Research Article

in

EMDR to Treat Functional Neurological Disorder: A Review

Advertisement

Abstract

Eye movement desensitization and reprocessing (EMDR) therapy is an established treatment for posttraumatic stress disorder (PTSD), but there is increasing evidence for its use beyond PTSD. EMDR can be effective at treating distressing memories not associated with PTSD, as well as somatic symptoms (like chronic pain), and as such could potentially be used as a treatment for patients with functional neurological disorder (FND). Searches were conducted for published peer-reviewed articles on the use of EMDR for FND. The databases selected and searched were Medline, Embase, Cochrane Library, CINAHL Plus, Web of Science, PsychINFO, PubMed, and Francine Shapiro Library. This review was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. Three relevant articles were found. The studies included are one case series and two case studies. Of the five participants included in the studies, four experienced functional non-epileptic attacks; and one experienced functional movement disorder. Four out of the five patients were successfully treated with EMDR. EMDR is potentially a useful treatment of FND, but further research, including controlled trials, is required. The authors propose that EMDR could be useful in treating patients with FND and comorbid PTSD, as well as patients without comorbid PTSD. We discuss the clinical implications and propose how EMDR could fit into the FND treatment pathway.

Functional neurological disorder (FND), sometimes called conversion disorder, is a common presentation in neurology clinics (Snijders, de Leeuw, Klumpers, Kappelle, & van Gijn, 2004). The term refers to neurological symptoms, such as limb weakness or numbness, fits, dystonia, gait disturbance, episodes of altered awareness, and cognitive symptoms like memory disturbances or mental fogginess, unexplained by the presence of disease or injury to the body. Common presentations include functional non-epileptic attacks (FNEA), where a person presents with fits that resemble epileptic seizures but do not have associated epileptic activity; or functional motor symptoms, also referred to as functional movement disorder, such as gait disturbance, tremors, or weakness affecting one side of the body. FND is referred to as functional neurological symptom disorder in the Diagnostic and Statistical Manual of Mental Disorders (5th ed.; DSM-5; American Psychiatric Association [APA], 2013), dissociative disorder in the International Statistical Classification of Diseases and Related Health Problems, 10th Revision ICD-10 (ICD-10; World Health Organization [WHO], 1992), and other names including conversion disorder, medically unexplained symptoms (MUS), and psychogenic disorder; historically, it was referred to as hysteria. In the case of FNEA, other terms include: functional seizures, psychogenic non-epileptic seizures, pseudoseizures, and dissociative seizures.

Identification and communication regarding the diagnosis has improved (LaFrance, Reuber, & Goldstein, 2013), but evidence-based psychological treatments are still not clearly established (Martlew, Pulman, Marson, & Cochrane Epilepsy Group, 2014; Ruddy & House, 2005). There is some evidence for the use of cognitive-behavioral therapy (CBT) and psychodynamic interpersonal therapy (PIT) for FNEA (Goldstein et al., 2010; Howlett & Reuber, 2009; LaFrance et al., 2014), and physiotherapy is the most-established treatment for functional motor symptoms (Nielsen, Stone, & Edwards, 2013; Nielsen et al., 2015). Not providing effective treatments for FND is associated with significant costs, as without treatment many patients will be referred unnecessarily to multiple medical specialties and undergo repeated unnecessary medical investigations (Ahmedani et al., 2013; Magee, Burke, Delanty, Pender, & Fortune, 2014). Additionally, it has been estimated that patients with FND have similar or greater levels of distress compared to those with neurological disease (Carson et al., 2011).

Patients with FND are heterogeneous in their presentations, with comorbid mental health difficulties prominent in some, but absent in others (Brown & Reuber, 2016; Kranick et al., 2011; Rusch, Morris, Allen, & Lathrop, 2001). Posttraumatic stress disorder (PTSD) or posttraumatic symptoms are present in some patients with FND (Fiszman, Alves-Leon, Nunes, D’Andrea, & Figueira, 2004; Pick, Mellers, & Goldstein, 2017). Psychological therapists may commonly see patients presenting with distress and “medically unexplained” physical symptoms in their clinical practice, which can lead to interpretations that the physical symptoms are a physical manifestation of their distress and that their symptoms are due to trauma, in line with conversion theory and neurobiological accounts of the impact of trauma on the body (van der Kolk, 2003). This interpretation may be relevant for some patients, but there are many patients who present in neurology clinics without identifiable trauma in their background (Brown & Reuber, 2016; Edwards & Bhatia, 2012), and alternative theories such as attention to and expectations regarding symptoms may be a more fitting explanation in those cases (Edwards, Adams, Brown, Pareés, & Friston, 2012). Additionally, a patient may have identifiable trauma in his or her background, but it may not be related to their FND symptoms, although it could be considered a vulnerability factor.

There is debate in the literature regarding whether patients with FNEA and patients with functional motor symptoms should be grouped together, with evidence pointing toward functional motor symptoms more commonly occurring after a physical event, such as illness or surgery (Pareés et al., 2014). It is suggested that the experience of novel sensory data, alongside psychological factors like experiencing the symptoms as threatening, can lead to the motor symptoms developing. Some argue that FNEA and functional motor symptoms should be considered as having different psychological profiles, whereas others argue they have common psychological profiles (Demartini et al., 2016; Hopp, Anderson, Krumholz, Gruber-Baldini, & Shulman, 2012). In a systematic review of psychological and psychiatric aspects of FNEA alone, the authors conclude that patients presenting with FNEA are more likely to report higher physical symptoms generally; experiences of trauma are common but not always present; trait dissociation can be more common in FNEA patients, but not universally; and that inconsistent findings across studies are probably a reflection of the heterogeneous nature of patients experiencing FNEA (Brown & Reuber, 2016).

Description of EMDR

EMDR therapy was developed by Francine Shapiro in 1987 with the first study published in 1989 (Shapiro, 1989). It is a psychological therapy that has integrated cognitive-behavioral, psychodynamic, experiential, and gestalt ideas. The fundamental premise is that psychological distress (and somatic expressions of distress) originates from upsetting memories in a person’s past, and that targeting those key memories will result in resolution of the psychological distress. It was originally designed to focus on any distressing memories, but in order to test the therapy on a group of patients where upsetting memories are a problem, Francine Shapiro initially focused on the treatment of PTSD. But while EMDR is well known as an intervention to treat PTSD, it has applications beyond PTSD (Shapiro, 1999; Tesarz et al., 2014).

EMDR is designed to be utilized only by suitably qualified practitioner psychologists or psychotherapists, who have undergone the 7-day EMDR training required and who receive EMDR supervision. It is an eight-phase treatment, where the EMDR phases are the most distinctive part of the treatment (but this constitutes only three of the phases: 4–6). The theory behind EMDR therapy is the Adaptive Information Processing (AIP) model, which suggests that our information processing system assimilates new experiences into already existing memory networks. The AIP model proposes that pathology can occur when adverse life experiences are stored incorrectly into a state-specific form that is unable to connect to other memory networks that hold adaptive information. This subsequently disturbs the neurological system and can cause some of the symptomology experienced. The proposed mechanism of the EMDR treatment is an assimilation of adaptive information from other memory networks linking into the network holding the isolated adverse event, which allows learning to take place with the now adaptively stored event (Solomon & Shapiro, 2008). There are several theories regarding why the eye movements (or dual attention to auditory or tactile stimuli) may facilitate emotional processing (Andrade, Kavanagh, & Baddeley, 1997; Stickgold, 2002; van den Hout, Muris, Salemink, & Kindt, 2001), but like other psychological therapies, the specific mechanisms of action are not clear. It has been suggested that the eye movements allow the person to stay in an optimal zone for processing (i.e., not too distressed) (Jeffries & Davis, 2013). EMDR incorporates aspects of many psychological therapeutic approaches, and it is likely many parts of EMDR contribute to its effectiveness, not a single part. There has been controversy regarding whether the eye movements within EMDR are a necessary part of treatment, with disagreement among researchers (Davidson & Parker, 2001; Jeffries & Davis, 2013).

EMDR therapy is now an established and recommended treatment for PTSD (Bisson et al., 2013; National Institute for Clinical Excellence, 2005). Its use beyond PTSD has also been utilized. There is now accumulating evidence for its effectiveness in treating other disorders, including chronic pain (Tesarz et al., 2014) and anxiety disorders (Shapiro, 1999). Accordingly, modified EMDR protocols have been developed to support therapists (e.g., Grant’s EMDR pain protocol) (Grant & Threlfo, 2002).

Rationale for Using EMDR to Treat Functional Neurological Disorder

The history of trauma in patients with functional neurological symptoms is often significant. High rates of trauma and abuse, ranging from 44%–100% to 23%–77%, respectively, have been reported by patients with FNEA, 15%–40% higher than those found in control groups (Fiszman et al., 2004). The extent to which trauma is involved (if at all) may not be completely clear, but evidence indicates an increased risk compared to the general population. This suggests that the AIP model can potentially be applied to functional neurological symptoms.

For patients with comorbid PTSD and FND, EMDR would arguably already be a treatment option as it is already a treatment for the former. The gap in treatment, therefore, remains in those who have no comorbid PTSD, and whether EMDR therapy would still serve as a possible treatment option. These patients may have experienced “big T” trauma (required for the ICD-10 and the DSM-5 diagnosis of PTSD [APA, 2013; WHO, 1992]), but not have sufficient PTSD symptoms to meet the threshold for diagnosis. Patients can also report “small t” traumas associated with the start of their symptoms, such as conflict within their family or at work. Additionally, “small t” traumas that occurred in childhood (e.g., bullying) can have lasting negative effects upon a person and are known vulnerability factors in the development of mental health difficulties (Lereya, Copeland, Costello, & Wolke, 2015; Shapiro, 2014). There is evidence that EMDR can be effective at treating non-PTSD upsetting memories (Cvetek, 2008). Furthermore, memories of physical ill health, investigations, or operations could also be seen as “small t” trauma and may relate to symptomology; many patients with FND report a physical trigger to the start of their symptoms (Demartini et al., 2016). The AIP model posits that most forms of pathology are based on unprocessed memories, suggesting that EMDR could be useful for people with FND without comorbid PTSD linked to “small t” trauma.

The AIP model suggests that due to the state-specific nature the adverse event is held in, external and internal stimuli can continue to trigger the experience, which can result in inappropriate symptomology. In regards to MUS generally, van Rood and de Roos (2009) propose a triggering stimuli may result in physical symptomology in two ways: a physical re-experience (e.g., pain) of the adverse event triggered by associations to the event (e.g., loud noise), or the meaning of the somatic complaint (e.g., “I am helpless” in relation to fatigue) may remind (consciously or unconsciously) the patient of a previous traumatic event associated with a similar meaning (e.g., being sexually assaulted)—a cognitive and emotional re-experiencing. Therefore, EMDR therapy could target the traumatic memory, an upsetting memory related to the somatic symptom, or the somatic symptom itself during the desensitization phase. The traumatic memory could be a serious accident or physical abuse that is re-experienced with the physical complaint. The somatic symptom memory could be the upsetting experiences that surround the somatic symptom or the traumatic consequences of the somatic symptom (e.g., memory of having a FNEA). Lastly, the somatic symptom could be experienced in session and used (e.g., sensations of numbness), rather than the memory of the experience (van Rood & de Roos, 2009).

A systematic review by van Rood and de Roos investigated the treatment of EMDR and MUS. It focused on MUS generally and included a wide variety of somatic symptoms, from phantom limb pain to body dysmorphic disorder. The study concluded tentatively that EMDR might be useful in the treatment of MUS patients where the complaint is etiologically linked to or maintained by trauma.

Objectives

This review aims to access the literature regarding EMDR and functional neurological symptoms in order to examine the evidence base regarding effectiveness. MUS included in the van Rood and de Roos systematic review was a broad and heterogeneous collection of disorders (van Rood & de Roos, 2009); this review aims to narrow the scope to just functional neurological symptoms, in order to create a clear rationale for EMDR in the specific area of FND.

Method

Eligibility Criteria

This review was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement (Moher, Liberati, Tetzlaff, Altman, & PRISMA Group, 2009) and is registered with PROSPERO (PROSPERO ID 2016: CRD42016050520).

Reports of prospective interventions were included and screened for. The criteria for inclusion was (a) intervention studies (case studies, case series, controlled studies, uncontrolled studies), (b) published in peer-reviewed journals, (c) EMDR is the treatment of primary interest, (d) patients must have FND, and (e) the aim of the intervention must be to reduce the symptomology (frequency or intensity) associated with the FND. Initially, single case studies were not included but due to the lack of new articles or studies since the previous systematic review, the eligibility criteria were expanded to include case studies despite the high risk of bias. No controlled trials were found.

Search Strategy

A search was conducted for published peer-reviewed articles on the use of EMDR for functional neurological symptoms. First, all selected databases were searched using an extensive series of keywords associated with EMDR and functional neurological symptoms. Some of the search terms used were: functional neurological disorder, functional movement disorder, myoclonic movement, dystonia, conversion disorder, non-epileptic seizures, psychogenic seizures, somatoform disorder, somatization, hysteria, and MUS. For a full list of the search terms, see the Appendix. The databases selected and searched were Medline, Embase, Cochrane Library, CINAHL Plus, Web of Science, PsychINFO, PubMed, and Francine Shapiro Library. The full text articles were retrieved from any promising articles found from the searches. One author reviewed these (LM), and then two authors (SC and JS) verified the included and excluded studies independently. The clinicaltrials.gov and WHO international clinical trials registry platforms were also searched to find any ongoing clinical trials, but there were none relating to EMDR and FND. The original searches were conducted between October 2016 and January 2017, and the searches were re-run in November 2017, with no relevant new articles discovered.

