Anna M. Cervantes-Arslanian
Boston University
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Publication
Featured researches published by Anna M. Cervantes-Arslanian.
Journal of Acquired Immune Deficiency Syndromes | 2017
Shibani S. Mukerji; Vikas Misra; David R. Lorenz; Anna M. Cervantes-Arslanian; Jennifer L. Lyons; Spyridon Chalkias; Alysse Wurcel; Deirdre Burke; Nagagopal Venna; Susan Morgello; Igor J. Koralnik; Dana Gabuzda
Background: Cerebrospinal fluid (CSF) viral escape is an increasingly recognized clinical event among HIV-1-infected adults. We analyzed longitudinal data and drug-resistance mutations to characterize profiles of HIV-1-infected patients on antiretroviral therapy with discordant CSF and plasma HIV-1 RNA levels. Methods: Forty-one cases of CSF escape defined as detectable CSF HIV-1 RNA when plasma levels were undetectable, or HIV-1 RNA >0.5-log higher in CSF than plasma were identified from Boston Hospitals and National NeuroAIDS Tissue Consortium (NNTC) from 2005 to 2016. Results: Estimated prevalence of CSF escape in Boston and NNTC cohorts was 6.0% and 6.8%, respectively; median age was 50, duration of HIV-1 infection 17 years, CD4 count 329 cells/mm3 and CD4 nadir 21 cells/mm3. Neurological symptoms were present in 30 cases; 4 had repeat episodes of CSF escape. Cases were classified into subtypes based plasma HIV-1 RNA levels in the preceding 24 months: high-level viremia (1000 copies/mL), low-level viremia (LLV: 51–999 copies/mL), and plasma suppression with CSF blip or escape (CSF RNA <200 or ≥200 copies/mL). High-level viremia cases reported more substance abuse, whereas LLV or plasma suppression cases were more neurosymptomatic (81% vs. 53%); 75% of repeat CSF escape cases were classified LLV. M184V/I mutations were identified in 74% of CSF samples when plasma levels were ⩽50 copies per milliliter. Conclusions: Characteristics frequently observed in CSF escape include HIV-1 infection >15 years, previous LLV, and M184V/I mutations in CSF. Classification based on preceding plasma HIV RNA levels provides a useful conceptual framework to identify causal factors and test therapeutics.
European Journal of Neurology | 2014
Elizabeth M. Sweeney; Kiran Thakur; Jennifer L. Lyons; Bryan Smith; Joshua Z. Willey; Anna M. Cervantes-Arslanian; M. K. Hickey; Ken Uchino; Diogo C. Haussen; S. Koch; Lee H. Schwamm; Mitchell S.V. Elkind; Russell T. Shinohara; Farrah J. Mateen
To our knowledge there are no studies reporting the use and short‐term outcomes of intravenous tissue plasminogen activator (IV‐TPA) for the treatment of acute ischaemic stroke (AIS) in people living with HIV.
Stroke | 2018
Mahmoud AbdelRazek; Jose Gutierrez; David Mampre; Anna M. Cervantes-Arslanian; Cora Ormseth; Diogo C. Haussen; Kiran Thakur; Jennifer L. Lyons; Bryan Smith; Owen O’Connor; Joshua Z. Willey; Farrah J. Mateen
Background and Purpose— Human immunodeficiency virus (HIV) infection has been shown to increase both ischemic and hemorrhagic stroke risks, but there are limited data on the safety and outcomes of intravenous thrombolysis with tPA (tissue-type plasminogen activator) for acute ischemic stroke in HIV-infected patients. Methods— A retrospective chart review of intravenous tPA-treated HIV patients who presented with acute stroke symptoms was performed in 7 large inner-city US academic centers (various search years between 2000 and 2017). We collected data on HIV, National Institutes of Health Stroke Scale score, ischemic stroke risk factors, opportunistic infections, intravenous drug abuse, neuroimaging findings, and modified Rankin Scale score at last follow-up. Results— We identified 33 HIV-infected patients treated with intravenous tPA (mean age, 51 years; 24 men), 10 of whom were stroke mimics. Sixteen of 33 (48%) patients had an HIV viral load less than the limit of detection while 10 of 33 (30%) had a CD4 count <200/mm3. The median National Institutes of Health Stroke Scale score at presentation was 9, and mean time from symptom onset to tPA was 144 minutes (median, 159). The median modified Rankin Scale score for the 33-patient cohort was 1 and for the 23-patient actual stroke cohort was 2, measured at a median of 90 days poststroke symptom onset. Two patients had nonfatal hemorrhagic transformation (6%; 95% confidence interval, 1%–20%), both in the actual stroke group. Two patients had varicella zoster virus vasculitis of the central nervous system, 1 had meningovascular syphilis, and 7 other patients were actively using intravenous drugs (3 cocaine, 1 heroin, and 3 unspecified), none of whom had hemorrhagic transformation. Conclusions— Most HIV-infected patients treated with intravenous tPA for presumed and actual acute ischemic stroke had no complications, and we observed no fatalities. Stroke mimics were common, and thrombolysis seems safe in this group. We found no data to suggest an increased risk of intravenous tPA-related complications because of concomitant opportunistic infections or intravenous drug abuse.
Neurosurgery Clinics of North America | 2018
Joseph D. Burns; Jennifer L. Fisher; Anna M. Cervantes-Arslanian
Primary intracerebral hemorrhage (ICH) is a common, devastating disease that lacks an effective specific treatment. Mortality is high, functional outcomes are poor, and these have not substantially changed for decades. There is, therefore, considerable opportunity for advancement in the management of ICH. In recent years, a significant amount of research has begun to address this gap. This article is aimed at updating neurologists on the most clinically relevant contemporary research.
Neurology | 2014
Ania Busza; Anna M. Cervantes-Arslanian; Carlos S. Kase
A 32-year-old right-handed woman from El Salvador was brought into the emergency department (ED) because of confusion, right-sided numbness, and word-finding difficulties.
Neurocritical Care | 2016
Joseph D. Burns; Rima S. Rindler; Christopher Carr; Helena Lau; Anna M. Cervantes-Arslanian; Deborah M. Green-LaRoche; Rony Salem; Carlos S. Kase
Stroke | 2018
Mahmoud AbdelRazek; Jose Gutierrez; David Mampre; Anna M. Cervantes-Arslanian; Cora Ormseth; Diogo C. Haussen; Kiran Thakur; Jennifer L. Lyons; Bryan Smith; Owen O’Connor; Joshua Z. Willey; Farrah J. Mateen
Neurology | 2018
Naillid Felipe; Sok Lee; Helena Lau; Ayshe Beesen; Melissa Mercado; Courtney Takahashi; Julie Shulman; Hugo Javier Aparicio; Thanh N. Nguyen; Jose R. Romero; Viken L. Babikian; David M. Greer; Anna M. Cervantes-Arslanian
Neurology | 2017
C. Frances Fan; Robert McInnis; Benjamin P. Linas; Ioana Bica; Anna M. Cervantes-Arslanian
Neurology | 2015
Deborah Green-LaRoche; Tudor Sturzoiu; Helena Lau; Anna M. Cervantes-Arslanian; Joseph D. Burns