Acessibilidade / Reportar erro

Training the trainers and disseminating information: a strategy to educate health professionals on epilepsy

Capacitações e multiplicadores: uma estratégia para educação de profissionais da área de saúde na epilepsia

Abstracts

PURPOSE: To evaluate the knowledge, attitudes and perceptions of epilepsy in primary care system health professionals prior to and after an educational intervention. METHODS: Educational interventions were delivered to three groups of people with an interest in epilepsy: 1. Information courses for physicians (241 subjects); 2. Social re-integration course for health professionals and community leaders (631 subjects); 3. "Training the Trainers" Course for physicians (11 subjects). The whole program is flexible and can be tailored for local or regional needs. For the evaluation of this process, health professionals completed a quantitative and qualitative questionnaire to assess their knowledge, attitudes and perception (KAP) of epilepsy prior to the training (pre-test) and 6 months after it (post-test). RESULTS: Comparison of knowledge scores prior to (mean=55.8, standard deviation=14.0) and after (mean=71.5, standard deviation=12.0) the intervention showed that physicians had improved knowledge after the training (t-test=7.8, p<0.001). The same pattern occurred with the health professionals: the knowledge score prior to (mean=22.3, standard deviation=12.5) and after (mean=36.6, standard deviation=12.5) the intervention showed that health professionals had improved knowledge after the training (t-test=12.4, p<0.001). Improvements in attitudes and perception also occurred after the courses. DISCUSSION: Training courses can promote increased knowledge, attitude and perception in a cost effective way in the primary care setting. However, a continuous education program is required to correct oversights and to improve the management of people with epilepsy.

training; educational courses; epilepsy; primary health care; education


OBJETIVO: Avaliar conhecimentos, atitudes e percepção sobre epilepsia de profissionais da saúde do sistema de atenção básica antes e depois de curso de capacitação. MÉTODO: Cursos de capacitação foram realizados em três grupos de profissionais de saúde: 1. cursos de capacitação para médicos (241 sujeitos); 2. cursos de inserção social para agentes comunitários de saúde (631 sujeitos); 3. cursos de replicadores para médicos (11 sujeitos). O programa de capacitação foi adaptado para as condições de cada local. Para avaliar o processo, foram aplicados questionários a respeito do seu conhecimento, sua atitude e percepção perante à epilepsia (KAP) antes dos cursos (pré-teste) e após a intervenção (pós-teste). RESULTADOS: A comparação feita a respeito do conhecimento com médicos mostrou que os mesmos melhoram seu conhecimento com os cursos (pré-teste: nota média=55.8; DP=14,0) vs. pós-teste: nota média=71,5; DP=12,0; t-test=7,8; p<0,001). O mesmo padrão ocorreu com os agentes comunitários de saúde: pré-teste: nota média=22.3; DP=12,5) vs. pós-teste: nota média=36,6; DP=12,5; t-test=12,4; p<0,001. Com relação a atitudes e percepção, foram observadas melhoras significativas depois da realização dos cursos. DISCUSSÃO: Os cursos de capacitação promovem melhoras no conhecimento, atitude e percepção, com baixo custo e de maneira efetiva, no sistema básico de saúde. Entretanto, um programa de educação continuada deve existir para que consiga corrigir os erros e melhorar o tratamento das pessoas com epilepsia.

treinamento; cursos de capacitação; epilepsia; sistema primário de saúde; educação


Training the trainers and disseminating information: a strategy to educate health professionals on epilepsy

Capacitações e multiplicadores: uma estratégia para educação de profissionais da área de saúde na epilepsia

Paula T. Fernandes, MSc, PhDI, II; Ana L.A. Noronha, MD, PhDI, II; Josemir W. Sander, MD, PhD, FRCPIII, IV; Gail S. Bell, MRCGP, MDIV; Li M. Li, MD, PhDI, II

IDepartment of Neurology, Faculty of Medicine, UNICAMP, Campinas, SP, Brazil

IIAssistência à Saúde de Pacientes com Epilepsia – ASPE, Campinas, SP, Brazil

IIIEpilepsy Institute of the Netherlands, SEIN, Heemstede, Achterweg 5, 2103 SW Heemstede, the Netherlands

IVDepartment of Clinical and Experimental Epilepsy, UCL Institute of Neurology, London UK

ABSTRACT

PURPOSE: To evaluate the knowledge, attitudes and perceptions of epilepsy in primary care system health professionals prior to and after an educational intervention.

