Decompensated Heart Failure with Mid-Range Ejection Fraction: Epidemiology and In-Hospital Mortality Risk Factors

Abstract

Background:

Recently, a new HF entity, with LVEF between 40-49%, was presented to comprehend and seek better therapy for HF with preserved LVEF (HFpEF) and borderline, in the means that HF with reduced LVEF (HFrEF) already has well-defined therapy in the literature.

Objective:

To compare the clinical-therapeutic profile of patients with HF with mid-range LVEF (HFmrEF) with HFpEF and HFrEF and to verify predictors of hospital mortality.

Method:

Historical cohort of patients admitted with decompensated HF at a supplementary hospital in Recife/PE between April/2007 - August/2017, stratified by LVEF (< 40%/40 - 49/≥ 50%), based on the guideline of the European Society of Cardiology (ESC) 2016. The groups were compared and Logistic Regression was used to identify predictors of independent risk for in-hospital death.

Results:

A sample of 493 patients, most with HFrEF (43%), HFpEF (30%) and HFmrEF (26%). Average age of 73 (± 14) years, 59% men. Hospital mortality 14%, readmission within 30 days 19%. In therapeutics, it presented statistical significance among the 3 groups, spironolactone, in HFrEF patients. Hospital death and readmission within 30 days did not make difference. In the HFmrEF group, factors independently associated with death were: valve disease (OR: 4.17, CI: 1.01-9.13), altered urea at admission (OR: 6.18, CI: 1.78-11.45) and beta-blocker hospitalization (OR: 0.29, CI: 0.08-0.97). In HFrEF, predictors were: prior renal disease (OR: 2.84, CI: 1.19-6.79), beta-blocker at admission (OR: 0.29, CI: 0.12-0.72) and ACEI/ ARB (OR: 0.21, CI: 0.09-0.49). In HFpEF, only valve disease (OR: 4.61, CI: 1.33-15.96) and kidney disease (OR: 5.18, CI: 1.68-11.98) were relevant.

Conclusion:

In general, HFmrEF presented intermediate characteristics between HFrEF and HFpEF. Independent predictors of mortality may support risk stratification and management of this group.

Keywords:
Heart Failure/physiopatology; Stroke Volume/physiology; Prognosis; Hospital Mortality; Epidemiology

Introduction

Heart failure (HF) is a clinical syndrome with high global prevalence, responsible for elevated mortality and readmission rates.¹ It is often categorized according to left ventricular ejection fraction (LVEF), historically defined as heart failure with reduced ejection fraction (HFrEF) and heart failure with preserved ejection fraction (HFpEF). Unlike HFrEF, whose therapy in terms of mortality reduction has been well-defined, HFpEF remains a syndrome that still poses diagnostic challenges, with no well-established treatment.² Most HFrEF clinical trials have included patients with EF < 35-40%, whereas HFpEF trials used EF > 50%, EF > 45% or EF > 40% as inclusion criteria. Other HF studies reported, within large populations, a broad proportion of patients with mid-range LVEF, between 40-50% still poorly characterized.^1-4

In 2013, the American Heart Association (AHA)⁵ proposed in its guidelines the inclusion of a new group, HF with borderline EF (EF: 41-49%). Recently, the European Society of Cardiology guidelines has emphasized this new classification, recognizing a new entity of HF with mid-range ejection fraction (HFmrEF), defined as the presence of signs and symptoms of heart failure, EF: 40-49%, elevated natriuretic peptides levels and at least 1 additional criterion: structural heart disease and/or diastolic dysfunction.⁶ Until now, there is no consensus on the most appropriate LVEF cut-off to differentiate the HF groups or the prognosis and the real benefits of the treatment in this particular group of HF with mid-range ejection fraction. In view of such a scenario, the objective of this study was to identify and compare the clinical and therapeutic profile of HF patients, stratifying them by LVEF, according with the 2016 European Society of Cardiology (ESC) guidelines, and to identify specific independent predictors of in-hospital mortality in each group.

