THA. Methods. Validated FE models of cemented (C-stem – stainless steel) and uncemented (Corail – titanium) THA were developed to match corresponding experimental model datasets; concordance correlation agreement of 0.78 & 0.88 for cemented & uncemented respectively. Comparison of the aforementioned stems was carried out reflecting decisions made in the current clinical practice. FE models of the implant positioned in varus, valgus, and neutral alignment were then developed and altered to represent five different bone defects according to the
First-time revision acetabular components have a 36% re-revision rate at 10 years in Australia, with subsequent revisions known to have even worse results. Acetabular component migration >1mm at two years following revision THA is a surrogate for long term loosening. This study aimed to measure the migration of porous tantalum components used at revision surgery and investigate the effect of achieving press-fit and/or three-point fixation within acetabular bone. Between May 2011 and March 2018, 55 patients (56 hips; 30 female, 25 male) underwent acetabular revision THR with a porous tantalum component, with a post-operative CT scan to assess implant to host bone contact achieved and Radiostereometric Analysis (RSA) examinations on day 2, 3 months, 1 and 2 years. A porous tantalum component was used because the defects treated (Paprosky IIa:IIb:IIc:IIIa:IIIb; 2:6:8:22:18; 13 with pelvic discontinuity) were either deemed too large or in a position preventing screw fixation of an implant with low coefficient of friction. Press-fit and three-point fixation of the implant was assessed intra-operatively and on postoperative imaging. Three-point acetabular fixation was achieved in 51 hips (92%), 34 (62%) of which were press-fit. The mean implant to host bone contact achieved was 36% (range 9–71%). The majority (52/56, 93%) of components demonstrated acceptable early stability. Four components migrated >1mm proximally at two years (1.1, 3.2, 3.6 and 16.4mm). Three of these were in hips with
Introduction. Acetabular revision surgery is becoming more prevalent with an estimated increase of 137% by 2030. It is challenging surgery especially in the presence of deficient bone loss. Several techniques of acetabular reconstruction are used world-wide. The greater the bone loss (Paprosky Type IIIA and IIIB, and AAOS Classification of Acetabular Bone Loss Type 3 and 4) the more complex are the reconstruction methods. There is however, insufficient literature comparing the contemporary techniques of revision acetabular reconstruction and their outcomes. Objectives. The purpose of this study was to systematically review the literature and to report clinical outcomes and survival of contemporary acetabular revision arthroplasty techniques (tantalum metal (TM) systems, uncemented revision jumbo cups, reinforced devices such as cages and rings, oblong cups and custom-made triflange cups). We specifically looked at outcomes when reconstruction was undertaken in the presence of bone loss. Methods. Full-text papers and those with an abstract in English published from January 2001 to October 2015, identified through international databases, Medline (PubMED), EMBASE, CINHAL, Web of Science, Cochrane and Google scholar databases, were reviewed. Studies reporting failure and complications following the use of tantalum metal systems, uncemented revision jumbo cups, reinforced devices as cages and rings, oblong cups and custom-made triflange cups, were included. Functional and radiological outcomes were also evaluated. Results. A total of 50 papers of level IV scientific evidence, comprising 2811 hips in total, fulfilled the inclusion criteria and were included. 1021 hips (291 of them classified
Introduction. The number of complex revision total hip arthroplasties (THA) is predicted to rise. The identification of acetabular bone defects prior to revision THA has important implications on technique and complexity of acetabular reconstruction.
