ADDITIONAL READING
- Adams BD, Baker R, Lopez JA, et al. Myelopro-liferative disorders and hyperviscosity syndrome.
Emerg Med Clin North Am
. 2009;27:459–476.
- Kremyanskaya M, Mascarenhas J, Hoffman R. Why does my patient have erythrocytosis?
Hematol Oncol Clin North Am.
2012;26(2):267–283.
- Landolfi R, Nicolazzi MA, Porfidia A, et al. Polycythemia vera.
Intern Emerg Med.
2010;5(5):375–384.
- McMullin MF. The classification and diagnosis of erythrocytosis.
Int J Lab Hematol
. 2008;30:447–459.
- Patnaik MM, Tefferi A. The complete evaluation of erythrocytosis: Congenital and acquired.
Leukemia
. 2009;23:834–844.
- Tefferi A. Polycythemia vera and essential thrombocythemia: 2012 update on diagnosis, risk stratification and management.
Am J Hematol.
2012;87(3):285–293.
CODES
ICD9
- 238.4 Polycythemia vera
- 289.0 Polycythemia, secondary
ICD10
- D45 Polycythemia vera
- D75.1 Secondary polycythemia
POLYNEUROPATHY
Sandra A. Deane
BASICS
DESCRIPTION
A peripheral nerve disorder in which many nerves throughout the body malfunction simultaneously:
- Acute polyneuropathy causes:
- Infectious (toxin producing bacteria, viruses)
- Autoimmune (Guillain–Barré)
- Toxic (heavy metals):
- Drugs:
- Anticonvulsants (phenytoin)
- Antibiotics (chloramphenicol, nitrofurantoin, sulfonamides)
- Chemotherapy (vinblastine, vincristine)
- Sedatives (hexobarbital and barbital)
- Cancer (multiple myeloma)
- Chronic polyneuropathy causes:
- Diabetes (most common)
- Alcohol abuse
- Nutritional deficiencies (Thiamine, B
12
)
- Hypothyroidism
- Liver failure
- Kidney failure
- Lung cancer
- Chronic inflammatory demyelinating polyneuropathy (CIDM)
EPIDEMIOLOGY
Incidence and Prevalence Estimates
- In US, the prevalence of polyneuropathy is ∼2% in the general population
- It is 8% in patients >55 yr of age
- The most common cause in US is diabetes and it occurs in ∼50% of diabetics on insulin
ETIOLOGY
- Myelin dysfunction:
- Parainfectious immune response triggered by antigens that cross-react with antigens in the peripheral nervous system:
- Encapsulated bacteria (
Campylobacter
sp., diphtheria)
- Viruses (enteric or influenza viruses, HIV)
- Vaccines (influenza)
- Guillain–Barré syndrome:
- Acute onset due to myelin dysfunction
- Rapidly progressive weakness and may lead to respiratory failure
- CIDM:
- Chronic illness of myelin dysfunction
- Symptoms may recur or progress over months and years
- Vasa nervosum compromise:
- Vascular supply to nerves compromised leading to nerve infarction
- Causes:
- Chronic atherosclerosis
- Vasculitis
- Infections
- Hypercoagulable states
- Axonopathy
- Primary dysfunction of the axon
- Most often the result of toxic–metabolic disorders:
- Diabetes
- Nutritional deficiencies
- Drugs/chemicals
DIAGNOSIS
SIGNS AND SYMPTOMS
- May be acute or chronic
- May be predominately sensory, motor, combined sensory–motor, or autonomic dysfunction
History
- More commonly affects lower extremities than upper extremities and begins distally
- Typical complaints:
- Dysaesthesias – numbness, burning, or tingling of the extremities
- Weakness of extremities
- Difficulty walking
- Autonomic symptoms:
- Constipation
- Loss of bowel/bladder control
- Sexual dysfunction
- Orthostatic dizziness
- Dry skin
- Decreased sweating
Physical-Exam
- Typically, findings are bilateral symmetrical and stocking glove distribution
- Typical findings:
- Decreased sensation
- Decreased vibratory and position sense
- Decreased motor function
- Decreased reflexes
- Muscle atrophy
- Fasciculations
- Paralysis
- Findings in specific types of polyneuropathy:
- Myelin dysfunction (Guillain–Barré – acute and CIDP – chronic):
- Muscle weakness greater than expected for degree of atrophy
- Paresthesias
- Greatly diminished reflexes
- Proximal and distal symptoms
- Ischemia to nerve (atherosclerosis, vasculitis, infectious, hypercoagulable):
- Painful, burning sensory disturbances
- Decreased pain and temperature sensation
- Muscle weakness proportional to atrophy
- Reflexes spared
- Usually spares proximal nerves
- Cranial nerve involvement rare
- Primary axon dysfunction (toxic-metabolic disorders):
- Have symptoms of either myelin dysfunction, ischemia, or combined
- Painful
- Distally symmetrical
- Stocking glove
- Lower extremities before upper
ESSENTIAL WORKUP
- Thorough past medical history and physical exam should be obtained to guide testing
- Initial lab testing:
- CBC
- Electrolytes
- Glucose
- Renal and liver function
- TSH
- ESR
- ANA
- Vitamin B
12
- Folate
- RPR
- HIV
- Hepatitis B and C
- Lyme
- CPK
- Serum protein electrophoresis
- Subsequent lab testing based on history:
- Heavy metal levels (history of exposure)
- Genetic testing for genetic neuropathies
- Serum antibody testing for immune-mediated neuropathies
DIAGNOSIS TESTS & NTERPRETATION
Imaging
Should be guided by history and physical findings
Diagnostic Procedures/Surgery
- Electromyography (EMG)
- Nerve conduction studies
- Lumbar puncture:
- Increased CSF protein level abnormal
- Diagnostic of Guillain–Barré syndrome and CIDP
- Skin or nerve biopsy
DIFFERENTIAL DIAGNOSIS
- Primarily to differentiate between various causes of polyneuropathy:
- Endocrine disease (diabetes)
- Infections (Guillain–Barré, Lyme disease, HIV, syphilis)
- Vitamin deficiency
- Cancer/paraneoplastic
- Toxins
- Liver disease
- Renal failure
- Genetic disorders
- Amyloidosis
- Other diseases with similar presentations:
- Polio
- Porphyria
- Spinal muscular atrophy
- Catecholamine disorders
- Psychological disorders
TREATMENT
PRE HOSPITAL
Primarily supportive care for ABCs
INITIAL STABILIZATION/THERAPY
- ABCs
- Respiratory support for respiratory failure
ED TREATMENT/PROCEDURES
- Pain control:
- Parenteral or oral narcotics
- Tricyclic antidepressants (amitriptyline)
- Anticonvulsants (gabapentin)
- Plasma exchange or IV immune globulin for acute myelin dysfunction
- Corticosteroids or antimetabolite drugs for chronic myelin dysfunction
- Supportive care for autonomic dysfunction (IVF, pressors)
- Measure Negative Inspiratory Force (NIF) if concerned about respiratory compromise (Normal is Ã-60 cm H
2
O)
FOLLOW-UP