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博来霉素与四环素作为兔胸膜硬化剂的疗效比较。

Effectiveness of bleomycin in comparison to tetracycline as pleural sclerosing agent in rabbits.

作者信息

Vargas F S, Wang N S, Lee H M, Gruer S E, Sassoon C S, Light R W

机构信息

Department of Medicine and Pathology, Veterans Administration Medical Center, Long Beach, Calif 90803.

出版信息

Chest. 1993 Nov;104(5):1582-4. doi: 10.1378/chest.104.5.1582.

Abstract

The two agents most commonly used for producing a pleurodesis are tetracycline and bleomycin. Tetracycline is no longer available due to more stringent requirements on the manufacturing process. The objective of this project was to determine whether bleomycin is an effective sclerosant in an experimental model in rabbits. The following medications were instilled intrapleurally in anesthetized male rabbits: tetracycline, 35 mg/kg, or bleomycin, 1.5 or 3.0 IU/kg diluted to a total volume of 1 ml with bacteriostatic saline solution. Twenty-eight days after the instillation, the animals were killed, and the pleural spaces were assessed grossly for evidence of pleurodesis and microscopically for evidence of fibrosis and inflammation. The intrapleural injection of bleomycin was ineffective in creating pleural fibrosis, either grossly or microscopically. The mean degree of gross pleurodesis in the six rabbits who received tetracycline was 2.7 +/- 1.5 (scale 0 to 4), while that in the rabbits who received the highest dose of bleomycin was 0.0 +/- 0.0. Based on this study, we recommend that bleomycin not be used as a pleural sclerosant in patients with nonneoplastic pleural disease, eg, those with pneumothorax, congestive heart failure or cirrhosis, and pleural effusion.

摘要

最常用于进行胸膜固定术的两种药物是四环素和博来霉素。由于对生产工艺的要求更加严格,四环素已不再可得。本项目的目的是确定博来霉素在兔实验模型中是否为一种有效的硬化剂。将以下药物经胸腔内注入麻醉的雄性兔体内:四环素,35毫克/千克,或博来霉素,1.5或3.0国际单位/千克,用抑菌生理盐水稀释至总体积1毫升。注入28天后,处死动物,大体评估胸膜腔有无胸膜固定术的证据,显微镜下评估有无纤维化和炎症的证据。胸腔内注射博来霉素在大体或显微镜下均未能有效造成胸膜纤维化。接受四环素的6只兔的大体胸膜固定术平均程度为2.7±1.5(0至4级),而接受最高剂量博来霉素的兔的大体胸膜固定术平均程度为0.0±0.0。基于本研究,我们建议博来霉素不应作为非肿瘤性胸膜疾病患者(如气胸、充血性心力衰竭或肝硬化合并胸腔积液患者)的胸膜硬化剂使用。

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