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SUBMITTED BY: Binamra Regmi
 Peripheral neuropathies are common in older people.
Peripheral neuropathy interferes with normal daily
activities and leads to increased risk of falls, injury
and poor quality of life. Management of peripheral
neuropathy often needs a multidisciplinary team
approach.
 Facial palsy
 Bell’s palsy
 Sarcoidosis
 Lyme disease
 Guillain-Barre syndrome
 Chronic inflammatory
 Demyelinating polyneuropathy
 Herpes zoster
 Carpal tunnel syndrome
 Ulnar nerve palsy
 Radial nerv palsy
 Meralgia paraesthetica
 Common personal nerve palsy
 Among adult patients referred for assessment of
peripheral neuropathy, a specific cause can be
identified in about 72% cases.
 Mononeuropathy is usually due to direct compression
or entrapment of the nerves but may be the first
manifestation of diabetic or vasculitic neuropathy.
 Multiple mononeuropathy (mononeuritis multiplex)
is caused by vascular, inflammatory, infiltration,
immune reactions and trauma.
 Causes of symmetrical polyneuropathy are more
extensive and complicated than those of
mononeuropathy, although relatively few diagnoses
account for a large number of cases (eg. diabetes
mellitus, alcohol over use).
 Motor signs include muscle wasting and weakness,
which in symmetrical polyneuropathy is usually distal
and symmetrical.The patient should be observed
standing and walking, rising onto their heels and toes,
the Romberg’s test and walking heel to toe. The skin
should be examined for trophic skin changes and ulcers
in the extremities.
 The clinical features often suggest a likely underlying
cause and point to the most appropriate
investigations. General laboratory tests and nerve
conduction studies should be performed as the first
stage of investigation in all patients. Subsequent
investigations will depend on the results of these
initial studies
 Basic laboratory investigations that should be
performed on all patients with peripheral neuropathy of
undetermined aetiology include urinalysis,
haemoglobin, white cell count, platelets, erythrocyte
sedimentation rate, fasting blood glucose, serum
electrolytes, serum proteins, vitamin B12, TSH, auto
antibodies, serum protein electrophoresis and
immunoelectrophoresis, serum creatinine, liver
function tests, chest radiographs and
electrophysiological studies.
 If these investigations do not provide information that
leads to a diagnosis, special investigations may be
required, such as cryoglobulins, HIV, anti Myelin-
Associated Glycoprotein (MAG) antibodies, urinary
heavy metals and lyme serology.
 Nerve conduction studies play a vital role in confirming
the presence of peripheral neuropathy and establishing
its cause. They help to determine whether a patient has
a mononeuropathy, mononeuritis multiplex or a
generalised neuropathy; whether the neuropathy is
symmetrical or asymmetrical; whether both sensory
and motor fibres are affected; and whether the
underlying pathology is of axonal degeneration or
demyelination.
 Electromyography is often useful in confirming the
presence of axonal degeneration. However, denervation
potentials may not appear until three weeks afer the
onset of axonal degeneration.
 Cerebrospinal fluid (CSF) examination is sometimes
useful in the investigation of peripheral neuropathy.
For example, in Guillain-Barré syndrome, CSF
protein concentration rises in the first week. In
chronic inflammatory demyelinating polyneuropathy,
oligoclonal IgG bands may be present. An increase in
white cell count may be seen in HIV and Lyme
disease.
 Quantitative sensory testing, autonomic function
studies, molecular genetics and nerve biopsy (eg.
sural) are some of the targeted investigations.
However, these are not routinely done and may need
referral to a specialised unit for further assessment.
 Management of polyneuropathy depends on the
underlying cause and its clinical presentations and
implications. Identification of the cause of the
peripheral neuropathy often leads to useful treatment
even if it is only the removal of the causative agent
(eg. stopping alcohol) or treatment of the underlying
condition (eg. diabetes, B12 deficiency, HIV, Lyme
disease).
 It is important to identify the impact of peripheral
neuropathy on a patient’s wellbeing. Aspects
commonly missed in evaluation and management
include anxiety and depression, breakdown of social
relationships and activities of daily life, sleep
disturbances, inability to engage in recreational
activities and negative feelings of self-worth.
 The older person is more likely to succumb to
peripheral neuropathy related to diabetes,
paraproteinaemia-associated malignancies and
chronic inflammatory neuropathies (eg. chronic
inflammatory demyelinating polyneuropathy).