Study Selection

The combination searching of both functional neurological symptoms (and its variant keywords) and EMDR totaled 108 references: 7 references from Medline with revisions, 18 references from Embase (14 were unique), 16 references from PsychINFO (13 were unique), 16 references from the Cochrane Library of Systematic Reviews, 3 references from the Cochrane Library of Controlled Trials, 14 references from CINAHL Plus (12 were unique), 24 references from Web of Science—one of which was later flagged by e-mail alert—(19 were unique), and 10 references from PubMed (0 were unique). Further screening of the references of any promising articles was carried out to search for more articles. This generated an additional two articles (Chemali & Meadows, 2004; Silver, Rogers, & Russell, 2008). Four articles were removed after full-text examination due to insufficient data (e.g., no clear pre-treatment and post-treatment data) or because they lacked original scientific data. All authors of the chosen three (Chemali & Meadows, 2004; Kelley & Benbadis, 2007; Silver et al., 2008) (Figure 1) were sent an e-mail enquiring of any further articles or ongoing projects they may have, but none responded.

Figure 1.
Flow diagram of search strategy and study selection.
sgremdr_12_3_118_fig01

Data Collection and Selected Studies

One author (LM) collected all the data from the articles, and two other authors (SC and JS) checked this independently if a problem arose. If any disagreements occurred, they were discussed and a conclusion was made between all three. Data were gathered regarding the characteristics of the participants and their presenting complaints; EMDR protocol used; EMDR targets used; length of treatment; therapist training level; how each study assessed the treatment, including assessor blinding and reliability; and the outcomes of the treatment, including symptom reduction and any outcome measures used. All articles were screened for report of any adverse events or safety problems. The overall quality of selected studies was assessed according to the Platinum Standard (PS) guidelines for EMDR evaluation (Hertlein & Ricci, 2004).

Results

An overview of the papers included in this systematic review is displayed in Table 1 according to authors, study type, participant, functional neurological symptoms, duration of symptoms, number of EMDR sessions, follow-up, and success of treatment. The studies included are one case series (Kelley & Benbadis, 2007) and two case studies (Chemali & Meadows, 2004; Silver et al., 2008). This totaled five participants. One of the case studies was part of a larger case series but the other participants did not fit the inclusion criteria (Silver et al., 2008). The literature search included studies from 1989 to 2016, although no studies that met the inclusion criteria were found from before 2004, and the most recent study was from 2008. The studies followed the same design of pre-treatment and post-treatment, and follow-up data. The follow-up period ranged from 3 months to 18 months after treatment.

Table 1.
Characteristics of the Studies and Study Participants Included in This Review
AuthorStudy TypeFunctional Neurological DisorderComorbiditiesDuration of SymptomNumber of EMDR SessionsFollow-upPrimary OutcomeSuccess of Treatment
Kelley and Benbadis (2007)Case seriesFNEAPTSD, major depression5 years618 monthsSeizure free+
FNEAPTSD, major depression, dependent personality disorder, unspecified learning disabilities2 years1 (EMDR discontinued due to patient unable to comply)NoneSeizures continued-
FNEAPTSD, mixed anxiety, and depressionMany years7NoneSeizure free+
Chemali and Meadows (2004)Case studyFNEAPTSD, borderline personality disorder3 years723 monthsSeizure free+
Silver et al. (2008)Case studyFunctional movement disorderPTSD, anxiety, depression35–40 years46 monthsMyoclonic movement free+

[i] Note. FNEA = functional non-epileptic attacks; PTSD = posttraumatic stress disorder.

Demographics of Participants

Four out of the five participants were female. The ages of participants ranged from 34 to 73 years, with a mean age of 47.8 years old. All were U.S.-based studies. All three participants of the case series are noted as White (Kelley & Benbadis, 2007), with the ethnic background of the other two participants unknown.

FND Presentation

Four participants experienced FNEA (Chemali & Meadows, 2004; Kelley & Benbadis, 2007); and one experienced functional myoclonic movement disorder (Silver et al., 2008). The duration of the symptoms varied among patients and disorders; the longest was the myoclonic movement case study of 35–40 years, while three of the FNEA participants had 2, 3, and 5 years’ symptom durations and the other participant with FNEA was described as having experienced fits for “many years.”

Comorbidities

A history of trauma with a diagnosis of PTSD was apparent in all five cases. This included war trauma (Silver et al., 2008) and childhood abuse (Chemali & Meadows, 2004; Kelley & Benbadis, 2007). Four of the five patients also had a diagnosis of depression, and one had a diagnosis of borderline personality disorder. As there is small sample size, it cannot be considered representative of the FND population.

Treatment

Patients were referred for EMDR due to ongoing and interfering functional neurological symptoms and because they had a comorbid diagnosis of PTSD. One patient requested EMDR based on familial advice (Chemali & Meadows, 2004).

The duration of treatment and frequency of EMDR sessions varied from case to case. The frequency varied from 1 to 72 sessions. Excluding the case consisting of 72 sessions, which is far greater than the others (and unusually long for an EMDR treatment), and examining only completed cases, the mean number of sessions was 5.7. Confusingly, in the case series (Kelley & Benbadis, 2007) patients also underwent “counseling sessions” from 10 to 20 months, consisting of trauma psychoeducation, behavioral, and supportive therapy techniques. The EMDR sessions were given after these preparatory sessions (Kelley & Benbadis, 2007). FNEA did not stop during this preparatory stage. It could be argued that the preparatory sessions were not separate from the EMDR treatment, as stabilization work is part of the EMDR protocol. Including the total number of psychological therapy sessions (both those classified as EMDR and as “counseling”), the mean number of treatment sessions increases to 17. Many of the patients were taking medications for their comorbidities, or for the functional neurological or somatic symptoms experienced. One of the patients was reported to be able to lower medication dosages after EMDR sessions (she stopped taking olanzapine, carbamazepine, and gabapentin, remaining on lamotrigine 275 mg and amitriptyline 20 mg daily, with clonazepam 0.5 mg twice a day in the process of being reduced) (Chemali & Meadows, 2004).

