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1.
Journal of Xi'an Jiaotong University(Medical Sciences) ; (6): 143-148, 2022.
Artículo en Chino | WPRIM | ID: wpr-1011616

RESUMEN

【Objective】 To report the early clinical effects and surgical complications of endoscopic spinal fusion technology (Endo-LIF) in the treatment of degenerative lumbar disease. 【Methods】 The clinical data of 31 patients with degenerative lumbar spine disease treated with Endo-LIF from June 2019 to May 2021 were retrospectively analyzed. All the 31 patients underwent endoscopic spinal fusion therapy. We recorded the operation time, hospital stay duration, postoperative complications, visual analogue scale for pain (VAS), oswestry dysfunction Index (ODI) and low back pain in the Chinese Orthopaedic Association Spine Group Surgery scoring standards before operation, immediately after operation, and the last follow-up to evaluate clinical efficacy. 【Results】 The operation time of the 31 patients was (134.80±34.98) min, the intraoperative blood loss was (100.13±18.49) mL, the hospital stay was (6.65±0.17) days, and the follow-up time was 6 to 18 (14±2.3) months. One patient had hematoma compression after surgery; he had incision made immediately to clear the hematoma and healed after bed rest. Two patients developed spinal hypertension and healed after bed rest. All the patients had no symptoms of nerve injury after operation, and the clinical symptoms were significantly relieved. We compared the perioperative VAS score and ODI index of all the patients, which were lower immediately after operation and at the last follow-up than those before the operation (P<0.05), and the difference was statistically significant. 【Conclusion】 Endo-LIF technology has good short-term clinical effects and the advantages of milder trauma, less blood loss, and quick recovery after surgery. It is a safe and minimally invasive lumbar fusion surgery.

2.
China Journal of Chinese Materia Medica ; (24): 528-532, 2013.
Artículo en Chino | WPRIM | ID: wpr-318662

RESUMEN

<p><b>OBJECTIVE</b>To study the protective effects of polysaccharides from Dendrobium huoshanense (DHP) against CCl4-induced liver injury in mice.</p><p><b>METHOD</b>Eighty male Kunming mice were randomly divided into normal control group, model control group, dextran control group, starch control group, hydrolyzate control group, three different dose of DPH groups consisting of high-dosage group, middle-dosage group and low-dosage group (200, 100, 50 mg x kg(-1)). Each group contained ten mice. The mice were treated with DHP via intragastric administration for 15 days before treatment of 50% CCl4 in olive oil for consecutive two days. Both alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities in serum and superoxide dismutase (SOD) activities and malondialdehyde (MDA) contents in liver tissues were determined in all groups. Immunohistochemistry was used to detect the expression of TNF-alpha in hepatic tissue. Hepatic histopathological examination was observed.</p><p><b>RESULT</b>DHP effectively decreased the activities of ALT and AST in serum and the contents of hepatic MDA, and restored hepatic SOD activities in acute liver injury mice. Liver tissue damage induced by CCl4 was ameliorated in mice with DHP administration through histopathology examination. Furthermore, the expression of TNF-alpha was greatly decreased in groups treated with polysaccharides.</p><p><b>CONCLUSION</b>DHP has a significantly hepatoprotective effect on CCl4-induced acute liver injury in mice. Protective effect of DHP on the liver may be related to its function of scavenging free radicals and inhibiting lipid peroxidation and TNF-alpha expression.</p>


Asunto(s)
Animales , Masculino , Ratones , Alanina Transaminasa , Sangre , Aspartato Aminotransferasas , Sangre , Tetracloruro de Carbono , Toxicidad , Enfermedad Hepática Inducida por Sustancias y Drogas , Sangre , Patología , Dendrobium , Química , Regulación de la Expresión Génica , Hígado , Metabolismo , Patología , Malondialdehído , Metabolismo , Polisacáridos , Química , Farmacología , Superóxido Dismutasa , Metabolismo , Factor de Necrosis Tumoral alfa , Metabolismo
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