Quality of life among epileptic patients in Qassim Region, KSA ============================================================== * Raghad M. Altwijri * Moath S. Aljohani * Haifa K. Alshammari ## Abstract **Objectives:** To explore the influence of epilepsy on quality of life (QoL) among people with epilepsy in Saudi Arabia, and its association with sociodemographic and clinical characteristic aspects in the Qassim region. **Methods:** A cross-sectional multi-centered study done in the Qassim region from June 2018 to May 2019. A self-administered questionnaire was provided to 216 participants who attended the neurology clinic. We used a validated Arabic version of the QoL in Epilepsy (QOLIE-31) to measure the QoL. **Results:** The mean of the overall QOLIE-31 score was 64.23 ± 17.8. we found that employment status had a significant influence on the overall score (*p*<0.001) and all other QOL domains (rho ranged from -.136 for energy fatigue to -.193 for social function) Patients with focal seizures were significantly higher in emotional wellbeing (rho=-.159), seizure worry (rho=-.226), cognitive function (rho=-.166) and overall score (*p*=0.010) than patients with the generalized type. Monotherapy patients have higher scores in total (*p*<0.001) and all subscales except seizure worry and emotional wellbeing than those on polytherapy. **Conclusion:** Employment status, type of seizure, and AED number are the most important factors affecting Saudi patient’s QoL. Many studies in multiple countries have tested quality of life (QoL) in epilepsy, and have highlighted areas of common concern. It has been shown that among Arabian people, epileptic patients are generally more susceptible to having higher levels of anxiety and depression.1 In Kenya, researchers have compared QoL between persons with epilepsy (PWE) and healthy people who have the same environment, social relationship, and living circumstances. These authors found that low education level, unemployment rate, unskilled employment, and low income were higher in PWE compared to their non-epileptic accompanying people.2 Despite the high prevalence rate in Saudi Arabia (6.54 per 1000),3 there has been limited research about the impact of QoL in epileptic patients. To better identify the factors that influence Saudi epilepsy patients, here we explore the influence of epilepsy on QoL among Saudi epileptic patients. ## Methods A cross-sectional study was carried out in the Neurology Clinic at King Fahad Specialist Hospital, King Saud Hospital and Buraidah Central Hospital in Qassim from June 2018 to May 2019. Our inclusion criteria included: patients diagnosed with epilepsy by a specialist, and able to complete the questionnaire. Patients with progressive central nervous system (CNS) disease, acute or severe chronic CNS diseases, disturbance of consciousness, language dysfunction, history of psychiatric illness, history of drug abuse, and patients whose type of seizure was not specified were excluded. Our study consisted of 228 epileptic patients, and we excluded 12 patients who were diagnosed as structural epilepsy, but seizure type was not specified. We used the PubMed database to search for prior related studies using the keywords “quality of life” “epilepsy”, and “QOLIE-31”, filtering for studies published in the last 5 years. A self-administered questionnaire included three main compartments: demographics (gender, age, marital status, educational level, employment status); clinical characteristics of the seizure [age of onset, duration of epilepsy, number of AEDs, and medical history of chronic diseases (e.g., diabetes, hypertension, asthma, and others)]; and the type of seizure. We used a validated Arabic version of the QOLIE-31 (developed by 1993, Rand, translated by Alaa Eldin Elsharkawy, 2015). It measures QoL in epileptic patients through 7 subscales: 5 items for seizure worry testing, 5 items for emotional role functioning, 4 items for energy/fatigue, 6 items for cognitive functioning, 3 items for medication effects, 5 items for social role functioning, 2 items for overall QoL, and one item for overall health. Each scale was converted into a 0–100 scale in which the value is distributed evenly for each question (the lower the score, the greater the disability). Official approval from the Regional Ethical Committee (20180601, June 3, 2018) and responsible authorities was obtained. The objectives of our study were clarified to the participants by stressing the importance of the data and its confidentiality. There