Literature DB >> 36191013

Every day mitral valve reconstruction: What has changed over the last 15 years?

Farnoosh Motazedian1, Roya Ostovar1, Martin Hartrumpf1, Filip Schröter1, Johannes M Albes1.   

Abstract

OBJECTIVE: Mitral valve reconstruction (MVR) is one of the cardiosurgical procedures which cannot be substituted by any intervention owing to the quality of the quasi-anatomical, physiological repair. However, technique and strategies have changed over the years. We looked at procedural characteristics and outcome in an all-comer, non-selected cohort of patients.
METHODS: 738 out of 1.977 patients were retrospectively analyzed receiving MVR with and without concomitant procedures. The cohort was divided into three periods. P1: 2004-2009 (134 pts.); P2: 2010-2014 (294 pts.), and P3: 2015-2019 (310 pts.).
RESULTS: Early mortality increased from P1 to P2 and decreased from P2 to P3 (9% P1, 13% P2, 10% P3). All patients received an annuloplasty-ring. In P1 resection measures dominated. In P3 artificial chordae were dominant. Age, BMI, and risk scores correlated with early mortality. Survival rates were 66% (5-years), 55% (10-years), 44% (15-years) in P1, 63% (5-years), 50% (10-years) in P2, and 80% (5-years) in P3. Odds ratio for reduced long-term survival were concomitant venous only bypass surgery (10-years 2,701, p = 0.026). 10-year survival was positively influenced by isolated MVR (0.246, p = 0.001), concomitant isolated arterial bypass (IMA) (0.153, p = 0.051), posterior leaflet measure (0.178, p<0.001), and use of artificial chordae (5-years 0.235, p<0.001).
CONCLUSION: Indication for ring implantation remained mandatory while preference changed alongside improved designs. Procedural characteristics changed from mainly resection maneuvers to predominant use of artificial chordae. Long-term results were negatively influenced by co-morbidities and positively influenced by posterior leaflet repair and artificial chordae. MVR underwent a qualitative evolution and remains a valuable cardiosurgical procedure.

Entities:  

Mesh:

Year:  2022        PMID: 36191013      PMCID: PMC9529113          DOI: 10.1371/journal.pone.0269537

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.752


Introduction

Mitral valve reconstruction (MVR) is one of the remaining cardiac surgical procedures that, due to the quality of the quasi-anatomical and thus physiological repair, cannot be replaced by any intervention. In the 1970s, Alain Carpentier introduced the systematic approach to mitral valve reconstruction into the clinical practice. The clarification of the underlying pathology types was accompanied by appropriate measures to treat them and thus to reconstruct the valve as anatomically and physiologically as possible [1-3]. This was clearly a breakthrough that far surpassed existing mitral repair maneuvers and thus opened the future of surgical repair not only of the mitral valve, but later also of the tricuspid and aortic valves. Today between half and two thirds of the mitral valves are being reconstructed in countries with an efficient health system [4]. Although the techniques invented and refined by Carpentier are still widely used, mitral valve reconstruction has gone through an evolutionary process over the years in which some techniques became obsolete or even died out while others flourished. We therefore examined both procedural features and outcome in an unselected group of patients who received MVR in our institution over the past 15 years.

Patients and methods

Of a total number of 1.977 mitral valve procedures 738 patients were retrospectively analyzed receiving MVR with and without any concomitant procedure from 2004 to 2019. Underlying pathologies leading to mitral regurgitation necessitating repair were distinguished between primary degenerative and secondary functional (ischemic) origin according to the current ESC-guidelines [5]. Patients who had to undergo a cardiac tumor resection were excluded, even if this tumor could be removed from the mitral valve and the valve left in place. Also excluded were patients with acute endocarditis, which led to resection measures on an otherwise preserved mitral valve. Furthermore, patients were excluded who did not want to participate in the study or they or their relatives were unable to undergo informed consent. Ethics vote was obtained by the Ethics Committee of our university. Owing to the entirely retrospective nature of the study, the necessity for written informed consent was waived. Late survival state was obtained in several cases by telephone contact. That was considered as oral and thus adequate consent by the ethics committee. (Sept. 2020; File No. E-01-20200709). The cohort was divided into three periods: Period one (P1): 2004–2009 (134 pts.); period two (P2) 2010–2014 (294 pts.); and period three (P3) 2015–2019 (310 pts.). Long-term results up to 15 years were obtained. Statistical evaluation was performed using Microsoft Excel 2010 and R® [6]. The descriptive statistics initially included all demographic items as well as perioperative parameters recorded during the patient stay and presented here as a mean value with standard deviation (95% confidence interval). Numerical data was tested for normal distribution before being compared with Student’s t-test or Mann-Whitney-U Test respectively. Categorical data was compared using Fisher’s exact test and Chi-squared test. To examine the existence of trends in categorical variables over the three time periods, Cochran-Armitage test for trend in proportions was used. In addition, a risk factor analysis was carried out to determine the odds ratio. Kendall’s Tau was used to correlate hospitalization time and a panel of typical risk factors. Differences were assumed to be significant if p<0.05. The patients were contacted by phone for follow up. No information could be obtained from 55/738 patients (93% follow-up). The survival times were calculated using the Kaplan-Meier method. The primary endpoint was all-cause mortality, the secondary endpoints were: recurrence rate requiring reoperation, early mortality and long-term survival in the years 2004–2009 (Period 1); 20010–2014 (Period 2); 2015–2019 (Period 3). Additional secondary endpoints were the type of surgery and the type and scope of other simultaneous surgical measures and their influence on early mortality and long-term survival.

