TY - JOUR
T1 - Mineralocorticoid receptor antagonist use in eligible patients following acute myocardial infarction
T2 - Real world data from the Acute Coronary Syndrome Israeli Surveys: 2004-2010
AU - Koifman, Edward
AU - Kopel, Eran
AU - Maor, Elad
AU - Fefer, Paul
AU - Matezky, Shlomi
AU - Tofler, Goeffrey
AU - Hamdan, Ashraf
AU - Grossman, Ehud
AU - Goldenberg, Ilan
AU - Klempfner, Robert
PY - 2013/10/9
Y1 - 2013/10/9
N2 - Background Following the EPHESUS trial in 2003, mineralocorticoid receptor antagonist (MRA) therapy received a class I indication for the management of eligible high-risk post-MI patients. Our goal was to examine temporal trends in MRA use in eligible post-myocardial infarction (MI) patients. Methods We investigated temporal trends and factors associated with MRA utilization among eligible patients enrolled in the biannual Acute Coronary Syndrome Israeli Surveys (ACSIS) 2004-2010. Results Among 7696 patients enrolled in the ACSIS surveys from 2004, 955 (12%) were eligible for MRA therapy. In this population, prescription of MRAs at discharge from the index event showed a modest increase from 21% to 25% over the six-year period, whereas utilization of other guideline recommended drugs, including angiotensin converting enzyme inhibitors/receptor blockers and β-blockers was > 2-fold higher. Multivariate logistic regression analysis showed that independent predictors of MRA prescription at discharge included a higher degree of left ventricular dysfunction (LVEF ≤ 30% vs. 31-40%: OR = 2.19; p = 0.02), history of heart failure prior to admission (OR = 1.92; p < 0.004), admission Killip ≥ II (OR = 1.78; p = 0.004), and an anterior location of the index MI (OR = 1.54; p = 0.03). MRA utilization was not associated with an increased risk for adverse events or rehospitalization at 30 days of follow-up. Conclusions In a real world setting, approximately one quarter of eligible post-MI patients are treated with an MRA following the index event, without a significant time-dependent change in this management strategy. MRAs are more likely to be underutilized in eligible lower-risk patients.
AB - Background Following the EPHESUS trial in 2003, mineralocorticoid receptor antagonist (MRA) therapy received a class I indication for the management of eligible high-risk post-MI patients. Our goal was to examine temporal trends in MRA use in eligible post-myocardial infarction (MI) patients. Methods We investigated temporal trends and factors associated with MRA utilization among eligible patients enrolled in the biannual Acute Coronary Syndrome Israeli Surveys (ACSIS) 2004-2010. Results Among 7696 patients enrolled in the ACSIS surveys from 2004, 955 (12%) were eligible for MRA therapy. In this population, prescription of MRAs at discharge from the index event showed a modest increase from 21% to 25% over the six-year period, whereas utilization of other guideline recommended drugs, including angiotensin converting enzyme inhibitors/receptor blockers and β-blockers was > 2-fold higher. Multivariate logistic regression analysis showed that independent predictors of MRA prescription at discharge included a higher degree of left ventricular dysfunction (LVEF ≤ 30% vs. 31-40%: OR = 2.19; p = 0.02), history of heart failure prior to admission (OR = 1.92; p < 0.004), admission Killip ≥ II (OR = 1.78; p = 0.004), and an anterior location of the index MI (OR = 1.54; p = 0.03). MRA utilization was not associated with an increased risk for adverse events or rehospitalization at 30 days of follow-up. Conclusions In a real world setting, approximately one quarter of eligible post-MI patients are treated with an MRA following the index event, without a significant time-dependent change in this management strategy. MRAs are more likely to be underutilized in eligible lower-risk patients.
KW - Acute myocardial infarction
KW - Heart failure
KW - Mineralocorticoid receptor antagonist
UR - http://www.scopus.com/inward/record.url?scp=84886260781&partnerID=8YFLogxK
U2 - 10.1016/j.ijcard.2013.06.091
DO - 10.1016/j.ijcard.2013.06.091
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C2 - 23890866
AN - SCOPUS:84886260781
SN - 0167-5273
VL - 168
SP - 3971
EP - 3976
JO - International Journal of Cardiology
JF - International Journal of Cardiology
IS - 4
ER -