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		<title>BMC Musculoskeletal Disorders - Latest articles</title>
		<link>http://www.biomedcentral.com/bmcmusculoskeletdisord/</link>
		<description>The latest articles from BMC Musculoskeletal Disorders (ISSN 1471-2474) published by 
				
				BioMed Central
		</description>
        <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
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				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2474/9/107"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2474/9/106"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2474/9/105"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2474/9/104"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2474/9/103"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2474/9/102"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2474/9/101"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2474/9/100"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2474/9/99"/>			    
            
				    <rdf:li rdf:resource="http://www.biomedcentral.com/1471-2474/9/98"/>			    
            
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		<item rdf:about="http://www.biomedcentral.com/1471-2474/9/107">
            
            <title>Post-traumatic glenohumeral cartilage lesions: a systematic review</title>
			<description>Background:
Any cartilage damage to the glenohumeral joint should be avoided, as these damages may result in osteoarthritis of the shoulder. To understand the pathomechanism leading to shoulder cartilage damage, we conducted a systematic review on the subject of articular cartilage lesions caused by traumas where non impression fracture of the subchondral bone is present.
Methods:
PubMed (MEDLINE), ScienceDirect (EMBASE, BIOBASE, BIOSIS Previews) and the COCHRANE database of systematic reviews were systematically scanned using a defined search strategy to identify relevant articles in this field of research. First selection was done based on abstracts according to specific criteria, where the methodological quality in selected full text articles was assessed by two reviewers. Agreement between raters was investigated using percentage agreement and Cohen's Kappa statistic. The traumatic events were divided into two categories: 1) acute trauma which refers to any single impact situation which directly damages the articular cartilage, and 2) chronic trauma which means cartilage lesions due to overuse or disuse of the shoulder joint.
Results:
The agreement on data quality between the two reviewers was 93% with a Kappa value of 0.79 indicating an agreement considered to be 'substantial'. It was found that acute trauma on the shoulder causes humeral articular cartilage to disrupt from the underlying bone. The pathomechanism is said to be due to compression or shearing, which can be caused by a sudden subluxation or dislocation. However, such impact lesions are rarely reported. In the case of chronic trauma glenohumeral cartilage degeneration is a result of overuse and is associated to other shoulder joint pathologies. In these latter cases it is the rotator cuff which is injured first. This can result in instability and consequent impingement which may progress to glenohumeral cartilage damage.
Conclusions:
The great majority of glenohumeral cartilage lesions without any bony lesions are the results of overuse. Glenohumeral cartilage lesions with an intact subchondral bone and caused by an acute trauma are either rare or overlooked. And at increased risk for such cartilage lesions are active sportsmen with high shoulder demand or athletes prone to shoulder injury.</description>
			<link>http://www.biomedcentral.com/1471-2474/9/107</link>
			
			 	<dc:creator>Heidi Ruckstuhl, Eling D de Bruin, Edgar Stussi and Benedicte Vanwanseele</dc:creator>
			
			<dc:source>BMC Musculoskeletal Disorders 2008, 9:107</dc:source>
			<dc:date>2008-07-23</dc:date>
			<dc:identifier>doi:10.1186/1471-2474-9-107</dc:identifier>
			
			
							
					<prism:publicationName>BMC Musculoskeletal Disorders</prism:publicationName>
					
			
							
					<prism:issn>1471-2474</prism:issn>
					
			
							
					<prism:volume>9</prism:volume>
					
			
							
					<prism:startingPage>107</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-23</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2474/9/106">
            
