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1 5% of subjects had left bundle-branch block (LBBB).
2  and patients with left bundle branch block (LBBB).
3 ight (RBBB) versus left bundle branch block (LBBB).
4 her complicated by left bundle-branch block (LBBB).
5 (MI) patients with left bundle-branch block (LBBB).
6 c HF patients with left bundle branch block (LBBB).
7 tients with LBBB or matched patients without LBBB.
8 rvedilol was seen in patients with CRT-D and LBBB.
9 %) developed RBBB, but no patients developed LBBB.
10 influence the mortality risk of TAVI-induced LBBB.
11 dle branch block (LBBB) versus those without LBBB.
12 een patients who did and did not develop new LBBB.
13  total of 233 patients (34.3%) developed new LBBB.
14  at AV delays of 40 ms was no different from LBBB.
15 7) were independent predictors of persistent LBBB.
16 th p < 0.001) compared with patients without LBBB.
17 MSI for detecting CAD in DCM with or without LBBB.
18 andard WMSI, particularly in the presence of LBBB.
19 sexes with LBBB, but not in patients without LBBB.
20 sponse to CRT-D therapy in patients with non-LBBB.
21 oximal LAD occlusions should cause RBBB, not LBBB.
22 roximal LAD septal perforator caused RBBB or LBBB.
23  better than QRS duration or the presence of LBBB.
24 t bundle-branch block (LBBB) and 308 had non-LBBB.
25 d more scar (2 [2-5] segments) compared with LBBB-1 and LBBB-2 (both 0 [0-1], P<0.05).
26 chronization therapy were most pronounced in LBBB-1 and worst in LBBB-3 patients.
27 ft ventricular free wall resulted in pattern LBBB-1.
28 septal deformation patterns were identified: LBBB-1=double-peaked systolic shortening (n=28); LBBB-2=
29                     In 24 canine hearts with LBBB (12 acute, 6 with heart failure, and 6 with myocard
30  (2 [2-5] segments) compared with LBBB-1 and LBBB-2 (both 0 [0-1], P<0.05).
31                This transformed into pattern LBBB-2 by additionally simulating septal hypocontractili
32 -1=double-peaked systolic shortening (n=28); LBBB-2=early systolic shortening followed by prominent s
33 population comprised 533 CRT-D patients with LBBB, 212 (40%) with complete left-sided reverse remodel
34 re 1281 (70%) with left bundle-branch block (LBBB), 228 (13%) with right bundle-branch block, and 308
35 g septal hypocontractility, and into pattern LBBB-3 by imposing additional left ventricular free wall
36  were most pronounced in LBBB-1 and worst in LBBB-3 patients.
37                                              LBBB-3 revealed more scar (2 [2-5] segments) compared wi
38 by prominent systolic stretching (n=34); and LBBB-3=pseudonormal shortening with less pronounced late
39 B, 5+/-2 versus 1+/-1; P=0.0004; NICD versus LBBB, 4+/-2 versus 1+/-1; P=0.001); (2) evidence of earl
40 ior or anterior fascicles: narrow QRS versus LBBB, 5+/-2 versus 1+/-1; P=0.0004; NICD versus LBBB, 4+
41 ents were performed in 22 dogs, 9 with acute LBBB, 7 with chronic LBBB combined with infarction (embo
42 nt, T or Q wave or left bundle branch block (LBBB) abnormalities between the prehospital and initial
43  LV pacing with short AV delay and intrinsic LBBB activation accurately predicted the optimal AV dela
44 traction pattern assessment to identify true LBBB activation provided important prognostic informatio
45 rain echocardiography (2DSE) may detect true LBBB activation.
46  registry of high-volume centers, persistent LBBB after CoreValve Revalving System transcatheter aort
47                         transient or absent) LBBB after TAVI with a balloon-expandable valve and its
48 pact of persistent left bundle-branch block (LBBB) after surgical aortic valve replacement.
49 ts with LLk and 72 consecutive patients with LBBB, all without prior myocardial infarction or sternot
50 th a lower mortality risk in both sexes with LBBB, although more pronounced among women.
