Translate this page into:
Playing soft, with tough players: Controlling adverse drug effects while tuning antiepileptic drugs, epilepsy & the person
-
Received: ,
This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
This article was originally published by Medknow Publications & Media Pvt Ltd and was migrated to Scientific Scholar after the change of Publisher.
Accumulated evidence over the past decades clearly indicates that successful treatment of epilepsy is based on antiepileptic drugs (AEDs). To be considered successful, it has to be an optimally weighted treatment when the efficacy, safety/tolerability and costs of one or more AEDs are calculated individually for each person with epilepsy. Dozens of AEDs were introduced with various positive neuropsychiatric effects and documented effectiveness in epilepsy12, but also with various adverse effects related to cognition, emotions, behaviour and somatic functions234. Epilepsy poses a substantial economic burden for health systems, individuals and their families, with AEDs being one of the major sources of expenditure5, including their adverse effects6.
In the study by Joshi et al7 in this issue, adverse effects, AEDs load, seizure frequency and biochemical alterations were found to be associated with the total number of AEDs prescribed. This study, although limited due to its cross-sectional design, showed us that various adverse effects were associated with number of AEDs rather than frequency of epileptic seizures. It also showed that polytherapy with a combination of three or more AEDs was probably associated with higher adverse effects and lower seizure control compared to both monotherapy and combination of two AEDs. However, no marked relationship of biochemical parameters with different AED regimens was observed. Taken together, the results of this study closely resemble data from randomized controlled trials primarily showing that adults taking AEDs mostly report more than one AED- related adverse effect, with even 83 per cent of people with epilepsy treated with polytherapy reporting two or more adverse effects389. In addition, the results agreed with a recent study that documented a considerable adverse effect of a higher drug load on cognition4. However, one previous cross-sectional study showed that adverse effects did not differ between monotherapy and polytherapy and did not correlate with AED load, what was considered to be a result of physicians’ intervention in individualizing treatment regimens10.
Here, I would like to reflect upon the ways in which Joshi et al7 could extend the study in future projects. First, the outcomes of the association of adverse effects and AEDs are shaped throughout the individualized treatment regimen, which should be studied in a follow up approach considering a network of the various factors. Thus, it would be important to evaluate various individual characteristics (e.g., behavioural, cognitive or social), which might be differently linked to adverse effects in monotherapy and polytherapy. The authors studied age, gender and biochemical parameters and the results were more or less the same to the previously reported ones. Second, an important aspect to include is how specific neurocognitive performances in an individual are linked to adverse effects of a particular AED. Different positive and negative cognitive and behavioural effects for AEDs were documented over the past two decades11, and studying prospectively cognitive functions in relations to adverse effects on individual levels would be important. Third, it was found that individual AEDs independently predicted some specific adverse effects, but not overall high adverse effect burden3. Thus, it would be interesting to study how two or more AEDs predict adverse effects in an individual, as well as their interactions in the case of polytherapy. Fourth, studying the severity of epilepsy beyond a simple measure of seizure frequency as linked to individual adverse effects is another necessary consideration. Recent data showed that the excitability levels in neural tissue mattered most when quantifying the outcomes of AEDs12. Finally, in the constellation of these various factors, it would be relevant to the study to which extent monotherapy and polytherapy influence the everyday living, whereas adverse effects could negatively affect the quality of life in epilepsy1314.
The second relevant point is that Joshi et al7 also evaluated the prescribed daily dose (PDD) and defined daily dose (DDD) for each AED included in the treatment regimen as an indicator for the AED load. It was reported that AED load did not have any correlation with the occurrence of adverse effects, although it was observed that the greater the number of prescribed AEDs, the higher the occurrence of adverse effects. This is an important finding for determining whether specific AED therapy is rational and it deserves an analysis of possible factors for these associations reported. There are some conflicting data on AED load and adverse effects; some authors have shown that AED toxicity may be related to total drug load rather than to the number of AEDs administered615, for example, Canevini et al10 provided evidence that adverse events did not differ between monotherapy and polytherapy and did not correlate with AED load.
Although these are hypothetical (i.e., research) considerations, but on the other hand, taking a clinical approach might lead us to further extend the research on adverse effects in a patient-centred way to optimize health outcomes in active epilepsy16. Dealing with a person suffering from epilepsy in a routine clinical practice is as fine as tuning a violin to play perfectly. The person her/himself, epilepsy and ADEs form a complex neuropsychopharmacological triangle. Epilepsy is ‘a disorder of the brain characterized by an enduring predisposition to generate epileptic seizures and by the neurobiologic, cognitive, psychological and social consequences of this condition’17, while AEDs act by reducing the excitability levels in neural tissue to reduce seizure severity and frequency34, each of these having a specific pharmacological profile2. Thus, we have the person, epilepsy, and the AEDs that might influence each other and each self to various degrees creating a unique predisposition (i.e., variance) at an individual level to develop specific adverse effects. Weighting these aspects with a person with epilepsy or his/her caregivers would be of significant relevance for successful treatment, which should be effective, safe and least-expensive.
References
- 2011. Effectiveness and safety of antiepileptic medications in patients with epilepsy Comparative Effectiveness Reviews No. 40. Rockville (MD): Agency for Healthcare Research and Quality (US); Available from http://www.ncbi.nlm.nih.gov/books/NBK83937/
- The challengesof treating epilepsy with 25 antiepileptic drugs. Pharmacol Res. 2016;107:211-9.
- [Google Scholar]
- Specific adverse effects of antiepileptic drugs – A true-to-life monotherapy study. Epilepsy Behav. 2016;54:150-7.
- [Google Scholar]
- Adverse cognitiveeffects of antiepileptic pharmacotherapy: Each additional drug matters. Eur Neuropsychopharmacol. 2015;25:1954-9.
- [Google Scholar]
- Adverse effects & drug load of antiepileptic drugs in patients with epilepsy: Monotherapy versus polytherapy. Indian J Med Res. 2017;145:317-26.
- [Google Scholar]
- Adverse antiepileptic drug effects: Toward a clinically and neurobiologically relevant taxonomy. Neurology. 2009;72:1223-9.
- [Google Scholar]
- New antiepileptic drugs: Comparison of key clinical trials. Epilepsia. 1999;40:590-600.
- [Google Scholar]
- Relationship between adverse effects of antiepileptic drugs, number of coprescribed drugs, and drug load in a large cohort of consecutive patients with drug-refractory epilepsy. Epilepsia. 2010;51:797-804.
- [Google Scholar]
- Psychiatric and Behavioural Disorders in Children with Epilepsy (ILAE Task Force Report): Adverse cognitive and behavioural effects of antiepileptic drugs in children. Epileptic Disord. 2016;18:S55-S67.
- [Google Scholar]
- Quantifying antiepileptic drug effects using intrinsic excitability measures. Epilepsia. 2016;57:e210-5.
- [Google Scholar]
- Quality of life of people with epilepsy: A European study. Epilepsia. 1997;38:353-62.
- [Google Scholar]
- Adverse effects of antiepileptic drugs and quality of life in pediatric epilepsy. Neurol India. 2015;63:353-9.
- [Google Scholar]
- Reappraisal of polytherapy in epilepsy: A critical review of drug load and adverse effects. Epilepsia. 1997;38:570-5.
- [Google Scholar]
- Optimizing health outcomes in active epilepsy. Neurology. 2002;58(8 Suppl 5):S9-20.
- [Google Scholar]
- The new ILAE report on terminology and concepts for organization of epileptic seizures: A clinician's critical view and contribution. Epilepsia. 2011;52:2155-60.
- [Google Scholar]