Primary studies included in this systematic review

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Publication Thread

This thread includes 2 references

Primary study

Unclassified

期刊 Iranian journal of pharmaceutical research : IJPR
Year 2014
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The purpose of this study was to examine the effect of intravenous magnesium sulfate on patients with COPD exacerbation requiring hospitalization. In this randomized clinical trial 30 patients with COPD exacerbation were studied. Patients were randomly assigned to group A (case) who concurrent with standard therapy received 2 g magnesium sulfate in normal saline infused in 20 minutes on days one to three and group B (control) who received standard medications and placebo. PEFR and FEV1 were measured by before, 45 minutes and third day of entering the study. Vital signs HR, BP, RR, temperature and SpO2 were monitored during hospitalization. 21 males and 9 females patients with mean age of 68 ± 9 years, case 67 ± 10 and control 70 ± 8 were studied (15 patients in each arm of study). The mean pretreatment FEV1 was 26% ± 12, and 35% ± 18 in case and control groups respectively (P=0.137). FEV1 after 45 minutes in case group was 27% ± 9 and control group 36% ± 20 (p=0.122). FEV1 after 3 days of study was 32% ± 17 in case and 41% ± 22 in control groups (P=0.205). The mean pretreatment PEFR was 126 ± 76 l/min in case and 142 ± 62 l/min in control groups (P=0.46). Changes in PEFR were not significant 45 min (p=0.540) and 3 days (p=0.733) of the administration of intravenous magnesium sulfate. Duration of hospital stay between the two groups did not show any significant difference. This study showed that administration of intravenous magnesium sulfate in hospitalized patients with COPD exacerbation neither revealed any significant bronchodilating effect nor reduced duration of hospital stay.

Primary study

Unclassified

期刊 Clinics (Sao Paulo, Brazil)
Year 2012
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OBJECTIVE: The potential influence of magnesium on exercise performance is a subject of increasing interest. Magnesium has been shown to have bronchodilatatory properties in asthma and chronic obstructive pulmonary disease patients. The aim of this study was to investigate the effects of acute magnesium IV loading on the aerobic exercise performance of stable chronic obstructive pulmonary disease patients. METHODS: Twenty male chronic obstructive pulmonary disease patients (66.2 + 8.3 years old, FEV1: 49.3+19.8%) received an IV infusion of 2 g of either magnesium sulfate or saline on two randomly assigned occasions approximately two days apart. Spirometry was performed both before and 45 minutes after the infusions. A symptom-limited incremental maximal cardiopulmonary test was performed on a cycle ergometer at approximately 100 minutes after the end of the infusion. RESULTS: Magnesium infusion was associated with significant reductions in the functional residual capacity (-0.41 l) and residual volume (-0.47 l), the mean arterial blood pressure (-5.6 mmHg) and the cardiac double product (734.8 mmHg.bpm) at rest. Magnesium treatment led to significant increases in the maximal load reached (+8 w) and the respiratory exchange ratio (0.06) at peak exercise. The subgroup of patients who showed increases in the work load equal to or greater than 5 w also exhibited significantly greater improvements in inspiratory capacity (0.29 l). CONCLUSIONS: The acute IV loading of magnesium promotes a reduction in static lung hyperinflation and improves the exercise performance in stable chronic obstructive pulmonary disease patients. Improvements in respiratory mechanics appear to be responsible for the latter finding.

Primary study

Unclassified

期刊 Archivos de bronconeumología
Year 2006
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目的:硫酸镁已被证明有哮喘的支气管扩张作用,但这种影响尚未明确慢性阻塞性肺疾病(COPD)的背景下成立的。为此,我们调查硫酸镁可能在COPD急性加重的支气管扩张作用。 病人与方法:我们研究了24例,加重慢性阻塞性肺病,要求加入到我们医院的肺病部门。所有患者基线肺活量和随后的随机双盲交叉设计群体。患者在输液20分钟1.5Ğ硫酸镁或安慰剂。那些接受硫酸镁的第一天服用安慰剂的第二天,反之亦然。肺活量,15,30,45分钟后,硫酸镁或安慰剂管理。最后,400微克沙丁胺醇的管理使用间隔15分钟后进行最后肺活量。所有患者还接受与糖皮质激素,静脉注射抗生素治疗,氧气治疗,并定期调度支气管扩张剂治疗(沙丁胺醇和溴化异丙托品,每6小时)。 结果:当我们相比绝对增加毫升,用力呼气容积的百分比增加1秒钟内得到应用,以增加与安慰剂后15,30,45分钟与硫酸镁(FEV 1),无显着差异。当我们比较管理沙丁胺醇后FEV1的绝对值和百分比增加,我们发现硫酸镁管理后显着更大的升幅。平均(SD)的FEV1绝对值增加0.18硫酸镁管理和0.081(0.42)长后,[修正] [0.01]后,安慰剂组的L(P = 0.004)。硫酸镁和7.06%(1.8%)后,安慰剂组(P = 0.008)后的FEV1的增幅为17.11%(3.7%)。 结论:静脉注射硫酸镁有没有在COPD急性加重患者的支气管扩张作用。然而,它确实提高吸入SS2-激动剂的支气管扩张作用。

Primary study

Unclassified

期刊 Archives of internal medicine
Year 1995
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背景:慢性阻塞性肺疾病急性加重的常见和难以治疗。我们试图确定硫酸镁的支气管扩张功效在这种情况下,因为该化合物是在急性哮喘很有帮助。 方法:受试者谁前来以下两种退伍军人事务部的紧急部门被随机双盲的方式接受或1.2克硫酸镁或安慰剂,20分钟后,他们第一次收到沙丁胺醇,2.5毫克喷雾。呼气流量峰值,呼吸困难的分数,通过脉搏血氧饱和度,最大吸气和呼气压力动脉血氧饱和度,以及生命体征45分钟硫酸镁或安慰剂治疗开始后进行监测。 结果:72两个人进行了研究。两组呼气流量峰值增加​​16.6%+ 27.7%(平均值+/-标准差)的初始沙丁胺醇治疗后,从121.2 +/- 55.7升/分钟至136.9 +/- 63.9升/分。从136.7 +/- 69.7升/分钟的最大呼气流量增加在输注开始至162.3 +/- 76.6升/分在30分钟时和161.3 +/- 78.7升/分,在45分钟内硫酸镁治疗。呼气峰流量为137.0 +/- 58.6升/分钟的静脉输注的开始,143.0 +/- 72.7升/分,在30分钟,和143.3 +/- 70.5升/分,在45分钟,在安慰剂组。从输液开始的呼气峰流速为30和45分钟后(计算为30年和45分钟值的方式)的区别是显著不同的两个群体(25.1 +/- 35.7升/分钟VS 7.4 + / - 33.3升/分; P = 0.3);差异也显著时表示增幅(22.4%+/- 28.5%和6.1%+/- 24.4%; P = 0.01)。有朝向住院硫酸镁组中的需求减少具有统计学不显着的趋势,与安慰剂组(28.1%对41.9%,P = 0.25)相比。有在其他参数有两种治疗没有显著的变化。 结论:硫酸镁,1.2克过β-受体激动剂给药后20分钟,是安全的,在慢性阻塞性肺疾病的急性恶化的治疗温和有效的,并且它的支气管扩张作用大于单独给予,持续一个β-受体激动剂的超出硫酸镁给药期间。