Cerebral palsy classification: Difference between revisions
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==Overview== | ==Overview== | ||
Cerebral palsy can be classified based on number of limbs involved, physiologically and functionally. Based on number of limbs involved cerebral palsy can be classified into monoplegia, hemiplegia, diplegia, paraplegia and quadriplegia. Physiologically, cerebral palsy can be divided into a spastic type (pyramidal), and an extrapyramidal type. The extrapyramidal types of cerebral palsy include athetoid, choreiform, ataxic, rigid, and hypotonic. The Manual Ability Classification System (MACS) and the Gross Motor Function Classification System (GMFCS) are two most commonly employed systems for functional classification of cerebral palsy. The Manual Ability Classification System (MACS) classifies children with cerebral palsy into five levels. The levels are based on the children’s self-initiated ability to handle objects and their need for assistance or adaptation to perform manual activities in everyday life. The Gross Motor Function Classification System (GMFCS) also classifies children with cerebral palsy into five levels. The levels are based on self-initiated movement abilities, in particular sitting and walking. | Cerebral palsy can be classified based on number of limbs involved, physiologically and functionally. Based on number of limbs involved cerebral palsy can be classified into [[monoplegia]], [[hemiplegia]], [[diplegia]], [[paraplegia]] and [[quadriplegia]]. Physiologically, cerebral palsy can be divided into a [[Spasticity|spastic type]] ([[pyramidal tract|pyramidal]]), and an [[extrapyramidal]] type. The [[extrapyramidal]] types of cerebral palsy include [[athetoid]], [[Athetosis|choreiform]], [[ataxic]], [[rigid]], and [[hypotonic]]. The Manual Ability Classification System (MACS) and the Gross Motor Function Classification System (GMFCS) are two most commonly employed systems for functional classification of cerebral palsy. The Manual Ability Classification System (MACS) classifies children with cerebral palsy into five levels. The levels are based on the children’s self-initiated ability to handle objects and their need for assistance or adaptation to perform manual activities in everyday life. The Gross Motor Function Classification System (GMFCS) also classifies children with cerebral palsy into five levels. The levels are based on self-initiated movement abilities, in particular sitting and walking. | ||
==Classification== | ==Classification== | ||
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===Physiologic classification=== | ===Physiologic classification=== | ||
Physiologically, cerebral palsy can be divided into a spastic type, which affects the corticospinal (pyramidal) | Physiologically, cerebral palsy can be divided into a [[Spasticity|spastic type]], which affects the [[corticospinal tracts]] ([[pyramidal tract|pyramidal]]) , and an [[extrapyramidal]] type, which affects the other regions of the developing brain. The [[extrapyramidal]] types of cerebral palsy include [[athetoid]], [[Athetosis|choreiform]], [[ataxic]], [[rigid]], and [[hypotonic]].<ref name="pmid26403442">{{cite journal |vauthors=Agarwal A, Verma I |title=Cerebral palsy in children: An overview |journal=J Clin Orthop Trauma |volume=3 |issue=2 |pages=77–81 |year=2012 |pmid=26403442 |pmc=3872805 |doi=10.1016/j.jcot.2012.09.001 |url=}}</ref> | ||
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{{familytree | | | | | | | | | A01 |A01=Cerebral palsy}} | {{familytree | | | | | | | | | A01 |A01=Cerebral palsy}} | ||
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{{familytree | | | | | C01 | | | | | | | | |!| |C01=Spastic}} | {{familytree | | | | | C01 | | | | | | | | |!| |C01=[[Spasticity|Spastic]]}} | ||
{{familytree | |,|-|-|-|+|-|-|-|.| | | | | |!| }} | {{familytree | |,|-|-|-|+|-|-|-|.| | | | | |!| }} | ||
{{familytree | D01 | | D02 | | D03 | | | | |!| D01=Spastic diplegia|D02=Spastic hemiplegia|D03=Spastic quadriplegia}} | {{familytree | D01 | | D02 | | D03 | | | | |!| D01=[[diplegia|Spastic diplegia]]|D02=[[hemiplegia|Spastic hemiplegia]]|D03=[[quadriplegia|Spastic quadriplegia]]}} | ||
{{familytree | | | | | | | | | | | |,|-|-|-|+|-|-|-|v|-|-|-|v|-|-|-|.|}} | {{familytree | | | | | | | | | | | |,|-|-|-|+|-|-|-|v|-|-|-|v|-|-|-|.|}} | ||
{{familytree | | | | | | | | | | | E01 | | E02 | | E03 | | E04 | | E05|E01=Athetoid|E02=Choreiform|E03=Rigid|E04=Ataxic|E05=Hypotonic|}} | {{familytree | | | | | | | | | | | E01 | | E02 | | E03 | | E04 | | E05|E01=[[Athetoid]]|E02=Choreiform|E03=Rigid|E04=[[Ataxic]]|E05=[[Hypotonic]]|}} | ||
{{familytree/end}} | {{familytree/end}} | ||
====Spastic==== | ====Spastic==== | ||