Only the case series included details on the therapists that undertook the EMDR therapy, both of which had Level II EMDR training (Kelley & Benbadis, 2007). Furthermore, the assessor in this study was separate to the therapist. This created a certain level of blinding. In one study, the therapist was also the assessor (Silver et al., 2008), which could have created bias in the outcome analysis. One study didn’t include details on the therapist or assessor (Chemali & Meadows, 2004). Activating the information processing system via “bilateral stimulation” was performed in different ways across the case studies. Eye movements were used in one study (Silver et al., 2008) and hand taps were used in the case series due to patients expressing discomfort with the repetitive eye movements (Kelley & Benbadis, 2007). One case study did not include details of the EMDR method used (Chemali & Meadows, 2004). The targets for the EMDR sessions were not stated in two of the three articles (Chemali & Meadows, 2004; Kelley & Benbadis, 2007). One specified it used the past war trauma as the target (Silver et al., 2008).

Outcome of Studies

The non-formal assessment of the clinically observed effect reported by the participants and therapists was the measurement used to decide the success of treatment. One study used standardized outcome measures to evaluate comorbid mental health difficulties (Silver et al., 2008).

Functional Non-Epileptic Attacks

The Kelley and Benbadis case series on FNEA only provided clinical observation to measure the success of the EMDR treatment. Of the three included case studies from the series (the participants who underwent EMDR processing sessions), two had successful treatment (case studies 2 and 7) as their FNEA were eliminated at post-treatment and follow-up. The patient that had unsuccessful treatment (case study 6) had only one EMDR desensitization session in which the patient experienced a FNEA. It should be noted that the patient also experienced fits (also considered to be FNEA) in their other “counseling” sessions. The case series included eight patients, all of which had a diagnosis of FNEA. Of the five patients not included in the review, two patients were seen for consultation only, two patients discontinued after two or three “counseling” sessions (with no EMDR sessions), and one patient became seizure free after the neurologist told him “You don’t have to do that anymore.” Therefore, they had a drop-out rate of 37.5% (three out of eight participants) before any therapy sessions. The participant described in the Chemali and Meadows’ study was FNEA-free at the end of treatment and at follow-up. She was able to reduce the medication prescribed by the end of treatment. No pharmacological changes were made between post-treatment and follow-up. However, between the end of treatment sessions and the follow-up session 3-months post-treatment, the patient experienced a severe depressive episode, was hospitalized, and was diagnosed with borderline personality disorder. In the follow-up period, it describes her attending dialectical behavioral therapy, but details regarding this were not provided. Therefore, the participant remaining FNEA-free at follow-up cannot be wholly accounted for by the EMDR treatment.

Functional Myoclonic Movement Disorder

The participant in Silver and colleagues’ study went from experiencing upper body shaking 20 times a day to 3 times or less per day after the first session, and at the end of treatment, no shaking was reported. The absence of shaking continued in the follow-ups at 1 month and 6 months. Data regarding level of depression and PTSD symptomatology were also measured using the Beck Depression Inventory (Beck, Ward, Mendelson, Mock, & Erbaugh, 1961), Beck Hopelessness Scale (Beck & Steer, 1988), and the Impact of Events Scale (Horowitz, Wilner, & Alvarez, 1979). Prior to treatment, he scored in the moderate ranges on the two former measures, and in the severe range on the latter. After treatment, he scored 0 on all the measures, indicating additional remission of PTSD and depression.

Platinum Standard Assessment

The overall quality of the studies was assessed using the Hertlein and Ricci’s (2004) PS criteria for EMDR studies to create a PS score, as shown in Figure 2. One point, 0.5, or 0 is awarded for each of the 13 PS criteria (e.g., clearly defined target symptoms or treatment adherence) and these are summed to give the PS score (with 13 being the best score possible). All of the studies in this review received low scores. This is mainly due to the fact they are case studies and therefore don’t meet many of the criteria, such as use of control group or effect size reporting. Some information was missing in all the studies (e.g., all studies provided no information on assessor training), which resulted in 0 scoring for the relevant criterion because it must be assumed that it was not considered in the research design. It remains possible, of course, that the studies followed the PS criteria more closely than their score suggests but the information was not included in the articles. The average PS score from the Hertlein and Ricci review of empirical studies of EMDR treating PTSD symptoms was 7.75. This suggests that the quality of the studies, and their design, included in this review is below average.

Figure 2.
Platinum standard score for included studies.
sgremdr_12_3_118_fig02

Limitations

The overall quality of the studies, according to the Hertlein and Ricci (2004) PS criteria for EMDR studies, was low. Important details regarding treatment given were missing, including therapist qualifications, EMDR targets, and that the EMDR method varied across the case studies, with some patients receiving “counseling” sessions prior to EMDR. Additionally, the sample of patients included in the case reports was varied in terms of age, prescribed medication, and comorbid difficulties, while blinding was variable.

Case studies are often subject to publication and reporting bias, which can skew results. As only case studies and one case series—with a small number of cases—were available, no meta-analyses could be carried out; only descriptive analysis performed. Consequently, clear estimates of the effect size of EMDR treatment cannot be determined. The case study design also means that results may be due to placebo or other factors.

The measurements of outcome in the case studies included in this review were limited. Subjective reporting of FND symptoms was the primary outcome for all studies and this can only be primarily measured by patient report. Only one case study used standardized outcome measures to assess comorbid mental health difficulties, when clearly mood and comorbid mental health difficulties are important to assess before and after treatment. Additionally, arguably when assessing outcome of patients with functional neurological symptoms, pre- and post-assessment regarding the impact of symptoms on day-to-day functioning would be an important treatment outcome to measure, and no study administered standardized measures assessing daily function. Nevertheless, although multimodal measurement is a criterion in the platinum standard guidelines for EMDR studies, no association has been found between multimodal measurement and treatment effect (Maxfield & Hyer, 2002).

Discussion

This article aimed to systematically review the evidence regarding the use of EMDR as a treatment for FND. Of the five patients treated across three studies, four patients were successfully treated for their conditions: three who experienced FNEA and one who experienced a functional movement disorder. Despite the limitations of the studies included, the successes outweigh the failures in this review, and therefore point to the potential promise of EMDR treatment, or at least an avenue of treatment that warrants further investigation. All patients treated had a history of trauma. This may be indicative of the proposed link between FND and trauma, or the association of PTSD with EMDR may have directed treatment for the patients toward EMDR. All studies found were published between 2004 and 2008. The lack of newer EMDR research with the FND population is surprising given the advancements in the literature and research of other physical conditions and EMDR treatment such as chronic pain (including phantom limb pain and migraines), in which observational and controlled trials have been administered (Shapiro, 2014; Tesarz et al., 2014). The stigma of FND or EMDR may be a reason for this lack of research, both subject to controversy (Davidson & Parker, 2001; Jeffries & Davis, 2013; Nicholson, Stone, & Kanaan, 2011; Wessely & White, 2004). Another potential reason is that FND research is focusing on other nonpharmacological treatments, such as physiotherapy and cognitive-behavioral therapy (Goldstein et al., 2015; Nielsen et al., 2015).

