y outcomeRivaroxaban was associated with a considerable reduction in riskof symptomatic venous thromboembolism compared withenoxaparin. Compared with enoxaparin, neitherdabigatrannor apixabanreduced the danger of symptomatic venousthromboembolism.No evidence of statistical heterogeneity for symptomatic venousthromboembolism was discovered among studies comparingrivaroxaban or apixaban Celecoxib with enoxaparin. Even so, there wasevidence of statistical heterogeneity for symptomatic venousthromboembolism among the dabigatran trials. The source of heterogeneity could not be identified afterinvestigating dabigatran every day dose, enoxaparin regimen, typeof surgery, adjudicating committee, or the presence of an outlierstudy. The effect on symptomatic venous thromboembolismcompared with enoxaparin was comparable with dabigatran dosesof 220 mgand 150 mg.
After including symptomatic venous thromboembolism eventsthat occurred throughout follow-up, the results had been comparable thanthose of the main analysis:rivaroxaban, dabigatran, and apixabancompared with enoxaparin.Secondary efficacy outcomesRivaroxaban was associated with a considerably lower danger ofsymptomatic deep vein thrombosis than was Celecoxib enoxaparin,whereas this trend was not considerable for symptomaticpulmonary embolism. Rivaroxabanalso decreased the danger for total venous thromboembolism orall cause deathas nicely as for majorvenous thromboembolism or venous thromboembolism relateddeath.Compared with enoxaparin, dabigatran was not related witha diverse danger of symptomatic deep vein thrombosisor pulmonary embolism.
Dabigatran was associated with a trend towards ahigher danger of total venous thromboembolism or all cause deaththan enoxaparinand Alogliptin a comparable riskof significant venous thromboembolism or venous thromboembolismrelated death. The danger of totalvenous HSP thromboembolism or all cause death was comparable betweendabigatran 220 mg and enoxaparinbut it was greater with the dabigatran 150 mg dose than withenoxaparin. Big venousthromboembolism or venous thromboembolism associated deathdid not differ considerably among the dabigatran 220 mg dailydose v enoxaparinor among thedabigatran 150 mg every day dose v enoxaparin.Apixaban decreased the danger of symptomatic deep veinthrombosis compared with enoxaparinbut was associated with a numerical improve in casesof pulmonary embolismwith borderline heterogeneity.
The results for pulmonary embolism werehomogeneous within the two pivotal studies on total kneereplacement surgery, in which the danger ofsymptomatic pulmonary embolism with apixaban wassignificantly greater than Alogliptin that with enoxaparin. On the contrary, apixaban was related witha lower danger of total venous thromboembolism or all cause deathand a trend towards a lower danger ofmajor venous thromboembolism or venous thromboembolismrelated deaththan enoxaparin..Main safety outcomeRivaroxaban was associated with a considerable improve in riskof clinically relevant bleeding. Dabigatrandid not show a considerable improve compared with enoxaparin. The danger was comparable in thecomparison of dabigatran 220 mg with enoxaparinand dabigatran 150 mg with enoxaparin. On the contrary, apixaban was associatedwith a considerably decreased danger of clinically relevant bleedingcompared with enoxaparin.
Noevidence of statistical heterogeneity was discovered for this outcomeamong studies comparing rivaroxaban, dabigatran, or apixabanwith enoxaparin.Secondary safety outcomesRivaroxaban was associated with a non-significant trend towardsa greater danger of significant bleeding than was enoxaparinandclinically relevant non-major bleeding. Compared with enoxaparin, dabigatran was associatedwith Celecoxib a comparable danger of significant bleedingand a non-significant trend towards a greater danger of clinicallyrelevant non-major bleeding.Apixaban showed a non-significant trend towards a low danger ofmajor bleeding than did enoxaparin,which was in the limit of statistical significance for clinicallyrelevant non-major bleeding. Nosignificant trends had been discovered in danger of death among the newanticoagulants and enoxaparin.
.Net clinical endpointNo statistically considerable differences had been discovered among thenew anticoagulants and enoxaparin on the net clinical endpoint. No evidence of statistical Alogliptin heterogeneity wasfound among studies.Major outcomes by sort of surgeryNo statistically considerable interaction of the sort of surgerywas discovered for symptomaticvenous thromboembolism, clinically relevant bleeding, and netclinical endpoint. Overall, the net clinical benefit ofthe new anticoagulants tended to be much better in total kneereplacement surgery than in total hip replacement surgery.Indirect comparisonsRivaroxaban tended to be associated with the lowest danger forsymptomatic venous thromboembolism, whereas apixabanseemed to achieve the lowest danger for clinically relevant bleeding. No differences had been discovered among treatment options onthe net clinical outcome.Absolute difference in events per 1000patients treatedThe numbers of symptomatic venous thromboembolic eventsavoided per 1000 patien
Tuesday, April 16, 2013
Grubby Facts About Alogliptin Celecoxib Revealed
Subscribe to:
Post Comments (Atom)
No comments:
Post a Comment