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1 rogressive muscle weakness was admitted with cardiogenic shock.
2 rcutaneous mechanical circulatory support in cardiogenic shock.
3 responsive and was found to be in a state of cardiogenic shock.
4 1 patients, 49 with septic shock and 22 with cardiogenic shock.
5 oronary intervention (PCI) in the setting of cardiogenic shock.
6 ematoma or hemorrhage, blood transfusion, or cardiogenic shock.
7 rrent pharmacological agents utilized during cardiogenic shock.
8 ical efficacy of these devices in refractory cardiogenic shock.
9 n patients with various causes of refractory cardiogenic shock.
10 be preferred over dopamine in patients with cardiogenic shock.
11 trength of association with and relevance to cardiogenic shock.
12 in the first 24 hours after the diagnosis of cardiogenic shock.
13 ous coronary intervention cardiac arrest and cardiogenic shock.
14 of pulmonary edema, myocardial ischemia, or cardiogenic shock.
15 owing admission to the ICU) of patients with cardiogenic shock.
16 lycation end products might be beneficial in cardiogenic shock.
17 gment elevation myocardial infarction and no cardiogenic shock.
18 ight represent a novel therapeutic target in cardiogenic shock.
19 old (p=.019) increase in 28-day mortality in cardiogenic shock.
20 advances in treatment and outcome in post-MI cardiogenic shock.
21 are being increasingly used in patients with cardiogenic shock.
22 he appropriate use of pVADs in patients with cardiogenic shock.
23 hypoxia, such as in hypovolemic, septic, or cardiogenic shock.
24 aorta producing left ventricular failure and cardiogenic shock.
25 ciated with an increased risk for developing cardiogenic shock.
26 ocirculatory flow was fully preserved during cardiogenic shock.
27 ds in the hospital prognosis associated with cardiogenic shock.
28 dered last resort to prevent or to reverse a cardiogenic shock.
29 ine its predictors among 30-day survivors of cardiogenic shock.
30 d inappropriate vasodilatation of persistent cardiogenic shock.
31 ied each year regardless of whether they had cardiogenic shock.
32 enal function, and survival in patients with cardiogenic shock.
33 sease and congestive HF, pulmonary edema, or cardiogenic shock.
34 ns included chest pain, pulmonary edema, and cardiogenic shock.
35 prospective European multinational study of cardiogenic shock.
36 al variables have been used to judge risk in cardiogenic shock.
37 inical parameters for risk stratification in cardiogenic shock.
38 osis is similar in patients with and without cardiogenic shock.
39 ggressive management of patients who develop cardiogenic shock.
40 ic bradycardia, symptomatic hypotension, and cardiogenic shock.
41 alance (18.9%-35.3%), pneumonia (4.4%-6.3%), cardiogenic shock (0.5%-1.5%), and acute respiratory fai
44 unterbalanced by 11 more per 1000 developing cardiogenic shock (1141 [5.0%] vs 885 [3.9%]; OR 1.30, 1
45 the high-risk unselected patient population (cardiogenic shock, 12.3%; cardiac arrest, 10.8%; and eld
46 , death presented with a higher incidence of cardiogenic shock (15 of 47 [32%] vs. 2 of 34 [6%]; p <
47 ty (5.7% CsA vs. 3.2% controls, p = 0.17) or cardiogenic shock (2.4% CsA vs. 1.5% controls, p = 0.33)
48 infarction (14.4% vs. 8.7%, p < 0.0001) and cardiogenic shock (2.56% vs. 0.38%, p < 0.0001) than tho
50 myocardial infarction (63.2% vs. 29.6%) and cardiogenic shock (29.0% vs. 2.2%); however, among in-ho
51 dobutamine or epinephrine in the presence of cardiogenic shock (2D) and atropine in the presence of s
53 more frequently presented with heart failure/cardiogenic shock (50% versus 7%; P<0.01), requiring int
55 had more major or life-threatening bleeding, cardiogenic shock, acute kidney injury (stage II or III)
56 t myocarditis with biventricular failure and cardiogenic shock, acutely manifested with hypotension a
58 t-ventricular assist device in patients with cardiogenic shock after acute myocardial infarction.
