コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 DEHEART trial (Bivalirudin Versus Heparin in ST-Segment and Non-ST-Segment Elevation Myocardial Infar
2 AD, leaflet redundancy, and T-wave inversion/ST-segment depression (all p < 0.0001) but not with mitr
4 th much higher biomarker thresholds, (2) new ST-segment depression of >=1 mm for the primary and >=0.
5 The implantable cardiac system detects early ST-segment deviation and alerts patients of a potential
6 were analyzed within a core laboratory; sum ST-segment deviation resolution >=50% was defined as suc
9 stents (<3.50 mm), among 1498 patients with ST-segment elevated myocardial infarction undergoing pri
10 tion, and presented more frequently with non-ST segment elevation acute coronary syndrome compared wi
11 lder than 18 years with unstable angina, non-ST segment elevation myocardial infarction (NSTEMI) or S
12 vely enrolled 27 patients with anterior wall ST segment elevation myocardial infarction (STEMI) and 4
13 elevation myocardial infarction (NSTEMI) or ST segment elevation myocardial infarction (STEMI), with
14 ina or urgent PCI for unstable angina or non-ST segment elevation myocardial infarction less than 30
15 raphy (ECG) showed signs of ongoing anterior ST segment elevation myocardial infarction, and emergent
16 raphy (ECG) showed signs of ongoing anterior ST segment elevation myocardial infarction, and emergent
17 in patients with unstable angina (UA) or non-ST-segment elevation (NSTE) myocardial infarction (MI).
18 syndrome (25%), which consisted of both non-ST-segment elevation acute coronary syndrome (14%) and S
19 ctive invasive strategy in patients with non-ST-segment elevation acute coronary syndrome (NSTE-ACS)
21 ease and stable ischaemic heart disease, non-ST-segment elevation acute coronary syndrome or ST-segme
22 ministration strategies in patients with non-ST-segment elevation acute coronary syndrome undergoing
23 ein IIb/IIIa Inhibition in Patients With Non-ST-Segment Elevation Acute Coronary Syndrome) trial.
24 e key in the management of patients with non-ST-segment elevation acute coronary syndrome, the optima
25 A total of 8,404 patients, with or without ST-segment elevation acute coronary syndrome, were rando
26 ein IIb/IIIa Inhibition in Patients With Non-ST-Segment Elevation Acute Coronary Syndrome; NCT0008989
27 compared with prasugrel in patients with non-ST-segment elevation acute coronary syndromes (NSTE-ACS)
28 isk of adverse outcomes versus men after non-ST-segment elevation acute coronary syndromes (NSTEACS)
29 concomitant clopidogrel presenting with non-ST-segment elevation acute coronary syndromes (NSTEACS)
30 myocardial infarction [STEMI], n = 399; non-ST-segment elevation acute coronary syndromes [NSTE-ACS]
32 Adult (>18 years) comatose survivors without ST-segment elevation after resuscitation from out-of-hos
33 as seen more commonly in admissions with non-ST-segment elevation AMI-CS, nonwhite race, and higher b
34 s with acute myocardial infarction including ST-segment elevation and non-ST-segment elevation were r
36 r access complication, and one had transient ST-segment elevation from air-embolism, without sequelae
37 arction (MI) (18.7% vs. 22.5%; p < 0.001) or ST-segment elevation MI (8.5% vs. 15.7%; p < 0.001).
