Division of Cardiology Győr, University of Pécs, Pecs, Hungary.
Department of Cardiology, Petz Aladár County Teaching Hospital, Gyor, Hungary.
Adv Ther. 2021 Jan;38(1):479-494. doi: 10.1007/s12325-020-01527-3. Epub 2020 Nov 5.
Our objective was to determine the effectiveness of a perindopril/indapamide (Per/Ind) single-pill combination (SPC) in a broad range of patient profiles, including subgroups with varying hypertension severity, age and cardiovascular risk profiles.
Patient data from four large prospective observational studies (FORTISSIMO, FORSAGE, PICASSO, ACES) were pooled. In each study, patients already treated for hypertension were switched to Per/Ind 10/2.5 mg SPC and systolic and diastolic blood pressure (SBP/DBP) measured at the 1-month (M1) and 3-month (M3) visits. Study endpoints included change in SBP and DBP from baseline to M1 and M3 and the percentage of patients achieving BP control (SBP/DBP < 140/90 mmHg for patients without diabetes or < 140/85 mmHg for patients with diabetes).
A total of 16,763 patients were enrolled and received Per/Ind (94% received the full dose of 10/2.5). Mean patient age was 61.4 years (36% were ≥ 65 years old), 57% were women, and 16% had isolated systolic hypertension (ISH). Mean baseline office SBP/DBP was 162/94 mmHg, and mean duration of hypertension was 11 years. Cardiovascular risk factors and comorbid conditions were common in this population. Significant mean reductions in SBP (- 23 mmHg) and DBP (- 11 mmHg) were observed at M1 compared with baseline (P < 0.001), which were maintained at M3 (- 30 mmHg and - 14 mmHg, respectively). At M3, BP control was achieved by 70% of patients (78% for ISH). In patients with SBP ≥ 180 mmHg at baseline (grade III hypertension), the mean SBP/DBP decrease was - 51/- 20 mmHg and 53% achieved BP control. Per/Ind was well tolerated with an overall rate of adverse events of 1.3%, most frequently cough and dizziness at rates of 0.3% and 0.2%, respectively.
In this hypertensive population including difficult-to-control patient subgroups, switching to Per/Ind 10/2.5 mg SPC led to rapid and important reductions in BP. BP control was achieved in 70% of patients overall in an everyday practice context.
我们的目的是确定培哚普利/吲达帕胺(培哚普利/吲达帕胺)单药复方(SPC)在广泛的患者人群中的疗效,包括不同严重程度、年龄和心血管风险特征的亚组。
四项大型前瞻性观察性研究(FORTISSIMO、FORSAGE、PICASSO、ACES)的患者数据进行了汇总。在每项研究中,已接受高血压治疗的患者转换为培哚普利/吲达帕胺 10/2.5 mg SPC,并在第 1 个月(M1)和第 3 个月(M3)测量收缩压和舒张压(SBP/DBP)。研究终点包括从基线到 M1 和 M3 的 SBP 和 DBP 的变化,以及达到血压控制的患者比例(无糖尿病患者的 SBP/DBP<140/90mmHg,糖尿病患者的 SBP/DBP<140/85mmHg)。
共纳入 16763 例患者,并接受培哚普利/吲达帕胺治疗(94%接受 10/2.5 的全剂量)。患者平均年龄为 61.4 岁(36%≥65 岁),57%为女性,16%患有单纯收缩期高血压(ISH)。平均基线诊室 SBP/DBP 为 162/94mmHg,高血压平均病程为 11 年。该人群中常见心血管危险因素和合并症。与基线相比,M1 时 SBP(-23mmHg)和 DBP(-11mmHg)显著降低(P<0.001),M3 时仍保持不变(分别为-30mmHg 和-14mmHg)。在 M3 时,70%的患者达到血压控制(ISH 为 78%)。在基线时 SBP≥180mmHg(三级高血压)的患者中,平均 SBP/DBP 下降为-51/-20mmHg,53%达到血压控制。培哚普利/吲达帕胺耐受性良好,总体不良事件发生率为 1.3%,最常见的不良事件是咳嗽和头晕,发生率分别为 0.3%和 0.2%。
在包括难以控制的亚组患者的高血压人群中,转换为培哚普利/吲达帕胺 10/2.5mg SPC 可迅速显著降低血压。在日常实践环境中,总体上有 70%的患者达到血压控制。