Differential symptomology of possible and confirmed Ebola virus disease infection in the Democratic Republic of the Congo: a retrospective cohort study
In its earliest phases, Ebola virus disease's rapid-onset, high fever, and gastrointestinal symptoms are largely indistinguishable from other infectious illnesses. We aimed to characterise the clinical indicators associated with Ebola virus disease to improve outbreak response. In this retrospe...
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Veröffentlicht in: | The Lancet infectious diseases 2023-01, Vol.23 (1), p.91-102 |
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creator | Nsio, Justus Ardiet, Denis-Luc Coulborn, Rebecca M Grellety, Emmanuel Albela, Manuel Grandesso, Francesco Kitenge, Richard Ngwanga, Dolla L Matady, Bibiche Manangama, Guyguy Mossoko, Mathias Ngwama, John Kombe Mbala, Placide Luquero, Francisco Porten, Klaudia Ahuka-Mundeke, Steve |
description | In its earliest phases, Ebola virus disease's rapid-onset, high fever, and gastrointestinal symptoms are largely indistinguishable from other infectious illnesses. We aimed to characterise the clinical indicators associated with Ebola virus disease to improve outbreak response.
In this retrospective analysis, we assessed routinely collected data from individuals with possible Ebola virus disease attending 30 Ebola health facilities in two provinces of the Democratic Republic of the Congo between Aug 1, 2018, and Aug 28, 2019. We used logistic regression analysis to model the probability of Ebola infection across 34 clinical variables and four types of possible Ebola virus disease exposures: contact with an individual known to have Ebola virus disease, attendance at any funeral, health facility consultation, or consultation with an informal health practitioner.
Data for 24 666 individuals were included. If a patient presented to care in the early symptomatic phase (ie, days 0–2), Ebola virus disease positivity was most associated with previous exposure to an individual with Ebola virus disease (odds ratio [OR] 11·9, 95% CI 9·1–15·8), funeral attendance (2·1, 1·6–2·7), or health facility consultations (2·1, 1·6–2·8), rather than clinical parameters. If presentation occurred on day 3 or later (after symptom onset), bleeding at an injection site (OR 33·9, 95% CI 12·7–101·3), bleeding gums (7·5, 3·7–15·4), conjunctivitis (2·4, 1·7–3·4), asthenia (1·9, 1·5–2·3), sore throat (1·8, 1·3–2·4), dysphagia (1·8, 1·4–2·3), and diarrhoea (1·6, 1·3–1·9) were additional strong predictors of Ebola virus disease. Some Ebola virus disease-specific signs were less prevalent among vaccinated individuals who were positive for Ebola virus disease when compared with the unvaccinated, such as dysphagia (–47%, p=0·0024), haematemesis (–90%, p=0·0131), and bleeding gums (–100%, p=0·0035).
Establishing the exact time an individual first had symptoms is essential to assessing their infection risk. An individual's exposure history remains of paramount importance, especially in the early phase. Ebola virus disease vaccination reduces symptom severity and should also be considered when assessing the likelihood of infection. These findings about symptomatology should be translated into practice during triage and should inform testing and quarantine procedures.
Médecins Sans Frontières and its research affiliate Epicentre. |
doi_str_mv | 10.1016/S1473-3099(22)00584-9 |
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In this retrospective analysis, we assessed routinely collected data from individuals with possible Ebola virus disease attending 30 Ebola health facilities in two provinces of the Democratic Republic of the Congo between Aug 1, 2018, and Aug 28, 2019. We used logistic regression analysis to model the probability of Ebola infection across 34 clinical variables and four types of possible Ebola virus disease exposures: contact with an individual known to have Ebola virus disease, attendance at any funeral, health facility consultation, or consultation with an informal health practitioner.
