TY - JOUR
T1 - Impact of a personalized, strike early and strong approach on non-HDL-cholesterol levels and outcome in patients with acute myocardial infarction
AU - for the FAST-NOTE (FAST track - NOvara Therapeutic carE pathway) Registry
AU - Patti, Giuseppe
AU - Cumitini, Luca
AU - Bosco, Manuel
AU - Marengo, Alessandra
AU - D'Amario, Domenico
AU - Mennuni, Marco
AU - Solli, Martina
AU - Grisafi, Leonardo
N1 - Publisher Copyright:
© 2024
PY - 2025/8/15
Y1 - 2025/8/15
N2 - Aims: We retrospectively evaluated the impact on non-HDL-cholesterol (non-HDL-C) levels of the systematic introduction in our institution of an individualized, pre-defined, strike early and strong (SES) strategy for lipid-lowering therapy (LLT) in patients with acute myocardial infarction (MI). Methods: We analyzed data from 500 consecutive patients admitted across three periods: Period A (N = 198, January–June 2019), when the non-HDL-C goal was <100 mg/dL and a stepwise LLT approach was indicated; Period B (N = 180, January–June 2021), when the non-HDL-C goal was <85 mg/dL and a stepwise approach was recommended; Period C (N = 122, January–June 2023), when the SES protocol was introduced. Primary endpoints were the percentage of patients reaching the non- HDL-C goal during follow-up and the incidence of major adverse cardiovascular events (MACE) at one year. Results: Compared to the other periods, the prevalence of prescription at discharge of potent statins, alone or in combination with ezetimibe, and PCSK9 inhibitors was greater in Period C. The achievement of the non-HDL-C goal in Period C was higher (87 % vs 67 % and 58 % in Periods A and B, respectively; p < 0.001). This achievement was associated with a lower occurrence of MACE (7 % vs. 13 % in patients not at target; log-rank p = 0.027). MACE incidence was the lowest in patients with early and sustained non-HDL-C < 85 mg/dL during follow-up. Conclusion: The systematic introduction of an individualized, SES approach for LLT in patients with acute MI led to higher achievement of the non-HDL-C goal and this translated into a lower risk of MACE.
AB - Aims: We retrospectively evaluated the impact on non-HDL-cholesterol (non-HDL-C) levels of the systematic introduction in our institution of an individualized, pre-defined, strike early and strong (SES) strategy for lipid-lowering therapy (LLT) in patients with acute myocardial infarction (MI). Methods: We analyzed data from 500 consecutive patients admitted across three periods: Period A (N = 198, January–June 2019), when the non-HDL-C goal was <100 mg/dL and a stepwise LLT approach was indicated; Period B (N = 180, January–June 2021), when the non-HDL-C goal was <85 mg/dL and a stepwise approach was recommended; Period C (N = 122, January–June 2023), when the SES protocol was introduced. Primary endpoints were the percentage of patients reaching the non- HDL-C goal during follow-up and the incidence of major adverse cardiovascular events (MACE) at one year. Results: Compared to the other periods, the prevalence of prescription at discharge of potent statins, alone or in combination with ezetimibe, and PCSK9 inhibitors was greater in Period C. The achievement of the non-HDL-C goal in Period C was higher (87 % vs 67 % and 58 % in Periods A and B, respectively; p < 0.001). This achievement was associated with a lower occurrence of MACE (7 % vs. 13 % in patients not at target; log-rank p = 0.027). MACE incidence was the lowest in patients with early and sustained non-HDL-C < 85 mg/dL during follow-up. Conclusion: The systematic introduction of an individualized, SES approach for LLT in patients with acute MI led to higher achievement of the non-HDL-C goal and this translated into a lower risk of MACE.
KW - Dyslipidemia
KW - Lipid-lowering therapies
KW - Major adverse cardiovascular events
KW - Myocardial infarction
KW - Non-HDL-C
KW - Strike early and strong
UR - https://www.scopus.com/pages/publications/105003937639
U2 - 10.1016/j.ijcard.2025.133327
DO - 10.1016/j.ijcard.2025.133327
M3 - Article
SN - 0167-5273
VL - 433
JO - International Journal of Cardiology
JF - International Journal of Cardiology
M1 - 133327
ER -