Treatment of Conversion Disorder



Treatment of Conversion Disorder


P. Rosebush

Michael F. Mazurek





INTRODUCTION

The condition we call “conversion disorder” (CD) was known to physicians at least as far back as the 16th century, and perhaps even earlier (1). By the late 19th century, it had become one of the first neurologic or psychiatric illnesses for which an effective treatment was available. An early breakthrough in this regard was the discovery by the Parisian neurologist Charcot that the symptoms of CD could be dramatically reversed with hypnosis. Soon afterward, the Viennese neurologist and neuroscientist Breuer recognized, through his successful treatment of the patient Anna O, that psychotherapeutic intervention could be even more effective than hypnosis, producing not merely an amelioration of symptoms, but an actual cure. This striking ability of psychotherapy to treat CD persuaded Breuer’s younger Viennese colleague, Freud, to break from neurology and establish psychiatry as an independent discipline.

By the late 1800s, CD had become one of the few neuropsychiatric conditions that was amenable to treatment. It is, therefore, ironic that CD has become an underrecognized and poorly treated cause of chronic disability. In our experience, there are two major reasons for this state of affairs: (i) the failure of physicians to make the diagnosis, and (ii) uncertainty about how the problem should be treated once a diagnosis has been made.


CURRENT STUDY

Over a 12-year period from 1992 to 2004, we have diagnosed CD in 45 patients, according to the Diagnostic and Statistical Manual of Mental Diseases, Fourth Edition (DSM-IV), which requires that the following diagnostic criteria be met:



  • A patient must have one or more symptoms or deficits affecting voluntary motor or sensory function that suggest a neurologic or other general medical condition.


  • Psychological factors are judged to be associated with the symptoms or deficit because the initiation or exacerbation of the symptoms or deficit is preceded by conflicts or other stressors.


  • The symptom or deficit is not intentionally produced or feigned.


  • The symptom or deficit cannot, after appropriate investigation, be fully explained by a general medical condition or by the direct effects of a substance, or as a culturally sanctioned behavior or experience.


  • The symptom or deficit causes clinically significant distress or impairment in social, occupational, or other important areas of functioning, or warrants medical evaluation.


This series did not include any individuals who were involved in litigation. The majority of patients were referred with a tentative diagnosis of conversion disorder, after extensive investigations failed to yield another condition that might account for their presentation, or when the course of a presumed condition, such as multiple sclerosis, was atypical. In a number of instances, we made the diagnosis after being asked to consider whether a rare metabolic or degenerative neuropsychiatric disorder might explain the clinical picture.


Nature of the Conversion Disorder

The frequency of CD type in the 45 patients was as follows:



  • Limb paralysis or immobility in 23 (50%); for 19, this was the predominant feature.


  • Seizurelike activity in 15 (37%); for 13, this was predominant.


  • Bizarre excessive movements such as dystonic posturing, choreoathetosis, or coarse tremulousness in 17 (38%); this was the primary manifestation in eight.


  • Speech disturbances in seven (15%); the main conversion feature in two.


  • Ataxia in five (11%); predominant in two.

In total, 20 patients (44%) manifested more than one type of neurologic abnormality and of these, almost half displayed more than two types of disturbance. Seventeen patients (38%) complained of sensory symptoms such as pain, shocklike sensations, vibrations, or paresthesias, and six (13%) endorsed cognitive problems in the form of poor concentration, “confusion,” disorientation, and memory impairment.


Burden of Illness

All patients were severely affected by their illness, as reflected in the following:



  • A period of complete inability to work, attend school, or care for children or family as before (40/45; 100%).


  • Being bedridden (13/45; 29%) or regularly using assistive devises such as a cane, walker, or wheelchair (13/45; 29%).


  • Daily dependence upon caregivers for feeding, dressing, mobilization, hygiene, toileting, or safety (22/45; 50%).


  • Long duration of symptoms: this was more than two years in 27 patients (60%).


  • A mean Global Assessment of Function (GAF) score of 35. This represents a score of 50 or less in all but one case, and 30 or less in 16 (35%). A score of 50 reflects serious impairment in social, occupational, or school functioning, and a score of 30, an inability to function in almost all areas.


