Abstract
Background
In precapillary pulmonary hypertension (PH), the incidence of different tricuspid regurgitation (TR) degree is poorly defined. The impact of TR severity on pulmonary artery pressure (PAP) assessment and clinical risk stratification in precapillary PH remains unclear.
Methods
A total of 207 patients diagnosed precapillary PH who underwent right heart catheterization (RHC) and echocardiography within 3 days were included. The severity of TR was graded as trace, mild, moderate and severe. Pearson correlation analysis was performed to evaluate the correlation between systolic PAP by echocardiography (sPAPECHO) and mean PAP by RHC (mPAPRHC) in different TR degree groups. The impact factors on risk stratification of precapillary PH were analyzed by logistic regression analysis.
Results
The proportion of None, Trace, Mild, Moderate and Severe TR group was 2.4%, 23.7%, 39.1%, 28.5% and 6.3% respectively. Right atrium (RA) area increased gradually with TR aggravation (p < 0.001). Moderate and Severe TR group had higher N-terminal pro-B-type natriuretic peptide (p < 0.001), right atrial pressure (RAP) (p = 0.018), right ventricular basal diameter (RVD)/left ventricular basal diameter (LVD) ratio (p < 0.001), larger right ventricle (RV) (p < 0.001) and lower tricuspid annular plane systolic excursion (p = 0.006) compared with Trace and Mild group. TR-sPAPECHO in Moderate TR group had the greatest correlation coefficient with mPAPRHC (0.742, p < 0.001) followed by Mild (0.635, p < 0.001) and severe group (0.592, p = 0.033), while there was no correlation in Trace TR group (0.308, p = 0.076). Multivariate logistic regression showed three significant independent echocardiography predictors of high-risk precapillary PH: RVD/LVD ratio (OR = 5.734; 95%CI1.502–21.889, p = 0.011), RA area (OR 1.054; 95% CI 1.004–1.107, p = 0.035) and systolic annular tissue velocity of the lateral tricuspid annulus (S’) (OR 0.735, 95% CI 0.569–0.949, p = 0.018).
Conclusions
Precapillary PH was not necessarily accompanied by significant TR. None or Trace TRaccounted for 26% in our population and TR-sPAPECHO was not applicable to estimate PAP in these patients. RVD/LVD ratio, RA area and S’ can independently predict the high-risk patients with precapillary PH. TR may play an indirect role in risk stratification by affecting these indicators.
Similar content being viewed by others
Explore related subjects
Find the latest articles, discoveries, and news in related topics.Background
Tricuspid regurgitation (TR) is generally considered highly prevalent and an important prognostic factor in patients with pulmonary hypertension (PH) [1]. Peak velocity of TR (TR Vmax) and its derived parameters systolic and mean pulmonary artery pressure (PAP) by Doppler echocardiography (sPAPECHO and mPAPECHO) are most commonly used for assessing PH. We previously investigated the accuracy and impact factors of TR in estimating PAP and have demonstrated sPAPECHO was superior than other TR-related methods in screening PH [2]. However, in precapillary PH, the true incidence of TR and the distribution of different TR degree are still poorly defined. The impact of TR severity on PAP assessment and clinical risk stratification in precapillary PH remains unclear.
This paper we want to investigate: i) the prevalence of TR in precapillary PH; and ii) the impact of TR severity on PAP estimation and clinical risk stratification in precapillary PH.
Methods
Subjects
We included consecutive patients admitted to China-Japan Friendship Hospital from November 2015 to October 2020, who were diagnosed precapillary PH by right heart catheterization (RHC) [mean PAP by RHC (mPAPRHC) ≥ 25 mmHg, pulmonary artery wedge pressure (PAWP) ≤ 15 mmHg and pulmonary vascular resistance (PVR) > 3WU at rest]. We excluded patients with one of the followings: echocardiography and RHC interval exceeded 3 days; either stenosis of right ventricular outflow tract or pulmonary artery; ventricular septal defect or patent ductus arteriosus; echocardiography images were of poor quality not suitable for analysis; primary valvular disease or pacemaker implantation. Patient’s demographic and clinical data were obtained from electronic medical records of our hospital. The institutional review board of China-Japan Friendship Hospital waived the need for written informed consent from patients as this study was a retrospective analysis of clinically acquired data. The original data will be shared on reasonable request by contacting the corresponding author. This study was approved by the Ethics Committee of China-Japan Friendship Hospital in Peking of China (No.2020–95-K59). Baseline assessment of eligible patients including World Health Organization (WHO) heart function class, the level of N-terminal pro-B-type natriuretic peptide (NT-proBNP) and 6-minute walk distance (6MWD) were recorded.
