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Anaesthesia for emergency caesarean section in a patient with Gitelman syndrome
Sarath Venugopalan1, Nitu Puthenveettil1, Sunil Rajan1
1Department of Anaesthesia and Critical Care, Amrita Institute of Medical Sciences, Kochi, Kerala, India.
Abstract:
Gitelman syndrome is a rare autosomal recessive salt-losing disorder of renal tubules, which results in hypokalemic metabolic alkalosis. Associated hypomagnesaemia and hypocalcaemia are also seen. Gitelman syndrome is a variant of renal Bartter's syndrome. Anaesthetic management of these obstetric patients is challenging and requires a careful multidisciplinary approach. Close monitoring of potassium and magnesium levels and their supplementation is required to avoid complications to mother and baby.
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