Psychiatric Comorbidity


Psychiatric

Twenty-seven patients (60%) met DSM-IV criteria for at least one other psychiatric illness in their lifetime. These disorders included: personality (n = 16; 35%); affective (n = 10; 22%); anxiety (n = 6; 13%); somatization (n = 9; 20%); posttraumatic stress (n = 2; 4%), and anorexia nervosa or bulimia (n = 3; 6%). Seventeen patients (38%) had received psychiatric treatment in the past for one of the aforementioned diagnoses. The identified comorbid conditions were active at the time of our assessments in 11 (24%). It is noteworthy that none of the patients had experienced psychotic symptoms or been diagnosed with schizophrenia, and over 75% had no history of any type of substance abuse.


Response to Treatment

Of the 45 patients assessed, 32 engaged in treatment, four were beginning treatment at the time of this report, and nine others had refused involvement in our program. Of those who refused treatment, only one enjoyed spontaneous improvement, and another, a 22-year-old woman, died from the complications of prolonged immobility secondary to leg paralysis. She had been bedridden for 4 years and developed contractures and recurrent infections, eventually succumbing to a pulmonary embolus. Efforts to engage her in psychiatric treatment were angrily rejected.

Twenty-six (81%) of the 32 patients who engaged in treatment had complete resolution of all conversion signs and symptoms, and no longer required care or use of assistive devices. The six other patients had partial, but functionally significant, improvement. They no longer required care from others and were able to return to work or school, but continued to experience symptoms or “episodes” intermittently.

All but two of the patients treated were hospitalized with an average length of stay of 8 weeks (range: 1 week to 6 months).


CASE STUDIES

Our approach in this article will be to describe in detail a number of these cases, with attention to the issues that helped give rise to the conversion symptoms and pointed the way to a successful therapeutic plan. This will be followed by a discussion of the barriers to diagnosis and treatment of this condition. We conclude with an attempt to summarize the principles of treatment that have proven effective in our patients.


Case 1: Conversion Disorder Presenting as Multiple Sclerosis

This 33-year-old married mother of two, BT, was well until the age of 30, when she began to experience leg weakness,
urinary retention, paresthesiae, and easy fatigability and muscle pain. She was referred to a neurologist, who recorded a number of abnormal findings including clonus, increased muscle tone, and absence of abdominal reflexes. She was diagnosed as having probable multiple sclerosis, and for the next three years was followed in the MS clinic of a teaching hospital. Over the first year of her illness, she deteriorated rapidly and lost control of her legs and bladder. Numerous investigations were undertaken, including magnetic resonance imaging (MRI) of the brain and spinal cord, electromyography (EMG), electroencephalography (EEG), evoked potentials (EVP), lumbar puncture, myelogram, cystoscopy, and cystometrogram. She was eventually referred to us for a second opinion because the severity of her disability seemed to be out of keeping with the persistent absence of lesions on repeat MRI scans.

When we initially assessed BT at age 33, she had been confined to a wheelchair for two years and was treating her “neurogenic bladder” with regular self-catheterization. She was taking 16 different medications for treatment of depression, muscle spasms, pain, constipation, and bladder dysfunction. We were not able to find any convincing abnormalities on neurologic examination.


Medical History

Prior to the age of 30, BT had no history of neurologic or psychiatric illness. There was no history of substance abuse. She did, however, have childhood asthma, for which she was reportedly hospitalized on multiple occasions before the age of 10.


Relevant Personal History

BT was raised in poverty by an abusive, alcoholic father and a mother who was “always sick” with “leg problems.” She had to assume care for her younger siblings and remembered feeling overwhelmed by their demands. During hospitalizations for asthma she enjoyed a respite from her responsibilities and the strife at home. BT fondly recalled the attention she received from nurses.

