UOS Dipartimentale per la Diagnosi e la Terapia delle Coagulopatie, A Bianchi Bonomi Hemophilia and Thrombosis Center, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Università degli Studi di Milano and Luigi Villa Foundation, Milan, Italy.
J Thromb Haemost. 2012 Apr;10(4):615-21. doi: 10.1111/j.1538-7836.2012.04653.x.
The European Network of Rare Bleeding Disorders (EN-RBD) was established to bridge the gap between knowledge and practise in the care of patients with RBDs.
To explore the relationship between coagulation factor activity level and bleeding severity in patients with RBDs.
PATIENTS/METHODS: Cross-sectional study using data from 489 patients registered in the EN-RBD. Coagulation factor activity levels were retrieved. Clinical bleeding episodes were classified into four categories according to severity.
The mean age of patients at data collection was 31 years (range, 7 months to 95 years), with an equal sex distribution. On linear regression analysis, there was a strong association between coagulation factor activity level and clinical bleeding severity for fibrinogen, factor (F) X, FXIII, and combined FV and FVIII deficiencies. A weaker association was present for FV and FVII deficiencies. There was no association between coagulation factor activity level and clinical bleeding severity for FXI. The coagulation factor activity levels that were necessary for patients to remain asymptomatic were: fibrinogen, > 100 mg dL(-1); FV, 12 U dL(-1); combined FV + VIII, 43 U dL(-1); FVII, 25 U dL(-1); FX, 56 U dL(-1) ; FXI, 26 U dL(-1); FXIII, 31 U dL(-1). Moreover, coagulation factor activity levels that corresponded with Grade III bleeding were: undetectable levels for fibrinogen, FV and FXIII, < 15 U dL(-1) for combined FV + VIII; < 8 U dL(-1) for FVI; < 10 U dL(-1) for FX; and < 25 U dL(-1) for FXI.
There is a heterogeneous association between coagulation factor activity level and clinical bleeding severity in different RBDs. A strong association is only observed in fibrinogen, FX and FXIII deficiencies.
欧洲罕见出血性疾病网络(EN-RBD)的成立旨在弥合 RBD 患者护理方面知识与实践之间的差距。
探究 RBD 患者凝血因子活性水平与出血严重程度之间的关系。
患者/方法:这是一项使用 EN-RBD 登记的 489 例患者数据的横断面研究。检索了凝血因子活性水平。根据严重程度将临床出血事件分为四类。
数据收集时患者的平均年龄为 31 岁(范围为 7 个月至 95 岁),性别分布均衡。线性回归分析显示,纤维蛋白原、因子(F)X、FXIII 和联合 FV 和 FVIII 缺乏症的凝血因子活性水平与临床出血严重程度密切相关。FV 和 FVII 缺乏症的相关性较弱。FXI 缺乏症与凝血因子活性水平和临床出血严重程度无关。使患者保持无症状所需的凝血因子活性水平为:纤维蛋白原,>100mg/dL(-1);FV,12U/dL(-1);联合 FV+VIII,43U/dL(-1);FVII,25U/dL(-1);FX,56U/dL(-1);FXI,26U/dL(-1);FXIII,31U/dL(-1)。此外,凝血因子活性水平与 III 级出血相对应的水平为:纤维蛋白原、FV 和 FXIII 水平不可检测,联合 FV+VIII<15U/dL(-1);FV<8U/dL(-1);FX<10U/dL(-1);FXI<25U/dL(-1)。
不同 RBD 患者的凝血因子活性水平与临床出血严重程度之间存在异质性关联。仅在纤维蛋白原、FX 和 FXIII 缺乏症中观察到强相关性。