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1 bradycardia, bronchospasm, and/or congestive heart failure).
2 as a critical determinant of arrhythmias in heart failure.
3 structural remodeling of chromatin underpins heart failure.
4 f 10 patients with CHD with AF had developed heart failure.
5 ardiomyopathy (DCM) is an important cause of heart failure.
6 l hypertension, obstructive sleep apnoea and heart failure.
7 ive therapy in older patients with ischaemic heart failure.
8 onto obesity-related cardiac remodeling and heart failure.
9 apy of choice for all patients with advanced heart failure.
10 tation is an effective therapy for end-stage heart failure.
11 modeling process, is a major risk factor for heart failure.
12 is considered a target for the treatment of heart failure.
13 nostic workup and treatment of patients with heart failure.
14 e with a first-time in-hospital diagnosis of heart failure.
15 ce hospitalization and mortality in systolic heart failure.
16 h as ventricular fibrillation and congestive heart failure.
17 ted the incidence and the mortality rates of heart failure.
18 lic target in a number of diseases including heart failure.
19 ptides decline with obesity in patients with heart failure.
20 eling response, which can ultimately lead to heart failure.
21 eutic target for pathological remodeling and heart failure.
22 generation of stem cell-based treatment for heart failure.
23 likelihood of depression in outpatients with heart failure.
24 T were among the top predictors for incident heart failure.
25 for morbidity and mortality in patients with heart failure.
26 by hyperglycemia is a major risk factor for heart failure.
27 to limiting progression of this condition to heart failure.
28 y, sleep disordered breathing and congestive heart failure.
29 s such as myocardial infarction, stroke, and heart failure.
30 urrently intensely studied as a biomarker in heart failure.
31 evated hs-TnT were older and had more severe heart failure.
32 MACE, including cardiovascular mortality and heart failure.
33 diseases, including cardiac hypertrophy and heart failure.
34 ion in t-tubule organization and accelerated heart failure.
35 nfarction, stroke, or hospital admission for heart failure.
36 and over time, these chronic loads can cause heart failure.
37 normalities, including pericardial edema and heart failure.
38 ht further improve outcomes in patients with heart failure.
39 of respiratory and autonomic dysfunction in heart failure.
40 ive hypertrophic cardiomyopathy and advanced heart failure.
41 g these CpGs novel epigenetic biomarkers for heart failure.
42 myocardial infarction, ischemic stroke, and heart failure.
43 iotensin system inhibitors for patients with heart failure.
44 sibility remains unresolved in patients with heart failure.
45 on (1.55, 1.33-1.80), hospital admission for heart failure (1.59, 1.36-1.86) and all-cause death (1.1
47 lar events (CVEs) including 281 (23.8%) with heart failure, 109 (9.2%) with atrial fibrillation, 89 (
48 e the most common noncardiac causes, whereas heart failure (22.5%) and arrhythmias (6.6%) were the mo
49 A), and cBIN1 level decreased in humans with heart failure, a condition with reduced cardiac muscle c
50 530 771, and 1 125 231 hospitalizations for heart failure, acute myocardial infarction, and pneumoni
53 r the composite outcome of incident ASCVD or heart failure after further stratifying by CAC (0, 1-100
54 ated with mortality or rehospitalization for heart failure after multivariate adjustment were increas
55 5'-nucleotidase (CD73) on the development of heart failure after transverse aortic constriction (TAC)
57 istration of MSCs should improve outcomes in heart failure, an entity in which excessive chronic infl
59 d that excessive leukocyte invasion leads to heart failure and death during acute myocardial ischemia
62 f cardiovascular events may be enhanced when heart failure and glucose intolerance coexist and may be
64 activation is an independent risk factor for heart failure and is considered a target for the treatme
67 5) and in a pig model with features of human heart failure and preserved ejection fraction with stern
