Advertisement for orthosearch.org.uk
Results 1 - 50 of 460
Results per page:
The Bone & Joint Journal
Vol. 102-B, Issue 2 | Pages 198 - 204
1 Feb 2020
Perlbach R Palm L Mohaddes M Ivarsson I Schilcher J

Aims. This single-centre observational study aimed to describe the results of extensive bone impaction grafting of the whole acetabular cavity in combination with an uncemented component in acetabular revisions performed in a standardized manner since 1993. Methods. Between 1993 and 2013, 370 patients with a median age of 72 years (interquartile range (IQR) 63 to 79 years) underwent acetabular revision surgery. Of these, 229 were more than ten years following surgery and 137 were more than 15 years. All revisions were performed with extensive use of morcellized allograft firmly impacted into the entire acetabular cavity, followed by insertion of an uncemented component with supplementary screw fixation. All types of reoperation were captured using review of radiographs and medical charts, combined with data from the local surgical register and the Swedish Hip Arthroplasty Register. Results. Among patients with possible follow-up of ten and 15 years, 152 and 72 patients remained alive without revision of the acetabular component. The number of deaths was 61 and 50, respectively. Of those who died, six patients in each group had a reoperation performed before death. The number of patients with a reoperation was 22 for those with ten-year follow-up and 21 for those with 15 years of follow-up. The Kaplan-Meier implant survival rate for aseptic loosening among all 370 patients in the cohort was 96.3% (95% confidence interval (CI) 94.1 to 98.5) after ten years and 92.8% (95% CI 89.2 to 96.6) after 15 years. Conclusion. Extensive bone impaction grafting combined with uncemented revision components appears to be a reliable method with favourable long-term survival. This technique offers the advantage of bone stock restoration and disputes the long-standing perception that uncemented components require > 50% of host bone contact for successful implant survival. Cite this article: Bone Joint J 2020;102-B(2):198–204


The Bone & Joint Journal
Vol. 95-B, Issue 2 | Pages 166 - 172
1 Feb 2013
Abolghasemian M Tangsataporn S Sternheim A Backstein D Safir O Gross AE

Trabecular metal (TM) augments are a relatively new option for reconstructing segmental bone loss during acetabular revision. We studied 34 failed hip replacements in 34 patients that were revised between October 2003 and March 2010 using a TM acetabular shell and one or two augments. The mean age of the patients at the time of surgery was 69.3 years (46 to 86) and the mean follow-up was 64.5 months (27 to 107). In all, 18 patients had a minor column defect, 14 had a major column defect, and two were associated with pelvic discontinuity. The hip centre of rotation was restored in 27 patients (79.4%). The Oxford hip score increased from a mean of 15.4 points (6 to 25) before revision to a mean of 37.7 (29 to 47) at the final follow-up. There were three aseptic loosenings of the construct, two of them in the patients with pelvic discontinuity. One septic loosening also occurred in a patient who had previously had an infected hip replacement. The augments remained stable in two of the failed hips. Whenever there was a loose acetabular component in contact with a stable augment, progressive metal debris shedding was evident on the serial radiographs. Complications included another deep infection treated without revision surgery. Good clinical and radiological results can be expected for bone-deficient acetabula treated by a TM cup and augment, but for pelvic discontinuities this might not be a reliable option.

Cite this article: Bone Joint J 2013;95-B:166–72.


The Bone & Joint Journal
Vol. 102-B, Issue 4 | Pages 423 - 425
1 Apr 2020
Hoggett L Cross C Helm A

Aims. Dislocation remains a significant complication after total hip arthroplasty (THA), being the third leading indication for revision. We present a series of acetabular revision using a dual mobility cup (DMC) and compare this with our previous series using the posterior lip augmentation device (PLAD). Methods. A retrospective review of patients treated with either a DMC or PLAD for dislocation in patients with a Charnley THA was performed. They were identified using electronic patient records (EPR). EPR data and radiographs were evaluated to determine operating time, length of stay, and the incidence of complications and recurrent dislocation postoperatively. Results. A total of 28 patients underwent revision using a DMC for dislocation following Charnley THA between 2013 and 2017. The rate of recurrent dislocation and overall complications were compared with those of a previous series of 54 patients who underwent revision for dislocation using a PLAD, between 2007 and 2013. There was no statistically significant difference in the mean distribution of sex or age between the groups. The mean operating time was 71 mins (45 to 113) for DMCs and 43 mins (21 to 84) for PLADs (p = 0.001). There were no redislocations or revisions in the DMC group at a mean follow-up of 55 months (21 to 76), compared with our previous series of PLAD which had a redislocation rate of 16% (n = 9) and an overall revision rate of 25% (n = 14, p = 0.001) at a mean follow-up of 86 months (45 to 128). Conclusion. These results indicate that DMC outperforms PLAD as a treatment for dislocation in patients with a Charnley THA. This should therefore be the preferred form of treatment for these patients despite a slightly longer operating time. Work is currently ongoing to review outcomes of DMC over a longer follow-up period. PLAD should be used with caution in this patient group with preference given to acetabular revision to DMC. Cite this article: Bone Joint J 2020;102-B(4):423–425


Orthopaedic Proceedings
Vol. 90-B, Issue SUPP_I | Pages 39 - 40
1 Mar 2008
Waddell J Chen X Griffith K Morton J Schemitsch E
Full Access

Fifty-five patients undergoing isolated acetabular revisions in fifty-seven hips were available for review. In thirty-three of fifty-seven hips there was no significant acetabular deficiency; of the remaining twenty-four hips twenty underwent allograft reconstruction and four autogenous bone grafting. Mean follow-up was four years with a range of three to seven years; there have been no femoral loosening, and three further surgical procedures for hip instability. All acetabular components at last review were soundly fixed with the exception of one patient who underwent excision arthroplasty at twelve months for deep infection. The purpose of this study was to review the functional outcome and the fate of the femoral stem and revised acetabular component following isolated ace-tabular revision. Findings of the current study demonstrate that isolated acetabular revision does not compromise the final functional nor radiographic outcome in acetabular revision in appropriately selected patients; the fate of the femoral component is not adversely influenced by this procedure. There is no need to remove the femoral component at the time of acetabular revision if the femoral component is well fixed and stable by pre- and intra-operative assessment. Prospectively entered data on fifty-seven hips (fifty-five patients) who have undergone isolated acetabular revision without femoral revision was available for review. All patients were assessed pre-operatively and post-operatively on an annual basis by means of physical examination, x-ray, SF-36 and WOMAC questionnaires. In thirty-three of fifty-seven hips there was no significant acetabular deficiency; of the remaining twenty-four hips, one had a segmental defect, thirteen had a cavitary defect and ten had a combined segmental and cavitary defect. Osteolysis existed in the proximal femur of two hips. Bone grafting in twenty-four hips consisted of morselized allograft in nine; combined structural and morselized allograft used in eleven and autogenous bone used in four acetabular defects. Autogenous bone grafting was done in two femoral osteolytic lesions. Mean follow-up was four years with a range of three to seven years. The mean duration of arthroplasty prior to revision was fourteen years (range four to twenty-three years). There were no nerve palsies, vascular injuries or intra-operative fractures in this patient group. All ace-tabular components at latest review were soundly fixed with the exception of one patient who underwent excision arthroplasty at twelve months for deep infection. Twenty-one of the twenty-four hips with bone grafting demonstrated positive radiographic signs of incorporation; the remaining threehips have a stable interface but no evidence of bone ingrowth. Three of the fifty-seven hips presented with hip dislocations after revision arthroplasty; two were managed by closed reduction; the third by open reduction and soft tissue repair


The Journal of Bone & Joint Surgery British Volume
Vol. 85-B, Issue 8 | Pages 1114 - 1119
1 Nov 2003
Elke R Berli B Wagner A Morscher EW

The need for supplementary screw fixation in acetabular revisions is still widely debated. We carried out 439 acetabular revisions over an eight-year period. In 171 hips with contained or small segmental defects, the Morscher press-fit cup was used. These revisions were followed prospectively. No screws were used for additional fixation. A total of 123 hips with a mean follow-up of 7.4 years (5 to 10.5) were available for clinical and radiological review. There was no further revision of a press-fit cup for aseptic loosening. Radiological assessment revealed osteolysis in three hips. Of the original 171 hips there was cranial and medial migration of up to 6 mm at two years in 44 (26%). No further migration was seen after the second post-operative year. Acetabular revision without screws is possible with excellent medium-term results in well selected patients


Orthopaedic Proceedings
Vol. 86-B, Issue SUPP_I | Pages 1 - 1
1 Jan 2004
Bargar W Blumenfeld T Taylor J
Full Access

A common finding in acetabular revisions is loss of medial bone stock. Using a standard cementless hemispherical component, alternatives for reconstruction include medialisation of the cup, medial particulate allograft with rim fixation on host bone, or use of a “mega-cup”. A cementless shell that has 6 mm of lateral augmentation is useful in restoring the joint centre while at the same time achieving implant stability and increasing host bone contact without loss of additional bone. From 1991 to 2000, a total of 142 acetabular revisions were performed with the Arthropor TM DP+6 implant (Joint Medical Products/J& J/DePuy). These patients have been prospectively followed bi-annually with Harris Hip Scores and monitoring of complications and radiographic findings. Average follow-up is 5 years (range 2 to 11 years). Implant survivorship is 100%. There have been seven re-operations: one for infection (debrided), two for femoral revision and four head/liner changes for recurrent dislocations. Dislocation incidence is 7.8%. The average Total Harris Score at 5 years is 74.3, with an average Harris Pain Score of 34.9 (out of a maximum of 44). Radiographic analysis showed frequent zone 3 radiolucent zones. Initial migration of > 2 mm with subsequent stabilisation occurred in 18%. The joint centre was restored to within 5 mm of the contralateral hip in 85% of cases. We have found this type of implant to be efficacious in the more common acetabular revisions where the loss of bone stock is mainly medial/cavitary, with an intact posterior column and small medial segmental defects


