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<title>Department of Orthopaedic Surgery Faculty Papers</title>
<copyright>Copyright (c) 2013 Thomas Jefferson University All rights reserved.</copyright>
<link>http://jdc.jefferson.edu/orthofp</link>
<description>Recent documents in Department of Orthopaedic Surgery Faculty Papers</description>
<language>en-us</language>
<lastBuildDate>Fri, 22 Feb 2013 17:17:56 PST</lastBuildDate>
<ttl>3600</ttl>








<item>
<title>Ulnar tunnel syndrome.</title>
<link>http://jdc.jefferson.edu/orthofp/43</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/43</guid>
<pubDate>Thu, 01 Nov 2012 11:49:19 PDT</pubDate>
<description>
	<![CDATA[
	<p>Ulnar tunnel syndrome could be broadly defined as a compressive neuropathy of the ulnar nerve at the level of the wrist. The ulnar tunnel, or Guyon's canal, has a complex and variable anatomy. Various factors may precipitate the onset of ulnar tunnel syndrome. Patient presentation depends on the anatomic zone of ulnar nerve compression: zone I compression, motor and sensory signs and symptoms; zone II compression, isolated motor deficits; and zone III compression; purely sensory deficits. Conservative treatment such as activity modification may be helpful, but often, surgical exploration of the ulnar tunnel with subsequent ulnar nerve decompression is indicated.</p>

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</description>

<author>Abdo Bachoura et al.</author>


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<item>
<title>Does the load-sharing classification predict ligamentous injury, neurological injury, and the need for surgery in patients with thoracolumbar burst fractures?: Clinical article.</title>
<link>http://jdc.jefferson.edu/orthofp/42</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/42</guid>
<pubDate>Wed, 03 Oct 2012 07:51:55 PDT</pubDate>
<description>
	<![CDATA[
	<p>OBJECT: The load-sharing score (LSS) of vertebral body comminution is predictive of results after short-segment posterior instrumentation of thoracolumbar burst fractures. Some authors have posited that an LSS > 6 is predictive of neurological injury, ligamentous injury, and the need for surgical intervention. However, the authors of the present study hypothesized that the LSS does not predict ligamentous or neurological injury.</p>
<p>METHODS: The prospectively collected spinal cord injury database from a single institution was queried for thoracolumbar burst fractures. Study inclusion criteria were acute (< 24 hours) burst fractures between T-10 and L-2 with preoperative CT and MRI. Flexion-distraction injuries and pathological fractures were excluded. Four experienced spine surgeons determined the LSS and posterior ligamentous complex (PLC) integrity. Neurological status was assessed from a review of the medical records.</p>
<p>RESULTS: Forty-four patients were included in the study. There were 4 patients for whom all observers assigned an LSS > 6, recommending operative treatment. Eleven patients had LSSs ≤ 6 across all observers, suggesting that nonoperative treatment would be appropriate. There was moderate interobserver agreement (0.43) for the overall LSS and fair agreement (0.24) for an LSS > 6. Correlations between the LSS and the PLC score averaged 0.18 across all observers (range -0.02 to 0.34, p value range 0.02-0.89). Correlations between the LSS and the American Spinal Injury Association motor score averaged -0.12 across all observers (range -0.25 to -0.03, p value range 0.1-0.87). Correlations describing the relationship between an LSS > 6 and the treating physician's decision to operate averaged 0.17 across all observers (range 0.11-0.24, p value range 0.12-0.47).</p>
<p>CONCLUSIONS: The LSS does not uniformly correlate with the PLC injury, neurological status, or empirical clinical decision making. The LSSs of only one observer correlated significantly with PLC injury. There were no significant correlations between the LSS as determined by any observer and neurological status or clinical decision making.</p>

