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1.
Arch Orthop Trauma Surg ; 127(7): 557-61, 2007 Sep.
Article in English | MEDLINE | ID: mdl-17106714

ABSTRACT

INTRODUCTION: Nonsteroidal anti-inflammatory drugs (NSAIDs) prevent heterotopic ossification but gastrointestinal complaints are frequently. Selective cyclooxygenase-2 (COX-2) inhibiting NSAID produce less gastrointestinal side effects. PATIENTS AND METHODS: A prospective two-stage study design for phase 2 clinical trials with 42 patients was used to determine if rofecoxib (a COX-2 inhibitor) 50 mg oral for 7 days prevents heterotopic ossification. A cemented primary THA was inserted for osteoarthroses. After 6 months heterotopic bone formation was assessed on AP radiographs using the Brooker classification. RESULTS: No heterotopic ossification was found in 81% of the patients, 19% of the patients had Brooker grade 1 ossification. CONCLUSION: Using a two-stage study design for phase 2 clinical trials, a 7-day treatment of a COX-2 inhibitor (rofecoxib) prevents effectively the formation of heterotopic ossification after cemented primary total hip arthroplasty.


Subject(s)
Arthroplasty, Replacement, Hip/adverse effects , Cyclooxygenase 2 Inhibitors/therapeutic use , Lactones/therapeutic use , Ossification, Heterotopic/prevention & control , Sulfones/therapeutic use , Adult , Aged , Aged, 80 and over , Female , Follow-Up Studies , Humans , Male , Middle Aged , Prospective Studies , Research Design
2.
Spine (Phila Pa 1976) ; 29(17): 1893-9; discussion 1900, 2004 Sep 01.
Article in English | MEDLINE | ID: mdl-15534411

ABSTRACT

STUDY DESIGN: Fifty-two patients with degenerative disc disease underwent single- or double-level anterior lumbar interbody fusion with SynCage and additional posterior fixation as treatment for degenerative disc disease and were prospectively followed for 4 years. OBJECTIVES: To test the clinical performance of anterior lumbar interbody fusion with SynCage, with emphasis on the safety and efficacy of the surgical procedure and the ability to restore anatomy and fuse the motion segment. SUMMARY OF BACKGROUND DATA: Anterior lumbar interbody fusion using femoral allograft and/or autologous bone has a high complication rate. With cage technology, some of these complications can be avoided. The design characteristics of the SynCage offer advantages in restoring and maintaining intervertebral height and restoration of lumbar lordosis. METHODS: Thirty-three patients underwent single-level and 19 patients double-level anterior lumbar interbody fusion with SynCage and additional posterior fixation (translaminar screws, n = 32 or pedicle screws, n = 10). Radiologic and functional results (VAS and Oswestry score) were evaluated. RESULTS: Intervertebral height was corrected from an average of 8.7 to 17.6 mm. Lordosis of the fused segment was significantly increased (average 10.6 degrees for the fused segment and 8 degrees for lumbosacral lordosis). After 2 years, there was radiologic evidence for fusion in 70 of 71 (98.6%) levels. Functional scores showed a significant improvement in pain and function up to the 2-year follow-up observation. At the 4-year follow-up observation, there was some loss of the initial improvement in VAS and Oswestry scores. Despite this loss, they remained significantly better than the preoperative scores. CONCLUSIONS: Anterior lumbar interbody fusion with SynCage and additional posterior fixation is a safe and effective procedure. Intervertebral height is corrected, and lumbosacral lordosis is restored. An initial improvement in VAS and Oswestry scores is partly lost at the 4-year follow-up observation, but 4-year results are still significantly better than the preoperative scores.


