Module 16: Advanced Extremities Flashcards

1
Q

Sprain Vs Fracture:
IAt preschool age- ligament is stronger than bone so if you see evidence of ligament injury look for a fracture.

A

Good to know

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Heel pain differential Diagnosis

A

There are numerous causes of heel pain
Most are due to:
-minor trauma
-repetative stress
-abnormal biomechanics
-subluxation

Important to rule out infection:
-consider osteomyelitis
-consider septic arthritis, nail puncture wound and ingrown toenail in this category.
-antalgic limp and pain, local tenderness and soft tissue swelling
-the calcaneus is the most common site
-there may be a history of puncture wound
-Xray may reveal bone changes, however bone destruction is not seen until 10-21 days
-

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is sever disease?

How do we treat it?

A

Sever’s disease is a painful condition of the heel that occurs in growing children. It happens when the tendon that attaches to the back of the heel (the Achilles tendon) pulls on the growth plate (the apophysis) of the bone of the heel (the calcaneus).

Treat it with?
Chiro management?
Find subluxation and correct it

Medical management:
RICE, NSAIDS, activity modification
-Achillies stretching
-Strengthening of the ankle dorsiflexors
-massage, ultrasound
-insertion od heel lift or heel cup- padding
-plantafascitis stretching.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Discuss a calcaneus stress fracture

A

Can occur after frequent running of strenuous activity
-generalised heel pain, diffuse tenderness and a limp
- a bone scan will be positive
-Xray showing a healing fracture
-medical management is with a below knee walking cast for 3-4 weeks.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What subluxation is in- toeing typically associated with as well as out- toeing?

A

In toeing is typically associated with an Anterior medial internal rotation tibia subluxation

Out toeing is typically associated with an Anterior lateral external rotation tibia subluxation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Fibula (proximal)
Can subluxate?
What other signs may you see?

A

Anterior Posterior Inferior
* Often asymptomatic
* May cause local pain
* Assessed similar to distal fibula
* May affect ankle, knee and hip joint
* WeakTFL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

List some generalised Swollen painful knee differential diagnosis?

List some localised swollen knee differential diagnosis?

A

Generalised:
1. Arthritis
2. Infection
3. RSD
4. Other rare conditions:
-Reactive synovitis due to femoral condyle lesion
-TB arthritis
meh

Localised:
1. Patella tendonitis
2. Osgood Schlager disease
4. Ligament sprain
5. Stress fractures of the patella
6. Bursitis
7. Direct Injury causing fracture can cause localised swelling
8. Tumours (benign and malignant)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Patellofemoral pain syndrome

What is it?
What are risk factors that may cause it?
What are common presenting symptoms?
What are differential diagnosis?

Whats your examination
Whats you Chiropractic management?

A

A condition in which the cartilage under the kneecap is damaged due to injury or overuse.
Patellofemoral Pain Syndrome (PFPS) is an umbrella term used for pain arising from the patellofemoral joint itself, or adjacent soft tissues. It is a chronic condition that tends to worsen with activities such as squatting, sitting, climbing stairs, and running.[1

Risk factors:
-Onset timing of vast muscles
-structural abnormalities
-muscle strength
-kinematic variables
-quadriceps angle

Common symptoms:
Pain + stiffness behind, underneath or around the patella. Achy but sharp at times.
-Usually gradual onset, but can be cause by trauma
-Stiffness or pain after prolonged sitting with knees flexed
-Swelling not usual
-popping or catching sensation may be described

DDX:
1. Intra-articular pathology
2. Plica syndrome
3. OSgood Schlager disease
4. Bursitis or tendinitis
5. neuroma
6. Other rare pathologies

Examination:
BLA

Chiro management:
-Identify vertebral subluxation -Especially pelvis and mid Lumbars
-Strengthen VMO
-Strengthen Core
-Increase stretches (eg lateral leg and hamstring)
-Modify activities:
-Avoid squatting
-change volume of activity
-change activity type (runners can swim or cycle)

