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The Rise and Fall of Gabapentin for Bipolar Disorder

A Case Study on Off-Label Pharmaceutical Diffusion

Datos Bibliográficos

ID9105129
AutoresCatherine A Fullerton (Harvard University, autor de correspondencia), Alisa B Busch (0000-0002-1828-9098, Harvard University, autor de correspondencia), Robert G Frank (0000-0003-1551-7072, Harvard University, autor de correspondencia), Richard G Frank
Año2010
Volumen48
Número4
Páginas372-379
Fecha de publicación2010-04-01
Peer ReviewedSí
Open AccessNo
TipoARTICLE
RevistaMedical Care (JOURNAL)
Identificadores de la revistaISSN: 0025-7079 • E-ISSN: 1537-1948
EditorialOvid Technologies (Wolters Kluwer Health) (PUBLISHER)
DOI10.1097/mlr.0b013e3181ca404e
PMID20195173
OpenAlexW2042746585
IdiomaEN
Citas recibidas1
Referencias citadas45

CONTEXT: Rising drug costs have increased focus on how new pharmaceuticals diffuse into the marketplace. The case of gabapentin use in bipolar disorder provides an opportunity to study the roles of marketing, clinical evidence, and prior authorization (PA) policy on off-label medication use. DESIGN: Observational study using Medicaid administrative and Verispan marketing data. We examined the association between marketing, clinical trials, and prior authorization on gabapentin use. SETTING AND PATIENTS: Florida Medicaid, bipolar disorder-diagnosed enrollees ages 18 to 64 for fiscal years 1994 to 2004. RESULTS: Gabapentin prescriptions increased from 8/1000 enrollees per quarter in 1994 to a peak of 387/1000 enrollees in 2002. Its uptake tracked marketing efforts towards psychiatrists. The publication of 2 negative clinical trials in 2000 and the discontinuation of marketing expenditures towards psychiatrists were associated with an end to the steep rise in gabapentin prescriptions. After these events gabapentin use remained between 319/1000 and 387/1000 enrollees per quarter until the PA policy, which was associated with a 45% decrease in prescriptions filled. After 1 year, scientific evidence and marketing discontinuation were associated with a 5.4 percentage point decrease in the predicted probability of filling a gabapentin prescription and the PA policy, a 7.1 percentage point decrease. CONCLUSIONS: Pharmaceutical marketing can influence off-label medication prescribing, particularly when pharmacologic options are limited. Evidence of inefficacy and/or the cessation of pharmaceutical marketing, and a restrictive formulary policy can alter prescriber behavior away from targeted pharmacologic treatments. These results suggest that both information and policy are important means in altering physician prescribing behavior

Alternative medicine · Context (archaeology) · Discontinuation · Family medicine · Formulary · Gabapentin · Health care · Marketing authorization · Medicaid · Medical prescription · Pharmaceutical industry · Pharmaceutical marketing · Prior authorization · Psychiatry · Medicine · Pharmaceutical Economics and Policy · Pharmaceutical industry and healthcare · Pharmaceutical studies and practices · Pharmacology

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    Open Access•Richard Grol, Jeremy M Grimshaw et al.•The Lancet•2003

  • Longitudinal Data Analysis for Discrete and Continuous Outcomes

    Scott L Zeger, Kung-Yee Liang et al.•Biometrics•1986

  • Models of technology diffusion

    Open Access•Paul A Geroski•Research Policy•2000

  • Longitudinal Racial/Ethnic Disparities in Antimanic Medication Use in Bipolar-I Disorder

    Alisa B Busch, Haiden A Huskamp et al.•Medical Care•2009

  • Changes Over Time and Disparities in Schizophrenia Treatment Quality

    Alisa B Busch, Anthony F Lehman et al.•Medical Care•2009

  • Prior Authorization Policies for Selective Cyclooxygenase-2 Inhibitors in Medicaid

    Michael A Fischer, Hailu Cheng et al.•Medical Care•2006

  • The Impact of Parity on Major Depression Treatment Quality in the Federal Employees’ Health Benefits Program After Parity Implementation

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Obras citantes distintas1
Citas por año0,06
Intervalo de citas2010 - 2010 (1)
Velocidad de citaciónhistorical
Altamente citadoNo
Tipos de citaNeutras: 1
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