In a recently published observational registry study, researchers have demonstrated that the utilizatio of evidence-based therapies in patients experiencing ST-elevation myocardial infarction is on the rise.
In a recently published observational registry study, researchers have demonstrated that the utilization of evidence-based therapies in patients experiencing ST-elevation myocardial infarction (STEMI) is on the rise; and further, this increased utilization is likely resulting in a gradual lowering of both short- and long-term mortality.
These findings from the SWEDEHEART/RIKS-HIA (the Register of Information and Knowledge about Swedish Heart Intensive Care Administration) investigators were published in a recent edition of the Journal of the American Medical Association.
According to the authors, "Only limited information is available on the speed of implementation of new evidence-based and guideline-recommended treatments and its association with survival in real life health care of patients with STEMI."
CLOPIDOGREL USE INCREASES
In respect to evidence-based drug therapy, researchers found that the use of aspirin, clopidogrel, beta-blockers, statins, angiotensin-converting enzyme (ACE) inhibitors, and glycoprotein IIb/IIIa inhibitors all statistically significantly increased over the study period. Most notably, use of clopidogrel increased from 0% to 82%, statins from 23% to 83%, and ACE inhibitor or angiotensin II receptor blockers from 39% to 69%.
In addition to the above evidence-based drug therapies, revascularization [bypass surgery or percutaneous coronary intervention (PCI)] and reperfusion (primary PCI or thrombolysis) strategies increased as well.
The investigators did note, "However, large variations existed between hospitals regarding the speed of implementation of new treatments."
Interestingly, major adverse cardiovascular events and mortality decreased over the same period of time. For example, the proportion of patients experiencing a new myocardial infarction dropped from 4% to 1%; hospital length-of-stays decreased, and estimated in-hospital, 30-day, and 1-year mortality decreased from 12.5% to 7.2%, 15.0% to 8.6%, and 21.0% to 13.3%, respectively (P<.001 for all). Moreover, the 12-year survival analyses showed that the observed decrease in mortality was sustained over time.
"...the improvement of outcome can be expressed as an average gain of at least 2.7 years of life in patients with STEMI in 2007 compared with 12 years earlier," the investigators noted.
While causality cannot be proven, the benefits seen in regard to cardiovascular outcomes reflect at least in part the greater utilization of evidence-based strategies by healthcare professionals, the authors concluded.
Get the latest industry news, event updates, and more from Managed healthcare Executive.
PBM-Offered Genomics Testing Could Reshape Prescribing of Medications
July 25th 2025Two PBMs, True Rx Health Strategies and Capital Rx, are using pharmacogenomics — how a person’s DNA affects their response to medications — to reduce the trial-and-error of prescribing medications, saving employers and patients time and money.
Read More
David Calabrese of OptumRx Talks Top Three Drugs in Pipeline, Industry Trends in Q2
July 1st 2020In this week's episode of Tuning Into The C-Suite podcast, MHE's Briana Contreras chatted with David Calabrese, R.Ph, MHP, who is senior vice president and chief pharmacy officer of pharmacy care services company, OptumRx. David is also a member of Managed Healthcare Executives’ Editorial Advisory Board. During the discussion, he shared the OptumRx Quarter 2 Drug Pipeline Insights Report of 2020. Some of the information shared includes the three notable drugs currently being reviewed or those that have been recently approved by the FDA. Also discussed were any interesting industry trends to watch for.
Listen
FDA Extends Review of Blenrep Combinations in Multiple Myeloma
July 24th 2025Last week, an FDA advisory committee against the risk-benefit profile of Blenrep in combination with other therapies. Regulators and reviewers were concerned about the ocular side effects and dosing and tolerability. The new action date is Oct. 23, 2025.
Read More
Sarepta to Pause Shipments of the Gene Therapy Elevidys
July 22nd 2025Sarepta officials said the temporary halt in shipments was done to maintain a productive working relationship with regulators while they address a safety labeling update about the risk of acute liver disease related to Elevidys.
Read More