Introduction. Acetabular revision surgery is challenging due to severe bone defects. Burch-Schneider anti-protrusion cages (BS cage: Zimmer-Biomet) is one of the options for acetabular revision, however higher dislocation rate was reported. A computed tomography (CT)-based navigation system indicates us the planned direction for implantation of a cemented acetabular cup during surgery. A large diameter femoral head is also expected to reduce the dislocation rate. The purpose of this study is to investigate short-term results of BS cage in acetabular revision surgery combined with the CT-based navigation system and the use of large diameter femoral head. Methods. Sixteen hips of fifteen patients who underwent revision THA using allografts and BS cage between September 2013 and December 2017 were included in this study with the follow-up of 2.7 (0.1–5.0) years. There were 12 women and three men with a mean age of 78.6 years (range, 59–61 years). The cause of acetabular revision was aseptic loosening in all hips. The failed acetabular cup was carefully removed, and acetabular bone defect was graded using the
Principles of bone preservation and restoration of biomechanical alignment should be followed during revision total hip arthroplasty (THA). Where possible, conservative femoral revision techniques and even reconstructive de-escalation involving using primary stems should be considered. This study aims to investigate the outcome of patients who have undergone conservative femoral revision THA in our Institution. We retrospectively identified patients from our Institution's revision arthroplasty database who had cemented, or un-cemented primary stems implanted during revision THA of a previous stemmed femoral implant. Our primary outcome measure was all-cause re-revision THA with a secondary outcome measure of improvement in Oxford hip score (OHS). Radiographic evidence of stem loosening and post-op complications were recorded. Between 02/12/2014 to 12/12/2019, there were 226 patients identified with a mean follow up of 2 years (1–5 years). The majority of cases were represented by
Trabecular metal (TM) augments are designed to support an uncemented socket in revision surgery when adequate rim fit is not possible. We have used TM augments in an alternative arrangement, to contain segmental defects to facilitate impaction bone grafting (IBG) and cementation of a cemented socket. However, there is a paucity of literature supporting the use of this technique. We present one of the largest studies to date, reporting early outcomes of patients from a tertiary centre. A single-centre retrospective analytical study of prospectively collected data was performed on patients who had undergone complex acetabular reconstruction using TM augments, IBG and a cemented cup. All patients operated between 2015 and 2019 were included. We identified 105 patients with a mean age of 74yrs. The mean follow-up was 2.3 years(1–5.5yrs). Our primary outcome measure was all-cause revision of the construct. The secondary outcome measures were, Oxford hip score (OHS), radiographic evidence of cup migration/loosening and post-op complications. Eighty-four out of 105 patients belonged to
Long-term success of cementless femoral revision is dependent on achieving initial axial and torsional stability by maximising canal fill at the time of implantation. We report on a minimum 10 years clinical and radiographic follow-up of 170 patients with extensively coated cementless revision femoral components. With a range of follow-up of 10 to 16 years and a mean of 13.2 years, a survivorship of greater than 95% was reported. Clinically, the average Postel-D’Aubigne pain and walking score improved from a preoperative score of 5.4 points to 10.8 points postoperatively. Eightytwo percent of the hips had radiographic evidence of a bone-ingrown prosthesis and 13.9% had evidence of stable fibrous fixation. Four percent of stems were unstable as seen on radiographs. Six stems were revised to larger extensively coated stems and one stem is causing pain and is unstable but has yet to be revised. The overall mechanical failure rate was 4.1%. Stress shielding was greatest in patients with stems larger than 16.5 mm and in osteoporotic bone (Dorr Type C). Nine percent of patients had significant thigh pain including all of the patients with unstable stems. In the presence of bone loss in the proximal metaphyseal region of the femur, fixation of the femoral component is predictable when optimising prosthetic-bone fit in the diaphyseal region of the femur using an extensively porous coated femoral component.
From 1992 to 1996, 142 consecutive hip revisions were performed with the use of an extended proximal femoral osteotomy. Twenty patients had insufficient follow-up or were followed elsewhere and were excluded from the review. The remaining 122 revisions included 83 women and 39 men. Average age at time of revision was 63.8 (26–84) years. Indications for revision were aseptic loosening (114), component failure (4), recurrent dislocation (2), femoral fracture (1), and second stage re-implantation for infection (1). The extended proximal femoral osteotomy gave easy access to the distal bone-cement or bone-prosthesis interface in all cases. It allowed neutral reaming of the femoral canal and implantation of the revision component in proper alignment. Varus remodelling of the proximal femur secondary to loosening was handled with relative ease implementing the osteotomy. Average time from the beginning of the osteotomy procedure to the complete removal of prosthesis and cement was thirty-five minutes. There were no non-unions of the osteotomised fragments at an average post-op follow- up of 2.6 years with no cases of proximal migration of the greater trochanteric fragment greater than 2 mm. There was evidence of radiographic union of the osteotomy site in all cases by 3 months. Stem fixation with bone ingrowth was noted in 112 (92%) of 122 hips, stable fibrous fixation was seen in nine (7%) and one stem (1%) was unstable and was subsequently revised. We have found that use of the osteotomy is an efficient, safe, and reliable technique in revision hip arthroplasty. The advantages include easier access to the fixation surface of the failed prosthesis without compromising the remaining bone stock, alteration of proximal bone deformities to allow neutral reaming of the femoral canal, predictable healing of the osteotomised fragment, proper tensioning of the abductors with distal advancement, decreased operative time, and enhanced exposure of the acetabulum.