Data for 24 666 individuals were included. If a patient presented to care in the early symptomatic phase (ie, days 0–2), Ebola virus disease positivity was most associated with previous exposure to an individual with Ebola virus disease (odds ratio [OR] 11·9, 95% CI 9·1–15·8), funeral attendance (2·1, 1·6–2·7), or health facility consultations (2·1, 1·6–2·8), rather than clinical parameters. If presentation occurred on day 3 or later (after symptom onset), bleeding at an injection site (OR 33·9, 95% CI 12·7–101·3), bleeding gums (7·5, 3·7–15·4), conjunctivitis (2·4, 1·7–3·4), asthenia (1·9, 1·5–2·3), sore throat (1·8, 1·3–2·4), dysphagia (1·8, 1·4–2·3), and diarrhoea (1·6, 1·3–1·9) were additional strong predictors of Ebola virus disease. Some Ebola virus disease-specific signs were less prevalent among vaccinated individuals who were positive for Ebola virus disease when compared with the unvaccinated, such as dysphagia (–47%, p=0·0024), haematemesis (–90%, p=0·0131), and bleeding gums (–100%, p=0·0035).
Establishing the exact time an individual first had symptoms is essential to assessing their infection risk. An individual's exposure history remains of paramount importance, especially in the early phase. Ebola virus disease vaccination reduces symptom severity and should also be considered when assessing the likelihood of infection. These findings about symptomatology should be translated into practice during triage and should inform testing and quarantine procedures.
Médecins Sans Frontières and its research affiliate Epicentre.</description><identifier>ISSN: 1473-3099</identifier><identifier>EISSN: 1474-4457</identifier><identifier>DOI: 10.1016/S1473-3099(22)00584-9</identifier><identifier>PMID: 36370717</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Asthenia ; Bleeding ; Cohort analysis ; Conjunctivitis ; Data collection ; Deglutition Disorders - epidemiology ; Democratic Republic of the Congo - epidemiology ; Diarrhea ; Disease Outbreaks - prevention & control ; Dysphagia ; Ebola virus ; Ebolavirus ; Ebolavirus - physiology ; Epidemics ; Exposure ; Gastrointestinal symptoms ; Glycoproteins ; Gums ; Health care facilities ; Health risks ; Hemorrhagic Fever, Ebola - prevention & control ; Humans ; Illnesses ; Immunization ; Infections ; Infectious diseases ; Patients ; Pharyngitis ; Registration ; Regression analysis ; Regression models ; Retrospective Studies ; Statistical analysis ; Symptomology ; Vaccination ; Vaccines ; Variables ; Viral diseases ; Viruses</subject><ispartof>The Lancet infectious diseases, 2023-01, Vol.23 (1), p.91-102</ispartof><rights>2023 Elsevier Ltd</rights><rights>Copyright © 2023 Elsevier Ltd. All rights reserved.</rights><rights>2023. Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c323t-287bfa27aca0c776862069b11e3426138ce8e7815c2c2bcef155f6aa56ff92a93</citedby><cites>FETCH-LOGICAL-c323t-287bfa27aca0c776862069b11e3426138ce8e7815c2c2bcef155f6aa56ff92a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1473309922005849$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36370717$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nsio, Justus</creatorcontrib><creatorcontrib>Ardiet, Denis-Luc</creatorcontrib><creatorcontrib>Coulborn, Rebecca M</creatorcontrib><creatorcontrib>Grellety, Emmanuel</creatorcontrib><creatorcontrib>Albela, Manuel</creatorcontrib><creatorcontrib>Grandesso, Francesco</creatorcontrib><creatorcontrib>Kitenge, Richard</creatorcontrib><creatorcontrib>Ngwanga, Dolla L</creatorcontrib><creatorcontrib>Matady, Bibiche</creatorcontrib><creatorcontrib>Manangama, Guyguy</creatorcontrib><creatorcontrib>Mossoko, Mathias</creatorcontrib><creatorcontrib>Ngwama, John Kombe</creatorcontrib><creatorcontrib>Mbala, Placide</creatorcontrib><creatorcontrib>Luquero, Francisco</creatorcontrib><creatorcontrib>Porten, Klaudia</creatorcontrib><creatorcontrib>Ahuka-Mundeke, Steve</creatorcontrib><title>Differential symptomology of possible and confirmed Ebola virus disease infection in the Democratic Republic of the Congo: a retrospective cohort study</title><title>The Lancet infectious diseases</title><addtitle>Lancet Infect Dis</addtitle><description>In its earliest phases, Ebola virus disease's rapid-onset, high fever, and gastrointestinal symptoms are largely indistinguishable from other infectious illnesses. We aimed to characterise the clinical indicators associated with Ebola virus disease to improve outbreak response.
