Current views on the diagnosis and management of hypokalaemia in children
Language English Country Norway Media print-electronic
Document type Journal Article, Review
PubMed
26972906
DOI
10.1111/apa.13398
Knihovny.cz E-resources
- Keywords
- Bartter syndrome, Children, Gitelman syndrome, Hypokalaemia, Steroidogenesis disorders,
- MeSH
- Child MeSH
- Genetic Diseases, Inborn complications MeSH
- Hypokalemia diagnosis etiology therapy MeSH
- Humans MeSH
- Disease Management MeSH
- Adrenal Cortex Diseases complications MeSH
- Check Tag
- Child MeSH
- Humans MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
UNLABELLED: Hypokalaemia is a common electrolyte disorder in children, caused by decreased potassium intake, increased gastrointestinal and urinary losses or transcellular shift. Patients with severe hypokalaemia may suffer from symptoms such as life-threatening cardiac arrhythmias. The aim of our study was to review the aetiology of hypokalaemia, suggest a diagnostic algorithm and discuss the management of patients with various aetiologies of hypokalaemia. CONCLUSION: Understanding the pathophysiology of hypokalaemic states, along with a detailed medical history, physical examination and specific laboratory tests are required for proper diagnosis and appropriate treatment.
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