The Journal of Bone & Joint Surgery British Volume
Vol. 91-B, Issue 9 | Pages 1148 - 1153
1 Sep 2009
Schreurs BW Keurentjes JC Gardeniers JWM Verdonschot N Slooff TJJH Veth RPH

We present an update of the clinical and radiological results of 62 consecutive acetabular revisions using impacted morsellised cancellous bone grafts and a cemented acetabular component in 58 patients, at a mean follow-up of 22.2 years (20 to 25). The Kaplan-Meier survivorship for the acetabular component with revision for any reason as the endpoint was 75% at 20 years (95% confidence interval (CI) 62 to 88) when 16 hips were at risk. Excluding two revisions for septic loosening at three and six years, the survivorship at 20 years was 79% (95% CI 67 to 93). With further exclusions of one revision of a well-fixed acetabular component after 12 years during a femoral revision and two after 17 years for wear of the acetabular component, the survivorship for aseptic loosening was 87% at 20 years (95% CI 76 to 97). At the final review 14 of the 16 surviving hips had radiographs available. There was one additional case of radiological loosening and four acetabular reconstructions showed progressive radiolucent lines in one or two zones. Acetabular revision using impacted large morsellised bone chips (0.5 cm to 1 cm in diameter) and a cemented acetabular component remains a reliable technique for reconstruction, even when assessed at more than 20 years after surgery


Orthopaedic Proceedings
Vol. 100-B, Issue SUPP_15 | Pages 51 - 51
1 Nov 2018
Negri S Regis D Sandri A Magnan B
Full Access

Introduction. The management of periprosthetic pelvic bone loss is a challenging problem in hip revision surgery. This study evaluates the minimum 10-year clinical and radiographic outcome of major column structural allografts combined with the Burch-Schneider antiprotrusio cage for acetabular reconstruction. Methods. From January 1992 to August 2005, 106 hips with periprosthetic osteolysis underwent acetabular revision using massive allografts and the Burch-Schneider antiprotrusio cage. Forty-five patients (49 hips) died for unrelated causes without further surgery. Fifty-nine hips in 59 patients underwent clinical and radiographic evaluation at an average follow-up of 15.1 years. There were 17 male and 42 female patients, with age ranging from 29 to 83 years (mean 59). Results. Ten hips required rerevision because of infection (3), aseptic loosening (6), and flange breakage (1). Moreover, 4 cages showed x-ray signs of instability with severe bone resorption. The survivorship of the Burch-Schneider cage at 21.9 years with removal for any reason or radiographic migration and aseptic or radiographic failure as the end points were 76.3 and 81.4, respectively. The average Harris hip score improved from 33.2 points preoperatively to 75.7 points at the latest follow-up (p < 0.001). Discussion. In hip revision surgery, severe deficiency of pelvic bone stock is a critical concern because of the difficulty in providing a stable and durable fixation of the prosthesis. Although antiprotrusio cages have a limited role in acetabular revision, the use in association with massive allografts in extended bone loss demonstrated highly successful long-term results, enabling bone stock restoration and cup stability


Orthopaedic Proceedings
Vol. 99-B, Issue SUPP_7 | Pages 56 - 56
1 Apr 2017
Engh C
Full Access

Porous-coated acetabular hemispherical components have proven successful in all but the most severe revision acetabular defects. A revision jumbo porous coated component has been defined as cup with minimum diameter of 66 mm in men and 62 mm in women. In published studies this size cup is used in 14–39% of acetabular revisions. The advantages of this technique are ease of use, most deficiencies can be treated without structural graft, host bone contact with the porous surface is maximised, and the hip center is generally normal. Jumbo cups are typically used in Paprosky type 2, 3A, and many 3B defects. Requirements for success include circumferential acetabular exposure, an intact posterior column, and much of the posterior wall. The cup should be stable with a press-fit between the ischium and anterior superior acetabulum with the addition of some superior lateral support. Additional support is provided with multiple dome or rim screws. Survivorship of the metal shell with revision for any reason has been reported to be 80%-96% at time frames from 15–20 years. The most common post-operative complication is dislocation


Orthopaedic Proceedings
Vol. 98-B, Issue SUPP_17 | Pages 114 - 114
1 Nov 2016
Gross A
Full Access

The indications for cementless acetabular fixation have been broadened because our data supports the use of trabecular metal cups even when there's limited bleeding host bone contact. Trabecular metal augments have allowed us to use cementless cups when there is segmental loss of bone. Surgical Technique: The acetabular bed is prepared. If there is less medial bone stock than 2 mm, then morselised allograft is impacted by reverse reaming. When reaming is complete and less than 50% bleeding host bone is available for cup stabilization, then a trabecular metal cup is indicated. Trabecular augments are used if the trabecular cup trial is not stable, or if it is uncovered by 40% or more. The conventional augments come in different sizes to accommodate the diameter of the cup and the size of the defect. Larger defects are addressed with anterior and posterior column augments, and superior defects with figure of seven augments. Augments are fixed with at least two screws. The interface between the cup and the augments should be stable, but some surgeons place a very thin layer of cement between the augment and cup so micromotion does not occur while ingrowth is occurring. We have used trabecular metal augments in 46 acetabular revisions in conjunction with a trabecular metal cup. Thirty-four cases have at least 2 years follow-up with an average of 64.5 months. There has been 4 cup loosenings with 3 re-revisions


Orthopaedic Proceedings
Vol. 93-B, Issue SUPP_I | Pages 40 - 40
1 Jan 2011
Brogan K Charity J Sheeraz A Hubble M Howell J
Full Access

There is evidence that recommends the retention of a well-fixed cement mantle at the time of revision hip arthroplasty. The cement-cement interface has been proven to have greater shear strength than a new bone-cement interface after removing a well-fixed cement mantle. This study reviewed a series of acetabular revision procedures with a minimum 2-year follow-up where the original cement mantle was left intact. From 1988 to 2004, 60 consecutive cement-in-cement revisions of the acetabular component were performed at our institution. Outcome was based on functional assessment using the Oxford, Charnley, and Harris scoring systems as well as radiographic analysis using the DeLee and Charnley criteria. In total 60 procedures were performed in 60 patients (40 female and 20 male), whose mean age at surgery was 75 years (range 40 to 99 years). 80% were performed for recurrent dislocation, 13.3% during femoral component revision, 5% for acetabular component wear, and 1.7% for pain. No case was lost to follow-up. There was one re-revision for aseptic cup loosening at 7 years, with 1 further case of radiological loosening identified at the latest review. There were 6 further cases of dislocation 4 of which were treated with further in-cement revisions. All other cases showed well-fixed components on radiographic analysis and no evidence of failure at the most recent follow up. The cement-in-cement technique already has a good body of evidence based on revision of the femoral component and this study shows that the technique can be applied to acetabular revisions as well with good functional and radiological results in the short to medium term


Orthopaedic Proceedings
Vol. 98-B, Issue SUPP_13 | Pages 4 - 4
1 Jun 2016
Mohammed R Siney P Purbach B Kay P
Full Access

Structural bulk autografts restore the severe bone loss at primary hip arthroplasty in dysplastic hips and have shown to have good long term outcomes. There are only a few reports of revision arthroplasty for these sockets that fail eventually. We report on a series of such primary hips which underwent cemented revision of the socket for aseptic loosening and their outcomes. A retrospective review was performed from our database to identify fifteen acetabular revisions after previous bulk autograft. The mean age at revision was 53.9 years (range 31–72.1). The mean duration between the primary and revision arthroplasty was 12.4 years (range 6.6 – 20.3). All procedures were done using trochanteric osteotomy and three hips also needed the femoral component revision. All fifteen hips needed re-bone grafting at the revision surgery to restore the new socket to the level of the true acetabulum. Of these ten hips had morsellised impaction allograft, and the remaining five also needing a structural bulk allograft. Two sockets underwent re-revision at mean 7.5 years for aseptic loosening. One patient had a dislocation that was reduced closed. At a mean follow up of 5.7 years, one socket showed superior migration, but was stable and did not need further intervention. Two other sockets also showed radiological evidence of loosening, and are being closely monitored. The medium term results of cemented acetabular revision in this younger age group are satisfactory, with repeat bone grafting being required to restore the true acetabular position. Though the primary arthroplasty with bulk bone graft recreates the acetabular bone stock, significant bone loss due to the mechanical loosening of the socket needs to be anticipated in revision surgery


Orthopaedic Proceedings
Vol. 100-B, Issue SUPP_5 | Pages 79 - 79
1 Apr 2018
Lee W Han C Yang I Park K
Full Access

