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康特格拉®带瓣同种异体移植物管道用于右心室流出道重建:一种可靠的解决方案。

The contegra® valved heterograft conduit for right ventricular outflow tract reconstruction: a reliable solution.

机构信息

Department of Pediatric and Congenital Cardiac Surgery, Mitera Children's Hospital, Athens, Greece.

出版信息

Hellenic J Cardiol. 2011 Nov-Dec;52(6):501-8.

Abstract

INTRODUCTION

The Contegra® bioprosthetic valved conduit, a glutaraldehyde-preserved valve-containing bovine jugular vein graft (Contegra, Medtronic Inc., Minneapolis MN, USA) introduced for clinical trials in 1998, is used for reconstruction of the right ventricular outflow tract (RVOT), mainly in children. This study evaluates our surgical experience with the Contegra® graft, emphasizing the assessment of conduit durability at mid-term follow up.

METHODS

The intermediate results of RVOT reconstruction utilizing the Contegra conduit were retrospectively analyzed in a series of 34 consecutive patients (25 male, 9 female), with a mean age of 10.9 ± 11.2 years (range 0.2-46 years). Included were 14 patients with tetralogy of Fallot (TOF) with pulmonary atresia, 11 with reoperation of previously corrected TOF, 5 with truncus arteriosus, 2 with TOF with absent pulmonary valve, 1 reoperation of previously repaired double outlet right ventricle with pulmonary atresia, and 1 undergoing a Ross procedure. Contegra conduit sizes varied in diameter between 12 and 22 mm (mean 18.3 ± 3.2 mm).

RESULTS

There were no hospital deaths. There was one early conduit replacement as a result of recurrent thrombosis. Four patients developed early thrombus formation in a valve cusp with complete resolution following anticoagulation therapy. At mean follow up of 85 months (range 6-136 months) and median follow up of 95 months, one patient required Contegra graft explantation in another institution (indications unknown). Freedom from reoperation for Contegra grafts was 94% at 11.4 years. Mean transpulmonary pressure gradients remained low (9.6 ± 5.3 mmHg postoperative, 19.6 ± 10.6 mmHg at follow up). Although there was a clear trend towards worsening of conduit valve insufficiency, this was neither statistically significant nor considered clinically so.

CONCLUSIONS

In our experience of 34 consecutive operations, the Contegra® valved conduit for RVOT reconstruction seems to be a reliable alternative to homograft conduits, with promising mid-term freedom from structural deterioration and reoperation.

摘要

介绍

康特格拉®生物瓣血管移植物是一种戊二醛保存的含瓣膜牛颈静脉移植物(康特格拉,美敦力公司,明尼苏达州明尼阿波利斯,美国),于 1998 年开始临床试验,用于右心室流出道(RVOT)的重建,主要用于儿童。本研究评估了我们使用康特格拉®移植物的手术经验,重点评估中期随访时移植物的耐久性。

方法

对 34 例连续患者(25 例男性,9 例女性)应用康特格拉移植物行 RVOT 重建的中间结果进行回顾性分析,患者平均年龄为 10.9 ± 11.2 岁(范围 0.2-46 岁)。包括 14 例法洛四联症伴肺动脉闭锁患者,11 例法洛四联症矫治术后再手术患者,5 例永存动脉干患者,2 例法洛四联症伴无肺动脉瓣患者,1 例曾行右心室双出口伴肺动脉闭锁矫治术后再次手术患者,1 例行罗斯手术患者。康特格拉移植物直径在 12-22mm 之间(平均 18.3 ± 3.2mm)。

结果

无院内死亡。1 例患者因复发性血栓形成早期更换移植物。4 例患者在瓣膜叶形成早期血栓形成,经抗凝治疗后完全消退。平均随访 85 个月(6-136 个月),中位随访 95 个月,1 例患者在另一机构行康特格拉移植物取出(原因不明)。康特格拉移植物无再手术率为 94%,随访 11.4 年。跨肺压梯度仍较低(术后 9.6 ± 5.3mmHg,随访时 19.6 ± 10.6mmHg)。尽管移植物瓣关闭不全有明显加重趋势,但无统计学意义,也无临床意义。

结论

在我们 34 例连续手术的经验中,康特格拉®RVOT 重建用带瓣血管移植物似乎是同种移植物的可靠替代品,具有良好的中期结构无恶化和无再手术的前景。

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