Rowena M. A. Packer
Sarah L. Hobbs
Emily J. Blackwell- 1Royal Veterinary College, London, United Kingdom
- 2Bristol Veterinary School, University of Bristol, Bristol, United Kingdom
Epilepsy is a common, complex and often challenging neurological disorder to treat in the dog, with 20–30% of dogs resistant to conventional medical therapies, and associated with cognitive and behavioral comorbidities and early death. Behavioral interventions are an emerging area of focus in the adjunctive treatment of drug-resistant human epilepsy patients, with studies indicating positive effects of a variety of interventions including relaxation-based techniques and behavioral therapy interventions. Behavioral interventions have the potential not only to improve seizure control, but also improve behavioral comorbidities and general quality of life in this hard to treat patient group. Despite striking similarities between human and canine epilepsy patients, including the recognition of co-morbid anxiety in epilepsy patients, behavioral interventions have yet to be studied in dogs. This is compounded by several licensed psychopharmaceutical agents for dogs being contra-indicated in epilepsy patients. We present evidence from human studies of the efficacy of behavioral interventions to improve seizure control, psychiatric comorbidities and quality of life, and propose that adapting such interventions for canine patients may be a valuable addition to the epilepsy management toolkit. There is a need for multi-center, double-blinded, placebo-controlled trials to confirm the effects of behavioral interventions on seizure frequency in veterinary medicine. In the absence of such evidence to date, the use of established behavioral medicine techniques to reduce stress and improve the mental health of these often sensitive and challenging patients is advocated, with a greater role for behaviorists in the management of epilepsy patients alongside neurologists and general practitioners.
Canine Epilepsy: Current Therapies and Challenges
Epilepsy is the most common chronic neurological presentation in first opinion practice for domestic dogs, with previous epidemiological studies estimating a prevalence of 0.6% of dogs affected in the UK alone (1). Epilepsy is a major risk to the health and welfare in dogs, with dogs at risk of developing behavioral changes such as anxiety and attention-deficit hyperactivity disorder (ADHD)-like behavior, cognitive impairments, reduced quality of life (QoL) from anti-epileptic drug (AED) side effects, complications of AED treatments and early death (2–7). Between 20 and 60% of dogs with IE die as a direct consequence of epilepsy (8). The condition is early onset, with most dogs experiencing their first seizure between 1 and 4 years of age, and is lifelong (9), requiring chronic medication. Medication with AEDs poses a fine balance between benefits and harms, with potentially adverse welfare consequences due to unpleasant side effects including excessive hunger, thirst, restlessness, lethargy, and ataxia (4). Their impact upon QoL may be considerable, with AED side-effects being cited as an important consideration for owners of epileptic dogs (4).
Despite advances in pharmacotherapy for canine idiopathic epilepsy (IE), with an increasing number of AEDs available to veterinarians managing these often challenging patients, a large proportion of this patient population continue to experience seizures while taking AEDs. At present, only a minority of canine epilepsy patients achieve significant periods of seizure freedom (10). Overall response rates (defined as >50% reduction in seizure frequency) to the first, second and third AEDs have been reported as 37.2, 10.7, and 6.1%, respectively (11); and thus many dogs continue to seizure chronically despite polytherapy. This parallels findings in human neurology, where up to 30% of epilepsy patients continue to seizure despite taking AEDs (12). Although AEDs remain the mainstay of epilepsy treatment in dogs, seizure control is often incomplete and their use is associated with a variety of quality of life inhibiting side effects including sedation, ataxia, polyphagia (5). Indeed, a recent meta-analysis of 90 canine epilepsy studies identified adverse effects associated with all nine of the most commonly used AEDs (13). The discovery of adjunctive therapies that effectively reduce seizure frequency in canine epilepsy patients, while avoiding additional side effects is of high priority. Non-pharmacological seizure control strategies are becoming increasingly common in both canine and human epilepsy, including dietary interventions [e.g., the ketogenic diet; (14, 15) and the use of dietary supplements (16)], and implantable neuromodulation devices [e.g., vagal nerve stimulators; (17, 18)]. Although non-pharmacological therapies including dietary and neuromodulation interventions have been demonstrated to improve seizure frequency in some patients, others still fail to achieve a significant level of seizure control following these adjunctive therapies (commonly considered a >50% reduction in dogs), and thus the search for additional adjunctive therapies for the epilepsy management tool-kit continues.
