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[What determines treatment results of the Frejka pillow treatment for congenital hip dislocation?].

The results of treatment of 1008 hips in 779 children were analyzed and their dependence on objective factors established. The major influence is attributed to the initial displacement of the femoral head; the greater it is the worse is the result. The age at the onset of treatment influences results only indirectly with displacement increasing in time. No other factor as sex, side involved (left, right or both), or family history seems to play a role.

Female↗

Acetabular dysplasia and hip dislocation after selective premature fusion of the triradiate cartilage. An experimental study in rabbits.

Premature fusion of the triradiate cartilage was obtained surgically in 10 three-week-old rabbits, and compared with isolated fusion of the ilio-ischial and of the ilio-pubic limbs of the triradiate cartilage in two further groups of 10 rabbits. Complete fusion caused acetabular dysplasia five weeks after operation in all animals and hip dislocation at nine weeks in half of them; ilio-ischial fusion had a comparable effect. Ilio-pubic fusion had only a minimal effect on acetabular development. The posterior position of the ilio-ischial limb in the acetabulum and its predominance in the formation of the triradiate cartilage in quadrupeds may have contributed to its decisive effect on acetabular development.

Acetabulum↗

A prosthesis augmentation device for the prevention of recurrent hip dislocation. A preliminary report.

At present, revision is the only standard option for cases of recurrent hip prosthesis dislocation. A device is described that contains the head of the femoral component, preventing dislocation, while only slightly restricting external rotation of the affected leg. The device can be inserted through a small incision, minimizing operation time. This device differs from others, e.g., the reversed acetabular cup, by being predrilled (with drill guide supplied), modular in design, and tailored to the dimensions of the cup site.

Aged↗

Fiber density in congenital muscle fiber type disproportion. II. Congenital muscle hypotonia and hip dislocation.

Our previous paper presenting electromyographic findings in patients with congenital fiber type disproportion myopathy, confirmed the myogenic character of the disease process. That group of patients was however fairly heterogenous regarding both the clinical features and the morphological changes in muscle fibers (e.g. cases with central cores). In the present study we have examined 13 children with hypotonia and muscle fiber type disproportion operated on in childhood for congenital hip dislocation. In all cases CNEMG and SFEMG with FD estimation was performed in biceps brachii and quadriceps femoris muscles. In all muscles examined either slight EMG changes indicative of myopathy or a normal EMG pattern was found. None of the patients demonstrated an evident increase in FD values. Normal FD and the recruitment pattern proportional to the force of contractures indicate that the normal number of motoneurons is preserved. Accordingly, our present findings confirm the conclusions of our previous paper.

Adolescent↗

[Results in surgically managed severe hip-dislocation fractures].

Following operative reconstruction in 11 German clinics working together on questions concerning osteosynthesis, 190 fractures of the hip socket were examined. The total results of all fracture types showed, with 60% very good to good, 15% satisfactory and 25% poor results, clear improvement as compared with purely conservative therapy. Practically two-thirds of the unsatisfactory results were due to traumatic injury followed by necrosis of the ball of the femoral head. Additional improvement of the results is possible by refined operative techniques, broader differentiation of the indications, and especially by a shortening of the interval between the time of accident and the osteosynthesis of the acetabulum.

Acetabulum↗

Treatment of congenital dislocated hip by arthroplasty with femoral shortening.

This was a retrospective study of 15 hips in 11 patients with complete congenital dislocation of the hip treated by total hip arthroplasty and femoral shortening with a subtrochanteric double chevron derotation osteotomy. The mean age at the time of surgery was 51 years (range, 21-74 years), and the mean followup was 5.5 years (range, 2-8.5 years). Functional evaluation using the modified Harris hip rating system showed an excellent result in five hips and a good result in seven hips (80% success rate). The location of the hip center was lowered by a mean of 8.3 cm (range, 5.7-10.4 cm). Leg length discrepancy in seven patients with unilateral involvement was reduced from a mean of 3.9 cm (range, 1.7-8.2 cm) before surgery to a mean of 1.4 cm at the latest followup (range, 0-4 cm). The Trendelenburg sign was assessed in 10 of 15 hips and was corrected from a positive preoperative status to a negative postoperative status in eight of these 10 hips. There were no cases of nonunion, dislocation, nerve palsy, or radiographic loosening. The only complications were a supracondylar fracture below the femoral component in a patient with severe osteoporosis 6 months after surgery and loosening of the cemented titanium metal backed acetabular component in the same patient 1.5 years after surgery. The current series showed that total hip arthroplasty in combination with a subtrochanteric double chevron derotation osteotomy has promising short to midterm results in the treatment of complete congenital dislocation of the hip in adults.

Adult↗

[Radiological study of the development of the hip joint in children with congenital hip dislocation treated by the Frejka cushion].

The changes in the radiological state of the hip joints between the 2-nd and the 21-st year of age in persons treated for congenital dysplasia of the hip with dislocation have been determined on the basis of the analysis of 3.005 X-razy pictures of 4 or 6 radiological parameters of 916 hip joints in 708 children and the total point evaluation. On comparing the rate of excellent, good and poor results in individual years of life, it has been concluded that marked and quick rebuilding occurs between the 2-nd and the 7-th year of age, and on the other hand, after 10 years of age the radiological state of the hip joint stabilizes.

Adolescent↗

Experiences in diagnosis and treatment of hip dislocation and dysplasia in populations screened by the ultrasound method of Graf.

Ultrasound investigation of the hip according to Graf is performed, whenever possible, as a routine screening test for hip dysplasia and dislocation in neonates. However, in spite of screening, hip dysplasia and/or dislocation is identified in a number of children after the third month of life only. The present study presents an analysis of reasons and causes. Between August 1999 and July 2001 children aged between six months and five years were documented, in whom the diagnosis of hip dysplasia or dislocation was made, despite normal ultrasound findings at primary investigation and who required non operative or operative treatment by a specialist surgeon working in Switzerland in paediatric orthopaedics. The study included 26 children (17 girls / 9 boys). Hip dysplasia and/or dislocation was diagnosed between the age of 6 days and 41 months. Twelve children had to be excluded from the sample (n = 26), four were infants who had basic neurological disorders or multiple anomalies and there were eight children from abroad whose original documentation could not be obtained. Analysis of the remaining 14 children showed that 43% were misdiagnosed (n = 6) and a treatment error occurred in 36% (n = 5) of cases. One child presented with a teratogenic hip dislocation. In two other infants with normal primary ultrasound findings, hip dysplasia was identified radiographically once the child started to walk. Delayed diagnosis can be the result of technical errors or misinterpretation. The six patients meeting the criteria of misinterpretation can be expressed as a rate of 0.04% of all births. However, even if the disorder is correctly diagnosed, its identification and treatment may be inadequate or fail to produce the desired results. This was the case for five of the children, that is, for a rate of 0.03% of births.

Bone Diseases, Developmental↗