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1901. Safety, Tolerability, and Efficacy of Fluoxetine as an Antiviral for Enterovirus D68 Associated Acute Flaccid Myelitis: A Retrospective Multicenter Cohort Study

BACKGROUND: Most patients with enterovirus (EV) D68-associated acute flaccid myelitis (AFM) have long-term disability. No effective therapies have been identified. Fluoxetine is the only FDA-approved medication with in vitro antiviral activity against EV-D68. This study retrospectively analyzed the...

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Detalles Bibliográficos
Autores principales: Messacar, Kevin, Sillau, Stefan, Hopkins, Sarah, Otten, Catherine, Wilson-Murphy, Molly, Wong, Brian, Santoro, Jonathan, Treister, Andrew, Tokhie, Harlori, Torres, Alcy, Zabrocki, Luke, Glanternik, Julia, Hurst, Amanda L, Martin, Jan, Schreiner, Teri, Makhani, Naila, DeBiasi, Roberta, Kruer, Michael, Tremoulet, Adriana H, Haren, Keith Van, Desai, Jay, Benson, Leslie, Gorman, Mark, Abzug, Mark, Tyler, Kenneth, Dominguez, Samuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254028/
http://dx.doi.org/10.1093/ofid/ofy210.1557
Descripción
Sumario:BACKGROUND: Most patients with enterovirus (EV) D68-associated acute flaccid myelitis (AFM) have long-term disability. No effective therapies have been identified. Fluoxetine is the only FDA-approved medication with in vitro antiviral activity against EV-D68. This study retrospectively analyzed the safety, tolerability, and efficacy of fluoxetine for EV-D68-associated AFM. METHODS: A multicenter cohort study of US children with AFM in 2015–2016 compared serious adverse events (SAEs), adverse effects, and outcomes between fluoxetine-treated patients and untreated controls with AFM. Fluoxetine was administered at the discretion of treating providers with data gathered retrospectively. The primary outcome was summative limb strength score (SLSS; sum of Medical Research Council strength in all four limbs). RESULTS: 56 patients with AFM from 12 centers met study criteria (Figure 1). Among 30 patients exposed to fluoxetine, no SAEs were reported and adverse effects were similar to controls (P = 0.16). The 28 patients treated with >1 dose of fluoxetine were more likely to have EV-D68 identified (57.1% vs. 14.3%, P = 0.001). Fluoxetine-treated patients had similar strength on initial examination compared with untreated controls (mean SLSS 12.9 vs. 14.3, P = 0.313), but more severe paralysis at nadir (mean SLSS 9.25 vs. 12.82, P = 0.023) and latest follow-up (mean SLSS 12.5 vs. 16.4, P = 0.005) (Figure 2). In propensity-adjusted analysis, SLSS from initial examination to latest follow-up decreased by 0.2 (95% CI: −1.8 to +1.4) in fluoxetine-treated patients and increased by 2.5 (95% CI: +0.7 to +4.4) in controls (P = 0.015). [Image: see text] [Image: see text] CONCLUSION: Fluoxetine was safely administered and relatively well-tolerated. Patients with AFM treated with fluoxetine were more likely to have EV-D68-associated disease and had more severe paralysis at nadir and poorer long-term outcomes. These data do not suggest a positive efficacy signal for fluoxetine as a potential antiviral therapy for AFM. DISCLOSURES: All authors: No reported disclosures.