The impact of a pharmacist-led educational interview on medication adherence of Saudi patients with epilepsy
Authors AlAjmi R, Al-Aqeel S, Baz S
Received 6 October 2016
Accepted for publication 20 March 2017
Published 18 May 2017 Volume 2017:11 Pages 959—964
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Colin Mak
Peer reviewer comments 2
Editor who approved publication: Dr Johnny Chen
Refah AlAjmi,1 Sinaa Al-Aqeel,1 Salah Baz2
1Clinical Pharmacy Department, College of Pharmacy, King Saud University, Riyadh, Kingdom of Saudi Arabia; 2Department of Neurosciences, King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia
Purpose: To evaluate the effectiveness of a pharmacist-led educational interview in terms of adherence to antiepileptic drug administration among adult patients with epilepsy.
Method: Sixty adult patients with epilepsy who fulfilled the inclusion criteria were recruited. A pharmacist-led educational interview was conducted with the intervention group (n=30). Patients in the control group (n=30) were interviewed and contacted 6 weeks after the initial visit without receiving any intervention. Antiepileptic drug adherence was measured during clinic visits, and 6 weeks afterwards using the 8-item Morisky Medication Adherence Scale. This prospective interventional study was conducted between September and December 2013.
Results: Only 29 control patients and 27 intervention patients completed the 6 weeks post-intervention adherence measurement. The adherence score average in the intervention group was 5.26±0.98 at baseline and improved to 6.7±0.823 (P<0.0001) after intervention. In the control group, the adherence score average was 5.76±1.806 at baseline and 5.83±1.627 at 6 weeks (P=0.792). While there was no statistically significant difference in adherence score between intervention and control groups at baseline, the post-intervention difference was significant (P=0.024).
Conclusion: Our study suggests that pharmacist-led educational interviews had a positive impact on medication adherence in patients with epilepsy.
Keywords: epilepsy, antiepileptic drugs, adherence
Epilepsy is a neurological disorder characterized by an enduring predisposition to epileptic seizures as well as the neurobiological, cognitive, psychological, and social consequences of this condition.1 Epilepsy is one of the most common neurological disorders worldwide with median incidence of 50.4 per 100,000 people per year (interquartile range [IQR]: 33.6–75.6). The median incidence for high-income countries is 45.0 per 100,000 people per year (IQR: 30.3–66.7) and 81.7 (IQR: 28.0–239.5) per 100,000 people per year for low- and middle-income countries.2 In the Kingdom of Saudi Arabia, the prevalence is 6.54 per 1,000 people per year.3
The World Health Organization defines medication adherence as the extent to which a patient’s behavior, in terms of taking medications, is in agreement with their provider’s recommendations.4 A consensus group5 described the process of medication adherence as initiation (ie, the patient takes the first dose of a prescribed medication), implementation (ie, the extent to which the patient’s actual dosing corresponds to the prescribed dosing regimen), and persistence (ie, the length of time on regimen between initiation and the last dose before discontinuation). Thus, non-adherence to medication can occur if a patient failed to initiate treatment, sub-optimally implemented the dosing regimen, and/or discontinued the treatment early.
Adherence is determined by many factors that can be grouped under five dimensions: social and economical, health system related, therapy related, condition related, and patient related.4 Determinants of adherence to antiepileptic drug (AED) regimens include the complexity of the drug regime, uncontrolled seizure, patients’ understanding about their illness, age, education level, and employment.6–8
Periods of adherence failure to AED regimens are associated with increased risk of seizure, status epilepticus, and mortality. There is a significantly higher incidence of emergency department visits, hospital admissions, injuries, and fractures than during periods of adherence – this results in higher resource utilization and costs.9–11
A recent review on strategies to improve adherence to antiepileptic medications identified three main types of interventions: educational, behavioral, and mixed.12 The assumption for educational interventions is that patients who understand their illness and its treatment will be more informed, have more control, and be more likely to adhere to treatment.13 This is particularly important given the evidence of lack of awareness about the medical condition and indications for AEDs among patients with epilepsy, and their needs for information and counseling.14,15 However, published evidence on the effectiveness of this approach reported mixed results.12
Previous evidence suggests that pharmacists with knowledge about pharmacotherapy and management of chronic diseases, and training in health education could contribute positively toward adherence to antidepressant and antidiabetic medications.16,17 A systematic review of published studies describing clinical services performed by pharmacists for patients with epilepsy, identified five studies that highlighted the positive impact of pharmacists’ interventions on knowledge, quality of life, and medication adherence in this group of patients.18
Considering the inconclusive evidence on the efficacy of educational interventions and the paucity of studies about pharmacists’ contributions to epilepsy management, this study evaluates the effectiveness of a pharmacist-led educational interview in terms of adherence to AED administration among adult patients with epilepsy.
