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1 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy).
2 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy).
3 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy).
4 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy).
5 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy).
6 CD) display a relatively limited response to cardiac resynchronization therapy.
7 implantable cardioverter-defibrillators and cardiac resynchronization therapy.
8 coronary sinus is the standard approach for cardiac resynchronization therapy.
9 patients with AF to maximize the benefits of cardiac resynchronization therapy.
10 r septal puncture is a feasible approach for cardiac resynchronization therapy.
11 e improvement in LV pump function induced by cardiac resynchronization therapy.
12 tivation, which may predict poor response to cardiac resynchronization therapy.
13 zations and has implications for delivery of cardiac resynchronization therapy.
14 te changes in RV function after temporary RV cardiac resynchronization therapy.
15 used for improved selection of patients for cardiac resynchronization therapy.
16 that this lead location should be avoided in cardiac resynchronization therapy.
17 y in selected patients who do not respond to cardiac resynchronization therapy.
18 e role of intrinsic conduction in optimizing cardiac resynchronization therapy.
19 rately predicts LV reverse remodeling during cardiac resynchronization therapy.
20 electrocardiographic selection criteria for cardiac resynchronization therapy.
21 a strong predictor of short-term response to cardiac resynchronization therapy.
22 ifferent in patients with and without active cardiac resynchronization therapy (-0.7 minutes [95% con
23 one antagonist (60.3% versus 34.5%, +25.1%), cardiac resynchronization therapy (66.3% versus 37.2%, +
24 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy), 801 patients with an
25 ry sinus lead implant or with nonresponse to cardiac resynchronization therapy and a suboptimal LV le
26 ith a new atrial lead placement as part of a cardiac resynchronization therapy and defibrillator impl
27 e feasibility of implementation of AVNS in a cardiac resynchronization therapy and defibrillator syst
28 did not influence the safety profile of the cardiac resynchronization therapy and defibrillator syst
29 venous anatomy for optimal implementation of cardiac resynchronization therapy and evaluation of left
30 ntly associated with long-term outcome after cardiac resynchronization therapy and had additive progn
31 to address this challenge including improved cardiac resynchronization therapy and imaging technologi
32 medication for left ventricular dysfunction, cardiac resynchronization therapy and revascularization
33 atients who will not receive the benefits of cardiac resynchronization therapy and whose clinical con
34 ization included impaired ejection fraction, cardiac resynchronization therapy, and institutional pra
35 of device monitoring, predicting response to cardiac resynchronization therapy, and the use of pacema
38 traventricular conduction delay treated with cardiac resynchronization therapy at our institution dur
40 ation, including those receiving concomitant cardiac resynchronization therapy between 2006 and 2010
41 ce understanding of the working mechanism of cardiac resynchronization therapy by comparing animal ex
42 duced activation and intrinsic conduction in cardiac resynchronization therapy by evaluating the acut
43 We investigated the electric mechanisms of cardiac resynchronization therapy by performing detailed
45 rt disease and right bundle branch block, RV cardiac resynchronization therapy carried multiple posit
47 c separation (MES) would improve response to cardiac resynchronization therapy compared with standard
48 implantable cardioverter defibrillators, and cardiac resynchronization therapy, consistent with evolv
50 d the quality of life (QOL) of patients with cardiac resynchronization therapy (CRT) and an implantab
51 d duration in echocardiographic responses to cardiac resynchronization therapy (CRT) and clinical out
52 linical trials have demonstrated benefit for cardiac resynchronization therapy (CRT) and implantable
