Aspirin Thromboprophylaxis After First-line Total Hip and Knee Replacement (TBP-ASPIR)

University Hospital, Strasbourg, France

Status: Unknown

Conditions: Hip and Knee Prosthesis Implantation

Study type: Observational

Funder types: Other

Identifiers

NCT05128214

8299

Details and patient eligibility

About

Annually, more than 100,000 total hip prostheses (THA) and more than 100,000 total knee prostheses (TKA) are implanted for osteoarthritis in France, and these figures are set to increase significantly in the future as in all industrialized countries. . Venous thrombosis is a potentially serious complication after PTH and PTG, justifying various prophylactic measures. In France, aggressive prophylaxis with low molecular weight heparin (LMWH) or direct oral anticoagulants (DOA) was until recently recommended, because this drug is considered to be the most effective, at the cost of a bleeding risk implicitly assumed but often poorly. evaluated. A recent publication suggests that the risk of bleeding is currently greater than the risk of a thromboembolic event.

More recently, foreign or international recommendations have broadened the range of these recommendations, notably by introducing aspirin as a possible prophylactic agent. While this molecule is potentially less effective than LMWHs or ADOs, it could decrease the risk of iatrogenic hemorrhage. The introduction of enhanced recovery procedures after surgery (RAAC) could decrease the risk of thrombosis without modifying the risk of bleeding, and thereby improve the cost-benefit ratio of aspirin, justifying its recent inclusion in the current French recommendations when The operated follows such a protocol.

Enrollment: 200 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult patient (≥ 18 years old);
• Patient operated on for a first-line total hip or knee replacement by the principal investigator;
• Patient not having expressed his opposition, after information, to the reuse of his data for the purposes of this research.

Exclusion criteria

• Subject having expressed opposition to participating in the study