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1 ssel myocardial infarction, or target vessel revascularization).
2 e stent thrombosis, stroke, or urgent vessel revascularization.
3 tal clinical outcomes compared with surgical revascularization.
4 omote macrophage recruitment and accelerated revascularization.
5 uided PCI, driven by a higher rate of repeat revascularization.
6 d ischemic limb events after lower extremity revascularization.
7 mortality, any myocardial infarction, or any revascularization.
8 arction, unstable angina, or urgent coronary revascularization.
9 [95% CI, 1.05-1.15]) was also observed with revascularization.
10 t-term adjunct to aspirin after endovascular revascularization.
11 ischemic stroke, or ischemia-driven coronary revascularization.
12 ntify an individual patient's risk of failed revascularization.
13 ndidates for optimal CAD medical therapy and revascularization.
14 02), compared with those undergoing surgical revascularization.
15 and composite major amputation or peripheral revascularization.
16 he importance of early recognition and early revascularization.
17 rade coronary artery disease (CAD) requiring revascularization.
18 acrophages but produced no defects in muscle revascularization.
19 suscitated cardiac arrest, heart failure, or revascularization.
20 ed prior to the widespread adoption of early revascularization.
21 ction, or clinically indicated target lesion revascularization.
22 utcomes of patients following carotid artery revascularization.
23 ator for up to 6 months after the qualifying revascularization.
24 ohort of patients with symptomatic PAD after revascularization.
25 , nonfatal myocardial infarction, and repeat revascularization.
26 g data on the performance versus deferral of revascularization.
27 c valve implants, 332 (20%) were assigned to revascularization.
28 nonfatal myocardial infarction, or coronary revascularization.
29 increase, potentially altering the need for revascularization.
30 h, myocardial infarction, or ischemia-driven revascularization.
31 varoxaban in peripheral artery disease after revascularization.
32 CAD in identifying patients unlikely to need revascularization.
33 ral myocardial infarction, and target lesion revascularization.
34 sts higher with endovascular versus surgical revascularization.
35 angiography (QCA) on the benefit of complete revascularization.
36 CE, MALE, and MALE including lower extremity revascularization.
37 s to identify those who do not need coronary revascularization.
38 nly 8% of site-level variation in receipt of revascularization.
39 of stroke, myocardial infarction, and repeat revascularization.
40 ), and across elective, urgent, and emergent revascularizations.
41 risk for ischemic events, including coronary revascularizations.
42 AD (0.5% versus 6.5%, P<0.0001), and receive revascularization (0.4% versus 5.8%, [adjusted odds rati
43 sociated with a higher risk of target vessel revascularization (18% versus 7.3%; OR, 3.04 [95% CI, 1.
44 ectomy (8%-IVSR vs. 7%-VSF), lower extremity revascularization (19%-IVSR vs. 16%-VSF), and aortic ane
45 re categorized as: 1) procedural (related to revascularization); 2) definite or probable stent thromb
46 nfarction (MI) who did not receive immediate revascularization; (2) patients who have undergone prima
47 ng ALI hospitalization included endovascular revascularization (39.2%, n=115), surgical bypass (24.6%
48 .43), and clinically indicated target lesion revascularization (5.2% versus 6.5%; P=0.30) did not dif
49 s 52%, and women were less likely to undergo revascularization (50.1% versus 53.6%, P<0.01) compared
50 ated myocardial infarction, or target lesion revascularization (a device-oriented composite endpoint
51 creases in antiplatelet therapy and coronary revascularization after implementation in patients with
56 sought to describe outcomes after peripheral revascularization and assess relationships between post-
58 patients with ACS treated with DAPT without revascularization and help support shared decision makin
61 iography was a better predictor for coronary revascularization and MACE and showed better agreement w
62 ss served as a better predictor for coronary revascularization and MACE than stenosis of 50% and grea
63 the predictive value of CT FFR for coronary revascularization and major adverse cardiac events (MACE
66 MI, nonfatal stroke, or urgent target vessel revascularization and superior in preventing BARC 3 (Ble
67 changes, optimal medical therapy, myocardial revascularization and the use of antiplatelet agents to
68 rt death, myocardial infarction, or coronary revascularization) and major vascular events (major coro
69 tiveness (clinically indicated target lesion revascularization) and safety (composite cardiac death a
70 angiographic findings, treatment (including revascularization), and clinical outcomes of patients wi
71 ember 2017 for MI, CHD (i.e., MI or coronary revascularization), and in Medicare for all-cause mortal
72 ent, 454 patients with at least 1 peripheral revascularization, and 236 patients with at least 1 ampu
75 cardiovascular events (MI, stroke, coronary revascularization, and cardiovascular death) in active v
77 myocardial infarction, unstable angina with revascularization, and heart failure hospitalization.
