TY - JOUR
T1 - Treatment responses for disseminated intravascular coagulation in 25 children treated with recombinant thrombomodulin
T2 - A single institution experience
AU - Yagasaki, Hiroshi
AU - Kato, Maiko
AU - Shimozawa, Katsuyoshi
AU - Hirai, Maiko
AU - Nishikawa, Eri
AU - Okuma, Hirotsugu
AU - Ishii, Wakako
AU - Imai, Yuki
AU - Matsumura, Masaharu
AU - Yonezawa, Ryuta
AU - Yoshikawa, Kayo
AU - Shichino, Hiroyuki
AU - Chin, Motoaki
AU - Mugishima, Hideo
PY - 2012/12
Y1 - 2012/12
N2 - Introduction: Recombinant thrombomodulin (rTM), which degrades factors Va and VIIIa by activating protein C, has been developed as a new drug for treating disseminated intravascular coagulation (DIC). Materials and methods: Since July 2009, we have treated 25 children with DIC using rTM (380 U/kg/day, or 130 U/kg/day for newborns) as a first-line therapy. Median duration of rTM administration was 5 consecutive days (range, 2-13 days). We employed DIC criteria of the Japan Welfare and Health Ministry. The first day on which rTM treatment was given was defined as day 1. Results: Median patients age was 3 years. Underlying diseases were hematological disorders (n = 13) and severe infection (n = 12). Overall, 20 of the 25 patients had recovered from DIC by day 7 and 22 of the 25 patients remained alive at day 28. Median Pediatric Logistic Organ Dysfunction score improved from 11 on day 1 to 2 on day 7 (p = 0.009). Laboratory data (median) on day 7 (prothrombin time (PT) ratio, 1.15; fibrin and fibrinogen degradation products (FDP), 9.6 mg/l; D-dimer, 1.6 mg/l FEU; antithrombin, 112%; protein C, 105%) were significantly improved compared to results on day 1 (PT ratio, 1.39; FDP, 21.6 mg/l; D-dimer, 6.4 mg/l FEU; antithrombin, 86%; protein C, 54%). Whereas, 5 patients failed to respond and serious bleeding events were observed in 2 newborns. Conclusion: The efficacy of rTM cannot be assessed from the present dataset, due to several limitations such as the small heterogenous patient cohort, and the lack of age- and disease-matched controls. Nevertheless, this case-series remains important in terms of enabling further prospective control studies to evaluate the efficacy of rTM in children.
AB - Introduction: Recombinant thrombomodulin (rTM), which degrades factors Va and VIIIa by activating protein C, has been developed as a new drug for treating disseminated intravascular coagulation (DIC). Materials and methods: Since July 2009, we have treated 25 children with DIC using rTM (380 U/kg/day, or 130 U/kg/day for newborns) as a first-line therapy. Median duration of rTM administration was 5 consecutive days (range, 2-13 days). We employed DIC criteria of the Japan Welfare and Health Ministry. The first day on which rTM treatment was given was defined as day 1. Results: Median patients age was 3 years. Underlying diseases were hematological disorders (n = 13) and severe infection (n = 12). Overall, 20 of the 25 patients had recovered from DIC by day 7 and 22 of the 25 patients remained alive at day 28. Median Pediatric Logistic Organ Dysfunction score improved from 11 on day 1 to 2 on day 7 (p = 0.009). Laboratory data (median) on day 7 (prothrombin time (PT) ratio, 1.15; fibrin and fibrinogen degradation products (FDP), 9.6 mg/l; D-dimer, 1.6 mg/l FEU; antithrombin, 112%; protein C, 105%) were significantly improved compared to results on day 1 (PT ratio, 1.39; FDP, 21.6 mg/l; D-dimer, 6.4 mg/l FEU; antithrombin, 86%; protein C, 54%). Whereas, 5 patients failed to respond and serious bleeding events were observed in 2 newborns. Conclusion: The efficacy of rTM cannot be assessed from the present dataset, due to several limitations such as the small heterogenous patient cohort, and the lack of age- and disease-matched controls. Nevertheless, this case-series remains important in terms of enabling further prospective control studies to evaluate the efficacy of rTM in children.
KW - Children
KW - Disseminated intravascular coagulation
KW - Hematological disorders
KW - Recombinant thrombomodulin
KW - Severe infection
UR - http://www.scopus.com/inward/record.url?scp=84870240523&partnerID=8YFLogxK
U2 - 10.1016/j.thromres.2012.10.004
DO - 10.1016/j.thromres.2012.10.004
M3 - Article
C2 - 23123162
AN - SCOPUS:84870240523
SN - 0049-3848
VL - 130
SP - e289-e293
JO - Thrombosis Research
JF - Thrombosis Research
IS - 6
ER -