BibTex format
@article{Murphy:2019:10.1001/jamacardio.2019.0886,
author = {Murphy, SA and Pedersen, TR and Gaciong, ZA and Ceska, R and Ezhov, MV and Connolly, DL and Jukema, JW and Toth, K and Tikkanen, MJ and Im, K and Wiviott, SD and Kurtz, CE and Honarpour, N and Giugliano, RP and Keech, AC and Sever, PS and Sabatine, MS},
doi = {10.1001/jamacardio.2019.0886},
journal = {JAMA Cardiology},
pages = {613--619},
title = {Effect of the PCSK9 inhibitor evolocumab on total cardiovascular events in patients with cardiovascular disease: A prespecified analysis from the FOURIER Trial},
url = {http://dx.doi.org/10.1001/jamacardio.2019.0886},
volume = {4},
year = {2019}
}
RIS format (EndNote, RefMan)
TY - JOUR
AB - Importance: The PCSK9 inhibitor evolocumab reduced low-density lipoprotein cholesterol and first cardiovascular events in the Further Cardiovascular Outcomes Research With PCSK9 Inhibition in Subjects With Elevated Risk (FOURIER) trial, but patients remain at high risk of recurrent cardiovascular events. Objective: To evaluate the effect of evolocumab on total cardiovascular events, given the importance of total number of cardiovascular events to patients, clinicians, and health economists. Design, Setting, and Participants: Secondary analysis of a randomized, double-blind clinical trial. The FOURIER trial compared evolocumab or matching placebo and followed up patients for a median of 2.2 years. The study included 27564 patients with stable atherosclerotic disease receiving statin therapy. Data were analyzed between May 2017 and February 2019. Main Outcomes and Measures: The primary end point (PEP) was time to first cardiovascular death, myocardial infarction, stroke, hospitalization for unstable angina, or coronary revascularization; the key secondary end point was time to first cardiovascular death, myocardial infarction, or stroke. In a prespecified analysis, total cardiovascular events were evaluated between treatment arms. Results: The mean age of patients was 63 years, 69% of patients were taking high-intensity statin therapy, and the median LDL-C at baseline was 92 mg/dL (to convert to millimoles per liter, multiply by 0.0259). There were 2907 first PEP events and 4906 total PEP events during the trial. Evolocumab reduced total PEP events by 18% (incidence rate ratio [RR], 0.82; 95% CI, 0.75-0.90; P < .001) including both first events (hazard ratio, 0.85; 95% CI, 0.79-0.92; P < .001) and subsequent events (RR, 0.74; 95% CI, 0.65-0.85). There were 2192 total primary events in the evolocumab group and 2714 total events in the placebo group. For every 1000 patients treated for 3 years, evolocumab prevented 22 first PEP events
AU - Murphy,SA
AU - Pedersen,TR
AU - Gaciong,ZA
AU - Ceska,R
AU - Ezhov,MV
AU - Connolly,DL
AU - Jukema,JW
AU - Toth,K
AU - Tikkanen,MJ
AU - Im,K
AU - Wiviott,SD
AU - Kurtz,CE
AU - Honarpour,N
AU - Giugliano,RP
AU - Keech,AC
AU - Sever,PS
AU - Sabatine,MS
DO - 10.1001/jamacardio.2019.0886
EP - 619
PY - 2019///
SN - 2380-6583
SP - 613
TI - Effect of the PCSK9 inhibitor evolocumab on total cardiovascular events in patients with cardiovascular disease: A prespecified analysis from the FOURIER Trial
T2 - JAMA Cardiology
UR - http://dx.doi.org/10.1001/jamacardio.2019.0886
UR - https://www.ncbi.nlm.nih.gov/pubmed/31116355
UR - http://hdl.handle.net/10044/1/70910
VL - 4
ER -