Baxter Presents Data at ASHP Meeting Indicating Machine Learning May Enhance Infusion Pump Programming Safety

* Data suggest machine learning and artificial intelligence could help hospitals align drug libraries more closely to clinical practices, which may advance infusion safety * Study conducted in partnership with MedAware, an expert in leveraging artificial intelligence (AI) technology to enhance medication safety monitoring

Baxter International Inc. (NYSE:BAX), a leader in innovative technology for medication delivery, announced new data from a retrospective study finding that machine learning, a type of artificial intelligence (AI) that uses algorithms to find patterns in large amounts of data, may help support clinical decision-making during the programming of smart infusion pumps.

The study, titled “Machine Learning Complements Smart Infusion Pump Safety Features,” was presented at the American Society of Health-System Pharmacists (ASHP) 2021 Midyear Clinical Meeting taking place Dec. 5 – Dec. 9, 2021. The study is part of a collaboration with MedAware that is intended to support Baxter’s development of next-generation dose error reduction software for integration directly into Baxter’s infusion pumps and hospital enterprise connectivity solutions.

“This study shows promise around the potential to enhance patient safety by using machine learning platforms to build and maintain smart infusion drug libraries that dynamically review infusions and signal possible infusion errors,” said Douglas M. Hansell, M.D., MPH, vice president of medical affairs for Baxter’s Medication Delivery business. “Baxter is eager to further explore the use of machine learning and other digital health platforms to generate real-time insights that support individualized clinical decisions.”

Smart infusion pumps use Dose Error Reduction Systems (DERS) to help prevent medication errors by checking programmed doses against preset limits specific to a drug. If a programmed dose is outside the limits, the pump alerts clinicians and can either require confirmation before beginning delivery (a soft limit) or not allow delivery at all (a hard limit).1 Dose limits must be meaningful and consistent with clinical practice to prevent alert fatigue, which can impact patient safety by leading to alerts being ignored or safety systems bypassed. However, developing meaningful DERS limits across all drugs and care areas within a hospital’s drug library, and then deploying those changes through thousands of pumps throughout the hospital, is challenging and requires detailed analysis and significant resources to maintain. This study examined whether machine learning and AI algorithms could inform adjustments to DERS limits.

The study used MedAware’s machine learning technology to analyze 3,823,367 infusions performed on 20,542 Baxter infusion pumps over a 10-month period. Algorithms were applied to the data set to replicate a potential machine-learning approach to optimizing infusion pump programming safety. These algorithms identified “outliers,” which included infusions deviating from commonly programmed doses/rates for specific drugs, uncommon drug concentrations, and patient weight entries outside of common weight ranges.

The analysis found 44,819 pump programming entries that were outliers to common programming patterns, of which 23% triggered DERS soft limits and 52% triggered DERS hard limits. Approximately 25% of these outliers were identified through MedAware’s machine learning technology but did not trigger DERS because the programming parameters were within DERS soft limits, so clinicians did not receive an alert during pump programming. These results reinforce the challenges associated with maintaining meaningful DERS limits. Study investigators concluded that machine learning could help inform future collaboration with hospitals around the development of more clinically relevant DERS limits that may help support increased infusion safety and reduce unnecessary alerts.

“We are thrilled to evaluate our medication safety monitoring technology within Baxter’s smart infusion pumps,” said Dr. Gidi Stein, co-founder and CEO of MedAware. “This study shows the significant potential of an AI-enabled, data-driven approach to mitigate alert fatigue and identify pump programming errors that would be difficult to find using conventional approaches and rule-based systems alone.”

Hot this week

Spartan Medical Broadens Single-Use Sterile Instrument Portfolio to Improve Outcomes, Increase Efficiency, and Generate Cost Savings

Spartan Medical products portfolio of single-use, sterile med tech includes micro and minor surgical convenience kits, kerrison rongeurs, spinal and general surgical retractors, dural repair kits, synthetic biologics, and a wide range of orthopedic pre-sterilized implants and devices.

Recor Medical Supports European Society of Cardiology’s Hypertension Guidelines

Record Medical notes the new guidelines, "2024 ESC Guidelines for the management of elevated blood pressure and hypertension," have been published online and recommend the consideration of renal denervation (RDN) as a safe and effective treatment option for patients who have uncontrolled resistant hypertension or those that have uncontrolled hypertension with a higher risk of cardiovascular disease, who express a preference to undergo RDN.

ConTIPI Medical Selects EVERSANA to Support U.S. Commercialization of Non-Surgical Medical Device ProVate for Women with Pelvic Organ Prolapse

EVERSANA is a leading provider of global commercial services to the life sciences industry, to support commercialization for the ProVate device in the United States to help women experiencing pelvic organ prolapse.

Boston Scientific Obtains CE Mark for ACURATE Prime Aortic Valve System

The ACURATE Prime aortic valve system is designed with several features to build upon the clinical performance of the ACURATE neo2™ platform including an additional valve size, which expands the treatment range to patients with a larger anatomy.

Noctrix Health Announces New CMS Reimbursement Codes and Payment for Nidra Tonic Motor Activation Therapy for Restless Legs Syndrome

Nidra TOMAC Tonic Motor Activation Therapy, which was authorized for marketing in the United States last year following its designation as a "Breakthrough Device" by the US Food & Drug Administration (FDA), remains the only clinically validated, non-pharmaceutical treatment available for patients with RLS.