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每日一次400微克丙酸氟替卡松滴鼻剂与安慰剂相比治疗成人双侧鼻息肉的疗效和耐受性。

Efficacy and tolerability of fluticasone propionate nasal drops 400 microgram once daily compared with placebo for the treatment of bilateral polyposis in adults.

作者信息

Keith P, Nieminen J, Hollingworth K, Dolovich J

机构信息

McMaster University Medical Centre, Hamilton, Ontario, Canada, Päijät-Häme Hospital, Lahti, Finland, GlaxoWellcome Research & Development, UK.

出版信息

Clin Exp Allergy. 2000 Oct;30(10):1460-8. doi: 10.1046/j.1365-2222.2000.00932.x.

Abstract

BACKGROUND

Chronic eosinophilic rhinosinusitis underlies a range of respiratory disorders including nasal polyposis. Surgical and medical methods are used to control polyps, with topical steroids commonly being used for their anti-inflammatory properties. Fluticasone propionate nasal drops (FPND) is a formulation developed specifically for an effective and well tolerated corticosteroid treatment of nasal polyposis.

OBJECTIVES

To assess efficacy and tolerability of FPND in the treatment of bilateral nasal polyposis in adults.

METHODS

This multicentre, randomized, parallel-group study compared FPND 400 microgram once daily (o.d.) with placebo for 12 weeks in adult patients with mild to moderate bilateral polyposis. The primary efficacy endpoint was visual assessment of polyp size by the physician at monthly clinic visits. Nasal blockage, rhinitis, peak nasal inspiratory flow (PNIF), olfactory function and requirement for polypectomy were also assessed at visits. The patients kept diary card records of symptoms, PNIF, and use of rescue antihistamine. Additional safety data were provided by a 12-week open extension, when all patients received FPND 400 microgram o.d.

RESULTS

After 12 weeks double-blind treatment with FPND (n = 52) or placebo (n = 52), polyp size was reduced in 27% and 16% of patients, respectively; clinical reduction of nasal blockage significantly favoured FPND over placebo (55% vs 22%; P = 0.002), and clinic PNIF had increased significantly with FPND (by 52 L/min vs -3 L/min for placebo; P < 0.001). Diary card measurements showed significant benefits of FPND vs placebo for daily PNIF, nasal blockage, rhinitis and use of loratadine rescue medication. Both treatments were well tolerated and no serious adverse events occurred during randomized treatment. Epistaxis was more frequent with FPND than placebo but was generally mild and did not result in withdrawals. Mean serum cortisol levels did not change significantly with either treatment.

CONCLUSION

This study showed FPND 400 microgram o.d. to be an effective and well tolerated treatment for bilateral nasal polyposis in adults.

摘要

背景

慢性嗜酸性粒细胞性鼻-鼻窦炎是包括鼻息肉病在内的一系列呼吸道疾病的基础。手术和药物方法用于控制息肉,局部用类固醇因其抗炎特性而常用。丙酸氟替卡松滴鼻剂(FPND)是一种专门为有效且耐受性良好地治疗鼻息肉病而开发的制剂。

目的

评估FPND治疗成人双侧鼻息肉病的疗效和耐受性。

方法

这项多中心、随机、平行组研究将400微克每日一次(o.d.)的FPND与安慰剂在患有轻度至中度双侧息肉病的成年患者中进行了12周的比较。主要疗效终点是医生在每月门诊就诊时对息肉大小的视觉评估。在就诊时还评估了鼻塞、鼻炎、鼻腔最大吸气流量(PNIF)、嗅觉功能和息肉切除术的需求。患者记录症状、PNIF和使用急救抗组胺药的日记卡。通过为期12周的开放延长期提供了额外的安全性数据,在此期间所有患者均接受400微克o.d.的FPND。

结果

在接受FPND(n = 52)或安慰剂(n = 52)进行12周双盲治疗后,息肉大小分别在27%和16%的患者中有所减小;FPND在临床上对鼻塞的改善明显优于安慰剂(55%对22%;P = 0.002),并且FPND使门诊PNIF显著增加(增加52升/分钟,而安慰剂为 -3升/分钟;P < 0.001)。日记卡测量结果显示,FPND在每日PNIF、鼻塞、鼻炎和使用氯雷他定急救药物方面相对于安慰剂有显著益处。两种治疗耐受性良好,随机治疗期间未发生严重不良事件。FPND组鼻出血比安慰剂组更频繁,但一般较轻,未导致退出研究。两种治疗方法下平均血清皮质醇水平均无显著变化。

结论

本研究表明,400微克o.d.的FPND是治疗成人双侧鼻息肉病的一种有效且耐受性良好的疗法。

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