Surgical management of chronic sialorrhea in pediatric patients: 10-year experience from one tertiary care institution

被引:27
|
作者
Formeister, Eric J. [1 ]
Dahl, John P. [1 ]
Rose, Austin S. [1 ]
机构
[1] Univ N Carolina, Sch Med, Dept Otolaryngol Head & Neck Surg, Chapel Hill, NC 27515 USA
关键词
Sialorrhea; Hypersalivation; Drooling; Submandibular gland excision; Parotid duct ligation; Botulinum toxin; BOTULINUM-TOXIN; EFFICACY; CHILDREN; INJECTION; LIGATION;
D O I
10.1016/j.ijporl.2014.06.005
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background: Chronic sialorrhea is a common problem for pediatric patients with disorders that affect swallowing. While many patients are successfully treated with medical therapies such as Robinul and Scopolamine, a number of such children are not able to tolerate the side effects of these medications. In these cases, surgical treatments can include Botulinum toxin A (Botox) injections into the major salivary glands, sublingual or submandibular gland excision (SMGE), submandibular duct ligation, parotid duct ligation (PDL), or any combination of the above procedures. The purpose of this study is to report on the 10-year experience with the surgical management of chronic sialorrhea at one tertiary care institution, and compare the efficacy of open surgical procedures versus Botox injections for reduction in salivary flow. Methods: A retrospective chart review identified 27 pediatric patients with chronic sialorrhea; 21 of whom underwent Botox injections and 15 of whom underwent surgical procedures. Preoperative and follow-up clinic notes were reviewed to determine the level and severity of drooling as well as the effectiveness of sialorrhea reduction, as assessed by the Teacher Drooling Scale (TDS). Results: 42% of those receiving Botox injections reported a reduction in drooling, with the average pre- and post-Botox TDS of 4.3 and 3.9, respectively (p = 0.02 by the Wilcoxon signed rank test). Nine of the patients receiving Botox injections (43%) required multiple injections, with an average duration of effect of 3.9 months, and 7 patients (33%) eventually required surgery. All of the children who underwent surgery (7 bilateral SMGE with PDL, 6 SMGE only, and 2 PDL only) experienced a reduction in drooling, with average pre- and post-operative TDS of 4.5 and 22, respectively. This reduction was significant by the Wilcoxon signed rank test (p = 0.001). Conclusions: The ten-year experience at our institution demonstrates the safety, efficacy and long-term control of drooling in the patients undergoing surgery for intractable sialorrhea. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1387 / 1392
页数:6
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