In view of the fact that little is known about the pre- and post-interventional coagulation management of phenprocoumon patients with reviparin at general practices in Germany, an observational study is being initiated to evaluate the effectiveness and tolerability of reviparin in the area of outpatient, general practice-based care in the context of bridging therapy. Patients for whom bridging therapy with low-molecular weight heparin (LMWH) was specified and for whom the LMWH reviparin was chosen for this purpose shall be investigated.
Study Type
OBSERVATIONAL
Enrollment
77
Research Facility 52
Berlin, Germany
Research facility 49
Berlin, Germany
Research facility 136
Essen, Germany
Research facility 139
Gladbeck, Germany
Patients without thromboembolic or bleeding complications in relation to Reviparin dosage
Documentation of the effect and the dosage of reviparin for the prevention of thromboembolic events in patients on oral anticoagulation (OAC) with phenprocoumon who need to undergo an elective surgical procedure or invasive investigation (target International Normalized Ratio (INR) between 2 and 3) and therefore receive bridging anticoagulation.
Time frame: 15 months
Documentation of the bridging regimen with reviparin used in Germany.
mean reviparin dose regimen measured in IU anti-Xa/ per day along with preoperative phenprocoumon withdrawal and postoperative re-onset over the related time course
Time frame: 15 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Research Facility 163
Herne, Germany
Research facility 123
Krefeld, Germany
Research Facility 82
Landsberg, Germany
Research facility 84
Leipzig, Germany
Research facility 70
Nossen, Germany
Research facility 119
Wachtendonk, Germany
...and 1 more locations