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Injection Laryngoplasty for Type I Laryngeal Cleft in Children

机译:注射喉成形术治疗儿童I型喉裂

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Objective. To review the 2-year, single-institution experience with injection laryngoplasty for diagnosis and treatment of type I laryngeal clefts (LC-I).Study Design. Case series with chart review. Setting. Tertiary care academic children's hospital.Subjects and Methods. Patients at our institution who underwent injection laryngoplasty for LC-I from January 2008 to December 2009. Outcome measures included patient demographics, surgical and anesthetic technique, effect on swallowing, and complications. Preoperative and postoperative swallowing evaluations were compared, and quality and duration of effects were calculated.Results. Sixteen children, 9 male and 7 female, underwent injection laryngoplasty for LC-I. Mean gestational age was 36.4 weeks (SD, 4.0 weeks; range, 27-41 weeks). Six patients had a major congenital anomaly (37.5%). Mean age at injection was 11.8 months (SD, 8.9 months; range, 2.9-33.5 months). Nine patients (56%) demonstrated complete resolution of penetration and aspiration on postoperative modified barium swallow (MBS), 4 patients (25%) had some improvement, and 3 patients (19%) showed no change. There were no complications. Mean duration of symptom improvement was 3.3 months (SD, 3.0 months; range, 0-11 months). Five patients went on to have definitive surgical LC-I repair.Conclusion. Injection laryngoplasty was found to have favorable results in this group of patients with LC-1. Most patients experienced complete resolution of aspiration on MBS, and no patients experienced complications. These findings support the further study of injection laryngoplasty for LC-1 as both a diagnostic and therapeutic technique. Longer follow-up intervals are necessary to elucidate the predictive value with regard to success of formal cleft repair.
机译:目的。回顾2年的单机构注射喉头成形术的诊断和治疗I型喉裂(LC-I)的经验。研究设计。案例系列与图表审查。设置。三级护理学业儿童医院。对象和方法。我们机构的患者从2008年1月至2009年12月接受了LC-1的注射喉成形术。结果指标包括患者的人口统计学资料,手术和麻醉技术,吞咽效果以及并发症。比较术前和术后吞咽评估,计算效果的质量和持续时间。 16名儿童(男9名,女7名)接受了LC-1注射喉成形术。平均胎龄为36.4周(标准差为4.0周;范围为27-41周)。六例患者患有严重的先天性异常(37.5%)。注射时的平均年龄为11.8个月(标准差为8.9个月;范围为2.9-33.5个月)。 9例患者(56%)表现出对改良型吞咽钡剂(MBS)的穿透和抽吸完全消退,4例患者(25%)有所改善,3例患者(19%)没有改变。没有并发症。症状改善的平均持续时间为3.3个月(标准差为3.0个月;范围为0-11个月)。五名患者接受了最终的LC-I外科手术修复。发现在这组LC-1患者中,注射喉成形术具有良好的效果。大多数患者在MBS上均可完全清除吸入,没有患者发生并发症。这些发现为LC-1作为诊断和治疗技术的注射喉成形术的进一步研究提供了支持。需要较长的随访时间来阐明正式裂隙修复成功的预测价值。

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