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Medical Studies/Studia Medyczne
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2/2023
vol. 39
 
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Original paper

Echocardiographic correlates of dyspnoea during acute decompensated heart failure treatment

Kamil Bugała
1
,
Leszek Drabik
2
,
Anna Niekurzak
3
,
Justyna Tyfel-Paluszek
1
,
Wojciech Płazak
2

  1. Department of Diagnostics, John Paul II Hospital, Krakow, Poland
  2. Department of Cardiac and Vascular Diseases, Jagiellonian University Medical College, Krakow, Poland
  3. Department of Internal Medicine, Angiology and Geriatrics, St. John Grande Hospital, Krakow, Poland
Medical Studies/Studia Medyczne 2023; 39 (2): 140–147
Online publish date: 2023/06/30
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Introduction

Acute decompensated heart failure (ADHF) is the most frequent manifestation of acute heart failure with significant, nearly 5% in-hospital mortality and 27.2% one-year mortality according to the ESC-HF-LT (European Society of Cardiology Heart Failure Long-Term) registry [1].
Dyspnoea is the most common complaint, present in over 90% of patients with ADHF, significantly reducing the quality of life and affecting long-term prognosis [2]. Being a subjective, emotional feeling, dyspnoea is difficult to objectify and evaluate clinically. Currently, there is no widely accepted precise diagnostic tool for dyspnoea assessment in ADHF. Several standardized measures of dyspnoea like the University of California – San Diego Shortness of Breath Questionnaire, the Edmonton symptom assessment scale, Borg dyspnoea scale, numeric rating scale, and the dyspnoea visual analogue scale (VAS), have been validated mainly for patients with chronic lung diseases, and their usefulness for ADHF patients is uncertain [3–5].
Removing fluid overload and congestion is a cornerstone of ADHF treatment. Routine management of heart failure exacerbation includes daily adjustment of decongestive therapy to signs and symptoms of hypervolaemia, bodyweight or fluid balance, renal function, and natriuretic peptides [6]. Therapy that is modified according to clinical signs, and symptoms of congestion like orthopnoea and peripheral oedema, has been shown to be mildly effective in reducing dyspnoea and preventing recurrence of ADHF after discharge in a post-hoc analysis of DOSE-AHF (Diuretic Optimization Strategy Evaluation in Acute Decompensated Heart Failure) and the CARESS-HF (Cardiorenal Rescue Study in Acute Decompensated Heart Failure) trials [7]. Moreover, ADHF management based on Swan-Ganz catheter measures was not superior to a standard approach in the ESCAPE (Evaluation Study of Congestive Heart Failure and Pulmonary Artery Catheterization Effectiveness) trial [8]. Echocardiography is recommended during ADHF treatment to define a patient’s haemodynamic state and its changes during hospitalization [9, 10]. Treatment of hypervolaemia using standardized echocardiographic protocols has been shown to reduce decongestion and improve prognosis during ADHF hospitalizations to a greater extent than standard therapy, in a study by Öhman et al. [11]. However, the correlation between echocardiographic parameters and severity of dyspnoea has not been precisely studied in ADHF. Guglin et al. [12] reported in a retrospective study in patients with ADHF a weak correlation between orthopnoea and dyspnoea on admission and invasively measured pulmonary artery pressures. Symptoms correlated inversely with left and right atrial size measured with echocardiography. Although acute changes in a few echocardiographic parameters predict clinical outcomes, their association with severity of dyspnoea and resolution of dyspnoea is largely unknown [13].

Aim of the research

Therefore, our study aimed to: (1) evaluate the association of dyspnoea intensity measured by the dyspnoea VAS with structural and functional parameters of the heart obtained by echocardiography in ADHF patients, and 2) to study the changes of these echocardiographic parameters depending on dyspnoea resolution during ADHF treatment.

Material and methods

Study population

In this prospective observational, single-centre study, we enrolled 34 consecutive adult patients hospitalized due to ADHF, which was defined as sudden worsening of the signs and symptoms of heart failure [14]. Patients were recruited in the Department of Cardiac and Vascular Diseases and Department of Diagnostics, Jagiellonian University Medical College, John Paul II Hospital in Krakow, Poland, between January 2018 and December 2020. Exclusion criteria included the following: other clinical phenotypes of acute heart failure (cardiogenic shock, pulmonary oedema), acute coronary syndrome, severe cardiac arrhythmias, venous thromboembolism, infection or sepsis at admission, kidney failure requiring dialysis, hyperthyroidism/ hypothyroidism, pregnancy, or puerperium.

