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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 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy).
5 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy).
6 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy).
7 nts with normalized ejection fractions after cardiac resynchronization therapy.
8 a strong predictor of short-term response to cardiac resynchronization therapy.
9 implantable cardioverter-defibrillators and cardiac resynchronization therapy.
10 coronary sinus is the standard approach for cardiac resynchronization therapy.
11 patients with AF to maximize the benefits of cardiac resynchronization therapy.
12 a are accumulating on the benefit of HBP for cardiac resynchronization therapy.
13 r septal puncture is a feasible approach for cardiac resynchronization therapy.
14 for >=4 weeks; and no Class I indication for cardiac resynchronization therapy.
15 e improvement in LV pump function induced by cardiac resynchronization therapy.
16 zations and has implications for delivery of cardiac resynchronization therapy.
17 used for improved selection of patients for cardiac resynchronization therapy.
18 that this lead location should be avoided in cardiac resynchronization therapy.
19 e registry, and patients with versus without cardiac resynchronization therapy.
20 ns were confirmed in 5 patient responders to cardiac resynchronization therapy.
21 undle branch block may respond positively to cardiac resynchronization therapy.
22 CD) display a relatively limited response to cardiac resynchronization therapy.
23 e coronary sinus is the mainstay approach of cardiac resynchronization therapy.
24 tivation, which may predict poor response to cardiac resynchronization therapy.
25 te changes in RV function after temporary RV cardiac resynchronization therapy.
26 e role of intrinsic conduction in optimizing cardiac resynchronization therapy.
27 electrocardiographic selection criteria for cardiac resynchronization therapy.
28 ifferent in patients with and without active cardiac resynchronization therapy (-0.7 minutes [95% con
29 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy), 801 patients with an
30 ry sinus lead implant or with nonresponse to cardiac resynchronization therapy and a suboptimal LV le
31 ith a new atrial lead placement as part of a cardiac resynchronization therapy and defibrillator impl
32 e feasibility of implementation of AVNS in a cardiac resynchronization therapy and defibrillator syst
33 did not influence the safety profile of the cardiac resynchronization therapy and defibrillator syst
34 ence of implantable cardiac defibrillator or cardiac resynchronization therapy and ejection fraction.
35 venous anatomy for optimal implementation of cardiac resynchronization therapy and evaluation of left
36 ntly associated with long-term outcome after cardiac resynchronization therapy and had additive progn
37 to address this challenge including improved cardiac resynchronization therapy and imaging technologi
39 medication for left ventricular dysfunction, cardiac resynchronization therapy and revascularization
40 ization included impaired ejection fraction, cardiac resynchronization therapy, and institutional pra
41 of device monitoring, predicting response to cardiac resynchronization therapy, and the use of pacema
44 traventricular conduction delay treated with cardiac resynchronization therapy at our institution dur
46 ation, including those receiving concomitant cardiac resynchronization therapy between 2006 and 2010
47 e reverse remodeling observed in women after cardiac resynchronization therapy, but this does not exp
48 ce understanding of the working mechanism of cardiac resynchronization therapy by comparing animal ex
49 duced activation and intrinsic conduction in cardiac resynchronization therapy by evaluating the acut
50 We investigated the electric mechanisms of cardiac resynchronization therapy by performing detailed
52 rt disease and right bundle branch block, RV cardiac resynchronization therapy carried multiple posit
54 c separation (MES) would improve response to cardiac resynchronization therapy compared with standard
55 implantable cardioverter defibrillators, and cardiac resynchronization therapy, consistent with evolv
57 on fraction 25% to 45%, and not eligible for cardiac resynchronization therapy could participate.
58 d the quality of life (QOL) of patients with cardiac resynchronization therapy (CRT) and an implantab
59 d duration in echocardiographic responses to cardiac resynchronization therapy (CRT) and clinical out
60 linical trials have demonstrated benefit for cardiac resynchronization therapy (CRT) and implantable
61 onship between echocardiographic response to cardiac resynchronization therapy (CRT) and the risk of
62 dyssynchrony indices to predict response to cardiac resynchronization therapy (CRT) appears to vary
64 of mitral regurgitation (MR) reduction with cardiac resynchronization therapy (CRT) are complex, and
68 ricular (LV) pacing improves the efficacy of cardiac resynchronization therapy (CRT) compared with co
74 filling to the optimal hemodynamic effect in cardiac resynchronization therapy (CRT) during adjustmen
75 s with congestive heart failure eligible for cardiac resynchronization therapy (CRT) either do not re
76 e electromechanical substrates responsive to cardiac resynchronization therapy (CRT) from unresponsiv
78 phology and duration on the effectiveness of cardiac resynchronization therapy (CRT) has been usually
80 e effect of reverse remodeling on APD during cardiac resynchronization therapy (CRT) has not been det
83 hocardiographic predictors of response after cardiac resynchronization therapy (CRT) have largely inv
87 icacy, safety, and long-term prognosis after cardiac resynchronization therapy (CRT) in elderly patie
89 V) ejection fraction and clinical outcome to cardiac resynchronization therapy (CRT) in mild heart fa
90 uency ablation improves effectiveness of the cardiac resynchronization therapy (CRT) in nonresponders
91 e conflicting data regarding the efficacy of cardiac resynchronization therapy (CRT) in patients with
92 ed controlled trial evaluating the effect of cardiac resynchronization therapy (CRT) in patients with
95 trial (RAFT) study demonstrated that adding cardiac resynchronization therapy (CRT) in selected pati
105 extend to patients with previously implanted cardiac resynchronization therapy (CRT) is unknown.
