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本文引用的文献

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Clinical implications of emerging pathogens in haemophilia: the variant Creutzfeldt-Jakob disease experience.血友病中新出现病原体的临床意义:变异型克雅氏病的经验
Haemophilia. 2006 Mar;12 Suppl 1:16-20; discussion 26-8. doi: 10.1111/j.1365-2516.2006.01196.x.
2
Emerging viral diseases and infectious disease risks.新出现的病毒性疾病和传染病风险。
Haemophilia. 2006 Mar;12 Suppl 1(Suppl 1):3-7; discussion 26-8. doi: 10.1111/j.1365-2516.2006.01194.x.
3
Clinical perspectives of emerging pathogens in bleeding disorders.出血性疾病中新兴病原体的临床观点。
Lancet. 2006 Jan 21;367(9506):252-61. doi: 10.1016/S0140-6736(06)68036-7.
4
Dendritic cells pulsed with hepatitis C virus NS3 protein induce immune responses and protection from infection with recombinant vaccinia virus expressing NS3.用丙型肝炎病毒NS3蛋白脉冲处理的树突状细胞可诱导免疫反应,并对感染表达NS3的重组痘苗病毒产生保护作用。
J Gen Virol. 2006 Jan;87(Pt 1):1-10. doi: 10.1099/vir.0.81423-0.
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Advances in chronic viral hepatitis.慢性病毒性肝炎的进展
Curr Opin Infect Dis. 2005 Oct;18(5):400-6. doi: 10.1097/01.qco.0000180163.84271.5e.
6
Transmissible Spongiform Encephalopathies. Managing risk in mammalian organs, cells and sera. 15-16 March 1999, San Diego, CA, USA.传染性海绵状脑病。管理哺乳动物器官、细胞和血清中的风险。1999年3月15 - 16日,美国加利福尼亚州圣地亚哥
IDrugs. 1999 Jun;2(6):564-6.
7
The public health impact of prion diseases.朊病毒疾病对公共卫生的影响。
Annu Rev Public Health. 2005;26:191-212. doi: 10.1146/annurev.publhealth.26.021304.144536.
8
Transfusion-transmitted virus is not present in factor IX concentrates commonly used to treat haemophilia B.常用于治疗乙型血友病的凝血因子IX浓缩物中不存在输血传播病毒。
Haemophilia. 2004 Nov;10(6):732-4. doi: 10.1111/j.1365-2516.2004.01048.x.
9
Successful treatment with cyclosporine and high-dose gamma immunoglobulin for persistent parvovirus B19 infection in a patient with refractory autoimmune hemolytic anemia.环孢素和大剂量γ-免疫球蛋白成功治疗一名难治性自身免疫性溶血性贫血患者的持续性细小病毒B19感染。
Int J Hematol. 2004 Oct;80(3):250-3. doi: 10.1532/ijh97.04017.
10
Inhibitors in congenital coagulation disorders.先天性凝血障碍中的抑制剂。
Br J Haematol. 2004 Nov;127(4):379-91. doi: 10.1111/j.1365-2141.2004.05168.x.

血液安全与抗血友病因子浓缩物的选择

Blood safety and the choice of anti-hemophilic factor concentrate.

作者信息

Valentino Leonard A, Oza Veeral M

机构信息

RUSH Hemophilia and Thrombophilia Center, Department of Pediatrics, Rush University Medical Center, Chicago, Illinois 60612, USA.

出版信息

Pediatr Blood Cancer. 2006 Sep;47(3):245-54. doi: 10.1002/pbc.20895.

DOI:10.1002/pbc.20895
PMID:16724312
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7168091/
Abstract

Hemophilia is a congenital disorder due to the deficiency of the activity of factor VIII (classical hemophilia A) or IX (Christmas disease or hemophilia B). Bleeding is common and may result in long-term complications or even death. Bleeding may be treated or prevented by infusion of factor concentrates however these drugs are not without risk. Clinicians often feel ill prepared to provide accurate and impartial information regarding these drugs. This review will provide the reader with an historical yet up to date perspective on blood safety as it relates to the choice of concentrates to treat hemophilia.

摘要

血友病是一种先天性疾病,由于缺乏凝血因子VIII(经典血友病A)或IX(克里斯马斯病或血友病B)的活性所致。出血很常见,可能导致长期并发症甚至死亡。输注凝血因子浓缩物可治疗或预防出血,然而这些药物并非没有风险。临床医生常常觉得没有充分准备好提供有关这些药物的准确和公正的信息。本综述将为读者提供一个与治疗血友病的浓缩物选择相关的血液安全方面的历史及最新观点。