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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.
28 septal deformation patterns were identified: LBBB-1=double-peaked systolic shortening (n=28); LBBB-2=
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
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
46 registry of high-volume centers, persistent LBBB after CoreValve Revalving System transcatheter aort
49 ts with LLk and 72 consecutive patients with LBBB, all without prior myocardial infarction or sternot
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.
59 nalysis showed that among 1000 patients with LBBB and chest pain, 929 would survive without major str
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
65 on fraction-matched control subjects without LBBB and no CAD (group B), and 10 normal control subject
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
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
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
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
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
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.
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
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
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
121 ) in patients with left bundle-branch block (LBBB), but the clinical impact of this testing strategy
124 t-IVT became shortened (NA by 7 +/- 3 s/min; LBBB by 9 +/- 4 s/min) and correlated with a fall in the
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
135 ar, the effects of left bundle branch block (LBBB), coronary artery disease (CAD), and total isovolum
137 ss I or II and ejection fraction </= 30% and LBBB derive substantial clinical benefit from CRT-D: a r
141 evelop a transient left bundle-branch block (LBBB) during exercise, but its prognostic significance i
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
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)
154 s patients with a QRSD 150 to 179 ms without LBBB had no improvement in survival with CRT-D, and thos
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
166 pulse conduction was significantly slower in LBBB+HF than in LBBB hearts (67+/-9 versus 44+/-16 ms, r
169 dian difference in CURE-SVD (range, 0-1) for LBBB-HF group versus narrow-QRS-HF group (-0.40; 95% con
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
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
184 ted with significantly larger scar size than LBBB is, and occlusion of a proximal LAD septal perforat
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
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
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.
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.
201 changes in ventricular activation induced by LBBB or CAD and is, by itself, a major determinant of pe
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
208 Patients without left bundle branch block (LBBB) or patients with smaller QRS duration (QRSd) respo
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
215 ection fraction was similar between RBBB and LBBB patients (24.9% vs. 25.0%; p = 0.98); however, RBBB
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
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
223 -CRT study, the clinical benefit of CRT-D in LBBB patients was not attenuated by prior history of IAT
227 and MBF reserve is homogeneously reduced in LBBB patients with left ventricular systolic dysfunction
229 eath was not significantly different between LBBB patients with or without history of IAT (HR: 0.50,
232 ve reperfusion therapy (13.6% vs. 2.6%) than LBBB patients without chest pain; they were also more li
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
244 for studies reporting raw data on new-onset LBBB post-TAVR and the need for PPI or mortality at 1-ye
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
257 LBBB and QRS duration less than 150 ms or no LBBB regardless of QRS duration, was associated with low
261 r small differences in age, exercise-induced LBBB remained associated with a higher risk of primary e
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
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
279 yses and inherent log-rank tests showed that LBBB was not associated with higher all-cause mortality,
288 1 with CAD (29 LBBB), and 60 without CAD (30 LBBB) were studied with echocardiography and cardiopulmo
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
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
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