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SKELETAL DISORDERS
PRESENTED BY : MS KAJAL
MSC(N) 1ST
YR.
CLEFT LIP AND CLEFT
PALATE
Presented by: Ms Kajal
M.Sc.N1st
yr
INTRODUCTION
 It is a congenital malformation resulting from the failure
of fusion of maxillary process during intrauterine
development.
 This defect may occur alone or together.
Definition
 CLEFT LIP (CHEILOSCHISIS): It is result from failure of fusion of
maxillary process with nose elevation on frontal prominence.
TYPES :
1. Partial / incomplete
2. Complete
3. Bilateral
4. Unilateral
CLEFT PALATE ( PALATOSCHISIS)
Its result from failure to fusion
of the hard palate with each
other and with the soft palate,
cleft lip usually occurs with
cleft palate.
TYPES:
1. Complete
2. Incomplete.
Child health nursing SKELETAL DISORDERS.pptx
ETIOLOGY / Causes
 Medication taken by mother. ( Ex- antimalarial,
anticonvulsion).
 Exposure of virus or chemicals.
 Maternal anemia
 Alcohol abuse
 Maternal smoking
PHYSIOLOGY
COMPLICATIONS
 Feeding difficulties.
 Respiratory infections.
 Ear infections and hearing
loss.
 Speech problem.
 Aspirate pneumonia.
DIAGNOSTIC EVALUATION
 Maternal use and
counselling
 After birth 
physical
examination.
MANAGEMENT
 SURGICAL MANAGEMENT :
FOR CLEFT LIP:
1. TENNISON  Randal triangular flap ( Z- plasty).
2. MILLARDS rotational advancement technique .
FOR CLEFT PALATE: required multiple surgery.
Child health nursing SKELETAL DISORDERS.pptx
LOGANS BOW:
 As part of a cleft lip
management to
maintain
postoperative
apposition and to
avoid excessive strain
after cheiloplasty for
a cleft lip.
MEDICAL MANAGEMENT.
 Antibiotics and analgesic.
NURSING MANAGEMENT:
 Maintaining adequate nutrition.
 Increasing family coping.
 Reducing the parents anxiety and guilt regarding
the newborns physical defects,
 preparing parents for the future repair of the
cleft lip and palate
DEVELOPMENTAL DYSPLASIA OF HIP
 DEFINITION: Its id refers to a variety of condition in which
the head of femur and acetabulum cavity are improperly
aligned and the femur head lies outside the hip socket or
acetabulum cavity.
DEGREE OF DDH
1. ACETABULAR DYSPLASIA OR PRELUXATION: mild
dislocation of hip joint to the acetabulum cavity.
2. SUBLUXATION : incomplete dislocation of hip joint.
3. COMPLETE DISLOCATION AND LUXATION : Complete
dislocation of hip joint.
ETIOLOGY
 common in females than male.
 Genetic factors.
 Intrauterine position.
 Maternal factors.
CLINICAL EVALUATION
 Shorting of legs.
 Asymmetry of legs.
 Gait abnormalities.
DIAGNOSIS
 BARLOW TEST
 ORTOLANI
 USG AND X- RAYS.
MANAGEMENT:
 Pavlik harness
 Brace- Von Rosen splint.
 SUREGERY: Closed reduction under
general anesthesia.
NURSING MANAGEMENT
 Maintain correct position of hip.
 Maintain physical mobility
 Educate and support parents.
CLUBFOOT (VARUS EQUINUS)
DEFINITION: A common deformity in which the foot is twisted out of its normal shape
or position.
Involving the ankle is known as TALIPES derived TALUS means ankle and PES means
FOOT.
TYPES:
1.TALIPES VARUS : There is an inversion or bending inward of foot.
2.TALIPES VALGUS: There is an eversion or bending outward of foot.
3.TALIPES EQUINUS: There is planter flexion and toes is lower than heel.
4.TALIPES CALCANEOUS: There is dorsiflexion and toes is higher than heel.
Child health nursing SKELETAL DISORDERS.pptx
ETIOLOGY
 Monozygotic twins
 Genetic factors
 Unknown
 Teratogen
CLINICAL FEATURES
 Adduction of forefoot.
 Development of lower legs is also affected.