51  mortality was 37.8% (n=88) in patients with LBBB and 24.0% (n=107) in patients without LBBB (P=0.002
52  were included in the study; 216 (43.5%) had LBBB and a QRSd >/=150 ms, 85 (17.1%) had LBBB and QRSd
53 ad LBBB and QRSd <150 ms, 92 (18.5%) had non-LBBB and a QRSd >/=150 ms, and 103 (20.8%) had non-LBBB
54 ith an improvement in survival in those with LBBB and a QRSD >/=180 ms (adjusted HR for death: 0.78;
55 95% CI: 0.68 to 0.91), but not in those with LBBB and a QRSD 150 to 179 ms (adjusted HR for death: 1.
56 in a community-based cohort of patients with LBBB and acute cardiopulmonary symptoms.
57                                         Both LBBB and CAD may do so by prolonging the total isovolumi
58 elf determined by the presence or absence of LBBB and CAD.
59 nalysis showed that among 1000 patients with LBBB and chest pain, 929 would survive without major str
60                          CRT-D patients with LBBB and complete left-sided reverse remodeling had a si
61 io, 3.79; confidence interval, 2.95-4.87 for LBBB and hazard ratio, 3.53; confidence interval, 2.14-5
62 d concentric remodeling), and 6 with chronic LBBB and heart failure (rapid pacing, LBBB+HF, and eccen
63                                           In LBBB and LBBB+HF animals, endocardial conduction was app
64                                              LBBB and NICD patients had similar right ventricular tot
65 on fraction-matched control subjects without LBBB and no CAD (group B), and 10 normal control subject
66                     Patients with persistent LBBB and no PPI at hospital discharge had a higher incid
67 ar synchrony) was observed for patients with LBBB and normal QRSd.
68 or the evaluation of the impact of new-onset LBBB and periprocedural PPI post-TAVR were sourced, resp
69 ated with better survival in both sexes with LBBB and QRS >/=130 ms, whereas there was no clear relat
70                         In patients with non-LBBB and QRS >/=160 ms, the hazard ratio for the primary
71 duration of 150 ms or greater, compared with LBBB and QRS duration less than 150 ms or no LBBB regard
72  of 150 ms or greater (20.9%), compared with LBBB and QRS duration of 120 to 149 ms (26.5%; adjusted
73 30.7%; HR, 1.34 [99% CI, 1.20-1.49]), and no LBBB and QRS duration of 120 to 149 ms (32.3%; HR, 1.52
74  of 150 ms or greater (38.6%), compared with LBBB and QRS duration of 120 to 149 ms (44.8%; adjusted
75 45.7%; HR, 1.16 [99% CI, 1.08-1.26]), and no LBBB and QRS duration of 120 to 149 ms (49.6%; HR, 1.31
76 ar mortality were lowest among patients with LBBB and QRS duration of 150 ms or greater (20.9%), comp
77 rd ratio [HR], 1.30 [99% CI, 1.18-1.42]), no LBBB and QRS duration of 150 ms or greater (30.7%; HR, 1
78 mission were also lowest among patients with LBBB and QRS duration of 150 ms or greater (38.6%), comp
79 ; adjusted HR, 1.18 [99% CI, 1.10-1.26]), no LBBB and QRS duration of 150 ms or greater (45.7%; HR, 1
80 ing CRT-D implantation in clinical practice, LBBB and QRS duration of 150 ms or greater, compared wit
81 then categorized as having either LBBB or no LBBB and QRS duration of either 150 ms or greater or 120
82 of 150 ms or longer compared with those with LBBB and QRS of 120 to 129 ms was similar between sexes
83                     Compared with women with LBBB and QRS of 120 to 129 ms, women with LBBB and QRS o
84 th LBBB and QRS of 120 to 129 ms, women with LBBB and QRS of 140 to 149 ms had a 27% lower mortality
85                                 Mortality in LBBB and QRS of 150 ms or longer compared with those wit
86                    REVERSE demonstrated that LBBB and QRS prolongation are markers of reverse remodel
87 ection fraction) was better in patients with LBBB and QRSd >/=150 ms (12 +/- 12%) than in those with
88  with LBBB and QRSd <150 ms (8 +/- 10%), non-LBBB and QRSd >/=150 ms (5 +/- 9%), and non-LBBB and QRS
89 -LBBB and QRSd >/=150 ms (5 +/- 9%), and non-LBBB and QRSd <150 ms (3 +/- 11%) (p < 0.0001).