Results

The proportion of mitral valve repair from all mitral valve procedures more than doubled from period 1 (22.1%) to period 2 (47.6%) and slightly decreased thereafter in period 3 (41.1%). Mitral valve pathology was of primary nature in 64,6% of all patients. Age remained quite stable (P1: 64.26 years, P2: 66.46 years, P3: 65.42 years), risk scores (EuroScore (ES), logistic ES (log. ES)) increased from P1 to P2 and decreased thereafter. Mean hospitalization time decreased (17.7 days P1; 17.5 days P2; 15.2 days P3) (Table 1).
Table 1

Demographic data.

Period 1Period 2Period 3p-value totalp-value Period 1 vs. 2p-value Period 1 vs. 3p-value Period 2 vs. 3
2004–20092010–20142015–2019
Age 64.26+/-11.2766.46+/-12.165.42+/-11.47 0.046 0.04 0.3230.323
Body Mass Index 26.46+/-4.1926.8+/-4.6527.11+/-4.660.582111
EuroSCORE (ES) 6.52+/-2.917.92+/-3.746.71+/-3.32 <0.001 <0.001 0.857 <0.001
logistic ES 11.93+/-11.5415.18+/-16.9810.54+/-13.14 <0.001 0.2630.216 <0.001
Hospitalization time 17.74+/-11.6817.45+/-13.8915.21+/-10.01 0.002 0.736 0.011 0.007
Male gender 58.21% [78]62.46% [183]63.55% [197]0.562111
Primary MV-pathology 66% [92]55% [163]73% [230] <0.001 0.0880.167 <0.001
Number of isolated procedures varied between 30 and 50% (48% P1, 31% P2, 40% P3). Minimal-invasive MVR did not play a major role in this non-selected cohort with only 13 patients mainly carried out in period 2. Early mortality increased from P1 to P2 and decreased from P2 to P3 (9% P1, 13% P2, 10% P3). Concomitant procedures were mostly coronary artery bypass graft as well as aortic valve replacement and endocardial cooled radiofrequency thermal atrial ablation (MAZE) was often performed (Table 2).
Table 2

Concomitant procedures.

Period 1Period 2Period 3P TotalP Period 1 vs. 2P Period 1 vs. 3P Period 2 vs. 3
2004–20092010–20142015–2019
CABG 34.33% [46]45.24% [133]27.42% [85] <0.001 0.0880.176 <0.001
Venous only CABG 14.18% [19]25.51% [75]15.16% [47] 0.001 0.025 0.903 0.007
CABG plus IMA 17.16% [23]17.69% [52]11.29% [35]0.06310.2510.102
IMA only 2.99% [4]2.04% [6]1.29% [4]0.399111
AV-Replacement 14.93% [20]19.39% [57]23.23% [72]0.1230.5860.1910.586
AV-Repair 0.75% [1]0.34% [1]0.97% [3]0.617111
MVR only 47.76% [64]31.29% [92]39.68% [123] 0.003 0.005 0.1390.078
MIS-MVR 0% [0]3.74% [11]0.65% [2] 0.004 0.1050.8730.058
TVR/Replacement 5.97% [8]11.9% [35]17.1% [53] 0.005 0.171 0.009 0.171
PFO/ASD 2.24% [3]1.7% [5]1.94% [6]0.938111
VSD 0% [0]1.02% [3]1.29% [4]0.54111
Aorta 1.49% [2]2.72% [8]3.87% [12]0.4310.9221
Electro 0.75% [1]1.02% [3]1.61% [5]0.748111
MAZE/LAA 3.73% [5]13.61% [40]10.97% [34] 0.009 0.011 0.044 0.388
MAZE only 18.66% [25]14.97% [44]10.32% [32] 0.046 0.4120.0720.22
LAA only 0% [0]0.68% [2]2.58% [8]0.060.470.3930.393
Re-OP 5.22% [7]4.08% [12]2.58% [8]0.3490.8440.7770.844
IABP 5.22% [7]10.54% [31]2.58% [8] <0.001 0.2140.259 <0.001
Carotis TEA 0% [0]0.68% [2]0.32% [1]0.789111
LV-Aneurysm 0% [0]0.34% [1]0% [0]0.5811

CABG = Coronary Artery Bypass Graft; IMA = Internal mammary artery; AV-Replacement = Aortic Valve Replacement, AV-Repair = Aortic Valve Repair; MVR = Mitral Valve Repair; MIS-MVR = Minimal-invasive MVR; TVR/Repair = Tricuspid Valve Replacement/repair; PFO/ASD = Persisting Foramen Ovale/Atrial Septal Defect; VSD = Ventricle Septal Defect; Aorta = Ascending Aorta wrapping or Replacement; Electro = Electrophysiological Implant; MAZE/LAA = Maze-Procedure (Atrial ablation) / Left Atrial Appendage; MAZE = Maze-Procedure (Atrial ablation); Re-OP = Redo-Operation; IABP = Intra aortic balloon pump; Carotis TEA = A. carotis interna thrombendarteriectomy; LV-Aneurysma = Left ventricular aneurysm