Patient management and evaluation

All study participants received conventional pharmacological treatment according to the current European Society of Cardiology guidelines for the treatment of ADHF [9]. Participation in the study did not result in any intrusion into the therapy, which was determined solely by the patient’s attending physician. A standardized questionnaire was used to collect patient demographic data, cardiovascular risk factors, comorbidities, and current treatment [15].
The usual diagnostic scheme, which included assessment of basic vital parameters (heart and respiratory rate, blood pressure, peripheral oxygen saturation (SpO2)), was introduced in all patients. A resting electrocardiogram was obtained at admission to exclude acute myocardial infarction changes or significant rhythm disturbances. Fluid balance and weights were monitored daily. Routine laboratory investigations were performed by standard methods. Additionally, serum N-terminal pro-B-type natriuretic peptide (NT-proBNP) was determined with electrochemiluminescence immunoassay (Roche Diagnostics, Mannheim, Germany) on the first day of treatment and at discharge.
A subjective assessment of the severity of dyspnoea was performed with a standardized 0–100 visual analogue dyspnoea scale [16]. The patients were asked to mark the level of dyspnoea on a linear scale on admission and during discharge, after lying down in the bed for 15 min. The cut-off point of the dyspnoea score was 50 points; values above 50 were defined as significant dyspnoea [3]. A significant improvement in dyspnoea was defined as dyspnoea score change ≥ 30 points, whereas values below 20 were considered as no improvement.

Echocardiographic evaluation

All the patients underwent transthoracic echocardiography on admission and on the day of discharge using Philips iE33 and Phillips Epiq ultrasound machines (Philips Healthcare, Eindhoven, Netherlands). The echocardiographic measurements were obtained according to the current guidelines [17, 18]. To evaluate the relationship between systemic circulation and dyspnoea, we analysed the following: left ventricular end-diastolic diameter (LVEDD), left ventricular ejection fraction (LVEF, measured with the Simpson biplane method); left ventricular outflow tract velocity-time-integral (LVOT-VTI), left atrial area (LAA); and the ratio of mitral peak velocity of early filling (E) to early diastolic mitral annular velocity (E’). In the assessment of mitral regurgitation (MR), vena contracta width (VC), proximal isovelocity surface area (PISA) radius, effective regurgitant orifice area (EROA), and mitral regurgitant volume (RV) were measured. As for pulmonary circulation, we evaluated right ventricular outflow tract diameter (RVOT), tricuspid annular plane systolic excursion (TAPSE), right atrial area (RAA), and tricuspid regurgitation peak gradient (TRPG).
The measurements were averaged from 3 consecutive cardiac cycles in patients with sinus rhythm and 3–5 consecutive cardiac cycles in those with atrial fibrillation. All examinations were performed per protocol by 2 independent researchers who analysed images offline using a dedicated workstation. The interobserver variability of echocardiographic measurements was below 10%. The study was approved by the Bioethical Committee of the Jagiellonian University in Cracow, Poland (No. 122.6120.294.2015). The study was conducted in accordance with the ethical guidelines of the 1975 Declaration of Helsinki. All the patients gave written informed consent.

Statistical analysis

The study was powered to have an 80% chance of detecting a 20-point difference in VAS at the a = 0.05 level. In order to demonstrate such a difference, 19 or more subjects were required based on the values of previous studies [19]. The continuous variables were presented as mean and standard deviation (SD), tested for normality of distribution using the Kolmogorov-Smirnov test, and then compared by Student’s t-test for independent data or the paired t-test, as appropriate. A p-value ≤ 0.05 (2-sided) was considered statistically significant. Categorical variables were presented as counts and percentages. Data were analysed using Statistica 13.1 software (StatSoft Inc., Tulsa, OK, USA).

