A Case of Vancomycin-Induced Agranulocytosis in a Hemodialysis Patient: Successful Treatment with G-CSF.
- Author:
Byung Oh LEE
1
;
Young Ok KIM
;
Ki Jo KIM
;
Myoung Beom KOH
;
Hyun Wha CHUNG
;
Sun Ae YOON
;
Hae Kyung LEE
;
Jong Wook LEE
;
Yoon Sik CHANG
;
Byung Kee BANG
Author Information
1. Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea. cmckyo@yahoo.co.kr
- Publication Type:Case Report
- Keywords:
Agranulocytosis;
Vancomycin;
Lupus nephritis;
G-CSF
- MeSH:
Adult;
Agranulocytosis*;
Catheterization;
Catheters;
Female;
Granulocyte Colony-Stimulating Factor*;
Humans;
Kidney Failure, Chronic;
Leukocyte Count;
Lupus Nephritis;
Neutrophils;
Renal Dialysis*;
Sepsis;
Staphylococcus;
Teicoplanin;
Vancomycin
- From:Korean Journal of Nephrology
2003;22(2):237-241
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Vancomycin induced agranulocytosis is a rare but life-threatening complication. We here report a case of vancomycin induced agranulocytosis in a patient with chronic renal failure. A 36-year-old woman receiving hemodialysis via jugular cannulation developed staphylococcus sepsis. The catheter was removed and she was started on vancomycin therapy (1.0 g/week). New catheter was inserted for next hemodialysis. Second sepsis of same organism developed 12 days after initial sepsis inspite of vancomycin therapy. We removed this catheter and continued vancomycin therapy. After 19 days of vancomycin treatment, the patient developed a severe agranulocytosis with white blood cell count of 1, 600/ mm3 and the complete absence of neutrophil. Vancomycin was discontinued and teicoplanin was substituted for vancomycin therapy and G-CSF (granulocyte colony stimulating factor) therapy was begun. White blood cell count including neutropil was completely recovered after 13 days of discontinuation of vancomycin.
