To determine the effect of methylprednisolone on respiratory failure in HIV-infected patients with presumed or confirmed pneumocystis carinii pneumonia who are stratified for presence or absence of respiratory failure at the time of randomization to the study.
HIV-infected children are randomized to receive adjunctive therapy with intravenous methylprednisolone or placebo. Treatment is administered for 10 days. Primary antipneumocystis therapy with TMP/SMX or systemic pentamidine is selected by the individual investigator and given for 21 days. Patients are stratified at the time of randomization by the presence or absence of respiratory failure.
Study Type
INTERVENTIONAL
Purpose
TREATMENT
UCSD Med Ctr / Pediatrics / Clinical Sciences
La Jolla, California, United States
Chicago Children's Memorial Hosp
Chicago, Illinois, United States
St Louis Univ School of Medicine
St Louis, Missouri, United States
Bellevue Hosp / New York Univ Med Ctr
New York, New York, United States
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Columbia Presbyterian Med Ctr
New York, New York, United States
Duke Univ Med Ctr
Durham, North Carolina, United States