Medically unexplained symptoms (somatisation, hypochondriasis, conversion disorder) Flashcards Preview

Year 5 - Psychiatry > Medically unexplained symptoms (somatisation, hypochondriasis, conversion disorder) > Flashcards

Flashcards in Medically unexplained symptoms (somatisation, hypochondriasis, conversion disorder) Deck (45)
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1
Q

Define functional symptoms.

A

Complex problems in the body with no detectable structural or physiological cause

2
Q

What % of consultations in GP are due to MUS?

A

Up to 20%

3
Q

Why is MUS important?

A

Associated with unnecessary costs and hospitalisations

Affects all ages

Investigation can cause harm

UK cost of MUS exceeds £3.1 billion each year

4
Q

Define MUS.

A

Persistent bodily complaints for which adequate examination doesn’t reveal sufficient explanatory structural or other specific pathology

5
Q

What are the main three categories of MUS symptoms?

A
  • Pain in different locations
  • Functional disturbance of organ systems
  • Complaints of fatigue and exhaustion
6
Q

What is the general criteria for diagnosing MUS?

A
  • Physical symptoms
  • For 3 months
  • Affecting functioning
  • Cannot be readily explained

Psychological and physical factors are often key, not just psychological.

7
Q

Rather than mind and body, what is a more useful classification of MUS?

A

Functional vs structural

Whereby functional is MUS. Medically unexplained can seem like a psychiatric issue (i.e. it’s all in the person’s head) and like not enough investigations can be done, when actually we know a lot about MUS/functional symptoms

Cartesian mind-body dualism is not useful

8
Q

Which MUS is CBT useful in?

A
  • Chronic fatigue syndrome
  • Irritable bowel syndrome
  • Chronic pain
  • Multiple somatisation disorder
9
Q

What are the risk factors for MUS?

A
  • Long term conditions associated with anxiety/depression
  • Childhood adversity/abuse
  • More common in women
  • In severe cases overlap with personality disorder
  • Recent infection, current physical illness, severe illness or death of close relative
10
Q

What % of patients with MUS go on to have an organic explanation for their presentation?

A

4-10%

75% remain unexplained at 1 year

11
Q

What % of patients with MUS have a coexistent psychiatric disorder?

A

30% (but could be 10-80%)

12
Q

How do patients and doctors with MUS often feel?

A

Patients:

  1. Very strong feelings
  2. Disbelieved and accused of fabricating symptoms

Doctors:

  1. Doctors feel challenged about competence
  2. They get called different negative terms - “frequent fliers”, “heart sink”

Physical disorders are seen as real and patients as victims, psychiatric disorders as ‘not real’ and patients responsible for symptoms

13
Q

What do patients say is the most useful and important factors in their recovery?

A

Whether the diagnosis and explanation they were given made sense to them – perhaps not immediately, but eventually.

14
Q

What are the key parts of the explanation of MUS?

A
  1. You have something common – you are not weird
  2. You do have something genuine – you are not imagining it
  3. You have symptoms that are potentially reversible
  4. It’s not your fault that you have these symptoms
  5. But you will need to put some effort into getting better
15
Q

Compare and contrast the somatoform disorders.

A

Somatization Disorder – patients believe they have been sickly most of their lives, complain of multitude of symptoms referred to numerous organ systems. Great concern about symptoms.

Conversion Disorder (now seen as dissociative symptoms) – loss of function, characterized by signs or symptoms inconsistent with what is known about anatomy and pathophysiology. Patients usually only have one symptom almost always neurological. They sometimes appear surprisingly unconcerned about their condition

Hypochondriasis – patient will believe, or strongly suspect, that they are ill with a very serious disease. Minor symptoms or anomalies support or augment their concern. The concern persists despite reassurance by doctors. Not so much concerned with the symptoms but the implied terrible and undiagnosed disease.

16
Q

What is somatisation disorder AKA?

A

Briquet’s Syndrome

17
Q

How common is somatisation disorder? Who is it more common in?

A

Lifetime prevalence is 0.1-0.2%

F:M 5-20-:1

Usually onset in teens (<30yrs)

18
Q

What are some theories for the aetiology of somatisation?

A

Biological: there is some evidence for faulty processing of sensory inputs in patients with this disorder. Genetics: 10 – 20 % 1st degree relatives

Psychosocial: a form of communication or as substitutions for repressed instinctual urges.