38 n-hospital reperfusion rates and outcomes of ST-segment elevation MI (STEMI) in renal transplant reci
40 ar risk of incident MI (0.8% annually), with ST-segment elevation MI constituting one-third of all ca
43 20% of MI cases and presented more often as ST-segment elevation MI versus MI not related to a stent
44 ntration was measured in 1,398 patients with ST-segment elevation MI who enrolled in a prospective co
45 h all-cause mortality in patients with acute ST-segment elevation MI who underwent primary percutaneo
48 % had ST-segment elevation MI, 74.3% had non-ST-segment elevation MI, and 8.9% had ventricular tachyc
49 ower EF were more likely to have experienced ST-segment elevation MI, have higher troponin values, an
52 SCAD patients more frequently presented with ST-segment elevation myocardial infarction (57% vs. 36%;
54 0; 95% CI: -0.98 to 1.58; p = 0.637) and non-ST-segment elevation myocardial infarction (ATE coeffici
55 without PCI or in those with a diagnosis of ST-segment elevation myocardial infarction (group by PCI
56 ISR PCI were less likely to present with non-ST-segment elevation myocardial infarction (MI) (18.7% v
57 cardiovascular (CV) events in patients with ST-segment elevation myocardial infarction (MI) and mult
58 complete revascularization in patients with ST-segment elevation myocardial infarction (MI) with mul
60 vation myocardial infarction (STEMI) and non-ST-segment elevation myocardial infarction (NSTEMI) pati
61 ruction commonly affects patients with acute ST-segment elevation myocardial infarction (STEMI) and i
62 cardiovascular (CV) events in patients with ST-segment elevation myocardial infarction (STEMI) and m
63 rt failure and non-fatal AMI at 12-months in ST-segment elevation myocardial infarction (STEMI) and n
67 e carry an increased risk of mortality after ST-segment elevation myocardial infarction (STEMI) compl
68 may have potentially refrained patients with ST-segment elevation myocardial infarction (STEMI) from
69 an alternative to mechanical reperfusion for ST-segment elevation myocardial infarction (STEMI) in se
71 percutaneous coronary intervention (PCI) for ST-segment elevation myocardial infarction (STEMI) may n
72 ical trial, we enrolled patients with either ST-segment elevation myocardial infarction (STEMI) or no
73 Singapore Myocardial Infarction Registry] of ST-segment elevation myocardial infarction (STEMI) patie
75 tated after cardiac arrest in the absence of ST-segment elevation myocardial infarction (STEMI) remai
87 moking is a well-established risk factor for ST-segment elevation myocardial infarction (STEMI); howe
88 CI full bivalirudin was administered in 612 (ST-segment elevation myocardial infarction [STEMI], n =
90 bstruction affects one-half of patients with ST-segment elevation myocardial infarction and confers a
92 lirudin Versus Heparin in ST-Segment and Non-ST-Segment Elevation Myocardial Infarction in Patients o
93 ation myocardial infarction (group by PCI or ST-segment elevation myocardial infarction interaction e
94 r CTA first in the diagnostic process in non-ST-segment elevation myocardial infarction is a safe gat
96 her this is true in a real-world prehospital ST-segment elevation myocardial infarction network using
99 ected patients presenting with suspected non-ST-segment elevation myocardial infarction to the emerge
100 orithm for rapid rule-out and rule-in of non-ST-segment elevation myocardial infarction using high-se
101 entation, with <=2 hours of symptoms or with ST-segment elevation myocardial infarction were excluded
102 mber 21, 2017, 440 patients, presenting with ST-segment elevation myocardial infarction within 6 h of
103 oing single-vessel FFR assessment (excluding ST-segment elevation myocardial infarction) from April 1
105 segment elevation acute coronary syndrome or ST-segment elevation myocardial infarction, with or with
109 patients resuscitated from VF/pVT OHCA with ST-segment elevation on their postresuscitation ECG, the