An emerging area in adjunctive therapies for drug-resistant human epilepsy patients is behavioral and psychological therapies. These interventions are based on accumulating evidence from animal models and clinical studies that there is a relationship between behavioral, physiological and psychological states and the probability of seizure occurrence, with a bidirectional relationship between seizures and psychological states (19). Interventions that alter behavioral or psychological states have been tested to determine whether they can reduce the occurrence of seizures in people with epilepsy, with success found with a variety of interventions. To date, this type of intervention for drug-resistant canine epilepsy patients remains entirely unexplored to the authors' knowledge, but offer much promise. There are striking similarities between canine and human epilepsy patients, with shared characteristics including spontaneous drug-resistance (20) and behavioral and cognitive comorbidities (2, 6, 7, 21). Many of the same drug and non-drug therapies (e.g., the MCT diet) have proven efficacious in both species, and as such, exploring behavioral interventions in dogs appears both logical and overdue. Potential benefits of behavioral interventions include their relatively low cost, lack of side effects and contra-indications with existing medications, and their non-invasive nature (22). As recently highlighted by Kanner (23), the treatment of epileptic seizure disorders is not restricted to the achievement of seizure-freedom, but must also include the management of co-morbid psychiatric and cognitive comorbidities (23). With the increasing recognition of behavioral and cognitive comorbidities in dogs with epilepsy (2, 6, 7, 21), the potential for behavioral interventions improving both seizure control and behavioral clinical outcomes warrants investigation in this area in canine patients.
Evidence for Behavioral Interventions for Epilepsy
Behavioral treatments for epilepsy in humans have been discussed since 1977 (24), but have not been subjected to investigation in rigorous clinical trials until recently, with the development of psychosocial treatment programs not keeping pace with the development of medical treatments (25). Despite this, behavioral techniques to control seizures have a long history with a multitude of empirical studies published on a variety of interventions. Many of these behavioral interventions target stress. Stress is increasingly recognized to have a major role in epilepsy, including: (i) acting as a risk factor for the development of epilepsy, (ii) being a trigger for the occurrence of seizures in some individuals with epilepsy, and (iii) exacerbating seizure frequency, and/or being an important component of a prodrome preceding a seizure in some individuals with epilepsy (26). Recent research has demonstrated that epilepsy is associated with elevated stress in both dogs with epilepsy and their owners (27); however, measures to counteract stress have yet to be explored in this population. Behavioral interventions to reduce stress and improve emotional state for people with epilepsy have included relaxation exercises including yoga and progressive muscle relaxation, biofeedback and cognitive behavioral therapy, which will now be briefly reviewed. Evidence is additionally summarized in Table 1.
Table 1. Evidence of the effects of behavioral interventions on seizure control in human epilepsy patients.
Relaxation-Based Techniques
Stress management techniques have been demonstrated to show strong preliminary evidence in seizure reduction in people with epilepsy. A well-studied technique is progressive muscle relaxation (PMR) which involves tensing and releasing different muscle groups in turn. In a recent multicenter randomized controlled trial (RCT), n = 66 adults with refectory epilepsy were randomized into one of two interventions; PMR with diaphragmatic breathing or control focused-attention activity with extremity movements. Participants underwent 12 weeks of double-blind treatment, and seizure frequency during this period was compared to the 8 week baseline phase before treatment commenced. In both groups, seizure frequency was significantly reduced from baseline; however, there was no difference in the efficacy of the two groups (26). PMR was more effective in reducing self-reported stress than focused attention (26). Prior to this RCT, several smaller studies demonstrated the promise of this technique. In a small study of epilepsy patients (n = 8), half underwent 3 weeks of PMR while half in the control arm underwent 3 weeks of quiet sitting, followed by 3 weeks of PMR. All subjects showed decreases in seizure frequency from baseline to treatment and improvements in well-being (28). In a further study of n = 18 adults with drug-resistant epilepsy, patients were split into three groups: contingent relaxation, attention control, and no-treatment (control) for 6 weeks. Patients in the contingent relaxation group were instructed to apply PMR techniques to situations or feelings associated with high risk of seizure activity. Results indicated that seizure frequency was significantly reduced in the PMR group (29). A further study compared the 8 week baseline seizure frequency for 12 participants with three subsequent 8 week follow-up periods, post PMR training. During the intervention period, PMR was practiced twice a day. By the third follow-up time point, the median seizure frequency for the group had decreased by 54% (31). Finally, in a study of n = 24 adults with epilepsy, a seizure frequency reduction of 29% was associated with six sessions of progressive relaxation training (n = 13) compared with just 3% in patients with six sessions of quiet sitting (n = 11) (30).