90 Sd >/=150 ms (12 +/- 12%) than in those with LBBB and QRSd <150 ms (8 +/- 10%), non-LBBB and QRSd >/=
91 ad LBBB and a QRSd >/=150 ms, 85 (17.1%) had LBBB and QRSd <150 ms, 92 (18.5%) had non-LBBB and a QRS
92 nd a QRSd >/=150 ms, and 103 (20.8%) had non-LBBB and QRSd <150 ms.
93 al deformation pattern is characteristic for LBBB and results from intraventricular dyssynchrony.
94 ents (group A; 27.4%) developed a persistent LBBB and the remaining 594 (group B; 72.6%) did not.
95 as an independent predictor in both RBBB and LBBB and, in addition, in LBBB, QRS/STT angle and ST J-p
96 tudy patients with left bundle branch block (LBBB) and 0, 1, 2, or >/=3 comorbidities, including rena
97 M-34 with CAD (20 normal activation [NA], 14 LBBB) and 25 without CAD (15 NA, 10 LBBB)-were studied.
98 Of these, 1175 had left bundle-branch block (LBBB) and 308 had non-LBBB.
99 erized by isolated left bundle branch block (LBBB) and a history of progressive left ventricular (LV)
100 ects of associated left bundle branch block (LBBB) and coronary artery disease (CAD) on peak cardiac
101 locity and pressure, with native conduction (LBBB) and during biventricular pacing at atrioventricula
102 etween that during left bundle branch block (LBBB) and LV pacing, reflects optimal resynchronization,
103 ween patients with left bundle-branch block (LBBB) and normal QRSd and if synchrony improved during p
104 mpact of new-onset left bundle branch block (LBBB) and permanent pacemaker implantation (PPI) after t
105 hree patients with DCM, 48 with CAD (16 with LBBB), and 25 without CAD (10 with LBBB) were studied.
106 al of 111 patients with DCM, 51 with CAD (29 LBBB), and 60 without CAD (30 LBBB) were studied with ec
107 hic morphology was left bundle branch block (LBBB), and in 15, it was nonspecific intraventricular co
108             Compared with women with no BBB, LBBB, and intraventricular conduction defect were strong
109                              The t-IVT, CAD, LBBB, and QRS duration were univariate predictors of exe
110  pulse pressure) compared with atrial pacing-LBBB, and this improvement correlated with mechanical re
111 uggest that only a minority of patients with LBBB are ultimately diagnosed with acute myocardial infa
112 tion >/= 140 ms may warrant consideration in LBBB as an indication for further diagnostic evaluation
113 % ]; P=0.009) increase than BiV-Opt, against LBBB as reference; BiV-Opt and biventricular pacing at A
114                                   Persistent LBBB at hospital discharge was associated with a decreas
115 that patients with left bundle branch block (LBBB) be treated with cardiac resynchronization therapy
116 fect of evolving ST segment, T or Q waves or LBBB between serially obtained prehospital and hospital
117                           In comparison with LBBB, biventricular pacing at separately preidentified h
118                        Only among those with LBBB, both sexes had better survival with longer QRS dur
119 creased significantly in CRT-D patients with LBBB but not in non-LBBB patients.
120 V pacing reduced QRS duration by 21+/-10% in LBBB but only by 5+/-12% in LBBB+HF hearts.
121 ) in patients with left bundle-branch block (LBBB), but the clinical impact of this testing strategy
122 ated with better survival in both sexes with LBBB, but not in patients without LBBB.
123 reased with stress (NA by 4.7 +/- 2.7 l/min; LBBB by 4.0 +/- 2.3 l/min; all p < 0.001).
124 t-IVT became shortened (NA by 7 +/- 3 s/min; LBBB by 9 +/- 4 s/min) and correlated with a fall in the
125 raction </=35%, QRS duration >/=120 ms) with LBBB by ECG were prospectively included.