 Difficulty in walking and running
MANAGEMENT
NON-OPERATIVE MANAGEMENT :
 Casting and splinting.
OPERATIVE MANAGEMENT:
 SALVAGE PROCEDURE: Tarsectomy ( removing one or more of the bone of
the tarsus).
NURSING MANAGEMENT:
 Maintain skin integrity
 Family support
 Promote healthy healing.
FRACTURE
DEFINITION: A break in the continuity of bone caused by trauma ,
twisting as a result of muscles spasm or indirect impairment of function
and bone decalcification.
CAUSES:
 Increase mobility.
 Insatiable curiosity.
 Immature level of motor coordination.
 Lack of calcium
 Fall from height
 Road traffic accident
CLASSIFICATION OF FRACTURE
Based on communication :
1. SIMPLE/ CLOSED FRACTURE.
2. COMPOUND/ OPEN FRACTURE.
3. COMPLETE FRACTURE.
4. INCOMPLETE FRACTURE.
5. SIMPLE/ CLOSED FRACTURE: Skin over the fracture are remain intact.
6. COMPOUND /OPEN FRACTURE: Bone is exposed destroy the continuity of the
bone.
7. COMPLETE FRACTURE: bone is broken across entirely, destroying continuity
of bone.
8. INCOMPLETE FRACTURE: Does not broken completely and destroy continuity
of bone.
CLASSIFICATION ON THE BASIC OF PATTERN
 TRANSVERSE FRACTURE: Bone is fracture straight across.
 OBLIQUE FEACTURE: Break extends in an oblique
direction.
 SPIRAL FRACTURE: Spiral fracture in which bone has been
twisted apart.
 LINEAR FRACTURE: The bone is fracture longitudinally
CLINICAL FEATURE
5P
 PAIN
 PALLOR
 PULSE
 PARESTHESIA
 PARALYSIS
 OTHER; SWELLING, MUSCLES SPASM,BRUISING.
DIAGNOSIS:
 Complete history
 X ray or CT scan
 Lab diagnosis.
COMMON SITES OF FRACTURE IN CHILDREN
 Clavicle
 Humerus
 Radius and ulna
 Femur
PROCESS OF BONE HEALING
 STAGE I: HEMATOMA FORMATION
 STAGE II: FIBRO CARTILAGE FORMATION
 STAGE III: CALLUS FORMATION
 STAGE IV: OSSIFICATION
 STAGE V : CONSOLIDATION AND REMODELILING
MANAGEMENT
 FRACTURE REDUCTION
 CAST
 TRACTION
NURSING MANAGEMENT:
 Promote comfort
 Maintain skin integrity
 To reduce pain
 Provide adequate fluid and nutrient.
DISORDERS OF SPINAL CORD
Spine has three types of curve:
1.KYPHOSIS
2.LORDOSIS
3.SCOLIOSIS
1.KYPHOSIS: It is a curving of the spine that cause a bowing or rounding of the
back, which leads to a hunchback or slouching posture.
ETIOLOGY:
 Certain endocrine disorder.
 Connective tissue disorder
 Infection ( POTS SPINE).
 Poliomyelitis.
 Spina bifida
CLINICAL FEATURES:
 Difficulty in breathing.
 Fatigue.
 Mild back pain
 Round back appearance
 Tenderness and stiffness in the spine.
DIAGNOSIS:
 X- ray.
 PFT (pulmonary function test).
 MRI
MANAGEMENT:
 BRACE THERAPY
 PHYSIOTHERAPHY
LORDOSIS
 Inward curvature of a portion of the lumbar and cervical vertebral
column.
ETIOLOGY:
 Congenital
 Neuromuscular problems.
 Surgery of spine.
CLINICAL FEATURES:
 Prominence of the buttocks.
 Back pain
 Pain down the legs.
MANAGEMENT:
 Physiotheraphy
 Bracing stabilizing
 Orthoplast jacket
NURSING MANAGEMENT:
 Assist for theraphy
 Counselling
 Psychological support
SCOLIOSIS
 Lateral curve of the spine, generally a sideway curve
greater than 10 degree is considered scoliosis.
ETIOLOGY:
 Congenital.