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</description>

<author>Kristen Radcliff et al.</author>


<category>Adult</category>

<category>Decision Making</category>

<category>Female</category>

<category>Humans</category>

<category>Ligaments</category>

<category>Lumbar Vertebrae</category>

<category>Male</category>

<category>Middle Aged</category>

<category>Neurologic Examination</category>

<category>Predictive Value of Tests</category>

<category>Retrospective Studies</category>

<category>Spinal Fractures</category>

<category>Spinal Fusion</category>

<category>Thoracic Vertebrae</category>

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<title>Duration of symptoms resulting from lumbar disc herniation: effect on treatment outcomes: analysis of the Spine Patient Outcomes Research Trial (SPORT).</title>
<link>http://jdc.jefferson.edu/orthofp/41</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/41</guid>
<pubDate>Tue, 25 Sep 2012 08:48:33 PDT</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: The purpose of the present study was to determine if the duration of symptoms affects outcomes following the treatment of intervertebral lumbar disc herniation.</p>
<p>METHODS: An as-treated analysis was performed on patients enrolled in the Spine Patient Outcomes Research Trial (SPORT) for the treatment of intervertebral lumbar disc herniation. Randomized and observational cohorts were combined. A comparison was made between patients who had had symptoms for six months or less (n = 927) and those who had had symptoms for more than six months (n = 265). Primary and secondary outcomes were measured at baseline and at regular follow-up intervals up to four years. The treatment effect for each outcome measure was determined at each follow-up period for the duration of symptoms for both groups.</p>
<p>RESULTS: At all follow-up intervals, the primary outcome measures were significantly worse in patients who had had symptoms for more than six months prior to treatment, regardless of whether the treatment was operative or nonoperative. When the values at the time of the four-year follow-up were compared with the baseline values, patients in the operative treatment group who had had symptoms for six months or less had a greater increase in the bodily pain domain of the Short Form-36 (SF-36) (mean change, 48.3 compared with 41.9; p < 0.001), a greater increase in the physical function domain of the SF-36 (mean change, 47.7 compared with 41.2; p < 0.001), and a greater decrease in the Oswestry Disability Index score (mean change, -41.1 compared with -34.6; p < 0.001) as compared with those who had had symptoms for more than six months (with higher scores indicating less severe symptoms on the SF-36 and indicating more severe symptoms on the Oswestry Disability Index). When the values at the time of the four-year follow-up were compared with the baseline values, patients in the nonoperative treatment group who had had symptoms for six months or less had a greater increase in the bodily pain domain of the SF-36 (mean change, 31.8 compared with 21.4; p < 0.001), a greater increase in the physical function domain of the SF-36 (mean change, 29.5 compared with 22.6; p = 0.015), and a greater decrease in the Oswestry Disability Index score (mean change, -24.9 compared with -18.5; p = 0.006) as compared with those who had had symptoms for more than six months. Differences in treatment effect between the two groups related to the duration of symptoms were not significant.</p>
<p>CONCLUSIONS: Increased symptom duration due to lumbar disc herniation is related to worse outcomes following both operative and nonoperative treatment. The relative increased benefit of surgery compared with nonoperative treatment was not dependent on the duration of the symptoms.</p>

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</description>

<author>Jeffrey A Rihn et al.</author>


<category>Adult</category>

<category>Aged</category>

<category>Disability Evaluation</category>

<category>Diskectomy</category>

<category>Female</category>

<category>Follow-Up Studies</category>

<category>Humans</category>

<category>Intervertebral Disc Displacement</category>

<category>Lumbar Vertebrae</category>

<category>Male</category>

<category>Middle Aged</category>

<category>Pain Measurement</category>

<category>Patient Satisfaction</category>

<category>Physical Therapy Modalities</category>

<category>Severity of Illness Index</category>

<category>Time Factors</category>

<category>Treatment Outcome</category>

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<item>
<title>The Impact of Epidural Steroid Injections on the Outcomes of Patients Treated for Lumbar Disc Herniation: A Subgroup Analysis of the SPORT Trial.</title>
<link>http://jdc.jefferson.edu/orthofp/40</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/40</guid>
<pubDate>Tue, 25 Sep 2012 08:38:37 PDT</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: The Spine Patient Outcomes Research Trial (SPORT) is a prospective, multicenter study of operative versus nonoperative treatment of lumbar intervertebral disc herniation. It has been suggested that epidural steroid injections may help improve patient outcomes and lower the rate of crossover to surgical treatment.</p>
<p>METHODS: One hundred and fifty-four patients included in the intervertebral disc herniation arm of the SPORT who had received an epidural steroid injection during the first three months of the study and no injection prior to the study (the ESI group) were compared with 453 patients who had not received an injection during the first three months of the study or prior to the study (the No-ESI group).</p>
<p>RESULTS: There was a significant difference in the preference for surgery between groups (19% in the ESI group compared with 56% in the No-ESI group, p < 0.001). There was no difference in primary or secondary outcome measures at four years between the groups. A higher percentage of patients changed from surgical to nonsurgical treatment in the ESI group (41% versus 12% in the No-ESI, p < 0.001).</p>
<p>CONCLUSIONS: Patients with lumbar disc herniation treated with epidural steroid injection had no improvement in short or long-term outcomes compared with patients who were not treated with epidural steroid injection. There was a higher prevalence of crossover to nonsurgical treatment among surgically assigned ESI-group patients, although this was confounded by the increased baseline desire to avoid surgery among patients in the ESI group. Given these data, we concluded that more studies are necessary to establish the value of epidural steroid injection for symptomatic lumbar intervertebral disc herniation.</p>
<p>LEVEL OF EVIDENCE: Therapeutic Level II. See Instructions for Authors for a complete description of levels of evidence.</p>

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</description>

<author>Kristen Radcliff et al.</author>


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<item>
<title>Passing the Boards: can USMLE and Orthopaedic in-Training Examination scores predict passage of the ABOS Part-I examination?</title>
<link>http://jdc.jefferson.edu/orthofp/39</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/39</guid>
<pubDate>Mon, 18 Jun 2012 09:50:07 PDT</pubDate>
<description>
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</description>

