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1.
Chin J Traumatol ; 20(5): 308-310, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28802782

ABSTRACT

Hypoxia leads to increased red blood cells and blood viscosity at high altitude while moderate trauma increases coagulation in blood. Under the above-mentioned conditions, venous sinus thrombosis is more likely to occur. A patient suffering bilateral acetabular fractures together with the gradual disturbance of consciousness was admitted to our hospital. Though computed tomography arteriogram (CTA) of the brain displayed normal blood vessels; bilateral thalamus and brainstem infarction were found on head computed tomography (CT) and Galen vein thrombosis on cerebral computed tomography venography (CTV). Dehydration and tracheotomy were immediately conducted with antiplatelet, anticoagulant and neurotrophic medicine administered to the patient. After three days' treatment, the patient's consciousness gradually improved and eventually became clear enough to leave the hospital. On follow-up, no dysfunction was documented.


Subject(s)
Acetabulum/injuries , Cerebral Veins , Fractures, Bone/complications , Venous Thrombosis/etiology , Humans , Male , Middle Aged , Tibet , Tomography, X-Ray Computed , Venous Thrombosis/diagnostic imaging
2.
Chin J Traumatol ; 18(1): 33-8, 2015.
Article in English | MEDLINE | ID: mdl-26169092

ABSTRACT

PURPOSE: To develop a novel injectable strontium-containing calcium phosphate cement with collagen. METHODS: A novel calcium phosphate bone cement (CPC) was prepared with the addition of strontium element, collagenl, and modified starch; the injectability, solidification time, microstructure, phase composition, compressive strength, anti-collapsibility and histological properties of material were evaluated. RESULTS: The results showed that the material could be injected with an excellent performance; the modified starch significantly improved the anti-washout property of cement; with the liquid to solid ratio of 0.3, the largest compressive strength of cement was obtained (48.0 MPa ± 2.3 MPa); histological examination of repair tissue showed that the bone was repaired after 16 weeks; the degradation of cement was consistent with the new bone growth. CONCLUSION: A novel injectable collagen-strontium-containing CPC with excellent compressive strength and suitable setting time was prepared, with addition of modified starch. The CPC showed a good anti-washout property and the degradation time of the cement met with the new bone growing. This material is supposed to be used in orthopedic and maxillofacial surgery for bone defects.


Subject(s)
Bone Cements/chemistry , Calcium Phosphates/chemistry , Collagen/chemistry , Strontium/chemistry , Animals , Bone Cements/therapeutic use , Compressive Strength , Histocompatibility Testing , Injections , Rabbits
3.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi ; 27(3): 317-9, 2011 Mar.
Article in Chinese | MEDLINE | ID: mdl-21638930

ABSTRACT

AIM: To determine the effect of bFGF on extracellular matrix and gene expression on the human de-generated nucleus pulposus cells. METHODS: The degenerated intervertebral disc cells were divided into 5 groups. A group: adding 100 pg/L bFGF, B group: adding 200 pg/LbFGF, C group: 500 pg/L bFGF, D group: 1000 pg/L bF-GF, E groups: control group, without interfering factors. The type II collagen and GAG mRNA expression were test, type II collagen content and glycosaminoglycan content of the supernatant were test. RESULTS: bFGF stimulated de-generated nucleus pulposus cells, collagen II, GAG mRNA, collagen type II and glycosaminoglycan expression of the extracellular matrix were increased significantly on the 7 days compared with the control group (P < 0. 05). type II collagen and GAG mRNA were significantly lower than the control group on 14 days, 21 days (P < 0.05). However,collagen type II and glycosaminoglycan expression of the extracellular matrix on 14 days, 21 days were still higher than normal (P <0.05). CONCLUSION: bFGF increase GAG and type II collagen mRNA expression, increased extracellular matrix type II collagen and GAG expression in short-term.


Subject(s)
Biomedical Research , Fibroblast Growth Factors/pharmacology , Glycosaminoglycans/metabolism , Intervertebral Disc Degeneration/drug therapy , Intervertebral Disc/metabolism , Intervertebral Disc/pathology , RNA, Messenger/drug effects , Collagen Type II/drug effects , Collagen Type II/metabolism , Extracellular Matrix/drug effects , Extracellular Matrix/metabolism , Humans , Intervertebral Disc/drug effects , Intervertebral Disc Degeneration/pathology , RNA, Messenger/metabolism
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