 Neuromuscular disorders
 Idiopathic causes
CLINICAL FEATURES:
 Backpain
 Fatique
DIAGNOSIS
 X-rays
 Bone scans
 MRI , CT
MANAGEMENT:
 Exercise
 Physical theraphy
Child health nursing SKELETAL DISORDERS.pptx
Child health nursing SKELETAL DISORDERS.pptx

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CRITICAL THINKING AND NURSING JUDGEMENT.pptxCRITICAL THINKING AND NURSING JUDGEMENT.pptx
CRITICAL THINKING AND NURSING JUDGEMENT.pptx
PoojaSen20

Child health nursing SKELETAL DISORDERS.pptx

  • 1. SKELETAL DISORDERS PRESENTED BY : MS KAJAL MSC(N) 1ST YR.
  • 2. CLEFT LIP AND CLEFT PALATE Presented by: Ms Kajal M.Sc.N1st yr
  • 3. INTRODUCTION It is a congenital malformation resulting from the failure of fusion of maxillary process during intrauterine development. This defect may occur alone or together.
  • 4. Definition CLEFT LIP (CHEILOSCHISIS): It is result from failure of fusion of maxillary process with nose elevation on frontal prominence. TYPES : 1. Partial / incomplete 2. Complete 3. Bilateral 4. Unilateral
  • 5. CLEFT PALATE ( PALATOSCHISIS) Its result from failure to fusion of the hard palate with each other and with the soft palate, cleft lip usually occurs with cleft palate. TYPES: 1. Complete 2. Incomplete.
  • 7. ETIOLOGY / Causes Medication taken by mother. ( Ex- antimalarial, anticonvulsion). Exposure of virus or chemicals. Maternal anemia Alcohol abuse Maternal smoking
  • 9. COMPLICATIONS Feeding difficulties. Respiratory infections. Ear infections and hearing loss. Speech problem. Aspirate pneumonia.
  • 10. DIAGNOSTIC EVALUATION Maternal use and counselling After birth physical examination.
  • 11. MANAGEMENT SURGICAL MANAGEMENT : FOR CLEFT LIP: 1. TENNISON Randal triangular flap ( Z- plasty). 2. MILLARDS rotational advancement technique . FOR CLEFT PALATE: required multiple surgery.
  • 13. LOGANS BOW: As part of a cleft lip management to maintain postoperative apposition and to avoid excessive strain after cheiloplasty for a cleft lip.
  • 14. MEDICAL MANAGEMENT. Antibiotics and analgesic. NURSING MANAGEMENT: Maintaining adequate nutrition. Increasing family coping. Reducing the parents anxiety and guilt regarding the newborns physical defects, preparing parents for the future repair of the cleft lip and palate
  • 15. DEVELOPMENTAL DYSPLASIA OF HIP DEFINITION: Its id refers to a variety of condition in which the head of femur and acetabulum cavity are improperly aligned and the femur head lies outside the hip socket or acetabulum cavity. DEGREE OF DDH 1. ACETABULAR DYSPLASIA OR PRELUXATION: mild dislocation of hip joint to the acetabulum cavity. 2. SUBLUXATION : incomplete dislocation of hip joint. 3. COMPLETE DISLOCATION AND LUXATION : Complete dislocation of hip joint.
  • 16. ETIOLOGY common in females than male. Genetic factors. Intrauterine position. Maternal factors. CLINICAL EVALUATION Shorting of legs. Asymmetry of legs. Gait abnormalities.
  • 17. DIAGNOSIS BARLOW TEST ORTOLANI USG AND X- RAYS. MANAGEMENT: Pavlik harness Brace- Von Rosen splint. SUREGERY: Closed reduction under general anesthesia. NURSING MANAGEMENT Maintain correct position of hip. Maintain physical mobility Educate and support parents.
  • 18. CLUBFOOT (VARUS EQUINUS) DEFINITION: A common deformity in which the foot is twisted out of its normal shape or position. Involving the ankle is known as TALIPES derived TALUS means ankle and PES means FOOT. TYPES: 1.TALIPES VARUS : There is an inversion or bending inward of foot. 2.TALIPES VALGUS: There is an eversion or bending outward of foot. 3.TALIPES EQUINUS: There is planter flexion and toes is lower than heel. 4.TALIPES CALCANEOUS: There is dorsiflexion and toes is higher than heel.