Following completion of high school, she married a man from a different ethnic background with a large extended family. There were culturally endorsed expectations that BT would care for her husband’s ill mother and grandmother, as well as help out with the family business. At the same time, she was expected to work full-time, care for their own children, and manage the household. BT attempted to keep up with these multiple demands for a number of years, but felt trapped, deprived, and inadequate. She particularly felt that she was neglecting her own children just as she had been neglected. Shortly before the development of her CD, BT was involved in a minor motor vehicle accident for which she was found to be at fault. While neither she nor anyone else was hurt, a young child was in the other vehicle and BT recalled hearing him cry. In the months that followed, she became “obsessed” with the cry of this child. It was over this period of time that she began to experience the leg weakness, paresthesiae, and bladder symptoms.

In trying to understand BT, why she developed CD when she did, and what issues would have to be addressed and resolved in psychotherapeutic treatment, we considered the factors below.


Predisposing Factors



  • Parental neglect and abuse which resulted in low self-esteem and chronically unmet needs.


  • Identification with a sick mother for whom she was prematurely responsible.


  • Repeated hospitalizations for asthma during which she was exposed to the only nurturing environment she knew as a child, and provided with relief from an abusive, neglectful home situation.


Precipitating Factors



  • Extreme fatigue secondary to overwork.


  • An increasing sense of being trapped, neglected, and taken advantage of in her marital and social situation.


  • A sense of inadequacy and failure as she took on more responsibilities and yet felt she did nothing very well.


  • A minor motor vehicle accident in which she heard a child crying. This seemed to personify her own needs as well as those of her own children, whom she thought she was neglecting.


Perpetuating Factors



  • Being cared for when she was ill, but not when she was well.


  • Being released from overwhelming responsibilities as a result of being disabled.


  • Not wanting to acknowledge her intense anger and other conflicted feelings about her family of origin as well as her marital situation.


  • Failure of physicians to accurately diagnose her condition earlier.


Approach to Treatment

At the time of our initial assessment, we asked BT to consider that “stress” and “pent-up emotions” might be playing at least some role in her condition. We presented her inability to walk in terms of a simple analogy, comparing her motor system to the engine of a car. If the car will not run, one possible explanation might be a breakdown of some vital engine part. Alternatively, there might be a disconnection between the ignition and an otherwise normal motor. In this case, the car can function if an appropriate starter signal can be restored. BT responded to this notion of a “mind-body disconnection” as an explanatory model for her inability to move her legs. We indicated to her that, in our opinion, her central nervous system “motor” was fundamentally
sound, and that she therefore had the potential for a complete recovery. We emphasized the importance of trying to understand what was causing the “disconnection” at the same time as she received physiotherapy for her motor dysfunction.

BT was hospitalized in our neuropsychiatry inpatient service for 6 months. During this time, all medications were tapered and discontinued. We discouraged self-catheterization and initiated physiotherapy three times a week with a focus upon learning to walk and regaining control over her motor function. Daily psychotherapy sessions were carried out. Much time was spent inquiring about her past life, earlier development, and why she had become who she was. She was also encouraged to talk about her life prior to her illness. Interventions typically involved helping her to correctly identify the feelings that had been aroused in different situations, both in her early life and later in her marriage. We acknowledged her ability to put her own needs aside and her strong sense of responsibility and compassion for others. At the same time, we pointed out the absence of an appropriate sense of entitlement to have her own needs met. Her self-esteem was low and she clearly harbored a deep sense of deprivation. She was also angered by others’ expectations of her. She felt intense, yet unexpressed, anger toward her husband for his role in creating and allowing a situation that recapitulated important aspects of her early life. BT saw herself as a victim and without any control. These unconscious feelings of anger had resulted in significant problems with intimacy as she distanced herself from others, including her husband and her own children, in order to avoid overt expression of her rage. The intensity of her rage—a word she began to use—often frightened her and, although she had no history of aggression, she was concerned that she might hurt someone. Feelings of rage eventually gave way to sadness and she developed a clinical depression, which was treated with antidepressant medication. Efforts to engage her husband in marital therapy were unsuccessful.


