- Research
- Open access
- Published:
Interpapillary muscle distance independently predicts recurrent mitral regurgitation
Journal of Cardiothoracic Surgery volume 19, Article number: 147 (2024)
Abstract
Objective
Ischaemic secondary mitral regurgitation (ISMR) after surgery is due to the displacement of papillary muscles resulting from progressive enlargement of the left ventricle end-diastolic diameter (LVEDD). Our aim was to prove that if the interpapillary muscle distance (IPMD) is surgically stabilized, an increase in LVEDD will not lead to a recurrence of ischaemic mitral regurgitation (MR).
Methods
Ninety-six patients with ISMR, who underwent surgical revascularisation and annuloplasty, were randomly assigned in a 1:1 ratio to undergo papillary muscle approximation (PMA). At the 5-year follow-up, we assessed the correlation between PMA and echocardiographic improvements, the effect size of PMA on echocardiographic improvements, and a prediction model for recurrent MR using inferential tree analysis.
Results
There was a significant correlation between PMA and enhancements in both the α and β angles (Spearman’s rho > 0.7, p < 0.01). The α angle represents the angle between the annular plane and either the A2 annular-coaptation line or the P2 annular-coaptation line. The β angle indicates the angle between the annular plane and either the A2 annular-leaflet tip line or the P2 annular-leaflet tip line. PMA led to substantial improvements in LVEDD, tenting area, α and β angles, with a large effect size (Hedge’s g ≥ 8, 95% CI ORs ≠ 1). The most reliable predictor of recurrent MR grade was the interpapillary distance, as only patients with an interpapillary distance greater than 40 mm developed ≥ 3 + grade MR. For patients with an IPMD of 40 mm or less, the best predictor of recurrent MR grade was LVEDD. Among the patients, only those with LVEDD greater than 62 mm showed moderate (2+) MR, while only those with LVEDD less than or equal to 62 mm had absent to mild (1+) MR.
Conclusion
Prediction of recurrent ischaemic MR is not independent of progressive LVEDD increase. PMA-based surgical procedure stabilises IPMD.
Introduction
The management of secondary ischemic mitral regurgitation (SIMR) is a topic of intense debate in the field of cardiac surgery. However, there is one aspect that is indisputable: the etiopathology of ischemic MR is predominantly caused by chordal tethering of the valvular leaflets, resulting from displacement of the papillary muscles. This displacement is a consequence of the gradual enlargement of the ischemic left ventricle [1]. Apparently, complete revascularisation of the ischemic myocardial segments could potentially resolve ischemic MR, assuming that the myocardial segments remain viable. This is often the scenario for moderate ischemic MR, which is likely due to moderate chronic myocardial ischemia. In this group of patients, only coronary revascularization is needed to satisfactorily resolve the MR without requiring additional procedures. However, such a simple approach is not suitable for higher degrees of MR, which are conceivably the result of more severe myocardial damage. This specific patient group is prone to exhibiting a coronary disease pattern that opposes full revascularisation and non-viable myocardial segments. This results in a progressive eccentric hypertrophy of the impaired ventricle, with gradual papillary muscle displacement and chordal tethering. In this situation, it is customary to supplement coronary revascularisation with a mitral procedure [1]. There is a significant inconsistency between observational and clinical experimental data regarding the best procedure for mitral treatment in this population subset. This subset of patients is more likely to present with a pattern of coronary disease that is hostile to complete revascularization, and myocardial segments that are not viable. The consequence is progressive eccentric hypertrophy of the impaired ventricle, with a gradual displacement of the papillary muscles alongside chordal tethering. For this subset of patients, the addition of a mitral procedure to coronary revascularization is customary [1]. Our group's latest meta-analysis focused on the most relevant data currently available (i.e. randomized controlled trials [RCT] and propensity-score matched cohorts only). We found that mitral valve replacement (MVR) increased operative mortality, but resulted in decreased recurrent MR and reoperation rates during follow-up when compared to mitral restrictive annuloplasty [2]. The final element of the evidence jigsaw is created by combining restrictive mitral annuloplasty (RMA) with papillary muscle approximation (PMA). In our group's PMA RCT-Analysis study [3], we compared RMA to PMA alongside RMA for treating severe ischemic MR (with complete revascularisation received by both groups). The inclusion of PMA led to favourable ventricular remodelling and performance 5 years later: left ventricle end-diastolic diameter (LVEDD) experienced an average decline of − 5.8 ± 4.1 mm compared to − 0.2 ± 2.3 mm in the group without PMA (p < 0.01); and left ventricular ejection fraction (LVEF) had an average increase of 8.8 ± 5.9% compared to 2.5 ± 4.3% in the group without PMA (p < 0.01). Over the 5-year period, the occurrence of moderate-severe MR reoccurred in 4.7% compared to 22.9% in those who had and did not have PMA, respectively (p = 0.01) [3]. However, there is limited understanding regarding the physiological basis behind the advantage of reapproximating the papillary muscles through surgery and whether particular effects of this procedure on the geometry or conformation of the mitral apparatus are responsible for its positive impact on adverse left ventricular remodeling and recurrence of mitral regurgitation.
