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find Author "刘瑛" 12 results
  • Genetic Polymorphism of Methicillin Resistant Staphylococcus Aureus Isolated from Hospital Acquired Pneumonia

    Objective To investigate the genetic polymorphism of methicillin resistant Staphylococcus aureus ( MRSA) isolated from hospital acquired pneumonia. Methods Seventy-four hospitalized patients were diagnosed as noscomial MRSA pneumonia from January 2007 to January 2008 in Xinhua Hospital, Shanghai Jiaotong Univesity. The genes of MRSA were amplified by random amplified polymorphic DNA typing ( RAPD) assay in 82 clinical isolates from these patients. Results Two to 15 amplified DNA fragments were observed in agarose gel and they were classified into 11 genotypes. Genotypes Ⅲ, Ⅵ and Ⅶ ( 32. 56% , 30. 23% and 13. 95% , respectively) were mainly isolated from the ICU. Both independent genotypes and overlapping genotpyes with those from ICU were identified in isolates from the departments of geriatrics, emergency and respiratory medicine. Outbreak or cluster cases ( 48. 65% ) were found in 36 of the 74 patients while all outbreak cases occurred in the ICU. Conclusions Noscomial MRSA pneumonia is easy to disseminate and small-scale outbreak may occur especially in ICU. RAPD is valuable for identification and prevention of the spread of MRSA in hospital.

    Release date:2016-09-14 11:24 Export PDF Favorites Scan
  • QRDR Mutations in Fluoroquinolon-Resistant Pseudomonas aeruginosa and Its Relationship with the Usage of Antibiotics in Nosocomial Pneumonia

    Objective To investigate the mutations of quinolone resistance determinational region ( QRDR) in fluoroquinolon-resistant Pseudomonas aeruginosa strains isolated from patients with nosocomial pneumonia. Methods Eight-four Pseudomonas aeruginosa strains isolated from patients with nosocomial pneumonia in Xinhua Hospital during January 2006 to December 2007, from whom fluoroquinolon-resistant resisitant ( case) and fluoroquinolon-susceptible ( control ) Pseudomona aeruginosa were identified. The mutation of QRDR was tested by restriction fragment length polymorphism ( RFLP) and gene sequencing.The relationship between QRDR mutations and clinical prescription was analyzed. Results Mutation in QRDR was found in 42 isolates among the 50 fluoroquinlon-resisitant isolates( 84. 0% ) , while no mutation was found in fluoroquinlon-susceptible isolates. The mutation in GyrB Ser464 was found in 34 isolates ( 68. 0% ) . There was statistical difference in the usage of β-lactams between the GyrB-Ser464-mutated group and the non-GyrB-Ser464-mutated group( OR = 11. 3, P = 0. 003 and OR = 3. 5, P = 0. 023) , also in the time of fluoroquinolon usage before isolated ( P = 0. 038) . Conclusions The mutation of QRDR is contributing to fluoroquindor-resisitance of Pseudomona aeruginosa, most of which lies in GyrB Ser464.Abuse of β-lactams and fluoroquinolon may be the risk factors of mutation in GyrB Ser464.

    Release date:2016-09-14 11:25 Export PDF Favorites Scan
  • 自身免疫性视神经病变

      自身免疫性视神经病变(AON)是指通过炎症性自身免疫机制损害一侧或双侧视神经而不伴有全身性自身免疫性疾病的一种排除诊断。患者一旦出现非典型的复发性视神经炎而无法用其它病因解释即应考虑AON。随诊过程中,必须留意全身症状并重复进行实验室检查,一旦其临床表现符合已知的自身免疫性疾病或胶原血管疾病(CVD)诊断标准,AON诊断将不再成立。部分找不到病因的视神经病变患者,特别是双眼发病或复发者,可以行皮肤活检辅助诊断。治疗AON的药物包括糖皮质激素、苯丁酸氮芥、环磷酰胺、甲氨喋呤、硫唑嘌呤、麦考酚酸吗乙酯及静脉注射免疫球蛋白等,但由于AON病例较为少见,目前还难以客观评价具体药物疗效。

    Release date:2016-09-02 05:41 Export PDF Favorites Scan
  • Effects of testosterone on optic nerve and retinal ganglion cells in experimenta l autoimmune encephalomyelitis

