Abstract:To assess and compare the growth of four microorganisms in solutions of intravenous anesthetics, known quanta of Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Candida albicans were inoculated into propofol, thiopental, a 1:1 mixture of propofol and thiopental, and normal saline. All microorganisms were taken from standard stock cultures and incubated for 24 h (48 h for C. albicans). Growth of microorganism in each drug was compared by counting the number of colony forming units (CFUs) gr… Show more
“…The literature contains numerous reports regarding the bactericidal and bacteriostatic properties of injectable and topical local anesthetics [45][46][47][48], however we were concerned whether chronic infusion of study drug would increase the likelihood of wound infection. None of the patients in the study experienced surgical site or catheter insertion site infections.…”
“…The literature contains numerous reports regarding the bactericidal and bacteriostatic properties of injectable and topical local anesthetics [45][46][47][48], however we were concerned whether chronic infusion of study drug would increase the likelihood of wound infection. None of the patients in the study experienced surgical site or catheter insertion site infections.…”
“…The key component, soybean oil, can cause lipid overload in those patients who are infused for a long duration (>3 days) of the formulation (5)(6)(7)(8)(9). The lipid emulsions support microbial growth, and they have to be handled under strict aseptic conditions to avoid bacterial contamination (10)(11)(12). Also, the emulsions need to be stored under controlled temperatures (4-22°C) (9).…”
This novel, lipid-free formulation exhibits improved in vitro properties without compromising in vivo effects, therefore representing a promising new alternative for propofol.
“…It is well-known that the contamination of syringes may increase the risk P R A C t i C e R e P O R t Am J Health-Syst Pharm-Vol 66 Nov 15, 2009 of infection, and several serious cases of such infection have been reported in the literature. [2][3][4][5][6][7][8][9][10][11][12][13] To minimize the risk of end-product contamination, United States Pharmacopeia (USP) chapter 797 requirements limit the storage of drugs in prefilled syringes to a one-hour period. 14 The two main factors that contribute to microbial contamination of drugs are the cleanliness of the work environment and the competency and care of the operator; however, no published data have quantified their respective impact.…”
High contamination rates were measured when the hub of syringes touched nonsterile environmental surfaces and fingers, whereas the drawn-air manipulation was associated with a lower risk of contamination. Working within a properly operating unidirectional airflow primary engineering control in an ISO class 5 cleanroom in accordance with USP chapter 797 requirements was demonstrated to be the best way to avoid bacterial or fungal contamination of injectable drugs directly resulting in patient infections.
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