Materials and methods
The study was conducted at the outpatient Epilepsy Clinic at King Faisal Specialist Hospital and Research Center (KFSH and RC) – a tertiary referral hospital in Riyadh, Kingdom of Saudi Arabia. The inclusion criteria for patients were a clinical diagnosis of epilepsy, age ≥18 years, current use of AEDs, and the ability to provide consent and complete the scale independently. Patients were excluded if they had any mental problems that impaired their ability to complete the scale or if they refused to participate. Patients who met the inclusion criteria were invited to participate in the study by one of the investigators (SB). Patients were given a participation information sheet that described the type of study, and the nature and purpose of the intervention. Those who agreed to participate signed the consent form. The Office of Research Affairs and Ethics Committee of KFSH and RC approved this study. Patients recruited in September 2013 were allocated to the control group, while those recruited in October through December 2013 were allocated to the intervention group. Participants did not receive incentives.
This study was designed as a prospective nonrandomized interventional study. The educational interview involved a 30-minute structured verbal face-to-face interview conducted by one of the researchers (RA) who is a pharmacist. All patients were educated according to the guidelines of the American Society of Health-System Pharmacists regarding pharmacist-conducted patient education and counseling.19 Patients in the intervention group were interviewed individually and privately, either in the clinic after the consultant’s examination or in the nurse’s room.
The educational content was divided into two parts. The first part included education about the medical aspects of epilepsy, and the second part included information about AEDs. Leaflets that contained the content of the educational interview were written in Arabic and were presented in a “question and answer” format, and given to the intervention group. This leaflet included educational information about the medical aspects of epilepsy including the definition of epilepsy, causes, description of brain seizure activity, diagnostic procedures, seizure observation, and classification; information about AEDs; and information about the importance of adherence and the consequences of non-adherence. The pharmacists also discussed methods to incorporate AED administration into their daily lives and to transform their daily routines into cues to take their AEDs. The most common cue was prayer times. In addition, the pharmacist provided a pill organizer to each participant and counseling about how to use it, and its usefulness.
For more assistance and support, participants were advised to visit an Epilepsy Support and Information Center (ESIC) – a non-profit regional office governed by KFSH and RC, under the “umbrella” of the International Bureau of Epilepsy, that provides information and support to epilepsy patients and their families. The leaflet also provided the web address for ESIC for patients to access online information. All participants received the usual care offered by their clinic. Patients in the control group did not receive an educational interview from the pharmacist, a pill organizer, or leaflets. They could access the ESIC, but the pharmacist did not encourage it.
The instrument used here consisted of a 2-part questionnaire. Part one included demographic data, and part two included medication adherence questions. Demographic characteristics included age, gender, marital status, occupational status, education, age of onset of epilepsy, seizure frequency, the time since the last seizure, and the number of AEDs taken. In this study, self-reported adherence was assessed using the 8-item Morisky Medication Adherence Scale (MMAS-8).20–22 The scale provides information on behavior related to low adherence that may be unintentional (eg, forgetfulness) or intentional (eg, stopped taking medications because they felt that their symptoms were under control). The scale contains items that seek to assess the extent of implementation of a dosing regimen and discontinuation of treatment.
