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Apixaban Reduces Hospitalizations in Patients With Venous Thromboembolism: An Analysis of the Apixaban for the Initial Management of Pulmonary Embolism and Deep‐Vein Thrombosis as First‐Line Therapy (AMPLIFY) Trial

BACKGROUND: In the Apixaban for the Initial Management of Pulmonary Embolism and Deep‐Vein Thrombosis as First‐Line Therapy (AMPLIFY) trial, apixaban was noninferior to enoxaparin/warfarin in preventing recurrent symptomatic venous thromboembolism (VTE) or venous thromboembolism–related death, with...

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Autores principales: Liu, Xianchen, Johnson, Margot, Mardekian, Jack, Phatak, Hemant, Thompson, John, Cohen, Alexander T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4845271/
https://www.ncbi.nlm.nih.gov/pubmed/26627879
http://dx.doi.org/10.1161/JAHA.115.002340
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author Liu, Xianchen
Johnson, Margot
Mardekian, Jack
Phatak, Hemant
Thompson, John
Cohen, Alexander T.
author_facet Liu, Xianchen
Johnson, Margot
Mardekian, Jack
Phatak, Hemant
Thompson, John
Cohen, Alexander T.
author_sort Liu, Xianchen
collection PubMed
description BACKGROUND: In the Apixaban for the Initial Management of Pulmonary Embolism and Deep‐Vein Thrombosis as First‐Line Therapy (AMPLIFY) trial, apixaban was noninferior to enoxaparin/warfarin in preventing recurrent symptomatic venous thromboembolism (VTE) or venous thromboembolism–related death, with significantly less bleeding. This analysis evaluated the effects of apixaban versus enoxaparin/warfarin on all‐cause hospitalizations during AMPLIFY. METHODS AND RESULTS: Of the 5365 patients included, 2676 received apixaban and 2689 received enoxaparin/warfarin. All‐cause hospitalizations during the treatment period after the index event were captured using dedicated case report forms. Outcomes included all‐cause hospitalizations and time from randomization to first hospitalization. Patients were censored at death, loss to follow‐up, or end of study, whichever came first. Treatment effects were assessed using Cox proportional hazards regression models. During the treatment period after the index event, 343 patients were hospitalized at least once: 153 (5.72%) in the apixaban group and 190 (7.07%) in the enoxaparin/warfarin group. Compared with enoxaparin/warfarin, apixaban significantly reduced all‐cause hospitalizations (hazard ratio 0.804, 95% CI=0.650–0.995, P=0.045). All‐cause hospitalization rates within the first 30 days after the index event were 2.28% and 3.35% in the apixaban and enoxaparin/warfarin groups, respectively (hazard ratio 0.676, 95% CI=0.488–0.935, P=0.018). For all patients, the average per‐patient estimated mean length of hospital stay was also shorter with apixaban than enoxaparin/warfarin (0.57 days versus 1.01 days, P<0.0001). CONCLUSIONS: Apixaban significantly reduced all‐cause hospitalizations versus enoxaparin/warfarin, and shortened the length of hospital stay in patients with acute venous thromboembolism. CLINICAL TRIAL REGISTRATION: URL: https://Clinicaltrials.Gov/. Unique identifier: NCT00643201.