In this retrospective analysis, we assessed routinely collected data from individuals with possible Ebola virus disease attending 30 Ebola health facilities in two provinces of the Democratic Republic of the Congo between Aug 1, 2018, and Aug 28, 2019. We used logistic regression analysis to model the probability of Ebola infection across 34 clinical variables and four types of possible Ebola virus disease exposures: contact with an individual known to have Ebola virus disease, attendance at any funeral, health facility consultation, or consultation with an informal health practitioner.
Data for 24 666 individuals were included. If a patient presented to care in the early symptomatic phase (ie, days 0–2), Ebola virus disease positivity was most associated with previous exposure to an individual with Ebola virus disease (odds ratio [OR] 11·9, 95% CI 9·1–15·8), funeral attendance (2·1, 1·6–2·7), or health facility consultations (2·1, 1·6–2·8), rather than clinical parameters. If presentation occurred on day 3 or later (after symptom onset), bleeding at an injection site (OR 33·9, 95% CI 12·7–101·3), bleeding gums (7·5, 3·7–15·4), conjunctivitis (2·4, 1·7–3·4), asthenia (1·9, 1·5–2·3), sore throat (1·8, 1·3–2·4), dysphagia (1·8, 1·4–2·3), and diarrhoea (1·6, 1·3–1·9) were additional strong predictors of Ebola virus disease. Some Ebola virus disease-specific signs were less prevalent among vaccinated individuals who were positive for Ebola virus disease when compared with the unvaccinated, such as dysphagia (–47%, p=0·0024), haematemesis (–90%, p=0·0131), and bleeding gums (–100%, p=0·0035).
Establishing the exact time an individual first had symptoms is essential to assessing their infection risk. An individual's exposure history remains of paramount importance, especially in the early phase. Ebola virus disease vaccination reduces symptom severity and should also be considered when assessing the likelihood of infection. These findings about symptomatology should be translated into practice during triage and should inform testing and quarantine procedures.
Médecins Sans Frontières and its research affiliate Epicentre.</description><subject>Asthenia</subject><subject>Bleeding</subject><subject>Cohort analysis</subject><subject>Conjunctivitis</subject><subject>Data collection</subject><subject>Deglutition Disorders - epidemiology</subject><subject>Democratic Republic of the Congo - epidemiology</subject><subject>Diarrhea</subject><subject>Disease Outbreaks - prevention & control</subject><subject>Dysphagia</subject><subject>Ebola virus</subject><subject>Ebolavirus</subject><subject>Ebolavirus - physiology</subject><subject>Epidemics</subject><subject>Exposure</subject><subject>Gastrointestinal symptoms</subject><subject>Glycoproteins</subject><subject>Gums</subject><subject>Health care facilities</subject><subject>Health risks</subject><subject>Hemorrhagic Fever, Ebola - prevention & control</subject><subject>Humans</subject><subject>Illnesses</subject><subject>Immunization</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Patients</subject><subject>Pharyngitis</subject><subject>Registration</subject><subject>Regression analysis</subject><subject>Regression models</subject><subject>Retrospective Studies</subject><subject>Statistical analysis</subject><subject>Symptomology</subject><subject>Vaccination</subject><subject>Vaccines</subject><subject>Variables</subject><subject>Viral diseases</subject><subject>Viruses</subject><issn>1473-3099</issn><issn>1474-4457</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkctu1TAQhi1ERS_wCCBLbMoi1Jc4TtggdNpCpUpIXNaW44xbV4kdbOdI50n6ujjnFBZsWHlkf_PP-P8Rek3Je0poc_Gd1pJXnHTdOWPvCBFtXXXP0Em5rqu6FvL5vj4gx-g0pQdCqKSkfoGOecMlkVSeoMdLZy1E8NnpEafdNOcwhTHc7XCweA4puX4ErP2ATfDWxQkGfNWHUeOti0vCg0ugE2DnLZjsgi8VzveAL2EKJursDP4G89KPpSiS69Mm-LvwAWscIceQ5rVxC2XAfYgZp7wMu5foyOoxwaun8wz9vL76sflS3X79fLP5dFsZzniuWCt7q5nURhMjZdM2jDRdTynwmjWUtwZakC0VhhnWG7BUCNtoLRprO6Y7fobOD7pzDL8WSFlNLhkYR-0hLEkxyUUri2hT0Lf_oA9hib5sVyghZCupWClxoEz5WYpg1RzdpONOUaLW5NQ-ObXGohhT--TUusibJ_WlLx7_7foTVQE-HgAodmwdRJWMA29gcLEYqIbg_jPiN4GMqqQ</recordid><startdate>202301</startdate><enddate>202301</enddate><creator>Nsio, Justus</creator><creator>Ardiet, Denis-Luc</creator><creator>Coulborn, Rebecca