首页> 外文OA文献 >Comparative Efficacy and Safety of Triple Therapy (Ramipril, Telmisartan, Hydrochlorothiazide) Vs Dual Anti Hypertensive Therapy (Ramipril or Telmisartan, Hydrochlorothiazide) in Stage 2 Hypertensive Patients
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Comparative Efficacy and Safety of Triple Therapy (Ramipril, Telmisartan, Hydrochlorothiazide) Vs Dual Anti Hypertensive Therapy (Ramipril or Telmisartan, Hydrochlorothiazide) in Stage 2 Hypertensive Patients

机译:三重治疗的比较疗效和安全性(Ramipril,Telmisartan,氢氯噻嗪)对2阶段高血压患者的双抗高血压治疗(Ramipril或Telmisartan,氢氯噻嗪)

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摘要

Aim: To evaluate the comparative efficacy and safety of ramipril5mg plus hydrochlorothiazide 12.5mg (R + HCTZ), telmisartan40mg plus hydrochlorothiazide12.5mg (T + HCTZ) and ramipril2.5mg plus telmisartan 20mg plus hydrochlorothiazide12.5mg(R + T + HCTZ) in patients with stage 2 hypertension.Materials and Methods: A prospective, open label, randomizedcomparative study was conducted to study the comparativeefficacy and safety of R+HCTZ (group 1), T+HCTZ ( group 2)andR+T+TCTZ (group3) in 88 patients with stage 2 hypertensionwithout co-morbid conditions. Echocardiography was done toassess left ventricular function. Patients were followed up to 24weeks and any ADR occurring in this period was recorded.Results: All the three treatment groups showed significant fallin both systolic and diastolic blood pressure compared to thebaseline scores (p<0.0001). Intergroup comparison did notreveal any significant difference. Total number of adverse drugevents reported were 15. Group III had higher percentage ADRs.Dry cough (8) was most common ADR. The echocardiographyparameters did not change from baseline values with all threetreatment regimens.Conclusion: All three medications were of equal efficacy inpatients with stage 2 hypertension without co morbid conditions,failing to prove superiority over each other.
机译:目的:评估ramipril的比较疗效和安全性5mg加氢氯噻嗪12.5mg(R + HCTZ),Telmisartan40mg加氢氯噻嗪12.5mg(t + hctz)和ramipril2.5mg Plus Telmisartan 20mg加氢氯噻嗪12.5mg(R + T + HCTZ)患者2阶段高血压。材料和方法:预期,开放标签,随机进行比较研究以研究比较R + HCTZ(第1组),T + HCTZ(第2组)和的功效和安全性在8阶段高血压患者中R + T + TCTZ(组3)没有共同病态的条件。超声心动图已完成评估左心室功能。患者随访24记录了几周和此期间发生的任何ADR。结果:所有三个治疗组均显示出明显的秋季在收缩系和舒张压血压中,与此相比基线评分(P <0.0001)。互动比较没有揭示任何显着差异。不良药物总数报告的事件是15.第三组的ADR百分比较高。干咳(8)是最常见的ADR。超声心动图参数与所有三个的基线值​​没有改变治疗方案。结论:所有三种药物都具有平等的疗效患者2阶段高血压没有CO病态条件,未能互相证明优势。

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    Bharat Bhushan;

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  • 年度 2014
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  • 原文格式 PDF
  • 正文语种 eng
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