Orthotics if excessive pronation

Patellofemoral (PF) pain is a common ailment of the lower extremity.
* A theorized cause for pain is patellar maltracking due to vasti muscle activation imbalance, represented as large vastus lateralis:vastus medialis (VL:VM) activation ratios.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Jake, aged 10, presents with right medial knee pain and limp.
* There is no fever or other illness.
* There has been no trauma.
* He is not a very active child–he is not involved in any jumping or running sports, and there has been no increase in recent physical exercise.
* Your knee examination is unremarkable.
* There is bilateral pronation. You adjust his talus, and his pelvis
and expect him to improve.
* 10dayslaterhereturnswiththesamesymptoms.Thepainhas increased in severity, and is now waking him from sleep. Pain medications are required throughout the day and night.
What do you suspect and why? What is your management?

A

Osteosacrcoma
Osteosarcoma is a type of bone cancer that begins in the cells that form bones. Osteosarcoma is most often found in the long bones — more often the legs, but sometimes the arms — but it can start in any bone.

-Often dismissed as growing pains
-becomes more constant and sever*
-Limp may develop
-Can be confused with injury or sprain
-May or may not be palpable mass, limited ROM, tenderness and warmth
-Most patients aren’t sick
-We must exercise some suspicion

Highest risk when Adolescent growth spurt (10-25 yrs)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Ewings Sarcoma
A cancer that most often occurs in and around the bones.
Ewing’s sarcoma typically occurs in children and young adults. It often begins in the legs, bones of the pelvis and arms.
Bone pain, localised swelling and tenderness are symptoms. In rare cases bone fractures may also be found.

Occurs ages 10-20

How does it present clinically?

A

Similar to Osteosacrcoma

  • similar to osteosarcoma.
  • Pain, swelling, limitation of motion, and tenderness, mild erythema.  may mimic a playground trauma.
     mild trauma may lead to ultimate diagnosis
     10-15% have pathologic fracture.
     many have limp
  • 61% have a tumour mass (one study)
  • 50% have pain for more than 6 months before diagnosis (another study)
  • With chest wall primaries, patients may present with respiratory distress.
  • With paraspinal or vertebral primary tumors may present cord compression.
  • not sick until late in disease.
  • if in the pelvis, symptoms and signs will be delayed.
  • typically present with gait abnormalities from root compression, bowel or bladder dysfunction, or back pain
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Maggie presents with John, age 4.
John is moving his right leg “differently” to the left He seems to be favoring the left leg.
He has been grumpier than usual.
The onset was today.
What are your first questions?

  1. What is the type of limp?
  2. What is the Diff. Dx?
  3. What is the Dx?
  4. What are the key points to take away?
A
  1. Has there been any trauma?
  2. Has there been an infection (URTI, digestive, other), or raised temperature/fever?

Maggie says that John is very active, and he is often climbing, falling, and bumping his body, but there has been no obvious fall. He has a cold last week, but there was no raise in temperature that she noticed?

Examination:
Gait: obvious decreased use of right leg.
Ankle/knee normal.
Hip – decreased internal rotation, normal otherwise
Temperature: 36.6, ear exam – normal, tongue – healthy colour, throat observation – normal, CSLN’s – normal.
Palpation of abdomen – no tenderness, no fecal impaction. Subluxation patterns – right pelvis subluxation, left C1/2 subluxation

Transient Synovitis
A non-specific, benign inflammation of the synovial lining (Do, 2000)
- most common age 3-6, causing an pain, stiffness and antalgic limp.
- It is a diagnosis of exclusion.
- Causes: often unknown, may include virus’s and trauma (Do, 2000)
History:
- acute onset of pain in anterior groin, anterior thigh, or knee. (non-traumatic anterior thigh or knee pain may be referred from the hip) - a history of URTI may be present, but systemic signs are absent.
Examination
- decrease in internal rotation of the hip may be seen.
- Use log roll test to help determine decrease in internal rotation (Leet 2000)
-occasional low grade fever (under 38)
Xray - NAD (except for the possibility of mild joint effusion indicated by medial joint space widening)

