POLLACK, C.V., F. DAVOUDI, D.B. DIERCKS, R.C. BECKER, S.K. JAMES, S.T. LIM, P.J. SCHULTE, Jindřich ŠPINAR, P.G. STEG, R.F. STOREY, A. HIMMELMANN, L. WALLENTIN a C.P. CANNON. Relative efficacy and safety of ticagelor vs clopidogrel as a function of time to invasive management in non-ST-segment elevation acute coronary syndrome in the PLATO trial. Clinical Cardiology. Hoboken: John Wiley and Sons Inc., 2017, roč. 40, č. 6, s. 390-398. ISSN 0160-9289. Dostupné z: https://dx.doi.org/10.1002/clc.22733.
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Základní údaje
Originální název Relative efficacy and safety of ticagelor vs clopidogrel as a function of time to invasive management in non-ST-segment elevation acute coronary syndrome in the PLATO trial
Autoři POLLACK, C.V. (840 Spojené státy), F. DAVOUDI (840 Spojené státy), D.B. DIERCKS (840 Spojené státy), R.C. BECKER (840 Spojené státy), S.K. JAMES (752 Švédsko), S.T. LIM (702 Singapur), P.J. SCHULTE (840 Spojené státy), Jindřich ŠPINAR (203 Česká republika, garant, domácí), P.G. STEG (250 Francie), R.F. STOREY (840 Spojené státy), A. HIMMELMANN (752 Švédsko), L. WALLENTIN (752 Švédsko) a C.P. CANNON (840 Spojené státy).
Vydání Clinical Cardiology, Hoboken, John Wiley and Sons Inc. 2017, 0160-9289.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30201 Cardiac and Cardiovascular systems
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 2.733
Kód RIV RIV/00216224:14110/17:00097701
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1002/clc.22733
UT WoS 000405393200007
Klíčová slova anglicky Non-ST-Segment Elevation Acute Coronary Syndromes (NSTE-ACS); Antiplatelet Therapy; P2Y(12) Receptor Antagonists; Clopidogrel; Ticagrelor; Angiography
Štítky EL OK
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Soňa Böhmová, učo 232884. Změněno: 13. 3. 2018 19:00.
Anotace
Background: Guidelines suggest that "upstream" P2Y(12) receptor antagonists should be considered in patients with non-ST-segment elevation acute coronary syndromes (NSTE-ACS). Hypothesis: Early use of ticagrelor in patients managed with an invasive strategy would be more effective than clopidogrel because of its more rapid onset of action and greater potency. Methods: In the PLATO trial, 6792 NSTE-ACS patients were randomized to ticagrelor or clopidogrel (started prior to angiography) and underwent angiography within 72 hours of randomization. We compared efficacy and safety outcomes of ticagrelor vs clopidogrel as a function of "early" (<3h) vs "late" (>= 3h) time to angiography. Adjusted Cox proportional hazards models evaluated interaction between randomized treatment and time from randomization to angiography on subsequent outcomes. Results: Overall, a benefit of ticagrelor vs clopidogrel for cardiovascular death/myocardial infarction/stroke was seen at day 7 (hazard ratio [HR]: 0.67, P = 0.002), day 30 (HR: 0.81, P = 0.042), and 1 year (HR: 0.80, P = 0.0045). There were no significant interactions in the <3h vs >= 3h groups at any timepoint. For major bleeding, overall there was no significant increase (HR: 1.04, 95% confidence interval: 0.85-1.27); but there was a significant interaction with no difference between ticagrelor and clopidogrel in the early group (HR: 0.79), but higher bleeding risk with ticagrelor in the late angiography group, at 7 days (HR: 1.51, P-int = 0.002). Patterns were similar at 30 days and 1 year. Conclusions: The benefit of ticagrelor over clopidogrel was consistent in those undergoing early and late angiography, supporting upstream use of ticagrelor
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