Preoperative computed tomography-imaging with patient-specific computer simulation in transcatheter aortic valve implantation: Design and rationale of the GUIDE-TAVI trial

被引:1
|
作者
Hegeman, Romy R. M. J. J. [1 ,6 ,8 ]
van Ginkel, Dirk-Jan [2 ]
Laengle, Severin [3 ]
Timmers, Leo [2 ]
Rensing, Benno J. W. M. [2 ]
de Kroon, Thomas L. [1 ]
Sonker, Uday [1 ]
Kelder, Johannes C. [4 ]
Mach, Markus [3 ,7 ]
Andreas, Martin [2 ,3 ]
Swaans, Martin J. [2 ]
ten Berg, Jurrien M. [2 ,5 ]
Klein, Patrick [1 ,6 ]
机构
[1] St Antonius Hosp, Dept Cardiothorac Surg, Nieuwegein, Netherlands
[2] St Antonius Hosp, Dept Cardiol, Nieuwegein, Netherlands
[3] Med Univ Vienna, Dept Cardiothorac Surg, Vienna, Austria
[4] St Antonius Hosp, Dept Epidemiol, Nieuwegein, Netherlands
[5] Cardiovasc Res Inst Maastricht, Maastricht, Netherlands
[6] Amsterdam Univ Med Ctr, Dept Cardiothorac Surg, Amsterdam, Netherlands
[7] Univ Freiburg, Fac Med, Heart Ctr Freiburg, Dept Cardiovasc Surg, Freiburg, Germany
[8] St Antonius Ziekenhuis Nieuwegein, Dept Cardiothorac Surg, Room 1-AF-36-2,E1 Cardiothoracale Chirurg,Koekoeks, NL-CM 3435 Nieuwegein, Netherlands
关键词
MILD PARAVALVULAR REGURGITATION; OUTCOMES;
D O I
10.1016/j.ahj.2023.12.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Transcatheter aortic valve implantation (TAVI) is an established treatment option for patients with severe aortic valve stenosis, but is still associated with relatively high rates of pacemaker implantation and paravalvular regurgitation. Routine preoperative computed tomography (CT) combined with patient-specific computer modelling can predict the interaction between the TAVI device and the patient's unique anatomy, allowing physicians to assess the risk for paravalvular regurgitation and conduction disorders in advance to the procedure. The aim of this trial is to assess potential improvement in the procedural outcome of TAVI by applying CT-based patient-specific computer simulations in patients with suitable anatomy for TAVI. Methods The GUIDE-TAVI trial is an international multicenter randomized controlled trial including patients accepted for TAVI by the Heart Team. Patients enrolled in the study will be randomized into 2 arms of each 227 patients. In patients randomized to the use of FEops HEARTGuide (FHG), patient-specific computer simulation with FHG is performed in addition to routine preoperative CT imaging and results of the FHG are available to the operator(s) prior to the scheduled intervention. In patients randomized to no use of FHG, only routine preoperative CT imaging is performed. The primary objective is to evaluate whether the use of FHG will reduce the incidence of mild to severe PVR, according to the Valve Academic Research Consortium 3. Secondary endpoints include the incidence of new conduction disorders requiring permanent pacemaker implantation, the difference between preoperative and final selected valve size, the difference between target and final implantation depth, change of preoperative decision, failure to implant valve, early safety composite endpoint and quality of life. Conclusions The GUIDE-TAVI trial is the first multicenter randomized controlled trial to evaluate the value of 3dimensional computer simulations in addition to standard preprocedural planning in TAVI procedures. (Am Heart J 2024;269:158-166.)
引用
收藏
页码:158 / 166
页数:9
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