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奈多罗米钠在中重度哮喘中对吸入性皮质激素的节省效应

[Inhaled corticotherapy sparing effect by sodium nedocromil in moderate to severe asthma].

作者信息

Murciano D, Braunstein G, Montagut A, Pariente R

机构信息

Service de Pneumologie, Hôpital Beaujon, Clichy.

出版信息

Rev Mal Respir. 1994;11(5):485-92.

PMID:7816992
Abstract

BACKGROUND

The increased use of high dose inhaled steroid in the treatment of asthma has revealed the risk of dose-dependent side effects. Nedocromil sodium is a non steroidal agent with anti-inflammatory properties.

OBJECTIVE

To demonstrate whether nedocromil sodium may have some therapeutic benefit in asthmatic patients treated with high dose inhaled steroids and whether it has an inhaled steroid sparing effect.

PATIENTS

134 adults with moderate to severe asthma not adequately controlled with high dose inhaled steroids (750 to 1,500 micrograms/day).

METHOD

After a two week baseline period, patients were randomized to receive either nedocromil sodium (4 mg qid) or placebo for 24 weeks in a double blind fashion. During the first 12 weeks of treatment, the dose of inhaled steroid was maintained constant whereas it was altered during the last 12 weeks according to asthma scores.

RESULTS

Among 108 patients reaching the reduction phase, a decrease of 250 micrograms of inhaled steroid or more was possible in 79% of patients on nedocromil sodium and in 60% of patients on placebo (p < 0.03). Symptoms scores were improved on both treatments during the 12 first weeks, more on nedocromil sodium than on placebo, treatment difference reaching significance for daytime asthma (p < 0.02). FEV1 improved during the trial for patients on nedocromil (from 69 +/- 18% to 74 +/- 21%; p < 0.005) whereas it did not for those on placebo.

CONCLUSION

Nedocromil sodium is effective in improving moderate to severe asthma in addition to inhaled steroid and has some steroid sparing effect in patients treated with high dose inhaled steroid.

摘要

背景

高剂量吸入性类固醇在哮喘治疗中的使用增加,已揭示了剂量依赖性副作用的风险。奈多罗米钠是一种具有抗炎特性的非甾体类药物。

目的

证明奈多罗米钠对接受高剂量吸入性类固醇治疗的哮喘患者是否可能具有某些治疗益处,以及它是否具有吸入性类固醇节省效应。

患者

134名中度至重度哮喘成年患者,高剂量吸入性类固醇(750至1500微克/天)未能充分控制病情。

方法

经过两周的基线期后,患者以双盲方式随机接受奈多罗米钠(4毫克,每日四次)或安慰剂治疗24周。在治疗的前12周,吸入性类固醇的剂量保持不变,而在最后12周根据哮喘评分进行调整。

结果

在108名进入减量阶段的患者中,79%接受奈多罗米钠治疗的患者和60%接受安慰剂治疗的患者吸入性类固醇减少了250微克或更多(p<0.03)。在最初的12周内,两种治疗的症状评分均有所改善,奈多罗米钠组比安慰剂组改善更多,白天哮喘的治疗差异具有显著性(p<0.02)。接受奈多罗米钠治疗的患者在试验期间FEV1有所改善(从69±18%提高到74±21%;p<0.005),而接受安慰剂治疗的患者则没有。

结论

奈多罗米钠除了吸入性类固醇外,对改善中度至重度哮喘有效,并且对接受高剂量吸入性类固醇治疗的患者具有一定的类固醇节省效应。

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