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dc.contributor.author Bagai A
dc.contributor.author Goodman SG
dc.contributor.author Cantor WJ
dc.contributor.author Vicaut E
dc.contributor.author Bolognese L
dc.contributor.author Cequier A
dc.contributor.author Chettibi M
dc.contributor.author Hammett CJ
dc.contributor.author Huber K
dc.contributor.author Janzon M
dc.contributor.author Lapostolle F
dc.contributor.author Lassen JF
dc.contributor.author Merkely, Béla Péter
dc.contributor.author Storey RF
dc.contributor.author Ten Berg JM
dc.contributor.author Zeymer U
dc.contributor.author Diallo A
dc.contributor.author Hamm CW
dc.contributor.author Tsatsaris A
dc.contributor.author El Khoury J
dc.contributor.author Van't Hof AW
dc.contributor.author Montalescot G
dc.date.accessioned 2018-06-15T07:43:38Z
dc.date.available 2018-06-15T07:43:38Z
dc.date.issued 2018
dc.identifier.citation pagination=56-64; journalVolume=196; journalTitle=AMERICAN HEART JOURNAL;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/5350
dc.identifier.uri doi:10.1016/j.ahj.2017.10.021
dc.description.abstract BACKGROUND: Among patients with STEMI in the ATLANTIC study, pre-hospital administration of ticagrelor improved post-PCI ST-segment resolution and 30-day stent thrombosis. We investigated whether this clinical benefit with pre-hospital ticagrelor differs by ischemic duration. METHODS: In a post hoc analysis we compared absence of ST-segment resolution post-PCI and stent thrombosis at 30 days between randomized treatment groups (pre- versus in-hospital ticagrelor) stratified by symptom onset to first medical contact (FMC) duration [</=1 hour (n = 773), >1 to </=3 hours (n = 772), and >3 hours (n = 311)], examining the interaction between randomized treatment strategy and duration of symptom onset to FMC for each outcome. RESULTS: Patients presenting later after symptom onset were older, more likely to be female, and have higher baseline risk. Patients with symptom onset to FMC >3 hours had the greatest improvement in post-PCI ST-segment elevation resolution with pre- versus in-hospital ticagrelor (absolute risk difference: </=1 hour, 2.9% vs. >1 to </=3 hours, 3.6% vs. >3 hours, 12.2%; adjusted p for interaction = 0.13), while patients with shorter duration of ischemia had greater improvement in stent thrombosis at 30 days with pre- versus in-hospital ticagrelor (absolute risk difference: </=1 hour, 1.3% vs. >1 hour to </=3 hours, 0.7% vs. >3 hours, 0.4%; adjusted p for interaction = 0.55). Symptom onset to active ticagrelor administration was independently associated with stent thrombosis at 30 days (adjusted OR 1.89 per 100 minute delay, 95%CI 1.20-2.97, P < .01), but not post-PCI ST-segment resolution (P = .41). CONCLUSIONS: The effect of pre-hospital ticagrelor to reduce stent thrombosis was most evident when given early within 3 hours after symptom onset, with delay in ticagrelor administration after symptom onset associated with higher rate of stent thrombosis. These findings re-emphasize the need for early ticagrelor administration in primary PCI treated STEMI patients.
dc.relation.ispartof urn:issn:0002-8703
dc.title Duration of ischemia and treatment effects of pre- versus in-hospital ticagrelor in patients with ST-segment elevation myocardial infarction: Insights from the ATLANTIC study.
dc.type Journal Article
dc.date.updated 2018-05-05T23:17:51Z
dc.language.rfc3066 en
dc.identifier.mtmt 3332929
dc.identifier.pubmed 29421015
dc.contributor.department SE/AOK/K/Városmajori Szív- és Érgyógyászati Klinika
dc.contributor.department SE/AOK/K/VAROSMAJOR_SZÍVÉRGYÓGY/Kardiológia Központ - Kardiológiai Tanszék
dc.contributor.institution Semmelweis Egyetem


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