July – September 2009 ISMP QuarterlyActionAgenda x Oneof themost important ways toprevent medication errors is tolearn about problems that haveoccurred in other organizations and tousethat information toprevent similar problems at your practicesite. Topromotesuch aprocess, thefollowing selected items fromtheJuly-September 2009 issues of theISMPMedication Safety Alert! havebeen prepared for an interdisciplinary committeetostimulatediscussion and action toreducetherisk of medication errors. Each itemincludes adescription of themedication safety problem, recommendations toreducetherisk of errors, and theissuenumber tolocateadditional informationas desired. Look for our high-alert medication icon under theissue number if theagendaiteminvolves oneor moremedications on the ISMPList of High-Alert Medications. TheAction Agendais alsoavailablefor downloadin aWord format (www.ismp.org/Newsletters/acutecare/articles/ActionAgenda0904.doc) that allows expansion of thecolumns in thetabledesignated for organizational documentation of an assessment, actions required, and assignments for each agendaitem. Many product-related problems can alsobeviewed in theISMPMedicationSafety Alert! section of our websiteat: http://www.ismp.org. Continuing education credit isavailablefor nurses at: www.ismp.org/Newsletters/acutecare/actionagendas.asp .Key: Problem No. (19) The Anesthesia Patient Safety Foundation (APSF) recently published an editorial regarding the continuing problem of opioidinduced respiratory depression. APSF identified inadequate monitoring of oxygenation and/or ventilation, in addition to failure to consider patient-specific characteristics, as causes for the continued occurrence of opioidinduced respiratory depression. (19) The auditory signal or beep issued by certain hospital point-of-care barcoding systems to indicate that the scanner successfully read a barcode may be misinterpreted as a signal that the correct patient and drug have been selected, particularly if the computer screen cannot be viewed clearly. April 23, 2009 —ISMP high-alert medication Recommendation Organization Action Required/ Assessment Assignment APSF offers recommendations for safe post-op opioid administration and monitoring Date Completed According to APSF, the following should be addressed in all patients receiving postoperative opioids: 1) Individualize each patient’s dose based on the patient’s history and physical status; 2) Make pulse oximetry routine; 3) Assess each patient’s need for supplemental oxygen; and 4) Consider capnography to monitor ventilation, particularly for patients receiving oxygen and/or at high risk for opioidinduced respiratory depression (e.g., depressed level of consciousness, preexisting respiratory impairment, sleep apnea, and very sick, elderly, or obese patients). What does a bar-coding scanner beep mean? Evaluate your point-of-care barcoding system to identify if any auditory signals could be misunderstood. Educate staff regarding the meaning of auditory signals related to bar-coding systems. For vendors of bar-coding systems, consider using different auditory signals to distinguish a correct drug that is scanned from an incorrect drug. Insulin errors ISMP MedicationSafetyAlert! QAA 1 July – September 2009 ISMP Problem No. (14) (16) (14, 15) QuarterlyActionAgenda Recommendation Organization Assessment Action Required/ Assignment Date Completed A renal transplant recipient Develop a medication preparation developed cardiopulmonary course and preceptor program for instability after receiving 100 units new residents and anesthesia, OR, instead of 10 units of regular insulin PACU, and pharmacy staff. In IV for the treatment of hyperkalemia. hospitals with OR pharmacy satellites, An anesthesiology resident drew 1 insulin dilution and dose preparation mL of U-100 insulin into a 10 mL should occur in the satellite syringe, added 9 mL of saline, and pharmacy, or an insulin minibag injected the entire contents. system (prediluted to 1 unit/ mL) may Inadequate hospital orientation and be used (however, insulin adherence training of residents in medication to plastic IV bags/tubing makes it preparation was a key contributing difficult to estimate exactly how much factor. insulin is reaching the patient). Plain D5W or hypotonic saline solutions post-op could result in acute hyponatremia and death in healthy children Two 6-year-old children died from Administration of hypotonic saline or severe postoperative hyponatremia. parenteral fluids without saline is In the first case, the rapid physiologically unsound and administration of plain D5W potentially dangerous for hospitalized (dextrose 5% in water) children. Thus, standards of practice postoperatively resulted in free should be established for water retention (also called water postoperative IV solutions used to intoxication). In the second case, the hydrate patients–particularly children. child received several