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Congenital dislocation of the hip in the older child. The effectiveness of overhead traction.

We studied the use of overhead traction in the treatment of congenital dislocation of the hip in thirty-five children (fifty hips) whose mean age at the time of the diagnosis was thirty-three months (range, eighteen to seventy-two months). None of the children had had any previous treatment. The mean time in traction was twenty-three days (range, eight to thirty-six days). Closed reduction was successful for relocation of the femoral head in thirty-eight of the fifty hips; twenty of these hips needed no additional treatment, sixteen were treated with an innominate osteotomy because of severe acetabular dysplasia, and two needed femoral derotation and an innominate osteotomy to correct persistent subluxation. In the remaining twelve hips, closed reduction failed at the outset and an open reduction was necessary. Femoral shortening also was performed in seven of the twelve hips to maintain concentric reduction. After a mean duration of follow-up of forty-eight months (range, thirty-two to sixty-five months), thirty-three hips were rated as class 1; seven, as class 2; four, as class 3; and five, as class 4, according to the criteria of Severin. The remaining hip could not be so classified. Avascular necrosis developed in two hips that had been treated with closed reduction followed by Salter osteotomy and in three hips that had been treated with primary open reduction. We found that preliminary overhead traction facilitated closed reduction of untreated congenitally dislocated hips in children who were eighteen to seventy-two months old.

Casts, Surgical↗

Treatment concepts for proximal femoral ischemic necrosis complicating congenital hip disease.

A retrospective review of fifty-three congenitally dislocated hips (in forty-four patients) in which ischemic necrosis developed was undertaken to assess patterns of growth disturbance and to establish treatment protocols. We utilized the Bucholz and Ogden classification of the four roentgenographic patterns of ischemic necrosis complicating the treatment of congenital hip disease. Patients with Type-I disease had transient ischemia with early recovery. Significant growth disturbances requiring surgical treatment were not observed. Limb-length discrepancy, increased height of the greater trochanter relative to the femoral neck and head, and problems with femoral head coverage were more likely to develop in hips with Type-II or Type-III ischemic necrosis. Equalization of limb lengths, trochanteric epiphyseodesis, and surgical means of improving femoral head coverage were also more commonly indicated in these patients. In patients with Type-IV disease, mild deformities of the femoral head and occasional limb-length discrepancies developed; other sequelae were uncommon and surgical intervention was rarely required.

Child, Preschool↗

[Treatment of congenital dislocation of the hip by Salter's innominate osteotomy. Study of the first 40 cases operated on at the Orthopedic Institute, Kassar Said, Tunisia].

1) Twenty-nine children aged 18 months to 7 years with 40 congenitally dislocated hips, were treated between 1964 and 1971. Six hips had a closed reduction, 34 had an open reduction and capsulorrhaphy, and all had an innominate osteotomy. 2) Complications of the treatment included 2 joint infections. Of 11 hips which were unstable post-operatively, more than half were due to errors of the operative technique, and 8 required further surgery. Avascular necrosis of the femoral head occured in 3 hips post-operatively, and another 3 showed irregular ossification of the femoral epiphysis. All 6 hips had had an open reduction, and were mainly in older children who had inadequate pre-operative traction. 18 hips were stiff post-operatively ; 17 had had an open reduction ; Seven of eleven were improved by traction and physiotherapy. 3) The average length of follow-up was 4 years. Although only 70 p. 100 of the hips were clinically satisfactory, 92 p. 100 had excellent or good anatomical results as seen on radiographs.

Child, Preschool↗

Radiological evaluation of asymmetrical limitation of hip abduction during the first year of life.

Asymmetrical limitation of abduction of the hip may be found on screening of children in the first year of life. The clinical features identified may occur in congenital dislocation of the hip but most infants do not have or develop hip dislocation. Radiological changes are present on the side of limitation of abduction and include a higher acetabular angle, retardation of femoral head epiphyseal development, pelvic obliquity and a rotational deformation of the pelvis in the transaxial plane. The appearances are postural deformities due to persistent infant positioning and are self-correcting. If aggressive treatment methods are to be avoided, the radiologist should not confuse these changes with those of congenital hip dislocation or subluxation.

Female↗

Congenital bilateral hip and knee dislocation treated without surgery: 18-year follow-up.

Report of an 18-year-old black girl successfully treated for congenital dislocation of the hips and knees is presented. Progress from date of birth, methods of treatment, and results are given. It is concluded that the condition is unusual, that dysplasia and intrauterine forces are the cause, that early treatment gives excellent results without surgery, and that follow-up through the entire growth period is essential.

Female↗

Results of congenital dislocation of the hip joint with open reduction followed up to an age of fifteen years or more.

Forty-three hips (35 patients) with congenital dislocation with open reduction were reviewed. They were under 7 years old at the time of open reduction and over 15 years old at the follow-up. According to Severin's classification, 11 hips were classified as Group I, 7 hips as Group II, and 20 hips as Group III. Avascular necrosis was observed in 20 hips, but no Kalamchi's groups III and IV. The findings were that the younger the patient's age at open reduction, the higher the incidence of avascular necrosis. The cases in which the cartilaginous acetabular floor was demonstrated to be thicker in preoperative arthrography tended to yield unsatisfactory results.

Adolescent↗

Acetabular development after closed reduction of congenital dislocation of the hip.

We reviewed the serial radiographs of 54 hips in 47 children treated by closed reduction for congenital dislocation of the hip and followed to at least 14 years of age, to determine the causes of acetabular dysplasia. We excluded hips with femoral head deformity or residual subluxation and compared the results with those from a control series of unaffected hips of patients with unilateral CDH. Acetabular development after the age of 11 or 12 years was significantly worse in Severin group III than in Severin group I hips on the affected side or Severin group III in unaffected control hips. One of the causes of acetabular dysplasia at maturity was found to be impairment of acetabular development after 11 or 12 years of age. This may be attributable to impaired secondary ossification in the acetabular rim. Our findings emphasise the importance of continuing the follow-up of patients treated for congenital dislocation of the hip until full skeletal maturity.