61 ermia in 20 consecutive patients admitted in cardiogenic shock after successful resuscitation from ou
63 pressure and cardiac output in patients with cardiogenic shock although potentially at the expense of
64 to each patient's needs based on severity of cardiogenic shock, amount of support needed, and the ove
65 a significant increase in the use of PCI for cardiogenic shock and a concomitant decrease in in-hospi
66 auses of death within the first 30 days were cardiogenic shock and anoxic brain injury after cardiac
68 y clinical factors that favored primary PCI, cardiogenic shock and delayed presentation were associat
69 The first two treated patients developed cardiogenic shock and died within a few days of T-cell i
70 Available data in animal models of post-MI cardiogenic shock and ischemia/reperfusion injury and sm
71 membrane oxygenation in patients with severe cardiogenic shock and little/no residual left ventricula
72 atients with acute coronary syndrome-related cardiogenic shock and may help therapeutic decision maki
73 may be prognostic biomarkers for survival in cardiogenic shock and might represent a novel therapeuti
75 zards models to test the association between cardiogenic shock and outcomes, adjusting for patient an
76 sought to evaluate the associations between cardiogenic shock and post-discharge mortality and all-c
77 djunct to revascularization in patients with cardiogenic shock and reduces infarct size when placed p
78 porary stabilization of otherwise refractory cardiogenic shock and serve as a bridge-to-decision ther
79 idity and mortality in post-MI patients with cardiogenic shock and warrants study a new treatment tha
80 rial extracorporeal membrane oxygenation for cardiogenic shock, and 3) extracorporeal cardiopulmonary
82 coronary intervention, those presenting with cardiogenic shock, and acute decompensated heart failure
83 es, higher peak troponin levels, in-hospital cardiogenic shock, and cardiology follow-up within 2 wee
84 shock survivors, identify the correlates of cardiogenic shock, and compare global quality of life an
85 ring more than 48 hours after randomization, cardiogenic shock, and congestive heart failure during t
86 with cardiogenic shock, the hemodynamics of cardiogenic shock, and hemodynamic effects of percutaneo
88 ST-segment-elevation myocardial infarction, cardiogenic shock, and multivessel disease, and were ass
89 nd point of death, congestive heart failure, cardiogenic shock, and reinfarction (adjusted odds ratio
90 mellitus, renal dysfunction, cardiac arrest, cardiogenic shock, and ST-segment elevation myocardial i
91 T-segment elevation myocardial infarction or cardiogenic shock, and those with no ST-segment elevatio
94 levels play a central role in patients with cardiogenic shock associated with proinflammatory and de
95 tients with acute anterior STEMI but without cardiogenic shock at 30 sites in 9 countries from June 2
96 was significantly higher among patients with cardiogenic shock at 60 days (9.6% vs. 5.5%) and 1 year
97 point of death, congestive heart failure, or cardiogenic shock at 90 days (adjusted HR, 2.4; 95% CI,
98 patients who underwent PCI in the setting of cardiogenic shock at one of 1429 National Cardiovascular
99 iods between 2001 and 2011, who did not have cardiogenic shock at the time of hospital presentation.
