The Hip

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Chapter 10 The Hip

The hip is a ball-and-socket joint in which the femoral head articulates deeply into the acetabulum. This deep fit, combined with thick ligamentous and muscular supporting structures, makes the hip extremely stable but relatively inaccessible. Therefore, the diagnosis of disorders of the hip is sometimes difficult.

Anatomy

The proximal portion of the femur consists of a head, neck, and greater and lesser trochanters. The axes of the neck and femoral shaft form an angle in the anteroposterior plane: the neck–shaft angle, or “angle of inclination.” This normally measures 125 to 130 degrees. An increase in this angle is termed coxa valga, and a decrease is termed coxa vara. The neck and shaft also form an angle in the transcondylar plane that is referred to as the angle of femoral torsion (Fig. 10-1). Normal femoral torsion is 40 degrees in children, and this decreases to 15 to 20 degrees in adults. Excessive femoral torsion is termed anteversion or antetorsion and is sometimes responsible for in-toeing. A decrease in the normal femoral torsion is termed retroversion or retrotorsion and may cause an out-toeing gait.

The vascular anatomy of the femoral head is of critical importance in many disorders of the hip. The main sources of blood supply are the retinacular and intramedullary vessels, both of which course from the intertrochanteric region proximally to nourish the femoral head (Fig. 10-2). Diseases or injuries that compromise the circulation may damage the viability of the femoral head and lead to avascular necrosis.

Among the nerves that supply the hip joint is the obturator nerve. This nerve also supplies a sensory branch to the medial side of the thigh and motor supply to some of the hip adductors. Irritation of this nerve from hip joint disease may result in referred pain along the inner aspect of the knee and thigh that may cause confusion with disorders of the knee joint. Therefore, complaints of pain in this area in the absence of physical findings in the knee should always draw attention to the hip joint.

Examination

Several bony landmarks are available for orientation on physical examination. The anterior and posterior superior iliac spines and iliac crest are easily palpable because they are not crossed by any muscles (Fig. 10-3). The proximal portion of the iliac crest lies at the level of the fourth lumbar vertebra. The greater trochanter is palpable laterally, and the pubic symphysis is palpable anteriorly. The femoral head lies approximately 2.5 cm distal and lateral to the point where the femoral artery passes beneath the inguinal ligament. This relationship should be recalled when performing venipuncture from the femoral vein. A needle passed through the vein may enter the hip joint and introduce infection into the hip. All femoral venipuncture sites should therefore be meticulously scrubbed and prepared before needle insertion.

Developmental Dysplasia of the Hip

Developmental dysplasia of the hip (DDH) is a term used to describe a spectrum of hip abnormalities in the young child. This can range from simple acetabular dysplasia without instability to complete dislocation of the femoral head. Congenital dysplasia of the hip is the most common subset of this disorder. (Other forms of DDH are commonly caused by neurologic or myopathic factors.)

DDH is frequently bilateral, and although the cause is unknown, heredity appears to play a role. Females are affected nine times more often than males, and although the condition may affect both hips, the left is three times more often involved. Firstborn children or children born by breech deliveries also have a higher incidence of the disorder. It is occasionally present in association with clubfoot and congenital muscular torticollis deformities.

The hip may be frankly dislocated at birth, or the child may simply be born with isolated hip dysplasia without instability (in which case the diagnosis may only be discovered incidentally on radiographic examination at some later date). In between is the minimally subluxable hip with inadequate coverage by the acetabulum, which will usually develop osteoarthritis in adulthood, commonly by the third or fourth decade.

Pathologically, abnormalities are seen in both the acetabulum and femoral head. The acetabulum may be shallower in contour and more vertically inclined than normal and result in insufficient coverage and inadequate containment of the femoral head. The femur is often excessively anteverted, and the hip joint capsule may also be lax. The major abnormalities are acetabular, however.

