2.Prevention and Management of Deep Fungal Infection by Fluconazole in the Patients with Severe Acute Pancreatitis
Jun YAN ; Chunhai GUO ; Ji WANG
Chinese Journal of Nosocomiology 2006;0(05):-
OBJECTIVE To investigate the clinical character of patients with severe acute pancreatitis(SAP)(infected) with deep fungal organisms and its prevention and treatment with fluconazole.METHODS Among 256(patients) with SAP,46 cases with SAP and deep fungal infection treated by fluconazole were selected as(fluconazole) treatment group,66 patients with suspicious deep fungal infection were randomized into 2 groups: fluconazole(prevention) group(42 cases) and control group(24 cases).RESULTS There were lower incidences of deep fungal(infection) in fluconazole prevention group than that in control one(P
3.Anesthesia effect in operation of whole lung lavage for treatment pneumoconiosis.
Zhi-Guo HAN ; Guo-Xuan MA ; Ji-Cheng WANG
Chinese Journal of Industrial Hygiene and Occupational Diseases 2010;28(1):61-62
Adult
;
Aged
;
Anesthesia
;
methods
;
Bronchoalveolar Lavage
;
methods
;
Female
;
Humans
;
Male
;
Middle Aged
;
Pneumoconiosis
;
surgery
;
Retrospective Studies
4.Integrated account audits management of medical insurance payment
Difei WANG ; Xiaojing WANG ; Boya ZHAO ; Xu GUO ; Lei JI
Chinese Journal of Hospital Administration 2013;29(8):606-609
Using the enterprise resource planning(ERP)management mode,the paper analyzed the present medical insurance payment audit accounts at public hospitals,and probed into the establishment of an information management platform for medical insurance payment audit accounts in the ERP environment.The purpose is to perfect the management of medical insurance payment audit accounts,increase the efficiency of hospital's working capital,strengthen the quality and efficiency of hospital management.
6.13 cases of Abamectin poisoning.
Yu-fei GUO ; Yi WANG ; Ji-xian ZHANG
Chinese Journal of Industrial Hygiene and Occupational Diseases 2010;28(6):472-472
Adult
;
Female
;
Humans
;
Insecticides
;
poisoning
;
Ivermectin
;
analogs & derivatives
;
poisoning
;
Male
;
Middle Aged
7.Expression and significance of Toll like receptor 2 and Toll like receptor 4 in chronic rhinosinusitis.
Xin WANG ; Wenjun JI ; Yuan XU ; Huamin GUO ; Chunyuan ZHAO
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2014;28(17):1285-1288
OBJECTIVE:
To explore the role of the innate immune factors TLR2 and TLR4 in the pathogenesis of chronic rhinosinusitis (CRS) by detecting their expression in different clinical types of CRS and the normal control group.
METHOD:
Immunohistochemistry was used to detect the expression of TLR2 and TLR4 respectively in 21 cases (chronic rhinosinusitis with nasal polyps, CRSwNP) group, 15 cases (chronic rhinosinusitis without nasal polyos, CRSsNP) group, 11 cases recurrent CRSwNP group and 13 cases control group. Positive cells were counted under the microscope artificially, Mann-Whitney U analysis was applied for the ranked data, and one-way anova analysis was adopted to analyze the experimental group and control group.
RESULT:
(1) TLR2 and TLR4 expression had the same characteristics. Expression mainly concentrated in parts of the whole layer of epithelial basement membrane, cytoplasm of glandular cells, very few inflammatory cells such as monocytes and plasma cells in the cytoplasm, sometimes unknown cell nuclei positive expression. (2) The glandular cells were stained manual counting and color grading. TLR2 and TLR4 packet application Wilcoxon rank test Mann-Whitney U test analysis was not statistically significant (P > 0.05), measurement data within the group variance statistical difference between the groups (P < 0.05).
CONCLUSION
The Nasal mucosa can produce the innate immune factors TLR2 and TLR4. The different expression of TLR2 and TLR4 in the various clinical types of CRS suggests that they play the certain role in the pathogenesis of CRS.
Chronic Disease
;
Epithelial Cells
;
immunology
;
metabolism
;
Female
;
Humans
;
Immunohistochemistry
;
Male
;
Nasal Mucosa
;
immunology
;
metabolism
;
Nasal Polyps
;
immunology
;
metabolism
;
Rhinitis
;
immunology
;
metabolism
;
Sinusitis
;
immunology
;
metabolism
;
Toll-Like Receptor 2
;
metabolism
;
Toll-Like Receptor 4
;
metabolism
8.Study on HPLC Fingerprint of Desmodium styracifolium and Its Preparations
Shengguo JI ; Nianxin GUO ; Yingchun LI ; Dong WANG
China Pharmacy 2007;0(27):-
OBJECTIVE:To establish RP-HPLC fingerprints of Desmodium styracifolium and its preparations in order to provide basis for the quality evaluation of them.METHODS:The separation was performed on ODS-C18(250 mm?4.6 mm,5 ?m) column with mobile phase consisted of methanol-20% phosphoric acid(gradient elution).The detection wavelength was set at 360 nm and flow rate was 1.0 mL?min-1.Column temperature was set at 25 ℃.The RP-HPLC fingerprint of D.styracifolium and its preparations were recorded.RESULTS:There were 13 common peak in RP-HPLC fingerprint of D.styracifolium and its preparations.CONCLUSION:The method is accurate,stable and reproducible for basis of quality evaluation and RP-HPLC finger print of D.styracifolium and its preparations.
9.THE EFFECT OF MSG ON THE EXPRESSION OF 5-HT IN GASTROENTERIC MUCOSA OF RAT
Fengqing JI ; Hongwei SHANG ; Xingcui WANG ; Chongji GUO
Acta Anatomica Sinica 2002;0(05):-
Objective To explore the effect of monosodium glutamate (MSG) on the expression of 5\|HT in gastroenteric mucosa of rat. Methods Immunohistochemical technique was used to detect the expression of 5\|HT. The immuno\|activity and the density of positive cells were measured by image analysis. Results The immuno\|activity and the density of 5\|HT positive cells(EC cell) in the experimental group are higher than that in control group. The effect by 120d is the most significant, followed by that of 52d. Statistical analysis showed a significant difference ( P
10.Determination of Ligustrazine in Rat's Plasma,Brain and Liver by HPLC
Lisheng WANG ; Aixian YUAN ; Jian HAN ; Xiujuan CHEN ; Ji GUO
China Pharmacy 2001;0(09):-
OBJECTIVE:To establish an HPLC method for the determination of the contents of Ligustrazine in rat's plasma,brain and liver.METHODS:Ligustrazine was separated on Hypersil ODS-C18 column with aspirin as internal standard.The mobile phase consisted of methanol-1.5% glacial acetic acid solution(45∶55,V/V)at a flow rate of 1.0 mL?min-1.The UV detection wavelength was 279 nm.RESULTS:The linear range of ligustrazine in rat's plasma,brain and liver was 0.006 25~7.813 ?g?mL-1,The lowest detectable limits were 0.5 ng?mL-1,1.55 ng?mL-1,and 1.55 ng?mL-1 and the average recoveries were 97.26%,96.44%,and 95.43% respectively with RSD at 3.40%,4.19% and 4.94%,respectively.CONCLUSION:With good linearity,precision and recovery,the method is sensitive and simple,and suitable for pharmacokinetic study and the research of Ligustrazine preparation.