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A randomized prospective clinical trial on the effectiveness of three treatment modalities for patients with lower denture problems - A 10 year follow-up study on patient satisfaction: a 10 year follow-up study on patient satisfaction

机译:三种前瞻性假牙问题患者治疗方式有效性的随机前瞻性临床试验-一项为期10年的患者满意度随访研究:一项为期10年的患者满意度随访研究

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摘要

Treatment of lower denture complaints of patients with an edentulous mandible with a height of at least 15 mm can consist of meticulous construction of a new set of dentures (CD), construction of a new set of dentures following preprosthetic surgery to enlarge the denture-bearing area (PPS), or construction of an implant-retained mandibular overdenture (IRO). The aim of this prospective randomized controlled clinical trial was to evaluate the satisfaction of the above mentioned treatment modalities in resolving lower denture related complaints. Ninety edentulous patients (Cawood class IV and V, mean mandibular height 20.7 +/- 2.7 mm) were randomly assigned to one of these treatment modalities. The main outcome parameters were denture satisfaction and chewing ability, which were assessed using validated self-administered questionnaires focusing on denture-related complaints and problems with chewing different types of food. These parameters were measured before treatment, and 1, 5 and 10 years after treatment. Differences among the three groups were tested by applying a one way analysis of variance and a Tukey's test for multiple comparison. At the I year evaluation, significantly better scores were observed in the two surgical groups (IRO, PPS) than in the CD group (P
机译:对高度至少为15 mm的无牙颌下颌患者的下颌义齿的治疗可以包括精心构建一套新义齿(CD),在义肢修复手术后建造一套新义齿以扩大义齿承载力区域(PPS)或植入物固定的下颌覆盖义齿(IRO)的构造。这项前瞻性随机对照临床试验的目的是评估上述治疗方式在解决下颌假牙相关主诉方面的满意度。 90名无牙颌患者(Cawood IV级和V级,下颌平均高度20.7 +/- 2.7 mm)被随机分配为这些治疗方式之一。主要结局参数是义齿满意度和咀嚼能力,这是使用经过验证的自我管理调查表进行评估的,该调查表侧重于义齿相关的投诉和咀嚼不同类型食物的问题。这些参数是在治疗前,治疗后1、5和10年测量的。通过应用方差的单向分析和多元比较的Tukey检验来测试三组之间的差异。在I年评估中,两个手术组(IRO,PPS)的观察结果明显好于CD组(P

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