Clinical Implications

This review demonstrates some promising evidence for the use of EMDR in treatment of FND with comorbid PTSD. This is not surprising given the proven effectiveness of EMDR to treat PTSD (Bisson et al., 2013; National Institute for Clinical Excellence, 2005). It suggests it may also be beneficial at treating associated somatic expressions, where there is a link between development of FND symptoms and traumatic experiences. Additionally, many patients with FND do not meet the criteria for a diagnosis of PTSD, but may have identifiable traumatic experiences in the background, such as experiences of childhood abuse (Fiszman et al., 2004; Myers, Perrine, Lancman, Fleming, & Lancman, 2013). The small amount of evidence from this review suggests EMDR could potentially be a helpful treatment for these presentations. Adding weight to this idea, EMDR is designed to treat traumatic memories (not just PTSD), so any presentation where the patient has identifiable trauma memories (whether “small t” or “big T” trauma) (Cvetek, 2008; Shapiro, 2014) that still distress him or her in the present day may be a suitable candidate for EMDR therapy (with or without comorbid PTSD).

An intriguing development of the usefulness of EMDR therapy is its use in treating somatic symptoms, such as chronic pain conditions like phantom limb pain, fibromyalgia, neuropathic pain, musculoskeletal pain, and headache (Tesarz et al., 2014). The target memories in EMDR treatment can be the pain itself or a distressing memory associated with the pain. de Jongh and colleagues demonstrated that in 64 patients—50% with PTSD, 50% without PTSD—there was no difference between groups in terms of reduction of vividness and emotionality associated with the target memory, suggesting that EMDR impacts on negative memories generally, not just those associated with PTSD (de Jongh, Ernst, Marques, & Hornsveld, 2013).

Therefore, we propose that EMDR therapy is possibly useful as a treatment for patients with FND in four possible ways: (a) comorbid PTSD associated with the FND; (b) distressing childhood trauma memories that may be relevant in terms of a person’s tendency to dissociate; (c) distressing memories associated with the FND symptoms, for example, memory of when the symptoms started (such as following a medical procedure); and (d) the FND symptoms (possibly using an adapted version of the pain protocol). This is summarized in Table 2. These potential uses of EMDR as a treatment for FND need to be properly researched, but we suggest that all four potential uses are examined.

Table 2.
Possible Uses of EMDR for Patients With Functional Neurological Disorder
1. Posttraumatic stress disorder
2. Childhood trauma memories
3. Distressing memories associated with FND
4. FND symptoms

It has been proposed that a one-treatment approach is not suitable for those with FND, and treatment should be individualized according to need (Agrawal, Gaynor, Lomax, & Mula, 2014; LaFrance, 2007). In Figure 3, we propose a FND pathway where EMDR treatment could potentially fit in. We suggest that after patients have had both neurological and neuropsychiatric assessment, they can attend group or individual psychoeducation regarding FND. Following this, depending on clinical need (and availability), they may then receive neuropsychiatric treatment, physiotherapy, psychological treatment (which could possibly include EMDR), and/or intensive inpatient or day-patient programs.

Figure 3.
Proposed functional neurological disorder care pathway, with possible role of EMDR.
sgremdr_12_3_118_fig03

The potentially short duration of EMDR therapy is useful, as is the nature of the therapy, which does not require the patient to speak in detail about associated distressing material. This could serve to reduce drop-out rates as difficulty identifying and discussing feelings can be a feature of patients with FNEA (Brown & Reuber, 2016). High drop-out rates were a problem in the Kelley and Benbadis case series (Kelley & Benbadis, 2007), but the study design included counseling sessions prior to the EMDR desensitization sessions, and this may have had the unintended consequence of causing people to disengage as they were not ready to consider possible links between their FND and past trauma. This was evidenced by one participant who dropped out prior to EMDR sessions, after the therapist suggested his FNEA were related to the death of his son.

Many patients with FND, in particular those with FNEA, have a general tendency to dissociate (Demartini et al., 2016; Pick et al., 2017). Although EMDR can be effective even when patients have dissociative tendencies, it should be noted that caution is required when working with this patient group. The desensitization phase requires accessing trauma memories, which may well trigger dissociation in the session. Clinicians using EMDR with patients who are highly dissociative, in particular patients with a diagnosis of dissociative identity disorder, need to have experience of working with this population, and be confident in their use of EMDR, in particular their ability to manage abreactions in session and the use of cognitive interweaves. Inadequate screening, preparation, or delivery of EMDR with this population can be destabilizing to patients’ mental health (Shapiro, 2001).

Future Research

The evidence presented from the case studies cannot be generalized, and clearly controlled trials are needed in order to properly establish EMDR therapy’s effectiveness with FND presentations. Given the small number of participants evaluated in the case studies presented, even an observational study with a larger sample size would be of benefit. Future trials would need to take into account the heterogeneous nature of the patients, perhaps examining subgroups of FND separately (e.g., FNEA vs. functional movement disorder), but then also the different presentations within each subgroup (e.g., associated with identifiable trauma or not). Non-trauma-based studies with FND patients are needed to determine whether the target can in fact be somatic symptom-based or needs to be a traumatic memory target. Van Rood and de Roos (van Rood & de Roos, 2009) noted in regards to a few studies on chronic pain that the pain as the target was not as effective as targeting the trauma (Mazzola et al., 2009; Wilensky, 2006).

In terms of measurement of outcomes, it will be important to examine not just reduction/resolution in FND symptoms, but also impact of symptoms on day-to-day functioning and mood.

Conclusions

Despite the limitations the case studies present, they offer a window into the possibilities that EMDR therapy could hold for patients suffering with FND. EMDR could potentially be a useful therapy for patients with FND, who have identifiable trauma in their background (with and without comorbid PTSD). Additionally, the burgeoning evidence for EMDR therapy’s effectiveness at treating chronic pain conditions suggests a utility for treating somatic symptoms alone, as well as the usefulness of targeting distressing memories associated with somatic symptoms. It is possible that EMDR could be used both as a treatment that targets distressing memories associated with the first experience of FND symptoms, as well as a treatment targeting FND symptoms alone, without targeting any traumatic or distressing memories. Further research, in particular controlled trials, is needed.

