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INTRODUCTION:- The term ‘mental handicap’ is now used for the condition ‘ mental
retardation’ at least 2-3 % of Indian population are mentally handicap in any one form.
The malfunctioning of the brain is poorly understood in most cases, but the
physiological alteration may be identified in some children. The cognitive and functional
ability are affected with limitation in adaptive ability and communication relationship self
direction health behaviour ,safety measure ,academic achievement ,leisure time utilization
and working capacity are altered in mentally handicapped children.
MENATAL HANDICAPS
A. Mental retardation
B. Cerebral palsy
MEANTAL RETARDATION
DEFINTION:-
MEASUREMENT OF IQ
Chronological age
a. Physical defects
1. Sensory disorder ( found in 20% cases)
Defect in vision
Defect in hearing
2. Motor defects
Spasticity
Ataxia( lack of coordination in doing voluntary activities)
Epilepsy ( seen in several mentally retarded children
b. Psychiatric disorder
Schizophrenia
Neurosis
Mood disorder
Personality disorder
Organic psychiatric disorder like dementia
Autism and over activity syndrome
Behaviour disorder like mannerism ,hand banging and hyperkinetic syndrome.
a. Antenatal causes
Deficiency of folic acid in mother
Viral infection to mother during the first trimester of pregnancy ( such as
pertussis, mumps rubella, syphilis etc.)
Exposure of pregnant ,female to radiations
Consumption of drugs ,chemical for intoxicants by mother like lead
,thalidiomide etc.
Placental dysfunction like hypothyroidism
Endocrine disorder like hypothyroidism
b. Intra natal causes
Birth asphyxia
Prolonged or difficult labour
Prematurity
Instrumental delivery
Birth injuries( head injury, intraventricular hemorrhage)
c. Post natal causes
Cranial injuries ( accident and child abuse)
Infection like meningitis and encephalitis
Intoxication (lead)
Kernicterus
d. Genetic cause
Chromosomal anomalies like down syndrome, klinefelter’s syndrome fragile
x-syndrome ,trisomy x, turner’s syndrome.
e. Metabolic disorders
Disorder of protein metabolism like phenylketonuria, maple syrup disease
,hartnup disease .
Disorder of carbohydrate metabolism like galactosemia, gargoylism
Disorder of purine metabolism like lesch-nyhan syndrome.
Disorder of urea cycle like aminosuccinic aciduria, citruttinuria.
Disorder of mucopolysaccharides like hurler’s syndrome.
Miscellaneous disorder like wilson’s , toni- fanconi syndrome.
f. Disease of brain
Tuberculosis sclerosis
Epilepsy
Neurofibromatosis
g. Cranial malfunction
Microcephaly
Anecephaly
Hydrocephaly
h. Psychiatric disorder
Autism
Rett’s syndrome
Childhood onset schizophrenia
Aspergerf’s syndrome
DIAGNOSTIC EVALAUTION
MANAGEMENT
There is no standard medical treatment of mental retardation ; however prevention is the best
approach. Prevention can be done at three levels:
1. Primary prevention
It consist of planned actions taken to reduce the incidence of mental retardation. It
involves strategies of health promotion and specific protection (identification of risk
factors and then removing them).
a. Health promotion
It includes:
i. Good antenatal care
ii. improving socioeconomic status of country
iii. education people
iv. family and genetics counselling
v. facilitating research to identify cause and risk factors of mental retardation
b. Specific protection
It includes:
i. Good prenatal, intra natal and postnatal care.
ii. Genetic counselling of high –risk mother.
iii. Avoiding child birth in late maternal age.
iv. Avoiding consanguineous marriage.
v. Avoiding marriage of mentally retarded.
vi. Medical measure for preventing maternal infection during pregnancy(like
rubella, syphilis and toxoplasmosis), toxaemia of pregnancy ,trauma
,malnutrition ,obstetric complications, smoking alcoholism ,etc, which have
adverse effects on fetal development.
vii. Prematurity and neonatal medical condition (like kernicterus) should be
promptly managed.