Acetabulum↗

One-stage treatment of congenital dislocation of the hip in older children.

We reviewed the results of a primary one-stage combined operation in 47 patients (55 hips) who were > or = 4 years and had congenital dislocation of the hip. At a mean follow-up of 7.5 years (2-16 years), 67% of the whole series had good or excellent clinical results, and 65% were good or excellent radiologically. Avascular necrosis occurred in four patients, and redislocation also occurred in four patients. We concluded that most of the children who are > or = 4 years and who have congenital dislocation of the hip can successfully be treated with an extensive one-stage operation consisting of open reduction combined with innominate osteotomy and femoral varus, derotation, and shortening osteotomy.

Adolescent↗

[Luxation of the hip and preventive examinations].

The present report on the possibilities and limitations of screening and its importance for the prevention of congenital hip dislocation is based on many years of practical experience in preventive medicine and equally extensive study of oblique presentation and congenital dislocation of the hip joint. The paper presents a review of the various forms of malformation of the hip and following a short discussion of the origins and prognoses of these various forms, deals with the various diagnoses. Two main examination periods are important for diagnosis: the neonatal period and the 4th month of life. In the neonatal period a hip joint is unstable if the Roser-Ortolani sign is positive. Other clinical symptoms are found in addition in the much rarer congenital dislocation of the hip. The advantage of examination in the neonatal period is that it enables the unstable hip joint to be treated immediately. As a rule this preventive treatment, involving little risk, results in normal development of the hip joint, instead of the possible defective development to hip dislocation. These possibilities in the neonatal period are limited by the degree of experience and the extent of cooperation between examiners and therapists. In the second main examination period, in the 4th month of life, the malformations which occur post partum should be identified. In contrast to the obviousness of the clinical hip joint findings in the neonatal period" clear clinical hip joint symptoms can only be expected in the 4th month of life with the most severe forms of hip dislocation.(ABSTRACT TRUNCATED AT 250 WORDS)

Age Factors↗

The surgical treatment of established congenital dislocation of the hip: results of surgery after planned delayed intervention following the appearance of the capital femoral ossific nucleus.

It has been proposed that the presence of the capital femoral ossific nucleus confers protection against ischemic injury or avascular necrosis (AVN) at the time of reduction of a congenitally dislocated hip. The current literature is contradictory. A prospective study was undertaken of the clinical and radiologic outcomes following closed or open reduction. Fifty hips were included in the study. These cases had presented late or had failed conservative treatment. In 28 hips treatment was intentionally delayed until the appearance of the ossific nucleus (but not beyond 13 months) and in 22 the ossific nucleus was present at clinical presentation. Six hips reached the age of 13 months without an ossific nucleus appearing and progressed to treatment. The significant AVN rate (more than grade 1) was 7% for closed reduction and 14% for open. However, the amended rate if hips were excluded that had failed Pavlik harness treatment was 0.0% and 9%, respectively (4% overall). Further surgical procedures were necessary in 57% of hips undergoing closed reduction and 41% after open, which compares favorably with other series. The authors conclude that the presence of the ossific nucleus is an important factor in the prevention of AVN, particularly after late closed reduction. Intentional delay in the timing of surgery does not condemn a hip to open surgery, but there is a comparable rate of secondary procedures becoming necessary, particularly after closed reduction. A simultaneous pelvic procedure may be appropriate after late closed reduction. The delayed strategy to await the appearance of the ossific nucleus for previously untreated dislocation allows a simple treatment algorithm to be employed that produces good clinical and radiologic outcomes.

Female↗

[Echography in the study of the neonatal hip: the diagnostic-therapeutic implications of type-IIa (borderline) findings].

Sonography (US) is a useful method in the early diagnosis of congenital hip dislocation; X-ray examination exhibits limitations due to high false-positive and false-negative rates. The advantages of US include: non-invasiveness, direct visualization of muscle and cartilage, dynamic demonstration of anatomical structures, and possible diagnosis in neonatal age. Therefore, US can be used as a screening or targeted diagnostic technique in selected newborns with clinical suspicion and/or risk factors. In this paper the authors report their experience in 1271 patients (721 females, 550 males), aged 1 day to 7 months, who were examined with US for the diagnosis of congenital hip dislocation. The newborns were divided into two groups at first examination: a) the screening group included 524 consecutive newborns (F = 266, M = 258) from S. Chiara Regional Hospital in Trento, and b) a selected group of 747 newborns (F = 455, M = 292) with clinical suspicion and/or risk factors, who had been selected in the Trento area. According to Graf's classification, the results of US in 2542 neonatal hips, were: 2346 (92.3%) normal hips, 171 (6.1%) type IIa hips, and 24 (1.6%) pathological hips. In the selected group (1494 hips) we observed: 1351 (90.4%) normal, 119 (8%) type IIa, and 24 (1.6%) pathological hips (IIb, IIc, D, III). In the screening group (1048 hips) we detected: 995 (95%) normal hips (Ia/Ib), 52 (4.9%) type IIa, and 1 (0.1%) pathological hips (D). Our experience suggests that US is a useful method in selected newborns with clinical suspicion of congenital hip dislocation and/or risk factors. US limitations consists in the dispersion of type IIa hips. Moreover, the need emerged for complete cooperation between pediatrician, radiologist, and orthopedist to optimize the cost/benefit ratio.

Female↗