Professional Documents
Culture Documents
Osteomyelitis
1. Clinical Picture
a. General Toxic features as fever pallor, sweating, nausea and vomiting and tackycardia.
b. Local - Severe pain (of sudden onset). -Swelling. – Pseudoparalysis.
c. redness & edema over the skin.
d. Localized tenderness over the bone (The earliest sign).
e. Sympathetic effusion of the adjacent joint.
2. Pathogenesis
3. Diagnosis
a. Laboratory:
i. CBC: ↑TLC & ↑ ESR & CRP.
ii. Blood culture (at time of fever).
iii. The most certain is to aspirate pus from metaphysis + C&S.
b. Radiographs:
• Soft tissue swelling.
• Hyperemia, demineralization of the bone.
• Lysis (when > 40% resorbed)
• Periosteal reaction
• Sclerosis (late)
c. X- Ray .
• 1st 2 weeks → -ve . End of 2nd wk → faint extra-cortical outline (periosteal new
bone formation) .
• After 3 weeks → chronic sequestrum.
d. U/S → Subperiosteal abcess + Joint effusion + U/S guided aspiratlon .
e. MRI.
• MRI T1 Dark
• T2 Bright/Mixed
f. CT scan (when M.R.l. is contraindicated )
a. General:
• Hospitalization, bed rest & immobilization (until inflammation subsides).
b. Medical :
• Analgesic. Antibiotics. Antipyretics + fluids.
• Early administration of high dose empiric broad spectrum antibiotics
(flucloxacillin, augmentin or vancomycin) + gentamycin for gram -ve
organisms then specific antibiotic according to culture and sensitivity.
• Parenterally for 1-2 wks then Oral for 4-6 weeks (minimum duration 6 weeks)
c.Surgical (Indications)
• Obvious collection of pus which must be drained.
• lf no improvement on antibiotics within 48 hours (from onset of fever) (we have
to interfere before chronicity = subperiosteal elevation)
• lf the patient is first seen after 48 hours.
• Procedure: Drainage of subperiosteal abscess + drill holes in the cortex (6-8
holes).
• Postoperative antibiotics for 6 weeks
5. Complications
• General:
o Toxemia.
o Septicemia & pyemia (if immunocompromised)
• Local :
o Chronic osteomyelitis
o Spread: suppurative arthritis (only if metaphysis is intra-capsular e.g. Hip joint).
o Disturbed bone growth (deformity and/or shortening).
o Pathological fractures
Osteonecrosis
1. Clinical picture
• Limp
• Antalgic gait
• Restricted ROM
• Tenderness around bone
• Joint deformity
• Muscle wasting
• Crescent Sign
• Snowcapping
• Areas of lucency
• Flattening of joint surface
2. Pathophysiology
• Vascular occlusion
• Altered lipid metabolism
• Intravascular coagulation
• Healing process
• Primary cell death
• Mechanical stress
3. Diagnosis
• X-ray
o May be the first test the doctor recommends.
o X-rays are not sensitive enough to detect bone changes in the early stages of the
disease.
o In later stages of osteonecrosis x rays may show bone damage, and once the
diagnosis is made they are often used to monitor disease progression.
•MRI
o Is the most sensitive method for diagnosing osteonecrosis in the early stages.
o Detects chemical changes in the bone marrow.
o May show diseased areas that are not yet causing any symptoms
• Bone Scan
• CT
• Biopsy
4. Management
• Offloading affected joints with use of crutches
• Immobilization
• Analgesia
• Bisphosphonates to delay femoral head collapse
• Stains in patients on high dose corticosteroids — reduced lipid deposition
• CORE DECOMPRESSION
o Indicated in stages I and II
o 8 — 10 mm anterolateral core of bone
o Filled with bone graft
o Decompresses medullary cavity, reduces pain
• REALIGNMENT OSTEOTOMY
o Indicated in stages III & IV
o Used to relocate necrotic area from weight bearing portion of femoral head
o Angular osteotomies more common • Multiple techniques for holding the
fixation
• ARTHROPLASTY
o Indicated in stage IV onwards
o Main aim is pain reduction
o Young patients will need revision
o Higher failure rates than in OA
o Hemi arthroplasty an option
Septic arthritis
1. Clinical picture
• Symptoms:
o Pain (night and rest pain are characteristic): severe , sudden, throbbing.
o Swelling at the joint area.
o lnability to move the joint.
