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晚期庞贝病患者的球部肌肉损伤:来自法国庞贝病登记处的观察。

Bulbar muscle impairment in patients with late onset Pompe disease: Insight from the French Pompe registry.

机构信息

Neurology Department, Raymond Poincaré University Hospital, Assistance Publique des Hopitaux de Paris, Garches, France.

Nord-Est-Ile-de-France Neuromuscular Reference Center, Fédération Hospitalo Universitaire PHENIX, Garches, France.

出版信息

Eur J Neurol. 2024 Oct;31(10):e16428. doi: 10.1111/ene.16428. Epub 2024 Aug 7.

Abstract

BACKGROUND AND PURPOSE

Late onset Pompe disease (LOPD) is a rare neuromuscular disorder caused by a deficit in acid alpha-glucosidase. Macroglossia and swallowing disorders have already been reported, but no study has focused yet on its frequency and functional impact on patients' daily life.

METHODS

We reviewed 100 adult LOPD patients followed in 17 hospitals in France included in the French national Pompe disease registry. The Swallowing Quality of Life Questionnaire and the Sydney Swallow Questionnaire were completed by patients, and a specialist carried out a medical examination focused on swallowing and assigned a Salassa score to each patient. Respiratory and motor functions were also recorded. Subgroup analysis compared patients with and without swallowing difficulties based on Salassa score.

RESULTS

Thirty-two percent of patients presented with swallowing difficulties, often mild but sometimes severe enough to require percutaneous endoscopic gastrostomy (1%). Daily dysphagia was reported for 20% of our patients and aspirations for 18%; 9.5% were unable to eat away from home. Macroglossia was described in 18% of our patients, and 11% had lingual atrophy. Only 15% of patients presenting with swallowing disorders were followed by a speech therapist. Swallowing difficulties were significantly associated with macroglossia (p = 0.015), longer duration of illness (p = 0.032), and a lower body mass index (p = 0.047).

CONCLUSIONS

Swallowing difficulties in LOPD are common and have significant functional impact. Increased awareness by physicians of these symptoms with systematic examination of the tongue and questions about swallowing can lead to appropriate multidisciplinary care with a speech therapist and dietitian if needed.

摘要

背景与目的

晚发性庞贝病(LOPD)是一种罕见的神经肌肉疾病,由酸性α-葡萄糖苷酶缺乏引起。巨舌症和吞咽障碍已有报道,但尚无研究专门关注其在患者日常生活中的频率和功能影响。

方法

我们回顾了法国 17 家医院的 100 名成年 LOPD 患者,这些患者均被纳入法国庞贝病登记处。患者完成了吞咽生活质量问卷和悉尼吞咽问卷,一名专家进行了重点关注吞咽的医学检查,并为每位患者分配了 Salassa 评分。还记录了呼吸和运动功能。亚组分析比较了根据 Salassa 评分存在和不存在吞咽困难的患者。

结果

32%的患者存在吞咽困难,通常为轻度,但有时严重到需要进行经皮内镜胃造口术(1%)。20%的患者报告日常吞咽困难,18%的患者存在误吸;9.5%的患者无法在家以外的地方进食。18%的患者描述有巨舌症,11%的患者有舌萎缩。仅 15%存在吞咽障碍的患者接受了言语治疗师的随访。吞咽困难与巨舌症(p=0.015)、疾病持续时间更长(p=0.032)和体重指数更低(p=0.047)显著相关。

结论

LOPD 中的吞咽困难很常见,且具有显著的功能影响。医生通过系统检查舌头和询问吞咽问题,提高对这些症状的认识,可以为患者提供适当的多学科治疗,包括言语治疗师和营养师。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cd3/11414798/d77399f03ecb/ENE-31-e16428-g001.jpg

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