A Prospective, Randomized Open-Label Study for Assessment of Antihypertensive Effect of Telmisartan Versus Cilnidipine Using Ambulatory Blood Pressure Monitoring (START ABPM Study).

IF 1.4 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Rahul Sawant, Sachin Suryawanshi, Mayur Jadhav, Hanmant Barkate, Sumit Bhushan, Tanmay Rane
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引用次数: 0

Abstract

Background: The antihypertensive agent telmisartan is an angiotensin II receptor blocker with a terminal elimination half-life of 24 h and has a high lipophilicity, thereby enhancing its bioavailability. Another antihypertensive agent, cilnidipine is a calcium antagonist and has dual mode of action on the calcium channels. This study aimed at determining effect of these drugs on ambulatory blood pressure (BP) levels.

Methods: A randomized, open-label, single-center study was conducted during 2021 - 2022 on newly diagnosed adult patients with stage-I hypertension, in a mega city of India. Forty eligible patients were randomized to telmisartan (40 mg) and cilnidipine (10 mg) groups, with once daily dose administered for 56 consecutive days. Ambulatory blood pressure monitoring (ABPM) (24 h) was performed pre- and post-treatment, and the ABPM-derived parameters were compared statistically.

Results: Statistically significant mean reductions were observed in all BP endpoints in telmisartan group but only in 24-h systolic blood pressure (SBP), daytime and nighttime SBP, and manual SBP and diastolic blood pressure (DBP) in cilnidipine group. The mean change from baseline to day 56 between two treatment groups showed statistical significance in last 6-h SBP (P = 0.01) and DBP (P = 0.014), and morning SBP (P = 0.019) and DBP (P = 0.028). The percent nocturnal drop within and between groups was statistically nonsignificant. Also, the between group mean SBP and DBP smoothness index differed nonsignificantly.

Conclusions: Telmisartan and cilnidipine once daily were effective and well tolerated in the treatment of newly diagnosed stage-I hypertension. Telmisartan provided sustained 24-h BP control and may offer advantages over cilnidipine in terms of BP reductions, particularly over the 18- to 24-h post-dose period or critical early morning hours.

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一项使用动态血压监测评估替米沙坦与西尼地平降压效果的前瞻性、随机、开放标签研究(START ABPM研究)。
背景:降压药替米沙坦是一种血管紧张素II受体阻滞剂,终末消除半衰期为24小时,具有高亲脂性,从而提高了其生物利用度。另一种降压药西尼地平是一种钙拮抗剂,对钙通道有双重作用。本研究旨在确定这些药物对动态血压(BP)水平的影响。方法:一项随机、开放标签、单中心研究于2021 - 2022年在印度一个大城市对新诊断的成年i期高血压患者进行了研究。40例符合条件的患者随机分为替米沙坦(40 mg)组和西尼地平(10 mg)组,每天一次,连续56天。治疗前后进行24 h动态血压监测(ABPM),并对ABPM衍生参数进行统计学比较。结果:替米沙坦组所有血压终点均有统计学意义的平均降低,而西尼地平组仅24小时收缩压(SBP)、白天和夜间收缩压、手动收缩压和舒张压(DBP)有统计学意义。两组患者术后6 h收缩压(P = 0.01)、舒张压(P = 0.014)、晨起收缩压(P = 0.019)、舒张压(P = 0.028)的平均变化均有统计学意义。夜间下降的百分比在组内和组间没有统计学意义。各组平均收缩压和舒张压平滑指数差异无统计学意义。结论:替米沙坦联合西尼地平每日1次治疗新诊断的i期高血压有效且耐受性良好。替米沙坦提供了持续的24小时血压控制,在血压降低方面可能比西尼地平更有优势,特别是在给药后18至24小时或关键的清晨时间。
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来源期刊
Cardiology Research
Cardiology Research CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
2.50
自引率
0.00%
发文量
42
期刊介绍: Cardiology Research is an open access, peer-reviewed, international journal. All submissions relating to basic research and clinical practice of cardiology and cardiovascular medicine are in this journal''s scope. This journal focuses on publishing original research and observations in all cardiovascular medicine aspects. Manuscript types include original article, review, case report, short communication, book review, letter to the editor.
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