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复杂先天性心脏病患儿术后肝损伤的影响。

Impact of hepatopathy in pediatric patients after surgery for complex congenital heart disease.

机构信息

Department for Pediatric Cardiology, University Heart & Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Cardiac Surgery for Congenital Heart Disease, University Heart & Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

PLoS One. 2021 Mar 25;16(3):e0248776. doi: 10.1371/journal.pone.0248776. eCollection 2021.

Abstract

Patients undergoing complex pediatric cardiac surgery in early infancy are at risk of postoperative secondary end-organ dysfunction. The aim of this study was to determine specific risk factors promoting the development of peri- and postoperative hepatopathy after surgery for congenital heart disease. In this retrospective study, we identified 20 consecutive patients operated between 2011 and 2019 from our institutional cohort who developed significant postsurgical hepatic dysfunction. These patients were compared to a control group of 30 patients with comparable initial cardiac conditions and STS-EACTS risk score. Patients who developed hepatopathy in the intensive care unit have chronic cholestasis and decreased liver synthesis. The impact of postoperative hepatopathy on morbidity was marked. In six patients (30%), liver transplantation was executed as ultima ratio, and two (10%) were listed for liver transplantation. The overall mortality related to postoperative hepatopathy is high: We found nine patients (45%) having severe hepatopathy and mostly multiple organ dysfunction who died in the postoperative course. According to risk analysis, postoperative right and left heart dysfunction in combination with a postoperative anatomical residuum needing a re-operation or re-intervention in the postoperative period is associated with a high risk for the development of cardiac hepatopathy. Furthermore, postoperative complications (pleural effusion, heart rhythm disorders, etc.), postoperative infections, and the need for parenteral nutrition also raise the risk for cardiac hepatopathy. Further investigations are needed to reduce hepatic complications and improve the general prognosis of such complex patients.

摘要

在婴儿早期接受复杂儿科心脏手术的患者存在术后次要终末器官功能障碍的风险。本研究旨在确定促进先天性心脏病手术后围手术期肝疾病发展的特定危险因素。在这项回顾性研究中,我们从机构队列中确定了 20 名连续接受手术的患者,这些患者在 2011 年至 2019 年期间接受了手术,他们出现了明显的术后肝功能障碍。这些患者与具有可比初始心脏状况和 STS-EACTS 风险评分的 30 名对照组患者进行了比较。在重症监护病房中出现肝疾病的患者存在慢性胆汁淤积和肝脏合成减少。术后肝疾病对发病率的影响显著。在六名患者(30%)中,肝移植作为最后的治疗手段,两名患者(10%)被列入肝移植名单。与术后肝疾病相关的总死亡率很高:我们发现 9 名患者(45%)患有严重肝疾病,并且大多数患有多器官功能障碍,在术后期间死亡。根据风险分析,术后右心和左心功能障碍以及术后解剖残余物需要手术或再次干预与心脏肝疾病的发展高风险相关。此外,术后并发症(胸腔积液、心律紊乱等)、术后感染和需要肠外营养也会增加心脏肝疾病的风险。需要进一步研究以减少肝脏并发症并改善此类复杂患者的总体预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbdc/7993827/cf460f4c38aa/pone.0248776.g001.jpg

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