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Characterization and prognostic impact of ischemic etiology in heart failure with reduced left ventricular ejection fraction
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Abstract
Introduction and objectives
Ischemic heart disease is the cause of 50-60% of cases of heart failure with reduced left ventricular ejection fraction (HF-rEF). The impact of ischemic etiology on left ventricular ejection fraction (LVEF) improvement and prognosis remains unclear. Our main objective was to analyze the differential clinical profile between ischemic and non-ischemic etiology, as well as its medium-to-long term prognosis.
Methods
Prospective study of a cohort of patients with HF-rEF in real clinical practice. A comparative analysis was performed between patients with HF-rEF of non-ischemic etiology (Group 1) and ischemic etiology (Group 2). Clinical, analytical, echocardiographic and therapeutic variables were analyzed, and the medium-to-long term impact in terms of mortality and hospital readmissions for HF was evaluated.
Results
409 patients were analyzed. 276 patients (67.5%) had non-ischemic etiology and 133 patients (32.5%) had ischemic etiology. Group 2 was older (65.8±13.3vs70.8±10.3;p<0.001), more men (68.1%vs86.5%;p<0.001), higher prevalence of arterial hypertension (62.3%vs76.7%;p = 0.004), diabetes mellitus (38.8%vs67.7%; p<0.001), dyslipemia (52.4%vs82.7%;p<0.001), chronic kidney disease (34.4%vs56.4%;p<0.001), anemia (24.3%vs47.4%;p<0.001) and vascular comorbidity (25.7%vs54.9%;p<0.001) and lower prevalence of atrial fibrillation (56.2%vs44.4%;p = 0.025). In Group 2 there was a lower proportion of de novo HF (60.1%vs45.1%;p = 0.004) with longer HF evolution time (24.4±48.8vs61.5±89.3; p<0.001), a lower proportion of patients improving LVEF at follow-up (51.6%vs21.1%;p<0.001) and a higher baseline NTproBNP concentration [4463(IQR 1976-10431)vs5746(IQR 2336.5-13789);p = 0.039]. Regarding baseline treatment, in Group 1 there was a higher prescription of mineralocorticoid receptor antagonists (78.3%vs63.9%;p = 0.002) and less ICD implantation (6.5vs14.3%;p = 0.01), with no differences in the rest of the treatment. With a mean follow-up of 60 months, Group 2 had a higher readmission rate (39%vs50.3%;p<0.01) and higher HF mortality (26.8%vs41%;p<0.01), with differences from early stages.
Conclusions
Patients with HF-rEF of ischemic etiology associate a greater number of comorbidities, a lower percentage of de novo HF, longer time of HF evolution, lower percentage of LVEF improvement and higher baseline NTproBNP.
Oxford University Press (OUP)
Title: Characterization and prognostic impact of ischemic etiology in heart failure with reduced left ventricular ejection fraction
Description:
Abstract
Introduction and objectives
Ischemic heart disease is the cause of 50-60% of cases of heart failure with reduced left ventricular ejection fraction (HF-rEF).
The impact of ischemic etiology on left ventricular ejection fraction (LVEF) improvement and prognosis remains unclear.
Our main objective was to analyze the differential clinical profile between ischemic and non-ischemic etiology, as well as its medium-to-long term prognosis.
Methods
Prospective study of a cohort of patients with HF-rEF in real clinical practice.
A comparative analysis was performed between patients with HF-rEF of non-ischemic etiology (Group 1) and ischemic etiology (Group 2).
Clinical, analytical, echocardiographic and therapeutic variables were analyzed, and the medium-to-long term impact in terms of mortality and hospital readmissions for HF was evaluated.
Results
409 patients were analyzed.
276 patients (67.
5%) had non-ischemic etiology and 133 patients (32.
5%) had ischemic etiology.
Group 2 was older (65.
8±13.
3vs70.
8±10.
3;p<0.
001), more men (68.
1%vs86.
5%;p<0.
001), higher prevalence of arterial hypertension (62.
3%vs76.
7%;p = 0.
004), diabetes mellitus (38.
8%vs67.
7%; p<0.
001), dyslipemia (52.
4%vs82.
7%;p<0.
001), chronic kidney disease (34.
4%vs56.
4%;p<0.
001), anemia (24.
3%vs47.
4%;p<0.
001) and vascular comorbidity (25.
7%vs54.
9%;p<0.
001) and lower prevalence of atrial fibrillation (56.
2%vs44.
4%;p = 0.
025).
In Group 2 there was a lower proportion of de novo HF (60.
1%vs45.
1%;p = 0.
004) with longer HF evolution time (24.
4±48.
8vs61.
5±89.
3; p<0.
001), a lower proportion of patients improving LVEF at follow-up (51.
6%vs21.
1%;p<0.
001) and a higher baseline NTproBNP concentration [4463(IQR 1976-10431)vs5746(IQR 2336.
5-13789);p = 0.
039].
Regarding baseline treatment, in Group 1 there was a higher prescription of mineralocorticoid receptor antagonists (78.
3%vs63.
9%;p = 0.
002) and less ICD implantation (6.
5vs14.
3%;p = 0.
01), with no differences in the rest of the treatment.
With a mean follow-up of 60 months, Group 2 had a higher readmission rate (39%vs50.
3%;p<0.
01) and higher HF mortality (26.
8%vs41%;p<0.
01), with differences from early stages.
Conclusions
Patients with HF-rEF of ischemic etiology associate a greater number of comorbidities, a lower percentage of de novo HF, longer time of HF evolution, lower percentage of LVEF improvement and higher baseline NTproBNP.
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