Venous Thromboembolism and Renal Impairment: Insights from the SWIss Venous ThromboEmbolism Registry (SWIVTER)

Author:

Spirk David1,Sebastian Tim2,Banyai Martin2,Beer Jürg H.3,Mazzolai Lucia4,Baldi Thomas5,Aujesky Drahomir6,Hayoz Daniel7,Engelberger Rolf P.7,Kaeslin Thomas8,Korte Wolfgang9,Escher Robert10,Husmann Marc2,Mollet Annette11,Szucs Thomas D.11,Kucher Nils2

Affiliation:

1. Institute of Pharmacology, University of Bern, Bern, Switzerland

2. Clinic of Angiology, University Hospital Zurich, Zurich, Switzerland

3. Department of Internal Medicine, Cantonal Hospital Baden, Baden, Switzerland

4. Clinic of Angiology, University Hospital Lausanne, Lausanne, Switzerland

5. Department of Internal Medicine, University Hospital Basel, Basel, Switzerland

6. Division of General Internal Medicine, Bern University Hospital, Bern, Switzerland

7. Department of Internal Medicine, Cantonal Hospital Fribourg, Villars-sur-Glâne, Switzerland

8. Department of Internal Medicine, Cantonal Hospital Obwalden, Sarnen, Switzerland

9. Department of Internal Medicine, Cantonal Hospital St. Gallen, St. Gallen, Switzerland

10. Department of Internal Medicine, Regional Hospital Burgdorf, Burgdorf, Switzerland

11. European Center of Pharmaceutical Medicine, University of Basel, Basel, Switzerland

Abstract

AbstractRenal impairment (RI) has increased substantially over the last decades. In the absence of data from confirmatory research, real-life data on anticoagulation treatment and clinical outcomes of venous thromboembolism (VTE) in patients with RI are needed. In the SWIss Venous ThromboEmbolism Registry (SWIVTER), 2,062 consecutive patients with objectively confirmed VTE were enrolled. In the present analysis, we compared characteristics, initial and maintenance anticoagulation, and adjusted 90-day clinical outcomes of those with (defined as estimated creatinine clearance < 30 mL/min) and without severe RI. Overall, 240 (12%) patients had severe RI; they were older, and more frequently had chronic and acute comorbidities. VTE severity was similar between patients with and without severe RI. Initial anticoagulation in patients with severe RI was more often performed with unfractionated heparin (44 vs. 24%), and less often with low-molecular-weight heparin (LMWH) (52 vs. 61%) and direct oral anticoagulants (DOACs; 4 vs. 12%). Maintenance anticoagulation in patients with severe RI was more frequently managed with vitamin K antagonists (70 vs. 60%) and less frequently with DOAC (12 vs. 21%). Severe RI was associated with increased risk of 90-day mortality (9.2 vs. 4.2%, hazard ratio [HR]: 2.27, 95% confidence interval [CI]: 1.41–3.65), but with similar risk of recurrent VTE (3.3 vs. 2.8%, HR: 1.19, 95% CI: 0.57–2.52) and major bleeding (2.1 vs. 2.0%, HR: 1.05, 95% CI: 0.41–2.68). In patients with severe RI, the use of LMWH versus any other treatment was associated with reduced mortality (HR: 0.37; 95% CI: 0.14–0.94; p = 0.036) and similar rate of major bleeding (HR: 0.59, 95% CI: 0.17–2.00; p = 0.39). Acute or chronic comorbidities rather than VTE severity or recurrence may explain increased early mortality in patients with severe RI. The higher rate of VTE recurrence, specifically fatal events, than major bleeding reinforces the need for effective anticoagulation in VTE patients with severe RI.

Publisher

Georg Thieme Verlag KG

Subject

Cardiology and Cardiovascular Medicine,Hematology

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