2. Secondary prevention
It involves early diagnosis and care case finding, followed by intervention to limit the
disability.
a. Early detection and treatment
It include early detection and treatment of preventable disorder which may
lead mental retardation like phenolketonuria (low phenylalanine diet must be
given to these patients), maple syrup urine disease ( lowbranched amino acid
diet is given to the child), hypothyroidism (thyroxin administration is
done),etc.
Early detection and treatment of sensory, motor and behavioural handicaps.
Early treatment of correctable disorders, e.g. infection (antibiotics are given),
skull configuration anomalies (surgical correction is done),etc.
Early recognition of presence of mental retardation. A delay is diagnosis may
cause unfortunate delay in rehabilitation.
3. Tertiary prevention
Tertiary prevention aims to limit disability and promote rehabilitation.
a. Disability limitation
Treatment of physical and psychological problem ( by drugs or
behavioural modification).
Institutional care of severe or profound mentally retarded .
Educational in special school, if educable.
Vocational training ,if educable.
Regular physiotherapy to treat associate defects.
b. Rehabilitation
Rehabilitation in vocational ,physical and social areas is the corner stone
of management of mentally retarded children. It depend on patient’s
intelligence level and his capacities.
COUNSELLING OF PARENTS
The parents of mentally retarded children require perseverance and patience, as they have to
make life long adjustments, counselling of parents helps them in taking proper care of the
child. It helps the parents and accept the child’s problem and plan his care accondingly.
CEREBRAL PALSY
Definition palsy is chronic non- progressive motor dysfunction caused to due to the motor
areas of brain( Blosser and Burns, 2004)
The word’ cerebral’ refers to cerebrum which is the affected area of brain and ‘palsy’
refers to disorder of movement.
In 2007, the incidence of cerebral palsy was estimated to be 2.12- 2.45 per 1000 live
births.
Cerebral palsy is caused by damage to the motor control centers of the developing brain
which can occurs during pregnancy, childhood or after birth up to the age of three years.
This results in activity limitation, which is often accompanied by disturbance of
sensation, depth perception and other sight based problem, communication impairment
and cognitive, epilepsy is found in about one third of cases.
A. Prenatal factors
i. Genetics and chromosomal anomalies
ii. Brain malformation
iii. Exposure to teratogens
iv. Multiple futuses
v. Intrauterine infection
vi. Placental problem causing insufficient nutrition and oxygen delivery to the
fetus
B. Birth factor
i. Preeclampsia
ii. Complicated labor and delivery
iii. Birth injury caused by direct head trauma
iv. Asphyxia secondary to card prolapsed or strangulation
C. Perinatal factor
i. Central nervous system infection
ii. Kernicterus
D. Childhood factors
i. Head trauma
ii. Meningitis
iii. Toxic ingestion like lead poisoning
iv. Shaken baby syndrome
v. Incidence causing hypoxia to brain like near drowning, choking due to foreign
body aspiration and poisoning.
Cerebral palsy is divided into four major classes according impairment and areas of brain thar
are damage. These four classes are:
a. Spastic hemiplegia
In this type one side of the body is affected.
Injury to the left side of the brain will cause right side deficit and vice
versa.
These patient are most ambulatory of all forms of spastic cerebral palsy
The affected persons have equines(limping instability) on the affected side
are prescribed ankle-foot orthosis to prevent equines.
b. Spastic diplegia
In this type, lower extremities are affected with little or no upper body
spasticity.
This is the most common form ,seen in 70-80% cases.
These patients have a ‘scissors gait’.
On the basis of gait analysis, patient are provided with walkers, crutches or
canes to help them in movement.
These patients may also have nearsightedness or strabismus.
c. Spastic monopleghia
One limb is affected
d. Spastic triplegia
Three limbs are affected
2. Spastic quadriplegia
Caused by damage to cerebellum.
Occurs in about 10% of cases.
Hypotonia and tremors may be present
Wide based gait.
Motors skill like writing, typing or using scissors might be affected.
3. Athetoid/ dyskinetics
Athetoid cerebral cerebral palsy involves mixed muscle tone- both hypertonia and
hypotonia are present along with constant involuntary motion.