RHC
Hemodynamic measurements were performed with a 7F Swan-Ganz catheter Philips Allura X-PERFD20 flat-plate angiography system (Baxter Inc) using Seldinger technique via right internal jugular vein pathway. The system was zeroed and referenced at patients’ heart level as previously described [3]. Right atrial pressure (RAP), systolic PAP (sPAPRHC), diastolic PAP and PAWP were measured and cardiac output (CO) was obtained using Fick’s method. mPAPRHC and PVR were calculated using standard formulas.
Echocardiography
Echocardiographic images were acquired using a GE Vivid E9 or E95 machine (GE Healthcare, General Electric Healthcare) equipped with M5S phased-array transducers. Analysis was performed independently by two blinded investigators using EchoPAC software (GE Healthcare version 201). Two-dimensional and Doppler echocardiography were performed according to the recommendations for cardiac chamber quantification guidelines by the American Society of Echocardiography (ASE) [4]. Specific measurements for right ventricle (RV) related parameters were as follows: area of the right atrium (RA) was measured in an apical four-chamber view; right ventricular basal diameter (RVD) and left ventricular basal diameter (LVD) were measured at end-diastole in the RV-focused apical four-chamber view calculating RVD/LVD ratio; right ventricular free wall thickness (RWT) was measured at end-diastole in the epigastric long-axis image. Echocardiographic assessment of TR involved a systematic and stepwise interrogation of TR from four main views: The RV inflow view from the parasternal long axis, the parasternal short-axis view at the level of the aortic valve, the apical four-chamber view and the parasternal four-chamber view. The color doppler was set to scale 63 cm/s, gain -5 dB and 17 frame per second. Determination of the severity of TR relied on integration of multiple qualitative and semiquantitative measures based on regurgitation jet area and vena contracta width (VC). The TR jet area was assessed from a sector that allowed visualization of the entire RA. The VC was measured at the narrowest diameter of color flow seen immediately beyond the area of flow convergence. The image was optimized by narrowing the sector width to enhance the frame rate and zooming in on the area of interest. The VC was measured as an average during four consecutive cardiac cycles. The severity of TR was graded as trace, mild (jet area < 5 cm2, VCTR < 3 mm), moderate (area 5–10 cm2, VCTR3-6.9 mm) and severe (jet area > 10cm2, VCTR ≥ 7 mm or a ratio of jet area to RA area more than 50%). When the results of jet area and VC were inconsistent, we mainly referred continuity equation method to calculate the TR volume (the blood flow through the tricuspid valve orifice in diastole minus the blood flow through the pulmonary valve orifice in systole). A small amount of TR which could not be detected in every section and regurgitant jet was just limited to the valve annulus with an area less than 2 cm2 was defined as Trace TR. TR Vmax was measured and the entire TR spectrum was traced to obtain the peak and mean pressure gradient (TR-PG and TR-mPG). sPAPECHO and mPAPECHO were calculated by adding the estimated RAP (eRAP) to TR-PG and TR-mPG respectively. eRAP is divided into three categories (3, 8, and 15 mmHg) based on the inferior vena cava diameter and its respiratory variation [5]. RV systolic function was assessed using multiple parameters, including tricuspid annular plane systolic excursion (TAPSE), systolic annular tissue velocity of the lateral tricuspid annulus (S’) and RV fractional area change (FAC). All parameters were repeatedly measured and averaged. TAPSE/TR-sPAPECHO ratio was also calculated.