In addition to PMR, another relaxation-based technique, yoga, has shown efficacy in seizure control for some patients with epilepsy. Yoga is an ancient Indian philosophy of life aimed at achieving the highest possible functional harmony between body and mind, which involves control of posture, breathing and meditation. Yoga may have an effect on the probability of seizure occurrence due to its effect on brain wave activity and arousal levels (39). It has been further suggested that yoga may stimulate the vagus nerve which may in turn decrease seizure frequency (40). Studies have demonstrated that certain types of yoga increase central parasympathetic activity and sensory motor rhythm and increase the sense of well-being (41, 42). In a study by Sathyaprabha and colleagues, 10 weeks of daily 60-min yoga practice (n = 18 epilepsy patients) was found to significantly decrease seizure frequency and parasympathetic dysfunction, compared to a group that practiced routine exercises involving sitting quietly for 20 min and simple physical exercises for 40 min who showed no reduction (n = 16) (32). In a further RCT by Lundgren et al. (22), drug-resistant epilepsy patients treated with either yoga (n = 8) or acceptance and commitment therapy (a cognitive technique; n = 10) experienced reduced seizure frequency and duration and increased quality of life compared to baseline (22).
Finally, training patients to relax using biofeedback has shown promise in controlling seizures. Biofeedback is a management tool where the patient is provided with visual or audio feedback to covert physiological responses occurring in their body, including changes in heart rate, skin conductivity or brain activity (from electroencephalography; EEG). Training may allow the patient to learn to actively control these bodily responses and use this biofeedback training as a countermeasure when they are aware a seizure is about to start (33). Negative amplitude shifts of cortical potential are related to seizure activity in epilepsy; regulation of the cortical potential with biofeedback has been successfully used to reduce the frequency of some patients' seizures (43). Galvanic Skin Response (GSR) is a sensitive measurement of autonomic arousal and physiological state which reflects one's behavior; a high skin resistance state reflects a state of relaxation and a low skin resistance state reflects a state of arousal. Nagai et al. found that GSR biofeedback training reduced seizure frequency in the biofeedback (n = 10) but not the sham control biofeedback (n = 8) group, thus demonstrating the promise of this technique (33). In addition, a meta-analysis of EEG biofeedback studies for epilepsy management found a 74% reduction in weekly seizures (44). This method is currently out of the scope of potential treatment techniques for canine patients, however if canine ambulatory EEG technology improves and becomes more widespread in the future, this may be another method to consider.
Behavioral Therapy Techniques
In addition to relaxation-based interventions, a variety of behavioral therapy based techniques have been trialed in humans with epilepsy, as techniques to improve both seizure control, treat psychiatric co-morbidities and more improve QoL more generally. In a crossover design study, Gillam compared the effect of two psychological approaches: one treatment focused on seizures, and involved training patients to identify factors that might precipitate seizures, to learn how to avoid these “triggers,” to try to interrupt seizures in the early stages of their occurrence, or to practice relaxation and breathing exercises, the other targeted psychological problems affecting the patients such as phobias, mild depression, and family tensions (34). Both techniques were effective in reducing psychological symptoms and seizure frequency, with the author concluding that the improved sense of self-control may have been more important than whether the intervention was targeted at psychological difficulties or seizures specifically. In a further study, Spector et al. (35) employed a group intervention in adults with drug-resistant epilepsy (n = 8). The intervention, based on a programme developed by Andrews and Reiter, “Taking Control of Your Epilepsy” (45) and recently updated in 2015 (46) involved a variety of measures including support and dealing with stigma, understanding epilepsy and antiepileptic drugs, identifying auras, identifying and avoiding triggers for seizures, channeling negative emotions into productive outlets, and dealing with stress (35). Following treatment there was a significant reduction in seizure frequency, which persisted at 8 week follow up (35).
Behavioral medicine in the form of cognitive behavioral therapy (CBT) has further been explored as an intervention for epilepsy, with mixed results to date. CBT emphasizes the influence of thoughts and their content on emotional state and treatment focuses on changing thought patterns and behavior. In a study of n = 37 adults with epilepsy, patients were assigned to either a 6 week CBT program or a control group. Seizure frequency was significantly reduced in the CBT group compared to the control (36). Conversely in earlier studies, although beneficial effects upon general QoL were found, positive effects on seizure frequency were not. A recent study assigned adults with epilepsy (n = 17) to either a treatment group (n = 7) consisting of 8 weekly 2-h group CBT sessions, or to a waitlist control group (n = 9). Although the treatment group showed improvements in QoL [as measured by the QOLIE-31 (47)], no significant reduction in seizure frequency was found in the CBT group (37). Similar findings were reported in an earlier study (38), where no evidence to support the use of CBT for seizure reduction was found. In that study, n = 27 adults with epilepsy were assigned to one of three groups: CBT, supportive counseling (attention-placebo control) and waiting list (no treatment control). No difference was found in seizure frequency between the three groups; however, ratings of psychological adjustment were found to improve for the two therapy groups (38).