Prognosis and treatment: (Do, 2000)
- self limiting and lasts 3 to 10 days,
- treatment is usually given to alleviate symptoms.
- rest, avoidance of weight bearing, anti- inflammatory therapy
Med MX:
Chiro Mx:
Rest and NSAIDS
Monitor for vascular necrosis Adjusting as indicated.
Nutrition to improve immune function and to regulate inflammation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q
  • A 2 year old male presents with fever and limp for two days.
  • He complains of pain and points to his right lower extremity.
  • The pain has become increasingly worse, and he is unable to sleep at night. His appetite is decreased. There is a recent history of an upper respiratory tract infection about two weeks ago, but no recent trauma. The pain is not known to migrate.
  • There is no history of cough, headache, abdominal pain, vomiting, diarrhea, hematuria, or known tick exposure. Family history is negative for sickle cell disease and arthritis.
  • Exam: VS T 39.5, P 120, R 18, BP 100/50.
  • He is thin appearing and refuses to walk.
  • HEENT exam is normal. His neck has good range of motion without pain.
  • Heart, lungs, abdomen, and genital exams are normal
  • He is lying with his right lower extremity externally rotated, abducted, and motionless.
  • He has severe discomfort with minimal internal and external rotation of the right hip despite attempts to distract him. His other joints and neurological exam are normal. There are no notable skin lesions.
  • What is your management plan?
A

You referred this patient- straight to E.D. – well done!

  • Laboratory studies revealed increased WBC’s.
  • Hip radiographs show widening of the acetabular
    space on the right.
  • An orthopedic surgeon was consulted.
  • An arthrocentesis of the right hip is performed which shows increased white blood cells.
  • Treatment with vancomycin and ceftriaxone is initiated after cultures are obtained.
  • Within three days of treatment onset, his fever declines and he slowly begins to ambulate.
  • He is discharged with home care.
  • His parents bring him back for you to continue his Chiropractic Management

Please fill in the gaps:
1. What is the type of limp?
2. What is the Diff. Dx?
Septic arthritis (Septic arthritis is an infection in the joint (synovial) fluid and joint tissues. Different types of bacteria, viruses, and fungi can infect a joint. )

Osteomyelitis (Osteomyelitis is inflammation or swelling that occurs in the bone. It can result from an infection somewhere else in the body that has spread to the bone, or it can start in the bone — often as a result of an injury.)

  1. What is the Dx?
  2. What are the key points to take away?

Septic Arthritis – overview
- an infection within the joint space.
- most often in the hip, knee, then ankle in the 0-3 age group.
In young child – difficult, signs vague, need suspicion
In older child – sickness, pain and fever
- posture: external rotation (10 degrees) and flexion (30-60), degrees
- decreased ROM
- point tenderness (anterior of the joint in septic arthritis)
recognition as a likely diagnosis and referral.
Lab tests (white cell count, ESR and CRP) - may be negative in an infant Bone scans - may show increased uptake
Ultrasound and radiography - may show joint effusion.
Confirmed with aspiration of the joint.
Drainage of the joint and antibiotics.

Osteomyelitis- overview
- an infection within the bone itself
- most often long bones, affecting the femur most commonly.
- not common, occur more often in late childhood (2009, Houghton)
Exam:
- local pain, swelling, warmth, erythema and tenderness
- systemic manifestations such as fever or malaise.
- Be aware that systemic response may be absent in an infant and toddler. - be aware hip ROM may be normal if hip joint itself is not affected
(2009, Houghton) MX: Referral for medical tests.
As for septic arthritis
MRI may be needed to permit the diagnosis of osteomyelitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Joan presents with Matt, aged 8.
Matt has a shortened stance on the right, and some pain at the front of the groin. The pain radiates slightly down towards the knee.
This has been present for months, but seems to be getting worse.
It is worse in the evenings after a lot of exercise.
* The examination is unremarkable except for some mild loss of internal rotation and abduction.

Please fill in the gaps:
1. What is the type of limp?
2. What is the Diff. Dx?
3. What is the Dx?
4. What are the key points to take away?
5. What is your management?

A

Mx: You referred for an xray – Well Done!