References

  1. Agrawal, N., Gaynor, D., Lomax, A., & Mula, M. (2014). Multimodular psychotherapy intervention for nonepileptic attack disorder: An individualized pragmatic approach. Epilepsy & Behavior, 41, 144–148. 10.1016/j.yebeh.2014.09.041
  2. Ahmedani, B. K., Osborne, J., Nerenz, D. R., Haque, S., Pietrantoni, L., Mahone, D., & Smith, B. J. (2013). Diagnosis, costs, and utilization for psychogenic non-epileptic seizures in a US health care setting. Psychosomatics, 54(1), 28–34. 10.1016/j.psym.2012.08.005
  3. American Psychiatric Association. (2013). Diagnostic and statistical manual of mental disorders (5th ed). Arlington, VA: American Psychiatric Publishing.
  4. Andrade, J., Kavanagh, D., & Baddeley, A. (1997). Eye-movements and visual imagery: A working memory approach to the treatment of post-traumatic stress disorder. British Journal of Clinical Psychology, 36(2), 209–223. 10.1111/j.2044-8260.1997.tb01408.x
  5. Beck, A. T., & Steer, R. A. (1988). Manual for the Beck Hopelessness Scale. San Antonio, TX: Psychological Corporation.
  6. Beck, A. T., Ward, C. H., Mendelson, M., Mock, J., & Erbaugh, J. (1961). An inventory for measuring depression. Archives of General Psychiatry, 4, 561–571. 10.1001/archpsyc.1961.01710120031004
  7. Bisson, J. I., Roberts, N. P., Andrew, M., Cooper, R., Lewis, C., & Cochrane Common Mental Disorders Group. (2013). Psychological therapies for chronic post-traumatic stress disorder (PTSD) in adults. In Bisson, J. I (Ed.), Cochrane Database of Systematic Reviews (Vol. 12). Chichester, UK: John Wiley & Sons, Ltd. 10.1002/14651858.CD003388.pub4
  8. Brown, R. J., & Reuber, M. (2016). Psychological and psychiatric aspects of psychogenic non-epileptic seizures (PNES): A systematic review. Clinical Psychology Review, 45, 157–182. 10.1016/j.cpr.2016.01.003
  9. Carson, A., Stone, J., Hibberd, C., Murray, G., Duncan, R., Coleman, R., … Sharpe, M. (2011). Disability, distress and unemployment in neurology outpatients with symptoms unexplained by organic disease. Journal of Neurology, Neurosurgery & Psychiatry, 82(7), 810–813. 10.1136/jnnp.2010.220640
  10. Chemali, Z., & Meadows, M. E. (2004). The use of eye movement desensitization and reprocessing in the treatment of psychogenic seizures. Epilepsy & Behavior, 5(5), 784–787. 10.1016/j.yebeh.2004.06.003
  11. Cvetek, R. (2008). EMDR treatment of distressful experiences that fail to meet the criteria for PTSD. Journal of EMDR Practice and Research, 2(1), 2–14.
  12. Davidson, P. R., & Parker, K. C. (2001). Eye movement desensitization and reprocessing (EMDR): A meta-analysis. Journal of Consulting and Clinical Psychology, 69(2), 305–316.
  13. de Jongh, A., Ernst, R., Marques, L., & Hornsveld, H. (2013). The impact of eye movements and tones on disturbing memories involving PTSD and other mental disorders. Journal of Behavior Therapy and Experimental Psychiatry, 44(4), 477–483. 10.1016/j.jbtep.2013.07.002
  14. Demartini, B., Goeta, D., Barbieri, V., Ricciardi, L., Canevini, M. P., Turner, K., … Gambini, O. (2016). Psychogenic non-epileptic seizures and functional motor symptoms: A common phenomenology? Journal of the Neurological Sciences, 368, 49–54. 10.1016/j.jns.2016.06.045
  15. Edwards, M. J., Adams, R. A., Brown, H., Pareés, I., & Friston, K. J. (2012). A Bayesian account of “hysteria.” Brain, 135(Pt 11), 3495–3512. 10.1093/brain/aws129
  16. Edwards, M. J., & Bhatia, K. P. (2012). Functional (psychogenic) movement disorders: Merging mind and brain. The Lancet. Neurology, 11(3), 250–260. 10.1016/S1474-4422(11)70310-6
  17. Fiszman, A., Alves-Leon, S. V., Nunes, R. G., D’Andrea, I., & Figueira, I. (2004). Traumatic events and posttraumatic stress disorder in patients with psychogenic nonepileptic seizures: A critical review. Epilepsy & Behavior, 5(6), 818–825. 10.1016/j.yebeh.2004.09.002
  18. Goldstein, L. H., Chalder, T., Chigwedere, C., Khondoker, M. R., Moriarty, J., Toone, B. K., & Mellers, J. D. (2010). Cognitive-behavioral therapy for psychogenic nonepileptic seizures: A pilot RCT. Neurology, 74(24), 1986–1994. 10.1212/WNL.0b013e3181e39658
  19. Goldstein, L. H., Mellers, J. D., Landau, S., Stone, J., Carson, A., Medford, N., … Chalder, T. (2015). Cognitive behavioural therapy vs standardised medical care for adults with Dissociative non-Epileptic Seizures (CODES): A multicentre randomised controlled trial protocol. BMC Neurology, 15(1), 98. 10.1186/s12883-015-0350-0
  20. Grant, M., & Threlfo, C. (2002). EMDR in the treatment of chronic pain. Journal of Clinical Psychology, 58(12), 1505–1520. 10.1002/jclp.10101
  21. Hertlein, K. M., & Ricci, R. J. (2004). A systematic research synthesis of EMDR studies: Implementation of the platinum standard. Trauma, Violence & Abuse, 5(3), 285–300. 10.1177/1524838004264340
  22. Hopp, J. L., Anderson, K. E., Krumholz, A., Gruber-Baldini, A. L., & Shulman, L. M. (2012). Psychogenic seizures and psychogenic movement disorders: Are they the same patients? Epilepsy & Behavior, 25(4), 666–669. 10.1016/j.yebeh.2012.10.007
  23. Horowitz, M., Wilner, N., & Alvarez, W. (1979). Impact of event scale: A measure of subjective stress. Psychosomatic Medicine, 41(3), 209–218. 10.1097/00006842-197905000-00004
  24. Howlett, S., & Reuber, M. (2009). An augmented model of brief psychodynamic interpersonal therapy for patients with nonepileptic seizures. Psychotherapy, 46(1), 125–138. 10.1037/a0015138
  25. Jeffries, F. W., & Davis, P. (2013). What is the role of eye movements in eye movement desensitization and reprocessing (EMDR) for post-traumatic stress disorder (PTSD)? A review. Behavioural and Cognitive Psychotherapy, 41(3), 290–300. 10.1017/S1352465812000793
  26. Kelley, S. D. M., & Benbadis, S. (2007). Eye movement desensitization and reprocessing in the psychological treatment of trauma-based psychogenic non-epileptic seizures. Clinical Psychology and Psychotherapy, 14, 135–144.
  27. Kranick, S., Ekanayake, V., Martinez, V., Ameli, R., Hallett, M., & Voon, V. (2011). Psychopathology and psychogenic movement disorders. Movement Disorders, 26(10), 1844–1850. 10.1002/mds.23830
  28. LaFrance, W. C. (2007). Treating patients with functional symptoms: One size does not fit all. Journal of Psychosomatic Research, 63(6), 633–635. 10.1016/j.jpsychores.2007.09.001
  29. LaFrance, W. C., Baird, G. L., Barry, J. J., Blum, A. S., Frank Webb, A., Keitner, G. I., … Szaflarski, J. P. (2014). Multicenter pilot treatment trial for psychogenic nonepileptic seizures: A randomized clinical trial. JAMA Psychiatry, 71(9), 997. 10.1001/jamapsychiatry.2014.817
