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Pregled bibliografske jedinice broj: 1047595

Alirocumab in Patients With Polyvascular Disease and Recent Acute Coronary Syndrome


(ODYSSEY OUTCOMES Committees and Investigators) Jukema, J. Wouter; Szarek, Michael; Zijlstra, Laurien E.; de Silva, H. Asita; Bhatt, Deepak L.; Bittner, Vera A.; Diaz, Rafael; Edelberg, Jay M.; Goodman, Shaun G.; Hanotin, Corinne et al.
Alirocumab in Patients With Polyvascular Disease and Recent Acute Coronary Syndrome // Journal of the American College of Cardiology, 74 (2019), 9; 1167-1176 doi:10.1016/j.jacc.2019.03.013 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 1047595 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Alirocumab in Patients With Polyvascular Disease and Recent Acute Coronary Syndrome

Autori
Jukema, J. Wouter ; Szarek, Michael ; Zijlstra, Laurien E. ; de Silva, H. Asita ; Bhatt, Deepak L. ; Bittner, Vera A. ; Diaz, Rafael ; Edelberg, Jay M. ; Goodman, Shaun G. ; Hanotin, Corinne ; Harrington, Robert A. ; Karpov, Yuri ; Moryusef, Angèle ; Pordy, Robert ; Prieto, Juan C. ; Roe, Matthew T. ; White, Harvey D. ; Zeiher, Andreas M. ; Schwartz, Gregory G. ; Steg, P. Gabriel

Kolaboracija
ODYSSEY OUTCOMES Committees and Investigators

Izvornik
Journal of the American College of Cardiology (0735-1097) 74 (2019), 9; 1167-1176

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
acute coronary syndrome ; alirocumab ; cerebrovascular disease ; death ; major adverse cardiac events ; peripheral artery disease ; cardiovascular event rates ; arterydisease ; pcsk9inhibition ; risk ; outpatients ; cholesterol ; management ; insights

Sažetak
BACKGROUND: Patients with acute coronary syndrome (ACS) and concomitant noncoronary atherosclerosis have a high risk of major adverse cardiovascular events (MACEs) and death. The impact of lipid lowering by proprotein convertase subtilisin-kexin type 9 inhibition in such patients is undetermined. OBJECTIVES: This pre-specified analysis from ODYSSEY OUTCOMES (Evaluation of Cardiovascular Outcomes After an Acute Coronary Syndrome During Treatment With Alirocumab) determined whether polyvascular disease influenced risks of MACEs and death and their modification by alirocumab in patients with recent ACS and dyslipidemia despite intensive statin therapy. METHODS: Patients were randomized to alirocumab or placebo 1 to 12 months after ACS. The primary MACEs endpoint was the composite of coronary heart disease death, nonfatal myocardial infarction, fatal or nonfatal ischemic stroke, or unstable angina requiring hospitalization. All-cause death was a secondary endpoint. RESULTS: Median follow-up was 2.8 years. Of 18, 924 patients, 17, 370 had monovascular (coronary) disease, 1, 405 had polyvascular disease in 2 beds (coronary and peripheral artery or cerebrovascular), and 149 had polyvascular disease in 3 beds (coronary, peripheral artery, cerebrovascular). With placebo, the incidence of MACEs by respective vascular categories was 10.0%, 22.2%, and 39.7%. With alirocumab, the corresponding absolute risk reduction was 1.4% (95% confidence interval [CI]: 0.6% to 2.3%), 1.9% (95% CI: -2.4% to 6.2%), and 13.0% (95% CI: -2.0% to 28.0%). With placebo, the incidence of death by respective vascular categories was 3.5%, 10.0%, and 21.8% ; the absolute risk reduction with alirocumab was 0.4% (95% CI: -0.1% to 1.0%), 1.3% (95% CI: -1.8% to 4.3%), and 16.2% (95% CI: 5.5% to 26.8%). CONCLUSIONS: In patients with recent ACS and dyslipidemia despite intensive statin therapy, polyvascular disease is associated with high risks of MACEs and death. The large absolute reductions in those risks with alirocumab are a potential benefit for these patients. (Evaluation of Cardiovascular Outcomes After an Acute Coronary Syndrome During Treatment With Alirocumab [ODYSSEY OUTCOMES]: NCT01663402) (C) 2019 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation.

