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Published on: November 10, 2017
Impact of high dose statin trials on hospital prescribers
Thomas I Barron1, Kathleen Bennett, John Feely
1Department of Pharmacology and Therapeutics, Trinity College Dublin, St Jame's Hospital, Dublin 8, Ireland. barront@tcd.ie
Insights
Hospital doctors increased atorvastatin prescribing doses after key studies showed its effectiveness. This shift reflects the impact of clinical trial results on medical practice for coronary heart disease prevention.
Area of Science:
- Cardiology
- Pharmacology
- Health Services Research
Background:
- PROVE-IT and REVERSAL studies demonstrated atorvastatin's superiority over pravastatin for secondary prevention of coronary heart disease (CHD).
- Intensive atorvastatin (80 mg/day) proved more effective than standard pravastatin (40 mg/day) in managing acute coronary syndromes and limiting atherosclerosis progression.
Purpose of the Study:
- To evaluate the influence of the PROVE-IT and REVERSAL trial findings on hospital physicians' prescribing habits for atorvastatin.
- To analyze changes in atorvastatin dosage prescribed by hospital doctors in the two years following these pivotal study publications.
Main Methods:
- Utilized a nationwide database of 18,894 patients with 23,750 hospital discharge prescriptions for atorvastatin (Sept 2002 - Dec 2005).
- Identified patients newly started, switched, or dose-titrated on atorvastatin by hospital prescribers.
- Analyzed monthly mean daily atorvastatin doses at discharge using segmented regression analysis.
Main Results:
- Observed a significant and sustained increase in the mean atorvastatin dose prescribed by hospital doctors.
- The average atorvastatin dose increased by 12 mg by December 2005.
- Prescribing of 20 mg, 40 mg, and 80 mg daily doses increased by 16.4%, 17.2%, and 8.8%, respectively.
Conclusions:
- The PROVE-IT and REVERSAL studies significantly influenced hospital prescribers' selection of atorvastatin dosage.
- The observed changes in prescribing patterns are likely attributable to the publication and effective promotion of these trial results.
Background:
The PROVE-IT and REVERSAL studies established that an intensive 80 mg/day dose of atorvastatin was superior to pravastatin 40 mg/day for the secondary prevention of coronary heart disease (CHD) following acute coronary syndromes and in limiting the progression of coronary atherosclerosis. We have evaluated the impact of the results from these studies on statin prescribing by hospital doctors in the 2 years following their publication.
Methods And Results:
Using a nationwide database, 18,894 patients receiving a total of 23,750 hospital discharge prescriptions for atorvastatin were identified between September 2002 and December 2005. From this cohort, patients newly commenced on, switched to, or dose titrated on atorvastatin by a hospital prescriber were identified. The mean daily atorvastatin dose on discharge was calculated for each month and the results were analysed using a segmented regression analysis. There was a significant and sustained increase in the mean atorvastatin dose used by hospital prescribers. This resulted in an increase of 12 mg, (95% CI 10.6, 13.4) in the mean dose prescribed by December 2005. This was attributable largely to a 16.4% (95% CI 13.5, 19.3), 17.2% (95% CI 14.0, 20.5) and 8.8% (95% CI 7.4, 10.2) increase in the prescribing of the 20 mg, 40 mg and 80 mg/day dosages, respectively.
Conclusion:
The PROVE-IT and REVERSAL studies have had a significant impact on hospital prescribers' choice of atorvastatin dose. It is likely that this has been the result of both the publication and effective promotion of results from these trials.
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