Criteria | Â | Â | Points |
---|---|---|---|
1. Underlined disease | Â | (+) | 1 |
 |  | (-) | 0 |
2. Symptom | (1) Bleeding tendency | (+) | 1 |
 |  | (-) | 0 |
 | (2) Symptom caused by organ dysfunction | (+) | 1 |
 |  | (-) | 0 |
3. Laboratory data | (1) Serum FDP (μg/ml) | 40 ≤ | 3 |
 |  | 20 ≤ < 40 | 2 |
 |  | 10 ≤ < 20 | 1 |
 |  | 10 > | 0 |
 | (2) Platelet (× 103/μl) | 50 ≥ | 3 |
 |  | 80 ≥ > 50 | 2 |
 |  | 120 ≥ > 80 | 1 |
 |  | 120 | 0 |
 | (3) Plasma fibrinogen (mg/dl) | 100 ≥ | 2 |
 |  | 150 ≥ > 100 | 1 |
 |  | 150 < | 0 |
 | (4) Prothrombin time/control | 1.67 ≤ | 2 |
 |  | 1.25 ≤ < 1.67 | 1 |
 |  | 1.25 > | 0 |
4. Supplemental data | (1) Detection of soluble fibrin monomer | Â | Â |
 | (2) Increase of D-dimer |  |  |
 | (3) Increase of thrombin-antithrombin complex |  |  |
 | (4) Increase of plasmin-a2-plasmin inhibitor complex |  |  |
 | (5) Exacerbation of FDP, platelet, fibrinogen within several days |  |  |
 | (6) Improvement of data with anticoagulant therapy |  |  |
Judgment* | Â | Â | Â |
1. Definite DIC | (1) Patients who do not have leukemia, pernicious anemia, liver cirrhosis, | More than 7 or 6 points with | |
 | or who are not under cancer chemotherapy | more than two of supplemental data | |
 | (2) Patients who have leukemia, pernicious anemia, or who are | More than 4 or 3 points with | |
 | under cancer chemotherapy points for bleeding tendency and platelet | more than two of supplemental data | |
 | are not included |  |  |
 | (3) Patients who have liver cirrhosis | More than 10 or 9 points with | |
 |  | more than two of supplemental data | |
2. Probable DIC | (1) Patients who do not have leukemia, pernicious anemia, liver cirrhosis, | 6 points | |
 | or who are not under cancer chemotherapy |  |  |
 | (2) Patients who have leukemia, pernicious anemia, or who are under | 3 points | |
 | cancer chemotherapy points for bleeding tendency and platelet are not included |  |  |
 | (3) Patients who have liver cirrhosis | 9 points |