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Dive into the research topics where Fritz Hefti is active.

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Featured researches published by Fritz Hefti.


Journal of Pediatric Orthopaedics B | 1999

Osteochondritis dissecans: a multicenter study of the European Pediatric Orthopedic Society.

Fritz Hefti; José Beguiristain; Ruediger Krauspe; Bjarne Möller-Madsen; Vincenzo Riccio; Christian Tschauner; Reinhard Wetzel; Reinhard Zeller

To assess of the value of conservative and operative treatment of osteochondritis dissecans of the knee, a multicenter study was performed. In 12 European countries, 798 cases of osteochondritis of the knee have been collected from 44 hospitals. Results were based on 452 patients with 509 affected knees with minimum follow-up was 1 year (mean follow-up, 3 years and 11 months) and sufficient data for evaluation: 61% were male patients; 39% female patients; 318 affected knees were found in juvenile patients; 191 affected knees were in adult or premature patients. The localization was the medial femoral condyle on the lateral side in 51% (typical site) of patients. Various other sites were involved. Of the 509 affected knees, 154 were treated conservatively, 355 were treated surgically (many with multiple operations). For evaluation, the initial situation (at the time of the diagnosis) was favorable in 198 patients (no effusion, diameter of the lesion < 20 mm and no gross dissection on imaging) and unfavorable (one of the parameters did not meet these prerequisites) in 311 patients. The results were better in young patients than in adult patients. However, in the adolescent group, 22% of patients had abnormal knee at follow-up. The classical localization has a better prognosis than an unusual one. Patients with a favorable situation at diagnosis have significantly better results after conservative treatment than those who have undergone operation. When there are signs of dissection, the results are better after operative than after conservative treatment.


Journal of Pediatric Orthopaedics B | 2000

Treatment approaches for congenital pseudarthrosis of tibia: results of the EPOS multicenter study. European Paediatric Orthopaedic Society (EPOS).

Franz Grill; Gérard Bollini; Pavel Dungl; John A. Fixsen; Fritz Hefti; Ernesto Ippolito; Bertil Romanus; Cosimo Tudisco; Shlomo Wientroub

&NA; This study was designed to analyze the different therapeutic methods used by European Paediatric Orthopaedic Society members from 13 countries for congenital pseudarthrosis of tibia. The treatment data of 340 patients who underwent 1287 procedures for this condition were analyzed. The essential findings were that the method of choice needed to approach the biological problem with the aims of: (1) resecting the pseudarthrosis to provide stability, the basic requirement for bony consolidation; (2) correcting length discrepancy and axial deformity; (3) achieving fusion; and (4) solving the additional problems around the main deformity such as alignment, leg length discrepancy and ankle valgus. The Ilizarov technique emerged as being the optimal method, having the highest rate of fusion (75.5%) of pseudarthrosis and rate of success in correction of the additional deformities. There was also consensus that surgery should be avoided before the third year of life.


Journal of Pediatric Orthopaedics B | 2005

The vertical expandable prosthetic titanium rib implant for the treatment of thoracic insufficiency syndrome associated with congenital and neuromuscular scoliosis in young children.

