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assisgnment.pptx
OUTLINE
 Introduction
 Definition and Types
 Epidemiology
 Etiology and Risk Factors
 Signs and Symptoms
 Diagnosis
 Treatment
 Complications and Prognosis
 Physiotherapy Treatment of Juvenile Arthritis
 Conclusion
Juvenile arthritis
 is a chronic autoimmune condition that affects children and
adolescents under the age of 16.
 It is characterized by joint inflammation, pain, and stiffness, which
can lead to long-term disability if left untreated.
 JIA ranges in severity. It affects the joints, as well as other structures
such as the eyes, skin, and organs.
 Juvenile arthritis is a broad term that encompasses several subtypes
of arthritis that occur in children.
 The most common form is called juvenile idiopathic arthritis (JIA),
previously known as juvenile rheumatoid arthritis (JRA).
Epidemiology
 JIA is the most common chronic heterogenous rheumatologic
condition in children.
 It is estimated that around 3 million children and young adults have
JIA. The global prevalence is believed to range from 3.8 to
400/100,000; the incidence is estimated to be 1.6 to 23/100,000.
 Females are at higher risk of JIA than males.
 The oligoarticular subtype is more common.
5
ETIOLOGY
 The exact cause of juvenile arthritis is unknown.
 a combination of
 genetic, a role, as certain genes have been associated with an
increased risk of developing the disease.
environmental,
immunological factors, dysregulation of the immune system,
specifically autoimmunity.
RISK FACTORS
 A family history of autoimmune diseases
 Genetic
 Exposure to infections or other environmental triggers
 Females
TYPES
1. Oligoarticular JIA:
Involves fewer than five joints in the first six months of disease
onset.
 It often affects the large joints, such as knees and ankles
is more common in girls.
2. Polyarticular JIA:
Affects five or more joints in the first six months of disease onset.
 can be further divided into rheumatoid factor (RF)-positive or RF-
negative subtypes based on the presence of a specific antibody.
3. Systemic JIA:
Involves inflammation in one or more joints, along with systemic
symptoms such as high fever, rash, and generalized enlargement of
lymph nodes.
4. Enthesitis-related arthritis:
Inflammation occurs at the sites where tendons and ligaments
attach to bones (entheses).
It is often associated with enthesitis, arthritis, and enthesopathy.
5. Psoriatic arthritis:
Presents with both joint inflammation and skin manifestations,
such as psoriasis or nail changes.
6. Other rare subtypes:
These include juvenile lupus, juvenile dermatomyositis, and
juvenile spondyloarthropathies
assisgnment.pptx
SIGN AND SYMPTOMS
 The signs and symptoms of juvenile arthritis vary depending on the
subtype and the individual child. Common features include:
 Joint pain: Persistent pain in one or more joints, which may be
worse in the morning or after periods of rest.
 Joint swelling: Affected joints may appear swollen, warm to the
touch, and tender.
 Joint stiffness: Stiffness and limited range of motion in the
affected joints, especially upon waking up in the morning or after
periods of inactivity.
 Fatigue: Generalized tiredness and lack of energy, which can
affect a child's daily activities.
 Systemic symptoms: Systemic JIA may present with high spiking
fevers, rash, and enlarged lymph nodes.
 Eye inflammation: Certain subtypes of juvenile arthritis, such as
oligoarticular JIA, can be associated with uveitis, an inflammation
of the eye.
 It is important to note that the symptoms may fluctuate in severity,
with periods of flare-ups and remission.
 The diagnosis is typically based on a combination of clinical findings,
medical history, physical examination, and laboratory tests.
 Laboratory tests commonly used in the diagnostic process include:
 Blood tests: such as CBC, ESR, CRP, RF, and ANA testing. These
tests help assess the presence of inflammation and autoimmune
markers.
 Joint fluid analysis:
 Imaging studies: X-rays and other imaging modalities, such as US
and MRI.
Eye examination
TREATMENT
 The management of juvenile arthritis aims to control symptoms,
prevent joint damage, and improve the child's quality of life.
 Treatment plans are individualized based on the subtype, disease
activity, and the child's specific needs.
 A multidisciplinary approach involving rheumatologists, physical
therapists, occupational therapists, and other healthcare professionals
is often necessary.
 Treatment options for juvenile arthritis include:
 Nonsteroidal anti-inflammatory drugs (NSAIDs):
 Disease-modifying antirheumatic drugs (DMARDs):
 Biologic agents:
 Corticosteroids
COMPLICATION
 Without appropriate treatment, juvenile arthritis can lead to significant
complications and long-term disability such as
 Joint damage,
 deformities, and
 growth disturbances are possible outcomes, particularly if the
disease remains uncontrolled.
 Children with systemic JIA may experience complications related to
systemic inflammation, such as pericarditis or macrophage activation
syndrome.
PROGNOSIS
 The prognosis for juvenile arthritis varies depending on the subtype,
disease severity, and the child's response to treatment.
 Early diagnosis and prompt initiation of appropriate therapy are
associated with better outcomes.
 Regular follow-up with a rheumatologist is essential to monitor
disease activity, adjust treatment as needed, and address any
emerging complications.
PHYSIOTHERAPY ASSESSMENT
 Assessment include a thorough examination of
 joint range of motion,
 muscle strength,
 posture, and
 functional abilities.
