Abstract

IntroductionIn a previous report, we demonstrated a favorable trend for supplementation with antithrombin (AT) concentrate at a dosage of 3,000 IU/day over 1,500 IU/day for the treatment of sepsis-associated disseminated intravascular coagulation (DIC) in patients with an AT activity of 70% or less. Since the survival difference did not reach statistical significance, we planned to examine the effects in a larger number of cases with severer disease.MethodsWe performed a non-randomized multi-institutional survey. In total, 307 septic DIC patients who had AT activity less than 40% and who had undergone AT substitution at a dose of either 1,500 IU/day or 3,000 IU/day for three consecutive days were analyzed. Of these, 259 patients received 1,500 IU/day (AT1500 group) and 48 patients received 3,000 IU/day (AT3000 group). The primary efficacy endpoints were recovery from DIC by day 7 and an all-cause mortality on day 28. Adverse bleeding events were also examined. A logistic regression analysis was conducted by using age, sex, body weight, initial AT activity, DIC score, platelet count, coadministration of heparin, recombinant thrombomodulin, suspected source of infection, surgery, and supplemented AT dose.ResultsSupplementation significantly decreased the DIC score in the AT3000 group, leading to the superior resolution of DIC, compared with the results in the AT1500 group (66.7% versus 45.2%, P = 0.007). In addition, the AT3000 group exhibited a better survival than the AT1500 group (77.1% versus 56.4%, P = 0.010). Bleeding events were observed in 6.96% (severe bleeding: 3.04%) in the AT1500 group and 6.52% (severe bleeding, 4.35%) in the AT3000 group (P = 1.000; severe bleeding, P = 0.648). A logistic regression analysis revealed that the use of AT3000 (odds ratio (OR), 2.419; P = 0.025), a higher initial platelet count (OR, 1.054; P = 0.027), and patient age (OR, 0.977; P = 0.045) were significantly correlated with an improved survival.ConclusionsThe AT3000 group exhibited significantly improved rates of survival and recovery from DIC without an increased risk of bleeding, compared with the AT1500 group, among the patients with sepsis-associated DIC and an AT activity of less than 40%.

Highlights

  • In a previous report, we demonstrated a favorable trend for supplementation with antithrombin (AT) concentrate at a dosage of 3,000 IU/day over 1,500 IU/day for the treatment of sepsis-associated disseminated intravascular coagulation (DIC) in patients with an AT activity of 70% or less

  • In a former study, we examined a total of 729 sepsisassociated DIC patients with AT activity levels of 70% or lower and reported that 3,000 IU/day of AT substitution for 3 days (AT3000) was a significant factor associated with an improvement in survival, compared with 1,500 IU/day of AT substitution (AT1500) (odds ratio (OR) 1.912; P = 0.026)

  • Fortyeight patients were treated with AT3000 for 3 days, and 259 patients were treated with AT1500 for 3 days

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Summary

Introduction

We demonstrated a favorable trend for supplementation with antithrombin (AT) concentrate at a dosage of 3,000 IU/day over 1,500 IU/day for the treatment of sepsis-associated disseminated intravascular coagulation (DIC) in patients with an AT activity of 70% or less. Excess clot formation, leading to malcirculation in organs and subsequent organ failure, is driven by activated coagulation, by impaired anticoagulant mechanisms, including the antithrombin (AT) and protein C system, and by the Previously, the results of a large-scale randomized controlled trial (RCT) known as KyberSept, which examined the effects and adverse events of high-dose AT for the treatment of severe sepsis, were published [5]. This trial demonstrated that AT did not provide survival benefit and instead increased the risk of bleeding. It may be too early to conclude that AT is not effective for sepsisassociated DIC

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