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重症肌无力危象中的自主神经功能障碍谱

The Spectrum of Autonomic Dysfunction in Myasthenic Crisis.

作者信息

Benjamin Rohit Ninan, Aaron Sanjith, Sivadasan Ajith, Devasahayam Suresh, Sebastin Amalan, Alexander Mathew

机构信息

Department of Neurology, Christian Medical College, Vellore, Tamil Nadu, India.

Department of Bioengineering, Christian Medical College, Vellore, Tamil Nadu, India.

出版信息

Ann Indian Acad Neurol. 2018 Jan-Mar;21(1):42-48. doi: 10.4103/aian.AIAN_270_17.

Abstract

BACKGROUND

Autoimmune autonomic dysfunction is described in Myasthenia Gravis. In myasthenic crisis, the spectrum of autonomic dysfunction is hitherto uncharacterized.

OBJECTIVE

The objective of this study is to describe the spectrum of autonomic dysfunction in myasthenic crises using the composite autonomic symptom scale 31 (COMPASS 31) autonomic symptom questionnaire and power spectral analysis of heart rate variability (HRV), which is a simple way of estimating general autonomic dysfunction.

METHODS

Adult patients with myasthenic crisis from January 1, 2014 to March 15, 2015, were prospectively included in this study. The COMPASS 31 questionnaire for symptoms of autonomic dysfunction and power spectral analysis of HRV were assessed. These were compared with the patient's demographic and clinical parameters and with previous literature. IRB approval was obtained.

RESULTS

Sixteen patients were included (M:F 3:1). 15/16 patents (93%) had autonomic dysfunction on COMPASS 31 questionnaire. The domains of involvement were gastrointestinal (80%), orthostatic (67.7%), pupillomotor (67.7%); sudomotor (33.3%), and vasomotor (13.3%). Parasympathetic dysfunction predominance was suggested by the symptom profile. HRV analysis showed a low frequency (LF) spectral shift suggesting slowed parasympathetic responsiveness (LF normalized unit (nu): high frequency [HF] nu mean 8.35, standard deviation ± 5.4, 95% confidence interval 2.2-12.5), which significantly exceeded the mean LF nu: HF nu ratios of the majority of previously reported noncrises myasthenic populations.

CONCLUSIONS

Myasthenic crisis has autonomic dysfunction involving multiple organ systems. Increased latency of parasympathetic reflexes is suggested. A comprehensive management protocol addressing different autonomic domains is required for holistic patient care.

摘要

背景

重症肌无力中存在自身免疫性自主神经功能障碍。在重症肌无力危象中,自主神经功能障碍的范围迄今尚未明确。

目的

本研究的目的是使用综合自主神经症状量表31(COMPASS 31)自主神经症状问卷和心率变异性(HRV)的功率谱分析来描述重症肌无力危象中自主神经功能障碍的范围,HRV功率谱分析是评估一般自主神经功能障碍的一种简单方法。

方法

前瞻性纳入2014年1月1日至2015年3月15日期间患有重症肌无力危象的成年患者。评估COMPASS 31自主神经功能障碍症状问卷和HRV功率谱分析。将这些结果与患者的人口统计学和临床参数以及以往文献进行比较。获得了机构审查委员会的批准。

结果

纳入16例患者(男∶女为3∶1)。16例患者中有15例(93%)在COMPASS 31问卷上存在自主神经功能障碍。受累领域包括胃肠道(80%)、直立性(67.7%)、瞳孔运动(67.7%)、泌汗(33.3%)和血管运动(13.3%)。症状特征提示以副交感神经功能障碍为主。HRV分析显示低频(LF)频谱偏移,提示副交感神经反应减慢(LF标准化单位[nu]∶高频[HF] nu平均值为8.35,标准差±5.4,95%置信区间2.2 - 12.5),这显著超过了大多数先前报道的非危象重症肌无力患者群体的平均LF nu∶HF nu比值。

结论

重症肌无力危象存在涉及多个器官系统的自主神经功能障碍。提示副交感神经反射潜伏期延长。需要一个针对不同自主神经领域的综合管理方案来进行全面的患者护理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c16/5909145/e95bee4fe54b/AIAN-21-42-g002.jpg

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