Treatment of Epilepsy Co-morbidities
As highlighted earlier, epilepsy treatment should not solely focus on seizure control. Behavioral interventions may reap benefits in addition to reduced seizure frequency. In a recent Cochrane review of psychological and behavioral treatments for health-related quality of life in epilepsy patients (rather than seizure frequency as the primary outcome) (48), 24 randomized controlled trials (RCTs) were included, of which 11 were considered psychological interventions including cognitive, behavioral and mindfulness-based interventions. The impact of these interventions on QoL, as measured by a validated scale [the QOLIE-31 (47)] was significant and exceeded the threshold of minimally important change, indicating a clinically meaningful post-intervention improvement of QoL (48). Overall QoL, including mental health should be taken seriously in addition to seizure frequency in epilepsy patients, with inter-ictal anxiety and depression found to have greater adverse effects on QoL than seizure frequency, severity or chronicity in people with epilepsy (49). With anxiety found more commonly as a comorbidity in drug-resistant dogs (2), finding appropriate treatments to reduce the effects of behavioral comorbidities and improve general QoL alongside improved seizure control should be the goal of epilepsy treatment.
Is there a Need for Behavioral Therapy in Canine Epilepsy Patients?
In addition to seizure control, there is an emerging need for therapies for co-morbid anxiety in dogs with epilepsy. Increases in anxiety following the onset of epilepsy have been documented in dogs with epilepsy (2); however, in a recent review on psychopharmacological options for the treatment of anxiety in dogs with IE, it was concluded that there is a scarcity of evidence of the effects of standard anxiolytic therapies in the IE population, with many drugs having pharmacokinetic interactions with AEDs, or contraindicated in these patients (50). Furthermore, patient response to anxiolytic medications may differ between healthy brains and epileptic brains. Although seizure reducing effects were documented in a recent study of imepitoin (an anti-consultant and anxiolytic), no changes in anxiety behavior were observed in dogs with IE (51), whereas positive effects on anxiety have been documented in otherwise healthy dogs with fear or anxiety problems (52). In addition to pharmaceutical interventions, some owners are already employing dietary therapies aimed at epilepsy and its comorbidities. In a recent study, 1 in 10 owners of epileptic dogs that were using dietary supplements reported that their aim was to improve behavioral problems associated with epilepsy (16). The use of behavioral therapy has been advocated in this population (50); however, its efficacy has yet to be ascertained with controlled trials, or indeed reported in case reports or series as yet.
Potential Behavioral Interventions for Canine Epilepsy Patients
Although some of the aforementioned behavioral interventions for human epilepsy patients rely upon methods based upon language or higher level cognitive processes, and may not be readily adapted to canine patients, the principles of other effective techniques may be used to design potential interventions. These include:
“Trigger” Management: As employed in several human behavioral intervention studies, the recognition, and subsequent avoidance of seizure triggers (seizure precipitating factors) may improve seizure control in epileptic patients (34, 35). Seizure triggers have recently been documented in two studies of canine epilepsy patients, with many of these precipitants psychological (53, 54), including general stress, changes in routine, unfamiliar places or people visiting. Developing methods to reliably identify seizure triggers and to teach owners to recognize these stimuli may allow for either their avoidance, or the use of behavioral therapy to systematically desensitize dogs to these stimuli using controlled exposure (where possible) under the guidance of a clinical animal behaviorist. Although it may not be possible to avoid all seizure triggers, some reduction in seizure frequency may be achieved by manipulation of the environment (55). In addition to canine patients diagnosed with idiopathic epilepsy, dogs with reflex epilepsy (i.e., seizure activity triggered by exposure to specific locations or situations) (56) are likely to strongly benefit from this behavioral management strategy.
Stress Reduction Therapies: The use of behavioral therapy principles to improve the mental health of dogs, including: improved consistency of dog-owner interactions, cessation of any punishment-based training or training devices [previously shown to be used by owners of epileptic dogs (7)], and improved predictability of the dog's life with enhanced feelings of control, may be a potential way to reduce overall stress and improve seizure control (57–59). Indeed, a previous human behavioral intervention study found no difference in seizure control between treatment programmes focused on general psychological problems vs. seizures themselves specifically, with the author concluding that the improved sense of self-control induced by either programme may have been more important than the specific type of intervention. Development of general stress reduction programmes for epilepsy patients has the potential to improve seizure control while also improving overall QoL of these patients by improving mental health.