The MMAS-8 has been used previously to assess medication adherence in epilepsy patients.23–25 The license to use the validated Arabic version of the MMAS-8 was obtained. The version is in modern standard Arabic language – the language used for reading and writing in Arab countries including Kingdom of Saudi Arabia. The MMAS is an 8-item questionnaire with seven items represented in a yes/no format. The final question is rated on a 5-point Likert scale. According to the MMAS scoring system, a score of 8 reflects high adherence, and 6 to <8 reflect medium adherence; scores <6 reflect low adherence.20
The questionnaire was administered to both the intervention and control groups at baseline as well as 6 weeks after the intervention. While baseline measurements were carried out at the clinic, adherence levels post-intervention were assessed via a phone call to both groups.
A pilot study indicated that a sample size of 27 subjects in each group was sufficient. The size was estimated based on an average MMAS of 5.2±1.6 with an expected adherence difference of within 24% at a significance level of 5%.
Descriptive analyses including the means and standard deviations (SDs) were calculated for all quantitative values. Differences between the group’s adherence levels were compared using a Wilcoxon signed rank test. The mean, median, and interquartile ranges were used for differences between adherence scores. Spearman’s correlation coefficient was used to assess the relationship between age, education level, duration of illness, number of seizure episodes, or number of AEDs and adherence score. Chi-square tests, Mann–Whitney U tests, and independent t-tests were used to test for differences in patients’ characteristics such as seizure frequency, as appropriate. The statistician was blinded to which group received the intervention. Analysis was conducted to determine the effect of intervention after 6 weeks. Statistical analysis was carried out using the Statistical Package for the Social Sciences (SPSS) version 19 software (IBM Corporation, Armonk, NY, USA).
Seventy patients were approached, and 60 agreed to participate; 30 were assigned to each group. Only 29 control patients and 27 intervention patients completed the 6 weeks post-intervention adherence measurement. The loss to follow-up was due to failure to reach the patients through a post-intervention phone call.
The participant characteristics are summarized in Table 1. The majority of participants were men aged <40 years, with a diagnosis of epilepsy for ≥10 years. The mean (±SD) number of AEDs were 2.34 (±0.93) and 2.03 (±1.05) for control and intervention groups, respectively. The average number of seizure episodes during the last 6 months ranged between 4.96 (±5.29) and 4.72(±3.26) for the intervention and control groups, respectively. There were no statistically significant differences in age, gender, educational status, marital status, or seizure frequencies between the intervention and control groups.
Table 1 Demographics and clinical characteristics of the study population
Only 12 participants (44.0%) used the pill organizer and incorporated it into their medication-taking behavior.
The adherence score average in the intervention group was 5.26±0.98 at baseline, and this improved to 6.7±0.823 (P<0.0001) after intervention. In the control group, the adherence score average was 5.76±1.806 at baseline and 5.83±1.627 at 6 weeks (P=0.792). While there was no statistically significant difference in adherence scores between intervention and control groups at baseline, the post-intervention difference was significant (P=0.024). There was no statistically significant correlation between medication adherence scores and age, education level, duration of illness, number of seizure episodes, or number of AEDs.
Table 2 shows the distribution of patients based on adherence level. At baseline, 40.7% of patients in the intervention group had medium adherence scores (MMAS-8 score, 6–8), and none were classified as having high adherence scores (MMAS-8 score, 8). Six weeks after intervention, 85.2% of patients in the intervention group had medium adherence scores (MMAS-8 score, 6 to <8) and 11.1% had high adherence scores (MMAS-8, score 8).
Table 2 Comparison of adherence level between control (N=29) and intervention (N=27) groups
The aim of this study was to investigate the effectiveness of pharmacist-led educational interview in epilepsy patients’ adherence to AED regimens. The adherence score improved significantly in the intervention group patients.
Compared with previous studies that used a MMAS-8 to measure medication adherence in patients with epilepsy,7,23,25 our participants had higher rates of moderate-to-low adherence (MMAS-8 score, <8). Two-thirds of our participants were on polytherapy, which is higher than rates reported in other studies.23,25 This is probably attributable to the nature of the clinic from which the patients were recruited (an epilepsy clinic in a tertiary referral center).
