- Original clinical investigation
- Open Access
Recombinant human soluble thrombomodulin administration improves sepsis-induced disseminated intravascular coagulation and mortality: a retrospective cohort study
Thrombosis Journal volume 11, Article number: 3 (2013)
Early treatment of disseminated intravascular coagulation (DIC) can be associated with improved patient outcomes. The Japanese Ministry of Health and Welfare (JMHW) and the International Society on Thrombosis and Haemostasis (ISTH) criteria are the most specific for diagnosis of septic DIC. The revised Japanese Association for Acute Medicine (JAAM) criteria are able to diagnose sepsis-induced DIC in the early stage. Recombinant human soluble thrombomodulin (rhTM) has recently been used for treating DIC. Previous studies have shown a benefit of using rhTM for D,IC diagnosed by the JMHW or ISTH criteria, but not the JAAM criteria. The purpose of this study was to sequentially evaluate coagulation biomarkers and the DIC score after giving rhTM treatment to patients with sepsis-induced DIC diagnosed according to the JAAM criteria.
We performed a retrospective cohort study. Critically ill patients were included if diagnosed with sepsis-induced DIC according to the JAAM criteria. They were either treated without rhTM (control group) or with rhTM (treatment group). The primary outcome was the DIC score on day 7. The secondary outcome was 28-day mortality from the start of DIC treatment. Changes in the results of coagulation tests were assessed over time from the start of treatment to day 7.
Twelve and 23 patients were assigned to the treatment and control groups, respectively. The DIC score on day 7 was significantly higher in the treatment group (3.3 ± 1.4) than in the control group (4.9 ± 1.8, p < 0.05). Estimated survival showed lower in treatment group than control group. There was significant difference between the control group and the treatment group (p < 0.05). The D-dimer level on day 7 was significantly lower in the treatment group (7.5 ± 4.1 μg/mL) than in the control group (30.9 ± 33.6 μg/mL, p < 0.05). Life-threatening bleeding did not occur. Our results indicated that rhTM improved sepsis-induced DIC and mortality.
Recombinant human soluble thrombomodulin may improve sepsis-induced DIC diagnosed according to the JAAM criteria without an increased bleeding risk.
Disseminated intravascular coagulation (DIC) is associated with high mortality in patients with severe sepsis. Excessive coagulation activation, inhibition of fibrinolysis, and consumption of coagulation inhibitors lead to a hypercoagulable state, resulting in fibrin deposition in microvessels and inflammatory reactions. Although the effectiveness of anticoagulant therapy in septic patients is still controversial worldwide, some studies have suggested that rapid diagnosis and early treatment of DIC improve outcomes for these patients. In particular, therapeutic intervention directly against coagulation and inflammation in DIC associated with severe sepsis is effective [1, 2], and it is generally accepted that early, aggressive treatment of the underlying disease is important.
Recently, the International Society on Thrombosis and Haemostasis (ISTH) criteria were proposed by the subcommittee of the ISTH. The revised Japanese Association for Acute Medicine (JAAM) criteria were proposed by the JAAM, and the Japanese Ministry of Health and Welfare (JMHW) criteria were proposed by the JMHW. These criteria have been used for clinical diagnosis of DIC [3–5]. The JAAM criteria have acceptable validity for diagnosis of DIC in the early phase of disease, and the scoring system can diagnose DIC with a higher sensitivity than can the criteria of the ISTH for overt DIC , thus enabling patients to receive early treatment.
The novel biological agent recombinant human soluble thrombomodulin (rhTM) was recently approved and has been used clinically for DIC treatment in Japan. The clinical effects of rhTM on DIC were previously examined in patients diagnosed according to the JMHW criteria in a multicenter randomized clinical trial conducted in Japan . This study revealed significantly better resolution of DIC in the rhTM treatment group than in the heparin treatment group. Only non-significant trends in favor of rhTM compared with heparin were observed for mortality in patients with sepsis-induced DIC . Yamakawa et al. showed that administration of rhTM reduced 28-day mortality in patients with severe sepsis .
However, the clinical effects of rhTM on patients diagnosed in the early stage of sepsis-induced DIC according to the JAAM criteria have not been assessed. Because the JAAM criteria show higher sensitivity for DIC diagnosis than do the ISTH criteria, and because early treatment of DIC may be associated with improved outcomes , rhTM treatment in patients diagnosed with sepsis-induced DIC according to the JAAM criteria may enhance clinical outcomes. Therefore, the purpose of this study was to sequentially evaluate coagulation biomarkers and the DIC score in rhTM treatment of patients with sepsis-induced DIC diagnosed according to the JAAM criteria.
