| Literature DB >> 28299152 |
Semeeh Akinwale Omoleke1, Ibrahim Mohammed2, Yauba Saidu3.
Abstract
The West African sub-continent is currently experiencing its first, and ironically, the largest and longest Ebola viral diseases (EVD) outbreak ever documented in modern medical history. The current outbreak is significant in several ways, including longevity, magnitude of morbidity and mortality, occurrence outside the traditional niches, rapid spread and potential of becoming a global health tragedy. The authors provided explicit insights into the current and historical background, drivers of the epidemic, societal impacts, status of vaccines and drugs development and proffered recommendations to halt and prevent future occurrences. The authors reviewed mainly five databases and a hand search of key relevant literature. We reviewed 51 articles that were relevant up until the 18th of August 2014. The authors supplemented the search with reference list of relevant articles and grey literature as well as relevant Internet websites. Article searches were limited to those published either in English or French. There are strong indications that the EVD may have been triggered by increased human activities and encroachment into the forest ecosystem spurred by increasing population and poverty-driven forest-dependent local economy. Containment efforts are being hampered by weak and fragile health systems, including public health surveillance and weak governance, certain socio-anthropological factors, fast travels (improved transport systems) and globalization. The societal impacts of the EBV outbreak are grave, including economic shutdown, weakening of socio-political systems, psychological distress, and unprecedented consumption of scarce health resources. The research and development (R&D) pipeline for product against EBV seems grossly insufficient. The outbreak of Ebola and the seeming difficulty to contain the epidemic is simply a reflection of the weak health system, poor surveillance and emergency preparedness/response, poverty and disconnect between the government and the people in many West African countries. Although interventions by the United Nations and other international development agencies could ultimately halt the epidemic, local communities must be engaged to build trust and create demand for the public health interventions being implemented in the Ebola-ravaged populations. In the intermediate and long term, post-Ebola rehabilitation should focus on strengthening of health systems, improving awareness about zoonosis and health behaviors, alleviating poverty and mitigating the impact of triggering factors. Finally, national governments and international development partners should mobilize huge resources and investments to spur or facilitate R&D of disease control tools for emerging and pernicious infectious diseases (not limited to EVD).Entities:
Keywords: Drivers of spread; Ebola viral disease; Globalization; West Africa; Zoonosis
Year: 2016 PMID: 28299152 PMCID: PMC5349256 DOI: 10.4081/jphia.2016.534
Source DB: PubMed Journal: J Public Health Afr ISSN: 2038-9922
Figure 1.Countries at risk of Ebola viral disease. Source: eLife 2014;3:e04395.[6]
Health system profiles of countries with Ebola viral diseases (EVD) outbreak and at-risk countries of EVD outbreaks.[6-1][1]
| Country | Total population, millions | Population at risk of EVD, millions | Current GDP, US $ billion | Physicians/1000 population | Hospital bed capacity | Health expenditure (% of GDP) | Healthcare system performance ranking |
|---|---|---|---|---|---|---|---|
| Angola | 21.47 | 0.28 | 121.7 | 0.166 | 0.8 | 3.474 | 181 |
| Burundi | 2.72 | 0.03 | 10.2 | 0.028 | 1.9 | 8.134 | 143 |
| Cameroon | 22.25 | 1.19 | 29.27 | 0.077 | 1.3 | 5.131 | 164 |
| Central African Republic | 4.62 | 0.9 | 1.54 | 0.048 | 1 | 3.7598 | 189 |
| Congo | 4.45 | 0.29 | 14.11 | 0.095 | 1.6 | 3.164 | 166 |
| Cote d'Ivoire | 20.32 | 0.46 | 30.91 | 0.144 | 0.4 | 7.064 | 137 |
