Restless Leg Syndrome
D.M.W. Dharmakeerthi (MD)
Senior Registrar in Clinical
Neurophysiology
Restless Leg Syndrome
•“The most common
disorder some have
never heard of.”
What are Restless legs?
 Neurological movement disorder
 Irresistible urge to move legs when at
rest
 Difficulty sleeping
 Involuntary periodic leg movements
 Uncomfortable sensation in limbs
subjective & difficult to describe
 Symptoms eased by movement
Why should we know about it?
 Excess 5 million in UK are sufferers (MEMO
2000)
 Estimated prevalence 2-15%
 Sufferers will present to primary care
 Important physical cause of sleep
disturbance
 Clinical diagnosis which can be made in
primary care
Why should we know about it?
 Unrecognised & under-diagnosed
 Incorrectly labeled as stress / anxiety
 Managed poorly
Wide spectrum
 Affects any age group
 More common in middle age + women
 Mild
 Minimal distress
 Severe
 Episodes occur >2 per week
 Can be disabling
Why is it important?
 Large impact on quality of life: (REST Study)
 Poor sleep
 Inability to get comfortable / relax
 Poor concentration / fatigue
 Pain
 Depression
 Problems in day to day functioning / employment
 Implications for partner
Common descriptive terms
used by patients
How do we diagnose RLS?
 International Restless Legs Syndrome
Study Group - 2003
Supporting Features
 Positive FHx (50-92%)
 Involuntary limb movements (80%)
 Sleep disturbance
Classification
 Primary
 No underlying cause found.
 Positive FHx >50%
 Earlier onset / slower progression
 Secondary
Sudden onset.
Often occurs after the age of 40
Most associated with specific medical
conditions or the use of certain drugs.
Pathophysiology
 Genetic
 Susceptibility loci identified on 3
chromosomes
 Genetic anticipation
 Positive FHx >50%
 Neurochemical
 Dopaminergic dysfunction - universal
response to dopaminergic agents
 Ferritin level - inverse relation between
severity and serum ferritin
Primary RLS
 Idiopathic.
 Familial in 25-75% of cases(AD).
 Progressive decrease in age at onset
with subsequent generations ( genetic
anticipation).
 Begins before approximately 40 to 45
years of age, and can even occur as
early as the first year of life.
Primary RLS
 Onset is often slow.
 RLS may disappear for months, or even
years.
 Often progressive and gets worse as
the person ages.
 RLS in children is often misdiagnosed
as growing pains.
Secondary RLS
 Iron deficiency
 Varicose vein
 folate deficiency
 magnesium deficiency
 sleep apnea
 uremia
 diabetes
 thyroid disease
Secondary RLS
 Auto-immune disorders (
Sjögren's syndrome, celiac disease and
rheumatoid arthritis)
 Acute intermittent porphyria
 Fibromyalgia
 Cholesterol peripheral microemboli.
 RLS can also worsen in pregnancy.
Neurologic conditions linked to
RLS
 Parkinson disease
 Spinal cerebellar atrophy
 Spinal stenosis
 Lumbosacral radiculopathy
 Charcot-Marie-Tooth disease type 2.
What investigations should we
do?
 Exclude secondary cause.
 Vascular dx / Neuropathy / nocturnal
cramp / anxiety
 Examination
 Neuro / vascular
 Bloods
 FBC, ferritin, B12, Folate, U&E, Glucose,
TFT, Auto immune screening etc.
What are the treatment
options?
 Non Pharmacological
 Preventative measures
 Symptomatic control
 Pharmacological
 PRN treatment - mild / intermittent
 Maintenance treatment - moderate / severe
 Majority of treatments used ‘off license’
Non pharmacological
treatment
 Preventative
 Avoid caffeine / alcohol / nicotine
 Avoid medication which may aggravate

SSRI / antihistamine / antiemetic / CaChannel blockers
 Keep active into evening
 Good sleep hygiene
 Symptom control
 Mental alerting activities
 Walking / stretching
 Massage
 Hot / cold bath
 Relaxation / biofeedback
Pharmacological options
Drug Advantage Disadvantage
Iron Helpful if serum
ferritin low
Slow response
Dopamine
agonist
Pramipexole /
ropinirole
High efficacy
(70-100%)
Less
augmentation
Daytime
sleepiness
Long term effect
not known
Dopaminergic
agent
Carbidopa /
levodopa
Can be used
PRN basis
Shown to be
effective
Up to 80%
develop
augmentation
Pharmacological options
Drug Advantage Disadvantage
Anticonvulsants
Gabapentin /
Carbamazepine
Useful in
neuropathy /
associated pain
Side effect profile
Benzos PRN use + help
sleep
Cognitive
impairment,
dependence
Opioids PRN use /
daytime use
Cognitive
impairment,
dependence
Rx Flow chart - RLS:UK
Mirapexin (pramipexole)
 First drug treatment / ONLY treatment
licensed in EU for RLS
 For use in moderate / severe disease
 Quick onset of symptom relief (<1/52)
 Start low dose 125mcg od
 Titrate up (max 750mcg od)
What should we be doing?
 Have raised awareness about diagnosis
 Exclude / treat secondary causes
 Symptoms generally mild +
reassurance & non-pharmacological
measures suffice
 In moderate / severe cases consider
onward referral
Useful Info
 Resources
 www.ekbom.org.uk
 www.restlesslegs.org.uk
 www.restlesslegs.com
 Review
 DTB Nov 2003
 Bandolier 118
Thank you

