Key result
Postoperative heparin is linked to ~69% higher post-kidney transplant bleeding risk, unlike intraoperative heparin.
Why the study?
Little is known about the bleeding risks associated with perioperative antithrombotic therapy after kidney transplantation despite its potential role in preventing thromboembolic complications.
Does perioperative antithrombotic therapy increase the incidence of early postoperative thromboembolic complications and bleeding in kidney transplantation recipients?
Cohort (n=2,000)
Yes
Does perioperative antithrombotic therapy increase the incidence of early postoperative thromboembolic complications and bleeding in kidney transplantation recipients?
p-value: p=0.006
Intraoperative heparin and antiplatelet therapy appear safe for preventing thromboembolic complications without increasing bleeding risk after kidney transplantation, whereas postoperative heparin infusion and vitamin K antagonists increase bleeding risk.
May support avoiding postoperative heparin and vitamin K antagonists; hypothesis-generating and should not yet change practice without RCTs.
Perioperative antithrombotic therapy could play a role in preventing thromboembolic complications (TEC) after kidney transplantation (KTx), but little is known on postoperative bleeding risks. This retrospective analysis comprises 2000 single-organ KTx recipients transplanted between 2011 and 2016 in the two largest transplant centers of the Netherlands. TEC and bleeding events were scored ≤7 days post-KTx. Primary analyses were for associations of antithrombotic therapy with incidence of TEC and bleeding. Secondary analyses were for associations of other potential risk factors. Mean age was 55 ± 14 years, 59% was male and 60% received a living donor kidney. Twenty-one patients (1.1%) had a TEC. Multiple donor arteries [OR 2.79 (1.15-6.79)] and obesity [OR 2.85 (1.19-6.82)] were identified as potential risk factors for TEC. Bleeding occurred in 88 patients (4.4%) and incidence varied significantly between different antithrombotic therapies (P = 0.006). Cardiovascular disease [OR 2.01 (1.18-3.42)], pre-emptive KTx [OR 2.23 (1.28-3.89)], postoperative heparin infusion [OR 1.69 (1.00-2.85)], and vitamin K antagonists [OR 6.60 (2.95-14.77)] were associated with an increased bleeding risk. Intraoperative heparin and antiplatelet therapy were not associated with increased bleeding risk. These regimens appear to be safe for the possible prevention of TEC without increasing the risk for bleeding after KTx.
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Berg et al. (2018) conducted a cohort in Kidney transplantation (n=2,000). Perioperative antithrombotic therapy vs. Different antithrombotic therapies or no therapy was evaluated on Incidence of thromboembolic complications (TEC) and bleeding ≤7 days post-transplantation (p=0.006). Intraoperative heparin and antiplatelet therapy did not increase bleeding risk after kidney transplantation, whereas postoperative heparin (OR 1.69; 95% CI 1.00-2.85) and vitamin K antagonists did.
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