Methods

Retrospective hospital-based cohort of patients admitted to a reference hospital of the Supplemental Healthcare System, in Recife/PE, between April 2007 and August 2017.

The sample included patients admitted with a diagnosis of decompensated heart failure, aged over 18 years, who had been hospitalized for at least 24 hours, in functional classes III and IV, according to the New York Heart Association (NYHA) functional classification⁷ and who had undergone echocardiography at the service or had recent echocardiographic data available (obtained within less than 3 months), including a description of the LVEF.

Based on the guideline of the European Society of Cardiology (ESC) 2016⁶ and on the Brazilian guidelines published in 2018,⁸ patients were divided into 3 distinct groups of HF, according to LVEF on echocardiogram: HFrEF (EF<40%), HFmrEF (EF: 40 - 49%) and HFpEF (≥ 50%).

LVEF was calculated by echocardiography, using the Teichholz’ M-mode volume method, or the modified Simpson’s formula for measurement of LV end-systolic and end-diastolic diameter, in the 4-chamber apical plane, in accordance with current guidelines, all performed in the echocardiography sector of the hospital.⁹

Data collection included hospital admission data, in-hospital mortality data and readmission within 30 days. The information were obtained from the consultation of medical records and complemented, whenever necessary, by contact with the assisting physician. A structured questionnaire was chosen as data collection instrument, including demographic and clinical variables, clinical exam at admission, complementary exams and the treatment adopted. The outcome of interest was in-hospital mortality.

The etiology of HF and the cause of decompensation were defined by the assistant physician on medical report. Ischemic, hypertensive, valvular, idiopathic, and other etiologies (lower proportion group or with no confirmed diagnosis by the assistant physician) were investigated.

Some continuous variables were changed into categories for analytical purposes;¹⁰ age (< 65 and ³ 65 years), systolic blood pressure (SBP < 115 mmHg and ³ 115 mmHg), heart rate (£ 80 bpm and > 80 bpm), serum creatinine (altered: > 1,3 mg/dl men and > 1,1 mg/dl women), plasma sodium (altered: < 130 mEq/l) and urea (altered: ³ 92 mg/dl). The presence of anemia was defined, according to the WHO criteria (Hb < 13.0 g/dL in men and Hb < 12.0 g/dL in women).¹¹

Statistical Analysis

Demographic and clinical characteristics of patients were analyzed using descriptive statistics: mean and standard deviation (SD) for quantitative variables and absolute and relative frequencies for qualitative variables. Data normality was verified using the Kolmogorov-Smirnov test. To compare the LVEF groups, in relation to the qualitative variables, the Qui-square test was utilized, and, for quantitative variables, analysis of variance methodology was used for normal distribution, Kruskal-Wallis test for not normal. Bivariate analysis, using Pearson’s Chi-square, was carried out as a strategy to assess the relation between the outcome (in-hospital death) and the independent variables, studied for each group individually. All variables related to in-hospital death with a p value < 0.20 in the bivariate analysis were considered for inclusion in multiple logistic regression model. The stepwise forward method was used to select the final model. Once the final model was chosen, calibration was assessed using Hosmer Lemeshow›s goodness of fit test. The IBM SPSS Statistics for Windows (Version 21.0. Armonk, NY: IBM. Corp.) software was used to perform statistical analysis. The level of significance assumed was 5%.

The research project was approved by the Ethics Committee in Research of the Catholic University of Pernambuco UNICAP/PE (CAAE: 70897517.8.0000.5206). The study was conducted in accordance with the principles of the Declaration of Helsinki.

Results

A sample of 599 patients was collected between January 2007 and March 2017. Out of these, 106 did not have any LVEF data available and were not included in the analysis. A total of 493 patients fulfilled the inclusion and exclusion criteria of the study.

