Intensive care due to myasthenia gravis: Risk factors and prognosis

IF 4.5 2区 医学 Q1 CLINICAL NEUROLOGY
Chris Myllynen, Anni Tuulasvaara, Sari Atula, Sini M. Laakso
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Abstract

Background and purpose

Exacerbation of myasthenia gravis (MG) with respiratory failure requires intensive care. We aimed to study the risk factors for intensive care unit admission for MG exacerbation and myasthenic crisis (MC) and the prognosis of people with MG (pwMG) thereafter.

Methods

This retrospective study investigated patients in the Helsinki and Uusimaa hospital district during the years 2008–2021. PwMG (International Classification of Diseases, 10th revision code G70.0) were identified through a data repository search, followed by a chart review of patient records. Risk factors for intensive care due to MG exacerbation were evaluated as compared with the patients only treated in the outpatient clinic and those treated in the neurological ward for MG exacerbation. The outcomes of patients in intensive care for any reason were also compared with those of patients in intensive care for exacerbation of bronchial asthma.

Results

Of 577 pwMG, 35 (6.1%) needed intensive care for MG within a median of 5.3 months from diagnosis. The mean (±SD) age at MG diagnosis was higher in the intensive care group (60.5 [±16.1] years) compared to the outpatient (48.3 [±20.9] years; p < 0.001) and neurological ward groups (53.4 [±20.8] years; p = 0.044). Thymoma (odds ratio [OR] 4.8, 95% confidence interval [CI] 1.19–19.43; p = 0.028) and female sex (OR 2.1, 95% CI 1.02–4.48; p = 0.045) were independent risk factors for intensive care. In-hospital mortality was 4% for MC patients. Six-month mortality after intensive care for MG exacerbation (14.3%) was twice that for asthma exacerbation (7.7%).

Conclusion

Our study shows an increased risk of intensive care treatment for patients with late-onset MG, female sex or thymoma, occurring usually within 6 months from diagnosis, which emphasises the importance of early treatment choices.

Abstract Image

重症肌无力导致的重症监护:风险因素和预后。
背景和目的:重症肌无力(MG)加重并伴有呼吸衰竭需要重症监护。我们旨在研究因重症肌无力加重和肌无力危象(MC)而入住重症监护室的风险因素,以及重症肌无力患者(pwMG)此后的预后:这项回顾性研究调查了2008-2021年间赫尔辛基和乌西马院区的患者。通过数据储存库搜索确定了马铃薯肌萎缩症患者(国际疾病分类第 10 次修订代码 G70.0),随后对患者病历进行了病历审查。与仅在门诊接受治疗的患者和因 MG 病情加重而在神经科病房接受治疗的患者相比,对因 MG 病情加重而接受重症监护的风险因素进行了评估。此外,还将因任何原因接受重症监护的患者的治疗结果与因支气管哮喘加重而接受重症监护的患者的治疗结果进行了比较:结果:在 577 名慢阻肺病人中,有 35 人(6.1%)在确诊后的中位数 5.3 个月内因慢阻肺病需要接受重症监护。与门诊患者(48.3 [±20.9] 岁;P 结论:我们的研究表明,晚发型 MG、女性或胸腺瘤患者接受重症监护治疗的风险增加,通常发生在确诊后 6 个月内,这强调了早期治疗选择的重要性。
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来源期刊
European Journal of Neurology
European Journal of Neurology 医学-临床神经学
CiteScore
9.70
自引率
2.00%
发文量
418
审稿时长
1 months
期刊介绍: The European Journal of Neurology is the official journal of the European Academy of Neurology and covers all areas of clinical and basic research in neurology, including pre-clinical research of immediate translational value for new potential treatments. Emphasis is placed on major diseases of large clinical and socio-economic importance (dementia, stroke, epilepsy, headache, multiple sclerosis, movement disorders, and infectious diseases).
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