Scientific Program

Conference Series Ltd invites all the participants across the globe to attend World Congress on Epilepsy and Brain Disorders Cape Town, South Africa.

Day 1 :

Keynote Forum

Ann Marie O’Connor

International Speaker, Canada

Keynote: Epilepsy surgery: Left selective Amygdalohippocampectomy
Conference Series Epilepsy Congress 2018 International Conference Keynote Speaker Ann Marie O’Connor photo
Biography:

Ann Marie O’Connor is an Education Assistant for Grades K-12, where she works primarily with students who suffer from FAS/ ADHD and ODD. She is also a Canadian Advocate for Epilepsy and former Vice President for the Edmonton and Northern Alberta Epilepsy Association, where she was on the Board of Directors for over 11 years. She has published two books and had several articles written on her behalf (Surgical Neurology International/Your Health Magazine/Spruce Grove Examiner) as well as she has been interviewed on Global Edmonton and Breakfast Television Edmonton. Her topics of discussion are Women and Epilepsy-Sex and Seizures-Depression-Side effects of R-Her surgery-Books published. In Canada alone, an average of 42 people a day learn that they have Epilepsy and over 50 million people worldwide suffer from the disorder. I can say that I Beat Epilepsy. It was 6:30 AM on December 03, 2002. I remember being wheeled down the hall at the University of Alberta Hospital in Edmonton, Alberta, Canada by the porter with the silence it felt like we were the only ones in the building. You could hear a pin drop. I had lived with epilepsy for almost 20 years of my life and that was about to change. Left selective Amygdalohippocampectomy is the surgery I was about to undergo and it is what cured me of my seizures. The left parahippocampalgyrus, left amygdale and left hippocampus were removed; structures within the left temporal lobe. I had 6 seizures 2 days before the surgery and I have not had one since. Since my surgery, I have accomplished some amazing tasks in my life. I have written two books, was asked to be a Canadian Advocate for Epilepsy in 2012 and have been a motivational speaker for over 8 years. Helping others is my passion, is my calling. I want to educate others internationally from a patient’s point of view, help them understand that they are not alone when it comes to living with epilepsy.

Abstract:

• Her energy and enthusiasm are contagious! Along with this her life experiences and talent make her a top candidate for your speaking engagement. I would be happy to communicate with you at any time regarding my sincere recommendation of Ann Marie. I know your audience will walk away energized and inspired. Chuck Carmen, Executive Director at Epilepsy Association of Central Florida, Inc. Orlando, Florida
• Ann speaks from the heart! Her personal experience has given her an awareness that is often unmatched and has helped her navigate a very complex journey. When working with Ann, we discovered a passionate and sincere woman who wanted nothing more than to be helpful and giving. Gary Collins, Toronto, Ontario, Epilepsy Canada
• I had the privilege of welcoming Ann to our grade 9 health class to give a presentation on Epilepsy and her own personal journey. This was an incredible addition to our health unit as it is something that wouldn't typically be covered in our curriculum, but very beneficial to our students. Ann is very comfortable and confident speaking to a group of teenagers, constantly encouraging student engagement and creating positive interactions. Ann presents her journey and diagnosis to the students in a way that made them feel as though they could ask her anything, students took a genuine interest in the topic. Jenaya Whalen Duffi eld School, Alberta, Canada Grade 8-9 Teacher
• Don't let epilepsy take control of you. Epilepsy is not easy but Ann Marie O’Connor is a survivor of epilepsy, she taught me that I should never give up on anything in life - Ann O’Connor did not give up! Ashlyn

Break: Networking and Refreshments Break with Group Photo
  • Epileptic Seizures | Chronic Disorder | Neurological Disorder | Seizure Disorders | Psychiatric / Psychological disorders | Pediatric Epilepsy | Alternative Treatments
Location: Cape Town, South Africa
Speaker

Chair

Guillermo Nicolás Jemar

TREMA Mental Health and Neurosciences, Argentina

Session Introduction

Guillermo Nicolás Jemar

TREMA Mental Health and Neurosciences, Argentina

Title: Clinical cognitive behavioral manifestations in epileptic patients
Speaker
Biography:

Guillermo Nicolás Jemar is a Doctor (National University of Córdoba Specialist in Psychiatry, Hospital José T. Borda and Maimónides University) and is a Specialist in Neuropsychiatry and Cognitive Neurology (University of Buenos Aires). He has done his Masters in Neuroscience (Maimónides University). He also has received an International Fellowship from the American Psychiatric Association (APA). And also an International Member of the European Psychiatric Association (EPA). He is the Director of the Senior Annual Course in Cognitive Neuroscience applied to Personality Disorders and psychopathies of the Argentine Society of Personality Disorders and Psychopathies, from the year 2016 to the present. Director of TREMA Mental Health and Neurosciences. He is the Founding Partner of the Ibero- Latin American Society of Neuroscience and Psychiatry (AINLANCYP) and Member of the psychoneuroimmunoendocrinology and Dual Pathology Chapters of the World Psychiatric Association (WPA). He is one of the founders and Treasurer of the Argentine Society of Disorders of Personality and Psychopathies (SATP). Vice-president of the Psychiatry Chapter of the Penitentiary Services of the Association of Argentine Psychiatrists (APSA).

