Wikananda I Made Fermi, Nurcahya I Gusti Ngurah Metta, Wijaya Putu Gede Pradipta Mahardika, Widiana I Gde Raka, Sindhughosa Dwijo Anargha
Faculty of Medicine, Udayana University, Denpasar, Indonesia.
Department of Internal Medicine Udayana University / Prof Dr IGNG Ngoerah Hospital, Denpasar, Indonesia.
Caspian J Intern Med. 2024 Winter;15(1):28-37. doi: 10.22088/cjim.15.1.2.
Besides being commonly used to treat high blood pressure, beta blockers are a family of drugs that are primarily used to regulate irregular cardiac rhythms. Nebivolol is a third generation of beta blockers, which is highly cardioselective, about three times as selective as bisoprolol. In this study, we aimed to evaluate Nebivolol's effectiveness and safety in comparison to other beta blockers.
We searched the online databases PubMed, ScienceDirect, and Cochrane Library for relevant RCTs evaluating Nebivolol's effect on hypertension management. Relative risk (WRR) and weighted mean difference (WMD), with a 95% confidence interval (CI) were utilized to quantify the impact of nebivolol medication in the treatment of hypertension using a random effects model.
Twelve RCTs are included in the study, the patient numbers in every attempt ranged from 42-273 and 1456 patients in all were included in this review. Nebivolol does not significantly reduce SBP, DBP and HR compared to other beta blockers (WMD -0.57 mmHg, 95% CI [-1.55; 0.42 mmHg] p=0.12; WMD -0.27 mmHg, 95% CI [-1.36; 0.82 mmHg] p=0.63 ; WMD 0.10 BPM, 95% CI [-4.11;1.31 BPM] p=0.96, respectively). Patients treated with Nebivolol has significantly lower LDL-C (WMD -8.88 mg/dL, 95% CI [-15.28; -2.48 mg/dL] p=0.007) and significantly higher HDL-C (WMD 2.30 mg/dL, 95% CI [0.75; 3.84 mg/dL] p=0.004.
According to this study's findings, nebivolol is well tolerated and decreases LDL-C. And higher HDL-C than other beta blocker agents. This review does not recommend nebivolol as first-line treatment in hypertension as Nebivolol does not significantly reduce blood pressure and HR of patients.
β受体阻滞剂除常用于治疗高血压外,还是一类主要用于调节心律失常的药物。奈必洛尔是第三代β受体阻滞剂,具有高度的心脏选择性,选择性约为比索洛尔的三倍。在本研究中,我们旨在评估奈必洛尔与其他β受体阻滞剂相比的有效性和安全性。
我们在在线数据库PubMed、ScienceDirect和Cochrane图书馆中搜索了评估奈必洛尔对高血压管理效果的相关随机对照试验(RCT)。采用随机效应模型,利用相对风险(WRR)和加权平均差(WMD)以及95%置信区间(CI)来量化奈必洛尔药物治疗高血压的影响。
该研究纳入了12项随机对照试验,每次试验的患者人数在42至273之间,本综述共纳入了1456例患者。与其他β受体阻滞剂相比,奈必洛尔在降低收缩压(SBP)、舒张压(DBP)和心率(HR)方面无显著差异(加权平均差分别为-0.57 mmHg,95%置信区间[-1.55;0.42 mmHg],p = 0.12;加权平均差为-0.27 mmHg,95%置信区间[-1.36;0.82 mmHg],p = 0.63;加权平均差为0.10次/分钟,95%置信区间[-4.11;1.31次/分钟],p = 0.96)。接受奈必洛尔治疗的患者低密度脂蛋白胆固醇(LDL-C)显著降低(加权平均差为-8.88 mg/dL,95%置信区间[-15.28;-2.48 mg/dL],p = 0.007),高密度脂蛋白胆固醇(HDL-C)显著升高(加权平均差为2.30 mg/dL,95%置信区间[0.75;3.84 mg/dL],p = 0.004)。
根据本研究结果,奈必洛尔耐受性良好,可降低低密度脂蛋白胆固醇,且高密度脂蛋白胆固醇水平高于其他β受体阻滞剂。由于奈必洛尔不能显著降低患者的血压和心率,本综述不推荐将奈必洛尔作为高血压的一线治疗药物。