            <title>Translation of the Neck Disability Index and validation of the Greek version in a sample of neck pain patients</title>
			<description>Background:
Neck pain is a highly prevalent condition resulting in major disability. Standard scales for measuring disability in patients with neck pain have a pivotal role in research and clinical settings. The Neck Disability Index (NDI) is a valid and reliable tool, designed to measure disability in activities of daily living due to neck pain. The purpose of our study was the translation and validation of the NDI in a Greek primary care population with neck complaints.
Methods:
The original version of the questionnaire was used. Based on international standards, the translation strategy comprised forward translations, reconciliation, backward translation and pre-testing steps. The validation procedure concerned the exploration of internal consistency (Cronbach alpha), test-retest reliability (Intraclass Correlation Coefficient), construct validity (exploratory factor analysis) and responsiveness (Spearman correlation coefficient, Standard Error of Measurement and Minimal Detectable Change) of the questionnaire. Data quality was also assessed through completeness of data and floor/ceiling effects.
Results:
The translation procedure resulted in the Greek modified version of the NDI. The latter was culturally adapted through the pre-testing phase. The validation procedure raised a large amount of missing data due to low applicability, which were assessed with two methods. Floor or ceiling effects were not observed. Cronbach alpha was calculated as 0.85, which was interpreted as good internal consistency. Intraclass correlation coefficient was found to be 0.93 (95% CI 0.84-0.97), which was considered as very good test-retest reliability. Factor analysis yielded one factor with Eigen value 4.48 explaining 44.77% of variance. The Spearman correlation coefficient (0.3;P=0.02) revealed some relation between change score in the NDI and Global Rating of Change (GROC). The SEM and MDC were calculated as 0.64 and 1.78 respectively.
Conclusions:
The Greek version of the NDI measures disability in patients with neck pain in a reliable, valid and responsive manner. It is considered a useful tool for research and clinical settings in Greek Primary Health Care.</description>
			<link>http://www.biomedcentral.com/1471-2474/9/106</link>
			
			 	<dc:creator>Marianna N Trouli, Howard T Vernon, Kyriakos N Kakavelakis, Maria D Antonopoulou, Aristofanis N Paganas and Christos D Lionis</dc:creator>
			
			<dc:source>BMC Musculoskeletal Disorders 2008, 9:106</dc:source>
			<dc:date>2008-07-22</dc:date>
			<dc:identifier>doi:10.1186/1471-2474-9-106</dc:identifier>
			
			
							
					<prism:publicationName>BMC Musculoskeletal Disorders</prism:publicationName>
					
			
							
					<prism:issn>1471-2474</prism:issn>
					
			
							
					<prism:volume>9</prism:volume>
					
			
							
					<prism:startingPage>106</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-22</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2474/9/105">
            
            <title>Effects of work ability and health promoting interventions for women with musculoskeletal symptoms: a 9-month prospective study    </title>
			<description>Background:
Women working in the public human service sector in 'overstrained' situations run the risk of musculoskeletal symptoms and long-term sick leave. In order to maintain the level of health and work ability and strengthen the potential resources for health, it is important that employees gain greater control over decisions and actions affecting their health - a process associated with the concept of self-efficacy. The aim of this study was to describe the effects of a self-efficacy intervention and an ergonomic education intervention for women with musculoskeletal symptoms, employed in the public sector. 
Methods:
The design of the study was a 9-month prospective study describing the effects of two interventions, a comprehensive self-efficacy intervention (n=21) and an ergonomic education intervention (n=21). Data were obtained by a self-report questionnaire on health- and work ability-related factors at baseline, and at ten weeks and nine months follow-up. Within-group differences over time were analysed.   
Results:
Over the time period studied there were small magnitudes of improvements within each group. Within the self-efficacy intervention group positive effects in perceived work ability were shown. The ergonomic education group showed increased positive beliefs about future work ability and a more frequent use of pain coping strategies.  
Conclusions:
Both interventions showed positive effects on women with musculoskeletal symptoms, but in different ways. Future research in this area should tailor interventions to participants' motivation and readiness to change. </description>
			<link>http://www.biomedcentral.com/1471-2474/9/105</link>
			
			 	<dc:creator>Agneta Larsson, Lena Karlqvist and Gunvor Gard</dc:creator>
			
			<dc:source>BMC Musculoskeletal Disorders 2008, 9:105</dc:source>
			<dc:date>2008-07-21</dc:date>
			<dc:identifier>doi:10.1186/1471-2474-9-105</dc:identifier>
			
			
							
					<prism:publicationName>BMC Musculoskeletal Disorders</prism:publicationName>
					
			
							