69 and pathophysiology of aortic stenosis with heart failure and reduced ejection fraction and summariz
71 initiated significantly later with comorbid heart failure and renal failure, with absence of fever o
72 rterial hypertension, diabetes mellitus, and heart failure), and a lower risk for 10-year mortality,
73 heart disease, 1.20 (95% CI: 1.01, 1.42) for heart failure, and 1.11 (95% CI: 1.04, 1.19) for a compo
74 ese risk markers in coronary artery disease, heart failure, and atrial fibrillation is discussed in d
79 atal or nonfatal stroke, hospitalization for heart failure, and hospitalization for acute coronary sy
80 CM but for both groups older age, congestive heart failure, and increased left ventricular end-systol
83 ar disease (including myocardial infarction, heart failure, and stroke) and all-cause mortality were
86 onal Class III or IV, previous admission for heart failure, and valve disease) and non-cardiac variab
87 onary artery (PA) pressures in patients with heart failure are associated with a high risk for hospit
88 ing the progression of diabetes mellitus and heart failure are closely intertwined, such that worseni
89 mammal (rat) and a large mammal (human) with heart failure are shown, demonstrating myocardial slice
93 cardial samples from patients with end-stage heart failure at time of transplant, with or without dia
94 uded myocardial infarction, new or worsening heart failure, atrial fibrillation, stroke, deep venous
95 penoid used in the treatment of glaucoma and heart failure based on its activity as a cyclic AMP boos
96 0 individuals with a first-time diagnosis of heart failure between 1995 and 2012; the annual incidenc
97 sity was associated with all-cause death and heart failure, but the result was not significant (P=0.0
98 hetic stimulation have been reported in left heart failure, but whether it would be beneficial for pu
99 ardiac surgery, anemia, respiratory failure, heart failure, cardiac arrest, metastatic cancer (requir
100 the evaluation of congenital heart disease, heart failure, cardiac masses, pericardial disease, and
102 The estimated absolute number of prevalent heart failure cases in the UK increased even more, by 23
103 -infected individuals have excess congestive heart failure (CHF) risk compared with uninfected people
105 hmias, eclampsia or preeclampsia, congestive heart failure (CHF), length of stay, preterm labor, anem
106 ere chronic kidney disease (CKD), congestive heart failure (CHF), or chronic liver disease (CLD) with
109 l strategies for Management of Patients with Heart failure) clinical cohort study, 496 patients with
111 bypass surgery leads to a lower incidence of heart failure compared with intensive lifestyle modifica
112 tes mellitus) are characteristic features of heart failure; conversely, neurohormonal systems activat
114 had a higher rate of hospital admission for heart failure decompensation in follow-up (HR, 1.66; 95%
115 pital status, known coronary artery disease, heart failure, diabetes mellitus, chronic kidney disease
116 noninvasive telemonitoring in patients with heart failure does not reduce mortality or hospitalizati
117 in greater improvements in QoL compared with heart failure education (P<0.01), including the Kansas C
118 e randomized to either a CST intervention or heart failure education, both delivered over 16 weeks.
119 al of 30% to 40% of patients with congestive heart failure eligible for cardiac resynchronization the
120 llitus, history of stroke, >1 g proteinuria, heart failure, estimated glomerular filtration rate <20
121 tential myocardial infarctions, strokes, and heart failure events in HealthLNK and compared them with
122 diovascular death, 17.5 versus 2.6, P<0.001; heart failure events, 22.4 versus 7.4, P<0.001); these r
125 hospital quartile of ICU use for congestive heart failure had a sensitivity of 50-60% and specificit
127 le is known whether PH heightens the risk of heart failure (HF) admission or mortality among chronic
128 r, molecular pathways underlying accelerated heart failure (HF) after MI in T2DM remain unclear.
