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.<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) ==
There are two main functions of the autonomic nervous system:
There are two main functions of the autonomic nervous system:


# Regulating visceral functions
* regulating visceral functions
# Maintaining homeostasis within the human body
* maintaining homeostasis within the human body
[[File:Sympathetic Nervous System.jpg|thumb|Sympathetic Nervous System]]
[[File:Sympathetic Nervous System.jpg|thumb|Figure 1. Sympathetic nervous system.]]


=== 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 the following:
 
* "Fight or flight" response: blood pressure and heart rate increase, glucose is poured into the bloodstream, and gastrointestinal peristalsis ceases.<ref name=":1" />
* 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.<ref name=":2">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]</ref>
* 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.<ref name=":2" />
[[File:Parasympathetic Innervation.png|right|frameless]]


* "fight or flight" response, which leads to increased blood pressure, heart rate and glucose production, cessation of gastrointestinal peristalsis, etc.<ref name=":1" />
* fibres from the SNS innervate many organs: the SNS provides physiological regulation over diverse body processes, including pupil diameter, gut motility (movement), and urinary output<ref name=":2">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]</ref>
* preparing the body for physical activity: there is "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"<ref name=":2" />[[File:Parasympathetic Innervation.png|thumb|Figure 2. Parasympathetic nervous system.|313x313px]]
=== Parasympathetic Nervous System (PNS) ===
=== Parasympathetic Nervous System (PNS) ===
The craniosacral axis is a starting point for the preganglionic cell bodies of the [[Parasympathetic System| Parasympathetic nervous system]] (PNS). It is characterised by long efferent pre-ganglionic fibres and short post-ganglionic fibres to effector organs. <ref name=":0" /> It is smaller than SNS and innervates only the head, the viscera, and the external genitalia.
The preganglionic cell bodies of the[[Parasympathetic System| parasympathetic nervous system]] (PNS) originate at the craniosacral axis. The PNS has long efferent preganglionic fibres but short postganglionic fibres to the effector organs.<ref name=":0" /> The PNS innervates the head, viscera, and external genitalia.
 
The functions of the PNS include: <ref name=":1" />


* Promoting the rest and digest process
Functions of the PNS include:<ref name=":1" />
* Lowering heart rate and blood pressure
* Gastrointestinal peristalsis or digestion restarting
[[File:Enteric nervous system.jpg|thumb|Enteric nervous system]]


* promoting "rest and digest"
* lowering heart rate and blood pressure
* facilitating gastrointestinal peristalsis
=== Enteric Nervous System (ENS) ===
=== Enteric Nervous System (ENS) ===
[[Enteric Nervous System (ENS)|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. <ref>Wang H, Foong JPP, Harris NL, Bornstein JC. [https://www.nature.com/articles/s41385-021-00443-1 Enteric neuroimmune interactions coordinate intestinal responses in health and disease.] Mucosal Immunol. 2022 Jan;15(1):27-39.</ref> It is an integral part of the parasympathetic nervous system as many of the ENS effector neurons are also innervated by [[Parasympathetic System|parasympathetic]] motor neurons.  
[[File:Enteric nervous system.jpg|thumb|Figure 3. Enteric nervous system.|380x380px]]The [[Enteric Nervous System (ENS)|enteric nervous system]] (ENS) is the largest, most complex unit within the peripheral nervous system. It innervates the gastrointestinal tract through a network of ganglion-rich nerve connections, extending from the oesophagus to the anal canal.<ref name=":5">Fleming MA 2nd, Ehsan L, Moore SR, Levin DE. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7495222/pdf/GRP2020-8024171.pdf The Enteric Nervous System and Its Emerging Role as a Therapeutic Target.] Gastroenterol Res Pract. 2020 Sep 8;2020:8024171. </ref><ref>Wang H, Foong JPP, Harris NL, Bornstein JC. [https://www.nature.com/articles/s41385-021-00443-1 Enteric neuroimmune interactions coordinate intestinal responses in health and disease.] Mucosal Immunol. 2022 Jan;15(1):27-39.</ref> While the ENS receives input from the central nervous system (CNS), it can act independently from the CNS because of local reflex circuits.  


ENS innervates the gastrointestinal (GI) tract and extends from the oesophagus to the anal canal. <ref>Fleming MA 2nd, Ehsan L, Moore SR, Levin DE. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7495222/pdf/GRP2020-8024171.pdf The Enteric Nervous System and Its Emerging Role as a Therapeutic Target.] Gastroenterol Res Pract. 2020 Sep 8;2020:8024171. </ref>  
Functions of the ENS include:<ref name=":5" />


The functions of the ENS include:
* propulsion of food
* blood flow regulation
* nutrient handling
* immunological defence


* Propulsion of food
== Autonomic Nervous System and Spinal Cord Injury (SCI) ==
* Nutrient handling
[[Spinal Cord Injury|Spinal cord injury]] can affect all three subsystems of the autonomic nervous system due to their anatomical location, loss of supraspinal influence, and sustained responses to afferent stimuli.<ref name=":0">Henke AM, Billington ZJ, Gater DR Jr. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9320320/pdf/jpm-12-01110.pdf Autonomic Dysfunction and Management after Spinal Cord Injury: A Narrative Review.] J Pers Med. 2022 Jul 7;12(7):1110.</ref> A number of pathophysiological responses from the ANS can occur after SCI, contributing to various complications and comorbidities.<ref name=":0" /><ref name=":1">Harding M. Autonomic Nervous System and Spinal Cord Injury Course. Plus, 2024.</ref>
* Blood flow regulation
* Immunological defense