Specific Relaxation Based Activities: There is growing evidence that dogs with epilepsy exhibit behavioral changes preceding a seizure event, which may represent the “prodromal” stage of the seizure cycle. In a study of n = 229 owners of dogs with epilepsy, 65% reported that dogs showed pre-seizure changes including included restlessness, clinginess and fearfulness (54). As implemented in human studies [e.g., Dahl et al. (29)], it is possible that applying acute relaxation based interventions during this pre-seizure stage may be effective in aborting impending seizure activity, if seizure generation is influenced by stress levels and cortical excitability can be dampened by relaxation based activities. At present, further research is needed to confirm the presence of this phase of the “seizure cycle” in dogs and whether this window of time for intervention exists. Relaxation sessions, aimed at reducing physiological arousal and thereby increasing the threshold for response to sensory signals, are used as a foundation for modifying context-specific behavior in many clinical behavior cases (60, 61) and daily relaxation outside of the prodromal phase may act as an anxiolytic if dogs are trained to effectively settle in a low arousal, positively valenced state.
Conclusions
Studies of behavioral interventions as tools to improve seizure control and QoL show great promise for human drug-resistant epilepsy patients. Despite the limitations of some of the early studies in this area, with small sample sizes commonplace, the fact that significant reductions in seizure frequency were found in such small samples provides compelling preliminary evidence for the strength of these interventions.
With great similarities exhibited between drug resistant human and canine epilepsy patients (62), trialing behavioral methods for this challenging population is timely and urgently needed. There are both challenges and opportunities in the use of behavioral methods, with important lessons to be learned from the past 40 years of human research in this field. Well-designed and powered studies are needed to successfully address whether behavioral treatments can increase seizure threshold and improve seizure control in drug resistant epilepsy patients. In both veterinary and human medicine there is a need for multi-center, double-blind, placebo-controlled trials to confirm the effects of behavioral interventions on seizure frequency.
In the absence of such evidence to date, the use of established behavioral medicine techniques to reduce stress and improve mental health of these often sensitive and challenging patients is advocated. Basic principles for all patients include the cessation of all punishment-based training techniques employed by owners. Greater education for owners on both overt and subtle signs of stress in their dog is essential for all behavioral interventions, and vets should either advise clients individually of these signs, or be able to direct owners to appropriate, evidence-based resources on this topic. We advocate a greater role for veterinary behaviorists in the management of epilepsy patients alongside neurologists and general practitioners, not only for epileptic patients with overt behavioral problems that owners actively seek treatment for (e.g., noise phobias), but also for expert opinion on a dog's behavioral husbandry and lifestyle with the aim of generally improving of the mental health and QoL of these sensitive patients.
Author Contributions
The idea for the manuscript was devised by RP. RP, SH, and EB all contributed ideas to and reviewed the final manuscript.
Funding
RP is supported by BBSRC grant number BB/P010881/1.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
This manuscript was approved for submission (CSS_01907).
References
1. Kearsley-Fleet L, O'Neill DG, Volk HA, Church DB, Brodbelt DC. Prevalence and risk factors for canine epilepsy of unknown origin in the UK. Vet Rec. (2013) 172:338. doi: 10.1136/vr.101133
2. Shihab N, Bowen J, Volk HA. Behavioral changes in dogs associated with the development of idiopathic epilepsy. Epilepsy Behav. (2011) 21:160–7. doi: 10.1016/j.yebeh.2011.03.018
3. Berendt M, Gredal H, Ersbøll AK, Alving J. Premature death, risk factors, and life patterns in dogs with epilepsy. J Vet Inter Med. (2007) 21:754–9. doi: 10.1111/j.1939-1676.2007.tb03017.x
4. Chang Y, Mellor DJ, Anderson TJ. Idiopathic epilepsy in dogs: owners' perspectives on management with phenobarbitone and/or potassium bromide. J Small Anim Pract. (2006) 47:574–81. doi: 10.1111/j.1748-5827.2006.00203.x
5. Wessmann A, Volk HA, Packer RMA, Ortega M, Anderson TJ. Quality-of-life aspects in idiopathic epilepsy in dogs. Vet Rec. (2016) 179:229. doi: 10.1136/vr.103355
6. Packer RMA, McGreevy PD, Salvin HE, Valenzuela MJ, Chaplin CM, Volk HA. Cognitive dysfunction in naturally occurring canine idiopathic epilepsy. PLoS ONE (2018) 13:e0192182. doi: 10.1371/journal.pone.0192182
7. Packer RMA, McGreevy PD, Pergande A, Volk HA. Negative effects of epilepsy and antiepileptic drugs on the trainability of dogs with naturally occurring idiopathic epilepsy. Appl Anim Behav Sci. (2018) 200:106–13. doi: 10.1016/j.applanim.2017.11.008
8. Mellersh CS. Genetic Testing in Canine and Feline Epilepsy. Birmingham: British Small Animal Veterinary Association Congress (2010).