With this secondary analysis of the PMA trial, our aim is to establish a predictive model that identifies the correlation between post-PMA parametric improvements and their impact on mitigating the effect of progressive LVEDD enlargement on recurrent ischemic MR in a hierarchical manner.
Methods
Study design
The initial PMA RCT was included, with an identification number of 202201143 from the institutional review board (IRB), in the Transcatheter Edge to Edge Mitral Valve Repair vs Standard Surgical Mitral Valve Operation for Secondary Mitral Valve Regurgitation project (TEERMISO). TEERMISO is a prospective comparison of surgical and percutaneous interventions for secondary MR. The TEERMISO protocol was registered in advance with identification number NCT05090540 on the Protocol Registration and Result System of ClinicalTrials.gov, along with declaration of conformity number 2222269v0. TEERMISO is recruiting from several centres, which include Hokkaido University Hospital in Japan, Mondor University Hospital in France, Biomedical Campus in Italy, Centre Cardiologique du Nord in France, and Aberdeen Royal Infirmary in the United Kingdom. Enrollment for TEERMISO will cease in December 2023, with overall results to be produced thereafter. The PMA RCT was a clinical trial that randomly selected patients with severe chronic ischemic MR. The patients were divided into two groups: those who underwent isolated RMA and those who underwent RMA plus PMA (the latter group will be referred to as the "PMA group" for simplicity). Both groups received complete coronary artery bypass grafting (CABG). The trial was conducted in a prospective manner. The study was originally planned to identify a 4 mm reduction in LVEDD at the end of the trial compared to the baseline (1 vs. 5 mm) between the groups, with an equal allocation ratio of 1:1, a standard deviation of 5 mm, a 5% α-error, and 90% power. The initial sample size calculation indicated 35 patients per group for follow-up. However, this number was raised to 48 per group to accommodate unexpected variability and potential loss of one-third of patients during the follow-up period. Patient selection for the PMA RCT took place in three central Italian regions (Lazio, Campania, Abruzzo), with all participants referred to the Bio-Medical Campus academic tertiary centre in Rome.
Enrolment started in May 2007 and finished in November 2010. The surgical procedures were carried out by three different surgeons, and the follow-up concluded in November 2015.
Patient consent was obtained after the assigned IRB approval number 202201173 in accordance with the research guidance. This study complies with the Declaration of Helsinki.
Eligibility
Adults with coronary artery disease affecting multiple arteries and moderate to severe ischemic mitral regurgitation were eligible to take part in the study. Severe mitral regurgitation (MR) was classified as an effective regurgitant orifice area (EROA) of at least 0.4 cm2 or greater, identified via transthoracic echocardiography (TTE). Eligible patients had coronary targets that were affected by proximal lesions of high grade, which compromise viable myocardium that is ischemic. Exclusion criteria comprised any echocardiographic evidence of structural mitral valve pathology, myxomatous disease, prior endocarditis, rheumatic valve disease, leaflet prolapse, additional planned valvular or aortic concomitant procedure (e.g. surgery on tricuspid valve or thoracic aorta), congenital heart disease, earlier cardiac surgery, pre-operative inotrope support or mechanical circulatory assistance, or chronic renal replacement therapy. Chronic renal insufficiency is defined as having creatinine ≥ 2. 5 mg/dL or chronic renal replacement therapy; hepatic cirrhosis or synthetic failure; pregnancy at the time of randomization; simultaneous disease limiting life expectancy to less than 2 years.
