The contribution of Ebola viral load at admission and other patient characteristics to mortality in a Médecins Sans Frontières (MSF) Ebola Case Management Centre (CMC), Kailahun, Sierra Leone, June -October, 2014.
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Authors
Fitzpatrick, GabrielVogt, Florian
Gbabai, Osman B Moi
Decroo, Tom
Keane, Marian
De Clerck, Hilde
Grolla, Allen
Brechard, Raphael
Stinson, Kathryn
Van Herp, Michel
Issue Date
2015-05-22Keywords
INFECTION CONTROLINFECTIOUS DISEASE
Local subject classification
EBOLA VIRUS
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The contribution of Ebola viral load at admission and other patient characteristics to mortality in a Médecins Sans Frontières (MSF) Ebola Case Management Centre (CMC), Kailahun, Sierra Leone, June -October, 2014. 2015: J. Infect. Dis.Publisher
Oxford University PressJournal
The Journal of infectious diseasesDOI
10.1093/infdis/jiv304PubMed ID
26002981Abstract
This paper describes patient characteristics, including Ebola viral load, associated with mortality in an MSF Ebola case management centre. Out of 780 admissions between June and October 2014, 525 (67%) were positive for Ebola with a known outcome. The crude mortality rate was 51% (270/525). Ebola viral load (whole blood sample) data was available on 76% (397/525) of patients. Univariate analysis indicated viral load at admission, age, symptom duration prior to admission and distance travelled to the CMC were associated with mortality (p value<0.05). The multivariable model predicted mortality in those with a viral load at admission greater than 10 million copies per millilitre (p value<0.05, Odds Ratio>10), aged 50 years or more (p value=0.08, Odds Ratio=2) and symptom duration prior to admission less than 5 days (p value=0.14). The presence of confusion, diarrhoea and conjunctivitis were significantly higher (p value<0.05) in Ebola patients who died. These findings highlight the importance viral load at admission has on mortality outcomes and could be used to cohort cases with viral loads greater than 10 million copies into dedicated wards with more intensive medical support to further reduce mortality.Item Type
Article In PressLanguage
enISSN
1537-6613Sponsors
No funding was obtained.ae974a485f413a2113503eed53cd6c53
10.1093/infdis/jiv304
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