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低钾性麻痹的临床特征和恢复模式。

Clinical features and recovery pattern of secondary hypokalaemic paralysis.

机构信息

Department of Neurology, Chiba Rosai Hospital, 2-16 Tatsumidai-Higashi, Ichihara-shi, Chiba, 290-0003, Japan.

Department of Neurology, Graduate School of Medicine, Chiba University, Chiba, Japan.

出版信息

J Neurol. 2023 Nov;270(11):5571-5577. doi: 10.1007/s00415-023-11923-8. Epub 2023 Aug 4.

Abstract

PURPOSE

Information regarding frequency, details of neurological signs and recovery patterns of patients with secondary hypokalaemic paralysis (HP) is limited. This study aimed to analyse the frequency, aetiology, clinical features and recovery patterns of patients with secondary HP.

METHODS

The clinical and laboratory records of 18 consecutive patients with secondary HP aged ≥ 18 years admitted to our hospital between April 2011 and March 2022 were reviewed. Patients with inherited hypokalaemic periodic paralysis were excluded.

RESULTS

Of the 18 patients, 16 had a common aetiology: chronic alcoholism, diarrhoea or an imbalanced diet. Initial symptoms, such as fatigue, were often atypical. Three patients had prominent asymmetric limb weakness and four had predominant upper limb weakness. On admission, the mean serum potassium and creatine kinase (CK) levels of the patients were 1.90 mmol/L and 4488 U/mL, respectively. Ten patients (56%) had decreased potassium levels after admission, despite potassium replacement treatment (rebound hypokalaemia). Twelve patients presented with increased CK levels even after 2-5 days (delayed hyperCKaemia). Low serum magnesium levels significantly correlated with rebound hypokalaemia.

CONCLUSIONS

Secondary HP can be caused by a variety of conditions, but mainly occurs due to lifestyle conditions/disorders. Secondary HP often presents with atypical symptoms, and the initial symptoms can be non-specific. Rebound hypokalaemia and delayed hyperCKaemia are common in secondary HP, despite potassium replacement. As such, careful serial monitoring is needed for patients with secondary HP.

摘要

目的

有关继发低钾性瘫痪(HP)患者的频率、神经体征细节和恢复模式的信息有限。本研究旨在分析继发 HP 患者的频率、病因、临床特征和恢复模式。

方法

回顾 2011 年 4 月至 2022 年 3 月期间我院收治的 18 例连续继发 HP 患者的临床和实验室记录,排除遗传性低钾性周期性瘫痪患者。

结果

18 例患者中,16 例有共同病因:慢性酒精中毒、腹泻或饮食失衡。初始症状常不典型,如疲劳。3 例患者有明显的不对称性肢体无力,4 例患者有明显的上肢无力。入院时,患者的平均血清钾和肌酸激酶(CK)水平分别为 1.90mmol/L 和 4488U/mL。尽管进行了补钾治疗(反弹性低钾血症),仍有 10 例(56%)患者在入院后血钾水平下降。即使在 2-5 天后(迟发性高 CK 血症),仍有 12 例患者 CK 水平升高。低血清镁水平与反弹性低钾血症显著相关。

结论

继发 HP 可由多种情况引起,但主要由生活方式紊乱引起。继发 HP 常表现为不典型症状,初始症状可能不具特异性。尽管进行了补钾治疗,但继发 HP 中常出现反弹性低钾血症和迟发性高 CK 血症。因此,需要对继发 HP 患者进行仔细的连续监测。

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