Porto-sinusoidal vascular disorder in surgical candidates for liver metastases: Prevalence, noninvasive diagnosis, and burden on surgical outcomes.

IF 4.7 2区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Liver Transplantation Pub Date : 2025-01-01 Epub Date: 2024-09-24 DOI:10.1097/LVT.0000000000000489
Elton Dajti, Matteo Serenari, Deborah Malvi, Gerti Dajti, Federico Ravaioli, Luigi Colecchia, Giovanni Marasco, Francesca Caputo, Matteo Renzulli, Francesco Vasuri, Amanda Vestito, Francesco Azzaroli, Giovanni Barbara, Matteo Ravaioli, Davide Festi, Antonietta D'Errico, Matteo Cescon, Antonio Colecchia
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引用次数: 0

Abstract

Chemotherapy can cause vascular and metabolic liver injury in patients with liver metastases, but scarce data are available. We aimed to (i) describe the prevalence of porto-sinusoidal vascular disorder (PSVD) among patients undergoing resection for liver metastases; and (ii) assess whether liver (LSM) and spleen stiffness measurements could diagnose PSVD and predict postoperative complications. This is a prospective single-center study enrolling consecutive patients undergoing hepatic resection for metastases at a tertiary center. For each patient, we evaluated previous exposure to chemotherapy, comorbidities, elastography, type of surgery, histological features at the resection specimen, morbidity (post-hepatectomy liver failure and major complications according to Clavien-Dindo), and 90-day survival. Sixty-eight patients were included, of whom 60 (88%) had received chemotherapy. Twenty-nine (44%) patients had PSVD. Spleen stiffness measurements <21 kPa (negative predictive value 87%) and >40 kPa (positive predictive value 100%) could accurately diagnose PSVD. PSVD significantly increased the risk of post-hepatectomy liver failure (22% vs. 45%) and major complications (11% vs. 31%). Preoperative LSM was associated with postoperative morbidity. The cutoff LSMs <4.5 and >8 kPa predicted the risk of clinically significant post-hepatectomy liver failure (0%, 11%, and 33% in LSM <4.5, 4.5-8, and >8 kPa, respectively) and major complications (0%, 25%, 44% in LSM <4.5, 4.5-8, and >8 kPa, respectively). PSVD is very common among patients undergoing liver surgery for metastases, and it is associated with increased morbidity. LSM and spleen stiffness measurements can correctly identify patients with PSVD and those at risk of clinically relevant postoperative complications.

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肝转移瘤手术候选者中的窦状门血管紊乱:发病率、无创诊断及对手术效果的影响。
背景和目的:化疗可导致肝转移患者的血管和肝脏代谢损伤,但相关数据却很少。我们的目的是:i)描述因肝转移而接受切除术的患者中门静脉血管紊乱(PSVD)的发生率;ii)评估肝脏(LSM)和脾脏硬度测量(SSM)是否能诊断 PSVD 并预测术后并发症:这是一项前瞻性单中心研究,在一家三级中心连续收治了接受肝转移切除术的患者。我们对每位患者的化疗前史、并发症、弹性成像、手术类型、切除标本的组织学特征、发病率[肝切除术后肝功能衰竭(PHLF)、根据Clavien-Dindo标准得出的主要并发症]和90天生存率进行了评估:共纳入 68 例患者,其中 60 例(88%)接受过化疗。29名患者(44%)患有 PSVD。SSM 40 kPa(PPV 100%)可准确诊断 PSVD。PSVD 会明显增加 PHLF(22 对 45%)和主要并发症(11 对 31%)的风险。术前 LSM 与术后发病率相关。LSM 8 kPa的临界值可预测有临床意义的PHLF风险(LSM 8 kPa分别为0%、11%和33%)和主要并发症风险(LSM 8 kPa分别为0%、25%和44%):PSVD在接受肝脏转移手术的患者中非常常见,而且与发病率的增加有关。LSM 和 SSM 可以正确识别 PSVD 患者和有临床相关术后并发症风险的患者。
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来源期刊
Liver Transplantation
Liver Transplantation 医学-外科
CiteScore
7.40
自引率
6.50%
发文量
254
审稿时长
3-8 weeks
期刊介绍: Since the first application of liver transplantation in a clinical situation was reported more than twenty years ago, there has been a great deal of growth in this field and more is anticipated. As an official publication of the AASLD, Liver Transplantation delivers current, peer-reviewed articles on liver transplantation, liver surgery, and chronic liver disease — the information necessary to keep abreast of this evolving specialty.
期刊最新文献
The impact of normothermic machine perfusion and acuity circles on waitlist time, mortality, and cost in liver transplantation: A multicenter experience. Ex-situ machine perfusion in clinical liver transplantation: Current practices and future directions. Prediction of portal venous pressure in living donor liver transplantation: A retrospective study. The clinical relevance of the new criteria for cirrhotic cardiomyopathy and future directions. Safety of acamprosate for alcohol use disorder after liver transplant: A pilot randomized controlled trial.
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