was no obligation to participate. Informed consent was provided to each participant before starting the questionnaire. Data were coded in the Excel sheet database using a unique identification number. The data information was saved in a password-protected laptop belonging to the Principal Investigator and CI, and all data were kept confidential. Only the research team had access to the database for analysis purposes. All aspects of the study were in accordance with the Helsinki declaration. The Statistical Package of Social Science (SPSS 23 for mac, IBM, Chicago, United States evaluation version) software was used for the analysis. Categorical variables were presented as frequencies (n) and proportions (%). T-tests and one-way analysis of variance (ANOVA) were used to compare the overall QOLIE-31 scores between the groups, and the Spearman correlation coefficient was used to measure its relation with the different subscales. We used a multiple linear regression model to control for confounders. Internal consistency reliability assessment of the Arabic version of the QOLIE-31 scale was assessed by Cronbach’s alpha. The final overall QOLIE-31 score was 0.885 ## Results The mean (±standard deviation) age of the participants was 30±12 years. **Table 1** shows the demographic and clinical characteristics of the participants. The overall mean QOLIE-31 score was 64.23±17.8 (maximum possible score=100). The highest domain score was for social function, while the seizure worry was the lowest (**Table 2**). View this table: [Table 1](http://nsj.org.sa/content/26/1/56/T1) Table 1 Participant demographics. View this table: [Table 2](http://nsj.org.sa/content/26/1/56/T2) Table 2 Mean QOLIE-31 subscale scores. **Table 3** shows the association between overall QOLIE-31 score and demographics and clinical characteristics. Employment status, the number of AED, and seizure type had a significant influence on QoL. While gender, marital status, age, and years since diagnosis did not differ significantly. View this table: [Table 3](http://nsj.org.sa/content/26/1/56/T3) Table 3 Relationships between overall QOLIE-31 score and demographics and clinical characteristics. **Table 4** demonstrates the Correlation between patients’ personal and clinical data with different QOL subscales. To adjusted for the confounder effects on the relation between QOL and patients’ personal and clinical data, a multiple linear regression model was conducted. It revealed that among all included factors, only 3 factors had an adjusted effect on patients’ QOL keeping all other factors constant. First was generalized seizures, as patients with generalized seizures showed a lower QOL score (by 7 points) than others after adjusting for all other factors (B=-7.0). Polytherapy was the second, as patients who receive multiple drugs recorded a lower adjusted QOL score (by about 10 points), keeping all other factors constant (B=9.4). Employment status was the third, as unemployed patients had a lower QOL (by about 6 points), keeping all other factors constant (B=6) (**Table 5**). View this table: [Table 4](http://nsj.org.sa/content/26/1/56/T4) Table 4 Correlation analysis for relation between patients personal and clinical data with different QOL subscales. View this table: [Table 5](http://nsj.org.sa/content/26/1/56/T5) Table 5 Multiple linear regression model to assess adjusted effect of epilepsy patients’ factors on their QOL ## Discussion In this study, we mainly assessed the QoL among PWE and its association with seizure type. The overall mean QOLIE-31 score of our sample (64.23±17.8) is consistent with the global mean QOLIE-31 score: 59.8±8.0.4 The highest domain score was for social function, and seizure worry was the lowest domain scores, which implies that seizure type is an important factor affecting QoL (**Table 2**). Also, Gaus et al. concluded that medication effects and seizure worry subscales were the most predictive elements for anxiety and depression.5 Consistent with the previous literature, employment status in our sample was significantly associated with the overall score and all the 7 subscale scores.6,7,8 Educated PWE are more likely to have a better understanding of their disease, seizure-triggering factors, and seizure management, which contribute to adherence to medications. Hence, this group will have better QoL. Unexpectedly, we found that the educational level was no longer significant after adjustment for confounders, which is also in line with the literature.9 On the other hand, other