CABG = Coronary Artery Bypass Graft; IMA = Internal mammary artery; AV-Replacement = Aortic Valve Replacement, AV-Repair = Aortic Valve Repair; MVR = Mitral Valve Repair; MIS-MVR = Minimal-invasive MVR; TVR/Repair = Tricuspid Valve Replacement/repair; PFO/ASD = Persisting Foramen Ovale/Atrial Septal Defect; VSD = Ventricle Septal Defect; Aorta = Ascending Aorta wrapping or Replacement; Electro = Electrophysiological Implant; MAZE/LAA = Maze-Procedure (Atrial ablation) / Left Atrial Appendage; MAZE = Maze-Procedure (Atrial ablation); Re-OP = Redo-Operation; IABP = Intra aortic balloon pump; Carotis TEA = A. carotis interna thrombendarteriectomy; LV-Aneurysma = Left ventricular aneurysm All patients in all periods received an annuloplasty-ring. While Edwards Classic™ (35.07%) and Livanova (previously Sorin™) Anuloflo™ (51.49%) were mostly used in P1 it gradually shifted until P3 to the Edwards Physio II (65.16%) and the St. Jude Rigid Saddle (25.48%). In P1 resection measures for the posterior leaflet as well as Wooler plasty dominated. In P2 artificial chordae came increasingly in use while resection measures decreased. In Period 3 artificial chordae were the dominant procedure (Table 3, Fig 1).
Table 3

Types of additional repair maneuvers.

Period 1Period 2Period 3P TotalP Period 1 vs. 2P Period 1 vs. 3P Period 2 vs. 3
2004–20092010–20142015–2019
AML11.94% [16]4.08% [12]5.16% [16] 0.005 0.014 0.039 0.662
PML54.48% [73]23.13% [68]21.29% [66] <0.001 <0.001 <0.001 0.656
Plication16.42% [22]13.61% [40]20% [62]0,1090,9030,9030.14
Resection45.52% [61]15.31% [45]6.13% [19] <0.001 <0.001 <0.001 <0.001
Artificial Chordae2.99% [4]22.45% [66]31.61% [98] <0.001 <0.001 <0.001 0.015
Other Chordae Measures8.21% [11]1.36% [4]0% [0] <0.001 0,002 <0.001 0.119
Wooler Plasty20.15% [27]2.04% [6]0.97% [3] <0.001 <0.001 <0.001 0.452
Patch2.99% [4]1.02% [3]0.97% [3]0.2070.7490.7491
Ring-Refixation0% [0]0.68% [2]0.32% [1]0.789111

AML = all measures on the anterior mitral leaflet; PML = all measures on the posterior mitral leaflet; Plication = Plication or inverse plication without resection; Resection: triangular or quadrangular resection on the leaflets. Artificial Chordae = Implantation of artificial chordae with stretched polytetrafluorethylen (Goretex™) from the papillary muscles to the AML and/or PML; Other Chordae Measures = other measures on the chordae or papillary muscles, i.e. repositioning, shortening, or resection. Wooler = Teflon-pledget-supported U-Suture on the anterior or posterior commissure; Patch = Implantation of a pericardium patch into the leaflet; Ring-Refixation = Refixationen of a partially detached annuloplasty-ring

Fig 1

Shift of additional reconstruction measures.

PML = Corrective measure on the posterior mitral leaflet; Resection = All types of resection measure on either leaflet; Wooler = Commissural reduction plasty according to Wooler; Plication = Plication on the leaflets without resection; AML = Corrective measure on the anterior mitral leaflet; Other Chord = Repositioning, shortening of the native chords, shortening of the origin of the chord by means of splitting or trimming or repositioning of the papillary muscle; Artif. Chordae = Chordae replacement with artificial chords.

Shift of additional reconstruction measures.

PML = Corrective measure on the posterior mitral leaflet; Resection = All types of resection measure on either leaflet; Wooler = Commissural reduction plasty according to Wooler; Plication = Plication on the leaflets without resection; AML = Corrective measure on the anterior mitral leaflet; Other Chord = Repositioning, shortening of the native chords, shortening of the origin of the chord by means of splitting or trimming or repositioning of the papillary muscle; Artif. Chordae = Chordae replacement with artificial chords. AML = all measures on the anterior mitral leaflet; PML = all measures on the posterior mitral leaflet; Plication = Plication or inverse plication without resection; Resection: triangular or quadrangular resection on the leaflets. Artificial Chordae = Implantation of artificial chordae with stretched polytetrafluorethylen (Goretex™) from the papillary muscles to the AML and/or PML; Other Chordae Measures = other measures on the chordae or papillary muscles, i.e. repositioning, shortening, or resection. Wooler = Teflon-pledget-supported U-Suture on the anterior or posterior commissure; Patch = Implantation of a pericardium patch into the leaflet; Ring-Refixation = Refixationen of a partially detached annuloplasty-ring High age, BMI, and risk scores correlated with early mortality (EM) (Age-EM: 71.54 Age- Control: 64.89%, P<0.001; BMI-EM: 28.12% BMI-Control: 26.72, P = 0.026; log. ES-EM: 30.98%, Log.ES-Control: 10.46%, P<0.001; ESII-EM: 16.99% ESII-Control: 4.63%, P<0.001). Concomitant bypass surgery, particularly without IMA as well as concomitant implantation or explantation of electrophysiological devices increased the risk for early mortality whereas isolated MVR and use of artificial chordae reduced it (Table 4).
Table 4

Procedure-dependent early mortality.

