Rivaroxaban prevents VTE after lower limb surgery

Roshini Claire Anthony
18 Apr 2020
Rivaroxaban prevents VTE after lower limb surgery

Rivaroxaban reduced venous thromboembolism (VTE) risk without increasing bleeding compared with enoxaparin in patients who underwent lower limb nonmajor orthopaedic surgery, the PRONOMOS* trial showed.

“This study represents a major step forward in our treatment of patients after many orthopaedic procedures because it proves that we can more effectively prevent thrombosis with a once-daily oral medication versus a daily injection with the same safety,” said study investigator Dr Nadia Rosencher from Paris University, Paris, France, who presented the findings at ACC.20/WCC.

The study included 3,604 adults (median age 41 years) scheduled for nonmajor orthopaedic surgery of the lower limbs with planned immobilization (>15 days) who were at risk for VTE. They were randomized to receive once-daily doses of oral rivaroxaban (10 mg; n=1,809, 66 percent male) or subcutaneous enoxaparin (4,000 IU; n=1,795, 64 percent male) with corresponding placebos. Patients received the trial drug for a mean 28.6 days, with about 60 percent receiving treatment for 2 weeks to 1 month.

The most common surgeries were knee ligament repair, ankle fracture, and knee arthroscopy (37.0, 15.1, and 9.0 percent, respectively). Almost 14 percent of patients received pre-surgery prophylactic low-molecular-weight heparin (LMWH).

Major VTE** was significantly reduced in the rivaroxaban vs enoxaparin group (0.2 percent vs 1.1 percent; risk ratio [RR], 0.25, 95 percent confidence interval, 0.09–0.75; pnoninferiority<0.001; psuperiority=0.01). [ACC.20, abstract 20-LB-20404-ACC; N Engl J Med 2020;doi;10.1056/NEJMoa1913808]

This reduction was driven by a significant decrease in symptomatic VTE with rivaroxaban vs enoxaparin (0.2 percent vs 0.6 percent; RR, 0.28).

Median time to a VTE event was 26 and 40 days in the rivaroxaban and enoxaparin groups, respectively.

Bleeding – comprising major*** and nonmajor clinically relevant bleeding (NMCRB) – occurred at a comparable rate in the rivaroxaban and enoxaparin groups (1.1 percent vs 1.0 percent; RR, 1.04; p=0.89). This finding was consistent when bleeding type was assessed separately (major bleeding: 0.6 percent vs 0.7 percent; RR, 0.81; p=0.62; NMCRB: 0.5 percent vs 0.3 percent; RR, 1.48; p=0.46).

Post hoc analysis showed a 52 percent lower incidence of events in the rivaroxaban vs enoxaparin group (net clinical benefit outcome# 0.8 percent vs 1.8 percent).

Substantial variation exists in the guidelines on thromboprophylaxis for patients undergoing nonmajor orthopaedic surgery. The US guidelines do not recommend routine thromboprophylaxis, while the European guidelines recommend a personalized LMWH strategy in certain patient groups.

“In patients deemed at risk, rivaroxaban could replace LMWH to prevent VTE during postoperative reduced mobility after nonmajor orthopaedic surgery,” said Rosencher. However, further research is necessary to establish the patient subgroups who would derive the most benefit from thromboprophylaxis, said Rosencher and colleagues.

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