53 onship between echocardiographic response to cardiac resynchronization therapy (CRT) and the risk of
54 dyssynchrony indices to predict response to cardiac resynchronization therapy (CRT) appears to vary
56 of mitral regurgitation (MR) reduction with cardiac resynchronization therapy (CRT) are complex, and
58 table cardioverter-defibrillators (ICDs) and cardiac resynchronization therapy (CRT) are treatments p
62 ricular (LV) pacing improves the efficacy of cardiac resynchronization therapy (CRT) compared with co
69 study was to define the extent and nature of cardiac resynchronization therapy (CRT) device usage out
70 filling to the optimal hemodynamic effect in cardiac resynchronization therapy (CRT) during adjustmen
71 s with congestive heart failure eligible for cardiac resynchronization therapy (CRT) either do not re
72 e electromechanical substrates responsive to cardiac resynchronization therapy (CRT) from unresponsiv
74 ographic dyssynchrony to predict response to cardiac resynchronization therapy (CRT) has been unclear
75 phology and duration on the effectiveness of cardiac resynchronization therapy (CRT) has been usually
77 e effect of reverse remodeling on APD during cardiac resynchronization therapy (CRT) has not been det
80 hocardiographic predictors of response after cardiac resynchronization therapy (CRT) have largely inv
81 er observational study in patients receiving cardiac resynchronization therapy (CRT) implantable card
84 icacy, safety, and long-term prognosis after cardiac resynchronization therapy (CRT) in elderly patie
86 V) ejection fraction and clinical outcome to cardiac resynchronization therapy (CRT) in mild heart fa
87 uency ablation improves effectiveness of the cardiac resynchronization therapy (CRT) in nonresponders
89 r (LV) pacing site on mechanical response to cardiac resynchronization therapy (CRT) in patients with
90 e conflicting data regarding the efficacy of cardiac resynchronization therapy (CRT) in patients with
91 ed controlled trial evaluating the effect of cardiac resynchronization therapy (CRT) in patients with
92 trial (RAFT) study demonstrated that adding cardiac resynchronization therapy (CRT) in selected pati
99 ining the criteria for patient selection for cardiac resynchronization therapy (CRT) may improve its
102 this study was to investigate the impact of cardiac resynchronization therapy (CRT) on right ventric
105 atory Heart Failure Trial) demonstrated that cardiac resynchronization therapy (CRT) reduced both mor
108 the left ventricular lead position (LVLP) on cardiac resynchronization therapy (CRT) response and cli
110 lar contraction (DHF) and its restoration by cardiac resynchronization therapy (CRT) using a canine t
111 of prospective randomized clinical trials of cardiac resynchronization therapy (CRT) versus implantab
112 d- 1990s, a pacemaker-based treatment termed cardiac resynchronization therapy (CRT) was developed to
114 nt studies have cast doubt on the benefit of cardiac resynchronization therapy (CRT) with defibrillat
115 table cardioverter-defibrillators (ICDs), or cardiac resynchronization therapy (CRT) with pacing capa
116 ed the hypothesis that patient selection for cardiac resynchronization therapy (CRT) would be enhance
117 se of left ventricular remodeling induced by cardiac resynchronization therapy (CRT), adjusting for t
118 ials have established the average benefit of cardiac resynchronization therapy (CRT), but estimating
119 for optimal outcome in patients treated with cardiac resynchronization therapy (CRT), but the influen
120 myocardial substrate of patients undergoing cardiac resynchronization therapy (CRT), in particular i
142 t bundle branch block (LBBB) be treated with cardiac resynchronization therapy (CRT); however, one-th
145 This trial was designed to determine whether cardiac-resynchronization therapy (CRT) with biventricul
146 The landmark trials of biventricular pacing (cardiac resynchronization therapy [CRT]) typically ran f
150 no survival benefit for patients undergoing cardiac resynchronization therapy defibrillator (CRT-D)
151 rade from VVIR stimulator (pacemaker, PM) to cardiac resynchronization therapy defibrillator (CRT-D).
