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1 endocardial stimulation strategy to achieve cardiac resynchronization.
2 Such changes can be reversed by cardiac resynchronization.
3 ion and in whom there are no indications for cardiac resynchronization, bradycardia support or antita
5 nical trials have demonstrated a benefit for cardiac resynchronization (CRT) and implantable cardiove
10 d Defibrillation in Heart Failure], CARE-HF (CArdiac REsynchronization-Heart Failure), MADIT-CRT [Mul
11 more had diabetes mellitus, kidney disease, cardiac resynchronization implantable cardioverter-defib
12 es (neurohormonal antagonists, diuretics and cardiac resynchronization in appropriate candidates).
15 focus on sudden cardiac death prevention and cardiac resynchronization, including published evidence
16 leaflets or their supporting structures (eg, cardiac resynchronization or transcatheter mitral valve
19 ifferent in patients with and without active cardiac resynchronization therapy (-0.7 minutes [95% con
20 d the quality of life (QOL) of patients with cardiac resynchronization therapy (CRT) and an implantab
21 d duration in echocardiographic responses to cardiac resynchronization therapy (CRT) and clinical out
22 linical trials have demonstrated benefit for cardiac resynchronization therapy (CRT) and implantable
23 dyssynchrony indices to predict response to cardiac resynchronization therapy (CRT) appears to vary
25 of mitral regurgitation (MR) reduction with cardiac resynchronization therapy (CRT) are complex, and
29 ricular (LV) pacing improves the efficacy of cardiac resynchronization therapy (CRT) compared with co
35 filling to the optimal hemodynamic effect in cardiac resynchronization therapy (CRT) during adjustmen
36 s with congestive heart failure eligible for cardiac resynchronization therapy (CRT) either do not re
37 e electromechanical substrates responsive to cardiac resynchronization therapy (CRT) from unresponsiv
39 phology and duration on the effectiveness of cardiac resynchronization therapy (CRT) has been usually
41 e effect of reverse remodeling on APD during cardiac resynchronization therapy (CRT) has not been det
44 hocardiographic predictors of response after cardiac resynchronization therapy (CRT) have largely inv
48 icacy, safety, and long-term prognosis after cardiac resynchronization therapy (CRT) in elderly patie
50 V) ejection fraction and clinical outcome to cardiac resynchronization therapy (CRT) in mild heart fa
51 uency ablation improves effectiveness of the cardiac resynchronization therapy (CRT) in nonresponders
52 e conflicting data regarding the efficacy of cardiac resynchronization therapy (CRT) in patients with
53 ed controlled trial evaluating the effect of cardiac resynchronization therapy (CRT) in patients with
56 trial (RAFT) study demonstrated that adding cardiac resynchronization therapy (CRT) in selected pati
68 ining the criteria for patient selection for cardiac resynchronization therapy (CRT) may improve its
71 this study was to investigate the impact of cardiac resynchronization therapy (CRT) on right ventric
72 vices included pacemakers (46%), ICDs (30%), cardiac resynchronization therapy (CRT) pacemakers (4%),
74 atory Heart Failure Trial) demonstrated that cardiac resynchronization therapy (CRT) reduced both mor
77 the left ventricular lead position (LVLP) on cardiac resynchronization therapy (CRT) response and cli
80 d- 1990s, a pacemaker-based treatment termed cardiac resynchronization therapy (CRT) was developed to
82 nt studies have cast doubt on the benefit of cardiac resynchronization therapy (CRT) with defibrillat
83 table cardioverter-defibrillators (ICDs), or cardiac resynchronization therapy (CRT) with pacing capa
84 ed the hypothesis that patient selection for cardiac resynchronization therapy (CRT) would be enhance
85 ials have established the average benefit of cardiac resynchronization therapy (CRT), but estimating
86 for optimal outcome in patients treated with cardiac resynchronization therapy (CRT), but the influen
87 myocardial substrate of patients undergoing cardiac resynchronization therapy (CRT), in particular i
110 t bundle branch block (LBBB) be treated with cardiac resynchronization therapy (CRT); however, one-th
112 table cardioverter-defibrillators (ICDs) and cardiac resynchronization therapy (ICD-CRT) than in pati
113 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy (MADIT-CRT) and to cre
114 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy (MADIT-CRT) showed tha
115 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy (MADIT-CRT) study by Q
116 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy (MADIT-CRT) study.