110 tients resuscitated from VF/pVT OHCA without ST-segment elevation on their postresuscitation ECG, the
113 ction including ST-segment elevation and non-ST-segment elevation were recruited between February 201
116 patency, the quantitative intracoronary ECG ST-segment elevation, and angina pectoris during the sam
117 ith acute coronary syndromes with or without ST-segment elevation, the incidence of death, myocardial
124 (RR, 0.84 [95% CI, 0.69-1.04]; P=0.11); non-ST-segment-elevation acute coronary syndrome (RR, 0.84 [
125 esions; (3) patients who have suffered a non-ST-segment-elevation acute coronary syndrome; and (4) pa
126 vation myocardial infarction (84.4%) and non-ST-segment-elevation acute coronary syndromes (71.5%) th
127 t IL-1 receptor antagonist, in patients with ST-segment-elevation acute myocardial infarction or hear
128 odels were created to explore all MI and non-ST-segment-elevation MI (NSTEMI) versus ST-segment-eleva
130 tion MI hospitalization was smaller than for ST-segment-elevation MI among both women and men (-1.9%
131 rst hospitalization for AMI overall, and for ST-segment-elevation MI and non-ST-segment-elevation MI
132 s -8.3% (95% CI, -8.0% to -8.6%).The AAPC in ST-segment-elevation MI changed among women in 2009 (200
137 all, and for ST-segment-elevation MI and non-ST-segment-elevation MI was identified by International
141 med for stable angina (66%), followed by non-ST-segment-elevation myocardial infarction (45%), and ST
142 was more frequently used among patients with ST-segment-elevation myocardial infarction (84.4%) and n
143 ning the infarct-related artery (IRA) in non-ST-segment-elevation myocardial infarction (MI) can be c
145 1.03); P=0.07; multivessel disease following ST-segment-elevation myocardial infarction (RR, 0.84 [95
148 nary intervention (PCI) for the treatment of ST-segment-elevation myocardial infarction (STEMI) has b
149 ival for overweight and obese patients after ST-segment-elevation myocardial infarction (STEMI) has b
150 imately half of the patients presenting with ST-segment-elevation myocardial infarction (STEMI) have
151 The optimal treatment strategy for treating ST-segment-elevation myocardial infarction (STEMI) in co
152 cardiovascular disease in general and acute ST-segment-elevation myocardial infarction (STEMI) in pa
153 of persistent T2 hyperintensity after acute ST-segment-elevation myocardial infarction (STEMI) is un
154 e ACS clinical presentation consisted of non-ST-segment-elevation myocardial infarction (STEMI) type
155 l patients and for patients with and without ST-segment-elevation myocardial infarction (STEMI) under
156 e direct immediate intervention and therapy, ST-segment-elevation myocardial infarction (STEMI) victi
158 ompared with clopidogrel among patients with ST-segment-elevation myocardial infarction (STEMI), thou
159 presentation and management of patients with ST-segment-elevation myocardial infarction (STEMI).
160 vately insured individuals hospitalized with ST-segment-elevation myocardial infarction (STEMI).
161 rse cardiac events (MACE) following an acute ST-segment-elevation myocardial infarction (STEMI).
162 rognostic utility in patients after an acute ST-segment-elevation myocardial infarction (STEMI).
163 Participants were stratified by AMI subtype (ST-segment-elevation myocardial infarction [STEMI] and n
164 o determine if timing of cell delivery after ST-segment-elevation myocardial infarction affects recov
165 mproves myocardial dynamics in patients with ST-segment-elevation myocardial infarction and is an ind
167 ete revascularization in patients with acute ST-segment-elevation myocardial infarction and multivess
168 complete revascularization in patients with ST-segment-elevation myocardial infarction and multivess
169 tructive nonculprit lesions in patients with ST-segment-elevation myocardial infarction and multivess
