Abstract
Background
Assessing right ventricular (RV) function is paramount for risk stratification, which remains challenging in patients with tricuspid regurgitation (TR). We assessed RV–pulmonary artery (PA) coupling and its predictability of outcomes after transcatheter tricuspid valve repair (TTVR).
Methods
Study participants comprised patients undergoing transcatheter tricuspid valve repair to treat symptomatic TR from June 2015 to July 2021. We calculated an RV–PA coupling ratio using a formula, which is dividing tricuspid annular plane systolic excursion (TAPSE) by echocardiographically estimated (ePASP) or invasively measured PASP (iPASP) at baseline. The primary outcome was all-cause mortality or heart failure rehospitalization within one year.
Results
The study participants (n = 206) were at high surgical risk (EuroSCORE II: 7.4 ± 4.8%). The primary outcome occurred in 57 patients within one year. The c-statistics for the outcome were 0.565 (95% CI 0.488–0.643) for TAPSE/ePASP and 0.695 (95% CI 0.631–0.759) for TAPSE/iPASP. The correlation between the ePASP and iPASP was attenuated in patients with massive/torrential TR compared to those with severe TR (interaction p = 0.01). In the multivariable Cox proportional model, TAPSE/iPASP was inversely associated with the risk of the primary outcome (per 0.1-point increase: adjusted-HR 0.67, 95% CI 0.56–0.82, p < 0.001), independent of baseline demographics. According to the TAPSE/iPASP quartiles (i.e., ≤ 0.316; 0.317–0.407; 0.408–0.526; ≥ 0.527), the event-free survival was 43.4%, 48.3%, 77.9%, and 85.4% at one year after TTVR.
Conclusion
RV–PA coupling predicts one-year mortality and heart failure rehospitalization after TTVR in patients with TR. The predictability is improved if invasively-measured PA pressure is included.
Graphical abstract
Assessing right ventricular (RV) function is paramount for risk stratification. The present analysis confirms that RV–PA coupling, measured as TAPSE/PASP, predicts one-year mortality and heart failure rehospitalization in patients undergoing TTVR. There is a significant interaction between TR severity and the correlation of ePASP with iPASP, and therefore the correlation is attenuated in patients with massive to torrential TR. The predictability of RV–PA coupling is improved if PA pressure is measured invasively and included in the formula.
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Introduction
Tricuspid regurgitation (TR) is associated with a dismal prognosis. TR can be treated less invasively through the use of recently developed transcatheter technologies [1, 2]. Assessing right ventricular (RV) function is paramount for risk stratification, which is, however, challenging in patients with TR. Although tricuspid annular plane systolic excursion (TAPSE) and RV fractional-area change (RVFAC) are common and easily obtainable parameters, these parameters are highly dependent on the volume status of the RV. Given that significant TR will lead to volume-overload and to pulmonary artery (PA) hypertension, the diagnostic accuracy for RV function using these parameters alone is limited.
RV–PA coupling seems more feasible for assessing RV function than other individual RV parameters, because it reflects the contractability of the RV under increased volume and afterload status in patients with TR. Brener et al. investigated RV–PA coupling, defined as the ratio between TAPSE and PA systolic pressure (PASP) as estimated by echocardiography, in patients undergoing transcatheter tricuspid valve treatment [3]. They reported that TAPSE/PASP was inversely associated with one-year mortality. However, echocardiography may miscalculate PASP in the presence of significant TR [4]. Instead, with the development of transcatheter interventions, a right-heart catheter has been increasingly recognized as a standard of care in the contemporary management of TR. Lurz et al. reported that invasively measured PASP (iPASP) may further discriminate clinical outcomes in patients undergoing TTVR beyond echocardiographically estimation of PASP [4]. Therefore, RV–PA coupling parameters using iPASP may provide a different cutoff value and better predictability of post-procedural outcomes than using echocardiographically estimated PASP (ePASP). This may be inducive in refining patient selection for TTVR in clinical practice.
In this context, we assessed RV–PA coupling parameters using ePASP or iPASP and compared them for outcome predictability.
Methods
Study populations
This is a retrospective analysis based on data from the Bonn registry, a prospective and consecutive data collection at the University Hospital of Bonn. All procedures were conducted in accordance with the Declaration of Helsinki and its amendments. Study participants comprised patients undergoing TTVR for the treatment of symptomatic TR from June 2015 to July 2021. All patients were deemed as being either ineligible or high risk for surgery. A standardized diagnostic workup was performed, including transesophageal echocardiography and left- and right-heart catheterization. In the present analysis, we included patients with sufficient information for the assessment of RV–PA coupling.
