| Literature DB >> 31318857 |
Robert Colebunders1, Joseph Nelson Siewe Fodjo1, Adrian Hopkins2, An Hotterbeekx1, Thomson L Lakwo3, Akili Kalinga4, Makoy Yibi Logora5, Maria-Gloria Basáñez6.
Abstract
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Year: 2019 PMID: 31318857 PMCID: PMC6638735 DOI: 10.1371/journal.pntd.0007407
Source DB: PubMed Journal: PLoS Negl Trop Dis ISSN: 1935-2727
Updated criteria for OAE [2].
| History of two or more unprovoked seizures, at least 24 hours apart (ILAE | |
| Onset of epilepsy between 3 and 18 years of age | |
| Normal psychomotor development prior to epilepsy onset | |
| No obvious cause of epilepsy identified in the individual during the 5 years preceding seizure onset, such as perinatal brain insult, head trauma, or previous infection of the central nervous system | |
| At least 3 years of residence in an onchocerciasis-endemic village with high epilepsy prevalence |
All five criteria must be met. Additional arguments in favour of OAE include a positive skin snip for Onchocerca volvulus microfilariae or seropositivity to Ov16 antigen confirming exposure to O. volvulus, head-nodding seizures and/or severe unexplained stunting with delayed or absence of external signs of sexual development, or presence of persons with such features in the village.
* ILAE: https://www.ilae.org/.
** An epilepsy prevalence threshold is not included because determining whether the point prevalence of epilepsy is above such a threshold would require conducting an epilepsy prevalence study, which can be complicated and costly or beyond what is feasible and may therefore lead to underreporting of OAE. However, if the epilepsy prevalence is known, a prevalence >2% should be considered as a high prevalence, given that the median epilepsy prevalence in sub-Saharan Africa is 1.4% [24].
Abbreviations: ILAE, International League Against Epilepsy; OAE, onchocerciasis-associated epilepsy.
Fig 1Collaboration between onchocerciasis elimination and mental health surveillance programmes.
In the proposed framework, onchocerciasis mapping efforts should encompass OAE surveillance using simple criteria (Table 2). High onchocerciasis prevalence and/or ongoing transmission warrants reinforcement of onchocerciasis elimination and epilepsy assessment. Detected epilepsy hotspots should become targets for improved management strategies in collaboration with mental health experts. ATS, alternative treatment strategy; CDTI, community-directed treatment with ivermectin; MMDP, morbidity management and disability prevention; NOEC, national onchocerciasis elimination committees; OAE, onchocerciasis-associated epilepsy.
Challenges, opportunities, and needs to fully recognise the public health importance of OAE and use its advocacy to strengthen onchocerciasis elimination programmes.
| Challenge | Needs |
|---|---|
| (1) Strengthen the evidence base to establish causality between | 1) Conduct fundamental research to establish causality and pathophysiological mechanism(s) of seizures, including NS [ |
| (2) Put OAE on the international development aid agenda | 2) Involve affected persons/communities, local leaders, and researchers in advocacy. In contrast with the notion that onchocerciasis no longer represents a public health concern, its substantial burden of disease due to OAE morbidity and mortality should be quantified and recognised |
| (3) Leverage funds and human resources, including community mobilisation, to implement biannual CDTI and vector control activities (including insecticidal and noninsecticidal approaches) | 3.1) Conduct prospective studies to investigate whether increasing CDTI frequency, with or without vector control (including noninsecticidal, community-directed antivectorial measures [ |
| (4) Improve healthcare infrastructure, implement epilepsy surveillance, and train epilepsy healthcare workers | 4.1) Strengthen peripheral health systems by developing community-based epilepsy treatment/care programmes |
Abbreviations: CDTI, community-directed treatment with ivermectin; NS, nodding syndrome; NTD, neglected tropical disease; OAE, onchocerciasis-associated epilepsy.