Legg-Calve-Perthes Disease
Overview
- Idiopathic avascular necrosis of the femoral head.
- Cause is unknown - however vascular supply of the femoral head is often tenuous, and always vulnerable due to its passage intracapsular along the femoral neck.
- Most common age 2-18, Most common 4-8 years, mean at 6. (Tach).
- More common in boys.
Clinical: Presenting complaint:
 Antalgic limp, with mild pain on the anteromedial aspect of the thigh and knee.  Insidious onset over several weeks, agg exercise, rel rest.
 Sometimes begins after trauma.
Exam: Screening exam normal, except for involved leg.
* Most prominent sign is stiffness ie loss of internal rotation and abduction
Limp is antalgic
Trendelenburg Sign may be present Mild atrophy may be present.

DDX:
leg calve- Perthes
Synovitis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

12 year old boy, Jacob presents with pain at the front of the left knee. He mother has noticed him walking “funny” over the past three months. His pain was intermittent, but it is now constant.
Examination:
Observation: Jacob appears overweight. ROM: - decreased internal rotation of the hip
- on flexion of the hip, the thigh rotates externally. Temperature, EENT, CSLN’s - all normal
Spinal: Subluxation patterns at the pelvis, T6, and Occiput. Extremity: Left ankle subluxation.
What is your management?

  1. What is the type of limp?
  2. What is the Diff. Dx?
  3. What is the Dx?
  4. What are the key points to take away?
A
  • Displacement of upper femoral epiphysis on metaphysis
  • The most common adolescent hip disorder.
  • Common in obese boys, Peak age 13 (boys) and 11 (girls) - Bilateral in 25% of cases, most slips are gradual
  • Risks:
    1. Increased weight
    2. Delayed skeletal maturation
    3. Constitutional disorders (esp endocrine/metabolic)
    4. Recent growth spurt
    5. Retroversion
    6. Trauma
    Clinical:
  • Pain is often referred to the knee, causing antalgic limp,
     occurs in 25% (Hawaii case based paeds)
  • Pain referred to knee is a risk factor for delay in diagnosis (Kocher 1999)
  • Acute slips: occur suddenly with no ability to walk due to pain
  • Longer standing slips may cause:
    1. out-toeing gait
    2. abductor lurch
    3. limb atrophy

Examination:
* Loss of internal hip rotation, may notice with gait.
* Test flexion of hip – look for obligate external rotation of the hip, a sign of SFCE (Leet, 2000)
* Often overweight
Imaging:
Frog leg view of hip.
Loss of normal r/ship between epiphysis and neck.
Klein’s line (line drawn along neck of femur, should intersect epiphysis)(Houghton 2009)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Antalgic gait Differential Diagnosis

A

When pain is present there is usually a shortened stance, hip is most common site - search for tenderness, guarding, decreased motion
If diagnosis not certain, xray, then bone scan
Most common causes: trauma, infections and inflammations, neoplasia.

  1. Trauma:
    Sprains, strains, contusions, Fractures (Occult Toddler’s fracture, stress fractures, Subluxation, overuse syndromes
  2. Infections and inflammations
    Septic arthritis, Osteomyelitis, Diskitis, Transient synovitis
    Others: Cellulitis, Post infectious reactive arthritis.
    Other rheum: Juvenile rheumatoid arthritis, Systemic lupus erythematosus
  3. Neoplasia Benign - Unicameral bone cyst, Osteoid osteoma, Osteoblastoma.
    Malignant - Osteosarcoma, Ewing’s sarcoma, Leukemia/lymphoma, Spinal cord tumors
  4. Acquired: – LCPD, - SCFE - Osteochondritis dissecans (knee, talus)
    - Osteochondritis - Kohler’s, Frieberg Disease, Severs disease
  5. Congenital - Developmental dysplasia of the hip, Sickle cell, Congenitally short femur, Clubfoot
  6. Neurologic - Cerebral palsy, especially mild hemiparesis, hereditary sensory motor neuropathies
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Antalgic Limp Differential Diagnosis
Based on age

Age 1-4:
* Infectious causes much more likely : 1. Septic arthritis 2. Osteomyelitis
* Non-infectious causes-

