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探讨舌下含服阿托品在治疗神经发育障碍患者流涎中的作用:一项回顾性研究。

Examining the Role of Sublingual Atropine for the Treatment of Sialorrhea in Patients with Neurodevelopmental Disabilities: A Retrospective Review.

作者信息

Petkus Kayla Durkin, Noritz Garey, Glader Laurie

机构信息

Division of Complex Care, Nationwide Children's Hospital, Columbus, OH 43205, USA.

Department of Pharmacy, Nationwide Children's Hospital, Columbus, OH 43205, USA.

出版信息

J Clin Med. 2023 Aug 11;12(16):5238. doi: 10.3390/jcm12165238.

Abstract

Sialorrhea is common in children with neurodevelopmental disabilities (NDD) and is reported in >40% of children with cerebral palsy (CP). It causes a range of complications, including significant respiratory morbidity. This single-center retrospective chart review aims to document sublingual atropine (SLA) utilization to guide further study in establishing its role in secretion management for children with NDD. A chart review was completed for patients with NDD ≤ 22 years of age treated with SLA at a free-standing children's hospital between 1 January 2016 and 1 June 2021. Descriptive statistics were generated to summarize findings. In total, 190 patients were identified, of which 178 met inclusion criteria. The average starting dose for SLA was 1.5 mg/day, or 0.09 mg/kg/day when adjusted for patient weight. Eighty-nine (50%) patients were prescribed SLA first line for secretion management while 85 (48%) patients tried glycopyrrolate prior to SLA. SLA was used after salivary Botox, ablation, and/or surgery in 16 (9%) patients. This study investigates SLA as a potential pharmacologic agent to treat sialorrhea in children with NDD. We identify a range of prescribing patterns regarding dosing, schedule, and place in therapy, highlighting the need for further evidence to support and guide its safe and efficacious use.

摘要

流涎在神经发育障碍(NDD)儿童中很常见,据报道,超过40%的脑瘫(CP)儿童存在流涎问题。它会引发一系列并发症,包括严重的呼吸道疾病。这项单中心回顾性病历审查旨在记录舌下阿托品(SLA)的使用情况,以指导进一步研究确定其在NDD儿童分泌物管理中的作用。对2016年1月1日至2021年6月1日期间在一家独立儿童医院接受SLA治疗的年龄≤22岁的NDD患者进行了病历审查。生成描述性统计数据以总结研究结果。总共确定了190例患者,其中178例符合纳入标准。SLA的平均起始剂量为1.5毫克/天,根据患者体重调整后为0.09毫克/千克/天。89例(5%)患者被一线开具SLA用于分泌物管理,而85例(48%)患者在使用SLA之前尝试过格隆溴铵。16例(9%)患者在接受唾液肉毒素注射、消融和/或手术后使用了SLA。本研究调查了SLA作为治疗NDD儿童流涎的潜在药物。我们确定了一系列关于给药剂量、给药方案和治疗地位的处方模式,突出了需要进一步的证据来支持和指导其安全有效使用的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46f5/10455410/8107fb66535b/jcm-12-05238-g001.jpg

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