Comparative effectiveness of risk mitigation strategies to prevent fetal exposure to mycophenolate

Author:

Sarayani AmirORCID,Albogami Yasser,Elkhider Mohannad,Hincapie-Castillo Juan MORCID,Brumback Babette A,Winterstein Almut GORCID

Abstract

BackgroundIn 2012, the US Food and Drug Administration approved a Risk Evaluation and Mitigation Strategy (REMS) programme including mandatory prescriber training and a patient/provider acknowledgement form to prevent fetal exposure to mycophenolate. Prior to the REMS, the teratogenic risk was solely mitigated via written information (black box warning, medication guide (MG period)). To date, there is no evidence on the effectiveness of the REMS.MethodsWe used a national private health insurance claims database to identify women aged 15–44 who filled ≥1 mycophenolate prescription. To compare fetal exposure during REMS with the MG period, we estimated the prevalence of pregnancy at treatment initiation in a pre/post comparison (analysis 1) and the rate of conception during treatment in a retrospective cohort study (analysis 2). Pregnancy episodes were measured based on diagnosis and procedure codes for pregnancy outcomes or prenatal screening. We used generalised estimating equation models with inverse probability of treatment weighting to calculate risk estimates.ResultsThe adjusted proportion of existing pregnancy per 1000 treatment initiations was 1.7 (95% CI 1.0 to 2.9) vs 4.1 (95% CI 3.2 to 5.4) during the REMS and MG period. The adjusted prevalence ratio and prevalence difference were 0.42 (95% CI 0.24 to 0.74) and −2.4 (95% CI −3.8 to −1.0), respectively. In analysis 2, the adjusted rate of conception was 12.5 (95% CI 8.9 to 17.6) vs 12.9 (95% CI 9.9 to 16.9) per 1000 years of mycophenolate exposure time in the REMS versus MG periods. The adjusted risk ratio and risk difference were 0.97 (95% CI 0.63 to 1.49) and −0.4 (95% CI −5.9 to 5.0), respectively. Sensitivity analyses on the estimated conception date demonstrated robustness of our findings.ConclusionWhile the REMS programme achieved less pregnancies at treatment initiation, it failed to prevent the onset of pregnancy during treatment. Enhanced approaches to ensure effective contraception during treatment should be considered.

Publisher

BMJ

Subject

Health Policy

Reference27 articles.

1. Examination of risk evaluation and mitigation strategies and drug safety in the US;Rodriguez-Monguio;Res Social Adm Pharm,2014

2. Food and Drug Administration (FDA) . Risk evaluation and mitigation strategies (REMS), 2018. Available: https://www.fda.gov/drugs/drug-safety-and-availability/risk-evaluation-and-mitigation-strategies-rems [Accessed 27 May 2019].

3. Risk evaluation and mitigation strategies (REMSs): are they improving drug safety? A critical review of REMSs requiring elements to Assure safe use (ETASU);Boudes;Drugs R D,2017

4. The US Food and Drug Administration's Risk Evaluation and Mitigation Strategy (REMS) Program - Current Status and Future Direction;Wu;Clin Ther,2016

5. Office of Inspector General/ Department of Health and Human Services . FDA lacks comprehensive data to determine whether risk evaluation and mitigation strategies improve drug safety (OEI-04-11-00510), 2013.

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