From the sample studied, most HF individuals (43%) were classified with LVEF < 40%, followed by 30% of with LVEF ≥ 50% and 26% with LVEF 40-49%. The age of the patients varied from 20 to 99 years, with a mean of 73 (SD = 14) years, 370 (75%) were 65 years old or more, with men accounting for the majority of them (59%), Functional Class (FC) IV (52%), ischemic etiology (52%), followed by hypertensive (19%) and idiopathic (9%) etiologies. The outcome in-hospital death was 14% of the sample. Nineteen percent of patients were readmitted within 30 days.

Among the most frequent comorbidities found, we can highlight: systemic arterial hypertension (SAH) in 87% of patients; diabetes mellitus (DM) in 51% and coronary insufficiency (CI) in 59%. In a comparative analysis, the groups were significantly distinct with regard to SAH and CI, being more frequent in HFmrEF patients; valve disease and alcoholism were more common in HFpEF and HFrEF, respectively. The main cause for decompensation was acute coronary syndrome - ACS (38%), followed by infection (33%) and arrhythmia (atrial fibrillation). In relation to pharmacological therapeutics during hospitalization, the use of beta-blockers was observed in 73% of patients, angiotensin converting enzyme inhibitors (ACEi) / angiotensin II receptor blockers (ARB) in 68% and aldosterone receptor antagonist spironolactone in 42%.

When the three groups were comparatively analyzed (Table 1), HFpEF and HFmrEF patients were older, with a prevalence of female patients, compared to the HFrEF group, which had a prevalence of males (68%). Ischemic and idiopathic etiologies were observed in a higher percentage of HFrEF and HFmrEF patients, whereas the hypertensive and valve etiologies were more frequent among those with HFpEF. ACS was the main cause for decompensation, being more frequent in HFmrEF (46%), followed by HFrEF (39%). Hypertension and CI were more prevalent among HFmrEF patients (93% and 67%, respectively), whereas valve disease accounted for a higher proportion in HFpEF, and alcoholism in the HFrEF and HFmrEF groups.

Table 1
Comparison of groups in relation to demographic, clinical, therapeutic, laboratory and outcome variables