129 nthracycline chemotherapy is associated with heart failure (HF) among survivors of non-Hodgkin lympho
136 idosis (ATTR) is an underrecognized cause of heart failure (HF) in older individuals, owing in part t
137 It is unknown whether the increased risk of heart failure (HF) in rheumatoid arthritis (RA) is indep
143 dorff-perfused hearts from control (CTL) and heart failure (HF) mice (HF induced by transaortic const
148 unclear how patients hospitalized for acute heart failure (HF) who are long-term chronic HF survivor
150 enic role of ischemic heart disease (IHD) in heart failure (HF) with reduced ejection fraction (HFrEF
152 therapy are known to have increased risks of heart failure (HF), but a radiation dose-response relati
154 olute rates and risk differences of incident heart failure (HF), coronary heart disease (CHD), and st
156 c sympathetic overstimulation, a hallmark of heart failure (HF), induces pathological signaling throu
157 or acute myocardial infarction (AMI) without heart failure (HF), it is unclear if beta-blockers are a
158 -blockers increase survival in patients with heart failure (HF), the mechanisms behind this protectio
168 flammation is a hallmark of chronic ischemic heart failure (HF); however, the pathophysiological role
169 3; 95% CI: 0.07 to 0.75), total mortality or heart failure hospitalization (aHR: 0.32; 95% CI: 0.12 t
170 y end point or day-30 all-cause mortality or heart failure hospitalization rate differed between the
172 ur-year survival that is free from death and heart failure hospitalization was higher for adherent pa
173 including myocardial infarction, stroke, and heart failure hospitalization, were compared between pat
175 occurrence of cardiovascular events (death, heart failure, hospitalization, arrhythmia, thromboembol
177 ), age (HR, 1.02, P = .001), and preexisting heart failure (HR, 1.85, P < .001) independently predict
178 rmal' range) showed strong associations with heart failure (HR: 2.04; 95% confidence interval [CI]: 1
179 s a potential pharmacotherapeutic target for heart failure, hypertension, and other cardiovascular di
180 outcomes were myocardial infarction, angina, heart failure, hypertension, arrhythmias, arterioscleros
181 measure mortality at 1 year in patients with heart failure in Africa, China, India, the Middle East,
182 essed cardiac hypertrophy and progression to heart failure in both vitamin D deficient and normal mic
184 Depletion of CTCF was sufficient to induce heart failure in mice, and human patients with heart fai
185 tation in food attenuates the development of heart failure in mice, more robustly in DCM, and partial
186 membrane oxygenation for acute decompensated heart failure in our ICU (67% of them had an intraaortic
187 tion therapy (CRT) is a potent treatment for heart failure in the setting of ventricular dyssynchrony
189 ian of 4.1 years, surgery patients had lower heart failure incidence than lifestyle modification pati
190 ty and gap junction coupling, as observed in heart failure, increase the probability of extreme DADs
191 bination drug recently approved for treating heart failure, inhibits stretch-induced hypertrophy, and
192 pitalization for management of decompensated heart failure, initiation of mechanical circulatory supp
198 resulting cerebral small vessel disease and heart failure may contribute to early cognitive decline
199 ents had persisting symptoms compatible with heart failure (median of 13 [range 0-76] in the Minnesot
200 pharmacotherapies for African Americans (eg, heart failure medications), disease management is less e
201 The authors hypothesized that the Seattle Heart Failure Model (SHFM) for overall survival and the
202 evant prediction models exist (SHFM [Seattle Heart Failure Model] and HMRS [HeartMate II Risk Score])
203 safety endpoint were age, anemia, congestive heart failure, multivessel disease, number of stents imp
204 rment has been detected in cardiomyopathies, heart failure, myocardial ischaemia, and hypertrophy.
206 nversely, neurohormonal systems activated in heart failure (norepinephrine, angiotensin II, aldostero
207 precursors, could be useful for treatment of heart failure, notably in the context of DCM, a disease
208 ter 1 year was related to a hazard ratio for heart failure of 0.77 (95% confidence interval, 0.60-0.9
209 point was defined as symptomatic congestive heart failure of New York Heart Association class III or
210 more pronounced in patients with congestive heart failure or ischemic heart disease than in those wi
211 acute coronary syndrome, stroke, congestive heart failure, or CVD death), and (ii) serious adverse e
212 malignant ventricular arrhythmias, end-stage heart failure, or death) compared with carriers of other
215 er risk of dying from myocardial infarction, heart failure, or stroke, respectively, than members of
218 esented with rapid development of congestive heart failure over 6 months, in sharp contrast to a prev
219 vascular disease, myocardial infarction, and heart failure over use of established and novel cardiova