Randomization
All enrolled patients provided written informed consent for the study and surgical procedure. Randomization was performed centrally and intra-operatively after sternotomy but before cannulation of the aorta to reduce the probability of including patients with unexpected surgical contraindications for mitral valve repair. After conducting checks, the treatment assignment was sent to the study coordinator and the intervention was carried out. Therefore, the primary efficacy analysis was conducted using the intention-to-treat approach.
Interventions
The standard RMA was supplemented with the standardized subvalvular repair, involving the reapproximation of both papillary muscles (PMs), to achieve correction of MR and restoration of the subvalvular apparatus using the following procedure:
- (1)
-
(2)
The realignment of the subvalvular apparatus in one plane in a standardised manner. both PMs to eliminate apical tenting of the anterior leaflet (Additional file 1: Fig. 2).
-
(3)
For PMs with anatomy types 1–3, both PMs are approximated using Goretex 4–0 stitch (CV-4, W.L. Gore & Associates, Newark, Delaware, USA). For PMs with anatomy types 4–5, a 4 mm Goretex graft (Gore & Associates, Newark, Delaware, USA) is used for approximation through the sling procedure (Additional file 1: Fig. 1).
In the parasternal short-axis view of the LV, end-diastolic and end-systolic interpapillary muscle distances (IPMD) were compared with preoperative values measured by transthoracic echocardiography. Comparing IPMD in physiological and pathological conditions is crucial for the procedure's success. In normal conditions, the distance between the interpapillary muscles measured in mid-systole is between 12.9 and 22.5Â mm. It should be noted that these measurements exhibit variability when adjusted for BSA and age. The BSA- and age-normalized value for IPMD is approximately 10.5Â mm plus or minus 3.3Â mm. The mean decrease in the interpapillary distance was 30%, with a subsequent decrease observed in the subsequent 6Â months post-surgery as a result of the advantageous reshaping of the left ventricle.
Coronary artery bypass surgery was conducted employing standard surgical approaches to achieve complete revascularisation using single or double internal thoracic artery (ITA) grafting. All patients were administered guideline-directed medical therapy to manage heart failure and coronary artery disease which included antiplatelet medication, neurohormonal antagonists, lipid-lowering agents, and appropriate cardiac resynchronization and defibrillator therapy. Patients were monitored for up to 5 years post-surgery. Details of the surgical procedure are in the supplementary material.
Endpoints of the secondary analysis
We established that a beneficial change occurred if there was a positive difference between the measurement of a specific echocardiographic parameter before the surgery and 5 years after. The parameters evaluated include the α-angle (tilt angle of the front leaflet), β-angle (tilt angle of the back leaflet), tenting area, interpapillary muscle distance (IPMD), LVEDD, left ventricle end-systolic diameter (LVESD), LVEF, and pulmonary artery systolic pressure (PAP). The main objective was to create a hierarchical model that forecasts the extent of recurring ischemic MR following surgical repair. As secondary objectives, we assessed the correlation of PMA with parametric improvements and the effect size of PMA on parametric improvements.
Statistical analysis
The correlation between PMA and improvements in parameters was analysed using Spearman’s rho. We defined the magnitude of correlation as low (rho 0–0.49), moderate (rho 0.50–0.69), or high (rho 0.70–1).
To evaluate the association between the differences in echocardiographic parameter measurements taken before surgery and 5 years after, and recurrent MR, we used logistic regression. All variables that demonstrated a significance level of p ≤ 0.2 in univariable regression were incorporated into the multivariable model.
A decision tree algorithm was used to identify the relationship between dependent and independent variables through recursive partitioning. If the null hypothesis of independence was rejected, the independent variable with the strongest correlation to the dependent variable was chosen. The data was then partitioned according to the selected independent variable and the process was repeated. The Strasser and Weber permutation test was used for conditional inference [4, 5]. Consistency was maintained with metrics and units. Fillers were removed for conciseness.
The statistical analyses were conducted using R Studio with the following packages: `stats’, `sjPlot’, `car’, `effectsize’, `ggplot2’, `ggfortify’, `tidyr’, `dplyr’, `binda’, `tidyverse’, `ctree’, `rpart’, and `rpart.plot’.
Results
Preoperative and operative variables
There were no differences between the RMA and PMA groups in terms of demographics, baseline characteristics, medications, and cardiac status before the operation (p > 0.05 for all) (Table 1). Moreover, the operative variables did not differ between the two groups (p > 0.05 for all) (Table 2). Operative mortality occurred in 7 patients (4 in the RA and 3 in the PMA groups). At 5-year follow-up, the cumulative rate of mortality was similar between groups (RA 29.2% vs. PMA 22.9%, p = 0.50).
