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3.
JAMA Neurol ; 73(6): 743-9, 2016 Jun 01.
Article in English | MEDLINE | ID: mdl-27111824

ABSTRACT

IMPORTANCE: Chronic traumatic encephalopathy (CTE) refers to pathologic changes that have been found in some individuals with a history of repetitive traumatic impact to the head (hereinafter referred to as head trauma). These changes cannot be assessed during the clinical evaluation of a living patient. OBSERVATIONS: The neuropathologic features, taxonomy, history, role of biomarkers in diagnosis, and existing criteria of CTE are reviewed. Previous criteria have been proposed to approach the living patient; however, a unified, specific approach is needed for the practicing clinician. We propose a new diagnostic construct for the clinical syndrome associated with repetitive exposure to head trauma: traumatic encephalopathy syndrome. This clinical paradigm will provide the framework for a diagnosis of probable, possible, and unlikely traumatic encephalopathy syndrome, with included discussion regarding the minimum exposure, nature of the clinical course, and additional clinical features needed for diagnosis. CONCLUSIONS AND RELEVANCE: While prospective longitudinal studies are ongoing to further elucidate the association of exposure to head trauma, clinical features, and the development of pathologic changes, a corresponding clinical construct for diagnosis is necessary.


Subject(s)
Chronic Traumatic Encephalopathy/diagnosis , Biomarkers/metabolism , Chronic Traumatic Encephalopathy/history , Chronic Traumatic Encephalopathy/physiopathology , Chronic Traumatic Encephalopathy/therapy , History, 20th Century , Humans , Longitudinal Studies
4.
Prim Care ; 40(4): 849-61, viii, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24209722

ABSTRACT

Radiological studies can confirm or rule out competing diagnoses for musculoskeletal injuries and pain. Obtaining a detailed history and physical examination is pivotal for localizing the pain generator and choosing the most appropriate imaging studies, based on the suspected injured tissue. Judicious use of imaging is important to avoid unnecessary radiation exposure, minimize cost, and avoid therapy targeting asymptomatic imaging abnormalities. This article compares and contrasts the diagnostic imaging commonly used for detecting musculoskeletal injuries.


Subject(s)
Musculoskeletal Diseases/diagnosis , Ankle Joint/diagnostic imaging , Ankle Joint/pathology , Foot/diagnostic imaging , Foot/pathology , Hip Joint/diagnostic imaging , Hip Joint/pathology , Humans , Knee Joint/diagnostic imaging , Knee Joint/pathology , Magnetic Resonance Imaging , Musculoskeletal Diseases/diagnostic imaging , Pelvis/diagnostic imaging , Pelvis/pathology , Shoulder Joint/diagnostic imaging , Shoulder Joint/pathology , Spinal Diseases/diagnosis , Spinal Diseases/diagnostic imaging , Tomography, X-Ray Computed
5.
PM R ; 4(1): 23-9, 2012 Jan.
Article in English | MEDLINE | ID: mdl-22093441

ABSTRACT

OBJECTIVE: To examine the relationship between ligamentum flavum thickness and clinical spinal stenosis. DESIGN: A validation study. SETTING: Clinical research laboratory. PATIENTS: A total of 119 subjects from the Michigan Spinal Stenosis Study (MSSS). METHODS: Two new measurement techniques were compared by use of magnetic resonance images of 4 asymptomatic subjects by 2 examiners. The technique with the best interrater reliability was then used to measure the ligamentum flavum at L4-L5 in 119 subjects in the MSSS who, on the basis of clinical examination without imaging, were thought to have lumbar stenosis, mechanical back pain, or no pain. These findings were related to other radiologic findings, demographics, clinical severity, and electrodiagnostic findings. MAIN OUTCOME MEASUREMENTS: Perpendicular on the inside of the spinal canal from the deepest point of concavity of the lamina to the edge of the ligament. RESULTS: The ligamentum flavum width measurement had high interrater (r = 0.774) and intrarater (r = 0.768) reliability. In 28 asymptomatic volunteers, ligamentum flavum width averaged 5.72 ± 0.95 mm, with the left side significantly thinner than the right (t = 2.117, P = .044), and thicker ligaments with age (r = 0.653, P < .001). Asymptomatic persons whom radiologists thought had stenosis had thicker ligaments (t = 2.273, P = .032). Persons with clinical stenosis (n = 48) and mechanical pain (n = 43) had ligament thickness similar to that of asymptomatic volunteers. Among patients with clinical stenosis, ligamentum flavum thickness did not relate to symptom severity (pedometer and laboratory ambulation tests, Pain Disability Index, and visual analog scale for pain). Most neurophysiological findings had no relationship with ligamentum flavum width, except the presence of limb fibrillation potentials related to a thinner ligament (t = 2.915, P = .004). CONCLUSIONS: The measurement technique is standardized for the ligamentum flavum for future use. Although the ligamentum flavum appears to get thicker with age, other factors, including clinical diagnosis, pain, and function, do not appear to relate to the ligamentum flavum width.


Subject(s)
Aging , Ligamentum Flavum/pathology , Lumbar Vertebrae , Magnetic Resonance Imaging/methods , Physical Examination/methods , Spinal Stenosis/diagnosis , Elasticity , Female , Humans , Hypertrophy , Ligamentum Flavum/physiopathology , Male , Middle Aged , Reproducibility of Results , Spinal Stenosis/physiopathology
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