Variables	Total	LVEF			p
		< 40%	40 – 49%	≥ 50%
Age – Mean (SD)	42.9 (13.6)	70.3 (14.4)+/++	75.2 (12.4)	74.6 (12,9)	0.003*
Age ≥ 65 years (%)	75.2	67.6	80.6	81.3
Male (%)	58.6	67.8	58.9	45.3	< 0.001*
FC IV (%)	52.3	55.3	52.4	47.9	0.392
Etiology (%)					< 0001*
Ischemic	52.3	57.1	56.3	41.8
Hipertensive	19.5	11.3	18.0	32.9
Idiopathic	8.6	10.4	11.7	3.4
Valve	11.5	8.0	10.2	17.8
Others	8.0	13.2	3.9	4.1
ACS-HF (%)	38.0	38.8	45.7	30.2	0.028*
Comorbidities
DM	50.7	44.9	58.1	52.7	0.050
SAH	87.2	82.7	93.8	88.0	0.011*
IC	58.6	60.7	67.4	48.0	0.003*
Valve disease	10.3	6.1	10.1	16.7	0.005*
Kidney disease	34.5	36.0	34.9	32.0	0.729
COPD/Asma	19.5	21.0	17.1	19.3	0.666
Neoplasia	8.1	5.1	10.9	10.0	0.103
Alcoholism	18.3	22.4	20.2	10.7	0.014*
Smoking	20.1	22.4	20.2	16.7	0.401
SBP (mmHg) – Mean (SD)	136.3 (31.8)	128.5 (27.9)+/++	139.2 (31.9)	145.0 (34.4)	< 0.001*
HR (bpm) – Mean (SD)	87,4 (20.8)	87.9 (21.6)	88,4 (20.6)	85.9 (19.6)	0.557
AF (%)	22.8	20.5	19.7	28.8	0.144
EDD – Median (P25 – P75)	58 (50-65)	65 (58 - 70)+/++	55 (52 – 62)+++	47 (45 – 85)	< 0.001*
SPAP - Median (P25 – P75)	46 (39-57)	45 (40 – 56)	42 (37 – 56)	48 (42 – 59)	0.870
Moderate/severe MR (%)	47.9	55.2	56.1	30.3	< 0.001*
Moderate/severe TR (%)	22.6	25.9	23.8	16.7	0.128
Increased RV (%)	19.6	30.2	12.9	11.0	< 0.001*
LVEF – Mean (SD)	43.2 (14.3)	30.2 (6.6)	44.4 (2.7)	60.7 (7,3)	-
Sodium Ad – Mean (SD)	137.2 (5.8)	137.6 (5.5)	137.1 (5.9)	136.7 (6.2)	0.387
Urea Ad – Mean (SD)	64.9 (39.6)	68.5 (42.9)	64.7 (40.7)	60.1 (32.6)	0.141
Creatinine Ad – Mean (DP)	1.5 (0.9)	1.4 (0.8)	1.4 (0.9)	1.5 (1.1)	0.681
Hb Ad – Mean (SD)	12.2 (2.3)	12.6 (2.3)+/++	11.9 (1.9)	11.8 (2.2)	0.002*
BNP Ad Median (P25–P75)	6,000	7,249	8,421	2,827	0.015*
	(2,769-15,927)	(3,473-19,610)+/++	(5,304-22,352)+++	(1,685-6,285)
B-blocker (%)	73.3	77.8	72.9	67.1	0.076
ACEi /ARB (%)	66.5	69.2	64.3	68.7	0.626
Digoxin (%)	22.0	28.6	17.2	16.8	0.008*
SPIR (%)	41.7	52.8	38.8	28.2	< 0.001*
In-hospital death (%)	14.0	18.2	12.4	12.0	0.173
Readmission within 30 d (%)	19.2	19.9	22.1	15.7	0.498

• ^*
  Statistically significant (p < 0.05);
• ⁺
  Statistically significant difference between G1 (< 40%) and G2 (40-49%);
• ⁺⁺
  Statistically significant difference between G1 (< 40%) and G3 (≥ 50%);
• ⁺⁺⁺
  Statistically significant difference between G2 (40-49%) and G3 (≥ 50%); A: p-value derived from ANOVA; χ: p-value derived from Pearson's Chi-Square test; K: p-value derived from Krukal-Wallis test.

In relation to systolic blood pressure (SBP) at admission, the values were lower in patients with HFrEF. As to heart rate (HR) and NYHA functional class VI, there were no statistical differences between the categories of HF.

With regard to the laboratory variables, the groups were distinct in terms of natriuretic peptides (NT-ProBNP) levels and anaemia, which were higher among patients with HFrEF and HFmrEF. LV end-diastolic diameter (LVEDD) values were higher among HFrEF patients compared to HFpEF patients. Moderate to severe mitral regurgitation (MR) was commonly observed in HFrEF and HFmrEF.

In-hospital pharmacological treatment of patients with DHF is presented in Chart 1. Beta-blockers, ACEi/ARB and Spironolactone were used in 78%, 69% and 53% of HFrEF patients, respectively. However, statistical significance was only observed in the Spironolactone variable, which is more commonly used in patients with HFrEF. No statistical difference was observed between the groups in terms of in-hospital death and readmission within 30 days.

Chart 1
Sample distribution, according to the drug administered during hospitalization.

According to the bivariate analysis, the variables that presented a significant association with in-hospital death for patients with HFrEF were: advanced age, valve disease, kidney disease, peripheral vascular disease (PVD), urea, aneamia, beta-blocker and ACEi/ARB; for HFmrEF: kidney disease, urea at admission, aneamia and beta-blocker; and for HFpEF: kidney disease, PVD and creatinine at admission.