Correlation of PMA with parametric improvements
A comparison of echocardiographic parameters preoperatively, at 1-year and 5-years follow-up is detailed in Table 3. The addition of PMA led to a significant improvement in all parameters for 5 years post-surgery (p < 0.01 for all). The improvement in the tethering angles (α-angle: rho 0.85; β-angle: rho 0.87) and tenting area (rho 0.75) correlated strongly with the addition of PMA. The ventricular diameters (LVEDD: rho 0.67; LVESD: rho 0.55) also improved moderately. The addition of PMA had a low correlation with improvements in PAP (rho 0.44) (Fig. 1).
Independent association of PMA to parametric improvements
Recurrent MR was found to be associated with the differences (Δs) between preoperative and 5-year postoperative values in all investigated parameters (Table 3) during univariable analysis. During multivariable analysis, the IPMD’s Δ was identified as the only independent factor related to the recurrence of 3–4 + MR with a significant effect size (odds ratio (OR) 2.55, 95% confidence interval (CI) 1.01 | 7.24). The difference of the tenting area was linked to recurrent MR independently, albeit with a reduced impact (OR 0.28, 95% CI 0.05 | 0.88) (Table 4).
Best predictors of recurrent IMR
The postoperative IPMD was found to be the most reliable indicator of recurrent MR severity. Patients with an IPMD > 40 mm experienced ≥ 3 + grade MR (11/20, 55%, p < 0.01). In patients with an IPMD ≤ 40 mm, a patient's LVEDD was the best predictor of the grade of recurrent MR.
Specifically, moderate (2+) MR was only present in patients with an LVEDD > 62 mm, while absent to mild (1+) MR was limited to patients with LVEDD ≤ 62 mm (as shown in Fig. 2).
Discussion
The initial analysis of the PMA randomised clinical trial's findings improves our understanding of the benefits of using PMA with RMA compared to using RMA alone for treating severe ischemic mitral regurgitation. The 5-year results indicate that the combination of papillary muscle surgery and annuloplasty was more effective than standard annuloplasty alone for the treatment of ischemic MR. This resulted in improved ventricular geometry, remodeling, and function. The research uncovered a significant difference between groups in the rank-based evaluation of left ventricular reverse remodeling after 5 years. The findings demonstrated a consistent and substantial enhancement in LVEDD, LV end-systolic diameter, and ejection fraction in the PMA cohort. On the other hand, the RMA alone group displayed progressive ventricular cavity enlargement and LV function decline, indicating inadequate counteraction or prevention of detrimental remodeling that occurred over time in ischemic MR [3].
In this second analysis, our objective is to thoroughly examine how reducing interpapillary distance through surgical approximation of papillary muscles can recover left ventricular geometry whilst mitigating the risk of recurrent MR.
Principal findings
The reappearance of ischemic MR after RMA ± CABG is traditionally thought to occur due to progressive LVEDD enlargement caused by chordal tethering. However, our findings illustrate that progressive LVEDD enlargement does not lead to the recurrence of ischemic MR, as long as the IPMD is surgically stabilized by adding PMA. Possibly, the combination of RMA and PMA provides a solution for both the valvular and sub-valvular mitral apparatus, similarly to MVR with chordal sparing.
