presentation11-240822162615-3d10cc7d (1).pdf

archanasenthil220124 182 views 57 slides Aug 23, 2024
Slide 1
Slide 1 of 57
Slide 1
1
Slide 2
2
Slide 3
3
Slide 4
4
Slide 5
5
Slide 6
6
Slide 7
7
Slide 8
8
Slide 9
9
Slide 10
10
Slide 11
11
Slide 12
12
Slide 13
13
Slide 14
14
Slide 15
15
Slide 16
16
Slide 17
17
Slide 18
18
Slide 19
19
Slide 20
20
Slide 21
21
Slide 22
22
Slide 23
23
Slide 24
24
Slide 25
25
Slide 26
26
Slide 27
27
Slide 28
28
Slide 29
29
Slide 30
30
Slide 31
31
Slide 32
32
Slide 33
33
Slide 34
34
Slide 35
35
Slide 36
36
Slide 37
37
Slide 38
38
Slide 39
39
Slide 40
40
Slide 41
41
Slide 42
42
Slide 43
43
Slide 44
44
Slide 45
45
Slide 46
46
Slide 47
47
Slide 48
48
Slide 49
49
Slide 50
50
Slide 51
51
Slide 52
52
Slide 53
53
Slide 54
54
Slide 55
55
Slide 56
56
Slide 57
57

About This Presentation

pina bifida is a birth defect that occurs when the neural tube doesn't form or close properly during pregnancy, resulting in defects in the spine and spinal cord. The neural tube is the structure that eventually develops into the baby's brain and spinal cord, and it begins to form early i...


Slide Content

Ms. Archana B
MSc Nursing 1
st
year
Dept of Medical Surgical Nursing
Ganga college of nursing
Coimbatore

SPINAL DEFECT
ANDDEFORMITIES

Anatomy and physiology of spinal cord

Spinal deformities
•An abnormal curve in your spine,
such as scoliosis or kyphosis

Type of spinal deformities
•Scoliosis
•Kyphosis
•lordosis

Scoliosis
•Scoliosis is an abnormal
lateral curvature of the
spine it is most often
diagnosed in childhood or
early adolescence

Incidence
The primary age of scoliosis is 10 to 15 years old
Occurring both gender
Scoliosis effect about 5 million peoples in India

Type of scoliosis
•Structural
•Non structural

Structural scoliosis
•Structural scoliosis is the most common type
of scoliosis
•This type of scoliosis affect the spinal structure
•It involves a side to side curvature

Type of structural
scoliosis
❖Idiopathic
❖neuromuscular

Idiopathicscoliosis
•Infantile scoliosis it is developed at the age of 0 to 3
years
•Juvenilescoliosis develops at the age of 4 to 10 years
•Adolescence scoliosis is develops at the age of 11 to
18 years

Neuromuscular scoliosis
•Neuromuscular is secondary neurological or muscular disease
•Neuromuscular scoliosis associated with cerebral palsy, spinal
cord trauma, muscular dystrophy, spinal muscular atrophy and
spina bifida.

Nonstructural scoliosis
•Nonstructural scoliosis is also known as functional
scoliosis result from a temporary cause and only involve
a side to side curvature of the spine that is no spine
rotation

Assessment
❖Cobbs angle
❖Sociometer
❖Adam forward bent test

Cobbs angle test
1.10degrees –minimum angulation
2.10-15 –Required regular check up
3.20-40 –Required brace
4.40-50 –Required surgery

Sociometer
•To measure asymmetry
•Used at 3areas
•Upper thoracic T3-T4
•Middle thoracic T5 –T12
•Thoracic lumbar area T12,L1-L2, L3
•More than 7 consider as abnormal

ADAM’s forward scale
•It can be used to make a distinction between structural scoliosis and
nonstructural scoliosis

On observation

Clinical manifestation
•Lateral deviation of spine
•Rib hump
•The intertemporal space is narrow

