Craig Allen1, Katherine Donegan1. 1. Vigilance and Risk Management of Medicines Division, Medicines and Healthcare Products Regulatory Agency (MHRA), London, UK.
Abstract
PURPOSE: The aim of this study was to assess the impact of regulatory action taken in June 2014 on the co-prescribing of renin-angiotensin system (RAS) blockers in UK primary care. METHODS: RAS blocker prescriptions, issued between 01/01/2009-30/06/2015, were extracted from the Clinical Practice Research Datalink to estimate the quarterly prevalence (number of patients with at least one co-prescription) and incidence (number of patients first receiving a RAS blocker co-prescription) of co-prescribing. Two different RAS blockers prescribed on the same day constituted a co-prescription. RESULTS: A total of 880 364 patients were prescribed a single RAS blocker during the study period. Prevalence of co-prescribing increased from 4812 patients per million person-years in Q1 2009 to 4865 in Q1 2010. A reduction then occurred decreasing to 2901 patients per million person-years in Q2 2014 when the EU review concluded and continued to decrease thereafter despite a continued increase in the prevalence of prescribing of a single RAS blocker. Incidence of new co-prescribing decreased from 454 patients per million person-years in Q1 2009 to 159 in Q2 2014, but remained relatively constant at ~119 patients per million person-years on average after the EU review concluded. A total of 96% of co-prescriptions were for an ACE inhibitor + ARB, and 4% accounted for an ACE inhibitor or ARB + renin inhibitor. CONCLUSIONS: Recently, there has been a decrease in the prevalence and incidence of RAS blocker co-prescribing. Reassuringly, overall co-prescribing reduced in line with recommendations, although there was a decreasing trend prior to this likely due in part to prior publication of the data used in the EU review.
PURPOSE: The aim of this study was to assess the impact of regulatory action taken in June 2014 on the co-prescribing of renin-angiotensin system (RAS) blockers in UK primary care. METHODS: RAS blocker prescriptions, issued between 01/01/2009-30/06/2015, were extracted from the Clinical Practice Research Datalink to estimate the quarterly prevalence (number of patients with at least one co-prescription) and incidence (number of patients first receiving a RAS blocker co-prescription) of co-prescribing. Two different RAS blockers prescribed on the same day constituted a co-prescription. RESULTS: A total of 880 364 patients were prescribed a single RAS blocker during the study period. Prevalence of co-prescribing increased from 4812 patients per million person-years in Q1 2009 to 4865 in Q1 2010. A reduction then occurred decreasing to 2901 patients per million person-years in Q2 2014 when the EU review concluded and continued to decrease thereafter despite a continued increase in the prevalence of prescribing of a single RAS blocker. Incidence of new co-prescribing decreased from 454 patients per million person-years in Q1 2009 to 159 in Q2 2014, but remained relatively constant at ~119 patients per million person-years on average after the EU review concluded. A total of 96% of co-prescriptions were for an ACE inhibitor + ARB, and 4% accounted for an ACE inhibitor or ARB + renin inhibitor. CONCLUSIONS: Recently, there has been a decrease in the prevalence and incidence of RAS blocker co-prescribing. Reassuringly, overall co-prescribing reduced in line with recommendations, although there was a decreasing trend prior to this likely due in part to prior publication of the data used in the EU review.