{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,2]],"date-time":"2026-06-02T05:17:50Z","timestamp":1780377470265,"version":"3.54.1"},"reference-count":15,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"6","content-domain":{"domain":["www.ahajournals.org"],"crossmark-restriction":true},"short-container-title":["JAHA"],"published-print":{"date-parts":[[2015,6,15]]},"abstract":"<jats:sec xml:lang=\"en\">\n            <jats:title>Background<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              Little is known about the incidence, predictors, or outcomes of intracranial hemorrhage (\n              <jats:styled-content style=\"fixed-case\">ICH<\/jats:styled-content>\n              ) in patients with non\u2013\n              <jats:styled-content style=\"fixed-case\">ST<\/jats:styled-content>\n              \u2010segment elevation acute coronary syndromes (\n              <jats:styled-content style=\"fixed-case\">NSTE ACS<\/jats:styled-content>\n              ). We aimed to determine the incidence and timing of\n              <jats:styled-content style=\"fixed-case\">ICH<\/jats:styled-content>\n              , characterize the location of\n              <jats:styled-content style=\"fixed-case\">ICH<\/jats:styled-content>\n              , and identify independent baseline predictors of\n              <jats:styled-content style=\"fixed-case\">ICH<\/jats:styled-content>\n              in\n              <jats:styled-content style=\"fixed-case\">NSTE ACS<\/jats:styled-content>\n              patients.\n            <\/jats:p>\n          <\/jats:sec>\n          <jats:sec xml:lang=\"en\">\n            <jats:title>Methods and Results<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              We pooled patient\u2010level data from 4 contemporary antithrombotic therapy trials. Multivariable modeling identified independent predictors of\n              <jats:styled-content style=\"fixed-case\">ICH<\/jats:styled-content>\n              .\n              <jats:styled-content style=\"fixed-case\">ICH<\/jats:styled-content>\n              s were adjudicated by a clinical events committee. Of 37\u00a0815 patients, 135 (0.4%) had an\n              <jats:styled-content style=\"fixed-case\">ICH<\/jats:styled-content>\n              . The median (25th, 75th percentiles) follow\u2010up was 332 (184, 434) days but differed across trials. Locations of\n              <jats:styled-content style=\"fixed-case\">ICH<\/jats:styled-content>\n              were intracerebral (50%), subdural (31%), subarachnoid (18.5%), and intraventricular (11%). Independent predictors of\n              <jats:styled-content style=\"fixed-case\">ICH<\/jats:styled-content>\n              were older age (\n              <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n              per 10\u00a0years, 1.61; 95%\n              <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n              , 1.35 to 1.91); prior stroke\/transient ischemic attack;\n              <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n              , 1.95; 95%\n              <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n              , 1.14 to 3.35), higher systolic blood pressure;\n              <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n              per 10\u00a0mm\u00a0Hg increase, 1.09; 95%\n              <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n              , 1.01 to 1.18), and larger number of antithrombotic agents (\n              <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n              per each additional agent, 2.06; 95%\n              <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n              , 1.49 to 2.84). Of all\n              <jats:styled-content style=\"fixed-case\">ICH<\/jats:styled-content>\n              s, 45 (33%) were fatal.\n            <\/jats:p>\n          <\/jats:sec>\n          <jats:sec xml:lang=\"en\">\n            <jats:title>Conclusions<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              In patients with\n              <jats:styled-content style=\"fixed-case\">NSTE ACS<\/jats:styled-content>\n              enrolled in recent clinical trials of antithrombotic therapies,\n              <jats:styled-content style=\"fixed-case\">ICH<\/jats:styled-content>\n              was uncommon. Patients with older age, prior transient ischemic attack\/stroke, higher systolic blood pressure, or larger number of antithrombotic agents were at increased risk. One\u2010third of patients with\n              <jats:styled-content style=\"fixed-case\">ICH<\/jats:styled-content>\n              died. These data may be useful to trialists and data and safety monitoring committees for trial conduct and monitoring.