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17篇 您的检索式:作者名="Preethi G"
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1Factors predicting adverse short-term outcomes in patients with acute cholangitis undergoing ERCP: A single center experience显示文摘AIM: To identify potential factors that can predict adverse short-term outcomes in patients with acute cholangitis undergoing endoscopic retrograde cholangiopancreatography(ERCP). METHODS: Retrospective analysis of consecutive patients admitted to our center for acute cholangitis and underwent ERCP from 2001 to 2012. Involvement of two or more organ systems was termed as organ failure(OF). Cardiovascular failure was defined based on a systolic blood pressure of < 90 mmHg despite fluid replacement and/or requiring vasopressor treatment; respiratory failure if the Pa02 /Fi02 ratio was < 300 mmHg and/or required mechanical ventilation; coagulopathy if the platelet count was < 80; and renal insufficiency if serum creatinine was > 1.9 mg/dL. Variables associated with short term adverse clinical outcomes defined as persistent OF and/or 30-d mortality was determined. RESULTS: A total of 172 patients(median age 62 years, 56.4% female) were included. The median door to ERCP time was 17 h. Bile duct stones were the most common etiology(n = 67, 39.2%). In multivariate analysis, factors that were independently associated with persistent OF and/or 30-d mortality included American Society of Anesthesiology(ASA) physical classification score > 3(OR = 7.70; 95%CI: 2.73-24.40), presence of systemic inflammatory response syndrome(OR = 3.67; 95%CI: 1.34-10.3) and door to ERCP time greater than 72 h(OR = 3.36; 95%CI: 1.12-10.20). Door to ERCP time greater than 72 h was also associated with 70% increase in the mean length of stay(P < 0.001). Every one point increase in the ASA physical classification and every 1 mg/dL increase in the preERCP bilirubin level was associated with a 34% and 2% increase in the mean length of hospital stay, respectively. Transfer status did not impact clinical outcomes. CONCLUSION: Higher ASA physical classification and delays in ERCP are associated with adverse clinical outcomes and prolonged length of hospital stay in patients with acute cholangitis undergoing ERCP.Udayakumar Navaneethan Norma G Gutierrez Ramprasad Jegadeesan Preethi GK Venkatesh Madhusudhan R Sanaka John J Vargo Mansour A Parsi 2014World Journal of Gastrointestinal Endoscopy2014,6,3:7
2印度亚拉文眼科模式(英文)显示文摘印度亚拉文医院是世界卫生组织合作单位,创造了“大规模、高质量、低成本”的眼科医疗模式,2005年,医院门诊量达163万多,手术超过22万例,其中白内障手术达16万多例,为世界之最。如何有效地借鉴印度亚拉文的模式为我所用,成为中国眼科界同仁日益热烈讨论的一个话题。本刊特邀印度亚拉文医院的主要负责人就该模式的特点撰文介绍。Srinivasan M Thulasiraj RD Preethi Pradhan Veni G 2006眼视光学杂志2006,8,2:6
3Reprint of “influence of chitosan-PEG binary template on the crystallite characteristics of sol-gel synthesised mesoporous nanotitania photocatalyst”显示文摘PREETHI T ABARNA B RAJARAJESWARI G R 2014Applied Surface Science2014,319,:1
4Structural modes of stabilization of permissive phosphorylation sites in protein kinases:distinct strategies in Ser/Thr and Tyr kinases显示文摘Krupa A Preethi G Srinivasan N 2004J Mol Biol2004,339,:1
5Structural modes of stabilization of permissive phosphorylation sites in protein kinases: Distinct strategies in Ser/qlar and Tyr kinases显示文摘KRUPA A PREETHI G SRINIVASAN N 2004J Mol Biol2004,339,5:1
6Structural modes of stabi- lization of permissive phosphorylation sites in protein kinases : distinct strategies in Ser/Thr and Tyr kinases显示文摘Krupa A Preethi G Srinivasan N 2004Journal of Molecular Biology2004,339,5:1
7Antitumor activity of Ruta graveolens extract 显示文摘Preethi K C Kuttan G Kuttan R 2006Asian Pae J Cancer Prey2006,7,3:1
8Structural modes of sta- bilization of permissive phosphorylation sites in protein kinases : dis- tinct strategies in Ser/Thr and Tyr kinases 显示文摘KRUPA A PREETHI G SRINIVASAN N 2004J Mol Biol2004,339,5:1
9Structural modes of stabilization of permissive phosphorylation sites in pro- tein kinases:Distinct strategies in Ser/Thr and Tyr kina- ses显示文摘Krupa A Preethi G Srinivasan N 2004J Mol Bio12004,339,:1
10Structural modes of stabilization of permissive phosphorylation sites in protein kinases:distinct strategies in Ser/Thr and Tyr kinases 显示文摘Krupa A Preethi G Srinivasan N 2004J Mol Biol2004,,10:1
11Structural modes of stabilization of permissive phosphorylation sites in protein kinases:distinct strategies in Ser/Thr and Tyr kinases显示文摘KRUPA A PREETHI G SRINIVASAN N 2004J Mol Biol2004,339,5:1
12Structural modes of stabilization of permissive phosphorylation sites in protein kinases: distinct strategies in Ser/Thr and Tyr kinases 显示文摘KRUPA A PREETHI G SRINIVASAN N 2004Journal of Molecular Biology2004,339,5:1
13Structural modes of stabilization of permissive phosphorylation sites in protein kinases: distinct strategies in ser/thrand tyr kinases显示文摘Krupa A Preethi G Srinivasan N 2004J Mol Biol2004,339,5:1
14Structural modes of stabilization of permissive phosphorylation sites in protein kinases:distinct strategies in Ser/Thr and Tyr kinases显示文摘KRUPA A PREETHI G SRINIVASAN N 2004J Mol Biol2004,339,5:1
15Evaluation of lipophilicity,antimi-crobial activity and mutagenicity of some novel ester prodrugs of metronidazole显示文摘Dubey S Jain V Preethi G 2009Indian J Chem2009,48,:1
16Structural modes of stabilization of permissive phosphorylation sites in protein kinases: distinct strategies in Ser/Thr and Tyr kinases显示文摘Krupa A Preethi G Srinivasan N 2004J Mol Biol2004,339,5:1
17Structural modes of stabilizati on of permissive phosphorylation sims in protein kinases: distinct strategies in Ser/Thr and Tyr kinases显示文摘KRUPA A PREETHI G SRINIVASAN N 2004J Mol Biol2004,339,:1
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