doses of Protocols should be established to furosemide and EDECRIN identify, treat, and monitor patients (ethacrynic acid), exacerbating the with hyponatremia, water intoxication, loss of sodium. In both cases, staff and/or SIADH. Consider establishing failed to recognize the signs of an interdisciplinary rapid-response hyponatremia. Children who receive team that allows healthcare workers hypotonic solutions are particularly (or patients/families) to summon a vulnerable to water intoxication clinical team to the bedside for a full because they are prone to evaluation when they fear something developing syndrome of is wrong and have expressed their inappropriate antidiuretic hormone concerns without adequate response. (SIADH), or the excessive release of ADH. Safety issues with elastomeric pain relief balls (ON-Q PainBuster and others) Safety issues have been identified Establish standard order sets for with the ON-Q PainBuster, an prescribing the pump and specific elastomeric pump used after surgery medications. Allow use of local to provide pain relief. The pump is anesthetics only. The Joint October 10, 2009 ISMP MedicationSafetyAlert! QAA 2 July – September 2009 ISMP QuarterlyActionAgenda Problem Recommendation usually filled and started in the OR without pharmacy involvement or knowledge. Patients have appeared on units where nurses have never seen the pump. The pain ball has been found unlabeled. Infusion rates may vary due to over- or under-filling of the balls; we’ve received one report of premature emptying of the pump. We have also received reports of using the pump to deliver medications other than local anesthetics, including vancomycin, fentaNYL, and morphine. Commission defines parenteral solutions in ON-Q pumps as IV admixtures, which should be prepared in the pharmacy except in urgent situations. The pharmacy should use a protocol that specifies the exact amount of solution to instill in the reservoir based on the duration of therapy. Always label the pump (drug, concentration, infusion rate, start date). Other safety strategies can be found at www.ismp.org/Newsletters/acutecare/ articles/20090716.asp). No. (19) FDA announced that it will be requiring stronger manufacturer warnings regarding severe tissue damage associated with accidental intraarterial administration or extravasation of IV prometh-azine. (17) A vial of generic sulfamethoxazole and trimethoprim injection was accidentally placed in a bin for EPINEPHrine injection. A technician took this vial from the EPINEPHrine bin and scanned the label on the bin, not the vial itself. The vial was placed in a ziplock bag with a October 10, 2009 Organization Assessment Action Required/ Assignment Date Completed IV promethazine update If possible, remove promethazine from the formulary and use alternatives such as 5-HT3 antagonists (e.g., ondansetron) when appropriate. If you MUST keep it on the formulary, administer the drug by deep IM injection only. Avoid IV use. Additional FDA recommendations can be found at: www.fda.gov/Drugs/DrugSafety/Post marketDrugSafetyInformationforPatie ntsandProviders/DrugSafetyInformati onforHeathcareProfessionals/ucm182 169.htm. Scan product, not storage container label To prevent mix-ups of products, scan the product label itself when removing drugs from bins, ADCs, or carousels. The drug storage bin labels should never be used to identify products. ISMP MedicationSafetyAlert! QAA 3 July – September 2009 ISMP Problem No. QuarterlyActionAgenda Recommendation Organization Assessment Action Required/ Assignment Date Completed barcode label. A pharmacist checked the item by scanning the barcode on the ziplock bag, not the vial. A technician then placed the item in an ADC, again scanning only the ziplock bag. (17) (15) (16, 17) Name mix-ups between VALTREX (valacyclovir) and VALCYTE (valganciclovir) Consider adding these drugs to your list of look-alike drug names, and take steps to reduce the risk of confusion, including: building software alerts to warn about possible confusion, requiring staff to match the prescribed drug with the patient’s medical history, using both the brand and generic names when prescribing or listing these drugs, requiring readback of all oral orders, and using tall man letters—valACYclovir and valGANCIclovir—when listing the drugs in computerized inventories. Name mix-ups between PROVERA (medroxyPROGESTERone), PROZAC (FLUoxetine), and PROSCAR (finasteride) A pharmacist misread a handwritten Consider adding these drugs to your order for Provera 10 mg PO daily list of look-alike drug names, and take and dispensed Prozac 10 mg, which steps to reduce the risk of confusion, the patient received until the next including: building software alerts to day. The handwritten order was warn about possible confusion, shown to several nurses, requiring prescribers to include the pharmacists, and physicians; one drug’s purpose on orders, and person