100 of death, malignant ventricular arrhythmia, cardiogenic shock, atrioventricular block, and reinfarct
102 vice effectiveness in 10 pigs that developed cardiogenic shock but survived massive PE after injectio
103 percentage points (95% CI, -5.3 to -1.9) and cardiogenic shock by -24 percentage points (95% CI, -4.3
104 atient features, treatments, and outcomes of cardiogenic shock by MI classification: ST-segment-eleva
107 In addition to known predictors of delay (cardiogenic shock, cardiac arrest, and prolonged door-in
108 e previously shown that neonates in profound cardiogenic shock caused by a severe Ebstein anomaly can
112 is considered to be a class I treatment for cardiogenic shock complicating acute myocardial infarcti
113 rial, we randomly assigned 600 patients with cardiogenic shock complicating acute myocardial infarcti
114 tly reduce 30-day mortality in patients with cardiogenic shock complicating acute myocardial infarcti
115 nds (1975 to 2005) in the incidence rates of cardiogenic shock complicating acute myocardial infarcti
116 in the incidence and hospital death rates of cardiogenic shock complicating acute myocardial infarcti
118 the hospital survival rate of patients with cardiogenic shock complicating acute myocardial infarcti
120 nderwent coronary artery bypass grafting for cardiogenic shock complicating acute myocardial infarcti
121 for acute decompensated heart failure (i.e., cardiogenic shock complicating chronic cardiomyopathy) h
122 mortality rates in patients with refractory cardiogenic shock complicating MI despite an open infarc
123 vanced glycation end products in humans with cardiogenic shock complicating myocardial infarction.
124 mized studies suggests that in patients with cardiogenic shock complicating ST-segment-elevation myoc
125 nts with multivessel disease presenting with cardiogenic shock complicating ST-segment-elevation myoc
126 dependent predictors for 28-day mortality in cardiogenic shock confirmed by receiver-operator charact
127 c dysfunction and mortality in patients with cardiogenic shock (CS) after acute myocardial infarction
128 s or risk factors for operative mortality in cardiogenic shock (CS) patients undergoing coronary arte
131 d multivariable adjusted odds of dying after cardiogenic shock declined during the most recent study
132 y, the use of IABP in the setting of PCI for cardiogenic shock decreased over time without a concurre
133 was observed for the subset of patients with cardiogenic shock, decreasing from 51.6% to 43.1% (p for
134 inhibitor in patients with MI and refractory cardiogenic shock despite establishment of an open infar
135 intractable refractory arrhythmic storm and cardiogenic shock despite optimal medical therapy were i
137 utcomes including death, cardiac arrest, and cardiogenic shock did not significantly change following
139 se-fatality rates for patients who developed cardiogenic shock during hospitalization for an acute my
141 On average, 3.7% of these patients developed cardiogenic shock during their acute hospitalization wit
144 ts who have acute myocardial infarction with cardiogenic shock, early revascularization of the culpri
145 elevation myocardial infarction (STEMI) and cardiogenic shock enrolled in the GUSTO (Global Utilizat
146 ular fibrillation, but increases the risk of cardiogenic shock, especially during the first day or so
147 licly reported outcomes), 2006-2007 (time 2: cardiogenic shock excluded on a trial basis), and 2008 a
148 ial basis), and 2008 and thereafter (time 3: cardiogenic shock excluded permanently) in New York and
152 atients (63.6+/-12.2 years; 81.7% male) with cardiogenic shock from acute myocardial infarction recei
155 ents with anoxic brain injury and refractory cardiogenic shock from public reporting has made them mo
156 creased substantially after the exclusion of cardiogenic shock from public reporting in New York, the
157 001 for time 3 vs 1]) after the exclusion of cardiogenic shock from public reporting in New York.
158 2006, New York began excluding patients with cardiogenic shock from the publicly reported percutaneou
167 (AMI) complicated by acute heart failure or cardiogenic shock have high mortality with conventional
171 reases in hospital survival in patients with cardiogenic shock, however, were observed from the mid-1
172 art Association class IV (HR=4.42; P=0.002), cardiogenic shock (HR=3.75; P=0.003), creatinine (HR=1.0
173 strongest predictors were diabetes mellitus, cardiogenic shock, hypertension, previous myocardial inf
174 ft ventricular ejection fraction in 27+/-9%; cardiogenic shock in 23%, and electrical storm in 62% of
175 eported data on the use of these devices for cardiogenic shock in a variety of different settings, in
176 ces (CF-VADs) in the treatment of refractory cardiogenic shock in Interagency Registry for Mechanical
177 ts with myocardial infarction complicated by cardiogenic shock in New York and Michigan, 905 (42.6%)
178 ncidence and hospital case-fatality rates of cardiogenic shock in patients hospitalized with acute my
179 refractory arrhythmic storm responsible for cardiogenic shock in patients resistant to antiarrhythmi
181 electively protected during severe states of cardiogenic shock in the absence of cardiac arrest.