| Democratic Republic of Congo | 67.51 | 11.7 | 30.63 | 0.107 | 0.8 | 5.586 | 188 |
| Equatorial Guinea | 0.76 | 0.01 | 15.57 | 0.302 | 2.1 | 4.736 | 171 |
| Ethiopia | 94.1 | 0.08 | 46.87 | 0.022 | 2.1 | 3.833 | 180 |
| Gabon | 1.67 | 0.31 | 19.34 | 0.292 | 6.3 | 5.117 | 139 |
| Ghana | 25.9 | 0.49 | 47.93 | 0.096 | 0.9 | 3.47 | 135 |
| Guinea | 11.75 | 1.4 | 6.19 | 0.1 | 0.3 | 6.3 | 161 |
| Liberia | 4.29 | 0.44 | 1.95 | 0.014 | 0.8 | 15.53 | 186 |
| Madagascar | 22.92 | 0.01 | 10.8 | 0.161 | 0.2 | 4.112 | 159 |
| Malawi | 16.63 | <0.01 | 3.7 | 0.019 | 1.3 | 9.158 | 185 |
| Mozambique | 25.83 | 0.07 | 15.32 | 0.04 | 0.7 | 6.423 | 184 |
| Nigeria | 173.6 | 2.07 | 521.8 | 0.395 | 0.53 | 6.07 | 187 |
| Sierra Leone | 6.09 | 0.43 | 4.93 | 0.022 | 0.4 | 15.08 | 191 |
| South Sudan | 11.3 | 0.03 | 13.8 | NA | NA | 2.55 | NA |
| Tanzania | 49.25 | 0.13 | 33.23 | NA | 0.7 | 6.992 | NA |
| Togo | 6.82 | 0.17 | 4.34 | 0.053 | 0.7 | 8.637 | 152 |
| Uganda | 37.58 | 0.98 | 21.48 | 0.117 | 0.5 | 7.973 | 147 |
EVD, Ebola viral disease; GDP, gross domestic product; NA, not available.
A summary of the inclusion and exclusion criteria.
| Criteria | Type |
|---|---|
| Inclusion criteria | |
| All publications until 18th August 2014 | Publication date |
| English and French | Publication language |
| Ebola, viral hemorrhagic disease, health systems, globalization, economy | Content |
| Letters, Editorials, Review Articles, Articles | Research design |
| Exclusion criteria | |
| Ebola Cases outside Africa | Scope |
Figure 2.Broad channels of short-term economic impact of Ebola. Adapted from: World Bank. 2014. The Economic Impact of the 2014 Ebola Epidemic: Short- and Medium-Term Estimates for West Africa. Washington, DC: World Bank.73 This is an adaptation of an original work by The World Bank. Views and opinions expressed in the adaptation are the sole responsibility of the author or authors of the adaptation and are not endorsed by The World Bank.
Research and development status of drugs.[95-10][1]
| Drug | Regulatory status | Remarks |
|---|---|---|
| Favipiravir | Approved in Japan the stock piling against Pandemic Influenza | Have been used in France to treat French nun who contracted while in Liberia |
| Lamivudine | Approved for the treatment of HIV/AIDS | A Liberian doctor reported that 13 of 15 patients he treated with Lamivudine out of desperation survived. This finding should be viewed with caution due to the limited sample size and other potential confounders |
| Brincidofovir | Currently being evaluated in Phase III for the treatment of cytomegalovirus and adenovirus | The drug has demonstrated in-vitro activity against Ebola virus and has been granted an emergency approval by USFDA as an investigational treatment for EVD. The drug was used by Texas doctors to treat the first case of Ebola diagnosed in US soil |
| BCX4430 | A broad spectrum antiviral agent originally developed for Hepatitis C | The drug has shown effectiveness against a range of flavi viruses and has received approval from USFDA to progress to Phase I evaluation in humans. |
USFDA, US Food and Drug Administration.
Status of Ebola vaccines under development in 2012.[82]
| Vaccine candidate | Basic R&D | Preclinical | Phase I | Phase II |
|---|---|---|---|---|
| Ebola virus recombinant protein subunit | + | + | ||
| VEE virus replicon particle | + | + | ||
| Kunjin virus replicon particle | + | |||
| Plasmid DNA prime/adenovirus-expressed protein boost | + | + | ||
| Plasmid DNA | + | + | ||
| VLP | + | + | ||
| Various adenovirus-vectored | + | + | ||
| Vesicular stomatitis virus-vectored | + | + | ||
| Paramyxovirus-vectored | + | |||
| CMV-vectored | + | |||
| Combination DNA/VLP | + | |||
| Multi-agent DNA | + | |||
| Vesicular stomatitis virus-vectored multi-agent vaccine (Lassa, Ebola, Marburg) | + | |||
| Prophylactic monoclonal antibodies | + |
R&D, research and development; VEE, Venezuelan equine encephalitis; VLP, virus-like particle; CMV, cytomegalovirus.