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自制腹透管尿毒症大鼠腹膜透析模型的建立 被引量:3

Establishment of peritoneal dialysis model in uremia rats with self-made peritoneal dialysis catheters
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摘要 目的:建立一种便利、成功率高的尿毒症大鼠腹膜透析模型.方法:采用医用硅胶吸痰管作为腹膜透析管,应用无菌输液接头,手术采用腹部正中切口,出口选在后背颈部(自制1组)或近尾部(自制2组),与传统的选材和手术方式(传统头皮针组,出口同自制1组)进行对照.结果:自制1组、传统头皮针组腹透管完好,无管道破损和渗漏;自制2组管道完全咬破损坏.自制1组出口处或隧道口感染3例,传统头皮针组6例.自制1组腹膜炎发生1例,传统头皮针组3例.自制1组第1日与第15日相比腹膜透析出液量无统计学差异(P>0.05),头皮针组差异有统计学意义(P<0.01),第1日自制1组与头皮针组相比无统计学差异(P>0.05),第15日自制1组与头皮针组相比存在统计学差异(P<0.05).自制1组腹透管大网膜完全包裹1例,部分包裹5例;传统头皮针组完全包裹4例,部分包裹6例.结论:正确的手术方式,是模型建立的基本保证,而透析管道的选材、接头稳固耐用是腹膜透析模型能否长期使用的关键. AIM: To develop an improved model of peritoneal dialysis in uremia rats. METHODS: Thirty SD rats were divided into three groups: experimental group 1, experimental group 2 and control group. In experimental groups, phlegm suction catheters were used as peritoneal dialysis catheters with tie-ins made from sterile transfuse connectors. The peritoneal dialysis catheters implanted into rats were tunneled subcutaneously to the nape (experimental group 1 ) or to the caudad part (experimental group 2). Rats with traditional operation mode and traditional operation materials belonged to the control group. RESULTS: Peritoneal dialysis catheters in rats in experimental group 1 were intact, whereas catheters in rats in experimental group 2 were broken. Three rats in experimental group 1 and six rats in control group had tunnel opening infections. One rat in experimental group 1 and 3 rats in control group had peritonitis. In experimental group 1, the amount of exchanged solution on the first day of peritoneal dialysis was not different with that on the fifteenth day (P 〉0.05 ), but in control group, the difference was significant ( P 〈0.01 ). There was no difference between experimental group 1 and control group in the amount of exchanged solution on the first day ( P 〉0.05 ), whereas there was significant difference on the fifteenth day ( P 〈0.05 ). Peritoneal dialysis catheters were completely wrapped by omentums in 1 rat in experimental group 1 and in 4 rats in control group. Catheters were partly wrapped in 5 rats in experimental group 1 and in 6 rats in control group. CONCLUSION: Correct operation modes, proper operation material and firm durable catheter fie-ins are the key factors for developing a successful model of peritoneal dialysis.
出处 《第四军医大学学报》 北大核心 2008年第8期749-751,共3页 Journal of the Fourth Military Medical University
关键词 腹膜透析 疾病模型 动物 尿毒症 透析管 大鼠 peritoneal dialysis disease models, animal uremia dialysis catheter rats
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参考文献9

  • 1Mortier S,Faict D,Schalkwijk CG,et al.long-term exposure to new peritoneal dialysis solutions:Effects on the peritoneal membrane[J].Kidney Int,2004,66(3):1257-1265.
  • 2Zareie M,Keuning ED,ter Wee PM,et al.Improved biocompatibility of bicarbonate/lactate-buffered PDF is not related to pH[J].Nephrol Dial Transplant,2006,21 (1):208 -216.
  • 3魏连波,吕瑞和,马志刚,叶任高,方敬爱.人参养荣汤对慢性肾功能衰竭腹膜透析营养不良大鼠模型的治疗作用[J].中国中西医结合肾病杂志,2000,1(1):18-20. 被引量:13
  • 4De Vriese AS,Tilton RG,Mortier S,et al.Myofibroblast tranedifferentiation of mesothelial cells is mediated by RAGE and contributes to peritoneal fibrosis in uraemia[J].Nephrol Dial Transplant,2006,21 (9):2549-2555.
  • 5Bammens B,Evenepeel P,Verbeke K,et al.Impairment of small intestinal protein assimilation in patients with end-stage renal disease:Extending the malnutrition-inflammation-atherosclerosis concept[J].Am J Clin Nutr,2004,80(6):1536-1543.
  • 6Tran L,Redela H,Avemethy NJ,et al.Lymphatic drainage of hypertonic solution from peritoneal cavity of anestheter-associatod infection[J].J Infect Dis,1993,168(4):897-867.
  • 7McDermid KP,Morck DW,Olson ME,et al.A porcine model of Staphylococcus epidennidis catheter-associated infection[J].J Infect Dis,1993,168(4):897-903.
  • 8Zweers MM,Deuma CE,de Waart DR,et al.The standard peritoneal permeability analysis in the rabbit:A longitudinal model for peritoneal dialysis[J].Perit Dial Int,1999,19 (1):56-64.
  • 9Slow S,Vasudevamurthy M,Fraser R,et al.Dimethylthetin treatment causes diffuse alveolar lung damage:A pilot study in a sheep model of Continuous Ambulatory Peritoneal Dialysis (CAPD)[J].Toxicol Pathol,2007,58 (5):285-290.

二级参考文献9

共引文献12

同被引文献21

  • 1何永成,栾韶东,陈海波,徐艺.非免疫性慢性肾功能衰竭大鼠模型的建立[J].宁夏医学杂志,2004,26(8):465-466. 被引量:2
  • 2周静,爱民,王朝阳,李兰城.腺嘌呤制作慢性肾功能衰竭大鼠疾病模型[J].内蒙古医学院学报,2004,26(4):248-249. 被引量:6
  • 3Zareie M,De Vriesc A S, Hekking I. H,et al. Immunopathological Changes in a Uraemic Rat Model for Peritoneal Dialysis [J]. Nephrol Dial Transplant, 2005,20( 7 ) : 1350-1361.
  • 4Nakamoto H, Kawaguchi Y, Suzuki H. ls technique survivalon peri|oneal dialysis better in Japan [ J ]. PeritDial hat, 2006,26(2) :1136-1139.
  • 5Lo W K. Peritoneal dialysis utilization and outcome: what are we facing [Jl. Perit Dial Int,2007,27 (2): 42 -44.
  • 6Izumotani T, lshimura E, Yamamoto T, et al. Correlation between peritoneal mesothelial cell cytology and peritoneal histopathology with respect to prognosis in patient s on continuous ambulatory peritoneal dialysis [J]. Nephron,2001,89 (1):43-49.
  • 7Kaneko K, Hamada C, Tomino Y. Peritoneal fibrosis intervention [ J ]. Perit Dial lnt, 2007, 27 ( 2 ) :82-87.
  • 8Diaz Buxo J A, Gotloib L. Agents that modulate peritoneal membrane structure and function [ J ]. Perit Dial Int, 2007,27( 1 ) :16-30.
  • 9Margetts P cytokines, peritoneum 2285 -2294 J, Kolb M, Yu L, et al. angiogenesis, and fibrosis J Pathol, 2002, Inflammatory in the rat 160 (6):2285-2294.
  • 10蓝天座,闵亚丽,朱春玲,郭碧林,卢涛.肾康注射液对单侧输尿管梗阻大鼠模型肾间质转化生长因子-β_1和骨形成蛋白-7表达的影响[J].中国药业,2008,17(10):20-21. 被引量:15

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