Practical management of new oral anticoagulants after total hip or total knee arthroplasty.

Within the past 5 years, the oral anticoagulants rivaroxaban, apixaban, and dabigatran etexilate have been approved for the prevention of venous thromboembolism in adult patients after elective hip or knee arthroplasty in the European Union and many other countries worldwide. These agents differ from the previously available anticoagulants because they selectively and directly inhibit a single factor in the coagulation cascade-rivaroxaban and apixaban inhibit Factor Xa, and dabigatran inhibits Factor IIa (thrombin)-potentially enhancing the predictability of their anticoagulant effect. Currently, although some guidelines provide recommendations for the use of rivaroxaban, dabigatran etexilate, and apixaban in clinical practice, there are still questions regarding the optimal practical management of patients receiving these agents. This article briefly reviews the practical limitations associated with conventional anticoagulants, discusses potential issues with the practical management of the newer oral anticoagulants, and provides clinical experience from a single institution where rivaroxaban and dabigatran etexilate have been used within their approved indications.

[Non-traumatic anterior knee dislocation in a patient with osteoarthritis of the knee]. / Atraumatische anteriore Kniegelenksluxation bei Pangonarthrose.

Complete knee dislocation is a rare and severe injury and usually follows high-energy trauma. Non-traumatic knee dislocations are exceedingly rare, while severe overweight appears to be the main cause of the knee dislocation. We here report on a spontaneous knee dislocation in a patient with severe osteoarthritis of the left knee. A 68-year-old woman was admitted to our hospital for an elective total knee replacement. One year prior to admission, a planned joint replacement was not performed due to an existing ulcus cruris. After healing of the ulcus cruris, the patient presented with progressive pain and instability of the left knee without any trauma. The clinical examination showed a multidirectional instability of the left knee with a restricted range of motion (ROM) with 0-0-40 degrees for extension and flexion. The performed radiological examination revealed an anterior knee dislocation of the left knee. Intraoperative findings suggest a non-traumatic aetiology. We suspect that osteoarthritis of the left knee has caused the dislocation. Therefore, we recommend, even in usually "harmless" osteoarthritis, close clinical and radiological follow-up examinations to detect and treat possible complications.

[Revision of unconstrained total knee arthroplasty - a technical analysis]. / Oberflächenersatzwechsel in der Knieendoprothetik - eine intraoperative Ursachenanalyse.

BACKGROUND: Total knee arthroplasty (TKA) revisions are increasing due to the rising numbers of primary cases, younger patients and an aging population. The technical demand of these procedures is incomparable higher than in primary cases. Also the expectable clinical results are inferior. Measures to improve the clinical results are desireable. PATIENTS/MATERIAL: 203 unconstrained knee arthroplasties were explanted in 2009 in a single centre. In 150 cases those were TKAs. Fractures were excluded. These cases were analysed with special attention to the reason for the failure. Clinical and radiological data were included. RESULTS: Survival of revised implants was in the mean 55 months (range: 0,5-125 months). In 46 cases components showed an aseptic loosening (30.7 %), 37 TKAs were unstable (24.7 %), in 26 cases stiffness was detected (17.3 %), and nine misplaced TKA components (five femoral, two tibial, two combined; total 6 %) as well as three broken inlays (2 %) were encountered. In 25 cases deep infection was observed (16.7 %) and four patients complained of an unspecific anterior knee pain (2.6 %). Three TKAs were removed for a two-staged procedure. In five cases an inlay exchange was performed and in another five cases a conversion from cruciate retaining to posterior stabilised state was performed. In 60 cases a rotating hinged TKA was implanted (40 %) and in 42 a pure hinge (28 %). In 45 cases a condylar constrained TKA system (CCK, 30 %) was used. Range of movement increased with the procedure. Plain radiographs were inferior in detecting all loosening in advance. CONCLUSION: This study demonstrated that in more than one third of the cases the revision could have been avoided and was due to technical errors during the primary procedure. Infection and arthrofibrosis were besides unspecific complaints less often observed than is described in the literature. This study supports the high demand on the technical issues during the primary procedure which should be conducted by experienced surgeons. Registry data from Germany should allow the provision of more specific information in the future.

[Histopathologic diagnostics in endoprosthetics: periprosthetic neosynovialitis, hypersensitivity reaction, and arthrofibrosis]. / Histopathologische Diagnostik in der Endoprothetik: Periprothetische Neosynovialitis, Hypersensitivitätsreaktion und Arthrofibrose.

The durability of endoprosthetic implants of the large joints has increased over the last decades. North American studies have shown a 10-year durability of 94% for prosthetic hip implants, and European studies have shown 10-year durabilities of 88-95%. Pathologists differentiate three etiological disease patterns for the"pathology of endoprosthetics" that lead to reduction of implant durability: 1) periprosthetic particle disease (aseptic loosening), 2) infection, and 3) arthrofibrosis. Four types of neosynovitis/periprosthetic membrane have been determined in a consensus classification: particle-induced type (type I), with a mean prosthesis durability (MPD) of 12 years; infectious type (type II), MPD 2.5 years; combined type (type III), MPD 4.2 years; and indeterminate type (type IV), MPD 5.5 years. There are three histopathologic degrees of arthrofibrosis; grade 1 always needs clinical information for diagnosis, whereas grades 2 and 3 are distinct histopathologic entities.

Cementless primary total hip arthroplasty with a tapered, proximally porous-coated titanium prosthesis: a 4- to 8-year retrospective review.

A consecutive series of 100 primary total hip arthroplasties were performed at a single institution on 87 patients using a cementless collared titanium press-fit stem. Of patients, 87% received a hemispheric porous-coated cup, and 13% received a nonmodular titanium fibermesh press-fit cup. Ten hips were excluded from the longer-term evaluation: 6 were lost to follow-up, and 4 patients were deceased. Ninety hips, with an average follow-up of 81 +/- 12 months, were retrospectively reviewed. The average postoperative hip score was 94, compared with an average preoperative hip score of 42. No postoperative infections were observed, but there were 2 cases of postoperative dislocation (2%) and 1 case of thigh pain (1%) at last follow-up. There were 2 revisions, both for cup failures. There were no femoral component loosenings or revisions. There was no evidence of stem subsidence or instability. These midterm results are encouraging with this stem design.