• Signs :
o Redness, swelling and discharging sinus (if neglected).
o Deformity (late)
o Hotness and tenderness on palpation.
o Complete loss of all movements (active & passive)
2. Pathophysiology
3. Diagnosis
• Laboratory:
o ↑TLC. ↑ ESR and CRP +ve.
o Joint aspiration +/- U/S guidance : as diagnostic and therapeutic.
• U/S : accurate for detection of effusion
• Radiology:
o Early: soft tissue shadow.
o Later: decreased joint space then complete obliteration bony ankylosis
4. Management
• General
o Bed rest + immobilization.
o Antibiotics
o Analgesics + fluids.
o Antipyretics.
• Specific: it is a surgical emergency
o Washout of the infected joint:
o ln knee, ankle and shoulder joints → arthroscopic washout or open arthrotomy
+ washout .
o ln hip joint sepsis → only open arthrotomy.
5. Complications
• Bone destruction.
• Pathological dislocation.
• Growth disturbance.
• Bony ankylosis.
• Toxemia, septicemia & pyemia.
Club foot
1. Clinical picture
• Heel is small and high.
• Deep creases appear posteriorly and medially.
• Abnormal thin calf.
• One or both feet are rotated inwards and downwards
• The soles of the feet face each other.
2. Pathology
• Deformity:
o Planter flexion of the foot at the ankle.
o inversion of the foot.
o Adduction of the forefoot
• Shortening of all ligaments on the medial side of the foot.
3. Diagnosis
• Presence of specific deformity (triad) at birth which cannot be corrected passively & consists
of:
o inversion of the foot → subtalar joint.
o Adduction of forefoot → tarso metatarsal joint.
o Equines (planter flexion) → ankle joint.
• Complete neurological examination must be done to exclude paralytic and spastic types of
deformity.
• IMAGING X-ray
o to assess progress of treatment:
o AP View:
✓ Talo-calcaneal angle (Kite’s angle) is decreased.
normal 20-40 degree, clubfoot angle almost parallel
✓ A line projecting the long axis of talus forward passes laterally.
• Lateral View:
➢ Tibio-calcaneal (Turco view)angle is obtuse
➢ Normal angle : 40 degree If less 20 degree
➢ shows deformity
4. Management
• Conservative:
✓ Correction of the deformity: -
✓ Starting from distal to proximal (begin in the 1st wk. of life)
• Maintenance of the correction by:-
✓ Adhesive strapping (in the 1st 2-3 wks).
✓ Plaster of Paris.
• To avoid recurrence of deformity use of a Denis Browne splint at night time is
recommended until age2 years.
• Splinting is not required during day time
DDH
1. Clinical picture
a. Neonates
• mother observes asymmetry, clicking hip or difficult in applying the napkins (
due to limited abduction).
• Ortlani test
o The examiner's thumb is placed over the patient's inner thigh.
o The index finger is gently placed over the greater trochanter.
o The hip is abducted, and gentle pressure is placed over the greater
trochanter.
o ln the presence of DDH, a clunk, similar to turning a light switch on or
off, is felt when the hip is reduced.
• Barlow test
o Performed with the hips in an adducted position, in which slight gentle
posterior pressure is applied to the hips.
o A clunk should be felt as the hip subluxes out of the acetabulum.
b. Infants and child
• Unilateral cases
o Asymetrical gluteal creases.
o Present with a limb (the affected leg tends to be short and externally
rotated Trendelenburg gait (after walking).
• Bilateral cases:
o Broad perineum and waddling gate.
c. Adolescent
• discomfort after exercise (X-ray may show dysplasia and possibly subluxation)
d. Adult
• pain is the usual complain as a result of degenerative osteoarthritis (X-ray may
show dysplasia and degenerative changes.)
• Trendelenburg gait: is an abnormal gait (as with walking) caused by weakness of
the abductor muscles of the lower limb, gluteus medius and gluteus minimus.
