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1 uideline for the Management of Patients With Valvular Heart Disease".
2 ry disease, 20% atrial fibrillation, and 17% valvular heart disease).
3 newer options for diagnosis and treatment of valvular heart disease.
4 l for identifying compounds likely to induce valvular heart disease.
5 idelines for the Management of Patients With Valvular Heart Disease.
6 echanism for development of the drug-induced valvular heart disease.
7 ercutaneous approaches for the correction of valvular heart disease.
8 gold standard for treatment of patients with valvular heart disease.
9 en a concordant decline in the prevalence of valvular heart disease.
10 heir development of effective treatments for valvular heart disease.
11 ive endocarditis in patients with underlying valvular heart disease.
12 pathway may play a role in the mechanism for valvular heart disease.
13 ge, body mass index, smoking, and history of valvular heart disease.
14 ogenesis are important in the development of valvular heart disease.
15 ike to be the ultimate solution for treating valvular heart disease.
16 alve matrix architecture that are evident in valvular heart disease.
17 tion, carcinoid tumors can cause right-sided valvular heart disease.
18 until it was reported to be associated with valvular heart disease.
19 weight loss may be associated with increased valvular heart disease.
20 receiving fenfluramine-phentermine developed valvular heart disease.
21 mmon type of inducible SMVT in patients with valvular heart disease.
22 Users of diet medications are at risk for valvular heart disease.
23 ssed the issue of longitudinal assessment of valvular heart disease.
24 e-phentermine therapy may be associated with valvular heart disease.
25 ffects, including pulmonary hypertension and valvular heart disease.
26 reasing recognition of nonrheumatic forms of valvular heart disease.
27 20 years have transformed the management of valvular heart disease.
28 siderably less attention than other forms of valvular heart disease.
29 proteomics, and metabolomics to the study of valvular heart disease.
30 scuss how these structures change in primary valvular heart disease.
31 t molecular pathways contributing to primary valvular heart disease.
32 vular heart diseases, and 30 (3.2%) isolated valvular heart disease.
33 vein graft remodeling, atherosclerosis, and valvular heart disease.
34 l heart disease, pulmonary hypertension, and valvular heart disease.
35 ilated left ventricular cardiomyopathies and valvular heart disease.
36 f coronary artery disease, hypertension, and valvular heart disease.
37 tions than previously appreciated, including valvular heart disease.
38 and quality of echocardiographic studies for valvular heart disease.
39 newer options for diagnosis and treatment of valvular heart disease.
40 clerosis, myocardial infarction, stroke, and valvular heart disease.
41 ociated with improved concordance in grading valvular heart disease.
42 ccredited laboratories for the evaluation of valvular heart disease.
43 s (289 male, 67+/-10 years) with ischemic or valvular heart disease.
44 Aortic stenosis is the most frequent valvular heart disease.
45 nowledge for the management of patients with valvular heart disease.
46 ion, and research in the field of structural valvular heart disease.
47 cardiomyopathy, ischemic heart disease, and valvular heart disease.
48 is that selective 5-HT2C agonism would avoid valvular heart disease.
49 heter therapies are being developed to treat valvular heart disease.
50 Aortic stenosis is the most common form of valvular heart disease.
51 ost challenging encountered in patients with valvular heart disease.
52 re more likely to have history of stroke and valvular heart disease.
53 guidance, and post-procedural assessment of valvular heart disease.
54 ntional surgery in the treatment of acquired valvular heart disease.
55 ic dysfunction, diastolic abnormalities, and valvular heart disease.
56 aortic stenosis is the most prevalent of all valvular heart diseases.
57 important treatment option for patients with valvular heart diseases.
58 urgitation (MR) is one of the most prevalent valvular heart diseases.