A

Age 1-4:
* Infectious causes much more likely : 1. Septic arthritis 2. Osteomyelitis
* Non-infectious causes-
3. Transient synovitis
4. Trauma (including Subluxation)
5. DDH (Perthes may present early, by age 3-4)

Age 4-10
1. Trauma is more likely in this age group
2. Perthes
3. Infection and
4. Transient synovitis

Age 11-16
-Trauma common
2. Slipped capitol femoral epiphesis
3. Neoplasia

All ages: cerebral palsy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

George 5 years of age:

A five year old boy George presents with abnormal gait.
His parents have noticed that he is clumsy when he runs where he falls often.
He runs on his tiptoes, which has occurred since he started walking.
Otherwise, he has no other problems. He is doing well in kindergarten despite his language difficulty.
His teacher notes that he has trouble getting up from a sitting position at school.
His parents deny that he has chronic fevers, leg pain, weight loss, seizures, skin rash, urinary or bowel incontinence, or frequent colds.
His past medical history, developmental history, family history, and birth history are all normal.
What are your differentials?

Exam:
His vital signs are normal. His height, weight and head circumference are at the 50th percentile.
He is alert, active, shy,well-nourished and slim in no distress.
His skin shows no neurocutaneous stigmata. His head is normocephalic and atraumatic.
His pupils are equal, round, reactive to light. No nystagmus is evident. His fundi are normal with sharp disk margins. His TMs are clear. His throat is normal with a uvula midline.
His lungs, heart, and abdomen are normal.
His back shows no sacral dimples.
Neurologic exam:
A standard cranial nerve exam reveals no deficits.
His strength is +4/5 in his deltoids, knee flexors and extensors; +5/5 in his biceps and triceps.
His calves are visibly enlarged with a firm, rubbery feeling.
He gets up to a standing position using a Gowers’ maneuver. No dysdiadochokinesia. Negative Romberg sign. Sensation to light touch is intact. His reflexes are +2/4 in his biceps, triceps, brachioradialis, patella and ankle.
His plantar reflex is downgoing (negative Babinski sign). No clonus is elicited.
Normal abdominal reflexes are present.
His gait is best described as a wide based waddling. When running, he tends to run on his toes. He is unable to jump.
A C1 ASL subluxation and S2 P-R subluxation is present.

A

**If bilateral:
* Neurological (pathology)
Neuromuscular disorder Myopathies
DMD (or other MD) Cerebral palsy

Neurological (dysfunction): Upper cervical
* Residual clubfoot deformity
* Congenital tendo-achilles contracture.
* Idiopathic heel cord contracture (habitual)

If Unilateral: cannot be habitual
-Neuromuscular
-CP (hemiplegia)
-LLD eg DDH

DIAGNOSIS: Muscular Dystrophy (rubbery)
Management: send to GP for Blood test
Creatinine Kynase
Genetic testing

18
Q

Trendelenburg gait

A
  • is non-painful
  • due to weakness of the abductor muscles and hip instability, causing a lateral sway of the shoulders.
  • If bilateral it produces a waddling gait.
    Cause - usually due to hip dysplasia or a neuromuscular disorder.
    Exam - Trendelenburg test
  • Neurological exam and Gower’s test.
  1. Developmental
    - DDH
    - Hip examination
    - Refer for standing hip x-ray
    - Leg length discrepancy
  2. Neuromuscular
    - Cerebral palsy, Muscular dystrophy, Poliomyelitis - Subluxation
19
Q

DEVELOPMENTAL HIP DYSPLASIA

we need to be very aggressive in our surveillance of this.

What is a late diagnosis?
What are the 2 types?
If a dislocation is allowed to occur it may result in?

What are the risk factors?

A

Late diagnosis is >3 months -increases chances of surgical intervention.

What are the 2 types? Typical -in a neurologically normal infant. and Teratologic- in which is congenital ie an underlying neuromuscular disorder.

