Connell Nathan T, Flood Veronica H, Brignardello-Petersen Romina, Abdul-Kadir Rezan, Arapshian Alice, Couper Susie, Grow Jean M, Kouides Peter, Laffan Michael, Lavin Michelle, Leebeek Frank W G, O'Brien Sarah H, Ozelo Margareth C, Tosetto Alberto, Weyand Angela C, James Paula D, Kalot Mohamad A, Husainat Nedaa, Mustafa Reem A
Hematology Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
Versiti Blood Research Institute, Medical College of Wisconsin, Milwaukee, WI.
Blood Adv. 2021 Jan 12;5(1):301-325. doi: 10.1182/bloodadvances.2020003264.
von Willebrand disease (VWD) is a common inherited bleeding disorder. Significant variability exists in management options offered to patients.
These evidence-based guidelines from the American Society of Hematology (ASH), the International Society on Thrombosis and Haemostasis (ISTH), the National Hemophilia Foundation (NHF), and the World Federation of Hemophilia (WFH) are intended to support patients, clinicians, and health care professionals in their decisions about management of VWD.
ASH, ISTH, NHF, and WFH formed a multidisciplinary guideline panel. Three patient representatives were included. The panel was balanced to minimize potential bias from conflicts of interest. The University of Kansas Outcomes and Implementation Research Unit and the McMaster Grading of Recommendations Assessment, Development and Evaluation (GRADE) Centre supported the guideline development process, including performing and updating systematic evidence reviews (through November 2019). The panel prioritized clinical questions and outcomes according to their importance to clinicians and patients. The panel used the GRADE approach, including GRADE Evidence-to-Decision frameworks, to assess evidence and make recommendations, which were subject to public comment.
The panel agreed on 12 recommendations and outlined future research priorities.
These guidelines make key recommendations regarding prophylaxis for frequent recurrent bleeding, desmopressin trials to determine therapy, use of antiplatelet agents and anticoagulant therapy, target VWF and factor VIII activity levels for major surgery, strategies to reduce bleeding during minor surgery or invasive procedures, management options for heavy menstrual bleeding, management of VWD in the context of neuraxial anesthesia during labor and delivery, and management in the postpartum setting.
血管性血友病(VWD)是一种常见的遗传性出血性疾病。为患者提供的管理方案存在显著差异。
美国血液学会(ASH)、国际血栓与止血学会(ISTH)、美国国家血友病基金会(NHF)和世界血友病联盟(WFH)发布的这些循证指南旨在支持患者、临床医生和医疗保健专业人员在血管性血友病管理方面做出决策。
ASH、ISTH、NHF和WFH组建了一个多学科指南小组。其中包括三名患者代表。该小组力求平衡,以尽量减少利益冲突导致的潜在偏差。堪萨斯大学结果与实施研究单位以及麦克马斯特推荐分级评估、制定与评价(GRADE)中心支持了指南制定过程,包括开展和更新系统证据综述(截至2019年11月)。该小组根据临床问题和结果对临床医生及患者的重要性进行了优先排序。该小组采用GRADE方法,包括GRADE证据到决策框架,来评估证据并提出建议,这些建议接受公众评议。
该小组就12项建议达成一致,并概述了未来的研究重点。
这些指南针对频繁复发性出血的预防、用于确定治疗方案的去氨加压素试验、抗血小板药物和抗凝治疗的使用、重大手术的目标血管性血友病因子(VWF)和凝血因子VIII活性水平、减少小手术或侵入性操作期间出血的策略、月经过多的管理方案、分娩期间神经轴麻醉情况下血管性血友病的管理以及产后管理等方面提出了关键建议。