Patients and study design
A retrospective analysis of all patients admitted to the intensive care unit (ICU) of Aichi Medical University Hospital between May 2008 and March 2011 was performed. Although the criteria for ICU admission were not standardized, all patients included in this study were diagnosed with sepsis-induced DIC according to the JAAM criteria. Administration of rhTM started within 48 h from the initiation of DIC treatment. Treatment with rhTM (0.06 or 0.02 mg/kg/day; patients who required renal replacement therapy for acute kidney injury [AKI] were drip-infused for 30 min once daily) was continued for 7 days. There was no difference in treatment strategy among all patients, equipment used, or number of physicians and nurses who took care of the patients during the study period. All patients were principally treated according to the strategy of the Surviving Sepsis Campaign Guidelines . Any patients who lacked the required laboratory data were excluded, and other exclusion criteria were as follows: acute pancreatitis, burns, treatment with danaparoid sodium, fatal or life-threatening bleeding (defined as intracranial or pulmonary bleeding) at the start of treatment for DIC, and age of ≤15 years. A patient flow diagram is shown in Figure 1.
Relevant clinical background, medication history, and laboratory data of all patients were collected at appropriate times during the treatment for sepsis. The variables compared between the two groups were age, sex, Acute Physiologic and Chronic Health Evaluation II (APACHE II) score, Sequential Organ Failure Assessment (SOFA) score, number of dysfunctional organs, shock (hypotension not reversed with fluid resuscitation), presence of AKI as defined by the Acute Kidney Injury Network , acute respiratory distress syndrome (ARDS), DIC score (calculated with the JAAM criteria) at the start of DIC treatment, maximum DIC score during DIC treatment, number of patients who fulfilled the ISTH criteria, platelet count, prothrombin time (PT) ratio, D-dimer level, antithrombin III (AT III) activity, renal replacement therapy, mechanical ventilation, use of vasopressors, administration of AT III, low-dose steroids, platelet concentrate, fresh frozen plasma transfusion, rate of positive blood culture, and site of infection. Patients were followed until day 28 after the start of DIC treatment.
Evaluation of clinical response
The DIC score and DIC resolution rate (rate of recovery from DIC) were assessed 7 days after the start of DIC treatment (or withdrawal) based on the JAAM criteria as the primary efficacy endpoint. Secondary endpoints were as follows: the 28-day mortality from the start of DIC treatment; severity of the patients’ conditions as calculated by the SOFA score from the start of treatment to day 28; and changes over time in the results of coagulation tests, such as the platelet count, D-dimer level, PT ratio, fibrinogen level, and AT III activity, were also assessed from the start of treatment to day 7. In addition, the presence of serious adverse events related to bleeding (defined as intracranial hemorrhage, gastrointestinal or respiratory tract bleeding that was uncontrollable by conservative treatments, and bleeding at a critical location, such as retinal hemorrhage, major hemarthrosis, spinal hemorrhage or any life-threatening bleeding) that led to discontinuation of the administrated study drug and abnormal changes in clinical laboratory test results related to the diagnosis of DIC were investigated.
Data are expressed as group means ± standard deviation or percentages, as appropriate. Continuous variables were compared between groups using the Student’s t-test. Noncontinuous variables were compared between groups using the Mann–Whitney test. Categorical variables were analyzed using the χ2 test or Fisher’s exact test, as appropriate. Univariate analysis of the time to DIC resolution and the mortality rate were compared using Wilcoxon’s test. In addition, stepwise multivariate Cox regression analysis was used to assess the covariates that were associated with time to mortality. Adjusted curves of time to mortality by associated covariates were estimated. Comparisons of DIC scores, SOFA scores, D-dimer level, platelet count, PT ratio, fibrinogen, and AT III activity between groups over time were analyzed by repeated measures analysis of variance (ANOVA) adjusted for the baseline values as a covariate, and by post hoc Bonferroni test. The last-observation-carried-forward method for missing data was used for the analysis. Missing samples occurred because some samples were not drawn. A p value of <0.05 was considered statistically significant. Statistical analyses, except for ANOVA and the post-hoc Bonferroni test, were performed using JMP for Windows version 5.0.1 software (SAS Institute, Inc, U.S.). ANOVAs and post hoc Bonferroni tests were performed using Microsoft Excel 2010 (Microsoft Corporation, U.S.).