  • The Sick Role (Parsons)
  • Illness Behaviour (Mechanic/Pilowsky)
  • Alexithymia – no words for moods
  • Culture / Family experience – early learning/attentional gain
  • Environment – secondary gain
19
Q

What do you call the lack of concern about the patients’ condition in conversion disorder?

A

La Belle indifference - a casual disregard for normally alarming symptoms

20
Q

Describe the usual onset of somatisation disorder.

A
  • Gradually fall in in teenage years (onset past 30 years is rare)
  • Common initial complaints are headache, dysmenorrhoea, abdominal pain
21
Q

What are the features of symptoms of somatisation disorder? What parts of the body are usually affected?

A

Multiple, recurrent and frequent changing

  • Patients are vague or dramatic, giving vague accounts and moving from one organ system to another
  • Have seen many doctors and hospitalized many times
  • Patients often fatigued, weak all over, plagued with headaches, dizzy spells and pain in the chest, heart beats wildly and dyspnea can occur
  • Pains in arms and legs, the back and many joints
  • Vague and poorly localized abdominal pain, nausea and bloating, constipation, irregular painful or heavy menstruation
22
Q

How do you manage somatisation disorder in a GP setting?

A
  1. Establish long-term relationship with one clinician
  2. Schedule regular follow ups e.g. every month
  3. Consider psychiatric consultation, group therapy or CBT
  4. +/- antidepressants for those with depressive symptoms
  5. Gradual and managed increase in exertion
23
Q

What is the prognosis of somatisation disorder?

A

Often chronic, presents at least once a year and a new symptom occurring when stressed

24
Q

What is the management of chronic fatigue syndrome?

A
  1. Combination of psychological and antidepressant treatment
  2. Gradual and managed increase in exertion
25
Q

What can sometimes affect the type of symptoms which occur in conversion disorder?

A

Generally a reflection of symptoms the patient has seen in another or has personally experienced

The symptom is like a ‘sign language’ saying what the patient cannot put into words

26
Q

When does conversion disorder usually occur?

A

Any time of life but usually adolescence and early adult life

Usually following a stressful life event

27
Q

What criteria must be fulfilled to diagnose conversion disorder?

A
  • Demonstrate with certainty that the symptoms clearly violate laws of anatomy and pathophysiology
  • No other explanation can be found
  • If in doubt, defer diagnosis and observe the patient over a period of time until clinical picture crystalises
28
Q

What are the differentials for conversion disorder?

A
  • MS
  • SLE
  • Polyarteretis nodosa
  • Sarcoidosis

These can all present in subtle and deceptive ways.

29
Q

What are the clinical features of conversion anaesthesia?

A

Conversion anaesthesia:

  • Anaesthesia of extremities (glove and stocking) with recise sharp boundaries often located at a joint
    • If asked yes/no to touch with eyes closed says no each time anaesthetic area is touched (i.e. they shouldn’t be saying anything)​
  • Hemianaesthesia bisecting the body
  • Lack of feelings in legs yet able to walk normally
  • Reflexes show no hyporeflexia
30
Q

What are the clinical features of conversion paralysis?

A

Conversion paralysis:

  • Weakness with precise boundaries
  • Hemiplegia in arm will cause it to hang lumply in side for a long time rather than be in typical flexion posture
  • Wrong way tongue sign
  • Weakened leg is dragged instead of circumducted
  • Hoover’s sign
  • Absent Babinski’s sign and no reflexes
31
Q

What is wrong way tongue sign?

A

Protruded tongue instead of deviating towards the hemiplegic side deviates instead to the normal side

32
Q

What is Hoover’s sign?

A

Hip flexure on normal side against resistance produces downward pressure in affected leg

33
Q

What are the clinical features of conversion seizures?

A

Conversion seizures

  • Grand mal seizures most common
  • Onset gradual rather than sudden
  • If patient cries out at onset it is usually intelligible screaming rather than an inarticulate cry
  • Movements during seizure appear purposeful (thrash around, strike at walls, break one piece of furniture) in contrast to the rhythmic tonic-clonic activity seen in grand mal seizures. - when you say their name they will look away purposefully rather than ignoring
  • Most don’t bite their tongue and only those with considerable medical sophistication may pass urine.
  • End gradually rather than abruptly and after patients are neither confused nor sleepy
  • If eyes open tend to look away from the observer
34
Q

What investigations can you do to confirm conversion seizures?

