Autonomic Nervous System and Spinal Cord Injury: Difference between revisions

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== Introduction ==
== Introduction ==
The [[Autonomic Nervous System|autonomic nervous system]] is a component of the peripheral nervous system that regulates involuntary physiological processes, including heart rate, blood pressure, respiration, digestion, and sexual arousal. It contains three anatomically distinct divisions: sympathetic, parasympathetic, and enteric nervous systems. Spinal cord injury may result in autonomic dysfunction due to broken connections between higher brain centres and the spinal cord or as a result of the impaired autonomic nervous system. <ref>Wulf MJ, Tom VJ. [https://www.frontiersin.org/articles/10.3389/fncel.2023.999253/full Consequences of spinal cord injury on the sympathetic nervous system.] Front Cell Neurosci. 2023 Feb 28;17:999253.</ref> This article provides a comprehensive review of the consequences of spinal cord injury on the autonomic nervous system.
The [[Autonomic Nervous System|autonomic nervous system]] is a component of the peripheral nervous system that regulates involuntary physiological processes, including heart rate, blood pressure, respiration, digestion, and sexual arousal. It contains three anatomically distinct divisions: the sympathetic, parasympathetic, and enteric nervous systems. Impairments of the autonomic nervous system in spinal cord injury may result in autonomic dysfunction. These are caused by disrupted connections between higher brain centres and the spinal cord.<ref>Wulf MJ, Tom VJ. [https://www.frontiersin.org/articles/10.3389/fncel.2023.999253/full Consequences of spinal cord injury on the sympathetic nervous system.] Front Cell Neurosci. 2023 Feb 28;17:999253.</ref> This article provides a comprehensive review of the impact of spinal cord injury on the autonomic nervous system.


== Anatomy of the Autonomic Nervous System (ANS) ==
== Anatomy of the Autonomic Nervous System (ANS) ==
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=== Sympathetic Nervous System (SNS) ===
=== Sympathetic Nervous System (SNS) ===
[[Sympathetic Nervous System]] (SNS) arises from the thoracolumbar regions of the spinal cord. The intermediolateral horns of the spinal cord are the location of the preganglionic cell bodies. The sympathetic nerves run parallel to the spinal cord on both sides of the vertebral column. <ref>Ken Hub. Sympathetic NS. Available from:https://www.kenhub.com/en/library/anatomy/sympathetic-nervous-system (accessed 17.3.2024)</ref>
The [[Sympathetic Nervous System|sympathetic nervous system]] (SNS) arises from the thoracolumbar regions of the spinal cord. There are three components in the sympathetic pathway: preganglionic neurons, sympathetic ganglia and postganglionic neurons.<ref name=":4" /> The preganglionic cell bodies are located in the intermediolateral horns of the spinal cord. The sympathetic nerves run parallel to the spinal cord on both sides of the vertebral column.<ref name=":4">Ken Hub. Sympathetic NS. Available from:https://www.kenhub.com/en/library/anatomy/sympathetic-nervous-system (accessed 17.3.2024)</ref>


The functions of the SNS include:
The functions of the SNS include:

Revision as of 08:07, 23 March 2024

Original Editor - Melanie Harding

Top Contributors - Ewa Jaraczewska, Jess Bell and Kim Jackson  

Introduction[edit | edit source]

The autonomic nervous system is a component of the peripheral nervous system that regulates involuntary physiological processes, including heart rate, blood pressure, respiration, digestion, and sexual arousal. It contains three anatomically distinct divisions: the sympathetic, parasympathetic, and enteric nervous systems. Impairments of the autonomic nervous system in spinal cord injury may result in autonomic dysfunction. These are caused by disrupted connections between higher brain centres and the spinal cord.[1] This article provides a comprehensive review of the impact of spinal cord injury on the autonomic nervous system.