METHODS: Educational interventions were delivered to three groups of people with an interest in epilepsy: 1. Information courses for physicians (241 subjects); 2. Social re-integration course for health professionals and community leaders (631 subjects); 3. "Training the Trainers" Course for physicians (11 subjects). The whole program is flexible and can be tailored for local or regional needs. For the evaluation of this process, health professionals completed a quantitative and qualitative questionnaire to assess their knowledge, attitudes and perception (KAP) of epilepsy prior to the training (pre-test) and 6 months after it (post-test).

RESULTS: Comparison of knowledge scores prior to (mean=55.8, standard deviation=14.0) and after (mean=71.5, standard deviation=12.0) the intervention showed that physicians had improved knowledge after the training (t-test=7.8, p<0.001). The same pattern occurred with the health professionals: the knowledge score prior to (mean=22.3, standard deviation=12.5) and after (mean=36.6, standard deviation=12.5) the intervention showed that health professionals had improved knowledge after the training (t-test=12.4, p<0.001). Improvements in attitudes and perception also occurred after the courses.

DISCUSSION: Training courses can promote increased knowledge, attitude and perception in a cost effective way in the primary care setting. However, a continuous education program is required to correct oversights and to improve the management of people with epilepsy.

Key words: training, educational courses, epilepsy, primary health care, education.

RESUMO

OBJETIVO: Avaliar conhecimentos, atitudes e percepção sobre epilepsia de profissionais da saúde do sistema de atenção básica antes e depois de curso de capacitação.

MÉTODO: Cursos de capacitação foram realizados em três grupos de profissionais de saúde: 1. cursos de capacitação para médicos (241 sujeitos); 2. cursos de inserção social para agentes comunitários de saúde (631 sujeitos); 3. cursos de replicadores para médicos (11 sujeitos). O programa de capacitação foi adaptado para as condições de cada local. Para avaliar o processo, foram aplicados questionários a respeito do seu conhecimento, sua atitude e percepção perante à epilepsia (KAP) antes dos cursos (pré-teste) e após a intervenção (pós-teste).

RESULTADOS: A comparação feita a respeito do conhecimento com médicos mostrou que os mesmos melhoram seu conhecimento com os cursos (pré-teste: nota média=55.8; DP=14,0) vs. pós-teste: nota média=71,5; DP=12,0; t-test=7,8; p<0,001). O mesmo padrão ocorreu com os agentes comunitários de saúde: pré-teste: nota média=22.3; DP=12,5) vs. pós-teste: nota média=36,6; DP=12,5; t-test=12,4; p<0,001. Com relação a atitudes e percepção, foram observadas melhoras significativas depois da realização dos cursos.

DISCUSSÃO: Os cursos de capacitação promovem melhoras no conhecimento, atitude e percepção, com baixo custo e de maneira efetiva, no sistema básico de saúde. Entretanto, um programa de educação continuada deve existir para que consiga corrigir os erros e melhorar o tratamento das pessoas com epilepsia.

Palavras-chave: treinamento, cursos de capacitação, epilepsia, sistema primário de saúde, educação.

Integral care for people with epilepsy includes seizure control, psychological support and social integration assuring adequate quality of life1. People with epilepsy and their families can be helped if measures are adopted to reduce stigma, increase awareness that epilepsy can be treated and rehabilitate those who suffer from epilepsy2,3.

Epilepsy is the most common serious neurological condition4. An epidemiological study in São Paulo State found a lifetime prevalence of epilepsy of 9.2/1,000 [95% CI 8.4-10.0]5. Stigma is present in our society, excluding people with epilepsy from social activities, particularly because of misinformation but also due to lack of appropriate attitudes held by health professionals3.

The treatment gap (lack of treatment or inadequate treatment) shows regional variation but, in general, inadequate or no treatment is a reality for a significant number of people with epilepsy. The majority of people with epilepsy can be classified as having problems of low complexity as seizures can be controlled with one low cost anti-epileptic drug (AED). These are the people with epilepsy who can effectively be treated in the primary care system6.

Nevertheless, in order for epilepsy to be managed in the primary care setting, knowledge about epilepsy needs to be enhanced among health professionals7. In addition to medical knowledge, a psychosocial approach is required to improve seizure control1. To some extent, a positive attitude held by health professionals helps to promote appropriate behaviour by patients8.

The phase II of the Demonstration Project on Epilepsy part of the Global Campaign Epilepsy Out of the Shadows-WHO-ILAE-IBE in Brazil, executed by ASPE, Assistência à Saúde de Pacientes com Epilepsia9, focused on educational interventions to improve knowledge, attitudes and perceptions of health professionals and school teachers. Here we describe the development of different modules of educational intervention and their results when applied to primary care health professionals.

