Jankowski R, Schrewelius C, Bonfils P, Saban Y, Gilain L, Prades J M, Strunski V
Department of Otorhinolaryngology, Head and Neck Surgery, Central Hospital, H. Poincaré University, F-54000 Nancy, France.
Arch Otolaryngol Head Neck Surg. 2001 Apr;127(4):447-52. doi: 10.1001/archotol.127.4.447.
To assess the efficacy and tolerability of once-daily treatment with budesonide aqueous nasal spray in patients with nasal polyps.
Randomized, double-blind, placebo-controlled, parallel-group study.
Sixteen hospital clinics.
One hundred eighty-three patients with moderate-sized nasal polyps causing clinically significant symptoms during a 1-week run-in period.
Patients were randomized to receive 1 of the following 4 budesonide aqueous nasal spray treatments: 128 microg once daily in the morning and placebo in the evening, 128 microg twice daily, 256 microg once daily in the morning and placebo in the evening, or placebo for 8 weeks. Nasal polyp size was scored and peak nasal inspiratory flow was measured at clinic visits at the beginning and end of the run-in period and after 4 and 8 weeks' treatment. Patients recorded daily peak nasal inspiratory flow, symptom scores (ie, blocked nose, runny nose, and sneezing) and sense of smell on diary cards.
Mean change in nasal polyp size at the end of treatment; mean changes in combined and individual symptom scores.
All doses of budesonide aqueous nasal spray significantly (P<.01) reduced polyp size; no significant differences were noted between the 4 treatment groups. The mean improvement in clinic peak nasal inspiratory flow at 8 weeks was 65.9 L/min with budesonide aqueous nasal spray, 128 microg twice daily; 71.6 L/min with budesonide aqueous nasal spray, 256 microg once daily; and 54.6 L/min with budesonide aqueous nasal spray, 128 microg once daily (all P<.001 vs placebo). Combined and individual symptom scores and sense of smell improved significantly in all budesonide-treated groups; the effect on symptoms became apparent within 1 to 2 days of the first dose. Budesonide aqueous nasal spray was well tolerated.
Doses of budesonide aqueous nasal spray, 128 microg once daily, were found to be effective in the treatment of nasal polyps, and doses of budesonide aqueous nasal spray, 256 microg once daily, did not show any significant additional efficacy.
评估布地奈德水鼻喷雾剂每日一次治疗鼻息肉患者的疗效和耐受性。
随机、双盲、安慰剂对照、平行组研究。
16家医院诊所。
183例中度鼻息肉患者,在为期1周的导入期内出现具有临床意义的症状。
患者被随机分配接受以下4种布地奈德水鼻喷雾剂治疗中的一种:每日上午128微克,晚上用安慰剂;每日两次,每次128微克;每日上午256微克,晚上用安慰剂;或用安慰剂治疗8周。在导入期开始和结束时以及治疗4周和8周后的门诊就诊时对鼻息肉大小进行评分,并测量鼻吸气峰流速。患者在日记卡上记录每日鼻吸气峰流速、症状评分(即鼻塞、流涕和打喷嚏)以及嗅觉。
治疗结束时鼻息肉大小的平均变化;综合和个体症状评分的平均变化。
所有剂量的布地奈德水鼻喷雾剂均显著(P<0.01)减小了息肉大小;4个治疗组之间未观察到显著差异。布地奈德水鼻喷雾剂每日两次、每次128微克治疗8周时,门诊鼻吸气峰流速的平均改善为65.9升/分钟;布地奈德水鼻喷雾剂每日一次、256微克治疗时为71.6升/分钟;布地奈德水鼻喷雾剂每日一次、128微克治疗时为54.6升/分钟(与安慰剂相比,所有P<0.001)。所有布地奈德治疗组的综合和个体症状评分以及嗅觉均有显著改善;对症状的影响在首剂后1至2天内显现。布地奈德水鼻喷雾剂耐受性良好。
发现每日一次128微克剂量的布地奈德水鼻喷雾剂对鼻息肉治疗有效,每日一次256微克剂量的布地奈德水鼻喷雾剂未显示出任何显著的额外疗效。