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The Journal of Bone & Joint Surgery British Volume
Vol. 89-B, Issue 6 | Pages 848 - 848
1 Jun 2007
Bennet GC


The Journal of Bone & Joint Surgery British Volume
Vol. 88-B, Issue 3 | Pages 380 - 381
1 Mar 2006
Sibinski M Sharma H Bennet GC

We examined differences in the rate of open reduction, operating time, length of hospital stay and outcome between two groups of children with displaced supracondylar fractures of the humerus who underwent surgery either within 12 hours of the injury or later.

There were 77 children with type-3 supracondylar fractures. Of these, in 43 the fracture was reduced and pinned within 12 hours and in 34 more than 12 hours after injury. Both groups were similar in regard to gender, age and length of follow-up. Bivariate and logistical regression analysis showed no statistical difference between the groups. The number of peri-operative complications was low and did not affect the outcome regardless of the timing of treatment.

Our study confirmed that the treatment of uncomplicated displaced supracondylar fractures of the humerus can be early or delayed. In these circumstances operations at night can be avoided.


The Journal of Bone & Joint Surgery British Volume
Vol. 87-B, Issue 7 | Pages 986 - 989
1 Jul 2005
McMurtry I Bennet GC Bradish C

We report 12 consecutive cases of vertical scapular osteotomy to correct Sprengel’s deformity, performed during a 16-year period, with a mean follow-up of 10.4 years. The mean increase in abduction of the shoulder was 53°. The cosmetic appearance improved by a mean of 1.5 levels on the Cavendish scale. Neither function nor cosmesis deteriorated with time. We recommend the procedure for correction of moderate deformities with a functional deficit.


The Journal of Bone & Joint Surgery British Volume
Vol. 83-B, Issue 1 | Pages 99 - 102
1 Jan 2001
Blyth MJG Kincaid R Craigen MAC Bennet GC

We have reviewed the incidence of bacteriologically or radiologically confirmed acute haematogenous osteomyelitis in children under 13 years of age resident in the area of the Greater Glasgow Health Board between 1990 and 1997. In this period there was a fall of 44% in the incidence of both acute and subacute osteomyelitis, mainly involving the acute form (p = 0.005). This mirrors the decline of just over 50% previously reported in the same population between 1970 and 1990. Using multiple regression analysis a decline in incidence of 0.185 cases per 100 000 population per year was calculated for the 28-year period (p > 0.001).

Staphylococcus was the most commonly isolated pathogen (70%). Only 20% of patients required surgery and there was a low rate of complications (10%). In general, patients with a subacute presentation followed a benign course and there were no complications or long-term sequelae in this group.

Haematogenous osteomyelitis in children in this area is becoming a rare disease with an annual incidence of 2.9 new cases per 100 000 population per year.


The Journal of Bone & Joint Surgery British Volume
Vol. 82-B, Issue 8 | Pages 1174 - 1176
1 Nov 2000
Bidwell JP Bennet GC Bell MJ Witherow PJ

We describe ten patients with Turner’s syndrome (karyotype 45, XO) who had leg lengthening for short stature. A high incidence of postoperative complications was encountered and many patients required intramedullary fixation as a salvage procedure. We discuss the reasons for this and highlight the differences between our findings and those of a similar series recently reported. In view of the considerable difficulties encountered, we do not recommend leg lengthening in Turner’s syndrome.


The Journal of Bone & Joint Surgery British Volume
Vol. 79-B, Issue 4 | Pages 700 - 700
1 Jul 1997
Bennet GC


The Journal of Bone & Joint Surgery British Volume
Vol. 78-B, Issue 6 | Pages 930 - 933
1 Nov 1996
Farrar MJ Bennet GC Wilson NIL Azmy A

Peripheral limb ischaemia is rare in children. We have treated only 12 infants and children with this condition in the past 15 years at the Royal Hospital for Sick Children in Glasgow.

There were nine neonates and three older children. Most were suffering from life-threatening illnesses or severe infection. Two were born with ischaemic arms with no apparent cause. We have analysed the factors leading to ischaemia, the outcome of the initial treatment and the later orthopaedic problems.

Two required amputation of both legs, one of an arm, two of feet and one of toes. Two had skin grafts. All surgery was performed after demarcation was well established and delayed closure was used after amputation.

Five children developed limb-length discrepancy or an angular deformity. To date two have required additional corrective surgery.