80 ity, ACS, ischemia-driven (unplanned) urgent revascularization, and noncardioembolic ischemic stroke
82 mposite end point), ischemia-driven coronary revascularization, and spontaneous myocardial infarction
83 cular death, myocardial infarction, coronary revascularization, and stroke through December 31, 2016.
84 l CABG is underused in contemporary surgical revascularization, and targeted referral of younger pati
85 ion, 180 strokes, 65 atrial fibrillation, 29 revascularizations, and 246 CVD deaths; 792 in the inter
87 y disease who have undergone lower-extremity revascularization are at high risk for major adverse lim
89 o determine whether the benefits of complete revascularization are sustained long-term and their impa
90 10-predictor BN accurately predicted failed revascularization: area under the receiver operating cha
91 tal myocardial infarction, and target vessel revascularization at 30 days (11.7% versus 12.9%, P=0.82
92 ents were more likely to be free from repeat revascularization at 6 years than HCR patients (88.2% ve
97 infarction, stroke, heart failure, coronary revascularization, atrial fibrillation, or CVD death, ir
99 o-severe intermittent claudication to either revascularization + best medical therapy + structured ex
101 ween females and males; however, the optimal revascularization beyond 5 years according to sex has no
103 ease death, myocardial infarction, or urgent revascularization by 23% (hazard ratio, 0.77; 95% CI, 0.
104 of EC apoptosis may promote ischemic tissue revascularization by preserving ECs within ischemic tiss
105 econdary outcomes including stroke, coronary revascularization, cardiovascular mortality, and all-cau
106 cluded any stroke, ischemic stroke, coronary revascularization, cardiovascular mortality, and all-cau
109 rdial infarction or ischemia-driven coronary revascularization (composite end point), cardiovascular
110 gher neutrophil count on admission and after revascularization correlates positively with major adver
111 adverse cardiovascular events after complete revascularization (CR) than after incomplete revasculari
112 used percutaneous coronary intervention for revascularization, deferred revascularization remained a
114 ve strategy with angiographic assessment and revascularization did not reduce clinical events among p
117 ability to manage their disease and hospital revascularization experience, open surgery first was ass
120 egies for atherosclerosis following coronary revascularization for patients with and without a tradit
121 -term cardiovascular and limb outcomes after revascularization for peripheral artery disease and, in
122 Rivaroxaban in Endovascular or Surgical Limb Revascularization for Peripheral Artery Disease) demonst
125 c evidence in support of medical therapy and revascularization for the management of patients with st
126 rgical technique, including bronchial artery revascularization, for incorporation into the overarchin
127 s with AMI who underwent inhospital coronary revascularization from January 2007 to December 2013 wer
128 is associated with altered expression of pro-revascularization genes in skeletal muscle and macrophag
129 of the 2016 patients (7.8%) in the complete-revascularization group as compared with 213 of the 2025
130 has previously been reported superior in the revascularization group at 1- and 2-year follow-up.