Introduction. Reinforcement ring with allograft bone is commonly used for acetabular reconstruction of bone defects because it can achieve stable initial fixation of the prosthesis. It is not clear whether the allograft bone can function as a viable host bone and provide long-standing structural support. The purpose of this study was to assess to long-term survival of the reinforcement rings and allograft bone incorporation after acetabular revisions. Methods. We retrospectively reviewed 39 hips (37 patients) who underwent reconstruction of the acetabulum with a Ganz reinforcement ring and allograft bone in revision total hip arthroplasty. There were 18 females and 19 males with a mean age of 55.9 years (35–74 years). The minimum postoperative follow-up period was 10 years (10∼17 years). We assessed the acetabular bone defect using the Paprosky's classification. We determined the rates of loosening of the acetabular reconstructions, time to aseptic loosening, integration of the allograft bone, resorption of the allograft bone, and survival rate. Aseptic loosening of the acetabular component was defined as a change in the cup migration of more than 5 mm or a change in the inclination angle of more than 5° or breakage of the acetabular component at the time of the follow-up. Graft integration was defined as trabecular remodelling crossing the graft-host interface. Resorption of the allograft bone was classified as minor (<1/3), moderate (1/3–1/2) or severe (>1/2). Kaplan-Meier survivorship analysis was performed for aseptic loosening of the acetabular component. The results. The acetabular bone defects were classified as follows: 8 type II hips (4 type IIB, 4 type IIC), and 31 type III hips (17 type IIIA, 14 type IIIB). Fourteen (35.9%) of 39 hips was defined as aseptic loosening of an acetabular component. Loosening was more frequent in type IIIB (57.1%) than in type IIIA hips (29.4%). Mean time to aseptic loosening of the acetabular reconstructions was 6.3 years in type IIIA and from 5 years in type IIIB defects, respectively. Allograft bone incorporation was satisfactory in 66.7% of hips. There was minor bone resorption in 14.3% and moderate bone resorption in 10.2%. In 9 hips (23.1%), severe resorption of the allograft bone was observed and early component loosening was observed in these cases. The survival rate of acetabular component at 10 years of follow-up was 63.6% (95% confidence interval, 49–77%) with aseptic loosening as endpoints. Conclusions. The long-term survival rate of acetabular revision using the reinforcement ring and allograft bone in the reconstruction of severe acetabular bone defects was unsatisfactorily low due to loosening of acetabular components. Because of unfavorable graft incorporation into a host bone, an alternative component and structural support may be employed in the reconstruction of severe acetabular bone defects


Orthopaedic Proceedings
Vol. 99-B, Issue SUPP_15 | Pages 103 - 103
1 Aug 2017
Gross A
Full Access

The indications for cementless acetabular fixation have been broadened because our data supports the use of trabecular metal cups even when there's limited bleeding host bone contact. Trabecular metal augments have allowed us to use cementless cups when there is segmental loss of bone. Surgical Technique: The acetabular bed is prepared. If there is less medial bone stock than 2mm, then morselised allograft is impacted by reverse reaming. When reaming is complete and less than 50% bleeding host bone is available for cup stabilisation, then a trabecular metal cup is indicated. Trabecular augments are used if the trabecular cup trial is not stable, or if it is uncovered by 40% or more. The conventional augments come in different sizes to accommodate the diameter of the cup and the size of the defect. Larger defects are addressed with anterior and posterior column augments, and superior defects with figure of seven augments. Augments are fixed with at least two screws. The interface between the cup and the augments should be stable, but some surgeons place a very thin layer of cement between the augment and cup so micromotion does not occur while ingrowth is occurring. We have used trabecular metal augments in 46 acetabular revisions in conjunction with a trabecular metal cup. Thirty-four cases have at least 2 years follow-up with an average of 64.5 months. There have been 4 cup loosenings with 3 re-revisions


Orthopaedic Proceedings
Vol. 105-B, Issue SUPP_12 | Pages 35 - 35
23 Jun 2023
Lavernia C Patron LP Lavernia CJ Gibian J Hong T Bendich I Cook SD
Full Access

Fracture of contemporary femoral stems is a rare occurrence. Earlier THR stems failed due to design issues or post manufacturing heat treatments that weakened the core metal. Our group identified and analyzed 4 contemporary fractured femoral stems after revision surgery in which electrochemical welds contributed to the failure.

All four stems were proximally porous coated titanium alloy components. All failures occurred in the neck region post revision surgery in an acetabular cup exchange. All were men and obese. The fractures occurred at an average of 3.6 years post THR redo (range, 1.0–6.5 years) and 8.3 years post index surgery (range, 5.5–12.0 years). To demonstrate the effect of electrocautery on retained femoral stems following revision surgery, we applied intermittent electrosurgical currents at three intensities (30, 60, 90 watts) to the polished neck surface of a titanium alloy stem under dry conditions.

At all power settings, visible discoloration and damage to the polished neck surface was observed. The localized patterns and altered metal surface features exhibited were like the electrosurgically-induced damage priorly reported.

The neck regions of all components studied displayed extensive mechanical and/or electrocautery damage in the area of fracture initiation. The use of mechanical instruments and electrocautery was documented to remove tissues in all 4 cases.

The combination of mechanical and electrocautery damage to the femoral neck and stem served as an initiation point and stress riser for subsequent fractures. The electrocautery and mechanical damage across the fracture site observed occurred iatrogenically during revision surgery. The notch effect, particularly in titanium alloys, due to mechanical and/or electrocautery damage, further reduced the fatigue strength at the fractured femoral necks. While electrocautery and mechanical dissection is often required during revision THA, these failures highlight the need for caution during this step of the procedure in cases where the femoral stem is retained.


Orthopaedic Proceedings
Vol. 97-B, Issue SUPP_1 | Pages 50 - 50
1 Feb 2015
Gross A
Full Access

The indications for cementless acetabular fixation have been broadened because our data supports the use of trabecular metal cups even when there's limited bleeding host bone contact. Trabecular metal augments have allowed us to use cementless cups when there is segmental loss of bone. Surgical Technique:. The acetabular bed is prepared. If there is less medial bone stock than 2mm, then morselised allograft is impacted by reverse reaming. When reaming is complete and less than 50% bleeding host bone is available for cup stabilization, then a trabecular metal cup is indicated. Trabecular augments are used if the trabecular cup trial is not stable, or if it is uncovered by 40% or more. The conventional augments come in different sizes to accommodate the diameter of the cup and the size of the defect. Larger defects are addressed with anterior and posterior column augments, and superior defects with figure of seven augments. Augments are fixed with at least two screws. The interface between the cup and the augments should be stable, but some surgeons place a very thin layer of cement between the augment and cup so micromotion does not occur while ingrowth is occurring. We have used trabecular metal augments in 46 acetabular revisions in conjunction with a TM cup. Thirty-four cases have at least 2 years follow-up with an average of 64.5 months. There has been 4 cup loosenings with 3 re-revisions


Orthopaedic Proceedings
Vol. 86-B, Issue SUPP_III | Pages 275 - 276
1 Mar 2004
dñImporzano M Pierannunzii L de Bellis U Fadigati P Milandri L
Full Access

Aims: This study evaluates the clinical results of acetabular revision with Lima SPH Anatomic cup in 63 cases, performed at our Institute since 1999. Methods: We have evaluated 63 acetabular revision with SPH Anatomic cup in retrospective way. All the cases were produced by aseptic loosening and bone loss was in stage I or II according to GIR classiþcation (simple acetabular enlargement or one wall defect). The evaluation occurred after 1 to 3.5 years. Results: Preoperative mean Harris Hip Score was 54 and at time of evaluation it was 91. No sign of loosening was found. The mean cranial elevation of centre of rotation was preoperatively 13 mm and postoperatively 9 mm. Conclusions: The good results obtained with this kind of cup can be explained through its peculiarities: the emispheric design with the cranial ßange permits a press-þt þxation in presence of sufþcient bone stock and an exact-þt þxation with screws when the wall defect is important. In our opinion the 18û automatic antiversion of the implant is helpful in cases in which there is a great posterior wall defect and a traditional cup could determinate a wrong, retroverted orientation of the acetabulum. As we can see, a cranial elevation of the centre of rotation is well tolerated because less than 1 cm, and many Authors agree with us upon this consideration. In conclusion SPH Anatomic cup is a good solution for acetabular revision with minimal to moderate bone loss


Orthopaedic Proceedings
Vol. 99-B, Issue SUPP_7 | Pages 127 - 127
1 Apr 2017
Gross A
Full Access

The indications for cementless acetabular fixation have been broadened because our data supports the use of trabecular metal cups even when there's limited bleeding host bone contact. Trabecular metal augments have allowed us to use cementless cups when there is segmental loss of bone. Surgical Technique: The acetabular bed is prepared. If there is less medial bone stock than 2 mm, then morselised allograft is impacted by reverse reaming. When reaming is complete and less than 50% bleeding host bone is available for cup stabilization, then a trabecular metal cup is indicated. Trabecular augments are used if the trabecular cup trial is not stable, or if it is uncovered by 40% or more. The conventional augments come in different sizes to accommodate the diameter of the cup and the size of the defect. Larger defects are addressed with anterior and posterior column augments, and superior defects with figure of seven augments. Augments are fixed with at least two screws. The interface between the cup and the augments should be stable, but some surgeons place a very thin layer of cement between the augment and cup so micromotion does not occur while ingrowth is occurring. We have used trabecular metal augments in 46 acetabular revisions in conjunction with a trabecular metal cup. Thirty-four cases have at least 2 years follow-up with an average of 64.5 months. There has been 4 cup loosenings with 3 re-revisions. Our most up to date data is 101 cases with an average follow-up of 3 years. There has been one infection that underwent a two stage revision. There are 4 loose cups – 3 revised


Orthopaedic Proceedings
Vol. 95-B, Issue SUPP_15 | Pages 191 - 191
1 Mar 2013
Hara K Kaku N Tabata T Tsumura H
Full Access