A
  • Post ictal Babinski’s sign
  • Post ictal prolactin elevation (take blood 15-30 minutes after seizure)

Many patients with epilepsy also have non-epileptic seizures, conversely patients who display non-epileptic seizures may also have epilepsy

35
Q

Give a feature of these other conversion disorders.

  1. Conversion deafness
  2. Conversion blindness + unilateral blindness
  3. Conversion aphonia
  4. Conversion syncope
  5. Conversion coma
A
  • Conversion deafness - the blink reflex to loud and unexpected sound is present
  • Conversion blindness - the pupillary reflex is present
  • Unilateral blindness - demonstrate that the peripheral fields are full in the unaffected eye and that the pupillary response is present in both eyes.
  • In conversion aphonia – ask patient to cough during examination of lungs. Cough is full and loud.
  • Conversion syncope - faint has a swooning character
  • Conversion coma – fluttering of eyelids when eyelashes lightly stroked, resistance to eyelid opening & abrupt closure when eyelids released & normal pupillary responses. Surprise touch to the face of an ice cube
36
Q

What is the prognosis with conversion disorder?

A

May be episodic or chronic course

Can remit spontaneously within weeks/months

37
Q

What is the management of conversion disorder?

A

1. Inform the patient- “I have good news: the examination and the tests have revealed no damage to the brain and nerves. Although we don’t always know the cause of symptoms it is known that patients recover usually within weeks.”

Never say “there is nothing wrong with you” as this will ruin the doctor-patient relationship.

2. Physiotherapy helps the patient providing an honourable way out of the symptoms.

38
Q

What are the clinical features of hypochondriasis? When does it usually begin?

A

Can begin from teenage to older years

  • Patients believe that they are sick with perhaps a life threatening illness
  • Patients may be willing to undergo dangerous tests e.g cardiac catheterization.
  • Symptoms change with time
  • They may bring photocopies of all their records with them
  • Reassurance does not work and leads to a fragile alliance which rarely lasts
  • Includes non-delusional dysmorphophobia - a preoccupation with an imagined bodily defect

Be alert to the possibility that minor symptoms do in fact indicate a serious disease

39
Q

What is a useful method for explaining somatisation/conversion to patients?

A

Drawing a timeline

Helps patients visualise

40
Q

What can be a trigger for hypochondriasis? What are some other aetiologies?

A

Witnessing or experiencing an illness can be a trigger – the post MI patient who becomes a “cardiac cripple”.

  • Faulty cognitive scheme of focusing on bodily sensations and misinterpreting them as serious
  • Entering the sick role as a “way out” of insurmountable problems
  • Variant in the presentation of anxiety/mood disorder
  • Displacement of aggressive and hostile wishes towards others, or expression of guilt or low self esteem
41
Q

How common is hypochondriasis?

A
  • Prevalence: 5%
  • F=M
  • Typically onset in 20’s
42
Q

What is the prognosis with hypochondriasis?

A

Tends to be chronic and lifelong

Doctors may cause iatrogenic harm

30-50% improve significantly

43
Q

What is the management of hypochondriasis?

A

CBT/ psychodynamic/ group therapy- patient untlikely to accept, although it may have some positive benefit

Consistency: offer patient regularly scheduled appointments, with the same therapist/doctor

Medication: some evidence that Fluoxetine 60-80 mg reduces concerns

Need to exclude depression especially in elderly where hypochondraical symptoms may predominate. Hypochondraical delusions will not respond to reassurance whereas they will briefly in hypochondriasis.

44
Q

Key point:

Associated pathology is rare and rarely missed, whereas psychiatric diagnoses are common and often missed

Agree levels of activity and tell them not to do more than agreed

Management…

A
  1. Regular scheduled appointments
  2. Perform a brief physical examination at each visit
  3. Look for signs of disease rather than relying on symptoms
  4. Avoid investigations and hospital admissions, unless clearly indicated, may decrease physical functioning
  5. Antidepressants can help (NNT 4), low dose may be helpful
  6. Advise activity rather than rest for back pain, fatigue & fibromyalgia (activity to be agreed, not to do more than agreed, and gradually increased)
45
Q

What is the NNT for antidepressants in MUS?

A

Only 4 so they are actually very effective

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