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HIP DISLOCATION
PRESNTED BYMAHAVEER SWARNKARM.Sc. Pediatric Nursing
In a normal hip,the head of the femur and the acetabulum are in close contact,
When abnormality either in the shape of the head of the femur, the shape of the acetabulum, or the supporting structures around them. As a result, the acetabulum and femur are not in close contact result hip dis location
INTRODUCTION
DEFINITION: Dislocation of hip refers to a hip with no
contact between the articulating surfaces of the hip.
Developmental dysplasia of hip is a spectrum of disorders related to abnormal development of hip that may develop at any time during fetal life ,infancy or childhood
CLASSIFICATION OF DDHTypical DDH: - occurs in otherwise normal
individuals or those without define syndromes or genetic conditions. Its risk factor such as oligohydramnios, breech presentation
Teratologic hip dislocation: usually have identifiable causes and occur before birth. It involves a neuromuscular defect such as arthrogryposis or myelodysplasia. The teratologic forms usually occur in utero and are much less common.
THREE DEGREE OF DDH
•Acetabular dysplasia (or preluxation) – •Subluxation•dislocation
ACETABULAR DYSPLASIA (OR PRELUXATION) –
this is the mildest form of DDH, in which there is neither subluxation nor
dislocation. Due to delay in acetabular development result it
is oblique and shallow, and allowing the ball of the hip too much mobility
The femoral head remains in the acetabulum.
Subluxation –The femoral head remains in contact with the
acetabulum, but a stretched capsule and ligamentum teres cause the head of the femur to be partially displaced. Pressure on the cartilaginous roof inhibits ossification and produces a flattening of the socket.
Dislocation – Hip dislocation refers to the state of the hip
when the femoral head is completely laterally displaced from under the acetabulum (MP=100%).
ETIOLOGY/ RISK FACTOR:- Exact cause is unknown, but certain
factors may be rsponsible such as Family history. If there is a parent,
brother or sister with DDH, then this makes it five times more likely than normal for a child to have DDH.
Gender- female baby > male
baby
Left hip > right hip -Oligohydramnios -not able to
move within the uterus as much.First born baby-uterus is
tighter and less elastic than future pregnancies
Breech position-this can put the legs in a position which increases the risk of DDH.
CONGENITAL MALFORMATIONS
Congenital torticollis
Metatarsus adductus
Chromosomal abnormalities
Neuromuscular disorders
POSTNATAL POSITIONINGhips in extension and adduction (e.g. papoose.
parent carrying baby on their hip) increases risk
X
INCIDENCE:-Hip instability-10/1000 live
birthIn breech presentation- 30-
60 %Left hip – 60 %Girls – 60%
PATHOPHYSIOLOGY
CLINICAL MANIFESTATIONS:-Neonates: positive Ortolani or Barlow sign.
Infant:
shortening of the thigh(The Galeazzi sign)
Asymmetry of the gluteal or thigh folds and positioning of the hip,
Limitation of abduction in affected hip joint
Klisic test positive.
The walking child: Limp, a waddling gait, or leg
length differance.affected side appears shorter
than normal extremitytoe-walk on the affected side.Trendlenberg sign is positive
Positive Galeazzi sign
Excessive Lordosis
DIAGNOSTIC EVALUATION: A. HistoryB. Physical examination -
Barlow testOrtolani testPositive Galeazzi sign
(allis sign)Klisic testTrendelenburg's sign
C. UltrasonographyD. Radiography
MANAGEMENT0-6 MONTHS: Pavlik harness for 6 weeks By maintain Ortoloni positive hip, It prevents hip extension
and adduction and permits flexion and abduction.
Children 6 months to 2 years of age:
goals in the treatment of the late-diagnosed patient are to obtain and maintain reduction of the hip without damaging the femoral head.
Closed or open reduction(some time before C.R. use skin traction)
The reduction is maintained in plaster cast for 12 weeks
abduction orthotic device for 2 months
CHILDREN OLDER THAN 2 YEARS OF AGE: Open reduction shortening osseotomy to
avoid excessive pressure on the proximal femur with reduction
acetabular procedure to adequately cover the femoral head.
COMPLICATIONS:-Avascular necrosisReduced hip functionDegenerative hip changesJoint malformationInability to reduce dislocationResults in growth arrest and eventual joint
destructionPostoperative complications-wound infection.
NURSING MANAGEMENT:1. Acute pain or discomfort related to orthopaedic device or
cast as evidence by child is crying continuous2. Risk for impaired skin integrity related to pressure of the
cast on the skin as evidence by child having rashes and redness on the skin
3. Altered Physical mobility related to lengthy treatment or orthopaedic device as evidence by child is not able to move
4. Diversnal activity deficient related to hospitalization or immobility as evidence by child look boredom
5. impaired bowel pattern related to immobility as evidence by decrease frequency of passing stool and hypoactive bowel sound
6. Knowledge Deficit of family caregiver related to home care of child in the orthopaedic device or cast as evidence by parents asking many questions regarding home care
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