Centers for Medicare & Medicaid Services Open Payments data, 2014-2016.4
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Rhee TG, Ross JS. Association Between Industry Payments to Physicians and Gabapentinoid Prescribing. JAMA Intern Med. 2019;179(10):1425–1428. doi:10.1001/jamainternmed.2019.1082
Gabapentin and pregabalin are γ-aminobutyric acid analogues.1 Gabapentin (Neurontin; Pfizer) was approved by the US Food and Drug Administration (FDA) in 1993 for seizure disorders and postherpetic neuralgia; it became available as a generic in 2004. Two extended-release versions are marketed as brand-name products: Gralise (Assertio Therapeutics) and Horizant (Arbor Pharmaceuticals). Pregabalin (Lyrica; Pfizer) was approved in 2004 for seizure disorders, postherpetic neuralgia, neuropathic pain, and fibromyalgia; a generic formulation is not available. Patient use of gabapentinoids has increased from 1.2% of US adults in 2002 to 3.9% in 2015,2 raising concerns about appropriate use.3 We examined associations between industry payments to physicians associated with gabapentinoids and physicians’ prescribing.
We used Centers for Medicare & Medicaid Services 2014 to 2016 Part D prescribing data linked to 2014 to 2016 Open Payments data.4,5 With Open Payments data, we identified general payments from industry to physicians associated with gabapentinoids, all of which were for the 3 brand-name products. We excluded research payments and payments associated with ownership and licensing fees because they are less likely to be associated with drug promotion. With Part D Prescriber data, we identified all gabapentinoid prescriptions. We linked the data sets at the physician level and categorized physicians as generalists (family medicine, general practice, internal medicine, pediatrics, and obstetrics and gynecology), pain medication specialists (anesthesiology, neuromusculoskeletal medicine, pain medicine, psychiatry and neurology, and pain-related physical medicine and rehabilitation), or other.
We estimated physician prescribing as the physician's proportion of prescription days filled for the 3 brand-name gabapentinoids in aggregate of all gabapentinoid prescription days filled. To account for the distribution of the data, we used Poisson regression models to examine the association between industry payments and physician prescribing. We conducted subgroup analyses by physician specialty and payment type, which were categorized as (1) food and beverages, gifts, and educational materials, or (2) speaker fees, consulting fees, honoraria, travel and lodging, or non-research grants. All analyses were conducted with Stata, version 15.1 MP/6-Core (StataCorp) and ArcMap, version 10.4.1. (Esri), and statistical significance was set as 2-sided P < .05. Because this study used publicly available data, the Yale University School of Medicine institutional review board exempted the study from review.
Between 2014 and 2016, the manufacturers of the 3 brand-name gabapentinoids made 509 874 general payments ($11.5 million) to 51 005 physicians; these physicians represented 14.4% of physicians who prescribed any gabapentinoid product under Part D during these years. The payments were most commonly made to physicians in the southern and eastern regions of the United States (Figure). Generalist physicians received 316 372 (62.0%) payments ($3.7 million), pain medication specialists 148 119 (29.1%) payments ($6.6 million), and other physicians 45 383 (8.9%) payments ($1.2 million). Of the payments, 486 322 (95.4%) were for food and beverages, gifts, or educational materials ($5.3 million) (Table).
Among physicians who prescribed any gabapentinoid, generic gabapentin (87.4%) and pregabalin (Lyrica, 12.4%) were most commonly prescribed. Physicians receiving payments from industry were more likely to prescribe the 3 brand-name gabapentinoids than generic gabapentin (incidence rate ratio, 1.91; 95% CI, 1.87-1.96; P < .001). Incidence rate ratios consistently demonstrated that physicians receiving payments from industry were more likely to prescribe brand-name gabapentinoids (ranging from 1.30 for pain medication specialists; 95% CI, 1.25-1.36; P < .001, to 2.76 for speaker fee payment type; 95% CI, 2.60-2.92; P < .001) (Table).
Among physicians who prescribed gabapentinoids, receipt of payments from industry was associated with a higher likelihood of prescribing brand-name products than generic gabapentin. Such prescribing increases spending for Medicare and beneficiaries because brand-name gabapentinoids typically cost several hundred dollars for a 1-month supply and accounted for nearly $2500 in mean Medicare spending per beneficiary in 2016 compared with less than $20 for a 1-month supply of gabapentin, or $89 in mean Medicare spending per beneficiary.6
Limitations of this study should be noted. The study was cross-sectional and thus cannot establish a cause-and-effect relationship between payment and prescribing. Also, we did not assess other potential factors in prescribing patterns, such as direct-to-consumer advertising, or prescription appropriateness. Nonetheless, our findings raise concerns about the reasons some physicians prescribe brand-name gabapentinoids and not less-expensive generic alternatives.
Accepted for Publication: March 13, 2019.
Corresponding Author: Taeho Greg Rhee, PhD, MSW, Department of Community Medicine and Health Care, School of Medicine, University of Connecticut Health Center, 263 Farmington Ave, Farmington, CT 06530 (email@example.com).
Published Online: July 8, 2019. doi:10.1001/jamainternmed.2019.1082
Author Contributions: Dr Rhee had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Concept and design: Both authors.
Acquisition, analysis, or interpretation of data: Both authors.
Drafting of the manuscript: Rhee.
Critical revision of the manuscript for important intellectual content: Both authors.
Statistical analysis: Rhee.
Obtained funding: Rhee.
Administrative, technical, or material support: Rhee.
Conflict of Interest Disclosures: Dr Rhee reported no financial or other relationship relevant to this article. In the past 36 months, Dr Ross has received research support through Yale University from Johnson & Johnson to develop methods of clinical trial data sharing, from Medtronic, Inc and the Food and Drug Administration (FDA) to develop methods for postmarket surveillance of medical devices (U01FD004585), from the FDA to establish Yale-Mayo Clinic Center for Excellence in Regulatory Science and Innovation program (U01FD005938), from the Blue Cross Blue Shield Association to better understand medical technology evaluation, from the Centers of Medicare & Medicaid Services to develop and maintain performance measures that are used for public reporting (HHSM-500-2013-13018I), from the Agency for Healthcare Research and Quality (R01HS022882), from the National Heart, Lung, and Blood Institute of the National Institutes of Health (NIH) (R01HS025164), and from the Laura and John Arnold Foundation to establish the Good Pharma Scorecard at Bioethics International and the Collaboration for Research Integrity and Transparency at Yale.
Funding/Support: Dr Rhee received funding support from the NIH (grant T32AG019134).
Role of the Funder/Sponsor: The NIH had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
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