Anatomy of the Autonomic Nervous System (ANS)[edit | edit source]

There are two main functions of the autonomic nervous system:

  1. Regulating visceral functions
  2. Maintaining homeostasis within the human body
Sympathetic Nervous System

Sympathetic Nervous System (SNS)[edit | edit source]

The sympathetic nervous system (SNS) arises from the thoracolumbar regions of the spinal cord. There are three components in the sympathetic pathway: preganglionic neurons, sympathetic ganglia and postganglionic neurons.[2] The preganglionic cell bodies are located in the intermediolateral horns of the spinal cord. The sympathetic nerves run parallel to the spinal cord on both sides of the vertebral column.[2]

The functions of the SNS include:

  • "Fight or flight" response: blood pressure and heart rate increase, glucose is poured into the bloodstream, and gastrointestinal peristalsis ceases.[3]
  • Innervating the tissues in almost every organ system by fibres from the SNS and providing physiological regulation over diverse body processes, including pupil diameter, gut motility (movement), and urinary output.[4]
  • Preparing the body for physical activity, a whole-body reaction affecting many organ systems throughout the body to redirect oxygen-rich blood to areas of the body needed during intense physical demand.[4]
Parasympathetic Innervation.png

Parasympathetic Nervous System (PNS)[edit | edit source]

The craniosacral axis is a starting point for the preganglionic cell bodies of the Parasympathetic nervous system (PNS). It is characterised by long efferent pre-ganglionic fibres and short post-ganglionic fibres to effector organs. [5] It is smaller than SNS and innervates only the head, the viscera, and the external genitalia.

The functions of the PNS include: [3]

  • Promoting the rest and digest process
  • Lowering heart rate and blood pressure
  • Gastrointestinal peristalsis or digestion restarting
Enteric nervous system

Enteric Nervous System (ENS)[edit | edit source]

Enteric nervous system (ENS) is the largest nervous system, which includes a network of ganglion-rich nerve connections capable of working independently of the central nervous system. [6] It is an integral part of the parasympathetic nervous system as many of the ENS effector neurons are also innervated by parasympathetic motor neurons.

ENS innervates the gastrointestinal (GI) tract and extends from the oesophagus to the anal canal. [7]

The functions of the ENS include:

  • Propulsion of food
  • Nutrient handling
  • Blood flow regulation
  • Immunological defense

ANS and Spinal Cord Injury (SCI)[edit | edit source]

After a spinal cord injury, all three subsystems of the autonomic nervous system are affected due to their anatomical location, loss of supraspinal influence, and sustained responses to afferent stimuli.[5] The pathophysiological responses from the ANS that contribute to the comorbidities and mortality of SCI include the following systems:[5][3]

  • Cardiovascular due to parasympathetic dominance with the weakening influence of the sympathetic nervous system in cervical and high thoracic levels of spinal cord injury. The following responses may occur:
    • Low resting arterial blood pressure
    • Postural hypotension
    • Autonomic dysreflexia (Acute hypertension)
    • Bradycardia or arrhythmia
  • Thermoregulatory as a result of the sympathetic nervous system subsiding, which inhibits sweating below the level of injury in high thoracic and cervical SCI. When the body attempts to dissipate heat, excess sweating may be present. It can cause the following pathologies:
    • Poikilothermia
      • Absorbing an encompassing temperature as a result of inability to regulate core body temperature
    • Quad fever (idiopathic hyperpyrexia)
    • Exercise-induced fever
    • Hyperhidrosis or hypohidrosis
  • Respiratory following dominance of the parasympathetic system over weakened supraspinal sympathetic drive. High cervical and thoracic spinal cord injury causes intercostal and abdominal muscle paralysis, which leads to neurogenic restrictive lung disease, which results in the following:
    • Bronchiolar constriction
    • Hyper-reactive airways
    • Increased mucus secretion
  • Gastrointestinal as a result of ENS impairment. ENS is influenced by SNS and PNS. PNS influence can lead to:
    • Acute and chronic increases in gastric acid secretions
    • High rates of biliary sludge, cholelithiasis and cholecystitis
    • Increased transit time at the distal colon
    • Reflex colorectal contractions
      • Constipation or bowel incontinence
  • Genitourinary due to increased uninhibited activation of the sympathetic and parasympathetic systems and the somatic nervous system, responsible for bladder storage and emptying. The results of the genitourinary system impairment are:
    • Bladder and bowel dysfunction
      • High bladder pressures and probable vesicoureteral reflux associated with hydroureter, hydronephrosis and urinary incontinence
    • Impaired sexual function affecting arousal, ejaculation, and orgasm
    • Problems during pregnancy, labour, and breastfeeding