Echocardiographic measurements
Doppler echocardiography was performed according to the current guidelines [5, 6]. TR severity was assessed using standard two-dimensional color Doppler methods integrating quantitative, semi-quantitative, and qualitative parameters according to the most recent guidelines. The TR jet was used to estimate TR peak gradient using the Bernoulli equation. The right atrial (RA) pressure was estimated by its size and collapsibility of the inferior vena cava. ePASP was then obtained by adding these two measures. TAPSE was measured as the peak excursion of the tricuspid annulus during the whole cardiac cycle in the apical four-chamber view. RV fractional area change (RVFAC) was calculated as (RV end-diastolic area − RV end-systolic area)/RV end-diastolic area × 100.
RV–PA coupling parameters
We calculated an RV–PA coupling ratio by dividing TAPSE by PASP at baseline. ePASP and iPASP were applied to the equation as a PA component (i.e., TAPSE/ePASP, TAPSE/iPASP). We also assessed RVFAC/ePASP and RVFAC/iPASP in sensitivity analyses. iPASP was obtained through a right heart catheter at baseline.
Outcome measures
The primary outcome was defined as a composite of mortality and rehospitalization due to heart failure within one year after TTVR. Each outcome was also assessed individually. We obtained clinical follow-up data through interviews at scheduled outpatient clinic visits, telephone interviews with their family, or documentation from the general practitioners.
Patient and public involvement
Patients or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
Statistical analysis
Continuous variables are reported as the mean ± standard deviation (SD) or medians with interquartile ranges (IQRs). T-tests are applied for normally-distributed variables and Mann–Whitney U test is conducted for non-normally distributed variables. Categorical variables are presented as numbers and percentages. Chi-square test is applied for the comparison. A test for Pearson’s correlation was conducted to assess the correlation of ePASP and iPASP, whereas a test for Spearman’s correlation was used for echocardiographic and invasive RA pressure measurements.
Given that the primary outcome is time-to-event data, we conducted a receiver operating characteristics (ROC) analysis using a Cox proportional model. The predictive accuracy of the outcome was evaluated using Harrell’s concordance index (Harrell’s C) [7, 8]. A smooth spline curve for hazard ratio (HR) of RV–PA coupling was depicted. The study participants were divided according to the quartiles of RV–PA coupling parameters. The Kaplan–Meier method was used for survival time analyses. A Cox proportional hazard model was conducted to assess the association of RV–PA coupling parameters with outcomes. Age, sex, EuroSCORE II, estimated glomerular filtration rate (eGFR), left ventricular (LV) ejection fraction, and chronic obstructive pulmonary disease were accounted in the model 1, while reduction in TR ≤ moderate at discharge was incorporated in the model 2 to adjust for the association [1, 3, 4, 9]. Furthermore, the association was tested among predefined subgroups (i.e., NYHA I/II or NYHA III/IV, LV ejection fraction ≤ 50% or > 50%, TR severity at baseline ≤ severe or ≥ massive, TR severity at discharge ≤ moderate or ≥ severe). All statistical analyses were performed using EZR version 1.37 (Saitama Medical Center, Jichi Medical University, Saitama, Japan), R version 3.5.2 (R Foundation for Statistical Computing), or IBM SPSS Statistics 26 (IBM Corporation, New York, USA).
Results
Study population
During the study period, a total of 206 patients met the inclusion criteria and were entered in the analysis. The mean age was 78.5 ± 7.1 years, and 58.3% were female. The study participants were at a high risk for surgery (EuroSCORE II: 9.0 ± 6.5%), and massive/torrential TR was observed in 100 (48.5%) of these patients. The majority of patients presented with atrial fibrillation (94.2%), preserved left ventricular ejection fraction (55.2 ± 10.1%), and a secondary etiology of TR (96.1%). All patients were treated either with transcatheter edge-to-edge repair (n = 185: 89.8%) or transcatheter annuloplasty (n = 21: 10.2%). No periprocedural death was observed. TTVR reduced the severity of TR (p < 0.001), with 78.0% of patients having TR 2+ or less at discharge.