					<prism:issn>1471-2474</prism:issn>
					
			
							
					<prism:volume>9</prism:volume>
					
			
							
					<prism:startingPage>105</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-21</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2474/9/104">
            
            <title>Clinical effectiveness of post-operative splinting after surgical release of Dupuytren's contracture: a systematic review</title>
			<description>Background:
Splinting after contracture release for Dupuytren's disease of the hand is widely advocated. The purpose of this systematic review was to evaluate the quantity and quality of evidence regarding the effectiveness of splinting in the post-surgical management of Dupuytren's contractures.
Methods:
Studies were identified by searching the electronic databases Medline, AMED, CINAHL and EMBASE. Studies were included if they met the following inclusion
criteria:  prospective or retrospective, experimental, quasi-experimental or observational studies investigating the effectiveness of static or dynamic splints worn day and/or night-time for at least 6 weeks after surgery and reporting either individual joint or composite finger range of motion and/or hand function.  The methodological quality of the selected articles was independently assessed by the two authors using the guidelines for evaluating the quality of intervention studies developed by McDermid.  
Results:
Four studies, with sample sizes ranging from 23 to 268, met the inclusion criteria for the systematic review.  Designs included retrospective case review, prospective observational and one controlled trial without randomisation.  Interventions included dynamic and static splinting with a mean follow-up ranging from 9 weeks to 2 years.  Pooling of results was not possible due to the heterogeneity of interventions (splint type, duration and wearing regimen) and the way outcomes were reported. 
Conclusions:
There is empirical evidence to support the use of low load prolonged stretch through splinting after hand  surgery and trauma, however only a few studies have investigated this specifically in Dupuytren's contracture. The low level evidence regarding the effect of  post-operative static and dynamic splints on final extension deficit in severe PIP joint contracture (>40 degrees) is equivocal, as is the effect of patient adherence on outcome.  Whilst total active extension deficit improved in some patients wearing a splint there were also deficits in composite finger flexion and hand function. The lack of data on the magnitude of this effect makes it difficult to interpret whether this is of clinical significance. There is a need for well designed controlled trials with proper randomisation to evaluate the  short-term and long-term effectiveness of  splinting following Dupuytren's surgery. </description>
			<link>http://www.biomedcentral.com/1471-2474/9/104</link>
			
			 	<dc:creator>Debbie Larson and Christina Jerosch-Herold</dc:creator>
			
			<dc:source>BMC Musculoskeletal Disorders 2008, 9:104</dc:source>
			<dc:date>2008-07-21</dc:date>
			<dc:identifier>doi:10.1186/1471-2474-9-104</dc:identifier>
			
			
							
					<prism:publicationName>BMC Musculoskeletal Disorders</prism:publicationName>
					
			
							
					<prism:issn>1471-2474</prism:issn>
					
			
							
					<prism:volume>9</prism:volume>
					
			
							
					<prism:startingPage>104</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-21</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2474/9/103">
            
            <title>Factor structure of the Shoulder Pain and Disability Index in patients with adhesive capsulitis</title>
			<description>Background:
The Shoulder Pain and Disability Index (SPADI) is a self-administered questionnaire that aims to measure pain and disability associated with shoulder disease. It consists of a pain section and a disability section with 13 items being responded to on visual analogue scales. Few researchers have investigated SPADI validity in specified diagnostic groups, although the selection of an evaluative instrument should be based on evidence of validity in the target patient group. The aim of the present study was to investigate factor structure of the SPADI in a study population of patients with adhesive capsulitis.
Methods:
The questionnaire was administered to 191 patients with adhesive capsulitis. Descriptive statistics for items and a comparison of scores for the two subscales were produced. Internal consistency was analyzed by use of the Cronbach alpha and a principal components analysis with varimax rotation was conducted. Study design was cross-sectional.
Results:
Two factors were extracted, but the factor structure failed to support the original division of items into separate pain and disability sections.
Conclusions:
We found minimal evidence to justify the use of separate subscales for pain and disability. It is our impression that the SPADI should be viewed as essentially unidimensional in patients with adhesive capsulitis.</description>
			<link>http://www.biomedcentral.com/1471-2474/9/103</link>
			