220 TnT levels in patients with chronic ischemic heart failure (P=0.0008, n=10, triple measurements).
221 Innate and adaptive immune cells modulate heart failure pathogenesis during viral myocarditis, yet
225 ement) demonstrated that ambulatory advanced heart failure patients selected for left ventricular ass
227 orthogonal to the main LV flow direction in heart failure patients with LBBB compared to those witho
229 d in improvement of patient health status in heart failure patients with low self-reported hrQoL, but
230 tients with left bundle branch block (LBBB), heart failure patients with narrow QRS and nonspecific i
232 al differences in mortality in patients with heart failure persisted after multivariable adjustment f
235 optimal cell population(s) for treatment of heart failure prompted implementation of a protocol for
236 w-up; p < 0.0001 vs. baseline) and Minnesota Heart Failure Questionnaire scores (56.2 +/- 26.8 vs. 31
237 13 [range 0-76] in the Minnesota Living with Heart Failure Questionnaire) and cardiac limitation on e
238 ts: ejection fraction, Minnesota Living with Heart Failure Questionnaire, 6-min walk test, major adve
239 art failure in mice, and human patients with heart failure receiving mechanical unloading via left ve
240 g Hospital Admission for Acute Decompensated Heart Failure Reduce Mortality and Readmissions?) demons
242 ving Treatment in Hospitalized Patients with Heart Failure) registry, 6,286 had a stable heart rate,
243 ictims remain at risk for infarct expansion, heart failure, reinfarction, repeat revascularization, a
247 r 2 inhibitors may reduce cardiovascular and heart failure risk in patients with type 2 diabetes mell
249 AKI associated with a 58% increased risk of heart failure (RR 1.58; 95% CI, 1.46 to 1.72) and a 40%
250 (RR: 0.67; 95% CI: 0.45 to 0.98), and 37% in heart failure (RR: 0.63; 95% CI: 0.43 to 0.99) compared
251 sus 29 kg/m(2)), worse Minnesota Living With Heart Failure score (48 versus 40), higher median N-term
253 rtions of patients of black race, those with heart failure signs at admission, and bleeding complicat
254 expertise from interventional cardiologists, heart failure specialists, cardiac surgeons, and cardiac
257 ses (acute myocardial infarction, congestive heart failure, stroke, pneumonia, and chronic obstructiv
258 death, nonfatal myocardial infarction [MI], heart failure, stroke, transient ischemic attack, periph
259 cute Congestion with Tolvaptan in Congestive Heart Failure) study was conducted to address the acute
260 uestionnaires were used to collect data: the Heart Failure Symptom Survey, the Interpersonal Support
261 ong individual and clinical characteristics, heart failure symptomatology, and subcomponents of socia
262 her individual and clinical characteristics, heart failure symptomatology, and the subcomponents of s
264 myopathy is an increasingly recognized acute heart failure syndrome precipitated by intense emotional
265 er among patients with a recent diagnosis of heart failure than among those with a longer-standing di
266 utic options for initial surgery and chronic heart failure that results from failed palliation are li
268 e randomly assigned 2157 patients with acute heart failure to receive a continuous intravenous infusi
269 We randomly assigned patients with advanced heart failure to receive either the new centrifugal cont
271 ata collected in the Sudden Cardiac Death in Heart Failure Trial (SCD-HeFT), which randomly assigned
272 vascular Improvements With MV-ASV Therapy in Heart Failure) trial investigated whether minute ventila
273 Effectiveness of Nesiritide in Decompensated Heart Failure) trial randomized 7,141 hospitalized patie
274 Impact on Global Mortality and Morbidity in Heart Failure) trial randomly assigned 8399 patients wit
277 mpaired cardiac force-frequency response and heart failure under some conditions but the mechanisms a
278 with recurrence and mortality were advanced heart failure, VT cycle length, and a left-sided-only pr
279 PANWARDS (platelets, albumin, no congestive heart failure, warfarin, age, race, diastolic blood pres
280 is probably due to immunosenescence, because heart failure was associated with increased senescent CD
282 associated with incident kidney failure and heart failure, we estimated GSTM1 copy number using exom
283 erved ejection fraction (HFpEF) (EF >/=50%), heart failure with borderline ejection fraction (HFbEF)
284 aptan in Patients Hospitalized for Worsening Heart Failure With Challenging Volume Management [SECRET
285 es in outcomes in patients hospitalized with heart failure with preserved ejection fraction (HFpEF) (
288 gh left atrial (LA) dysfunction is common in heart failure with preserved ejection fraction (HFpEF),
289 ts with hypertensive heart disease (HHD) and heart failure with preserved ejection fraction (HFpEF).
290 METHODS AND We randomized 12 subjects with heart failure with preserved ejection fraction to oral K
291 comes in the I-Preserve trial (Irbesartan in Heart Failure With Preserved Ejection Fraction) accordin
293 ection fraction (HFbEF) (EF 41% to 49%), and heart failure with reduced ejection fraction (HFrEF) (EF
294 the first study to evaluate elamipretide in heart failure with reduced ejection fraction and demonst
295 lly over time among ambulatory patients with heart failure with reduced ejection fraction who were en
296 efficacy of many therapies for patients with heart failure with reduced ejection fraction, such as an
298 s, are under investigation for patients with heart failure with reduced left ventricular ejection fra
299 resent in approximately 50% of patients with heart failure with reduced left ventricular ejection fra
300 there was an initial decrease in PAC use in heart failure, with a nadir in 2009 followed by a subseq
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