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Propofol and postoperative infections
1Department of Pharmacy Services, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia. sklar@kfshrc.edu.sa
Abstract:
The package insert for propofol states in several places the importance of strict aseptic technique in the preparation and handling of the drug, and the potential for infection if these procedures are not followed. In the US, the product has been reformulated to contain disodium edetate 0.005% as a microbial growth retardant to inhibit the growth of microorganisms in the event of accidental contamination. However, this new formulation is not considered an antimicrobially preserved product under USP standards. What effect, if any, this has had on the risk of postoperative infections is not known. Strict aseptic technique is still required when handling the new formulation. When propofol is used as an anesthetic, it is recommended that the dose be prepared just prior to administration, and that the infusion be completed within 6 hours after the ampul or vial is opened. Any unused portion of propofol must be discarded at the end of the procedure or at 6 hours, whichever occurs sooner. In the ICU, if propofol is administered directly from its original container, the tubing and any unused portion must be discarded after 12 hours. If propofol is transferred to another container, administration lines and unused drug should be discarded after 6 hours. The occurrence of postoperative infections is usually thought to be related to the surgeon or the surgical procedure. However, based on the available microbiologic and clinical evidence, the use of propofol appears to be an additional risk factor. Hospital personnel involved in the preparation and handling of propofol must be educated on, and adhere to, the recommendations outlined by the manufacturer to prevent further outbreaks of infections.
Insights
Strict aseptic technique is crucial when handling propofol, even with its new formulation. Propofol use may increase the risk of postoperative infections, necessitating adherence to manufacturer guidelines.
Area of Science:
- Anesthesiology
- Infectious Disease
- Pharmaceutical Science
Background:
- Propofol's package insert emphasizes strict aseptic technique to prevent infections.
- A reformulated propofol in the US contains disodium edetate as a microbial growth retardant.
- This new formulation is not classified as an antimicrobially preserved product under USP standards.
Purpose of the Study:
- To evaluate the impact of the reformulated propofol on the risk of postoperative infections.
- To highlight the continued importance of aseptic technique in propofol handling.
- To underscore propofol as a potential risk factor for postoperative infections.
Main Methods:
- Review of package insert recommendations for propofol preparation and handling.
- Analysis of microbiologic and clinical evidence regarding propofol and infection risk.
- Examination of USP standards for antimicrobially preserved products.
Main Results:
- The effect of the reformulated propofol on postoperative infection risk is currently unknown.
- Strict aseptic technique remains essential despite the new formulation.
- Specific time limits for propofol use after opening are recommended (6 hours for transferred solutions, 12 hours for direct administration from original container in ICU).
Conclusions:
- Propofol use is identified as an additional risk factor for postoperative infections.
- Hospital personnel require education on and adherence to manufacturer guidelines for propofol handling.
- Preventing outbreaks of infection requires rigorous aseptic practices during propofol preparation and administration.