			 	<dc:creator>Einar Kristian Tveita, Leiv Sandvik, Ole Marius Ekeberg, Niels Gunnar Juel and Erik Bautz-Holter</dc:creator>
			
			<dc:source>BMC Musculoskeletal Disorders 2008, 9:103</dc:source>
			<dc:date>2008-07-17</dc:date>
			<dc:identifier>doi:10.1186/1471-2474-9-103</dc:identifier>
			
			
							
					<prism:publicationName>BMC Musculoskeletal Disorders</prism:publicationName>
					
			
							
					<prism:issn>1471-2474</prism:issn>
					
			
							
					<prism:volume>9</prism:volume>
					
			
							
					<prism:startingPage>103</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-17</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2474/9/102">
            
            <title>Prevalence of widespread pain and associations with work status - a population study
</title>
			<description>Background:
This population study based on a representative sample from a Swedish county investigates the prevalence, duration, and determinants of widespread pain (WSP) in the population using two constructs and estimates how WSP affects work status. In addition, this study investigates the prevalence of widespread pain and its relationship to pain intensity, gender, age, income, work status, citizenship, civil status, urban residence, and health care seeking. 
Methods:
A cross-sectional survey using a postal questionnaire was sent to a representative sample (n = 9952) of the target population (284,073 people, 18-74 years) in a county (Ostergotland) in the southern Sweden. The questionnaire was mailed and followed by two postal reminders when necessary. 
Results:
The participation rate was 76.7% (n = 7637); the non-participants were on the average younger, earned less money, and male. Women had higher prevalences of pain in 10 different predetermined anatomical regions. WSP was generally chronic (90-94%) and depending on definition of WSP the prevalence varied between 4.8-7.4% in the population. Women had significantly higher prevalence of WSP than men and the age effect appeared to be stronger in women than in men. WSP was a significant negative factor - together with age 50-64 years, low annual income, and non-Nordic citizen - for work status in the community and in the group with chronic pain. Chronic pain but not the spreading of pain was related to health care seeking in the population. 
Conclusion:
This study confirms earlier studies that report high prevalences of widespread pain in the population and especially among females and with increasing age. Widespread pain is associated with prominent effects on work status.</description>
			<link>http://www.biomedcentral.com/1471-2474/9/102</link>
			
			 	<dc:creator>Bjorn Gerdle, Jonas Bjork, Lars Coster, K-g Henriksson, Chris Henriksson and Ann Bengtsson</dc:creator>
			
			<dc:source>BMC Musculoskeletal Disorders 2008, 9:102</dc:source>
			<dc:date>2008-07-15</dc:date>
			<dc:identifier>doi:10.1186/1471-2474-9-102</dc:identifier>
			
			
							
					<prism:publicationName>BMC Musculoskeletal Disorders</prism:publicationName>
					
			
							
					<prism:issn>1471-2474</prism:issn>
					
			
							
					<prism:volume>9</prism:volume>
					
			
							
					<prism:startingPage>102</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-15</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2474/9/101">
            