studies have found an association.10,11 Gender, age, and marital status were not associated with the overall score or any of the seven subscale scores. Although this is consistent with a study carried out in Japan,8 such an association was detected among an Australian sample,6 where they found that PWE older than 65 years have higher overall scores. While in China, Wang et al. used the same measuring scale and found that married PWE had a better QoL than unmarried PWE in young and middle-aged patients.12 Pimpalkhute et al. reported that the overall score means did not differ significantly within groups for sociodemographic factors among Indian patients.13 Also, a systematic review found that age, gender, and marital status were not associated with health-related QoL (HRQoL), and the relationship between educational level and employment status remains controversial.14 Different beliefs and socioeconomic factors among countries might account for these differing results. In our sample, PWE on monotherapy has higher scores in total and all subscales, except seizure worry and emotional wellbeing, than those on polytherapy. This is in line with the findings of other studies,15 which might be because those receiving monotherapy are more adherent than those receiving multiple AED. Another possible justification is that people who are receiving polytherapy have difficulty controlling their seizures. Considering the type of seizures, participants with generalized type were found to have significantly lower scores in emotional wellbeing, seizure worry, cognitive function, and overall QoL than participants with focal type, which is similar to findings in other studies.16 However, an Iranian study did not find such an association.17 In comparison to other Arabic studies, marital status and gender do not have an impact on QoL among Tunisian and Iraqi patients, which is in line with our findings. Employment status was not significantly affected by Iraqi and Tunisian samples. Seizure type has no significant impact on Tunisian PWE. In Iraq, age and educational level significantly affect QOL.18-20 All of these cited studies used the Short Form (SF-36) health survey. Another study conducted in the United Arab Emirates used the World Health Organization Quality of Life abbreviated scale (WHOQOL-BREF), and found no significant differences between QoL and sociodemographic and clinical characteristics.21 None of these studies have used the same scale as we have, making it difficult to compare findings. Although our sample was collected from more than one center in the Qassim region, the size is not sufficient to generalize our results. Other limitations were that we did not measure the seizure frequency; many studies have found that higher seizure frequencies have a negative influence on QoL. Further research is also needed to measure AED level and seizure frequency to assess whether medication adherence or the difficulty in controlling the seizure can also cause a negative impact among Saudi patients. In conclusion, as in many countries, epilepsy negatively impacts the QoL of Saudi patients. Moreover, employment status, type of seizure, and AED number were the most important factors considered. Current study results have encouraged the application of behavioral intervention in practice. Therapists should consider other factors, as well as QOLIE31 and its domains, thereby adapting therapy to the patient’s specific needs. Authorship entitlement Excerpts from the Uniform Requirements for Manuscripts Submitted to Biomedical Journals updated November 2003. Available from [www.icmje.org](http://www.icmje.org) The international Committee of Medical Journal Editors has recommended the following criteria for authorship; these criteria are still appropriate for those journals that distinguish authors from other contributors. Authorship credit should be based on 1) substantial contributions to conception and design, or acquisition of data, or analysis and interpretation of data; 2) intellectual content; and 3) final approval of the version to be published. Authors should meet conditions 1, 2, and 3. Acquisition of funding, collection of data, or general supervision of the research group, alone, does not justify authorship. An author should be prepared to explain the order in which authors are listed. ## Footnotes * **Disclosure.