Comparison of cefuroxime with or without intranasal fluticasone for the treatment of rhinosinusitis - The CAFFS trial: A randomized controlled trial

被引:106
作者
Dolor, RJ
Witsell, DL
Hellkamp, AS
Williams, JW
Califf, RM
Simel, DL
机构
[1] Duke Univ, Med Ctr, Duke Clin Res Inst, Durham, NC 27705 USA
[2] Durham Vet Affairs Med Ctr, Dept Med, Durham, NC USA
[3] Durham Vet Affairs Med Ctr, Dept Surg, Div Internal Med, Durham, NC USA
[4] Duke Univ, Med Ctr, Div Otolaryngol, Durham, NC USA
[5] Univ Texas, Hlth Sci Ctr, Audie L Murphy Div, S Texas Vet Affairs Hlth Care Syst, San Antonio, TX USA
[6] Univ Texas, Hlth Sci Ctr, Div Internal Med, San Antonio, TX USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2001年 / 286卷 / 24期
关键词
D O I
10.1001/jama.286.24.3097
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context It is not known whether intranasal corticosteroids are beneficial to treat acute rhinosinusitis in patients with a history of chronic or recurrent sinus symptoms. Objective To assess whether the addition of an intranasal corticosteroid to antibiotic therapy affects the speed and rate of recovery of such patients with acute rhinosinusitis. Design, Setting, and Patients A double-blind, randomized, placebo-controlled multicenter trial of 95 patients (median age, 39 years) with a history of recurrent sinusitis or chronic rhinitis and evidence of acute infection by sinus radiograph or nasal endoscopy, which was conducted from October 1998 through April 2000 at 22 sites (12 primary care and 10 otolaryngology). Intervention Two puffs (total dose, 200 mug) of fluticasone propionate (n=47) or placebo nasal spray (n=48) in each nostril once daily for 21 days; all received 2 puffs of xylometazoline hydrochloride in each nostril twice daily for 3 days and 250 mg of cefuroxime axetil twice daily for 10 days. Main Outcome Measure Time to clinical success (patient reported cured or much improved) during telephone follow-up at 10, 21, and 56 days. Results A total of 88 patients (93%) completed follow-up. Patients recorded their symptoms, work assessment, and compliance during the 3-week treatment phase. Patients receiving fluticasone achieved a significantly higher rate of clinical success than patients receiving placebo (93.5% vs 73.9%; P=.009). Patients treated with fluticasone improved significantly more rapidly (median of 6.0 days to clinical success) vs patients in the placebo group (median of 9.5 days; P=.01). Conclusions The addition of fluticasone to xylometazoline and antimicrobial therapy with cefuroxime improves clinical success rates and accelerates recovery of patients with a history of chronic rhinitis or recurrent sinusitis who present for treatment of acute rhinosinusitis.
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页码:3097 / 3105
页数:9
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