Intensive Care Unit-Like Care of Nonhuman Primates with Ebola Virus Disease.


Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
16 08 2021
Historique:
received: 05 06 2020
accepted: 18 12 2020
pubmed: 29 12 2020
medline: 2 2 2022
entrez: 28 12 2020
Statut: ppublish

Résumé

Ebola virus disease (EVD) supportive care strategies are largely guided by retrospective observational research. This study investigated the effect of EVD supportive care algorithms on duration of survival in a controlled nonhuman primate (NHP) model. Fourteen rhesus macaques were challenged intramuscularly with a target dose of Ebola virus (1000 plaque-forming units; Kikwit). NHPs were allocated to intensive care unit (ICU)-like algorithms (n = 7), intravenous fluids plus levofloxacin (n = 2), or a control group (n = 5). The primary outcome measure was duration of survival, and secondary outcomes included changes in clinical laboratory values. Duration of survival was not significantly different between the pooled ICU-like algorithm and control groups (8.2 vs 6.9 days of survival; hazard ratio; 0.50; P = .25). Norepinephrine was effective in transiently maintaining baseline blood pressure. NHPs treated with ICU-like algorithms had delayed onset of liver and kidney injury. While an obvious survival difference was not observed with ICU-like care, clinical observations from this model may aid in EVD supportive care NHP model refinement.

Sections du résumé

BACKGROUND
Ebola virus disease (EVD) supportive care strategies are largely guided by retrospective observational research. This study investigated the effect of EVD supportive care algorithms on duration of survival in a controlled nonhuman primate (NHP) model.
METHODS
Fourteen rhesus macaques were challenged intramuscularly with a target dose of Ebola virus (1000 plaque-forming units; Kikwit). NHPs were allocated to intensive care unit (ICU)-like algorithms (n = 7), intravenous fluids plus levofloxacin (n = 2), or a control group (n = 5). The primary outcome measure was duration of survival, and secondary outcomes included changes in clinical laboratory values.
RESULTS
Duration of survival was not significantly different between the pooled ICU-like algorithm and control groups (8.2 vs 6.9 days of survival; hazard ratio; 0.50; P = .25). Norepinephrine was effective in transiently maintaining baseline blood pressure. NHPs treated with ICU-like algorithms had delayed onset of liver and kidney injury.
CONCLUSIONS
While an obvious survival difference was not observed with ICU-like care, clinical observations from this model may aid in EVD supportive care NHP model refinement.

Identifiants

pubmed: 33367826
pii: 6047590
doi: 10.1093/infdis/jiaa781
pmc: PMC8366444
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

632-642

Subventions

Organisme : NIAID NIH HHS
ID : T32 AI007291
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL116275
Pays : United States

Informations de copyright

Published by Oxford University Press for the Infectious Diseases Society of America 2020.

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Auteurs

Paul W Blair (PW)

Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Austere Environments Consortium for Enhanced Sepsis Outcomes, Henry M. Jackson Foundation, Bethesda, Maryland, USA.

Mark G Kortepeter (MG)

University of Nebraska Medical Center, Omaha, Nebraska, USA.

Lydia G Downey (LG)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Cristian S Madar (CS)

Tripler Army Medical Center, Honolulu, Hawaii, USA.

Isaac L Downs (IL)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Karen A Martins (KA)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Franco Rossi (F)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Janice A Williams (JA)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Annie Madar (A)

Tripler Army Medical Center, Honolulu, Hawaii, USA.

Christopher W Schellhase (CW)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Jeremy J Bearss (JJ)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Xiankun Zeng (X)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Sina Bavari (S)

Edge BioInnovation Consulting and Management, Frederick, Maryland, USA.

Veronica Soloveva (V)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Jay B Wells (JB)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Kelly S Stuthman (KS)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Nicole L Garza (NL)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Sean A Vantongeren (SA)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Ginger C Donnelly (GC)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Jesse Steffens (J)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Jennifer Kalapaca (J)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Perry Wiseman (P)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Joseph Henry (J)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Shannon Marko (S)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Mark Chappell (M)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Luis Lugo-Roman (L)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Elliot Ramos-Rivera (E)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Christian Hofer (C)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Eugene Blue (E)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Joshua Moore (J)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Jimmy Fiallos (J)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Darrel Wetzel (D)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

William D Pratt (WD)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Tami Unangst (T)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Adele Miller (A)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

James J Sola (JJ)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Ronald B Reisler (RB)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

Anthony P Cardile (AP)

Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

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