152 anted implantable cardioverter defibrillator/cardiac resynchronization therapy defibrillator (hazard
153 vival outcomes in patients with an ICD and a cardiac resynchronization therapy defibrillator enrolled
155 P% independently correlate with mortality in cardiac resynchronization therapy defibrillator patients
156 - 7%) who met enrollment criteria received a cardiac resynchronization therapy defibrillator, and 980
157 er implantable cardioverter defibrillator or cardiac resynchronization therapy defibrillator, New Yor
158 eductions in left atrial volume (LAV) with a cardiac resynchronization therapy-defibrillator (CRT-D)
159 antable cardioverter-defibrillator (ICD) and cardiac resynchronization therapy-defibrillator (CRT-D)
160 ator Registry, we defined a cohort of 45,392 cardiac resynchronization therapy-defibrillator (CRT-D)
161 at women have better outcomes than men after cardiac resynchronization therapy-defibrillator (CRT-D)
162 ilure, atrial fibrillation/flutter, having a cardiac resynchronization therapy-defibrillator device,
163 omized controlled trials have shown that the cardiac resynchronization therapy-defibrillator improves
164 than 20% of Medicare beneficiaries receiving cardiac resynchronization therapy defibrillators (CRT-D)
165 men have been under-represented in trials of cardiac resynchronization therapy-defibrillators (CRT-D)
168 cited publications on predicting response to cardiac resynchronization therapy define response using
171 patients who had an upgrade to or a revised cardiac resynchronization therapy device (18.7%; 95% con
172 ; QRS, 181+/-25 ms; all mean+/-SD) underwent cardiac resynchronization therapy device implantation.
173 an implantable cardioverter-defibrillator or cardiac resynchronization therapy device, and were based
174 confirmed, AVNS software was uploaded to the cardiac resynchronization therapy device, tested, and op
176 ntable cardioverter-defibrillator (including cardiac resynchronization therapy devices) and were foll
177 implantable cardioverter-defibrillators, and cardiac resynchronization therapy devices, via the prema
178 ilure, and a QRS duration <120 milliseconds, cardiac resynchronization therapy did not improve clinic
179 e cardioverter defibrillator without or with cardiac resynchronization therapy enrolled in the Sensit
183 g implantable cardioverter-defibrillator and cardiac resynchronization therapy) for patients with hea
184 implantable cardioverter defibrillators and cardiac resynchronization therapy have also been reporte
185 ia believed to define a positive response to cardiac resynchronization therapy have been used in the
186 table cardioverter-defibrillators (ICDs) and cardiac resynchronization therapy (ICD-CRT) than in pati
187 DS AND Enrolled patients had dual chamber or cardiac resynchronization therapy ICDs, history of >/=1
188 diac defibrillator implant and 37% underwent cardiac resynchronization therapy implant) were compared
189 acteristics, QLV/QRS duration (QLV ratio) at cardiac resynchronization therapy implant, and data abou
191 evascularization, sex, diabetes, age, use of cardiac resynchronization therapy, implantable cardiover
192 ticoagulant therapy for atrial fibrillation, cardiac resynchronization therapy, implantable cardiover
196 hood of a response to medical therapy and to cardiac resynchronization therapy in heart failure.
197 ow early after defibrillator implantation or cardiac resynchronization therapy in patients with chron
198 o compare the effects of active and inactive cardiac resynchronization therapy in patients with sever
199 rk studies of antiarrhythmic drugs, ICD, and cardiac resynchronization therapy in the primary and sec
202 ne of the reasons for patient nonresponse to cardiac resynchronization therapy is a suboptimal left v
204 ween different methods to define response to cardiac resynchronization therapy is poor 75% of the tim
207 dy demonstrates clinical feasibility of dual cardiac resynchronization therapy lead delivery to optim
208 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy (MADIT-CRT) and to cre
209 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy (MADIT-CRT) showed tha
210 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy (MADIT-CRT) study by Q
211 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy (MADIT-CRT) study.
212 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy (MADIT-CRT) study.
213 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy (MADIT-CRT) Trial to d
214 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy (MADIT-CRT) trial who
215 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy (MADIT-CRT) trial.