CLINICAL FEATURES

There are no symptoms in the newborn, but most cases are detectable at birth. The clinical picture of the unstable hip will range from minimal findings to obvious frank dislocation, depending on the age of the child. In the newborn, provocative maneuvers, such as Barlow’s and Ortolani’s tests, are commonly used to detect instability. The tests are similar. The Ortolani test refers to the gentle reduction of the dislocated hip by abduction of the flexed hip (Fig. 10-5). This is often accompanied by a soft “clunk,” sometimes called the click of entry. In Barlow’s test, the hip is purposely dislocated by gentle downward pressure of the flexed, adducted hip. With posterior pressure, the femoral head will be displaced out of the acetabulum if the hip is unstable, sometimes called the click of exit. The head is then reduced by gentle abduction of the flexed hip by performing Ortolani’s maneuver. Barlow’s test should not be performed excessively, because it could make the problem worse. Occasionally, this maneuver may result only in a sensation of excessive gliding without an obvious dislocation. This may be an indicator that the hip is subluxable and therefore unstable. Soft clicks sometimes felt during abduction–adduction movements are not considered pathologic unless other findings are present.

If the diagnosis is made late, the hip is less flexible, and the ability to reduce the dislocated hip by the provocative maneuvers is lessened. At this time, the physical findings may include asymmetry of the skin folds and limited abduction (Fig. 10-6). If the hip is dislocated, it may not be reducible, and other signs may be present, such as shortening of the extremity (Fig. 10-7).

If weight bearing has begun, a painless limp is often the initial symptom of dislocation. Hip motion, especially abduction, is limited, and abnormal piston mobility or “telescoping” may be present. The Trendelenburg test is usually positive. This test takes advantage of the fact that normally, when standing on one leg, contraction of the abductor muscles on the side bearing weight will cause the opposite side of the pelvis to be elevated. If the hip is dislocated, these muscles no longer work effectively, and when the child stands on the affected leg, the opposite side of the pelvis drops downward instead. This causes the typical waddling gait caused by abductor weakness.

The roentgenographic examination is usually not very helpful when the patient is younger than 3 months of age unless a complete dislocation is present. After this age, a delay in the ossification of the femoral head is frequently noted (Fig. 10-8). The acetabulum may be more inclined vertically, and the acetabular index is often increased. If subluxation or dislocation has occurred, upward and outward displacement of the femoral head will be seen.

Ultrasonography is useful in congenital hip dysplasia, especially in high-risk infants (such as those who are breech delivered or who have a positive family history) or those with uncertain clinical findings. Among its benefits is the elimination of exposure to radiation. Magnetic resonance imaging (MRI) may eventually be helpful, but the diagnosis can usually be established by other means.

TREATMENT

Referral is indicated if there is any suggestion of instability in the hip of the newborn. Treatment is initiated as soon as possible and varies with the age of the patient and the degree of dysplasia. Early detection is of utmost importance, because conservative treatment is more likely to succeed in the infant. The more the child’s age exceeds the weight-bearing age, the more likely it is that surgery will be necessary, and the less likely that a normal functional result will ensue. Whenever any doubt exists, treatment and follow-up are indicated.

The objective of treatment is to reduce the femoral head into the acetabulum and maintain that reduction. By maintaining the hip in the reduced position, normal development of the hip joint structures and deepening of the acetabulum are encouraged. A variety of external devices are available for the treatment of hip dysplasia or dislocation, the most functional of which is the Pavlik harness (Fig. 10-9). The brace is usually worn for several weeks until the hip is stable.

Failure to obtain or maintain a stable reduction necessitates surgical intervention. The objective is to reduce the hip by either closed or open methods and maintain the reduction by casting or osteotomy.

Legg–Calvé–Perthes Disease

Perthes’ disease, or coxa plana, is a self-limited disorder of the hip in which a portion of the ossific nucleus of the femoral head undergoes avascular necrosis. Eventually, the infarcted, necrotic bone is absorbed and replaced by normal bone. The etiology is unknown. The disorder usually occurs between the ages of 4 and 10 years but may affect children as young as 2 or as old as 12. Males are four times more commonly affected than females. Fifteen percent of cases are bilateral, and the condition is rare in African Americans.

The disease is frequently divided into three stages. The early stage of the disease is characterized by synovitis of the hip joint and early ischemic changes in the ossific nucleus of the femoral head. Roentgenograms taken at this stage reveal joint swelling that may result in lateral displacement of the femoral head. An increase in the opacity of the ossific nucleus is usually present (Fig. 10-10).

