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地塞米松单次给药对唑来膦酸治疗后急性期反应的影响:一项随机对照试验。

Effect of single-dose dexamethasone on acute phase response following zoledronic acid: a randomized controlled trial.

机构信息

Bone & Joint Research Group, University of Auckland, Private Bag 92019, Auckland, 1142, New Zealand.

Division of Endocrinology and Metabolism, University of Calgary, 1820 Richmond Road SW, Calgary, Alberta, T2T 5C7, Canada.

出版信息

Osteoporos Int. 2017 Jun;28(6):1867-1874. doi: 10.1007/s00198-017-3960-0. Epub 2017 Feb 23.

Abstract

UNLABELLED

Zoledronic acid provokes an inflammatory reaction, or acute phase response, in some individuals. We examined whether treatment with dexamethasone could prevent this response. A single dose of dexamethasone 4 mg, given at the time of zoledronic acid infusion, did not influence the incidence or severity of the acute phase response.

INTRODUCTION

The potent bisphosphonate zoledronic acid (ZOL) is used to treat osteoporosis, Paget's disease, and hypercalcemia of malignancy. This medication can provoke an inflammatory reaction, known as the acute phase response (APR). We examined whether glucocorticoid treatment at the time of first exposure to ZOL prevents the development of APR.

METHODS

This double-blind, randomized, controlled trial assessed 40 adults receiving ZOL 5 mg intravenously for the first time. Participants received oral dexamethasone 4 mg (n = 20) or placebo (n = 20) at the time of ZOL infusion. Oral temperature was measured at baseline and three times a day for 3 days following infusion. Symptoms of APR were assessed via questionnaire at baseline then daily for 3 days and again at day 15 post-infusion. Use of rescue medications (paracetamol or ibuprofen) in the 3 days following infusion was evaluated. Primary outcome was between-group difference in temperature change from baseline.

RESULTS

There was no significant difference in temperature change (p = 0.95) or symptom score (p = 0.42) in the 3 days following ZOL between dexamethasone and placebo recipients. Eleven (55%) in the dexamethasone group and 10 (50%) placebo recipients experienced a temperature increase of ≥1 °C (p = 0.99). Seven (35%) in the dexamethasone group and 9 (45%) in the placebo group experienced an increase in symptom score of ≥3 points (p = 0.75). Thirteen (65%) dexamethasone recipients and 12 (60%) in the placebo group required rescue medications (p = 0.99). Dexamethasone was well-tolerated.

CONCLUSIONS

A single dose of dexamethasone 4 mg does not influence the incidence or severity of APR following first exposure to ZOL.

TRIAL REGISTRATION

ACTRN12615000794505.

摘要

未注明

唑来膦酸在一些个体中会引发炎症反应或急性期反应。我们研究了地塞米松治疗是否可以预防这种反应。在唑来膦酸输注时给予单次 4 毫克地塞米松剂量并不影响急性期反应的发生率或严重程度。

引言

强效双膦酸盐唑来膦酸(ZOL)用于治疗骨质疏松症、佩吉特病和恶性高钙血症。这种药物会引起炎症反应,称为急性期反应(APR)。我们研究了首次使用 ZOL 时糖皮质激素治疗是否可以预防 APR 的发生。

方法

这项双盲、随机、对照试验评估了 40 名首次接受静脉注射 ZOL 5 毫克的成年人。参与者在 ZOL 输注时接受口服地塞米松 4 毫克(n=20)或安慰剂(n=20)。在输注后 3 天内,每天测量三次基础体温。在输注后 3 天内通过问卷评估 APR 症状,并在第 15 天再次评估。评估输注后 3 天内使用救援药物(对乙酰氨基酚或布洛芬)的情况。主要结局是两组之间从基线开始的体温变化差异。

结果

地塞米松组和安慰剂组在 ZOL 输注后 3 天内的体温变化(p=0.95)或症状评分(p=0.42)无显著差异。地塞米松组 11 名(55%)和安慰剂组 10 名(50%)患者的体温升高≥1°C(p=0.99)。地塞米松组 7 名(35%)和安慰剂组 9 名(45%)患者的症状评分升高≥3 分(p=0.75)。地塞米松组 13 名(65%)和安慰剂组 12 名(60%)患者需要使用救援药物(p=0.99)。地塞米松耐受性良好。

结论

单次 4 毫克地塞米松剂量不会影响首次接触 ZOL 后的 APR 发生率或严重程度。

试验注册

ACTRN12615000794505。

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