170 us coronary intervention in 93 patients with ST-segment-elevation myocardial infarction and multivess
171 nger age categories and in patients with non-ST-segment-elevation myocardial infarction and stable an
172 rfusion times and mortality in patients with ST-segment-elevation myocardial infarction are influence
173 ions in time to reperfusion in patients with ST-segment-elevation myocardial infarction as well as in
174 riage of survivors of cardiac arrest without ST-segment-elevation myocardial infarction at the point
175 vely investigated 215 patients admitted with ST-segment-elevation myocardial infarction between April
176 ention among 95 925 patients presenting with ST-segment-elevation myocardial infarction between Janua
177 patients who have undergone primary PCI for ST-segment-elevation myocardial infarction but have resi
178 scoring model was developed and validated on ST-segment-elevation myocardial infarction cohorts from
179 infarction and multivessel disease; and the ST-segment-elevation myocardial infarction culprit vesse
181 Routine thrombus aspiration during PCI for ST-segment-elevation myocardial infarction did not impro
182 During Primary PCI), 440 patients with acute ST-segment-elevation myocardial infarction from 11 UK ho
183 by 9254 operators at 1538 hospitals for non-ST-segment-elevation myocardial infarction from 2009 to
184 cardiovascular magnetic resonance following ST-segment-elevation myocardial infarction have recently
185 ive sample of patients in China admitted for ST-segment-elevation myocardial infarction in 2001, 2006
186 patients with LV dysfunction after extensive ST-segment-elevation myocardial infarction in terms of g
187 ely 4% to 5%, a figure comparable to that of ST-segment-elevation myocardial infarction in the era of
188 igher rates of reperfusion for patients with ST-segment-elevation myocardial infarction in the interv
189 re performed in 1119 patients discharged for ST-segment-elevation myocardial infarction included in a
190 lor maintenance therapy after revascularized ST-segment-elevation myocardial infarction is associated
191 ndings support efforts to implement regional ST-segment-elevation myocardial infarction networks focu
192 , admitted with acute myocardial infarction (ST-segment-elevation myocardial infarction or type I non
193 milar number had acute presentation (49% non-ST-segment-elevation myocardial infarction or unstable a
194 d, single-blind, controlled trial randomized ST-segment-elevation myocardial infarction patients 1:1
196 r obstruction, which occurs in around 50% of ST-segment-elevation myocardial infarction patients post
198 provides better prognostic stratification of ST-segment-elevation myocardial infarction patients trea
199 and led to a relevant decrease in TA use in ST-segment-elevation myocardial infarction patients unde
202 mized, Phase III STEM-AMI OUTCOME trial, 161 ST-segment-elevation myocardial infarction patients were
203 ND In this prospective study, 88 consecutive ST-segment-elevation myocardial infarction patients were
204 tions and the documented survival benefit in ST-segment-elevation myocardial infarction patients who
205 of a prospective trial which randomized 696 ST-segment-elevation myocardial infarction patients with
207 reserve-guided complete revascularization in ST-segment-elevation myocardial infarction patients with
208 selective use of CMR for risk prediction in ST-segment-elevation myocardial infarction patients with
209 METHODS AND Hospitals (n=167 with 23 498 ST-segment-elevation myocardial infarction patients) wer
210 its robust risk stratification of discharged ST-segment-elevation myocardial infarction patients, but
211 eluting stent (SES) at 12-month follow-up in ST-segment-elevation myocardial infarction patients.
212 ognostic value over clinical risk factors in ST-segment-elevation myocardial infarction patients.
213 elop and validate a CMR-based risk score for ST-segment-elevation myocardial infarction patients.
