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接受孟鲁司特治疗哮喘的患者中的变应性肉芽肿性血管炎。

Churg-Strauss syndrome in patients receiving montelukast as treatment for asthma.

作者信息

Wechsler M E, Finn D, Gunawardena D, Westlake R, Barker A, Haranath S P, Pauwels R A, Kips J C, Drazen J M

机构信息

Departments of Medicine, Brigham & Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.

出版信息

Chest. 2000 Mar;117(3):708-13. doi: 10.1378/chest.117.3.708.

Abstract

STUDY OBJECTIVES

We previously reported eight patients who developed Churg-Strauss syndrome in association with zafirlukast treatment for asthma and postulated that the syndrome resulted from unmasking of a previously existing condition due to corticosteroid withdrawal and not from a direct drug effect. The availability of montelukast, a new leukotriene receptor antagonist with a different molecular structure, permitted us to test this hypothesis. Our goals were to ascertain whether the Churg-Strauss syndrome developed in patients taking montelukast and other novel asthma medications, and to describe potential mechanisms for the syndrome.

DESIGN

Case series.

SETTING

Outpatient and hospital practices of pulmonologists in the United States and Belgium.

PATIENTS

Four adults (one man, three women) who received montelukast as treatment for asthma; two women who received salmeterol/fluticasone therapy, but not montelukast.

RESULTS

Churg-Strauss syndrome developed in the four asthmatic patients who received montelukast. In each case, there was a long history of difficult-to-control asthma characterized by multiple exacerbations that had required frequent courses of oral systemic corticosteroids or high doses of inhaled corticosteroids for control. Two other asthmatics who received fluticasone and salmeterol but not montelukast therapy developed the same syndrome with tapering doses of oral or high doses of inhaled corticosteroids.

CONCLUSIONS

The occurrence of Churg-Strauss syndrome in asthmatic patients receiving leukotriene modifiers appears to be related to unmasking of an underlying vasculitic syndrome that is initially clinically recognized as moderate to severe asthma and treated with corticosteroids. Montelukast does not appear to directly cause the syndrome in these patients.

摘要

研究目的

我们之前报告了8例在使用扎鲁司特治疗哮喘过程中发生Churg-Strauss综合征的患者,并推测该综合征是由于停用皮质类固醇后使先前存在的疾病暴露所致,而非药物的直接作用。孟鲁司特是一种具有不同分子结构的新型白三烯受体拮抗剂,其应用使我们能够验证这一假设。我们的目标是确定服用孟鲁司特及其他新型哮喘药物的患者是否会发生Churg-Strauss综合征,并描述该综合征的潜在机制。

设计

病例系列研究。

地点

美国和比利时肺科医生的门诊及医院诊疗机构。

患者

4名接受孟鲁司特治疗哮喘的成年人(1名男性,3名女性);2名接受沙美特罗/氟替卡松治疗但未使用孟鲁司特的女性。

结果

接受孟鲁司特治疗的4例哮喘患者发生了Churg-Strauss综合征。每例患者均有长期难以控制的哮喘病史,其特点是多次发作,需要频繁使用口服全身性皮质类固醇或高剂量吸入性皮质类固醇来控制。另外2名接受氟替卡松和沙美特罗治疗但未使用孟鲁司特的哮喘患者,在逐渐减少口服剂量或高剂量吸入皮质类固醇时也发生了同样的综合征。

结论

接受白三烯调节剂治疗的哮喘患者发生Churg-Strauss综合征似乎与潜在血管炎综合征的暴露有关,该综合征最初在临床上被认为是中度至重度哮喘并接受皮质类固醇治疗。孟鲁司特似乎不会直接导致这些患者发生该综合征。

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