接种 COVID-19 疫苗后治疗危重格林-巴利综合征病例的经验

IF 1.7 4区 医学 Q3 DEVELOPMENTAL BIOLOGY
Chunying Zhu, Huan Wang, Yingfu Zhang, Wentao Wang, Jia Wang, Wei Li
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引用次数: 0

摘要

背景 本研究报告了一例有神经乳头炎病史的病例。在接种 COVID-19 疫苗 2 个月内,患者出现急性腹泻、进行性肌无力、突发性呼吸和心脏症状,随后出现危重的格林-巴利综合征(GBS)。接着,我们进行了六个周期的人免疫球蛋白治疗(剂量为 400 毫克/千克-天,连续静脉注射 5 天)和三次血浆置换(PE,30 毫升/千克),然后使用甲基强的松龙琥珀酸钠。结果患者的意识恢复正常,可以进行正常交流。肌力逐渐恢复,但仍无法独立站立。结论对于曾患根管炎的患者,接种 COVID-19 疫苗可能会增加对 GBS 的易感性。因此,建议延长这些患者的疫苗接种间隔,并确保持续评估任何可能增加的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Experience of treatment in critical Guillain-Barre Syndrome case after COVID-19 vaccination

Experience of treatment in critical Guillain-Barre Syndrome case after COVID-19 vaccination

Experience of treatment in critical Guillain-Barre Syndrome case after COVID-19 vaccination

Background

The current study reported a case with a history of neuroradiculitis. Within 2 months of the COVID-19 vaccine, critical Guillain-Barre Syndrome (GBS) appeared after acute diarrhea, progressive myasthenia, and sudden respiratory and cardiac symptoms.

Methods

The syndrome was addressed with measures, such as endotracheal intubation and cardiopulmonary resuscitation vasoactive drugs. Next, we conducted six cycles of human immunoglobulin treatment (dose of 400 mg/kg·d intravenously for 5 days consecutively) and three times plasma exchange (PE, 30 ml/kg), followed by methylprednisolone sodium succinate. Rehabilitation training was carried out continuously.

Results

The consciousness of the patient returned to normal, wherein he carried out normal communication. The muscle strength recovered gradually but still could not stand independently. Presently, he is recovering at home.

Conclusions

For patients with previous radiculitis, COVID-19 vaccination may increase the susceptibility to GBS. Thus, it is recommended to extend the vaccination interval for these patients and ensure that any potential increased risk is continually assessed.

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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
78
审稿时长
6-12 weeks
期刊介绍: International Journal of Developmental Neuroscience publishes original research articles and critical review papers on all fundamental and clinical aspects of nervous system development, renewal and regeneration, as well as on the effects of genetic and environmental perturbations of brain development and homeostasis leading to neurodevelopmental disorders and neurological conditions. Studies describing the involvement of stem cells in nervous system maintenance and disease (including brain tumours), stem cell-based approaches for the investigation of neurodegenerative diseases, roles of neuroinflammation in development and disease, and neuroevolution are also encouraged. Investigations using molecular, cellular, physiological, genetic and epigenetic approaches in model systems ranging from simple invertebrates to human iPSC-based 2D and 3D models are encouraged, as are studies using experimental models that provide behavioural or evolutionary insights. The journal also publishes Special Issues dealing with topics at the cutting edge of research edited by Guest Editors appointed by the Editor in Chief. A major aim of the journal is to facilitate the transfer of fundamental studies of nervous system development, maintenance, and disease to clinical applications. The journal thus intends to disseminate valuable information for both biologists and physicians. International Journal of Developmental Neuroscience is owned and supported by The International Society for Developmental Neuroscience (ISDN), an organization of scientists interested in advancing developmental neuroscience research in the broadest sense.
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