Dapsone-Trimethoprim for Pneumocystis carinii Pneumonia in the Acquired Immunodeficiency Syndrome

  1. GIFFORD S. LEOUNG, M.D.;
  2. JOHN MILLS, M.D.;
  3. PHILIP C. HOPEWELL, M.D.;
  4. WALTER HUGHES, M.D.; and
  5. CONSTANCE WOFSY, M.D.
  1. San Francisco, California; and Memphis, Tennessee

    Abstract

    All patients with the acquired immunodeficiency syndrome and a first episode of Pneumocystis carinii pneumonia seen at the San Francisco General Hospital between November 1984 and April 1985 were evaluated for oral treatment with dapsone (100 mg/d) plus trimethoprim (20 mg/kg body weight · d). All 15 patients who met the entry criteria improved clinically and radiographically within 3 to 10 days after starting treatment. Repeat pulmonary function tests and gallium lung scans after 3 weeks of therapy also showed improvement. Although side effects occurred in 14 patients, in only 2 were they severe enough to require stopping therapy. Both of these patients had worsening skin rash, and dapsonetrimethoprim therapy was stopped after 10 days. When compared with trimethoprim-sulfamethoxazole or pentamidine used to treat P. carinii pneumonia in similar patients, oral dapsone-trimethoprim is at least as effective, seems to be better tolerated, and may have a lower frequency of serious side effects.

    Article and Author Information

    • ▸From the Medical Service, San Francisco General Hospital Medical Center, and the Department of Medicine, University of California, San Francisco, San Francisco, California; and St. Jude Children's Research Hospital, Memphis, Tennessee.

    • ▸Requests for reprints should be addressed to Philip C. Hopewell, M.D.; Chest Service, Room 5K1, San Francisco General Hospital, 1001 Potrero Avenue; San Francisco, CA 94110.

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