PMA affects normal spatial relationships of the components of MV in patients with SIMR
The erroneous assumption that the leaflet tethering in ischemic MR resulted from apical displacement of the papillary muscles was initially made due to the use of tethering lengths (2D parameters) in earlier studies to evaluate the 3D displacement of the muscles [6,7,8,9,10,11,12,13,14]. However, subsequent studies looking at the effect of LVEDD enlargement in ischemic MR with a 3D assessment challenged this notion. Experimental induction of acute ischemic MR did not displace the papillary muscles at the apex. Instead, it restricted the distance between the posterior commissure and the posterior papillary muscle, according to reports [15,16,17]. Moreover, three-dimensional evidence reveals that experimental models studying non-acute ischemic MR yield fitting results. In cases of sub-acute or chronic ischemic MR, an enlarged LVEDD results in decreased mitral annulus to posterior papillary muscle distance compared to the control group (3.16 ± 0.41 cm vs. 3.82 ± 0.53 cm respectively, p = 0.01). This change in shape resulted from two different forces affecting the posterior papillary muscle—a force towards the back (0.58 ± 0.4 cm compared to 1.39 ± 0.46 cm in the control and ischemic groups, p < 0.01) and a force from the side (0.66 ± 0.55 cm compared to 1.19 ± 0.70 cm in the control and ischemic groups, p < 0.01). On the other hand, the ischemic enlargement of the LVEDD did not significantly shift the anterior papillary muscle. Hence, 3D data contradicts the idea that ischemic MR is caused by displacement of the apical papillary muscle and points instead to displacement of the posterior papillary muscle in the posterolateral region as the primary cause. This hypothesis is supported by studies that have attempted to rectify the sub-valvular vectors. Balloon repositioning of a posterior papillary muscle, which was displaced, along an anteroseptal vector resulted in reduced tethering and MR [18, 19]. The Coapsys device (Myocor Inc, Maple Grove, Minnesota), which redirects the posterior papillary muscle with an anteroseptal vector, yielded comparable results [20]. Additionally, repositioning the posterior papillary muscle towards the right fibrous trigone (anteroseptal vector) decreased leaflet tethering [21]. Conversely, pulling the posterior papillary muscle towards the posterior commissure was unsuccessful in correcting ischemic MR as confirmed by the evidence [22].
RMA worsens posterolateral tethering by pulling the annulus further from the displaced posterior papillary muscle [23]. This can result in residual and recurrent regurgitation [24]. Numerous surgical groups have published clinical evidence that supports these experimental findings. For instance, our PMA trial's primary analysis revealed that PMA decreases recurrent MR by moving the posterior papillary muscle towards the anterior septum instead of the ventricular base [3, 25]. Our findings align with those of other surgical groups [26,27,28,29,30,31].
Most clinicians prefer valve replacement over repair to treat ischemic mitral regurgitation based on the results of the CTSN trial [24, 32]. However, the trial's comparison of MVR to RMA alone (without PMA) is insufficient in this context, as demonstrated. Therefore, a trial comparing MVR versus RMA combined with PMA would be advantageous.
The optimal treatment for ISMR remains a topic of debate. Our analysis underscores the need to effectively address both the valvular and subvalvular components of the mitral valve to prevent the recurrence of mitral regurgitation, which results from sustained ventricular geometrical distortion. Limiting the annular diameter or solely focusing on the leaflets through procedures like transcatheter therapies [31,32,33,34] may prove inadequate in attaining LV geometry restoration and preventing adverse remodeling consequences.
Currently, no published or ongoing trials have been developed to evaluate the clinical impact of the modulation of the IPMD in ISMR [33,34,35,36,37,38,39]. The present and previous studies from other groups appear to endorse the theory that restoring the functional spatial relationships between the various components of the mitral valve apparatus is vital in ensuring long-lasting outcomes post-surgery [3, 25,26,27,28,29,30,31].
Repairing the mitral valve using valvular techniques to avoid future surgeries is crucial in patients with small preoperative ventricular dimensions during standard surgical procedures [24]. Additionally, individuals who have undergone transcatheter edge-to-edge repair (TEER) should receive RMA [33] .
The CTSN trial showed that RMA provides clear benefits for patients with smaller left ventricular size [24]. Out of the 74 patients with severe ISMR who underwent the RMA procedure and did not have persistent or recurring mitral regurgitation, their left ventricle measured significantly smaller (43 ± 26 mL/m2) 2 years post-procedure as compared to those who had recurring mitral regurgitation following RMA (63 ± 27 mL/m2). Moreover, their left ventricle was smaller than anticipated in comparison to patients who had gone through MVR (61 ± 39 mL/m2) [24].
Hamasi et al. [33] investigated the prognostic significance of altered mitral valve geometry in patients receiving TEER or medical therapy (GDMT). In heart failure patients with severe secondary mitral regurgitation, a significant anteroposterior mitral annular diameter and higher effective regurgitatant orifice area (EROA) proved to be strong echocardiographic indicators for heart failure hospitalization and mortality risk. These findings are applicable to patients who have received treatment with GDMT alone or with the additional TEER procedure. The Alfieri stitch does not prevent recurrence of MR regurgitation, highlighting the need to treat an increased anteroposterior diameter with RMA.