Introduction. In the case of bipolar hemiarthroplasty, surgeons are often faced with only migration of outer head and severe osteolysis in acetabulum without loosening of femoral component. There has been much debate regarding the merits of removing or retaining stable femoral components in such cases. The purpose of this study was to determine whether revision of an isolated acetabular component without the removal of a well-fixed femoral component [Fig. 1] could be successfully performed. Materials and methods. Thirty-four hips of 33 patients who were followed up for a minimum of 1 year were examined. There were 29 women and 4 men. The average time from primary operation to revision surgery was 12.5 years (range, 0.0 to 17.9 years), and the average follow-up time after revision was 5 years (range, 1.1 to 15.2 years). The average age of the patients at the time of the index revision was sixty-four years (range, thirty-two to seventy-eight years). The reason for acetabular revision was migration of outer head in twenty-eight hips, disassembly of bipolar cup in four hips and recurrent dislocation in two hips. Of the thirty-four femoral components, twenty-seven were cementless and seven were cemented. In nine hips, we performed bone grafting to osteolysis of the proximal femur around the stem. Acetabular components were revised to an acetabular reinforcement ring with a cemented cup in 26 hips, to cementless acetabular components in 8 hips, and to cemented cup in 1 hip. Results. The average Japan Orthopaedic Association hip score improved from 50.7 to 86.1 points after revision surgery. One femoral component (3%) was revised because of periprosthetic fracture, three years after the index acetabular revision and eighteen years after the initial bipolar hemiarthroplasty. Radiographic evaluation of the thirty-three femoral components that were not revised demonstrated no evidence of loosening or subsidence. There were no dislocation or deep infection. Thirty-three (97%) of the acetabular components were judged to be stable at the final follow-up. A nonprogressive radiolucent line of less than 2 mm was observed in one case. Conclusion. We recommend that isolated acetabular revision be considered in cases of failed bipolar hemiarthroplasty with a well-fixed femoral component


The Journal of Bone & Joint Surgery British Volume
Vol. 86-B, Issue 4 | Pages 492 - 497
1 May 2004
Schreurs BW Bolder SBT Gardeniers JWM Verdonschot N Slooff TJJH Veth RPH

This study presents the clinical and radiological results of 62 consecutive acetabular revisions in 58 patients, at a mean of 16.5 years follow-up (15 to 20). The Kaplan-Meier survivorship for the cup with end-point revisions for any reason, was 79% at 15 years (95% confidence interval (CI); 67 to 91). Excluding two revisions for septic loosening at three and six years, and one revision of a well-fixed cup after 12 years in the course of a femoral revision, the survivorship was 84% at 15 years (95% CI; 73 to 95). At review there were no additional cases of loosening, although seven acetabular reconstructions showed radiolucent lines in one or two zones. Acetabular revision using impacted large morsellised bone chips (0.7 cm to 1.0 cm) and a cemented cup, is a reliable technique of reconstruction, when assessed at more than 15 years


Orthopaedic Proceedings
Vol. 86-B, Issue SUPP_I | Pages 80 - 80
1 Jan 2004
Reddy VRM Dorairajan A Krikler SJ
Full Access

Aims: To study clinical and radiological outcome of acetabular revision in THR with porous, hydroxyapatite-coated cups. Methods: 50 acetabular revisions (48 patients) operated by single surgeon were reviewed. Uncemented, hydroxyapatite coated cup (Mallory/Head, Biomet) was used. Preoperative acetabular bone loss graded by Paprosky’s classification (grade 1: 12, grade 2a: 26, grade 2b: 8, 2c: 2, grade 3a: 2). Acetabulum alone was revised in 22 hips. Duration of follow up: 35 months (24–52). Clinical outcome assessment was done using Merle d’Aubigne and Postel score & QALY index questionnaire. Radiological assessment by standard X-rays taken at the latest review date. No case was lost to follow up. Results: Merle d’Aubigne & Postel scores improved from 2.1, 2.7 and 2.4 (pre-operative) to 5.0, 4.3 and 4.5 (post-operative) respectively with significant improvement in QALYs scores. Radiological assessment showed no mechanical failures. Good trabecular formation between HA-coating and the bone seen in the majority. Non-progressive radiolucency < 1mm in 6 cases, superior migration > 2 mm in 3 cups where bone graft was used, and < 2mm migration in 9 cups was noted. 2 cases had rerevision for recurrent dislocation. Conclusions: Hydroxyapatite coating on the implant may enhance bony ongrowth at bone-implant interface giving additional stability. Good midterm results obtained in our study using hydroxyapatite-coated components favour the use of this type of cup in acetabular revisions for moderate bone loss, but a long-term follow up is essential


Orthopaedic Proceedings
Vol. 85-B, Issue SUPP_II | Pages 115 - 115
1 Feb 2003
Khaleel A Dutta A Scott WA Crabtree S
Full Access

To evaluate large/Jumbo acetabular cups in revision surgery, 52 cups in 48 patients were reviewed; mean age was 71. 6 years and mean follow up 6 years. Average Harris Hip Score was 85. Excellent bony incorporation was seen in all but the failures, of which there were three, 1 due to infection and 2 due to aseptic loosening. Major complications included 2 intraoperative fractures. Intermediate results of acetabular revisions, using large cups, without bone grafting are encouraging


Orthopaedic Proceedings
Vol. 84-B, Issue SUPP_II | Pages 155 - 155
1 Jul 2002
Khaleel A Dutta A Scott WA Crabtree S
Full Access

Aim: to evaluate the use of large acetabular cup in revision surgery without structural bone graft. Materials/methods: Patients who had revision hip surgery at Greenwich Hospital between 1991 and 1994 were reviewed. All patients had complete clinical and radiological follow up. Large cup was the press fit Mathys Isoelastic cup. No patient had any structural bone grafting. Failure was defined as need for surgery and/or poor clinical outcome. Objective clinical assessment was done using the Harris Hip score. Radiological assessment was carried out using RC Johnston’s criteria for uncemented cups. Results: 52 revised cups in 48 patients were reviewed. Mean age was 71.6yrs, 21 males and 27 females. Mean follow up was 6 years (4 to 8 years). Average cup size was 64 mm (62 to 66). Diagnosis at index operation was 10 Rheumatoid, and 42 osteoarthrosis. Average Harris Hip Score was 85 (excellent 35, good 11, fair 3, poor 3). Radiological assessment showed excellent bony incorporation in all but the failures. There were 3 failures, 1 due to infection (revision was for infected primary THR), and 2 due to aseptic loosening in rheumatoid patients (both had significant cup malposition at revision). The major complications included 2 intraoperative fractures. Conclusion: Intermediate term results of acetabular revisions, using large cups, without structural bone grafting, in our hands, are encouraging. Cup position at revision appears crucial for long-term survival


Orthopaedic Proceedings
Vol. 90-B, Issue SUPP_III | Pages 514 - 514
1 Aug 2008
Atilla B
Full Access

The most challenging aspect of acetabular revision is the management of bone loss compromising implant fixation and stability. Several options, including both nonbiologic and biologic fixation, are available for acetabular revision. Biologic fixation is considered the best solution for revision surgery because it aims to restore the detoriated bone stock by using structural or cancellous allografts and a cemented polyethylene cup with impaction grafting with or without an antiprotrusio cage. With this technique, reliable and durable fixation of cemented acetabular components depend on the incorporation of allografts. Impaction grafting with use of morselized bone is a biological fixation alternative as defined by Sloof in 1984. He reported 94% survival in 11 years. Best results of this technique are obtained in contained or cavitary defects because the skeleton, while weakened, is basically intact. In these defects the anterior and posterior columns and the peripheral supporting bone for the acetabular component are intact. However, uncontained, or segmental, defects are more of a challenge. If the patient has a large segmental defect and there is no possibility of placing the implant against host bone or of restoring nearly normal anatomy, then the use of a structural bone graft may be indicated. In our revision arthroplasty series, despite the success of impaction grafting on the femoral side and on cavitary defects of the acetabulum, we had early loosening in segmentary defects with mesh or structural allograft reconstruction of the acetabular wall and impaction. Retrospectively, we have compared the survival of acetabular cup revisions with impaction grafting technique with or without reconstruction cages in 40 hips of 39 patients. There were 15 hips without cage support and 25 hips with cage reconstruction. Patient demographics and preoperative hip scores were comparable in each group. After 4 years of follow-up we have evaluated 26.3% aseptic loosening in impaction grafting alone, and 8.3% loosening in impaction with cage reconstruction. We have concluded that the metal cage allows for a better stability, protects the cancellous graft micromotion and eventually leading to a better incorporation in segmentary defects. Impaction of the cancellous bone cubes without a cage support in segmentary acetabular defects may prone to fail because of the micromotion between the cement and the graft which is not contained in stable walls


Orthopaedic Proceedings
Vol. 100-B, Issue SUPP_4 | Pages 11 - 11
1 Apr 2018
Kwong L Billi F Keller S Kavanaugh A Luu A Ward J Salinas C Paprosky W
Full Access