Patient have trioble holding themselves in upright steady position for siting or
walking.
Difficulty in holding object, especially small ones requiring fine motor control like
tooth brush or pencil.
10% patients have this type of cerebral palsy.
4. Mixed type
Symptoms of more than one form exist in these patients.
CLINICAL FEATURES
DIAGNOSTIC EVALUATION
The diagnostic of cerebral palsy has historically rested on the patients history and physical
examination. Once diagnosed with cerebral palsy, further diagnostic tests are optional. The
American academy of neurology suggested that neuroimaging with CT or MRI is also
capable of revealing treatable condition such as hydrocephalus , porencephaly, arteriovenous
nalformation and subdural hemotomas.
MANAGEMENT
Treatment for cerebral cerebral palsy is lifelong multi- dimensional process focused on the
maintenance of associated condition. Treatment may include one or more of the following:
1. Physical therapy
2. Occupational therapy
3. Speech therapy
4. Drug to control seizures pain , or relax muscle spasm(e.g. benzodiazepines, baclofen
and intrathecal phenol/baclofen), hyperbaric oxygen and the use of botox to relax
contracting muscles.
5. Surgery to correct anatomical abnormalities to release tight muscles.
6. Communication aids such as computers with attached voice synthesizers.
Treatment is usually symptomatic and focus on helping the person to develop as many
motor skills as possible.
1. Physical therapy
Physiotherapy program are designed to improve gait and voluntary movements,
together with stretching program to limit contractures. Life- long physiotherapy is
crucial to maintain muscle tone, bone structure, and prevent dislocation of the joint.
2. Occupational therapy
It helps adults and children maximize their functioning adopt to their limitation and
live as independently as possible. Occupational therapy enables individual with
cerebral palsy to participate in activities of daily living that are meaningful to them.
Occupational therapist work closely with families in order to address their concern
and priorities for their child. Occupational therapist may address issued related to
sensory ,cognitive or motor impairment resulting from cerebral palsy that affect the
child’s participation in self –care, productivity or leisure.
3. Speech therapy
It help control the muscle of the mouth and jaw, and helps improve communication .
speech therapy often start before a child begins school and continues throughout the
school year.
4. Biofeedback
It is an alternative therapy in which people with cerebral palsy learn to control their
affected muscle. Some people learn ways to reduce tension with this technique.
5. Massage therapy
It is designed to help relax tense muscle, strengthen muscle, and keep joint flexible.
6. Drug therapy
Botulinum toxin a injection are given in to muscle that are spastic or sometimes
dystonic, the aim being to reduce the muscle hypertonus that can be painful, a
reduction in muscle tone can also facilitate bracing and the use of othotics. Most often
lower exrimities muscle are injected and reinjection is needed every 4-6 months.
7. Surgery and orthosis
Surgery usually involves one or a combination of following:
Loosening of tight muscle and releasing fixed joints, most often performed on
the hops , knees, hamstrings and ankles.
Straightening abnormal twists of the legs bones, i.e. femur and tibia. This is a
secondary complication caused by the spastics muscle generating abnormal
forces on the bones.
Cutting nerves of the limbs most affected by spasm. This procedure , called
rhizotomy(‘rhizo’ meaning root and ‘tomy’ meaning a cutting off) reduce
spasms and allows more flexibility and control of the affected limb and joints.
Orthotic devices such as ankle-foot orthosis are often prescribed to minimize
gait. Irregularities and increase speed.
PROGNOSIS
Cerebral palsy is not a progressive disorder (means the brain damage does not
worsen), but the symptoms can become more severe more over severe over time
due to subdural damage. A person with the disorder may improve somewhat
during childhood if or she receive extensive care from specialties, but once bones
and muscularity become more established, orthopaedic surgery may be required.
SUMMARY :-
CONCLUSION:-
SUBMITTED TO: -
SUBMITTED BY: -
MR. P. K. MASIH
MS. JAMUNA KUMARI
ASSOCIATE PROFESSOR
M.Sc. NSG FINAL YEAR
CHILD HEALTH NURSING
CHILD HEALTH NURSING