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伊曲康唑对变应性支气管肺曲霉病的辅助治疗

Adjunctive therapy of allergic bronchopulmonary aspergillosis with itraconazole.

作者信息

Denning D W, Van Wye J E, Lewiston N J, Stevens D A

机构信息

Department of Medicine, Santa Clara Valley Medical Center, San Jose, CA 95128.

出版信息

Chest. 1991 Sep;100(3):813-9. doi: 10.1378/chest.100.3.813.

Abstract

Itraconazole is a new orally active antifungal triazole with impressive activity against Aspergillus spp. Six patients with allergic bronchopulmonary aspergillosis (ABPA), aged 14 to 49 years, were treated with oral itraconazole (200 mg twice daily) for a mean of 3.9 months (range, one to six months; three patients continue on therapy). Two patients received two courses. Three patients had underlying cystic fibrosis, and three had severe asthma; four of the six required continuous high-dose systemic prednisone (mean, 43 mg/day; confidence interval [CI], 23 to 63 mg/day) at the start of therapy. In those treated for two months or longer, the mean total serum IgE level fell from 2,462 U/ml (CI, 752 to 4,202 U/ml) to 502 U/ml (CI, 123 to 880 U/ml) during each course, and the mean daily steroid dosage was decreased to a mean of 24 mg/day (CI, 11 to 37 mg/day). All patients experienced improvement in pulmonary function during the trial, with mean FEV, increasing from 1.43 to 1.77L/sec and mean FVC from 2.3 to 2.9 L in those treated for two months or longer. The mean steady-state serum concentration of itraconazole was 5.1 micrograms/ml (range, 1.8 micrograms/ml to 7.3 micrograms/ml); the patient with the lowest concentrations had the least significant clinical response. Cultures of sputum from two of three patients became negative for A fumigatus during therapy. No adverse clinical effects occurred except loss of libido in one patient. We conclude that oral itraconazole may be an effective adjunctive therapy in ABPA, possibly by clearing the airway of Aspergillus, and that randomized trials of this agent are warranted to better define its usefulness in this disorder.

摘要

伊曲康唑是一种新型口服活性抗真菌三唑类药物,对曲霉菌属具有显著活性。6例年龄在14至49岁的变应性支气管肺曲霉菌病(ABPA)患者接受口服伊曲康唑治疗(每日2次,每次200mg),平均治疗3.9个月(范围为1至6个月;3例患者继续接受治疗)。2例患者接受了两个疗程的治疗。3例患者患有潜在的囊性纤维化,3例患有重度哮喘;6例患者中有4例在治疗开始时需要持续高剂量全身应用泼尼松(平均43mg/天;置信区间[CI]为23至63mg/天)。在治疗两个月或更长时间的患者中,每个疗程期间血清总IgE水平平均从2462U/ml(CI为752至4202U/ml)降至502U/ml(CI为123至880U/ml),每日类固醇剂量平均降至24mg/天(CI为11至37mg/天)。所有患者在试验期间肺功能均有改善,治疗两个月或更长时间的患者平均第一秒用力呼气容积(FEV₁)从1.43L/秒增加至1.77L/秒,平均用力肺活量(FVC)从2.3L增加至2.9L。伊曲康唑的平均稳态血清浓度为5.1μg/ml(范围为1.8μg/ml至7.3μg/ml);浓度最低的患者临床反应最不明显。3例患者中有2例在治疗期间痰培养烟曲霉转阴。除1例患者出现性欲减退外,未发生不良临床效应。我们得出结论,口服伊曲康唑可能是ABPA的一种有效辅助治疗方法,可能是通过清除气道中的曲霉菌,并且有必要对该药物进行随机试验以更好地确定其在这种疾病中的效用。

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