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肝硬化和可治愈性肝病患者中Baveno VII再补偿标准的验证与扩展

Validation and expansion of Baveno VII recompensation criteria in patients with cirrhosis and curable liver disease.

作者信息

Tonon Marta, Gagliardi Roberta, Pompili Enrico, Barone Anna, Zaccherini Giacomo, Zilio Gianluca, Baldassarre Maurizio, Accetta Antonio, Carrello Daniele, Calvino Valeria, Iannone Giulia, Incicco Simone, Zeni Nicola, Gambino Carmine Gabriele, Caraceni Paolo, Angeli Paolo, Piano Salvatore

机构信息

Unit of Internal Medicine and Hepatology, Department of Medicine, University of Padova.

Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, Italy; Unit of Semeiotics, Liver and Alcohol-related diseases, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Italy.

出版信息

J Hepatol. 2025 Apr 12. doi: 10.1016/j.jhep.2025.04.018.

Abstract

BACKGROUND AND AIMS

Baveno-VII consensus recently defined recompensation in patients with decompensated cirrhosis achieving etiological cure. However, incidence, predictors and clinical significance of recompensation are poorly known. This study aimed to evaluate the incidence and prognostic impact of recompensation in patients with decompensated cirrhosis.

METHODS

Outpatients with cirrhosis and curable etiologies (alcohol, HCV, HBV) were consecutively included and followed up. Recompensation was defined according to Baveno VII criteria. Additionally, expanded recompensation criteria were evaluated for patients on low dose diuretics and/or lactulose/rifaximin for ≥12 months. In 160 patients, inflammatory cytokines (IL-6,IL-1β, IL-10) were measured in serum samples. An external cohort was used to validate study findings.

RESULTS

298 out of 525 decompensated cirrhotic outpatients achieved an effective etiological treatment and 21 (7%) achieved recompensation (Baveno-VII criteria), while 112 patients achieved expanded recompensation criteria (37.6%). MELD score (sHR=0.89; p<0.001), BMI (sHR=0.93; p=0.020), hemoglobin (sHR=1.14; p=0.010) and further decompensation (sHR=0.50; p=0.001) were independent predictors of recompensation. In multivariable analysis, mortality risk was not significantly different between patients achieving recompensation and compensated patients (HR=0.97; p=0.947), while decompensated patients had the highest mortality risk (HR=4.96; p<0.001). Mortality risk was not significantly different between patients meeting expanded recompensation criteria and Baveno-VII criteria (HR=0.97; p=0.938). Serum IL-6, IL-1beta and IL-10 were significantly higher in decompensated patients than in compensated and recompensated patients.

CONCLUSION

Baveno-VII criteria identify cirrhotic patients with a good prognosis, but fewer than 10% of decompensated patients achieve recompensation. Expanding these criteria to include patients receiving minimal decompensation treatment identifies those with similarly low mortality risk.

IMPACT AND IMPLICATIONS

In recent years, growing evidence has shown that achieving an etiological cure can significantly improve the prognosis of decompensated patients, leading to the development of the concept of recompensation. Baveno VII recently proposed a definition for recompensation; however, data on the clinical impact of this condition remain limited. In this study we evaluated Baveno VII criteria and developed and validated expanded Baveno VII criteria for recompensation. Our findings demonstrates that recompensation is associated with improved survival, reduced hyperdynamic circulation and decreased systemic inflammation in outpatients with decompensated cirrhosis. These results are valuable for hepatologists and researchers aiming to refine patient management strategies and risk stratification in cirrhosis care.

摘要

背景与目的

巴韦诺 VII 共识最近对失代偿期肝硬化病因治愈患者的再代偿进行了定义。然而,再代偿的发生率、预测因素及临床意义尚不清楚。本研究旨在评估失代偿期肝硬化患者再代偿的发生率及其预后影响。

方法

连续纳入病因可治愈(酒精性、丙型肝炎病毒、乙型肝炎病毒)的肝硬化门诊患者并进行随访。根据巴韦诺 VII 标准定义再代偿。此外,对使用低剂量利尿剂和/或乳果糖/利福昔明≥12 个月的患者评估扩展的再代偿标准。在 160 例患者中,检测血清样本中的炎性细胞因子(白细胞介素 -6、白细胞介素 -1β、白细胞介素 -10)。使用外部队列验证研究结果。

结果

525 例失代偿期肝硬化门诊患者中,298 例实现了有效的病因治疗,21 例(7%)实现了再代偿(巴韦诺 VII 标准),而 112 例患者达到了扩展的再代偿标准(37.6%)。终末期肝病模型(MELD)评分(标准化风险比[sHR]=0.89;p<0.001)、体重指数(BMI)(sHR=0.93;p=0.020)、血红蛋白(sHR=1.14;p=0.010)及进一步失代偿(sHR=0.50;p=0.001)是再代偿的独立预测因素。在多变量分析中,实现再代偿的患者与代偿患者的死亡风险无显著差异(风险比[HR]=0.97;p=0.947),而失代偿患者的死亡风险最高(HR=4.96;p<0.001)。达到扩展再代偿标准的患者与符合巴韦诺 VII 标准的患者的死亡风险无显著差异(HR=0.97;p=0.938)。失代偿患者血清白细胞介素 -6、白细胞介素 -1β和白细胞介素 -10 显著高于代偿和再代偿患者。

结论

巴韦诺 VII 标准可识别预后良好的肝硬化患者,但失代偿患者中实现再代偿的不到 10%。将这些标准扩展至包括接受最小化失代偿治疗的患者,可识别出死亡风险同样较低的患者。

影响与意义

近年来,越来越多的证据表明病因治愈可显著改善失代偿患者的预后,从而产生了再代偿的概念。巴韦诺 VII 最近提出了再代偿的定义;然而,关于这种情况临床影响的数据仍然有限。在本研究中,我们评估了巴韦诺 VII 标准,并制定和验证了扩展的巴韦诺 VII 再代偿标准。我们的研究结果表明,再代偿与失代偿期肝硬化门诊患者生存率提高、高动力循环减轻及全身炎症反应降低相关。这些结果对于旨在优化肝硬化护理中患者管理策略和风险分层的肝病学家和研究人员具有重要价值。

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