The pathophysiological responses from the ANS can also be present during procedures or when pain or injury occurs. The examples include:[3]

  • Surgery
  • Invasive investigational procedures such as urodynamic studies.
  • Stretches
  • Fractures
  • UTIs
ASIA ISCoS

Assessment of ANS in SCI[edit | edit source]

International Standards to document Autonomic Function following SCI (ISAFSCI) was published in 2009 and revised in 2012. ISAFSCI is also referred to as the Autonomic Standards. The American Spinal Injury Association (ASIA) and the International Spinal Cord Society (ISCoS) recommendations for the Autonomic Standards include the following:[8]

  • Using Autonomic Standards in conjunction with the full International Standards for Neurological Classification of SCI (ISNCSCI) following the initial injury
  • Tracking the association between changes in ANS function correspondent with changes in the neurological level of injury (NLI) and completeness of injury as classified by the ASIA Injury Severity (AIS) scale
  • Tracking changes in autonomic functions following clinical intervention or during a clinical trial

Autonomic Standards Assessment Form include the following:[3]

  • Autonomic control of the heart
  • Autonomic control of blood pressure
  • Autonomic control of sweating
  • Temperature regulation
  • Autonomic and somatic control of a bronchopulmonary system
  • The lower urinary tract
  • Bowel and sexual function
  • Urodynamics

At the ASIA e-Learning Center, you can learn more about the impact of ANS impairment on organ system function and how to use the ISAFSCI.

Function of the ANS in SCI[edit | edit source]

Autonomic Function Assessment[edit | edit source]

The following systems are assessed, and impairments are documented:

  1. Cardiovascular, thermoregulation, sudomotor control, bronchopulmonary, lower urinary tract:[3]
Autonomic Function Assessment
Scoring:

2-Normal Function 1-Reduced/AlteredFunction 0-Complete loss of control NT-not tested

Normal (2) Reduced/Altered (1) Complete loss of control (0) Comments
Heart rate 61-99bmp
  • Below 60bpm (Bradycardia)
  • Above 100bpm (Tachycardia)
  • Measured in supine and seated
  • Arrhythmias should be defined
  • When the pulse is not tested, the reason should be given
Systolic blood pressure (SBP) 91-138mmHg
  • SBP under 90 (Hypotension)
  • Fall of more than 20 millimetres of mercury within 10 minutes of sitting up (Orthostatic hypotension)
  • The heart rate is less than 60 bpm, and the systolic blood pressure is less than 90 (Neurogenic shock)
  • Increase in the systolic blood pressure of more than 20 mmHg above the baseline (Autonomic dysreflexia)
  • BP above 140 (supine hypertension)
  • Measured in supine and seated
  • The patient's baseline must be known to determine whether it is actually autonomic dysreflexia.
Diastolic blood pressure (DBP) 62-89 mmHg
  • Under 60 mmHg (Hypotension)
  • Fall of more than 10 within 10 minutes of sitting up (Orthostatic hypotension)
  • More than 90 mmHg (Hypertension)
  • Measured in supine and seated
  • When blood pressure is not tested, a reason should be noted
Core Body Temperature 36.4-37.6°C

(97.5-99.7 °F)