• Wadling gate: is a form of gait abnormality.
• The "waddling" is due to the weakness of the proximal muscles of the pelvic
girdle. The patient uses circumduction to compensate for gluteal weakness.
2. Pathology
• Acetabulum
o Shallow (looks like a saucer instead of a cup)
o The roof slopes too steeply
o Anteverted
• Femoral head
o Dislocated(post. and sup.)
o Delayed ossific center
• Femoral neck : Unduly anteverted
• Capsule
o Stretched
o ± hourglass by iliopsoas
• Limbus
o Superiorly the acetabular labrum and its capsular edge may be pushed into the
socket by the dislocated femoral head .
o This fibrocartilagenous structure may obstruct closed reduction.
• Lig. Teres
o Elongated
o Hypertrophied
3. Diagnosis
• Ultrasound:
o It has been of significant benefit in the assessment and treatment of children
with hip dysplasia. Used to control and monitor hip stability and as screening
test between 4-6 weeks particularly in at risk patient.
• x-ray:
o Had little value before the age of 1 year old as the head of femur is
cartilagenous till this age.
o At the age of 1 yr or older:
o Shallow acetabulum.
o Ossification center of the head is displaced upwards & outwards.
4. Management
• Neonate
o Most of neonates with instability sign at birth, spontaneously
corrected, so it is better to wait till 3 weeks before intervention.
o After 3 weeks → reduction & splinting in abduction.
o lf U/S confirm the diagnosis of CHD → VonRosen splint for 3-6 months
is a must.
• At the age of 6 months to 6 years:
o Reduction in plaster cast with maintained abduction for 6 wks.
o After 6 wks → replace the cast with splint that prevent adduction but
allow movement.
o Follow up by serial X-ray films.
a. lf failed reduction → surgery is performed either:
b. Open reduction followed by fixation by plaster cast Or
c. If the acetabulum is markedly shallow, it can be deepened by a
concomitatnt pelvic osteotomy
• After the age of 6 years:
o Unilateral dislocation → operative reduction + corrective osteotomy.
o Bilateral dislocation: -
o Painless not noticed waddling → better to avoid operative reduction.
o lf there is noticed waddling → operative reduction + corrective
osteotomy.
Osteosarcoma
1. Clinical picture
• Symptoms .
o General –
o Local: -
o Swelling.
➢ Pathological fracture is uncommon because the patient is bed ridden due to pain).
• Signs .
o Local:
✓ lnspection: -
✓ Swelling.
✓ Local tenderness.
2. Pathology
Site :
➢ Metaphysis of long bone (rule of 80).
Cell of Origin:
➢ Osteoblasts → osteogenic.
Macroscopic picture:
➢ Osteosarcoma destroys and replaces the normal bone.
➢ The tumor rapidly infiltrates towards the bone marrow early, but it respects the epiphyseal
cartilage and hence does not invade the epiphysis or the joint.
3. Diagnosis
4. Treatment
1. First AID
• General → lf poly-traumatized patient.
o Primary Survey
✓ This includes a pre-hospital phase and a hospital phase.
ABCDE
A - Airway:
Assessment: if the patient is able to speak freely, his airway is patent.
Action:
1. Clear airway.
2. Protect airway: oropharyngeal airway, tracheal intubation or
cricothyroidotomy.
3. Cervical spine control.
B- Breathing:
Assessment: inspection, palpation, percussion and auscultation
Action: e.g. Needle decompression for tension pneumothorax
C- Circulation :
Assessment: general examination for hemorrhagic, cardiogenic or neurogenic
shock.
Action:
1. Control bleeding.
2. Restore the lost blood.
D- Disability:
Assessment:
AVPU evaluation (alert, vocal, painful stimulation
unresponsive), followed by Glasgow coma scale in the secondary survey.
E- Exposure:
✓ insert Foley's catheter and nasogastric tube
✓ Radiological assessment .
✓ AMPLE history (may be done in the secondary survey).
o Secondary Survey
After establishment of the general condition of patient, 2ry survey has to be
done.
II. Fixation
III. Rehabilitation