214 pectively collected data on 5665 consecutive ST-segment-elevation myocardial infarction PCI patients
215 aseline differences, clinical outcomes after ST-segment-elevation myocardial infarction PCI were simi
216 oup analysis, we included 1653 patients with ST-segment-elevation myocardial infarction randomized to
218 available process measure for patients with ST-segment-elevation myocardial infarction requiring int
219 2017, treatment times of 2063 patients with ST-segment-elevation myocardial infarction requiring int
220 n 1 h after pPCI in patients presenting with ST-segment-elevation myocardial infarction scheduled for
221 in the Netherlands, enrolling patients with ST-segment-elevation myocardial infarction scheduled to
222 r is recommended in patients presenting with ST-segment-elevation myocardial infarction scheduled to
223 e analysis of bivalirudin versus UFH for non-ST-segment-elevation myocardial infarction to date, biva
224 MVO in a cohort of consecutive patients with ST-segment-elevation myocardial infarction treated with
225 cardiac mortality in patients with high-risk ST-segment-elevation myocardial infarction treated with
226 econdary prevention therapy in patients with ST-segment-elevation myocardial infarction undergoing pe
227 7, we included all consecutive patients with ST-segment-elevation myocardial infarction undergoing pe
228 d with reduced infarct size in patients with ST-segment-elevation myocardial infarction undergoing pe
229 ects of NAC on infarct size in patients with ST-segment-elevation myocardial infarction undergoing pe
230 tor antagonists are delayed in patients with ST-segment-elevation myocardial infarction undergoing pr
233 platelet aggregation (IPA) in patients with ST-segment-elevation myocardial infarction undergoing pr
234 n a head-to-head comparison in patients with ST-segment-elevation myocardial infarction undergoing pr
235 ticagrelor versus prasugrel in patients with ST-segment-elevation myocardial infarction undergoing pr
237 g with an acute coronary syndrome, including ST-segment-elevation myocardial infarction were enrolled
240 A total of 122 P2Y(12)-naive patients with ST-segment-elevation myocardial infarction were randomly
241 gh-risk patients with unstable angina or non-ST-segment-elevation myocardial infarction who did not u
242 ospective cohort of unselected patients with ST-segment-elevation myocardial infarction with paired a
243 levation myocardial infarction or type I non-ST-segment-elevation myocardial infarction), and own a s
246 ccurs in a large proportion of patients with ST-segment-elevation myocardial infarction, adversely af
247 reperfusion strategy for patients with acute ST-segment-elevation myocardial infarction, aiming at re
248 2015 included 120 cases; 75% presented with ST-segment-elevation myocardial infarction, and 80% had
249 O-PCI) in patients with multivessel disease, ST-segment-elevation myocardial infarction, and cardioge
250 d with acute congestive heart failure or non-ST-segment-elevation myocardial infarction, and had mult
251 ikely to include high-risk features, such as ST-segment-elevation myocardial infarction, cardiogenic
254 r ejection fraction <30% within 4 days after ST-segment-elevation myocardial infarction, primary vent
255 henotype were observed, particularly for non-ST-segment-elevation myocardial infarction, reflecting a
256 utaneous coronary intervention for extensive ST-segment-elevation myocardial infarction, the effects
258 patients with cardiogenic shock complicating ST-segment-elevation myocardial infarction, there may be
260 going percutaneous coronary intervention for ST-segment-elevation myocardial infarction, we did not f
281 versus placebo in 120 patients with anterior ST-segment-elevation myocardial infarctions resulting in
282 ing analyses of patients with large anterior ST-segment-elevation myocardial infarctions, bone marrow
285 rgency coronary angiography in patients with ST-segment elevations on ECG after OHCA, while the role
286 ach is that it captures small changes in the ST segment over time that cannot be detected by visual i
287 rticularly without a persistent elevation of ST-segment reflected in an electrocardiogram or in blood
288 in the culprit artery (P=0.020), incomplete ST-segment resolution (P=0.037), and higher troponin (P=
289 farct-related artery before pPCI or complete ST-segment resolution 1 h after pPCI in patients present
292 vasive strategy was associated with improved ST-segment resolution and enhanced outcomes within 1 yea
293 ehospital pharmacoinvasive strategy, similar ST-segment resolution and rescue rates were observed wit
296 Angiographic recanalization before PCI, ST-segment resolution, infarct size by magnetic resonanc
297 cardiac monitoring with real-time alarms for ST-segment shift that exceeds a subject's self-normative
298 c monitor with real-time alarms for abnormal ST-segment shifts to reduce pre-hospital delay during AC
299 distinct (P wave, PR segment, QRS interval, ST segment, T wave, and TP segment) and 2 composite, con
300 -wave onset to R-peak, R-peak to R-wave end, ST-segment, T-wave onset to T-peak, and T-peak to T-wave