山东大学学报 (医学版) ›› 2020, Vol. 58 ›› Issue (1): 91-93.doi: 10.6040/j.issn.1671-7554.0.2019.1228
• • 上一篇
王亚杰1,闻蓓2,施浩宇3,商亮1,董康迪1,李乐平1
WANG Yajie1, WEN Bei2, SHI Haoyu3, SHANG Liang1, DONG Kangdi1, LI Leping1
摘要: 目的 本文旨在探讨合并血友病的外科患者围手术期管理。 方法 分析一名胃癌合并轻型血友病A的患者术后出血的临床特点、诊断及治疗过程,同时对围手术期合并血友病的处理要点进行文献复习。 结果 通过组织多学科会诊,深入了解病情,血液检查发现患者凝血因子Ⅷ活性降低,确诊该患者合并轻型血友病A。并对患者进行输注重组凝血因子Ⅷ治疗,其出血症状得到治愈。 结论 对于血友病患者的围术期管理,目前替代疗法是最主要的治疗方案。首选重组FⅧ制剂,并根据手术类型、损伤程度等,适当延长替代治疗时间。患者应在血友病中心进行登记,进行长期随访。
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[1] Bolton-Maggs PH, Pasi KJ. Haemophilias A and B[J]. Lancet, 2003, 361(9371): 1801-1809. [2] 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(2017年版)[J]. 中华血液学杂志, 2017, 38(5): 364-370. Thrombosis and Hemostasis Group, Hematology Society of Chinese Medical Association, Hemophilia Treatment Center Collaborative Network of China. Consensus of Chinese experts on diagnosis and treatment of hemophilia(version 2017)[J]. Chinese Journal of Hematology, 2017, 38(5): 364-370. [3] Wong T, Recht M. Current options and new developments in the treatment of haemophilia[J]. Drugs, 2011, 71(3): 305-320. [4] Tanaka KA, Key NS, Levy JH. Blood coagulation: hemostasis and thrombin regulation[J]. Anesth Analg, 2009, 108(5): 1433-1446. [5] Blanchette VS, Key NS, Ljung LR, et al. Definitions in hemophilia: communication from the SSC of the ISTH[J]. J Thromb Haemost, 2014, 12(11): 1935-1939. [6] Nakagawa N, Fujinaga M, Chikagawa Y, et al. Mild hemophilia A diagnosed in an adult patient on the occasion of postoperative bleeding following a second knee surgery[J]. Rinsho Ketsueki, 2019, 60(5): 398-400. [7] Kitamura T, Sato T, Ikami E, et al. A case of a patient who is diagnosed with mild acquired hemophilia a after tooth extraction died of acute subdural hematoma due to head injury[J]. Case Reports in Dentistry, 2018, 2018:1-3. doi:10.1155/2018/7185263. [8] Ishikawa N, Furukawa K, Yokoi K, et al. Mild hemophilia a diagnosed in a 55-year-old patient after pancreatoduodenectomy for carcinoma of the papilla of vater[J]. Journal of Nippon Medical School, 2007, 74(5): 372-376. [9] 张之南, 郝玉书, 赵永强, 等. 血液病学[M]. 2版. 北京: 人民卫生出版社, 2011: 1309-1323. [10] Mannucci PM, Tuddenham EG. The hemophilias-from royal genes to gene therapy[J]. New England Journal of Medicine, 2001, 344(23): 1773-1779. [11] 张威, 毛建华. 血友病A治疗研究新进展[J]. 中华血液学杂志, 2018, 39(1): 83-86. ZHANG Wei, MAO Jianhua. Advances of hemophilia A treatment[J]. Chinese Journal of Hematology, 2018, 39(1): 83-86. [12] Srivastava A, Brewer AK, Mauser-Bunschoten EP, et al. Guidelines for the management of hemophilia[J]. Haemophilia, 2013, 19(1): e1-e47. [13] Escobar MA, Brewer A, Caviglia H, et al. Recommendations on multidisciplinary management of elective surgery in people with haemophilia[J]. Haemophilia, 2018, 24(5): 693-702. [14] Benson G, Auerswald G, Dolan G, et al. Diagnosis and care of patients with mild haemophilia: practical recommendations for clinical management[J]. Blood Transfus, 2018, 16(6): 535-544. [15] 张雪芹, 程彦, 房云海, 等. 血友病A手术前漏诊16例临床分析[J]. 社区医学杂志, 2014, 12(17): 35-36. ZHANG Xueqin, CHENG Yan, FANG Yunhai, et al. Clinical analysis of 16 cases of hemophilia A missed diagnosis before operation[J]. Journal of Community Medicine, 2014, 12(17): 35-36. |
[1] | 张文慧,陈昀,常亚丽,周亚伟,房云海,张心声,郭农建. 山东省55例血友病A患者基因检测及分析[J]. 山东大学学报 (医学版), 2019, 57(12): 57-61. |
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