\n            <\/jats:p>\n          <\/jats:sec>\n          <jats:sec xml:lang=\"en\">\n            <jats:title>Clinical Trial Registration<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              URL:\n              <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"https:\/\/www.clinicaltrials.gov\/\">https:\/\/www.clinicaltrials.gov\/<\/jats:ext-link>\n              . Unique identifiers: TRACER: NCT00527943, PLATO: NCT00391872, APPRAISE\u20102: NCT00831441, TRILOGY ACS: NCT00699998.\n            <\/jats:p>\n          <\/jats:sec>","DOI":"10.1161\/jaha.114.001512","type":"journal-article","created":{"date-parts":[[2015,6,19]],"date-time":"2015-06-19T03:00:12Z","timestamp":1434682812000},"update-policy":"https:\/\/doi.org\/10.1161\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":22,"title":["Meta\u2010Analysis of Intracranial Hemorrhage in Acute Coronary Syndromes: Incidence, Predictors, and Clinical Outcomes"],"prefix":"10.1161","volume":"4","author":[{"given":"Kenneth W.","family":"Mahaffey","sequence":"first","affiliation":[{"name":"Department of Medicine, Stanford University, Stanford, CA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rebecca","family":"Hager","sequence":"additional","affiliation":[{"name":"Duke Clinical Research Institute, Durham, NC"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Daniel","family":"Wojdyla","sequence":"additional","affiliation":[{"name":"Duke Clinical Research Institute, Durham, NC"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Harvey D.","family":"White","sequence":"additional","affiliation":[{"name":"Green Lane Cardiovascular Service, Auckland, New Zealand"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Paul W.","family":"Armstrong","sequence":"additional","affiliation":[{"name":"Division of Cardiology, University of Alberta, Edmonton, Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"John H.","family":"Alexander","sequence":"additional","affiliation":[{"name":"Duke Clinical Research Institute, Durham, NC"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pierluigi","family":"Tricoci","sequence":"additional","affiliation":[{"name":"Duke Clinical Research Institute, Durham, NC"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Renato D.","family":"Lopes","sequence":"additional","affiliation":[{"name":"Duke Clinical Research Institute, Durham, NC"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E. Magnus","family":"Ohman","sequence":"additional","affiliation":[{"name":"Duke Clinical Research Institute, Durham, NC"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Matthew T.","family":"Roe","sequence":"additional","affiliation":[{"name":"Duke Clinical Research Institute, Durham, NC"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robert A.","family":"Harrington","sequence":"additional","affiliation":[{"name":"Department of Medicine, Stanford University, Stanford, CA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lars","family":"Wallentin","sequence":"additional","affiliation":[{"name":"Department of Medical Sciences, Uppsala Clinical Research Center, Uppsala University, Uppsala, Sweden"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"e_1_3_5_2_2","doi-asserted-by":"publisher","DOI":"10.1056\/NEJMoa1109719"},{"key":"e_1_3_5_3_2","doi-asserted-by":"publisher","DOI":"10.1056\/NEJMoa0904327"},{"key":"e_1_3_5_4_2","doi-asserted-by":"publisher","DOI":"10.1056\/NEJMoa1105819"},{"key":"e_1_3_5_5_2","doi-asserted-by":"publisher","DOI":"10.1056\/NEJMoa1205512"},{"key":"e_1_3_5_6_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.ahj.2009.07.001"},{"key":"e_1_3_5_7_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.ahj.2009.01.003"},{"key":"e_1_3_5_8_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.ahj.2010.04.022"},{"key":"e_1_3_5_9_2","doi-asserted-by":"publisher","DOI":"10.1161\/01.CIR.98.14.1376"},{"key":"e_1_3_5_10_2","doi-asserted-by":"publisher","DOI":"10.1056\/NEJMoa0706482"},{"key":"e_1_3_5_11_2","first-page":"45","article-title":"Enoxaparin vs unfractionated heparin in high\u2010risk patients with non\u2010ST\u2010segment elevation acute coronary syndromes managed with an intended early invasive strategy: primary results of the SYNERGY randomized trial","volume":"292","author":"Ferguson JJ","year":"2004","unstructured":"Ferguson JJ, Califf RM, Antman EM, Cohen M, Grines CL, Goodman S, Kereiakes DJ, Langer A, Mahaffey KW, Nessel CC, Armstrong PW, Avezum A, Aylward P, Becker RC, Biasucci L, Borzak S, Col J, Frey MJ, Fry E, Gulba DC, Guneri S, Gurfinkel E, Harrington R, Hochman JS, Kleiman NS, Leon MB, Lopez\u2010Sendon JL, Pepine CJ, Ruzyllo W, Steinhubl SR, Teirstein PS, Toro\u2010Figueroa L, White H; SYNERGY Trial Investigators . Enoxaparin vs unfractionated heparin in high\u2010risk patients with non\u2010ST\u2010segment elevation acute coronary syndromes managed with an intended early invasive strategy: primary results of the SYNERGY randomized trial. 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