  • 35.1-36.3 °C (95.1-97.4 °F)
  • 37.7 - 37.9 °C(99.8- 100.2°F) [Elevated]
  • The core temperature of less than 35°C (95°F )[Hypothermia]
  • The core temperature of more than 38 °C (100.4 °F) [Hyperthermia]
Temperature measurements must be taken under the following conditions:
  • an air temperature of between 20 and 25 °C (68-77 °F)
  • 30 to 50% humidity,
  • patient wearing a single layer of clothing
  • after a 10-minute rest
  • no acute illness or infection
Sudomotor control Sweating over all the skin surfaces
  • Diminished sweating, whether above or below the neurological level (Hypohidrosis)
  • Excessive sweating, either above or below the neurological level (Hyperhidrosis)
  • No sweating, either above or below the neurological level (Anhidrosis)
  • Records the sweating response to high ambient heat or exercise only
  • Where sweating is not tested, the reason must be given.
  • Sweating associated with autonomic dysreflexia, orthostatic hypotension, or mental stress would not be scored.
Respiration Normal voluntary breathing
  • Unable to voluntarily breathe
  • Requires full ventilatory support
  • Voluntary breathing requires partial ventilatory support
  • Impaired voluntary respiration but does not require ventilatory support
  • Unknown or unable to assess
Lower urinary tract Reduced or altered in the following functions:
  • Sensation of the need for bowel movement
  • The ability to prevent stool leakage or continence
  • Voluntary sphincter contraction.
  • Genital arousal, either erection or lubrication.
  • Orgasm and ejaculation in the male
  • The sensation of menses in the female
  • Not tested is recorded when you are unable to assess due to pre-existing or concomitant problems

2. Temperature regulation:

Individuals with a lesion at T6 and above:

  • Lacking the descending sympathetic control to respond appropriately to environmental changes in temperature [3]
  • Become adversely affected by the lack of afferent and efferent thermoregulatory information[9]
  • Feel a greater impact of the internal and external heat load, resulting in a greater potential for exercise-induced hyperthermia [9]
  • Sweating, going red, vasodilation, and faster breathing are less effective due to no response below the lesion, resulting in fever [3]

The following techniques can be successful in restoring normal body temperature:[9]

  • Wearing cooling garments or other cooling devices
    • Cooling vest
    • Refrigerated headpiece
    • Cooling device on the feet
  • Water spray and artificial sweat
  • Ice slurry
  • The use of a cold cloth or a fan[3]

3. Orthostatic hypotension

Orthostatic hypotension occurs due to the interruption of efferent pathways from the brain stem's vasomotor centre to the sympathetic nerves involved in vasoconstriction.

  • Symptoms may include dizziness, nausea, light-headedness, or faintness.
  • Physical signs include paleness, excessive sweating, or a loss of consciousness.

SCI and ANS Symptoms Management[edit | edit source]

General Rules[edit | edit source]

Be aware...........

-of the system impairments in SCI. Educate yourself and your patients

-of the less obvious or even silent symptoms

-that suctioning or insertion of a nasogastric tube can commonly induce bradycardia and apnoea

Autonomic Dysreflexia[edit | edit source]

"Sudden bouts of hypertension triggered by noxious afferent stimuli below the level of lesion, above the outflow to the splanchnic and renal vascular beds (T5– T6)". [3]-- Melanie Harding

As a result of noxious afferent stimuli below the level of the lesion, the following occurs:[3]

  • A widespread activation of the sympathetic nervous system demonstrated by an increase in norepinephrine release.
  • Vasoconstriction in the majority of vascular beds below the level of injury: muscle, skin, kidneys, and presumably also the splanchnic vascular bed
  • The increase in arterial blood pressure activates the baroreceptors. It acts to buffer the vasoconstriction through dilation of vascular beds above the lesion level (with intact central control) and through a reduction in HR (vagal innervation to the heart is unaffected by SCI).

Signs[edit | edit source]

The signs of AD include:

  • Piloerection (goosebumps)
  • Chills or shivering
  • Pounding headache
  • Paresthesia
  • Flushing
  • Diaphoresis(sweating) above the lesion level
  • Nasal congestion
  • Anxiety (feeling of impending doom)
  • Malaise
  • Nausea

Watch this video to learn more about Autonomic Dysreflexia:

[10]

Triggering Factors[edit | edit source]

  • Irritation of the urinary bladder
    • Catheterisation and manipulation or blockage of an indwelling catheter
    • Urinary tract infection
    • Detrusor sphincter dyssynergia and bladder percussion
    • Distended/overfull bladder
  • Gastrointestinal tract distension, constipation, anal fissures, haemorrhoids.
  • Stimuli that would be noxious if pain sensation was preserved, such as:
    • Bone fractures or joint displacements, pressure sores, ingrown toenails
    • Sexual activity/orgasm may induce AD in both sexes
    • During pregnancy and delivery and breastfeeding
    • Cystoscopy, UDS, vibration or electrostimulation for ejaculation
    • Electrical stimulation or stretching of muscles or neural tissue

