Acute Hypocalcemia and Metabolic Alkalosis in Children on Cation-Exchange Resin Therapy
Background. Sodium polystyrene sulfonate (SPS) is a chelating agent used for the treatment of hyperkalemia. SPS has a wide range of exchange capacity requiring close monitoring of serum electrolytes. We observed two patients who developed acute hypocalcemia and increased metabolic alkalosis after in...
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Series: | Case Reports in Nephrology |
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doaj-176983a4008143a69ec6e3dc6d957e642020-11-24T23:23:09ZengHindawi LimitedCase Reports in Nephrology2090-66412090-665X2017-01-01201710.1155/2017/65826136582613Acute Hypocalcemia and Metabolic Alkalosis in Children on Cation-Exchange Resin TherapyAadil Kakajiwala0Kevin T. Barton1Elisha Rampolla2Christine Breen3Madhura Pradhan4Division of Pediatric Nephrology, Washington University in St. Louis School of Medicine, St. Louis, MO, USADivision of Pediatric Nephrology, Washington University in St. Louis School of Medicine, St. Louis, MO, USADivisions of Nephrology, The Children’s Hospital of Philadelphia, Philadelphia, PA, USADivisions of Nephrology, The Children’s Hospital of Philadelphia, Philadelphia, PA, USADivisions of Nephrology, The Children’s Hospital of Philadelphia, Philadelphia, PA, USABackground. Sodium polystyrene sulfonate (SPS) is a chelating agent used for the treatment of hyperkalemia. SPS has a wide range of exchange capacity requiring close monitoring of serum electrolytes. We observed two patients who developed acute hypocalcemia and increased metabolic alkalosis after initiating SPS therapy. We report these cases to draw attention to the potential risk of this medication in pediatric patients. Case Diagnosis/Treatment. Two children with chronic kidney disease on dialysis were started on SPS for hyperkalemia. Within a week after initiation of the medication, both patients developed hypocalcemia on routine labs without overt clinical manifestations. The hypocalcemia was rapidly corrected with oral supplementation and discontinuation of SPS. Conclusions. Severe hypocalcemia can develop after SPS therapy. The metabolic alkalosis in these patients associated with the hypocalcemia put them at increased risk for complications. Hence, careful attention must be paid to the state of calcium metabolism in all patients receiving SPS. Often calcium supplementation is required to maintain normal calcium levels.http://dx.doi.org/10.1155/2017/6582613 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Aadil Kakajiwala Kevin T. Barton Elisha Rampolla Christine Breen Madhura Pradhan |
spellingShingle |
Aadil Kakajiwala Kevin T. Barton Elisha Rampolla Christine Breen Madhura Pradhan Acute Hypocalcemia and Metabolic Alkalosis in Children on Cation-Exchange Resin Therapy Case Reports in Nephrology |
author_facet |
Aadil Kakajiwala Kevin T. Barton Elisha Rampolla Christine Breen Madhura Pradhan |
author_sort |
Aadil Kakajiwala |
title |
Acute Hypocalcemia and Metabolic Alkalosis in Children on Cation-Exchange Resin Therapy |
title_short |
Acute Hypocalcemia and Metabolic Alkalosis in Children on Cation-Exchange Resin Therapy |
title_full |
Acute Hypocalcemia and Metabolic Alkalosis in Children on Cation-Exchange Resin Therapy |
title_fullStr |
Acute Hypocalcemia and Metabolic Alkalosis in Children on Cation-Exchange Resin Therapy |
title_full_unstemmed |
Acute Hypocalcemia and Metabolic Alkalosis in Children on Cation-Exchange Resin Therapy |
title_sort |
acute hypocalcemia and metabolic alkalosis in children on cation-exchange resin therapy |
publisher |
Hindawi Limited |
series |
Case Reports in Nephrology |
issn |
2090-6641 2090-665X |
publishDate |
2017-01-01 |
description |
Background. Sodium polystyrene sulfonate (SPS) is a chelating agent used for the treatment of hyperkalemia. SPS has a wide range of exchange capacity requiring close monitoring of serum electrolytes. We observed two patients who developed acute hypocalcemia and increased metabolic alkalosis after initiating SPS therapy. We report these cases to draw attention to the potential risk of this medication in pediatric patients. Case Diagnosis/Treatment. Two children with chronic kidney disease on dialysis were started on SPS for hyperkalemia. Within a week after initiation of the medication, both patients developed hypocalcemia on routine labs without overt clinical manifestations. The hypocalcemia was rapidly corrected with oral supplementation and discontinuation of SPS. Conclusions. Severe hypocalcemia can develop after SPS therapy. The metabolic alkalosis in these patients associated with the hypocalcemia put them at increased risk for complications. Hence, careful attention must be paid to the state of calcium metabolism in all patients receiving SPS. Often calcium supplementation is required to maintain normal calcium levels. |
url |
http://dx.doi.org/10.1155/2017/6582613 |
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