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Sodium-Thiosulfate Induced Life-Threatening Metabolic Acidosis Limiting Treatment of Calciphylaxis
1Department of Internal Medicine, SUNY Upstate Medical University, Syracuse, NY, USA.
Insights
Calcific uremic arteriolopathy (CUA) treatment is limited by severe metabolic acidosis from sodium thiosulfate (STS). This rare condition has high mortality, necessitating research into safer therapeutic approaches.
Area of Science:
- Nephrology
- Dermatology
- Vascular Medicine
Background:
- Calcific uremic arteriolopathy (CUA) is a rare, painful skin disorder in hemodialysis patients caused by calcium dysregulation, leading to vascular stenosis and thrombosis.
- CUA presents with non-healing wounds, sepsis risk, and high mortality, with limited effective therapies.
- Prevalence is approximately 4% in hemodialysis patients, often associated with end-stage renal disease.
Observation:
- A case report details a 53-year-old male with end-stage renal disease on hemodialysis and warfarin, presenting with non-healing leg cellulitis.
- Skin biopsy confirmed CUA; conventional treatments (calcitriol, cinacalcet) failed.
- Intravenous sodium thiosulfate (STS) was initiated, leading to life-threatening metabolic acidosis and subsequent death within 12 weeks.
Findings:
- Sodium thiosulfate (STS) therapy for CUA, while potentially useful, is frequently complicated by high anion gap metabolic acidosis.
- The patient developed severe acidosis requiring bicarbonate, highlighting a critical treatment limitation.
- CUA carries an 80% mortality rate within 6 months, with metabolic acidosis as a major adverse effect.
Implications:
- Current CUA treatment options are limited, particularly regarding the safe use of sodium thiosulfate due to acidosis risk.
- Further research is crucial to establish optimal dosing and frequency of STS to mitigate adverse effects.
- Developing safer and more effective therapies for CUA is essential given its high mortality and severe patient impact.
Abstract:
BACKGROUND Calcific uremic arteriolopathy (CUA) is a rare and incredibly painful cutaneous disorder secondary to microvascular involvement in which calcium dysregulation leads to stenosis of medium sized arterial blood vessels along with endothelial dysregulation and thrombosis. Ultimately, these patients are at high risk for non-healing wounds with risk of death from sepsis and multi-organ failure. It is a poorly understood condition with limited therapies that do not offer mortality benefit. Prevalence is about 4% in hemodialysis patients. Sodium thiosulfate (STS) can be used in hemodialysis patients but therapy is often limited by the development of high anion gap metabolic acidosis. CASE REPORT A 53-year-old male who had end stage renal disease and who was on hemodialysis and taking warfarin for bio-prosthetic mitral valve replacement and atrial fibrillation presented with non-healing right lower extremity cellulitis which had failed outpatient treatment. A skin biopsy of the lesion was consistent with CUA. The patient failed to improve on calcitriol and cinacalcet and was started on intravenous STS. Subsequently, he developed life threatening metabolic acidosis requiring a bicarbonate drip. He died 12 weeks after his initial diagnosis of CUA. CONCLUSIONS This article seeks to describe how the treatment of CUA; a rare disease with high mortality, is limited by the development of metabolic acidosis when using STS therapy. There is an 80% mortality rate within 6 months from CUA with major adverse effect of a high anion gap metabolic acidosis. Further research is needed in the field of establishing optimal dosing and frequency.
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