<author>Gregg R Klein et al.</author>


<category>Certification</category>

<category>Humans</category>

<category>Orthopedics</category>

<category>Predictive Value of Tests</category>

<category>Specialty Boards</category>

<category>United States</category>

</item>






<item>
<title>Isolated Polyethylene Exchange versus Acetabular Revision for Polyethylene Wear</title>
<link>http://jdc.jefferson.edu/orthofp/38</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/38</guid>
<pubDate>Tue, 20 Mar 2012 07:45:30 PDT</pubDate>
<description>
	<![CDATA[
	<p>Polyethylene wear and osteolysis are not uncommon in THA mid- and long-term. In asymptomatic patients the dilemma faced by the orthopaedic surgeon is whether to revise the cup and risk damage to the supporting columns and even pelvic discontinuity or to perform isolated polyethylene exchange and risk a high rate of postoperative recurrent instability and dislocation that will necessitate further surgery. We retrospectively reviewed 62 patients (67 hips) who underwent revision arthroplasty for polywear and osteolysis. Thirty-six hips had isolated polyethylene exchange, while 31 had full acetabular revision. The minimum followup was 2 years (mean, 2.8 years; range, 2-5 years). Three of 36 hips with a retained cup grafted through the cup holes failed within 5 years due to acetabular loosening. One of 31 hips with full revision underwent re-revision for aseptic cup loosening at 5 months postoperatively. Although we do not recommend prophylactic revision of all cups for polywear and osteolysis, the patient may be warned of the possibility of an approximate 10% failure rate when retaining the acetabular component. We do, however, advocate cup extraction in the following situations: damage to the locking mechanism, erosion of the femoral head through the liner and into the cup damaging the metal, and a malpositioned component that may jeopardize the stability of the revision. Level of Evidence: Level II, prognostic study. See the Guidelines for Authors for a complete description of levels of evidence.</p>

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</description>

<author>Camilo Restrepo et al.</author>


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<item>
<title>An organ culture system to model early degenerative changes of the intervertebral disc.</title>
<link>http://jdc.jefferson.edu/orthofp/37</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/37</guid>
<pubDate>Fri, 24 Feb 2012 08:00:17 PST</pubDate>
<description>
	<![CDATA[
	<p>ABSTRACT: INTRODUCTION: Back pain, a significant source of morbidity in our society, is related to the degenerative changes of the intervertebral disc. At present, the treatment of disc disease consists of therapies that are aimed at symptomatic relief. This shortcoming stems in large part from our lack of understanding of the biochemical and molecular events that drive the disease process. The goal of this study is to develop a model of early disc degeneration using an organ culture. This approach is based on our previous studies that indicate that organ culture closely models molecular events that occur in vivo in an ex vivo setting. METHODS: To mimic a degenerative insult, discs were cultured under low oxygen tension in the presence of TNF-α, IL-1β and serum limiting conditions. RESULTS: Treatment resulted in compromised cell survival and changes in cellular morphology reminiscent of degeneration. There was strong suppression in the expression of matrix proteins including collagen types 1, 2, 6 and 9, proteoglycans, aggrecan and fibromodulin. Moreover, a strong induction in expression of catabolic matrix metalloproteinases (MMP) 3, 9 and 13 with a concomitant increase in aggrecan degradation was seen. An inductive effect on NGF expression was also noticed. Although similar, nucleus pulposus and annulus fibrosus tissues showed some differences in their response to the treatment. CONCLUSIONS: Results of this study show that perturbations in microenvironmental factors result in anatomical and gene expression change within the intervertebral disc that may ultimately compromise cell function and induce pathological deficits. This system would be a valuable screening tool to investigate interventional strategies aimed at restoring disc cell function.</p>

