Effects of six-week clarithromycin therapy in corticosteroid-dependent asthma: A randomized, double-blind, placebo-controlled pilot study

被引:16
|
作者
Gotfried, MH
Jung, R
Messick, CR
Rubinstein, I
Garey, KW
Rodvold, KA
Danziger, LH
机构
[1] Univ Illinois, Dept Pharm Practice, Coll Pharm, Chicago, IL 60612 USA
[2] Univ Arizona, Phoenix, AZ USA
[3] Univ Colorado, Hlth Sci Ctr, Dept Clin Pharm, Denver, CO 80202 USA
[4] Clin Res Pharm Coordinating Ctr, Clin Res Pharm, Vet Affairs Cooperat Study Program, Albuquerque, NM USA
[5] Univ Houston, Coll Pharm, Dept Clin Sci & Adm, Houston, TX USA
关键词
clarithromycin; corticosteroid-dependent asthma; steroid-sparing effect; prednisone;
D O I
10.1016/S0011-393X(04)90000-8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Although corticosteroids such as prednisone are efficacious for the treatment of severe asthma, chronic administration of oral corticosteroid therapy is associated with significant adverse effects. Previous studies have shown that clarithromycin is effective in reducing bronchial hyperresponsiveness and allergen-induced bronchoconstriction. However, the effect of long-term clarithromycin therapy in patients with prednisone-dependent asthma is uncertain. \ Objective: This study was conducted to determine the effects of oral clarithromycin on prednisone daily dosage, pulmonary function, quality of life (QOL), and asthmatic symptoms in patients with corticosteroid-dependent asthma. Methods: This 14-week, prospective, randomized, double-blind, placebo-controlled pilot study was conducted at Pulmonary Associates (Phoenix, Arizona) and the University of Illinois at Chicago Medical Center (Chicago, Illinois). Patients aged 18 to 75 years with an established diagnosis of asthma and who had been receiving greater than or equal to5 mg/d of prednisone for the preceding 6 months were enrolled. After a 4-week data-collection period, patients received clarithromycin 500 mg BID for 6 weeks, followed by a 4-week follow-up period. The effects of clarithromycin therapy on prednisone dosage requirements, pulmonary function (as assessed using spirometry), QOL, and asthmatic symptoms (nocturnal asthma, shortness of breath, chest discomfort, wheezing, and cough) were assessed. Results: Fourteen patients (9 men, 5 women; mean [SD] age, 62 [13] years) completed the study and were included in the final analysis. One patient withdrew from the study due to clarithromycin-related nausea. After 6 weeks of clarithromycin therapy, patients were able to tolerate a significant reduction in mean (SD) prednisone dosage from baseline (30% [18%]; P = 0.020). Pulmonary function, QOL, and asthmatic symptoms did not significantly worsen despite reduction in prednisone dose. All patients who completed the study tolerated clarithromycin therapy. Conclusions: In this pilot study of patients with corticosteroid-dependent asthma, 6-week clarithromycin 500 mg BID was clinically effective in allowing a reduction in prednisone dosage, without worsening pulmonary function, QOL, or asthmatic symptoms. In addition, clarithromycin was well tolerated, with only 1 patient discontinuing therapy due to treatment-related nausea. Copyright (C) 2004 Excerpta Medica, Inc.
引用
收藏
页码:1 / 12
页数:12
相关论文
共 50 条
  • [31] Effects of coenzyme Q10 in MSA, a randomized, placebo-controlled, double-blind pilot study
    Apetauerova, D.
    Lamont, S.
    Kakullavarapu, J.
    Scala, S.
    MOVEMENT DISORDERS, 2006, 21 : S523 - S523
  • [32] Effects of coenzyme Q10 in MSA, a randomized, placebo-controlled, double-blind pilot study
    Apetauerova, Diana
    Lamont, Sharon
    Kakullavarapu, Jyotsna
    Scala, Stephanie
    NEUROLOGY, 2007, 68 (12) : A50 - A50
  • [33] Treatment of functional dyspepsia with sertraline:A double-blind randomized placebo-controlled pilot study
    Victoria PY Tan
    Tin K Cheung
    Wai M Wong
    Roberta Pang
    Benjamin CY Wong
    World Journal of Gastroenterology, 2012, (42) : 6127 - 6133
  • [34] Treatment of functional dyspepsia with sertraline: A double-blind randomized placebo-controlled pilot study
    Tan, Victoria P. Y.
    Cheung, Tin K.
    Wong, Wai M.
    Pang, Roberta
    Wong, Benjamin C. Y.
    WORLD JOURNAL OF GASTROENTEROLOGY, 2012, 18 (42) : 6127 - 6133
  • [35] Rifaximin for the treatment of active pouchitis: A randomized, double-blind, placebo-controlled pilot study
    Isaacs, Kim L.
    Sandler, Robert S.
    Abreu, Maria
    Picco, Michael F.
    Hanauer, Stephen B.
    Bickston, Stephen J.
    Present, Daniel
    Farraye, Francis A.
    Wolf, Douglas
    Sandborn, William J.
    INFLAMMATORY BOWEL DISEASES, 2007, 13 (10) : 1250 - 1255
  • [36] Reversal of Immunoparalysis in Humans In Vivo A Double-Blind, Placebo-controlled, Randomized Pilot Study
    Leentjens, Jenneke
    Kox, Matthijs
    Koch, Rebecca M.
    Preijers, Frank
    Joosten, Leo A. B.
    van der Hoeven, Johannes G.
    Netea, Mihai G.
    Pickkers, Peter
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2012, 186 (09) : 838 - 845
  • [37] A randomized, double-blind, placebo-controlled pilot study of simvastatin in aneurysmal subarachnoid hemorrhage
    Chou, Sherry H. -Y.
    Smith, Eric E.
    Badjatia, Neeraj
    Nogueira, Raul G.
    Sims, John R., II
    Ogilvy, Christopher S.
    Rordorf, Guy A.
    Ayata, Cenk
    STROKE, 2008, 39 (10) : 2891 - 2893
  • [38] OXYTOCIN TREATMENT OF ALCOHOL DEPENDENCE: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED PILOT STUDY
    Garbutt, J. C.
    Casey, R.
    Garcia, N.
    Kampov-Polevoy, A. B.
    Leserman, J.
    Gallop, R.
    Stansbury, M.
    Pedersen, C.
    ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2014, 38 : 214A - 214A
  • [39] Double-blind, randomized, placebo-controlled pilot study of leflunomide in systemic lupus erythematosus
    Tam, LS
    Li, EK
    Wong, CK
    Lam, CWK
    Szeto, CC
    LUPUS, 2004, 13 (08) : 601 - 604
  • [40] Efficacy of artichoke leaf extract in the treatment of patients with functional dyspepsia:: a six-week placebo-controlled, double-blind, multicentre trial
    Holtmann, G
    Adam, B
    Haag, S
    Collet, W
    Grünewald, E
    Windeck, T
    ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 18 (11-12) : 1099 - 1105