10. Packer RM, Shihab NK, Torres BB, Volk HA. Clinical risk factors associated with anti-epileptic drug responsiveness in canine epilepsy. PLoS ONE (2014) 9:e106026. doi: 10.1371/journal.pone.0106026
11. Packer RMA, Shihab NK, B.Torres BJ, Volk HA. Responses to successive anti-epileptic drugs in canine idiopathic epilepsy. Vet Rec. (2015) 176:203. doi: 10.1136/vr.102934
12. Kwan P, Brodie MJ. Early identification of refractory epilepsy. N Engl J Med. (2000) 342:314–9. doi: 10.1056/NEJM200002033420503
13. Charalambous M, Shivapour SK, Brodbelt DC, Volk HA. Antiepileptic drugs' tolerability and safety – a systematic review and meta-analysis of adverse effects in dogs. BMC Vet Res. (2016) 12:79. doi: 10.1186/s12917-016-0703-y
14. Law TH, E.Davies SS, Pan Y, Zanghi B, Want E, Volk HA. A randomised trial of a medium-chain TAG diet as treatment for dogs with idiopathic epilepsy. Br J Nutr. (2015) 114:1438–47. doi: 10.1017/S000711451500313X
15. Martin K, Jackson CF, Levy RG, Cooper PN. Ketogenic diet and other dietary treatments for epilepsy. Cochr Database Syst Rev. (2016) 2:CD001903. doi: 10.1002/14651858.CD001903.pub3
16. Berk BA, Packer RMA, Law TH, Volk HA. Investigating owner use of dietary supplements in dogs with idiopathic epilepsy. Res Vet Sci. (2018) 119:276–84. doi: 10.1016/j.rvsc.2018.07.004
17. Muñana KR, Vitek SM, Tarver WB, Saito M, Skeen TM, N.Sharp JH, et al. Use of vagal nerve stimulation as a treatment for refractory epilepsy in dogs. J Am Vet Med Assoc. (2002) 221:977–83. doi: 10.2460/javma.2002.221.977
18. Morris GL, Mueller WM. Long-term treatment with vagus nerve stimulation in patients with refractory epilepsy. Neurology (1999) 53:1731. doi: 10.1212/WNL.53.8.1731
20. Löscher W. Animal models of intractable epilepsy. Progr Neurobiol. (1997) 53:239–58. doi: 10.1016/S0301-0082(97)00035-X
21. Jokinen TS, Tiira K, Metsähonkala L, Seppälä EH, Hielm-Björkman A, Lohi H, Laitinen-Vapaavuori O. Behavioral abnormalities in lagotto romagnolo dogs with a history of benign familial juvenile epilepsy: a long-term follow-up study. J Vet Inter Med. (2015) 29:1081–7. doi: 10.1111/jvim.12611
22. Lundgren T, Dahl J, Yardi N, Melin L. Acceptance and commitment therapy and yoga for drug-refractory epilepsy: a randomized controlled trial. Epilepsy Behav. (2008) 13:102–8. doi: 10.1016/j.yebeh.2008.02.009
23. Kanner AM. Management of psychiatric and neurological comorbidities in epilepsy. Nat Rev Neurol. (2016) 12:106. doi: 10.1038/nrneurol.2015.243
24. Mostofsky DI, Balaschak BA. Psychobiological control of seizures. Psychol Bull. (1977) 84:723–50. doi: 10.1037/0033-2909.84.4.723
25. Mittan RJ. Psychosocial treatment programs in epilepsy: a review. Epilepsy Behav. (2009) 16:371–80. doi: 10.1016/j.yebeh.2009.08.031
26. Haut SR, Lipton RB, Cornes S, Dwivedi AK, Wasson R, Cotton S, et al. Behavioral interventions as a treatment for epilepsy. A multicenter randomized controlled trial. Neurology (2018) 90: e963–70. doi: 10.1212/WNL.0000000000005109
27. Packer RMA, Volk HA, Fowkes RC. Physiological reactivity to spontaneously occurring seizure activity in dogs with epilepsy and their carers. Physiol Behav. (2017) 177:27–33. doi: 10.1016/j.physbeh.2017.04.008
28. Rousseau A, Hermann B, Whitman S. Effects of progressive relaxation on epilepsy: analysis of a series of cases. Psychol Rep. (1985) 57:1203–12. doi: 10.2466/pr0.1985.57.3f.1203