126                    Left bundle branch block (LBBB) causes left ventricular (LV) dyssynchrony which is
127 h acute myocardial infarction, regardless of LBBB chronicity, and that a significant proportion of pa
128 n 22 dogs, 9 with acute LBBB, 7 with chronic LBBB combined with infarction (embolization; LBBB plus m
129 low direction in heart failure patients with LBBB compared to those without LBBB during early but not
130 tal activation time (LVTAT) in patients with LBBB compared with heterogeneous activation sequences an
131                                Assessment of LBBB contraction pattern was superior to time-to-peak in
132   Two-thirds of patients (63%) had a typical LBBB contraction pattern.
133                         Absence of a typical LBBB contraction was independently associated with incre
134 al 4-chamber view determined whether typical LBBB contraction was present.
135 ar, the effects of left bundle branch block (LBBB), coronary artery disease (CAD), and total isovolum
136                         Most data pertain to LBBB delays.
137 ss I or II and ejection fraction </= 30% and LBBB derive substantial clinical benefit from CRT-D: a r
138  50.5 years of age on average at the time of LBBB diagnosis.
139 e achieved for patients with normal QRSd and LBBB during biventricular and LV pacing.
140 patients with LBBB compared to those without LBBB during early but not late diastole.
141 evelop a transient left bundle-branch block (LBBB) during exercise, but its prognostic significance i
142                                Use of strict LBBB ECG criteria was not independently associated with
143  IAT during follow-up in 1,264 patients with LBBB enrolled in the MADIT-CRT (Multicenter Automatic De
144 in-hospital survival of 29,585 patients with LBBB enrolled in the National Registry of MI 2 June 1994
145 RT-D patients with left bundle branch block (LBBB) enrolled in MADIT-CRT (Multicenter Automatic Defib
146 erter defibrillator-CRT in patients with non-LBBB, especially when the QRS duration is <160 ms.
147                                Patients with LBBB experienced a 25.3-mL/m(2) mean reduction in left v
148 stolic function in left bundle-branch block (LBBB)-failing hearts despite different electrical activa
149  and hemodynamics were obtained in dogs with LBBB-failing hearts during right atrial, LV, and BiV sti
150  prior conduction disturbances developed new LBBB following TAVI with a balloon-expandable valve, alt
151 d syndrome, including: 1) history of typical LBBB for >5 years; 2) LV ejection fraction (EF) >50%; 3)
152 with a suspected acute coronary syndrome and LBBB for urgent reperfusion therapy.
153      The latter 2 groups were defined as non-LBBB groups.
154 s patients with a QRSD 150 to 179 ms without LBBB had no improvement in survival with CRT-D, and thos
155 T-D, and those with a QRSD 150 to 179 ms and LBBB had only a modest improvement.
156 ors of all-cause mortality were TAVI-induced LBBB (hazard ratio [HR], 1.54; confidence interval [CI],
157 mong patients with left bundle branch block (LBBB) (hazard ratio [HR]: 0.58; p < 0.001) and no signif
158 t to patients with left bundle branch block (LBBB), heart failure patients with narrow QRS and nonspe
159  was significantly slower in LBBB+HF than in LBBB hearts (67+/-9 versus 44+/-16 ms, respectively), an
160 s optimal timing of LV stimulation in canine LBBB hearts.
161 ntional epicardial CRT in compromised canine LBBB hearts.
162 rker of diastolic mechanical dyssynchrony in LBBB hearts.
163                                  In LBBB and LBBB+HF animals, endocardial conduction was approximatel
164 l infarction than in eccentrically remodeled LBBB+HF hearts (19% versus 10%).
165 n by 21+/-10% in LBBB but only by 5+/-12% in LBBB+HF hearts.
166 pulse conduction was significantly slower in LBBB+HF than in LBBB hearts (67+/-9 versus 44+/-16 ms, r
167 hronic LBBB and heart failure (rapid pacing, LBBB+HF, and eccentric remodeling).
168 LBBB with tachypacing-induced heart failure (LBBB+HF, n=6).
169 dian difference in CURE-SVD (range, 0-1) for LBBB-HF group versus narrow-QRS-HF group (-0.40; 95% con
170  however, there was no sex difference in non-LBBB (HR: 0.95; 95% CI: 0.85 to 1.06; p = 0.37).