If dislocation is allowed to occur this results in:
1. Acetabular dysplasia and maldirection
2. Excessive femoral anteversion (torsion)
3. Hip muscle contractures

Risk factors:
-first born
-female gender
-high birth weight
-family history
-breech position

20
Q

List the tests used to screen for hip dysplasia and understand how they work:

A
  • Barlow test – No longer used!
  • Ortolanitest
    https://www.youtube.com/watch?v=4-9FsXgDRDI

https://www.youtube.com/watch?v=Qn-bWuvm0Pk

  • Hip abduction
  • Supine leg length
  • Galeazzi’s sign
  • Klisic test
  • Thomas test
  • Asymmetric thigh creases
21
Q

Hip screening after 10 weeks of age? what to look for?

A

Barlow and Ortolani is no longer useful
Prescence of hip contracture with Thomas test suggests dislocated hip- refer to a paediatrician/ ultrasound assessment

Look for:
-Uneven knee height
-Supine short leg
-Limitations of abduction of the hip

If present refer for ultrasound assessment of hips

22
Q

What are some signs an older child may have DDH

A

Complaints of:
-Delayed walking
-Limping
-Waddling
-Increased lumbar lordosis
-Toe walking
-Leg length discrepancy - may indicate an unrecognised DDH .

23
Q
  • A well 20 month old girl comes to see you having started to walk at 18 months of age and the parents are concerned that their daughter has a limp.
  • What tests/examination of her hips should you do?
  • How would you manage this case?
    a) Treat and monitor for resolution of limp
    b) Refer immediately for pelvic xray
    c) Xray only if hip examination tests are abnormal
  • Whattests/examinationofherhipsshouldyoudo?
A

Xray

  1. Supine straight leg length
  2. Allis/Galeazzi sign
  3. Hip abduction
  4. Thomas test
24
Q

Ultrasound or radiographs?
When to do each for DDH

A
  • Radiographs are utilized to screen for DDH after age 4 to 6 months, when ultrasonography becomes more challenging and less reliable because of ossification of the femoral heads.
  • The ossific nucleus of the femoral head does not appear until 3–7 mo of age, and it may be further delayed in DDH.
  • Hip stability as well as acetabular development may be assessed accurately in neonates and young infants by dynamic ultrasonography.
25
Q

Radiographic evaluation

What degrees is considered normal for a acetabular index – angle

A

The maximal normal measurement for the acetabular index is 30 degrees
up to age 4 months and 25 degrees up to age 2 years.

Know this!

26
Q

Radiographic findings of DDH

A

Radiographic findings of DDH include an
1. upward slanting sourcil (roof of the acetabulum)
2. small capital femoral epiphysis
3. superolateral subluxation of the femoral head

An 8-month-old girl demonstrates bilateral DDH, with the left hip worse than the right hip.
1. Note upward slanting sourcil bilaterally.
2. The right femoral head is concentrically located within its dysplastic
acetabula.
3. The left femoral head is superolaterally dislocated.

27
Q

An anteroposterior radiograph in a 1-year-old girl demonstrates

A

Radiographic findings of DDH include an
1. upward slanting sourcil (roof of the acetabulum)
2. small capital femoral epiphysis
3. superolateral subluxation of the femoral head

  1. left-sided developmental dysplasia of the hip
  2. upward slanting sourcil
  3. superolaterally subluxed femoral head
  4. delayed ossification of the left capital femoral epiphysis
28
Q

What is the medical management under 6 months of age of DDH?

A

The Pavlik harness is well established as the orthosis of choice for infants under 6 months of age with DDH superseding multiple preceding devices

  • The harness is often worn for 3 to 6 weeks following successful reduction; both clinical examination and ultrasonography are performed to evaluate the effectiveness of therapy.
  • Aim is to allow hip movement (“dynamic splintage”) within a non-pathological range
     This reduces the hip and corrects the acetabular dysplasia whilst also minimising the risk of
    femoral head avascular necrosis (AVN)
  • Use of the Pavlik harness is contraindicated when there is
     major muscle imbalance e.g. myelomeningocele (L2 to L4 functional level)  major joint stiffness
     ligamentous laxity e.g. Ehlers-Danlos syndrome
29
Q

What is the medical management over 6 months of age and under 2 years of DDH?