The independent risk factors obtained by multivariate analysis for in-hospital death are shown in Table 2. In the worst outcomes, previous kidney disease was associated with HFrEF and HFpEF. Previous valve disease was related to HFmrEF and HFpEF, and increased urea levels, exclusively in HFmrEF. The use of medication, such as beta-blockers and ACEi/ARB, were associated with a better evolution in HFmrEF and HFrEF, respectively.

Table 2
Results of Multivariate analysis for the in-hospital death outcome – p-value

Variables	EF < 40%	P-value	EF 40 – 49%	P-value	EF ≥ 50%	p-value
	OR (CI95%)		OR (CI95%)		OR (CI95%)
Sex - Male	-	-		0.373	-	-
Age ≥ 65 years		0.087	-	-		0.182
FC IV		0.223		0.090	-	-
Etiology	-	-		0.768	-	-
IC PR	-	-		0.494	-	-
Valve disease PR		0.084	4.17 (1.01-9.13)	0.047	4.61 (1.33-15.96)	0.016
Kidney disease PR	2.84 (1.9-6.79)	0.019		0.192	5.18 (1.68-11.98)	0.004
COPD/Asma PR		0.724	-	-	-	-
PVD PR		0.120	-	-		0.049
Sodium ALT		0.974		0.199	-	-
Urea ALT		0.914	6.18 (1.78-11.45)	0.004		0.911
Creatinine ALT	-	-	-	-		0.412
Aneamia		0.222		0.274	-	-
BB INT.	0.29 (0.12-0.72)	0.008	0.29 (0.08-0.97)	0.045	-	-
ACEi/ARB INT.	0.21 (0.09-0.49)	0.001	-	-	-	-
SPIR. INT		0.260		0.182	-	-
Furos. INT		0.068		0.077	-	-

• Note: OR: odds ratio; CI95%: 95% confidence interval.

It is worthy to highlight that HFrEF was associated with higher in-hospital mortality rates in patients with previous kidney disease (Odds Ratio (OR): 2.84, CI:1.19-6.79) and showed a 3.5 higher risk of in-hospital death for patients under no beta-blocker therapy and an almost 5 times higher risk for those under no treatment with ACE inhibitors or ARBs. HFmrEF was associated with higher in-hospital mortality rates for valve disease (OR: 4.17, CI: 1.01-9.13) and to altered levels of urea at admission (OR:6.18, CI:1.78-11.45), and the likelihood of death increased by 3.5 times in patients under no beta-blocker therapy. In relation to HFpEF patients, there was an association with valve disease (OR: 4.61, CI: 1.33-15.96) and kidney disease (OR: 5.18, CI: 1.68-11.98).

Discussion

Clinical Profile

The ICD¹² classification is already well-defined, and its categorization according to LVEF measured by echocardiography is used to characterize the syndrome clinically and, particularly, to orientate the treatment. LVEF through echocardiography is considered easy to perform, of lower cost and can be applied at the bedside, when necessary. However, there are several limitations concerning its estimation, both technical (dependent observer, two-dimensional evaluation, intra- and inter-observer variability and inadequate acoustic window) and non-technical (mitral regurgitation, aortic stenosis, arrhythmias, myocarditis and Takotsubo syndrome), which may generate inaccurate measurements.¹³ Cardiac magnetic resonance imaging is considered the gold standard for assessing left ventricular (LV) systolic function,¹⁴ but it is not easily available in daily clinical practice. Although echocardiography does not seem to be the ideal method, it remains a practical and accessible tool for estimation of LVEF and the choice exam in all studies that have focused on HF treatment so far.^15-17 It is worthy to note that classifying HF patients is more complex than simply stratifying them by LVEF cut-off values because these patients have a high burden of cardiovascular and non-cardiovascular comorbidities, which may interact on different levels of LVEF, and may influence prognosis more than the LVEF category.

