Hannover Medical School, Department of Gastroenterology, Hepatology, Infectious Diseases and Endocrinology, Hannover, Germany.
German Center for Infection Research (DZIF), Hannover-Braunschweig, Hannover, Germany.
Aliment Pharmacol Ther. 2024 Oct;60(8):1021-1032. doi: 10.1111/apt.18204. Epub 2024 Aug 27.
Non-selective beta-blockers (NSBB) are a well-established treatment in patients with clinically significant portal hypertension. However, their potential role after insertion of a transjugular intrahepatic portosystemic shunt (TIPS) still needs to be determined. Of note, recent studies suggested that favourable anti-inflammatory effects of NSBB might be independent from pressure reduction. This study aimed to evaluate whether NSBB-treatment is associated with amelioration of systemic inflammation (SI), hepatic decompensation and survival after TIPS-insertion.
In a retrospective study comprising 305 consecutive patients, we investigated the impact of NSBB-intake at TIPS-placement on periinterventional cirrhosis-associated complications and continued NSBB-treatment after discharge on complications including hepatic decompensation and mortality during 1-year follow-up, employing multivariable competing-risk-analyses. In a prospective cohort including 45 patients, we performed a comprehensive analysis of SI analysing 48 soluble inflammatory markers (SIMs) at baseline plus 3 and 6 months after TIPS-insertion.
Overall, 175 (57.4%) patients received NSBB-therapy prior to TIPS-insertion; upon discharge, this decreased to 131 (22.9%), with 36 (27.5%) discontinuing NSBB within 1-year follow-up. Neither NSBB-therapy at TIPS-insertion nor treatment-continuation after discharge were associated with lower risks for hepatic decompensation, individual cirrhosis-associated complications or mortality neither in the periinterventional period nor during follow-up. Similarly, in the prospective cohort NSBB-intake was not linked to lower levels or a more prominent change of WBC, CRP or any other SIM at any of the investigated time points.
NSBB-therapy at the time of TIPS-insertion and its (dis-)continuation afterwards seems to have no significant impact on SI, development of hepatic decompensation and survival.
非选择性β受体阻滞剂(NSBB)是治疗临床显著门静脉高压症患者的有效方法。然而,其在经颈静脉肝内门体分流术(TIPS)后应用的潜在作用仍有待确定。值得注意的是,最近的研究表明,NSBB 的有利抗炎作用可能与其降压作用无关。本研究旨在评估 TIPS 置入时使用 NSBB 治疗是否与改善全身炎症(SI)、肝功能失代偿和 TIPS 置入后的生存率有关。
在一项回顾性研究中,我们纳入了 305 例连续患者,研究了 TIPS 放置时使用 NSBB 对围手术期与肝硬化相关并发症的影响,以及出院后继续使用 NSBB 治疗对包括肝功能失代偿和 1 年随访期间死亡率在内的并发症的影响,采用多变量竞争风险分析。在一项包括 45 例患者的前瞻性队列研究中,我们对 SI 进行了全面分析,在 TIPS 置入前、后 3 个月和 6 个月检测了 48 种可溶性炎症标志物(SIM)。
总体而言,175 例(57.4%)患者在 TIPS 置入前接受了 NSBB 治疗;出院时,这一比例降至 131 例(22.9%),其中 36 例(27.5%)在 1 年随访期间停止使用 NSBB。TIPS 置入时使用 NSBB 治疗或出院后继续使用 NSBB 治疗,在围手术期或随访期间,均与肝功能失代偿、单个肝硬化相关并发症或死亡率的风险降低无关。同样,在前瞻性队列中,NSBB 摄入与任何时间点的白细胞计数(WBC)、C 反应蛋白(CRP)或任何其他 SIM 的水平降低或更明显的变化无关。
TIPS 置入时使用 NSBB 治疗及其(停用)后,似乎对 SI、肝功能失代偿和生存率没有显著影响。