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<title>Journal of Bone and Joint Surgery - British Volume Children's Orthopaedics</title>
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<title>Journal of Bone and Joint Surgery - British Volume</title>
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<link>http://www.jbjs.org.uk</link>
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<title><![CDATA[[Children's Orthopaedics] Operative treatment of congenital torticollis]]></title>
<link>http://www.jbjs.org.uk/cgi/content/short/90-B/7/934?rss=1</link>
<description><![CDATA[
<p>There were 47 patients with congenital muscular torticollis who underwent operative release. After a mean follow-up of 74 months (60 to 90), they were divided into two groups, one aged one to four years (group 1) and the other aged five to 16 years (group 2). The outcomes were assessed by evaluating the following parameters: deficits of lateral flexion and rotation, craniofacial asymmetry, surgical scarring, residual contracture, subjective evaluation and degree of head tilt.</p>
<p>The craniofacial asymmetry, residual contracture, subjective evaluation and overall scores were similar in both groups. However, group 2 showed superior results to group 1 in terms of the deficits of movement, surgical scarring and degree of head tilt.</p>
<p>It is recommended that operative treatment for congenital muscular torticollis is postponed until the patient can comply successfully with post-operative bracing and an exercise programme.</p>
]]></description>
<dc:creator><![CDATA[Shim, J. S., Jang, H. P.]]></dc:creator>
<dc:date>2008-06-30</dc:date>
<dc:identifier>info:doi/10.1302/0301-620X.90B7.20339</dc:identifier>
<dc:title><![CDATA[[Children's Orthopaedics] Operative treatment of congenital torticollis]]></dc:title>
<dc:publisher>British Editorial Society of Bone and Joint Surgery</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>90-B</prism:volume>
<prism:endingPage>939</prism:endingPage>
<prism:publicationDate>2008-07-01</prism:publicationDate>
<prism:startingPage>934</prism:startingPage>
<prism:section>Children's Orthopaedics</prism:section>
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<title><![CDATA[[Children's Orthopaedics] Perthes' disease: PROGNOSIS IN CHILDREN UNDER SIX YEARS OF AGE]]></title>
<link>http://www.jbjs.org.uk/cgi/content/short/90-B/7/940?rss=1</link>
<description><![CDATA[
<p>Children presenting with Perthes&rsquo; disease before their sixth birthday are considered to have a good prognosis. We describe 166 hips in children in this age group. The mean age at onset of the disease was 44 months (22 to 72). Mild forms (Catterall I and II) were treated conservatively and severe forms (Catterall III and IV) either conservatively or operatively. The aim of the former treatment was to restrict weight-bearing. Operative treatment consisted of innominate osteotomy and was indicated by a Conway type-B appearance on the bone scan. All the patients were followed to skeletal maturity with a mean follow-up of 11 years (8 to 15).</p>
<p>The end results were evaluated radiologically using the classifications of Stulberg and Mose. A total of 50 hips were Catterall grade-I or grade-II, 65 Catterall grade-III and 51 Catterall grade-IV. All hips with mild disease had a good result at skeletal maturity. Of the hips with severe disease 78 (67.3%) had good (Stulberg I and II), 26 (22.4%) fair (Stulberg III) and 12 (10.3%) poor results (Stulberg IV and V). Of the Catterall grade-III hips 38 were treated conservatively of which 31 (81.6%) had a good result, six (15.8%) a fair and one (2.6%) a poor result. Operative treatment was carried out on 27 Catterall grade-III hips, of which 21 (77.8%) had a good, four (14.8%) a fair and two (7.4%) a poor result. By comparison conservative treatment of 19 Catterall grade-IV hips led to ten (52.7%) good, seven (36.8%) fair and two (10.5%) poor results. Operative treatment was carried out on 32 Catterall grade-IV hips, of which 16 (50.0%) had a good, nine (28.1%) a fair and seven (21.9%) a poor result.</p>
<p>We confirm that the prognosis in Perthes&rsquo; disease is generally good when the age at onset is less than six years. In severe disease there is no significant difference in outcome after conservative or operative treatment (p &gt; 0.05). Catterall grade-III hips had a better outcome according to the Stulberg and Mose criteria than Catterall grade-IV hips, regardless of the method of treatment.</p>
]]></description>
<dc:creator><![CDATA[Canavese, F., Dimeglio, A.]]></dc:creator>
<dc:date>2008-06-30</dc:date>
<dc:identifier>info:doi/10.1302/0301-620X.90B7.20691</dc:identifier>
<dc:title><![CDATA[[Children's Orthopaedics] Perthes' disease: PROGNOSIS IN CHILDREN UNDER SIX YEARS OF AGE]]></dc:title>
<dc:publisher>British Editorial Society of Bone and Joint Surgery</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>90-B</prism:volume>
<prism:endingPage>945</prism:endingPage>
<prism:publicationDate>2008-07-01</prism:publicationDate>
<prism:startingPage>940</prism:startingPage>
<prism:section>Children's Orthopaedics</prism:section>