== ANS and Spinal Cord Injury (SCI) ==
* '''Cardiovascular dysfunction''': SCI (particularly cervical and high thoracic injuries) can result in parasympathetic dominance and reduced sympathetic influence (i.e. sympathetic blunting). This imbalance can lead to various cardiovascular complications, including:
After a [[Spinal Cord Injury|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.<ref name=":0">Henke AM, Billington ZJ, Gater DR Jr. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9320320/pdf/jpm-12-01110.pdf Autonomic Dysfunction and Management after Spinal Cord Injury: A Narrative Review.] J Pers Med. 2022 Jul 7;12(7):1110.</ref> The pathophysiological responses from the ANS that contribute to the comorbidities and mortality of SCI include the following systems:<ref name=":0" /><ref name=":1">Harding M. Autonomic Nervous System and Spinal Cord Injury. Plus Course 2024</ref>
** low resting arterial blood pressure
** postural hypotension
** autonomic dysreflexia (sudden, acute hypertension in response to specific stimuli)
** bradycardia or arrhythmia
* '''Thermoregulatory dysfunction''': commonly occurs in individuals with high thoracic and cervical SCI, primarily because of sympathetic dysfunction or blunting. This affects the ability of the body to redistribute warm blood from the core to the periphery and inhibits sweating below the level of injury. When the body attempts to dissipate heat, excess sweating may occur, and the skin may appear flushed above the injury.<ref name=":0" /> Thermoregulatory dysfunction is associated with:<ref name=":0" />
** poikilothermia<ref name=":0" />
*** an individual with an SCI takes on "the ambient temperature around them due to the inability to regulate core body temperature"
** quad fever (idiopathic hyperpyrexia)
*** "an extreme elevation in body core temperature beyond 40.8°C (105.4°F) in a patient with spinal cord injury"<ref>Ali S, Ganesan D, Sundaramoorthy V. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298584/ Quad fever in a case of cervical cord injury-a rare case report]. Asian J Neurosurg. 2022 Jun 28;17(1):85-87. </ref>
** exercise-induced fever
** hyperhidrosis (excess sweating) or hypohidrosis (reduced sweating)
* '''Respiratory dysfunction''': associated with parasympathetic dominance and blunted supraspinal sympathetic drive in individuals with high cervical and thoracic SCI:<ref name=":0" />  
** bronchiolar constriction: associated with unopposed vagal influence on the bronchial tree, as well as hyper-reactive airways and increased secretion of mucus
** individuals with high thoracic and cervical SCI are unable to cough / clear pulmonary secretions voluntarily and are at risk of:
*** atelectasis
*** pneumonia
*** mucus plugging
**during exercise, inspiratory effort is limited by ventilatory insufficiency, bronchoconstriction and mucus production


* 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:  
* '''Gastrointestinal dysfunction''': as mentioned above, while the ENS can act independently, it is usually influenced by the SNS and PNS. PNS dominance and sympathetic blunting in SCI can lead to:<ref name=":0" />
** Low resting arterial blood pressure
** acute and chronic increases in gastric acid secretions
** Postural hypotension
** high rates of biliary sludge, cholelithiasis and cholecystitis
** Autonomic dysreflexia (Acute hypertension)
** increased transit time at the distal colon
** Bradycardia or arrhythmia
** reflex colorectal contractions
* 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:
*** constipation or bowel incontinence
** Poikilothermia
* '''Genitourinary dysfunction''': after SCI, there is increased uninhibited activation of the sympathetic, parasympathetic and the somatic nervous systems, which are responsible for bladder storage and emptying. The results of genitourinary dysfunction include:<ref name=":0" />
*** Absorbing an encompassing temperature as a result of inability to regulate core body temperature
** bladder and bowel dysfunction
** Quad fever (idiopathic hyperpyrexia)
*** detrusor sphincter dyssynergia: high bladder pressures and likely vesicoureteral reflux, which is associated with hydroureter, hydronephrosis and urinary incontinence
** Exercise-induced fever
** impaired sexual function affecting fertility (usually preserved in females), arousal, lubrication, ejaculation, and orgasm
** Hyperhidrosis or hypohidrosis
** problems during pregnancy, labour, and breastfeeding
* 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:
For more information on these pathophysiological responses, please see [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9320320/pdf/jpm-12-01110.pdf Autonomic Dysfunction and Management after Spinal Cord Injury: A Narrative Review.]
** 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:<ref name=":1" />
Pathophysiological responses from the ANS can occur during procedures or with pain or injury. Events that may trigger pathophysiological responses include:<ref name=":1" />


