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September 18, 2012; 79 (12) Articles

Neurologic outcomes in retinopathy-negative cerebral malaria survivors

Douglas G. Postels, Terrie E. Taylor, Malcolm Molyneux, Kara Mannor, Peter W. Kaplan, Karl B. Seydel, Yamikani F. Chimalizeni, Kondwani Kawaza, Gretchen L. Birbeck
First published August 22, 2012, DOI: https://doi.org/10.1212/WNL.0b013e31826aacd4
Douglas G. Postels
From the International Neurologic and Psychiatric Epidemiology Program (D.G.P., G.L.B.), College of Osteopathic Medicine (T.E.T., K.B.S.), and Department of Epidemiology (K.M.), Michigan State University, East Lansing; Malawi-Liverpool-Wellcome Trust Clinical Research Programme (M.M.), College of Medicine, Blantyre, Malawi; Department of Neurology (P.W.K.), Johns Hopkins University School of Medicine, Baltimore, MD; and Blantyre Malaria Project (Y.F.C., K.K.), University of Malawi College of Medicine, Blantyre, Malawi.
MD
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Terrie E. Taylor
From the International Neurologic and Psychiatric Epidemiology Program (D.G.P., G.L.B.), College of Osteopathic Medicine (T.E.T., K.B.S.), and Department of Epidemiology (K.M.), Michigan State University, East Lansing; Malawi-Liverpool-Wellcome Trust Clinical Research Programme (M.M.), College of Medicine, Blantyre, Malawi; Department of Neurology (P.W.K.), Johns Hopkins University School of Medicine, Baltimore, MD; and Blantyre Malaria Project (Y.F.C., K.K.), University of Malawi College of Medicine, Blantyre, Malawi.
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Malcolm Molyneux
From the International Neurologic and Psychiatric Epidemiology Program (D.G.P., G.L.B.), College of Osteopathic Medicine (T.E.T., K.B.S.), and Department of Epidemiology (K.M.), Michigan State University, East Lansing; Malawi-Liverpool-Wellcome Trust Clinical Research Programme (M.M.), College of Medicine, Blantyre, Malawi; Department of Neurology (P.W.K.), Johns Hopkins University School of Medicine, Baltimore, MD; and Blantyre Malaria Project (Y.F.C., K.K.), University of Malawi College of Medicine, Blantyre, Malawi.
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Kara Mannor
From the International Neurologic and Psychiatric Epidemiology Program (D.G.P., G.L.B.), College of Osteopathic Medicine (T.E.T., K.B.S.), and Department of Epidemiology (K.M.), Michigan State University, East Lansing; Malawi-Liverpool-Wellcome Trust Clinical Research Programme (M.M.), College of Medicine, Blantyre, Malawi; Department of Neurology (P.W.K.), Johns Hopkins University School of Medicine, Baltimore, MD; and Blantyre Malaria Project (Y.F.C., K.K.), University of Malawi College of Medicine, Blantyre, Malawi.
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Peter W. Kaplan
From the International Neurologic and Psychiatric Epidemiology Program (D.G.P., G.L.B.), College of Osteopathic Medicine (T.E.T., K.B.S.), and Department of Epidemiology (K.M.), Michigan State University, East Lansing; Malawi-Liverpool-Wellcome Trust Clinical Research Programme (M.M.), College of Medicine, Blantyre, Malawi; Department of Neurology (P.W.K.), Johns Hopkins University School of Medicine, Baltimore, MD; and Blantyre Malaria Project (Y.F.C., K.K.), University of Malawi College of Medicine, Blantyre, Malawi.
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Karl B. Seydel
From the International Neurologic and Psychiatric Epidemiology Program (D.G.P., G.L.B.), College of Osteopathic Medicine (T.E.T., K.B.S.), and Department of Epidemiology (K.M.), Michigan State University, East Lansing; Malawi-Liverpool-Wellcome Trust Clinical Research Programme (M.M.), College of Medicine, Blantyre, Malawi; Department of Neurology (P.W.K.), Johns Hopkins University School of Medicine, Baltimore, MD; and Blantyre Malaria Project (Y.F.C., K.K.), University of Malawi College of Medicine, Blantyre, Malawi.
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Yamikani F. Chimalizeni
From the International Neurologic and Psychiatric Epidemiology Program (D.G.P., G.L.B.), College of Osteopathic Medicine (T.E.T., K.B.S.), and Department of Epidemiology (K.M.), Michigan State University, East Lansing; Malawi-Liverpool-Wellcome Trust Clinical Research Programme (M.M.), College of Medicine, Blantyre, Malawi; Department of Neurology (P.W.K.), Johns Hopkins University School of Medicine, Baltimore, MD; and Blantyre Malaria Project (Y.F.C., K.K.), University of Malawi College of Medicine, Blantyre, Malawi.
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Kondwani Kawaza
From the International Neurologic and Psychiatric Epidemiology Program (D.G.P., G.L.B.), College of Osteopathic Medicine (T.E.T., K.B.S.), and Department of Epidemiology (K.M.), Michigan State University, East Lansing; Malawi-Liverpool-Wellcome Trust Clinical Research Programme (M.M.), College of Medicine, Blantyre, Malawi; Department of Neurology (P.W.K.), Johns Hopkins University School of Medicine, Baltimore, MD; and Blantyre Malaria Project (Y.F.C., K.K.), University of Malawi College of Medicine, Blantyre, Malawi.
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Gretchen L. Birbeck
From the International Neurologic and Psychiatric Epidemiology Program (D.G.P., G.L.B.), College of Osteopathic Medicine (T.E.T., K.B.S.), and Department of Epidemiology (K.M.), Michigan State University, East Lansing; Malawi-Liverpool-Wellcome Trust Clinical Research Programme (M.M.), College of Medicine, Blantyre, Malawi; Department of Neurology (P.W.K.), Johns Hopkins University School of Medicine, Baltimore, MD; and Blantyre Malaria Project (Y.F.C., K.K.), University of Malawi College of Medicine, Blantyre, Malawi.
MD
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Citation
Neurologic outcomes in retinopathy-negative cerebral malaria survivors
Douglas G. Postels, Terrie E. Taylor, Malcolm Molyneux, Kara Mannor, Peter W. Kaplan, Karl B. Seydel, Yamikani F. Chimalizeni, Kondwani Kawaza, Gretchen L. Birbeck
Neurology Sep 2012, 79 (12) 1268-1272; DOI: 10.1212/WNL.0b013e31826aacd4

