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培哚普利对有跌倒史老年人姿势不稳的影响:一项随机对照试验。

The effect of perindopril on postural instability in older people with a history of falls-a randomised controlled trial.

机构信息

Department of Medicine for the Elderly, NHS Tayside, Dundee, UK.

Division of Molecular and Clinical Medicine, School of Medicine, University of Dundee, Dundee, UK.

出版信息

Age Ageing. 2018 Jan 1;47(1):75-81. doi: 10.1093/ageing/afx127.

DOI:10.1093/ageing/afx127
PMID:28985263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5860560/
Abstract

DESIGN

double-blind, parallel group, placebo-controlled randomised trial.

METHODS

we recruited people aged >65 years with at least one fall in the previous year. Participants received 4 mg perindopril or placebo daily for 15 weeks. The primary outcome was the between-group difference in force-plate measured anteroposterior (AP) sway at 15 weeks. Secondary outcomes included other measures of postural sway, limits of stability during maximal forward, right and left leaning, blood pressure, muscle strength, 6-min walk distance and falls. The primary outcome was assessed using two-way ANOVA, adjusted for baseline factors.

RESULTS

we randomised 80 participants. Mean age was 78.0 (SD 7.4) years; 60 (75%) were female. About 77/80 (96%) completed the trial. At 15 weeks there were no significant between-group differences in AP sway with eyes open (mean difference 0 mm, 95% CI -8 to 7 mm, P = 0.91) or eyes closed (mean difference 2 mm, 95% CI -7 to 12 mm, P = 0.59); no differences in other measures of postural stability, muscle strength or function. About 16/40 (42%) of patients in each group had orthostatic hypotension at follow-up. The median number (IQR) of falls was 1 (0,4) in the perindopril versus 1 (0,2) in the placebo group (P = 0.24).

CONCLUSIONS

perindopril did not improve postural sway in older people at risk of falls.

CLINICAL TRIALS REGISTRATION

ISRCTN58995463.

摘要

设计

双盲、平行组、安慰剂对照随机试验。

方法

我们招募了年龄在 65 岁以上且在前一年至少跌倒过一次的患者。参与者每天接受 4 毫克培哚普利或安慰剂治疗 15 周。主要结局是 15 周时力板测量的前后(AP)摆动的组间差异。次要结局包括其他姿势摆动测量、最大向前、向右和向左倾斜时的稳定性极限、血压、肌肉力量、6 分钟步行距离和跌倒。主要结局采用双向方差分析进行评估,并根据基线因素进行调整。

结果

我们随机分配了 80 名参与者。平均年龄为 78.0(SD 7.4)岁;60 名(75%)为女性。大约 77/80(96%)完成了试验。在 15 周时,睁眼时 AP 摆动(平均差异 0 毫米,95%CI-8 至 7 毫米,P=0.91)或闭眼时(平均差异 2 毫米,95%CI-7 至 12 毫米,P=0.59)两组间无显著差异;其他姿势稳定性、肌肉力量或功能测量也无差异。随访时,每组约有 16/40(42%)的患者出现体位性低血压。培哚普利组(中位数(IQR)为 1(0,4))和安慰剂组(中位数(IQR)为 1(0,2))的跌倒中位数(IQR)(P=0.24)。

结论

培哚普利不能改善有跌倒风险的老年人的姿势摆动。

临床试验注册

ISRCTN58995463。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1615/5860560/91bf6e96b85d/afx127f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1615/5860560/91bf6e96b85d/afx127f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1615/5860560/91bf6e96b85d/afx127f01.jpg

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