During the study period, although 49 patients were diagnosed with DIC, only 35 patients met the requirements of our study. Fourteen patients were excluded (acute pancreatitis, 2; burns, 12). Twelve patients were treated with rhTM for DIC (treatment group) and 23 patients were treated without rhTM (control group). All patients were regarded as having been infected with pathogens. Baseline characteristics and therapeutic interventions of the study population are shown in Table 1. Twenty-four patients were male. The duration of rhTM administration was 3 to 7 days (5.83 ± 1.26 days). Baseline characteristics, including severity of underlying disease, DIC scores, and treatment excluding rhTM administration showed no significant differences between the control and treatment groups. The ratio of patients diagnosed with DIC according to the ISTH criteria was 39.1% (9 of 23) for the control group and 41.7% (5 of 12) for the treatment group.
On day 7, the DIC score was significantly lower in the treatment group (3.3 ± 1.4) than in the control group (4.9 ± 1.8, p < 0.05, Figure 2). The DIC resolution rate was significantly higher in the treatment group (58.3%) than in the control group on day 7 (26.1% p = 0.079, Figure 3). While three patients in the control group died before 7 days, no patient in the treatment group died before 7 days.
The 28-day mortality rate in the control group was 33.3% (8 of 23 patients) compared with 8.3% (1 of 12 patients) in the treatment group (p = 0.075 by Wilcoxon’s test). We performed Cox regression analysis to adjust for the baseline variables of patients. We assessed a total of 11 possible confounders related to outcome: age, sex, APACHE II score, SOFA score, fulfilled ISTH criteria at the start of DIC treatment, AKI, ARDS, use of AT III, platelet concentrate, fresh frozen plasma, and administration of rhTM. Consequently, two prognostic variables were selected: AKI and administration of rhTM. After adjusting for AKI and rhTM administration was identified as an independent significant predictor of the probability of 28-day mortality (adjusted hazard ratio, 0.089 to 0.904; P = 0.026) (Table 2). The survival curves of the prediction model calculated by Cox regression analysis are shown in Figure 4. Estimated survival showed higher in treatment group than control group. There was significant difference between the control and the treatment groups (p < 0.05). The SOFA score was not significantly different between the two groups (Figure 5). In the coagulation tests, D-dimer level was significantly lower on day 7 (7.5 ± 4.1 μg/ml in the treatment group vs 30.9 ± 33.6 μg/ml in the control group; p < 0.01), while the platelet count, PT ratio, and fibrinogen levels were not significantly different at day 7 between the groups (Figure 6). AT III was used when the physician considered that it was required. AT III was administrated at a concentration of1500 IU per day for less than 3 days. AT III was not administrated after day 4. AT III activity was not significantly different at day 7 between the two groups, and showed a significant difference compared with the maximum level and day 7 in the control group (Figure 7).
Until 28 days after the start of DIC treatment, one serious adverse event related to bleeding occurred in the control group (4.3%) and no serious adverse events occurred in the treatment group (0%) within 28 days. No clear correlation was shown between these adverse events and the treatment used. There was no significant difference in the incidence of these adverse events between the two groups (p = 1.00).
The results of this study provide evidence that rhTM may have a beneficial effect on coagulation in patients with sepsis-induced DIC diagnosed according to the JAAM criteria. We showed a significant decrease in the DIC score in the treatment group compared with that in the control group. The DIC resolution rate was higher and the mortality rate was lower in the treatment group than in the control group. Bleeding showed no significant difference between the two groups.
Early treatment of DIC may be associated with improved outcomes . In our study, the number of patients who fulfilled the ISTH criteria did not show a significant difference between the two groups. In the present study, approximately half of the patients were in the early phase of DIC compared with the diagnosis according to the ISTH criteria. Mortality has been shown to be correlated with the maximum DIC score . In our study, the maximum DIC score, APACHE II score, SOFA score, AKI, and ARDS showed no significant differences between the control and treatment groups at baseline. Therefore, it was considered reasonable to compare the two groups.