METHOD

The development of educational modules followed three main steps: 1. identification of target groups; 2. definition of the objective of the intervention; 3. definition of the teaching contents. The overall goal was to educate health care workers to provide bio-psycho-social management for people with epilepsy and to provide self-sustained education within the network. The primary care setting, particularly in the Family Physician Program model, includes a team of multi-disciplinary professionals, which can be divided into physicians and other health professionals, particularly health agents and community leaders. The courses were developed for these three groups:

Module 1. Information courses for physicians – This course is of eight hours duration and can be delivered to 35-40 people at a time. The main purpose is to provide pragmatic information on the management of people with epilepsy, including:

– The nature of epilepsy.

– Epilepsy diagnosis.

– Epileptic seizures.

– Treatment.

– Epilepsy in special situations (women, older people, and children).

– Myths and beliefs.

– Psycho-social aspects (stigma, quality of life).

For physicians, the main diagnostic aspect of this module is centred on three questions: is it epilepsy? (yes or no); is the seizure partial or generalized?; what is the cause of epilepsy? (symptomatic, idiopathic, or cryptogenic). With regard to the second question, the professional is advised to ask directly whether the patient has absence spells or myoclonic jerks, as the answer has implications for choosing the antiepileptic drug. The answers to these questions provide a framework of epilepsy management. Where doubt persists, patients should be referred to neurologists.

Module 2. Social re-integration course for health professionals and community leaders – This course is of three hours duration and can be delivered to 60 to 80 people at a time. The objective is to educate these professionals on the main bio-psycho-social aspects of epilepsy to promote the dissemination of correct information in the community. After this course, the health care workers should be able to provide and articulate social support to people with epilepsy. The themes covered are: epilepsy (definition, prevalence, seizures and treatments), psycho-social aspects (social difficulties, prejudice and stigma) and strategies to deal with prejudice and stigma. The aim is to promote advocacy groups for people with epilepsy to enable social re-integration. This module highlighted the importance of working in groups for people with epilepsy, enabling the professionals to set up advocacy groups in their communities, to empower patients and their families on their rights and duties as citizens.

In addition to these educational courses, we devised a course to provide self-sustained education within the healthcare network. This aims to train a physician to provide education to the rest of the team.

Module 3. "Training the trainers" course for physicians – This course is of 20 hours duration (three days) and can be delivered to up to 30 people at a time. It is important that there is a prior agreement with the site health manager to allow the information courses to run, and that there is a supply of support materials. This module aims to prepare physicians to pass on the information on epilepsy to other health staff, providing a self-sustained education program within their health network. This course covers the following aspects: medical aspects (epilepsy diagnosis, epileptic seizures and prevalent syndromes, special situations, treatment with anti-epileptic drugs (AEDs), differential diagnosis, investigations; psychological aspects (self-esteem, self-confidence, depression, anxiety, stigma and quality of life); social aspects (social inclusion).

Participants received teaching material to enable them to run information courses in their communities. This consists of a CD with the lectures as power-point presentations, a booklet with the main aspects taught in the module and a guideline for AED prescription with four first line AEDs (carbamazepine, sodium valproate, phenobarbital and phenytoin). Specific booklets were also prepared for the other courses.

The whole program is flexible and can be tailored for local or regional needs. For the evaluation of this process, health professionals completed a quantitative and qualitative questionnaire regarding their knowledge, attitudes and perception (KAP) of epilepsy prior to the training (pre-test) and 6 months after it (post-test). This questionnaire was developed following a standard process for its elaboration and validation10. Briefly, the steps of the process are the following:

– Definition of the theme of interest: A literature review was undertaken and the current knowledge of epilepsy in the primary care setting was established.

– Delimitation of the population: Multi-disciplinary primary care health workers (physicians, nurses, psychologists, social workers, dentists, physical therapists), divided into physicians and non-physicians.

– Definition of item: We defined which type of possible answer (for example, multiple choice, true or false, scale) would best fit each question.

– Designing the questionnaire: The items of the questionnaire were elaborated by a panel of experts in the field of epilepsy. Different questionnaires were designed for the different target populations: physicians and non-physicians. The questionnaire for physicians included questions regarding medical management (drugs, diagnosis and investigations), in addition to attitudes and perceptions.

Each question in the knowledge section of the questionnaire was given a score for the correct answer, and the final grade was based on the total score achieved, as a percentage between zero and 100 (see appendix appendix ), so that we could compare the performance prior to and after the training. We did not identified the respondents, thus a non-paired t-test was used to assess significance of the score achieved prior to and after the training.

