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首页> 外文期刊>European Archives of Oto-Rhino-Laryngology >A prospective, randomised, placebo-controlled trial of postoperative oral steroid in allergic fungal sinusitis
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A prospective, randomised, placebo-controlled trial of postoperative oral steroid in allergic fungal sinusitis

机译:术后口服类固醇治疗过敏性真菌性鼻窦炎的前瞻性,随机,安慰剂对照试验

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摘要

The aim of this study is to determine the effectiveness of postoperative oral steroid in controlling disease in patients with allergic fungal sinusitis (AFS). The study design includes prospective, randomised, double-blind, placebo-controlled trial using oral prednisolone. Twenty-four patients diagnosed with AFS underwent sinus surgery (endoscopic sinus surgery with or without open surgery) to completely excise disease. Patients were randomised to receive either oral steroid (n = 12) or placebo (n = 12) soon after surgery. All patients were also administered itraconazole and steroid nasal spray in the postoperative period. Subjective evaluation of symptom relief and objective evaluation by rigid nasal endoscopy at 6 and 12 weeks following surgery was performed. After 12 weeks, the code was broken and the two groups of patients were identified to note their response to treatment. At 6 weeks, complete relief of preoperative symptoms was obtained in eight patients who had received oral steroid and none who had received placebo (p = 0.001). Partial relief of preoperative symptoms was obtained in four who had received oral steroid and eight who had received placebo. Nasal endoscopy revealed that 8 of 12 patients who had received oral steroid and 1 patient who had received placebo were disease free (p = 0.009). At 12 weeks, complete symptom relief was obtained by all patients who received oral steroid but only one who received placebo (p = 0.0001). Nasal endoscopy at 12 weeks revealed that all 12 patients who had received oral steroid and only 1 patient (the same patient) who had received placebo were disease free (p = 0.0001). In conclusion, postoperative oral steroid in a tapering dose produces significant subjective and objective improvement of patients with AFS. It is also effective in preventing early recurrence. Inclusion of postoperative oral steroid therapy for at least 12 weeks is recommended in all patients who undergo excisive surgery for AFS. Keywords Allergic fungal sinusitis - Postoperative oral steroid - Randomised-controlled trial
机译:这项研究的目的是确定术后口服类固醇在控制过敏性真菌鼻窦炎(AFS)患者疾病中的有效性。研究设计包括使用口服泼尼松龙的前瞻性,随机,双盲,安慰剂对照试验。 24名诊断为AFS的患者接受了鼻窦手术(内窥镜鼻窦手术(有或没有开放手术))以完全切除疾病。患者在手术后不久随机接受口服类固醇(n = 12)或安慰剂(n = 12)。所有患者在术后均接受伊曲康唑和类固醇鼻喷雾剂治疗。术后6周和12周通过硬性鼻内窥镜检查对症状缓解进行主观评估,并进行客观评估。 12周后,密码被打破,确定了两组患者以记录他们对治疗的反应。在6周时,有8例接受口服类固醇激素治疗的患者完全没有缓解术前症状(p = 0.001)。四名接受口服类固醇激素治疗的患者和八名接受安慰剂的患者术前症状得到部分缓解。鼻内窥镜检查显示,接受口服类固醇治疗的12例患者中有8例接受安慰剂,其中1例患者无疾病(p = 0.009)。在第12周时,所有接受口服类固醇激素治疗的患者均能完全缓解症状,但只有一名接受安慰剂的患者(p = 0.0001)。鼻内窥镜检查在第12周时发现,所有12例接受口服类固醇治疗的患者和1例接受安慰剂的患者(同一患者)均无疾病(p = 0.0001)。总之,术后逐渐减少剂量的口服类固醇激素可对AFS患者产生明显的主观和客观改善。在预防早期复发方面也有效。对于所有接受过AFS兴奋性手术的患者,建议在术后至少接受12周口服类固醇激素治疗。关键词过敏性真菌性鼻窦炎-术后口服类固醇-随机对照试验

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