Hristo Kirov, Murat Mukharyamov, Angelique Runkel, Tulio Caldonazo, Torsten Doenst
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引用次数: 0
Abstract
Different techniques allow implantation of biological aortic valve prostheses larger than associated with classic annulus sizing. We described a replica-based technique (upsizing) before that utilizes the patient's root anatomy. We here evaluate the safety and efficacy of upsizing compared with standard sizing using the Epic Supra bioprosthesis.We assessed 958 patients undergoing aortic valve replacement with the Epic Supra bioprosthesis between 2010 and 2023. Upsizing was defined as implantation of a prosthesis larger than the measured annular size without enlarging the annulus. We assessed hemodynamic and standard outcome parameters. Mean follow-up was 44.5 ± 31.2 months. Propensity score matching was used to adjust for baseline differences.Patient anatomy allowed upsizing in 62% of patients. Demographics and outcomes (perioperative mortality, reoperation, bleeding, and pacemaker implantation) were comparable between the matched groups. Immediate postoperative and long-term pressure gradients were consistently and significantly lower in the upsizing groups across all annular sizes (upsizing vs. control: 23 mm; 12.9 ± 8.2 vs. 14.0 ± 5.6 mm Hg, p = 0.029; 25 mm; 10.8 ± 4.0 vs. 13.0 ± 4.4 mm Hg, p < 0.001; 27 mm; 10.8 ± 4.0 vs. 13.0 ± 4.4 mm Hg, p < 0.001). Differences persisted at long-term follow-up but were less pronounced for the 25-mm annular size and greatest in the 27-mm group (8.5 ± 4.5 vs. 12.5 ± 5.5 mm Hg; p < 0.001). Long-term survival was numerically higher in the upsizing groups with statistical significance in annular size 25 mm.Implanting a larger Epic Supra prosthesis than classically recommended ("upsizing") is safe and associated with improved immediate- and long-term hemodynamics without increasing pacemaker, perioperative, or long-term mortality risks.
不同的技术允许植入比传统环尺寸更大的生物主动脉瓣假体。我们之前描述了一种基于复制的技术(放大),它利用了患者的根解剖结构。我们在此评估使用Epic Supra生物假体与标准假体相比,放大假体的安全性和有效性。我们评估了2010年至2023年间使用Epic Supra生物假体进行主动脉瓣置换术的958例患者。放大定义为植入假体大于测量的环尺寸而不扩大环。我们评估了血流动力学和标准结局参数。平均随访44.5±31.2个月。倾向评分匹配用于调整基线差异。患者解剖允许62%的患者增大尺寸。人口统计学和结果(围手术期死亡率、再手术、出血和起搏器植入)在匹配组之间具有可比性。在所有环空尺寸中,增大组的术后即刻和长期压力梯度一致且显著降低(增大组与对照组:23 mm; 12.9±8.2 vs. 14.0±5.6 mm Hg, p = 0.029; 25 mm; 10.8±4.0 vs. 13.0±4.4 mm Hg, p p p p)
期刊介绍:
The Thoracic and Cardiovascular Surgeon publishes articles of the highest standard from internationally recognized thoracic and cardiovascular surgeons, cardiologists, anesthesiologists, physiologists, and pathologists. This journal is an essential resource for anyone working in this field.
Original articles, short communications, reviews and important meeting announcements keep you abreast of key clinical advances, as well as providing the theoretical background of cardiovascular and thoracic surgery. Case reports are published in our Open Access companion journal The Thoracic and Cardiovascular Surgeon Reports.