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Hemophilia gene therapy knowledge and perceptions: Results of an international survey

机译:血友病基因治疗知识和看法:国际调查结果

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Background Hemophilia gene therapy is a rapidly evolving therapeutic approach in which a number of programs are approaching clinical development completion. Objective The aim of this study was to evaluate knowledge and perceptions of a variety of health care practitioners and scientists about gene therapy for hemophilia. Methods This survey study was conducted February 1 to 18, 2019. Survey participants were members of the ISTH, European Hemophilia Consortium, European Hematology Association, or European Association for Hemophilia and Allied Disorders with valid email contacts. The online survey consisted of 36 questions covering demographic information, perceptions and knowledge of gene therapy for hemophilia, and educational preferences. Survey results were summarized using descriptive statistics. Results Of the 5117 survey recipients, 201 responded from 55 countries (4% response rate). Most respondents (66%) were physicians, and 59% were physicians directly involved in the care of people with hemophilia. Among physician respondents directly involved in hemophilia care, 35% lacked the ability to explain the science of adeno‐associated viral gene therapy for hemophilia, and 40% indicated limited ability or lack of comfort answering patient questions about gene therapy for hemophilia based on clinical trial results to date. Overall, 75% of survey respondents answered 10 single‐answer knowledge questions correctly, 13% incorrectly, and 12% were unsure of the correct answers. Conclusions This survey highlighted knowledge gaps and educational needs related to gene therapy for hemophilia and, along with other inputs, has informed the development of “Gene Therapy in Hemophilia: An ISTH Education Initiative.”
机译:背景技术血友病基因治疗是一种迅速发展的治疗方法,其中许多计划正在接近临床发展完成。目的本研究的目的是评估对血友病学基因治疗的各种卫生医生和科学家的知识和看法。方法采用该调查研究于2019年2月1日至18日进行。调查参与者是ISTH的成员,欧洲血友病联盟,欧洲血液学协会或欧洲血友病协会和有效的电子邮件联系人的联合障碍。在线调查包括36个问题,包括血友病的人口统计信息,知觉和基因治疗的知识和教育偏好。调查结果总结了使用描述性统计数据。 5117调查接受者的结果,201来自55个国家(4%的回复率)。大多数受访者(66%)是医生,59%的医生直接参与血友病的人。在直接参与血友病护理的医生受访者中,35%缺乏解释血友病的腺相关病毒基因治疗科学的能力,40%指示有限的能力或缺乏基于临床试验的血友病学基因治疗的舒适性应答患者问题结果到目前为止。总体而言,75%的调查受访者正确地回答了10个单答知识问题,13%不正确,12%不确定正确的答案。结论这项调查强调了与血友病的基因治疗相关的知识差距和教育需求,以及其他投入,已知出“在血友病中的基因治疗:一项教育倡议”。

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