M</creator><creator>Grellety, Emmanuel</creator><creator>Albela, Manuel</creator><creator>Grandesso, Francesco</creator><creator>Kitenge, Richard</creator><creator>Ngwanga, Dolla L</creator><creator>Matady, Bibiche</creator><creator>Manangama, Guyguy</creator><creator>Mossoko, Mathias</creator><creator>Ngwama, John Kombe</creator><creator>Mbala, Placide</creator><creator>Luquero, Francisco</creator><creator>Porten, Klaudia</creator><creator>Ahuka-Mundeke, Steve</creator><general>Elsevier Ltd</general><general>Elsevier Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>0TZ</scope><scope>3V.</scope><scope>7QL</scope><scope>7RV</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8C2</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>202301</creationdate><title>Differential symptomology of possible and confirmed Ebola virus disease infection in the Democratic Republic of the Congo: a retrospective cohort study</title><author>Nsio, Justus ; Ardiet, Denis-Luc ; Coulborn, Rebecca M ; Grellety, Emmanuel ; Albela, Manuel ; Grandesso, Francesco ; Kitenge, Richard ; Ngwanga, Dolla L ; Matady, Bibiche ; Manangama, Guyguy ; Mossoko, Mathias ; Ngwama, John Kombe ; Mbala, Placide ; Luquero, Francisco ; Porten, Klaudia ; Ahuka-Mundeke, Steve</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c323t-287bfa27aca0c776862069b11e3426138ce8e7815c2c2bcef155f6aa56ff92a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Asthenia</topic><topic>Bleeding</topic><topic>Cohort analysis</topic><topic>Conjunctivitis</topic><topic>Data collection</topic><topic>Deglutition Disorders - epidemiology</topic><topic>Democratic Republic of the Congo - epidemiology</topic><topic>Diarrhea</topic><topic>Disease Outbreaks - prevention & control</topic><topic>Dysphagia</topic><topic>Ebola virus</topic><topic>Ebolavirus</topic><topic>Ebolavirus - physiology</topic><topic>Epidemics</topic><topic>Exposure</topic><topic>Gastrointestinal symptoms</topic><topic>Glycoproteins</topic><topic>Gums</topic><topic>Health care facilities</topic><topic>Health risks</topic><topic>Hemorrhagic Fever, Ebola - prevention & control</topic><topic>Humans</topic><topic>Illnesses</topic><topic>Immunization</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Patients</topic><topic>Pharyngitis</topic><topic>Registration</topic><topic>Regression analysis</topic><topic>Regression models</topic><topic>Retrospective Studies</topic><topic>Statistical analysis</topic><topic>Symptomology</topic><topic>Vaccination</topic><topic>Vaccines</topic><topic>Variables</topic><topic>Viral diseases</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nsio, Justus</creatorcontrib><creatorcontrib>Ardiet, Denis-Luc</creatorcontrib><creatorcontrib>Coulborn, Rebecca M</creatorcontrib><creatorcontrib>Grellety, Emmanuel</creatorcontrib><creatorcontrib>Albela, Manuel</creatorcontrib><creatorcontrib>Grandesso, Francesco</creatorcontrib><creatorcontrib>Kitenge, Richard</creatorcontrib><creatorcontrib>Ngwanga, Dolla L</creatorcontrib><creatorcontrib>Matady, Bibiche</creatorcontrib><creatorcontrib>Manangama, Guyguy</creatorcontrib><creatorcontrib>Mossoko, Mathias</creatorcontrib><creatorcontrib>Ngwama, John Kombe</creatorcontrib><creatorcontrib>Mbala, Placide</creatorcontrib><creatorcontrib>Luquero, Francisco</creatorcontrib><creatorcontrib>Porten, Klaudia</creatorcontrib><creatorcontrib>Ahuka-Mundeke, Steve</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Pharma and Biotech Premium PRO</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing & Allied Health Database</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Lancet Titles</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>The Lancet infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nsio, Justus</au><au>Ardiet, Denis-Luc</au><au>Coulborn, Rebecca M</au><au>Grellety, Emmanuel</au><au>Albela, Manuel</au><au>Grandesso, Francesco</au><au>Kitenge, Richard</au><au>Ngwanga, Dolla L</au><au>Matady, Bibiche</au><au>Manangama, Guyguy</au><au>Mossoko, Mathias</au><au>Ngwama, John