Abedi Farshad, Omidkhoda Navid, Arasteh Omid, Ghavami Vahid, Hosseinzadeh Hossein
Department of Clinical Pharmacy, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Biostatistics, School of Health, Mashhad University of Medical Sciences, Mashhad, Iran.
Drug Res (Stuttg). 2023 Jan;73(1):5-16. doi: 10.1055/a-1879-3111. Epub 2022 Oct 10.
Pulmonary hypertension (PH) is a pathophysiological disorder, which involves multiple clinical conditions such as the upregulation of the Rho/ROCK signaling pathway. On the other hand, fasudil as a Rho kinase inhibitor has been investigated in the treatment of PH in some clinical studies.
The present systematic review and meta-analysis aimed to evaluate the human clinical trials regarding the efficacy of fasudil in the management of PH.
Databases were searched with pre-defined search terms, up to December 2021. Efficacy measures were such as mean pulmonary arterial pressure (mPAP), systolic PAP (sPAP), pulmonary vascular resistance (PVR), systolic vascular resistance (SVR) and cardiac index (CI).
A total of 12 studies involving 575 PH patients were included in our research. Eight short-term trials and four mid-term trials were found (no clinical trials on the long-term effects). Short-term trials had a before-after study design and measuring pulmonary hemodynamic parameters' intervention revealed a statistically significant improvement of mPAP, sPAP, PVR, SVR, and CI in the meta-analysis of five eligible studies. Three mid-term trials also revealed improvement in some pulmonary hemodynamic parameters with fasudil and in another mid-term trial, fasudil significantly decreased rehospitalization and mortality in PH patients. No serious adverse effects with fasudil were reported in these trials.
Fasudil therapy is efficacious and probably safe in the improvement of some hemodynamics in PH patients along short and mid-term periods. However, long-term randomized controlled trials comparing fasudil with placebo and other treatments are warranted for confirmation of these benefits.
肺动脉高压(PH)是一种病理生理紊乱,涉及多种临床情况,如Rho/ROCK信号通路的上调。另一方面,法舒地尔作为一种Rho激酶抑制剂,已在一些临床研究中用于治疗PH。
本系统评价和荟萃分析旨在评估关于法舒地尔治疗PH疗效的人体临床试验。
使用预定义的检索词检索数据库,检索截至2021年12月的文献。疗效指标包括平均肺动脉压(mPAP)、收缩期肺动脉压(sPAP)、肺血管阻力(PVR)、体循环血管阻力(SVR)和心脏指数(CI)。
我们的研究共纳入12项涉及575例PH患者的研究。发现8项短期试验和4项中期试验(无关于长期影响的临床试验)。短期试验采用前后对照研究设计,在5项符合条件的研究的荟萃分析中,测量肺血流动力学参数的干预显示mPAP、sPAP、PVR、SVR和CI有统计学意义的改善。3项中期试验也显示法舒地尔可改善一些肺血流动力学参数,在另一项中期试验中,法舒地尔显著降低了PH患者的再住院率和死亡率。这些试验中未报告法舒地尔有严重不良反应。
法舒地尔治疗在短期和中期改善PH患者的一些血流动力学方面有效且可能安全。然而,需要进行长期随机对照试验,将法舒地尔与安慰剂及其他治疗方法进行比较,以证实这些益处。