TY - JOUR
T1 - Impact of a personalized, strike early and strong lipid-lowering approach on low-density lipoprotein-cholesterol levels and cardiovascular 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:
© The Author(s) 2025.
PY - 2025/3/1
Y1 - 2025/3/1
N2 - Aims Considering the lack of evidence, we evaluated the impact on cardiovascular outcome of the systematic introduction in our institution of a personalized strike early and strong (SES) approach for lipid-lowering therapy (LLT) in patients admitted for acute myocardial infarction (MI). Methods and results We retrospectively analysed data from 500 consecutive patients hospitalized across three periods: Period A (N = 198, January–June 2019), when the low-density lipoprotein cholesterol (LDL-C) goal was <70 mg/dL and a stepwise LLT approach was recommended; Period B (N = 180, January–June 2021), when the LDL-C goal was <55 mg/dL and a stepwise approach was recommended; Period C (N = 122, January–June 2023), when the LDL-C goal was <55 mg/dL and our SES protocol was implemented. Primary endpoints were achievement of the LDL-C goal during follow-up and 1-year incidence of major adverse cardiovascular events (MACE). Compared to the other periods, in Period C, there was a higher use of potent statins, alone or in combination with ezetimibe, and of proprotein convertase subtilisin/kexin type 9 inhibitor inhibitors at discharge. This translated into higher achievement of the LDL-C goal (83% vs. 55% in Period A and 43% in Period B; P < 0.001) and reduced incidence of MACE (3% vs. 12% and 11%; P = 0.026). MACE rates were lowest in patients with early and sustained LDL-C <55 mg/dL and in those achieving both LDL-C <55 mg/dL and ≥50% LDL-C reduction. Conclusion The systematic introduction of a personalized, SES strategy for LLT in patients with acute MI led to greater achievement of LDL-C goal and lower risk of MACE at 1 year vs. the stepwise approach. The systematic introduction in patients with acute myocardial infarction of a personalized, SES lipid-lowering approach led to greater achievement of the LDL-C goal during follow-up and to lower risk of MACE at 1 year vs. the stepwise approach. LDL-C, low-density lipoprotein cholesterol; MACE, major adverse cardiovascular events; PCSK9i, proprotein convertase subtilisin/kexin type 9 inhibitor; SES, strike early and strong.
AB - Aims Considering the lack of evidence, we evaluated the impact on cardiovascular outcome of the systematic introduction in our institution of a personalized strike early and strong (SES) approach for lipid-lowering therapy (LLT) in patients admitted for acute myocardial infarction (MI). Methods and results We retrospectively analysed data from 500 consecutive patients hospitalized across three periods: Period A (N = 198, January–June 2019), when the low-density lipoprotein cholesterol (LDL-C) goal was <70 mg/dL and a stepwise LLT approach was recommended; Period B (N = 180, January–June 2021), when the LDL-C goal was <55 mg/dL and a stepwise approach was recommended; Period C (N = 122, January–June 2023), when the LDL-C goal was <55 mg/dL and our SES protocol was implemented. Primary endpoints were achievement of the LDL-C goal during follow-up and 1-year incidence of major adverse cardiovascular events (MACE). Compared to the other periods, in Period C, there was a higher use of potent statins, alone or in combination with ezetimibe, and of proprotein convertase subtilisin/kexin type 9 inhibitor inhibitors at discharge. This translated into higher achievement of the LDL-C goal (83% vs. 55% in Period A and 43% in Period B; P < 0.001) and reduced incidence of MACE (3% vs. 12% and 11%; P = 0.026). MACE rates were lowest in patients with early and sustained LDL-C <55 mg/dL and in those achieving both LDL-C <55 mg/dL and ≥50% LDL-C reduction. Conclusion The systematic introduction of a personalized, SES strategy for LLT in patients with acute MI led to greater achievement of LDL-C goal and lower risk of MACE at 1 year vs. the stepwise approach. The systematic introduction in patients with acute myocardial infarction of a personalized, SES lipid-lowering approach led to greater achievement of the LDL-C goal during follow-up and to lower risk of MACE at 1 year vs. the stepwise approach. LDL-C, low-density lipoprotein cholesterol; MACE, major adverse cardiovascular events; PCSK9i, proprotein convertase subtilisin/kexin type 9 inhibitor; SES, strike early and strong.
KW - Dyslipidemia
KW - LDL-C
KW - Lipid-lowering therapies
KW - Major adverse cardiovascular events
KW - Myocardial infarction
KW - Strike early
KW - and strike strong
UR - https://www.scopus.com/pages/publications/105001193849
U2 - 10.1093/ehjcvp/pvaf004
DO - 10.1093/ehjcvp/pvaf004
M3 - Article
SN - 2055-6837
VL - 11
SP - 143
EP - 154
JO - European Heart Journal - Cardiovascular Pharmacotherapy
JF - European Heart Journal - Cardiovascular Pharmacotherapy
IS - 2
ER -