RV–PA coupling parameters
Variables regarding echocardiography and right heart catheterization are listed in Table 1. The median values of TAPSE, ePASP, and TAPSE/ePASP were 17.0 mm (IQR 15.0, 20.0 mm), 45.0 mmHg (IQR 36.3, 53.0 mmHg), and 0.392 mm/mmHg (IQR 0.287, 0.514 mm/mmHg). The median time from baseline echocardiography to invasive right heart catheterization was one day (IQR − 1, 5 days). The invasively-measured PASP (i.e., iPASP) was 42.0 mmHg (IQR 35.0, 52.0 mmHg), and the median of TAPSE/iPASP was 0.408 mm/mmHg (IQR 0.316, 0.526 mm/mmHg).
Prediction for outcomes according to RV–PA coupling parameters
With the median follow-up duration of 201 days (IQR 98–424 days), 29 patients had died, and 40 patients had experienced rehospitalization due to heart failure, resulting in 57 cases of the primary outcome. The associations of right heart parameters with the primary outcome are listed in Supplemental Table 1. Compared to TAPSE/ePASP, TAPSE/iPASP showed better predictability for the primary outcome (Fig. 1A): the c-statistics was 0.565 (95% CI 0.488–0.643) for TAPSE/ePASP and increased to 0.695 (95% CI 0.631–0.759) when iPASP was applied to the formula (i.e., TAPSE/iPASP) (p < 0.001). The trend was consistent for RV–PA coupling using RVFAC (Fig. 1B). RVFAC itself was not associated with the primary outcome (Supplemental Table 1). Similarly, RVFAC/ePASP was not predictive for the outcome, while RVFAC/iPASP predicted the primary endpoint. As shown in Fig. 1, integrating the iPASP measurement led to a better prediction for the outcome (c-statistics: 0.495 for RVFAC/ePASP [95% CI 0.411–0.578]; c-statistics for RVFAC/iPASP: 0.643 [95% CI 0.566–0.719]).
In addition, we separately conducted ROC analyses in patients with severe and those with massive/torrential TR. TAPSE/iPASP showed a better discrimination irrespective of the TR severity, whereas the difference in Harrell’s C was numerically higher in patients with more advanced TR (delta c-statistics: 0.102 ± 0.035 in severe TR, p = 0.003; delta c-statistics: 0.179 ± 0.056 in massive/torrential TR, p = 0.001).
Correlation between echocardiographic and invasive PA pressures
There was a significant correlation between ePASP and iPASP in the total cohort (correlation coefficient 0.50, p < 0.001), whereas the correlation was attenuated in patients with massive to torrential TR (severe TR: correlation coefficient 0.588, p < 0.001; massive to torrential TR: correlation coefficient 0.337, p = 0.001; interaction p = 0.01) (Fig. 2). A similar trend was observed in the correlation between TR pressure gradient and iPASP (severe TR: correlation coefficient 0.546, p < 0.001; massive to torrential TR: correlation coefficient 0.331, p = 0.001; interaction p = 0.035).
In addition, the echocardiographic RA pressure (median 15 mmHg [IQR 8–15 mmHg]) was modestly correlated with the invasive measurement (median 13 mmHg [IQR 9–18 mmHg]) (correlation coefficient 0.165, p value = 0.023) (Fig. 3). The RA pressure was likely to be underestimated in patients with the echocardiographic measurement of 3 and 8 mmHg. The miscalculation was also observed in patients with the echocardiographic RA pressure of 15 mmHg: a quarter of patients showed less than 10 mmHg of the invasive measurement, whereas another quarter showed more than 20 mmHg of the invasively-measured RA pressure.
Clinical implication of TAPSE/iPASP
We divided the study participants according to TAPSE/iPASP (quartile 1: ≤ 0.316; quartile 2: 0.317–0.407, quartile 3: 0.408–0.526, quartile 4: ≥ 0.527). The baseline characteristics are listed in Table 1. Patients with lower TAPSE/iPASP were more likely to be male, having prior coronary artery bypass graft surgery, higher PA resistance and RA pressure, compared to patients with higher TAPSE/iPASP mm/mmHg. TR reduction to ≤ 2+ at discharge was consistently observed regardless of TAPSE/iPASP (Supplemental Table 2).