The significance of papillary muscles was confirmed by the Osaka group’s study [40]. Kainuma et al. discovered that resolution of leaflet tethering cannot be achieved by RMA alone and that the IPMD is primarily responsible for the reappearance of mitral regurgitation. Left ventricle reverse remodelling conducted after RMA reduced the IPMD from 31 ± 6 to 25 ± 5 mm, thereby potentially compensating for the greater angle of the posterior leaflet and augmenting its advantages [40].
Limitations
This research study encompasses all limitations outlined for the primary analysis [3], alongside supplementary limitations that are characteristic of secondary analyses [41]. The authors also acknowledge that the evidence supporting PMA as an adjunct to RMA is currently not strong, being backed only by one RCT and a few observational analyses. It is necessary to conduct further RCTs to establish PMA as a recommended procedure.
Conclusion
During the research, surgery of the papillary muscles for SIMR led to significant enhancements in the left ventricle's geometry and distortion, ultimately restoring the normal spatial relationships between all parts of the mitral valve. This procedure has effectively lowered the risk of mitral regurgitation recurrence. Furthermore, it was discovered that surgical stabilization of the IPMD can decrease the connection between the gradual rise in the LVEDD and recurring ischemic MR. Further randomised multicentre clinical trials with a minimum follow-up of 5Â years are required to directly compare patients undergoing either PMA alongside RMA and MVR, or transcatheter edge-to-edge repair, for the management of SIMR.
Availability of data and materials
Drs Nappi, Gambardella, had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. The data underlying this article will be shared on reasonable request to the corresponding author.
References
Kron JL, LaPar DJ, Acker MA, et al. 2016 update to The American Association for Thoracic Surgery (AATS) consensus guidelines: Ischemic mitral valve regurgitation. J Thorac Cardiovasc Surg. 2017;153:97–114.
Nappi F, Antoniou GA, Nenna A, Michler R, Benedetto U, Avtaar Singh SS, Gambardella IC, Chello M. Treatment options for ischemic mitral regurgitation: a meta-analysis. J Thorac Cardiovasc Surg. 2022;163:607–22.
Nappi F, Lusini M, Spadaccio C, Nenna A, Covino E, Acar C, Chello M. Papillary muscle approximation versus restrictive annuloplasty alone for severe ischemic mitral regurgitation. J Am Coll Cardiol. 2016;67:2334–46.
Hothorn T, Zeileis A. Partykit: a modular toolkit for recursive partitioning in R. J Mach Learn Res. 2015;16(118):3905–9.
Strasser H, Weber C. On the asymptotic theory of permutation statistics. Math Methods Statist. 1999;8:220–50.
Dal Bianco JP, Aikawa E, Bischoff J, et al. Active adaptation of the tethered mitral valve: insights into a compensatory mechanism for functional mitral regurgitation. Circulation. 2009;120:334–42.
Agricola E, Oppizzi M, Pisani M, Meris A, Maisano F, Margonato A. Ischemic mitral regurgitation: mechanisms and echocardiographic classification. Eur J Echocardiogr. 2008;9:207–21.
Yiu SF, Enriquez-Sarano M, Tribouilloy C, Seward JB, Tajik AJ. Determinants of the degree of functional mitral regurgitation in patients with systolic left ventricular dysfunction: a quantitative clinical study. Circulation. 2000;102:1400–6.
Levine RA, Hagege AA, Judge DP, Padala M, Dal-Bianco JP, Aikawa E, et al. Mitral valve disease–morphology and mechanisms. Nat Rev Cardiol. 2015;12:689–710.
Uemura T, Otsuji Y, Nakashiki K, Yoshifuku S, Maki Y, Yu B, et al. Papillary muscle dysfunction attenuates ischemic mitral regurgitation in patients with localized basal inferior left ventricular remodeling: insights from tissue Doppler strain imaging. J Am Coll Cardiol. 2005;46:113–9.
Kumanohoso T, Otsuji Y, Yoshifuku S, Matsukida K, Koriyama C, Kisanuki A, et al. Mechanism of higher incidence of ischemic mitral regurgitation in patients with inferior myocardial infarction: quantitative analysis of left ventricular and mitral valve geometry in 103 patients with prior myocardial infarction. J Thorac Cardiovasc Surg. 2003;125:135–43.