Management[edit | edit source]

  • Sit the patient up
  • Loosen any tight clothing or constrictive devices
  • Rule out bladder problem
    • If no urinary catheter is in place, catheterise the patient
    • If there is a urinary catheter, check the system along its entire length for blockages, twists, kinks or obstructions and correct placement
    • If the catheter seems to be blocked, report to the nurse or carer to gently irrigate the bladder with a small amount of body temperature normal saline
  • Rule out faecal impaction
    • The carer/nurse should check the rectum for stool, using a local anaesthetic jelly as a lubricant
    • Gentle manual evacuation is recommended
  • If no obvious cause is found, emergency medical care is advised
  • Monitor blood pressure and pulse every 2-5 minutes until the patient has stabilized
  • Use of an antihypertensive agent is recommended when the systolic blood pressure is at or above 150 mm Hg; medicating with a short-acting antihypertensive is of utmost importance
  • The individual's symptoms and blood pressure should be monitored for at least 2 hours after the episode to ensure that the elevation of blood pressure does not repeat

Complications of Unmanaged AD[edit | edit source]

When untreated, AD can cause complications leading to comorbidities and mortality in patients with a spinal cord injury:

  • Pulmonary embolism
  • Stroke
  • Combined immunodeficiency(CIDS)
  • Clinically significant infectious complications
  • Seizures
  • Retinal haemorrhage or detachment
  • Pulmonary oedema
  • Renal insufficiency
  • Myocardial infarction

Resources[edit | edit source]

References[edit | edit source]

  1. Wulf MJ, Tom VJ. Consequences of spinal cord injury on the sympathetic nervous system. Front Cell Neurosci. 2023 Feb 28;17:999253.
  2. 2.0 2.1 Ken Hub. Sympathetic NS. Available from:https://www.kenhub.com/en/library/anatomy/sympathetic-nervous-system (accessed 17.3.2024)
  3. 3.00 3.01 3.02 3.03 3.04 3.05 3.06 3.07 3.08 3.09 3.10 Harding M. Autonomic Nervous System and Spinal Cord Injury. Plus Course 2024
  4. 4.0 4.1 Alshak MN, M Das J. Neuroanatomy, Sympathetic Nervous System. [Updated 2023 May 8]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK542195/ [last access 17.03.2024]
  5. 5.0 5.1 5.2 Henke AM, Billington ZJ, Gater DR Jr. Autonomic Dysfunction and Management after Spinal Cord Injury: A Narrative Review. J Pers Med. 2022 Jul 7;12(7):1110.
  6. Wang H, Foong JPP, Harris NL, Bornstein JC. Enteric neuroimmune interactions coordinate intestinal responses in health and disease. Mucosal Immunol. 2022 Jan;15(1):27-39.
  7. Fleming MA 2nd, Ehsan L, Moore SR, Levin DE. The Enteric Nervous System and Its Emerging Role as a Therapeutic Target. Gastroenterol Res Pract. 2020 Sep 8;2020:8024171.
  8. Wecht JM, Krassioukov AV, Alexander M, Handrakis JP, McKenna SL, Kennelly M, Trbovich M, Biering-Sorensen F, Burns S, Elliott SL, Graves D, Hamer J, Krogh K, Linsenmeyer TA, Liu N, Hagen EM, Phillips AA, Previnaire JG, Rodriguez GM, Slocum C, Wilson JR. International Standards to document Autonomic Function following SCI (ISAFSCI): Second Edition. Top Spinal Cord Inj Rehabil. 2021 Spring;27(2):23-49
  9. 9.0 9.1 9.2 Grossmann F, Flueck JL, Perret C, Meeusen R, Roelands B. The Thermoregulatory and Thermal Responses of Individuals With a Spinal Cord Injury During Exercise, Acclimation and by Using Cooling Strategies-A Systematic Review. Front Physiol. 2021 Apr 1;12:636997.
  10. Dr Matt & Dr Mike. Autonomic Dysreflexia. Available from:https://www.youtube.com/watch?v=eocOmytfg8s [last accessed 18/3/2024]