*Spastic cerebral palsy is the most common form of cerebral palsy.<ref name="pmid25755853">{{cite journal |vauthors=Shamsoddini A, Amirsalari S, Hollisaz MT, Rahimnia A, Khatibi-Aghda A |title=Management of spasticity in children with cerebral palsy |journal=Iran J Pediatr |volume=24 |issue=4 |pages=345–51 |year=2014 |pmid=25755853 |pmc=4339555 |doi= |url=}}</ref> | *Spastic cerebral palsy is the most common form of cerebral palsy.<ref name="pmid25755853">{{cite journal |vauthors=Shamsoddini A, Amirsalari S, Hollisaz MT, Rahimnia A, Khatibi-Aghda A |title=Management of spasticity in children with cerebral palsy |journal=Iran J Pediatr |volume=24 |issue=4 |pages=345–51 |year=2014 |pmid=25755853 |pmc=4339555 |doi= |url=}}</ref> | ||
*Spastic cerebral palsy is usually associated with injury to the pyramidal tracts in the immature brain. | *Spastic cerebral palsy is usually associated with injury to the [[pyramidal tract|pyramidal tracts]] in the immature [[brain]]. | ||
*Spasticity is caused due to exaggeration of the normal muscle passive stretch reflex. | *Spasticity is caused due to exaggeration of the normal [[muscle]]passive [[stretch reflex]]. | ||
*Histologically altered muscle function leads to the deposition of type I collagen in the endomysium of the affected muscle, leading to thickening and fibrosis, the degree of which correlated to the severity of the spasticity. | *Histologically altered muscle function leads to the deposition of [[type I collagen]] in the [[endomysium]] of the affected [[muscle]], leading to thickening and [[fibrosis]], the degree of which correlated to the severity of the [[spasticity]]. | ||
*Simultaneous co-contraction of normally antagonistic muscle groups leads to fatigue, loss of dexterity and coordination, and balance difficulties. | *Simultaneous co-contraction of normally antagonistic muscle groups leads to [[fatigue]], loss of [[dexterity]] and coordination, and balance difficulties. | ||
====Athetoid==== | ====Athetoid==== | ||
*Athetoid cerebral palsy is caused by an injury to the extrapyramidal tracts. | *Athetoid cerebral palsy is caused by an injury to the [[extrapyramidal|extrapyramidal tracts]]. | ||
*Athetoid cerebral palsy is characterized by dyskinetic, purposeless movements that may be exacerbated by environmental stimulation. | *Athetoid cerebral palsy is characterized by [[dyskinetic]], purposeless movements that may be exacerbated by environmental stimulation. | ||
*With the improvements in prevention of Rh incompatibility leading to kernicterus, the incidence of athetoid cerebral palsy is decreasing. | *With the improvements in prevention of [[Rh incompatibility]] leading to [[kernicterus]], the incidence of athetoid cerebral palsy is decreasing. | ||
*Dystonia, characterized by an increased overall tone and distorted positioning in response to voluntary movements, or hypotonia also can occur with athetoid cerebral palsy. | *[[Dystonia]], characterized by an increased overall [[tone]] and distorted positioning in response to voluntary movements, or [[hypotonia]] also can occur with athetoid cerebral palsy. | ||
====Choreiform==== | ====Choreiform==== | ||
*Choreiform cerebral palsy is characterized by continual purposeless movements of the patient's wrists, fingers, toes, and ankles. | *Choreiform cerebral palsy is characterized by continual purposeless movements of the patient's [[wrist|wrists]], [[fingers]], [[toes]], and [[ankle|ankles]]. | ||
*This continuous movement can make bracing and sitting difficult. | *This continuous movement can make bracing and [[sitting]] difficult. | ||
====Rigid==== | ====Rigid==== | ||
*Patients with rigid cerebral palsy are the most hypertonic of all cerebral palsy patients. | *Patients with rigid cerebral palsy are the most [[hypertonic]] of all cerebral palsy patients. | ||
*Hypertonicity occurs in the absence of hyperreflexia, spasticity, and clonus, which are common in spastic cerebral palsy. | *[[Hypertonicity]] occurs in the absence of [[hyperreflexia]], [[spasticity]], and [[clonus]], which are common in spastic cerebral palsy. | ||
*Patients with rigid cerebral palsy have a “cogwheel” or “lead pipe” muscle stiffness that often requires surgical release. | *Patients with rigid cerebral palsy have a “cogwheel” or “lead pipe” [[stiffness|muscle stiffness]] that often requires surgical release. | ||
====Ataxic==== | ====Ataxic==== | ||
*Ataxic cerebral palsy is a very rare type. | *Ataxic cerebral palsy is a very rare type. | ||
*Ataxic cerebral palsy is characterized by the disturbance of coordinated movement as a result of an injury to the developing cerebellum. | *Ataxic cerebral palsy is characterized by the disturbance of coordinated movement as a result of an injury to the developing [[cerebellum]]. | ||
*It is important to distinguish true ataxia from spasticity because with treatment many children with ataxia are able to improve their gait function without surgery. | *It is important to distinguish true [[ataxia]] from spasticity because with treatment many children with [[ataxia]] are able to improve their [[gait]] function without surgery. | ||