RESULTS

The results are presented separately for the three modules.

Module 1. Information courses for physicians – The information courses were provided in different towns of Brazil: Campinas, Rio de Janeiro and São José do Rio Preto in the Southeast; Anápolis, Campo Grande in the Central-west; Cabedelo, Sousa, Patos, in Northeast Brazil, Joinville and Londrina in South Brazil.

Questionnaires were completed by 241 physicians (194 subjects in the pre-test and 47 subjects in both pre and post-test). Table 1 shows the main characteristics of the subjects.

Comparison of knowledge scores achieved prior to (mean=55.8, standard deviation=14.0) and after the course (mean=71.5, standard deviation=12.0) showed that the knowledge of physicians was improved after the training (t-test=7.8, p<0.001) (Fig 1).


The pre and post-information results on attitude and perception about epilepsy for physicians are presented in Tables 2 and 3.

Module 2. Social re-integration course to health agents and community leaders – This module was run in Campinas, São José do Rio Preto, in the Southeast region, Anápolis, in the Central-West, Cabedelo, João Pessoa, Patos and Sousa, in the Northeast region. Altogether 631 non-graduate health professionals (Table 4) completed the questionnaires (484 pre-test and 147 both pre and post-test).

Comparison of knowledge scores prior to (mean= 22.3, standard deviation=12.5) and after the course (mean=36.6, standard deviation=12.5) showed that health agents had improved knowledge after the training (t-test=12.4, p<0.001) (Fig 2).


The subjects’ pre- and post-test results on attitude and perception about epilepsy for the second module are presented in Tables 5 and 6.

Module 3. Training the Trainers Course for physicians – This module was provided in Campinas with the support of Unicamp, the Division of Mental Health of the Brazilian Ministry of Health and the Pan-American Health Organization (PAHO). Physicians in 11 Brazilian towns participated.

Following this course, eleven physicians were enabled to be trainers.

Figure 3 shows the outcome of this activity, with follow-up activity carried out by five of eleven participants.


In the towns of Londrina, Joinville, Vitória da Conquista and Campo Grande, the physicians delivered information courses to the team of primary care health workers in the Family Physician Program. The physician from Cabedelo in Paraiba state went further by cooperating with local and State Health Departments in promoting a large scale information course for 610 health professionals, of whom 140 were physicians including 25 trainers. These professionals were from all over the state. This course was delivered by four ASPE personnel with the assistance of PAHO.

Contact was lost with the physicians from Imperatriz and Belém. In the other towns, no further activities were carried out mainly due to lack of cooperation by local health administrators.

In all modules, participants expressed their opinions or wrote comments about the course. The general opinion was that the teaching methodology was simple with pragmatic information, which helped to simplify the management and treatment of epilepsy. The participants therefore felt more confident after completing the courses.

DISCUSSION

Here we describe information courses for primary health care professionals, aiming to improve the management of people with epilepsy in the context of the Brazilian Demonstration Project of the Global Campaign Against Epilepsy. We found that in the public health context, information courses can promote better management of epilepsy, including most common medical, psychological and social aspects associated with epilepsy, through increased knowledge, attitude and perception.

In Brazil, medical services for epilepsy particularly at primary care level are often of poor quality mainly due to the lack of knowledge and information7. For this reason, providing basic information and knowledge about the condition to primary care teams may lead to improvements in epilepsy care at this level7.

The results were largely positive, and showed that the modules seem to improve knowledge, and change attitudes towards and perception of epilepsy, as shown by the significant differences between the pre-test and post-test scores in the modules. On average physicians improved by 16%; and health agents improved by 14%. It is important to highlight that the interval between the questionnaires was six months in each group. Thus these data suggest that people retain knowledge. Nevertheless, the knowledge of health agents even after the training was still below 50%, and some questions were still answered inappropriately by some physicians. These facts reinforce the necessity of continuous education in order to correct oversights and improve the management of people with epilepsy.

The qualitative assessment of the training the trainers’ module suggests that these low cost courses are highly effective and can quickly expand the information programme. Originally 11 physicians were trained and, after the course, these professionals trained a further 810 new health professionals, including workers of the primary care teams. This module allows a fast and effective expansion of the information courses covering health staff in many areas of the country.