Yu HY, Su MY, Liao TY, Peng HH, Lin FY, Tseng WY. Functional mitral regurgitation in chronic ischemic coronary artery disease: analysis of geometric alterations of mitral apparatus with magnetic resonance imaging. J Thorac Cardiovasc Surg. 2004;128:543–51.
D’Ancona G, Biondo D, Mamone G, Marrone G, Pirone F, Santise G, et al. Ischemic mitral valve regurgitation in patients with depressed ventricular function: cardiac geometrical and myocardial perfusion evaluation with magnetic resonance imaging. Eur J Cardiothorac Surg. 2008;34:964–8.
Veronesi F, Corsi C, Sugeng L, Caiani EG, Weinert L, Mor-Avi V, et al. Quantification of mitral apparatus dynamics in functional and ischemic mitral regurgitation using real-time 3-dimensional echocardiography. J Am Soc Echocardiogr. 2008;2:347–54.
Gorman JH, Gorman RC, Jackson BM, et al. Annuloplasty ring selection for chronic ischemic mitral regurgitation: lessons from the ovine model. Ann Thorac Surg. 2003;76:1556–60.
Timek TA, Lai DT, Bothe W, et al. Geometric perturbations in multiheaded papillary tip positions associated with acute ovine ischemic mitral regurgitation. J Thorac Cardiovasc Surg. 2015;150:232–7.
Lai DT, Timek TA, Tibayan FA, et al. The effects of mitral annuloplasty rings on mitral valve complex 3-D geometry during acute left ventricular ischemia. Eur J Cardiothorac Surg. 2002;22:808–16.
Hung J, Solis J, Guerrero JL, et al. A novel approach for reducing ischemic mitral regurgitation by injection of a polymer to reverse remodel and reposition displaced papillary muscles. Circulation. 2008;118:S263–9.
Hung J, Chaput M, Guerrero JL, et al. Persistent reduction of ischemic mitral regurgitation by papillary muscle repositioning: structural stabilization of the papillary muscle-ventricular wall complex. Circulation. 2007;116:I259–63.
Mishra YK, Mittal S, Jaguri P, Trehan N. Coapsys mitral annuloplasty for chronic functional ischemic mitral regurgitation: 1-year results. Ann Thorac Surg. 2006;81:42–6.
Jensen H, Jensen MO, Smerup MH, Vind-Kezunovic S, Ringgaard S, Andersen NT, et al. Impact of papillary muscle relocation as adjunct procedure to mitral ring annuloplasty in functional ischemic mitral regurgitation. Circulation. 2009;120:S92–8.
Langer F, Rodriguez F, Ortiz S, et al. Subvalvular repair: the key to repairing ischemic mitral regurgitation? Circulation. 2005;112:383–9.
Yu HY, Su MY, Chen YS, Lin FY, Tseng WYI. Mitral tetrahedron as a geometrical surrogate for chronic ischemic mitral regurgitation. Am J Physiol Heart Circ Physiol. 2005;289:218–1225.
Goldstein D, Moskowitz AJ, Gelijns AC, et al. Two-year outcomes of surgical treatment of severe ischemic mitral regurgitation. N Engl J Med. 2016;374:344–53.
Nappi F, Spadaccio C, Nenna A, Lusini M, Fraldi M, Acar C, Chello M. Is subvalvular repair worthwhile in severe ischemic mitral regurgitation? Subanalysis of the Papillary Muscle Approximation trial. J Thorac Cardiovasc Surg. 2017;153:286–95.
Kron IL, Green GR, Cope JT. Surgical relocation of the posterior papillary muscle in chronic ischemic mitral regurgitation. Ann Thorac Surg. 2002;74:600–1.
Bothe W, Doenst T. Ring-noose-string technique allows adjustable papillary muscle repositioning during minimally invasive mitral valve repair in patients with functional/ischemic mitral regurgitation. J Thorac Cardiovasc Surg. 2016;64:447–9.
Langer F, Groesdonk HV, Kunihara T, Schafers HJ. Dynamic RING STRING for ischemic mitral regurgitation: papillary muscle repositioning and modification of the septal-lateral diameter in the loaded beating heart under echocardiographic guidance. J Thorac Cardiovasc Surg. 2011;141:1315–6.
Ueno T, Sakata R, Iguro Y, Nagata T, Otsuji Y, Tei C. New surgical approach to reduce tethering in ischemic mitral regurgitation by relocation of separate heads of the posterior papillary muscle. Ann Thorac Surg. 2006;81:2324–5.
