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Enhancing case definitions for surveillance of human monkeypox in the Democratic Republic of Congo

BACKGROUND: Human monkeypox (MPX) occurs at appreciable rates in the Democratic Republic of Congo (DRC). Infection with varicella zoster virus (VZV) has a similar presentation to that of MPX, and in areas where MPX is endemic these two illnesses are commonly mistaken. This study evaluated the diagno...

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Autores principales: Osadebe, Lynda, Hughes, Christine M., Shongo Lushima, Robert, Kabamba, Joelle, Nguete, Beatrice, Malekani, Jean, Pukuta, Elisabeth, Karhemere, Stomy, Muyembe Tamfum, Jean-Jacques, Wemakoy Okitolonda, Emile, Reynolds, Mary G., McCollum, Andrea M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593177/
https://www.ncbi.nlm.nih.gov/pubmed/28892474
http://dx.doi.org/10.1371/journal.pntd.0005857
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author Osadebe, Lynda
Hughes, Christine M.
Shongo Lushima, Robert
Kabamba, Joelle
Nguete, Beatrice
Malekani, Jean
Pukuta, Elisabeth
Karhemere, Stomy
Muyembe Tamfum, Jean-Jacques
Wemakoy Okitolonda, Emile
Reynolds, Mary G.
McCollum, Andrea M.
author_facet Osadebe, Lynda
Hughes, Christine M.
Shongo Lushima, Robert
Kabamba, Joelle
Nguete, Beatrice
Malekani, Jean
Pukuta, Elisabeth
Karhemere, Stomy
Muyembe Tamfum, Jean-Jacques
Wemakoy Okitolonda, Emile
Reynolds, Mary G.
McCollum, Andrea M.
author_sort Osadebe, Lynda
collection PubMed
description BACKGROUND: Human monkeypox (MPX) occurs at appreciable rates in the Democratic Republic of Congo (DRC). Infection with varicella zoster virus (VZV) has a similar presentation to that of MPX, and in areas where MPX is endemic these two illnesses are commonly mistaken. This study evaluated the diagnostic utility of two surveillance case definitions for MPX and specific clinical characteristics associated with laboratory-confirmed MPX cases. METHODOLOGY/PRINCIPAL FINDINGS: Data from a cohort of suspect MPX cases (identified by surveillance over the course of a 42 month period during 2009–2014) from DRC were used; real-time PCR diagnostic test results were used to establish MPX and VZV diagnoses. A total of 333 laboratory-confirmed MPX cases, 383 laboratory-confirmed VZV cases, and 36 cases that were determined to not be either MPX or VZV were included in the analyses. Significant (p<0.05) differences between laboratory-confirmed MPX and VZV cases were noted for several signs/symptoms including key rash characteristics. Both surveillance case definitions had high sensitivity and low specificities for individuals that had suspected MPX virus infections. Using 12 signs/symptoms with high sensitivity and/or specificity values, a receiver operator characteristic analysis showed that models for MPX cases that had the presence of ‘fever before rash’ plus at least 7 or 8 of the 12 signs/symptoms demonstrated a more balanced performance between sensitivity and specificity. CONCLUSIONS: Laboratory-confirmed MPX and VZV cases presented with many of the same signs and symptoms, and the analysis here emphasized the utility of including 12 specific signs/symptoms when investigating MPX cases. In order to document and detect endemic human MPX cases, a surveillance case definition with more specificity is needed for accurate case detection. In the absence of a more specific case definition, continued emphasis on confirmatory laboratory-based diagnostics is warranted.
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spelling pubmed-55931772017-09-15 Enhancing case definitions for surveillance of human monkeypox in the Democratic Republic of Congo Osadebe, Lynda Hughes, Christine M. Shongo Lushima, Robert Kabamba, Joelle Nguete, Beatrice Malekani, Jean Pukuta, Elisabeth Karhemere, Stomy Muyembe Tamfum, Jean-Jacques Wemakoy Okitolonda, Emile Reynolds, Mary G. McCollum, Andrea M. PLoS Negl Trop Dis Research Article BACKGROUND: Human monkeypox (MPX) occurs at appreciable rates in the Democratic Republic of Congo (DRC). Infection with varicella zoster virus (VZV) has a similar presentation to that of MPX, and in areas where MPX is endemic these two illnesses are commonly mistaken. This study evaluated the diagnostic utility of two surveillance case definitions for MPX and specific clinical characteristics associated with laboratory-confirmed MPX cases. METHODOLOGY/PRINCIPAL FINDINGS: Data from a cohort of suspect MPX cases (identified by surveillance over the course of a 42 month period during 2009–2014) from DRC were used; real-time PCR diagnostic test results were used to establish MPX and VZV diagnoses. A total of 333 laboratory-confirmed MPX cases, 383 laboratory-confirmed VZV cases, and 36 cases that were determined to not be either MPX or VZV were included in the analyses. Significant (p<0.05) differences between laboratory-confirmed MPX and VZV cases were noted for several signs/symptoms including key rash characteristics. Both surveillance case definitions had high sensitivity and low specificities for individuals that had suspected MPX virus infections. Using 12 signs/symptoms with high sensitivity and/or specificity values, a receiver operator characteristic analysis showed that models for MPX cases that had the presence of ‘fever before rash’ plus at least 7 or 8 of the 12 signs/symptoms demonstrated a more balanced performance between sensitivity and specificity. CONCLUSIONS: Laboratory-confirmed MPX and VZV cases presented with many of the same signs and symptoms, and the analysis here emphasized the utility of including 12 specific signs/symptoms when investigating MPX cases. In order to document and detect endemic human MPX cases, a surveillance case definition with more specificity is needed for accurate case detection. In the absence of a more specific case definition, continued emphasis on confirmatory laboratory-based diagnostics is warranted. Public Library of Science 2017-09-11 /pmc/articles/PMC5593177/ /pubmed/28892474 http://dx.doi.org/10.1371/journal.pntd.0005857 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Osadebe, Lynda
Hughes, Christine M.
Shongo Lushima, Robert
Kabamba, Joelle
Nguete, Beatrice
Malekani, Jean
Pukuta, Elisabeth
Karhemere, Stomy
Muyembe Tamfum, Jean-Jacques
Wemakoy Okitolonda, Emile
Reynolds, Mary G.
McCollum, Andrea M.
Enhancing case definitions for surveillance of human monkeypox in the Democratic Republic of Congo
title Enhancing case definitions for surveillance of human monkeypox in the Democratic Republic of Congo
title_full Enhancing case definitions for surveillance of human monkeypox in the Democratic Republic of Congo
title_fullStr Enhancing case definitions for surveillance of human monkeypox in the Democratic Republic of Congo
title_full_unstemmed Enhancing case definitions for surveillance of human monkeypox in the Democratic Republic of Congo
title_short Enhancing case definitions for surveillance of human monkeypox in the Democratic Republic of Congo
title_sort enhancing case definitions for surveillance of human monkeypox in the democratic republic of congo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593177/
https://www.ncbi.nlm.nih.gov/pubmed/28892474
http://dx.doi.org/10.1371/journal.pntd.0005857
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