    Objective:To observe the effects of testosterone on optic nerve an d retinal ganglion cells (RGC) in experimental autoimmune encephalomyelitis (EAE ). Methods:Fourty one female Wistar rats were randomly divide d into 3 groups: the normal group (10 rats), the untreated control group (15 rats) and the testos terone group (16 rats). The rats in the first two groups were fed with 1% ethano l every day, and the rats in the testosterone group were fed with methyltestoste rone (0.25 mg/kg) every day. On the 20th day, EAE model was induced in the untre ated control group and the testosterone group by injecting guinea pig spinal cor d homogenate in complete Freund's adjuvant and bordetella pertussis vaccine. RGC were labeled with flurogold (FG) by injecting it in superior colliculus and lat eral geniculate body 7 days before establishing EAE model. All rats were fed wit h drugs continuously, and after 1430 days, rats in normal group and rats in un t reated control and testosterone groups who had symptoms within 48~72 hours were observed by light microscopy and flash visual evoked potential (FVEP) to detect the functional and morphological changes of optic nerve. The number of RGC was counted by fluorescence microscopy,and apoptosis of RGC was observed by termina l deoxynucleotidyl transferasemediated biotinylated UTP nick end labeling (TUN E L) Results:EAE rats presented weakness or paralysis of tail a nd hind limbs 10 days after establishing EAE model. Compared with the rats in the untreated contr ol group, the rats in the testosterone group had longer disease delitescence and lower clinical score (P=0.042). Extensive demyelination of optic nerves wi th the circuitous configuration was found in the untreated control group; while mild demyelination of optic nerves with regular figure was found in the testosterone group. In the testosterone group, the latency of N1、P and N2 wave was shorter w hile the amplitude ofN1-P and P-N2was higher than that in the untreated cont rol group (Plt;0.05). The number of RGC was (2284plusmn;132), (934plusmn;78, and (1725 plusmn;95)cells/mm2 in the normal, untreated control and testosterone groups, respectively; w hich was higher in testosterone group than that in untreated control group (P=0.028). The number of TUNEL positive cells was (4.02plusmn;0.16), (24.44plusmn;2.22), and (9.84plusmn;2.36) cells per high power field (times;400) in the 3 grou ps, respectively; wh ich was less in testosterone group than that in untreated control group (P=0.025). Conclusions:Testosterone may reduce the incidence and clinical score of EAE, inhibit the apoptosis of RGC, alleviate the demyelinatio n of optic nerves, and improved the conduction function of optic nerves.

    Release date:2016-09-02 05:48 Export PDF Favorites Scan
  • Value of ice test in diagnosis of myasthenia gravis

    Objective To investigate the value of ice test in the diagnosis of ptosis of myasthenia gravis(MG). Methods A total of 32 patients with myasthenic ptosis and 33 with nonmyasthenic ptosis underwent ice and rest test which were performed alternately twice within 1 day on each patient. Besides, neostigmine test was performed on the patients with myasthenic ptosis after ice and rest test . Two observers who didnrsquo;t know the clinical diagnosis were asked to evaluate the improvement of eyelid elevation by measuring the width between the midpoints of upper and lower eyelid with a 20mm steel rule (precision of 0.5 mm). The average of margin of palpebral fissure width after double ice or rest tests subtrac ted from the one before the tests in one patient was the standard of the improve ment of eyelid elevation. Results Ice and rest test improved myasthenic ptosis but not nonmyasthenic ptosis with the specificity of 100% in both of the tests. In addition, ice test improved myasthenic ptosis more effectively with a higher sensitivity of 78%, and it could also improve the palpebral fissure width in pa i tents with complete myasthenic ptosis apparently. Compared with the neostigmine test, ice test had lower sensitivity, cost shorter time, didnt need injection which avoided the discomfort, and had no side effects. Conclusion Ice test is a simple and safe means with high sensitivity and specificity to diagnose myasthenic ptosis, which is valuable in clinical application. (Chin J Ocul Fundus Dis, 2006,22:382-384)

    Release date:2016-09-02 05:51 Export PDF Favorites Scan
  • 视神经疾病的基因治疗新进展

    视神经由视网膜神经节细胞(RGC)轴索组成,因其周围无Schwann细胞,故损伤后不能再生。对于大多数可导致RGC发生不可逆损伤的视神经疾病,即使给予对因治疗,其视功能预后也较差;而对于遗传性视神经疾病,至今尚无有效的治疗方法。因此,相关的基因治疗研究便逐步受到重视和得以广泛开展,并有望成为某些视神经疾病的可供选择的治疗方法之一。

    Release date:2016-09-02 05:51 Export PDF Favorites Scan
  • Efficacy and Safety of Linagliptin for Type 2 Diabetes Mellitus: A Meta-analysis