Introduction. The objective of this study was to compare the performance of the Explant Acetabular Cup Removal System (Zimmer), which has been the favored system for many surgeons during hip revision surgery, and the new EZout Powered Acetabular Revision System (Stryker). Methods. 54mm Stryker Trident® acetabular shells were inserted into the foam acetabula of 24 composite hemi-pelvises (Sawbones). The hemi-pelvises were mounted on a supporting apparatus enclosing three load cells. Strain gauges were placed on the hemipelvis, on the posterior and the anterior wall, and on the internal ischium in proximity to the acetabular fossa. A thermocouple was fixed onto the polar region of the acetabular component. One experienced orthopaedic surgeon and one resident performed mock revision surgery 6 times each per system. Results. Statistical analysis was conducted using Tukey's range test (HSD). The maximum force transferred to the implant was more than 4X lower with the EZout System regardless the surgeon experience (p=1.0E-08). Overall, recorded strains were lower for the EZout System with the higher decrease in strain (5X) observed at the posterior wall region(p=2E-08). The temperature at the interface was higher for the EZout System but never more than 37°C. Total removal time was on average reduced by a third with the EZout System (p=0.01). The calculated torque was lower for the EZout System. The amount of foam left on the cup after removal, which mimics the compromised bone, was 2.5X higher on average for the Explant System with most of the foam concentrated in the polar region. Lastly, it was observed that the polar region of each implant was reached by rotating the EZout System handpiece within a very narrow cylinder of space centered along the axis of the acetabular component compared to the Explant System, which required movement of the pivoting osteotomes within a large cone-shaped operating envelope. Discussion. Quantitatively, the EZout System required lower force, producing lower strains in the surrounding composite bone. Higher impact forces and associated increased strains may increase fracture risk. Qualitatively, the Explant System required a greater cone of movement than the EZout System requiring more space for the surgeon to leverage the handle of the tool. In addition, both surgeon and resident felt substantially greater exhaustion after using the Explant System vs. the EZout System. The resident compensated for the increased workload of the Explant with time, the experienced surgeon with force. The learning curve for both experienced surgeon and resident was also much shorter with the EZout System as shown by the close force values between the experienced surgeon and resident. Conclusion. Based on the results of this in vitro model, the EZout Powered Acetabular Removal System may be a reasonable alternative to manual removal techniques


The Journal of Bone & Joint Surgery British Volume
Vol. 88-B, Issue 5 | Pages 586 - 591
1 May 2006
Wang J Fong C Su Y Yu H

Failure of total hip arthroplasty with acetabular deficiency occurred in 55 patients (60 hips) and was treated with acetabular revision using morsellised allograft and a cemented metal-backed component. A total of 50 patients (55 hips) were available for clinical and radiological evaluation at a mean follow-up of 5.8 years (3 to 9.5). No hip required further revision of the acetabular component because of aseptic loosening. All the hips except one had complete incorporation of the allograft demonstrated on the radiographs. A complete radiolucent line of > 1 mm was noted in two hips post-operatively. A good to excellent result occurred in 50 hips (91%). With radiological evidence of aseptic loosening of the acetabular component as the end-point, the survivorship at a mean of 5.8 years after surgery was 96.4%. The use of impacted allograft chips in combination with a cemented metal-backed acetabular component and screw fixation can achieve good medium-term results in patients with acetabular bone deficiency


Orthopaedic Proceedings
Vol. 91-B, Issue SUPP_II | Pages 208 - 208
1 May 2009
Hekal W Desai A Farhan M
Full Access

Aim of the study: To assess the results of the uncemented oblong shaped Bofor cup in acetabular revision. Methods & materials: A prospective study from January 2001 to July 2006.15 cases of acetabular revision in 14 patients is studied. Paprosky classification for the acetabular defects is used. Final outcome assessed clinically and radiologically. Both Harris hip and Oxford hip functional scoring is used to assess the patients. None of the cases are lost in follow up. Results: The average follow-up was 36 months (range 8–52 months). All the cases were of aseptic loosening. 1case of type 2a, 6 cases of type 2b, 5 cases of type 2c, 3cases of type 3 defect and 4 cases with medial wall defect were noted. Stem was revised in 8 cases. In 4 cases auto graft from iliac crest was used. allograft was not used in any cases. In 12 cases 15 degree hooded insert was used. Average HHS improved from 30 points (range 20–38) to 84 points (range 70–90). Average OHS improved from 24 points (range 18–40) to 82 points (range 74–92). There were no cases of dislocation& infection.1 patient had sciatic nerve neuropraxia.1 case of severe Ankylosing spondylitis failed which was revised. Conclusion: Assemytical shape and design of the Boforcup makes it an useful cup for segmental and cavitatory acetabular defects. Pre operative classification of acetabular defects is inconsistent and unreliable. Allograft usage is not essential for these defects


Orthopaedic Proceedings
Vol. 90-B, Issue SUPP_II | Pages 298 - 298
1 Jul 2008
Carter RL Meek RMD Grigoris P
Full Access

Introduction: This study is a prospective series using a porous-coated cobalt-chromium alloy cup augmented with screw fixation for acetabular revisions. Methods: Between August 1997 and December 2001, eighty-five consecutive cementless acetabular revisions (81 patients) were performed. The mean age at operation was 64 years. Using the AAOS classification of acetabular defects there was one type I defect, 25 type two defects and 59 type III defects. Eighty-three cases were available for review (98%) with an average follow up of 6 years 6 months (range 3 months – 110 months). Clinical outcome was measured using the Charnley Hip Score and radiological assessment by plain radiographic measurement. Results: The Charnley Hip Score had improved from a pre-operative average of 7.52 (range 4–11) to the latest score of 14.84 (range 8 – 18). Significant cup migration occurred in only one case, which did not require revision. Sixteen cases demonstrated non-progressive radiolucent lines in one or two Delee and Charnley zones but none extended to all three zones. There were no cases of significant osteolysis. There were five dislocations none requiring re-operation; one revision was carried out for deep infection and one liner exchange at time of stem revision for subsidence. The results of Kaplan-Meier survival analysis using revision for all causes as the endpoint was 98.8% (95% confidence limits 0.964 to 1) at seventy-three months. Discussion: This press fit porous-coated cobalt-chromium alloy cup augmented with screw fixation for acetabular revision surgery produced excellent midterm results. Changes in cup design and material should only be undertaken with consideration of such results


Orthopaedic Proceedings
Vol. 92-B, Issue SUPP_I | Pages 185 - 186
1 Mar 2010
Timperley J Brogan K Charity J Sheeraz A Hubble M Howell J Gie G
Full Access

There is evidence that recommends the retention of a well-fixed cement mantle at the time of revision hip arthroplasty. The cement-cement interface has been proven to have a greater shear strength than a new bone-cement interface after removing the old cement mantle. This study reviewed a series of acetabular revision procedures with a minimum 2 year follow-up where the original cement mantle was left intact. From 1988 to 2004, 61 consecutive cement-in-cement revisions of the acetabular component were performed at our institution. Outcome was based on functional assessment using the Oxford, Charnley, and Harris scoring systems as well as radiographic analysis using the DeLee and Charnley criteria. In total 61 procedures were performed in 59 patients (40 female and 19 male), whose mean age at surgery was 75 years (range 40 to 99 years). 47 hips (77%) were performed for recurrent dislocation, 12 for polyethylene wear associated with other reasons for revision (aseptic stem loosening in 8, stem fracture in 2, femoral periprosthetic fracture in 1, subluxation in 1), 1 for unexplained pain, and 1 for disarticulation (intraprosthetic dislocation) of a constrained liner. No case was lost to follow-up. There was a significant improvement in the functional scores from the pre-operative status with the patients maintaining a low level of pain. There was one re-revision for aseptic cup loosening at 7 years, with 1 further case of radiological loosening identified at the latest review. There were 6 further cases of dislocation 4 of which were treated with further in-cement revisions. All other cases showed well-fixed components on radiographic analysis and no evidence of failure at the most recent follow up. The cement-in-cement revision technique can be used in selected cases of acetabular revision surgery, providing satisfactory functional outcomes backed up by good radiographic results. Blood loss and surgical time are also significantly decreased


Orthopaedic Proceedings
Vol. 92-B, Issue SUPP_I | Pages 16 - 16
1 Mar 2010
Brogan KRFS Charity JP Sheeraz A Hubble MJ Howell JR
Full Access

Purpose: There is evidence that recommends the retention of a well-fixed cement mantle at the time of revision hip arthroplasty. The cement-cement interface has been proven to have a greater shear strength than a new bone-cement interface after removing the old cement mantle. Method: This study reviewed a series of acetabular revision procedures with a minimum 2-year follow-up where the original cement mantle was left intact. From 1988 to 2004, 63 consecutive cement-in-cement revisions of the acetabular component were performed at our institution. Outcome was based on functional assessment using the Oxford, Charnley, and Harris scoring systems as well as radiographic analysis using the DeLee and Charnley criteria. Results: In total 63 procedures were performed in 61 patients (40 female and 21 male), whose mean age at surgery was 74 years (range 40 to 99 years). 47 hips (75%) were performed for recurrent dislocation, 13 for aseptic loosening, 1 for pain, 1 for excessive shortening, and 1 for disarticulation of a constrained liner. No case was lost to follow-up. There was a significant improvement in the functional scores from the pre-operative status with the patients maintaining a low level of pain. There was one re-revision for aseptic cup loosening at 7 years, with 1 further case of radiological loosening identified at the latest review. There were 6 further cases of dislocation 5 of which were treated with further in-cement revisions. All other cases showed well-fixed components on radiographic analysis and no evidence of failure at the most recent follow up. Conclusion: The cement-in-cement revision technique can be used in selected cases of acetabular revision surgery, providing satisfactory functional outcomes backed up by good radiographic results. Blood loss and surgical time are also significantly decreased


Orthopaedic Proceedings
Vol. 93-B, Issue SUPP_IV | Pages 449 - 449
1 Nov 2011
Cho Y Kim K Chun Y Rhyu K Song J Yoo M
Full Access