Revision of total hip arthroplasty (THA) is being performed with increasing frequency. However, outcomes of repeated revisions have been rarely reported in the literature, especially for severe defects. Cup revision can be a highly complex operation depending on the bone defect. In acetabular defects like
Revision total hip arthroplasty (THA) presents with increasing challenges, potentially compromising the integrity of a revision. The objective of this study was to assess radiologic outcomes of patients who underwent revision THA with a modular tapered stem (Reclaim, DePuy Synthes). This study retrospectively examined all revision Reclaim THAs between 2012 and 2016. Radiologic assessment compared x-rays at two time points: immediately after surgery and the most recent x-ray available. Leg length discrepancy, subsidence and line-to-line fit was assessed. Significant subsidence was considered ≥10mm. Adequate line-to-line fit was considered ≥30mm of bicortical contact. Descriptive statistics included clinical factors (i.e. age,
Aims. Severe acetabular bone loss and pelvic discontinuity (PD) present particular challenges in revision total hip arthroplasty. To deal with such complex situations, cup-cage reconstruction has emerged as an option for treating this situation. We aimed to examine our success in using this technique for these anatomical problems. Patients and Methods. We undertook a retrospective, single-centre series of 35 hips in 34 patients (seven male, 27 female) treated with a cup-cage construct using a trabecular metal shell in conjunction with a titanium cage, for severe acetabular bone loss between 2011 and 2015. The mean age at the time of surgery was 70 years (42 to 85) and all patients had an acetabular defect graded as
Objectives. In order to address acetabular defects, porous metal revision acetabular components and augments have been developed, which require fixation to each other. The fixation technique that results in the smallest relative movement between the components, as well as its influence on the primary stability with the host bone, have not previously been determined. Methods. A total of 18 composite hemipelvises with a
Although the introduction of ultraporous metals in the forms of acetabular components and augments has substantially improved the orthopaedic surgeon's ability to reconstruct severely compromised acetabuli, there remain some revision THAs that are beyond the scope of cups, augments, and cages. In situations involving catastrophic bone loss, allograft-prosthetic composites or custom acetabular components may be considered. Custom components offer the potential advantages of immediate, rigid fixation with a superior fit individualised to each patient. These custom triflange components require a preoperative CT scan with three-dimensional (3-D) reconstruction using rapid prototyping technology, which has evolved substantially during the past decade. The surgeon can fine-tune exact component positioning, determine location and length of screws, modify the fixation surface with, for example, the addition of hydroxyapatite, and dictate which screws will be locked to enhance fixation. The general indications for using custom triflange components include: (1) failed prior salvage reconstruction with cage or porous metal construct augments, (2) large contained defects with possible discontinuity, (3) known pelvic discontinuity, and (4) complex multiply surgically treated hips with insufficient bone stock to reconstruct using other means. We previously reported on our center's experience with 23 patients (24 hips) treated with custom triflange components with minimum 2-year follow-up. This method of reconstruction was used in a cohort of patients with
Aims. Reconstruction of the acetabulum after failed total hip arthroplasty
(THA) can be a surgical challenge in the presence of severe bone
loss. We report the long-term survival of a porous tantalum revision
acetabular component, its radiological appearance and quality of
life outcomes. Patients and Methods. We reviewed the results of 46 patients who had undergone revision
of a failed acetabular component with a
Aims. Few reconstructive techniques are available for patients requiring
complex acetabular revisions such as those involving
