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LETTER

Comparison of Oral Agents for Treatment of Pneumocystis carinii Pneumonia

right arrow Mark A. Perazella, MD

1 March 1997 | Volume 126 Issue 5 | Page 407


TO THE EDITOR:

Safrin and colleagues [1] provide a useful comparison of the efficacy and tolerability of three oral antibiotic regimens (trimethoprim-sulfamethoxazole, dapsone-trimethoprim, and clindamycin-primaquine) used to treat Pneumocystis carinii pneumonia in patients with the acquired immunodeficiency syndrome (AIDS). Rash, nausea and vomiting, myelosuppression, and hepatotoxicity accounted for most of the toxic reactions associated with these regimens. Surprisingly, hyperkalemia occurred in only one of their patients, who was treated with either trimethoprim-sulfamethoxazole or dapsone-trimethoprim. This lack of hyperkalemia makes the results of this study clearly different from the results of previous studies done in patients with AIDS who received trimethoprim-containing regimens [2, 3]; in these studies, hyperkalemia developed in 20% to 53% of patients.

In the study by Safrin and colleagues, the absence of hyperkalemia in patients treated with a trimethoprim-containing regimen may be related to the dosage of trimethoprim used. Trimethoprim was prescribed at a lower dose (10 to 20 mg/kg of body weight per day) than was used in other studies (20 mg/kg per day) [2, 3]. However, because one study showed that standard-dose trimethoprim-sulfamethoxazole (320 mg/d) was associated with hyperkalemia in 62.5% of hospitalized patients who did not have AIDS [4], it is unlikely that the lower dose completely explains the absence of hyperkalemia. Alternatively, the patients in the study by Safrin and colleagues [1] may have had significantly lower serum potassium concentrations at baseline. It is possible that these concentrations increased significantly with trimethoprim relative to baseline but did not reach a level consistent with hyperkalemia. Therefore, it would be of interest to know 1) the baseline and follow-up serum or plasma potassium concentrations in these patients and 2) the potassium concentration that was used to define hyperkalemia.


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Yale University School of Medicine, New Haven, CT 06520


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1. Safrin S, Finkelstein DM, Feinberg J, Frame P, Simpson G, Wu A, et al. Comparison of three regimens for treatment of mild to moderate Pneumocystis carinii pneumonia in patients with AIDS. A double-blind, randomized trial of oral trimethoprim-sulfamethoxazole, dapsone-trimethoprim, and clindamycin-primaquine. Ann Intern Med. 1996; 124:792-802.

2. Medina I, Mills J, Leoung G, Hopewell PC, Lee B, Modin G, et al. Oral therapy for Pneumocystis carinii pneumonia in the acquired immunodeficiency syndrome. A controlled trial of trimethoprim-sulfamethoxazole versus trimethoprim-dapsone. N Engl J Med. 1990; 323:776-82.

3. Velazquez H, Perazella MA, Wright FS, Ellison DH. Renal mechanism of trimethoprim-induced hyperkalemia. Ann Intern Med. 1993; 119:296-301.

4. Alappan R, Perazella MA, Buller GK. Hyperkalemia in hospitalized patients treated with trimethoprim-sulfamethoxazole. Ann Intern Med. 1996; 124:316-20.

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