Common Pediatric Hip Problem Prepared by Pediatric Orthopedic gruop Surgeons KKUH.

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Common Pediatric Hip Problem Prepared by Pediatric Orthopedic gruop Surgeons KKUH

Transcript of Common Pediatric Hip Problem Prepared by Pediatric Orthopedic gruop Surgeons KKUH.

Page 1: Common Pediatric Hip Problem Prepared by Pediatric Orthopedic gruop Surgeons KKUH.

Common Pediatric Hip Problem

Prepared by

Pediatric Orthopedic gruop SurgeonsKKUH

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Common Pediatric Hip problems

DDHSCFEPerthe’s

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DDH

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Nomenclature

• CDH : Congenital Dislocation of the Hip• DDH : Developmental Dysplasia of the Hip

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Pediatric Hips Dislocation

• Types:– Idiopathic isolated pathology– Teratologic:

• Neurologic as: patient with C.P or MMC• Muscular as: Arthrogryposis• Syndromatic as: Larsen syndrome

– Miscellaneous:• Complication to hip septic arthritis• Traumatic

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Pediatric Hips Dislocation

• Note delivery in its self (OBGY Dr.) does not dislocate a hip

• DDH occurs in the 3ed trimester • Teratologic usually in the 1st trimester

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Normal pelvis

adult child

CHILDADULT

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DDH

Normal hip Dislocated hip

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Patterns of disease

1) Dislocated 2) Dislocatable3) Sublaxated 4) Acetabular dysplasia

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Causes (multi factorial)

• Hormonal – Relaxin, oxytocin

• Familial – Lig.laxity diseases

• Genetics– F 4-6x > M– Twins 40%

• Mechanical – Pre natal– Post natal

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Mechanical Causes

• Pre natal– Breach , oligohydrominus , primigravida , twins (torticollis , metatarsus adductus )

• Post natal– Swaddling , strapping

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Infants at Risk• Positive family history: 10X• A baby girl: 4-6 X• Breach presentation: 5-10 X• Torticollis: CDH in 10-20% of cases• Foot deformities:

– Calcaneo-valgus and metatarsus adductus• Knee deformities:

– hyperextension and dislocation – Parents who are relatives (consanguinity)

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DDH

• When risk factors are present the infant should be reviewed:– Clinically– Radiologically

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Examination

• The infant should be– Quiet– Comfortable

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DDH

• Look:– External rotation– Lateralized contour– Shortening– Asymmetrical skin

folds• Anterior – posterior

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DDH

• Move– Limited abduction

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DDH

• Special test (depending on the age):– Galiazzi sign– Ortolani, Barlow test only till 4-6 m of age– Hamstring Stretch test – Trendelenburg sign older comprehending child– Limping:

• Unilateral one sided limping• Bilateral waddling gait (Trendelenburg gait)

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DDH- Giliazi test

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DDH- Ortolani test

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DDH- Barlow test

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DDH- Hamstring Stretch Test

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DDH- Trendelenburg Test

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DDH- Investigations

• 3w -3m U/S

• > 3months X-ray pelvis (AP + abduction)

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DDH

• The pathology is of 2 componants:– Femoral head position.– Acetabular development.

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Femoral Head Position

Normal hip Dislocated hip

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Acetabular Development

Normal hip Dislocated hip

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DDH- Radiology> 6m: reliable & ossification center normally appears (5-6m) of age, if

delayed or did not appear it’s one of the signs of DDH

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Treatment - Aims

A concentrically, reduced, stable, painless, mobile hip joint.

•Obtain concentric reduction•Maintain concentric reduction•In a non-traumatic fashion•Without disrupting the blood supply to femoral headThat is why:

Refer to pediatric orthopedic surgeon

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DDH- Treatment

• Method depends on age• The earlier started:

– Its easier– Better the results (higher remodeling potential)– Treatment is mainly non-operative

• Should be detected EARLY• Either surgical or non-surgical

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Treatment• Birth – 6m

– In OPD: reduce + maintain with Pavlik harness or hip spica (H.S)• 6-12 m:

– GA + closed (? Open) reduction + maintain with H.S• 12 - 18 m:

– GA + open reduction + maintain with H.S 6w, then B.S cast for months • 18 – 24 m:

– GA + open reduction + acetabuloplasty + H.S 6w, then B.S cast 6w • 2-8 years:

– GA + open reduction + acetabuloplasty + femoral shortening + H.S 6w, B.S 4-6w

• Above 8 years:– GA +open reduction + acetabuloplasty (advanced) + femoral shortening +

H.S

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Pavlik Harness

• Maximum to start it is 6m of age, if older use other method

• Is kept on for 6w continuous, then use a rigid abduction splint

• This is to achieve stable reduction• It’s a dynamic splint

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Abduction splint

• It’s a rigid splint• This is to maintain the reduction & wait for

improvement of the acetabular cover to be < 30° & with concavity

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Normal Hip Arthrogram

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Hip Arthrogram Guided Reduction

Dislocate view Reduced view

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Hip Spica

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Broom-Stick Cast

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Example: Open reduction & Acetabuloplasty

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Example: Open reduction & Acetabuloplasty & Femoral Shortening

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DDH

• Late complications if not treated:– Severe pain (hip area, back)– Early hip arthritis – LLD (leg length discrepancy) – Pelvic inequality (tilt)– Early Lumbar spine degeneration

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SCFE

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SCFE

• Slipped Capital Femoral Epiphysis• At the level of physis • Its considered as Salter-Harris fracture, type-1• So it is an emergency

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SCFE- Top View

Anterior slippage

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SCFE

• Types:– Radiological:

• Acute < 3w • Chronic > 3w, can see start of callus formation• Acute on chronic

– Clinical:• Unstable can not weight bear on that limb• Stable can put weight (walk)

• When its acute or unstable urgent surgery

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SCFE

• Causes:– Hormonal hypothyroid, abnormal G.H,

hypogonadisum – Metabolic Chronic renal failure – Mechanical (obesity)– Trauma– Unknown

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SCFE

• Typically:– 8 – 12y old – Male– Obese– Black

• 20 - 25 % to affect the other hip, within 18m post affection

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SCFE

• History:– Pain hip, anterior thigh, knee– Duration of C/O (more or less than 3w)– Gait painful or painless – Trauma minor or none– Any known hormonal or metabolic issues

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SCFE

• Examination:– The limb is in ext. rotation– With hip flexion the limb goes in spontaneous ext.

rotation– Limited int. rotation & abduction– Painful hip R.O.M– Gait can or can not (antalgic) weight bear on

affected limb

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SCFE

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SCFE

• Investigation:– XR pelvis:

• AP standing & frog lateral• See the actual slip • Positive “Klein Line”• Or just wide physis pre slip phase

– XR knee is normal– MRI in unusual or unclear presentations

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SCFE- XR AP

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SCFE- XR Frog Lateral

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SCFE- Chronic

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SCFE- Kline’s Line

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SCFE- Kline’s Line

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SCFE

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SCFE- Example 1

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SCFE- Example 2

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SCFE

• Severity:– Depends on degree of slip– The metaphysis is divided to 3 (1/3)– The more the slip the worsted the severity

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SCFE- Severity

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SCFE

• Treatment:– Acute or chronic its an emergency refer to

Orthopedic urgently– Aim prevent further slippage & fuse the physis

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SCFE

• Treatment:– Acute:

• Emergency in-situ fixation (no reduction done)• Using 1 or 2 (6mm) screws• Pin threads pass the physis, & stops 5mm before the

articular surface to prevent “Chondrolysis”• Do hormonal essay if any abnormality refer to

endocrine

– Chronic salvage corrective osteotomies

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SCFE

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SCFE

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SCFE

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SCFE

• Complications:– Chondrolysis that causes early hip OA– Femoral AVN– FAI ( Femoral Acetabular Impingement) – If not treated coxa vara or valga– Stiff hip joint– LLI (leg length inequality) – Pelvic obliquity – Early Lumbar spine degeneration

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SCFE- Chondrolysis

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SCFE- Chondrolysis

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SCFE- AVN

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Legg-Calve-Perth’s Disease(LCP)

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Perth’s Disease

• It is vascularity of head of femur (AVN) of an unknown cause.

• So a patient with SCA & femoral AVN does not have Perth’s disease.

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Perth’s Disease

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Legg-Calve-Perth’s Disease

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Perth’s Disease

• Typically: – 4-8 years old– males– obese – Bil in 10 – 12% of patients

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Perth’s Disease

• Theories of its cause:– Minor trauma (hyperactive child)– A.V malformation– Virus infection

• Most agree its multifactorial

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Perth’s Disease

• Severity depends on how much of the head is involved

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Perth’s Disease

• Stages (weeks-years per stage):– Vasculitis– Fragmentation– Reossification / Healing– Reossified / Healed

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Perth’s Disease

• Prognosis:– < 6y of age:

• Good prognosis (heals well)• Usually conservative treatment

– > 9y of age:• Usually bad prognosis• Needs surgical treatment (may be >1 operation)

– 6-9 y of age:• Various outcomes• Majority of patients present in this age gp

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Perth’s DiseaseAt 3y of age 5y 7y 9y

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Perth’s Disease

• History:– Pain hip, anterior thigh, knee– Antalgic gait– Trauma minor or none– URTI few weeks earlier– C/O since weeks to months

• The usual a minor trauma few months ago with initial antalgic gait & now pain is better but still limping

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Perth’s Disease

• Examination:– Antalgic gait– Restricted hip ROM in all directions, esp. with more

sever head involvement– Worse restriction for internal rotation & abduction– Knee normal – Thigh muscle wasting (disuse)

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Perth’s Disease

• Investigation:– XR pelvis AP standing & frog lateral– XR knee is normal– MRI:

• In unusual presentations• Vary early in the disease even before classical XR changes

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Perth’s Disease XR changes

AP standing Frog lateral

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Perth’s Disease XR changesSubchondral fracture,

one of the 1st signs of LCP,best seen on frog lat XR

Metaphyseal cysts

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Perth’s Disease XR changes

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Perth’s Disease

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Perth’s Disease

• Treatment:– Refer to Orthopedic Dr. as an urgent case.– Vary controversial, depending on age, stage &

classification. – Aim have a painless, contained, mobile hip joint

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Perth’s Disease

• Treatment:– But basic guidelines:

• Pain relief (may) admit, skin traction few days, analgesia• Increase hip ROM P.T, mobilize PWB or NWB• Keep hips abducted:

– So head will mold better in the acetabulum, and less body weight on the femoral heads.

– By abduction splint or casting (Broom-Stick cast or Spica cast)

• While keeping the head contained:– Do containment osteotomy in the fragmentation stage. – If came in late reossification stage wait till heals then do salvage

surgery

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Perth’s Disease

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Perth’s Disease

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Perth’s Disease

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Perth’s Disease

• Complications:– Abduction hinge may need Chelectomy– Heals in coxa magna (big), brevia (short), plana

(wide)– Stiff hip joint– LLI (leg length inequality) – Pelvic obliquity – Early hip OA – Early Lumbar spine degeneration

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Perth’s Disease Abduction Hinge

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Remember

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Common Pediatric Hip problems:

DDHSCFE

Perthe’s