The spline curve depicts the linear association of TAPSE/iPASP with the primary endpoint (Fig. 4). TAPSE/iPASP was inversely associated with the primary outcome (per 0.1-point increase: adjusted-HR 0.67, 95% CI 0.56–0.82, p < 0.001) in the multivariable Cox proportional model (Table 2). Other parameters associated with the outcome were sex (male: adjusted-HR 2.26, 95% CI 1.21–4.20, p = 0.01) and eGFR (per 1 ml/min/1.73 m2 increase: adjusted-HR 0.98, 95% CI 0.97–0.99, p = 0.008).
The association of TAPSE/iPASP with the outcome remained significant after adjusting for the TR reduction (Table 2). Also, the observed association was consistent among the predefined subgroups, including NYHA functional class, LV ejection fraction, the severity of TR at baseline, and the reduction in TR at discharge (Supplemental Fig. 1).
Event-free survival curves were estimated and depicted using a Kaplan–Meier method (Fig. 5). According to the TAPSE/iPASP quarters (i.e., ≤ 0.316; 0.317–0.407; 0.408–0.526; ≥ 0.527), the event-free survivals were 43.4%, 48.3%, 77.9%, and 85.4% at one year after TTVR. Similar findings were observed for each outcome. The event-free survival from heart failure rehospitalization were 52.0%, 61.8%, 86.4%, and 87.3%, whereas survival from death were 65.0%, 82.1%, 85.9%, and 90.6% at one-year follow-up after TTVR.
Discussion
This study assessed RV–PA coupling measured by the ratio of TAPSE and PASP in patients undergoing TTVR. The main findings can be summarized as follows (graphical abstract):
-
1.
RV–PA coupling, measured as TAPSE/PASP, predicted adverse outcomes after TTVR in patients with TR.
-
2.
The prediction for outcomes was improved if invasively measured PASP (i.e., iPASP) was applied to the formulas.
-
3.
There was a significant interaction between TR severity and the correlation of ePASP with iPASP. The correlation was attenuated in patients with massive to torrential TR.
-
4.
TAPSE/iPASP was associated with event-free survival after TTVR, independent of baseline demographics or TR reduction after TTVR.
According to current guidelines [5, 6], RV function is one of the main variables to weigh the indication of surgical or transcatheter tricuspid valve treatment in patients with TR. Despite the promising data and potential prognostic benefit of less invasive transcatheter technologies[2], concomitant RV dysfunction might pose challenges in the diagnosis and management of TR [4, 10]. Many TR patients receive appropriate clinical attention too late and appear with developed RV failure with multiple organ failures at the timing of interventions [9]. In the present study, patients represented a high surgical risk profile with the EuroSCORE II of 9.0 ± 6.5%. We found no periprocedural mortality, and TR reduction to 2+ or less was observed in 78% of patients, which is comparable to previous reports [11, 12]. Although an adequate reduction in TR may lead to an improved outcome [2, 13], the prognostic benefit of TR treatment may also be affected by concomitant RV function [14, 15]. Furthermore, TR reduction with TTVR might be linked to a risk of afterload mismatch of the RV after the procedure, especially in patients with inherent RV impairment [16].
RV–PA coupling is increasingly recognized as a more accurate parameter of RV systolic function, where RV parameters are indexed to a measurement of afterload (e.g., PASP) [15, 17]. The coupling of RV functional parameters (e.g., TAPSE, RVFAC) and PA pressure indicates that RV can compensate for an increased afterload of the pulmonary artery. The concept has recently widely been validated in patients with various types of diseases and also in patients with TR [3, 9,10,11,12]. Brener et al. reported that echocardiography-assessed RV–PA coupling (TAPSE/ePASP) was discriminative for one-year mortality in patients undergoing TTVR in a multicenter cohort [3]. Our findings are in line with the earlier studies and expand them by demonstrating better prediction for outcomes by applying TAPSE/iPASP (c-statistics 0.695) compared to TAPSE/ePASP (c-statistics 0.565). Furthermore, a similar association was observed in the RVFAC/ePASP and RVFAC/iPASP. The risk of outcomes was stratified by the TAPSE/iPASP. HF rehospitalization or all-cause mortality at one year were estimated in 56.6% for the first quartile of TAPSE/iPASP, whereas the event rate was 14.6% for patients in the fourth quartile of TAPSE/iPASP.
