Another Tragic Parenteral Nutrition Compounding Error
Problem: In our newsletter two weeks ago, we highlighted a tragic story about contaminated parenteral nutrition (PN) from a compounding pharmacy that led to nine deaths.1 Around the same time, another tragic outcome with PN was making the headlines, this one involving a 6-week old infant who died late in 2010 after receiving a PN solution that contained 60 times more sodium than prescribed.2-4 While these events are dissimilar—one involves bacterial contamination, the other a data entry error—both demonstrate the need for stepped up safety for sterile compounding.
Summary of 2010 event. The infant had been born prematurely, weighing less than 1 kg at birth but thriving at 6 weeks. His nutritional requirements were being supported with PN. According to news reports, on the day of the event, the infant’s physician prescribed a total of 14.7 mEq of sodium chloride and 982 mg of calcium in the infant’s PN. (The other products in the PN, the total volume of the solution, and the prescribed rate of infusion were not disclosed in media reports.) The order was faxed to the pharmacy after midnight, at which time a pharmacy technician made an error when entering the order into automated compounder software. Apparently, the technician accidentally entered the prescribed dose of calcium (“982” mg) into the mEq field for sodium. The technician then prepared the PN, which contained a total of 982 mEq of sodium, using an automated IV compounder. The technician affixed the printed label to the PN, which showed the erroneous sodium content.2-4
Unfortunately, the error was not detected when a pharmacist checked the final product. Furthermore, a different label that listed the sodium content as 14.7 mEq, the originally prescribed amount, was applied directly over the label produced by the compounder software that had listed the actual amount of sodium (982 mEq) in the solution. Thus, the nurse who eventually started administration of the PN solution was unable to detect the error.2-4
A few hours after the PN was started, routine lab studies showed that the infant’s sodium level was abnormally high. The infant’s physician assumed the study results were inaccurate and asked for the lab test to be redone. This was never accomplished before the infant experienced a cardiac arrest and died.4
Possible causes of the event. News reports do not indicate the vendor of the automated compounder and related order entry software in use at the time of the error. However, according to Pharmacy Purchasing & Products,5 Baxa compounders and Abacus software are by far the most widely used in hospitals. Thus, we have evaluated how this event could have happened if the Abacus order entry system had been used at the time of the error. This way, we can help a majority of our readers identify how this error could happen in their organization.
Abacus software is not interactive with the pharmacy order entry system; thus, screening for dose irregularities (and drug interactions, incompatibilities, etc.) does not occur. However, the software comes with two types of dose warnings:
- Baxa Only Warning Limits, which are extremely high, catastrophic dose limits established and installed by Baxa personnel for typical products used to compound neonatal, pediatric, and adult PN. The entry of doses above these limits results in a hard stop warning that cannot be bypassed. Any modifications to these limits must be requested through Baxa.
- Template Institutional Warning Limits, which are suggested dose limits intended for organizations to review and modify as desired. These dose limits are designed as templates that the customer can use to establish more restrictive dose limits, as the Baxa Only Warning Limits are so high that a fatal dosing error could easily be entered into the system without issuing a warning.
The Baxa catastrophic dose limits are not distinctively weight-based. For example, all dose limits set for neonates are based on a 10 kg infant. However, the institutional warning templates provided with the software allow users to define and install more appropriate weight-based dose limits. The Abacus software can employ multiple sets of dose warning limits for adults, pediatric patients, and neonates, each associated with specific rules regarding how PN orders are processed and how the components of PN are calculated. Since the Abacus software can also be used for sterile preparations that are not directly infused (e.g., cardioplegia solutions, dialysates), users can create non-PN templates into which these orders can be entered. These non-PN templates do not employ the catastrophic dose limit warnings provided by the vendor.
In the 2010 event described above, the sodium dose of 982 mEq would have been entered into the Abacus software. The Baxa Only Warning Limit for sodium is set at 385 mEq for neonates. Thus, you would expect the system to warn the user with a hard stop after entering the 982 mEq dose. One possible scenario that would allow this entry to be made without a hard stop dose warning is if the PN order had been entered into a non-PN patient type template that the user had created without dose limits. Another possibility is if an adult application of the software was purposely used to enter the neonatal PN (the Abacus adult catastrophic sodium limit is 1,000 mEq). A final possibility is that a different vendor’s software system was used that did not employ catastrophic dose warnings or user-defined dose warnings with a hard stop.
