In order to keep AEDs in proper working condition and in keeping with regulatory requirements, AED manufacturers may provide software updates for their devices in the field.
Typically, these AED upgrades occur for one of two reasons:
1. Corrective Actions:
Corrective actions occur when device manufacturers identify a potentially problematic issue in their product, requiring a change to AEDs that have already been shipped and deployed in the field. Commonly, corrective actions do not compel customers to ship the device back to the manufacturer but, instead, require customers to install new software (or firmware) onto the device to ensure that the AED is functioning properly. The customer can complete most field corrective actions without assistance from a manufacturer representative, however, the number of steps required and the degree of difficulty varies from manufacturer to manufacturer.
In extreme cases, a product recall involves removing potentially problematic devices from the field until the faults are fixed. Usually, recalls are voluntary and initiated by the manufacturer, but the FDA also has the power to compel companies to recall faulty AEDs. An AED recall can happen for many reasons, including if the device is faulty, poses a health risk, or both.
2. Updates in AED Science: The CPR ratio of compressions-to-breaths changed from 15:2 to 30:2.
- AED unit “shock” delivery was adjusted from stacked shocks (3 shocks in a row) to a “shock” followed by two minutes of CPR, then another shock, and so on.
Examples of field upgrades and Corrective Action
All AED units have had and will continue to require software upgrades, but the methodology and process of performing the upgrade vary by AED vendor. For instance,
In March 2011, AED manufacturer Defibtech issued a “Field Safety Notice” as a result of two faults on its DDU-100 series. The first fault, which the company estimated as happening in 1 in 400,000 devices, involved the AED canceling its charge as it prepared to deliver the shock. The second condition involved a subset of devices failing to charge in the lead-up to a shock when used in very high humidity conditions. The company provided a free software update that could be performed by customers in the field by installing a small software data card (5) into their AED(s) to rectify both of these malfunctions. (6)
- In April 2009, ZOLL Medical Corporation announced field corrective action for about 180,000 of its ZOLL AED Plus® AEDs. The company had determined that some of the devices manufactured before February 12, 2009, had some issues with battery compatibility, and the AEDs’ self-test software was unable to detect defective batteries. This meant that the identified subset of AEDs carried a risk of failing to deliver a shock during the treatment of Sudden Cardiac Arrest (SCA). ZOLL provided a free software update that was downloadable from the company’s website. The new software, when installed, enabled the AED to detect battery defects and alert the user to install fresh batteries. (7)
In 2005, AED manufacturer Physio Control issued an upgrade on two of its models, the LIFEPAK CR® Plus and LIFEPAK EXPRESS, to enable the AEDs to meet the threshold set by 2005 AHA AED and ECC Guidelines. In the new guidelines, the AHA had recommended a single shock followed by CPR as the preferred sequence for helping SCA patients. In response, Physio Control’s upgrades replaced the pre-programmed series of “stacked shocks” (up to three shocks in a row before performing CPR) with a single shock, followed by two minutes of CPR. Another change involved modifying the voice prompt from “Start CPR” to “Provide chest compressions and rescue breaths.” Physio Control offered the upgrade in two forms. The Basic Upgrade Package came via CD that contained upgrade software, which could be loaded using a computer, costing $30 (or $140 if a USB connection cable was included).
- The Premium Upgrade Package provided the customer with a service representative to perform the upgrade for them alongside preventative maintenance checks. This option cost a minimum of $275. (8)
Challenges of Today’s Upgrade Processes
Although the internet, better device technology, and computing advances have made getting and installing upgrades on AEDs easier, there are several challenges with the process that remain.
Cost of the Upgrade or the Equipment Required to Upgrade the AED’s Software
A significant challenge relates to the price of upgrade equipment such as USB adapters, Bluetooth and IrDA readers, and installation CDs that may be required to upgrade units in the field. For example, ZOLL sells the USB IrDA adapter that connects the AED to the computer for $105. Physio Control’s installation CD and IrDA cable combo go for $140. These costs, which are similar to their peers across the AED market, can be prohibitive for institutions and homes with limited resources. Particularly, financial stress may be applied to the owners of multiple AEDs that are located in different geographical regions, thus requiring their own upgrade kits. Additionally, for many AED devices, the new software installation process requires the use of a compatible laptop or PC, which is another substantial investment.