Anna K. Hell; Robert M. Campbell; Fritz Hefti

Expansion thoracoplasty and vertical expandable prosthetic titanium rib (VEPTR; Synthes Spine Co., West Chester, Pennsylvania, USA) implantation is a new method for the treatment of thoracic insufficiency syndrome and congenital spinal deformity in children. The longitudinal rib implant expands the thorax and indirectly corrects spinal deformity, thus allowing spinal, thoracic and probably lung growth. VEPTR has been used since 1989 in San Antonio, USA, and was introduced to Europe in 2002. This paper describes the preliminary experience with the European patients. Fifteen children with progressive scoliosis had a VEPTR implantation at a mean age of 6 years (11 months to 12 years). Nine children had thoracic insufficiency syndrome due to unilateral unsegmented bars (n=4), absent ribs (n=1), hemivertebrae (n=2) or bilateral fused ribs (n=2). Six children had severe thoracolumbar scoliosis and pelvic obliquity due to neuromuscular scoliosis. After VEPTR implantation, families and patients reported improvement of the thoracic insufficiency syndrome and better sitting abilities in the neuromuscular patients, as well as radical cosmetic improvement. There were three complications (skin breakage, lumbar hook displacement, rib fracture) after performing fifteen primary VEPTR implantations and 13 expansion surgeries in eight patients. Our experience suggests that expansion thoracoplasty and VEPTR implantation is a safe and efficient method for the treatment of thoracic insufficiency syndrome in young children with severe scoliosis.


Journal of Pediatric Orthopaedics B | 2000

Congenital pseudarthrosis of the tibia: history, etiology, classification, and epidemiologic data.

Fritz Hefti; Gérard Bollini; Pavel Dungl; John A. Fixsen; Franz Grill; Ernesto Ippolito; Bertil Romanus; Cosimo Tudisco; Shlomo Wientroub

&NA; Congenital pseudarthrosis of the tibia is a rare disease with a variable history. The pseudarthrosis is usually not present at birth (and therefore is not truly congenital) but occurs during the first decade of life. Paget in 1891 was the first to describe a case. The etiology is unknown. Neurofibromatosis plays a role in approximately 50% of patients. In the others, hereditary and mechanical factors are debated. Various (morphologic) classification systems have been proposed (Andersen, Boyd, Crawford). Because the appearance changes during the course of the disease, all classification systems have limited value: the determining factor is the stage of the disease at which it was classified. Because of the rarity of the disease and the variability of its history, the European Pediatric Orthopaedic Society decided to carry out a multicenter study on this disease. This paper presents the epidemiologic data on the patients involved. Data have been gathered on 340 patients from 13 countries. Two hundred patients were male (58.8%), 140 were female (41.2%). The right side was affected in 165 patients (48.5%) and the left side in 172 (50.6%); 3 patients had bilateral disease. Symptoms of neurofibromatosis were present in 54.7%. Histologic examinations in 192 patients showed a nonspecific appearance in 45.3%; in 15.6% the ultrastructure resembled fibrous dysplasia, and in 39% there was histologic evidence of neurofibromatosis. Most of the lesions were initially localized in the middle or distal third of the tibia. In 29% the localization changed during the course of the disease.


Journal of Pediatric Orthopaedics B | 2000

Free vascular fibular transfer in congenital pseudoarthrosis of the tibia: results of the EPOS multicenter study. European Paediatric Orthopaedic Society (EPOS).

Bertil Romanus; Gérard Bollini; Pavel Dungl; John A. Fixsen; Franz Grill; Fritz Hefti; Ernesto Ippolito; Cosimo Tudisco; Shlomo Wientroub

&NA; This paper presents a review of the literature, describes the principal authors (B.R.) personal experience and provides the results of the European Paediatric Orthopaedic Society (EPOS) multicenter study. The objective is to evaluate the present status and future role of free vascular fibular transfer in treating congenital pseudoarthrosis of the tibia. Variables such as the selection of cases, age at operation, technical surgical details and postoperative results will be considered. The data on the EPOS study were incomplete at the time of writing, but the considerable amount of information already amassed is a valuable contribution to this updated report.


Journal of Pediatric Orthopaedics B | 2000

Functional results at the end of skeletal growth in 30 patients affected by congenital pseudoarthrosis of the tibia.