* [[Functional Electrical Stimulation Cycling for Spinal Cord Injury|Functional electrical stimulation]]
* [[Functional Electrical Stimulation Cycling for Spinal Cord Injury|functional electrical stimulation]]
* surgery
* invasive investigational procedures, such as urodynamic studies
* stretches
* fractures
* [[Urinary Tract Infection|urinary tract infection (UTI)]]
== Assessment of the Autonomic Nervous System in Spinal Cord Injury ==
[[File:ASIA ISCoS Autonomic Standards Assessment Form.jpg|thumb|Figure 4. ASIA ISCoS Autonomic Standards Assessment Form.]]The International Standards to document Autonomic Function following SCI (ISAFSCI) was published in 2009 and revised in 2012. The ISAFSCI is also referred to as the Autonomic Standards. [[American Spinal Injury Association (ASIA) Impairment Scale|The American Spinal Injury Association]] (ASIA) and the International Spinal Cord Society (ISCoS) recommendations for the Autonomic Standards include the following:<ref name=":6">Wecht JM, Krassioukov AV, Alexander M, Handrakis JP, McKenna SL, Kennelly M, et al. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152176/pdf/i1082-0744-27-2-23.pdf International Standards to document Autonomic Function following SCI (ISAFSCI): Second Edition]. Top Spinal Cord Inj Rehabil. 2021 Spring;27(2):23-49</ref>


* Surgery
* using Autonomic Standards in conjunction with the full International Standards for Neurological Classification of SCI (ISNCSCI) following the initial injury
* Invasive investigational procedures such as urodynamic studies.
* 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"<ref name=":6" />
* Stretches
* tracking changes in autonomic functions following clinical interventions or during clinical trials
* Fractures
* [[Urinary Tract Infection|UTIs]]
[[File:ASIA ISCoS Autonomic Standards Assessment Form.jpg|thumb|ASIA ISCoS]]


== Assessment of ANS in SCI ==
The '''Autonomic Standards Assessment Form''' includes the following:<ref name=":1" />
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. [[American Spinal Injury Association (ASIA) Impairment Scale|The American Spinal Injury Association]] (ASIA) and the International Spinal Cord Society (ISCoS) recommendations for the Autonomic Standards include the following:<ref>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. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152176/pdf/i1082-0744-27-2-23.pdf International Standards to document Autonomic Function following SCI (ISAFSCI): Second Edition]. Top Spinal Cord Inj Rehabil. 2021 Spring;27(2):23-49</ref>


* Using Autonomic Standards in conjunction with the full International Standards for Neurological Classification of SCI (ISNCSCI) following the initial injury
* autonomic control of the heart
* 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
* autonomic control of blood pressure
* Tracking changes in autonomic functions following clinical intervention or during a clinical trial
* autonomic control of sweating (sudomotor control)
* temperature regulation
* autonomic and somatic control of the bronchopulmonary system
* lower urinary tract
* bowel and sexual function
* urodynamics
Table 1 describes each area in detail, highlighting what constitutes normal function, reduced or altered function and a complete loss of control. You can also learn more about the impact of ANS impairment on the function of organ systems and how to use the ISAFSCI at the [https://asia-spinalinjury.org/learning/ ASIA e-Learning Center].
{| class="wikitable"
|+'''Table 1. Autonomic Function Assessment'''<ref name=":6" />
|
| colspan="3" |Scoring:
2 = Normal Function


'''Autonomic Standards Assessment Form''' include the following:<ref name=":1" />
1 = Reduced / Altered Function


* Autonomic control of the heart
0 = Complete loss of control
* 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 [https://asia-spinalinjury.org/learning/ ASIA e-Learning Center], you can learn more about the impact of ANS impairment on organ system function and how to use the ISAFSCI.
NT = not tested
 
|
== '''Function of the ANS in SCI''' ==
 
=== '''Autonomic Function Assessment''' ===
The following systems are assessed, and impairments are documented:
 
# '''Cardiovascular, thermoregulation, sudomotor control, bronchopulmonary, lower urinary tract:'''<ref name=":1" />
 
{| class="wikitable"
|+'''Autonomic Function Assessment'''
!
! colspan="3" |Scoring:
2-Normal Function
1-Reduced/AlteredFunction
0-Complete loss of control
NT-not tested
!
|-
|-
!
!
Line 130: Line 121:
!'''Comments'''
!'''Comments'''
|-
|-
!Heart rate
|Heart rate
!61-99bmp
|61-99 beats per minute (bpm)
!
|
* Below 60bpm (Bradycardia)
* Below 60 bpm (bradycardia)
* Above 100bpm (Tachycardia)
* Above 100 bpm (tachycardia)
!
|
!
|
* Measured in supine and seated
* Measured in supine and seated