107 ining the criteria for patient selection for cardiac resynchronization therapy (CRT) may improve its
110 this study was to investigate the impact of cardiac resynchronization therapy (CRT) on right ventric
111 vices included pacemakers (46%), ICDs (30%), cardiac resynchronization therapy (CRT) pacemakers (4%),
113 atory Heart Failure Trial) demonstrated that cardiac resynchronization therapy (CRT) reduced both mor
116 the left ventricular lead position (LVLP) on cardiac resynchronization therapy (CRT) response and cli
119 of prospective randomized clinical trials of cardiac resynchronization therapy (CRT) versus implantab
120 d- 1990s, a pacemaker-based treatment termed cardiac resynchronization therapy (CRT) was developed to
122 nt studies have cast doubt on the benefit of cardiac resynchronization therapy (CRT) with defibrillat
123 table cardioverter-defibrillators (ICDs), or cardiac resynchronization therapy (CRT) with pacing capa
124 ed the hypothesis that patient selection for cardiac resynchronization therapy (CRT) would be enhance
125 ials have established the average benefit of cardiac resynchronization therapy (CRT), but estimating
126 for optimal outcome in patients treated with cardiac resynchronization therapy (CRT), but the influen
127 myocardial substrate of patients undergoing cardiac resynchronization therapy (CRT), in particular i
150 t bundle branch block (LBBB) be treated with cardiac resynchronization therapy (CRT); however, one-th
153 The landmark trials of biventricular pacing (cardiac resynchronization therapy [CRT]) typically ran f
157 no survival benefit for patients undergoing cardiac resynchronization therapy defibrillator (CRT-D)
158 rade from VVIR stimulator (pacemaker, PM) to cardiac resynchronization therapy defibrillator (CRT-D).
159 anted implantable cardioverter defibrillator/cardiac resynchronization therapy defibrillator (hazard
160 vival outcomes in patients with an ICD and a cardiac resynchronization therapy defibrillator enrolled
161 e revision, replacement, upgrade, or initial cardiac resynchronization therapy defibrillator implant.
162 ization with a cardioverter-defibrillator or cardiac resynchronization therapy defibrillator implante
164 P% independently correlate with mortality in cardiac resynchronization therapy defibrillator patients
165 stem upgrade or an initial implantation of a cardiac resynchronization therapy defibrillator were ran
166 er implantable cardioverter defibrillator or cardiac resynchronization therapy defibrillator, New Yor
167 at women have better outcomes than men after cardiac resynchronization therapy-defibrillator (CRT-D)
168 eductions in left atrial volume (LAV) with a cardiac resynchronization therapy-defibrillator (CRT-D)
169 omized controlled trials have shown that the cardiac resynchronization therapy-defibrillator improves
170 than 20% of Medicare beneficiaries receiving cardiac resynchronization therapy defibrillators (CRT-D)
171 ices included 38 dual-chamber pacemakers, 17 cardiac resynchronization therapy defibrillators, and 2
172 men have been under-represented in trials of cardiac resynchronization therapy-defibrillators (CRT-D)
177 ; QRS, 181+/-25 ms; all mean+/-SD) underwent cardiac resynchronization therapy device implantation.
178 an implantable cardioverter-defibrillator or cardiac resynchronization therapy device, and were based
179 confirmed, AVNS software was uploaded to the cardiac resynchronization therapy device, tested, and op
182 ntable cardioverter-defibrillator (including cardiac resynchronization therapy devices) and were foll
183 implantable cardioverter-defibrillators, and cardiac resynchronization therapy devices, via the prema
184 ilure, and a QRS duration <120 milliseconds, cardiac resynchronization therapy did not improve clinic
185 We postulated that this effect might limit cardiac resynchronization therapy efficacy in patients w
186 e cardioverter defibrillator without or with cardiac resynchronization therapy enrolled in the Sensit
189 g implantable cardioverter-defibrillator and cardiac resynchronization therapy) for patients with hea
190 iovascular implantable electronic devices or cardiac resynchronization therapy, given the natural his
191 table cardioverter-defibrillators (ICDs) and cardiac resynchronization therapy (ICD-CRT) than in pati
192 DS AND Enrolled patients had dual chamber or cardiac resynchronization therapy ICDs, history of >/=1
193 diac defibrillator implant and 37% underwent cardiac resynchronization therapy implant) were compared
194 acteristics, QLV/QRS duration (QLV ratio) at cardiac resynchronization therapy implant, and data abou
196 evascularization, sex, diabetes, age, use of cardiac resynchronization therapy, implantable cardiover
197 , implantable cardioverter defibrillator and cardiac resynchronization therapy implantation, LVEF imp
201 on, atrioventricular conduction disease, and cardiac resynchronization therapy in 68 (46%), 56 (38%),
202 hood of a response to medical therapy and to cardiac resynchronization therapy in heart failure.
