Treatment of Chronic Rhinosinusitis With Nasal Polyposis With Oral Steroids Followed by Topical Steroids A Randomized Trial

被引:133
作者
Vaidyanathan, Sriram
Barnes, Martyn
Williamson, Peter
Hopkinson, Pippa
Donnan, Peter T.
Lipworth, Brian [1 ]
机构
[1] Ninewells Hosp, Div Med Sci, Ctr Cardiovasc & Lung Biol, Asthma & Allergy Res Grp, Dundee DD1 9SY, Scotland
关键词
GLUCOCORTICOID-RECEPTOR; DOUBLE-BLIND; FLUTICASONE; SPRAY; STANDARDIZATION; BUDESONIDE; DIAGNOSIS; EFFICACY; RHINITIS; THERAPY;
D O I
10.7326/0003-4819-154-5-201103010-00003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Chronic rhinosinusitis (CRS) with nasal polyposis is common. The long-term efficacy and safety of approaches to medical management are not well-known. Objective: To evaluate the efficacy and safety of a 2-week regimen of oral steroid therapy followed by 26 weeks of sequential topical steroid maintenance therapy. Design: Parallel randomized trial with computer-generated block randomization and central allocation. Patients and investigators were blinded to group assignment. (ClinicalTrials.gov registration number: NCT00788749) Setting: A specialty rhinology clinic in Tayside, Scotland. Patients: 60 adults with CRS and moderate-sized or larger nasal polyps who were referred by their primary physicians for specialty care. Interventions: Patients were randomly assigned in a 1: 1 ratio to receive oral prednisolone, 25 mg/d, or placebo for 2 weeks, followed in both groups by fluticasone propionate nasal drops, 400 mu g twice daily, for 8 weeks and then fluticasone propionate nasal spray, 200 mu g twice daily, for 18 weeks. Measurements: Polyp grading (primary outcome), hyposmia score, quality of life, symptoms, nasal patency, adrenal function, and bone turnover. Results: The mean decrease in polyp grade from baseline to 2 weeks was 2.1 units (SD, 1.1) in the prednisolone group and 0.1 unit (SD, 1.0) in the placebo group (mean difference between groups, -1.8 units [95% CI, -2.4 to -1.2 units]; P < 0.001). The difference between groups was -1.08 units (CI, -1.74 to -0.42 unit; P = 0.001) at 10 weeks and -0.8 unit (CI, -1.8 to 0.2 unit; P = 0.11) at 28 weeks. The mean decrease in hyposmia score from baseline to 2 weeks was 31.12 mm (SD, 30.1) in the prednisolone group and 1.41 mm (SD, 30.6) in the placebo group (mean difference between groups, -28.33 mm [CI, -42.71 to -13.96 mm]; P = 0.002). The difference between groups was -16.06 mm (CI, -30.99 to -1.13 mm; P = 0.03) at 10 weeks and -12.13 mm (CI, -30.55 to 6.29 mm; P = 0.19) at 28 weeks. Prednisolone therapy resulted in transient suppression of adrenal function and increase in bone turnover after 2 weeks, with a return to baseline at 10 and 28 weeks. Limitations: Patients were referred from primary care to a single-center rhinology clinic, which limits the generalizability of results. Serial measurements of surrogates of nasal inflammation (such as nitric oxide or cytokine levels) were not performed. Conclusion: Initial oral steroid therapy followed by topical steroid therapy seems to be more effective over 6 months than topical steroid therapy alone in decreasing polyp size and improving olfaction in patients referred for specialty care of CRS with at least moderate nasal polyposis.
引用
收藏
页码:293 / 302
页数:10
相关论文
共 28 条
[1]   ATS/ERS recommendations for standardized procedures for the online and offline measurement of exhaled lower respiratory nitric oxide and nasal nitric oxide, 2005 [J].
American Thoracic Society ;
European Respiratory Society .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2005, 171 (08) :912-930
[2]   Important research questions in allergy and related diseases: 3-chronic rhinosinusitis and nasal polyposis - a GA2LEN study [J].
Bachert, C. ;
Van Bruaene, N. ;
Toskala, E. ;
Zhang, N. ;
Olze, H. ;
Scadding, G. ;
Van Drunen, C. M. ;
Mullol, J. ;
Cardell, L. ;
Gevaert, P. ;
Van Zele, T. ;
Claeys, S. ;
Hallden, C. ;
Kostamo, K. ;
Foerster, U. ;
Kowalski, M. ;
Bieniek, K. ;
Olszewska-Ziaber, A. ;
Nizankowska-Mogilnicka, E. ;
Szczeklik, A. ;
Swierczynska, M. ;
Arcimowicz, M. ;
Lund, V. ;
Fokkens, W. ;
Zuberbier, T. ;
Akdis, C. ;
Canonica, G. ;
Van Cauwenberge, P. ;
Burney, P. ;
Bousquet, J. .
ALLERGY, 2009, 64 (04) :520-533
[3]   Chronic rhinosinusitis patients mucosa have a greater burden with polyps or polypoid of illness [J].
Banerji, Aleena ;
Piccirillo, Jay F. ;
Thawley, Stanley E. ;
Levitt, Robert G. ;
Schechtman, Kenneth B. ;
Kramper, Maggie A. ;
Hamilos, Daniel L. .
AMERICAN JOURNAL OF RHINOLOGY, 2007, 21 (01) :19-26
[4]   Effects of levocetirizine as add-on therapy to fluticasone in seasonal allergic rhinitis [J].
Barnes, ML ;
Ward, JH ;
Fardon, TC ;
Lipworth, BJ .
CLINICAL AND EXPERIMENTAL ALLERGY, 2006, 36 (05) :676-684
[5]   A short course of oral prednisone followed by intranasal budesonide is an effective treatment of severe nasal polyps [J].
Benítez, P ;
Alobid, I ;
de Haro, J ;
Berenguer, J ;
Bernal-Sprekelsen, M ;
Pujols, L ;
Picado, C ;
Mullol, J .
LARYNGOSCOPE, 2006, 116 (05) :770-775
[6]  
Crapo RO, 2000, AM J RESP CRIT CARE, V161, P309
[7]   Systemic bioavailability of fluticasone propionate administered as nasal drops and aqueous nasal spray formulations [J].
Daley-Yates, PT ;
Baker, RC .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2001, 51 (01) :103-105
[8]  
Fokkens W., 2007, Rhinol Suppl, P1
[9]   MEASURING HEALTH-RELATED QUALITY-OF-LIFE [J].
GUYATT, GH ;
FEENY, DH ;
PATRICK, DL .
ANNALS OF INTERNAL MEDICINE, 1993, 118 (08) :622-629
[10]   INTRANASAL DRUG DELIVERY BY SPRAY AND DROPS [J].
HARDY, JG ;
LEE, SW ;
WILSON, CG .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1985, 37 (05) :294-297