Abstract

BackgroundThe safety profile of anti-epileptic drugs (AEDs) is an important consideration for the regulatory bodies, owners and prescribing clinicians. Information on their adverse effects still remains limited. A systematic review including a meta-analytic approach was designed to evaluate existing evidence for the safety profile of AEDs in canine patients. Electronic searches of PubMed, CAB Direct and Google scholar were carried out without date or language restrictions. Conference proceedings were also searched. Peer-reviewed full-length studies reporting adverse effects of AEDs in epileptic and healthy non-epileptic dogs were included. Studies were allocated to three groups based on their design. Individual studies were evaluated based on the quality of evidence (study design, study group sizes, subject enrolment quality and overall risk of bias) and the outcome measures reported (proportion of specific adverse effects for each AED, prevalence and 95 % confidence interval of the affected population in each study and comparative odds ratio of adverse effects for AEDs).ResultsNinety studies, including six conference proceedings, reporting clinical outcomes of AEDs’ adverse effects were identified. Few studies were designed as blinded randomised controlled clinical trials. Many studies included low canine populations with unclear criteria of subject enrolment and short treatment periods. Direct comparisons suggested that imepitoin and levetiracetam might have a better safety profile than phenobarbital, whilst the latter might have a better safety profile than potassium bromide. However, none of these comparisons showed a statistically significant difference. Comparisons between other AEDs were not possible as a considerable amount of studies lacked power calculations or adequate data to allow further statistical analysis. Individual AED assessments indicated that levetiracetam might be one of the safest AEDs, followed by imepitoin and then phenobarbital and potassium bromide; these findings were all supported by a strong level of evidence. The safety profile in other AEDs was variable, but weak evidence was found to permit firm conclusions or to compare their safety to other AEDs.ConclusionsThis systematic review provides objective evaluation of the most commonly used AEDs’ adverse effects. Adverse effects usually appeared mild in all AEDs and subsided once doses and/or serum levels were monitored or after the AED was withdrawn. Although phenobarbital might be less safe than imepitoin and levetiracetam, there was insufficient evidence to classify it as an AED with a high risk of major adverse effects. It is important for clinicians to evaluate both AEDs’ effectiveness and safety on an individual basis before the selection of the appropriate monotherapy or adjunctive AED therapy.

Highlights

  • The safety profile of anti-epileptic drugs (AEDs) is an important consideration for the regulatory bodies, owners and prescribing clinicians

  • AEDs are evaluated on the grounds of their effectiveness and safety through clinical trials and experimental laboratory studies before they are approved for use in patients by the regulatory authorities, e.g. the European Medicines Agency (EMA) or the US Food and Drug Administration (FDA) [2]

  • Description of studies By 29 December 2015, the search strategy had identified a total of 368 unique citations; 347 from the electronic searches of PubMed, CAB Abstracts, Google Scholar and manual searches from the publications’ reference lists, 16 from manual searching of major conference proceedings and 6 unpublished studies included as part of published data

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Summary

Introduction

The safety profile of anti-epileptic drugs (AEDs) is an important consideration for the regulatory bodies, owners and prescribing clinicians. Information on their adverse effects still remains limited. AEDs are evaluated on the grounds of their effectiveness and safety through clinical trials and experimental laboratory studies before they are approved for use in patients by the regulatory authorities, e.g. the European Medicines Agency (EMA) or the US Food and Drug Administration (FDA) [2]. The safety profile of drugs is an important consideration for their approval by the authorities and use by prescribing clinicians on their clients’ animals [2, 3] It affects clinicians’ decisions to prescribe specific AED(s), as serious adverse effects can lead to chronic complications or even death. The benefits of an effective AED may be outweighed by its adverse effects, and the latter should be always taken into consideration

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