Investigation
•Physicalexamination
•X-ray
•CT scan
•MRI

Medical
management

Halo traction

SPIROMETRY EXERCISE

Nutrition therapy
•Healthy fats like
•avocados,
•coconuts,
•egg yolk,
•and lots of nuts
High-quality protein from grass-fed
animals. Herbal teas and fresh
vegetable juices

Surgical management
•Spinal fusion
•Expanding rod

Nursing management
•Check the patient conscious level
•Check vital signs
•Check the patient intake and output
•Check the bowel pattern
•Encourage the patient intake of protein rich diet.
•Check the fluids therapy

Kyphosis

Definition
•General term used excessive backward convexity
of the spine
•Kyphosis is found in children

Causes
•Habitual bed poster
•Arthritis
•Rheumatism
•Lung affection
•Neuromuscular weakness
•Tuberculosis
•Spondylitis
•Congenital anomalies

Types of kyphosis
•Round kyphosis
•Angular kyphosis

Round kyphosis
•Gentle backpack curvature of
spinal Colum mostly seen
elderly and in post-menopausal
women who have osteoporosis

Angular kyphosis
•A sharp prominence of spinal
•Commonly seen in tuberculosis or
some vertebral fractures

Diagnostic evaluation
•The syndrome is diagnosed 10-15 years of age
•Complete x ray from shoulder to pelvis

Management
•Exercise

Medical management
•Non steroid
•Ibuprofen
•Naproxen

Lordosis
Lordosis is the inward curvature of the
portion

ETIOLOGY
❖Poor poster
❖Congenital problem of vertebrae
❖Back surgery
❖Hip problem
❖Rickets may leads to lordosis

Clinical manifestation
•Back pain
•Pain down the leg

Dignosticevaluation
•X-ray
•Bone scan
•Ct scan MRI scan
•Blood investigation

Management
•Brace
•Exercise

Spinal defects

Etiology
•Genetics
•maternally age above 35 years below 20 years environmental
•folic acid deficiency

Classification

Spina bifida
occulta
Spina bifida occulta is a
mild form of spina bifida
where there is a small
defect in the spinal
vertebrae, but the spinal
cord and nerves are not
exposed. It often causes no
symptoms and is usually
found incidentally during
imaging for other reasons

Spina bifida cystica
•Defect in the closure of
posterior vertebral arch
with proportion of spinal
cord and meninges through
the defect

meningocele
Meningocele is a
form of spina bifida
where a fluid-filled
sac containing the
spinal cord’s
protective coverings
protrudes through a
spinal defect. The
spinal cord stays in
place but can cause
complications.
Surgery is usually
needed to repair it.

Myelomeningocele
Myelomeningocele is
a severe form of
spina bifida where
both the spinal cord
and its protective
coverings protrude
through an opening
in the spine. It often
requires surgical
intervention and can
cause significant
neurological issues

Clinical features
Spina bifida occulta
•Dimple in the skin
•Growth of hair Over malformed vertebra
•Once child starting grow ,he may develop foot weekness
•Weakness’ of bowel sphincter
•Disturbance of bladder

meningocele
External cystic defect
•Weakness of leg
•Lack of spincture control

myelomeningocele
•Herniation mass
•Hydrocephalus
•Loss of motor control

Diagnostic evaluation
•Ultrasound
•Fetal MRI
•Amniocenteses
•CT scan

Management
➢Laminectomy –closer of the defect with in
24-48 hours of birth

Nursing management
•Prevention of infection
•Prevention of injury in the sac
•Prevention of skin breaks
•Prevention of urinary tract infection
•Providing adequate nutrition

Complications
•Frequently UTI
•Hydrocephalus
•Loss of bladder and bowel control
•Meningitis
•Paralysis of the leg

Prevention
•Genetics counselling
•Folic acid supplements
•It severely defect is detected in early pregnancy
therapeutic abortion may consider