Risk stratification
We identified high-risk subjects according to a simplified risk stratification in pulmonary artery hypertension (PAH), which was modified based on the 2015 European Society of Cardiology (ESC)/European Respiratory Society (ERS) PH guidelines, published by 2018 World Symposium on PH [6] and also supported by 2021 Chinese guidelines for diagnosis and treatment of PH [7]. This simplified method made the risk stratification more clear, simple and convenient for clinical application. Patients were classified as low (< 5%), medium (5%-10%) or high-risk (> 10%) according to their 1-year expected mortality rate. High risk variables included WHO functional class IV; 6MWD < 165 m; B-type natriuretic peptide (BNP) > 300 ng/L, NT-proBNP > 1400 ng/L or RAP > 14 mmHg; cardiac index (CI) < 2.0L/min/m2 or oxygen saturation of mixed venose blood (SvO2) < 60%. Patients with at least 2 high risk variables including CI or SvO2 were defined as high risk. We analyzed echocardiographic parameters by logistic regression to investigate the risk prediction value of TR in precapillary PH. We put morphological indexes of right heart (RA area, RV, RVD/LVD ratio, RWT)and left heart [left atrium diameter (LAD), left ventricular internal diameter at end-diastole (LVIDd)], RV function indexes (S’ and FAC), left ventricular ejection fraction (LVEF), TR-sPAPECHO and TR severity into the equation. Since TAPSE and S’ both reflect the long axis motion of RV free wall and the repeatability of S’ was better than TAPSE in our previous study [8], we just put S’ into the equation.
Statistical analysis
SPSS 24.0 software was used for statistical analysis (Chicago, IL, USA). The missing data was deleted. Normal distribution was assessed by the Shapiro–Wilk test. Continuous variables were expressed as mean ± standard deviation with normal distribution or as median (interquartile range) for variables without normal distribution. Categorical variables were expressed as frequency and percentage. Comparisons of parameters among four groups were performed by a one-way analysis of variance (ANOVA) when normally distributed or nonparametric test when not normally distributed. Categorical variables were described as frequencies and percentages, which were compared using χ2 test. Probabilities of P < 0.05 were considered statistically significant. Pearson correlation analysis was performed to evaluate the correlation between sPAPECHO and mPAPRHC. The impact factors on risk stratification of precapillary PH were analyzed by Multivariate logistic regression analysis. Intraobserver and interobserver reproducibility were assessed in randomly selected 28 subjects. Interobserver reproducibility was tested by two independent observers. Interobserver and intraobserver reproducibility were evaluated by means of intraclass correlation coefficient (ICC).
Results
Baseline characteristics
A total of 207 patients diagnosed precapillary PH by RHC were finally included as shown in Fig. 1. One hundred one subjects were diagnosed chronic thromboembolic PH (48.8%), 81 were PAH (81, 39.1%), and 25 (12.1%) were lung diseases or of other etiology. Typical images of color and continuous-wave Doppler in different TR groups were shown in Fig. 2. The proportion of None, Trace, Mild, Moderate and Severe TR was 2.4%, 23.7%, 39.1%, 28.5% and 6.3% respectively, as shown in Fig. 3. There were only 5 patients without TR and the number was small. Considering None or Trace TR had similar effects on cardiac structure, function and clinical significance and the difference between them was little, we classified 5 None TR cases into the Trace group. Baseline demographics and clinical characteristics of the four groups were described in Table 1and Fig. 4. There were no differences in age, sex and body surface area (BSA) among the four groups. Although the proportion of patients with WHO heart function III or IV class and 6MWD did not differ among the four groups (p = 0.370, 0.772 respectively), NT-proBNP, the sensitive indicator of heart failure increased significantly from Trace TR to Moderate and above (p < 0.001). However, there was no significant difference in plasma NT-proBNP level between moderate and severe TR group (P = 0.915).
