9 research outputs found
There’s life in the old dog yet: vitamin C as a therapeutic option in endothelial dysfunction
Mineralisation patterns in the subchondral bone plate of the humeral head
PURPOSE: Pathologic changes of the glenohumeral joint, like a long-standing overloading or an accident often lead to severe glenohumeral osteoarthritis, and a glenohumeral joint replacement could be necessary. Joint instability and glenoid loosening are the most common post-operative complications, which can be caused by eccentric loading of the glenoid, if the humeral head is malcentered. If these malcentered cases could be identified pre-operatively, the pathologic position of the humeral head could be fixed intra-operatively and complication may be prevented. Computed tomography osteoabsorptiometry (CT-OAM) is a useful method to determine the distribution of mineralisation in the subchondral bone as a marker for the long-term loading history of a joint. The objective of this study was to gain information about the mineralisation distribution in the subchondral bone plate of the humeral head. METHODS: By the use of CT-OAM, the distribution of the subchondral mineralisation of 69 humeral heads was investigated and groups of mineralisation patterns were built. To evaluate if differences in age exist, the mean values of the two groups were compared using t test. RESULTS: 49 humeral heads (71% of 69 specimens) showed bicentric subchondral mineralisation patterns with ventral and dorsal maxima, 20 humeral heads (29% of 69 specimens) could be classified as monocentric with a centro-dorsal maximum. We found no statistical significant difference between the age of the monocentric and the bicentric group on a significance level of 95%. CONCLUSION: We could show that stress distribution at the humeral head is typically bicentric with a ventral and dorsal maximum. However, other mineralisation patterns may occur under pathologic circumstances. The pre-operative identification of such cases by the use of CT-OAM could help to improve the post-operative results in shoulder surgery
Insufficient sensitivity of joint aspiration during the two-stage exchange of the hip with spacers
Improved pre-operative diagnostic accuracy for low-grade prosthetic joint infections using second-generation multiplex Polymerase chain reaction on joint fluid aspirate
Procedure for single-stage implant retention for chronic periprosthetic infection using topical degradable calcium-based antibiotics
Oral rivaroxaban for the treatment of symptomatic pulmonary embolism.
BACKGROUND:
A fixed-dose regimen of rivaroxaban, an oral factor Xa inhibitor, has been shown to be as effective as standard anticoagulant therapy for the treatment of deep-vein thrombosis, without the need for laboratory monitoring. This approach may also simplify the treatment of pulmonary embolism.
METHODS:
In a randomized, open-label, event-driven, noninferiority trial involving 4832 patients who had acute symptomatic pulmonary embolism with or without deep-vein thrombosis, we compared rivaroxaban (15 mg twice daily for 3 weeks, followed by 20 mg once daily) with standard therapy with enoxaparin followed by an adjusted-dose vitamin K antagonist for 3, 6, or 12 months. The primary efficacy outcome was symptomatic recurrent venous thromboembolism. The principal safety outcome was major or clinically relevant nonmajor bleeding.
RESULTS:
Rivaroxaban was noninferior to standard therapy (noninferiority margin, 2.0; P=0.003) for the primary efficacy outcome, with 50 events in the rivaroxaban group (2.1%) versus 44 events in the standard-therapy group (1.8%) (hazard ratio, 1.12; 95% confidence interval [CI], 0.75 to 1.68). The principal safety outcome occurred in 10.3% of patients in the rivaroxaban group and 11.4% of those in the standard-therapy group (hazard ratio, 0.90; 95% CI, 0.76 to 1.07; P=0.23). Major bleeding was observed in 26 patients (1.1%) in the rivaroxaban group and 52 patients (2.2%) in the standard-therapy group (hazard ratio, 0.49; 95% CI, 0.31 to 0.79; P=0.003). Rates of other adverse events were similar in the two groups.
CONCLUSIONS:
A fixed-dose regimen of rivaroxaban alone was noninferior to standard therapy for the initial and long-term treatment of pulmonary embolism and had a potentially improved benefit-risk profile. (Funded by Bayer HealthCare and Janssen Pharmaceuticals; EINSTEIN-PE ClinicalTrials.gov number, NCT00439777.)