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<title><![CDATA[[Children's Orthopaedics] The outcome of surgical intervention for early deformity in young ambulant children with bilateral spastic cerebral palsy]]></title>
<link>http://www.jbjs.org.uk/cgi/content/short/90-B/7/946?rss=1</link>
<description><![CDATA[
<p>We reviewed the outcome in 24 children with bilateral spastic cerebral palsy aged seven years or younger for whom surgery was recommended between 1999 and 2005 following gait analysis. A total of 13 children (operative group) had surgery and the remaining 11 (control group) did not, for family or administrative reasons. The operative group had at least two post-operative gait analyses at yearly intervals, with eight children having a third and six children a fourth. The control group had a second analysis after a mean interval of 1.5 years (95% confidence interval 1.1 to 1.9). In the operative group, the Gillette gait index, the ranges of movement in the lower limb joint and knee extension in stance improved following surgery, and this was maintained overall at the second post-operative analysis. The minimum knee flexion in stance in the control group increased between analyses.</p>
<p>These results suggest that surgical intervention in selected children can result in improvements in gait and function in the short to medium term compared with non-operative management.</p>
]]></description>
<dc:creator><![CDATA[Gough, M., Schneider, P., Shortland, A. P.]]></dc:creator>
<dc:date>2008-06-30</dc:date>
<dc:identifier>info:doi/10.1302/0301-620X.90B7.20577</dc:identifier>
<dc:title><![CDATA[[Children's Orthopaedics] The outcome of surgical intervention for early deformity in young ambulant children with bilateral spastic cerebral palsy]]></dc:title>
<dc:publisher>British Editorial Society of Bone and Joint Surgery</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>90-B</prism:volume>
<prism:endingPage>951</prism:endingPage>
<prism:publicationDate>2008-07-01</prism:publicationDate>
<prism:startingPage>946</prism:startingPage>
<prism:section>Children's Orthopaedics</prism:section>
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<title><![CDATA[[Children's Orthopaedics] Callus distraction for humeral nonunion with bone loss and limb shortening caused by chronic osteomyelitis]]></title>
<link>http://www.jbjs.org.uk/cgi/content/short/90-B/6/795?rss=1</link>
<description><![CDATA[
<p>Nonunion of the humerus with bone loss and shortening due to osteomyelitis is rare but difficult to treat. We describe our experience with a callus distraction technique using a monolateral external fixator for the treatment of this condition.</p>
<p>Between October 1994 and January 2004, 11 patients were treated. There were seven males and four females, with a mean age of 14 years (10 to 17). The mean bone loss was 1.9 cm (1 to 2.7) and the mean length discrepancy in the upper limb was 5.6 cm (3.5 to 8.0).</p>
<p>The mean follow-up was for 106 months (54 to 166). The mean external fixation index was 34.8 days/cm (29.8 to 40.5). The mean lengthening was 9.5 cm (5.5 to 13.4). There were seven excellent results, three good and one poor. There were nine excellent functional results and two good.</p>
<p>The treatment of humeral nonunion with bone loss and shortening due to osteomyelitis by callus distraction is a safe and effective means of improving function and cosmesis.</p>
]]></description>
<dc:creator><![CDATA[Liu, T., Zhang, X., Li, Z., Zeng, W., Peng, D., Sun, C.]]></dc:creator>
<dc:date>2008-06-06</dc:date>
<dc:identifier>info:doi/10.1302/0301-620X.90B6.20392</dc:identifier>
<dc:title><![CDATA[[Children's Orthopaedics] Callus distraction for humeral nonunion with bone loss and limb shortening caused by chronic osteomyelitis]]></dc:title>
<dc:publisher>British Editorial Society of Bone and Joint Surgery</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>90-B</prism:volume>
<prism:endingPage>800</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>795</prism:startingPage>
<prism:section>Children's Orthopaedics</prism:section>
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<item rdf:about="http://www.jbjs.org.uk/cgi/content/short/90-B/6/801?rss=1">
<title><![CDATA[[Children's Orthopaedics] Is there a role for lengthening flexor hallucis and flexor digitorum longus tendons in surgery for club foot?: A PRELIMINARY REPORT]]></title>
<link>http://www.jbjs.org.uk/cgi/content/short/90-B/6/801?rss=1</link>
<description><![CDATA[
<p>Most cases of club foot (congenital talipes equinovarus) respond to non-operative treatment but resistant cases may need surgery. It is broadly accepted that lengthening of tendo Achillis, the tendon of tibialis posterior and capsulotomy of the ankle and subtalar joints are necessary during surgical release, but there is no consensus as to whether lengthening of the tendons of flexor hallucis longus and flexor digitorum longus is required.</p>
<p>We randomised 13 children with severe bilateral club foot deformities to undergo lengthening of the flexor hallucis longus and flexor digitorum longus tendons on one side and simple decompression on the other. We found no difference in the deformities of the toes between the lengthened and non-lengthened sides at a mean follow-up of four years (2 to 6).</p>