Early mortality respective treatmentEarly mortality controlOdds ratio [mortality]P
Artificial Chordae 4.17% [7/168]12.98% [74/570]0.292 <0.001
Other Chordae Measures 0% [0/15]11.2% [81/723]00.393
CABG 17.8% [47/264]7.17% [34/474]2.799 <0.001
Venous CABG only 20.57% [29/141]8.71% [52/597]2.709 <0.001
CABG with IMA 15.45% [17/110]10.19% [64/628]1.610.135
IMA only 7.14% [1/14]11.05% [80/724]0.621
AV-Replacement 13.42% [20/149]10.36% [61/589]1.3410.304
AV-Repair 20% [1/5]10.91% [80/733]2.0380.442
MV-Replacement 11.11% [1/9]10.97% [80/729]1.0141
MVR only 3.23% [9/279]15.69% [72/459]0.179 <0.001
MIS-MVR 0% [0/13]11.17% [81/725]00,38
TVR/Replacement 16.67% [16/96]10.12% [65/642]1.7740.078
PFO/ASD 0% [0/14]11.19% [81/724]00.385
VSD 0% [0/7]11.08% [81/731]01
Aorta 9.09% [2/22]11.03% [79/716]0.8071
Electro 55.56% [5/9]10.43% [76/729]10.671 0.001
MAZE/LAA 5.06% [4/79]11.68% [77/659]0.4030.086
LAA only 0% [0/10]11.13% [81/728]00.612

CABG = Coronary Bypass; IMA = Internal mammary artery; AV-Replacement = Aortic Valve Replacement, AV-Repair = Aortic Valve Repair; MVR = Mitral Valve Repair; MIS-MVR = Minimal-invasive MVR; TVR/Replacement = Tricuspid valve repair/replacement; PFO/ASD = Persisting Foramen Ovale/Atrial Septal Defect; VSD = Ventricle Septal Defect; Aorta = Aortic wrapping or replacement; Electro = Electrophysiological implant; MAZE/LAA = Maze-Procedure (Atrial ablation) / Left Atrial Appendage

CABG = Coronary Bypass; IMA = Internal mammary artery; AV-Replacement = Aortic Valve Replacement, AV-Repair = Aortic Valve Repair; MVR = Mitral Valve Repair; MIS-MVR = Minimal-invasive MVR; TVR/Replacement = Tricuspid valve repair/replacement; PFO/ASD = Persisting Foramen Ovale/Atrial Septal Defect; VSD = Ventricle Septal Defect; Aorta = Aortic wrapping or replacement; Electro = Electrophysiological implant; MAZE/LAA = Maze-Procedure (Atrial ablation) / Left Atrial Appendage Freedom from early or late redo-procedures for the mitral valve was 91% in P1, 96% in P2, and 97% in P3 (P1 vs. P2 P = 0.008; P1 vs. P3 P = 0.006; P2 vs. P3 P = 0.195). Early mitral valve replacement after initial repair were most often performed. MV-Replacement after MVR early: Mean interval 91 days; MV-Replacement after MVR late: Mean interval 927 days; MVR after MVR early: Mean interval 13.67 days; MVR after MVR late: Mean interval 317 days. Survival rates (93% follow-up) were 66% (5-years), 55% (10 years), 44% (15 years) in P1, 63% (5 years), 50% (10 years) in P2, and 80% (5 years) in Period 3. General survival was 70% after 5 years, 56% after 10 years, and 45% after 15 years. 5-year survival was better in the recent period than in both previous periods. The differences between Period 1 and 2, Period 1 and 3, and Period 2 and 3 were significant (p<0.001). Odds ratios for reduced long-term survival were concomitant venous bypass surgery (5-years 1.871, p = 0.004; 10 years 2,701, p = 0.026); concomitant tricuspid valve surgery (10-years 4.699, p = 0.04). Survival was positively influenced by isolated MVR (5-years 0.375, p<0.001; 10-years 0.246, p = 0.001), concomitant isolated arterial bypass (IMA) (10-years 0.153, p0.051); posterior leaflet procedures (5 years 0.568, p = 0.005; 10 years 0.178, p<0.001), and use of artificial chordae (5-years 0.235, p<0.001) (Table 5, Fig 2).
Table 5

Odds ratios of 5- and 10-year survival.

5-Year Survival10-Year Survival
ORPORp
Gender 0.86 [0.597–1.24]0.4750.839 [0.49–1.435]0.612
Anterior Mitral leaflet 0.773 [0.352–1.699]0.6540.286 [0.114–0.717] 0.011
Posterior Mitral leaflet 0.355 [0.229–0.55] 0 0.137 [0.077–0.243] 0
Plication 0.46 [0.267–0.792] 0.006 0.419 [0.213–0.826] 0.018
Resection 0.461 [0.278–0.764] 0.003 0.151 [0.083–0.277] 0
Patch 0.492 [0.098–2.46]0.4850.31 [0.043–2.243]0.245
Ring-Refixation 0.296 [0.014–6.193]0.5181.602 [0.076–33.749]1
Wooler Plasty 0.612 [0.262–1.426]0.3440.213 [0.094–0.479] 0
Artificial Chordae 0.342 [0.199–0.589] 0 1.725 [0.573–5.198]0.465
Other Chordae Measures 0.892 [0.211–3.777]10.307 [0.061–1.557]0.152
CABG 1.912 [1.325–2.758] 0.001 2.17 [1.239–3.801] 0.009
Venous CABG only 2.292 [1.481–3.549] 0 2.358 [1.14–4.875] 0.027
CABG plus IMA 1.253 [0.782–2.006]0.4141.815 [0.843–3.909]0.171
IMA only 0.366 [0.077–1.743]0.3290.204 [0.033–1.245]0.092
AV-Replacement 2.084 [1.326–3.274] 0.002 1.76 [0.867–3.573]0.157
AV-Repair 1.495 [0.209–10.701]12.253 [0.115–44.117]1
MV-Replacement 0.741 [0.183–2.998]0.7460.24 [0.063–0.918] 0.039
MVR 0.663 [0.229–1.921]0.6270.307 [0.039–2.438]0.47
MVR only 0.242 [0.156–0.375] 0 0.202 [0.115–0.355] 0
MIS-MVR 0.069 [0.004–1.176] 0.007 0.313 [0.019–5.072]0.423
TVR/Replacement 2.363 [1.341–4.161] 0.004 4.023 [1.198–13.507] 0.014
PFO/ASD 0.892 [0.211–3.777]10.468 [0.077–2.853]0.597
VSD 0.744 [0.067–8.258]10.957 [0.039–23.748]1
Aorta 0.532 [0.167–1.696]0.4231.921 [0.228–16.22]1
Electro 19.951 [1.118–356.183] 0.004 4.239 [0.236–76.139]0.342
MAZE/LAA 0.743 [0.408–1.353]0.4092.212 [0.638–7.665]0.309
LAA only 0.245 [0.029–2.047]0.2510.957 [0.039–23.748]1