Recent total knee arthroplasty (TKA) designs have featured more anatomical morphologies and shorter tibial keels. However, several reports have raised concerns about the impact of these modifications on implant longevity. The aim of this study was to report the early performance of a modern, cemented TKA design. All patients who received a primary, cemented TKA between 2012 and 2017 with a minimum two-year follow-up were included. The implant investigated features an asymmetrical tibial baseplate and shortened keel. Patient demographic details, Knee Society Scores (KSS), component alignment, and the presence of radiolucent lines at final follow-up were recorded. Kaplan-Meier analyses were performed to estimate survivorship.Aims
Methods
Purpose:. Acetabular bone loss during revision total hip arthroplasty (THA) poses a challenge for reconstruction as segmental and extensive cavitary defects require structural support to achieve prosthesis stability. Trabecular metal (TM) acetabular augments structurally support hemispherical cups. Positive short-term results have been encouraging, but mid- to long-term results are largely unknown. The purpose of this study was to determine the continued efficacy of TM augments in THA revisions with significant pelvic bone loss. Methods:. Radiographs and medical records of 51 patients who had undergone THA revision with the use of a TM augment were retrospectively reviewed. Acetabular defects were graded according to the
Using an institutional database we have identified over 1000 femoral revisions using extensively porous-coated stems. Using femoral re-revision for any reason as an endpoint, the survivorship is 99 ± 0.8% (95% confidence interval) at 2 years, 97 ± 1.3% at 5 years, 95.6 ± 1.8% at 10 years, and 94.5 ± 2.2% at 15 years. Similar to Moreland and
A pelvic discontinuity occurs when the superior
and inferior parts of the hemi-pelvis are no longer connected, which
is difficult to manage when associated with a failed total hip replacement.
Chronic pelvic discontinuity is found in 0.9% to 2.1% of hip revision
cases with risk factors including severe pelvic bone loss, female
gender, prior pelvic radiation and rheumatoid arthritis. Common
treatment options include: pelvic plating with allograft, cage reconstruction,
custom triflange implants, and porous tantalum implants with modular augments.
The optimal technique is dependent upon the degree of the discontinuity,
the amount of available bone stock and the likelihood of achieving
stable healing between the two segments. A method of treating pelvic
discontinuity using porous tantalum components with a distraction
technique that achieves both initial stability and subsequent long-term
biological fixation is described. Cite this article:
Aims. Loss or absence of proximal femoral bone in revision total hip
arthroplasty (THA) remains a significant challenge. While the main
indication for the use of proximal femoral replacements (PFRs) is
in the treatment of malignant disease, they have a valuable role
in revision THA for loosening, fracture and infection in patients
with bone loss. Our aim was to determine the clinical outcomes,
implant survivorship, and complications of PFRs used in revision
THA for indications other than malignancy. Patients and Methods. A retrospective review of 44 patients who underwent revision
THA using a PFR between 2000 and 2013 was undertaken. Their mean
age was 79 years (53 to 97); 31 (70%) were women. The bone loss
was classified as
Impaction bone grafting for the reconstitution
of bone stock in revision hip surgery has been used for nearly 30 years.
Between 1995 and 2001 we used this technique in acetabular reconstruction,
in combination with a cemented component, in 304 hips in 292 patients
revised for aseptic loosening. The only additional supports used
were stainless steel meshes placed against the medial wall or laterally
around the acetabular rim to contain the graft. All
Introduction and Purposes. Custom made acetabular prosthesis are a valid option for the reconstruction after the resection of pelvic tumors. They should guarantee a stable and reliable reconstruction for the expected survival of the patient. Nevertheless in many cases periacetabular metastatic lesions have been compared to high grade (IIIA-B)
We maintain a database on 1000 femoral revisions using extensively porous-coated stems. Using femoral rerevision for any reason as an endpoint, the survivorship is 99 ± 0.8% (95% confidence interval) at 2 years, 97 ± 1.3% at 5 years, 95.6 ± 1.8% at 10 years, and 94.5 ± 2.2% at 15 years. Similar to Moreland and