171 RT-D patients with left bundle branch block (LBBB) (HR: 0.51 [95% CI: 0.35 to 0.76], p < 0.001).
172 s effect on hearts with RBBB than those with LBBB (i.e., 5.5 +/- 1.1% vs. 29.5 +/- 5.0% increase in d
173 le, we describe the evolving epidemiology of LBBB in acute coronary syndromes and discuss controversi
174                                     Isolated LBBB in animals causes cardiac remodeling due to mechani
175 hanical dyssynchrony is induced by RBBB than LBBB in failing hearts, and the corresponding impact of
176 w-onset persistent left bundle branch block (LBBB) in patients undergoing transcatheter aortic valve
177  patients with non-left bundle branch block (LBBB; including right bundle branch block, intraventricu
178                    However, the existence of LBBB-induced cardiomyopathy in humans remains uncertain.
179 rvations support the existence of a specific LBBB-induced cardiomyopathy resolved by CRT.
180                                              LBBB, intraventricular conduction defect, and RBBB combi
181                                 TAVI-induced LBBB is an independent predictor of mortality.
182         Additionally, longer QRS duration in LBBB is associated with better survival in both sexes.
183                                 In contrast, LBBB is most commonly caused by nonischemic pathologies.
184 ted with significantly larger scar size than LBBB is, and occlusion of a proximal LAD septal perforat
185 tients develop new left bundle-branch block (LBBB), its effect on clinical outcome is unclear.
186 , and dyslipidemia, and had more often a non-LBBB (left bundle branch block) wide QRS complex, and lo
187 py candidates with left bundle branch block (LBBB)-like electrocardiogram morphology (left ventricula
188              It is unclear whether new-onset LBBB may also impact the prognosis of patients after tra
189 d with resynchronization pacemakers, 13 with LBBB (mean QRS, 171 ms) and 9 with normal QRSd <120 ms (
190 investigate whether the absence of a typical LBBB mechanical activation pattern by 2DSE was associate
191 t arrhythmias with left bundle-branch block (LBBB) morphology.
192                                      Not all LBBB-morphology EIVA can be dismissed, and not all RBBB-
193 2.73 [95% CI, 1.78 to 4.13]; P < 0.001), but LBBB-morphology EIVA was not (hazard ratio, 0.82 [CI, 0.
194          Inclusion of patients with isolated LBBB-morphology EIVA, which often is idiopathic, may con
195                                Patients with LBBB-morphology EIVAs had a mortality rate (2.5%) simila
196 o heart failure patients (narrow QRS [n=18], LBBB [n=11], NICD [n=23]) underwent 3-dimensional electr
197 ed dogs with acute left bundle-branch block (LBBB, n=10) and chronic LBBB with tachypacing-induced he
198 tion were compared among patients with RBBB, LBBB, nonspecific LV conduction delay, and QRS <120 ms.
199 ith STEMI or a new left branch bundle block (LBBB), of which 1,654 (60%) presented < or =12 hours.
200 all-cause 1-year mortality and (2) new-onset LBBB on the need for PPI at 1-year follow-up.
201 changes in ventricular activation induced by LBBB or CAD and is, by itself, a major determinant of pe
202 were acquired in heart failure patients with LBBB or matched patients without LBBB.
203 er reason, then categorized as having either LBBB or no LBBB and QRS duration of either 150 ms or gre
204  centers in Italy, we analyzed those without LBBB or pacemaker at admission (879 patients [82.9%]).
205 e the impact of (1) periprocedural new-onset LBBB or PPI post-TAVR on cardiac mortality and all-cause
206 ersistent ST-segment elevation as opposed to LBBB or Q waves.
207 mong patients with left bundle-branch block (LBBB) or longer QRS duration.
208   Patients without left bundle branch block (LBBB) or patients with smaller QRS duration (QRSd) respo
209       At rest, t-IVT was 8 s/min longer with LBBB (p < 0.001), was unaffected by CAD, and did not cor
210 h LBBB and 24.0% (n=107) in patients without LBBB (P=0.002).