There was a discrete predominance of patients with HFrEF at this institution, in consonance with previous studies, which indicates that the profile of supplemental health care patients is pretty much similar to those from international registries¹⁰ and that it differs from Brazilian data when HFmrEF reaches the absolute majority.¹⁸ The predominance in our study of older individuals with ischemic etiology is also compatible with data from developed countries.^19-21 In-hospital death, which occurred in 14% of the population studied, is in accordance with data from the Brazilian registry of acute HF patients admitted to public and private hospitals.¹⁸

Twenty-six percent of the population presented HFmrEF, which corroborates the estimated range, from 10-20%, in recent studies.^22,23 These patients were aged over 65 years (80%), with a higher proportion of females, similarly to the HFpEF profile. As for ischemic etiology, HFmrEF had a prevalence of 56 % and was closer in value to the HFrEF group. Hypertensive etiology showed intermediate values in relation to the other two groups.

DHF associated with ACS was more prevalent among HFmrEF patients (46%) compared to those from the other two groups. In Brazil, recent data have shown that the main cause of DHF is poor medication adherence;¹⁸ other studies presented different results.²³ Data from OPTIMIZE-HF,²⁴ a comprehensive European registry, were consistent with those reported in this study, which can be justified by differences between the profile and data of the population seen at supplemental health system and in the public health system.

HFmrEF presented with high comorbidity rates, such as diabetes mellitus, hypertension, IC and MI, and showed intermediate values for valve disease, kidney disease and alcoholism. It is also interesting to stress that left ventricular end-diastolic diameter values were intermediate, which indicates a possible transition stage between the other two HF groups. The similarities between HFmrEF and HFpEF suggest that HFmrEF may represent recovered or early stages of HFrEF,^25,26 but other long-term echocardiographic follow-up studies in these patients are needed.

Mortality and Prognostic Factors

In-hospital mortality in HFmrEF was similar in absolute values to HFpEF but lower than HFrEF, although the study has no sufficient statistical power to prove this difference. The same pattern was observed in hospital readmission rates. The “benignity” of HFpEF has been documented in the literature.²⁷ Data from the OPTIMIZE registry have shown lower in-hospital mortality rates in HFpEF patients. Nevertheless, the criterion adopted in this study was HFpEF (EF ≥ 40%),²⁸ and thus included those patients currently classified as HFmrEF, which poses limitations to comparisons. A meta-analysis involving over 60,000 patients reported lower mortality in HFpEF (EF ≥ 50%) compared to HFrEF. However, the evaluation itself does not make a distinction between outpatients or patients with DHF, which may influence the outcomes.²⁹ Only a handful of published studies have focused on patients with HFmrEF which, comparable to the sample of this study, have shown an intermediate group with mortality rates similar to those in the other HF groups.³⁰ Consequently, the population data shown is this report are consistent with recently published studies that used data from hospitalized patients.³⁰ When the outcomes were analyzed, after the one-year follow-up evaluation, including death by any cause and admission due to HF, there were similarities between HFmrEF and HFpEF, with HFrEF patients presenting the worst prognosis.³¹ It was not possible to establish comparisons with national data due to the scarcity of publications.

In general, heart failure mortality prediction scores have limited accuracy.¹⁰ The BIOSTAT-CHF³² emerged as a comprehensive European program designed to develop and validate risk prediction models, in an attempt to minimize this problem. The authors highlighted the small percentage of models validated in a separate cohort and the fact these models performed only moderately (c-statistic values 0.71 and 0.63 for mortality and HF hospitalization, respectively). Using a multivariable model (249), they found that the strongest predictors of mortality were urea and serum sodium. It is interesting to highlight that there was no significant difference between patients with acute or chronic HF. An LVEF cut-off of 45% was used to distinguish HFrEF from HFpEF, and no similarities were found between the risk factors of the population studied and the validation cohort, which has also included a small percentage of patients with an LVEF greater than 45%. The LVEF cut-off adopted may be a limiting factor for extrapolation of any findings to the HFmrEF group.³²

