Knowledge , Attitudes and Practices of Schoolchildren Towards Epilepsy in Bindura District, Zimbabwe: Implications for school health promotion Ignicious Murambidzi James January Introduction • Epilepsy represents a considerable public health affecting about 50 million people globally with more than 80% living in developing countries (de Boer, Mula & Sander, 2007) • Treatment gaps for active epilepsy exceeded 75% in most low-income countries and less than 10% in high income countries (Meyer, Dua, Ma, Saxena & Birbeck 2010) • Different perceptions and understanding of epilepsy, lack of prioritization, poor medical supply chain, lack of knowledge on epilepsy, stigma and discrimination all contribute to treatment gaps (ILAE,IBE, WHO 2003; Scott, Lhatoo & Sander, 2001) Introduction • Social stigma and discrimination was reported to be more devastating for persons with epilepsy than the seizures themselves (De Boer, Mula & Sander, 2008) • Widespread attitudinal and institutional barriers and prejudices against PWE in education, employment, marriage and other socio economic activities (Atadzhanov et al , 2010) Introduction • KAP studies on epilepsy among teachers noted that teachers lack basic first aid knowledge on seizure management (Mielke, et al. 1997; Birbeck, et al. 2006; Sanya,et al 2005) • Studies on adolescents reported little knowledge about epilepsy and seizures, and perceptions that reflected stigma (MacLeod, & Austin,2003; Austin, Shafer, Deering, 2002) • Study Rationale • The Demonstration Project on Epilepsy in Zimbabwe reported high community prevalence of epilepsy of 13.3/1000 and wide treatment gap 93% (ILAE,IBE WHO, 2003) • Poor understanding of epilepsy, beliefs in supernatural causes, stigma and discrimination notably contributed to the delay in seeking treatment, underutilization of formal health services. Rationale • The study sought to contribute to the knowledge base on community’s perception, attitudes, and practices on epilepsy • Study focused on schoolchildren - reflect their communities’ present and future characteristics. • look forward to developing culturally sensitive and effective educational materials targeting children as social change agents Study purpose Aim - obtain baseline data on the knowledge, attitudes and practices of schoolchildren with respect to epilepsy Objectives • To assess school children’s knowledge of epilepsy • To describe the attitudes and practices of school children with respect to epilepsy. • To discuss the implications of the prevailing knowledge levels, attitudes and practices on the education and management of epilepsy in Zimbabwe. Methods • A total of 523 school going children from three secondary schools in Bindura District Mashonaland Central Province, Zimbabwe • Multi-stage sampling was adopted • The subjects responded to a self administered questionnaire in either English or Shona (local translation) language. • 14-item questionnaire was adapted from a study among secondary school children Cameroon, in 2010 (Njamnshi et al, 2010) • Medical Research Council of Zimbabwe (IRB) reviewed and approved the study Results Sex 229 females 282 males Age 127 (12-14 yrs) 262 (15-17yrs) 124 (18yrs) Mean age 16 years (sd 2) Level 202 (F 1-2) Location 174 (Rural) 226 (F 3-4) 69 (F 5-6) 218 (urban) 131 (CFA ) Results Familiarity with epilepsy • About 87% had heard about epilepsy. • The primary source of information were friends and school (54.7% and 51.4% respectively). • Up to 63% knew someone with epilepsy while 55.04% had witnessed a seizure. • Participants from rural and commercial farming areas were likely to know someone with epilepsy or had witnessed a seizure (P = 0.001) Results Knowledge about epilepsy • There was patchy information on the causes of epilepsy with 28% correctly identifying epilepsy as a brain disorder • 26% reported not knowing the causes of epilepsy. • A number of misconceptions were reported on the causes of epilepsy which included, blood disorder (29%), witchcraft (18%). • No significant differences between knowledge and age, school location and religion Results Practices • On epilepsy first aid, 47% would call for help, 46% would take the person away from danger, 34 % would put something soft under the head for protection • However harmful practices were also common with 17% reporting putting a spoon or cloth in the mouth, 16% pouring cold water and 16% reporting physical restraining • Correct practices were significantly related to age (18+, p= 0.044 ) education (upper level, p=0.002) and school location (urban, p=0.039) Results - Attitudes • Most of the participants had positive attitudes toward persons with epilepsy • Upon knowing someone has epilepsy, 47% reported that will treat him/ her as before. • 51% reported that they would relate more closely and learn more about epilepsy. • Respondents reported having no objections to their children either associating (62%) or marrying (64%) people who sometimes have seizures or fits. • About 80% believed epilepsy is not a hindrance to education. Discussion • Participants were familiar with epilepsy, a result which has also been reported in other African studies (Ndoye, et al. 2005; Njamnshi, et al. 2009) • This could be attributed to the high prevalence of epilepsy in the region • Peers (54.7%) and school (51.3%) were the main primary sources of information thus educational interventions targeting peers and school teachers could be more effective Conclusion • Where, when, and how can children, people with epilepsy and their families receive information??? • Extensive one-on-one from health care providers have practical challenges (Gilliam et al., 2009;) • On delivery of information to young people, Lewis et al. (2010) found that this population wanted to receive information in an ageappropriate format and not during clinic visit Conclusion Way forward • Peer driven programmes can be a powerful and effective strategy to educate and reduce stigma. • Engage youths in the development of campaigns to increase efficacy. • Employ multifaceted approaches, including edutainment, peer education, strengthening school health promotion and media Study Limitations • Study was conducted in one district out of the 65 districts in the country. Given the diverse socio cultural differences, generalisation of study findings are limited • The quantitative nature of the study using structured questions with yes or no answers does not permit exploration of the reasons why the respondents hold particular views about epilepsy. References • Atadzhanov.M, Haworth.A, Chomba.E.N, Mbewe.E.K, & Birbeck.G.L; (2010), Epilepsy associated stigma in Zambia: What factors predict greater felt stigma in a highly stigmatized population?; Epilepsy & Behavior 19, 414–418 • Austin JK, Shafer PO, Deering JB. ( 2002) Epilepsy familiarity, knowledge, and perceptions of stigma: report from a survey of adolescents in the general population. Epilepsy & Behaviour 2002;3:368–75. • Birbeck, GL., Chomba E., Atadzhanov M., Mbewe, E., Haworth, A., 2006; Zambian teachers: What do they know about epilepsy and how can we work with them to decrease stigma?, Epilepsy & Behavior 9 (2006) 275–280 References • de Boer, H.M., Mula., M & Sander W.S, 2008, The global burden and stigma of epilepsy, Epilepsy & Behavior 12 540– 546 • Gilliam, F., P. E. Penovich, C. A. Eagan, J. M. Stern, D. M. Labiner, M. Onofrey, G. L. Holmes, E. Mathis, and J. Cramer. 2009. 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