* Arrhythmias should be defined  
* Arrhythmias should be defined
* When the pulse is not tested, the reason should be given
* A reason must be given when the pulse is not tested
|-
|-
|Systolic blood pressure (SBP)
|Systolic blood pressure (SBP)
|91-138mmHg
|91-138 mmHg
|
|
* SBP under 90 (Hypotension)
* SBP under 90 mmHg (hypotension)
* Fall of more than 20 millimetres of mercury within 10 minutes of sitting up (Orthostatic hypotension)
* Fall of more than 20 millimetres of mercury (mmHg) 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)
* Heart rate is less than 60 bpm, and the SBP is less than 90 mmHg (neurogenic shock - most common within the first 30 days of injury)
* Increase in the systolic blood pressure of more than 20 mmHg above the baseline (Autonomic dysreflexia)
* increase in the SBP of more than 20 mmHg above the baseline (autonomic dysreflexia)
* BP above 140 (supine hypertension)
* SBP above 140 mmHg (supine hypertension)
|
|
|
|
* Measured in supine and seated
* Measured in supine and seated
* The patient's baseline must be known to determine whether it is actually autonomic dysreflexia.
* The patient's baseline must be known to determine whether measurements reflect autonomic dysreflexia
* A reason must be given when the blood pressure is not measured
|-
|-
|Diastolic blood pressure (DBP)
|Diastolic blood pressure (DBP)
|62-89 mmHg
|62-89 mmHg
|
|
* Under 60 mmHg (Hypotension)  
* DBP under 60 mmHg (hypotension)
* Fall of more than 10 within 10 minutes of sitting up (Orthostatic hypotension)
* Fall of DBP of more than 10 mmHg within 10 minutes of sitting up (orthostatic hypotension)
* More than 90 mmHg (Hypertension)  
* DBP more than 90 mmHg (hypertension)
|
|
|
|
* Measured in supine and seated
* Measured in supine and seated
* When blood pressure is not tested, a reason should be noted
* A reason must be given when the blood pressure is not measured
|-
|-
|Core Body Temperature
|Core body temperature
|36.4-37.6°C
|36.4-37.6°C
(97.5-99.7 °F)
(97.5-99.7 °F)
|
|
* 35.1-36.3 °C (95.1-97.4 °F)
* 35.1-36.3 °C (95.1-97.4 °F) (reduced)
* 37.7 - 37.9 °C(99.8- 100.2°F) [Elevated]
* 37.7-37.9 °C (99.8- 100.2°F) (elevated)
* The core temperature of less than 35°C (95°F )[Hypothermia]
* A core temperature of less than 35°C (95°F )(hypothermia)
* The core temperature of more than 38 °C  (100.4 °F) [Hyperthermia]
* A core temperature of more than 38 °C  (100.4 °F) (hyperthermia)
|
|
|Temperature measurements must be taken under the following conditions:
|Temperature measurements must be taken under the following conditions:


* an air temperature of between 20 and 25 °C (68-77 °F)
* an air temperature of between 20 and 25 °C (68-77 °F)
* 30 to 50% humidity,
* 30 to 50% humidity
* patient wearing a single layer of clothing  
* patient is wearing a single layer of clothing
* after a 10-minute rest  
* after a 10-minute rest  
* no acute illness or infection  
* no acute illness or infection present
|-
|-
|Sudomotor control
|Sudomotor control
|Sweating over all the skin surfaces
|Sweating over all the skin surfaces
|
|
* Diminished sweating, whether above or below the neurological level (Hypohidrosis)
* Diminished sweating, whether above or below the neurological level (hypohidrosis)
* Excessive sweating, either above or below the neurological level (Hyperhidrosis)
* Excessive sweating, either above or below the neurological level (hyperhidrosis)
|
|
* No sweating, either above or below the neurological level (Anhidrosis)
* No sweating, either above or below the neurological level (anhidrosis)
|
|
* Records the sweating response to high ambient heat or exercise only
* Records the sweating response to high ambient heat or exercise only
* Where sweating is not tested, the reason must be given.  
* When sweating is not tested, a reason must be given.
* Sweating associated with autonomic dysreflexia, orthostatic hypotension,  or mental stress would not be scored.
* Sweating that is associated with autonomic dysreflexia, orthostatic hypotension,  or mental stress would not be scored
|-
|-
|Respiration
|Respiration
Line 206: Line 198:
|
|
|-
|-
|Lower urinary tract
|Lower urinary tract, bowel and sexual function
|
|
|
|Reduced or altered in the following functions:
* Awareness of the need to empty the bladder
 
* Ability to prevent leakage (urinary continence)
* Sensation of the need for bowel movement
* Bladder emptying metho
* The ability to prevent stool leakage or continence
* Sensation of the need for a bowel movement
* Voluntary sphincter contraction.
* Ability to prevent stool leakage or achieve continence
* Genital arousal, either erection or lubrication.
* Voluntary sphincter contraction
* Orgasm and ejaculation in the male
* Genital arousal, either erection or lubrication
* The sensation of menses in the female 
* Orgasm and ejaculation in males
* Sensation of menses in females
|
|
|
|
* Not tested is recorded when you are unable to assess due to pre-existing or concomitant problems
* Not tested is recorded when you are unable to assess due to pre-existing or concomitant problems
|}
|}
'''2. Temperature regulation:'''


===== Temperature Regulation =====
Individuals with a lesion at T6 and above:
Individuals with a lesion at T6 and above:


* Lacking the descending sympathetic control to respond appropriately to environmental changes in temperature <ref name=":1" />
* lack the descending sympathetic control to respond appropriately to environmental changes in temperature<ref name=":1" />
* Become adversely affected by the lack of afferent and efferent thermoregulatory information<ref name=":3">Grossmann F, Flueck JL, Perret C, Meeusen R, Roelands B. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049141/pdf/fphys-12-636997.pdf 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.</ref>
* can be adversely affected by the lack of afferent and efferent thermoregulatory information<ref name=":3">Grossmann F, Flueck JL, Perret C, Meeusen R, Roelands B. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049141/pdf/fphys-12-636997.pdf 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.</ref>
* Feel a greater impact of the internal and external heat load, resulting in a greater potential for exercise-induced hyperthermia <ref name=":3" />  
* can be more affected by internal and external heat load, so there is a greater potential for exercise-induced hyperthermia<ref name=":3" />  
* Sweating, going red, vasodilation, and faster breathing are less effective due to no response below the lesion, resulting in  fever <ref name=":1" />
* sweating, vasodilation, and faster breathing are less effective measures to reduce heat as there is no response below the lesion; this can lead to fever<ref name=":1" />