            <title>The effect on the extracellular matrix of the deep fascia in response to leg lengthening</title>
			<description>Background:
Whereas the alterations of diverse tissues in cellular and molecular levels have been investigated during leg lengthening via microscopy and biochemical studies, little is known about the response of deep fascia. This study aims to investigate the changes of the extracellular matrix in deep fascia in response to leg lengthening.
Methods:
Animal model of leg lengthening was established in New Zealand white rabbits. Distraction was initiated at a rate of 1 mm/day and 2 mm/day in two steps, and preceded until increases of 10% and 20% in the initial length of tibia had been achieved. Alcian blue stain and picrosirius-polarization method were used for the study of the extracellular matrix of deep fascia samples. Leica DM LA image analysis system was used to investigate the quantitative changes of collagen type I and III.
Results:
Alcian blue stain showed that glycosaminoglycans of fascia of each group were composed of chondroitin sulphate and heparin sulphate, but not of keratan sulphate. Under the polarization microscopy, the fascia consisted mainly of collagen type I. After leg lengthening, the percentage of collagen type III increased. The most similar collagen composition of the fascia to that of the normal fascia was detected at a 20% increase in tibia length achieved via a distraction rate of 1 mm/d.
Conclusion:
The changes in collagen distribution and composition occur in deep fascia during leg lengthening. Although different lengthening schemes resulted in varied matrix changes, the most comparable collagen composition to be demonstrated under the scheme of a distraction rate of 1 mm/day and 20% increase in tibia length. Efficient fascia regeneration is initiated only in certain combinations of the leg load parameters including appropriate intensity and duration time, e.g., either low density distraction that persist a relatively short time or high distraction rates.</description>
			<link>http://www.biomedcentral.com/1471-2474/9/101</link>
			
			 	<dc:creator>Hai-Qiang Wang, Xin-Kui Li, Zi-Xiang Wu, Yi-Yong Wei and Zhuo-Jing Luo</dc:creator>
			
			<dc:source>BMC Musculoskeletal Disorders 2008, 9:101</dc:source>
			<dc:date>2008-07-09</dc:date>
			<dc:identifier>doi:10.1186/1471-2474-9-101</dc:identifier>
			
			
							
					<prism:publicationName>BMC Musculoskeletal Disorders</prism:publicationName>
					
			
							
					<prism:issn>1471-2474</prism:issn>
					
			
							
					<prism:volume>9</prism:volume>
					
			
							
					<prism:startingPage>101</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-09</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2474/9/100">
            
            <title>Ipsilateral free semitendinosus tendon graft transfer for reconstruction of chronic tears of the Achilles tendon</title>
			<description>Background:
Many techniques have been developed for the reconstruction of the Achilles tendon in chronic tears. In presence of a large gap (greater than 6 centimetres), tendon augmentation is required.
Methods:
We present our method of minimally invasive semitendinosus reconstruction for the Achilles tendon using one para-midline and one midline incision.
Results:
The first incision is a 5 cm longitudinal incision, made 2 cm proximal and just medial to the palpable end of the residual tendon. The second incision is 3 cm long and is also longitudinal but is 2 cm distal and in the midline to the distal end of the tendon rupture. The distal and proximal Achilles tendon stumps are mobilised. After trying to reduce the gap of the ruptured Achilles tendon, if the gap produced is greater than 6 cm despite maximal plantar flexion of the ankle and traction on the Achilles tendon stumps, the ipsilateral semitendinosus tendon is harvested. The semitendinosus tendon is passed through small incisions in the substance of the proximal stump of the Achilles tendon, and it is sutured to the Achilles tendon. It is then passed beneath the intact skin bridge into the distal incision, and passed from medial to lateral through a transverse tenotomy in the distal stump. With the ankle in maximal plantar flexion, the semitendinosus tendon is sutured to the Achilles tendon at each entry and exit point
Conclusion:
This minimally invasive technique allows reconstruction of the Achilles tendon using the tendon of semitendinosus preserving skin integrity over the site most prone to wound breakdown, and can be especially used to reconstruct the Achilles tendon in the presence of large gap (greater than 6 centimetres).</description>
			<link>http://www.biomedcentral.com/1471-2474/9/100</link>
			
			 	<dc:creator>Nicola Maffulli, Umile Giuseppe Longo, Nikolaos Gougoulias and Vincenzo Denaro</dc:creator>
			
			<dc:source>BMC Musculoskeletal Disorders 2008, 9:100</dc:source>
			<dc:date>2008-07-08</dc:date>
			<dc:identifier>doi:10.1186/1471-2474-9-100</dc:identifier>
			
			
							
					<prism:publicationName>BMC Musculoskeletal Disorders</prism:publicationName>
					
			
							
					<prism:issn>1471-2474</prism:issn>
					
			
							
					<prism:volume>9</prism:volume>
					
			
							
					<prism:startingPage>100</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-08</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2474/9/99">
            