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</description>

<author>Ravi K Ponnappan et al.</author>


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<item>
<title>Reactive oxygen and nitrogen species induce protein and DNA modifications driving arthrofibrosis following total knee arthroplasty.</title>
<link>http://jdc.jefferson.edu/orthofp/36</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/36</guid>
<pubDate>Thu, 09 Feb 2012 10:57:35 PST</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: Arthrofibrosis, occurring in 3%-4% of patients following total knee arthroplasty (TKA), is a challenging condition for which there is no defined cause. The hypothesis for this study was that disregulated production of reactive oxygen species (ROS) and nitrogen species (RNS) mediates matrix protein and DNA modifications, which result in excessive fibroblastic proliferation.</p>
<p>RESULTS: We found increased numbers of macrophages and lymphocytes, along with elevated amounts of myeloperoxidase (MPO) in arthrofibrotic tissues when compared to control tissues. MPO expression, an enzyme that generates ROS/RNS, is usually limited to neutrophils and some macrophages, but was found by immunohistochemistry to be expressed in both macrophages and fibroblasts in arthrofibrotic tissue. As direct measurement of ROS/RNS is not feasible, products including DNA hydroxylation (8-OHdG), and protein nitrosylation (nitrotyrosine) were measured by immunohistochemistry. Quantification of the staining showed that 8-OHdg was significantly increased in arthrofibrotic tissue. There was also a direct correlation between the intensity of inflammation and ROS/RNS to the amount of heterotopic ossification (HO). In order to investigate the aberrant expression of MPO, a real-time oxidative stress polymerase chain reaction array was performed on fibroblasts isolated from arthrofibrotic and control tissues. The results of this array confirmed the upregulation of MPO expression in arthrofibrotic fibroblasts and highlighted the downregulated expression of the antioxidants, superoxide dismutase1 and microsomal glutathione S-transferase 3, as well as the significant increase in thioredoxin reductase, a known promoter of cell proliferation, and polynucleotide kinase 3'-phosphatase, a key enzyme in the base excision repair pathway for oxidative DNA damage.</p>
<p>CONCLUSION: Based on our current findings, we suggest that ROS/RNS initiate and sustain the arthrofibrotic response driving aggressive fibroblast proliferation and subsequent HO.</p>

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</description>

<author>Theresa A Freeman et al.</author>


</item>






<item>
<title>Reactive oxygen and nitrogen species induce protein and DNA modifications driving arthrofibrosis following total knee arthroplasty.</title>
<link>http://jdc.jefferson.edu/orthofp/35</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/35</guid>
<pubDate>Wed, 01 Feb 2012 13:27:11 PST</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: Arthrofibrosis, occurring in 3%-4% of patients following total knee arthroplasty (TKA), is a challenging condition for which there is no defined cause. The hypothesis for this study was that disregulated production of reactive oxygen species (ROS) and nitrogen species (RNS) mediates matrix protein and DNA modifications, which result in excessive fibroblastic proliferation. RESULTS: We found increased numbers of macrophages and lymphocytes, along with elevated amounts of myeloperoxidase (MPO) in arthrofibrotic tissues when compared to control tissues. MPO expression, an enzyme that generates ROS/RNS, is usually limited to neutrophils and some macrophages, but was found by immunohistochemistry to be expressed in both macrophages and fibroblasts in arthrofibrotic tissue. As direct measurement of ROS/RNS is not feasible, products including DNA hydroxylation (8-OHdG), and protein nitrosylation (nitrotyrosine) were measured by immunohistochemistry. Quantification of the staining showed that 8-OHdg was significantly increased in arthrofibrotic tissue. There was also a direct correlation between the intensity of inflammation and ROS/RNS to the amount of heterotopic ossification (HO). In order to investigate the aberrant expression of MPO, a real-time oxidative stress polymerase chain reaction array was performed on fibroblasts isolated from arthrofibrotic and control tissues. The results of this array confirmed the upregulation of MPO expression in arthrofibrotic fibroblasts and highlighted the downregulated expression of the antioxidants, superoxide dismutase1 and microsomal glutathione S-transferase 3, as well as the significant increase in thioredoxin reductase, a known promoter of cell proliferation, and polynucleotide kinase 3'-phosphatase, a key enzyme in the base excision repair pathway for oxidative DNA damage. CONCLUSION: Based on our current findings, we suggest that ROS/RNS initiate and sustain the arthrofibrotic response driving aggressive fibroblast proliferation and subsequent HO.</p>

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</description>

<author>Theresa A Freeman et al.</author>


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<item>
<title>Concave pit-containing scaffold surfaces improve stem cell-derived osteoblast performance and lead to significant bone tissue formation.</title>
<link>http://jdc.jefferson.edu/orthofp/34</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/34</guid>
<pubDate>Wed, 01 Feb 2012 13:26:50 PST</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: Scaffold surface features are thought to be important regulators of stem cell performance and endurance in tissue engineering applications, but details about these fundamental aspects of stem cell biology remain largely unclear.</p>
<p>METHODOLOGY AND FINDINGS: In the present study, smooth clinical-grade lactide-coglyolic acid 85:15 (PLGA) scaffolds were carved as membranes and treated with NMP (N-metil-pyrrolidone) to create controlled subtractive pits or microcavities. Scanning electron and confocal microscopy revealed that the NMP-treated membranes contained: (i) large microcavities of 80-120 microm in diameter and 40-100 microm in depth, which we termed primary; and (ii) smaller microcavities of 10-20 microm in diameter and 3-10 microm in depth located within the primary cavities, which we termed secondary. We asked whether a microcavity-rich scaffold had distinct bone-forming capabilities compared to a smooth one. To do so, mesenchymal stem cells derived from human dental pulp were seeded onto the two types of scaffold and monitored over time for cytoarchitectural characteristics, differentiation status and production of important factors, including bone morphogenetic protein-2 (BMP-2) and vascular endothelial growth factor (VEGF). We found that the microcavity-rich scaffold enhanced cell adhesion: the cells created intimate contact with secondary microcavities and were polarized. These cytological responses were not seen with the smooth-surface scaffold. Moreover, cells on the microcavity-rich scaffold released larger amounts of BMP-2 and VEGF into the culture medium and expressed higher alkaline phosphatase activity. When this type of scaffold was transplanted into rats, superior bone formation was elicited compared to cells seeded on the smooth scaffold.</p>
<p>CONCLUSION: In conclusion, surface microcavities appear to support a more vigorous osteogenic response of stem cells and should be used in the design of therapeutic substrates to improve bone repair and bioengineering applications in the future.</p>

