Literature DB >> 24616240

Methodological gaps in the assessment of risk minimization interventions: a systematic review.

Inna Gridchyna1, Anne-Marie Cloutier, Lenhangmbong Nkeng, Camille Craig, Sarah Frise, Yola Moride.   

Abstract

INTRODUCTION: Since the introduction of therapeutic risk management regulatory guidance, an increase in the number of risk minimization interventions (RMIs) published in the literature has been observed. Methods used to evaluate their effectiveness remain, however, poorly examined.
OBJECTIVE: This paper aimed to conduct a literature review on the methods of evaluation of effectiveness of RMIs and to identify methodological gaps.
METHODS: The search was conducted using MEDLINE and Embase between 1 January 2000 and 31 December 2010, and updated on 1 April 2013. The following characteristics were extracted from each study: target population for the RMI, target population for the assessment of effectiveness, study design, data sources, and effectiveness outcome(s).
RESULTS: A total of 188 unique RMIs were identified in the literature, of which effectiveness was evaluated in only 65 (34.6%) at the time of publication. The largest proportion of studies reviewed (n = 49, 75.4%) attempted to evaluate changes in behavior through prescribing or laboratory test practices. One quarter of studies evaluated the effect of RMIs on the occurrence of adverse events. Only a minority of studies used robust designs, such as randomized controlled trials (n = 6, 9.2%) or a quasi-experimental design with a parallel comparison group (n = 8, 12.3%).
CONCLUSION: Lack of robust methodological design used in published studies on RMI effectiveness evaluation is an important methodological gap in the evaluation of RMI effectiveness.
© 2014 The Authors. Pharmacoepidemiology and Drug Safety published by John Wiley & Sons, Ltd. © 2014 The Authors. Pharmacoepidemiology and Drug Safety published by John Wiley & Sons, Ltd.

Keywords:  REMS; effectiveness; pharmacoepidemiology; risk minimization intervention; therapeutic risk management

Mesh:

Substances:

Year:  2014        PMID: 24616240     DOI: 10.1002/pds.3596

Source DB:  PubMed          Journal:  Pharmacoepidemiol Drug Saf        ISSN: 1053-8569            Impact factor:   2.890


  14 in total

Review 1.  Study design, process and outcome indicators of post-authorization studies aimed at evaluating the effectiveness of risk minimization measures in the EU PAS Register.

Authors:  Andreea Farcas; Madalina Huruba; Cristina Mogosan
Journal:  Br J Clin Pharmacol       Date:  2018-12-27       Impact factor: 4.335

2.  Evaluation of the Effectiveness of Additional Risk Minimization Measures for Voriconazole in the EU: Findings and Lessons Learned from a Healthcare Professional Survey.

Authors:  Joanna Lem; Muhammad Younus; Jalal A Aram; Shahrzad Moosavi; Klaus Freivogel; Anne Lewis; Rachel E Sobel
Journal:  Pharmaceut Med       Date:  2019-04

3.  Integrating risk minimization planning throughout the clinical development and commercialization lifecycle: an opinion on how drug development could be improved.

Authors:  Elaine H Morrato; Meredith Y Smith
Journal:  Ther Clin Risk Manag       Date:  2015-02-26       Impact factor: 2.423

4.  A multinational, drug utilization study to investigate the use of dexmedetomidine (Dexdor®) in clinical practice in the EU.

Authors:  Mary Weatherall; Riku Aantaa; Giorgio Conti; Chris Garratt; Pasi Pohjanjousi; Michael A Lewis; Nicholas Moore; Susana Perez-Gutthann
Journal:  Br J Clin Pharmacol       Date:  2017-05-10       Impact factor: 4.335

5.  Study Design and Evaluation of Risk Minimization Measures: A Review of Studies Submitted to the European Medicines Agency for Cardiovascular, Endocrinology, and Metabolic Drugs.

Authors:  Giampiero Mazzaglia; Sabine M J Straus; Peter Arlett; Daniela da Silva; Heidi Janssen; June Raine; Enrica Alteri
Journal:  Drug Saf       Date:  2018-02       Impact factor: 5.606

Review 6.  A review of studies evaluating the effectiveness of risk minimisation measures in Europe using the European Union electronic Register of Post-Authorization Studies.

Authors:  Pareen Vora; Esther Artime; Montse Soriano-Gabarró; Nawab Qizilbash; Vineet Singh; Alex Asiimwe
Journal:  Pharmacoepidemiol Drug Saf       Date:  2018-04-16       Impact factor: 2.890

7.  Advancing the field of pharmaceutical risk minimization through application of implementation science best practices.

Authors:  Meredith Y Smith; Elaine Morrato
Journal:  Drug Saf       Date:  2014-08       Impact factor: 5.606

8.  Evaluation of Risk-Minimization Activities for Cyproterone Acetate 2 mg/Ethinylestradiol 35 µg: A Cross-Sectional Physician Survey.

Authors:  Kimberly H Davis; Alex Asiimwe; Laurie J Zografos; David J McSorley; Elizabeth B Andrews
Journal:  Pharmaceut Med       Date:  2017-08-28

9.  Measuring the impact of medicines regulatory interventions - Systematic review and methodological considerations.

Authors:  Thomas Goedecke; Daniel R Morales; Alexandra Pacurariu; Xavier Kurz
Journal:  Br J Clin Pharmacol       Date:  2017-12-20       Impact factor: 4.335

10.  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

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