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吉兰-巴雷综合征的心血管自主神经评估:一项纵向研究。

Cardiovascular Autonomic Assessment in Guillain-Barré Syndrome: A Longitudinal Study.

作者信息

Tan Cheng-Yin, Shahrizaila Nortina, Tan Hui-Ting, Goh Khean-Jin, Tan Maw-Pin

机构信息

Division of Neurology, Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

Division of Geriatric Medicine, Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

出版信息

Neurol India. 2022 Sep-Oct;70(5):1856-1859. doi: 10.4103/0028-3886.359191.

Abstract

BACKGROUND

Severe dysautonomia is typically seen during acute phase of Guillain-Barré syndrome (GBS).

OBJECTIVE

To investigate the relationship of cardiovascular autonomic dysfunction with motor recovery in GBS.

MATERIALS AND METHODS

Consecutive GBS patients presented to our hospital were recruited. Clinical assessment was evaluated with the Medical Research Council (MRC) sum score and GBS disability score (GDS). All patients had series of autonomic testing on admission and after treatment at 6 and 24 weeks. Both computation-dependent tests (heart rate variability [HRV] and baroreflex sensitivity [BRS]) and autonomic maneuvers were performed. Age- and gender-matched healthy controls (HC) were recruited. The data obtained at admission, 6 weeks and 24 weeks were compared within groups for statistical difference.

RESULTS

Six patients (4 men; mean age 39.5 ± 14.3 years) were recruited over one year. Five had GBS and one Miller Fisher syndrome. The mean MRC sum score and GDS on admission were 52.3 ± 4.3 and 3.5 ± 0.8 respectively. During admission, time-domain average RR interval (AVNN) and BRS were significantly poorer among cases compared to HC. Active standing 30:15 ratio and cold pressor test at admission were also significantly abnormal when compared with HC. All the autonomic parameters had normalized by 6 weeks and these were significant for the high frequency-HRV, BRS, and active standing 30:15 ratio. For MRC and GDS, there were significant improvements in the scoring over a period of 24 weeks.

CONCLUSIONS

Dysautonomia in GBS improved gradually and in keeping with motor and disability recovery.

摘要

背景

严重自主神经功能障碍通常在吉兰-巴雷综合征(GBS)急性期出现。

目的

研究GBS患者心血管自主神经功能障碍与运动恢复之间的关系。

材料与方法

招募我院连续收治的GBS患者。采用医学研究委员会(MRC)总分和GBS残疾评分(GDS)进行临床评估。所有患者在入院时以及治疗后6周和24周进行了一系列自主神经功能测试。同时进行了依赖计算的测试(心率变异性[HRV]和压力反射敏感性[BRS])以及自主神经动作。招募了年龄和性别匹配的健康对照(HC)。对入院时、6周和24周获得的数据进行组内比较以分析统计学差异。

结果

在一年多的时间里招募了6名患者(4名男性;平均年龄39.5±14.3岁)。其中5例为GBS,1例为米勒-费雪综合征。入院时MRC总分和GDS平均分别为52.3±4.3和3.5±0.8。入院期间,与HC相比,病例组的时域平均RR间期(AVNN)和BRS明显较差。与HC相比,入院时主动站立30:15比值和冷加压试验也明显异常。所有自主神经参数在6周时均恢复正常,高频-HRV、BRS和主动站立30:15比值尤为显著。对于MRC和GDS,在24周期间评分有显著改善。

结论

GBS中的自主神经功能障碍逐渐改善,与运动和残疾恢复一致。

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