Severe Neutropenia Associated with Sustained-Release Procainamide
- A. GRAY ELLRODT, M.D.;
- GLEN H. MURATA, M.D.;
- MARY S. RIEDINGER, R.N.;
- MORGAN E. STEWART, M.S.;
- CAROL MOCHIZUKI, Pharm.D.; and
- RICHARD GRAY, M.D.
Abstract
Neutropenia is a rare complication of procainamide therapy. However, over a period of 20 months, 8 patients developed severe neutropenia while taking a sustained-release preparation of the drug. Seven patients presented with fever and constitutional symptoms and one patient was asymptomatic. Bone marrow examinations showed myeloid aplasia or maturation arrest in 5 patients and myeloid hyperplasia in 1. Neutropenia resolved within 30 days of drug withdrawal, and all patients survived. A case-control study showed a significant association between sustained-release procainamide therapy and severe neutropenia in 5 of 114 patients (4.4%) recovering from open-heart surgery (Mantel-Haenszel chi square = 13.84; p < 0.001). Thus, life-threatening neutropenia may be common with sustained-release procainamide preparations.
Article and Author Information
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▸From the Department of Medicine, Cedars-Sinai Medical Center, UCLA School of Medicine; Los Angeles, California.
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▸Requests for reprints should be addressed to A. Gray Ellrodt, M.D.; Department of Medicine, Cedars-Sinai Medical Center, 8700 Beverly Boulevard; Los Angeles, CA 90048.
- © 1984 American College of Physicians
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