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Adjunctive Dexamethasone for Tuberculous Meningitis in HIV-Positive Adults

Authors:
Joseph Donovan, Nguyen D. Bang, Darma Imran, Ho D.T. Nghia, Erlina Burhan, Dau T.T. Huong, Nguyen T.T. Hiep, Lam H.B. Ngoc, Dang V. Thanh, Nguyen T. Thanh, Anna L.S. Wardhani, Kartika Maharani et al

Abstract

The ACT HIV trial was a double-blind, randomized, placebo-controlled study evaluating adjunctive dexamethasone in 520 HIV-positive adults with tuberculous meningitis across Vietnam and Indonesia. Participants received a 6–8-week tapering course of intravenous and oral dexamethasone or placebo alongside standard 12-month antituberculosis chemotherapy and antiretroviral therapy (ART). At 12-month follow-up, death occurred in 44.1% (dexamethasone) vs. 49.0% (placebo) (HR = 0.85; 95% CI: 0.66–1.10; P = 0.22)no, statistically significant survival benefit. Secondary outcomes (neurologic disability, IRIS, AIDS-defining events, open-label steroid use, serious adverse events) also showed no difference. Serious neurologic adverse events were fewer in the dexamethasone group, but overall serious adverse event rates were similar (~74%). Subgroup analyses (disease severity, CSF diagnosis, ART status, CD4 count) failed to identify a clearly benefiting population. Authors conclude that routine adjunctive dexamethasone offers no survival or secondary benefit in HIV-associated tuberculous meningitis

Keywords: ACT HIV trial tuberculous meningitis HIV coinfection dexamethasone adjunctive corticosteroids randomized controlled trial neuroinflammation CD4 count ART initiation immune reconstitution
DOI: https://doi.ms/10.00420/ms/6278/FJDRJ/NSN | Volume: 389 | Issue: 15 | Views: 0
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