实用医学杂志 ›› 2024, Vol. 40 ›› Issue (4): 543-548.doi: 10.3969/j.issn.1006-5725.2024.04.018

• 药物与临床 • 上一篇    下一篇

沙库巴曲缬沙坦治疗慢性肾脏病5期难治性高血压患者的临床观察

宁燕虹1,2,徐苑珊1,李晓华1,李仕华1,杨桢华1,廖蕴华1,潘玲1()   

  1. 1.广西医科大学第一附属医院肾内科 (南宁 530021 )
    2.南宁市第二人民医院肾内科 (南宁 530031 )
  • 收稿日期:2023-08-24 出版日期:2024-02-25 发布日期:2024-03-08
  • 通讯作者: 潘玲 E-mail:nnpanling008@sina.com
  • 基金资助:
    广西自然科学基金项目(2022GXNSFAA035458);广西医疗卫生适宜技术开发与推广应用项目(S2018045)

An observational study on the treatment of chronic kidney disease stage 5 with resistant hypertension with sacubitril/valsartan

Yanhong NING1,2,Yuanshan XU1,Xiaohua LI1,Shihua LI1,Zhenhua YANG1,Yunhua LIAO1,Ling. PAN1()   

  1. *.Department of Nephrology,the First Affiliated Hospital of Guangxi Medical University,Nanning 530021,China
    *.Department of Nephrology,the Second Nanning People′s Hospital,Nanning 530031,China
  • Received:2023-08-24 Online:2024-02-25 Published:2024-03-08
  • Contact: Ling. PAN E-mail:nnpanling008@sina.com

摘要:

目的 评估沙库巴曲缬沙坦治疗慢性肾脏病(CKD)5期合并难治性高血压患者的心血管获益及安全性。 方法 一项真实世界的观察性研究,选取2020年9月至2022年3月广西医科大学第一附属医院诊治的CKD5期合并难治性高血压患者,分为观察组(沙库巴曲缬沙坦)和对照组(ACEI或ARB),两组患者均接受规律透析及CKD5期常规药物治疗,随访至少3个月。比较两组患者之间的基线资料、疗效及安全性指标的差异,观察不良事件发生情况。 结果 研究共纳入110例患者,观察组及对照组各55例。两组患者按1∶1进行倾向性评分匹配,基线资料比较提示两组之间性别、年龄、透析龄、基础病因、透析模式及血压水平差异无统计学意义(P > 0.05);观察组治疗3个月后的收缩压(SBP)、舒张压(DBP)、心率、B型钠尿肽前体(pro-BNP)、心功能Ⅳ级比例较前下降,左室射血分数(LVEF)< 50%比例较治疗前减少(P < 0.05)。观察组患者治疗前后的DBP降幅、BNP降幅比对照组下降更明显,且LVEF差值及左室舒张末期内径差值更大(P < 0.05)。两组治疗前后的血钾、肝肾功能水平差异无统计学意义(P > 0.05)。随访期间仅对照组有1例出现高钾血症,两组均未出现低血压及其他不良反应。 结论 沙库巴曲缬沙坦治疗CKD5期高血压患者的心血管获益明显,在降压、改善心功能、减轻容量负荷等方面均有疗效,且不良事件少,安全性也较高。

关键词: 沙库巴曲缬沙坦, CKD5期, 高血压, 疗效, 安全性

Abstract:

Objective The aim of this study was to evaluate the efficacy and side effects of sacubitril/valsartan in the treatment of patients with chronic kidney disease (CKD) at stage 5 with resistant hypertension, and to explore the cardiovascular benefits and security of medical in the patients. Methods Patients with CKD5 resistant hypertension diagnosed and treated in the First Affiliated Hospital of Guangxi Medical University from September 2020 to March 2022 were selected and divided into the observation group (treated with routine treatment of kidney disease at end-stage and sacubitril/valsartan) and control group (include droutine treatment of renal disease at end-stage and ACEI or ARB drugs) according to treatment strategy. The patients in both two groups were treated with adequate dialysis treatment and conventional drug treatment of renal disease at end-stage. The patients were followed up for at least 3 months,the clinical efficacy of three months after treated with sacubitril/valsartan was observed, and the efficacy indicators and security indicators and adverse cardiovascular events were observed, the occurrence of adverse effects during the period of drug use were compared with the control group. Results A total of 110 patients were included in this study and there were 55 cases in each group.There were no significant differences in gender, age, age of dialysis, etiology, dialysis mode and blood pressure between the two groups (P > 0.05). The Systolic blood pressure (SBP), diastolic blood pressure (DBP), b-type urinary natriuretic peptide precursor (Pro-BNP) and cardiac function grade in the observation group after treatment was significantly decreased compared with before treatment. The left ventricular ejection fraction (LVEF) and the ratio of LVEF < 50% in the observation group was significantly reduced after treatment (P < 0.05). SBP, DBP and Pro-BNP decreased 3 months after treatment compared with the baseline before treatment,and improved significantly in the first month after treatment(P < 0.05). The decrease of DBP and BNP before and after treatment was significantly different between the two groups, and the decrease of DBP and BNP was more significant in the observation group(P < 0.05). The difference of LVEF and left ventricular end diastolic diameter (LVEDD)between the two groups before and after treatment was statistically significant, and the improvement was more obvious in the observation group (P < 0.05). There were no significant differences in the safety indicators of serum potassium, estimated glomerular filtration rate (eGFR) and liver function between two groups before and after treatment (P > 0.05). In terms of adverse reactions, only 1 case in the control group developed hyperkalemia within 3 months of follow-up, and no hypotension or other adverse reactions occurred in the two groups. Conclusions The treatment of patients with CKD stage 5 hypertension with sacubitril/valsartan has obvious cardiovascular benefits. Sacubitril/Valsartan has efficacy in lowering blood pressure, improving cardiac function and reducing volume load, with less adverse events and higher safety than control group.

Key words: sacubitril/valsartan, CKD 5, hypertension, curative effect, security

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