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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 […]

74/Survival after cardiac resynchronisation therapy – An 18-year experience in the United Kingdom

F Leyva (Presenting Author) - Aston University, Birmingham, UK; A Zegard - Aston University, Birmingham, UK; O Okafor - Aston University, Birmingham, UK; J DeBono - Queen Elizabeth Hospital, Birmingham, UK; D McNulty - Queen Elizabeth Hospital, Birmingham, UK; A Ahmed - Aston University, Birmingham, UK; H Marshall - Queen Elizabeth Hospital, Birmingham, UK; D Ray - NHS Digital and Farr Institute, London, UK; T Qiu - Aston University, Birmingham, UK
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Published Online: Oct 3rd 2008 European Journal of Arrhythmia & Electrophysiology. 2019;5(Suppl. 1):abstr74
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Aims: Randomised, controlled trials have shown that cardiac resynchronisation therapy (CRT) prolongs survival in patients with heart failure (HF). No studies have explored survival after CRT in relation to individuals in the general population (relative survival, RS). We sought to determine observed and RS after CRT in a nationwide cohort undergoing CRT.

Methods and results: A national administrative database was used to quantify observed mortality for patients undergoing CRT. Relative survival (RS) was quantified using life tables. In 50,084 patients (age: 72.1 ± 11.6 years [mean ± SD]) undergoing with (CRT-D) (n=25,273) or without (CRT-P) defibrillation (n=24,811) over 8.8 years (median follow-up 2.7 years (interquartile range [IQR]: 1.3–4.8), expected survival decreased with age. Device type, male sex, ischaemic heart disease, diabetes and chronic kidney disease predicted excess mortality. In multivariate analyses, excess mortality (analogue of RS) was lower after CRT-D than after CRT-P in all patients (adjusted hazard ratio [aHR]: 0.80; 95% confidence interval [CI] 0.76–0.84) as well as in subgroups with (aHR:0.79;95% CI 0.74–0.84) or without (aHR:0.82;95% CI 0.74–0.91) ischaemic heart disease. A Charlson co-morbidity index (CCI) ≥3 portended a higher excess mortality (aHR: 3.04; 95% CI 2.76–3.34). RS was higher in 2015–7 than in 2009–11 (aHR:0.64;95% CI 0.59–0.69).

Conclusions: Reference RS data after CRT is presented. Sex, ischaemic heart disease, diabetes, chronic kidney disease and CCI were major determinants of RS after CRT. CRT-D was associated with a higher RS than CRT-P in patients with or without ischaemic heart disease. RS after CRT improved from 2009 to 2017.

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