  30. LaFrance, W. C., Reuber, M., & Goldstein, L. H. (2013). Management of psychogenic nonepileptic seizures. Epilepsia, 54(Suppl 1), 53–67. 10.1111/epi.12106
  31. Lereya, S. T., Copeland, W. E., Costello, E. J., & Wolke, D. (2015). Adult mental health consequences of peer bullying and maltreatment in childhood: Two cohorts in two countries. The Lancet Psychiatry, 2(6), 524–531. 10.1016/S2215-0366(15)00165-0
  32. Magee, J. A., Burke, T., Delanty, N., Pender, N., & Fortune, G. M. (2014). The economic cost of nonepileptic attack disorder in Ireland. Epilepsy & Behavior, 33, 45–48. 10.1016/j.yebeh.2014.02.010
  33. Martlew, J., Pulman, J., Marson, A. G., & Cochrane Epilepsy Group. (2014). Psychological and behavioural treatments for adults with non-epileptic attack disorder. In Martlew, J (Ed.), Cochrane database of systematic reviews (p. CD00637018). Chichester, UK: John Wiley & Sons, Ltd. 10.1002/14651858.CD006370.pub2
  34. Maxfield, L., & Hyer, L. (2002). The relationship between efficacy and methodology in studies investigating EMDR treatment of PTSD. Journal of Clinical Psychology, 58(1), 23–41.
  35. Mazzola, A., Calcagno, M. L., Goicochea, M. T., Pueyrredòn, H., Leston, J., & Salvat, F. (2009). EMDR in the treatment of chronic pain. Journal of EMDR Practice and Research, 3(2), 66–79.
  36. Moher, D., Liberati, A., Tetzlaff, J., Altman, D. G., & PRISMA Group. (2009). Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement. PLoS Medicine, 6(7), e1000097. 10.1371/journal.pmed.1000097
  37. Myers, L., Perrine, K., Lancman, M., Fleming, M., & Lancman, M. (2013). Psychological trauma in patients with psychogenic nonepileptic seizures: Trauma characteristics and those who develop PTSD. Epilepsy & Behavior, 28(1), 121–126. 10.1016/j.yebeh.2013.03.033
  38. National Institute for Clinical Excellence. (2005). Post-traumatic stress disorder (PTSD): The treatment of PTSD in adults and children. Understanding NICE guidance–information for people with PTSD, their advocates and carers, and the public. Retrieved from https://www.nice.org.uk/guidance/cg26/resources/posttraumatic-stress-disorder-ptsd-the-treatment-of-ptsd-in-adults-and-children-pdf-193439629
  39. Nicholson, T. R., Stone, J., & Kanaan, R. A. (2011). Conversion disorder: A problematic diagnosis. Journal of Neurology, Neurosurgery & Psychiatry, 82(11), 1267–1273. 10.1136/jnnp.2008.171306
  40. Nielsen, G., Ricciardi, L., Demartini, B., Hunter, R., Joyce, E., & Edwards, M. J. (2015). Outcomes of a 5-day physiotherapy programme for functional (psychogenic) motor disorders. Journal of Neurology, 262(3), 674–681. 10.1007/s00415-014-7631-1
  41. Nielsen, G., Stone, J., & Edwards, M. J. (2013). Physiotherapy for functional (psychogenic) motor symptoms: A systematic review. Journal of Psychosomatic Research, 75(2), 93–102. 10.1016/j.jpsychores.2013.05.006
  42. Pareés, I., Kojovic, M., Pires, C., Rubio-Agusti, I., Saifee, T. A., Sadnicka, A., … Edwards, M. J. (2014). Physical precipitating factors in functional movement disorders. Journal of the Neurological Sciences, 338(1-2), 174–177. 10.1016/j.jns.2013.12.046
  43. Pick, S., Mellers, J. D., & Goldstein, L. H. (2017). Dissociation in patients with dissociative seizures: Relationships with trauma and seizure symptoms. Psychological Medicine, 47(7), 1–15. 10.1017/S0033291716003093
  44. Ruddy, R., & House, A. (2005). Psychosocial interventions for conversion disorder. Cochrane Database of Systematic Reviews, 4(4), CD005331-CD005331. 10.1002/14651858.CD005331.pub2
  45. Rusch, M. D., Morris, G. L., Allen, L., & Lathrop, L. (2001). Psychological treatment of nonepileptic events. Epilepsy & Behavior: E&B, 2(3), 277–283.
  46. Shapiro, F. (1989). Efficacy of the eye movement desensitization procedure in the treatment of traumatic memories. Journal of Traumatic Stress, 2(2), 199–223.
  47. Shapiro, F. (1999). Eye movement desensitization and reprocessing (EMDR) and the anxiety disorders: Clinical and research implications of an integrated psychotherapy treatment. Journal of Anxiety Disorders, 13(1-2), 35–67.
  48. Shapiro, F. (2001). Eye movement desensitization and reprocessing: Basic principles, protocols, and procedures (2nd ed.). New York, NY: Guilford Press.
  49. Shapiro, F. (2014). The role of eye movement desensitization and reprocessing (EMDR) therapy in medicine: Addressing the psychological and physical symptoms stemming from adverse life experiences. The Permanente Journal, 18(1), 71–77. 10.7812/TPP/13-098
  50. Silver, S. M., Rogers, S., & Russell, M. (2008). Eye movement desensitization and reprocessing (EMDR) in the treatment of war veterans. Journal of Clinical Psychology, 64(8), 947–957. 10.1002/jclp.20510
  51. Snijders, T. J., de Leeuw, F. E., Klumpers, U. M., Kappelle, L. J., & van Gijn, J. (2004). Prevalence and predictors of unexplained neurological symptoms in an academic neurology outpatient clinic—an observational study. Journal of Neurology, 251(1), 66–71. 10.1007/s00415-004-0273-y
  52. Solomon, R. M., & Shapiro, F. (2008). EMDR and the adaptive information processing model: Potential mechanisms of change. Journal of EMDR Practice and Research, 2(4), 315–325. 10.1891/1933-3196.2.4.315
  53. Stickgold, R. (2002). EMDR: A putative neurobiological mechanism of action. Journal of Clinical Psychology, 58(1), 61–75. 10.1002/jclp.1129
  54. Tesarz, J., Leisner, S., Gerhardt, A., Janke, S., Seidler, G. H., Eich, W., & Hartmann, M. (2014). Effects of eye movement desensitization and reprocessing (EMDR) treatment in chronic pain patients: A systematic review. Pain Medicine, 15(2), 247–263. 10.1111/pme.12303
  55. van den Hout, M., Muris, P., Salemink, E., & Kindt, M. (2001). Autobiographical memories become less vivid and emotional after eye movements. British Journal of Clinical Psychology, 40(Pt 2), 121–130. 10.1348/014466501163571
  56. van der Kolk, B. A. (2003). The neurobiology of childhood trauma and abuse. Child and Adolescent Psychiatric Clinics of North America, 12(2), 293–317. 10.1016/S1056-4993(03)00003-8
  57. van Rood, Y. R., & de Roos, C. (2009). Medically unexplained symptoms and somatoform disorders. Journal of EMDR Practice and Research, 3(4), 248–263.
  58. Wessely, S., & White, P. D. (2004). There is only one functional somatic syndrome. British Journal of Psychiatry, 185(2), 95–96. 10.1192/bjp.185.2.95
  59. Wilensky, M. (2006). Eye movement desensitization and reprocessing (EMDR) as a treatment for phantom limb pain. Journal of Brief Therapy, 5(1), 31–44.
  60. World Health Organization. (1992). The ICD-10 classification of mental and behavioral disorders: Clinical descriptions and diagnosis guidelines. Retrieved from http://www.who.int/classifications/icd/en/bluebook.pdf