Cosimo Tudisco; Gérard Bollini; Pavel Dungl; John Fixen; Franz Grill; Fritz Hefti; Bertil Romanus; Shlomo Wientroub

&NA; From a multicentric study on Congenital Pseudoarthrosis of the tibia (CPT) conducted on 340 patients, we evaluated the functional results on a group of thirty patients who were at the end of skeletal growth (age ≤ 16 years). The prognosis of CPT is very much related to the radiologic classification. Crawford type 2 and Crawford type 4 pseudoarthrosis have a worse prognosis, with a lower percentage of fusion at the site of pseudoarthrosis. Crawford 4 patients have the worst functional results. Most of them showed a severe leg length discrepancy, needed a permenent brace, with an ankle joint function fair or poor. The presence of fibula pseudoarthrosis seems to be responsible for most of the worst functional results. The level of deformity caused by either the natural course of the disease or its treatment, is decisive in the evalution of the functional results.


Journal of Pediatric Orthopaedics B | 2000

The fibula in congenital pseudoarthrosis of the tibia: the EPOS multicenter study. European Paediatric Orthopaedic Society (EPOS).

David Keret; Gérard Bollini; Pavel Dungl; John A. Fixsen; Franz Grill; Fritz Hefti; Ernesto Ippolito; Bertil Romanus; Cosimo Tudisco; Shlomo Wientroub

&NA; Fibular involvement in congenital pseudoarthrosis of the tibia (CPT) can be either a rare isolated pathology or is in association with the tibial changes. Out of 282 patients with CPT who had complete radiographic work‐up, 62% (almost two thirds) demonstrated fibular pathology: 36% had true fibular pseudoarthrosis and the rest, i.e., 26% had fibular hypoplasia or dysplastic fibula. Neurofibromatosis was found in 62% of the patients with fibular pathology. The typical radiological features of tibial pseudoarthrosis are often missing in patients with fibular pathology. It is most probably because fibular changes precede the tibial involvement. In 250 patients with tibial surgical treatment, the highest rate of fusion occurred in patients with fibular involvement compared with those with normal fibula.


Journal of Pediatric Orthopaedics B | 1996

Relation of femoral to tibial torsion in children measured by ultrasound.

Marek Pasciak; Thomas M. Stoll; Fritz Hefti

To study the relation between femoral and tibial torsion, we measured their values by ultrasound (US) in 97 normal children in two groups (aged 6 and 15 years). Anteversion was measured between the anterior aspect of the femoral neck and the axis of the femoral condyles, and tibial torsion as the difference of the proximal to the distal posterior tibial planes. The mean value of anteversion was 37 degrees in the younger group and 24 degrees in the older group. The mean value of tibial torsion was 18 degrees in both groups. We found neither side- nor sex-dependent differences in both age groups. There was no relation between both values.


Journal of Pediatric Orthopaedics B | 2011

Supracondylar stress fracture of the femur in a child.

Martin Bachmann; Mark S. Gaston; Fritz Hefti

We describe the unique case of a supracondylar-supraphyseal femoral stress fracture in a healthy 13-year-old boy. The importance of careful history taking is emphasized particularly in regard to asking about new, repetitive activities. The important differential diagnosis in this anatomical region is neoplastic disease and the use of imaging, particularly MRI scanning will yield useful information but is not definitive. Regular follow-up and repeat imaging must be undertaken where the diagnosis of stress fracture is made so that the diagnosis can be ultimately confirmed with the appearance of a healing fracture. Active management in lower limb stress fractures with immobilization is also emphasized as it is apparent that such fractures often do not follow a benign course. Immobilization will also help ensure compliance to treatment and follow-up, which can sometimes be difficult in this patient population.


Orthopade | 2004

Treatment of congenital scoliosis with the vertical expandable prosthetic titanium rib implant

Hell Ak; Fritz Hefti; Campbell Rm

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Pavel Dungl

Charles University in Prague

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Cosimo Tudisco

University of Rome Tor Vergata

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John A. Fixsen

Great Ormond Street Hospital

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Ernesto Ippolito

University of Rome Tor Vergata

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Mark S. Gaston

Royal Hospital for Sick Children

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David Keret

Boston Children's Hospital

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Robert M. Campbell

Children's Hospital of Philadelphia

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