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使用中的静脉混合输液中的微粒和微生物污染

Particulate and microbial contamination in in-use admixed intravenous infusions.

作者信息

Yorioka Katsuhiro, Oie Shigeharu, Oomaki Masafumi, Imamura Akihisa, Kamiya Akira

机构信息

Department of Pharmacy, Saiseikai Yamaguchi University Hospital, Japan.

出版信息

Biol Pharm Bull. 2006 Nov;29(11):2321-3. doi: 10.1248/bpb.29.2321.

Abstract

We compared particulate and microbial contamination in residual solutions of peripheral intravenous admixtures after the termination of drip infusion between intravenous fluids admixed with glass ampoule drugs and those admixed with pre-filled syringe drugs. The mean number of particles>or=1.3 microm in diameter per 1 ml of residual solution was 758.4 for fluids (n=60) admixed with potassium chloride in a glass ampoule (20 ml volume), 158.6 for fluids (n=63) admixed with potassium chloride in a pre-filled syringe (20 ml volume), 736.5 for fluids (n=66) admixed with sodium chloride in a glass ampoule (20 ml volume), 179.2 for fluids (n=15) admixed with sodium chloride in a pre-filled syringe (20 ml volume), 1884.5 in fluids (n=30) admixed with dobutamine hydrochloride in 3 glass ampoules (5 ml volume), and 178.9 (n=10) in diluted dobutamine hydrochloride in pre-filled syringes (50 ml volume: For these samples alone, particulate and microbial contamination were evaluated in sealed products.) Thus, for potassium chloride or sodium chloride for injection, the number of particles>or=1.3 microm in diameter in the residual intravenous solution was significantly higher for fluids admixed with glass ampoule drugs than for those admixed with pre-filled syringe drugs (p<0.0001). For dobutamine hydrochloride for injection, the number of particles>or=1.3 microm in diameter in the residual intravenous solution was estimated to be higher for fluids admixed with its glass ampoule drug than for those admixed with its pre-filled syringe drug. Observation of the residual solutions of fluids admixed with potassium chloride, sodium chloride, or dobutamine hydrochloride in glass ampoules using an electron microscope with an X-ray analyzer showed glass fragments in each residual solution. Therefore, for the prevention of glass particle contamination in peripheral intravenous admixtures, the use of pre-filled syringe drugs may a useful method. No microbial contamination was observed in any of the residual solutions of 5 types of admixture.

摘要

我们比较了静脉输液中玻璃安瓿药物混合液和预充式注射器药物混合液在滴注结束后外周静脉混合液残留溶液中的微粒和微生物污染情况。每1 ml残留溶液中直径≥1.3微米的微粒平均数量,对于与玻璃安瓿(20 ml容量)中的氯化钾混合的液体(n = 60)为758.4,对于与预充式注射器(20 ml容量)中的氯化钾混合的液体(n = 63)为158.6,对于与玻璃安瓿(20 ml容量)中的氯化钠混合的液体(n = 66)为736.5,对于与预充式注射器(20 ml容量)中的氯化钠混合的液体(n = 15)为179.2,对于与3个玻璃安瓿(5 ml容量)中的盐酸多巴酚丁胺混合的液体(n = 30)为1884.5,对于预充式注射器(50 ml容量:仅对这些样品在密封产品中评估微粒和微生物污染)中稀释的盐酸多巴酚丁胺为178.9(n = 10)。因此,对于注射用氯化钾或氯化钠,与玻璃安瓿药物混合的液体在残留静脉溶液中直径≥1.3微米的微粒数量显著高于与预充式注射器药物混合的液体(p < 0.0001)。对于注射用盐酸多巴酚丁胺,与玻璃安瓿药物混合的液体在残留静脉溶液中直径≥1.3微米的微粒数量估计高于与预充式注射器药物混合的液体。使用带有X射线分析仪的电子显微镜观察与玻璃安瓿中的氯化钾、氯化钠或盐酸多巴酚丁胺混合的液体的残留溶液,发现每个残留溶液中都有玻璃碎片。因此,为防止外周静脉混合液中的玻璃颗粒污染,使用预充式注射器药物可能是一种有用的方法。在5种混合液的任何残留溶液中均未观察到微生物污染。

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