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牛颈静脉管道植入术后早期不良结局的风险因素:管道过大对结局的影响。

Risk factors for early adverse outcomes after bovine jugular vein conduit implantation: influence of oversized conduit on the outcomes.

机构信息

Division of Pediatric Cardiac Surgery, Department of Thoracic and Cardiovascular Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

出版信息

Interact Cardiovasc Thorac Surg. 2022 Sep 9;35(4). doi: 10.1093/icvts/ivac197.

Abstract

OBJECTIVES

We investigated potential risk factors for early failure of bovine jugular vein conduit (Contegra®) implantation for right ventricular outflow tract (RVOT) reconstruction.

METHODS

A single-centre retrospective review of 115 consecutive patients (54 males) who underwent RVOT reconstruction with Contegra between 2016 and 2019 was performed. Overall survival, explantation-free survival and freedom from significant RVOT lesions (valve regurgitation ≥ moderate or flow velocity ≥3.5 m/s) were investigated.

RESULTS

Median age, body weight and Contegra diameter were 10.3 months [interquartile range (IQR) 5.7-26.9 months], 7.8 kg (IQR 6.3-12.4 kg) and 14 mm (IQR 12-16 mm), respectively. During the median follow-up duration of 25.1 months, there were 7 deaths, 34 significant RVOT lesions, 10 endocarditis episodes and 15 explantations. Overall survival and explantation-free survival at 3 years were 94.8% and 78.4%, respectively. Significant RVOT lesions (n = 34) comprised 20 stenoses, 8 regurgitations and 6 combined lesions. Freedom from significant RVOT lesions at 3 years was 62.6%. Cox regression identified higher indexed Contegra size (Contegra diameter/body weight, mm/kg) as the only risk factor for decreased time to explantation or death (hazard ratio 2.32, P < 0.001) and time to significant RVOT lesions development (hazard ratio 2.75, P < 0.001). The cut-off value of indexed Contegra size for significant RVOT lesions at 12 months was 1.905 mm/kg (sensitivity, 0.75; specificity, 0.78; area under the curve, 0.82).

CONCLUSIONS

Outcomes of RVOT reconstruction using Contegra were acceptable. However, oversized Contegra should be avoided when possible.

IRB APPROVAL DATE

26 October 2020.

IRB REGISTRATION NUMBER

S2020-2505-0001.

摘要

目的

我们研究了牛颈静脉移植物(康特格拉®)用于右心室流出道(RVOT)重建的早期失败的潜在危险因素。

方法

对 2016 年至 2019 年间接受 RVOT 重建的 115 例连续患者(54 例男性)进行了单中心回顾性研究。研究了总体存活率、无移植物取出存活率和无明显 RVOT 病变(瓣膜反流≥中度或流速≥3.5m/s)的存活率。

结果

中位年龄、体重和康特格拉直径分别为 10.3 个月[四分位距(IQR)5.7-26.9 个月]、7.8kg(IQR 6.3-12.4kg)和 14mm(IQR 12-16mm)。在中位随访 25.1 个月期间,有 7 例死亡,34 例出现明显 RVOT 病变,10 例心内膜炎发作和 15 例移植物取出。3 年时的总生存率和无移植物取出生存率分别为 94.8%和 78.4%。34 例明显的 RVOT 病变包括 20 例狭窄、8 例反流和 6 例联合病变。3 年时无明显 RVOT 病变的生存率为 62.6%。Cox 回归分析发现,较大的康特格拉指数(康特格拉直径/体重,mm/kg)是导致移植物取出或死亡时间缩短的唯一危险因素(风险比 2.32,P<0.001)和 RVOT 明显病变发展时间(风险比 2.75,P<0.001)。12 个月时康特格拉指数大小的临界值为 1.905mm/kg(敏感性为 0.75;特异性为 0.78;曲线下面积为 0.82)。

结论

使用康特格拉进行 RVOT 重建的结果是可以接受的。然而,当可能时,应避免使用过大的康特格拉。

IRB 批准日期:2020 年 10 月 26 日。

IRB 注册号:S2020-2505-0001。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99b7/9514799/73382e6d56dc/ivac197f5.jpg

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