Peripheral neuropathy in older people
Peripheral neuropathy in older people

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Peripheral neuropathy in older people

  • 2.  Peripheral neuropathies are common in older people. Peripheral neuropathy interferes with normal daily activities and leads to increased risk of falls, injury and poor quality of life. Management of peripheral neuropathy often needs a multidisciplinary team approach.
  • 3.  Facial palsy  Bell’s palsy  Sarcoidosis  Lyme disease  Guillain-Barre syndrome  Chronic inflammatory
  • 4.  Demyelinating polyneuropathy  Herpes zoster  Carpal tunnel syndrome  Ulnar nerve palsy  Radial nerv palsy  Meralgia paraesthetica  Common personal nerve palsy
  • 5.  Among adult patients referred for assessment of peripheral neuropathy, a specific cause can be identified in about 72% cases.
  • 6.  Mononeuropathy is usually due to direct compression or entrapment of the nerves but may be the first manifestation of diabetic or vasculitic neuropathy.
  • 7.  Multiple mononeuropathy (mononeuritis multiplex) is caused by vascular, inflammatory, infiltration, immune reactions and trauma.
  • 8.  Causes of symmetrical polyneuropathy are more extensive and complicated than those of mononeuropathy, although relatively few diagnoses account for a large number of cases (eg. diabetes mellitus, alcohol over use).
  • 9.  Motor signs include muscle wasting and weakness, which in symmetrical polyneuropathy is usually distal and symmetrical.The patient should be observed standing and walking, rising onto their heels and toes, the Romberg’s test and walking heel to toe. The skin should be examined for trophic skin changes and ulcers in the extremities.
  • 10.  The clinical features often suggest a likely underlying cause and point to the most appropriate investigations. General laboratory tests and nerve conduction studies should be performed as the first stage of investigation in all patients. Subsequent investigations will depend on the results of these initial studies
  • 11.  Basic laboratory investigations that should be performed on all patients with peripheral neuropathy of undetermined aetiology include urinalysis, haemoglobin, white cell count, platelets, erythrocyte sedimentation rate, fasting blood glucose, serum electrolytes, serum proteins, vitamin B12, TSH, auto antibodies, serum protein electrophoresis and immunoelectrophoresis, serum creatinine, liver function tests, chest radiographs and electrophysiological studies.
  • 12.  If these investigations do not provide information that leads to a diagnosis, special investigations may be required, such as cryoglobulins, HIV, anti Myelin- Associated Glycoprotein (MAG) antibodies, urinary heavy metals and lyme serology.
  • 13.  Nerve conduction studies play a vital role in confirming the presence of peripheral neuropathy and establishing its cause. They help to determine whether a patient has a mononeuropathy, mononeuritis multiplex or a generalised neuropathy; whether the neuropathy is symmetrical or asymmetrical; whether both sensory and motor fibres are affected; and whether the underlying pathology is of axonal degeneration or demyelination.
  • 14.  Electromyography is often useful in confirming the presence of axonal degeneration. However, denervation potentials may not appear until three weeks afer the onset of axonal degeneration.
  • 15.  Cerebrospinal fluid (CSF) examination is sometimes useful in the investigation of peripheral neuropathy. For example, in Guillain-Barré syndrome, CSF protein concentration rises in the first week. In chronic inflammatory demyelinating polyneuropathy, oligoclonal IgG bands may be present. An increase in white cell count may be seen in HIV and Lyme disease.
  • 16.  Quantitative sensory testing, autonomic function studies, molecular genetics and nerve biopsy (eg. sural) are some of the targeted investigations. However, these are not routinely done and may need referral to a specialised unit for further assessment.
  • 17.  Management of polyneuropathy depends on the underlying cause and its clinical presentations and implications. Identification of the cause of the peripheral neuropathy often leads to useful treatment even if it is only the removal of the causative agent (eg. stopping alcohol) or treatment of the underlying condition (eg. diabetes, B12 deficiency, HIV, Lyme disease).
  • 18.  It is important to identify the impact of peripheral neuropathy on a patient’s wellbeing. Aspects commonly missed in evaluation and management include anxiety and depression, breakdown of social relationships and activities of daily life, sleep disturbances, inability to engage in recreational activities and negative feelings of self-worth.
  • 19.  The older person is more likely to succumb to peripheral neuropathy related to diabetes, paraproteinaemia-associated malignancies and chronic inflammatory neuropathies (eg. chronic inflammatory demyelinating polyneuropathy).