Several DIC markers were assessed. It was difficult to assess the platelet count and AT III activity because they varied widely among the patients, and platelet concentrate was used for approximately half of the patients in the two groups. However, we consider that the contribution of rhTM administration to the increases in platelet counts was not large because there was no significant difference in improvement in the platelet counts between the two groups. In addition, we consider that the contribution of platelet concentrate to the DIC score was not large because the platelet count was <80,000/μl after the use of platelet concentrate at approximately day 7. Although AT III activity decreased from days 3 to 7 in the control group, it did not decrease with rhTM administration. This suggests that rhTM improves sepsis-induced DIC by not decreasing AT III activity. Recombinant human soluble thrombomodulin decreases thrombin-antithrombin complex compared with heparin . Therefore, in the present study, AT III activity did not decrease in the treatment group.
The sensitivity of a low fibrinogen level for the diagnosis of DIC according to ISTH criteria was 28% and hypofibrinogenemia has been detected in severe cases of DIC only . Although rhTM improves fibrinogen levels in animal studies [12, 13], fibrinogen levels were normal in all patients in the present study. Therefore, fibrinogen levels showed no significant differences between the control and treatment groups.
D-dimer levels were significantly decreased in the treatment group compared with the control group on day 7. In a phase III trial of rhTM for patients with DIC, Saito et al. showed that the rate of change in D-dimer levels in the rhTM group was significantly greater than that in the heparin group, suggesting that rhTM is superior to heparin in the attenuation of the hypercoagulable state . Yamakawa et al. showed that rhTM decreased fibrin degradation products in patients with DIC who fulfilled the ISTH criteria . Therefore, it is thought that rhTM affects the treatment of not only overt DIC, but also the early phase of DIC as diagnosed by the JAAM criteria. Recombinant human soluble thrombomodulin directly inhibits thrombin and produces activated protein C (APC), and it induces 50-fold increased inhibition of prothrombinase compared with heparin, thus producing an anti-thrombin effect [12, 14]. Although it is considered that regulation of coagulation and activation of fibrinolysis are mechanisms of decreasing D-dimer levels, rhTM does not affect the fibrinolytic system . Therefore, rhTM suppresses the hypercoagulative state in patients with sepsis-induced DIC. As a result, the D-dimer level was decreased and the PT ratio did not decrease in the treatment group in our study.
Although the accuracy of the mortality rate was questionable because of the small sample size, Cox regression analysis indicated that 28-day mortality of the patients treated with rhTM was significantly improved compared with that in the patients treated without rhTM.
In our study, the SOFA score did not show a significant difference on days 7 or 28. Although Yamakawa et al. showed that rhTM did not decrease the SOFA score on day 7 compared with the control group, organ damage was improved on days 21 and 28 by rhTM administration, and the 28-day mortality was significantly improved. They investigated patients with DIC diagnosed according to the ISTH criteria. However, in the present study, we investigated patients with DIC diagnosed according to the JAAM criteria. SOFA score might have been nonsignificant because of the small sample size.
Several animal studies have demonstrated a reduction in mortality with the administration of rhTM in severe sepsis models. Iba et al. showed that changes in coagulation abnormalities were reduced and that mortality was decreased by the concomitant administration of rhTM and antithrombin in rats with lipopolysaccharide infusion-induced sepsis, which are similar results to our study. Therefore, decreased mortality is expected, not only in patients with overt DIC, but also in patients in the early phase of DIC as diagnosed by the JAAM criteria. D-dimer levels are decreased by recombinant APC ; however, APC does not reduce the 28-day mortality . Recombinant human soluble thrombomodulin treatment might have the same effect. Further evaluation of the effects of rhTM is necessary.
Bleeding is the most significant adverse event associated with the administration of rhTM, as it is with recombinant human APC . Sadaka et al. reported that life-threatening bleeding was higher in the APC group than in the placebo group . In the present study, the PT ratio and bleeding were not significant between the two groups. Moreover, life-threatening bleeding did not occur. Recombinant human soluble thrombomodulin was considered not to increase the risk of bleeding based on our study results. Clinical doses of APC and rhTM do not affect the clotting time [12, 20]. Therefore, PT is not a predictive factor of bleeding by rhTM. This is supported by the fact that there was no significant difference in bleeding between the two groups; the anticoagulative effect of rhTM depends on the amount of thrombin available. Accordingly, after controlling thrombin generation by rhTM administration, rhTM does not work in excess and generation of further APC decreases. Recombinant human soluble thrombomodulin has been shown to have a wider safety margin and a favorable antithrombotic profile with less bleeding than heparin in animals and in in vitro experiments .