The following techniques can be successful in restoring normal body temperature:<ref name=":3" />
The following techniques can be successful in restoring normal body temperature in individuals with SCI:<ref name=":3" />


* Wearing cooling garments or other cooling devices
* wearing cooling garments or other cooling devices
** Cooling vest
** cooling vest
** Refrigerated headpiece
** refrigerated headpiece
** Cooling device on the feet
** cooling device on the feet
* Water spray and artificial sweat
* water spray and artificial sweat
* Ice slurry
* ice slurry
* The use of a cold cloth or a fan<ref name=":1" />
* using a cold cloth or a fan<ref name=":1" />


'''3.''' '''Orthostatic hypotension'''
===== Orthostatic Hypotension =====
[[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:<ref name=":1" />


[[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


* Symptoms may include dizziness, nausea, light-headedness, or faintness.
== Autonomic Nervous System Symptom Management in Spinal Cord Injury ==
* Physical signs include paleness, excessive sweating, or a loss of consciousness.
 
== SCI and ANS Symptoms Management ==


=== General Rules ===
=== General Rules ===
'''Be aware'''...........
'''Be aware'''...........


-of the system impairments in SCI. Educate yourself and your patients
* of the system impairments in SCI - educate yourself and your patients
 
* of the less obvious or even silent symptoms
-of the less obvious or even silent symptoms
* that suctioning or insertion of a nasogastric tube can commonly induce bradycardia and apnoea in individuals with SCI
 
-that suctioning or insertion of a nasogastric tube can commonly induce bradycardia and apnoea


=== Autonomic Dysreflexia ===
=== Autonomic Dysreflexia ===
<blockquote>"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)". <ref name=":1" />-- Melanie Harding</blockquote>As  a result of noxious afferent stimuli below the level of the lesion, the following occurs:<ref name=":1" />
<blockquote>"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)"<ref name=":1" /> -- Melanie Harding</blockquote>It most commonly occurs in individuals with SCI at or above T6.<ref name=":6" /> Noxious afferent stimuli below the level of the lesion can cause the following:<ref name=":1" />


* A widespread activation of the sympathetic nervous system demonstrated by an increase in norepinephrine release.
* widespread activation of the sympathetic nervous system, demonstrated by the increased release of norepinephrine (noradrenaline)
* Vasoconstriction in the majority of vascular beds below the level of injury: muscle, skin, kidneys, and presumably also the splanchnic vascular bed
* 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).
* an increase in arterial blood pressure, which activates the baroreceptors; this acts to buffer the vasoconstriction through dilation of vascular beds above the lesion level (where there is intact central control) and through a reduction in heart rate


==== Signs ====
==== Signs of Autonomic Dysreflexia ====
The signs of AD include:
The signs of autonomic dysreflexia include:


* Piloerection (goosebumps)
* piloerection (goosebumps)
* Chills or shivering
* chills or shivering
* Pounding headache
* pounding headache
* Paresthesia
* paraesthesia
* Flushing
* flushed skin
* Diaphoresis(sweating) above the lesion level
* diaphoresis (sweating) above the lesion level
* Nasal congestion
* nasal congestion
* Anxiety (feeling of impending doom)
* anxiety (feeling of impending doom)
* Malaise
* malaise
* Nausea
* nausea
Watch this video to learn more about [[Autonomic Dysreflexia]]:
Please watch this optional video if you would like to learn more about [[Autonomic Dysreflexia]]:


{{#ev:youtube|v=eocOmytfg8s|300}}<ref>Dr Matt & Dr Mike. Autonomic Dysreflexia. Available from:https://www.youtube.com/watch?v=eocOmytfg8s [last accessed 18/3/2024]</ref>
{{#ev:youtube|v=eocOmytfg8s|300}}<ref>Dr Matt & Dr Mike. Autonomic Dysreflexia. Available from:https://www.youtube.com/watch?v=eocOmytfg8s [last accessed 18/3/2024]</ref>


==== Triggering Factors ====
==== Potential Triggers for Autonomic Dysreflexia ====
 
The following factors can trigger autonomic dysreflexia in individuals with SCI:
* Irritation of the urinary bladder
* irritation of the urinary bladder
** Catheterisation and manipulation or blockage of an indwelling catheter
** catheterisation and manipulation or blockage of an indwelling catheter
** Urinary tract infection  
** urinary tract infection
** Detrusor sphincter dyssynergia and bladder percussion
** detrusor sphincter dyssynergia and bladder percussion
** Distended/overfull bladder
** distended / overfull bladder
* Gastrointestinal tract distension, constipation, anal fissures, haemorrhoids.
* gastrointestinal tract distension, constipation, anal fissures, haemorrhoids.
* Stimuli that would be noxious if pain sensation was preserved, such as:
* stimuli that would be noxious if pain sensation was preserved, such as:
** Bone fractures or joint displacements, pressure sores, ingrown toenails
** bone fractures or joint displacements, pressure sores, ingrown toenails
** Sexual activity/orgasm may induce AD in both sexes
** sexual activity / orgasm may induce autonomic dysreflexia in both sexes
** During pregnancy and delivery and breastfeeding
** during pregnancy, delivery and breastfeeding
** Cystoscopy, UDS, vibration or electrostimulation for ejaculation
** cystoscopy, urodynamic studies (UDS), vibration or electrostimulation for ejaculation
** Electrical stimulation or stretching of muscles or neural tissue
** electrical stimulation or stretching of muscles or neural tissue
 
