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1例抗信号识别颗粒免疫介导坏死性肌病的住院康复治疗及功能转归

INPATIENT REHABILITATION AND FUNCTIONAL OUTCOME OF A CASE OF ANTI-SRP IMMUNE-MEDIATED NECROTIZING MYOPATHY.

作者信息

Chen Nicole, Yamin Thein Khin, San Tay San

机构信息

From the Department of Rehabilitation Medicine, Changi General Hospital, Singapore.

出版信息

J Rehabil Med Clin Commun. 2024 Oct 17;7:40653. doi: 10.2340/jrm-cc.v7.40653. eCollection 2024.

Abstract

OBJECTIVE

Immune-mediated necrotizing myopathy associated with anti-signal recognition particle antibodies is a rare and debilitating condition characterized by significant muscle weakness and resultant disability. Although there are existing recommendations for physical therapy and exercise for patients with myositis in current literature, effective rehabilitation guidelines for such patients have not been fully established.

CASE REPORT

A 42-year-old woman presented with subacute onset proximal upper and lower limb weakness and dysphagia. She was diagnosed with anti-SRP immune-mediated necrotizing myopathy and was promptly initiated on aggressive immunosuppressive therapy. Despite this, she had significant impairment in function, including the inability to ambulate.

INTERVENTION AND OUTCOME

The patient underwent an intensive structured inpatient rehabilitation programme consisting of strength and endurance exercises combined with functional exercises and robot-assisted gait training. This resulted in major improvements in objective outcomes including Functional Independence Measure, Modified Barthel Index, 10-metre-walk test and 6-minute-walk test scores. The programme was well tolerated by the patient with no adverse events.

CONCLUSION

This case details the crucial role of a structured rehabilitation programme in the holistic management of a patient with anti-SRP immune-mediated necrotizing myopathy. It also highlights the use of robotics in gait training, resulting in successful functional outcomes for the patient.

摘要

目的

与抗信号识别颗粒抗体相关的免疫介导坏死性肌病是一种罕见且使人衰弱的疾病,其特征为严重的肌肉无力及由此导致的残疾。尽管当前文献中有针对肌炎患者的物理治疗和运动的现有建议,但此类患者的有效康复指南尚未完全确立。

病例报告

一名42岁女性出现亚急性起病的近端上下肢无力及吞咽困难。她被诊断为抗SRP免疫介导坏死性肌病,并立即开始接受积极的免疫抑制治疗。尽管如此,她仍有明显的功能障碍,包括无法行走。

干预与结果

患者接受了一项强化的结构化住院康复计划,包括力量和耐力训练、功能训练以及机器人辅助步态训练。这导致了客观结果的显著改善,包括功能独立性测量、改良巴氏指数、10米步行测试和6分钟步行测试得分。该计划患者耐受性良好,未出现不良事件。

结论

本病例详细阐述了结构化康复计划在抗SRP免疫介导坏死性肌病患者整体管理中的关键作用。它还强调了机器人技术在步态训练中的应用,为患者带来了成功的功能恢复结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5974/11497626/d9e023a1c9d1/JRMCC-7-40653-g001.jpg

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