59 CV disease, heart failure, arrhythmias, and valvular heart diseases.
60 art disease, 1.07 (95% CI, 0.89 to 1.30) for valvular heart disease, 1.07 (95% CI, 0.96 to 1.19) for
63 a; Rhythm Disorders and Thromboembolism; and Valvular Heart Disease.(1-104) * To view the full manusc
64 on for ischemic heart disease (9.9% v 9.7%), valvular heart disease (2.9% v 2.8%), conduction abnorma
65 mic heart disease (410-414, 36.0, and 36.1), valvular heart disease (394-397, 424, 35), congestive he
66 4%), pulmonary vascular disease (1.2%-7.1%), valvular heart disease (5.0%-9.8%), and renal failure (7
67 (0 of 3 patients) vs those without multiple valvular heart disease (6 of 8 patients [75.0%]) and in
68 ysplasia (ARVD, 17%), postmyocarditis (14%), valvular heart disease (8%), congenital heart disease (2
69 were being evaluated for stable angina (53), valvular heart disease (8), atypical chest pain (12), or
70 tic stenosis (AS) is the most common form of valvular heart disease, affecting 2% of those over age 6
71 coronary artery disease (aHR, 1.051.151.27), valvular heart disease (aHR, 1.221.321.43), peripheral v
72 al advances is providing unique solutions to valvular heart disease also requiring revascularization,
73 al therapeutic molecular targets for primary valvular heart disease and discuss key knowledge gaps th
74 itial association between the development of valvular heart disease and drugs stems from observations
75 eart disease, arrhythmia, heart failure, and valvular heart disease and formulate practice-based reco
77 our understanding of the pathophysiology of valvular heart disease and in the surgical techniques fo
79 of the atrium is described in patients with valvular heart disease and is associated with an increas
81 y common and unexpected finding in end-stage valvular heart disease and may be associated with repair
82 ngs advance our understanding of this common valvular heart disease and may reveal novel therapeutic
83 t be explained by ischemic, hypertensive, or valvular heart disease and often results in sudden cardi
84 y multivariate analyses, in subjects free of valvular heart disease and preexisting cardiovascular di
85 Mitral regurgitation (MR) is the most common valvular heart disease and presents unique challenges fo
86 view of the current and future management of valvular heart disease and propose treatment approaches
88 emonstrates that the Lewis rat is a model of valvular heart disease and that streptococcal M protein
89 une responses against cardiac myosin lead to valvular heart disease and the infiltration of the heart
90 ady been undertaken to inhibit EndMT in both valvular heart disease and vein graft remodeling, with p
91 ral regurgitation (MR) is the most prevalent valvular heart disease and, when left untreated, it conf
92 ase, diabetes mellitus, atrial fibrillation, valvular heart disease, and antihypertensive medication
94 rest in establishing best practices in TAVR, valvular heart disease, and cardiovascular implantable e
95 an emphasis on nonischemic cardiomyopathies, valvular heart disease, and COVID-19 disease cardiac man
97 ting factors, such as renal artery stenosis, valvular heart disease, and ischemia, should be strongly
98 ase including metabolic syndrome, left-sided valvular heart disease, and ischemic heart disease are c
99 Mitral regurgitation (MR) is the most common valvular heart disease, and mitral valve surgery is the
100 xperts, including reduced ejection fraction, valvular heart disease, and other cardiomyopathies.
101 as chest pain, congestive heart failure, and valvular heart disease, and preoperative risk assessment
102 ardial infarction, congestive heart failure, valvular heart disease, and stroke or transient ischemic
103 erial revascularization, rheumatic and other valvular heart disease, and symptomatic bradyarrhythmia;
104 tions are now available for the treatment of valvular heart disease, and their efficacy and safety ha
105 vention, Rhythm Disorders & Thromboembolism, Valvular Heart Disease, and Vascular Medicine (1-100).
106 tabolic & Lipid Disorders, Rhythm Disorders, Valvular Heart Disease, and Vascular Medicine (1-100).
107 vention, Rhythm Disorders & Thromboembolism, Valvular Heart Disease, and Vascular Medicine (1-100).
108 ders & Lipids, Rhythm Disorders, Statistics, Valvular Heart Disease, and Vascular Medicine (1-63).
109 tabolic & Lipid Disorders, Rhythm Disorders, Valvular Heart Disease, and Vascular Medicine (1-84).
110 urodegenerative Disorders, Rhythm Disorders, Valvular Heart Disease, and Vascular Medicine (1-86).
114 The role of diabetes in the development of valvular heart disease, and, in particular, the relation
115 fects, 80 (8.5%) simultaneous congenital and valvular heart diseases, and 30 (3.2%) isolated valvular
116 ease, or Group 2 PH, includes heart failure, valvular heart diseases, and congenital heart diseases.
117 l similarities between coronary and calcific valvular heart disease (aortic stenosis [AS] and mitral
118 and comorbidities such as renal failure and valvular heart disease are independent predictors for AF
119 herapeutic options for calcific vascular and valvular heart disease are invasive transcatheter proced
121 myopathy, while the main divergences were in valvular heart disease, arrhythmias, and aortic disease.