Difficult Process of Reaching the Initial AED Owner
The typical sales and supply chain process of AED units sold in the United States can lead to challenges locating units after the initial transaction. Commonly, AED units are sold to large distribution companies that then resell the devices to a group of smaller, local distributors who, in turn, sell the AED unit to its eventual owner. While each party requires tracking of AED sales, every time the AED is sold and changes hands from one party to the next, the AED, its location, and its most up-to-date responsible party become more challenging to track. Thus, the AED manufacturers often face challenges when trying to spread information on recalls to all their customers. Furthermore, it is also the case that an AED has gone unused for so long, the owner isn’t attentive to their AED’s functionality status.
Difficult Process of Reaching Responsible Parties in the Future
After buying an AED:
- Customers may resell their devices as their business contracts and expands through normal operations.
- The business might move, changing addresses.
- Responsible parties might change over time as company employees retire or are terminated.
- Customers who are “found” but not expecting or prepared to perform a new task are unresponsive to communication, making it hard for AED manufacturers and their distributors to track them down when updates or recalls are required.
- Sometimes an AED has gone unused for so long that the owner isn’t cognizant of the AED’s functionality status
The Process can be Cumbersome and Inconvenient
After a customer is notified of a possible need to upgrade their AED, their first step is to verify whether an upgrade is required or not; this can often be complex for laypeople.
Difficulty Performing the Upgrade on Affected Units
Once a unit has been identified as requiring an upgrade, the customer may need to purchase equipment, find a computer with which to download the latest AED software, and then manually install the software on the AED unit. Even technically savvy owners can struggle with the steps, order of operations, and time-consuming processes. With each layer of friction imposed on obtaining the new software, fewer AED owners make the necessary changes. Performing these steps on one AED can be frustrating; performing them on hundreds – or thousands – of AEDs requires full-time support.
Upgrade Process for Different AED Brands
Each AED manufacturer provides a unique “in-field” upgrade protocol, and individual AED owners should consult their manufacturer for more information including whether an AED requires an upgrade and, if so, what the upgrade process entails.
- Cardiac Science: https://www.cardiacscience.com/support/
- Defibtech: http://www.defibtech.com/support/us-support
- HeartSine: https://heartsine.com/support/
- Philips: https://www.usa.philips.com/healthcare/solutions/emergency-care-resuscitation/automated-external-defibrillators#_Contact
- Physio Control: https://www.physio-control.com
- ZOLL Medical: https://www.zoll.com/medical-products/automated-external-defibrillators/aed-plus/2015-guidelines-upgrade/
(1) “2015 Guidelines Summary Heartsine Samaritan® PAD Automated External Defibrillators”, Heartsine.Com, 2015, https://heartsinelive.s3.amazonaws.com/uploads/2016/03/2015-Guidelines-Summary-HeartSine-samaritan®-PAD-Automated-External-Defibrillators.pdf.
(6) Defibtech.Com, 2011. http://www.defibtech.com/sites/defibview.com/files/FA11-int.pdf.
(7) “ZOLL Conducting ‘Corrective Action’ On 180,000 Aeds — Occupational Health & Safety”, Occupational Health & Safety, 2009, https://ohsonline.com/articles/2009/04/04/zoll-conducting-corrective-action-on-180000-aeds.aspx.
(8) “LIFEPAK CR® Plus AED and LIFEPAK EXPRESS® AED Upgrade Information”, Physio-Control.Com, 2005, https://www.physio-control.com/uploadedFiles/learning/aha-guidelines/CRPlus_Express.pdf.
(9) “Automated External Defibrillator: Implementing an AED Program”, Heart.Org, 2019, https://cpr.heart.org/idc/groups/heart-public/@wcm/@ecc/documents/downloadable/ucm_480036.pdf.