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</description>

<author>Antonio Graziano et al.</author>


<category>Adult</category>

<category>Animals</category>

<category>Cells, Cultured</category>

<category>Enzyme-Linked Immunosorbent Assay</category>

<category>Fluorescent Antibody Technique</category>

<category>Humans</category>

<category>Immunocompromised Host</category>

<category>Immunoenzyme Techniques</category>

<category>Lactic Acid</category>

<category>Middle Aged</category>

<category>Osteoblasts</category>

<category>Osteogenesis</category>

<category>Polyglycolic Acid</category>

<category>Pyrrolidinones</category>

<category>Rats</category>

<category>Rats, Wistar</category>

<category>Stem Cells</category>

<category>Stromal Cells</category>

<category>Tissue Engineering</category>

<category>Tissue Scaffolds</category>

<category>Vascular Endothelial Growth Factor A</category>

<category>Young Adult</category>

</item>






<item>
<title>Molecular diagnostics in periprosthetic joint infection.</title>
<link>http://jdc.jefferson.edu/orthofp/33</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/33</guid>
<pubDate>Tue, 20 Dec 2011 09:42:20 PST</pubDate>
<description>
	<![CDATA[
	<p>Periprosthetic joint infection (PJI) is a significant and costly challenge to the orthopedic community. The lack of a gold standard for diagnosis remains the biggest obstacle in the detection and subsequent treatment of PJI. Molecular markers in the serum and joint fluid aspirate hold immense promise to enhance the development of a firm diagnostic criterion. The primary goal is one marker with high sensitivity and specificity. Here, we review our current research efforts in the field of molecular markers: C-reactive protein, erythrocyte sedimentation rate, white blood cells, and leukocyte esterase. Each marker has been studied to determine its sensitivity, specificity, and positive and negative predictive values in diagnosing PJI.</p>

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</description>

<author>Javad Parvizi et al.</author>


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<item>
<title>Femoroacetabular Impingement: Saving the Joint</title>
<link>http://jdc.jefferson.edu/orthofp/32</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/32</guid>
<pubDate>Mon, 22 Aug 2011 06:29:59 PDT</pubDate>
<description>
	<![CDATA[
	<p>Many factors have been linked to the development of osteoarthritis (OA)  of the hip, but often, cases are still considered “idiopathic.”  Femoroacetabular impingement (FAI) has been suggested as a possible  etiologic factor for the otherwise “idiopathic” cases. It is theorized  that the subtle morphologic abnormalities seen at the head-neck junction  and acetabulum in FAI may lead to labral tears, chondral damage, and  subsequent progression of OA. Prevalence of FAI has been suggested to be  as high as 14% in the general population. It often presents in young  active patients that subject their hip joint to repetitive micro trauma  associated with impingement of the osseous deformity within normal  ranges of motion. Current surgical treatment options for FAI include  arthroscopy, open surgical dislocation, or mini-open direct anterior  osteoplasty. All methods are directed at correcting the osseous  abnormalities and associated pathologies in hopes of delaying the  progression of OA and the need for hip replacement. Limited short term  follow-up data has shown significant improvement in pain and function  following each of the three procedures. However, long term follow-up and  comparative studies are necessary to evaluate the efficacy of each of  the surgical approaches in delaying the progression of osteoarthritis.</p>

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</description>

<author>Ronald Huang et al.</author>


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<item>
<title>The infected hip: A treatment algorithm</title>
<link>http://jdc.jefferson.edu/orthofp/31</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/31</guid>
<pubDate>Mon, 01 Aug 2011 09:19:43 PDT</pubDate>
<description>
	<![CDATA[
	<p>The management of periprosthetic joint infection following total joint  arthroplasty is presently a major challenge to orthopedic surgeons.  Despite various treatment options available, the two-stage revision  procedure is most often chosen in North America because of a high  success rate, especially in cases involving resistant organisms.  Sometimes the use of antibiotics alone, irrigation with debridement, or a  one-stage exchange may be a more appropriate treatment option. Various  factors such as the status of a patient’s immune system, time of onset  of the infection, as well as susceptibility of causative microorganism  should be considered as they play an important role in effectiveness of  treatment. When surgery presents a great risk to patients due to their  level of health, and infection is caused by a low-virulent antimicrobial  susceptible pathogen, antibiotic suppression alone may be the best  treatment option. If the patient can successfully undergo surgery then  an irrigation and debridement procedure may be preferred, especially  with an acute onset of symptoms. If onset of symptoms is much later as  in chronic cases, or irrigation and debridement procedure is  unsuccessful, then resection of all components and reimplantation is  necessary. In a two-stage revision, placement of an antibiotic-loaded  spacer is needed to eradicate the infection before reimplantation takes  place. There are rare cases in which salvage procedures, such as  arthrodesis or amputation, are necessary to completely eradicate an  uncontrollable infection in immunocompromised patients.</p>