211 ile range, 253-725) days in patients without LBBB (P=0.90).
212 ] index: 0.80 +/- 0.03 vs. 0.58 +/- 0.09 for LBBB, p < 0.04; CURE 0-->1 is dyssynchronous-->synchrono
213 ICD) were significantly (P < 0.001) lower in LBBB patients (0.47; P < 0.001) than in non-LBBB patient
214  LBBB patients (0.47; P < 0.001) than in non-LBBB patients (1.24; P = 0.257).
215 ection fraction was similar between RBBB and LBBB patients (24.9% vs. 25.0%; p = 0.98); however, RBBB
216                      Sixty-three symptomatic LBBB patients (group A), 10 left ventricular ejection fr
217 < 0.001) and no significant effect among non-LBBB patients (HR: 1.05; p = 0.82, p for the difference
218  CRT-D was significantly increased among non-LBBB patients (HR: 3.62; p = 0.002, p for the difference
219                                          Non-LBBB patients (n=537; 30%) were divided into 2 groups ba
220 ystolic volume index (P<0.0001), whereas non-LBBB patients had smaller decreases (6.7 mL/m(2); P=0.18
221 rams from the LV free wall were later in the LBBB patients in absolute terms (155 ms [SD 23] versus 6
222                                              LBBB patients typically demonstrated (1) a single LV bre
223 -CRT study, the clinical benefit of CRT-D in LBBB patients was not attenuated by prior history of IAT
224                                       In non-LBBB patients with a normal PR interval, implantation of
225                                       In non-LBBB patients with a prolonged PR interval, CRT-D treatm
226 ta support the use of CRT-D in MADIT-CRT non-LBBB patients with a prolonged PR interval.
227  and MBF reserve is homogeneously reduced in LBBB patients with left ventricular systolic dysfunction
228                                       In non-LBBB patients with normal PR, CRT-D therapy was associat
229 eath was not significantly different between LBBB patients with or without history of IAT (HR: 0.50,
230             Long-term survival was better in LBBB patients with QRSd >/=150 ms (p = 0.02), but this d
231 ctor (P=0.006) of SPECT perfusion defects in LBBB patients without CAD.
232 ve reperfusion therapy (13.6% vs. 2.6%) than LBBB patients without chest pain; they were also more li
233                               In contrast to LBBB patients, narrow QRS and NICD patients are characte
234 y increase subsequent arrhythmic risk in non-LBBB patients.
235 y in CRT-D patients with LBBB but not in non-LBBB patients.
236 tion fraction with CRT-D in LBBB than in non-LBBB patients.
237 vasodilator MCE and SPECT were undertaken in LBBB patients.
238 ger scar size than left bundle branch block (LBBB) patients do.
239                             Among those with LBBB, patients with a QRSD >/=180 ms had a greater adjus
240 nefit was larger in concentrically remodeled LBBB plus myocardial infarction than in eccentrically re
241 LBBB combined with infarction (embolization; LBBB plus myocardial infarction, and concentric remodeli
242 all discriminate effectively between LLk and LBBB populations.
243  well they discriminated between the LLk and LBBB populations.
244  for studies reporting raw data on new-onset LBBB post-TAVR and the need for PPI or mortality at 1-ye
245                                    New-onset LBBB post-TAVR is a marker of an increased risk of cardi
246                                    New-onset LBBB post-TAVR was associated with a higher risk of PPI
247              Nearly half of MI patients with LBBB present without chest pain.
248 onary syndrome and left bundle branch block (LBBB) present a unique diagnostic and therapeutic challe
249  benefit was observed in patients with a non-LBBB QRS pattern (right bundle-branch block or intravent
250 r in both RBBB and LBBB and, in addition, in LBBB, QRS/STT angle and ST J-point depression in aVL wer
251 tion 26+/-7%) with left bundle-branch block (LBBB; QRS duration 174+/-18 ms) were atriobiventricularl
252 th a fall in the QRS duration (NA: r = 0.87; LBBB: r = 0.91), and CO increased with stress (NA by 4.7
253 m follow-up of MADIT-CRT study patients with LBBB randomized to CRT-D, there were differences in HF o
254 nto left, right, and indetermined-type BBBs (LBBB, RBBB, and intraventricular conduction defect, resp
255                             In patients with LBBB receiving implantable cardioverter defibrillator-CR
256 RS duration and survival in patients without LBBB regardless of patient sex.
257 LBBB and QRS duration less than 150 ms or no LBBB regardless of QRS duration, was associated with low
258 n patients without left bundle branch block (LBBB) regardless of patient sex.
