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Blood pressure normalization in a large population of hypertensive patients treated with perindopril/indapamide combination: results of the OPTIMAX trial

机译:培哚普利/吲达帕胺联合治疗的大量高血压患者的血压正常化:OPTIMAX试验结果

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Objective: To determine if the fixed-dose perindopril/indapamide combination (Per/Ind) normalizes blood pressure (BP) in the same fraction of hypertensive patients when treated in everyday practice or in controlled trials. Methods: In this prospective trial, 17 938 hypertensive patients were treated with Per 2 mg/Ind 0.625 mg for 3–6 months. In Group 1 Per/Ind was initiated in newly diagnosed patients (n = 7032); in Group 2 Per/Ind replaced previous therapy in patients already treated but having either their BP still uncontrolled or experiencing side-effects (n = 7423); in Group 3 Per/Ind was added to previous treatment in patients with persistently high BP (n = 3483). BP was considered normalized when ≤ 140/90 mm Hg. A multivariate analysis for predictors of BP normalization was performed. Results: Subjects were on average 62 years old and had a baseline BP of 162.3/93.6 mm Hg. After treatment with Per/Ind, BP normalization was reached in 69.6% of patients in the Initiation group, 67.5% in the Replacement Group, and 67.4% in the Add-on Group (where patients were more frequently at risk, diabetic, or with target organ damage). Mean decreases in systolic BP of 22.8 mm Hg and in diastolic BP of 12.4 mm Hg were recorded. Conclusions: This trial was established to reflect everyday clinical practice, and a treatment strategy based on the Per/Ind combination, administered as initial, replacement, or add-on therapy, led to normalization rates that were superior to those observed in Europe in routine practice. These results support recent hypertension guidelines which encourage the use of combination therapy in the management of arterial hypertension.
机译:目的:确定在日常实践或对照试验中,固定剂量的培哚普利/吲达帕胺联合使用(Per / Ind)是否能使相同比例的高血压患者的血压(BP)正常化。方法:在这项前瞻性试验中,对17 938名高血压患者进行了每2 mg / Ind 0.625 mg的治疗,持续3-6个月。在第1组中,新诊断的患者开始使用Per / Ind(n = 7032);在第2组中,Per / Ind替代了已经接受治疗但血压仍未得到控制或出现副作用的患者中的先前治疗(n = 7423);在第3组中,对于持续高BP(n = 3483)的患者,在以前的治疗中加入Per / Ind。当≤140/90 mm Hg时,血压被认为是正常的。对BP正常化的预测因素进行了多元分析。结果:受试者平均62岁,基线血压为162.3 / 93.6 mm Hg。在使用Per / Ind治疗后,起始组中有69.6%的患者BP正常化,替代组中有67.5%的患者,附加组中有67.4%的患者达到了BP正常化(在这些患者中,患病风险更高,患糖尿病或患有糖尿病的频率更高)目标器官损伤)。记录平均收缩压降低22.8 mm Hg,舒张压平均降低12.4 mm Hg。结论:该试验的建立是为了反映日常临床实践,并且基于Per / Ind组合的治疗策略(作为初始,替代或附加治疗)使正常化率优于欧洲常规情况实践。这些结果支持了最近的高血压指南,该指南鼓励在动脉高血压的治疗中使用联合疗法。

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