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Updated: Feb 2, 2026

Measurement of Factor V Activity in Human Plasma Using a Microplate Coagulation Assay
Published on: September 9, 2012
The prognosis of disseminated intravascular coagulation associated with hematologic malignancy and its response to
Naoki Kurita1, Tatsuhiro Sakamoto1, Takayasu Kato1
1Department of Hematology, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8577, Japan.
Introduction:
Disseminated intravascular coagulation (DIC) is a lethal complication in patients with hematologic malignancies (HMs). DIC can be induced by the HM itself, but also by HM-associated secondary infection; however, whether difference of triggering factor impacts the outcome of DIC in HM patients remains unknown. The objective of this study is to clarify the difference between HM-induced DIC and infection-induced DIC in HM patients regarding treatment response and prognosis.
Methods:
HM-induced DIC (158 episodes) and infection-induced DIC in HM patients (83 episodes) from a single center were retrospectively analyzed. Recombinant human thrombomodulin (rhTM) was administered in 149 episodes, while the remaining received conventional therapies.
Results:
In HM-induced DIC, improvement by day 7 was 46% (95% confidence interval [CI], 38-54), and rhTM enhanced the improvement (hazard ratio [HR], 1.7; 95% CI, 1.1-2.4). In contrast, improvement of infection-induced DIC was significantly worse (29%; 95% CI, 20-39 on day 7), and this was not influenced by rhTM (HR, 1.0; 95% CI, 0.50-2.2). Thirty-day survival in HM-induced DIC and infection-induced DIC was 87% (95% CI, 81-92) and 53% (95% CI, 42-63), respectively, and was not affected by treatment. A DIC score (Japanese Ministry of Health and Welfare criteria) of ≥5 was a predictor of worse survival in both types of DIC (HR, 2.5; 95% CI, 1.5-3.9).
Conclusions:
This study showed the inadequacy of current therapeutic strategies for secondary infection-induced DIC, the prognosis of which was significantly worse than HM-induced DIC, and the limited efficacy of rhTM only in the improvement of HM-induced DIC.
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