4.3 Article

Rivaroxaban in the Treatment of PICC-associated Upper Extremity Venous Thrombosis

Journal

CLINICAL THERAPEUTICS
Volume 39, Issue 9, Pages 1882-1888

Publisher

ELSEVIER
DOI: 10.1016/j.clinthera.2017.07.041

Keywords

bleeding; resolution; rivaroxaban; thrombosis; upper limb; vitamin K antagonists

Funding

  1. Clinical Research Award of the First Affiliated Hospital of Xi'an Jiaotong University, China [XJTU1AHCR2014-019]
  2. new medical technology project of the First Affiliated Hospital of Xi'an Jiaotong University, China
  3. new medical technology project of Medical School of Xi'an Jiaotong University, China

Ask authors/readers for more resources

Purpose: Peripherally inserted central catheters (PICCs) are frequently used for prolonged drug administration, but their use is commonly complicated by the development of upper extremity deep venous thrombosis (UEDVT) requiring anticoagulation. Here, we compared the efficacy and safety profile of rivaroxaban (20 mg/d) with low molecular weight (LMW) heparin and vitamin K antagonists in the treatment of PICC-associated UEDVT. Methods: Patients (N = 84) with PICC-associated UEDVT were studied. All had UEDVT identified by ultrasound scanning. Further ultrasound images were obtained at 1, 2, and 3 months after the start of treatment. Forty-four patients were treated with rivaroxaban and 40 with initial LMW heparin and vitamin K antagonist with continuation of vitamin K antagonists alone once international normalized ratio was therapeutic Findings: In the rivaroxaban group mean (SD) age was 51 (16) years and 57% were men, whereas in the other group respective values were 50 (16) years and 56%. All patients were receiving treatment for cancer. Resolution of thrombus had occurred in 53.5% at 1 month, 76.1% at 2 months, and 92.6% at 3 months in the rivaroxaban-treated patients. Corresponding values in the LMW heparin/vitamin antagonist treated patients were 34.2%, 55.5%, and 88.5%, respectively. Differences between groups were significant at 1 month (P < 0.01) and 2 months (P < 0.05). There were no major bleeds in either group, and cumulative bleeding rates by 3 months were 7.3% in the rivaroxaban group and 11.4% in the LMW heparin/vitamin K antagonist group. (C) 2017 Elsevier HS Journals, Inc. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available