Tysonstensgaard3040

043) but not cartilage injury (P=0.186). Residents in the spaced retraining group decreased their task completion time (163.2 ± 23.9 s) whereas the task time in the control group increased (351.3 ± 25.5 s). The same pattern was found with the camera path length. Conclusions Implementing a spaced retraining schedule in 1 week resulted in a reduced task completion time and camera path length, but no significant reduction in cartilage injury. It appears that introducing a spaced retraining schedule in order to retain arthroscopic skills acquired through massed learning may be advantageous.Purpose To evaluate the 3D ZTE MRI technique and compare with 3D CT for the assessment of the glenoid bone. Methods ZTE MRI using multiple resolutions and multislice CT was performed on six shoulder specimens before and after creation of glenoid defects and ten glenohumeral instability patients. Two musculoskeletal radiologists independently generated 3D volume rendered images of the glenoid en face. Postprocessing times and glenoid widths were measured. Intermodality and interrater agreement was assessed. Results Intraclass correlation coefficients (ICCs) for intermodality assessment showed almost perfect agreement for both readers, ranging from 0.949-0.991 for the ex vivo study and 0.955-0.987 for the in vivo patients. Excellent interobserver agreement for both the ex vivo (ICCs ≥ 0.98) and in vivo (ICCs ≥ 0.92) studies was demonstrated. For the ex vivo study, Bland-Altman analyses for CT vs MRI demonstrated a mean difference of 0.6-1 mm at 1.0 mm3 MRI resolution, 0.3-0.6 mm at 0.8 mm3 MRI resolution, and 0.3-0.6 mm at 0.6 mm3 MRI resolution for both readers. For the in vivo study, Bland-Altman analyses for CT vs MRI demonstrated a mean difference of 0.6-0.8 mm at 1.0 mm3 MRI resolution, 0.5-0.6 mm at 0.8 mm3 MRI resolution, and 0.4-0.8 mm at 0.7 mm3 MRI resolution for both readers. Mean post-processing times to generate 3D images of the glenoid ranged from 32-46 seconds for CT and 33-64 seconds for ZTE MRI. Conclusions 3D ZTE MRI can potentially be considered as a new technique to determine glenoid width and can be readily incorporated into the clinical workflow.Purpose To elucidate whether the presence or location of ulnar styloid fractures (USFs) in adults with distal radius fracture (DRF) can predict the presence of traumatic triangular fibrocartilage complex (TFCC) injuries. Methods From 2005 to 2018, an arthroscopic evaluation was performed to detect TFCC injuries associated with DRF. The presence and location of USFs were evaluated using computed tomography. TFCC injuries were classified in accordance with Palmer's classification. All wrists were divided into Group A (DRF without USF) and Group B (DRF with USF). The incidence of TFCC injuries in the two groups was compared. Group B was then divided into two subgroups in accordance with the USF location the tip or middle fracture subgroup, and the base fracture subgroup. Data were analyzed with significance set at p less then .05. Results One hundred thirty-eight patients were enrolled in this study. Group A included 42 wrists in 42 patients, while Group B included 96 wrists in 96 patients. There were significant differences between the two groups regarding the incidence of traumatic TFCC injuries (p=0.036) and TFCC 1B injury (p=0.002), though there were no differences between the two groups regarding age, sex, injured side, direction of displacement, and type of DRF. Within Group B, the tip and middle fracture subgroup included 37 wrists in 37 patients, while the base fracture group included 59 wrists in 59 patients; significant difference was observed between the two subgroups regarding the incidences of TFCC 1B injuries (p=0.044). Conclusions The presence of USF associated with DRF predicted the presence of frequently occurring traumatic TFCC injury and TFCC 1B injury. Moreover, the location of USFs was a predictive factor for TFCC 1B injury in adults with DRF. On the other hand, traumatic TFCC injury had occurred in adults with DRF, regardless of the presence of USF.Purpose To compare patient functional scores and rates of achieving Minimum Clinical Important Differences (MCID) and Patient Acceptable Symptomatic State (PASS) between patients with a hypotrophic labrum to those with a normal labrum width at a minimum 1-year follow-up from arthroscopic treatment of Femoroacetabular Impingement Syndrome (FAIS). eIF inhibitor Methods Data from consecutive patients who underwent primary hip arthroscopy between November 2015 and July 2018 for the treatment of FAIS were analyzed. Baseline demographic data, preoperative patient reported outcome measures (PROMs), and minimum 1-year PROMs including Hip Outcome Score-Activities of Daily Living (HOS-ADL), HOS-Sports Subscale (HOS-SS), modified Harris Hip Score (mHHS), international Hip Outcome Tool 12 questions (iHOT-12), and visual analog scale (VAS) for pain and satisfaction were recorded. The labrum size was determined using an arthroscopic probe at the 12 to 2 o'clock position with a hypotrophic labrum being defined as 0.05 for all). Conclusions Patients with an intraoperative finding of labral hypotrophy achieve 1-year meaningful clinical outcome at the same rate as those with normal labral width following arthroscopic labral repair.Canine parvovirus (CPV) non-structural protein-1 (NS1) plays crucial roles in CPV replication and transcription, as well as pathogenic effects to the host. However, the mechanism was not fully understood. Lack of NS1 antibody is one of the restricting factors for NS1 function investigation. To prepare NS1 monoclonal antibody (mAb), the NS1 epitope (AA461 ~ AA650) gene was amplified by PCR, and inserted into pGEX-4T-1vector to construct the prokaryotic expression vector of GST-tag-fused NS1 epitope gene. The NS1 fusion protein was expressed in E. coli, and purified with GSH-magnetic beads, and then used to immunize BALB/c mice. The mouse splenic lymphocytes were isolated and fused with myeloma cells (SP 2/0) to generate hybridoma cells. After several rounds of screening by ELISA, a hybridoma cell clone (1B8) stably expressing NS1 mAb was developed. A large amount of NS1 mAb was prepared from mouse ascites fluid. The isotype of NS1 mAb was identified as IgG1, which can specifically bind NS1 protein in either CPV-infected cells or NS1 vector-transfected cells, indicating the NS1 mAb is effective in detecting NS1 protein.