    ObjectiveTo systematically review the efficacy and safety of linagliptin in the treatment of type 2 diabetes. MethodsWe searched The Cochrane Library, EMbase, PubMed, CNKI, CBM, VIP and WanFang data to collect randomized controlled trials (RCTs) on linagliptin versus placebo for type 2 diabetes from inception to January 2015. Two reviewers independently screened literature, extracted data and assessed the risk of bias of included studies. Then meta-analysis was performed using RevMan 5.3 software. ResultsA total of 16 RCTs were included. The results of meta-analysis showed:The linagliptin monotherapy group was superior to the placebo group in reducing HbA1c (MD=-0.76, 95%CI -0.85 to -0.66) and FPG (MD=-1.12, 95%CI -1.28 to -0.95), and there were no statistical differences in the incidence of overall adverse events (OR=0.86, 95%CI 0.70 to 1.06) and hypoglycemic (OR=1.19, 95%CI 0.36 to 4.01) between the two groups. The linagliptin combination treatment group (combined with other oral antihyperglycemic drugs) was superior to the placebo combination treatment group in reducing HbA1c (MD=-0.61, 95%CI -0.67 to -0.56) and FPG (MD=-0.79, 95%CI -0.96 to -0.63), and there was no statistical difference in the incidence of overall adverse events between the two groups (OR=1.07, 95%CI 0.92 to 1.24), however, the incidence of hypoglycaemic in the linagliptin combination treatment group was higher than that in the placebo combination treatment group (OR=1.55, 95%CI 1.19 to 2.02). ConclusionLinagliptin is effective and safe in the treatment of type 2 diabetes. Due to the limited quantity and quality of included studies, more high quality studies are needed to verify the above conclusion.

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  • Quality assessment of systematic reviews on community interventions in China

    ObjectivesTo assess the characteristics, methodological and reporting qualities of systematic reviews on community interventions in China.MethodsThe Cochrane Library, PubMed, EMbase, Web of Science, CNKI, VIP, WanFang Data and CBM databases were searched for studies of community interventions from inception to August 2017. Two reviewers independently screened literature, extracted data and assessed the methodological and reporting quality by AMSTAR tool and PRISMA checklist. Data analysis was performed by SPSS 20.0 software.ResultsA total of 18 systematic reviews of community interventions were included. The average AMSTAR score was 4.67±1.68, and all studies did not provide the list of included and excluded studies or a statement on conflict of interests. The average PRISMA score was 16.42±3.65, and over 50.0% of the included systematic reviews did not perform protocol and registration, search, additional analyses, risk of bias of included studies and funding.ConclusionsThe evidence shows that the reporting and methodological quality of meta-analyses of community interventions in China is insufficient. The combination of results, quality of individual research and the evaluation of publication bias should be paid more attention to improve methodological quality. The reporting of meta-analyses of community interventions in China should follow the PRISMA checklist.

    Release date:2018-07-18 02:49 Export PDF Favorites Scan
  • Risk Factors and Genotyping of Nosocomial Pneumonia Due to Extended Spectrum β-Lactamase Producing EscherichiaColi and KlebsiellaPneumoniae

    Objective To analyze the current drug resistance and risk factors of hospital acquired pneumonia( HAP) due to extended spectrumβ-lactamase ( ESBLs) producing Escherichia coli and Klebsiella pneumoniae, and to estimate the prevalence trend of ESBLs producing strains. Methods FromApril 2007 to January 2008, 140 patients of Xinhua Hospital with HAP due to E. coli and K. pnermoniae were enrolled.Among them, 88 patients were with ESBLs producing strains and 52 patients were with non-ESBLs producing strains. Risk factors were analyzed by comparing between these patients. The rate of drug resistance was determined by antibiotic sensitive test. Fifty-three ESBLs producing strains were genotyped by random amplified polymorphic DNA ( RAPD) . Results The rate of drug resistance of ESBLs producing strains washigher than that of non-ESBLs producing strains. ICU stay, use of third- and forth-generation cehpalosporin were found to be the independent risk factors by multivariate analysis with logistic regression. By RAPD, 37 ESBLs producing E. coli strains were divided into 27 types and 16 ESBLs producing K. pneumoniae strains were divided into 13 types. Conclusions ICU stay, use of third-generation and forth-generation cehpalosporin remain as major risk factors in the HAP due to ESBLs producing E. coli and K. pneumoniae.RAPD is an economic, quick and credible method for epidemic analysis

    Release date:2016-08-30 11:53 Export PDF Favorites Scan
  • 特发性颅内压增高症

    特发性颅内压增高症好发于育龄期肥胖妇女,以头痛和视盘水肿为主要表现,脑脊液循环障碍导致颅内压增高,脑静脉窦阻塞或狭窄可能在其中发挥重要作用 ;内分泌功能失调可能也起到一定作用。

    Release date:2016-09-02 05:46 Export PDF Favorites Scan
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