Theoretically, it should be possible for the information module to be used to provide basic epilepsy education to the whole primary care system in Brazil, which consists of around 60,000 Basic Health Units (BHU). The Family Physician Program currently has about 25,000 teams distributed over 5,000 locations11. Each team comprises a physician, a nurse, a nurse assistant, and four to six health agents, and provides health care for an average of 1,000 families. This represents health care for over 79 million people. We suggest the use of large scale information courses run either regionally or at state level, to disseminate basic information. Running the courses in each state is more feasible than a regional approach because of political boundaries. A mathematical exercise can illustrate how 25,000 teams can be provided with basic information. Using the large scale information course conducted in the state of Paraíba (attended by 610 health professionals, including delivering the "training the trainers" module for 25 physicians) as an example, and assuming that each trainer would then run three courses for 35 primary care physicians per course, this would provide education for 2,625 physicians. Thus, in theory, it only would require only 10 large scale information courses to reach all the physicians of the 25,000 teams of Family Physician Program.

The information courses showed that health professionals can improve their knowledge, attitude and perceptions regarding epilepsy. These modules (1 and 2) showed a decrease of doubt in all aspects of epilepsy, especially the perception of epilepsy: the negative beliefs and myths about this condition were better comprehended and the doubts decreased a lot. The physicians (module 1) learned how to diagnosis and to manage patients with epilepsy, minimising neurologist referral, and learned about specific issues concerning women, causes and investigations. The other health professionals (module 2) could understand certain aspects about epilepsy, including perceptions, implications for women, diagnosis of epilepsy and beliefs.

Epilepsy should be regarded as a public health problem, and most cases are of low medical complexity which, according to the WHO, should easily be managed at primary care level. We believe that this is possible if resources are directed towards making treatment and rehabilitation accessible for patients via a broad action based on the Primary Health Care. The psycho-social and economic impact of epilepsy demands a broad and sustained medical and social action.

In conclusion, training courses can promote increased knowledge, attitude and perception in a cost effective way in the primary care setting. However, a continuous education program is required to improve the management of people with epilepsy.

Dr. Li Li Min - Department of Neurology / UNICAMP - Cx. Postal 6111 - 13083-970 Campinas SP - Brazil. E-mail: limin@fcm.unicamp.br or li@aspebrasil.org; Site: http://www.aspebrasil.org

  • 1. Suurmeijer TP, Reuvekamp MF, Aldenkamp BP. Social functioning, psychological functioning, and quality of life in epilepsy. Epilepsia 2001;42:1160-1168.
  • 2. Baker G. The psychosocial burden of epilepsy. Epilepsia 2002;43:26-30.
  • 3. Fernandes PT, L LM. Estigma na epilepsia. 1-207. 2005. Departamento de Neurologia - FCM/UNICAMP. PhD Thesis.
  • 4. Sander JW. Global campaign against epilepsy: overview of the demonstration projects. Epilepsia 2002;43(Suppl 6):34-36.
  • 5. Noronha ALA, Borges A, Marques LH, et al. Prevalence and pattern of epilepsy treatment in different social-economic classes in Brazil. Epilepsia, **(*):16, 2007, doi:10.1111/j.1528-1167.2006.00974.
  • 6. Noronha AL, Marques LH, Borges MA, Cendes F, Guerreiro CA, Min LL. Assessment of the epilepsy treatment gap in two cities of south-east of Brazil. Arq Neuropsiquiatr 2004;62:761-763.
  • 7. Kendall S, Thompson D, Couldridge L. The information needs of carers of adults diagnosed with epilepsy. Seizure 2004;13:499-508.
  • 8. DiIorio C, Shafer PO, Letz R, Henry T, Schomer DL, Yeager K. Project EASE: a study to test a psychosocial model of epilepsy medication management. Epilepsy Behav 2004;5:926-936.
  • 9. Li LM, Sander JW. National demonstration project on epilepsy in Brazil. Arq Neuropsiquiatr 2003;61:153-156.
  • 10. Bunchaft G, Cavas CST. Sob medida: um guia de elaboração de medidas do comportamento e suas aplicações. 2002.
  • 11. Oliveira AMF, Zanolli MLA ampliação do programa de saúde da família no Brasil: conquistas e desafios. 2006. Boletim da Faculdade de Ciências Médicas da Unicamp.

appendix

Publication Dates

  • Publication in this collection
    29 Nov 2007
  • Date of issue
    June 2007
Academia Brasileira de Neurologia - ABNEURO R. Vergueiro, 1353 sl.1404 - Ed. Top Towers Offices Torre Norte, 04101-000 São Paulo SP Brazil, Tel.: +55 11 5084-9463 | +55 11 5083-3876 - São Paulo - SP - Brazil
E-mail: revista.arquivos@abneuro.org