A recent Swedish HF registry has reported that chronic kidney disease is a strong predictor of mortality in both HFmrEF and HFrEF patients.³³ However, in the population assessed here, renal involvement, whether due to previous kidney disease or to increased urea at admission, was the only mortality predictor that revealed similarities between the 3 HF groups. Similarly, urea has been strongly associated to in-hospital death risk in traditional scores, such as BIOSTAT³² and ADHERE.¹⁰ The persistence of urea in all these models indicates its prognostic strength. Thus it should be the object of more attention by those who monitor patients with HF, due to the higher death risk among HFmrEF individuals (6 times more), for instance. It is possible to suggest that the presence of valve disease as a factor of worse prognosis in HF patients with LVEF greater than 40% indicates that it could be the etiology of heart failure. At the same time, it involves clinical characteristics and challenges, especially among the elderly population, due to the small number of randomized clinical trials. Consequently, treatment is also less well established.

It is necessary to highlight the efficacy of medication, since recent international publications, as observed by this study, originally in Brazil, have demonstrated significant benefits of beta-blockers both in HFrEF³² and HFmrEF,³⁴ thus suggesting benefits in all HF patients with an ejection fraction less than or equal to 49%. This fact has not been registered in randomized clinical trials which have included exclusively patients with systolic HF.^17,35 A recent meta-analysis involving 11 randomized studies and over 14,000 patients on the use of beta-blockers has confirmed their benefits in patients with EF < 50% and sinus rhythm.³⁶ As for ACEI/ARB, it is important to point out that the results only remained among HFmrEF patients, with a 5 times increased mortality among those who did not receive the medication. In the OPTIMIZE-HF registry, although the use of ACEI/ARB has been associated with less mortality and hospital readmission within 30- and 90-days in HFrEF patients, such benefit has not been observed among the HFmrEF and HFpEF groups.²⁸ In a subanalysis of CHARM, the benefit of candesartan was also seen in patients with HFmrEF.³⁷ Furthermore, in spite of the results of the TOPCAT trial, studies have found benefits of spironolactone in patients with EF between 45-49%,³⁸ which was not observed in this study's population. Therefore, HFmrEF signals a transition behavior or a “gray area” in which a better characterization of this group may soon bring prognostic and therapeutic benefits.

Limitations

The study is based on patients with a clinical picture of decompensated heart failure, and their physical and laboratory variables were collected at admission on a database. Thus information was collected retrospectively. Other potentially relevant variables, such as natriuretic peptide levels, were not selected in the multivariate model because data was not available in all patients.

Conclusion

The demographic/clinical profiles of HFmrEF are intermediate, between those of HFpEF and HFrEF. Kidney disease was the only risk factor for death in HFrEF and HFpEF, whereas valve disease and increased urea levels were associated with HFmrEF. The use of ACEI/ARB and beta-blockers, already established as mortality reducing drugs in HFrEF, has been independently related to better evolution in this HF group. The benefits of the beta-blockers in HFmrEF have also been reported, which indicates this conduct in the intermediate scenario, since there have been no recommendations based on guidelines.

• Sources of Funding
  There were no external funding sources for this study.

• Study Association
  This article is part of the Thesis of monograph of the work of conclusion of the residency in cardiology submitted by Gabriela Paiva Cavalcanti, from Real Hospital Português de Beneficência de Recife.

• Ethics approval and consent to participate
  This study was approved by the Ethics Committee of the Centro de Pesquisa da Universidade Católica de Pernambuco under the protocol number 70897517.8.0000.5206. All the procedures in this study were in accordance with the 1975 Helsinki Declaration, updated in 2013. Informed consent was obtained from all participants included in the study.

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Publication Dates

• Publication in this collection
  24 Oct 2019
• Date of issue
  Jan-Feb 2020

History

• Received
  18 Dec 2017
• Reviewed
  23 Oct 2018
• Accepted
  01 Nov 2018