Outcome and Follow-up

Six months after admission, BT was no longer using the wheelchair. She walked with a cane and required assistance in going up and down stairs. At this point she was discharged and seen in twice-weekly psychotherapy by one of us (PR) for the next 2 years. Antidepressant medication was continued during this time. Eight months after discharge, she was walking normally, and within a year she had returned to her factory job. She soon assumed full-time hours and began to coach baseball in her spare time. She initiated a separation from her husband and maintained full custody of her children. At 5-year follow-up, she had remarried, and at 10-year follow-up, continued to work full-time with no relapses of her CD or hospitalizations for other reasons.


Case 2: CD Presenting as a Neurometabolic Disorder

This 13-year-old girl, HN, was healthy and developing normally until the age of 9, when she began to complain of a range of medical symptoms, including excessive fatigability, headache, gastrointestinal disturbances, and weakness. She was hospitalized for investigations, initially at her local hospital and later for a full year on the pediatric service of a major out-of-province teaching hospital. At times she required tube feeding. Extensive testing failed to yield a diagnosis. Meanwhile, she continued to clinically deteriorate to the point where she was confined to a wheelchair. She was eventually referred to us with the provisional diagnosis of an inherited neurometabolic disorder, with the hope that we might be able to provide biochemical and genetic characterization of her problem.

When we initially assessed her at the age of 13, HN was completely unable to walk. She had been confined to a wheelchair for one year, and had not attended school for two. She was reluctant to go outside, claiming that it made her feel “nervous.” Despite the fact that she had not been diagnosed with any specific psychiatric disorder, several selective serotonin reuptake inhibitor antidepressant medications had been prescribed over the previous 3 years. She had no response and repeatedly developed akathisia with use of these agents.

We observed HN interacting with hospital staff prior to our initial formal assessment. When not in her wheelchair, she was in bed, requiring assistance with toileting, feeding, and turning. With any effort to move her legs, she displayed striking “overflow” choreoathetotic movements of her head, arms, and torso. Otherwise, her neurologic examination showed no convincing abnormalities. There were striking inconsistencies between what she could do when distracted and what she was purportedly able to do in response to specific requests.


Investigations

In view of the clinical history, we undertook fairly extensive investigations, including a cranial MRI, EMG, muscle biopsy, EEG, evoked potentials, ophthalmologic assessment, cognitive testing, and various enzyme analyses, all of which yielded normal results.


Relevant Personal History

HN came from a stable, well-adjusted family and had a normal upbringing. By temperament she was shy, anxious, and easily frightened. At age 9, six months prior to her first bout of illness, she had witnessed the unprovoked and repeated stabbing of a classmate by another classmate’s mother. She and the child who was assaulted were alone in the school cloakroom at the time. HN did not reveal this history herself and when asked about it replied, “It didn’t really bother me because I was busy tying up my shoes.” Shortly after this horrific event, her dog, which had always
provided her with a sense of protection, died. Despite these events, she denied experiencing any stress other than that caused by her illness.

In arriving at a formulation we considered the following:


Predisposing Factors



  • An anxious temperament.


Precipitating Factors



  • Witnessing a life-threatening assault.


  • Death of a pet.


Perpetuating Factors



  • Failure to consider a diagnosis of CD.


  • Ongoing secondary gain of being able to avoid almost all social situations, including the added social and interpersonal expectations that would naturally have begun to occur around this age.


Approach to Treatment

While comfortable having a neurologic assessment, HN was initially very upset about seeing a psychiatrist and voiced her concern that our involvement meant she was “crazy” and “imagining everything.” Despite this, she did not resist hospitalization and listened intently to our explanation that she was suffering from a stress-related illness that had caused her to lose control of her legs. We emphasized that investigations had indicated that the “hard-wiring” required for walking was intact, but that her brain was having difficulty “cueing up” the motor program that would normally allow her to walk and use her legs normally. We likened this to a CD player having problems “reading” the information on a particular compact disc, making it impossible to play the recorded music. We explained that stress can be present and affect the body without any real emotional awareness. We put it in terms of stress disturbing the “cueing” function in the brain, with the result that some of the motor “programs” may not get “played” properly. An important, explicitly stated goal of psychotherapy was that she would become more conscious of how life events made her feel so that the “short-circuiting” to her body might be interrupted.

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Sep 12, 2016 | Posted by in PSYCHIATRY | Comments Off on Treatment of Conversion Disorder

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