Jensen D M, Machicado G A, Tapia J I, Kauffman G, Franco P, Beilin D
Gastroenterology. 1983 Mar;84(3):573-9.
One of the most promising nonoperative techniques for control of variceal hemorrhage is sclerosis via the fiberoptic endoscope. Many questions remain, however, about sclerosing agents, guidelines for effective use, and limitations of endoscopic techniques. A reproducible large animal model of esophageal varices would facilitate the critical evaluation of techniques for variceal hemostasis or sclerosis. Our purpose was to develop a large animal model of esophageal varices. Studies in pigs and dogs are described which led to the development of a reproducible canine model of esophageal varices. For the final model, mongrel dogs had laparotomy, side-to-side portacaval shunt, inferior vena cava ligation, placement of an ameroid constrictor around the portal vein, and liver biopsy. The mean (+/- SE) pre- and postshunt portal pressure increased significantly from 12 +/- 0.4 to 23 +/- 1 cm saline. Weekly endoscopies were performed to grade the varix size. Two-thirds of animals developed medium or large sized esophageal varices after the first operation. Three to six weeks later, a second laparotomy with complete ligation of the portal vein and liver biopsy were performed in animals with varices (one-third of the animals). All dogs developed esophageal varices and abdominal wall collateral veins of variable size 3-6 wk after the first operation. After the second operation, the varices became larger. Shunting of blood through esophageal varices via splenic and gastric veins was demonstrated by angiography. Sequential liver biopsies were normal. There was no morbidity or mortality. Ascites, encephalopathy, or spontaneous variceal bleeding did not occur. We have documented the lack of size change and the persistence of medium to large esophageal varices and abdominal collateral veins in all animals followed for more than 6 mo. Variceal bleeding could be induced by venipuncture for testing endoscopic hemostatic and sclerosis methods. We suggest other potential uses of this reproducible canine model of esophageal varices.
控制静脉曲张出血最有前景的非手术技术之一是通过纤维内镜进行硬化治疗。然而,关于硬化剂、有效使用指南以及内镜技术的局限性仍存在许多问题。一种可重复的大动物食管静脉曲张模型将有助于对静脉曲张止血或硬化技术进行严格评估。我们的目的是建立一种大动物食管静脉曲张模型。本文描述了在猪和狗身上进行的研究,这些研究促成了一种可重复的犬类食管静脉曲张模型的建立。对于最终模型,杂种狗接受了剖腹手术、端侧门腔分流术、下腔静脉结扎术、在门静脉周围放置阿梅氏缩窄环以及肝脏活检。分流术前和术后门静脉平均压力(±标准误)从12±0.4显著增加至23±1厘米盐水柱。每周进行内镜检查以对静脉曲张大小进行分级。三分之二的动物在首次手术后出现中等或大尺寸的食管静脉曲张。三至六周后,对有静脉曲张的动物(动物总数的三分之一)进行第二次剖腹手术,完全结扎门静脉并进行肝脏活检。所有狗在首次手术后3 - 6周均出现食管静脉曲张和大小不一的腹壁侧支静脉。第二次手术后,静脉曲张变得更大。血管造影显示血液通过脾静脉和胃静脉经食管静脉曲张分流。连续的肝脏活检结果正常。无发病率或死亡率。未出现腹水、脑病或自发性静脉曲张出血。我们记录了所有随访超过6个月的动物中食管静脉曲张和腹部侧支静脉的大小没有变化且持续存在。通过静脉穿刺诱导静脉曲张出血可用于测试内镜止血和硬化方法。我们提出了这种可重复的犬类食管静脉曲张模型的其他潜在用途。