216 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy (MADIT-CRT), patients
219 er Automatic Defibrillator Implantation With Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
220 er Automatic Defibrillator Implantation With Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
221 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
222 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
223 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
224 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
225 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
226 er Automatic Defibrillator Implantation With Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
228 ay optimization of biventricular pacemakers (cardiac resynchronization therapy) may maximize hemodyna
232 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy patients by QRS morpho
233 Electric left ventricular lead position in cardiac resynchronization therapy patients was a signifi
234 ant (20 patients), for stabilization pending cardiac resynchronization therapy/percutaneous coronary
235 ared ICD versus no ICD, whereas one compared cardiac resynchronization therapy plus a defibrillator v
237 patients from the Predictors of Response to Cardiac Resynchronization Therapy (PROSPECT) study with
238 MES-guided placement of the RV lead improves cardiac resynchronization therapy responders compared wi
245 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy], REVERSE [Resynchroni
246 comparison to other AV delay methods used in cardiac resynchronization therapy (SMART-AV) trial prosp
247 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy) study patients with l
248 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy) study, the echocardio
254 ted Left Ventricular Lead Placement to Guide Cardiac Resynchronization Therapy [TARGET] study); ISRCT
255 ioverter-defibrillator (ICD) with or without cardiac resynchronization therapy, the subcutaneous ICD
256 ted Left Ventricular Lead Placement to Guide Cardiac Resynchronization Therapy]), the LV lead was pos
257 Automatic Defibrillator Implantation Trial: Cardiac Resynchronization Therapy) to evaluate whether t
260 METHODS AND Forty consecutive patients with cardiac resynchronization therapy underwent intracardiac
264 ead ECGs during left bundle branch block and cardiac resynchronization therapy were analyzed in 202 c
265 reduction of left ventricular volumes after cardiac resynchronization therapy were most pronounced i
266 t failure management with medical as well as cardiac resynchronization therapy when indicated is an e
267 timulation (PNS) is a common complication of cardiac resynchronization therapy when left ventricular
269 ardioverter-defibrillator (ICD) therapy with cardiac resynchronization therapy with a defibrillator (
270 th clinical outcomes in patients who receive cardiac resynchronization therapy with a defibrillator (
271 y symptomatic heart failure (HF) who receive cardiac resynchronization therapy with a defibrillator (
272 This study aimed to evaluate the effect of cardiac resynchronization therapy with a defibrillator (
273 ere are limited data regarding the effect of cardiac resynchronization therapy with a defibrillator (
274 phology identifies patients who benefit from cardiac resynchronization therapy with a defibrillator (
275 omplete left-sided reverse remodeling due to cardiac resynchronization therapy with a defibrillator (
276 (single-chamber, 19.8%; dual-chamber, 41.3%; cardiac resynchronization therapy with a defibrillator [
277 In heart failure patients undergoing either cardiac resynchronization therapy with a defibrillator o
278 ons in India who had class I indications for cardiac resynchronization therapy with an ICD and were u
279 on delay) did not have clinical benefit from cardiac resynchronization therapy with defibrillator (CR
280 isk of heart failure (HF) or death comparing cardiac resynchronization therapy with defibrillator (CR
282 r ejection fraction (LVEF) super-response to cardiac resynchronization therapy with defibrillator (CR
283 outcome analysis that compared the effect of cardiac resynchronization therapy with defibrillator (CR
285 of patients with both conditions who receive cardiac resynchronization therapy with defibrillator (CR
287 of renal function on long-term outcomes with cardiac resynchronization therapy with defibrillator amo
288 428 patients at least 65 years old receiving cardiac resynchronization therapy with defibrillator fro
292 predicted outcomes; however, no benefit from cardiac resynchronization therapy with defibrillator was
293 older patients with heart failure receiving cardiac resynchronization therapy with defibrillator, di
294 enal function, derive long-term benefit from cardiac resynchronization therapy with defibrillator, wi
295 sk was further attenuated in the subgroup of cardiac resynchronization therapy with implantable cardi
296 205 patients with heart failure referred for cardiac resynchronization therapy with QRS >/=120 ms and
297 DIT-CRT) showed that early intervention with cardiac-resynchronization therapy with a defibrillator (
298 urces on receipt of a heart failure therapy, cardiac-resynchronization therapy with defibrillation (C
299 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy) with speckle-tracking
300 he hypothesis that an incremental benefit to cardiac resynchronization therapy would be gained by ech
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