Results

Patient characteristics

The clinical characteristics of the study group on admission are shown in Table 1. At admission, all the patients were dyspnoeic, with a mean dyspnoea score of 82.40 ±8.81. N-terminal pro-B-type natriuretic peptide (NT-proBNP) was elevated in all the patients (Figure 1 A). During the treatment, a significant reduction in the dyspnoea score (of 34.10% to 45.00 ±10.95, p < 0.001) and in NT-proBNP (of 43.4%) was observed (Figure 1 A).

Comparison of groups according to the severity of dyspnoea on admission

Patients with significant dyspnoea had a higher respiratory rate and NT-proBNP compared with those without severe dyspnoea (Figure 1 B, Table 2). In the echocardiographic examination (Table 2), in the group with significant dyspnoea, RAA, RVOT, vena cava inferior diameter, and tricuspid valve regurgitation were larger, whereas the right ventricular systolic function was worse compared with the patients without significant dyspnoea. The severity of mitral valve regurgitation was higher in patients with significant dyspnoea. Of note, the dyspnoea score was not associated with LVEDD, LAA, LVEF, LVOT-VTI, mitral E/E’ ratio, and TRPG.

Comparison of groups according to the improvement in dyspnoea during ADHF treatment

Regardless of the resolution of dyspnoea score during ADHF treatment (≥ 30 points or ≤ 20 points), improvement in LVEF and the reduction of right ventricular dimension, left atrial size, mitral and tricuspid regurgitation, and vena cava diameter was observed (Table 3). We did not observe a change in LVOT-VTI and TAPSE in the group with or without a significant reduction of dyspnoea score during the ADHF treatment.
Of note, in the group of patients with a significant reduction of dyspnoea score during the treatment (≥ 30 points), a significant decrease of LVEDD, RAA, mitral E/E’ ratio, and TRPG was observed (Figure 2). Also, a decrease in NT-proBNP and an increase in SpO2 were observed only in the group with significant dyspnoea score reduction (Figure 1 C).

