雷特综合征患者的误吸、呼吸系统并发症及相关医疗资源利用

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Nazia Rashid, Jonathan D Darer, Charles Ruetsch, Xiaoyun Yang
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引用次数: 0

摘要

背景:Rett综合征(RTT)患者有较高的误吸风险,下呼吸道感染(LRTI)和呼吸衰竭(RF)的发生率也很高。方法:对89例有或无误吸证据的RTT患者进行回顾性比较队列分析,使用EHR结构化和抽象的临床记录数据。已知或疑似误吸的个体(按临床文献)(病例)与对照组进行误吸危险因素、RF、LRTI和住院率的比较。结果:符合条件的患者中,误吸病例25例(28.1%)。有和没有吸痰的RTT患者RF累积率分别为60.0%和6.3%。在6个月的基线期间,与对照组相比,误吸病例更有可能存在危险因素,包括癫痫(54.5%对4.5%)、吞咽困难(40.9%对0%)、胃食管反流(31.8%对0.0%)、脊柱侧弯(31.8%对4.5%)和呕吐(18.2%对0.0%)。与非误吸组相比,误吸组发生LRTI(50%比5.0%)和≥1次住院的可能性更大(75.0%比35.0%)(均为p)。结论:已知或怀疑误吸的RTT患者发生LRTI、RF和住院的风险增加。提供者应监测误吸,并制定预防措施,个人误吸危险因素,即使在没有误吸症状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aspiration, respiratory complications, and associated healthcare resource utilization among individuals with Rett syndrome.

Background: Individuals with Rett syndrome (RTT) are at high risk for aspiration and also experience high rates of lower respiratory tract infections (LRTI) and respiratory failure (RF).

Methods: A retrospective comparative cohort analysis was performed among 89 individuals with RTT with and without evidence of aspiration, using EHR structured and abstracted clinical notes data. Individuals with known or suspected aspiration (per clinical documentation) (cases) were compared to controls on aspiration risk factors, RF, LRTI, and hospitalization.

Results: Of eligible individuals, 25 (28.1%) were aspiration cases. The cumulative rate of RF among RTT individuals with and without aspiration was 60.0% and 6.3%, respectively. Aspiration cases were more likely to have risk factors compared to controls during the 6-month baseline including epilepsy (54.5% vs. 4.5%), dysphagia (40.9% vs. 0%), GERD (31.8% vs. 0.0%), scoliosis (31.8% vs. 4.5%), and vomiting (18.2% vs. 0.0%). Aspiration cases were more likely to have LRTI (50% vs. 5.0%) and ≥ 1 inpatient admissions than non-aspiration controls (75.0% vs. 35.0%) (all p < 0.05).

Conclusions: Individuals with RTT with known or suspected aspiration are at increased risk of LRTI, RF, and inpatient admissions. Providers should monitor aspiration and institute preventative measures among individuals with aspiration risk factors even in the absence of aspiration symptoms.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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