Meaningful use stage 2 e-prescribing threshold and adverse drug events in the Medicare Part D population with diabetes

Author:

Powers Christopher1,Gabriel Meghan Hufstader2,Encinosa William3,Mostashari Farzad4,Bynum Julie5

Affiliation:

1. Centers for Medicare and Medicaid Services, Office of Enterprise Data and Analytics, 7500 Security Boulevard, Mailstop B2-29-04, Baltimore, MD

2. Office of the National Coordinator for Health Information Technology, 200 Independence Avenue SW Suite 745H.2.5, Washington, DC 20201

3. Center for Delivery, Organization and Markets, Agency for Healthcare Research and Quality, 540 Gaither Road, Rockville, MD 20850

4. Aledade, 7315 Wisconsin Ave Suite 423W, Bethesda, MD 20814

5. The Dartmouth Institute for Health Policy and Clinical Practice, Geisel School of Medicine at Dartmouth, 35 Centerra Parkway, Lebanon, NH 03766

Abstract

Abstract Evidence supports the potential for e-prescribing to reduce the incidence of adverse drug events (ADEs) in hospital-based studies, but studies in the ambulatory setting have not used occurrence of ADE as their outcome. Using the “prescription origin code” in 2011 Medicare Part D prescription drug events files, the authors investigate whether physicians who meet the meaningful use stage 2 threshold for e-prescribing (≥50% of prescriptions e-prescribed) have lower rates of ADEs among their diabetic patients. Risk of any patient with diabetes in the provider’s panel having an ADE from anti-diabetic medications was modeled adjusted for prescriber and patient panel characteristics. Physician e-prescribing to Medicare beneficiaries was associated with reduced risk of ADEs among their diabetes patients (Odds Ratio: 0.95; 95% CI, 0.94-0.96), as were several prescriber and panel characteristics. However, these physicians treated fewer patients from disadvantaged populations.

Publisher

Oxford University Press (OUP)

Subject

Health Informatics

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