185 3 calendar year periods: 2002-2005 (time 1: cardiogenic shock included in publicly reported outcomes
186 The current pharmacological treatment for cardiogenic shock includes inotropes, vasopressors and d
187 ulatory support devices for the treatment of cardiogenic shock, including current evidence, contraind
189 bypass graft surgery, myocardial infarction/cardiogenic shock, injury, and infection/septic shock.
193 h acute myocardial infarction complicated by cardiogenic shock is associated with a high in-hospital
197 onducting randomized trials in patients with cardiogenic shock, lack of clear guidelines on indicatio
198 isease, New York Heart Association class IV, cardiogenic shock, left main coronary stenosis, and valv
201 h acute myocardial infarction complicated by cardiogenic shock (mean [SD] age at randomization, 66 [1
202 d at testing the hypothesis that patients in cardiogenic shock might benefit from mild therapeutic hy
204 tion between hemodynamic variables and early cardiogenic shock mortality in critically ill patients.
205 nfection/septic shock, myocardial infarction/cardiogenic shock (n=1705), and coronary artery bypass g
207 low cytometry was significantly increased in cardiogenic shock nonsurvivors (137.02+/-7.48 mean fluor
209 rongest predictors of in-hospital death were cardiogenic shock (odds ratio, 6.01; 95% confidence inte
210 he rivaroxaban group; this patient died from cardiogenic shock on day 50 after a type A aortic dissec
214 -0.89]; P = .002) and the 2194 patients with cardiogenic shock or cardiac arrest (41.5% vs 46.7%; OR,
215 e most pronounced for the 6081 patients with cardiogenic shock or cardiac arrest (prereporting: 44.2%
217 28 non-ST-elevation patients with MI without cardiogenic shock or HF at presentation treated at 609 h
218 into clinical practice for the treatment of cardiogenic shock or refractory nontolerated ventricular
219 ve heart failure (OR, 1.7; 95% CI, 1.3-2.2), cardiogenic shock (OR, 5.4; 95% CI, 2.7-10.9), and fluid
220 56 to 0.71) or concomitant cardiac arrest or cardiogenic shock (OR: 0.58, 95% CI: 0.47 to 0.70).
221 rt failure (OR: 1.33; 95% CI: 1.17 to 1.52), cardiogenic shock (OR: 1.26; 95% CI: 1.08 to 1.48), and
222 ith a preimplantation profile of 1 (critical cardiogenic shock) or 2 (progressive decline) were asses
223 acute outcomes (death, reinfarction, stroke, cardiogenic shock, or congestive heart failure) among pa
224 cardiovascular death, myocardial infarction, cardiogenic shock, or heart failure) and secondary outco
226 onship between hemodynamic variables and the cardiogenic shock outcome in critically ill patients.
231 ew is to discuss four sub-classifications of cardiogenic shock patients (acute myocardial infarction,
232 stics, the risk of death remained higher for cardiogenic shock patients in the first 60 days after di
233 ion (ECMO) has allowed approximately half of cardiogenic shock patients to receive an implantable lef
235 did not affect microcirculation variables in cardiogenic shock patients with little/no residual left
237 EDLINE search was conducted with MeSH terms: cardiogenic shock, percutaneous mechanical circulatory s
238 tation after cardiac arrest, presentation in cardiogenic shock, presentation in heart failure, presen
239 e in patients with myocardial infarction and cardiogenic shock prior to cardiogenic shock resolution.