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Abstract

Objectives: Patients surviving retinopathy-positive cerebral malaria (CM) are at high risk for the development of epilepsy, developmental disabilities, and behavioral abnormalities. We aimed to establish whether retinopathy-negative CM is also a risk factor for these outcomes.

Methods: Between 2005 and 2007, survivors of CM and concurrently hospitalized controls in Blantyre, Malawi, were followed to assess the development of neurologic abnormalities. At discharge and every 3 months thereafter, incident cases of epilepsy and developmental disabilities were ascertained using screening questionnaires and confirmatory neurologic examinations. Incident cases of epilepsy and developmental disabilities were compared in retinopathy-negative CM survivors to controls and retinopathy-positive CM survivors.

Results: Thirty-five retinopathy-negative CM survivors were enrolled. Their neurologic outcomes were compared to 132 retinopathy-positive CM survivors and 272 controls. Compared to survivors of retinopathy-positive CM, children without malaria retinopathy have an equal odds of adverse neurologic outcome (odds ratio [OR] = 1.0, 95% confidence interval [CI] 0.4–2.2). Eleven of 35 survivors of retinopathy-negative CM had at least 1 adverse neurologic outcome compared to 2 of 272 controls (OR 61.9, 95% CI 13.0–295.5). In retinopathy-negative CM survivors, a Blantyre Coma Scale score ≤1 on admission was associated with an adverse outcome.

Conclusions: Compared with controls, children surviving either retinopathy-negative or -positive CM are at similar high risk for adverse neurologic outcomes. Studies to evaluate preventive and therapeutic strategies in children with both retinopathy-negative and -positive CM are needed to improve mortality, morbidity, or both.

GLOSSARY

CI=
confidence interval;
CM=
cerebral malaria;
OR=
odds ratio

Footnotes

  • Study funding: Supported by grants NIH/NINDS K23 NS046086-01 (G.L.B.), NIH/NIAID R01 AI034969-10AI (T.E.T.), and the Wellcome Trust 074125/Z/04/Z (M.E.M.).

  • Editorial, page 1196

  • Received January 11, 2012.
  • Accepted March 28, 2012.
  • Copyright © 2012 by AAN Enterprises, Inc.
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  • RETINOPATHY IN MALARIA-?PROGNOSTIC SIGNIFICANCE
    • Khichar SHUBHAKARAN, Associate Professor Neurology, Dr. S. N. Medical College Jodhpurdrkhicharsk@gmail.com
    Submitted October 01, 2012
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