Key result
Among patients with type 2 diabetes post-myocardial infarction, only 49.0% initiated β-blocker therapy within 30 days of discharge, with heart failure (OR 0.45) predicting lower initiation.
Cohort (n=341)
Absolute Event Rate: 49% vs 51%
Beta-blockers are significantly underutilized (only 49% initiation) in patients with type 2 diabetes following myocardial infarction, with comorbidities like heart failure paradoxically predicting non-use.
May indicate underuse in high-risk T2D post-MI; leaves open whether addressing HF-related concerns improves initiation rates.
Background: Beta-blockers remain important for secondary prevention after myocardial infarction (MI). Despite clinical guideline recommendations, underutilization of this pharmacotherapy continues in patients with type 2 diabetes (T2DM) compared to the general post-MI population. Objective: This study aimed to (1) quantify the proportion of T2DM patients utilizing β-blocker therapy within 30 days of hospital discharge after MI and (2) identify clinical and demographic characteristics predicting initiation of β-blocker therapy. Methods: A retrospective cohort of US employed, commercially insured individuals was assembled using de-identified enrollment files, medical claims, and pharmacy claims from 2007 to 2009. Inclusion criteria were the following: (1) type 2 diabetes, (2) ≥18 years old, (3) continuous eligibility, (4) MI. Multivariable logistic regression with adjusted odds ratios (OR adj ) using manual backward elimination was used to identify predictors of β-blocker initiation within 30 days of discharge from index hospitalization. Results: Of 341 T2DM patients, 167 (49.0%) were new users and 174 (51.0%) were nonusers of β-blockers within 30 days of post-MI hospital discharge. Patients on a calcium channel blocker (OR adj 2.63) and patients taking 1 to 5 medications (OR adj 3.59) were more likely to initiate β-blockers post-MI. Patients with heart failure (OR adj 0.45) or an arrhythmia (OR adj 0.44) were less likely to initiate β-blockers as well as patients with renal failure not taking a diuretic (OR adj 0.17). Conclusions: These results confirm previous findings that β-blockers are underutilized in T2DM patients post-MI. Predictors from the regression model can guide future research investigating how this deviation from guidelines is attributed to prescriber versus patient behavior.
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Hickson et al. (2016) conducted a cohort in Type 2 diabetes post-myocardial infarction (n=341). β-blocker therapy vs. No β-blocker therapy was evaluated on Initiation of β-blocker therapy within 30 days of hospital discharge. Among patients with type 2 diabetes post-myocardial infarction, only 49.0% initiated β-blocker therapy within 30 days of discharge, with heart failure (OR 0.45) predicting lower initiation.
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