4 results on '"Yu-Feng Su"'
Search Results
2. Intraoperative intracranial pressure and cerebral perfusion pressure for predicting surgical outcome in severe traumatic brain injury
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Shiuh-Lin Hwang, Yu-Feng Su, Sui-Sum Kung, Tzuu-Yuan Huang, Ann-Shung Lieu, and Tai-Hsin Tsai
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Adult ,Male ,medicine.medical_specialty ,Adolescent ,Intracranial pressure ,Traumatic brain injury ,medicine.medical_treatment ,Intraoperative Period ,Young Adult ,Hematoma ,medicine ,Humans ,Cerebral perfusion pressure ,Aged ,Severe traumatic brain injury ,Medicine(all) ,Aged, 80 and over ,lcsh:R5-920 ,integumentary system ,business.industry ,musculoskeletal, neural, and ocular physiology ,Glasgow Outcome Scale ,Glasgow Coma Scale ,Retrospective cohort study ,General Medicine ,Middle Aged ,medicine.disease ,humanities ,nervous system diseases ,Surgery ,nervous system ,Brain Injuries ,Cerebrovascular Circulation ,Anesthesia ,Female ,Decompressive craniectomy ,lcsh:Medicine (General) ,business - Abstract
Intraoperative intracranial pressure (ICP) and cerebral perfusion pressure (CPP) were evaluated for use as prognostic indicators after surgery for severe traumatic brain injury (TBI), and threshold ICP and CPP values were determined to provide guidelines for patient management. This retrospective study reviewed data for 66 patients (20 females and 46 males) aged 13–83 years (average age, 48 years) who had received decompressive craniectomy and hematoma evacuation for severe TBI. The analysis of clinical characteristics included Glascow Coma Scale score, trauma mechanism, trauma severity, cerebral hemorrhage type, hematoma thickness observed on computed tomography scan, Glasgow Outcome Scale score, and mortality. Patients whose treatment included ICP monitoring had significantly better prognosis (p
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- 2013
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3. Effect of Aspirin and Indomethacin on Prostaglandin E2 Synthesis in C6 Glioma Cells
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Shiuh-Lin Hwang, Ann-Shung Lieu, Chi-Yun Cheng, Yu-Feng Su, Kung-Shing Lee, Shen-Long Howng, Yan-Fen Hwang, Joon-Khim Loh, and Chih-Lung Lin
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Time Factors ,aspirin ,medicine.medical_treatment ,Pharmacology ,C6 glioma ,Dinoprostone ,Immunoenzyme Techniques ,indomethacin ,Tumor Cells, Cultured ,medicine ,Humans ,Tumor growth ,Prostaglandin E2 ,Medicine(all) ,chemistry.chemical_classification ,lcsh:R5-920 ,Aspirin ,prostaglandin E2 ,Dose-Response Relationship, Drug ,Brain Neoplasms ,business.industry ,Anti-Inflammatory Agents, Non-Steroidal ,Immunosuppression ,Glioma ,General Medicine ,Dose–response relationship ,Enzyme ,chemistry ,lipids (amino acids, peptides, and proteins) ,lcsh:Medicine (General) ,business ,Intracellular ,brain tumor ,medicine.drug - Abstract
Prostaglandin E2 (PGE2) plays an important role in immunosuppression and tumor growth. PGE2 inhibitors such as aspirin and indomethacin suppress experimental tumor growth. Little is known of the relationship between PGE2 synthesis in brain tumors and the dose of aspirin or indomethacin. The present study was undertaken to evaluate the effect of different doses of aspirin and indomethacin on PGE2 synthesis in C6 glioma cells. C6 glioma cells were incubated with different concentrations (2, 4, and 8 microM) of aspirin and indomethacin for 1, 2, 4, 6, 8, 12, and 24 hours. Intracellular PGE2 concentration was measured by enzyme immunoassay. Each concentration of aspirin and indomethacin effectively inhibited PGE2 synthesis. Concentrations of 2, 4, and 8 microM of aspirin significantly inhibited PGE2 production at 6, 4, and 1 hour, respectively, and the inhibition persisted for more than 24 hours (p0.05). Concentrations of 2 and 4 microM of indomethacin were effective at 4 and 2 hours (p0.05), respectively. However, inhibition was not observed beyond 12 hours (p0.05). Indomethacin 8 microM was effective at 1 hour and the inhibition persisted beyond 24 hours (p0.05). Our study demonstrates that aspirin and indomethacin inhibit PGE2 synthesis in C6 glioma cells and that low-dose aspirin is as effective as high-dose aspirin. This study may encourage future clinical use of low-dose aspirin in the prevention or treatment of brain tumors.
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4. Analysis of Surgically Treated Intraspinal Tumors in Southern Taiwan
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Chih-Jen Wang, Yu-Feng Su, Tzuu-Yuan Huang, Chih-Zen Chang, Kung-Shing Lee, Ann-Shung Lieu, Shiuh-Lin Hwang, Chun-Po Yen, Sheng-Long Howng, Yen-Fen Hwang, Aij-Lie Kwan, Joon-Khim Loh, and Chih-Lung Lin
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Adult ,Male ,medicine.medical_specialty ,Adolescent ,Spinal Cord Neoplasm ,Taiwan ,Metastasis ,medicine ,Paralysis ,Humans ,intraspinal tumor ,Spinal Cord Neoplasms ,Neoplasm Metastasis ,Aged ,Aged, 80 and over ,Medicine(all) ,lcsh:R5-920 ,Gastrointestinal tract ,Lung ,business.industry ,Medical record ,General Medicine ,Middle Aged ,medicine.disease ,Surgery ,medicine.anatomical_structure ,spinal metastasis ,statistics ,Hepatocellular carcinoma ,Female ,medicine.symptom ,lcsh:Medicine (General) ,business ,Lumbosacral joint - Abstract
The medical records of 117 patients with spinal tumors who underwent surgery with pathologic confirmation from January 1999 to April 2004 at Kaohsiung Medical University Hospital were reviewed. Data from this review were compared with those obtained from the same institution 10 years earlier (covering the period 1988‐1995) and from other reported series. There were 69 male and 48 female patients aged from 13 to 87 years old (mean age, 51.9). The most common pathologic findings were metastasis in 45.3% (53/117), nerve sheath tumors in 28.2% (33/117), menin‐giomas in 12% (14/117) and neuroepithelial tumors in 6% (7/117). The peak ages at diagnosis were 41‐50 years and 61–70 years. A slight male predominance was noted for all tumors, except meningiomas. Motor weakness, even paralysis, was the major clinical presentation (64–86%), followed by sensory deficits (50%) and pain (42%). The location of tumors was most often in the thoracic (50.4%; 59/117), lumbosacral (27.4%; 32/117) and cervical spine (22.2%; 26/117) segments. Among the metastatic tumors, the lung (22.6%) and breast (15.1%) were the most common primary sites of origin, followed by unknown origin, the liver (hepatocellular carcinoma), the gastrointestinal tract and the nasopharynx (nasopharyngeal cancer).
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