259 ere is no sex difference in patients without LBBB, regardless of QRS duration.
260                                          How LBBB-related effects on LV diastolic function may contri
261 r small differences in age, exercise-induced LBBB remained associated with a higher risk of primary e
262 chrony and impact of CRT in pure RBBB versus LBBB remains largely unknown.
263  hearts with acute left bundle branch block (LBBB) showed that endocardial left ventricular (LV) paci
264 inical composite score improved with CRT for LBBB subjects (odds ratio, 0.530; P=0.0034) but not for
265 odds ratio, 0.530; P=0.0034) but not for non-LBBB subjects (odds ratio, 0.724; P=0.21).
266                                   However in LBBB, systolic amplitude proved to be the only significa
267  increase in ejection fraction with CRT-D in LBBB than in non-LBBB patients.
268 after TAVI is higher in patients who develop LBBB than in patients who do not.
269                             In those without LBBB, the mortality difference was modest and did not di
270                             In patients with LBBB, there was a continuous relationship between broade
271 tion, (2) multiple left bundle-branch block (LBBB)-type VTs, and (3) an abnormal endocardial substrat
272 mmend that patients with new or presumed new LBBB undergo early reperfusion therapy, data suggest tha
273 ts with narrow QRS and NICD to patients with LBBB using high-density electroanatomic activation maps.
274 cardiac effects of left bundle-branch block (LBBB) using myocardial contrast echocardiography (MCE) t
275 ery wide QRSD with left bundle branch block (LBBB) versus those without LBBB.
276                                  In 52 of 66 LBBB VTs, the origin was from the RV perivalvular region
277                           On the other hand, LBBB was associated with a higher short-term rate of pac
278                                              LBBB was more frequent after implantation of the Medtron
279 yses and inherent log-rank tests showed that LBBB was not associated with higher all-cause mortality,
280                                    New-onset LBBB was observed in 61 patients (30.2%) after TAVI, and
281  90% sensitivity and 82% specificity whether LBBB was present or not.
282                                    New-onset LBBB was the only factor associated with PPI following T
283                    Left bundle branch block (LBBB) was present in 65 patients, right bundle branch bl
284 he mortality differences in patients without LBBB were attenuated in both sexes.
285 rom the cohort, 70 cases of exercise-induced LBBB were identified.
286                                Patients with LBBB were less likely to experience at least one VT/VF e
287               Those with RBBB (compared with LBBB) were more likely to have ischemic heart disease (7
288 1 with CAD (29 LBBB), and 60 without CAD (30 LBBB) were studied with echocardiography and cardiopulmo
289  (16 with LBBB), and 25 without CAD (10 with LBBB) were studied.
290 [NA], 14 LBBB) and 25 without CAD (15 NA, 10 LBBB)-were studied.
291 tients with a QRSD >/=180 ms with or without LBBB, whereas patients with a QRSD 150 to 179 ms without
292  associated with a higher rate of persistent LBBB, which in turn determined higher risks for complete
293 proach among clinically stable patients with LBBB who do not have electrocardiographic findings highl
294                                Patients with LBBB who experienced a first VTE had no change in the ri
295 y should be considered for all patients with LBBB who have symptoms consistent with MI.
296                          Among patients with LBBB who received CRT-D, mortality is lower in women tha
297 bundle-branch block (LBBB, n=10) and chronic LBBB with tachypacing-induced heart failure (LBBB+HF, n=
298 independent predictor of incident HF only in LBBB, with more pronounced risk at QRS >/= 140 ms than a
299 mong patients with left bundle branch block (LBBB), women had a 21% lower mortality risk than men (HR
300                          Among patients with LBBB, women receiving CRT-D had a lower relative death r

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