Literature DB >> 23656443

Improving the effect of FDA-mandated drug safety alerts with Internet-based continuing medical education.

Carl N Kraus1, Alan T Baldwin, R G McAllister.   

Abstract

The US Food and Drug Administration (FDA) requires risk communication as an element of Risk Evaluation and Mitigation Strategies (REMS) to alert and educate healthcare providers about severe toxicities associated with approved drugs. The educational effectiveness of this approach has not been evaluated. To support the communication plan element of the ipilimumab REMS, a Medscape Safe Use Alert (SUA) letter was distributed by Medscape via email and mobile device distribution to clinicians specified in the REMS. This alert contained the FDA-approved Dear Healthcare Provider (DHCP) letter mandated for distribution. A continuing medical education (CME) activity describing ipilimumab toxicities and the appropriate management was simultaneously posted on the website and distributed to Medscape members. Data were collected over a 6-month period regarding the handling of the letter and the responses to pre- and post-test questions for those who participated in the CME activity. Analysis of the answers to the pre- and posttest questions showed that participation in the CME activity resulted in an improvement in correct answer responses of 47%. Our experience shows that there are likely distinct information sources that are utilized by different HCP groups. The ready availability of a brief CME activity was utilized by 24,063 individuals, the majority of whom showed enhanced understanding of ipilimumab toxicity by improvement in post-test scores, educational data that are not available via implementation of standard safety alert communications. These results demonstrate that improvement in understanding of specific drug toxicities is enhanced by a CME intervention.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23656443     DOI: 10.2174/1574886311308010003

Source DB:  PubMed          Journal:  Curr Drug Saf        ISSN: 1574-8863


  4 in total

1.  Quality of Reporting on the Evaluation of Risk Minimization Programs: A Systematic Review.

Authors:  Andrea M Russell; Elaine H Morrato; Rebecca M Lovett; Meredith Y Smith
Journal:  Drug Saf       Date:  2020-05       Impact factor: 5.606

2.  Adherence to risk evaluation and mitigation strategies (REMS) requirements for monthly testing of liver function.

Authors:  Christopher M Blanchette; Anthony P Nunes; Nancy D Lin; Kathleen M Mortimer; Joshua Noone; Krishna Tangirala; Stephen Johnston; Benjamin Gutierrez
Journal:  Drugs Context       Date:  2015-02-10

3.  The RIMES Statement: A Checklist to Assess the Quality of Studies Evaluating Risk Minimization Programs for Medicinal Products.

Authors:  Meredith Y Smith; Andrea Russell; Priya Bahri; Peter G M Mol; Sarah Frise; Emily Freeman; Elaine H Morrato
Journal:  Drug Saf       Date:  2018-04       Impact factor: 5.606

4.  Healthcare professionals' pharmacovigilance knowledge and adverse drug reaction reporting behavior and factors determining the reporting rates.

Authors:  Müberra Devrim Güner; Perihan Elif Ekmekci
Journal:  J Drug Assess       Date:  2019-01-05
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.