A
  • Children over 6 months but less than 2 years of age are often treated with a spica cast following closed or open reduction.
  • Recurrent dislocation may occur in up to 8% of patients and is more common in those with bilateral or right-sided DDH, decreased abduction in the spica cast, and large pelvic width

Birth
* When an unstable hip is recognized at birth, maintenance of the hip in the position of flexion and abduction (“human” position) for 1–2 mo is usually sufficient.

1-6 months
* During this age, a true dislocation may develop. As a consequence, treatment is directed toward reduction of the femoral head into the acetabulum. Pavlik harness is the treatment of choice in this age group.

6–18 Months.
* In the older infant, surgical closed reduction is the major method of treatment.

18 Months–8 Years.
* After 18 mo of age, the progressive deformities are so severe that open reduction followed by pelvic (innominate) osteotomy or femoral osteotomy, or both, are necessary to realign the hip.

30
Q

What is the most severe complication of DDH

How often should we as chiropractors check hips

A
  • The most important and severe complication of DDH is avascular necrosis of the CFE.
  • Infants should have their hips reassessed after a minimum of 4-6 weeks during the first year when being seen by a chiropractor. I would say every other visit?
31
Q

Management summary for the chiropractor

0-2 weeks

4-8 weeks

8-10 weeks

A

0-2 weeks of age
* Most clicking hips (positive Barlow) will resolve without treatment (799 out of 800) – only severe cases will need a harness.
* Positive Ortolani test indicates need for immediate orthopaedic referral

4-8 weeks of age
* Ortolani test is clinically useful during this age range and positive tests indicate need for ultrasound assessment

8-10 weeks plus
* Ortolani tests are no longer clinically useful, don’t look for clicks anymore, look for limited abduction of hip joint and uneven knees.

32
Q

Case study: 2 week old Charlie
* Two week old Charlie is brought to your office because he has positional preference and his mother is concerned that he may develop a funny shaped head.
* Is there any relationship between torticollis and DDH?
* When you examine Charlie’s hip joints as part of your routine physical examination what tests are you going to perform?
* What history information suggests Charlie is more likely to have DDH?

A

*
Hip assessment at 2 weeks of age.
Ortolani test
Thomas test
Allis test/Galezzi sign
Supine leg length

  • What would a positive Barlow test then positive Ortolani test indicate? +ve hip dysplasia
  • How would you manage this baby? Ultrasound to Confirm
  • What would a negative Barlow and positive Ortolani test indicate? +ve hip dysplasia?
  • How would you manage this baby? Ultrasound
  • What finding with Thomas test is clinically important at this age? Unilateral?
  • How would you manage a 2 week old baby with unilateral loss of hip
    flexor contracture?
  • When would you next plan to assess Charlie’s hip joints? every 4-6 weeks- send to GP for referral for Hip ultrasound
33
Q
  • 7 week old Isla has been brought to see you because she has difficulty breast feeding, doesn’t sleep well and is generally unsettled.
  • When you examine Isla’s hip joints as part of your routine physical examination what tests are you going to perform?
A

Hip assessment at 7 weeks of age.

Ortolani test
Thomas test
Allis test/Galezzi sign
Supine leg length

  • What would a positive Barlow test then positive Ortolani test indicate? +ve hip dysplasia
  • How would you manage this baby? refer for Xray? or ultrasound? know when to do each.
  • What would a negative Barlow and positive Ortolani test indicate?
  • How would you manage this baby?
  • What finding with Thomas test is clinically important at this age? Because after 6 weeks they should reduced and also its unilateral.
  • How would you manage a 7 week old baby with unilateral hip flexor contracture?
    Xray?
34
Q

A mother presents with her 6 week old baby, Indigo.
She has noticed that when Indigo is breathing there is difficulty, and one side of the abdomen bulges, but the other doesn’t.
What anatomy is involved? What might be the cause? What’s your diagnosis??

Further examination reveals:
* Position of right arm is in adduction, internal rotation and forearm pronation.
* Biceps reflex is absent.
* Moro is absent on affected side.
Now, what is your diagnosis?

A

What anatomy is involved? C3,4,5 keeps the diaphragm alive.