Pausch J, Sequeira Gross T, Müller L, et al. Subannular repair for functional mitral regurgitation type IIIb in patients with ischaemic versus dilated cardiomyopathy. Eur J Cardiothorac Surg. 2021;60(1):122–30.
Harmel E, Pausch J, Gross T, et al. Standardized subannular repair improves outcomes in type IIIb functional mitral regurgitation. Ann Thorac Surg. 2019;108(6):1783–92.
Acker MA, Parides MK, Perrault LP, et al. Mitral-valve repair versus replacement for severe ischemic mitral regurgitation. N Engl J Med. 2014;370:23–32.
Namazi F, Delgado V, Pio S, et al. Prognostic implications of mitral valve geometry in patients with secondary mitral regurgitation: the COAPT trial. Eur Heart J Cardiovasc Imaging. 2022;23(11):1540–51.
Mack MJ, Lindenfeld J, Abraham WT, Kar S, Lim DS, Mishell JM, et al. COAPT investigators 3-year outcomes of transcatheter mitral valve repair in patients with heart failure. J Am Coll Cardiol. 2021;77(8):1029–40.
Okuno T, Praz F, Kassar M, et al. Surgical versus transcatheter repair for secondary mitral regurgitation: a propensity score matched cohorts comparison. J Thorac Cardiovasc Surg. 2021;S0022–5223(21):01128–34.
Nappi F, Avtaar Singh SS. Subannular repair or transcatheter edge-to-edge repair for secondary mitral regurgitation? More data for international guidelines. JTCVS Open. 2022;10:176–80.
Praz F, Spargias K, Chrissoheris M, et al. Compassionate use of the PASCAL 536 transcatheter mitral valve repair system for patients with severe mitral regurgitation: a multicentre, prospective, 537 observational, first-in-man study. Lancet. 2017;390:773–80.
Webb JG, Hensey M, Szerlip M, et al. 1- year outcomes for transcatheter repair in patients with mitral regurgitation 541 from the clasp study. JACC Cardiovasc Interv. 2020;13:2344–57.
A Multicenter, randomized, controlled study to assess mitral vAlve reconsTruc- Tion for advancEd insufficiency of functional or iscHemic ORigiN (MATTER- HORN). ClinicalTrials.gov identifier: NCT02371512. Accessed 8 March 2022. https://clinicaltrials.gov/ct2/show/NCT02371512
Kainuma S, Funatsu T, Kondoh H, et al. Beneficial effects of restrictive annuloplasty on subvalvular geometry in patients with functional mitral regurgitation and advanced cardiomyopathy. J Thorac Cardiovasc Surg. 2018;156(2):630-638.e1.
Wickham RJ. Secondary analysis research. J Adv Pract Oncol. 2019;10:395–400.
Funding
This research received no external funding.
Author information
Authors and Affiliations
Contributions
Drs Nappi and Gambardella contributed equally. Concept and design: Nappi, Gambardella. Methodology, Nappi, Gambardella. Statistical analysis, Gambaredella. Acquisition, analysis, or interpretation of data; Nappi, Gambardella, Spadaccio, Avtaar Singh, Shingu, Kunihara, Wakasa. Drafting of the manuscript: , Nappi, Gambardella. Critical revision of the manuscript for important intellectual content: All authors. Supervision: Nappi, Spadaccio, Shingu, Kunihara, Wakasa. Other - protocol review: Nappi, Gambardella, Spadaccio
Corresponding author
Ethics declarations
Ethics approval
Head of the study Doctor Francesco Nappi. Approval Number assigned by the IRB: IRB-MTP_2022_07_202201173.. Date: 12 July 2022.
Informed Consent
Written informed consent was provided by all patients.
Competing interests
The authors declare no conflict of interest.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Additional file 1:
Supplementary Figure 1. Combined papillary muscle approximation and restrictive mitral annuloplasty. Supplementary Figure 2. The anatomy of the PMs (papillary muscles) is the key to surgical correction.
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
Gambardella, I., Spadaccio, C., Singh, S.S.A. et al. Interpapillary muscle distance independently predicts recurrent mitral regurgitation. J Cardiothorac Surg 19, 147 (2024). https://doi.org/10.1186/s13019-024-02631-z
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s13019-024-02631-z