Abstract:

During recent years, the Neurosciences have provided valuable studies and empirical information about atypical clinical presentations in epileptic patients, who most oft en attend interconsultation with Neuropsychiatry. Among these Manifestations, impulsiveness and disruptive behaviors are those that generate clinical disquisitions between epilepsy and the basic structuring of the subject's personality. Alterations in higher brain functions, especially mnesic failures, but also depletion in attention and cognitive decline in general are manifestations that limit social cognition and patients' relationship life. It is also known that sensoperceptive alterations appear when there are psychotic symptoms, among which the delusional ideation of a mystical type is more frequent. Th e cognitive decline is marked by the course of thought, and evolutionarily the content of it. Patients are losing agility, their language becomes sticky, reduced and persevering, losing the fl uidity that leads to free and easy association. In the present paper we propose to analyze the sign symptomatology of the epileptic patient that presents alterations in the structuring of the personality, failure in the control of the impulses and in the behavior and cognitive decline characterized by progressive loss of the superior cerebral functions and sensoperceptive alterations

 

Speaker
Biography:

Claire Lownie graduated with her medical degree (MBBCh) from Wits University in 2003. She completed her internship at Groote Schuur Hospital (2004) and her community service at a district hospital in Kokstad (2005). In 2006, she was diagnosed with a Stage-4 Malignant Melanoma. Thereafter, Dr Lownie worked for several years as a clinical trial coordinator, research programme manager and ultimately Trauma Programme Manager at Milpark Hospital. She completed a Master of Science in Emergency Medicine degree (MSc Med Emergency Medicine) and worked clinically in various private Emergency Departments. In 2012 Dr Lownie left Netcare to work in the corporate pharmaceutical environment. The combination of personal and professional experiences piqued her interest in Psychiatry and mental health. She subsequently completed her specialist training in the Department of Psychiatry at Wits Universit and obtained her specialist fellowship (FC Psych SA) through the Colleges of Medicine of South Africa in May 2018. Dr Lownie currently runs her private practice in Bryanston. She treats a variety of mental illnesses and is passionate about working with children and adolescents.

Abstract:

Aim & Objective: Conduct Disorder is a serious psychiatric disorder with onset in childhood and adolescence and antisocial behaviour which may continue into adulthood. Characteristic externalising behaviours have the potential to negatively impact

on the wellbeing of the individual as well as on societal interactions. Th e aim of this study was to review the records of children and adolescents with a diagnosis of Conduct Disorder at a local specialised psychiatric hospital to identify possible associated factors.

Method: Clinical fi les at Th e Tara, H. Moross Centre’s Child and Adolescent Clinic were reviewed and those with Conduct Disorder were identifi ed. Variables in the dataset included gender, referral source, age at symptom onset, age when diagnosis was made, schooling, co-morbid diagnoses, pregnancy/ birth history, perinatal complications, attachment, primary caregiver, milestones, discipline style, exposure to violence/ abuse/ neglect, social circumstances, other conditions that may be a focus of clinical attention (“V” or “Z” codes), family psychiatric history and interventions. Descriptive and comparative statistical analyses of the data were performed.

Result: A total of 953 fi les were reviewed, of which 107 (11.2%) of the mental health care users were diagnosed with having Conduct Disorder. Associated factors included: (1) having a parent as the primary caregiver seemed to have been a protective

factor; while (2) exposure to violence, abuse or neglect, having a family history of Antisocial Personality Disorder, or having 2 or more “V” or “Z” codes, were signifi cantly more oft en associated with severe conduct disordered features.

Conclusion: Considering these factors associated with an increased risk, may help to develop strategies for earlier detection and intervention in children and adolescents at risk.

Temitope Farombi

University College Hospital, Nigeria

Title: Hormal profile of females with epilepsy in Nigeria

Time : 12:30-13:00

Speaker
Biography:

Temitope Farombi MD, FMCP (Neurology), is a graduate of University of Ibadan. She trained in internal medicine at the University College Hospital (UCH) and Neurology at UCH Ibadan Nigeria. Obtained a master’s degree in Clinical Neuroscience at King’s College London. Temitope is a Consultant Neurologist at the Chief Tony Anenih Geriatric center University college hospital, the first geriatric center in West Africa sub-region. The Temitope practice specializes in the critical care neurology of the elderly, movement disorders, Dementia, and headaches. Temitope was a visiting scholar to the Northwestern University Chicago, USA and has published articles in scientific journals.

Abstract:

Aim: Th e uncommon occurrence of peri-menstrual (C1) catamenial epilepsy in our routine epilepsy clinic, and the absence of a statistical diff erence in the frequency of clinically signifi cant sexual dysfunction between female with epilepsy (FEW) and their matched controls informed this study. We compared the sex hormones between FWE and their age-matched controls. We postulated that a diff erence in etiology, with a higher prevalence of structural etiology in sub-Saharan Africa, may be associated with an unexpected hormonal profi le.

