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Warnings Without Guidance

Patient Responses to an FDA Warning About Ezetimibe

Bibliographic Data

ID9104299
AuthorsWilliam H Shrank (Brigham and Women's Hospital, corresponding author), Niteesh K Choudhry (0000-0001-7719-2248, Harvard University, corresponding author), Angela Tong (0000-0002-4733-3414, Harvard University), Jessica Myers, Jessica A Myers (Harvard University), Michael A Fischer (0000-0002-4685-164X, Brigham and Women's Hospital, corresponding author), Kellie Swanton (Harvard University), Julie Slezak (CVS Health (United States)), Troyen A Brennan (CVS Health (United States)), Joshua N Liberman (0000-0002-4907-812X, CVS Health (United States)), Susan Moffit (A. Alfred Taubman Health Care Center), J Avorn (0000-0003-0255-2346, Harvard University, corresponding author), Daniel Carpenter (0000-0002-5694-3927, Harvard University)
Year2012
Volume50
Issue6
Pages479-484
Publication date2012-06-01
Peer ReviewedYes
Open AccessNo
TypeARTICLE
VenueMedical Care (JOURNAL)
Journal identifiersISSN: 0025-7079 • E-ISSN: 1537-1948
PublisherOvid Technologies (Wolters Kluwer Health) (PUBLISHER)
DOI10.1097/mlr.0b013e31825517b6
PMID22581012
OpenAlexW2325016397
LanguageEN
References cited14

BACKGROUND: In January 2008, the Food and Drug Administration (FDA) communicated concerns about the efficacy of ezetimibe, but did not provide clear clinical guidance, and substantial media attention ensued. We investigated the proportion of patients who discontinued therapy and switched to a clinically appropriate alternative after the FDA communication. METHODS: Using claims data from a national pharmacy benefits manager, we created a rolling cohort of new users of ezetimibe between January 2006 and August 2008 and created a supply diary for each patient in the year after cohort entry. A patient was identified as nonpersistent if a gap of 90 days was seen in the diary. Using segmented linear regression, we compared rates of nonpersistence before and after the FDA communication and assessed patient-level characteristics associated with discontinuation. Among nonpersistent patients, we determined whether a patient made a clinically appropriate switch in the subsequent 90 days by adding a new cholesterol-lowering medication or by increasing the dose of an existing one. We used a weighted t test to compare the rates of appropriate switching before and after the communication. RESULTS: Among 867,027 new ezetimibe users, 407,006 (46.9%) were nonpersistent in the first year. After the FDA communication, the monthly level of ezetimibe nonpersistence increased by 5.7 percentage points (P<0.0001). Younger patients, those who lived in low-income zip codes, and female patients were less likely to discontinue therapy (P<0.0001 for all). Among nonpersistent patients, rates of clinically appropriate switching increased from 10.8% before to 16.5% after the FDA warning (P = 0.004). CONCLUSIONS: A substantial increase in ezetimibe nonpersistence rates was seen after an FDA communication regarding its efficacy and following associated media attention, and a small proportion of patients made a clinically appropriate switch after discontinuation. Further consideration is needed to deliver messages that promote appropriate use of chronic therapy rather than simply reduce use

Cholesterol · Cohort · Cohort study · Discontinuation · Ezetimibe · Family medicine · Food and drug administration · Medical emergency · Emergency Medicine · Health Systems, Economic Evaluations, Quality of Life · Internal Medicine · Medication Adherence and Compliance · Medicine · Pharmacovigilance and Adverse Drug Reactions · Pharmacy

  • Segmented regression analysis of interrupted time series studies in medication use research

    Open Access•Anita K Wagner, Stephen B Soumerai et al.•Journal of Clinical Pharmacy and…•2002

Citation velocityhistorical
Highly citedNo
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