Department of Haemostasis and Thrombosis, National Institute of Blood Disease and Bone Marrow Transplantation.
Clin Appl Thromb Hemost. 2011 Nov-Dec;17(6):E131-7. doi: 10.1177/1076029610391650. Epub 2011 Jan 19.
To determine the frequency of inherited bleeding disorders, its complications, and treatment modalities available for its treatment.
Cross-sectional study.
Patients with a history of bleeding tendency were tested for confirmation of the diagnosis. History and clinical findings were recorded. Laboratory analysis included prothrombin time (PT), activated partial thromboplastin time (APTT), bleeding time (BT), and fibrinogen assay. Patients with prolonged APTT were tested for factors VIII (FVIII) and IX (FIX). If FVIII was low, von Willebrand factor: antigen (vWF:Ag) and von Willebrand factor:ristocetin cofactor (vWF:RCo) were performed. When PT and APTT both were prolonged, FV, FX, and FII were tested. Platelet aggregation studies were done when there was isolated prolonged BT. Urea clot solubility test was done when all coagulation tests were normal. All patients with hemophilia A and B were evaluated for inhibitors.
Of the 376 patients, inherited bleeding disorder was diagnosed in 318 (85%) cases. Median age of patients was 16.4 years. Hemophilia A was the commonest inherited bleeding disorder that was observed in 140 (37.2%) followed by vWD 68 (18.0%), platelet function disorders 48 (12.8%), and hemophilia B in 33 (8.8%) cases. We also found rare congenital factor deficiencies in 13 (3.4%), low VWF in 11 (3.0%) participants and 5 (1.3%) in female hemophilia carriers. Hemarthrosis was the most frequent symptom in hemophilia A and B (79.7%) involving knee joint. Inhibitor was detected in 21 (15%) cases. Fresh frozen plasma/cryoprecipitate were the most common modality of treatment. In 58 patients, no abnormality was detected in coagulation profile.
Hemophilia A and vWD are the most common congenital bleeding disorders in this study. Hemarthrosis involving knee joint was the most common complication. Inhibitor was detected in a significant number of patients. Plasma is still the most common modality of treatment.
确定遗传性出血性疾病的频率、其并发症以及可用于治疗的治疗方法。
横断面研究。
对有出血倾向病史的患者进行测试以确认诊断。记录病史和临床发现。实验室分析包括凝血酶原时间(PT)、活化部分凝血活酶时间(APTT)、出血时间(BT)和纤维蛋白原测定。APTT 延长的患者检测因子 VIII(FVIII)和 IX(FIX)。如果 FVIII 降低,进行血管性血友病因子:抗原(vWF:Ag)和血管性血友病因子:瑞斯托霉素辅因子(vWF:RCo)检测。当 PT 和 APTT 均延长时,检测 FV、FX 和 FII。当孤立性 BT 延长时进行血小板聚集研究。当所有凝血试验均正常时进行尿素凝块溶解度试验。所有血友病 A 和 B 患者均评估抑制剂。
在 376 名患者中,318 名(85%)诊断为遗传性出血性疾病。患者的中位年龄为 16.4 岁。血友病 A 是最常见的遗传性出血性疾病,共 140 例(37.2%),其次是血管性血友病 68 例(18.0%)、血小板功能障碍 48 例(12.8%)和血友病 B 33 例(8.8%)。我们还发现了 13 例(3.4%)罕见的先天性因子缺乏症、11 例(3.0%)低 vWF 和 5 例(1.3%)女性血友病携带者。关节内血肿是血友病 A 和 B 最常见的症状(79.7%),涉及膝关节。21 例(15%)患者检测到抑制剂。新鲜冷冻血浆/冷沉淀是最常见的治疗方式。在 58 名患者中,凝血谱未发现异常。
在本研究中,血友病 A 和血管性血友病是最常见的先天性出血性疾病。膝关节关节内血肿是最常见的并发症。在相当数量的患者中检测到抑制剂。血浆仍然是最常见的治疗方式。