Why the study?
Does ischaemic aetiology of heart failure worsen long-term clinical outcomes compared to non-ischaemic aetiology in patients undergoing cardiac resynchronisation therapy?
Cohort (n=119)
No
Does ischaemic aetiology of heart failure worsen long-term clinical outcomes compared to non-ischaemic aetiology in patients undergoing cardiac resynchronisation therapy?
Hazard Ratio: 2.698 (95% CI 1.092–6.667)
Absolute Event Rate: 34.6% vs 20.9%
p-value: p=0.032
Ischaemic aetiology of heart failure is an independent predictor of higher cardiovascular mortality and hospitalisation after CRT compared to non-ischaemic aetiology, despite similar short-term reverse remodelling benefits.
OBJECTIVE: To examine the impact of heart failure (HF) aetiology on long-term outcome after cardiac resynchronisation therapy (CRT). DESIGN: Prospective cohort study. SETTING: University hospital. PATIENTS: 119 patients (44% with ischaemic and 56% non-ischaemic aetiology) who underwent CRT. INTERVENTIONS: Clinical follow-up for 39 (24) months. MAIN OUTCOME MEASURES: Cardiovascular mortality, HF and cardiovascular hospitalisation were compared by Kaplan-Meier curves between the two groups, followed by Cox regression analysis for prognostic predictor(s). RESULTS: 41 (34%) patients died, in whom cardiovascular causes were identified in 32 (27%) patients. The ischaemic group had a higher cardiovascular mortality (log-rank chi(2) = 4.293, p = 0.038) and cardiovascular hospitalisation (log-rank chi(2) = 5.123, p = 0.024) when compared with the non-ischaemic group, though no difference was found in HF hospitalisation (log-rank chi(2) = 0.019, p = 0.892). At three months, left ventricular reverse remodelling occurred in 52% of the ischaemic group and 55% of the non-ischaemic group (chi(2) = 0.128, p = 0.720). By Cox regression analysis, ischaemic aetiology and absence of reverse remodelling at three months were independent predictors of cardiovascular mortality (HR = 2.698, p = 0.032; HR = 3.541, p = 0.030) and cardiovascular hospitalisation (HR = 1.905, p = 0.015; HR = 2.361, p = 0.004). Furthermore, these two factors had an incremental value in predicting cardiovascular mortality when compared with either alone (left ventricular reverse remodelling, log-rank chi(2) = 10.275 vs 6.311, p = 0.05; Ischaemic aetiology, log-rank chi(2) = 10.275 vs 4.293, p<0.05). CONCLUSION: Ischaemic aetiology of HF is an independent predictor of higher cardiovascular mortality and hospitalisation after CRT. This may implicate the progressive nature of coronary heart disease leading to a worse outcome despite similar short-term benefits of CRT.
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Zhang et al. (2008) conducted a cohort in Heart failure (n=119). Ischemic etiology vs. Non-ischemic etiology was evaluated on Cardiovascular mortality (HR 2.698, 95% CI 1.092-6.667, p=0.032).
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