We wanted to evaluate the clinical and radiological results of acetabular revision using the acetabular reinforcement ring and allograft impaction in patients with severe acetabular bony defect. 41 hips revision arthroplasty using reinforcement ring were performed between April 1997 and October 2005 and were followed up for more than two years. The cause of primary arthroplasty was AVN in 18 cases, secondary osteoarthritis (OA) in 17 cases, fracture in cases and primary OA in 1 case. The cause of revision arthroplasty was acetabular cup loosening in 20 cases, massive osteolysis in 14 cases, infection in 4 cases, liner dissociation in 2 cases, and recurrent dislocation in 1 case. The average period between primary and revision arthroplasty was 11.4 years (range 0.6 to 29.1 years). Acetabular defects were classified based on the AAOS classification and Paprosky classification system. All were treated with autografts or allografts. Muller ring was used in 18 cases, Burch-Schneider ring was used in 14 cases, and Ganz ring in 9 cases. Clinical evaluations were performed according to the Harris hip score (HHS), and the radiographic results were evaluated by progression of acetabular component loosening, union of bone grafts, periacetabular osteolysis, and migration of the hip center. The mean preoperative Harris hip score of 64.9 was improved to 91.8 points at the latest follow-up. There were 39 cases of type 3 defect, 2 cases of type 4 defect according to the AAOS classification and 8 cases of type 2B defect, 3 cases of type 2C defect, 28 cases of type 3A defect, and 2 cases of type 3B defect according to Paprosky classification. Radiographically, the bone grafts were well united except one case. The mean preoperative hip center of rotation which was vertically 32.3mm, horizontally 33.2 mm migrated to vertically 26 mm, horizontally 33.2 mm postoperatively and it was statistically significant. The mean preoperative abductor lever arm of 41.7 mm changed to 45 mm postoperatively which was statistically insignificant. However the mean preoperatiave body lever arm of 89.4 mm changed to 96.9 mm postoperatively which was statistically significant. Postoperative complications were cup loosening in 1 case, dislocation in 2 cases, and recurrence of deep infection in 1 case. Clinically and radiographically, acetabular reconstruction using reinforcement ring showed very promising short term result. We conclude that reinforcement ring can provide stable support for grafted bone in severe bone defect. But meticulous surgical technique to get initial firm stability of ring and optimal indication in mandactory for the successful result


Orthopaedic Proceedings
Vol. 91-B, Issue SUPP_I | Pages 53 - 54
1 Mar 2009
Fink B Grossmann A Schubring S Fuerst M
Full Access

In acetabular revision press-fit cups usually are used in smaller defects and contact to the host bone should be more than 50 %. Due to the thin wall thickness and the surface design the cementless press-fit cup Allofit S has a specific characteristic during implantation. Therefore this cup was used for revision with greater acetabular defects and analysed in a prospective study. The press-fit in these cases was 4 mm and additional 2 or 3 screws into the Os ilium were used. 64 cups were were followed prospectively for 38.3 months with a minimum of 24 months and examined clinically (Harris-Hip-Score) and radiographically for migration (Method of Nunn et al.) and loosening (Method of Delee and Charnley). Corresponding to Nunn et al. and Blum et al., cup migration was defined to be a change of position greater than 3 mm or referring to Cordero-Ampuero et al. and Dickob et al. a change of inclination greater than 5 degrees. There were 25 revisions of the cup and 39 complete exchanges of the prosthesis due to 54 aseptic and 10 septic loosenings (two-step revision with spacer and cementless reimplantation). There were acetabular defects of type Paprosky 2A in 12 cases, of type 2B in 15 cases, type 2C in 19 cases, type 3A in 16 cases and type 3 B in 2 cases. The average age of the patients was 70.9 ± 8.9 years. The Harris-Hip-Score increased from 45.4 ± 14.9 points preoperatively to 81.8 ± 17.5 points one year and 82.3 ± 17.1 points two years postoperative. There was no loosing or significant migration of the cups. The Allofit S press-fit cup shows good result in cup revisions with greater acetabular defects when using a press-fit of 4 mm and additional 2 or 3 screws. In these cases it seems to be a good and cheeper alternative to specific implants like trabecular metal cups


Orthopaedic Proceedings
Vol. 92-B, Issue SUPP_I | Pages 112 - 112
1 Mar 2010
Min B Song K Cho C Bae K Lee K
Full Access

It is still unclear whether it is best, when revision surgery is required for replacement of an acetabular component, to treat femoral focal osteolysis with bone-grafting or instead to leave it untreated because the defect is too small and uncontained; the concern is to prevent bone graft from escaping into the hip joint. We hypothesized that progression of osteolysis can halted if the cause of particulate generation is removed and the femoral component is well osseointegrated. We prospectively followed 21 patients (24 hips) who underwent acetabular revision and curetting of proximal femoral osteolysis. These patients were followed for the minimum 3 years (mean, 4.3 years; range, 3–7.4 years). At the time of the latest follow-up examination, all hips were judged to be stable and to have well-fixed acetabular cups and femoral stems. No hips had significant progression of the osteolytic defect through the follow-up period and none demonstrated any new osteolytic lesion. Provided that a femoral component is bone ingrown with osseointegration sufficient to provide long-term stability, that the osteolytic defect is in the proximal aspect of the femur, and that the defect is uncontained, simple curettage is an effective alternative to additional bone-grafting


Orthopaedic Proceedings
Vol. 86-B, Issue SUPP_III | Pages 209 - 209
1 Mar 2004
Schreurs B
Full Access

Aims: To reconstruct acetabular bone stock loss in revision hip surgery, from 1979 on we have used a biologic reconstruction method with tightly impacted cancellous allografts in combination with a cemented polyethylene cup. Methods: This studies presents the clinical and radiological results of 62 consecutive acetabular revisions in 58 patients at a mean of 16.5 years (15–20 years) followup. The Kaplan-Meier survivorship for the cup with end-point revisions for any reason was 79% at fifteen years followup (95% C.I.: 67–91%). Results: Excluding two revisions for septic loosening at 3 and 6 years, the survivorship with end point aseptic loosening was 84% at fifteen years years (95% C.I.: 73–95%). At review there were no additional radiological loosenings, although 7 acetabular reconstructions showed radiolucent lines in one or two zones. Conslusions: This acetabular bone impaction technique using large morselized bone chips (range 0.7–1.0 cm) and a cemented cup is a reliable reconstruction technique, even after a 15–20 years followup


Orthopaedic Proceedings
Vol. 99-B, Issue SUPP_15 | Pages 101 - 101
1 Aug 2017
Gross A
Full Access

Acetabular cages are necessary when an uncemented or cemented cup cannot be stabilised at the correct anatomic level. Impaction grafting with mesh for containment of bone graft is an alternative for some cases in centers that specialise in this technique.

At our center we use three types of cage constructs –

Conventional cage ± structural or morselised bone grafting. This construct is used where there is no significant bleeding host bone. This construct is susceptible to cage fatigue and fracture, This reconstruction is used in young patients where restoration of bone stock is important.

Conventional cage in combination with a porous augment where contact with bleeding host bone can be with the ilium and then by the use of cement that construct can be unified. The augment provides contact with bleeding host bone and if and when ingrowth occurs, the stress is taken off the cage.

Cup-Cage Construct – in this construct there must be enough bleeding host bone to stabilise the ultra-porous cup which functions like a structural allograft supporting and eventually taking the stress off the cage. This construct is ideal for pelvic discontinuity with the ultra-porous cup, i.e., bridging and to some degree distracting the discontinuity. If, however, the ultra-porous cup cannot be stabilised against some bleeding host bone, then a conventional stand-alone cage must be used.

In our center the cup-cage reconstruction is our most common technique where a cage is used, especially if there is a pelvic discontinuity.

Acetabular bone loss and presence of pelvic discontinuity were assessed according to the Gross classification. Sixty-seven cup-cage procedures with an average follow-up of 74 months (range, 24–135 months; SD, 34.3) months were identified; 26 of 67 (39%) were Gross Type IV and 41 of 67 (61%) were Gross Type V (pelvic discontinuity). Failure was defined as revision surgery for any cause, including infection.

The 5-year Kaplan-Meier survival rate with revision for any cause representing failure was 93% (95% confidence interval, 83.1–97.4), and the 10-year survival rate was 85% (95% CI, 67.2–93.8). The Merle d'Aubigné-Postel score improved significantly from a mean of 6 pre-operatively to 13 post-operatively (p < 0.001). Four cup-cage constructs had non-progressive radiological migration of the ischial flange and they remain stable.


The Journal of Bone & Joint Surgery British Volume
Vol. 91-B, Issue 7 | Pages 870 - 876
1 Jul 2009
Kosashvili Y Backstein D Safir O Lakstein D Gross AE

Pelvic discontinuity with associated bone loss is a complex challenge in acetabular revision surgery. Reconstruction using ilio-ischial cages combined with trabecular metal acetabular components and morsellised bone (the component-cage technique) is a relatively new method of treatment. We reviewed a consecutive series of 26 cases of acetabular revision reconstructions in 24 patients with pelvic discontinuity who had been treated by the component-cage technique. The mean follow-up was 44.6 months (24 to 68). Failure was defined as migration of a component of > 5 mm. In 23 hips (88.5%) there was no clinical or radiological evidence of loosening at the last follow-up. The mean Harris hip score improved significantly from 46.6 points (29.5 to 68.5) to 76.6 points (55.5 to 92.0) at two years (p < 0.001). In three hips (11.5%) the construct had migrated at one year after operation. The complications included two dislocations, one infection and one partial palsy of the peroneal nerve. Our findings indicate that treatment of pelvic discontinuity using the component-cage construct is a reliable option


Orthopaedic Proceedings
Vol. 98-B, Issue SUPP_22 | Pages 60 - 60
1 Dec 2016
Gross A
Full Access

Acetabular cages are necessary when an uncemented or cemented cup cannot be stabilised at the correct anatomic level. Impaction grafting with mesh for containment of bone graft is an alternative for some cases in centers that specialise in this technique.

