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As proven in a clinical study involving over 1,700 patients undergoing hip fracture surgery, ARIXTRA significantly reduced the risks of VTE* and proximal DVT vs enoxaparin sodium.
*VTE, the primary endpoint, was a composite of documented DVT and/or documented symptomatic PE reported up to day 11.
- Patient population: 1,711 patients enrolled in the study
- Study design: Randomized, multicenter, double-blind clinical trial in patients undergoing hip fracture surgery
- Duration of thromboprophylaxis: 5 to 9 days
- Primary efficacy outcome: VTE up to day 11, defined as DVT detected by mandatory bilateral venography, documented symptomatic DVT, or documented symptomatic PE
In this study, incidence of proximal DVT was 0.9% (6/650) with ARIXTRA therapy vs 4.3% (28/646) with enoxaparin sodium.
DVT involving popliteal or more proximal veins reported up to day 11.
Postoperative Prophylaxis |

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ARIXTRA |

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ARIXTRA Evidence-Based Conclusion |
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Incidence of VTE |

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8.3% |

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Statistically significant (P<.001) |
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Proximal DVT§ |

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0.9% |

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Statistically significant (P<.001) |
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SafetyMajor bleeding|| |

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2.2% |

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Comparable |
VTE, the primary endpoint, was a composite of documented DVT and/or documented symptomatic PE reported up to day 11.
§DVT involving popliteal or more proximal veins reported up to day 11.
||Bleeding leading to reoperation; nonfatal bleeding involving a critical organ; fatal bleeding; or bleeding index >2. Bleeding index was defined as the number of whole blood or packed red blood cell (PRBC) units transfused + [(prebleeding)-(postbleeding)] hemoglobin (g/dL) values.
Now, there is more clinical evidence in hip fracture surgery. Click here to find out more about extended prophylaxis in hip fracture surgery.
Click here for important safety information.
Please see full prescribing information, including BOXED WARNING for Spinal/Epidural Hematomas.
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