122 holds immense potential for the treatment of valvular heart disease as adjuncts to surgical intervent
123 rticle reviews unique advantages emerging in valvular heart disease as the technology of invasive car
124 ations for clinicians to diagnose and manage valvular heart disease as well as supporting documentati
125 s less frequent in patients who had multiple valvular heart disease before TAVI (0 of 3 patients) vs
126 mended first-line test for the assessment of valvular heart disease, but cardiovascular magnetic reso
127 es have much promise as biomarkers in common valvular heart disease, but the impact of their measurem
128 third-degree atrioventricular block, severe valvular heart disease, cardiomyopathy, and pulmonary or
129 lve stenosis (AVS), which is the most common valvular heart disease, causes a progressive narrowing o
130 cardiomyopathy, hypertensive heart disease, valvular heart disease, cerebrovascular disease or nonca
132 e models, the use of diuretics, a history of valvular heart disease, coronary disease, advancing age,
135 African American, and to have hypertension, valvular heart disease, diabetes, hypothyroidism, AIDS,
136 olesterol; history of myocardial infarction, valvular heart disease, diabetes, lung disease, and use
138 m surrounding the diagnosis and treatment of valvular heart disease, driven in part by emerging percu
141 been the standard of care for patients with valvular heart disease for many decades, but transcathet
142 American College of Cardiology guidelines on valvular heart disease generated considerable controvers
146 cture: Many recommendations from the earlier valvular heart disease guidelines have been updated with
147 patients (52.6% of those with congenital or valvular heart disease) had received corrective cardiac
148 As populations age worldwide, the burden of valvular heart disease has grown exponentially, and so h
151 lions of individuals with coronary artery or valvular heart disease have been given a new chance at l
152 k and benefit of mechanical interventions in valvular heart disease have been primarily described amo
155 io 2.27; 95% CI, 1.03 to 5.04; P = .043) and valvular heart disease (hazard ratio 3.01; 95% CI, 1.05
156 2), atrial fibrillation HR 1.54 (1.36-1.73), valvular heart disease HR 1.23 (1.05-1.44), thromboembol
159 ameters such as age, left atrial dilatation, valvular heart disease, impaired renal function, and ser
161 fenfluramine (phen-fen) on the prevalence of valvular heart disease in 226 obese subjects enrolled in
163 es were dilated cardiomyopathy in 119 (53%), valvular heart disease in 34 (15%), arrhythmogenic right
164 ary heart disease in 278 participants (52%), valvular heart disease in 42 (8%), hypertension in 140 (
166 on, history of congestive heart failure, and valvular heart disease in Cox proportional hazards model
170 Because streptococcal M proteins produced valvular heart disease in Lewis rats and have been linke
171 fic aortic stenosis (CAS) is the most common valvular heart disease in older adults and has no effect
172 egurgitation (MR) is the most common type of valvular heart disease in patients over the age of 75 in
173 ent, progression and regression of carcinoid valvular heart disease in patients with carcinoid syndro
174 the pulmonic position in 2000, treatment for valvular heart disease in the outflow position has becom
175 contributing to altered profiles of acquired valvular heart disease in the past few decades include a
179 e (DAVD) has become the most common cause of valvular heart disease in the Western world, causing sig
180 se is increasing in importance as a cause of valvular heart disease in urban centers in the United St
181 tricuspid regurgitation are the most common valvular heart diseases in patients with heart failure a
182 c stenosis is perhaps the most common of all valvular heart diseases in the developed nations of the
183 uropean Society of Cardiology guidelines for valvular heart disease included changes in the definitio
203 th observed in patients with hypertension or valvular heart diseases is called maladaptive or patholo
204 anaemia, chronic kidney disease, presence of valvular heart disease, left ventricular ejection fracti
205 hypertension, sex, left atrial enlargement, valvular heart disease, left ventricular ejection fracti
206 rol ratio, prevalent coronary heart disease, valvular heart disease, left ventricular hypertrophy, an
207 en high-risk surgical candidates with native valvular heart disease (mainly mitral with severe MAC) o
208 Pathologic left ventricular remodeling and valvular heart disease may contribute to the clinical pr
211 sex) and clinical (diabetes, smoking status, valvular heart disease, medications, indications for cat
212 stress in the aortic valve, with functional valvular heart disease, mimicking the clinical syndrome.
213 CTRCEs included newly emerging arrhythmias, valvular heart diseases (moderate and more), myocardial
215 7 ESC/EACTS Guidelines for the management of valvular heart disease on antithrombotic therapy in pati
217 s generally well tolerated, with no observed valvular heart disease or pulmonary arterial hypertensio
218 er, decreased ejection fraction, presence of valvular heart disease or the use of concomitant medicat
219 tory of coronary artery disease, MI, CHF, or valvular heart disease (OR 1.6 [95% CI 0.9-2.6]), revisi
220 ng conditions (for example, hypertension and valvular heart disease) or coronary artery disease.