A similar prior event. In our September 6, 2007 newsletter,6 we described an error in which an infant died from a 1,000-fold overdose of zinc that resulted from an error while entering a PN order into an automated compounder software system. In this case, the pharmacist entering the order accidentally chose “mg” instead of “mcg” from a pull-down list when entering the dose of zinc. At the time, the software system did not warn pharmacists about massive overdoses. Another similarity between this case and the most recent event is that the PN order arrived in the pharmacy later in the evening/night, when less staff were available.
Safe Practice Recommendations
If your organization prepares PN using an automated compounder and associated order entry software, please consider the following recommendations to avoid potential harm to your patients. Most recommendations are also applicable in organizations that use automated compounder-associated software for PN computations alone (not actual compounding) and/or prepare PN solutions manually.
Compound PN orders during the day. Policies that require pharmacists to compound PN during the day shift should be established and enforced to maximize the safety with which these solutions are prepared and dispensed. If using an IV compounding pharmacy to prepare PN solutions, the order should be transmitted to the pharmacy during the day shift so it can be checked by a hospital pharmacist with PN expertise before it is sent to be compounded. Pharmacy staff should be aware of patients who are receiving PN and check if orders have not been received by the established time.
Standardize the format of PN orders. Synchronize the order and format of listing ingredients in PN order sets, the pharmacy computer system, the compounder software, and the PN label to help prevent errors caused by jumping back and forth.
Maximize decision support. Install, test, and maximize automated dose-limit warnings in the pharmacy computer system and automated compounder order entry system, particularly for high-alert medications such as PN and its ingredients. If your PN software supports warning limits, fully implement them. Turning off warning limits is like driving without a seat belt. However, DO NOT rely solely on the catastrophic dosing limits established by software vendors. Vendor-established dose limits, such as the Baxa Only Warning Limits, will still allow a potentially fatal dose to be entered into the software without issuing a warning. Organizations need to define more restrictive weight-based dosing limits applicable to their patient populations. These warnings should function as a hard stop without the ability to proceed until the dose has been reviewed via a peer review process. Organizations should also print all alerts encountered during the order entry process so the person checking the order entry can also view and respond to the alerts. Reinforce the importance of reacting to the alerts with all staff.
Label products and use critical thinking skills. Produce product labels and associated work labels used by pharmacy staff to compound solutions that include the actual dose/strength of the base solution and each additive, not just the volume amounts needed to prepare the products. Encourage technicians who compound products to focus not only on the volumes needed to prepare the solution but also on the dose of the additives and the concentration of the solutions. Apply easy-to-read labels that print from the compounder order entry system to compounded products to ensure the label lists the actual contents. These labels should follow the format of the prescriber’s order.
Carry out effective redundancies. Several verification processes should occur in the pharmacy: 1) before order entry into the automated compounding software to verify that the PN order is appropriate for the patient (e.g., based on weight, height, disease state, lab values), 2) after initial order entry into the automated compounding software to match it to the verified order, 3) before injecting any additives that must be added manually, and 4) once the PN has been compounded. Verification of manual additives should include inspection of the actual vials and filled syringes prior to admixture (the “pullback” method is not recommended). Final verification of the compounded PN should include review of the original order, product label, and work label, as well as comparison of the expected weight/specific gravity with the actual weight/specific gravity. If different than expected or off by 3% or more, the product should be prepared again.6 If PN compounding is outsourced, a pharmacist should verify the appropriateness of the order before sending it to the pharmacy and verify that the product received matches the verified prescriber order. Before administering PN, nurses should also independently compare the label on the solution with the physician’s order.
- ISMP. TPN-related deaths call for FDA guidance and pharmacy board oversight of USP Chapter <797>. ISMP Medication Safety Alert! 2011;16(7):1-3.
- Perez A. Couple says Park Ridge Hospital killed their baby. NBC Chicago. April 6, 2011.
- Janssen K. Lawsuit says Park Ridge Hospital’s negligence caused baby’s death. Chicago Sun Times. April 6, 2011.
- Rhodes D. Parents sue Park Ridge Hospital after death of infant. Chicago Tribune. April 05, 2011.
- PP&P. The 5th annual state of automation; automated compounding devices. Pharmacy Purchasing & Products (PP&P). 2010;7(8).
- ISMP. Fatal 1,000-fold overdoses can occur, particularly to neonates, by transposing mcg and mg. ISMP Medication Safety Alert! 2007;12(18):1-4.