Method: An observational study carried out at the University College Hospital, Oyo State – a tertiary hospital in South- Western Nigeria involving seventy-five FWE and forty-five age-matched controls. Samples for hormonal evaluation at preovulatory phase – on the 10th–13th day of the cycle and luteal phase – on the 21st–24th day were taken

Result: FWE had lower FSH levels when compared to controls, p: 0.012. In the pre-ovulatory phase, Further stratification shows a higher FSH level among FWE on medication, p: 0.003. Controls had similar LH/FSH ratio with FWE on medication while FWE not on medication having a higher LH/FSH ratio, p: 0.026. In the mid-luteal phase, FSH level was lowest in FEW not on medication), FWE on medication had higher levels but lower when compared to the control group, p: 0.002. FEW had lower progesterone levels when compared with the control group, p: 0.004 with no difference with the use of AEDs. The E/P ratio showed a reverse picture with FWE having higher values when compared to controls, p: 0.002. There was no significant difference in the levels of LH, LH/FSH ratio, estrogen, E/P ratio, and testosterone between FWE and controls.

Conclusion: Menstrual abnormalities and abnormal FSH and progesterone are commoners in FWE than controls in our population.

Break: Lunch Break 13:00-14:00 @ Restaurant
Biography:

Jason Labuschagne completed his MBBCh in 1999 and obtained his MMED in Neurosurgery in 2006. He is currently the head of Paediatric Neurosurgery at the Nelson Mandela Children’s Hospital and a lecturer in the Department of Neurosurgery at the University of the Witwatersrand.

Abstract:

Vagus nerve Stimulation (VNS) has been shown to be effective in reducing seizure frequency. Traditionally, the left Vagus nerve is stimulated in ongoing cycles along with user-initiated stimulation by passing a magnet across the implanted device at the time of the perceived seizure onset. However, manual application of the magnet at the time of the perceived seizure may not be feasible for a variety of reasons. An automated method to initiate stimulation at the start of the seizure would be beneficial in these circumstances. Approximately 70% of focal onset seizures are associated with tachycardia. One method of delivering stimulation is to use the detected tachycardia to initiate automated stimulation. A prospective, unblinded, single-center study was performed. Ten subjects all of whom were younger than twelve years of age, who could not perform manual stimulation were treated using the AspireSR VNS therapy device. Baseline seizure frequency data was collected along with postbaseline seizure frequency data. Quantitative seizure severity, pre and post insertion, was collected, using the Hague Seizure Severity Scale. Baseline and postbaseline quality of life data, using the QOLCE-55 questionnaire were obtained. Responder rate, along with the Engel and McHugh classification of outcomes were collected. Adverse events were systematically collected and reported. Our minimum period of six months follow up data is reported.

Elzette Struwig

University of Pretoria, South Africa

Title: The Ketogenic Diet (KD) for the management of Refractory Epilepsy

Time : 15:30-16:00

Speaker
Biography:

Elzette Struwig completed her dietetics degree at the University of Pretoria, South Africa, after which she worked internationally in the development of ketogenic diet and ketogenic diet products for epilepsy. She has also undergone her Ketogenic diet training at Matthew’s Friends KwetoCollege in the UK. Elzette is now the director of Metabolic Med, a ketogenic diet and low-carbohydrate, high-fat dietetics practice in Pretoria, South Africa.

Abstract:

The Ketogenic Diet (KD) is a high fat, adequate protein and low carbohydrate diet. Th e hallmark of the KD is the production of ketone bodies by the liver which becomes the brain’s primary source of energy. Th e KD has been applied in individuals with refractory or also known as drug-resistant epilepsy since the 1920s. Th e diet was discovered by the observation of decreased seizure frequency during episodes of fasting. In 1921, Dr. Wilder at Mayo clinic suggested the KD for the long-term management of epilepsy. In terms of this suggestion, it was stated that the benefi ts of fasting could be recreated through the implementation of a KD. Additionally, the KD could be sustained for a much longer period as it compensates for the clear disadvantages associated with a prolonged period of fasting. Initial anti-seizure drug (as standalone therapy) control seizures in approximately half of patients with newly diagnosed epilepsy. Th e remaining half of the patients, normally those suff erring from drug-resistant/refractory/intractable epilepsy, may benefi t from the KD. Systemic reviews of KD therapies in children with refractory epilepsy suggest that 33 - 56% of children achieve ≥50% seizure reduction and approximately 16% achieve seizure freedom. Th e KD and variants thereof has shown promising results in those (from infancy to adulthood) suff erring from refractory epilepsy and should be recommended by medical professionals aft er two trials of anti-seizure medication has proven to be unsuccessful.

 

  • Workshop
Location: Cape Town, South Africa
Speaker

Chair

Adriaan Du Plessis

Nulife Counselling & Wellness, South Africa