131 l therapy + structured exercise therapy (the revascularization group) or best medical therapy + struc
133 group), patients who underwent endovascular revascularization had significantly lower in-hospital mo
134 medical therapy, the role of coronary artery revascularization has decreased and is largely confined
135 P=0.01) and increased risk of target vessel revascularization (hazard ratio, 1.82; 95% CI, 1.10-2.94
136 ity at 1 year compared with angiography-only revascularization (hazard ratio: 0.57; 95% confidence in
137 to 1.40) and major amputation or peripheral revascularization (hazard ratio: 8.13; 95% confidence in
138 e-varying myocardial infarction and coronary revascularization (hazard ratios: SB, 1.00, 1.11, 1.27;
141 ent CHD events (ie, recurrent MI or coronary revascularization), heart failure hospitalization, and a
142 <0.001) but not MALE or MALE/lower extremity revascularization (HR, 1.02 [95% CI, 0.84-1.23], P=0.824
143 nd an increased risk of MALE/lower extremity revascularization (HR, 1.08 [95% CI, 1.04-1.11]; P<0.001
144 In multivariable modeling, smoking, prior revascularization, hypertension, unstable angina, female
145 revascularization (CR) than after incomplete revascularization (ICR) in patients with multivessel dis
146 ction [MI], or ischemia-driven target lesion revascularization [ID-TLR]) as well as its individual co
147 ction [MI], or ischemia-driven target lesion revascularization [ID-TLR]), and target lesion failure (
148 ategy consisting of coronary angiography and revascularization (if appropriate) added to medical ther
152 vel minimally invasive procedure for carotid revascularization in high-risk patients that is associat
153 on, we provide practical recommendations for revascularization in patients with high-risk multivessel
155 ical trials that have assessed the effect of revascularization in patients with stable coronary disea
156 coprimary outcome was reduced with complete revascularization in the 2,479 patients with QCA stenosi
157 that were caused by both the need for repeat revascularization in the left anterior descending artery
158 n without a diagnostic angiogram or trial of revascularization in the preceding 90 days regardless of
159 d the need for first and subsequent coronary revascularizations in statin-treated patients with eleva
160 uring follow-up but a higher total number of revascularizations including the randomized treatment.
162 use death, any myocardial infarction, or any revascularization; individual components of the composit
166 migrate to the areas of damage and stimulate revascularization largely by paracrine activation of ang
167 ete versus 76% (95% CI, 74-80) with complete revascularization (log-rank test: P=0.02) after off-pump
169 ssel disease, stress echocardiography-guided revascularization may not be significantly different to
170 was large site-level variation in the use of revascularization (median rate, 41.7% [interquartile ran
171 irectly associated with timely initiation of revascularization, missed, misdiagnosis or late diagnosi
174 which was a composite of SVG occlusion, SVG revascularization, myocardial infarction in myocardial t
175 ere observed in total (first and subsequent) revascularizations (negative binomial rate ratio, 0.64 [
176 revealed a hazard ratio incomplete/complete revascularization of 1.19 (95% CI, 1.01-1.39; P=0.04).
177 ate the severity of stenosis, and that after revascularization of a CTO, the index of ischemia may in
178 Eluting Absorbable Polymer Stent System for Revascularization of Coronary Arteries; n=1398) is a pro
179 r angioplasty is the preferred treatment for revascularization of femoropopliteal lesions in peripher
181 , migration to areas of vascular damage, and revascularization of ischemic areas in pathologic condit
184 Although clinical evidence indicates that revascularization of the ischemic brain regions is cruci
185 howed complete local tumor control, 1 showed revascularization of the scleral melt, and 1 required or
187 nfarct expansion after stroke, the effect of revascularization on poststroke neuroinflammation and th
188 freedom from clinically driven target-lesion revascularization or access-circuit thrombosis during th
189 ardiovascular events, while prior peripheral revascularization or amputation is associated with great
190 icantly associated with a lower incidence of revascularization or endovascular surgery and lower extr
192 e or probable stent thrombosis, or unplanned revascularization or rehospitalization for progressive a
193 is, PAD events (critical limb ischemia, limb revascularization, or amputation for ischemia) and VTE (
194 , any stroke, any myocardial infarction, any revascularization, or Bleeding Academic Research Consort
195 ardial infarction, nonfatal stroke, coronary revascularization, or hospitalization for unstable angin
197 ardial infarction, nonfatal stroke, coronary revascularization, or unstable angina requiring hospital
201 tack, heart failure hospitalization, cardiac revascularization, peripheral arterial disease intervent
204 dial infarction with initial angiography and revascularization plus guideline-based medical therapy (
205 terventions were combination of endovascular revascularization plus supervised exercise (n = 106) or
207 ovascular events either following a coronary revascularization procedure (percutaneous coronary inter
208 was associated with an increased hazard of a revascularization procedure during follow-up (HR 2.50; 9