==== Management ====


* Sit the patient up  
==== Management of Autonomic Dysreflexia ====
* Loosen any tight clothing or constrictive devices
Management of autonomic dysreflexia includes the following:
* Rule out bladder problem
* sit the patient up
** If no urinary catheter is in place, catheterise the patient
* loosen any tight clothing or constrictive devices
** If there is a urinary catheter, check the system along its entire length for blockages, twists, kinks or obstructions and correct placement
* rule out a bladder problem
** 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
** if no urinary catheter is in place, catheterise the patient
* Rule out faecal impaction
** if there is a urinary catheter, check the system along its entire length for blockages, twists, kinks or obstructions and correct placement
** The carer/nurse should check the rectum for stool, using a local anaesthetic jelly as a lubricant
** if the catheter seems to be blocked, report this to the nurse or carer, so they can gently irrigate the bladder with a small amount of body temperature normal saline
** Gentle manual evacuation is recommended
* 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
* 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
* monitor blood pressure and pulse every 2-5 minutes until the patient has stabilised
* 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
* 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 the 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
* the individual's symptoms and blood pressure should be monitored for at least 2 hours after the episode to ensure there is no further elevation in blood pressure


==== Complications of Unmanaged AD ====
==== Complications of Unmanaged Autonomic Dysreflexia ====
When untreated, AD can cause complications leading to comorbidities and mortality in patients with a spinal cord injury:
When untreated, autonomic dysreflexia can cause complications / comorbidities or mortality in patients with a spinal cord injury, including:


* [[Pulmonary Embolism|Pulmonary embolism]]
* [[Pulmonary Embolism|pulmonary embolism]]
* [[Stroke]]
* [[stroke]]
* Combined immunodeficiency(CIDS)  
* combined immunodeficiency (CIDS)
* Clinically significant infectious complications
* clinically significant infectious complications
* Seizures
* seizures
* Retinal haemorrhage or detachment  
* retinal haemorrhage or detachment
* [[Pulmonary Oedema|Pulmonary oedema]]
* [[Pulmonary Oedema|pulmonary oedema]]
* Renal insufficiency
* renal insufficiency
* Myocardial infarction
* myocardial infarction


== Resources ==
== Resources ==
*[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7495222/pdf/GRP2020-8024171.pdf The Enteric Nervous System and Its Emerging Role as a Therapeutic Target.]
*Fleming MA 2nd, Ehsan L, Moore SR, Levin DE. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7495222/pdf/GRP2020-8024171.pdf The Enteric Nervous System and Its Emerging Role as a Therapeutic Target.] Gastroenterol Res Pract. 2020 Sep 8;2020:8024171.
*[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9320320/pdf/jpm-12-01110.pdf Autonomic Dysfunction and Management after Spinal Cord Injury: A Narrative Review]
*Henke AM, Billington ZJ, Gater DR Jr. [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9320320/pdf/jpm-12-01110.pdf Autonomic Dysfunction and Management after Spinal Cord Injury: A Narrative Review.] J Pers Med. 2022 Jul 7;12(7):1110.
*[https://asia-spinalinjury.org/learning/ ASIA e-Learning Center]
*[https://asia-spinalinjury.org/learning/ ASIA e-Learning Center]
*[https://asia-spinalinjury.org/wp-content/uploads/2022/02/ISAFSCI-Autonomic-General-and-Sacral-Exam-Worksheets.pdf General Autonomic Function]
*[https://asia-spinalinjury.org/wp-content/uploads/2022/02/ISAFSCI-Autonomic-General-and-Sacral-Exam-Worksheets.pdf General Autonomic Function]
Line 334: Line 325:


<references />
<references />
[[Category:Course Pages]]
[[Category:Spinal cord injury]]
[[Category:Rehabilitation]]
[[Category:ReLAB-HS Course Page]]

Latest revision as of 11:05, 25 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.[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:

  • regulating visceral functions
  • maintaining homeostasis within the human body
Figure 1. 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 the following:

  • "fight or flight" response, which leads to increased blood pressure, heart rate and glucose production, cessation of gastrointestinal peristalsis, etc.[3]
  • fibres from the SNS innervate many organs: the SNS provides physiological regulation over diverse body processes, including pupil diameter, gut motility (movement), and urinary output[4]
  • preparing the body for physical activity: there is "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]
    Figure 2. Parasympathetic nervous system.

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

The preganglionic cell bodies of the parasympathetic nervous system (PNS) originate at the craniosacral axis. The PNS has long efferent preganglionic fibres but short postganglionic fibres to the effector organs.[5] The PNS innervates the head, viscera, and external genitalia.

Functions of the PNS include:[3]

  • promoting "rest and digest"
  • lowering heart rate and blood pressure
  • facilitating gastrointestinal peristalsis

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

Figure 3. Enteric nervous system.

The enteric nervous system (ENS) is the largest, most complex unit within the peripheral nervous system. It innervates the gastrointestinal tract through a network of ganglion-rich nerve connections, extending from the oesophagus to the anal canal.[6][7] While the ENS receives input from the central nervous system (CNS), it can act independently from the CNS because of local reflex circuits.