<p>We conclude that routine lengthening of the tendons of flexor hallucis longus and flexor digitorum longus during soft-tissue surgery for resistant club foot is not necessary.</p>
]]></description>
<dc:creator><![CDATA[Lahoti, O., Bajaj, S.]]></dc:creator>
<dc:date>2008-06-06</dc:date>
<dc:identifier>info:doi/10.1302/0301-620X.90B6.19727</dc:identifier>
<dc:title><![CDATA[[Children's Orthopaedics] Is there a role for lengthening flexor hallucis and flexor digitorum longus tendons in surgery for club foot?: A PRELIMINARY REPORT]]></dc:title>
<dc:publisher>British Editorial Society of Bone and Joint Surgery</dc:publisher>
<prism:number>6</prism:number>
<prism:volume>90-B</prism:volume>
<prism:endingPage>802</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>801</prism:startingPage>
<prism:section>Children's Orthopaedics</prism:section>
</item>

<item rdf:about="http://www.jbjs.org.uk/cgi/content/short/90-B/5/657?rss=1">
<title><![CDATA[[Children's Orthopaedics] The assessment of the ulnar nerve at the elbow by ultrasonography in children]]></title>
<link>http://www.jbjs.org.uk/cgi/content/short/90-B/5/657?rss=1</link>
<description><![CDATA[
<p>We evaluated the morphological changes to the ulnar nerve of both elbows in the cubital tunnel by sonography in a total of 237 children, of whom 117 were aged between six and seven years, 66 between eight and nine years, and 54 between ten and 11 years. We first scanned longitudinally in the extended elbow and then transversely at the medial epicondyle with the elbow extended to 0&deg;. We repeated the scans with the elbow flexed at 45&deg;, 90&deg;, and 120&deg;. There were no significant differences in the area of the ulnar nerve, but the diameter increased as the elbow moved from extension to flexion in all groups. More importantly, the ulnar nerve was subluxated anteriorly on to the medial epicondyle by 1.5% to 1.9% in extended elbows, by 5.9% to 7.9% in those flexed to 45&deg;, by 40.0% to 44% in those flexed to 90&deg;, and by 57.4% to 58.1% in those flexed to 120&deg;, depending on the age group. Sonography clearly and accurately showed the ulnar nerve and was useful for localising the nerve before placing a medial pin. Because the ulnar nerve may translate anteriorly onto the medial epicondyle when the elbow is flexed to 90&deg; or more, it should never be overlooked during percutaneous medial pinning.</p>
]]></description>
<dc:creator><![CDATA[Shen, P.-C., Chern, T.-C., Wu, K.-C., Tai, T.-W., Jou, I.-M.]]></dc:creator>
<dc:date>2008-04-30</dc:date>
<dc:identifier>info:doi/10.1302/0301-620X.90B5.19820</dc:identifier>
<dc:title><![CDATA[[Children's Orthopaedics] The assessment of the ulnar nerve at the elbow by ultrasonography in children]]></dc:title>
<dc:publisher>British Editorial Society of Bone and Joint Surgery</dc:publisher>
<prism:number>5</prism:number>
<prism:volume>90-B</prism:volume>
<prism:endingPage>661</prism:endingPage>
<prism:publicationDate>2008-05-01</prism:publicationDate>
<prism:startingPage>657</prism:startingPage>
<prism:section>Children's Orthopaedics</prism:section>
</item>

<item rdf:about="http://www.jbjs.org.uk/cgi/content/short/90-B/4/488?rss=1">
<title><![CDATA[[Children's Orthopaedics] Refracture after Ilizarov osteosynthesis in atrophic-type congenital pseudarthrosis of the tibia]]></title>
<link>http://www.jbjs.org.uk/cgi/content/short/90-B/4/488?rss=1</link>
<description><![CDATA[
<p>We investigated patterns of refracture and their risk factors in patients with congenital pseudarthrosis of the tibia after Ilizarov osteosynthesis. We studied 43 cases in 23 patients. Temporal and spatial patterns of refracture and refracture-free survival were analysed in each case. The refracture-free rate of cumulative survival was 47% at five years and did not change thereafter. Refracture occurred at the previous pseudarthrosis in 16 of 19 cases of refracture. The risk of refracture was significantly higher when osteosynthesis was performed below the age of four years, when the tibial cross-sectional area was narrow, and when associated with persistent fibular pseudarthrosis. Refracture occurs frequently after successful osteosynthesis in these patients. Delaying osteosynthesis, maximising the tibial cross-sectional area and stabilising the fibula may reduce the risk of refracture.</p>
]]></description>
<dc:creator><![CDATA[Cho, T.-J., Choi, I. H., Lee, S. M., Chung, C. Y., Yoo, W. J., Lee, D. Y., Lee, J. W.]]></dc:creator>
<dc:date>2008-03-31</dc:date>
<dc:identifier>info:doi/10.1302/0301-620X.90B4.20153</dc:identifier>
<dc:title><![CDATA[[Children's Orthopaedics] Refracture after Ilizarov osteosynthesis in atrophic-type congenital pseudarthrosis of the tibia]]></dc:title>
<dc:publisher>British Editorial Society of Bone and Joint Surgery</dc:publisher>
<prism:number>4</prism:number>
<prism:volume>90-B</prism:volume>
<prism:endingPage>493</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>488</prism:startingPage>
<prism:section>Children's Orthopaedics</prism:section>
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