We acknowledge several limitations of our observational study design. This study was not a randomized controlled trial, and we compared two groups retrospectively. A small number of patients was included in this study. Finally, this study was carried out in a single institution. Further multicenter, prospective, randomized trials are necessary to fully evaluate the effects of rhTM.
Recombinant human soluble thrombomodulin administration may improve sepsis-induced DIC diagnosed according to the JAAM criteria without an increased bleeding risk. Further clinical investigations are necessary to fully evaluate the effect of rhTM.
Disseminated intravascular coagulation
Subcommittee of the international society on thrombosis and haemostasis
Japanese association for acute medicine
Japanese ministry of health and welfare
Recombinant human soluble thrombomodulin
Intensive care unit
Acute kidney injury
- APACHE II:
Acute physiologic and chronic health evaluation II
Sequential organ failure assessment
Acute respiratory distress syndrome
- AT III:
Analysis of variance
Activated protein C.
Wada H, Wakita Y, Nakase T, Shimura M, Hiyoyama K, Nagaya S, Mori Y, Shiku H: Outcome of disseminated intravascular coagulation in relation to the score when treatment was begun, Mie DIC Study Group. Thromb Haemost 1995, 74: 848-852.
Dhainaut JF, Yan SB, Jpyce DE, Pettila V, Basson B, Brandt T, Sundin DP, Levis M: Treatment effects of drotrecogin alfa (activated) in patients with severe sepsis with or without overt disseminated intravascular coagulation. J Thromb Haemost 2004, 2: 1924-1933. 10.1111/j.1538-7836.2004.00955.x
Taylor FB, Toh CH, Hoots WK, Wada H, Levi M: Towards definition, clinical and laboratory criteria, and a scoring system for disseminated intravascular coagulation. Thromb Haemost 2001, 86: 1327-1330.
Kobayashi N, Maekawa T, Takada M, Tanaka H, Gonmori H: Criteria for diagnosis of DIC based on the analysis of clinical and laboratory findings in 345 DIC patients collected by the Research Committee on DIC in Japan. Bibl Haematol 1983, 49: 265-275.
Gando S, Saitoh D, Ogura H, Mayumi T, Koseki K, Ikeda T, Ishikura H, Iba T, Ueyama M, Eguchi Y, Ohtomo Y, Okamoto K, Kushimoto S, Endo S, Shimazaki S: Natural history of disseminated intravascular coagulation diagnosed based on the newly established diagnostic criteria for critically ill patients: results of a multicenter, prospective survey. Crit Care Med 2006, 34: 625-631.
Gando S, Wada H, Asakura H, Iba T, Eguchi Y, Okamoto K, Ohtomo Y, Kawasugi K, Koga S, Koseki K, Tsuji H, Mayumi T, Murata A, Nakagawa M, Endo S: Evaluation of new Japanese diagnostic criteria for disseminated intravascular coagulation in critically ill patients. Clin Appl Thromb Haemost 2005, 11: 71-76. 10.1177/107602960501100108
Saito H, Maruyama I, Shimazaki S, Yamamoto Y, Aikawa N, Ohno R, Hirayama A, Matsuda T, Asakura H, Nakashima M, Aoki N: Efficacy and safety of recombinant human soluble thrombomodulin (ART-123) in disseminated intravascular coagulation: results of a phase III, randomized, double-blind clinical trial. J Thromb Haemost 2007, 5: 31-41. 10.1111/j.1538-7836.2006.02267.x
Yamakawa K, Fujimi S, Mohri T, Matsuda H, Nakamori Y, Hirose T, Tasaki O, Ogura H, Kuwagata Y, Hamasaki T, Shimazu T: Treatment effects of recombinant human soluble thrombomodulin in patients with severe sepsis: a historical control study. Crit Care 2011, 15: R123. Epub 10.1186/cc10228