Acknowledgments.

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Appendices

Appendix

List of search terms used in database search:

Functional neurological symptom* OR Medically unexplained symptom* OR Psychogenic movement disorder* OR Functional symptom* OR Hysteria OR Conversion disorder*, ([Psychogenic non-epileptic and seizure*) or attack*) OR ((Non-epileptic and attack*] or disorder*) OR Non-organic, myoclonic movement* OR (dystonia or tremor* or dysphonia or “sensory disturb*” or “hemisensory syndrome*”) OR Gait disorder* OR Movement disorder* OR Functional paralysis OR Blackout* OR ((Functional and movement disorder*) or weakness disorder*) OR somatization OR somatisation OR exp somatoform disorder/ AND “Eye movement desensitisation reprocessing” OR “Eye movement desensitization reprocessing” OR “Eye movement desensitisation” OR “Eye movement desensitization” OR EMDR

Figures

Figure 1.
Flow diagram of search strategy and study selection.
sgremdr_12_3_118_fig01View in Context
Figure 2.
Platinum standard score for included studies.
sgremdr_12_3_118_fig02View in Context
Figure 3.
Proposed functional neurological disorder care pathway, with possible role of EMDR.
sgremdr_12_3_118_fig03View in Context

Tables

Table 1.
Characteristics of the Studies and Study Participants Included in This Review
AuthorStudy TypeFunctional Neurological DisorderComorbiditiesDuration of SymptomNumber of EMDR SessionsFollow-upPrimary OutcomeSuccess of Treatment
Kelley and Benbadis (2007)Case seriesFNEAPTSD, major depression5 years618 monthsSeizure free+
FNEAPTSD, major depression, dependent personality disorder, unspecified learning disabilities2 years1 (EMDR discontinued due to patient unable to comply)NoneSeizures continued-
FNEAPTSD, mixed anxiety, and depressionMany years7NoneSeizure free+
Chemali and Meadows (2004)Case studyFNEAPTSD, borderline personality disorder3 years723 monthsSeizure free+
Silver et al. (2008)Case studyFunctional movement disorderPTSD, anxiety, depression35–40 years46 monthsMyoclonic movement free+

[i] Note. FNEA = functional non-epileptic attacks; PTSD = posttraumatic stress disorder.

View in Context
Table 2.
Possible Uses of EMDR for Patients With Functional Neurological Disorder
1. Posttraumatic stress disorder
2. Childhood trauma memories
3. Distressing memories associated with FND
4. FND symptoms
View in Context
Article usage
Article Usage
Period Abstract Full PDF Total
Apr 2024 41 229 30 300
Mar 2024 54 123 23 200
Feb 2024 67 138 30 235
Jan 2024 56 156 15 227
Dec 2023 50 89 16 155
Nov 2023 34 126 25 185
Oct 2023 48 106 22 176
Sep 2023 29 74 20 123
Aug 2023 152 108 20 280
Jul 2023 66 99 15 180
Jun 2023 55 116 26 197
May 2023 51 100 20 171
Apr 2023 67 106 22 195
Mar 2023 67 157 29 253
Feb 2023 38 147 21 206
Jan 2023 37 119 32 188
Dec 2022 35 131 24 190
Nov 2022 33 110 23 166
Oct 2022 53 138 34 225
Sep 2022 49 100 28 177
Aug 2022 18 109 17 144
Jul 2022 41 105 17 163
Jun 2022 42 84 18 144
May 2022 51 119 25 195
Apr 2022 40 139 30 209
Mar 2022 42 130 27 199
Feb 2022 40 142 19 201
Jan 2022 49 121 25 195
Dec 2021 28 102 10 140
Nov 2021 29 97 14 140
Oct 2021 37 104 9 150
Sep 2021 25 102 19 146
Aug 2021 24 88 15 127
Jul 2021 19 104 24 147
Jun 2021 15 172 14 201
May 2021 23 170 16 209
Apr 2021 20 186 16 222
Mar 2021 32 177 24 233
Feb 2021 27 161 17 205
Jan 2021 32 138 24 194
Dec 2020 31 141 12 184
Nov 2020 61 116 19 196
Oct 2020 29 57 7 93
Sep 2020 36 59 12 107
Aug 2020 26 50 12 88
Jul 2020 23 49 6 78
Jun 2020 14 54 13 81
May 2020 28 82 12 122
Apr 2020 21 83 12 116
Mar 2020 21 56 13 90
Feb 2020 30 48 5 83
Jan 2020 17 62 10 89
Dec 2019 26 26 4 56
Nov 2019 89 2 0 91
Oct 2019 76 1 1 78
Sep 2019 77 0 0 77
Aug 2019 70 0 2 72
Jul 2019 46 0 4 50
Jun 2019 58 0 1 59
May 2019 57 0 1 58
Apr 2019 82 0 7 89
Mar 2019 72 4 5 81
Feb 2019 65 5 3 73
Jan 2019 64 1 2 67
Dec 2018 55 4 6 65
Nov 2018 50 7 3 60
Oct 2018 69 7 12 88
Sep 2018 107 13 16 136
Aug 2018 61 13 18 92