METAANALYSIS OF PROPHYLACTIC TREATMENTS AGAINST PNEUMOCYSTIS-CARINII PNEUMONIA AND TOXOPLASMA ENCEPHALITIS IN HIV-INFECTED PATIENTS

Citation
Hc. Bucher et al., METAANALYSIS OF PROPHYLACTIC TREATMENTS AGAINST PNEUMOCYSTIS-CARINII PNEUMONIA AND TOXOPLASMA ENCEPHALITIS IN HIV-INFECTED PATIENTS, Journal of acquired immune deficiency syndromes and human retrovirology, 15(2), 1997, pp. 104-114
Citations number
37
Categorie Soggetti
Immunology,"Infectious Diseases
ISSN journal
10779450
Volume
15
Issue
2
Year of publication
1997
Pages
104 - 114
Database
ISI
SICI code
1077-9450(1997)15:2<104:MOPTAP>2.0.ZU;2-X
Abstract
In a meta-analysis, we examined the efficacy of aerosolized pentamidin e, trimethoprim-sulfamethoxazole, and dapsone or dapsone/pyrimethamine for the prevention of Pneumocystis carinii pneumonia and toxoplasma e ncephalitis in patients with HIV infection. Of 22 trials, 13 compared trimethoprim-sulfamethoxazole with aerosolized pentamidine, nine compa red dapsone alone or in combination with pyrimethamine with aerosolize d pentamidine, and eight compared trimethoprim-sulfamethoxazole with d apsone/pyrimethamine. In total, 1484 patients were treated with trimet hoprim-sulfamethoxazole, 1548 patients with dapsone/pyrimethamine or d apsone, and 1800 patients with aerosolized pentamidine. For dapsone/py rimethamine versus aerosolized pentamidine, the risk ratio for P. cari nii pneumonia was 0.90 (95% confidence interval [CI], 0.71-1.15), and for toxoplasma encephalitis it was 0.72 (95% CI, 0.54-0.97). For trime thoprim-sulfamethoxazole versus aerosolized pentamidine, the risk rati o of P. carinii pneumonia was 0.59 (95% CI, 0.45-0.76), and for toxopl asma encephalitis it was 0.78 (95% CI, 0.55-1.11). For trimethoprim-su lfamethoxazole versus dapsone/pyrimethamine, the risk ratio of P. cari nii pneumonia was 0.49 (95% CI, 0.26-0.92), and for toxoplasma encepha litis it was 1.17 (95% CI, 0.68-2.04). Although current evidence does not allow a definitive recommendation, administration of trimethoprim- sulfamethoxazole for prophylaxis of P. carinii pneumonia and toxoplasm osis in patients with HIV infection is consistent with the available d ata.