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Dive into the research topics where A. Catterall is active.

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Featured researches published by A. Catterall.


Journal of Bone and Joint Surgery-british Volume | 2000

Test of stability as an aid to decide the need for osteotomy in association with open reduction in developmental dysplasia of the hip

H. G. Zadeh; A. Catterall; A. Hashemi-Nejad; R. E. Perry

After open reduction for developmental dysplasia of the hip (DDH), a pelvic or femoral osteotomy may be required to maintain a stable concentric reduction. We report the clinical and radiological outcome in 82 children (95 hips) with DDH treated by open reduction through an anterior approach in which a test of stability was used to assess the need for a concomitant osteotomy. The mean age at the time of surgery was 28 months (9 to 79) and at the latest follow-up, 17 years (12 to 25). All patients have been followed up until closure of the triradiate cartilage with a mean period of 15 years (8 to 23). At the time of open reduction before closure of the joint capsule, the position of maximum stability was assessed. A hip which required flexion with abduction for stability was considered to need an innominate osteotomy. If only internal rotation and abduction were required, an upper femoral derotational and varus osteotomy was carried out. For a ‘double-diameter’ acetabulum with anterolateral deficiency, a Pemberton-type osteotomy was used. A hip which was stable in the neutral position required no concomitant osteotomy. Overall, 86% of the patients have had a satisfactory radiological outcome (Severin groups I and II) with an incidence of 7% of secondary procedures for persistent dysplasia including one hip which redislocated. The results were better (p = 0.04) in children under the age of two years. Increased leg length on the affected side was associated with poor acetabular development and recurrence of joint dysplasia (p = 0.01). The incidence of postoperative avascular necrosis was 7%. In a further 18%, premature physeal arrest was noted during the adolescent growth spurt (Kalamchi-MacEwen types II and III). Both of these complications were also associated with recurrence of joint dysplasia (p = 0.01). Studies with a shorter follow-up are therefore likely to underestimate the proportion of poor radiological results.


Clinical Orthopaedics and Related Research | 1991

A Method of Assessment of the Clubfoot Deformity

A. Catterall

The literature on clubfeet is inadequate because a common method language for assessing the deformity is lacking. Different severities of clubfoot deformity will give different results for a standard procedure: a less severe deformity can be corrected by limited releases, whereas a severe deformity requires radical procedures. This paper presents a language of assessment that has been used for a number of years. The importance of developing a language of assessment to be able to identify the various types of clubfoot deformity is important if the treatment of this condition is to develop within the field of pediatric orthopedics.


Journal of Bone and Joint Surgery, American Volume | 2010

Legg-Calvé-Perthes disease.

A. Catterall

Legg–Calve–Perthes disease is caused by infarction of the upper femoral epiphysis complicated by trabecular fracture and associated with a process of repair (Fig. 27.1) [1]. The infarct may be variable in extent and the disorder also varies in its outcome: at best the effects may be limited to a childhood limp which can resolve spontaneously. At worst, if the femoral head segmental collapses and subsequent deformity fails to remodel well, it may lead to shortening, stiffness, and premature hip arthritis.


Journal of Bone and Joint Surgery-british Volume | 2005

The management of avascular necrosis after slipped capital femoral epiphysis

M. M. Mullins; M. Sood; A. Hashemi-Nejad; A. Catterall

Avascular necrosis is a serious complication of slipped capital femoral epiphysis and is difficult to treat. The reported incidence varies from 3% to 47% of patients. The aims of treatment are to maintain the range of movement of the hip and to prevent collapse of the femoral head. At present there are no clear guidelines for the management of this condition and treatment can be difficult and unrewarding. We have used examination under anaesthesia and dynamic arthrography to investigate avascular necrosis and to determine the appropriate method of treatment. We present 20 consecutive cases of avascular necrosis in patients presenting with slipped capital femoral epiphysis and describe the results of treatment with a mean follow-up of over eight years (71 to 121 months). In patients who were suitable for joint preservation (14), we report a ten-year survivorship of the hip joint of 75% and a mean Harris hip score of 82 (44 to 98).


Acta Orthopaedica Scandinavica | 1984

Effects of vascular occlusion on the femoral head in growing rabbits

Paul T. Calvert; J. Kernohan; Derek C. J. Sayers; A. Catterall

Temporary vascular occlusion of the femoral head in 6-week-old rabbits was produced by a closed means in a hip spica; the hips were maintained for 24 h in the position of flexion, abduction and internal rotation. All animals developed necrosis of the capital femoral epiphysis, best seen histologically at 2 weeks, and this subsequently recovered. Despite marked histological changes only one hip developed radiographic changes.


Journal of Bone and Joint Surgery-british Volume | 2016

A protocol for the use of closed reduction in children with developmental dysplasia of the hip incorporating open psoas and adductor releases and a short-leg cast: Mid-term outcomes in 113 hips.