117 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy (MADIT-CRT) Trial to d
118 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy (MADIT-CRT) trial who
119 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy (MADIT-CRT), patients
121 The landmark trials of biventricular pacing (cardiac resynchronization therapy [CRT]) typically ran f
122 er Automatic Defibrillator Implantation With Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
123 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
124 er Automatic Defibrillator Implantation With Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
125 ted Left Ventricular Lead Placement to Guide Cardiac Resynchronization Therapy [TARGET] study); ISRCT
126 ry sinus lead implant or with nonresponse to cardiac resynchronization therapy and a suboptimal LV le
127 ith a new atrial lead placement as part of a cardiac resynchronization therapy and defibrillator impl
128 e feasibility of implementation of AVNS in a cardiac resynchronization therapy and defibrillator syst
129 did not influence the safety profile of the cardiac resynchronization therapy and defibrillator syst
130 ence of implantable cardiac defibrillator or cardiac resynchronization therapy and ejection fraction.
131 venous anatomy for optimal implementation of cardiac resynchronization therapy and evaluation of left
132 ntly associated with long-term outcome after cardiac resynchronization therapy and had additive progn
133 to address this challenge including improved cardiac resynchronization therapy and imaging technologi
135 medication for left ventricular dysfunction, cardiac resynchronization therapy and revascularization
138 traventricular conduction delay treated with cardiac resynchronization therapy at our institution dur
139 ation, including those receiving concomitant cardiac resynchronization therapy between 2006 and 2010
140 ce understanding of the working mechanism of cardiac resynchronization therapy by comparing animal ex
141 duced activation and intrinsic conduction in cardiac resynchronization therapy by evaluating the acut
142 We investigated the electric mechanisms of cardiac resynchronization therapy by performing detailed
144 rt disease and right bundle branch block, RV cardiac resynchronization therapy carried multiple posit
146 c separation (MES) would improve response to cardiac resynchronization therapy compared with standard
148 on fraction 25% to 45%, and not eligible for cardiac resynchronization therapy could participate.
149 no survival benefit for patients undergoing cardiac resynchronization therapy defibrillator (CRT-D)
150 rade from VVIR stimulator (pacemaker, PM) to cardiac resynchronization therapy defibrillator (CRT-D).
151 anted implantable cardioverter defibrillator/cardiac resynchronization therapy defibrillator (hazard
152 vival outcomes in patients with an ICD and a cardiac resynchronization therapy defibrillator enrolled
153 e revision, replacement, upgrade, or initial cardiac resynchronization therapy defibrillator implant.
154 ization with a cardioverter-defibrillator or cardiac resynchronization therapy defibrillator implante
156 P% independently correlate with mortality in cardiac resynchronization therapy defibrillator patients
157 stem upgrade or an initial implantation of a cardiac resynchronization therapy defibrillator were ran
158 er implantable cardioverter defibrillator or cardiac resynchronization therapy defibrillator, New Yor
159 than 20% of Medicare beneficiaries receiving cardiac resynchronization therapy defibrillators (CRT-D)
160 ices included 38 dual-chamber pacemakers, 17 cardiac resynchronization therapy defibrillators, and 2
162 ; QRS, 181+/-25 ms; all mean+/-SD) underwent cardiac resynchronization therapy device implantation.
163 an implantable cardioverter-defibrillator or cardiac resynchronization therapy device, and were based
164 confirmed, AVNS software was uploaded to the cardiac resynchronization therapy device, tested, and op
167 implantable cardioverter-defibrillators, and cardiac resynchronization therapy devices, via the prema
168 ilure, and a QRS duration <120 milliseconds, cardiac resynchronization therapy did not improve clinic
169 We postulated that this effect might limit cardiac resynchronization therapy efficacy in patients w
170 e cardioverter defibrillator without or with cardiac resynchronization therapy enrolled in the Sensit
171 DS AND Enrolled patients had dual chamber or cardiac resynchronization therapy ICDs, history of >/=1
172 diac defibrillator implant and 37% underwent cardiac resynchronization therapy implant) were compared
173 acteristics, QLV/QRS duration (QLV ratio) at cardiac resynchronization therapy implant, and data abou
175 , implantable cardioverter defibrillator and cardiac resynchronization therapy implantation, LVEF imp
179 on, atrioventricular conduction disease, and cardiac resynchronization therapy in 68 (46%), 56 (38%),
180 hood of a response to medical therapy and to cardiac resynchronization therapy in heart failure.
181 ow early after defibrillator implantation or cardiac resynchronization therapy in patients with chron
182 neficial in specific subpopulations, such as cardiac resynchronization therapy in patients with inter
183 o compare the effects of active and inactive cardiac resynchronization therapy in patients with sever
184 rk studies of antiarrhythmic drugs, ICD, and cardiac resynchronization therapy in the primary and sec
186 ne of the reasons for patient nonresponse to cardiac resynchronization therapy is a suboptimal left v
188 dy demonstrates clinical feasibility of dual cardiac resynchronization therapy lead delivery to optim
190 ith a cardiac implantable electronic device (cardiac resynchronization therapy or implantable cardiov
192 Data from a multicenter registry of 725 cardiac resynchronization therapy patients (median follo
193 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy patients by QRS morpho
194 Electric left ventricular lead position in cardiac resynchronization therapy patients was a signifi
195 ared ICD versus no ICD, whereas one compared cardiac resynchronization therapy plus a defibrillator v
196 iovascular implantable electronic device and cardiac resynchronization therapy programming strategies
201 MES-guided placement of the RV lead improves cardiac resynchronization therapy responders compared wi
203 in smaller hearts contributes to the better cardiac resynchronization therapy response in women.