** Authors have no conflict of interests, and the work was not supported or funded by any drug company. * Received June 28, 2020. * Accepted September 10, 2020. * Copyright: © Neurosciences Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. ## References 1. Al-Khateeb JM, Al-Khateeb AJ (2014) Research on psychosocial aspects of epilepsy in Arab countries:a review of literature. Epilepsy Behav 31:256–262. 2. Kinyanjui DW, Kathuku DM, Mburu JM (2013) Quality of life among patients living with epilepsy attending the neurology clinic at Kenyatta National Hospital, Nairobi, Kenya:a comparative study. Health Qual Life Outcomes 11:98. 3. Al Rajeh S, Awada A, Bademosi O, Ogunniyi A (2001) The prevalence of epilepsy and other seizure disorders in an Arab population:a community-based study. Seizure 10:410–414. [PubMed](http://nsj.org.sa/lookup/external-ref?access_num=11700993&link_type=MED&atom=%2Fnsj%2F26%2F1%2F56.atom) 4. Saadi A, Patenaude B, Mateen FJ (2016) Quality of life in epilepsy-31 inventory (QOLIE-31) scores:A global comparison. Epilepsy Behav 65:13–17. 5. Gaus V, Kiep H, Holtkamp M, Burkert S, Kendel F (2015) Gender differences in depression, but not in anxiety in people with epilepsy. Seizure 32:37–42. 6. Peterson CL, Walker C, Coleman H, Shears G (2019) Reported service needs at diagnosis of epilepsy and implications for quality of life. Epilepsy Behav 100:106527. 7. Gu XM, Ding CY, Wang N, Xu CF, Chen ZJ, Wang Q, et al. (2016) Influence of Occupational Status on the Quality of Life of Chinese Adult Patients with Epilepsy. Chin Med J (Engl) 129:1285–1290. 8. Kubota H, Awaya Y (2010) Assessment of health-related quality of life and influencing factors using QOLIE-31 in Japanese patients with epilepsy. Epilepsy Behav 18:381–387. [PubMed](http://nsj.org.sa/lookup/external-ref?access_num=20646964&link_type=MED&atom=%2Fnsj%2F26%2F1%2F56.atom) 9. Camara-Lemarroy CR, Hoyos M, Ibarra-Yruegas BE, Diaz-Torres MA, De Leon R (2017) Affective symptoms and determinants of health-related quality of life in Mexican people with epilepsy. Neurol Sci 38:1829–1834. 10. Saadi A, Patenaude B, Nirola DK, Deki S, Tshering L, Clark S, et al. (2016) Quality of life in epilepsy in Bhutan. Seizure 39:44–48. 11. Muche EA, Ayalew MB, Abdela OA (2020) Assessment of Quality of Life of Epileptic Patients in Ethiopia. Int J Chronic Dis 2020:8714768. 12. Wang FL, Gu XM, Hao BY, Wang S, Chen ZJ, Ding CY (2017) Influence of Marital Status on the Quality of Life of Chinese Adult Patients with Epilepsy. Chin Med J (Engl) 130:83–87. 13. Pimpalkhute SA, Bajait CS, Dakhale GN, Sontakke SD, Jaiswal KM, Kinge P (2015) Assessment of quality of life in epilepsy patients receiving anti-epileptic drugs in a tertiary care teaching hospital. Indian J Pharmacol 47:551–554. 14. Taylor RS, Sander JW, Taylor RJ, Baker GA (2011) Predictors of health-related quality of life and costs in adults with epilepsy:a systematic review. Epilepsia 52:2168–2180. [CrossRef](http://nsj.org.sa/lookup/external-ref?access_num=10.1111/j.1528-1167.2011.03213.x&link_type=DOI) [PubMed](http://nsj.org.sa/lookup/external-ref?access_num=21883177&link_type=MED&atom=%2Fnsj%2F26%2F1%2F56.atom) 15. Nagarathnam M, Vengamma B, Shalini B, Latheef S (2017) Stigma and Polytherapy:Predictors of Quality of Life in Patients with Epilepsy from South India. Ann Indian Acad Neurol 20:233–241. 16. Hawari I, Syeban Z, Lumempouw SF (2007) Low education, more frequent of seizure, more types of therapy, and generalized seizure type decreased quality of life among epileptic patients. Medical Journal of Indonesia 16:101–103. 17. Ashjazadeh N, Yadollahikhales G, Ayoobzadehshirazi A, Sadraii N, Hadi N (2014) Comparison of the health-related quality of life between epileptic patients with partial and generalized seizure. Iran J Neurol 13:94–100. 18. Mrabet H, Mrabet A, Zouari B, Ghachem R (2004) Health-related quality of life of people with epilepsy compared with a general reference population:a Tunisian study. Epilepsia 45:838–843. [PubMed](http://nsj.org.sa/lookup/external-ref?access_num=15230710&link_type=MED&atom=%2Fnsj%2F26%2F1%2F56.atom) 19. Hamid H, Kasasbeh AS, Suleiman MJ, Cong X, Liu H, Mohiuddin S, et al. (2013) Neuropsychiatric symptoms, seizure severity, employment, and quality of life of Jordanians with epilepsy. Epilepsy Behav 27:272–275. 20. Shakir M, Al-Asadi JN (2012) Quality of life and its determinants in people with epilepsy in basrah, iraq. Sultan Qaboos Univ Med J 12:449–457. 21. Alsaadi T, Kassie S, El Hammasi K, Shahrour TM, Shakra M, Turkawi L, et al. (2017) Potential factors impacting health-related quality of life among patients with epilepsy:Results from the United Arab Emirates. Seizure 53:13–17.