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</description>

<author>Bahar Adeli et al.</author>


</item>






<item>
<title>Potent inhibition of heterotopic ossification by nuclear retinoic acid receptor-γ agonists.</title>
<link>http://jdc.jefferson.edu/orthofp/30</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/30</guid>
<pubDate>Fri, 03 Jun 2011 07:08:37 PDT</pubDate>
<description>
	<![CDATA[
	<p>Heterotopic ossification consists of ectopic bone formation within soft tissues after surgery or trauma. It can have debilitating consequences, but there is no definitive cure. Here we show that heterotopic ossification was essentially prevented in mice receiving a nuclear retinoic acid receptor-γ (RAR-γ) agonist. Side effects were minimal, and there was no significant rebound effect. To uncover the mechanisms of these responses, we treated mouse mesenchymal stem cells with an RAR-γ agonist and transplanted them into nude mice. Whereas control cells formed ectopic bone masses, cells that had been pretreated with the RAR-γ agonist did not, suggesting that they had lost their skeletogenic potential. The cells became unresponsive to rBMP-2 treatment in vitro and showed decreases in phosphorylation of Smad1, Smad5 and Smad8 and in overall levels of Smad proteins. In addition, an RAR-γ agonist blocked heterotopic ossification in transgenic mice expressing activin receptor-like kinase-2 (ALK2) Q207D, a constitutively active form of the receptor that is related to ALK2 R206H found in individuals with fibrodysplasia ossificans progressiva. The data indicate that RAR-γ agonists are potent inhibitors of heterotopic ossification in mouse models and, thus, may also be effective against injury-induced and congenital heterotopic ossification in humans.</p>

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</description>

<author>Kengo Shimono et al.</author>


<category>Activin Receptors, Type I</category>

<category>Animals</category>

<category>Bone Morphogenetic Proteins</category>

<category>Cell Differentiation</category>

<category>Chondrogenesis</category>

<category>Humans</category>

<category>Mesenchymal Stem Cell Transplantation</category>

<category>Mesenchymal Stem Cells</category>

<category>Mice</category>

<category>Mice, Knockout</category>

<category>Mice, Mutant Strains</category>

<category>Mice, Nude</category>

<category>Mice, Transgenic</category>

<category>Ossification, Heterotopic</category>

<category>Receptors, Retinoic Acid</category>

<category>Signal Transduction</category>

</item>






<item>
<title>Neurologic improvement after thoracic, thoracolumbar, and lumbar spinal cord (conus medullaris) injuries</title>
<link>http://jdc.jefferson.edu/orthofp/29</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/29</guid>
<pubDate>Fri, 18 Feb 2011 07:27:24 PST</pubDate>
<description>
	<![CDATA[
	<p>Study Design. Retrospective. Objective. With approximately 10,000 new spinal cord injury (SCI) patients in the United States each year, predicting public health outcomes is an important public health concern. Combining all regions of the spine in SCI trials may be misleading if the lumbar and sacral regions (conus) have a neurologic improvement at different rates than the thoracic or thoracolumbar spinal cord.</p>
<p>Summary of Background Data. Over a 10-year period between January 1995 to 2005, 1746 consecutive spinal injured patients were seen, evaluated, and treated through a level 1 trauma referral center. A retrospective analysis was performed on 150 patients meeting the criteria of T4 to S5 injury, excluding gunshot wounds. One-year follow-up data were available on 95 of these patients.</p>
<p>Methods. Contingency table analyses (chi-squared statistics) and multivariate logistic regression. Variables of interest included level of injury, initial American Spinal Injury Association (ASIA), age, race, and etiology.</p>
<p>Results. A total of 92.9% of lumbar (conus) patients neurologically improved one ASIA level or more compared with 22.4% of thoracic or thoracolumbar spinal cord-injured patients. Only 7.7% of ASIA A patients showed neurologic improvement, compared with 95.2% of ASIA D patients; ASIA B patients demonstrated a 66.7% improvement rate, whereas ASIA C had a 84.6% improvement rate. When the two effects were considered jointly in a multivariate analysis, ASIA A and thoracic/thoracolumbar patients had only a 4.1% rate of improvement, compared with 96% for lumbar (conus) and incomplete patients (ASIA B-D) and 66.7% to 72.2% for the rest of the patients. All of these relationships were significant to P < 0.001 (chi-square test). There was no link to age or gender, and race and etiology were secondary to region and severity of injury.</p>
<p>Conclusion. Thoracic (T4-T9) SCIs have the least potential for neurologic improvement. Thoracolumbar (T10-T12) and lumbar (conus) spinal cord have a greater neurologic improvement rate, which might be related to a greater proportion of lower motor neurons. Thus, defining the exact region of injury and potential for neurologic improvement should be considered in future clinical trial design. Combining all anatomic regions of the spine in SCI trials may be misleading if different regions have neurologic improvement at different rates. Over a ten-year period, 95 complete thoracic/thoracolumbar SCI patients had only a 4.1% rate of neurologic improvement, compared with 96.0% for incomplete lumbar (conus) patients and 66.7% to 72.2% for all others.</p>