29. Dahl JA, Melin L, Lund L. Effects of a contingent relaxation treatment program on adults with refractory epileptic seizures. Epilepsia (1987) 28:125–32. doi: 10.1111/j.1528-1157.1987.tb03637.x
30. Puskarich CA, Whitman S, Dell J, Hughes JR, Rosen AJ, Hermann BP. Controlled examination of effects of progressive relaxation training on seizure reduction. Epilepsia (1992) 33:675–80. doi: 10.1111/j.1528-1157.1992.tb02346.x
31. Whitman S, Dell J, Legion V, Eibhlyn A, Statsinger J. Progressive relaxation for seizure reduction. J Epilepsy (1990) 3:17–22. doi: 10.1016/0896-6974(90)90073-8
32. Sathyaprabha TN, Satishchandra P, Pradhan C, Sinha S, Kaveri B, Thennarasu K, et al. Modulation of cardiac autonomic balance with adjuvant yoga therapy in patients with refractory epilepsy. Epilepsy Behav. (2008) 12:245–52. doi: 10.1016/j.yebeh.2007.09.006
33. Nagai Y, Goldstein LH, P.Fenwick BC, Trimble MR. Clinical efficacy of galvanic skin response biofeedback training in reducing seizures in adult epilepsy: a preliminary randomized controlled study. Epilepsy Behav. (2004) 5:216–23. doi: 10.1016/j.yebeh.2003.12.003
34. Gillham RA. Refractory Epilepsy: an evaluation of psychological methods in outpatient management. Epilepsia (1990) 31:427–32. doi: 10.1111/j.1528-1157.1990.tb05498.x
35. Spector S, Tranah A, Cull C, Goldstein LH. Reduction in seizure frequency following a short-term group intervention for adults with epilepsy. Seizure (1999) 8:297–303. doi: 10.1053/seiz.1999.0292
36. McLaughlin DP, McFarland K. A randomized trial of a group based cognitive behavior therapy program for older adults with epilepsy: the impact on seizure frequency, depression and psychosocial well-being. J Behav Med. (2011) 34:201–7. doi: 10.1007/s10865-010-9299-z
37. Au A, Chan F, Li K, Leung P, Li P, Chan J. Cognitive-behavioral group treatment program for adults with epilepsy in Hong Kong. Epilepsy Behav. (2003) 4:441–6. doi: 10.1016/S1525-5050(03)00149-5
38. Tan SY, Bruni J. Cognitive-behavior therapy with adult patients with epilepsy: a controlled outcome study. Epilepsia (1986) 27:225–33. doi: 10.1111/j.1528-1157.1986.tb03533.x
40. Brown RP, Gerbarg PL. Sudarshan kriya yogic breathing in the treatment of stress, anxiety, and depression: part I—neurophysiologic model. J Alternat Complement Med. (2005) 11:189–201. doi: 10.1089/acm.2005.11.189
41. Deepak KK, Manchanda SK, Maheshwari MC. Meditation improves clinicoelectroencephalographic measures in drug-resistant epileptics. Biofeedback Self Regul. (1994) 19:25–40. doi: 10.1007/BF01720668
42. Rajesh B, Jayachandran D, Mohandas G, Radhakrishnan K. A pilot study of a yoga meditation protocol for patients with medically refractory epilepsy. J Alternat Complement Med. (2006) 12:367–71. doi: 10.1089/acm.2006.12.367
43. Nagai Y, Goldstein LH, Critchley HD, P.Fenwick BC. Influence of sympathetic autonomic arousal on cortical arousal: implications for a therapeutic behavioural intervention in epilepsy. Epilepsy Res. (2004) 58:185–93. doi: 10.1016/j.eplepsyres.2004.02.004
44. Tan G, Thornby J, Hammond DC, Strehl U, Canady B, Arnemann K, et al. Meta-analysis of EEG biofeedback in treating epilepsy. Clin EEG Neurosci. (2009) 40:173–9. doi: 10.1177/155005940904000310
45. Reiter J, Andrews D, Janis C. Taking Control of Your Epilepsy2. A Workbook for Patients and Professionals. Santa-Rosa, CA: The Basic Publishing Company (1987).
46. Reiter JM, Andrews D, Reiter C, LaFrance W Jr. Taking Control of Your Seizures: Workbook Treatments That Work. New York, NY: Oxford University Press (2015).
