Abstract

Data collected during the 2012 Ebola virus disease (EVD) epidemic in the Democratic Republic of the Congo were analysed for clinical signs, symptoms and case fatality of EVD caused by Bundibugyo virus (BDBV), establishment of differential diagnoses, description of medical treatment and evaluation of the quality of clinical documentation. In a quantitative observational prospective study, global epidemiological data from 52 patients (34 patients within the community, 18 patients treated in the Ebola Treatment Centre) were entered anonymously into a database, subsequently matched and analysed. Relevant findings include an over-representation of females among community EVD cases (85.3%) and of community EVD cases in the age group of 15-54 years (82.4%). All ETC patients had fever (55.6% of all 18 ETC patients during their hospital stay) or self-reported fever (88.2% upon admission) at some point of time during their illness. Major symptoms of ETC patients during hospital stay included asthenia (82.4%), anorexia (82.4%), myalgia (70.6%), sore throat/difficulty swallowing (70.6%), arthralgia (76.5%) and nausea (70.6%). Gastrointestinal signs and symptoms (nausea, diarrhoea, vomiting) (76.4%) as well as general pain (94.1%) were frequent in ETC patients. The median duration of EVD was 18 days, while the mean incubation period was 11.3 days. Differential diagnosis of EVD included malaria (28.3%), intestinal parasitosis (10.9%), and infectious syndrome (10.9%). There was also an important variation in clinical evolvement. Quality of documentation was adversely affected by the way patient file contents were transferred from inside to outside the high-risk zone, entailing a mean mismatch value of 27.3% between patient file contents inside vs. outside the high-risk zone. This study adds further description of EVD (frequently non-specific signs and symptoms, non frequent bleeding, a long incubation period, long duration of disease) and emphasizes the need for improving clinical monitoring and documentation in EVD outbreak settings.

Highlights

  • Ebolavirus disease (EVD) is an acute severe disease with a high case fatality risk (CFR)

  • As clinical documentation has previously been shown to be poor in outbreaks due to filoviruses [5, 13], we evaluated the quality of the documentation

  • Compared with national demographic data [16] females were significantly overrepresented among EVD cases in the community (50.2% in the general population vs. 85.3% in community cases, p

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Summary

Introduction

Ebolavirus disease (EVD) is an acute severe disease with a high case fatality risk (CFR). Four ebolaviruses have been identified prior to 2007: Ebolavirus (EBOV), Sudan virus (SUDV), Taï Forest virus (TAFV) and Reston virus (RESTV). EBOV and SUDV are associated with large outbreaks in Equatorial and Western Africa with high CFRs [1,2,3]. In 2007, a newly identified ebolavirus, Bundibugyo virus (BDBV), was discovered during an outbreak in Uganda [4, 5]. Out of 43 cases ä, 17 were fatal (CFR 40%) [4]. The most frequent sign was non–bloody diarrhoea (81%), the most frequent symptom asthenia (77%), while only seven patients (27%) showed haemorrhagic signs [5]. No further outbreak of EVD caused by BDBV was observed until 2012. No further outbreak of EVD caused by BDBV was observed until 2012. [6,7,8,9]

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