Speech correcting surgery

  • 文章类型: Journal Article
    目的:唇裂和/或腭裂(CL/P)修复后,儿童可能发展为咽喉功能不全(VPI)导致言语缺陷,需要额外的言语矫正手术。这项研究检查了Sommerlad的CL/P腭成形术后VPI和言语矫正手术的发生率,及其与各种临床特征的关联。
    方法:在乌得勒支的Wilhelmina儿童医院进行了一项回顾性队列研究,对2008年至2017年登记的380名CL/P患者的儿童记录进行了回顾性分析。纳入标准包括CL/P的诊断,根据Sommerlad的技术进行原发性腭成形术,和5岁以上的语言评估。裂缝类型和宽度之间的关联,存在其他遗传性疾病和术后并发症(腭裂开,瘘管)使用比值比和卡方检验进行评估。
    结果:共纳入239例患者。VPI率为52.7%(n=126),在119例患者(49.8%)中进行了言语矫正手术。严重裂隙型,如更高的Veau分类所示,与明显较高的言语矫正手术率相关(p=0.033)。在裂隙宽度>10毫米的患者中进行了更多的言语矫正手术,与裂隙宽度≤10mm的患者相比(p<0.001)。与没有口瘘的患者相比,口鼻瘘的患者接受了更多的言语矫正手术(p=0.004)。在有和没有遗传疾病的患者之间,言语矫正手术的发生率没有统计学上的显着差异(p=0.890)。
    结论:裂隙形态的变化,裂隙宽度和口鼻瘘等并发症与不同的言语结局相关。未来的研究应该集中在为CL/P患者的言语矫正手术创建多变量预测模型。
    OBJECTIVE: After cleft lip and/or palate (CL/P) repair, children may develop velopharyngeal insufficiency (VPI) leading to speech imperfections, necessitating additional speech correcting surgery. This study examines the incidence of VPI and speech correcting surgery after Sommerlad\'s palatoplasty for CL/P, and its association with various clinical features.
    METHODS: A retrospective cohort study was performed in the Wilhelmina Children\'s Hospital in Utrecht and child records from 380 individuals with CL/P registered from 2008 to 2017 were retrospectively reviewed. Inclusion criteria comprised the diagnosis of CL/P, primary palatoplasty according to Sommerlad\'s technique, and speech assessment at five years or older. Association between cleft type and width, presence of additional genetic disorders and postoperative complications (palatal dehiscence, fistula) were assessed using odds ratios and chi squared tests.
    RESULTS: A total of 239 patients were included. The VPI rate was 52.7% (n = 126) and in 119 patients (49.8%) a speech correcting surgery was performed. Severe cleft type, as indicated by a higher Veau classification, was associated with a significant higher rate of speech correcting surgeries (p = 0.033). Significantly more speech correcting surgeries were performed in patients with a cleft width >10 mm, compared to patients with a cleft width ≤10 mm (p < 0.001). Patients with oronasal fistula underwent significantly more speech correcting surgeries than those without fistula (p = 0.004). No statistically significant difference was found in the incidence of speech correcting surgery between patients with and without genetic disorders (p = 0.890).
    CONCLUSIONS: Variations in cleft morphology, cleft width and complications like oronasal fistula are associated with different speech outcomes. Future research should focus on creating a multivariable prediction model for speech correcting surgery in CL/P patients.
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  • 文章类型: Systematic Review
    目的:在腭裂患者中,软腭通常使用直线腭成形术闭合,Z-腭成形术,或者用颊瓣进行腭成形术。目前,尚不清楚哪种手术技术在言语结局方面更优越。这篇综述的目的是研究每种软腭成形术技术的言语矫正手术(SCS)的发生率,并确定与该结果相关的变量。
    方法:根据PRISMA指南进行了系统的文献检索。纳入和排除标准用于关注软腭成形术后SCS的发生率。其他变量,如手术修改,裂隙形态,综合征,腭成形术的年龄,报告了瘘管和咽喉功能评估。使用改良的新渥太华量表(NOS)进行质量评估。荟萃分析的汇总估计值是使用随机效应模型计算的。
    结果:共发现29项研究,其中54项被纳入分析。直线腭成形术后SCS的汇总估计比例为19%(95%CI15-24),Z-pal成形术后6%(95%CI4-9),术后有7%的颊侧皮瓣(95%CI4-11)。
    结论:在接受Z-pal移植的患者中,与直线pal移植相比,SCS发生率较低。我们提出了一组最小的结果参数,理想情况下应将其纳入有关left裂修复后语音结果的未来研究中。
    结论:目前文献报道了关于腭裂修复的高度异质性数据。我们推荐的参数集可以解决这种不一致性,并且可以使中心间比较成为可能并且质量更好。
    OBJECTIVE: In cleft palate patients, the soft palate is commonly closed using straight-line palatoplasty, Z-palatoplasty, or palatoplasty with buccal flaps. Currently, it is unknown which surgical technique is superior regarding speech outcomes. The aim of this review is to study the incidence of speech correcting surgery (SCS) per soft palatoplasty technique and to identify variables which are associated with this outcome.
    METHODS: A systematic literature search was carried out according to the PRISMA guidelines. Inclusion and exclusion criteria were applied to focus on the incidence of SCS after soft palatoplasty. Additional variables like surgical modification, cleft morphology, syndrome, age at palatoplasty, fistula and assessment of velopharyngeal function were reported. A modified New-Ottawa Scale (NOS) was used for quality appraisal. Pooled estimates from the meta-analysis were calculated using a random-effects model.
    RESULTS: One thousand twenty-nine studies were found of which 54 were included in the analysis. The pooled estimate proportion of SCS after straight-line palatoplasty was 19% (95% CI 15-24), after Z-palatoplasty 6% (95% CI 4-9), and after palatoplasty with buccal flaps 7% (95% CI 4-11).
    CONCLUSIONS: A lower SCS rate was found in patients receiving Z-palatoplasty when compared to straight-line palatoplasty. We propose a minimum set of outcome parameters which ideally should be included in future studies regarding speech outcomes after cleft palate repair.
    CONCLUSIONS: Current literature reports highly heterogenous data regarding cleft palate repair. Our recommended set of parameters may address this inconsistency and could make intercenter comparison possible and of better quality.
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