Dellinger RP, Levy MM, Carlet JM, Bion J, Parker MM, Jaeschke R, Reinhart K, Angus DC, Brun-Buisson C, Beale R, Calandra T, Dhainaut JF, Gerlach H, Harvey M, Marini JJ, Marshall J, Ranieri M, Ramsay G, Sevransky J, Thompson BT, Townsend S, Vender JS, Zimmerman JL, Vincent JL: Surviving Sepsis Campaign: international guidelines for management of severe sepsis and septic shock: 2008. Crit Care Med 2008, 36: 296-327. 10.1097/01.CCM.0000298158.12101.41
Mehta RL, Kellum JA, Shah SV, Molitoris BA, Ronco C, Warnock DG, Levin A: Acute kidney injury network: report of an initiative to improve outcomes in acute kidney injury. Crit Care 2007, 11: R31. Epub 10.1186/cc5713
Levi M, Toh CH, Thachil J, Watson HG: Guidelines for the diagnosis and management of disseminated intravascular coagulation. Br J Haematol 2009, 145: 24-33. 10.1111/j.1365-2141.2009.07600.x
Mohri M, Gonda Y, Oka M, Aoki Y, Gomi K, Kiyota T, Sugihara T, Yamamoto S, Ishida T, Maruyama I: The antithrombotic effects of recombinant human soluble thrombomodulin (rhsTM) on tissue factor-induced disseminated intravascular coagulation in crab-eating monkeys (Macaca fascicularis). Blood Coagul Fibrinolysis 1997, 8: 274-283. 10.1097/00001721-199707000-00003
Iba T, Nakarai E, Takayama T, Nakajima K, Saraoka T, Ohno Y: Combination effect of antithrombin and recombinant human soluble thrombomodulin in a lipopolysaccharide induced rat sepsis model. Crit Care 2009, 13: R203. 10.1186/cc8210
Van de Wouwer M, Collen D, Conway EM: Thrombomodulin-protein C-EPCR system integrated to regulate coagulation and inflammation. Arterioscler Thromb Vasc Biol 2004, 24: 1374-1383. 10.1161/01.ATV.0000134298.25489.92
Nakazono O, Suzuki M, Sata M, Sugimoto E, Suzuki H: Anticoagulant activities of recombinant human soluble thrombomodulin (ART-123). Jpn Pharmacol Ther 2006, 34: 347-353.
Bernard GR, Vincent JL, Laterre PF, LaRosa SP, Dhainaut JF, Lopez-Rodriguez A, Steingrub JS, Garber GE, Helterbrand JD, Ely EW, Fisher CJ Jr: Efficacy and safety of recombinant human activated protein C for severe sepsis. N Engl J Med 2001, 344: 699-709. 10.1056/NEJM200103083441001
Benstetter M, Haubenreisser S: Xigris (drotrecogin alfa (activated)) to be withdrawn due to lack of efficacy. http://www.webcitation.org/62icYBgm1
Gentry CA, Gross KB, Sud B, Drevets DA: Adverse outcomes associated with the use of drotrecogin alfa (activated) in patients with severe sepsis and baseline bleeding precautions. Crit Care Med 2009, 37: 19-25. 10.1097/CCM.0b013e318192843b
Sadaka F, O’Brien J, Migneron M, Stortz J, Vanston A, Taylor RW: Activated protein C in septic shock: a propensity-matched analysis. Crit Care 2011, 15: R89. Epub 10.1186/cc10089
Wang Y, Thiyagarajan M, Chow N, Singh I, Guo H, Davis TP, Zlokovic BV: Differential neuroprotection and risk for bleeding from activated protein C with varying degrees of anticoagulant activity. Stroke 2009, 40: 1864-1869. 10.1161/STROKEAHA.108.536680
We thank Hidefumi Kato, Syoshiro Okada, Masayuki Haniuda, and Yoshihiro Fujiwara for serving as advisors of our study.
The authors declare that they have no competing interests.
TK, TS, MK, MH, TH, KM, and TN contributed to the study conception and design, collected and assembled the study data, contributed to the writing and revising of the manuscript, and provided final approval of the manuscript. TK and TS performed the statistical analysis. All authors read and approved the final manuscript.
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Kato, T., Sakai, T., Kato, M. et al. Recombinant human soluble thrombomodulin administration improves sepsis-induced disseminated intravascular coagulation and mortality: a retrospective cohort study. Thrombosis J 11, 3 (2013) doi:10.1186/1477-9560-11-3
- Disseminated intravascular coagulation
- Intensive care unit
- Critically ill patient
- Multiple organ failure
- DIC score