207 ith an indication for permanent pacemaker or cardiac resynchronization therapy that underwent LBBP fo
208 METHODS AND Forty consecutive patients with cardiac resynchronization therapy underwent intracardiac
212 t failure management with medical as well as cardiac resynchronization therapy when indicated is an e
213 timulation (PNS) is a common complication of cardiac resynchronization therapy when left ventricular
215 omplete left-sided reverse remodeling due to cardiac resynchronization therapy with a defibrillator (
216 ardioverter-defibrillator (ICD) therapy with cardiac resynchronization therapy with a defibrillator (
217 th clinical outcomes in patients who receive cardiac resynchronization therapy with a defibrillator (
218 y symptomatic heart failure (HF) who receive cardiac resynchronization therapy with a defibrillator (
219 This study aimed to evaluate the effect of cardiac resynchronization therapy with a defibrillator (
220 (single-chamber, 19.8%; dual-chamber, 41.3%; cardiac resynchronization therapy with a defibrillator [
221 In heart failure patients undergoing either cardiac resynchronization therapy with a defibrillator o
222 ons in India who had class I indications for cardiac resynchronization therapy with an ICD and were u
223 of patients with both conditions who receive cardiac resynchronization therapy with defibrillator (CR
225 on delay) did not have clinical benefit from cardiac resynchronization therapy with defibrillator (CR
226 isk of heart failure (HF) or death comparing cardiac resynchronization therapy with defibrillator (CR
228 r ejection fraction (LVEF) super-response to cardiac resynchronization therapy with defibrillator (CR
230 of renal function on long-term outcomes with cardiac resynchronization therapy with defibrillator amo
231 428 patients at least 65 years old receiving cardiac resynchronization therapy with defibrillator fro
235 predicted outcomes; however, no benefit from cardiac resynchronization therapy with defibrillator was
236 older patients with heart failure receiving cardiac resynchronization therapy with defibrillator, di
237 enal function, derive long-term benefit from cardiac resynchronization therapy with defibrillator, wi
238 ion to implantable cardiac defibrillators or cardiac resynchronization therapy with defibrillators de
239 sk was further attenuated in the subgroup of cardiac resynchronization therapy with implantable cardi
240 205 patients with heart failure referred for cardiac resynchronization therapy with QRS >/=120 ms and
241 he hypothesis that an incremental benefit to cardiac resynchronization therapy would be gained by ech
243 ay optimization of biventricular pacemakers (cardiac resynchronization therapy) may maximize hemodyna
244 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy) study patients with l
245 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy) study, the echocardio
250 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy) with speckle-tracking
251 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy), 801 patients with an
252 onal classes I/II with medical treatment (or cardiac resynchronization therapy), including 6 patients
256 ization included impaired ejection fraction, cardiac resynchronization therapy, and institutional pra
257 of device monitoring, predicting response to cardiac resynchronization therapy, and the use of pacema
258 e reverse remodeling observed in women after cardiac resynchronization therapy, but this does not exp
259 implantable cardioverter defibrillators, and cardiac resynchronization therapy, consistent with evolv
260 iovascular implantable electronic devices or cardiac resynchronization therapy, given the natural his
261 evascularization, sex, diabetes, age, use of cardiac resynchronization therapy, implantable cardiover
263 ioverter-defibrillator (ICD) with or without cardiac resynchronization therapy, the subcutaneous ICD
264 mogeneous loading conditions, such as during cardiac resynchronization therapy, then triggers a rever
268 at women have better outcomes than men after cardiac resynchronization therapy-defibrillator (CRT-D)
269 omized controlled trials have shown that the cardiac resynchronization therapy-defibrillator improves
270 men have been under-represented in trials of cardiac resynchronization therapy-defibrillators (CRT-D)
292 ant (20 patients), for stabilization pending cardiac resynchronization therapy/percutaneous coronary
295 ted Left Ventricular Lead Placement to Guide Cardiac Resynchronization Therapy]), the LV lead was pos
296 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy], REVERSE [Resynchroni
298 DIT-CRT) showed that early intervention with cardiac-resynchronization therapy with a defibrillator (
299 urces on receipt of a heart failure therapy, cardiac-resynchronization therapy with defibrillation (C