In the second, regenerative stage, or fragmentation stage, the necrotic area begins to be replaced by viable bone. This phase lasts from 1 to 2 years. The roentgenographic appearance during this stage is one of fragmentation and compression of the femoral head with secondary widening of the femoral neck.

Reossification and healing occur in the third stage, which varies in duration beyond 1 year. The roentgenogram in this stage shows a disappearance of the rarefaction while normal bone continues to reform. The final roentgenographic appearance depends on several factors, including the age of the patient and the degree of involvement. The femoral head may end up normal in shape or irregular and flat (coxa plana) because of the collapse of the osteonecrotic bone and overlying cartilage. The end result may be osteoarthritis if coxa plana develops.

TREATMENT AND PROGNOSIS

Referral is indicated whenever the diagnosis is suspected. Treatment recommendations continue to evolve. The ultimate goal of treatment is to prevent deformity of the femoral head while healing is progressing. If a deformity can be prevented, the chances of degenerative joint disease developing at a later date are lessened. The initial goals of treatment are the relief of pain and maintenance of joint motion, which are accomplished by rest to control synovitis. Many children younger than 6 years of age with minimal involvement have a good prognosis and require only symptomatic care. The older child who is at risk for having a poor outcome may require treatment. In these children, treatment is aimed at keeping the femoral head centered in the acetabulum. If the head is contained in the acetabulum while it is re-forming, the acetabulum will “mold” the head and prevent significant deformity from occurring. These goals of treatment are usually accomplished by the use of an abduction brace that allows motion but contains the head in the acetabulum (Fig. 10-11). The brace must be worn continuously for up to 2 years, although the results of specific forms of treatment remain inconclusive, and some investigators advocate only nighttime bracing. Surgery may be necessary in select cases.

The prognosis depends on the age of the patient, the degree of involvement, and the adequacy of treatment. Young patients with minimal involvement who are treated early do very well with few sequelae. Patients over 8 years of age frequently have some permanent restriction of motion, a slight limp, and a more irregular or flattened femoral head. A few patients will later develop degenerative arthritis.

Slipped Capital Femoral Epiphysis

Slipped capital femoral epiphysis is a disorder of unknown cause in which weakening of the epiphyseal plate of the upper femur occurs and results in upward and anterior displacement of the femoral neck. The actual amount of displacement varies. In most cases, the slippage is gradual, and some elements of healing are usually present. The condition is seen most commonly in boys between the ages of 11 and 16 years during their rapid growth spurt. The disorder is bilateral in 25% of cases and frequently occurs in two distinct body types. The first is the slender, tall, rapidly growing boy, and the second is the large, obese boy with underdeveloped sexual characteristics. The presence of the disorder in these two body types suggests a hormonal cause, but none has been proved.

CLINICAL FEATURES

The onset is generally gradual, and symptoms usually occur even when little displacement is present. Mild discomfort in the hip, groin, and knee and a painful limp with activity are the most common initial complaints. Symptoms have often been present for several weeks. Examination reveals tenderness over the hip joint capsule. An external rotation (toeing-out) deformity of the lower extremity may be present, and internal rotation, abduction, and flexion are usually restricted. Pain is present at the extremes of motion, and the hip tends to rotate externally and abduct as it is flexed (Whitman’s sign).

In the early “preslipping” stage, the roentgenogram characteristically reveals irregular widening of the epiphyseal plate and joint swelling (Fig. 10-12). As displacement occurs, a line drawn along the superior or anterior neck of the femur will transect less of the femoral head than normal. This may be more readily seen on the lateral view. More severe degrees of slippage are usually easily diagnosed.

A condition similar to slipped capital femoral epiphysis is termed acute traumatic separation of the upper femoral epiphysis (Fig. 10-13). This is actually an epiphyseal fracture and has a much poorer prognosis than the gradual slippage that occurs in slipped capital femoral epiphysis.

Transient Synovitis (Irritable Hip)

Transient synovitis is a self-limited, nonspecific inflammation of the synovium of the hip joint that occurs in children. It is the most common cause of pain in the hip in children younger than 10 years of age. The cause is unknown, but a viral infection is suspected. Its importance lies in its similarity to other hip joint disorders, especially septic arthritis. The diagnosis is one of exclusion.