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Published on: January 21, 2020
Plasmapheresis-induced hypercalcaemia
Anas-Alwogud Abdelmogheth1, Islam El-Baroudy, Saif Al-Yaaruby
1Department of Child Health, Sultan Qaboos University Hospital, Muscat, Oman.
This case study reports hypercalcaemia, a rare complication, in a child treated for Guillain-Barré syndrome (GBS) using plasmapheresis. The study highlights the need for monitoring calcium levels during GBS treatment.
Area of Science:
- Neurology
- Pediatrics
- Nephrology
Background:
- Guillain-Barré syndrome (GBS) is an acute inflammatory polyradiculoneuropathy potentially leading to severe motor paralysis.
- Hypercalcaemia is an uncommon complication in GBS patients.
- Plasmapheresis is a standard treatment for ventilated GBS patients, involving extracorporeal blood purification.
Purpose of the Study:
- To report a rare case of hypercalcaemia associated with plasmapheresis in a pediatric patient with GBS.
- To investigate the potential link between plasmapheresis and hypercalcaemia in the absence of other underlying causes.
Main Methods:
- Case report of an 8-year-old child with GBS symptoms including neurological deficits.
- Treatment involved intravenous immunoglobulin and plasmapheresis.
- Laboratory monitoring for electrolyte imbalances, specifically calcium levels.
Main Results:
- The patient experienced favorable outcomes following treatment with intravenous immunoglobulin and plasmapheresis.
- A laboratory observation revealed hypercalcaemia during plasmapheresis therapy.
- No underlying cause for hypercalcaemia was identified, suggesting a potential association with the treatment.
Conclusions:
- Hypercalcaemia can occur in pediatric GBS patients treated with plasmapheresis, even without an apparent underlying etiology.
- This case underscores the importance of vigilant laboratory monitoring for hypercalcaemia in GBS patients undergoing plasmapheresis.
- Further research and data collection are needed to understand and confirm this association and explore potential mechanisms.
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