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Ventricular fibrillation (VF) is characterized by rapid (>300 beats a per minute), irregular electrical activation with variable electrocardiographic waveforms that prevents coordinated myocardial contraction, resulting in immediate loss of cardiac output.1 It most commonly occurs in the context of coronary artery disease.2,3 Resuscitation efforts are critically time-dependent: with each minute of untreated VF, the survival rate declines […]

55/Prognosis of incidental left bundle branch block

A Zegard (Presenting Author) – Aston University, Birmingham, UK; O Okafor – Aston University, Birmingham, UK; J DeBono – Queen Elizabeth Hospital, Birmingham, UK; R Steeds – Queen Elizabeth Hospital, Birmingham, UK; L Hudsmith – Queen Elizabeth Hospital, Birmingham, UK; B Stegemann – Medtronic Inc, Maastricht, The Netherlands; A Jani – Queen Elizabeth Hospital, Birmingham, UK; H Marshall – Queen Elizabeth Hospital, Birmingham, UK; B Holloway – Queen Elizabeth Hospital, Birmingham, UK; Qiu – Aston University, Birmingham, UK; F Leyva – Aston University, Birmingham, UK
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Published Online: Oct 4th 2008 European Journal of Arrhythmia & Electrophysiology. 2019;5(Suppl. 1):abstr55
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Article

Background: Incidental LBBB (iLBBB) is a frequent cause for cardiology referrals. In such instances, there may be uncertainty as to its prognosis and need for clinical follow-up. Cardiovascular magnetic resonance (CMR) is the gold-standard for myocardial phenotyping.

Objectives: To determine the utility of CMR in the risk stratification of patients with iLBBB.

Methods: CMR was used to identify the myocardial phenotype of patients with iLBBB. We compared outcomes of patients with an iLBBB with (iLBBBCMR+) or without (iLBBBCMR–) an abnormal CMR scan with healthy controls as well as age- and sex-matched individuals in the general population (life tables).

Results: In patients with iLBBB (n=199, aged 62.9 ± 12.6 years (mean ± SD), CMR was abnormal in 136 (68.4%) and was attributed to ischaemic (30 [15.1%]), non-ischaemic (94 [47.2%]) causes, hypertension (24 [12.1%]) and aortic valve disease (7 [3.5%]). Over 4 (2.5–5.3) years (median [interquartile range]), iLBBBCMR+ had a higher risk of total mortality or major adverse cardiac events (adjusted hazard ratio [aHR]: 8.48, 95% confidence interval [C.I.] 2.56–28.1, p<0.001), total mortality (aHR: 4.96, 95% C.I. 1.44–17.1, p=0.011) and total mortality or heart failure hospitalisation (aHR: 7.75, 95% C.I. 2.31–26.0, p=0.001) compared with controls. iLBBBCMR- had a similar risk of all endpoints. iLBBBCMR- patients had a similar survival to controls and the general population.

Conclusions: Over two thirds of patients with a iLBBB had an abnormal myocardial phenotype on CMR. Outcomes in iLBBBCMR+ were poor. Survival in iLBBBCMR- was comparable to the general population.

 

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