Our results suggest that educational interview could positively impact the medication adherence of patients with epilepsy. Previous evidence on the effectiveness of educational interventions in terms of medication adherence in patients with epilepsy is mixed.12 Li et al26 found that self-reported adherence remarkably improved in participants who received intensive education, consultation services, and repeated reminders, while unchanged adherence levels were reported in the non-intervention cohort. Peterson et al27 reported a positive impact on patient adherence to AEDs among those who received counseling, a pill organizer, and other reminder techniques, measured using blood tests and refill frequencies.
In another study, there was no significant difference in adherence to AEDs based on detectable drug levels or by self-reporting between the intervention and control groups, 1 year after a day-long health educational program.28 Dash et al23 investigated the effect of a structured one-on-one educational program administered by an epilepsy nurse over four sessions each lasting at least 30 minutes. They found that self-reported adherence scores were significantly improved in the intervention group with no significant change in the control group.
The current study’s findings suggest that pharmacists can improve the utilization of treatment by educating patients with epilepsy. Similar research, albeit limited in number, shows similar directions. A randomized controlled trial comparing AEDs education provided by a pharmacist with AEDs plus behavioral intervention, found that adherence increased greatly from baseline in both groups, but without significant differences.29 In a before/after study conducted in adults with epilepsy,30 a single 30-minute consultation with a pharmacist was associated with improved self-reported adherence 2 months after the intervention.
We did not assess the feasibility and costs of implementing such an intervention into pharmacists’ routine care for patients with epilepsy. Published evidence suggests that adherence-enhancing interventions are cost-effective or cost-saving.31,32 However, more studies on the cost-effectiveness of pharmacist-delivered interventions to improve adherence are needed.
Although our study found a statistically significant difference in adherence score between baseline and 6 weeks after the educational interview, the clinical impact remains unclear. The level at which non-adherence becomes clinically significant varies between medications, and the needed adherence rate is unknown for many medications.33 Research examining the level at which non-adherence rates to AEDs becomes clinically significant is needed.
This study is one of the very few studies29,30 that has examined the efficacy of pharmacist-led educational interview in patients with epilepsy. It does have some obvious limitations. The study was a prospective interventional study with no randomization. This might introduce selection bias. The majority of participants have had a clinical diagnosis of epilepsy for >10 years; thus, we cannot generalize our findings to newly diagnosed patients with epilepsy. The difference in collection periods between control and intervention groups is also a weakness. The fact that less than half of the participants used the pill organizer, limited our ability to assess the impact of this simple intervention. Previous studies have shown that reminder packaging has a positive impact on medication adherence.34 We also used a self-reported adherence measure. Self-reported measures have several advantages.33,35,36 Self-reporting may be considered the most practical method of measuring adherence in clinical settings. They also provide a reasonably accurate estimate of adherence. Other advantages include low cost, ease of administration, and flexibility in timing and mode of administration. Also, self-reports can explain underlying issues that contribute to non-adherence. However, self-reported measures of adherence have several potential disadvantages.33,35,36 First, many self-reporting measures have not been rigorously tested for convergent or criterion validity, internal consistency, and test–retest reliability. Second, there is a chance of social desirability and memory biases. Patients could have reported themselves as being more adherent than they actually were, and non-adherence may have been underreported due to memory deficit and poor patient recall of information. Here, one of the authors who interviewed patients to obtain self-report adherence data also delivered the adherence-enhancing intervention. This might have increased socially desirable responses.35 Third, when using self-reporting measures to assess the efficacy of adherence-enhancing interventions, intervention participants may be disproportionately influenced to self-report faithful adherence compared to control arm participants.35
A pharmacist-led educational intervention had a positive impact on medication adherence in epilepsy patients. This study paves the way for conducting a randomized controlled trial with longer follow-up and more rigorous protocols for measurement of medication adherence to confirm the findings.
Use of the ©MMAS is protected by US and International copyright laws. Permission for use is required. A license agreement is available from Donald E. Morisky, MMAS Research (MORISKY) 16636 159th Place SE, Renton WA 98058, firstname.lastname@example.org. This research project was supported by a grant from the Research Center of the Female Scientific and Medical Colleges, Deanship of Scientific Research, King Saud University, Riyadh, Kingdom of Saudi Arabia.
The authors report no conflicts of interest in this work.
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