CABG = Coronary Bypass; IMA = Internal mammary artery; AV-Replacement = Aortic Valve Replacement, AV-Repair = Aortic Valve Repair; MVR = Mitral Valve Repair; MIS-MVR = Minimal-invasive MVR; TVR/Replacement = Tricuspid valve repair/replacement; PFO/ASD = Persisting Foramen Ovale/Atrial Septal Defect; VSD = Ventricle Septal Defect; Aorta = Aortic wrapping or replacement; Electro = Electrophysiological implant; MAZE/LAA = Maze-Procedure (Atrial ablation) / Left Atrial Appendage

Fig 2

Odds ratios for long-term survival (5- and 10 years).

MIC = Minimal invasive; MVR = Mitral valve repair; LAA = Left atrial appendage closure; PML = posterior mitral leaflet; IMA = Internal mammary artery; MAZE = Atrial ablation therapy; AML = Anterior mitral leaflet; CABG = Coronary artery bypass graft; AV-Replacement = Aortic valve replacement; TVR/Replacement = Tricuspid valve repair or replacement; Electro = Electrophysiological device.

Odds ratios for long-term survival (5- and 10 years).

MIC = Minimal invasive; MVR = Mitral valve repair; LAA = Left atrial appendage closure; PML = posterior mitral leaflet; IMA = Internal mammary artery; MAZE = Atrial ablation therapy; AML = Anterior mitral leaflet; CABG = Coronary artery bypass graft; AV-Replacement = Aortic valve replacement; TVR/Replacement = Tricuspid valve repair or replacement; Electro = Electrophysiological device. CABG = Coronary Bypass; IMA = Internal mammary artery; AV-Replacement = Aortic Valve Replacement, AV-Repair = Aortic Valve Repair; MVR = Mitral Valve Repair; MIS-MVR = Minimal-invasive MVR; TVR/Replacement = Tricuspid valve repair/replacement; PFO/ASD = Persisting Foramen Ovale/Atrial Septal Defect; VSD = Ventricle Septal Defect; Aorta = Aortic wrapping or replacement; Electro = Electrophysiological implant; MAZE/LAA = Maze-Procedure (Atrial ablation) / Left Atrial Appendage

Discussion

Ever since Carpentier has propagated the mandatory use of an annuloplasty-ring in order to stabilize the reconstruction result it became the procedure the overwhelming majority of all surgeons adhered to owing to the clear and steadily growing body of evidence regarding the benefit of the ring [1-3]. Indeed, our study mirrored this indicating that ring implantation remained mandatory throughout the entire observation period. However, preference towards certain rings changed alongside improved designs. Those design changes comprised on one hand the very shape of the ring propagating the “saddle-shape” as being a design improvement with positive implications on hemodynamic performance but on the other hand on design changes intended to facilitate implantation itself [7-9]. These particular changes comprised wider rings with multi-layer fabric to allow for better stitching and more secure anchoring. Stiff or moderately flexible rings appeared to stabilize the annulus significantly better than highly flexible ones [10, 11] so that the use of the latter did not play a role in this study. Procedural characteristics for the valvular apparatus changed markedly from mainly classical resection maneuvers to predominant use of artificial chordae [12-18]. In the early years the classical recommendations such as reshaping of the posterior leaflet by resection or plication maneuvers as well as reshaping of the annulus by appropriate rings were mostly followed but measures such as Wooler plasty, Paneth plasty, or Alfieri Stitch were still performed [19, 20]. However, they did not exhibit such robust evidence in the literature regarding a beneficial effect on long-term patency as posterior leaflet correction and/or artificial chordae. We did not perform the Paneth plasty, which are meant to reduce the diameter of the anulus but favored instead the annuloplasty-ring as an implant from the early days on. Alfieri-Stich was neither performed because of the, in our eyes, “non-anatomical” approach. The patients who had received a Wooler plasty, however, fared quite well and the presence of a Wooler plasty positively influenced long-term survival even after 10 years. This, however, was quite probably not due to the Wooler plasty itself but owing to the mandatory annuloplasty ring, these patients also received. It cannot be ruled out, however, that intraoperative quality control also played a role regarding long-term stability. Transesophageal echocardiography (TEE) was not yet mandatory in period 1. Surgeons mainly relied on intraoperative filling of the left ventricle with saline to estimate the success of the reconstruction and no intraoperative quality control was thus performed while the heart was beating. Direct correction in case of an insufficient result was thus not an option [21-23]. The widespread introduction of artificial chordae was a relevant evolutionary step that our godfather Alain Carpentier had not foreseen. Perhaps this is because the most suitable material for these chordae, expanded polytetrafluoroethylene, Goretex ™, was not yet available in the 1970s. Artificial chordae were soon adopted by the majority of surgeons and gained worldwide acceptance. Indeed, that was apparent also in our cohorts over the years. Although early and intermediate results up to five years were quite favorable for valves repaired with artificial chordae this benefit disappeared in the long-term results (10-year survival). It must be noted, however, that artificial chordae came into wider use but in the second and third period so that long-term results on a larger scale are not yet available. We noticed a steep increase in repair from period 1 to period 2 possibly owing to the experience gained with repair strategies in the early years in our institution. From period 2 to period 3 a slight decrease of the proportion of repair maneuvers was noted declining from 48% to 41%. This shift was not due to a more restrictive policy regarding repair surgery but was instead non-intentional and can be explained by a higher morbidity of the patients resulting in a higher proportion of patients with complex redo-surgery or endocarditis. The increase in patients with primary mitral regurgitation from period 1 to period 3 cannot be readily explained. It is conceivable that, because of demographic change, patients with restrictive mitral valve pathology presented with increasing multimorbidity, so that the indication for repair in patients with secondary mitral valve pathology became more defensive. Only 13 minimally invasive mitral valve repair procedures were carried out mainly in period 2. The true minimally invasive approach was indeed not favored in our clinic until very recently because of lack of center-wide, multi-surgeon expertise. Leaflet repair strategies especially concerning the posterior leaflet remained a frequent procedure demonstrating excellent results even in the long-term. Why is it so? The posterior leaflet has a much less complex movement and serves mainly as an abutment for the very mobile anterior leaflet. Thus, a stable coaptation for the anterior leaflet can be rather easily achieved with appropriate measures on the posterior leaflet such as quadrangular resection, plication or cleft-closure accompanied by remodeling the often v-shaped distorted posterior anulus back to its distinct anteriorly flattened circle, the “smiley” mouth. In contrast, any reshaping measure of the highly mobile anterior leaflet is much more prone to frustrating results (Fig 3). While co-morbidities negatively influenced survival early as well as late [24, 25], it was interesting to see that patients with concomitant venous only coronary bypass surgery fared worse than the others (Fig 3).
Fig 3

