Azapağası Ebru, Kendirli Tanıl, Perk Oktay, Kutluk Gültekin, Öz Tunçer Gökçen, Teber Serap, Çobanoğlu Nazan
Department of Pediatric Intensive Care, Ankara University Medical Faculty, Ankara, Turkey.
Department of Pediatric Neurology, Ankara University Medical Faculty, Ankara, Turkey.
J Pediatr Intensive Care. 2020 Sep;9(3):196-200. doi: 10.1055/s-0040-1708552. Epub 2020 Apr 7.
Sialorrhea is a frequent problem and may lead to aspiration in patients with swallowing dysfunction. We aimed to assess the effectiveness and safety of sublingual atropine sulfate treatment in pediatric patients with sialorrhea. The medical records of patients who had received sublingual atropine sulfate between January 2015 and January 2016 were reviewed retrospectively. The demographic properties, diagnosis, invasive or noninvasive mechanical ventilation need, and the presence of tracheotomy were assessed. Response rates to sublingual atropine were measured using the Teacher Drooling Scale (TDS). Pre and post-treatment drooling scores were compared. Atropine sulfate ampoule was administered at 20 µg/kg/dose. Minimum dose was 0.25 mg, while maximum dose was 0.03 mg/kg.Thirty-five pediatric patients with sialorrhea who had received sublingual atropine sulfate were identified; however, TDS scores had been recorded in only 20 of them. The median age of the patients was 25 months (3-78 months; 7 girls, 13 boys). Sixteen (80%) patients were on invasive mechanical ventilation and seven (30%) had tracheotomy. Nineteen patients had a neurodevelopmental disorder and only one patient had oral and esophageal lesions due to corrosive material intake. The median TDS score prior to sublingual atropine sulfate treatment was 5, and it decreased to 3 on the second day of treatment, a change that was statistically significant ( < 0.001). No side effects were observed. Sublingual atropine sulfate is safe and effective in the short-term treatment of sialorrhea; however, randomized placebo controlled and long-term follow-up studies are necessary.
流涎是一个常见问题,可能导致吞咽功能障碍患者发生误吸。我们旨在评估硫酸阿托品舌下给药治疗小儿流涎的有效性和安全性。回顾性分析了2015年1月至2016年1月期间接受硫酸阿托品舌下给药的患者的病历。评估了人口统计学特征、诊断、有创或无创机械通气需求以及气管切开情况。使用教师流涎量表(TDS)测量对硫酸阿托品的反应率。比较治疗前后的流涎评分。硫酸阿托品安瓿以20μg/kg/剂量给药。最小剂量为0.25mg,最大剂量为0.03mg/kg。确定了35例接受硫酸阿托品舌下给药的小儿流涎患者;然而,其中只有20例记录了TDS评分。患者的中位年龄为25个月(3 - 78个月;7名女孩,13名男孩)。16例(80%)患者接受有创机械通气,7例(30%)患者进行了气管切开。19例患者患有神经发育障碍,只有1例患者因摄入腐蚀性物质而有口腔和食管病变。硫酸阿托品舌下给药治疗前的中位TDS评分为5分,治疗第二天降至3分,这一变化具有统计学意义(<0.001)。未观察到副作用。硫酸阿托品舌下给药在短期治疗流涎方面安全有效;然而,需要进行随机安慰剂对照和长期随访研究。