Joseph M. Hoxworth

Joseph M. Hoxworth

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Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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31 March 2000 in Arthritis Research & Therapy
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Journal Article
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RGRaphaela Goldbach-Mansky
Raphaela Goldbach-Mansky
JLJennifer Lee
Jennifer Lee
AMAngela McCoy
Angela McCoy
JHJoseph M. Hoxworth
Joseph M. Hoxworth
CYCheryl Yarboro
Cheryl Yarboro
HEHani El-Gabalawy
Hani El-Gabalawy
An inception cohort of 238 patients having peripheral joint synovitis of less than 12 months duration was evaluated clinically and followed prospectively for 1 year to determine the clinical significance of a number of rheumatoid arthritis (RA) associated autoantibodies. Serum samples collected at the time of the initial evaluation were tested for rheumatoid factor (RF) and antibodies to Sa (anti-Sa), RA-33, (pro)filaggrin [antifilaggrin antibody (AFA)], cyclic citrullinated peptide (anti-CCP), calpastatin, and keratin [antikeratin antibody (AKA)]. RF had a sensitivity of 66% and a specificity of 87% for RA. Anti-Sa, AFA, and anti-CCP all had a specificity of more than 90%, but a sensitivity of less than 50% for this diagnosis. Overall, there was a high degree of correlation between AFA, AKA, anti-Sa or anti-CCP, this being highest between anti-Sa and anti-CCP (odds ratio, 13.3; P < 0.001). Of the 101 patients who were positive for at least one of these four autoantibodies, 57% were positive for only one. Finally, anti-SA identified a subset of predominantly male RA patients with severe, erosive disease. Anti-SA, AFA and anti-CCP are all specific for early RA but, overall, have little additional diagnostic value over RF alone. Although these antibodies may preferentially recognize citrullinated antigens, the modest degree of concordance between them in individual patient sera suggests that it is unlikely a single antigen is involved in generating these responses.

4 February 2013 in The Laryngoscope
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Journal Article
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MHMichael L. Hinni
Michael L. Hinni
MZMatthew A. Zarka
Matthew A. Zarka
JHJoseph M. Hoxworth
Joseph M. Hoxworth

8 October 2008 in American Journal of Neuroradiology
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Journal Article
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JHJoseph M. Hoxworth
Joseph M. Hoxworth
APA.C. Patel
A.C. Patel
EBE.P. Bosch
E.P. Bosch
KNK.D. Nelson
K.D. Nelson
SUMMARY: A 53-year-old woman with superficial siderosis underwent spinal MR imaging, which demonstrated a large cervicothoracic epidural fluid collection compatible with a CSF leak. Conventional and dynamic CT myelography failed to localize the dural tear because of rapid equilibration of myelographic contrast between the thecal sac and the extradural collection. The superior temporal resolution of digital subtraction myelography precisely localized the CSF leak preoperatively and led to the successful surgical correction of the dural tear.

1 September 2012 in American Journal of Roentgenology
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Journal Article
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JHJoseph M. Hoxworth
Joseph M. Hoxworth
TTTerrence L. Trentman
Terrence L. Trentman
AKAmy L. Kotsenas
Amy L. Kotsenas
KTKent R. Thielen
Kent R. Thielen
KNKent D. Nelson
Kent D. Nelson
DDDavid W. Dodick
David W. Dodick
OBJECTIVE. The objective of our study was to review the clinical utility of digital subtraction myelography for the diagnosis of spinal CSF leaks in patients with spontaneous intracranial hypotension (SIH) and those with superficial siderosis. MATERIALS AND METHODS. Procedure logs from 2007 to 2011 were reviewed to identify cases in which digital subtraction myelography was performed to diagnose spinal CSF leaks. Electronic medical records were reviewed to obtain information regarding diagnosis and outcome. For patients to be included in the study, preprocedural spinal MRI had to show an extradural fluid collection spanning more than one vertebral level and postmyelographic CT had to confirm the presence of an active CSF leak. If digital subtraction myelography successfully showed the site of the CSF leak, the location was documented. RESULTS. Eleven patients (seven men and four women; mean age, 49.0 years) underwent digital subtraction myelography during the study period. Six patients had SIH and five pa...

1 March 2015 in Journal of Neurosurgery: Spine
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Journal Article
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KTKent R. Thielen
Kent R. Thielen
JSJohn C. Sillery
John C. Sillery
JMJonathan M. Morris
Jonathan M. Morris
JHJoseph M. Hoxworth
Joseph M. Hoxworth
FDFelix E. Diehn
Felix E. Diehn
PLPatrick H. Luetmer
Patrick H. Luetmer
OBJECT: Precise localization and understanding of the origin of spontaneous high-flow spinal CSF leaks is required prior to targeted treatment. This study demonstrates the utility of ultrafast dynamic CT myelography for the precise localization of high-flow CSF leaks caused by spiculated spinal osteophytes. METHODS: This study reports a series of 14 patients with high-flow CSF leaks caused by spiculated spinal osteophytes who underwent ultrafast dynamic CT myelography between March 2009 and December 2010. There were 10 male and 4 female patients, with an average age of 49 years (range 37–74 years). The value of ultrafast dynamic CT myelography in depicting the CSF leak site was qualitatively assessed. RESULTS: In all 14 patients, ultrafast dynamic CT myelography was technically successful at precisely demonstrating the site of the CSF leak, the causative spiculated osteophyte piercing the dura, and the relationship of the implicated osteophyte to adjacent structures. Leak sites included 3 cervical, 11 thoracic, and 0 lumbar levels, with 86% of the leaks occurring from C-5 to T-7. Information obtained from the ultrafast dynamic CT myelogram was considered useful in all treated CSF leaks. CONCLUSIONS: Spinal osteophytes piercing the dura are a more frequent cause of high-flow CSF leaks than previously recognized. Ultrafast dynamic CT myelography adds value beyond standard dynamic myelography or digital subtraction myelography in the diagnosis and anatomical characterization of high-flow spinal CSF leaks caused by these osteophytes. This information allows for appropriate planning for percutaneous or surgical treatment.

1 March 1999 in Brain Research
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Journal Article
Closed access
JHJoseph M. Hoxworth
Joseph M. Hoxworth
KXKui Xu
Kui Xu
YZYinong Zhou
Yinong Zhou
WLW.DAvid Lust
W.DAvid Lust
JLJoseph C LaManna
Joseph C LaManna