Echocardiography may miscalculate PASP in the presence of significant TR. The discordance between ePASP and iPASP was pronounced in patients with massive to torrential TR, inferring that PASP estimated by TR pressure gradient is likely underestimated because of a laminar flow of TR owing to a huge coaptation defect [4]. Lurz et al. reported that the diagnostic accuracy of ePASP to detect PA hypertension was only 55%. In the present study, the ePASP was somewhat higher than the iPASP, suggesting a possibility that the equation of ePASP itself may not be optimal in TR patients. Another explanation may be related to the estimation of RA pressure by echocardiography. An RA pressure estimation based on inferior vena cava diameters may not be correlated with the invasively measured RA pressure [18]. The diameter and shape of inferior vena cava are affected by RA pressure but are generally highly varied in individuals [19]. Assuming that patients with lower RV–PA coupling parameters are likely to have inferior outcomes even after treating TR, assessing PA and RA pressures will be critical. In line with the most recent European guideline [20], our findings underline that invasive cardiac catheterization is needed to directly assess right-heart pressures, thereby proceeding with clinical decision-making of TR [5].
Limitations
Several limitations to our study should be acknowledged. First, the single-center, retrospective nature of this study, and the small sample size may limit the generalizability of the results. Nevertheless, the present study cohort represents data from one of the high-volume centers for TTVR. Second, no follow-up data on RV–PA coupling using iPASP was available. An early change in RV–PA coupling was reported in the most recent study, which needs to be validated in future studies using invasive measurements of right heart pressures. Also, factors associated with a change in RV–PA coupling following TTVR should be elucidated in further investigations. Third, the study cohort was regarded as one homogenous group, but we did not assess more detailed etiology of TR (i.e., atrial or ventricular secondary TR, cardiac implantable electronic device lead-induced TR). Fourth, since two different PASP values (echocardiographic and invasive) were measured at different times, patients might have been subjected to different hemodynamic influences. Finally, TAPSE reflects the longitudinal RV function but does not account for global RV function or might overestimate RV function in the presence of TR [10]. Nonetheless, the current analysis showed comparable c-statistics between the RV–PA coupling using TAPSE and RVFAC, which implies their feasibility in clinical practice for risk stratification in patients with TR. Magnetic resonance tomography might be more accurate for assessing function [10]. Nevertheless, impaired renal function or implanted pacemaker lead may limit its clinical use or feasibility of measurements. In contrast, TAPSE is the most commonly used and easily reproducible marker of RV function in clinical practice. Therefore, TAPSE/iPASP can be generalizable in each individual and each hospital.
Conclusion
The present analysis confirmed that RV–PA coupling, measured as TAPSE/PASP, predicts one-year mortality and heart failure rehospitalization in patients undergoing TTVR. There was a significant interaction between TR severity and the correlation of ePASP with iPASP: the correlation was attenuated in patients with massive to torrential TR. The prediction for outcomes was improved if iPASP was measured and included in the formula. TAPSE/iPASP discriminated the event-free survival of patients with TR, independent of their baseline characteristics or TR reduction after TTVR.
Availability of data and material
The data underlying this article will be shared on reasonable request to the corresponding author.
References
Wild MG, Löw K, Rosch S et al (2022) Multicenter experience with the transcatheter leaflet repair system for symptomatic tricuspid regurgitation. JACC Cardiovasc Interv 15:1352–1363
Lurz P, Stephan von Bardeleben R, Weber M et al (2021) Transcatheter edge-to-edge repair for treatment of tricuspid regurgitation. J Am Coll Cardiol 77:229–239
Brener MI, Lurz P, Hausleiter J et al (2022) Right ventricular-pulmonary arterial coupling and afterload reserve in patients undergoing transcatheter tricuspid valve repair. J Am Coll Cardiol 79:448–461
Lurz P, Orban M, Besler C et al (2020) Clinical characteristics, diagnosis, and risk stratification of pulmonary hypertension in severe tricuspid regurgitation and implications for transcatheter tricuspid valve repair. Eur Heart J 41:2785–2795
Vahanian A, Beyersdorf F, Praz F et al (2021) ESC/EACTS guidelines for the management of valvular heart disease. Eur Heart J 43:561–632