====Hypotonic==== | ====Hypotonic==== | ||
*Hypotonic cerebral palsy is characterized by weakness in conjunction with low muscle tone and normal deep tendon reflexes. | *Hypotonic cerebral palsy is characterized by weakness in conjunction with [[hypotonia|low muscle tone]] and normal [[deep tendon reflex|deep tendon reflexes]]. | ||
*Many children who ultimately develop spastic or ataxic cerebral palsy pass through a hypotonic stage lasting 1 or 2 years before the true nature of their brain injury becomes apparent. | *Many children who ultimately develop spastic or ataxic cerebral palsy pass through a hypotonic stage lasting 1 or 2 years before the true nature of their [[brain injury]] becomes apparent. | ||
*Persistent hypotonia can lead to difficulties with sitting balance, head positioning, and communication. | *Persistent [[hypotonia]] can lead to difficulties with sitting balance, head positioning, and communication. | ||
===Functional Classification of Cerebral Palsy=== | ===Functional Classification of Cerebral Palsy=== |
Latest revision as of 16:35, 6 October 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aditya Ganti M.B.B.S. [2]
Overview
Cerebral palsy can be classified based on number of limbs involved, physiologically and functionally. Based on number of limbs involved cerebral palsy can be classified into monoplegia, hemiplegia, diplegia, paraplegia and quadriplegia. Physiologically, cerebral palsy can be divided into a spastic type (pyramidal), and an extrapyramidal type. The extrapyramidal types of cerebral palsy include athetoid, choreiform, ataxic, rigid, and hypotonic. The Manual Ability Classification System (MACS) and the Gross Motor Function Classification System (GMFCS) are two most commonly employed systems for functional classification of cerebral palsy. The Manual Ability Classification System (MACS) classifies children with cerebral palsy into five levels. The levels are based on the children’s self-initiated ability to handle objects and their need for assistance or adaptation to perform manual activities in everyday life. The Gross Motor Function Classification System (GMFCS) also classifies children with cerebral palsy into five levels. The levels are based on self-initiated movement abilities, in particular sitting and walking.
Classification
Topographical Distribution
Based on number of limbs involved cerebral palsy can be classified into 4 subtypes
TYPE | Involved Limb |
---|---|
Monoplegia | One extremity involved, usually lower |
Hemiplegia | Both extremities on the same side involved
Usually, upper extremity involved more than lower extremity |
Paraplegia | Both lower extremities equally involved |
Diplegia | Lower extremities more involved than upper extremities
Fine-motor/sensory abnormalities in upper extremity |
Quadriplegia | All extremities involved equally
Normal head/neck control |
Double hemiplegia | All extremities involved, upper more than lower |
Physiologic classification
Physiologically, cerebral palsy can be divided into a spastic type, which affects the corticospinal tracts (pyramidal) , and an extrapyramidal type, which affects the other regions of the developing brain. The extrapyramidal types of cerebral palsy include athetoid, choreiform, ataxic, rigid, and hypotonic.[1]
Cerebral palsy | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Pyramidal | Extrapyramidal | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Spastic | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Spastic diplegia | Spastic hemiplegia | Spastic quadriplegia | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Athetoid | Choreiform | Rigid | Ataxic | Hypotonic | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
Spastic
- Spastic cerebral palsy is the most common form of cerebral palsy.[2]
- Spastic cerebral palsy is usually associated with injury to the pyramidal tracts in the immature brain.
- Spasticity is caused due to exaggeration of the normal musclepassive stretch reflex.
- Histologically altered muscle function leads to the deposition of type I collagen in the endomysium of the affected muscle, leading to thickening and fibrosis, the degree of which correlated to the severity of the spasticity.
- Simultaneous co-contraction of normally antagonistic muscle groups leads to fatigue, loss of dexterity and coordination, and balance difficulties.
Athetoid
- Athetoid cerebral palsy is caused by an injury to the extrapyramidal tracts.
- Athetoid cerebral palsy is characterized by dyskinetic, purposeless movements that may be exacerbated by environmental stimulation.
- With the improvements in prevention of Rh incompatibility leading to kernicterus, the incidence of athetoid cerebral palsy is decreasing.