Restless

  • 1.
    Restless Leg Syndrome D.M.W.Dharmakeerthi (MD) Senior Registrar in Clinical Neurophysiology
  • 2.
    Restless Leg Syndrome •“Themost common disorder some have never heard of.”
  • 3.
    What are Restlesslegs?  Neurological movement disorder  Irresistible urge to move legs when at rest  Difficulty sleeping  Involuntary periodic leg movements  Uncomfortable sensation in limbs subjective & difficult to describe  Symptoms eased by movement
  • 4.
    Why should weknow about it?  Excess 5 million in UK are sufferers (MEMO 2000)  Estimated prevalence 2-15%  Sufferers will present to primary care  Important physical cause of sleep disturbance  Clinical diagnosis which can be made in primary care
  • 5.
    Why should weknow about it?  Unrecognised & under-diagnosed  Incorrectly labeled as stress / anxiety  Managed poorly
  • 6.
    Wide spectrum  Affectsany age group  More common in middle age + women  Mild  Minimal distress  Severe  Episodes occur >2 per week  Can be disabling
  • 7.
    Why is itimportant?  Large impact on quality of life: (REST Study)  Poor sleep  Inability to get comfortable / relax  Poor concentration / fatigue  Pain  Depression  Problems in day to day functioning / employment  Implications for partner
  • 8.
  • 9.
    How do wediagnose RLS?  International Restless Legs Syndrome Study Group - 2003
  • 10.
    Supporting Features  PositiveFHx (50-92%)  Involuntary limb movements (80%)  Sleep disturbance
  • 11.
    Classification  Primary  Nounderlying cause found.  Positive FHx >50%  Earlier onset / slower progression  Secondary Sudden onset. Often occurs after the age of 40 Most associated with specific medical conditions or the use of certain drugs.
  • 12.
    Pathophysiology  Genetic  Susceptibilityloci identified on 3 chromosomes  Genetic anticipation  Positive FHx >50%  Neurochemical  Dopaminergic dysfunction - universal response to dopaminergic agents  Ferritin level - inverse relation between severity and serum ferritin
  • 13.
    Primary RLS  Idiopathic. Familial in 25-75% of cases(AD).  Progressive decrease in age at onset with subsequent generations ( genetic anticipation).  Begins before approximately 40 to 45 years of age, and can even occur as early as the first year of life.
  • 14.
    Primary RLS  Onsetis often slow.  RLS may disappear for months, or even years.  Often progressive and gets worse as the person ages.  RLS in children is often misdiagnosed as growing pains.
  • 15.
    Secondary RLS  Irondeficiency  Varicose vein  folate deficiency  magnesium deficiency  sleep apnea  uremia  diabetes  thyroid disease
  • 16.
    Secondary RLS  Auto-immunedisorders ( Sjögren's syndrome, celiac disease and rheumatoid arthritis)  Acute intermittent porphyria  Fibromyalgia  Cholesterol peripheral microemboli.  RLS can also worsen in pregnancy.
  • 17.
    Neurologic conditions linkedto RLS  Parkinson disease  Spinal cerebellar atrophy  Spinal stenosis  Lumbosacral radiculopathy  Charcot-Marie-Tooth disease type 2.
  • 18.
    What investigations shouldwe do?  Exclude secondary cause.  Vascular dx / Neuropathy / nocturnal cramp / anxiety  Examination  Neuro / vascular  Bloods  FBC, ferritin, B12, Folate, U&E, Glucose, TFT, Auto immune screening etc.
  • 19.
    What are thetreatment options?  Non Pharmacological  Preventative measures  Symptomatic control  Pharmacological  PRN treatment - mild / intermittent  Maintenance treatment - moderate / severe  Majority of treatments used ‘off license’
  • 20.
    Non pharmacological treatment  Preventative Avoid caffeine / alcohol / nicotine  Avoid medication which may aggravate  SSRI / antihistamine / antiemetic / CaChannel blockers  Keep active into evening  Good sleep hygiene  Symptom control  Mental alerting activities  Walking / stretching  Massage  Hot / cold bath  Relaxation / biofeedback
  • 21.
    Pharmacological options Drug AdvantageDisadvantage Iron Helpful if serum ferritin low Slow response Dopamine agonist Pramipexole / ropinirole High efficacy (70-100%) Less augmentation Daytime sleepiness Long term effect not known Dopaminergic agent Carbidopa / levodopa Can be used PRN basis Shown to be effective Up to 80% develop augmentation
  • 22.
    Pharmacological options Drug AdvantageDisadvantage Anticonvulsants Gabapentin / Carbamazepine Useful in neuropathy / associated pain Side effect profile Benzos PRN use + help sleep Cognitive impairment, dependence Opioids PRN use / daytime use Cognitive impairment, dependence
  • 23.
    Rx Flow chart- RLS:UK
  • 24.
    Mirapexin (pramipexole)  Firstdrug treatment / ONLY treatment licensed in EU for RLS  For use in moderate / severe disease  Quick onset of symptom relief (<1/52)  Start low dose 125mcg od  Titrate up (max 750mcg od)
  • 25.
    What should webe doing?  Have raised awareness about diagnosis  Exclude / treat secondary causes  Symptoms generally mild + reassurance & non-pharmacological measures suffice  In moderate / severe cases consider onward referral
  • 26.
    Useful Info  Resources www.ekbom.org.uk  www.restlesslegs.org.uk  www.restlesslegs.com  Review  DTB Nov 2003  Bandolier 118
  • 27.