At our center we use three types of cage constructs:

Conventional cage ± structural or morselised bone grafting. This construct is used where there is no significant bleeding host bone. This construct is susceptible to cage fatigue and fracture. This reconstruction is used in young patients where restoration of bone stock is important.

Conventional cage in combination with a porous augment where contact with bleeding host bone can be with the ilium and then by the use of cement that construct can be unified. The augment provides contact with bleeding host bone and if and when ingrowth occurs, the stress is taken off the cage.

Cup Cage Construct – in this construct there must be enough bleeding host bone to stabilise the ultra-porous cup which functions like a structural allograft supporting and eventually taking the stress off the cage. This construct is ideal for pelvic discontinuity with the ultra-porous cup, i.e., bridging and to some degree distracting the discontinuity. If, however, the ultra-porous cup cannot be stabilised against some bleeding host bone, then a conventional stand-alone cage must be used.

In our center the cup cage reconstruction is our most common technique where a cage is used, especially if there is a pelvic discontinuity.


Orthopaedic Proceedings
Vol. 98-B, Issue SUPP_17 | Pages 102 - 102
1 Nov 2016
Gross A
Full Access

Acetabular cages are necessary when an uncemented or cemented cup cannot be stabilised at the correct anatomic level. Impaction grafting with mesh for containment of bone graft is an alternative for some cases in centers that specialise in this technique.

At our center we use three types of cage constructs –

Conventional cage ± structural or morselised bone grafting. This construct is used where there is no significant bleeding host bone. This construct is susceptible to cage fatigue and fracture. This reconstruction is used in young patients where restoration of bone stock is important.

Conventional cage in combination with a porous augment where contact with bleeding host bone can be with the ilium and then by the use of cement that construct can be unified. The augment provides contact with bleeding host bone and if and when ingrowth occurs, the stress is taken off the cage.

Cup Cage Construct – in this construct there must be enough bleeding host bone to stabilise the ultra-porous cup which functions like a structural allograft supporting and eventually taking the stress off the cage. This construct is ideal for pelvic discontinuity with the ultra-porous cup, i.e., bridging and to some degree distracting the discontinuity. If, however, the ultra-porous cup cannot be stabilised against some bleeding host bone, then a conventional stand-alone cage must be used.

In our center the cup cage reconstruction is our most common technique where a cage is used, especially if there is a pelvic discontinuity.


Orthopaedic Proceedings
Vol. 103-B, Issue SUPP_10 | Pages 39 - 39
1 Aug 2021
Rajan A Leong J Singhal R Siney P Shah N Board T
Full Access

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 Paprosky grade IIb, IIc or IIIa. Kaplan-Meier survivorship for all-cause revision was 96.36% (CI, 90.58–100.00) at 2 years with 3 failures. Two were due to early infection which required two-stage re-revision. The third was due to post-operative acetabular fracture which was then re-revised with TM augment, bone graft and large uncemented cup. Pre-op and post-op matched OHS scores were available for 60 hips(57%) with a mean improvement of 13 points. Radiographic analysis showed graft incorporation in all cases with no evidence of cup loosening. The mean vertical cup migration was 0.5mm (Range −5 to 7mm). No other complications were recorded.

This study shows that reconstruction of large acetabular defects during revision THA using a combination of TM augments to contain the acetabulum along with IBG to preserve the bone stock and a cemented socket is a reliable and safe technique with low revision rates and satisfactory clinical and radiographic results. Long term studies are needed to assess the possibility of preservation and regeneration of bone stock.


Orthopaedic Proceedings
Vol. 101-B, Issue SUPP_5 | Pages 30 - 30
1 Apr 2019
Perticarini L Medetti M Benazzo FM
Full Access

BACKGROUND

Total hip revision surgery in cases with previous multiple reconstructive procedures is a challenging treatment due to difficulties in treatment huge bone defects with standard revision prosthetic combinations. A new specially made production system in Electron-Beam Melting (EBM) technology based on a precise analysis of patients' preoperative CT scans has been developed.

METHODS

Objectives of design customization in difficult cases are to correctly evaluate patient's anatomy, to plan a surgical procedure and to obtain an optimal fixation to a poor bone stock. The 3D Printing (EBM) technology permits to create an extremely flexible patient matching implant and instrument, with material performances not viable with standard manufacturing process. Dedicated visual 3D tools and instrumentations improve implants congruency according to preoperative plan. Primary stability is enhanced and tailored on patient's anatomy by means of press-fit, iliac stems and the high friction performances of Trabecular Titanium matrix. The use of bone screws and their position is designed to enhance primary stability, even in critical bone conditions, avoiding implant stress shielding and allowing bone integration. 4 cases (2 men and 2 women) of acetabular customized implants were performed. Mean age at surgery was 51.5 years (range 25–72). Patients were reviewed clinically and radiographically at follow-up.


The Bone & Joint Journal
Vol. 99-B, Issue 5 | Pages 607 - 613
1 May 2017
Mäkinen TJ Abolghasemian M Watts E Fichman SG Kuzyk P Safir OA Gross AE

Aims. It may not be possible to undertake revision total hip arthroplasty (THA) in the presence of massive loss of acetabular bone stock using standard cementless hemispherical acetabular components and metal augments, as satisfactory stability cannot always be achieved. We aimed to study the outcome using a reconstruction cage and a porous metal augment in these patients. Patients and Methods. A total of 22 acetabular revisions in 19 patients were performed using a combination of a reconstruction cage and porous metal augments. The augments were used in place of structural allografts. The mean age of the patients at the time of surgery was 70 years (27 to 85) and the mean follow-up was 39 months (27 to 58). The mean number of previous THAs was 1.9 (1 to 3). All patients had segmental defects involving more than 50% of the acetabulum and seven hips had an associated pelvic discontinuity. . Results. Three failures were observed in two hips, both of which had undergone a previous resection of a tumour affecting the acetabulum. Other complications included a late arterial injury, a sciatic nerve palsy, a dislocation treated with a femoral revision, a deep infection treated with irrigation and debridement and a fracture of the greater trochanter treated conservatively. The mean Oxford Hip Score significantly increased from 13.9 (2 to 23) to 28.7 (13 to 38) (p < 0.00001). The mean vertical distance between the centre of rotation of the hip and its normal location decreased from 30 mm to 10 mm. Conclusions. Acceptable early survivorship can be achieved using this novel technique, but it may be unsuitable for use in patients who have previously undergone the resection of a tumour involving the acetabulum. Cite this article: Bone Joint J 2017;99-B:607–13


Orthopaedic Proceedings
Vol. 86-B, Issue SUPP_III | Pages 275 - 275
1 Mar 2004
Perka C Tohtz S
Full Access

Aim: The purpose of this study was to assess the results with use of an oval cementless acetabular component for revision total hip arthroplasty. Methods: 30 hips had an acetabular revision with an cementless oval acetabular component. No patient was lost to follow-up, but one died during the study period. All defects were classiþed during surgery according the AAOS classiþcation. All patients were evaluated radiographically and clinically and were followed for an average of thirty-six months (range, twenty four to fourty eight months). In 21 of the 30 hips no additional bone grafting was necessary. Results: There were 17 segmental defects (type 1), 12 combined defects (type III) and one case of pelvic discontinuity (type IV). At the time of follow-up, 27 (93.1%) of 29 cups were stable. One of the loosening affected the patient with pelvic discontinuity, the other a patient with a combined segmental defect including the medial wall. The average Harris Hip Score improved from 39 points (range: 15–73 points) preoperatively to 89 points (range 68–96 points) postoperatively. Complications included three dislocations without recurrency. The radiological follow-up examinations revealed good osteointegration of 27 implants. All postoperatively remaining defects were completly þlled in by bone at the follow up. Conclusion: The asymmetrical shape of the BOFOR enhanced the primary stabilty on the lateral columns with three point anchorage. We recommend this device when a patient has an oblong-shaped acetabular defect and the surgeon wants to correct an elevated hip center. However, the medial wall of the acetabulum (Kohlerñs line) should be intact


The Bone & Joint Journal
Vol. 97-B, Issue 10 | Pages 1338 - 1344
1 Oct 2015
te Stroet MAJ Keurentjes JC Rijnen WHC Gardeniers JWM Verdonschot N Slooff TJJH Schreurs BW

We present the results of 62 consecutive acetabular revisions using impaction bone grafting and a cemented polyethylene acetabular component in 58 patients (13 men and 45 women) after a mean follow-up of 27 years (25 to 30). All patients were prospectively followed. The mean age at revision was 59.2 years (23 to 82).

We performed Kaplan–Meier (KM) analysis and also a Competing Risk (CR) analysis because with long-term follow-up, the presence of a competing event (i.e. death) prevents the occurrence of the endpoint of re-revision.

A total of 48 patients (52 hips) had died or had been re-revised at final review in March 2011. None of the deaths were related to the surgery. The mean Harris hip score of the ten surviving hips in ten patients was 76 points (45 to 99).

The KM survivorship at 25 years for the endpoint ‘re-revision for any reason’ was 58.0% (95% confidence interval (CI) 38 to 73) and for ‘re-revision for aseptic loosening’ 72.1% (95% CI 51 to 85). With the CR analysis we calculated the KM analysis overestimates the failure rate with respectively 74% and 93% for these endpoints. The current study shows that acetabular impaction bone grafting revisions provide good clinical results at over 25 years.

Cite this article: Bone Joint J 2015;97-B:1338–44.