What might be the cause? What’s your diagnosis??
Birth injury ie forceps, assisted delivery

Diagnosis: Brachial plexus injury
Klumpkes palsy

35
Q

Signs:
 Infant loses arm abduction and external rotation and forearm supination.  Position of arm is in adduction, internal rotation and forearm pronation.  Biceps reflex is absent.
 Moro is absent on affected side.
 May have sensory impairment on the outer aspect of arm
* Power in the forearm and the hand grasp are preserved unless the lower part of the plexus is also injured - the presence of the hand grasp is a favourable prognostic sign.

What is it?

Prognosis of the 2 palsy’s?

A

Erbs palsy
* The injury is limited to the 5th and 6th cervical nerves.

If the phrenic nerve (3/4/5 cervical roots) is involved, alteration of breathing may occur.
 This leads to laboured breathing and a lack of abdomen bulge on the involved side.
 Ultrasound confirms an elevated diaphragm.
 Increased risk of pneumonia which may be the presenting issue.

C3,4,5 keeps the diaphragm alive!

Prognosis:
If recovery has not started by 3 months there is likely to be residual functional defecit.

36
Q

What is Panner’s disease (Osteochondrosis of the Capitellum)

A

-abnormal ossification or necrosis and degeneration of the distal humeral ossification centre.

-A common cause of lateral 1 sided elbow pain
in children younger than 10
-presents with lateral sided elbow pain without pinpoint tenderness (vague)

Xray shows: fragmentation of the entire humeral capitellum
-irregular areas of radadiolucencies with areas of sclerosis

37
Q

Osteochondritis of the capitellum of the humorous

A

Initial symptoms are typically pain, stiffness, and occasionally mechanical symptoms – similar to Panner disease (Tachdjian)

In addition:
 loose bodies in the joint
 stiffness, catching pain and possible deformity.  decreased ROM of elbow.
Diff Dx with Panner Disease:
 occurs in older children, greater level of symptoms  more likely to require surgical treatment.

Xray:
1. loose fragments, flattening of humeral capitelum and subchondral cysts (Steheli)
2. cannot be distinguished from Panner disease, other than by the skeletal age of the patient. (Tachdjian)

38
Q

Little leaguers elbow

A

Broad term for a group of disorders at the elbow in young active children (D0, 2003) Overuse injury due to excessive valgus stress. (Do, 2003)
Highest risk in pitchers or football quarterbacks who throw excessively.(Do, 2003) May also occur in racquet sports (Staheli)

Mechanisms: (Do, 2003)
 Excessive medial strain may cause microfractures at medial epicondylar epiphysis,
 excessive strain of the medial collateral ligament, or compression of the radiocapitellar column.

Clinical: (Do, 2003)
 Initial - swelling and pain at the medial epicondyle with throwing activities or on the valgus stress test.
 Pain relieved by rest
 Continued stress may lead to avulsion fracture of epiphysis.
Management
 Adjust as required (spine/extremities)  Rest
 Ice
 Stretching

 Sequence, (not timing) is important: CRITOE
* Capitellum,
* Radial Head
* Internal (medial) epicondyle
* Trochlea
* Olecranon
* External (lateral) epicondyle

39
Q

Supracondylar fracture

A
  • Distal humeral metaphyseal region proximal to the elbow)
  • Most common elbow fracture
  • Commonly ages 3-10
    FOOSH injury
     arm held in pronation and resists flexion
     neurovascular injury common in severe displacement.  flow through brachial artery may be affected
    – treat as a medical emergency.

 Compartment syndrome can develop in 24 hours
Medical emergency

40
Q

Scaphoid Fractures
Predominately found in boys aged 12 +
-MRI is best sensitivity (99-100%), Radiographs only detect 54%

So what would you do in regards to imaging if you suspected a child had a scaphoid fracture?

A

Send for Xray is a PA, lateral, pronated oblique, ulnar deviated PA

MRI is the optimal second test assessing a possible scaphoid fracture after a negative radiograph

If the fracture is seen on an Xray they should be sent for a CT for further assessment of the fracture and for surgical planning.

FINITO