            <title>Muscle performance and ankle joint mobility in long-term patients with diabetes</title>
			<description>Background:
Long-term patients with diabetes and peripheral neuropathy show altered foot biomechanics and abnormal foot loading. This study aimed at assessing muscle performance and ankle mobility in such patients under controlled conditions.
Methods:
Forty six long-term diabetes patients with (DN) and without (D) peripheral neuropathy, and 21 controls (C) were examined. Lower leg muscle performance and ankle mobility were assessed by means of a dedicated equipment, with the patient seated and the examined limb unloaded. 3D active ranges of motion and moments of force were recorded, the latter during maximal isometric contractions, with the foot blocked in different positions.
Results:
All patients showed reduced ankle mobility. In the sagittal and transversal planes reduction vs C was 11% and 20% for D, 20% and 21% for DN, respectively.Dorsal-flexing moments were significantly reduced in all patients and foot positions, the highest reduction being 28% for D and 37% for DN. Reductions of plantar-flexing moments were in the range 12&#8211;15% for D (only with the foot blocked in neutral and in dorsal-flexed position), and in the range 10&#8211;24% for DN. In all patients, reductions in the frontal and transversal planes ranged 14&#8211;41%.
Conclusion:
The investigation revealed ankle functional impairments in patients with diabetes, with or without neuropathy, thus suggesting that other mechanisms besides neuropathy might contribute to alter foot-ankle biomechanics. Such impairments may then play a role in the development of abnormal gait and in the onset of plantar ulcers.</description>
			<link>http://www.biomedcentral.com/1471-2474/9/99</link>
			
			 	<dc:creator>Claudia Giacomozzi, Emanuela D'Ambrogi, Stefano Cesinaro, Velio Macellari and Luigi Uccioli</dc:creator>
			
			<dc:source>BMC Musculoskeletal Disorders 2008, 9:99</dc:source>
			<dc:date>2008-07-04</dc:date>
			<dc:identifier>doi:10.1186/1471-2474-9-99</dc:identifier>
			
			
							
					<prism:publicationName>BMC Musculoskeletal Disorders</prism:publicationName>
					
			
							
					<prism:issn>1471-2474</prism:issn>
					
			
							
					<prism:volume>9</prism:volume>
					
			
							
					<prism:startingPage>99</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-04</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.biomedcentral.com/1471-2474/9/98">
            
            <title>Tibial tubercle osteotomy for access during revision knee arthroplasty: Ethibond suture repair technique</title>
			<description>Background:
Tibial Tubercle Osteotomy has shown much promise in revision total knee replacement. Methods of repair previously described include screw and wire fixation. Both methods have significant complications.
Methods:
This article describes suture fixation of the osteotomy using Ethibond sutures placed medially with a lateral periosteal hinge.
Results:
This method of fixation relies upon an adequate osteotomy segment including the entire insertion of the patella tendon. The lateral periosteal hinge is maintained and adds to the stability of the construct. A minimum of two number 5 Ethibond sutures are passed medially through drill holes to secure the osteotomy segment. No post-operative immobilisation is required.
Conclusion:
Ethibond sutures provide adequate fixation of the tibial tubercle osteotomy segment in revision knee arthroplasty with reduced risk of complication as compared to conventional fixation methods.</description>
			<link>http://www.biomedcentral.com/1471-2474/9/98</link>
			
			 	<dc:creator>Crawford R Deane, Nicholas A Ferran, Adel Ghandour and Rhidian L Morgan-Jones</dc:creator>
			
			<dc:source>BMC Musculoskeletal Disorders 2008, 9:98</dc:source>
			<dc:date>2008-06-30</dc:date>
			<dc:identifier>doi:10.1186/1471-2474-9-98</dc:identifier>
			
			
							
					<prism:publicationName>BMC Musculoskeletal Disorders</prism:publicationName>
					
			
							
					<prism:issn>1471-2474</prism:issn>
					
			
							
					<prism:volume>9</prism:volume>
					
			
							
					<prism:startingPage>98</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-06-30</prism:publicationDate>
					

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