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首页> 外文期刊>International Journal of Hypertension >Efficacy of Diltiazem for the Control of Blood Pressure in Puerperal Patients with Severe Preeclampsia: A Randomized, Single-Blind, Controlled Trial
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Efficacy of Diltiazem for the Control of Blood Pressure in Puerperal Patients with Severe Preeclampsia: A Randomized, Single-Blind, Controlled Trial

机译:Diltiazem对葛根患者严重先兆子痫患者血压控制的疗效:随机,单盲,受控试验

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摘要

Background. Postpartum preeclampsia is a serious disease related to high blood pressure that occurs commonly within the first six days after delivery. Objective. To evaluate if diltiazem improves blood pressure parameters in early puerperium patients with severe preeclampsia. Methodology. A randomized, single-blind longitudinal clinical trial of 42 puerperal patients with severe preeclampsia was carried out. Patients were randomized into two groups: the experimental group (n?=?21) received diltiazem (60?mg) and the control group (n?=?21) received nifedipine (10?mg). Both drugs were orally administered every 8 hours. Systolic, diastolic, and mean blood pressures as well as the heart rate were recorded and analyzed (two-way repeated measures ANOVA) at baseline and after 6, 12, 18, 24, 30, 36, 42, and 48?hours. Primary outcome measures were all the aforementioned blood pressure parameters. Secondary outcome measures included the number of hypertension and hypotension episodes along with the length of stay in the intensive care unit. Results. No statistical differences were found between groups (diltiazem vs. nifedipine) regarding basal blood pressure parameters. Interarm differences in blood pressure (systolic, diastolic, and mean) and heart rate were statistically significant between treatment groups from 6 to 48 hours. Patients in the diltiazem group had lower blood pressure levels than patients in the nifedipine group. Significantly, patients who received diltiazem had fewer hypertension and hypotension episodes and stayed fewer days in the intensive care unit than those treated with nifedipine. Conclusions. Diltiazem controlled arterial hypertension in a more effective and uniform manner in patients under study than nifedipine. Patients treated with diltiazem had fewer collateral effects and spent less time in the hospital. This trial is registered with NCT04222855.
机译:背景。产后葡萄球菌列痫是一种严重的疾病,与高血压有关,其在递送后的前六天内通常发生。客观的。评估Diltiazem是否改善了严重预胰蛋白早期卵培养患者的血压参数。方法。进行了42例患有严重先兆子痫患者的随机的单盲纵临临床试验。患者随机分为两组:实验组(N?=β21)接受了Diltiazem(60〜Mg)和对照组(N?=Δ21)接受硝苯地平(10?Mg)。两种药物每8小时口服给药。在基线和6,12,18,24,30,36,42和48℃下记录和分析(双向重复测量Anova)的收缩压,舒张和平均血压以及心率(双向重复测量Anova)。主要结果措施是所有上述血压参数。二次结果措施包括高血压和低血压发作的数量以及重症监护病房的逗留时间。结果。在关于基础血压参数的基团(Diltiazem vs. Nifedipine)之间没有发现统计差异。血压(收缩压,舒张性和平均值)和心率差异在治疗组之间的统计学意义为6至48小时。患有尼堤查组的患者比硝苯地平组的患者较低。值得注意的是,接受Diltiazem的患者具有较少的高血压和低血压发作,并在重症监护手册中保持较少的日子,而不是用硝苯地平治疗的病例。结论。 Diltiazem在研究中以比硝苯地平进行更有效和更均匀的方式控制动脉高血压。用Diltiazem治疗的患者在医院的抵押品效应较少,并在较少的时间内度过。此试验在NCT04222855中注册。

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