Procedure-related survival.

MVR = Mitral valve repair; Resection = All types of resection measure on either leaflet; CABG = Coronary artery Bypass Graft; IMA = Internal mammary artery.

Procedure-related survival.

MVR = Mitral valve repair; Resection = All types of resection measure on either leaflet; CABG = Coronary artery Bypass Graft; IMA = Internal mammary artery. This can, however, be explained. These patients were too sick to be deemed fit for the use of a mammary artery in the eyes of the surgeon carrying out the procedure. Such a surgical decision was made upon the general clinical appraisal of the patient and not concrete facts such as the EuroSCORE. Thus, the underlying reasons for such a decision remained somehow elusive. This finding gains additional validation when looking at the fate of the patients who indeed had received LIMA only bypass surgery. They fared significantly better than the control. These patients only had a 1-vessel disease and received an artery for prognostic reasons, i.e. profiting from it because of a better life expectancy in the eyes of the surgeon (Fig 3). At the other end of the spectrum were those patients receiving aortic valve replacement, concomitant tricuspid valve repair or even replacement or those requiring electrophysiological implants. These patients fared worse early as well as late indicating the higher morbidity at the time of surgery. In general, early mortality risks were typically dependent on the patient’s individual situation. Procedural success and stability increased over the three periods and long-term results were very acceptable. The patients of period 3 demonstrated a superior 5-year survival than that of the two previous groups. Whether this is due to a more precise indication and/or better perioperative management in this latter period is speculative. It remains to be seen whether this trend will continue significantly after 10 or 15 years, respectively (Fig 4).
Fig 4

Cohort-Survival.

Limitations

This study is of retrospective nature and thus naturally subject to the typical limitations. Mitral valve pathologies could only be roughly obtained. In almost all cases, however, we were able to differentiate between primary or secondary nature from the still available documents (surgery, echocardiography). The procedures were carried out upon the discretion of the respective surgeon and not prospectively assigned in a randomized fashion. Long-term follow-up was not complete. We tried best to reach all patients but particularly in the rural regions the whereabouts of some patients remained elusive despite all efforts. We used many different rings in the last 15 years. However, not all of the available rings were used at respective times. Thus, the selection is incomplete and is even somehow biased as the clinics policy always was and is to reduce the number of implants to a reasonable minimum for budgetary purposes.

