Criteria

Assessment of current diagnostic criteria for Guillain-Barre syndrome[87][148]

Required features

  • Progressive weakness in both arms and legs

  • Areflexia (or hyporeflexia).

Features supportive of diagnosis

  • Progression of symptoms over days to 4 weeks

  • Relative symmetry

  • Mild sensory signs or symptoms

  • Cranial nerve involvement, especially bilateral facial weakness

  • Recovery beginning 2 to 4 weeks after progression ceases

  • Autonomic dysfunction

  • Absence of fever at onset

  • Typical cerebrospinal fluid (CSF) and electromyogram/nerve conduction studies features.

Features casting doubt on the diagnosis

  • Asymmetric weakness

  • Persistent bladder and bowel dysfunction

  • Bladder or bowel dysfunction at onset

  • >50 mononuclear leukocytes/mm³ or presence of polymorphonuclear leukocytes in CSF

  • Distinct sensory level.

Features that rule out the diagnosis

  • Hexacarbon abuse

  • Abnormal porphyrin metabolism

  • Recent diphtheria infection

  • Lead intoxication

  • Other similar conditions: poliomyelitis, botulism, hysterical paralysis, toxic neuropathy.

Electrophysiologic classification of Guillain-Barre syndrome[108][112]

Neurophysiologic criteria for acute inflammatory demyelinating polyradiculoneuropathy (AIDP), acute motor-sensory axonal neuropathy (AMSAN), and acute motor axonal neuropathy (AMAN).

At least 3 sensory nerves and 3 motor nerves with multisite stimulation F waves, and bilateral tibial H reflexes, need to be evaluated.

AIDP

At least 1 of the following in each of at least 2 nerves, or at least 2 of the following in 1 nerve if all others inexcitable and distal compound muscle action potential (dCMAP) >10% lower limit of normal (LLN):

  • Motor conduction velocity <90% LLN (85% if dCMAP <50% LLN)

  • Distal motor latency >110% upper limit of normal (ULN) (>120% if dCMAP <100% LLN)

  • Proximal compound muscle action potential (pCMAP)/dCMAP ratio <0.5 and dCMAP >20% LLN

  • F-response latency >120% ULN.

Newer criteria have been proposed for AIDP, which increase the sensitivity of diagnosis, and include:[114]

  • At least 1 of the following in at least 2 nerves: mean corpuscular volume <70% LLN; distal motor latency >150% ULN; F-response latency >120% ULN, or >150% ULN (if distal CMAP <50% of LLN); or

  • F-wave absence in 2 nerves with dCMAP ≥20% LLN or greater, with an additional parameter, in 1 other nerve; or

  • pCMAP/dCMAP ratio <0.7 (excluding the tibial nerve) in 2 nerves, with an additional parameter in 1 other nerve.

AMSAN

  • Diminution of muscle and sensory action potentials[64]

  • None of the features of AIDP except 1 demyelinating feature allowed in 1 nerve if dCMAP <10% LLN

  • Sensory action potential amplitudes less than LLN.

AMAN

  • Reduction in distally evoked motor action potential amplitudes, early signs of denervation on needle, normal action potential on sensory nerves, and relatively preserved motor nerve conduction velocity.[51][67][68]

  • None of the features of AIDP except 1 demyelinating feature allowed in 1 nerve if dCMAP <10% LLN

  • Sensory action potential amplitudes normal.

Inexcitable

  • dCMAP absent in all nerves or present in only 1 nerve with dCMAP <10%.

Miller-Fisher syndrome

  • Reduced or absent sensory action potential response without slowing of sensory conduction velocity.[149]

Electrodiagnostic criteria for acute inflammatory demyelinating polyradiculoneuropathy[113]

Different sets of criteria have been published, including the following (sensitivity 64% to 72%):

  • 150% prolongation of motor distal latency above ULN

  • 70% slowing of motor conduction velocity below LLN

  • 125% (150% if the distal negative-peak CMAP amplitude was 80% of LLN) prolongation of F wave latency above ULN

  • Abnormal temporal dispersion (peak CMAP duration increase) in ≥2 nerves.

Hughes Scale[150]

0 - healthy

1 - minor symptoms or signs of neuropathy but capable of manual work

2 - able to walk without support of a stick but incapable of manual work

3 - able to walk with a stick, appliance, or support

4 - confined to bed or chairbound

5 - requiring assisted ventilation

6 - dead

Identification of patients with GBS at risk of respiratory failure using the 20/30/40 rule[125]

In patients with no bulbar dysfunction, or with mild bulbar dysfunction without aspiration risk, the 20/30/40 rule should be used.

Intensive care unit monitoring and elective intubation should be considered if any of the following is present:

  • Vital capacity <20 mL/kg (odds ratio 15.0)

  • Maximal inspiratory pressure worse than -30 cmH₂O

  • Maximal expiratory pressure <40 cmH₂O

  • Reduction of 30% or more of vital capacity, maximal inspiratory pressure, or maximal expiratory pressure.


Tracheal intubation: animated demonstration
Tracheal intubation: animated demonstration

How to insert a tracheal tube in an adult using a laryngoscope.



Bag-valve-mask ventilation: animated demonstration
Bag-valve-mask ventilation: animated demonstration

How to use bag-valve-mask apparatus to deliver ventilatory support to adults. Video demonstrates the two-person technique.


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