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</description>

<author>James S. Harrop, MD et al.</author>


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<item>
<title>Limitations of the Knee Society Score in evaluating outcomes following revision total knee arthroplasty.</title>
<link>http://jdc.jefferson.edu/orthofp/28</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/28</guid>
<pubDate>Wed, 01 Dec 2010 12:19:04 PST</pubDate>
<description>
	<![CDATA[
	<p>BACKGROUND: Traditionally, the results of revision total knee arthroplasty have been determined with use of surgeon-based measures such as the Knee Society rating system. Recently, outcome and quality-of-life measures have shifted toward a greater emphasis on patient-based evaluation. The aim of our study was to determine the validity and responsiveness of the Knee Society rating system compared with the Short Form-36 health survey (SF-36), Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), and a four-question 4-point Likert scale satisfaction questionnaire following revision total knee arthroplasty.</p>
<p>METHODS: A total of 152 patients underwent revision total knee arthroplasty at our institution, between August 2003 and January 2007, and had a two-year follow-up evaluation after revision surgery. The SF-36, WOMAC, Knee Society rating system, and satisfaction scores were completed preoperatively and postoperatively. Spearman correlation coefficients were calculated to determine the degree of correlation for each outcome scale. The SF-36, WOMAC, and patient satisfaction were correlated with the Knee Society rating system.</p>
<p>RESULTS: Both before and after surgery, the correlation among items of the Knee Society rating system displayed low to negligible levels of association. The Knee Society rating system pain score showed modest levels of convergent construct validity with the WOMAC and SF-36. However, the Knee Society functional score displayed negligible to low correlation with its WOMAC functional counterpart preoperatively. The Knee Society pain and functional scores, respectively, showed marked and moderate association with satisfaction. The change in the Knee Society pain and functional scores had moderate association with the SF-36 and WOMAC counterparts, except low correlation was displayed between the pain scores for the Knee Society rating system and the SF-36. The Knee Society rating system pain score was found to be the most responsive of the measures with a standardized response mean of 1.6, whereas the Knee Society rating system functional score was found to be the least responsive at 0.7.</p>
<p>CONCLUSIONS: Currently, there is no so-called gold standard that optimally reflects the status of the knee, as well as the patient, prior to and following revision total knee arthroplasty. Ideally, numerous assessment scales should be administered to the patient in order to accurately reflect the patient characteristics for the purpose of academic study, but from a practical standpoint, this may not be feasible. We encourage further research and development of a simple and concise standardized questionnaire for use before and after revision total knee arthroplasty.</p>

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</description>

<author>Elie Ghanem et al.</author>


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<item>
<title>Mast cells and hypoxia drive tissue metaplasia and heterotopic ossification in idiopathic arthrofibrosis after total knee arthroplasty.</title>
<link>http://jdc.jefferson.edu/orthofp/27</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/27</guid>
<pubDate>Tue, 28 Sep 2010 12:44:05 PDT</pubDate>
<description>
	<![CDATA[
	<p>ABSTRACT: BACKGROUND: Idiopathic arthrofibrosis occurs in 3-4% of patients who undergo total knee arthroplasty (TKA). However, little is known about the cellular or molecular changes involved in the onset or progression of this condition. To classify the histomorphologic changes and evaluate potential contributing factors, periarticular tissues from the knees of patients with arthrofibrosis were analyzed for fibroblast and mast cell proliferation, heterotopic ossification, cellular apoptosis, hypoxia and oxidative stress. RESULTS: The arthrofibrotic tissue was composed of dense fibroblastic regions, with limited vascularity along the outer edges. Within the fibrotic regions, elevated numbers of chymase/fibroblast growth factor (FGF)-expressing mast cells were observed. In addition, this region contained fibrocartilage and associated heterotopic ossification, which quantitatively correlated with decreased range of motion (stiffness). Fibrotic, fibrocartilage and ossified regions contained few terminal dUTP nick end labeling (TUNEL)-positive or apoptotic cells, despite positive immunostaining for lactate dehydrogenase (LDH)5, a marker of hypoxia, and nitrotyrosine, a marker for protein nitrosylation. LDH5 and nitrotyrosine were found in the same tissue areas, indicating that hypoxic areas within the tissue were associated with increased production of reactive oxygen and nitrogen species. CONCLUSIONS: Taken together, we suggest that hypoxia-associated oxidative stress initiates mast cell proliferation and FGF secretion, spurring fibroblast proliferation and tissue fibrosis. Fibroblasts within this hypoxic environment undergo metaplastic transformation to fibrocartilage, followed by heterotopic ossification, resulting in increased joint stiffness. Thus, hypoxia and associated oxidative stress are potential therapeutic targets for fibrosis and metaplastic progression of idiopathic arthrofibrosis after TKA.</p>

