Critical Illness Polyneuropathy (CIP): Difference between revisions

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== Diagnostic Procedures  ==
== Diagnostic Procedures  ==
Medical Research Council (MRC)
Electromyography
Biopsy


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Revision as of 12:04, 13 June 2018

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Definition
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Critical Illness Polyneuropathy (CIP) is one of three classifications of Intensive care -unit acquired weakness (ICUAW), the others being Critical Illness Myopathy (CIM) and Critical Illness Neuromyopathy (CINM)[1]. ICUAW is defined as 'a clinically detected weakness in critically ill patients in whom there is no plausable aetiology other than critical illness' [2]

Clinically Relevant Anatomy
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Pathological Process[edit | edit source]

The pathophysiology for CIP remains unclear and complex, with human studies highlighting axonal degeneration [3].It has been thought that the mechanism may involve:

  1. Microvascular alterations: Increase in E- Selectin expression, vasodilation, increased capillary permeability, extravasation and endoneural oedema which results in hypoxia.
  2. Metabolic alterations: Production of toxic factors such as cytokines, hyperglycaemia, hormone imbalance, hypoalbuminemia, amina acid deficiency and activation of proteolytic pathways.
  3. Electrical alterations: Ion channel dysfunction, cell depolarisation, inexcitability, altered calcium homeostasis and changes in excitation-contraction coupling.
  4. Bionenergetic failure: Anti-oxident depletion, an increase in reactive oxygen species, mitochrondial dysfunction and apoptosis.
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https://youtu.be/eH-eHuz6i-k

Risk Factors

  • Sepsis
  • SIRS
  • Multi Organ Failure (MOF)
  • Female Gender
  • Duration of Organ Dysfunction
  • Duration of ICU Stay
  • Ionotropic Support
  • Renal Failure
  • Low Serum Albumin
  • Hyperglycemia
  • Neuromuscular Blockades
  • Corticosteroids

Clinical Presentation[edit | edit source]

Visser (2006) [4] reports that the clinical features of CIP typically include:

  • Muscle Weakness: Predominantly in the lower extremities. This should be suspected if there is reduced limb movement following a painful stimulus to the distal limb. Flaccid weakness can be observed symmetrically.
  • Absent Facial Weakness: Cranial nerves are rarely affected.
  • Muscle Wasting: Observed in one third of patients
  • Reduced Muscle Reflexes: Reflexes are usually present at the start of the disease, but decrease over time.
  • Difficulty in Weaning from Ventillator
  • Sensory Loss: Although difficult to assess with a sedated or intubated patient.
  • Impaired Consciousness: Suggested of an encephalopathy is also usually present

Diagnostic Procedures[edit | edit source]

Medical Research Council (MRC)

Electromyography

Biopsy


Outcome Measures[edit | edit source]

add links to outcome measures here (see Outcome Measures Database)

Management / Interventions
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add text here relating to management approaches to the condition

Differential Diagnosis
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add text here relating to the differential diagnosis of this condition

Resources
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add appropriate resources here

References[edit | edit source]

  1. Appleton, R. and Kinsella, J., 2012. Intensive care unit-acquired weakness. Continuing Education in Anaesthesia, Critical Care and Pain12(2), pp.62-66.
  2. Stevens, R.D., Marshall, S.A., Cornblath, D.R., Hoke, A., Needham, D.M., de Jonghe, B., Ali, N.A. and Sharshar, T., 2009. A framework for diagnosing and classifying intensive care unit-acquired weakness. Critical care medicine37(10), pp.S299-S308.
  3. Zhou, C., Wu, L., Ni, F., Ji, W., Wu, J. and Zhang, H., 2014. Critical illness polyneuropathy and myopathy: a systematic review. Neural regeneration research9(1), p.101.
  4. Visser, L.H., 2006. Critical illness polyneuropathy and myopathy: clinical features, risk factors and prognosis. European journal of neurology13(11), pp.1203-1212.