Writing Committee Members, Otto CM, Nishimura RA et al (2020) ACC/AHA guideline for the management of patients with valvular heart disease: a report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice guidelines. J Thorac Cardiovasc Surg 2021(162):e183–e353
Stamatelopoulos K, Mueller-Hennessen M, Georgiopoulos G, Cathepsin S et al (2022) Levels and survival among patients with non-ST-segment elevation acute coronary syndromes. J Am Coll Cardiol 80:998–1010
Mangesius J, Thomas S, Katie B et al (2020) Hypofractionated and single-fraction radiosurgery for brain metastases with sex as a key predictor of overall survival. https://www.researchsquare.com/article/rs-41042/v1. Accessed 1 Sept 2022 (in review)
Tanaka T, Kavsur R, Sugiura A et al (2021) Prognostic impact of hepatorenal function in patients undergoing transcatheter tricuspid valve repair. Sci Rep 11:14420
Kresoja K-P, Rommel K-P, Lücke C et al (2021) Right ventricular contraction patterns in patients undergoing transcatheter tricuspid valve repair for severe tricuspid regurgitation. JACC Cardiovasc Interv 14:1551–1561
Nickenig G, Weber M, Lurz P et al (2019) Transcatheter edge-to-edge repair for reduction of tricuspid regurgitation: 6-month outcomes of the TRILUMINATE single-arm study. Lancet Lond Engl 394:2002–2011
Davidson CJ, Lim DS, Smith RL et al (2021) Early feasibility study of cardioband tricuspid system for functional tricuspid regurgitation. JACC Cardiovasc Interv 14:41–50
Sugiura A, Tanaka T, Kavsur R et al (2021) Leaflet configuration and residual tricuspid regurgitation after transcatheter edge-to-edge tricuspid repair. JACC Cardiovasc Interv 14:2260–2270
Schlotter F, Miura M, Kresoja K-P et al (2021) Outcomes of transcatheter tricuspid valve intervention by right ventricular function: a multicentre propensity-matched analysis. EuroIntervention J Eur Collab Work Group Interv Cardiol Eur Soc Cardiol. 17:e343–e352
Sugiura A, Kavsur R, Spieker M et al (2022) Impact of right ventricular-pulmonary arterial coupling on clinical outcomes of tricuspid regurgitation. EuroIntervention J Eur Collab Work Group Interv Cardiol Eur Soc Cardiol. 18:852–861
Hagemeyer D, Merdad A, Ong G, Fam NP (2022) Acute afterload mismatch after transcatheter tricuspid valve repair. JACC Case Rep 4:519–522
Brener MI, Grayburn P, Lindenfeld J et al (2021) Right ventricular-pulmonary arterial coupling in patients with HF secondary MR: analysis from the COAPT trial. JACC Cardiovasc Interv 14:2231–2242
Albani S, Mesin L, Roatta S et al (2022) Inferior vena cava edge tracking echocardiography: a promising tool with applications in multiple clinical settings. Diagn Basel Switz 12:427
Ranard LS, Vahl TP, Chung CJ et al (2022) Impact of inferior vena cava entry characteristics on tricuspid annular access during transcatheter interventions. Catheter Cardiovasc Interv Off J Soc Card Angiogr Interv. 99:1268–1276
Galiè N, Humbert M, Vachiery J-L et al (2016) 2015 ESC/ERS guidelines for the diagnosis and treatment of pulmonary hypertension: the Joint Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT). Eur Heart J 37:67–119
Acknowledgements
We thank Dr. Meghan Lucas (scientific coordinator for the Heart Center Bonn, Bonn, Germany) for proofreading the manuscript.
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Open Access funding enabled and organized by Projekt DEAL. This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
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Marcel Weber has received lecture or proctoring fees from Abbott and Edwards. Georg Nickenig has received research funding from the Deutsche Forschungsgemeinschaft, the German Federal Ministry of Education and Research, Abbott, Edwards Lifesciences, Medtronic, and St Jude Medical and has received honoraria for lectures or advisory boards from Abbott, Edwards Lifesciences, Medtronic, and St Jude Medical. The other authors have no conflicts of interest.
Ethics approval
The study was a retrospective analysis based on data from the Bonn registry, which was approved by the ethics committees of the individual centers. The study was conducted in accordance with the Declaration of Helsinki.
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All patients provided written informed consent to participate in the registry.
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Supplementary file1 Supplemental Figure 1. Association of TAPSE/iPASP with primary outcome according to predefined subgroups. (PDF 44 kb)
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Sugiura, A., Tanaka, T., Kavsur, R. et al. Refining accuracy of RV–PA coupling in patients undergoing transcatheter tricuspid valve treatment. Clin Res Cardiol 113, 177–186 (2024). https://doi.org/10.1007/s00392-023-02339-5
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DOI: https://doi.org/10.1007/s00392-023-02339-5