thought the order was for requiring staff to match the prescribed Proscar. drug with the patient’s medical history. Name mix-ups between KAPIDEX (dexlansoprazole) and CASODEX (bicalutamide) There have been numerous reports Consider adding Kapidex and of errors due to name confusion Casodex to your list of look-alike drug between Kapidex and Casodex with names, and take steps to reduce the both handwritten and oral risk of confusion, including: building prescriptions. ISMP also learned software alerts to warn about possible there is a foreign acetaminophen confusion, requiring staff to match the ISMP continues to receive reports of mix-ups between Valtrex and Valcyte. The generic names for these two drugs are also strikingly similar, and both the brand and generic names of the products start with the prefix “val.” Both have uses associated with cytomegalovirus (CMV) and may be used in immunosuppressed patients with human immunodeficiency virus (HIV) or transplant patients. October 10, 2009 ISMP MedicationSafetyAlert! QAA 4 July – September 2009 ISMP QuarterlyActionAgenda Problem Recommendation and propoxyphene containing product called Capadex available in Australia, New Zealand, and online. prescribed drug with the patient’s medical history, requiring prescribers to include the drug’s purpose on prescriptions, and requiring read-back of all oral orders. No. (18) A physician ordered QUALAQUIN (quinine sulfate) 324 mg for leg cramps for a newly admitted patient. The pharmacist selected a 324 mg tablet from a list of products on the computer screen. However, he selected quinidine extended release 324 mg instead of quinine. This error continued for 2 weeks. Fortunately the patient was not adversely affected. Mix-ups between quinidine and quinine are common. (16) Pentacel is a 2-vial vaccine product that requires mixing of the two components before administration. Only the DTaP/IPV vial carries the brand name Pentacel. Clinicians may think only the vial labeled Pentacel is needed. ISMP has contacted the vaccine manufacturer to suggest labeling changes. (17) Ohio pharmacist Eric Cropp was sentenced to 6 months in prison, 6 months of home confinement, and other criminal penalties for making a human error that caused the death of a child. During an independent check, Eric failed to detect that a pharmacy technician had used too much 23.4% rather than 0.9% Organization Assessment Action Required/ Assignment Date Completed Quinine-quinidine mix-ups still happen The only approved indication for quinine is to treat uncomplicated Plasmodium falciparum malaria, (rarely encountered in the US). Quinine should not be available for leg cramps and should be removed from the formulary. If malaria is encountered, access the drug from an outside source. Use tall man letters for quiNIDine and stock it only in the available 300 mg strength (extended release and immediate release). PENTACEL (diphtheria and tetanus toxoids, acellular pertussis [DTaP], inactivated poliovirus [IPV], and Haemophilus b [Hib] conjugate) October 10, 2009 Educate staff who will be administering vaccines to children about the need to mix the two vials. If feasible, have pharmacy add auxiliary labeling to the product before dispensing it. Require documentation of the NDC number, lot number, and expiration date for each component in the vaccine log. Ohio government sentences pharmacist to jail time Review your procedures for checking pharmacy-prepared infusions of highalert medications to ensure that the process is reliable. Ensure that technicians preparing IV infusions are well trained regarding the types of products being used and the appropriate use of 23.4% sodium chloride. Whenever possible, use ISMP MedicationSafetyAlert! QAA 5 July – September 2009 ISMP Problem No. sodium chloride as a diluent when preparing a chemotherapy infusion. Human factor research shows that, under moderate stress, we fail to detect an error about 20% of the time. (19) A recent article suggests that onceweekly levothyroxine may be as effective as daily dosing. This new dosing regimen may lead to errors in which the weekly dose is taken daily. Errors may be difficult to detect since daily administration is the norm, doses vary between patients, and a weekly dose may be the same as a daily dose for some patients. October 10, 2009 QuarterlyActionAgenda Recommendation Organization Assessment Action Required/ Assignment Date Completed standard, premixed base solutions (such as 0.9% sodium chloride) instead of preparing base solutions by hand. Restrict access to hypertonic sodium chloride vials. Educate staff about human factors and a Just Culture. Caution regarding once-weekly levothyroxine Provide education to physicians regarding the potential for error with this weekly dosing regimen. Patient education should include emphasis of the weekly dosing schedule and the potential for a dosing error. ISMP MedicationSafetyAlert! QAA 6