Neurological Counterparts of Hyponatremia: Pathological Mechanisms and Clinical Manifestations

被引:0
作者
Manuel Alfredo Podestà
Irene Faravelli
David Cucchiari
Francesco Reggiani
Silvia Oldani
Carlo Fedeli
Giorgio Graziani
机构
[1] Humanitas Clinical and Research Center,Nephrology and Dialysis Unit
[2] University of Milan,Department of Pathophysiology and Transplantation (DEPT), Dino Ferrari Centre, Neuroscience Section
[3] Neurology Unit,Emergency Department
[4] IRCCS Foundation Ca’Granda Ospedale Maggiore Policlinico,undefined
[5] Humanitas Clinical and Research Center,undefined
[6] Istituto Clinico Humanitas IRCCS,undefined
来源
Current Neurology and Neuroscience Reports | 2015年 / 15卷
关键词
Hyponatremia; Osmotic demyelination syndrome; Central nervous system; Pathogenesis; Therapy;
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摘要
Hyponatremia, defined as a serum sodium concentration <135 mEq/L, represents the most frequent electrolyte disorder in older hospitalized patients. Early recognition of hyponatremia is mandatory, since it represents an independent risk factor that increases hospital mortality by 40 %. Delayed correction of hyponatremia may worsen brain edema, resulting in different degrees of neural damage. However, an overly rapid correction of serum sodium levels can lead to osmotic demyelination syndrome (ODS), a dreadful neurological picture. In recent years, hyponatremia and ODS have received growing attention both in terms of clinical management and pathophysiology, leading to the discovery of new drugs and treatment algorithms. In this review, we recapitulate the pathogenetic background, clinical manifestations, and treatment guidelines of hyponatremia, focusing on the neurological alterations. Neurological symptoms may be neglected when they manifest as early signs of mild hyponatremia, while brain damage can irremediably affect patients’ conditions in the context of ODS.
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