240 culatory support in patients with refractory cardiogenic shock providing a bridge to long-term mechan
243 of patients undergoing PCI in the setting of cardiogenic shock received an IABP and 6.7% received O-M
244 n to ventricular arrhythmias, heart failure, cardiogenic shock, recurrent myocardial infarction, and
245 an emergency setting in patients with acute cardiogenic shock refractory to conventional therapy irr
246 tments are insufficient for the treatment of cardiogenic shock refractory to inotropic support, there
249 he mortality rate associated with refractory cardiogenic shock remains markedly elevated, with INTERM
254 ort, the independent predictors of MACE were cardiogenic shock, renal disease, history of peripheral
255 refractory arrhythmic storm responsible for cardiogenic shock resistant to antiarrhythmic drugs.
256 otensin-aldosterone system blockers prior to cardiogenic shock resolution (27.3% vs 16.9%; adjusted h
258 gy, pathophysiology, causes, and outcomes of cardiogenic shock; reviews contemporary best medical, su
261 SAVR was associated with higher risk of cardiogenic shock, severe bleeding, and acute kidney inj
262 ected left main artery as the target vessel, cardiogenic shock, severely depressed left ventricular f
263 gently revascularize Occluded Coronaries for cardiogenic shocK (SHOCK) trial registry were included.
264 gently revascularize Occluded Coronaries for cardiogenic shocK (SHOCK) trial showed significantly imp
265 gently Revascularize Occluded Coronaries for Cardiogenic Shock (SHOCK) trial, an international random
266 vice (pVAD) in patients in severe refractory cardiogenic shock (SRCS) despite intra-aortic balloon pu
267 se in acute myocardial infarction (AMI) with cardiogenic shock, ST elevation acute coronary syndromes
269 and small case series of human patients with cardiogenic shock suggest its promise as a potential the
271 s with acute myocardial infarction (AMI) and cardiogenic shock survive hospitalization; little is kno
272 oal was to describe the functional status of cardiogenic shock survivors, identify the correlates of
273 disease and acute myocardial infarction with cardiogenic shock, the 30-day risk of a composite of dea
274 hey group using ECMO for therapy of advanced cardiogenic shock, the application of ECMO is described.
275 e the contemporary outcomes of patients with cardiogenic shock, the hemodynamics of cardiogenic shock
276 el disease, acute myocardial infarction, and cardiogenic shock to one of two initial revascularizatio
278 rnational Study in Unstable MI Patients With Cardiogenic Shock [TRIUMPH]) with planned enrollment of
279 imilar to that of historical controls not in cardiogenic shock undergoing elective revascularization.
280 nd adequate cardiac support in patients with cardiogenic shock unresponsive to inotropes/vasopressors
281 cute myocardial infarction, unstable angina, cardiogenic shock, ventricular arrhythmia, atrioventricu
282 onia (n=1 in the dulaglutide 0.75 mg group); cardiogenic shock; ventricular fibrillation; and an unkn
286 Until recently, there were few options if cardiogenic shock was refractory to vasopressors or intr
287 ansplantation, INTERMACS profile 1 (critical cardiogenic shock) was present in 207 patients, INTERMAC
288 tricular fibrillation arrest and presence of cardiogenic shock were associated strongly with mortalit
289 with septic shock and not patients with pure cardiogenic shock were characterized by a rapid and prof
291 with non-ventricular fibrillation arrest or cardiogenic shock were included, and patients with concu
293 complicating physiology (eg, hypovolemia or cardiogenic shock), while invasive hemodynamic monitorin
296 almost two thirds of hospital survivors with cardiogenic shock who were treated with early revascular
297 s used to assemble a cohort of patients with cardiogenic shock with similar baseline characteristics
299 ly effective, facilitating rapid reversal of cardiogenic shock without device-related complications.
300 e [<75 years vs >/=75 years] and presence of cardiogenic shock [yes vs no]) to heparin (70 U/kg) or b
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