Department of Cardiac Surgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Department of Cardiac Surgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Ann Thorac Surg. 2022 Dec;114(6):2314-2321. doi: 10.1016/j.athoracsur.2021.10.033. Epub 2021 Nov 25.
A novel polymeric pulmonary valved conduit, resistant to calcification and structural valve deterioration, may provide a more durable therapy option for the pediatric population by preventing loss of right ventricular function and increasing freedom from valve-related reintervention and mortality.
This was a prospective, multicenter, single-arm study evaluating safety and performance of an investigational novel expanded polytetrafluoroethylene-based valve. Patients met study inclusion/exclusion criteria, had a signed informed consent, had pre- and postoperative evaluation via transthoracic echocardiography, and 6-month cardiac magnetic resonance imaging.
Seventeen patients were enrolled from 3 sites. Median age was 12 years (range, 6-17 years) with 52.9% male. Body surface area ranged from 0.82 to 1.57 m. There has been no mortality and 100% freedom from device related reinterventions. Baseline compared with 6-month cardiac magnetic resonance imaging (in 11 of 16 patients with available data) suggests favorable right ventricular remodeling (right ventricular end-diastolic volume, 123 ± 37 to 94 ± 25 mL/m) with no significant change in ejection fraction. Through current follow-up, no patient has a right ventricular outflow tract gradient >20 mm Hg (mean, 11.2 ± 4.3 mm Hg). No evidence of worsening valvular insufficiency was observed throughout postoperative serial transthoracic echocardiogram evaluations. No pulmonary regurgitation above baseline (≤ mild) was observed. No patient developed endocarditis. No thrombus or calcification was identified.
This preliminary evaluation of a novel expanded polytetrafluoroethylene-based valved conduit suggests promising valve function with no thromboembolic or infectious complications, no valve related reinterventions, no valve-related adverse events or unexpected findings, improved right ventricular volumes, and encouraging hemodynamic performance through current follow-up.
一种新型的聚合物肺动脉带瓣管道,具有抗钙化和结构瓣膜退化的特性,可能为儿科患者提供更持久的治疗选择,防止右心室功能丧失,并增加免于瓣膜相关再干预和死亡率。
这是一项前瞻性、多中心、单臂研究,评估一种新型膨体聚四氟乙烯(ePTFE)瓣膜的安全性和性能。患者符合研究纳入/排除标准,签署知情同意书,术前和术后均通过经胸超声心动图进行评估,并在 6 个月时进行心脏磁共振成像(CMR)检查。
来自 3 个中心的 17 名患者入选。中位年龄为 12 岁(范围,6-17 岁),52.9%为男性。体表面积为 0.82-1.57m。无死亡病例,100%免于器械相关再干预。与基线相比,6 个月心脏磁共振成像(在 16 名患者中有 11 名提供了可用数据)提示右心室重塑良好(右心室舒张末期容积从 123±37 降至 94±25mL/m),射血分数无显著变化。截至目前的随访中,没有患者的右心室流出道梯度>20mmHg(平均为 11.2±4.3mmHg)。术后系列经胸超声心动图评估未见瓣膜功能不全加重的证据。未观察到任何高于基线的(≤轻度)肺动脉瓣反流。没有患者发生感染性心内膜炎。没有血栓或钙化。
新型 ePTFE 带瓣管道的初步评估表明,该瓣膜具有良好的功能,无血栓栓塞或感染并发症,无瓣膜相关再干预,无瓣膜相关不良事件或意外发现,右心室容积改善,且目前的随访中血流动力学表现令人鼓舞。