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[肌萎缩侧索硬化症的对症治疗]

[Symptomatic treatment of amyotrophic lateral sclerosis].

作者信息

Bak S, Bak L

机构信息

Odense Universiteshospital, neurologisk afdeling N.

出版信息

Ugeskr Laeger. 1994 Jul 11;156(28):4138-40.

PMID:7520644
Abstract

During a twelve year period 58 patients with motor neurone disease were admitted to the Department of Neurology, Odense University Hospital. The medical records were reviewed and different aspects of symptomatic treatment for these patients were recorded retrospectively. After the first admission 55% of the patients received out-patient treatment, while 31% had no further contact to the Department of Neurology. Forty-nine patients developed bulbar symptoms. Of these patients 41% were referred to a laryngologist, 27% were referred to a speech therapist and 10% to a nutritionist. Seven patients had a gastrostomy, while feeding tube was used by at least six patients. At the time of follow up 49 patients had died, 63% in hospital. At least 22 patients were treated with morphine in the last period of their lives. In order to improve the symptomatic treatment in motor neurone disease we suggest that these patients are treated at the neurological departments by interdisciplinary teams with particular interest in motor neurone disease.

摘要

在12年期间,58例运动神经元病患者被收治于欧登塞大学医院神经内科。回顾了病历并对这些患者对症治疗的不同方面进行了回顾性记录。首次入院后,55%的患者接受门诊治疗,而31%的患者未再与神经内科联系。49例患者出现延髓症状。在这些患者中,41%被转诊至耳鼻喉科医生处,27%被转诊至言语治疗师处,10%被转诊至营养师处。7例患者进行了胃造口术,至少6例患者使用了饲管。随访时49例患者已死亡,63%死于医院。至少22例患者在生命的最后阶段接受了吗啡治疗。为了改善运动神经元病的对症治疗,我们建议这些患者在神经内科由对运动神经元病特别感兴趣的多学科团队进行治疗。

相似文献

1
[Symptomatic treatment of amyotrophic lateral sclerosis].[肌萎缩侧索硬化症的对症治疗]
Ugeskr Laeger. 1994 Jul 11;156(28):4138-40.
2
[5-year experience with a clinic for amyotrophic lateral sclerosis].[一家肌萎缩侧索硬化症诊所的5年经验]
Tidsskr Nor Laegeforen. 1997 May 20;117(13):1892-5.
3
[Survival in amyotrophic lateral sclerosis].[肌萎缩侧索硬化症的生存情况]
Srp Arh Celok Lek. 1997 Jan-Feb;125(1-2):19-23.
4
Differentiation between primary lateral sclerosis and amyotrophic lateral sclerosis: examination of symptoms and signs at disease onset and during follow-up.原发性侧索硬化与肌萎缩侧索硬化的鉴别:疾病发作时及随访期间症状和体征的检查
Arch Neurol. 2007 Feb;64(2):232-6. doi: 10.1001/archneur.64.2.232.
5
A retrospective review of specialist palliative care involvement in motor neurone disease.对专科姑息治疗介入运动神经元病的回顾性研究。
Ir Med J. 2012 Nov-Dec;105(10):335-8.
6
Outcomes research in amyotrophic lateral sclerosis: lessons learned from the amyotrophic lateral sclerosis clinical assessment, research, and education database.肌萎缩侧索硬化症的疗效研究:从肌萎缩侧索硬化症临床评估、研究与教育数据库中汲取的经验教训。
Ann Neurol. 2009 Jan;65 Suppl 1:S24-8. doi: 10.1002/ana.21556.
7
[Amyotrophic lateral sclerosis: mechanical ventilation--or not right?].[肌萎缩侧索硬化症:机械通气——是否正确?]
Ned Tijdschr Geneeskd. 2004 Mar 13;148(11):509-13.
8
[Epidemiological and clinical aspects of amyotrophic lateral sclerosis in neurological clinic of Dakar].[达喀尔神经科诊所肌萎缩侧索硬化症的流行病学与临床特征]
Dakar Med. 2004;49(3):167-71.
9
Presentation of ALS to the otolaryngologist/head and neck surgeon: getting to the neurologist.肌萎缩侧索硬化症患者转诊至耳鼻喉科医生/头颈外科医生处:转诊至神经科医生。
Neurology. 1999;53(8 Suppl 5):S22-5; discussion S35-6.
10
[Association of amyotrophic lateral sclerosis and multiple sclerosis].肌萎缩侧索硬化症与多发性硬化症的关联
Rev Neurol (Paris). 1993;149(5):351-3.

引用本文的文献

1
Enteral tube feeding for amyotrophic lateral sclerosis/motor neuron disease.肠内管饲用于肌萎缩侧索硬化/运动神经元病。
Cochrane Database Syst Rev. 2023 Aug 10;8(8):CD004030. doi: 10.1002/14651858.CD004030.pub4.
2
Enteral tube feeding for amyotrophic lateral sclerosis/motor neuron disease.肌萎缩侧索硬化症/运动神经元病的肠内管饲喂养
Cochrane Database Syst Rev. 2011 Jan 19;2011(1):CD004030. doi: 10.1002/14651858.CD004030.pub3.