- Dystonia, characterized by an increased overall tone and distorted positioning in response to voluntary movements, or hypotonia also can occur with athetoid cerebral palsy.
Choreiform
- Choreiform cerebral palsy is characterized by continual purposeless movements of the patient's wrists, fingers, toes, and ankles.
- This continuous movement can make bracing and sitting difficult.
Rigid
- Patients with rigid cerebral palsy are the most hypertonic of all cerebral palsy patients.
- Hypertonicity occurs in the absence of hyperreflexia, spasticity, and clonus, which are common in spastic cerebral palsy.
- Patients with rigid cerebral palsy have a “cogwheel” or “lead pipe” muscle stiffness that often requires surgical release.
Ataxic
- Ataxic cerebral palsy is a very rare type.
- Ataxic cerebral palsy is characterized by the disturbance of coordinated movement as a result of an injury to the developing cerebellum.
- It is important to distinguish true ataxia from spasticity because with treatment many children with ataxia are able to improve their gait function without surgery.
Hypotonic
- Hypotonic cerebral palsy is characterized by weakness in conjunction with low muscle tone and normal deep tendon reflexes.
- Many children who ultimately develop spastic or ataxic cerebral palsy pass through a hypotonic stage lasting 1 or 2 years before the true nature of their brain injury becomes apparent.
- Persistent hypotonia can lead to difficulties with sitting balance, head positioning, and communication.
Functional Classification of Cerebral Palsy
The Manual Ability Classification System (MACS) and the Gross Motor Function Classification System (GMFCS) are two most commonly employed systems for functional classification of cerebral palsy.[3]
Manual Ability Classification System
The Manual Ability Classification System (MACS) classifies children with cerebral palsy into five levels. The levels are based on the children’s self-initiated ability to handle objects and their need for assistance or adaptation to perform manual activities in everyday life.[4]
Does the child handle most kind of daily activities independently ( during play and leisure, eating and dressing) | |||||||||||||||||||||||||||||||||||||||||||
Yes | No | ||||||||||||||||||||||||||||||||||||||||||
Does the child handle even more difficult tasks with fair speed and accuracy and does not need alternative ways to perform | Does the child perform number of mannual tasks which commonly need to prepared or adapted and help is needed occasionally | ||||||||||||||||||||||||||||||||||||||||||
Yes | No | Yes | No | ||||||||||||||||||||||||||||||||||||||||
Level 1 Handles objects easily and successfully | Level 2 Handles most objects with reduced quality and speed of acheivement | Level 3 Handles objects with difficulty but needs preparation | Can the child perform easy activites with frequent support | ||||||||||||||||||||||||||||||||||||||||
Yes | No | ||||||||||||||||||||||||||||||||||||||||||
Level 4 Handles easy activites with limitations and support | Level 5 Cannot handle daily activites has severely limited abilities to perform even simple actions | ||||||||||||||||||||||||||||||||||||||||||
Gross Motor Function Classification System
The Gross Motor Function Classification System (GMFCS) also classifies children with cerebral palsy into five levels. The levels are based on self-initiated movement abilities, in particular sitting and walking.[5]
Level | Description |
---|---|
1 |
|
2 |
|
3 |
|
4 |
|
5 |
|
References
- ↑ Agarwal A, Verma I (2012). "Cerebral palsy in children: An overview". J Clin Orthop Trauma. 3 (2): 77–81. doi:10.1016/j.jcot.2012.09.001. PMC 3872805. PMID 26403442.
- ↑ Shamsoddini A, Amirsalari S, Hollisaz MT, Rahimnia A, Khatibi-Aghda A (2014). "Management of spasticity in children with cerebral palsy". Iran J Pediatr. 24 (4): 345–51. PMC 4339555. PMID 25755853.
- ↑ Compagnone E, Maniglio J, Camposeo S, Vespino T, Losito L, De Rinaldis M, Gennaro L, Trabacca A (2014). "Functional classifications for cerebral palsy: correlations between the gross motor function classification system (GMFCS), the manual ability classification system (MACS) and the communication function classification system (CFCS)". Res Dev Disabil. 35 (11): 2651–7. doi:10.1016/j.ridd.2014.07.005. PMID 25062096.
- ↑ Paulson A, Vargus-Adams J (2017). "Overview of Four Functional Classification Systems Commonly Used in Cerebral Palsy". Children (Basel). 4 (4). doi:10.3390/children4040030. PMC 5406689. PMID 28441773.
- ↑ Carnahan KD, Arner M, Hägglund G (2007). "Association between gross motor function (GMFCS) and manual ability (MACS) in children with cerebral palsy. A population-based study of 359 children". BMC Musculoskelet Disord. 8: 50. doi:10.1186/1471-2474-8-50. PMC 1919364. PMID 17584944.