209 s with a first open surgical or endovascular revascularization procedure in the lower extremities or
212 nation therapy resulted in a lower number of revascularization procedures during follow-up but a high
215 , fatal coronary events, silent infarctions, revascularization procedures, or resuscitated cardiac ar
216 h symptomatic PAD undergoing lower extremity revascularization randomized to rivaroxaban 2.5 mg twice
218 16 were used to compare mortality and repeat revascularization rates for HCR and conventional CABG af
219 Prespecified analyses examined all coronary revascularizations, recurrent revascularizations, and re
220 nonculprit lesions with the aim of complete revascularization reduced major cardiovascular (CV) even
221 ultivessel coronary artery disease, complete revascularization reduced major CV outcomes to a greater
223 rivaroxaban to aspirin after lower extremity revascularization regardless of concomitant clopidogrel,
224 intervention for revascularization, deferred revascularization remained associated with a higher risk
225 imary patency and freedom from target lesion revascularization remained superior compared with conven
227 before invasive treatment for IC, but early revascularization remains widespread, especially in pati
230 ry disease who had undergone lower-extremity revascularization, rivaroxaban at a dose of 2.5 mg twice
231 he brain even following early and successful revascularization.SIGNIFICANCE STATEMENT This study addr
232 stolic blood pressure (SBP) after successful revascularization (SR) via endovascular therapy (EVT) is
234 (ISCHEMIA) and Complete versus Culprit-Only Revascularization Strategies to Treat Multivessel Diseas
237 re randomly assigned to one of the following revascularization strategies: either percutaneous corona
238 ermine the association between an FFR-guided revascularization strategy and all-cause mortality at 1
242 was no interaction between sex and coronary revascularization strategy regarding mortality and renal
246 was a composite of nonfatal AMI, unscheduled revascularization, stroke, all-cause death, heart failur
247 e composite of myocardial infarction, repeat revascularization, stroke, or death (termed major cardio
248 CVD events (myocardial infarction, coronary revascularization, stroke, or death), and whether it was
250 the BioFreedom stent group had target lesion revascularization than those in the Orsiro stent group (
251 these results uncover a role of ALX/FPR2 in revascularization that may be amenable to therapeutic ta
252 after 1 year and higher rates of subsequent revascularization that were caused by both the need for
254 ifferent to complete angiographically guided revascularization, thereby reducing the need for electiv
255 utcomes of primary patency and target lesion revascularization (TLR) estimated with Kaplan-Meier anal
256 he COMPLETEs trial (Complete vs Culprit-Only Revascularization to Treat Multi-Vessel Disease After Ea
257 In the COMPLETE (Complete vs Culprit-only Revascularization to Treat Multi-vessel Disease After Ea
258 s myocardial infarction, coronary or carotid revascularization, transient ischemic attack, or stroke.
259 ed, randomized Hybrid Trial (Hybrid Coronary Revascularization Trial) was initiated to examine whethe
263 ypass Surgery for Effectiveness of Left Main Revascularization) trials; the Fourth Universal Definiti
264 d of undergoing endovascular versus surgical revascularization using a logistic regression model.
265 ches for randomized trials comparing routine revascularization versus an initial conservative strateg
267 te-level, and procedural factors, FFR-guided revascularization was associated with a 43% lower risk o
278 with stable ischemic heart disease, routine revascularization was not associated with improved survi
279 ographic findings were all well-balanced and revascularization was performed equally effective, the a
280 914) hospitalizations for ALI, endovascular revascularization was performed in 5008 (47.8%) and surg
281 between sexes, whereas prior lower extremity revascularization was reported less frequently in women
282 d 365-day clinically indicated target lesion revascularization was significantly lower with DCS (7.2%
284 Four-year MI rates in patients undergoing revascularization were more frequent with the invasive v
285 on myocardial infarction who did not undergo revascularization were randomized to prasugrel or clopid
286 peripheral artery disease who had undergone revascularization were randomly assigned to receive riva
288 infarction, or ischemia-driven target lesion revascularization) were assessed and compared after perc
289 freedom from clinically driven target lesion revascularization when compared with PTA (Kaplan-Meier e
290 n initial invasive strategy (angiography and revascularization when feasible) and medical therapy or
292 (myocardial infarction, ischemic stroke, and revascularization with coronary artery bypass graft surg
294 ructive coronary artery disease benefit from revascularization with percutaneous coronary interventio
295 at substantial risk for long-term MACE after revascularization with percutaneous coronary interventio
297 her than the target lesion, or target lesion revascularization within 1 year, analyzed by intention-t
298 s unlikely to have high-grade CAD or require revascularization within 90 days and unlikely to experie
300 iod, there was a temporal increase in use of revascularization within 90 days of hospitalization-endo