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血友病患者关节评估及治疗的研究进展 被引量:3

Research progress in joint evaluation and treatment of patients with hemophilia
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摘要 血友病是一组X连锁隐性遗传性出血性疾病。以自发性出血或者轻微外伤后过度出血为主要临床表现,其中关节出血最常见。反复的关节出血可引起退行性关节病,因此早期进行关节评估极为重要。目前,凝血因子替代治疗仍是血友病的首选治疗,但是患者经反复多次替代治疗后,可产生相应的凝血因子抑制物,影响疗效。多项针对血友病的新治疗方案已取得显著进展,但其安全性仍待进一步研究。笔者拟就血友病多种关节评估及治疗方法进行综述,分析其优、缺点,以期为血友病患者选择合适的诊疗方案提供参考。 Hemophilia is an X-linked recessive hereditary bleeding disorder.The main clinical manifestations were spontaneous bleeding or excessive bleeding after minor trauma,among which joint bleeding represents the most commonly reported type of hemorrhage in patients.Repeated bleeding episodes may lead to degenerative arthropathy,so early joint assessment is extremely important.At present,blood coagulation factors replacement therapy is still the preferred treatment for hemophilia,but repeated usage can produce corresponding blood coagulation factors inhibitors and affect the therapeutic effect.Several new treatments have made significant progress,but their safety remains to be further studied.This paper reviews various joint evaluation methods and treatment methods of hemophilia,and analyzes their advantages and disadvantages,in order to provide reference for appropriate diagnosis and treatment schemes for hemophilia patients.
作者 王稳 胡群 Wang Wen;Hu Qun(Department of Pediatric Hematology,Tongji Hospital,Tongji Medical College of Huazhong University of Science and Technology,Wuhan 430030,Hubei Province,China)
出处 《国际输血及血液学杂志》 CAS 2021年第5期456-460,共5页 International Journal of Blood Transfusion and Hematology
基金 Hemophilia Experiences,Results,and Opportunities(HERO)基金(2018033)。
关键词 血友病A 血友病B 关节积血 日常生活活动 药物疗法 基因治疗 Hemophilia A Hemophilia B Hemarthrosis Activities of daily living Drug therapy Gene therapy
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  • 1郭晔,张磊,竺晓凡,杨仁池.儿童血友病429例临床回顾分析[J].中国实用儿科杂志,2006,21(4):292-295. 被引量:37
  • 2林强,余卫,梁继祥,朱海峰,孟薇,徐瑞燚,赵永强.血友病患者关节病变的X线和核磁共振影像比较[J].中国医学科学院学报,2006,28(6):828-831. 被引量:6
  • 3中华医学会血液学分会血栓与止血学组,中国血友病协作组.血友病诊断与治疗中国专家共识(2013年版).中华血液学杂志,2013,34:461-463.
  • 4Gupta S, Siddiqi AE, Soucie JM, et al. The effect of secondary prophylaxis versus episodic treatment on the range of motion of target joints in patients with haemophilia. Br J Haematol, 2013, 161:424-433.
  • 5Poon MC, Luke KH. Haemophilia care in China: achievements of a decade of World Federation of Hemophilia treatment centre twinning activities. Haemophilia, 2008,14:879-888.
  • 6Srivastava A, Brewer AK, Mauser-Bunschoten EP, et al. Guide- lines for the management of hemophilia. Haemophilia, 2013,19: e1-e47.
  • 7Towner D, Castro MA, Eby-Wilkens E, et al. Effect of mode of delivery in nulliparous women on neonatal intracranial injury. N Engl J Med, 1999, 341:1709-1714.
  • 8Ljung R, Chambost H, Stain AM, et al. Haemophilia in the first years of life. Haemophilia, 2008,14 Suppl 3:188-195.
  • 9Maclean PS, Richards M, Williams M, et al. Treatment related factors and inhibitor development in children with severe haemo- philia A. Haemophilia, 2011,17:282-287.
  • 10Wang XF, Zhao YQ, Yang RC, et al. The prevalence of factor VIII inhibitors and genetic aspects of inhibitor development in Chinese patients with haemophilia A.Haemophilia, 2010,16:632- 639.

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