Abstract

Drug–drug interactions (DDIs) are a serious problem in the healthcare system, leading to excess healthcare utilization and costs. We conducted a second prospective randomized, controlled trial to further establish the real-world clinical utility of a novel assay that objectively identifies potentially serious DDIs in real-world patients. Re-recruiting primary care physicians (PCPs) from our first randomized, controlled, simulated-patients study on DDIs, we experimentally introduced a definitive, urine-based mass spectrometry test intervention that the physicians could use when caring for their eligible patients. Patients were eligible if taking four or more prescription medications or suspected of taking other non-prescribed substances with potential medication interactions. The primary outcome was whether DDI testing changed clinical care. We explored a secondary outcome to see if the change in practice improved symptoms in patients with potential DDIs. A total of 169 control and 162 intervention patients were enrolled in the study, and their medical records were abstracted. In real-world patients, intervention physicians identified and/or treated a DDI at 3.0x the rate in their patient population compared to controls (21.6% vs. 7.1%, p < 0.001). Intervention physicians were more likely to discontinue or adjust the interacting agent compared to controls (62.9% vs. 8.3%, p = 0.001), and patient-reported symptoms also significantly declined (29.6% vs. 20.1%, p = 0.045). These results were nearly identical to concurrent measurements that used simulated patients, wherein intervention was more likely to both make a DDI diagnosis (56.3% vs. 21.6%, p < 0.001) and stop the interacting medications (58.3% versus 26.6%, p < 0.001). Bringing a new diagnostic test to market, particularly for an under-recognized clinical problem, requires robust data on both clinical validity and clinical utility. The results of this follow-up study showed that the use of DDI testing in real-world patients significantly improved (1) primary care patient management of drug interactions and (2) patient outcomes.

Highlights

  • Drug–drug interactions (DDIs) are underdiagnosed, accounting for more than 30% of all adverse drug events (ADEs) [1,2,3], which cost the collective healthcare system an estimated USD 30.1 billion [4,5,6,7]

  • Physician management of drug interactions was examined in order to determine which factors were significant in detecting or treating DDIs

  • The same multivariate regression model was used to evaluate the management of the consenting patients, and here we found that only the use of the DDI test improved DDI detection or treatment (O.R. 4.1; 95% C.I. 2.0–8.5)

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Summary

Introduction

Drug–drug interactions (DDIs) are underdiagnosed, accounting for more than 30% of all adverse drug events (ADEs) [1,2,3], which cost the collective healthcare system an estimated USD 30.1 billion [4,5,6,7]. The number of patients taking five or more prescription drugs has more than doubled between 1988 and 2018 [8], while past research confirms that the risk of an ADE or DDI increases with polypharmacy [9], highlighting the urgent need for a DDI test with demonstrable clinical utility. Aegis Sciences Corporation has analytically and clinically validated a urine- or oralfluid-based DDI test. The DDI test (InterACT RxTM) utilizes a sensitive and specific liquid chromatography–mass spectrometry-based method to detect 150 unique interacting substances. The urine-based test detects prescription and nonprescription substances that are commonly prescribed or ingested by patients with common comorbid medical conditions and are capable of impacting prescription medication pharmacokinetics (e.g., drug absorption and/or metabolism) or pharmacodynamics. In addition to providing objective information regarding ingested substances, the test results describe the interaction severities (e.g., moderate, severe, contraindicated) and provide clinical descriptions of the interactions

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