Jiang Lili, Ran Jing, Zhu Yu, Pan Lupin, Yang Bayi, Ran Xue, Ran Ying, Ding Hejun, Yang Jurong, Wu Shaofa
Department of Nephrology, The Third Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Department of Nephrology, Youyang Hospital, a Branch of The First Affiliated Hospital of Chongqing Medical University, China.
PLoS One. 2025 Sep 4;20(9):e0330038. doi: 10.1371/journal.pone.0330038. eCollection 2025.
Hypertension is associated with elevated mortality rates among individuals on maintenance hemodialysis (MHD). However, there is limited information regarding the efficacy and safety of sacubitril-valsartan (SV) in MHD patients suffering from hypertension. Consequently, this study aims to evaluate the efficacy and safety of SV in this specific patient population.
We retrospectively reviewed the data of MHD patients with hypertension who were receiving SV treatment at our hospital from January 1, 2023 to June 30, 2024. The SV dose ranged from 50 mg twice daily to 200 mg twice daily. Blood pressure measurements were compared at baseline and during follow-up intervals to assess therapeutic efficacy. Safety evaluations included comprehensive monitoring of treatment-emergent adverse events throughout the observation period.
A total of 64 MHD patients hypertension (mean age = 54.11 years; male proportion = 73.4%) were ultimately included in the study. After three months of treatment with SV, the mean reductions in systolic blood pressure, diastolic blood pressure, and pulse pressure were 21.06 ± 15.82 mmHg (P < 0.001), 8.41 ± 13.09 mmHg (P < 0.001), and 12.65 ± 13.17 mmHg (P < 0.001), respectively. With respect to safety, new-onset intradialytic hypotension was observed in three patients. The study also included twelve patients with hyperkalemia. Importantly, no patients reported experiencing cough, angioedema, or abnormal liver biochemistry. Among the 64 subjects, none required a dose reduction or discontinuation of SV due to these adverse effects.
In MHD patients with hypertension, SV demonstrates a preliminary ability to lower blood pressure and appears safe. Further prospective randomized studies are warranted to validate our findings.
高血压与维持性血液透析(MHD)患者的死亡率升高有关。然而,关于沙库巴曲缬沙坦(SV)在患有高血压的MHD患者中的疗效和安全性的信息有限。因此,本研究旨在评估SV在这一特定患者群体中的疗效和安全性。
我们回顾性分析了2023年1月1日至2024年6月30日在我院接受SV治疗的高血压MHD患者的数据。SV剂量范围为每日两次50毫克至每日两次200毫克。在基线和随访期间比较血压测量值,以评估治疗效果。安全性评估包括在整个观察期内对治疗中出现的不良事件进行全面监测。
共有64例高血压MHD患者(平均年龄 = 54.11岁;男性比例 = 73.4%)最终纳入研究。用SV治疗三个月后,收缩压、舒张压和脉压的平均降低值分别为21.06±15.82 mmHg(P < 0.001)、8.41±13.09 mmHg(P < 0.001)和12.65±13.17 mmHg(P < 0.001)。在安全性方面,有3例患者出现了新的透析中低血压。该研究还包括12例高钾血症患者。重要的是,没有患者报告出现咳嗽、血管性水肿或肝生化异常。在这64名受试者中,没有人因这些不良反应而需要减少SV剂量或停药。
在患有高血压的MHD患者中,SV显示出初步的降压能力且似乎是安全的。需要进一步的前瞻性随机研究来验证我们的发现。