Treatment of chronic pulmonary aspergillosis by voriconazole in nonimmunocompromised patients

被引:130
作者
Camuset, Juliette
Nunes, Hilario
Dombret, Marie-Christine
Bergeron, Anne
Henno, Priscilla
Philippe, Bruno
Dauriat, Gaelle
Mangiapan, Gilles
Rabbat, Antoine
Cadranel, Jacques
机构
[1] Hop Tenon, APHP, Dept Pneumol & Resp Intens Care, F-75970 Paris, France
[2] Avicenne Hosp, APHP, Dept Pneumol, Bobigny, France
[3] Hop Xavier Bichat, Dept Pneumol, APHP, Paris, France
[4] St Louis Hosp, Dept Pneumol, APHP, Paris, France
[5] George Pompidou European Univ, Dept Pneumol, APHP, Paris, France
[6] Foch Hosp, Dept Pneumol, Suresnes, France
[7] Beaujon Hosp, Dept Pneumol, Clichy, France
[8] Intercommune Hosp Ctr, Dept Pneumol, Creteil, France
[9] Hop Hotel Dieu, Dept Pneumol, APHP, Paris, France
关键词
aspergillosis; lung disease; triazole;
D O I
10.1378/chest.06-2441
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: There is no recognized medical treatment for chronic pulmonary aspergillosis (CPA) apart from surgery in patients with simple aspergilloma. To evaluate the efficacy of voriconazole in this setting, we conducted a retrospective multicenter study over a 3-year period. Methods: For inclusion in the study, patients had to have received voriconazole for treatment of confirmed or probable CPA with a follow-up of at least 6 months. Clinical, radiologic, and mycologic data were collected at baseline, every 2 to 3 months, and at the end of treatment or at the date point. Results: Twenty-four patients were included in the study, among which 9 patients presented with chronic cavitary pulmonary aspergillosis and 15 presented with chronic necrotizing pulmonary aspergillosis (CNPA). Voriconazole was given as a first-line treatment to 13 patients. The median duration of treatment and follow-up were 6.5 and 10 months, respectively. Three patients had to stop treatment with voriconazole because of toxicity. Symptoms and imagery findings were improved in 16 of 24 patients and 17 of 24 patients, respectively, at the end of follow-up. Mycology, which was positive at baseline in 21 of 23 patients, was negative in IS of 19 patients at the end of follow-up; serologic test results were also negative in 6 of 19 evaluable patients, all of whom had CNPA. Improved radioclinical findings and mycologic eradication were observed at the end of folow-up in 11 of 19 patients (58%). Patients in whom the disease was controlled had a significantly longer median duration of treatment than patients in whom it was uncontrolled (9 vs 6 months, respectively; p = 0.04). Conclusion: Voriconazole provides effective treatment of CPA with an acceptable level of toxicity.
引用
收藏
页码:1435 / 1441
页数:7
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