Functions of the ENS include:[6]

  • propulsion of food
  • blood flow regulation
  • nutrient handling
  • immunological defence

Autonomic Nervous System and Spinal Cord Injury (SCI)[edit | edit source]

Spinal cord injury can affect all three subsystems of the autonomic nervous system due to their anatomical location, loss of supraspinal influence, and sustained responses to afferent stimuli.[5] A number of pathophysiological responses from the ANS can occur after SCI, contributing to various complications and comorbidities.[5][3]

  • Cardiovascular dysfunction: SCI (particularly cervical and high thoracic injuries) can result in parasympathetic dominance and reduced sympathetic influence (i.e. sympathetic blunting). This imbalance can lead to various cardiovascular complications, including:
    • low resting arterial blood pressure
    • postural hypotension
    • autonomic dysreflexia (sudden, acute hypertension in response to specific stimuli)
    • bradycardia or arrhythmia
  • Thermoregulatory dysfunction: commonly occurs in individuals with high thoracic and cervical SCI, primarily because of sympathetic dysfunction or blunting. This affects the ability of the body to redistribute warm blood from the core to the periphery and inhibits sweating below the level of injury. When the body attempts to dissipate heat, excess sweating may occur, and the skin may appear flushed above the injury.[5] Thermoregulatory dysfunction is associated with:[5]
    • poikilothermia[5]
      • an individual with an SCI takes on "the ambient temperature around them due to the inability to regulate core body temperature"
    • quad fever (idiopathic hyperpyrexia)
      • "an extreme elevation in body core temperature beyond 40.8°C (105.4°F) in a patient with spinal cord injury"[8]
    • exercise-induced fever
    • hyperhidrosis (excess sweating) or hypohidrosis (reduced sweating)
  • Respiratory dysfunction: associated with parasympathetic dominance and blunted supraspinal sympathetic drive in individuals with high cervical and thoracic SCI:[5]
    • bronchiolar constriction: associated with unopposed vagal influence on the bronchial tree, as well as hyper-reactive airways and increased secretion of mucus
    • individuals with high thoracic and cervical SCI are unable to cough / clear pulmonary secretions voluntarily and are at risk of:
      • atelectasis
      • pneumonia
      • mucus plugging
    • during exercise, inspiratory effort is limited by ventilatory insufficiency, bronchoconstriction and mucus production
  • Gastrointestinal dysfunction: as mentioned above, while the ENS can act independently, it is usually influenced by the SNS and PNS. PNS dominance and sympathetic blunting in SCI can lead to:[5]
    • 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 dysfunction: after SCI, there is increased uninhibited activation of the sympathetic, parasympathetic and the somatic nervous systems, which are responsible for bladder storage and emptying. The results of genitourinary dysfunction include:[5]
    • bladder and bowel dysfunction
      • detrusor sphincter dyssynergia: high bladder pressures and likely vesicoureteral reflux, which is associated with hydroureter, hydronephrosis and urinary incontinence
    • impaired sexual function affecting fertility (usually preserved in females), arousal, lubrication, ejaculation, and orgasm
    • problems during pregnancy, labour, and breastfeeding

For more information on these pathophysiological responses, please see Autonomic Dysfunction and Management after Spinal Cord Injury: A Narrative Review.

Pathophysiological responses from the ANS can occur during procedures or with pain or injury. Events that may trigger pathophysiological responses include:[3]

Assessment of the Autonomic Nervous System in Spinal Cord Injury[edit | edit source]

Figure 4. ASIA ISCoS Autonomic Standards Assessment Form.

The International Standards to document Autonomic Function following SCI (ISAFSCI) was published in 2009 and revised in 2012. The 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:[9]

  • 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"[9]
  • tracking changes in autonomic functions following clinical interventions or during clinical trials

The Autonomic Standards Assessment Form includes the following:[3]

  • autonomic control of the heart
  • autonomic control of blood pressure
  • autonomic control of sweating (sudomotor control)
  • temperature regulation
  • autonomic and somatic control of the bronchopulmonary system
  • lower urinary tract
  • bowel and sexual function
  • urodynamics

Table 1 describes each area in detail, highlighting what constitutes normal function, reduced or altered function and a complete loss of control. You can also learn more about the impact of ANS impairment on the function of organ systems and how to use the ISAFSCI at the ASIA e-Learning Center.

Table 1. Autonomic Function Assessment[9]
Scoring:

2 = Normal Function

1 = Reduced / Altered Function

0 = Complete loss of control

NT = not tested

Normal (2) Reduced/Altered (1) Complete loss of control (0) Comments
Heart rate 61-99 beats per minute (bpm)
  • Below 60 bpm (bradycardia)
  • Above 100 bpm (tachycardia)
  • Measured in supine and seated
  • Arrhythmias should be defined
  • A reason must be given when the pulse is not tested
Systolic blood pressure (SBP) 91-138 mmHg
  • SBP under 90 mmHg (hypotension)
  • Fall of more than 20 millimetres of mercury (mmHg) within 10 minutes of sitting up (orthostatic hypotension)
  • Heart rate is less than 60 bpm, and the SBP is less than 90 mmHg (neurogenic shock - most common within the first 30 days of injury)
  • increase in the SBP of more than 20 mmHg above the baseline (autonomic dysreflexia)
  • SBP above 140 mmHg (supine hypertension)
  • Measured in supine and seated
  • The patient's baseline must be known to determine whether measurements reflect autonomic dysreflexia
  • A reason must be given when the blood pressure is not measured
Diastolic blood pressure (DBP) 62-89 mmHg
  • DBP under 60 mmHg (hypotension)
  • Fall of DBP of more than 10 mmHg within 10 minutes of sitting up (orthostatic hypotension)
  • DBP more than 90 mmHg (hypertension)
  • Measured in supine and seated
  • A reason must be given when the blood pressure is not measured
Core body temperature 36.4-37.6°C

