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A retrospective study evaluating the tolerability and effectiveness of adjunctive antihypertensive drugs in patients with inadequate response to initial treatment

机译:回顾性研究评估辅助降压药对初始治疗反应不足的患者的耐受性和有效性

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摘要

Real‐world tolerability and effectiveness of nebivolol as first add‐on therapy were compared with hydrochlorothiazide, metoprolol, and amlodipine. Medical records of hypertensive adults initiating nebivolol, hydrochlorothiazide, metoprolol, or amlodipine as first add‐on therapy between December 16, 2010 and July 21, 2011 were retrospectively abstracted (N = 1600; 400/treatment). Outcomes included medication‐related side‐effect rates and blood pressure (BP) reduction and control. Compared with nebivolol, metoprolol and amlodipine had significantly higher side‐effect rates (incidence rate ratio [95% CI]: 1.82 [1.14‐2.92] and 2.67 [1.69‐4.21]), respectively); the hydrochlorothiazide‐nebivolol rate ratio was not significant (1.61 [0.95‐2.71]). All treatments reduced BP at 2 months. Metoprolol, amlodipine, and hydrochlorothiazide were associated with significantly lower odds of achieving 2‐month BP control than nebivolol (odds ratios [95% CI]: 0.34 [0.23‐0.51], 0.51 [0.35‐0.75] and 0.66 [0.44‐0.99], respectively). In a real‐world setting, nebivolol as first add‐on therapy was associated with fewer side effects than metoprolol or amlodipine and with a higher BP control rate than hydrochlorothiazide, metoprolol, or amlodipine.
机译:将奈必洛尔作为首次附加治疗的真实世界耐受性和有效性与氢氯噻嗪,美托洛尔和氨氯地平进行了比较。回顾性分析了2010年12月16日至2011年7月21日开始使用奈比洛尔,氢氯噻嗪,美托洛尔或氨氯地平作为首次附加治疗的高血压成年人的病历(N = 1600; 400 /疗程)。结果包括与药物有关的副作用发生率以及血压的降低和控制。与奈比洛尔相比,美托洛尔和氨氯地平具有更高的副作用发生率(发生率[95%CI]:1.82 [1.14-2.92]和2.67 [1.69-4.21])。氢氯噻嗪-奈比洛尔比率并不显着(1.61 [0.95-2.71])。所有治疗均在2个月时降低BP。美托洛尔,氨氯地平和氢氯噻嗪与奈必洛尔相比,实现2个月BP控制的几率显着降低(几率[95%CI]:0.34 [0.23-0.51],0.51 [0.35-0.75]和0.66 [0.44-0.99] , 分别)。在现实世界中,奈必洛尔作为首次附加治疗的副作用比美托洛尔或氨氯地平少,并且与氢氯噻嗪,美托洛尔或氨氯地平相比,血压控制率更高。

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