Ranta Susanna, Heyman Mats M, Jahnukainen Kirsi, Taskinen Mervi, Saarinen-Pihkala Ulla M, Frisk Tony, Söderhäll Stefan, Petrini Pia, Mäkipernaa Anne M-T
aChildren's Hospital, Helsinki University Central Hospital, Helsinki, Finland bChildhood Cancer Research Unit, Karolinska Institute cDepartment of Blood Coagulations Disorders, Karolinska University Hospital, Stockholm, Sweden dUnit of Coagulation Disorders, Division of Haematology, Department of Medicine, Helsinki University Central Hospital, Helsinki, Finland.
Blood Coagul Fibrinolysis. 2013 Oct;24(7):749-56. doi: 10.1097/MBC.0b013e328363b147.
Children with acute lymphoblastic leukemia (ALL) have several risk factors for deep venous thromboses (DVTs) such as central venous catheters and asparaginase (ASP), related antithrombin (AT) deficiency. After introduction of a new standard and intermediate-risk ALL treatment protocol with prolonged continuous ASP treatment, two symptomatic DVTs in 10 patients were observed at the Children's Hospital, Helsinki, Finland. To prevent further thrombotic complications yet ensuring continuous exposure to ASP, an AT substitution strategy was adopted in Helsinki. The same ALL treatment protocol is used without AT substitution in the other Nordic countries. In this retrospective study, we describe the effect of prolonged ASP treatment on AT and fibrinogen levels in children without AT substitution in Stockholm, Sweden (n = 39) and the AT substitution in children with AT activity below 0.55 kIU/l in Helsinki (n = 36, intervention group). The intervention group is compared with children treated similarly earlier in Helsinki without AT substitution (n = 10). The median lowest AT activity during the ASP treatment without AT substitution was 0.55 kIU/l. Fibrinogen level of 1.0 g/l or less was found in 14% of all routine samples during the ASP treatment. In the intervention group, 23 (64%) received AT concentrate. Two (20%) children had symptomatic DVT before initiation of the AT substitution and two (6%) thereafter. We conclude that most children are exposed to low AT activity during ASP treatment predisposing to thrombosis. The effect of prophylactic AT substitution remains unclear.
急性淋巴细胞白血病(ALL)患儿存在多种深静脉血栓形成(DVT)的风险因素,如中心静脉导管和天冬酰胺酶(ASP),以及相关的抗凝血酶(AT)缺乏。在引入一种新的标准和中危ALL治疗方案并延长持续ASP治疗后,芬兰赫尔辛基儿童医院观察到10例患者出现了2例有症状的DVT。为预防进一步的血栓并发症同时确保持续使用ASP,赫尔辛基采用了AT替代策略。其他北欧国家使用相同的ALL治疗方案但不进行AT替代。在这项回顾性研究中,我们描述了在瑞典斯德哥尔摩未进行AT替代的儿童(n = 39)中延长ASP治疗对AT和纤维蛋白原水平的影响,以及在赫尔辛基AT活性低于0.55 kIU/l的儿童(n = 36,干预组)中进行AT替代的影响。将干预组与赫尔辛基早期未进行AT替代的类似治疗儿童(n = 10)进行比较。在未进行AT替代的ASP治疗期间,最低AT活性中位数为0.55 kIU/l。在ASP治疗期间,所有常规样本中有14%的纤维蛋白原水平为1.0 g/l或更低。在干预组中,23例(64%)接受了AT浓缩物。2例(20%)儿童在开始AT替代前出现有症状的DVT,之后有2例(6%)出现。我们得出结论,大多数儿童在ASP治疗期间暴露于低AT活性,易发生血栓形成。预防性AT替代的效果仍不明确。