P. Mathew et Me. Conley, EFFECT OF INTRAVENOUS GAMMA-GLOBULIN (IVIG) ON THE PLATELET COUNT IN PATIENTS WITH WISKOTT-ALDRICH SYNDROME, Pediatric allergy and immunology, 6(2), 1995, pp. 91-94
The ability of IVIG to increase platelet counts in patients with idiop
athic thrombocytopenic purpura suggests its potential usefulness in ot
her disease states characterized by low platelet counts. This possibil
ity was evaluated in nine patients with the Wiskott-Aldrich syndrome (
WAS) who received IVIG, at a dose of 400 mg/kg every 4 weeks. The mean
platelet count prior to institution of IVIG was 32,000/cumm (range 2,
400 to 98,000). Following administration of IVIG, the platelet count r
anged between 5,000 and 85,000/cumm. There were no immediate increases
in platelet counts after IVIG infusion in any patient who had serial
platelet counts. During treatment, patients were not given any routine
platelet transfusions for low platelet counts. However, while on IVIG
, two patients showed a good response to platelet transfusion prior to
surgical procedures. In conclusion, chronic IVIG therapy does not app
ear to affect platelet counts in patients with the Wiskott-Aldrich syn
drome.