(97.5-99.7 °F)

  • 35.1-36.3 °C (95.1-97.4 °F) (reduced)
  • 37.7-37.9 °C (99.8- 100.2°F) (elevated)
  • A core temperature of less than 35°C (95°F )(hypothermia)
  • A 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 is wearing a single layer of clothing
  • after a 10-minute rest
  • no acute illness or infection present
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
  • When sweating is not tested, a reason must be given.
  • Sweating that is 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, bowel and sexual function
  • Awareness of the need to empty the bladder
  • Ability to prevent leakage (urinary continence)
  • Bladder emptying metho
  • Sensation of the need for a bowel movement
  • Ability to prevent stool leakage or achieve continence
  • Voluntary sphincter contraction
  • Genital arousal, either erection or lubrication
  • Orgasm and ejaculation in males
  • Sensation of menses in females
  • Not tested is recorded when you are unable to assess due to pre-existing or concomitant problems
Temperature Regulation[edit | edit source]

Individuals with a lesion at T6 and above:

  • lack the descending sympathetic control to respond appropriately to environmental changes in temperature[3]
  • can be adversely affected by the lack of afferent and efferent thermoregulatory information[10]
  • can be more affected by internal and external heat load, so there is a greater potential for exercise-induced hyperthermia[10]
  • sweating, vasodilation, and faster breathing are less effective measures to reduce heat as there is no response below the lesion; this can lead to fever[3]

The following techniques can be successful in restoring normal body temperature in individuals with SCI:[10]

  • wearing cooling garments or other cooling devices
    • cooling vest
    • refrigerated headpiece
    • cooling device on the feet
  • water spray and artificial sweat
  • ice slurry
  • using a cold cloth or a fan[3]
Orthostatic Hypotension[edit | edit source]

Orthostatic hypotension occurs due to the interruption of efferent pathways from the brain stem's vasomotor centre to the sympathetic nerves involved in vasoconstriction:[3]

  • symptoms may include dizziness, nausea, light-headedness, or faintness
  • physical signs include paleness, excessive sweating, or a loss of consciousness

Autonomic Nervous System Symptom Management in Spinal Cord Injury[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 in individuals with SCI

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

It most commonly occurs in individuals with SCI at or above T6.[9] Noxious afferent stimuli below the level of the lesion can cause the following:[3]

  • widespread activation of the sympathetic nervous system, demonstrated by the increased release of norepinephrine (noradrenaline)
  • vasoconstriction in the majority of vascular beds below the level of injury: muscle, skin, kidneys, and presumably also the splanchnic vascular bed
  • an increase in arterial blood pressure, which activates the baroreceptors; this acts to buffer the vasoconstriction through dilation of vascular beds above the lesion level (where there is intact central control) and through a reduction in heart rate

Signs of Autonomic Dysreflexia[edit | edit source]

The signs of autonomic dysreflexia include:

  • piloerection (goosebumps)
  • chills or shivering
  • pounding headache
  • paraesthesia
  • flushed skin
  • diaphoresis (sweating) above the lesion level
  • nasal congestion
  • anxiety (feeling of impending doom)
  • malaise
  • nausea

Please watch this optional video if you would like to learn more about Autonomic Dysreflexia:

[11]

Potential Triggers for Autonomic Dysreflexia[edit | edit source]

The following factors can trigger autonomic dysreflexia in individuals with SCI:

  • 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 autonomic dysreflexia in both sexes
    • during pregnancy, delivery and breastfeeding
    • cystoscopy, urodynamic studies (UDS), vibration or electrostimulation for ejaculation
    • electrical stimulation or stretching of muscles or neural tissue

Management of Autonomic Dysreflexia[edit | edit source]

Management of autonomic dysreflexia includes the following:

  • sit the patient up
  • loosen any tight clothing or constrictive devices
  • rule out a 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 this to the nurse or carer, so they can 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 stabilised
  • 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 the utmost importance
  • the individual's symptoms and blood pressure should be monitored for at least 2 hours after the episode to ensure there is no further elevation in blood pressure

Complications of Unmanaged Autonomic Dysreflexia[edit | edit source]

When untreated, autonomic dysreflexia can cause complications / comorbidities or mortality in patients with a spinal cord injury, including:

  • 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 Course. Plus, 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 5.3 5.4 5.5 5.6 5.7 5.8 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. 6.0 6.1 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.
  7. 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.
  8. Ali S, Ganesan D, Sundaramoorthy V. Quad fever in a case of cervical cord injury-a rare case report. Asian J Neurosurg. 2022 Jun 28;17(1):85-87.
  9. 9.0 9.1 9.2 9.3 Wecht JM, Krassioukov AV, Alexander M, Handrakis JP, McKenna SL, Kennelly M, et al. International Standards to document Autonomic Function following SCI (ISAFSCI): Second Edition. Top Spinal Cord Inj Rehabil. 2021 Spring;27(2):23-49
  10. 10.0 10.1 10.2 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.
  11. Dr Matt & Dr Mike. Autonomic Dysreflexia. Available from:https://www.youtube.com/watch?v=eocOmytfg8s [last accessed 18/3/2024]