S. Tennant; Deborah M. Eastwood; Peter Calder; Aresh Hashemi-Nejad; A. Catterall

AIMS Our aim was to assess the effectiveness of a protocol involving a standardised closed reduction for the treatment of children with developmental dysplasia of the hip (DDH) in maintaining reduction and to report the mid-term results. METHODS A total of 133 hips in 120 children aged less than two years who underwent closed reduction, with a minimum follow-up of five years or until subsequent surgery, were included in the study. The protocol defines the criteria for an acceptable reduction and the indications for a concomitant soft-tissue release. All children were immobilised in a short- leg cast for three months. Arthrograms were undertaken at the time of closed reduction and six weeks later. Follow-up radiographs were taken at six months and one, two and five years later and at the latest follow-up. The Tönnis grade, acetabular index, Severin grade and signs of osteonecrosis were recorded. RESULTS A total of 67 hips (51%) were Tönnis grade 3/4 hips. By 12 months, 20 reductions (15%) had not been maintained, and these required open reduction. In all, 55% of these were Severin 1; the others were Severin 2, due to minor acetabular dysplasia. Of the 113 successful closed reductions, 98 hips (87%) were Severin 1. Surgery for residual DDH was offered for ten hips. Osteonecrosis was seen in 32 hips (29%) but was transient in 28. In total, two children (1.5%) had severe osteonecrosis. Bilateral dislocations were significantly more likely to fail and most Tönnis 4 hips failed. CONCLUSION Closed reduction, with concomitant adductor and psoas release when required and the use of a short leg plaster of Paris cast for three months, can produce good mid-term results in children with DDH aged less than two years. This protocol is not recommended for Tönnis 4 hips. Cite this article: Bone Joint J 2016;98-B:1548-53.


Acta Orthopaedica | 2017

Radiographic classifications in Perthes disease

Stefan Huhnstock; Svein Svenningsen; Else Merckoll; A. Catterall; Terje Terjesen; Ola Wiig

Background and purpose — Different radiographic classifications have been proposed for prediction of outcome in Perthes disease. We assessed whether the modified lateral pillar classification would provide more reliable interobserver agreement and prognostic value compared with the original lateral pillar classification and the Catterall classification. Patients and methods — 42 patients (38 boys) with Perthes disease were included in the interobserver study. Their mean age at diagnosis was 6.5 (3–11) years. 5 observers classified the radiographs in 2 separate sessions according to the Catterall classification, the original and the modified lateral pillar classifications. Interobserver agreement was analysed using weighted kappa statistics. We assessed the associations between the classifications and femoral head sphericity at 5-year follow-up in 37 non-operatively treated patients in a crosstable analysis (Gamma statistics for ordinal variables, γ). Results — The original lateral pillar and Catterall classifications showed moderate interobserver agreement (kappa 0.49 and 0.43, respectively) while the modified lateral pillar classification had fair agreement (kappa 0.40). The original lateral pillar classification was strongly associated with the 5-year radiographic outcome, with a mean γ correlation coefficient of 0.75 (95% CI: 0.61–0.95) among the 5 observers. The modified lateral pillar and Catterall classifications showed moderate associations (mean γ correlation coefficient 0.55 [95% CI: 0.38–0.66] and 0.64 [95% CI: 0.57–0.72], respectively). Interpretation — The Catterall classification and the original lateral pillar classification had sufficient interobserver agreement and association to late radiographic outcome to be suitable for clinical use. Adding the borderline B/C group did not increase the interobserver agreement or prognostic value of the original lateral pillar classification.


Journal of Bone and Joint Surgery-british Volume | 1971

THE NATURAL HISTORY OF PERTHES' DISEASE

A. Catterall


Clinical Orthopaedics and Related Research | 1981

Legg-Calvé-Perthes syndrome.

A. Catterall


Journal of Bone and Joint Surgery-british Volume | 1999

Lateral shelf acetabuloplasty in Perthes’ disease: A REVIEW AT THE END OF GROWTH

K. Daly; C. Bruce; A. Catterall

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A. Hashemi-Nejad

Royal National Orthopaedic Hospital

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C. Bruce

Royal National Orthopaedic Hospital

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H. G. Zadeh

Royal National Orthopaedic Hospital

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K. Daly

Royal National Orthopaedic Hospital

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M. J. K. Bankes

Royal National Orthopaedic Hospital

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R. E. Perry

Royal National Orthopaedic Hospital

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Aresh Hashemi-Nejad

Royal National Orthopaedic Hospital

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C. J. Coates

Royal National Orthopaedic Hospital

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Deborah M. Eastwood

Royal National Orthopaedic Hospital

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G. S. Biring

Royal National Orthopaedic Hospital

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