47. Cramer JA, Perrine K, Devinsky O, Bryant-Comstock L, Meador K, Hermann B. Development and cross-cultural translations of a 31-item quality of life in epilepsy inventory. Epilepsia (1998) 39:81–8. doi: 10.1111/j.1528-1157.1998.tb01278.x
48. Michaelis R, Tang V, Wagner JL, Modi AC, LaFrance WC Jr, Goldstein LH, et al. Psychological treatments for people with epilepsy. Cochr Database Syst Rev. (2017) 4:CD002029. doi: 10.1002/14651858.CD012081.pub2
49. Johnson EK, Jones JE, Seidenberg M, Hermann BP. The relative impact of anxiety, depression, and clinical seizure features on health-related quality of life in epilepsy. Epilepsia (2004) 45:544–50. doi: 10.1111/j.0013-9580.2004.47003.x
50. Watson F, Rusbridge C, Packer RMA, Casey RA, Heath S, Volk HA. A review of treatment options for behavioural manifestations of clinical anxiety as a comorbidity in dogs with idiopathic epilepsy. Vet J. (2018) 238:1–9. doi: 10.1016/j.tvjl.2018.06.001
51. Packer RMA, De Risio L, Volk HA. Investigating the potential of the anti-epileptic drug imepitoin as a treatment for co-morbid anxiety in dogs with idiopathic epilepsy. BMC Vet Res. (2017) 13:90. doi: 10.1186/s12917-017-1000-0
52. McPeake KJ, Mills DS. The use of imepitoin (Pexion™) on fear and anxiety related problems in dogs – a case series. BMC Vet Res. (2017) 13:173. doi: 10.1186/s12917-017-1098-0
53. Forsgård J, Metsähonkala E, Kiviranta A, Cizinauskas S, Junnila J, Laitinen-Vapaavuori O, et al. Seizure-precipitating factors in dogs with idiopathic epilepsy. In: Berendt M, editor. 31st Annual Symposium of the ESVN-ECVN. Copenhagen (2018).
54. Finnegan S, Volk HA, Asher L, Daley M, Packer R. Identification of owner-perceived seizure triggers and behavioural predictors prior to seizure activity in dogs with idiopathic epilepsy. In: Berendt M, editor. 31st Annual Symposium of the ESVN-ECVN. Copenhagen (2018).
55. Thompson P, Baxendale S (eds.). Non-Pharmacological Treatment of Epilepsy. Oxford: Blackwell (1996).
56. Shell L, Scariano R, Rishniw M. Features of stimulus-specific seizures in dogs with reflex epilepsy: 43 cases (2000–2014). J Am Vet Med Assoc. (2016) 250:75–8. doi: 10.2460/javma.250.1.75
57. Beerda B, Schilder MBH, van Hooff JARAM, de Vries HW. Manifestations of chronic and acute stress in dogs. Appl Anim Behav Sci. (1997) 52:307–19. doi: 10.1016/S0168-1591(96)01131-8
58. Ziv G. The effects of using aversive training methods in dogs—A review. J Vet Behav. (2017) 19:50–60. doi: 10.1016/j.jveb.2017.02.004
59. Casey RA, Twells C, Blackwell E. An investigation of the relationship between measures of consistency in owners and the occurrence of ‘behavior problems' in the domestic dog. J Vet Behavior Clin Appl Res. (2007) 2:83–84. doi: 10.1016/j.jveb.2007.10.008
60. Blackwell E, Casey R, Bradshaw J. Controlled trial of behavioural therapy for separation-related disorders in dogs. Vet Rec. (2006) 158:551. doi: 10.1136/vr.158.16.551
61. Overall K. Manual of Clinical Behavioral Medicine for Dogs and Cats. St Louis: Elsevier Inc. (2013).
Keywords: canine, epilepsy, behavior therapy, relaxation, drug-resistant
Citation: Packer RMA, Hobbs SL and Blackwell EJ (2019) Behavioral Interventions as an Adjunctive Treatment for Canine Epilepsy: A Missing Part of the Epilepsy Management Toolkit? Front. Vet. Sci. 6:3. doi: 10.3389/fvets.2019.00003
Received: 12 December 2018; Accepted: 09 January 2019;
Published: 28 January 2019.
Edited by:
Luisa De Risio, Animal Health Trust, United KingdomReviewed by:
Daisuke Hasegawa, Nippon Veterinary and Life Science University, JapanSarah A. Moore, The Ohio State University, United States
Copyright © 2019 Packer, Hobbs and Blackwell. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Rowena M. A. Packer, rpacker@rvc.ac.uk