Subject(s)
Internal Fixators , Intervertebral Disc Displacement/surgery , Lumbar Vertebrae/surgery , Spinal Fusion/methods , Adult , Bone Screws , Bone Transplantation , Equipment Design , Female , Follow-Up Studies , Humans , Intervertebral Disc Displacement/complications , Low Back Pain/etiology , Lumbar Vertebrae/diagnostic imaging , Male , Middle Aged , Pain Measurement , Postoperative Complications , Prospective Studies , Radiography , Recurrence , Sacrum , Severity of Illness Index , Spinal Fusion/instrumentation , Treatment Outcome
3.
Clin Orthop Relat Res ; (421): 143-50, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15123939

ABSTRACT

In a one-surgeon study the clinical and radiographic results of 30 cementless bipolar hip prostheses in 24 patients younger than 55 years were evaluated. Eleven noncoated prostheses (Noncoated Group) and 19 hydroxyapatite-coated prostheses (Hydroxyapatite Group) were compared after a mean followup of 10.4 years. The Harris hip score increased from a preoperative average of 41 points to 76 points at final followup (Noncoated Group, 70 points; Hydroxyapatite Group, 80 points). Thigh or groin pain was present in 15 patients (16 hips) (Noncoated Group, 55%; Hydroxyapatite Group, 53%). Radiographically, subsidence was the major problem at the noncoated prostheses (Noncoated Group, 91%; Hydroxyapatite Group, 5%), whereas osteolysis mainly was seen at the hydroxyapatite-coated prostheses (Noncoated Group, 18%; Hydroxyapatite Group, 89%). The obtained aseptic revision rate of 27% (Noncoated Group, 27%; Hydroxyapatite Group, 26%) is too high to use this implant in young patients. The large amounts of polyethylene wear debris generated by the bipolar system play an important role in this limited success. In the initially well-fixed hydroxyapatite-coated prostheses the sealing effect of a hydroxyapatite coating creates high concentrations of polyethylene in the limited joint space, resulting in massive proximal femoral osteolysis. Consequently, a hydroxyapatite coating introduces a new failure mechanism. Therefore, hydroxyapatite does not improve the outcome of a cementless bipolar hemiarthroplasty in the long-term.


Subject(s)
Arthroplasty, Replacement, Hip , Coated Materials, Biocompatible , Durapatite , Hip Prosthesis , Osteoarthritis, Hip/surgery , Prosthesis Failure , Adolescent , Adult , Female , Follow-Up Studies , Humans , Male , Middle Aged , Osteoarthritis, Hip/diagnostic imaging , Prospective Studies , Prosthesis Design , Radiography , Time Factors , Treatment Outcome
4.
Arch Orthop Trauma Surg ; 122(1): 17-23, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11995874

ABSTRACT

Surgical treatment of giant cell tumor of bone has always been a difficult problem because of its local aggressive behavior. Oncologic results and functional outcome are reported here in a retrospective study of 36 patients, treated by various surgical procedures. The average age at the time of diagnosis was 34 years, and the median follow-up period was 7 years. Twenty-three patients were treated by intralesional excision with local adjuvant therapy, and 11 patients by extralesional excision. Two patients received radiotherapy only. Seven local tumor recurrences (30%) were encountered after intralesional procedures, while local tumor control was the rule after extralesional excision. Intralesional excision with local adjuvant therapy resulted in significantly better functional results compared with extralesional excision. Wide excision was associated with a poor functional outcome and marginal excision with a good functional outcome. For the treatment of giant cell tumor of bone, intralesional excision with local adjuvant therapy is recommended because of a good functional outcome. When applying cryosurgery as the local adjuvant, more vigorous freezing may be necessary to improve local tumor control.


Subject(s)
Bone Neoplasms/diagnosis , Bone Neoplasms/surgery , Cryosurgery/methods , Giant Cell Tumors/diagnosis , Giant Cell Tumors/surgery , Orthopedic Procedures/methods , Adolescent , Adult , Biopsy, Needle , Bone Neoplasms/mortality , Child , Disease-Free Survival , Female , Follow-Up Studies , Giant Cell Tumors/mortality , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Neoplasm Staging , Recovery of Function , Retrospective Studies , Survival Rate , Tomography, X-Ray Computed , Treatment Outcome
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