Conclusion

Mitral valve repair underwent a qualitative evolution in the last 15 years. It became clear that the use of a ring as well as artificial chordae and appropriate reshaping of the leaflets, particularly the posterior one, were keys to success. Thus, proving that the combination of the best well established old-fashioned techniques such as leaflet resection measures and mandatory use of rings as well as the most useful modern approaches such as artificial chordae and modern saddle-shaped ring designs is in the best interest of the patient. Co-morbidities and thus, the necessity to perform concomitant procedures in more than half of the entire cohort markedly influenced survival. However, almost half of the patients are alive after 15 years. Mitral valve repair is one of the few remaining primary cardiosurgical procedures and it will remain in our hands as long as we are able to provide a reliable, stable and long-lasting anatomical repair surpassing the results of any interventional strategy [26-30]. Luckily, the complexity of the mitral valves plays into our cards in this regard. Thus, mitral valve repair is still and for the years to come one of the most valuable cardiosurgical procedures. 18 Feb 2022
PONE-D-21-35308
Everyday mitral valve reconstruction. What has changed over the last 15 years?
PLOS ONE Dear Dr. Albes Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. ==============================
Please ensure that your decision is justified on PLOS ONE’s publication criteria and not, for example, on novelty or perceived impact. For Lab, Study and Registered Report Protocols: These article types are not expected to include results but may include pilot data. ============================== Please submit your revised manuscript by 4/3/2022 . If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file. Please include the following items when submitting your revised manuscript:
A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'. A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'. An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'. If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter. If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols. We look forward to receiving your revised manuscript. Kind regards, Alessandro Leone, MD Academic Editor PLOS ONE Journal Requirements: When submitting your revision, we need you to address these additional requirements. 1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf 2. Please update your submission to use the PLOS LaTeX template. The template and more information on our requirements for LaTeX submissions can be found at http://journals.plos.org/plosone/s/latex. 3. Please provide additional details regarding participant consent. In the ethics statement in the Methods and online submission information, please ensure that you have specified what type you obtained (for instance, written or verbal, and if verbal, how it was documented and witnessed). If your study included minors, state whether you obtained consent from parents or guardians. If the need for consent was waived by the ethics committee, please include this information 4. We note that you have stated that you will provide repository information for your data at acceptance. Should your manuscript be accepted for publication, we will hold it until you provide the relevant accession numbers or DOIs necessary to access your data. If you wish to make changes to your Data Availability statement, please describe these changes in your cover letter and we will update your Data Availability statement to reflect the information you provide Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice [Note: HTML markup is below. Please do not edit.] Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #1: Yes Reviewer #2: Yes ********** 2. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: Yes Reviewer #2: Yes ********** 3. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #1: Yes Reviewer #2: Yes ********** 4. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #1: Yes Reviewer #2: Yes ********** 5. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: Dear the authors of the manuscript entitled "Everyday mitral valve reconstruction. What has changed over the last 15 years?" Thank you for writing this retrospective study which evaluates the change in the paradigm of mitral valve reconstruction over a three periods of time I valued the way you presented this study and the results and discussion parts I think this study provided outcomes after mitral valve reconstruction and also provided the changes in the method of surgical techniques utilized One major issue which I believe is adding the mitral valve pathologies in these patients, which I think is very related to the outcomes studied Otherwise I have no concerns Thank you Reviewer #2: This paper describes the evolution of mitral valve repair over many year. The evolution peroid was divided into three phases. I have the following notice: 1. In the results in line 100-102 the was a decrease in MVR in P3. Can you explain it please? 2. Only 13 minimally invasive MVR? 3. Some of the abbreviation are known German abbreviation used with English meaning like MIC (minimal invasive Chirurgie) for minimally invasive. Could you please correct this? 4. From line 200 to 203: you wrote. (These particular changes 201 comprised wider rings with multi-layer fabric to allow for better stitching and more secure 202 anchoring. Stiff or moderately flexible rings appeared to stabilize the annulus significantly 203 better than highly flexible ones so that the use of the latter did not play a role in this study). Can you please give an evidence or a reference to this sentence.! In general, the paper proves the thought of cardiac surgeons the use of artificial chordae is dominating the field of mitral surgery. The only unexplainable finding is he very low number of minimally invasive procedure which could be a center decision to avoid such an approach but with still no explanation. This nice collection needs some improvement before publication beside a language editing. Best regards ********** 6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #1: Yes: Salah Eldien Altarabsheh Reviewer #2: No [NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.] While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.
15 Mar 2022 Dear Reviewers, Thank you for your thoughtful comments and suggestions, which we would like to respond to as follows: Reviewer #1: Mitral valve pathologies are indeed important. I am sure you know from your own experience that it is somewhat problematic to determine the exact underlying pathology in a retrospective study with an almost historical cohort going back to 2004, with few meaningful echocardiographic findings properly documented or with not much in the surgeon's protocol or in the letter from the referring hospital. Thus, pathologies were not the primary focus of interest in this retrospective study. However, on your advice, we reviewed all the data still available and obtained as much information as possible. In the end, we were able to distinguish quite well between primary and secondary nature of the origin of mitral valve regurgitation by considering the morphology as primary origin if the valve leaflets and other aspects directly affected the valve apparatus or as secondary origin if the valves were tethered and/or the annulus was asymmetrically distorted. In the remaining cases, whose pathological origin was still unclear, we assumed that it was a secondary condition if bypass surgery was performed at the same time. Indeed, our results show differences between patients with measures on the valves themselves (resection, reconstruction, repair) and those with concomitant bypass surgery. In this way, we were able to investigate, at least indirectly, the importance of the type of mitral valve regurgitation (primary or secondary origin) on outcome. We included mitral valve pathologies in Table 1 and referred to them in the Patients and Methods section (lines 72-5) and in the Results (line 107), Discussion (245-9), and Limitations (lines 291-3). We also cited the 2021 ESC guidelines, which contain the current mitral valve pathology systematics [5]. Reviewer #2: 1. The slight decrease between period 2 and 3 was indeed apparent. After noticing a steep increase in repair from period 1 to period 2 possibly owing to the experience gained with repair strategies in the early years in our institution a slight decrease of the proportion of repair maneuvers was noted declining from 48% to 41%. This shift was not due to a more restrictive policy regarding repair surgery but was instead non-intentional and can be explained by a higher morbidity of the patients resulting in a higher proportion of patients with complex redo-surgery or endocarditis. We explained the slight decrease of the proportion of mitral valve repair and added a respective statement in the Discussion (lines 239-44). 2. Only 13 minimally invasive mitral valve repairs were performed mainly in period 2. The true minimally invasive approach was not favored in our hospital until recently because of the lack of center-wide expertise performed by multiple surgeons. So, you are correct. This was a center decision at the time, which has now been changed after several experienced surgeons had been trained in the meantime with minimally invasive mitral valve repair with left mini-thoracotomy at other institutions with high experience and volume. We added a respective statement in the discussion (lines 250-2) 3. We have erased the term MIC in tables, legends, and figure 2 and replaced it by MIS-MVR. 4. We added respective literature evidence regarding our statement: These particular changes comprised wider rings with multi-layer fabric to allow for better stitching and more secure anchoring. Stiff or moderately flexible rings appeared to stabilize the annulus significantly better than highly flexible ones [10,11]. Thank you again for your valuable comments. Johannes M. Albes, MD, PhD, MBA Submitted filename: Response to Reviewers.docx Click here for additional data file. 24 May 2022 Everyday mitral valve reconstruction. What has changed over the last 15 years? PONE-D-21-35308R1 Dear Dr. Johannes Prof. Dr. Albes , We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements. Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication. An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org. If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org. Kind regards, Chengming Fan, MD, PhD Academic Editor PLOS ONE Additional Editor Comments (optional): Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation. Reviewer #1: All comments have been addressed Reviewer #2: All comments have been addressed ********** 2. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #1: Yes Reviewer #2: Yes ********** 3. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: Yes Reviewer #2: Yes ********** 4. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #1: Yes Reviewer #2: Yes ********** 5. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #1: Yes Reviewer #2: Yes ********** 6. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: Dear the authors I want to thank you for taking into consideration for my as well as the reviewer's comments which are all meant to improve the quality of the manuscript I have no concerns about the manuscript in its current status Reviewer #2: no comment more needed to be added. the authors has adressed all our concerns in the revised version of the paper ********** 7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #1: Yes: Salah Eldien Altarabsheh Reviewer #2: No 20 Jun 2022 PONE-D-21-35308R1 Every day mitral valve reconstruction: What has changed over the last 15 years? Dear Dr. Albes: I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department. If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org. If we can help with anything else, please email us at plosone@plos.org. Thank you for submitting your work to PLOS ONE and supporting open access. Kind regards, PLOS ONE Editorial Office Staff on behalf of Dr. Chengming Fan Academic Editor PLOS ONE
  29 in total