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spelling pubmed-48452712016-04-27 Apixaban Reduces Hospitalizations in Patients With Venous Thromboembolism: An Analysis of the Apixaban for the Initial Management of Pulmonary Embolism and Deep‐Vein Thrombosis as First‐Line Therapy (AMPLIFY) Trial Liu, Xianchen Johnson, Margot Mardekian, Jack Phatak, Hemant Thompson, John Cohen, Alexander T. J Am Heart Assoc Original Research BACKGROUND: In the Apixaban for the Initial Management of Pulmonary Embolism and Deep‐Vein Thrombosis as First‐Line Therapy (AMPLIFY) trial, apixaban was noninferior to enoxaparin/warfarin in preventing recurrent symptomatic venous thromboembolism (VTE) or venous thromboembolism–related death, with significantly less bleeding. This analysis evaluated the effects of apixaban versus enoxaparin/warfarin on all‐cause hospitalizations during AMPLIFY. METHODS AND RESULTS: Of the 5365 patients included, 2676 received apixaban and 2689 received enoxaparin/warfarin. All‐cause hospitalizations during the treatment period after the index event were captured using dedicated case report forms. Outcomes included all‐cause hospitalizations and time from randomization to first hospitalization. Patients were censored at death, loss to follow‐up, or end of study, whichever came first. Treatment effects were assessed using Cox proportional hazards regression models. During the treatment period after the index event, 343 patients were hospitalized at least once: 153 (5.72%) in the apixaban group and 190 (7.07%) in the enoxaparin/warfarin group. Compared with enoxaparin/warfarin, apixaban significantly reduced all‐cause hospitalizations (hazard ratio 0.804, 95% CI=0.650–0.995, P=0.045). All‐cause hospitalization rates within the first 30 days after the index event were 2.28% and 3.35% in the apixaban and enoxaparin/warfarin groups, respectively (hazard ratio 0.676, 95% CI=0.488–0.935, P=0.018). For all patients, the average per‐patient estimated mean length of hospital stay was also shorter with apixaban than enoxaparin/warfarin (0.57 days versus 1.01 days, P<0.0001). CONCLUSIONS: Apixaban significantly reduced all‐cause hospitalizations versus enoxaparin/warfarin, and shortened the length of hospital stay in patients with acute venous thromboembolism. CLINICAL TRIAL REGISTRATION: URL: https://Clinicaltrials.Gov/. Unique identifier: NCT00643201. John Wiley and Sons Inc. 2015-12-01 /pmc/articles/PMC4845271/ /pubmed/26627879 http://dx.doi.org/10.1161/JAHA.115.002340 Text en © 2015 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research
Liu, Xianchen
Johnson, Margot
Mardekian, Jack
Phatak, Hemant
Thompson, John
Cohen, Alexander T.
Apixaban Reduces Hospitalizations in Patients With Venous Thromboembolism: An Analysis of the Apixaban for the Initial Management of Pulmonary Embolism and Deep‐Vein Thrombosis as First‐Line Therapy (AMPLIFY) Trial
title Apixaban Reduces Hospitalizations in Patients With Venous Thromboembolism: An Analysis of the Apixaban for the Initial Management of Pulmonary Embolism and Deep‐Vein Thrombosis as First‐Line Therapy (AMPLIFY) Trial
title_full Apixaban Reduces Hospitalizations in Patients With Venous Thromboembolism: An Analysis of the Apixaban for the Initial Management of Pulmonary Embolism and Deep‐Vein Thrombosis as First‐Line Therapy (AMPLIFY) Trial
title_fullStr Apixaban Reduces Hospitalizations in Patients With Venous Thromboembolism: An Analysis of the Apixaban for the Initial Management of Pulmonary Embolism and Deep‐Vein Thrombosis as First‐Line Therapy (AMPLIFY) Trial
title_full_unstemmed Apixaban Reduces Hospitalizations in Patients With Venous Thromboembolism: An Analysis of the Apixaban for the Initial Management of Pulmonary Embolism and Deep‐Vein Thrombosis as First‐Line Therapy (AMPLIFY) Trial
title_short Apixaban Reduces Hospitalizations in Patients With Venous Thromboembolism: An Analysis of the Apixaban for the Initial Management of Pulmonary Embolism and Deep‐Vein Thrombosis as First‐Line Therapy (AMPLIFY) Trial
title_sort apixaban reduces hospitalizations in patients with venous thromboembolism: an analysis of the apixaban for the initial management of pulmonary embolism and deep‐vein thrombosis as first‐line therapy (amplify) trial
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4845271/
https://www.ncbi.nlm.nih.gov/pubmed/26627879
http://dx.doi.org/10.1161/JAHA.115.002340
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