203 ow early after defibrillator implantation or cardiac resynchronization therapy in patients with chron
204 neficial in specific subpopulations, such as cardiac resynchronization therapy in patients with inter
205 o compare the effects of active and inactive cardiac resynchronization therapy in patients with sever
206 rk studies of antiarrhythmic drugs, ICD, and cardiac resynchronization therapy in the primary and sec
207 onal classes I/II with medical treatment (or cardiac resynchronization therapy), including 6 patients
209 ne of the reasons for patient nonresponse to cardiac resynchronization therapy is a suboptimal left v
212 dy demonstrates clinical feasibility of dual cardiac resynchronization therapy lead delivery to optim
213 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy (MADIT-CRT) and to cre
214 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy (MADIT-CRT) showed tha
215 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy (MADIT-CRT) study by Q
216 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy (MADIT-CRT) study.
217 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy (MADIT-CRT) Trial to d
218 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy (MADIT-CRT) trial who
219 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy (MADIT-CRT), patients
221 er Automatic Defibrillator Implantation With Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
222 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
223 er Automatic Defibrillator Implantation With Cardiac Resynchronization Therapy [MADIT-CRT]; NCT001802
225 ay optimization of biventricular pacemakers (cardiac resynchronization therapy) may maximize hemodyna
228 ith a cardiac implantable electronic device (cardiac resynchronization therapy or implantable cardiov
231 Data from a multicenter registry of 725 cardiac resynchronization therapy patients (median follo
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
236 iovascular implantable electronic device and cardiac resynchronization therapy programming strategies
241 MES-guided placement of the RV lead improves cardiac resynchronization therapy responders compared wi
243 in smaller hearts contributes to the better cardiac resynchronization therapy response in women.
247 omatic Defibrillator Implantation Trial With Cardiac Resynchronization Therapy], REVERSE [Resynchroni
248 omatic Defibrillator Implantation Trial with Cardiac Resynchronization Therapy) study patients with l
249 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 ith an indication for permanent pacemaker or cardiac resynchronization therapy that underwent LBBP fo
256 ioverter-defibrillator (ICD) with or without cardiac resynchronization therapy, the subcutaneous ICD
257 ted Left Ventricular Lead Placement to Guide Cardiac Resynchronization Therapy]), the LV lead was pos
258 mogeneous loading conditions, such as during cardiac resynchronization therapy, then triggers a rever
260 METHODS AND Forty consecutive patients with cardiac resynchronization therapy underwent intracardiac
264 reduction of left ventricular volumes after cardiac resynchronization therapy were most pronounced i
265 t failure management with medical as well as cardiac resynchronization therapy when indicated is an e
266 timulation (PNS) is a common complication of cardiac resynchronization therapy when left ventricular
268 omplete left-sided reverse remodeling due to cardiac resynchronization therapy with a defibrillator (
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 (single-chamber, 19.8%; dual-chamber, 41.3%; cardiac resynchronization therapy with a defibrillator [
275 In heart failure patients undergoing either cardiac resynchronization therapy with a defibrillator o
276 ons in India who had class I indications for cardiac resynchronization therapy with an ICD and were u
277 of patients with both conditions who receive cardiac resynchronization therapy with defibrillator (CR
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 renal function on long-term outcomes with cardiac resynchronization therapy with defibrillator amo
286 428 patients at least 65 years old receiving cardiac resynchronization therapy with defibrillator fro
290 predicted outcomes; however, no benefit from cardiac resynchronization therapy with defibrillator was
291 older patients with heart failure receiving cardiac resynchronization therapy with defibrillator, di
292 enal function, derive long-term benefit from cardiac resynchronization therapy with defibrillator, wi
293 ion to implantable cardiac defibrillators or cardiac resynchronization therapy with defibrillators de
294 sk was further attenuated in the subgroup of cardiac resynchronization therapy with implantable cardi
295 205 patients with heart failure referred for cardiac resynchronization therapy with QRS >/=120 ms and
296 DIT-CRT) showed that early intervention with cardiac-resynchronization therapy with a defibrillator (
297 urces on receipt of a heart failure therapy, cardiac-resynchronization therapy with defibrillation (C
298 r Automatic Defibrillator Implantation Trial-Cardiac Resynchronization Therapy) with speckle-tracking
299 he hypothesis that an incremental benefit to cardiac resynchronization therapy would be gained by ech