RHC and echocardiography parameters
RHC and echocardiography parameters were shown in Table 2. There were significant differences among the four groups in sPAPRHC, mPAPRHC, and PVR (p = 0.004, 0.014, < 0.001 respectively), which was mainly for the difference between Trace TR and other TR groups (p < 0.05 respectively). Patients with mild to severe TR had higher sPAP and PVR compared with patients with Trace TR. However, it’s not that the more severe the regurgitation, the higher the sPAP and PVR. Moderate and Severe TR group had higher RAP than Trace and Mild TR group (p = 0.018). The similar results were also found in TR-sPAPECHO, TR-mPAPECHO and eRAP (p < 0.001, < 0.001, < 0.001 respectively). In the morphology of the right heart by echocardiography, RA area increased gradually with TR aggravation (p < 0.001), which was the most obvious. Secondly, Moderate and Severe TR group had larger RV, smaller LVIDd and higher RVD/LVD ratio than Trace and Mild TR group (p < 0.001, < 0.001 respectively). Thirdly, patients with Mild TR and above had a thicker RV wall than those with Trace TR (p = 0.006). In RV function by echocardiography, TAPSE in moderate and severe TR group decreased compared with Trace and Mild group (p = 0.006). TAPSE/TR-sPAP ECHO ratio representing a non-invasive assessment of RV-PA coupling also decreased with the increase of TR (p < 0.001). No statistical differences were found in S’ and FAC.
Reproducibility analysis
The interobserver ICC was 0.884 (95% CI: 0.723–0.953) for VCTR and 0.906 (95% CI: 0.631–0.970) for the TR jet area. The intraobserver ICC was 0.918 (95% CI: 0.832–0.961) for VCTR and 0.921 (95% CI: 0.701–0.975) for the jet area.
Association between TR-sPAPECHO and mPAPRHC in four groups
In our previous study [2], Bland–Altman analysis demonstrated low bias between RHC and TR-derived parameters with wide limits of agreements. In our patients, TR-sPAPECHO in Moderate TR group had the greatest correlation coefficient with mPAPRHC (0.742, p < 0.001) followed by Mild TR group (0.635, p < 0.001) and severe group (0.592, p = 0.033). In Trace TR group, 5 had no TR and 15 were with insufficient quality of TR signals, totally accounting for 9.7% of the whole population. We evaluated the correlation between sPAPECHO and mPAPRHC in other 34 patients and no correlation was seen in Trace TR group (0.308, p = 0.076).
Echocardiography predictors for high-risk precapillary PH
There were 37 high-risk precapillary PH patients. The results of the logistic regression were presented in Table 3. Multivariate logistic regression showed three significant independent echocardiography predictors of high-risk precapillary PH: RVD/LVD (OR = 5.734; 95%CI1.502–21.889, p = 0.011), RA area (OR 1.054; 95% CI 1.004–1.107, p = 0.035) and S’(OR 0.735, 95% CI 0.569–0.949, p = 0.018).
Discussion
In our study, we reported the distribution of TR in patients with precapillary PH, and found that up to 26% of patients had only trace or none of TR, even though the PAP and PVR significantly increased and the right heart significantly enlarged. On the one hand, it showed that PH was not necessarily accompanied by significant TR; on the other hand, it also suggested that routine TR-related methods could not be used to estimate PAP in these patients. Meanwhile, we must pay attention to the preliminary screening of PH in combination with other indirect signs and the estimated mean pressure by pulmonary regurgitation (PR), so as to avoid misdiagnosing. In meta-analysis by Wang et al. [9], 33.9% to 56% of the PH patients were without TR. However, in another study by Chen et al. [10], 96.5% of the PH patients had TR. Due to different etiology, classification and severity of PH, the results of TR distribution varied wildly. The patients selected in this study were diagnosed precapillary PH with relatively high PAP and PVR. Mild and moderate TR groups accounted for about two-thirds of our precapillary PH patients, in which TR-sPAPECHO were highly correlated with mPAPRHC the gold standard for measuring PAP. The correlation coefficient in severe TR group was 0.592 (p = 0.033) not as good as Moderate (0.742, p < 0.001) and Mild TR group (0.635, p < 0.001), while TR-sPAPECHO could also be used to estimate PAP in severe TR group. We reviewed our 13 patients with severe TR and found that there were no obvious characteristic dagger-shaped spectrum in all of them. The reason may be that TR in our precapillary PH patients was secondary and functional, while dagger-shaped spectrum with an early peak pressure and rapid decay was often seen in intrinsic tricuspid valve disease as shown by Fox et al. [11]. We are not quite sure about this and will further study this phenomenon. There was no correlation in Trace TR group accounting for 26% of our population, therefore TR-sPAPECHO was not applicable to assess PAP in these patients. Patients with PH are often accompanied by pulmonary artery dilatation and PR. PAP assessment by PR is also a good selection in PH patients, which has been confirmed by our previous findings [12].
We also found that there were no significant differences in WHO heart function class and exercise tolerance (6MWD) among patients with different degree of TR, while NT-proBNP was significantly different among the four groups. It indicated that heart function class and exercise tolerance may depend more on the compensation ability of RV function relative to the increased load. NT-proBNP was significantly related to the degree of TR. TR significantly increased RAP leading to intracardiac volume expansion and filling pressure overload of the right heart. The resulting end-diastolic wall stress prompted ventricular and atrial myocardium to produce more NT-proBNP [13], which is much more sensitive and commonly elevated before patients had exercise intolerance and dyspnea that are neither specific nor sensitive for predicting heart function. In terms of right heart function, the routine parameters S' and FAC had no significant differences in different degrees of TR groups, while TAPSE was lower in patients with moderate and severe TR. On the one hand, it may be because these parameters have a certain load dependency [14] and TR can induce overestimations of RV systolic function to the increased blood volume [15]. On the other hand, it may also suggested that the factors affecting the compensation and decompensation of RV function in PH patients were complex, and TR was not a decisive factor. Preload and afterload, the etiology and length of the disease, and RV-pulmonary artery coupling all affect RV function, which should be comprehensively considered in clinical practice. In our study, TAPSE/TR-sPAPECHO representing a non-invasive assessment of RV-PA coupling decreased with the increase of TR, which can be obtained from routine indicators, more convenient for clinical use and may be helpful in evaluating RV function.
Previous studies have shown that TR was an important echocardiographic index affecting prognosis [1, 16,17,18]. Referring to the risk stratification in patients with PAH, we found that the echocardiographic parameters that can independently predict the high-risk patients with precapillary PH were RVD/LVD ratio, RA area and S', which reflected right heart remodeling and RV longitudinal systolic function. The degree of TR was not an independent predictor of high-risk precapillary PH. However, the more severe the TR was, the more obvious the expansion of RA and RV was. RAP and NT-proBNP also increased with TR aggravation. So we believe that TR may play an indirect role in risk stratification of precapillary PH by affecting these indicators.
Study limitations
A significant limitation of this study is the retrospective nature and the small number of patients from a single-center. So studies involving a larger number of patients will be needed to verify our findings. A selection bias was also in our study since TR-sPAPECHO was the most convenient and commonly used method as the main screening method to decide whether RHC is indicated or not. In this study, only conventional parameters were used to evaluate RV remodeling and RV function by echocardiography. However, in these subjects all the three-dimensional images and two-dimensional dynamic images that could be used for speckle tracking were also collected. In the future, we will further analyze these data to study the impact of TR on RV function. In clinical practice, echocardiography and RHC could not be performed at the same time. The interval selected for this study was within 3 days so as to minimize its impact on the measurements.
Conclusions
Precapillary PH was not necessarily accompanied by significant TR. None (2.4%) or Trace TR accounted for 26% in our population and TR-sPAPECHO was not applicable to estimate PAP in these patients. The correlation coefficient between TR-sPAPECHO and mPAPRHC in severe TR group was not as good as Moderate and Mild TR group, while TR-sPAPECHO could still be used to estimate PAP in this group. RVD/LVD ratio, RA area and S' can independently predict the high-risk patients with precapillary PH. TR may play an indirect role in risk stratification of precapillary PH by affecting these indicators.
Availability of data and materials
The original data will be shared on reasonable request by contacting the corresponding author.
Abbreviations
- TR:
-
Tricuspid regurgitation
- PH:
-
Pulmonary hypertension
- PAP:
-
Pulmonary artery pressure
- RHC:
-
Right heart catheterization
- sPAPECHO :
-
Systolic pulmonary artery pressure by echocardiography
- mPAPRHC :
-
Mean pulmonary artery pressure by right heart catheterization
- RA:
-
Right atrium
- RAP:
-
Right atrial pressure
- RVD:
-
Right ventricular basal diameter
- LVD:
-
Left ventricular basal diameter
- RV:
-
Right ventricle
- S’:
-
Systolic annular tissue velocity of the lateral tricuspid annulus
- TR Vmax:
-
Peak velocity of tricuspid regurgitation
- mPAPECHO :
-
Mean pulmonary artery pressure by echocardiography
- PAWP:
-
Pulmonary artery wedge pressure
- PVR:
-
Pulmonary vascular resistance
- WHO:
-
World Health Organization
- NT-proBNP:
-
N-terminal pro-B-type natriuretic peptide
- 6MWD:
-
6-Minute walk distance
- sPAPRHC :
-
Systolic pulmonary artery pressure by right heart catheterization
- CO:
-
Cardiac output
- ASE:
-
American Society of Echocardiography
- RWT:
-
Right ventricular free wall thickness
- VC:
-
Vena contracta
- TR-PG:
-
Peak pressure gradient of tricuspid regurgitation
- TR-mPG:
-
Mean pressure gradient of tricuspid regurgitation
- eRAP:
-
Estimated right atrial pressure
- TAPSE:
-
Tricuspid annular plane systolic excursion
- FAC:
-
Fractional area change of right ventricle
- PAH:
-
Pulmonary artery hypertension
- BNP:
-
B-type natriuretic peptide
- CI:
-
Cardiac index
- SvO2:
-
Oxygen saturation of mixed venose blood
- LAD:
-
Left atrium diameter
- LVIDd:
-
Left ventricular internal diameter at end-diastole
- LVEF:
-
Left ventricular ejection fraction
- ANOVA:
-
One-way analysis of variance
- BSA:
-
Body surface area
- ICC:
-
Intraclass correlation coefficient
References
Mukai J, Tanaka H, Sano H, Yokota S, Suto M, Takada H, et al. Associations between functional tricuspid regurgitation and long-term outcomes for patients with pulmonary hypertension. Int J Cardiovasc Imaging. 2020;36(7):1261–9.
Lv GJ, Li AL, Tao XC, Zhai YN, Zhang Y, Lei JP, et al. The accuracy and influencing factors of Doppler echocardiography in estimating pulmonary artery systolic pressure: comparison with right heart catheterization: a retrospective cross-sectional study. BMC Med Imaging. 2022;22(1):91.
Krishnan A, Markham R, Savage M, Wong YW, Walters D. Right heart catheterisation: how to do it. Heart Lung Circ. 2019;28(4):e71–8.
Lang RM, Badano LP, Mor-Avi V, Afilalo J, Armstrong A, Ernande L, et al. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J Am Soc Echocardiogr. 2015;28(1):1-39.e14.
Galiè N, Humbert M, Vachiery JL, Gibbs S, Lang I, Torbicki A, et al. 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 Respir J. 2015;46(4):903–75.
Galiè N, Channick RN, Frantz RP, Grünig E, Jing ZC, Moiseeva O, et al. Risk stratification and medical therapy of pulmonary arterial hypertension. Eur Respir J. 2019;53(1):1801889.
Working Group on Pulmonary Embolism and Pulmonary Vascular Disease of Chinese Medical Association Respiratory Branch; Pulmonary Embolism and Pulmonary Vascular Disease Working Committee of Respiratory Doctor Branch of Chinese Medical Doctor Association; National Collaborative Group on Prevention and Treatment of Pulmonary Embolism and Pulmonary Vascular Disease; Expert Group of the National Pulmonary Hypertension Standardization System Construction Project. Chinese guidelines for diagnosis and treatment of pulmonary hypertension. Natl Med J China. 2021;101(1):11–51.
Li AL, Zhai YN, Zhai ZG, Xie WM, Wan J, Tao XC, et al. Echocardiographic study of right ventricular dysfunction in patients with chronic thromboembolic pulmonary hypertension: Comparison of the right ventricular free wall longitudinal strain and conventional parameters. Chin J Ultrasonogr. 2018;27(4):559–64.
Wang N, Fulcher J, Abeysuriya N, McGrady M, Wilcox I, Celermajer D, et al. Tricuspid regurgitation is associated with increased mortality independent of pulmonary pressures and right heart failure: a systematic review and meta-analysis. Eur Heart J. 2019;40(5):476–84.
Chen L, Larsen CM, Le RJ, Connolly HM, Pislaru SV, Murphy JG, et al. The prognostic significance of tricuspid valve regurgitation in pulmonary arterial hypertension. Clin Res J. 2018;12(4):1572–80.
Fox DJ, Khattar RS. Carcinoid heart disease: presentation, diagnosis, and management. Heart. 2004;90(10):1224–8.
Li AL, Zhai YN, Tao XC, Zhang Y, Li L, Lv GJ, et al. The Accuracy and the Cutoff Value of Different Echocardiographic Methods in Screening Pulmonary Hypertension. Chinese J Ultrasound Med. 2021;37(10):1116–9.
Mueller C, McDonald K, de Boer RA, Maisel A, Cleland JGF, Kozhuharov N, et al. Heart Failure Association of the European Society of Cardiology practical guidance on the use of natriuretic peptide concentrations. Eur J Heart Fail. 2019;21(6):715–31.
Dandel M, Hetzer R. Evaluation of the right ventricle by echocardiography: particularities and major challenges. Expert Rev Cardiovasc Ther. 2018;16(4):259–75.
Dandel M, Knosalla C, Kemper D, Stein J, Hetzer R. Assessment of right ventricular adaptability to loading conditions can improve timing of listing to transplantation in patients with pulmonary arterial hypertension. J Heart Lung Trasplant. 2015;34(3):319–28.
Medvedofsky D, Aronson D, Gomberg-Maitland M, Thomeas V, Rich S, Spencer K, et al. Tricuspid regurgitation progression and regression in pulmonary arterial hypertension: implications for right ventricular and tricuspid valve apparatus geometry and patients outcome. Eur Heart J Cardiovasc Imaging. 2017;18(1):86–94.
Gerçek M, Rudolph V. Secondary Tricuspid Regurgitation: Pathophysiology, Incidence and Prognosis. Front Cardiovasc Med. 2021;8:701243.
Schneider M, König A, Geller W, Dannenberg V, Winter MP, Thomas Binder T, et al. Severe tricuspid regurgitation: prognostic role of right heart remodelling and pulmonary hypertension. Eur Heart J Cardiovasc Imaging. 2022;23(2):246–54.
Acknowledgements
The authors would like to thank the Pulmonary Vascular Disease Team and the Cardiology Team of China‐Japan Friendship Hospital for their support of this study.
Funding
The study was funded by Capital Health Development Research Project (2020–2-4063), Chinese Academy of Medical Sciences (CAMS) Innovation Fund for Medical Sciences (CIFMS) (2021-I2M-1–049) and National Key Clinical Specialty Construction Project (2020-QTL-009). The funding body had no role in the design of the study, collection, analysis, and interpretation of data and in writing the manuscript.
Author information
Authors and Affiliations
Contributions
LAL created the idea and designed the study. LAL and LJH collected and analyzed the data, wrote and submitted the manuscript. LAL, LL and ZYN performed echocardiography. ZY and CAH helped organize the data. TXC provided the data of RHC. GQ and XWM helped collect the cases. ZZG gave support to the study. All authors have given approval to the final version of the manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
This study complied with the Declaration of Helsinki. The institutional review board of China-Japan Friendship Hospital waived the need for written informed consent from patients as this study was a retrospective analysis of clinically acquired data. This study was approved by the Ethics Committee of China-Japan Friendship Hospital in Peking of China (No.2020–95-K59). All methods were carried out in accordance with relevant guidelines and regulations.
Consent for publication
Not applicable
Competing interests
The authors declare no financial and non-financial competing interests.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Li, J., Li, A., Zhai, Y. et al. Prevalence and risk prediction value of tricuspid regurgitation by echocardiography in precapillary pulmonary hypertension. BMC Pulm Med 22, 409 (2022). https://doi.org/10.1186/s12890-022-02207-4
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s12890-022-02207-4