  • 20. ETIOLOGY Monozygotic twins Genetic factors Unknown Teratogen CLINICAL FEATURES Adduction of forefoot. Development of lower legs is also affected. Difficulty in walking and running
  • 21. MANAGEMENT NON-OPERATIVE MANAGEMENT : Casting and splinting. OPERATIVE MANAGEMENT: SALVAGE PROCEDURE: Tarsectomy ( removing one or more of the bone of the tarsus). NURSING MANAGEMENT: Maintain skin integrity Family support Promote healthy healing.
  • 22. FRACTURE DEFINITION: A break in the continuity of bone caused by trauma , twisting as a result of muscles spasm or indirect impairment of function and bone decalcification. CAUSES: Increase mobility. Insatiable curiosity. Immature level of motor coordination. Lack of calcium Fall from height Road traffic accident
  • 23. CLASSIFICATION OF FRACTURE Based on communication : 1. SIMPLE/ CLOSED FRACTURE. 2. COMPOUND/ OPEN FRACTURE. 3. COMPLETE FRACTURE. 4. INCOMPLETE FRACTURE. 5. SIMPLE/ CLOSED FRACTURE: Skin over the fracture are remain intact. 6. COMPOUND /OPEN FRACTURE: Bone is exposed destroy the continuity of the bone. 7. COMPLETE FRACTURE: bone is broken across entirely, destroying continuity of bone. 8. INCOMPLETE FRACTURE: Does not broken completely and destroy continuity of bone.
  • 24. CLASSIFICATION ON THE BASIC OF PATTERN TRANSVERSE FRACTURE: Bone is fracture straight across. OBLIQUE FEACTURE: Break extends in an oblique direction. SPIRAL FRACTURE: Spiral fracture in which bone has been twisted apart. LINEAR FRACTURE: The bone is fracture longitudinally
  • 25. CLINICAL FEATURE 5P PAIN PALLOR PULSE PARESTHESIA PARALYSIS OTHER; SWELLING, MUSCLES SPASM,BRUISING. DIAGNOSIS: Complete history X ray or CT scan Lab diagnosis.
  • 26. COMMON SITES OF FRACTURE IN CHILDREN Clavicle Humerus Radius and ulna Femur PROCESS OF BONE HEALING STAGE I: HEMATOMA FORMATION STAGE II: FIBRO CARTILAGE FORMATION STAGE III: CALLUS FORMATION STAGE IV: OSSIFICATION STAGE V : CONSOLIDATION AND REMODELILING
  • 27. MANAGEMENT FRACTURE REDUCTION CAST TRACTION NURSING MANAGEMENT: Promote comfort Maintain skin integrity To reduce pain Provide adequate fluid and nutrient.
  • 28. DISORDERS OF SPINAL CORD Spine has three types of curve: 1.KYPHOSIS 2.LORDOSIS 3.SCOLIOSIS 1.KYPHOSIS: It is a curving of the spine that cause a bowing or rounding of the back, which leads to a hunchback or slouching posture. ETIOLOGY: Certain endocrine disorder. Connective tissue disorder Infection ( POTS SPINE). Poliomyelitis. Spina bifida
  • 29. CLINICAL FEATURES: Difficulty in breathing. Fatigue. Mild back pain Round back appearance Tenderness and stiffness in the spine. DIAGNOSIS: X- ray. PFT (pulmonary function test). MRI
  • 30. MANAGEMENT: BRACE THERAPY PHYSIOTHERAPHY
  • 31. LORDOSIS Inward curvature of a portion of the lumbar and cervical vertebral column. ETIOLOGY: Congenital Neuromuscular problems. Surgery of spine. CLINICAL FEATURES: Prominence of the buttocks. Back pain Pain down the legs.
  • 32. MANAGEMENT: Physiotheraphy Bracing stabilizing Orthoplast jacket NURSING MANAGEMENT: Assist for theraphy Counselling Psychological support
  • 33. SCOLIOSIS Lateral curve of the spine, generally a sideway curve greater than 10 degree is considered scoliosis. ETIOLOGY: Congenital. Neuromuscular disorders Idiopathic causes CLINICAL FEATURES: Backpain Fatique
  • 34. DIAGNOSIS X-rays Bone scans MRI , CT MANAGEMENT: Exercise Physical theraphy