Operative Care Line, Michael E. DeBakey VA Medical Center, Department of Surgery, Baylor College of Medicine, Houston, Texas2Department of Cardiovascular Surgery, Texas Heart Institute, Houston.
Hines Cooperative Studies Program Coordinating Center, Hines, Illinois.
JAMA Surg. 2014 Jun;149(6):507-13. doi: 10.1001/jamasurg.2013.4150.
Surgical clinical trials have played a critical role in shaping clinical practice, yet their launch and conduct remain challenging. Innovative approaches to carrying out such studies can not only help transform how trials produce definitive evidence but also move the field toward increased participation in trials.
To review a recently launched pilot program aimed at enhancing patient enrollment and improving surgical trial operations at individual sites and nationally.
After a solicitation to create a national network focused on making the conduct of clinical trials more efficient, 10 Department of Veterans Affairs (VA) sites were selected. These sites, collectively called the Cooperative Studies Program (CSP) Network of Dedicated Enrollment Sites (NODES), were evaluated with regard to their previous participation in CSP multisite trials, the strength of the local clinical research environment, and presentation of innovative plans to coordinate and enhance the operations of local CSP studies and share best practices with other centers. Node accountability was also emphasized and involved metrics that tracked productivity and efficiency.
Building from available CSP experience in a range of clinical trials, including ones involving surgical interventions, NODES provides VA surgeons with resources for facilitating timely study initiation, determining patient availability, and addressing enrollment barriers. Such resources are particularly important for surgical studies, which often face challenges in patient recruitment and retention. In addition, NODES can maintain qualified and trained personnel at sites to support surgeons with limited time to fulfill the numerous administrative and regulatory responsibilities that often fall to the investigators.
The VA's approach to enhancing trial efficiency may reinvigorate interest in surgical trials by offering a redesigned cooperative framework that builds on a core of high-yield sites and could mitigate traditional limitations of surgical trials.
外科临床试验在塑造临床实践方面发挥了关键作用,但它们的启动和实施仍然具有挑战性。开展此类研究的创新方法不仅有助于改变试验产生明确证据的方式,还可以推动该领域增加对试验的参与。
审查最近启动的一个试点计划,旨在提高患者入组率,并改善各站点和全国范围内的外科试验操作。
在征集建立一个专注于提高临床试验效率的全国性网络后,选择了 10 个退伍军人事务部(VA)站点。这些站点统称为合作研究计划(CSP)专用入组站点(NODES)网络,根据他们以前参与 CSP 多站点试验、当地临床研究环境的实力以及提出协调和加强当地 CSP 研究运营并与其他中心分享最佳实践的创新计划进行评估。节点问责制也得到了强调,并涉及跟踪生产力和效率的指标。
利用 CSP 在各种临床试验中的现有经验,包括涉及外科干预的试验,NODES 为 VA 外科医生提供了便利及时启动研究、确定患者可用性和解决入组障碍的资源。这些资源对于外科研究尤其重要,因为外科研究通常在患者招募和保留方面面临挑战。此外,NODES 可以在站点保留合格和培训有素的人员,以支持时间有限的外科医生履行通常由调查员承担的众多行政和监管职责。
VA 提高试验效率的方法通过提供一个基于高产站点核心的重新设计的合作框架,可能重振对外科试验的兴趣,并减轻外科试验的传统局限性。