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</description>

<author>Theresa A Freeman et al.</author>


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<item>
<title>Use of orthogonal or parallel plating techniques to treat distal humerus fractures.</title>
<link>http://jdc.jefferson.edu/orthofp/26</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/26</guid>
<pubDate>Wed, 15 Sep 2010 12:07:13 PDT</pubDate>
<description>
	<![CDATA[
	<p>Distal humerus fractures continue to be a complex fracture to treat. This article describes two surgical techniques that can be used to tackle these difficult fractures: Parallel plating and orthogonal plating. Both techniques have yielded excellent outcomes after open reduction and internal fixation; yet each has its own set of unique considerations. However, the key to successful treatment of these difficult fractures regardless of technique remains obtaining anatomic reduction with stable fixation and the implementation of early motion.</p>

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</description>

<author>Joshua M. Abzug et al.</author>


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<item>
<title>Current concepts: Neonatal brachial plexus pals</title>
<link>http://jdc.jefferson.edu/orthofp/25</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/25</guid>
<pubDate>Thu, 05 Aug 2010 08:05:51 PDT</pubDate>
<description>
	<![CDATA[
	<p>Neonatal brachial plexus palsy may be decreasing in incidence; however, conflicting reports exist. Regardless, neonatal brachial plexus palsy has an incidence of 1 to 2 per 1000 live births making this a frequent occurrence.  The majority of infants with brachial plexus palsy spontaneously recover in the first 2 months of life and subsequently progress to near complete recovery of motion and strength.  However, those infants who do not have substantial recovery by age 3 months will have permanent limited range of motion, less strength, and a decrease in size and girth of the involved extremity. Currently, debate continues about the timing and type of surgical intervention. This article provides an update based on recent literature regarding the anatomy, epidemiology, diagnosis, classification schemes, and treatment options for neonatal brachial plexus palsy.</p>

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</description>

<author>Joshua M. Abzug, MD et al.</author>


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<item>
<title>Correlation of C2 fractures and vertebral artery injury.</title>
<link>http://jdc.jefferson.edu/orthofp/24</link>
<guid isPermaLink="true">http://jdc.jefferson.edu/orthofp/24</guid>
<pubDate>Mon, 12 Jul 2010 07:23:07 PDT</pubDate>
<description>
	<![CDATA[
	<p>STUDY DESIGN: Retrospective review of prospectively collected data.</p>
<p>SUMMARY OF BACKGROUND DATA: Vertebral artery injuries (VAI) occur commonly after cervical spine trauma. No study has yet examined the association between VAI and specific variants of C2 fractures.</p>
<p>OBJECTIVE: To evaluate the incidence of VAI (as defined by magnetic resonance imaging/angiography [MRI/A]) in subtypes of C2 fractures. To define the association between the incidence, morphology, and severity of C2 fractures, based on fracture angulation and comminution, and the occurrence of VAI.</p>
<p>METHODS: Patients admitted to the hospital with C2 fractures between October 2006 and December 2008 to a tertiary care referral center were identified through a prospectively maintained database. Computed tomography (CT) and MRI/A studies were individually reviewed to evaluate the specific C2 fracture type and the occurrence of VAI. Fracture displacement and angulation were measured. Incidence of VAI was compared between different types and subtypes of C2 fractures. The effects of displacement and angulation of the fracture, morphology of foramen transversarium fracture, patient age, and patient gender on VAI were also analyzed.</p>
<p>RESULTS: One hundred one patients were identified with C2 fractures that met inclusion criteria, and 18 (17.8%) had VAI by MRI/A. There was no correlation between fracture types and VAI. However, in subtype analysis, there was a correlation of VAI with traumatic spondylolisthesis of axis (TSA) and greater degree of angulation (P = 0.0023), communition fracture (P = 0.0341), and presence of bone fragment(s) within the foramen transversarium (P = 0.0075). Multivariate logistic regression indicated that age, gender and the presence of fragments within foramen transversarium were associated with greater risk of VAI.</p>
<p>CONCLUSION: Vertebral artery injuries are more likely to occur in C2 fractures with comminuted fractures involving the foramen transversarium, with fractures manifesting bony fragment(s) within the foramen transversarium, or with fractures having greater angulation. These risk factors should be considered when a patient presents with isolated axis fracture.</p>

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<author>Tao Ding et al.</author>


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