超声内镜引导门静脉压力梯度测量在肝定向治疗前评估肝功能中的作用。

IF 1.7 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Ahmed Telbany, Youssef Soliman, Gagandeep Singh, Khaled Abouelezz, Toufic Kachaamy
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引用次数: 0

摘要

肝脏定向治疗,如切除、消融和栓塞,作为多学科肿瘤治疗的一部分,为原发性和转移性肝脏肿瘤患者提供了潜在的治疗选择。然而,这些治疗具有显著的肝功能失代偿风险,特别是对于潜在的肝脏疾病和化疗相关的脂肪性肝炎。准确评估肝功能和门脉高压(PH)是候选人选择的关键。虽然Child-Pugh评分和终末期肝病模型是常用的,但它们有很大的局限性。肝静脉压梯度(HVPG)测量仍然是评估PH值的金标准,但它是有创的,并没有广泛应用。内镜超声(EUS)引导门静脉压力梯度(PPG)测量已成为一种有前途的微创替代方法。在早期研究中,EUS-PPG显示了出色的技术成功率、安全性以及与HVPG的相关性。通过提供直接的门静脉压力测量,EUS-PPG在肝脏定向治疗前的预后和风险分层方面比现有方法有几个优势,特别是在检测窦前高血压方面。此外,它在评估新辅助治疗的反应和指导辅助治疗方面具有潜在的应用价值。然而,还需要在更大的前瞻性队列中验证其预测性能和成本效益,并确定其与无创肝功能评估相比的准确性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of endoscopic ultrasound-guided portal pressure gradient measurement in assessing liver function before liver-directed therapies.

Liver-directed therapies such as resection, ablation, and embolization offer potentially curative options for patients with primary and metastatic liver tumors as part of multidisciplinary oncology care. However, these treatments pose significant hepatic decompensation risks, particularly with underlying liver disease and chemotherapy-associated steatohepatitis. Accurate assessment of liver function and portal hypertension (PH) is critical for candidate selection. While Child-Pugh score and model for end-stage liver disease are commonly used, they have substantial limitations. Hepatic venous pressure gradient (HVPG) measurement remains the gold standard for assessing PH but is invasive and not widely available. Endoscopic ultrasound (EUS) guided portal pressure gradient (PPG) measurement has emerged as a promising minimally invasive alternative. EUS-PPG demonstrates excellent technical success rates, safety profile, and correlation with HVPG in early studies. By providing direct portal pressure measurement, EUS-PPG offers several advantages over existing methods for prognostication and risk stratification prior to liver-directed therapies, particularly in detecting presinusoidal hypertension. Furthermore, it has potential applications in assessing response to neoadjuvant treatments and guiding adjuvant therapies. However, research is needed to validate its predictive performance and cost-effectiveness in larger prospective cohorts and to establish its accuracy compared to non-invasive assessment of liver function.

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