Review 1.  Outcomes of mitral valve repair using artificial chordae.

Authors:  Michael Ibrahim; Christopher Rao; Maria Savvopoulou; Roberto Casula; Thanos Athanasiou
Journal:  Eur J Cardiothorac Surg       Date:  2013-08-29       Impact factor: 4.191

2.  Intraoperative TEE during mitral valve repair: does it predict early and late postoperative mitral valve dysfunction?

Authors:  Y Saiki; H Kasegawa; M Kawase; H Osada; E Ootaki
Journal:  Ann Thorac Surg       Date:  1998-10       Impact factor: 4.330

3.  MitraClip: a word of caution regarding an all too liberal indication and delayed referral to surgery in case of failure.

Authors:  Roya Ostovar; Michael Erb; Filip Schroeter; Michael Zytowski; Ralf-Uwe Kuehnel; Martin Hartrumpf; Johannes Maximilian Albes
Journal:  Eur J Cardiothorac Surg       Date:  2021-04-29       Impact factor: 4.191

4.  A new reconstructive operation for correction of mitral and tricuspid insufficiency.

Authors:  A Carpentier; A Deloche; J Dauptain; R Soyer; P Blondeau; A Piwnica; C Dubost; D C McGoon
Journal:  J Thorac Cardiovasc Surg       Date:  1971-01       Impact factor: 5.209

Review 5.  Transcatheter Mitral Valve Repair With MitraClip for Symptomatic Functional Mitral Valve Regurgitation.

Authors:  Rodrigo Mendirichaga; Vikas Singh; Vanessa Blumer; Manuel Rivera; Alex P Rodriguez; Mauricio G Cohen; William W O'Neill; Sammy Elmariah
Journal:  Am J Cardiol       Date:  2017-05-30       Impact factor: 2.778

6.  The edge-to-edge technique: a simplified method to correct mitral insufficiency.

Authors:  F Maisano; L Torracca; M Oppizzi; P L Stefano; G D'Addario; G La Canna; M Zogno; O Alfieri
Journal:  Eur J Cardiothorac Surg       Date:  1998-03       Impact factor: 4.191

7.  Functional and Degenerative Mitral Regurgitation: One Ring Fits All?

Authors:  Konstantinos Sideris; Johannes Boehm; Bernhard Voss; Thomas Guenther; Ruediger S Lange; Ralf Guenzinger
Journal:  Thorac Cardiovasc Surg       Date:  2019-09-23       Impact factor: 1.827

8.  Transesophageal Echocardiography, Mortality, and Length of Hospitalization after Cardiac Valve Surgery.

Authors:  Emily J MacKay; Mark D Neuman; Lee A Fleisher; Prakash A Patel; Jacob T Gutsche; John G Augoustides; Nimesh D Desai; Peter W Groeneveld
Journal:  J Am Soc Echocardiogr       Date:  2020-03-26       Impact factor: 5.251

9.  Clinical performance of a three-dimensional saddle-shaped, rigid ring for mitral valve repair.

Authors:  Nicolas Doll; Ventsislav Sheytanov; Louis Labrousse; Michael W A Chu; Pierluigi Stefàno; Aleš Mokrácek; Olivier Baron; Shuzhen Li; Ralf Günzinger
Journal:  Eur J Cardiothorac Surg       Date:  2019-02-01       Impact factor: 4.191

10.  Results for tricuspid valve surgery in adults with congenital heart disease other than Ebstein's anomaly†.

Authors:  Mauro Lo Rito; Maria Grandinetti; Giulia Muzio; Alessandro Varrica; Alessandro Frigiola; Angelo Micheletti; Massimo Chessa; Alessandro Giamberti
Journal:  Eur J Cardiothorac Surg       Date:  2019-10-01       Impact factor: 4.191

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.