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患有安格曼综合征个体的医疗负担:安格曼综合征自然史研究的结果。

Healthcare burden among individuals with Angelman syndrome: Findings from the Angelman Syndrome Natural History Study.

机构信息

Ovid Therapeutics Inc., New York, New York.

Division of Genetics & Genomics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.

出版信息

Mol Genet Genomic Med. 2019 Jul;7(7):e00734. doi: 10.1002/mgg3.734. Epub 2019 May 14.

DOI:10.1002/mgg3.734
PMID:31090212
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6625091/
Abstract

BACKGROUND

The objective of this study is to describe healthcare resource utilization (HRU) and supportive therapy utilization (STU) among individuals with Angelman syndrome (AS), and to compare such usage by molecular etiology.

METHODS

Participants were categorized into deletion and non-deletion genotypes. Statistical differences were assessed using an independent samples t test.

RESULTS

Data were available on 302 individuals. Mean age of participants was 5.5 years, 92% of whom were less than 13 years, and 71% had the deletion etiology. About 68% of participants had at least one hospitalization since birth to enrollment in the study; the average number of hospitalizations during that time period was 2.3 and average length of stay was 4.5 days. The most common reasons for hospitalization were seizures, lower respiratory infections, and surgery. The most common reasons for surgery were myringotomy, strabismus surgery, tonsillectomy or adenoidectomy, and gastrostomy tube insertion/fundoplication. Anticonvulsants, gastroesophageal reflux disease, sleep, and behavioral medications were the most commonly prescribed drugs. STU was high among individuals with AS.

CONCLUSIONS

This study shows that individuals with AS have high HRU/STU, and apart from a few differences, HRU/STU was similar across molecular etiology. These results reflect usage in younger individuals and studies that describe HRU/STU in older individuals are needed.

摘要

背景

本研究旨在描述安格曼综合征(AS)患者的医疗资源利用(HRU)和支持性治疗利用(STU)情况,并按分子病因学进行比较。

方法

参与者分为缺失型和非缺失型基因型。采用独立样本 t 检验评估统计学差异。

结果

共有 302 名参与者的数据可用。参与者的平均年龄为 5.5 岁,92%的参与者年龄小于 13 岁,71%的参与者存在缺失病因。大约 68%的参与者自出生以来至参加研究期间至少有一次住院治疗;在此期间,平均住院次数为 2.3 次,平均住院时间为 4.5 天。住院的最常见原因是癫痫发作、下呼吸道感染和手术。手术最常见的原因是鼓膜切开术、斜视手术、扁桃体切除术或腺样体切除术以及胃造口管插入/胃底折叠术。抗癫痫药、胃食管反流病、睡眠和行为药物是最常开的药物。AS 患者的 STU 很高。

结论

本研究表明,AS 患者的 HRU/STU 较高,除了少数差异外,HRU/STU 与分子病因学相似。这些结果反映了年轻患者的使用情况,需要对年龄较大的患者进行 HRU/STU 描述研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b21/6625091/4a2e67933e35/MGG3-7-e00734-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b21/6625091/4a2e67933e35/MGG3-7-e00734-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b21/6625091/4a2e67933e35/MGG3-7-e00734-g001.jpg

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Orphanet J Rare Dis. 2017 Oct 16;12(1):164. doi: 10.1186/s13023-017-0716-z.
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