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首页> 外文期刊>International journal of otolaryngology >Randomized Clinical Trial Comparing Bucket Handle and Cartilage Tympanoplasty Techniques for the Reconstruction of Subtotal or Anterior Tympanic Membrane Perforation
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Randomized Clinical Trial Comparing Bucket Handle and Cartilage Tympanoplasty Techniques for the Reconstruction of Subtotal or Anterior Tympanic Membrane Perforation

机译:比较桶柄和软骨鼓膜成形术重建小鼓或前鼓膜穿孔的随机临床试验

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Objective. The purpose of the study is to compare the clinical outcome of the two techniques of Bucket Handle Tympanoplasty and Cartilage Tympanoplasty in achieving success in graft survival as well as acceptable auditory results. 60 patients who suffered chronic otitis media with anterior perforation of the tympanic membrane were chosen. The patients were randomly assigned using Block Randomization Method of two groups including patients who underwent Bucket Handle Tympanoplasty () or those that underwent Cartilage Tympanoplasty (). The patients were followed up for 1, 3, 6, and 12 months postoperatively. Results. The mean PTA was lower in Bucket Handle Tympanoplasty group as case group compared to Cartilage Tympanoplasty group as the control (). No significant statistical differences had identified passing through the time, in terms of PTA outcome ( Value = 0.547) and SRT outcome ( Value = 0.352), between Bucket Handle Tympanoplasty group and the Cartilage Tympanoplasty group. In total, postoperative tympanic membrane perforation was found in 10.0% of patients in Cartilage Tympanoplasty group and 13.3% in Bucket Handle Tympanoplasty group with no difference (). Conclusions. Hearing improvements in both methods were similar. Registration Number. The trial is registered with IRCT2016022626773N1.
机译:目的。该研究的目的是比较桶柄鼓膜成形术和软骨鼓膜成形术这两种技术在获得移植物存活成功和可接受的听觉效果方面的临床效果。选择60例患有慢性中耳炎并鼓膜前穿孔的患者。使用分组随机分组法将患者随机分为两组,包括接受过桶柄鼓膜成形术的患者()或接受过软骨鼓膜成形术的患者()。术后1、3、6、12个月对患者进行随访。结果。病例组的桶把手鼓膜成形术组的平均PTA低于对照组的软骨鼓膜成形术组()。在桶柄鼓膜成形术组和软骨鼓膜成形术组之间,在时间上没有发现明显的统计学差异,无论是PTA结局(值= 0.547)还是SRT结局(值= 0.352)。总体而言,在鼓室鼓膜成形术组中有10.0%的患者术后鼓膜穿孔,在桶柄鼓膜成形术组中有13.3%的患者无差异()。结论。两种方法的听觉改善相似。注册号码。该试验已在IRCT2016022626773N1中注册。

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