Ciprofloxacin-Associated Hemolytic-Uremic Syndrome

Author:

Allan David S1,Thompson Cheryl M2,Barr Robert M3,Clark William F4,Chin-Yee Ian H5

Affiliation:

1. David S Allan MSc MD, Hematology Fellow, University of Western Ontario, London, Ontario, Canada

2. Cheryl M Thompson BSc Pharm, Pharmacist, London Health Sciences Centre, London, Ontario

3. Robert M Barr MD FRCPC, Division of Hematology, London Health Sciences Centre

4. William F Clark MD FRCPC, Division of Nephrology, London Health Sciences Centre

5. Ian H Chin-Yee MD FRCPC, Division of Hematology, London Health Sciences Centre

Abstract

OBJECTIVE: To report the first case of ciprofloxacin-associated hemolytic-uremic syndrome (HUS). CASE SUMMARY: A 53-year-old white man was treated with chemotherapy for acute lymphoblastic leukemia. Four weeks after initiation of treatment, he recovered his blood cell counts, but developed fever and was prescribed oral ciprofloxacin 500 mg twice daily. After 4 doses, he developed the typical features of HUS manifested by microangiopathic hemolytic anemia, oliguric renal failure, and thrombocytopenia. The medication was withdrawn, and he received 5 sessions of plasma exchange. He recovered completely and has normal renal function. DISCUSSION: Secondary HUS or its related syndrome, thrombotic thrombocytopenic purpura (TTP), is uncommon, but has been reported in association with cancer, chemotherapy, and a variety of medications. Our case represents a possible adverse drug reaction to ciprofloxacin according to the Naranjo probability scale. It is the first reported case of HUS associated with ciprofloxacin. CONCLUSIONS: Ciprofloxacin use was followed by HUS in our patient and was possibly causally related. Early detection, discontinuation of the offending medication, and treatment of HUS/TTP is critical.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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