In a randomised prospective study, 20 patients with intra-articular fractures of the distal radius underwent arthroscopically- and fluoroscopically-assisted reduction and external fixation plus percutaneous pinning. Another group of 20 patients with the same fracture characteristics underwent fluoroscopically-assisted reduction alone and external fixation plus percutaneous pinning. The patients were evaluated clinically and radiologically at follow-up of 24 months. The Disabilities of the Arm, Shoulder, and Hand (DASH) questionnaire and modified Mayo wrist score were used at 3, 9, 12 and 24 months postoperatively. In the arthroscopically- and fluoroscopically-assisted group, triangular fibrocartilage complex tears were found in 12 patients (60%), complete or incomplete scapholunate ligament tears in nine (45%), and lunotriquetral ligament tears in four (20%). They were treated either arthroscopically or by open operation. Patients who underwent arthroscopically- and fluoroscopically-assisted treatment had significantly better supination, extension and flexion at all time points than those who had fluoroscopically-assisted surgery. The mean DASH scores were similar for both groups at 24 months, whereas the difference in the mean modified Mayo wrist scores remained statistically significant. Although the groups are small, it is clear that the addition of arthroscopy to the fluoroscopically-assisted treatment of intra-articular distal radius fractures improves the outcome. Better treatment of associated intra-articular injuries might also have been a reason for the improved outcome.
The aim of this prospective study is to investigate the effectiveness of a new method for arthroscopic all-inside meniscus repair (Clearfix meniscal screw system-Innovasive Devices Inc.).This system consists of delivery cannulae,screw implants and a screw driver.After tear debridement a screw is located on the driver and passed through the cannula to the insertion site, holding the two sides of the tear together under linear compression.In this study, 46 patients (48 repairs)are included, mean age 32,7 years,with a follow-up ranging from 6 to 48 months (average 18,8 months).Only longitudinal lesions in the red/red zone or red/white areas were repaired. Ligament stabilizing procedures were done in 39 patients (84,8%) who had ACL deficient knees,.Thirty-four (71%) injuries were considered chronic (injury to repair time more than 4 weeks) and 14 (29%) injuries were considered acute (injury to repair time less than 4 weeks).The evaluation of the results was based on the clinical examination,the “OAK ” knee evaluation scheme and the MRI.Criteria for clinical success included absence of joimt line tenderness, swelling and a negative Mc Murray test.Thirteen out of 48 repairs (27%) were considered as failures according to the above mentioned criteria.The average time for the procedure was 8 minutes.Postoperatively there were no complications directly associated with the device.Magnetic resonance imaging, however,showed a persisting grade III and IV lesion in 72,8% of the patients (n=35) according to Reicher classification. Though the system offers two main advantages,that is the absence of serious complications and the reduced operative time, the failure rate in this study is quite high. This clinical study is in agreement with the recent experimental studies referring to the limited pull-out strength of this device.