Izvorni jezik
Engleski



POVEZANOST RADA


Ustanove:
Klinička bolnica "Merkur",
Medicinski fakultet, Rijeka,
Medicinski fakultet, Zagreb,
Klinička bolnica "Sveti Duh",
KBC "Sestre Milosrdnice",
Opća bolnica Varaždin,
Opća bolnica "Dr. Josip Benčević",
Klinička bolnica "Dubrava",
Klinički bolnički centar Zagreb,
Klinički bolnički centar Rijeka,
Sveučilište u Zagrebu,
Sveučilište u Rijeci,
Opća bolnica Dubrovnik,
Thalassoterapia Opatija,
Fakultet za dentalnu medicinu i zdravstvo, Osijek

Profili:

Avatar Url Viktor Peršić (autor)

Poveznice na cjeloviti tekst rada:

doi

Citiraj ovu publikaciju:

(ODYSSEY OUTCOMES Committees and Investigators) Jukema, J. Wouter; Szarek, Michael; Zijlstra, Laurien E.; de Silva, H. Asita; Bhatt, Deepak L.; Bittner, Vera A.; Diaz, Rafael; Edelberg, Jay M.; Goodman, Shaun G.; Hanotin, Corinne et al.
Alirocumab in Patients With Polyvascular Disease and Recent Acute Coronary Syndrome // Journal of the American College of Cardiology, 74 (2019), 9; 1167-1176 doi:10.1016/j.jacc.2019.03.013 (međunarodna recenzija, članak, znanstveni)
(ODYSSEY OUTCOMES Committees and Investigators) (ODYSSEY OUTCOMES Committees and Investigators) Jukema, J., Szarek, M., Zijlstra, L., de Silva, H., Bhatt, D., Bittner, V., Diaz, R., Edelberg, J., Goodman, S. & Hanotin, C. (2019) Alirocumab in Patients With Polyvascular Disease and Recent Acute Coronary Syndrome. Journal of the American College of Cardiology, 74 (9), 1167-1176 doi:10.1016/j.jacc.2019.03.013.
@article{article, author = {Jukema, J. Wouter and Szarek, Michael and Zijlstra, Laurien E. and de Silva, H. Asita and Bhatt, Deepak L. and Bittner, Vera A. and Diaz, Rafael and Edelberg, Jay M. and Goodman, Shaun G. and Hanotin, Corinne and Harrington, Robert A. and Karpov, Yuri and Moryusef, Ang\`{e}le and Pordy, Robert and Prieto, Juan C. and Roe, Matthew T. and White, Harvey D. and Zeiher, Andreas M. and Schwartz, Gregory G. and Steg, P. Gabriel}, year = {2019}, pages = {1167-1176}, DOI = {10.1016/j.jacc.2019.03.013}, keywords = {acute coronary syndrome, alirocumab, cerebrovascular disease, death, major adverse cardiac events, peripheral artery disease, cardiovascular event rates, arterydisease, pcsk9inhibition, risk, outpatients, cholesterol, management, insights}, journal = {Journal of the American College of Cardiology}, doi = {10.1016/j.jacc.2019.03.013}, volume = {74}, number = {9}, issn = {0735-1097}, title = {Alirocumab in Patients With Polyvascular Disease and Recent Acute Coronary Syndrome}, keyword = {acute coronary syndrome, alirocumab, cerebrovascular disease, death, major adverse cardiac events, peripheral artery disease, cardiovascular event rates, arterydisease, pcsk9inhibition, risk, outpatients, cholesterol, management, insights} }
@article{article, author = {Jukema, J. Wouter and Szarek, Michael and Zijlstra, Laurien E. and de Silva, H. Asita and Bhatt, Deepak L. and Bittner, Vera A. and Diaz, Rafael and Edelberg, Jay M. and Goodman, Shaun G. and Hanotin, Corinne and Harrington, Robert A. and Karpov, Yuri and Moryusef, Ang\`{e}le and Pordy, Robert and Prieto, Juan C. and Roe, Matthew T. and White, Harvey D. and Zeiher, Andreas M. and Schwartz, Gregory G. and Steg, P. Gabriel}, year = {2019}, pages = {1167-1176}, DOI = {10.1016/j.jacc.2019.03.013}, keywords = {acute coronary syndrome, alirocumab, cerebrovascular disease, death, major adverse cardiac events, peripheral artery disease, cardiovascular event rates, arterydisease, pcsk9inhibition, risk, outpatients, cholesterol, management, insights}, journal = {Journal of the American College of Cardiology}, doi = {10.1016/j.jacc.2019.03.013}, volume = {74}, number = {9}, issn = {0735-1097}, title = {Alirocumab in Patients With Polyvascular Disease and Recent Acute Coronary Syndrome}, keyword = {acute coronary syndrome, alirocumab, cerebrovascular disease, death, major adverse cardiac events, peripheral artery disease, cardiovascular event rates, arterydisease, pcsk9inhibition, risk, outpatients, cholesterol, management, insights} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


Citati:





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