Orthopaedic Proceedings
Vol. 96-B, Issue SUPP_8 | Pages 59 - 59
1 May 2014
Schmalzried T
Full Access

Hemispheric, porous-ingrowth revision acetabular components (generally with multiple screw fixation) have demonstrated versatility and durability over 25 years. Jumbo cups (minimum diameter of 62mm in women, 66mm in men, or 10mm larger than the normal contra-lateral acetabulum) are utilised in the majority of revisions with acetabular bone loss, with or without bone grafting, or other augmentation. The popularity of jumbo cups is due to their relative ease of use and the reliability of the result. With up to 20 year follow-up, and failure defined as cup revision for aseptic loosening or radiographic evidence of loosening, implant survival was 97.3% (95% confidence interval [CI], 89.6% to 99.3%) at ten years and 82.8% (95% CI, 59% to 97.6%) at fifteen years. Instability is decreased in association with larger diameter bearings. Revisions associated with wear of non-crosslinked polyethylene increased in the second decade. Cross-linked polyethylene and ultra-porous materials will likely increase both the durability and the utility of jumbo cups


Orthopaedic Proceedings
Vol. 86-B, Issue SUPP_III | Pages 311 - 311
1 Mar 2004
Schreurs B Bolder S Gardeniers J Buma P Slooff T
Full Access

Aims: To test the outcome of acetabular revisons with impacted morsellized bone grafts and a cemented cup at a minimum follow-up of 15 years. Methods: Between 1979–1986 62 acetabular revisions (58 patients) were performed with impacted bone grafts and a cemented cup. Two cases (2 hips) were lost to FU. The average age at operation was 59.1 years. The indication was aseptic in 56 and septic loosening in 4 hips. Defects were AAOS-classiþed as ñcavitaryñ in 37 and ñcombinedñ 23 cases. Femoral-head allografts were used. Acetabular re-revisions were determined, the HHS obtained and radiographs analyzed. Results: Nineteen cases (20 hips) died within þfteen years after the operation, none had a re-revision. Eleven acetabular re-revisions were performed: 2 septic loosenings (3 and 6 years p.o.), 7 aseptic loosenings (6, 9, 11, 12, 13, 14, 14 year p.o.) and two for cup wear (12 and 17 yrs p.o.). The average HHS at follow-up was 86 (50–100). There were no additional radiographic failures. Using Kaplan-Meier analysis the survival with endpoint revision for any reason was 79% at 15 years and 71% at 20 years; for aseptic loosening of the cup 84% at 15 years and 84% at 20 years. Conclusions: This technique is attractive to reconstruct acetabular bone stock loss


Orthopaedic Proceedings
Vol. 86-B, Issue SUPP_I | Pages 68 - 68
1 Jan 2004
Bobak P Wroblewski BM Siney P Fleming P
Full Access

We report the result of 49 revisions for aseptic cup loosening using freeze-dried allografts.

We assessed the results according to the primary pathology, severity of bone loss, direction of socket migration before revision, method of bone grafting, socket position, graft incorporation and socket loosening.

Patient’s mean age at revision was 56 years 8 months. At a mean follow up of 7 years and 5 months four cups have been revised for aseptic loosening. Five sockets have migrated but remained stable while six showed full demarcation but have not migrated.

The other 34 remained stable and show radiographic evidence of graft incorporation.


The Journal of Bone & Joint Surgery British Volume
Vol. 70-B, Issue 5 | Pages 838 - 838
1 Nov 1988
Archibald D Protheroe K Stother I Campbell A


Orthopaedic Proceedings
Vol. 101-B, Issue SUPP_12 | Pages 36 - 36
1 Oct 2019
Bedard NA Brown TS Lewallen DG Trousdale RT Berry DJ Abdel MP
Full Access

Introduction. Many surgeons are reluctant to use a constrained liner at the time of acetabular component revision given concerns this might result in early acetabular component loosening. We hypothesized that with appropriate initial implant stabilization of highly porous acetabular components with supplemental screw fixation, constrained liners could be safely used at the time of acetabular revision. Methods. We retrospectively identified 148 revision total hip arthroplasties (THAs) where a constrained liner of one design was cemented into a newly placed highly porous acetabular component fixed with supplemental screws (mean 5 screws). Mean age at revision THA was 69 years, with 68% being female. The most common indications for revision were two-stage re-implantation (33%), recurrent dislocation (30%), and aseptic loosening (22% acetabular; 9% acetabular/femoral component). Mean follow-up was 8 years. Results. There were no failures at the bone-implant interface, and there were no revisions for aseptic loosening of the acetabular component. Furthermore, all acetabular components were bone ingrown on radiographic analysis. The 10-year survivorships free from any acetabular revision and free from any reoperation were 75% and 67%, respectively. Overall, 33 hips (22%) required revision or reoperation for infection/wound complications (n=12), dislocation (n=11), periprosthetic femur fracture (n=4), femoral loosening (n=3), and other (n=3). The 10-year survivorship free from dislocation was 84% overall, which was similar to the 85% 10-year survivorship free from dislocation for those specifically revised for instability (p=0.9). Conclusions. Implanting a constrained liner at the time of acetabular revision in high-risk patients resulted in no cases of aseptic acetabular component loosening in this large series. This is likely related to the fact that a highly porous acetabular component was utilized with a large number of supplemental screws in each case. Such information is valuable as these data favor a paradigm shift when compared to some traditionally-held tenets. For any tables or figures, please contact the authors directly


Orthopaedic Proceedings
Vol. 94-B, Issue SUPP_XXV | Pages 40 - 40
1 Jun 2012
Delport H Mulier M Gelaude F Clijmans T
Full Access

The number of joint revision surgeries is rising, and the complexity of the cases is increasing. In 58% of the revision cases, the acetabular component has to be revised. For these indications, literature decision schemes [Paprosky 2005] point at custom pre-shaped implants. Any standard device would prove either unfeasible during surgery or inadequate in the short term. Studies show that custom-made triflanged implants can be a durable solution with good clinical results. However, the number of cases reported is few confirming that the device is not in widespread use.

Case Report

A patient, female 50 yrs old, diagnosed having a pseudotumor after Resurfacing Arthroplasty for osteo-arthritis of the left hip joint. The revision also failed after 1 y and she developed a pelvic discontinuity. X-ray and Ct scans were taken and sent to a specialized implant manufacturer [Mobelife, Leuven, Belgium]. The novel process of patient-specific implant design comprises three highly automated steps.

In the first step, advanced 3D image processing presented the bony structures and implant components. Analysis showed that anterior column was missing, while the posterior column was degraded and fractured. The acetabular defect was diagnosed being Paprosky 3B. The former acetabular component migrated in posterolateral direction resulting in luxation of the joint. The reconstruction proposal showed the missing bone stock and anatomical joint location.

In the second step, a triflanged custom acetabular metal backing implant was proposed. The bone defect (35ml) is filled with a patient-specific porous structure which is rigidly connected to a solid patient-specific plate. The proposed implant shape is determined taking into account surgical window and surrounding soft tissues. Cup orientation is anatomically analyzed for inclination and anteversion. A cemented liner fixation was preferred (Biomet Advantage 48mm). Screw positions and lengths are pre-operatively planned depending on bone quality, and transferred into surgery using jig guiding technology (Materialise NV, Leuven, Belgium).

In the third step, the implant design was evaluated in a fully patient-specific manner in dedicated engineering (FEA) software. Using the novel automated CT-based methodology, patient-specific bone quality and thickness, as well as individualised muscle attachments and muscle and joint forces were included in the evaluation.

Implants and jig were produced with Additive Manufacturing techniques under ISO 13485 certification, using respectively Selective Laser Melting (SLM) techniques [Kruth 2005] in medical grade Ti6Al4V material, and the Selective Laser Sintering technique using medical grade epoxy monomer. The parts were cleaned ultrasonically, and quality control was performed by optical scanning [Atos2 scanning device, GOM Intl. AG, Wilden, Switzerland]. Sterilization is performed in the hospital.

CONCLUSION

A unique combination of advanced 3D planning, patient-specific designed and evaluated implants and drill guides is presented. This paper illustrates, by means of a clinical case, the novel tools and devices that are able to turn reconstruction of complex acetabular deficiencies into a reliable procedure.


Orthopaedic Proceedings
Vol. 99-B, Issue SUPP_3 | Pages 37 - 37
1 Feb 2017
Beckmann N Jaeger S Janoszka M Klotz M Schwarze M Bitsch R
Full Access

Introduction

Revision Total Hip Arthroplasties (THA) have a significantly higher failure rate than primary THA's and the most common cause is aseptic loosening of the cup. To reduce this incidence of loosening various porous metal implants with a rough surface and a porous architecture have been developed which are said to increase early osteointegration. However, for successful osteointegration a minimal micromotion between the implant and the host bone (primary stability) is beneficial. It has not been previously determined if the primary stability for the new Gription® titanium cup differs from that of the old Porocoat® titanium cup.

Material and Methods

In 10 cadaveric pelvises, divided into 20 hemipelvises, bilateral THA's were performed by an experienced surgeon (RGB) following the implant manufacturer's instructions and with the original surgical instruments provided by the company. In randomized fashion the well established Porocoat® titanium implant was implanted on one side of each each hemipelvis whereas on the corresponding opposite side the modified implant with a Gription® coating was inserted. Radiographs were taken to confirm satisfactory operative results. Subsequently, the hemipelvis and cups were placed in a biomechanical testing machine and subjected to physiological cyclic loading.

Three-dimensonal loading corresponded to 30% of the load experienced in normal gait was imposed reflecting the limited weight bearing generally prescribed postoperatively. The dynamic testing took place in a multi-axial testing machine for 1000 cycles. Relative motion and micromotion were quantified using an optical measurement device (Pontos, GOM mbh, Braunschweig, Germany). Statistical evaluation was performed using the Wilcoxon signed-rank test.