221 ailure, such as pre-existing cardiomyopathy, valvular heart disease, or congenital heart disease.
222 or impact on the management of patients with valvular heart disease over the next several years.
225 ered as the mechanism of VT in patients with valvular heart disease, particularly if the arrhythmia o
226 ts (N=114, 49%) compared with (ischemic and) valvular heart disease patients (N=26, 17%; P<0.001).
228 ry artery disease, congestive heart failure, valvular heart disease, pericardial disease, conduction
229 k score based on hypertension, age 75 years, valvular heart disease, peripheral vascular disease, obe
231 , hypertension treatment, diabetes mellitus, valvular heart disease, prevalent myocardial infarction,
232 ask Force on the management of patients with valvular heart disease proscribe the use of bioprostheti
233 linically relevant 5-HT-related pathologies (valvular heart disease, pulmonary arterial hypertension)
234 disease (CAD), cardiomyopathies, significant valvular heart disease, pulmonary hypertension, and arrh
235 stive heart failure, ischemic heart disease, valvular heart disease, pulmonary hypertension, and cong
236 used on hemodynamic measurements to evaluate valvular heart disease, pulmonary hypertension, cardiomy
237 hts into hemodynamic changes associated with valvular heart diseases, pulmonary hypertension phenotyp
238 AS without coronary artery disease or other valvular heart disease, scheduled for surgical aortic va
240 Future studies are needed to confirm whether valvular heart disease, specifically AS, may be an overl
241 ferences are observed across the spectrum of valvular heart disease, starting with pathophysiology an
242 METHODS AND We enrolled 335 consecutive valvular heart disease subjects who underwent echocardio
244 , out-of-hospital cardiac arrest, left-sided valvular heart disease, the advocacy potential of these
245 rature beyond the pandemic are novel data on valvular heart disease, the increasing use of artificial
246 n investigated for its role in production of valvular heart disease, the most serious sequelae of gro
247 allenges inherent in translating research on valvular heart disease to viable molecular targets that
248 ease, chronic obstructive pulmonary disease, valvular heart disease, tobacco use, and alcohol abuse.
249 gh surgery was the mainstay of treatment for valvular heart disease, transcatheter valve therapies ha
250 The overall proportion of women enrolled in valvular heart disease trials was 41.1%, with no signifi
252 tudy was to evaluate the association between valvular heart disease (VHD) and maternal and fetal outc
254 The occurrence of fenfluramine-associated valvular heart disease (VHD) has raised concerns that ot
263 with atrial fibrillation (AF) and coexisting valvular heart disease (VHD) is of substantial interest.
265 art valves, significant mitral stenosis, and valvular heart disease (VHD) requiring intervention were
266 ege of Cardiology/American Heart Association valvular heart disease (VHD) stage prevalence, progressi
267 psed since the original Euro Heart Survey on valvular heart disease (VHD) was conducted with multiple
268 nt of pulmonary arterial hypertension (PAH), valvular heart disease (VHD), and related cardiopathies.
273 or in mediating the heart valve fibroplasia [valvular heart disease (VHD)] and primary pulmonary hype
276 essants fenfluramine and dexfenfluramine and valvular heart disease was first described in patients f
277 rditis, coronary artery disease, stroke, and valvular heart disease were also observed for multiple c
282 diabetes, left ventricular hypertrophy, and valvular heart disease were predictive of increased risk
283 gy/American Heart Association guidelines for valvular heart disease were released to help guide the c
284 e for a variety of safety concerns including valvular heart disease which was the cause for the withd
285 amyloid deposits in patients with AF without valvular heart disease, which represents the most common
286 ith heart failure and identify patients with valvular heart disease who have myocardial decompensatio
287 LVEF may remain normal amongst patients with valvular heart disease who have significant myocardial d
288 , valve tissues from rheumatic patients with valvular heart disease who required valve replacement we
289 fraction < or =35%) and without significant valvular heart disease who underwent PET/FDG study at th
290 ed age, with chronic kidney disease, or with valvular heart disease will be discussed as well as the
291 Mitral valve prolapse (MVP) is a common valvular heart disease with a prevalence of >2% in the g
292 prevalent phenotype in patients affected by valvular heart disease with a well-recognized cluster of