医用一次性新型溶药器的研制与实验研究  

Development and clinical application of disposable medical dissolving drug apparatus

作　　者：徐雪芬[1] 傅新文[2] 刘勇[3] 叶英武[1] 周鸿 李鸿艳[3] 肖邦华 叶芸[5] 

机构地区：[1]江西省胸科医院哮喘科,江西南昌330006 [2]江西省人民医院检验科,江西南昌330006 [3]南昌大学公共卫生学院流行病与卫生统计学系 [4]江西省疾病控制中心检验科,江西南昌330006 [5]安远县人民医院检验科,江西安远342100

出　　处：《护理管理杂志》2007年第3期51-52,共2页Journal of Nursing Administration

摘　　要：目的减少粉针剂瓶药物的溶解环节,避免或减少微粒污染对人体造成的危害。方法分别用注射器和溶药器等量、等次稀释同批号对氨基水杨酸钠(2 g×6瓶)粉针剂瓶药物各30份。分别抽取样本检测稀释后药液微粒直径数,比较两种稀释方法所需的操作时间。结果溶药器与注射器稀释粉针剂瓶药物所检测的微粒直径总数量、操作所需的时间,差异均具有统计学意义(P<0.01)。结论新型溶药器稀释粉针剂瓶药物优于注射器稀释法。Objective To approach into reducing dissolving links of bottled pulvis drugs with venoclysis for preventing microparticles contamination injuring the body, Methods 60 bottled sodium para - aminosalicylate, divided into 2 groups, were diluted by the disposable medical dissolving drug apparatus and traditional standardization injector for single use only respectively. The diameters and numbers of the microparticles in the diluted liquid were detected for each 2 bottles with random sampling. The costs and spent time were contrasted between the two methods. Results The microparticles in the diluted agent and the colonial numbers of syringe were significantly statistical different between above two methods respectively （ P 〈 0, 01 ）. Conclusion The method of disposable medical dissolving drug apparatus is superior to that of traditional standardization injector in dissolving bottled pulvis drugs.

关 键 词：新型溶药器 注射器 微粒检测 

分 类 号：D472[政治法律—政治学]