 It helps the physiotherapist develop an individualized treatment plan
tailored to the child's specific needs
 Aim of physiotherapy management
 to reduce the pain
 to improve joint mobility and ROM
 to improve the muscle strength and balance
 to improve posture and alignment
 to achieve functional independence
 to promotes physical fitness
 patient education
 Physiotherapy management include
 ROM exercises
 Strengthening Exercises
 Heat therapy
 Cold therapy
 Transcutaneous electrical nerve stimulation (TENS)
 Ultrasound therapy
 Assistive Devices
 Functional Training
 Education and Home Exercise Program

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assisgnment.pptx

  • 2. OUTLINE Introduction Definition and Types Epidemiology Etiology and Risk Factors Signs and Symptoms Diagnosis Treatment Complications and Prognosis Physiotherapy Treatment of Juvenile Arthritis Conclusion
  • 3. Juvenile arthritis is a chronic autoimmune condition that affects children and adolescents under the age of 16. It is characterized by joint inflammation, pain, and stiffness, which can lead to long-term disability if left untreated. JIA ranges in severity. It affects the joints, as well as other structures such as the eyes, skin, and organs.
  • 4. Juvenile arthritis is a broad term that encompasses several subtypes of arthritis that occur in children. The most common form is called juvenile idiopathic arthritis (JIA), previously known as juvenile rheumatoid arthritis (JRA).
  • 5. Epidemiology JIA is the most common chronic heterogenous rheumatologic condition in children. It is estimated that around 3 million children and young adults have JIA. The global prevalence is believed to range from 3.8 to 400/100,000; the incidence is estimated to be 1.6 to 23/100,000. Females are at higher risk of JIA than males. The oligoarticular subtype is more common. 5
  • 6. ETIOLOGY The exact cause of juvenile arthritis is unknown. a combination of genetic, a role, as certain genes have been associated with an increased risk of developing the disease. environmental, immunological factors, dysregulation of the immune system, specifically autoimmunity.
  • 7. RISK FACTORS A family history of autoimmune diseases Genetic Exposure to infections or other environmental triggers Females
  • 8. TYPES 1. Oligoarticular JIA: Involves fewer than five joints in the first six months of disease onset. It often affects the large joints, such as knees and ankles is more common in girls. 2. Polyarticular JIA: Affects five or more joints in the first six months of disease onset. can be further divided into rheumatoid factor (RF)-positive or RF- negative subtypes based on the presence of a specific antibody.
  • 9. 3. Systemic JIA: Involves inflammation in one or more joints, along with systemic symptoms such as high fever, rash, and generalized enlargement of lymph nodes. 4. Enthesitis-related arthritis: Inflammation occurs at the sites where tendons and ligaments attach to bones (entheses). It is often associated with enthesitis, arthritis, and enthesopathy.
  • 10. 5. Psoriatic arthritis: Presents with both joint inflammation and skin manifestations, such as psoriasis or nail changes. 6. Other rare subtypes: These include juvenile lupus, juvenile dermatomyositis, and juvenile spondyloarthropathies
  • 12. SIGN AND SYMPTOMS The signs and symptoms of juvenile arthritis vary depending on the subtype and the individual child. Common features include: Joint pain: Persistent pain in one or more joints, which may be worse in the morning or after periods of rest. Joint swelling: Affected joints may appear swollen, warm to the touch, and tender. Joint stiffness: Stiffness and limited range of motion in the affected joints, especially upon waking up in the morning or after periods of inactivity.
  • 13. Fatigue: Generalized tiredness and lack of energy, which can affect a child's daily activities. Systemic symptoms: Systemic JIA may present with high spiking fevers, rash, and enlarged lymph nodes. Eye inflammation: Certain subtypes of juvenile arthritis, such as oligoarticular JIA, can be associated with uveitis, an inflammation of the eye. It is important to note that the symptoms may fluctuate in severity, with periods of flare-ups and remission.
  • 14. The diagnosis is typically based on a combination of clinical findings, medical history, physical examination, and laboratory tests. Laboratory tests commonly used in the diagnostic process include: Blood tests: such as CBC, ESR, CRP, RF, and ANA testing. These tests help assess the presence of inflammation and autoimmune markers. Joint fluid analysis: Imaging studies: X-rays and other imaging modalities, such as US and MRI. Eye examination
  • 15. TREATMENT The management of juvenile arthritis aims to control symptoms, prevent joint damage, and improve the child's quality of life. Treatment plans are individualized based on the subtype, disease activity, and the child's specific needs. A multidisciplinary approach involving rheumatologists, physical therapists, occupational therapists, and other healthcare professionals is often necessary.
  • 16. Treatment options for juvenile arthritis include: Nonsteroidal anti-inflammatory drugs (NSAIDs): Disease-modifying antirheumatic drugs (DMARDs): Biologic agents: Corticosteroids
  • 17. COMPLICATION Without appropriate treatment, juvenile arthritis can lead to significant complications and long-term disability such as Joint damage, deformities, and growth disturbances are possible outcomes, particularly if the disease remains uncontrolled. Children with systemic JIA may experience complications related to systemic inflammation, such as pericarditis or macrophage activation syndrome.
  • 18. PROGNOSIS The prognosis for juvenile arthritis varies depending on the subtype, disease severity, and the child's response to treatment. Early diagnosis and prompt initiation of appropriate therapy are associated with better outcomes. Regular follow-up with a rheumatologist is essential to monitor disease activity, adjust treatment as needed, and address any emerging complications.
  • 19. PHYSIOTHERAPY ASSESSMENT Assessment include a thorough examination of joint range of motion, muscle strength, posture, and functional abilities. It helps the physiotherapist develop an individualized treatment plan tailored to the child's specific needs
  • 20. Aim of physiotherapy management to reduce the pain to improve joint mobility and ROM to improve the muscle strength and balance to improve posture and alignment to achieve functional independence to promotes physical fitness patient education
  • 21. Physiotherapy management include ROM exercises Strengthening Exercises Heat therapy Cold therapy Transcutaneous electrical nerve stimulation (TENS)
  • 22. Ultrasound therapy Assistive Devices Functional Training Education and Home Exercise Program