Whats New in the Patient Safety World
April 2012
Problems with Ketofol
The increasingly popular practice of mixing ketamine and propofol together for use in patient procedures has come under fire recently. The practice stems from the idea that using lower doses of both agents together can provide adequate patient sedation with less toxicity. The May 2011 issue of The Annals of Emergency Medicine had several articles addressing the use of this combination for procedural sedation/analgesia. The article by Green et al. (Green 2011) nicely summarizes the pros and cons of use of this combination.
But ISMP has recently warned about some safety issues associated with this practice (ISMP 2012). They are especially concerned about sterility, since the mixing of these two drugs often takes place in the emergency room under less-than-ideal circumstances for sterility. They caution against puncturing single-dose vials multiple times, ensuring that the proper expiration date is included on the syringe label, and that the medication is appropriately disposed of after use. They also note that there is no standardized concentration or volume of each drug in the combination and that there is little literature on the compatibility of these two agents. Moreover, look-alike/sound-alike issues may occur. Because ketofol does not appear in standard drug dictionaries or CPOE lists it would be easy to choose the wrong drug from a list. Similarly, a syringe filled with ketofol might be mistaken for a syringe filled with just propofol. ISMP recommends that, if you use ketofol, you conduct a FMEA (failure mode and effects analysis) to determine your vulnerabilities.
A second paper (Andolfatto 2010) has also raised safety issues about ketofol. Contrary to the widely-held view that the combination is safer than individual drugs, the authors found in a randomized controlled trial that ketofol does not result in a reduced incidence of adverse respiratory events compared to propofol alone. In an emergency department setting they found that ketofol resulted in adverse respiratory events in 30% of patients, compared to 32% of patients receiving propofol alone. Deep levels of sedation were common and several patients required bag/mask ventilation. Moreover, several patients receiving ketofol developed recovery agitation, the side effect that had largely displaced ketamine from frequent use in the past.
So evidence has raised significant safety concerns to the use of this combination. Be very wary. You may not even know what areas of your organization may be using this potentially dangerous combination. Use your pharmacy IT systems to identify patients in whom both agents were used but bear in mind that many EDs, ORs, and radiology suites (the 3 areas most likely to use this combination) are not connected to the main hospital IT systems so you may need to do some good old detective work to find out who is using it.