Key result
Substantial site-level variability exists in anticoagulant choice for acute myocardial infarction (median OR 4.70 for LMWH vs UFH), with no differences in risk-adjusted bleeding or mortality across hospital phenotypes.
Why the study?
Does the choice of anticoagulant strategy impact clinical outcomes in patients with acute myocardial infarction treated with an early invasive strategy?
Observational (n=63,796)
Yes
Does the choice of anticoagulant strategy impact clinical outcomes in patients with acute myocardial infarction treated with an early invasive strategy?
There is substantial hospital-level variability in the choice of anticoagulants for AMI patients undergoing PCI, but this variability does not translate into differences in risk-adjusted clinical outcomes.
Answers are grounded in this paper and cite their sources.
Variability in AMI anticoagulant choice should not change practice; leaves open optimal selection and unmeasured confounders.
BACKGROUND: During a myocardial infarction, no single best approach of systemic anticoagulation is recommended, likely due to a lack of comparative effectiveness studies and trade-offs between treatments. METHODS AND RESULTS: We investigated the patterns of use and site-level variability in anticoagulant strategies (unfractionated heparin [UFH] only, low-molecular-weight heparin [LMWH] only, UFH+LMWH, any bivalirudin) of 63 796 patients with a principal diagnosis of myocardial infarction treated with an early invasive strategy with percutaneous coronary intervention at 257 hospitals. About half (47%) of patients received UFH only, 6% UFH+LMWH, 7% LMWH only, and 40% bivalirudin. Compared with UFH, the median odds ratio was 2.90 for LMWH+UFH, 4.70 for LMWH only, and 3.09 for bivalirudin, indicating that 2 "identical" patients would have a 3- to 4-fold greater likelihood of being treated with anticoagulants other than UFH at one hospital compared with another. We then categorized hospitals as low- or high-users of LMWH and bivalirudin. Using hierarchical, multivariate regression models, we found that low bivalirudin-using hospitals had higher unadjusted bleeding rates, but the risk-adjusted and anticoagulant-adjusted bleeding rates did not differ across the hospital anticoagulation phenotypes. Risk-standardized mortality and risk-standardized length of stay also did not differ across hospital phenotypes. CONCLUSIONS: We found substantial site-level variability in the choice of anticoagulants for invasively managed acute myocardial infarction patients, even after accounting for patient factors. No single hospital-use pattern was found to be clinically superior. More studies are needed to determine which patients would derive the greatest benefit from various anticoagulants and to support consistent treatment of patients with the optimal anticoagulant strategy.
No takes yet. Share an insight, caveat, or question.
Arnold et al. (2015) conducted an observational in Acute myocardial infarction (n=63,796). Anticoagulant strategies other than UFH (LMWH, bivalirudin) vs. Unfractionated heparin (UFH) only was evaluated on Likelihood of being treated with LMWH only vs UFH at different hospitals (site-level variability) (median OR 4.70). Substantial site-level variability exists in anticoagulant choice for acute myocardial infarction (median OR 4.70 for LMWH vs UFH), with no differences in risk-adjusted bleeding or mortality across hospital phenotypes.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: