Methods: Between January 2015 and January 2017, a total of 282 consecutive patients (250 males, 32 females; mean age: 46±10 years; range, 18 to 66 years) with advanced heart failure who were referred for heart transplantation were retrospectively analyzed. The patients were divided into two groups as severe (n=84) and non-severe functional mitral regurgitation (n=198). Patients" medical histories, demographic characteristics, echocardiographic evaluations, and findings of right heart catheterization were recorded.
Results: The two groups were similar in terms of left ventricular ejection fraction, the New York Heart Association functional class, Interagency Registry for Mechanically Assisted Circulatory Support profile, and the duration of heart failure (p>0.05). Both groups were also similar with respect to tricuspid annular plane systolic excursion and right ventricular stroke work index. Functional mitral regurgitation was the only statistically significant variable in the univariate analysis for tricuspid annular plane systolic excursion (odds ratio [OR]: 0.58; 95% confidence interval [CI] 0.34-0.97; p=0.04), with no significant effect in the multivariate analysis. In the univariate analysis for right ventricular stroke work index, pulmonary arterial systolic pressure (OR: 0.77; 95% CI 0.67-0.88; p<0.001) was a significant variable and also had a significant effect in the multivariate analysis (OR: 0.92; 95% CI 0.87-0.97; p=0.003). In the tertile analyses, there were no significant differences between the two groups with respect to tricuspid annular plane systolic excursion and right ventricular stroke work index.
Conclusion: We found no significant difference in right ventricular functions between the severe and non-severe functional mitral regurgitation groups in patients with advanced heart failure who had relatively short follow-up. Right ventricle can maintain its normal function at early stage. Adaptive remodeling of right ventricle may have an effect on these findings. Severe functional mitral regurgitation may be associated with adverse effects on advanced heart failure by increasing the right ventricular afterload.
Right ventricular (RV) dysfunction has adverse effects on the course of disease and mortality in the presence of chronic HF. Several parameters contribute to RV dysfunction including a longer duration of HF, pulmonary hypertension which as defined by a mean pulmonary artery pressure (PAPm) ≥25 mmHg regardless of the cause, and increased pulmonary vascular resistance (PVR) which, in turn, lead to elevated right-sided filling pressures in patients with HF.[5,6] Moreover, the presence of RV dysfunction may have an adverse effect on eligibility of patients for further therapies. Therefore, RV function must be taken into account in the pre-transplant evaluation.[7]
Echocardiography is the first-choice imaging technique to evaluate RV function. Tricuspid annular plane systolic excursion (TAPSE) is a straightforward and practical parameter for RV function.[8] Echocardiographic evaluation of the RV can be challenging due to its complex geometrical structure, resulting in inaccurate assessments, as well as considerable interobserver variability.
Right heart catheterization (RHC) still remains to be the gold standard to assess RV function, particularly for patients awaiting assist device implantation or transplantation. In addition, the guidelines of the International Society for Heart and Lung Transplantation (ISHLT) recommend serial RHC at three-month intervals in heart transplant candidates.[9] Right ventricular stroke work index (RVSWI) is one of the parameters of RHC to assess RV function, while PVR, pulmonary arterial elastance (PaE), pulmonary arterial capacitance (PaC) provide information on pulmonary afterload, the evaluation of which is as significant as that of RV function in patients with AdHF.[10-13]
Functional mitral regurgitation (FMR) is secondary to left ventricular (LV) remodeling without organic mitral valve disease. It has additive effects on LV filling and pulmonary arterial pressures in patients with HF.[14]
In the present study, we aimed to investigate the effects of severe FMR on the echocardiographic and RHC parameters such as TAPSE and RVSWI among potential heart transplant recipients.
Echocardiographic variables
Echocardiographic evaluation of patients
was made according to the American College of
Cardiology/American Heart Association (ACC/AHA)
guidelines for the echocardiographic assessment of
the right heart.[8] The LVEF was d etermined by the
biplane Simpson's method. The following parameters
were measured: the sizes of the left atrium (LA), LV and RV, the ratio of early transmitral flow velocity
(E)-to-early diastolic mitral annular velocity (e")
and deceleration time (DT) of the mitral E wave,
pulmonary arterial systolic pressure (PAPs), PVR,
TAPSE, systolic tricuspid velocity, and plethora.
To differentiate severe FMR from moderate FMR,
the effective regurgitant orifice area (EROA) and
regurgitant volume (RV") were calculated using the
proximal isovelocity surface area (PISA) method.
Severe FMR was defined as an EROA of ≥20 mm²
and an RV of ≥30 mL.[15-17] In addition, FMR was
evaluated with PISA measurement in 146 patients
(70 of whom with severe, 76 of whom with moderate
FMR) and also by conventional methods, such as
vena contracta (VC) and visual classification; in
the presence of inconsistent results between the
methods, the visual classification results were taken
into account. The PISA could not be measured in
136 patients, most of whom (82%) had mild and
mild-to-moderate FMR and, thus, FMR was visually
classified as non-severe FMR. Of 136 patients,
18% had moderate and severe FMR on the basis
of visual classification, and due to eccentric and
wall impinging jet, PISA could not be measured.
To differentiate between severe FMR and moderate
FMR, VC and a pulmonary vein flow pattern through transesophageal echocardiography were
assessed. Systolic flow reversal in the pulmonary
vein and a VC ≥0.7 cm was defined as a severe
FMR. Tricuspid regurgitation (TR) was evaluated
with color flow Doppler and a TR VC ≥0.7 cm was
recognized as severe TR. The PAPs was calculated
using TR velocity plus RA pressure (4 × [peak
systolic TR velocity at end-expiration]2 + RA
pressure). The RA pressure was estimated from
inferior vena cava (IVC) and its collapsibility. The
IVC diameter <2.1 cm that collapsed >50% with a
sniff suggested a normal RA pressure (5 mmHg),
IVC diameter >2.1 cm that collapsed <50% with a
sniff suggested an elevated RA pressure (15 mmHg)
and IVC diameters >2.1 cm without collapse (<50%),
RA pressure was upgraded to 20 mmHg. When
uncertainty existed, secondary findings of elevated
RA pressure were assessed.
Hemodynamic variables
Right heart catheterization was performed using
a Swan-Ganz catheter and LV and aortic pressures
were assessed using a pigtail catheter under
hemodynamic and fluoroscopic guidance according
to the 2015 European Society of Cardiology/
European Respiratory Society (ESC/ERS) guidelines for the diagnosis and treatment of pulmonary
hypertension.[9] Pulmonary arterial systolic, mean and
diastolic pressures (PAPs, PAPm, PAPd), pulmonary
capillary wedge pressure (PCWP), mean right
atrial pressure (RAPm), transpulmonary pressure
gradient (TPG), diastolic pulmonary gradient
(DPG), P VR, P aE [ PaE= ( PAPm-PCWP)/SV], P aC
[PaC= SV/(PAPs-PAPd)], RVSWI [RVSWI= (PAPm-
RAPm)xSVIx0.0136], systolic blood pressure (SBP)
and diastolic blood pressure (DBP), LV end-diastolic
pressure (LVEDP), transsystemic gradient (TSG),
systemic vascular resistance (SVR), cardiac output
(CO) by the direct Fick method, cardiac index (CI),
stroke volume (SV), stroke volume index (SVI)
and left ventricle stroke work index [LVSWI =
(mean aortic pressure-PAWP)xSVIx0.0136] were
measured.
RV functional analysis
The RV function was evaluated using both
echocardiographic and RHC parameters. A TAPSE
of >2.0 cm suggests normal biventricular function,
while a TAPSE of ≤1.5 cm suggests RV dysfunction
according to the ACC/AHA guidelines for the
echocardiographic assessment of the right heart in
adults.[8,18] The cut-off value o f RVSWI in patients
with AdHF has not been reported, while the normal
range of RVSWI for healthy individuals is considered
to be 5 to 10 gxm/m2/beat. Some previous studies
have shown that an RVSWI of <5 gxm/m2/beat
reflects RV dysfunction.[19,20] In this study, RV
dysfunction was defined as a TAPSE of ≤1.5 cm and
an RVSWI of <5 gxm/m2/beat.
Statistical analysis
Statistical analysis was performed using the
IBM SPSS version 21.0 software (IBM Corp.,
Armonk, NY, USA). Continuous variables were
presented in mean ± standard deviation (SD)
or median (interquartile range [IQR]), while
categorical variables were presented in number
and frequency. The two groups were compared
using the Student t-test or Wilcoxon rank-sum
test for continuous variables and Fisher exact
test for categorical variables. Multivariate logistic
regression models were used to analyze the data.
In the multivariate analysis, covariates such as
severe FMR, PAP, PVR, LVEF, and the duration
of HF were identified according to their clinical
and biological plausibility and in association with
RV dysfunction which was shown in previous
studies.[5,9,10,14,15] We also performed univariate
analysis and, then, variables with a p value of <0.10 were included in the multivariate model.
Tertile analyses were made according to TAPSE
and RVSWI. A two-tailed p value of < 0.05 was
considered statistically significant.
Table 1. Baseline characteristics of the patients
Echocardiographic findings
Echocardiographic parameters are shown in
Table 2. There was no significant difference in
the LVEF between the two groups (p=0.44). The
LA diameter, LV end-diastolic diameter and LV
end-systolic diameter were found to be higher in
patients with severe FMR, compared to those with
non-severe FMR (p<0.01). Although higher PAPs and
PVR and a higher incidence of severe TR were found
in patients with severe FMR (p<0.01, p<0.01, p=0.01,
respectively), TAPSE and ST (systolic velocity of the
tricuspid annulus) which reflect RV function were
similar in both groups (p=0.57, p=0.91).
Table 2. Echocardiographic parameters
Hemodynamic characteristics
Findings of left and RHC are shown in Table 3.
Patients with severe FMR had significantly lower
CO, CI, SV, SVI, and LVSWI (p=0.04, p=0.04,
p=0.01, p<0.01, p<0.01, respectively). Systemic
vascular resistance was similar in the two groups
(p=0.81). Patients with severe FMR had significantly
increased PAPs, PAPm, PAPd, PCWP, and TPG
(p=0.01, p<0.01, p<0.01, p=0.04 and p=0.01, respectively). Severe FMR was associated with an
increased PVR, PaE and a decreased PaC (p=0.02,
p<0.01, p<0.01, respectively), but not with RVSWI
(p=0.44).
Table 3. Findings of left and right heart catheterization
Univariate and multivariate analyses for TAPSE
and RVSWI
Univariate and multivariate analysis results for
TAPSE are shown in Table 4. The presence of a
TAPSE of ≤1.5 cm and an RVSWI of <5 gxm/m2/beat
was accepted as RV dysfunction.[8,18-20] Accordingly,
multivariate logistic regression analysis was performed
to identify RV dysfunction. In addition, PAPs, PAPd,
PVR, LVEF and the duration of HF were included
in the multivariate analysis. The only statistically
significant variable in the univariate logistic regression
analysis for TAPSE was severe FMR (odds ratio
[OR]: 0.58; 95% confidence interval [CI] 0.34-0.97;
p=0.04) and, therefore, we did not perform multivariate
analysis for TAPSE.
Table 4. Univariate and multivariate analyses for TAPSE
Both univariate and multivariate regression analysis results for RVSWI are shown in Table 5. In the univariate logistic regression analysis for RVSWI, PAPs (OR: 0.77; 95% CI 0.67-0.88; p<0.001), PAPm (OR: 0.74; 95% CI 0.63-0.85; p<0.001), PAPd (OR: 0.67; 95% CI 0.55-0.83; p<0.001), and PVR (OR: 0.38; 95% CI 0.20-0.75; p=0.005) were significant variables, while PAPs (OR: 0.95; 95% CI 0.92-0.98; p<0.001) also had a significant effect in the multivariate logistic regression analysis and PAPm was not included in the multivariate study due to collinearity.
Table 5. Univariate and multivariate analyses for RVSWI
The tertile analyses according to TAPSE and
RVSWI
Table 6 shows TAPSE tertiles in patients with
severe and non-severe FMR. In the light of previous
studies, the patients were classified into three tertiles
according to TAPSE and RVSWI.[8,18-21] The TAPSE
tertiles were defined as low (TAPSE ≤1.5 cm), middle (1.6-1.9 cm), high (TAPSE ≥2.0 cm). In the severe
FMR group, 40 (44.4%) patients, 37 (41.1%) patients,
and 13 (14.4%) patients fell into the low, middle, and
high TAPSE tertiles, respectively.
Table 6. TAPSE tertiles in patients with severe and non-severe FMR
Table 7 shows RVSWI tertiles in patients with severe and non-severe FMR. Similarly, the patients were classified into three RVSWI tertiles (low: RVSWI <5 gxm/m2/beat; middle: RVSWI 5-10 gxm/m2/beat; high: RVSWI >10 gxm/m2/beat). In the severe FMR group, 14 (20.3%) patients were in the low RVSWI tertile, 41 (59.4%) patients were in the middle RVSWI tertile, and 14 (20.3%) patients were in the high RVSWI tertile. There were no significant differences between the two FMR groups with respect to the TAPSE (p=0.56, p=0.42, p=0.35, respectively) and RVSWI (p=0.05, p=0.13, p=0.85, respectively) tertiles.
Table 7. RVSWI tertiles in patients with severe and non-severe FMR
Advanced heart failure represents the last phase of HF. Standard treatments are frequently inadequate; heart transplantation and MCS devices are potential treatment options in selected patients. Right ventricular dysfunction is a significant parameter for the selection of patients. We examined the effect of FMR on RV function which is an important comorbidity in patients with AdHF. We found no significant differences between the non-severe FMR and severe FMR groups in terms of TAPSE and RVSWI, reflecting the right heart systolic function (p=0.57, p=0.44, respectively). Although there were no significant differences in TAPSE and RVSWI between the two FMR groups in the univariate, multivariate and tertile analyses, the patients with severe FMR had significantly higher PVR, PaE and significantly lower PaC than the patients with non-severe FMR (p=0.01, p=0.02, p<0.01, respectively). The severe FMR group had also higher PAPs, PAPm and PAPd, as well as increased PCWP and decreased CO, CI, SV, SVI and LVSWI, as expected. The only statistically significant variable in the univariate logistic regression analysis for TAPSE was severe FMR. In the univariate logistic regression analysis for RVSWI, PAPs, PAPd, and PVR were significant variables, while PAPs had also a significant effect in the multivariate analysis.
Previous studies have shown that AdHF accompanied by severe FMR is associated with dyspnea, exercise intolerance, and an increased risk for mortality due to increased pulmonary pressures.[14,22,23] Cappola et al.[24] reported that PAPm and PVR were the strongest predictors of mortality, with mortality rates almost doubled when PVR was ≥3 WU. In our study, the mean PAPm was 37.4±10.3 mmHg and the mean PVR was 4.4±2.6 WU and significantly increased PAPm and PVR were found in the severe FMR group, indicating the negative effects of severe FMR on PAP and PVR in heart transplant candidates.
Nishikawa and Tanemoto[25] showed that an increased PVR of 2.3 WU in patients with AdHF accompanied by severe FMR decreased to 1.7 WU after mitral annuloplasty. Another study reported significant improvements in ejection fraction (EF) and the NYHA functional class after mitral valve repair or replacement surgery, as well as significant decreases in PAPs and PCWP among patients with an EF <35% and severe FMR.[26] The authors speculated that a surgery for secondary MR in selected patients with a low EF could be an alternative to cardiac transplantation. A retrospective study on MitraClip® treatment in patients with AdHF found decreased PAP and PVR and improvements in the NYHA functional class and reported that MitraClip® t reatment m ight be beneficial as a bridge-to-transplant in patients on the transplantation list.[27] There were also some case reports where MitraClip® t reatment was found to be effective in patients with severe FMR, resulting in removal from the waiting list for transplantation.[28,29]
Many hemodynamic parameters reflecting pulmonary vascular remodeling have been studied, one of which is PVR though its relationship with CO limits its diagnostic value. New parameters such as PaC and PaE have been proposed, as PVR may be higher in patients with a low CO. While PVR reflects the resistive component of the RV afterload, PaC reflects its dynamic component.[30] Dragu et al.[11] found that PaC was a strong independent hemodynamic marker in HF and could contribute to increased mortality rates associated with reactive pulmonary hypertension (PAH). In addition, several studies have reported that, for the assessment of RV afterload, evaluating PVR together with PaC may be more appropriate than evaluating these two parameters separately.[11,12,31] Amin et al.[13] proposed that, in addition to PVR, PaE calculation might be useful to recognize the changes in the RV afterload early and precisely. We also assessed RV afterload along with PVR, PaE, and PaC and found that PaC was significantly lower in the severe FMR group, while PVR and PaE were significantly higher.
In this study, RV afterload which was defined by PCWP, was significantly increased in patients with severe FMR, but RV function was similar in the two groups, which can be explained with adaptive remodeling of the RV due to RV-pulmonary artery coupling which is defined as the RV adaptation to chronic overload. Our patient group consisted of patients diagnosed with HF within a maximum of four years. The RV function would be preserved at the early stage of overload, but maladaptation may occur over time, resulting in RV dysfunction. Therefore, despite the increased pulmonary afterload, RV function could appear normal in early stage of the disease.
This study has some limitations. It is a retrospective study presenting a single tertiary center experience; therefore, the study cohort may not represent the overall AdHF population. While quantitative measurements were used for classification to differentiate severe FMR from moderate FMR, mild and mild-to-moderate mitral regurgitation were visually classified as non-severe FMR, since PISA could not be measured in most patients. Proportionate versus disproportionate mitral regurgitation could not be evaluated due to the absence of end-diastolic volume measurements. As no prognostic data were available, we could not assess the relationship of mitral regurgitation and RV dysfunction with prognosis. Similarly, as the duration of mitral regurgitation was unavailable, its effect on our results could not be identified. Although conditions that directly affect primarily RV were excluded, RV could not have been assessed with cardiac magnetic resonance imaging to evaluate intrinsic RV dysfunction. Of note, the present study was performed before amendments in the criteria of pulmonary hypertension; therefore, we used a PABm of >25 mmHg to define pulmonary hypertension.
In conclusion, right ventricular function as assessed by the right ventricular stroke work index and tricuspid annular plane systolic excursion was similar between the patients with severe and non-severe functional mitral regurgitation. However, the patients with severe functional mitral regurgitation had significantly higher pulmonary afterload as assessed by pulmonary vascular resistance, pulmonary arterial capacitance, and pulmonary arterial elastance. Given that the relatively short follow-up of the patients with advanced heart failure (approximately eight months), it can be speculated that right ventricular function, which appeared to be preserved at an early stage, may worsen in the presence of an increased afterload over time due to constant pressure overload. Thus, treatment of severe functional mitral regurgitation with percutaneous techniques or surgery in the early period may be considered to protect right ventricular function in the long term.
Ethics Committee Approval: The study protocol was approved by the Health Science Univercity, Kartal Koşuyolu High Specialization Training and Research Hospital Ethics Committee (date: 25.09.2018; no: 2018.6/15-114). The study was conducted in accordance with the principles of the Declaration of Helsinki.
Patient Consent for Publication: A written informed consent was obtained from each patient.
Data Sharing Statement: The data that support the findings of this study are available from the corresponding author upon reasonable request.
Author Contributions: Idea/concept: B.G.S., C.D., N.O.; Design: Z.B., S.C.E.; Control/supervision: C.K., M.K.K., N.O.; Data collection and/or processing: B.G.S., A.K., S.U., R.B.A., A.H.; Analysis and/or interpretation: R.D.A., B.G.S., Z.B.; Literature review: O.Y.A., A.K., H.C.T.; Writing the article: B.G.S., S.C.E.; Critical review: C.K., M.K.K., N.O.; References and fundings: A.K., O.Y.A.; Materials: B.G.S.
Conflict of Interest: The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.
Funding: The authors received no financial support for the research and/or authorship of this article.
1) Xanthakis V, Enserro DM, Larson MG, Wollert KC, Januzzi
JL, Levy D, et al. Prevalence, neurohormonal correlates, and
prognosis of heart failure stages in the community. JACC
Heart Fail 2016;4:808-15.
2) Bjork JB, Alton KK, Georgiopoulou VV, Butler J,
Kalogeropoulos AP. Defining advanced heart failure: A
systematic review of criteria used in clinical trials. J Card
Fail 2016;22:569-77.
3) Fang JC, Ewald GA, Allen LA, Butler J, Westlake
Canary CA, Colvin-Adams M, et al. Advanced (stage
D) heart failure: A statement from the Heart Failure
Society of America Guidelines Committee. J Card Fail
2015;21:519-34.
4) Crespo-Leiro MG, Metra M, Lund LH, Milicic D, Costanzo
MR, Filippatos G, et al. Advanced heart failure: A position
statement of the Heart Failure Association of the European
Society of Cardiology. Eur J Heart Fail 2018;20:1505-35.
5) Rao SD, Adusumalli S, Mazurek JA. Pulmonary hypertension
in heart failure patients. Card Fail Rev 2020;6:e05.
6) Elming MB, Hammer-Hansen S, Voges I, Nyktari E, Raja
AA, Svendsen JH, et al. Right ventricular dysfunction
and the effect of defibrillator implantation in patients
with nonischemic systolic heart failure. Circ Arrhythm
Electrophysiol 2019;12:e007022.
7) Kochav SM, Flores RJ, Truby LK, Topkara VK. Prognostic
Impact of Pulmonary Artery Pulsatility Index (PAPi) in
patients with advanced heart failure: Insights from the
ESCAPE trial. J Card Fail 2018;24:453-9.
8) Rudski LG, Lai WW, Afilalo J, Hua L, Handschumacher
MD, Chandrasekaran K, et al. Guidelines for the
echocardiographic assessment of the right heart in adults:
A report from the American Society of Echocardiography
endorsed by the European Association of Echocardiography,
a registered branch of the European Society of Cardiology,
and the Canadian Society of Echocardiography. J Am Soc
Echocardiogr 2010;23:685-713.
9) 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 Heart J 2016;37:67-119.
10) Cameli M, Lisi M, Righini FM, Tsioulpas C, Bernazzali S,
Maccherini M, et al. Right ventricular longitudinal strain
correlates well with right ventricular stroke work index
in patients with advanced heart failure referred for heart
transplantation. J Card Fail 2012;18:208-15.
11) Dragu R, Rispler S, Habib M, Sholy H, Hammerman H,
Galie N, et al. Pulmonary arterial capacitance in patients
with heart failure and reactive pulmonary hypertension. Eur
J Heart Fail 2015;17:74-80.
12) Dupont M, Mullens W, Skouri HN, Abrahams Z, Wu Y,
Taylor DO, et al. Prognostic role of pulmonary arterial
capacitance in advanced heart failure. Circ Heart Fail
2012;5:778-85.
13) Amin A, Taghavi S, Esmaeilzadeh M, Bakhshandeh H,
Naderi N, Maleki M. Pulmonary arterial elastance for
estimating right ventricular afterload in systolic heart failure.
Congest Heart Fail 2011;17:288-93.
14) Bursi F, Barbieri A, Grigioni F, Reggianini L, Zanasi V,
Leuzzi C, et al. Prognostic implications of functional mitral
regurgitation according to the severity of the underlying
chronic heart failure: A long-term outcome study. Eur J Heart
Fail 2010;12:382-8.
15) Grigioni F, Enriquez-Sarano M, Zehr KJ, Bailey KR,
Tajik AJ. Ischemic mitral regurgitation: Long-term outcome
and prognostic implications with quantitative Doppler
assessment. Circulation 2001;103:1759-64.
16) Lancellotti P, Moura L, Pierard LA, Agricola E, Popescu
BA, Tribouilloy C, et al. European Association of
Echocardiography recommendations for the assessment
of valvular regurgitation. Part 2: Mitral and tricuspid
regurgitation (native valve disease). Eur J Echocardiogr
2010;11:307-32.
17) Coats AJS, Anker SD, Baumbach A, Alfieri O, von Bardeleben
RS, Bauersachs J, et al. The management of secondary
mitral regurgitation in patients with heart failure: A joint position statement from the Heart Failure Association (HFA),
European Association of Cardiovascular Imaging (EACVI),
European Heart Rhythm Association (EHRA), and European
Association of Percutaneous Cardiovascular Interventions
(EAPCI) of the ESC. Eur Heart J 2021;42:1254-69.
18) López-Candales A, Rajagopalan N, Saxena N, Gulyasy B,
Edelman K, Bazaz R. Right ventricular systolic function is
not the sole determinant of tricuspid annular motion. Am J
Cardiol 2006;98:973-7.
19) Ibe T, Wada H, Sakakura K, Ito M, Ugata Y, Yamamoto
K, et al. Right ventricular stroke work index. Int Heart J
2018;59:1047-51.
20) Imamura T, Kinugawa K, Kinoshita O, Nawata K, Ono
M. High pulmonary vascular resistance in addition to low
right ventricular stroke work index effectively predicts
biventricular assist device requirement. J Artif Organs
2016;19:44-53.
21) Tello K, Axmann J, Ghofrani HA, Naeije R, Narcin N, Rieth
A, et al. Relevance of the TAPSE/PASP ratio in pulmonary
arterial hypertension. Int J Cardiol 2018;266:229-35.
22) Rosenkranz S, Gibbs JS, Wachter R, De Marco T, Vonk-
Noordegraaf A, Vachiéry JL. Left ventricular heart failure
and pulmonary hypertension. Eur Heart J 2016;37:942-54.
23) Giannini C, Fiorelli F, Colombo A, De Carlo M, Weisz
SH, Agricola E, et al. Right ventricular evaluation to
improve survival outcome in patients with severe functional
mitral regurgitation and advanced heart failure undergoing
MitraClip therapy. Int J Cardiol 2016;223:574-80.
24) Cappola TP, Felker GM, Kao WH, Hare JM, Baughman KL,
Kasper EK. Pulmonary hypertension and risk of death in
cardiomyopathy: Patients with myocarditis are at higher risk.
Circulation 2002;105:1663-8.
25) Nishigawa K, Tanemoto K. Restrictive mitral annuloplasty
for functional mitral regurgitation in patients with end-stage
cardiomyopathy. Circ J 2011;75:538-9.
26) Rukosujew A, Klotz S, Welp H, Bruch C, Ghezelbash F,
Schmidt C, et al. Surgery of secondary mitral insufficiency
in patients with impaired left ventricular function. J
Cardiothorac Surg 2009;4:36.
27) Geis NA, Pleger ST, Bekeredjian R, Chorianopoulos E,
Kreusser MM, Frankenstein L, et al. Haemodynamic effects
of percutaneous mitral valve edge-to-edge repair in patients
with end-stage heart failure awaiting heart transplantation.
ESC Heart Fail 2018;5:892-901.
28) Godino C, Scotti A, Agricola E, Pivato CA, Chiarito M, Stella
S, et al. Young patient with advanced heart failure no longer
a candidate for heart transplantation after MitraClip®
procedure. J Heart Valve Dis 2017;26:234-6.
29) Ferraro P, Biondi-Zoccai G, Giordano A. Transcatheter mitral
valve repair with mitraclip for significant mitral regurgitation
long after heart transplantion. Catheter Cardiovasc Interv
2016;88:144-9.