Kombe</au><au>Mbala, Placide</au><au>Luquero, Francisco</au><au>Porten, Klaudia</au><au>Ahuka-Mundeke, Steve</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential symptomology of possible and confirmed Ebola virus disease infection in the Democratic Republic of the Congo: a retrospective cohort study</atitle><jtitle>The Lancet infectious diseases</jtitle><addtitle>Lancet Infect Dis</addtitle><date>2023-01</date><risdate>2023</risdate><volume>23</volume><issue>1</issue><spage>91</spage><epage>102</epage><pages>91-102</pages><issn>1473-3099</issn><eissn>1474-4457</eissn><abstract>In its earliest phases, Ebola virus disease's rapid-onset, high fever, and gastrointestinal symptoms are largely indistinguishable from other infectious illnesses. We aimed to characterise the clinical indicators associated with Ebola virus disease to improve outbreak response.
In this retrospective analysis, we assessed routinely collected data from individuals with possible Ebola virus disease attending 30 Ebola health facilities in two provinces of the Democratic Republic of the Congo between Aug 1, 2018, and Aug 28, 2019. We used logistic regression analysis to model the probability of Ebola infection across 34 clinical variables and four types of possible Ebola virus disease exposures: contact with an individual known to have Ebola virus disease, attendance at any funeral, health facility consultation, or consultation with an informal health practitioner.
Data for 24 666 individuals were included. If a patient presented to care in the early symptomatic phase (ie, days 0–2), Ebola virus disease positivity was most associated with previous exposure to an individual with Ebola virus disease (odds ratio [OR] 11·9, 95% CI 9·1–15·8), funeral attendance (2·1, 1·6–2·7), or health facility consultations (2·1, 1·6–2·8), rather than clinical parameters. If presentation occurred on day 3 or later (after symptom onset), bleeding at an injection site (OR 33·9, 95% CI 12·7–101·3), bleeding gums (7·5, 3·7–15·4), conjunctivitis (2·4, 1·7–3·4), asthenia (1·9, 1·5–2·3), sore throat (1·8, 1·3–2·4), dysphagia (1·8, 1·4–2·3), and diarrhoea (1·6, 1·3–1·9) were additional strong predictors of Ebola virus disease. Some Ebola virus disease-specific signs were less prevalent among vaccinated individuals who were positive for Ebola virus disease when compared with the unvaccinated, such as dysphagia (–47%, p=0·0024), haematemesis (–90%, p=0·0131), and bleeding gums (–100%, p=0·0035).
Establishing the exact time an individual first had symptoms is essential to assessing their infection risk. An individual's exposure history remains of paramount importance, especially in the early phase. Ebola virus disease vaccination reduces symptom severity and should also be considered when assessing the likelihood of infection. These findings about symptomatology should be translated into practice during triage and should inform testing and quarantine procedures.
Médecins Sans Frontières and its research affiliate Epicentre.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>36370717</pmid><doi>10.1016/S1473-3099(22)00584-9</doi><tpages>12</tpages></addata></record> |
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source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Asthenia Bleeding Cohort analysis Conjunctivitis Data collection Deglutition Disorders - epidemiology Democratic Republic of the Congo - epidemiology Diarrhea Disease Outbreaks - prevention & control Dysphagia Ebola virus Ebolavirus Ebolavirus - physiology Epidemics Exposure Gastrointestinal symptoms Glycoproteins Gums Health care facilities Health risks Hemorrhagic Fever, Ebola - prevention & control Humans Illnesses Immunization Infections Infectious diseases Patients Pharyngitis Registration Regression analysis Regression models Retrospective Studies Statistical analysis Symptomology Vaccination Vaccines Variables Viral diseases Viruses |
title | Differential symptomology of possible and confirmed Ebola virus disease infection in the Democratic Republic of the Congo: a retrospective cohort study |
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