Rapid Deployment Aortic Replacement (RADAR) Registry in Spain: a protocol

被引:6
作者
Bautista-Hernandez, Victor [1 ,2 ]
Cal-Purrinos, Natalia [3 ]
Arribas-Leal, Jose M. [4 ]
Carnero-Alcazar, Manuel [5 ]
Gutierrez-Diez, Jose F. [6 ]
Cuenca-Castillo, Jose J. [1 ]
机构
[1] Xerencia Xest Integrada A Coruna XXIAC, Dept Cardiovasc Surg, La Coruna, Spain
[2] Inst Invest Biomed A Coruna INIBIC, Congenital & Struct Heart Dis, La Coruna, Spain
[3] Xerencia Xest Integrada A Coruna XXIAC, Fdn Prof Novoa Santos, La Coruna, Spain
[4] Hosp Virgen Arrixaca, Dept Cardiovasc Surg, Murcia, Spain
[5] Hosp Clin San Carlos, Dept Cardiovasc Surg, Madrid, Spain
[6] Hosp Marques de Valdecilla, Dept Cardiovasc Surg, Santander, Spain
来源
BMJ OPEN | 2017年 / 7卷 / 01期
关键词
INTERMEDIATE-SURGICAL-RISK; VALVE-REPLACEMENT; ELDERLY-PATIENTS; TRANSCATHETER; STENOSIS; OUTCOMES; IMPLANTATION; MULTICENTER; SOCIETY; DISEASE;
D O I
10.1136/bmjopen-2016-011437
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Rapid deployment valves (RDV) represent a newly introduced approach to aortic valve replacement which facilitates surgical implantation and minimally invasive techniques, shortens surgical times and shows excellent haemodynamic performance. However, evidence on their safety, efficacy and potential complications is mostly fitted with small-volume and retrospective studies. Moreover, no current guidelines exist. To improve our knowledge on this technology, The Rapid Deployment Aortic Replacement (RADAR) Registry will be established across Spain with the aim of assessing RDV outcomes in the real-world setting. Methods and analysis The RADAR Registry is designed as a product registry that would provide information on its use and outcomes in clinical practice. This multicentre, prospective, national effort will initially involve 4 centres in Spain. Any patient undergoing cardiac surgery for aortic valve replacement and receiving an RDV as an isolated operation or in combination with other cardiac procedures may be included. Participation is voluntary. Data collection is equal to information obtained during standard care and is prospectively entered by the participating physicians perioperatively and during subsequent follow-up visits. The primary outcome assessed is in-hospital and up to 5years of follow-up, prosthetic valve functioning and clinical status. Secondary outcomes are to perform subgroup analysis, to compare outcomes with other existing approaches and to develop future clinical guidelines. The follow-up assessments are timed with routine clinical appointments. Dissociated data will be extracted and collectively analysed. Initial target sample size for the registry is 500 participants entered with complete follow-up information. Different substudies will be implemented within the registry to investigate specific populations undergoing aortic valve replacement. Ethics and dissemination The protocol is approved by all local institutional ethics committees. Findings will be shared by the participant hospitals, policymakers and the academic community to promote quality monitoring and efficient use of this technology.
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页数:5
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