Discussion

The main findings of the present study are that: 1) the severity of dyspnoea in ADHF patients is connected with right heart function and structure and mitral regurgitation severity, but not directly with left ventricular ejection fraction and dimension; 2) improvement in dyspnoea during treatment is associated mainly with the reduction in left ventricular filling pressure and right ventricular afterload; and 3) dyspnoea may remain unchanged despite the treatment-induced improvement in LVEF, mitral, and tricuspid regurgitations, right ventricle size, and filling pressure.
Although the feeling of dyspnoea in ADHF is multifactorial, our results suggest that changes in pulmonary circulation are essential for its occurrence, because mitral insufficiency increases pulmonary capillary wedge pressure (PCWP), and pulmonary hypertension causes right ventricular and right atrial enlargement [20]. We observed mitral E/E’ ratio reduction, but without normalization, and it is worth emphasizing that even a suboptimal change in left ventricular feeling pressure resulted in a decrease of right ventricular afterload and a subsequent dyspnoea reduction. This observation is enhanced with data from studies with lung ultrasonography, where resolution of lung congestion, dyspnoea, and a decrease in NT-proBNP correlated with left ventricular feeling pressure [11, 21]. In the MEDIA-DHF (Metabolic Road to Diastolic Heart Failure) study, patients with acute heart failure and reduced ejection fraction shared a similar phenotype of venous congestion and right ventricular dysfunction with those with preserved ejection fraction [22].
It is noteworthy that we observed a similar pattern of several echocardiographic parameters during ADHF treatment as in the ESCAPE trial, including a reduction in the right atrial, right ventricular, and inferior vena cava diameters and improvement in the severity of mitral regurgitation [8]. Interestingly we observed a reduction in left ventricular size, which has been shown to reduce the risk of death or heart failure rehospitalization after an ADHF episode [8]. Because this phenomenon was observed only in patients with significant dyspnoea decrease during decongestive therapy, we assume that this group has the lowest prevalence of residual pulmonary congestion.
Treatment of ADHF is associated with a decrease in left- and right-sided heart pressures in invasive measurements, the change of which has been shown to be concordant with echocardiographic assessment, particularly for right atrial pressure, pulmonary artery systolic pressure, and IVC diameter measurement and TRPG, respectively [8, 13]. Our study showing the impact of LV filling pressure as assessed by echo, left ventricular diastolic dysfunction, and secondary pulmonary hypertension on the feeling of dyspnoea emphasizes observations of the detrimental effect of residual pulmonary congestion on quality of life in ADHF [7]. However, previous research was not unambiguous in this aspect. In a Finnish study, a decrease in the mitral E/E’ ratio preceded early decongestion, evaluated with lung ultrasonography, and was associated with lower 6-month mortality in patients with acute heart failure [23]. Conversely, the study based on data from the ESCAPE trial suggested a weak correlation between echocardiographic parameters and the severity of dyspnoea [8, 24].
Nevertheless, these were patients with a starting LVEF below 30%, probably chronically adapted pulmonary congestion. High loss to follow-up rates, in-hospital, and early mortality in ADHF might also have biased results of studies on echocardiographic correlates of dyspnoea in heart failure [12].
Therapy of ADHF using rapid cardiothoracic ultrasound protocols, e.g. CaTUS, based on cardiac filling pressures, inferior vena cava diameter, and lung assessment, have been shown to reduce symptoms and natriuretic peptides faster than standard management without ultrasound guidance [11]. A recent study showed the POCUS (point-of-care ultrasound) algorithm relying on mitral flow, mitral annular velocities, and lung ultrasound to have high accuracy in diagnosing dyspnoea secondary to ADHF in the emergency department [25]. Furthermore, therapy based on echo-derived cardiac filling pressures resolves congestion faster and more effectively and may result in a greater improvement in dyspnoea [26]. Knowledge about the complex relationship between echocardiographic parameters, natriuretic peptides, and reported dyspnoea may help clinicians to differentiate the source of dyspnoea and to monitor the course of ADHF treatment.
Plasma NT-proBNP has been shown to correlate with mitral E’, right ventricular systolic function, and the severity of tricuspid regurgitation in patients with dyspnoea enrolled in the PRIDE (ProBNP Investigation of Dyspnoea in the Emergency Department) study [27]. In another study on dyspnoea in emergency departments, NT-proBNP measurements had high diagnostic accuracy for LVEF < 40% and diastolic dysfunction in ADHF and pulmonary congestion [28, 29].
Also, we enrolled patients with ischaemic and non-ischaemic heart failure and a high prevalence of atrial fibrillation, as reported in other ADHF studies [1, 12]. None of the patients was lost to follow-up, despite reported high in-hospital mortality [1] or incomplete long-term observations in other trials on dyspnoea in ADHF [12]. Finally, we believe that objectification and categorization of dyspnoea with VAS may be helpful for the development of protocols for other heart failure clinical trials.
Limitations: The study findings are limited by the sample size. However, the number of patients was sufficient to detect the intergroup differences based on the results of power calculation.
Our study reflects standard treatment for ADHF in a university hospital. The study duration was limited to the in-hospital phase of ADHF, and long-term observation might elucidate different dyspnoea-related factors [30]. Exercise echocardiography testing might have revealed other associations with dyspnoea, unavailable to detect in the resting examination; however, its use in the acute phase may be associated with additional risk for the patient [31]. We did not perform right heart catheterization because the aim of the study was to find easy to assess bedside tools valuable in the prognostication of dyspnoea relief. Of note, echocardiography parameters depend on heart rate and atrial fibrillation (AF) episodes. AF increases heart rate, deteriorates LVEF, and reduces mitral regurgitation parameters during episode [32]. Similarly, the impact on circulation haemodynamics may have adrenergic stimulation, connected with stress due to hospitalization and dyspnoea [33]. No change in heart rhythm was observed in our study group (AF or sinus rhythm from admission to discharge); the level of stress on admission and during hospitalization was stable.

Conclusions

We have shown that dyspnoea severity in ADHF patients is determined mainly by the mitral regurgitation severity and the right heart structure and function, whereas dyspnoea decrease during treatment is associated mainly with the reduction of left ventricular filling pressure and right ventricular systolic pressure. The relationship between dyspnoea severity and echocardiographic parameters may help clinicians to monitor the course of ADHF treatment.

Acknowledgments

The study was supported by Jagiellonian University Medical College (grant No. K/2DS/007820).

Conflict of interest

The authors declare no conflict of interest.

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Copyright: © 2023 Jan Kochanowski University in Kielce This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
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