Francisco Diniz Affonso da CostaI,II; Daniele de Fátima Fornazari ColatussoII; Gustavo Luis do Santos MartinII; Kallyne Carolina Silva ParraII; Mariana Cozer BottaII; Eduardo Mendel Balbi FilhoII; Myrian VelosoII; Gabriela MiottoII; Andreia Dumsch de Aragon FerreiraII; Claudinei ColatussoII
DOI: 10.21470/1678-9741-2017-0145
ABSTRACT
Introduction: Current guidelines state that patients with severe mitral regurgitation should be treated in reference centers with a high reparability rate, low mortality rate, and durable results.ACC = American College of Cardiology
AF = Atrial fibrillation
AVR = Aortic valve replacement
CABG = Coronary artery bypass grafting
CAD = Coronary artery disease
CI = Confidence intervals
COPD = Chronic obstructive pulmonary disease
CPB = Cardiopulmonary bypass
DDLV = Diastolic dimension of the left ventricle
ECC = Extended extracorporeal circulation
FD = Fibroelastic deficiency
HR = Hazard ratios
INC-Cardio = Instituto de Neurologia e Cardiologia de Curitiba
LV = Left ventricle
LVEF = Left ventricular ejection fraction
MD = Myxomatous degeneration
MR = Mitral regurgitation
MVR = Mitral valve repair
NYHA = New York Heart Association
RA = Right atrial
RD = Rheumatic disease
RV = Right ventricular
SAM = Systolic anterior motion
SD = Standard deviation
SDLV = Systolic dimension of the left ventricle
SIH/SUS = Hospital Information System - Ministry of Health
STS = Society of Thoracic Surgeons
TEE = Transesophageal echocardiography
TR = Tricuspid regurgitation
USA = United States of America
INTRODUCTION
Mitral valve repair (MVR) is considered the best surgical option for most patients with severe mitral regurgitation (MR), including elderly patients with associated comorbidities and higher operative risks[1,2]. In fact, recent guidelines for management of valvular heart diseases indicate that asymptomatic patients with preserved left ventricular function should be redirected to "reference centers" and surgery should be considered only when the probability of the repair is high, and the operative mortality is low[3,4].
The Society of Thoracic Surgeons (STS) database demonstrates that despite an increasing adoption of conservative operations in the last decade, the overall rate of MVR in the United States of America (USA) is still only around 70%, and probably restricted to simpler repairs involving prolapse of the posterior cusp, in most centers[5]. In Brazil, MVR is performed even more infrequently, and although the statistical estimates are somewhat imprecise, the incidence of MVR appears to be in a disappointingly range of 1520% (Hospital Information System - Ministry of Health [SIH/SUS]).
Our surgical group, working in two different institutions, has been involved in mitral valve repair since the late 1980's. The Instituto de Neurologia e Cardiologia de Curitiba (INC-Cardio) is a new private health institution in Curitiba, and since its inception in 2004, we have had the opportunity to establish a heart valve team that enabled us not only to perform all valvular operations with intraoperative transesophageal echocardiography (TEE) control, but also to prospectively follow our patients at ambulatory level in an adequate manner. The aim of this study was to analyze our global experience with all surgically treated patients presented with any form of organic mitral valve insufficiency at this institution.
METHODS
This study was approved by the Institutional Research Ethical Committee (number 1.061.245) and registered at Plataforma Brasil (number CAAE 42.708015.2.0000.5227). We retrospectively analyzed all patients operated at INC-Cardio from January 2004 to March 2017 who had the diagnosis of organic MR as the primary indication for surgery. Patients with concomitant procedures such as tricuspid repair, ablation for atrial fibrillation (AF), and coronary artery bypass grafting (CABG) were included. However, patients with concomitant aortic valve replacement (AVR) or functional MR due to ischemic cardiomyopathy were excluded from the analysis.
The etiology of the disease was based in echocardiographic findings and confirmed at the operation by visual inspection. Patients with degenerative disease were subdivided in fibroelastic deficiency (FD), moderate myxomatous degeneration (MD), and Barlow disease, according to the degree of myxomatous changes. Typically, patients with normally sized and thin cusps, except for the prolapsing segment, were considered FD; while those with voluminous, aneurysmal and thickened cusps, with massive annular dilatation and often displaced posterior cusp attachment, were categorized as Barlow disease. Valves with intermediary changes in this spectrum were labeled as MD. Rheumatic disease (RD) patients were included if they had pure MR or mixed lesions with at least moderate degree of MR.
Surgical Technique
All operations were performed by a single surgeon (FDAC), most commonly through full sternotomy or, in the last few years, using a right minithoracotomy approach in selected cases. When midline sternotomy was used, cardiopulmonary bypass (CPB) was instituted with central aortic and bicaval cannulation. We routinely employed moderate systemic hypothermia (32ºC), and myocardial protection was obtained with intermittent antegrade cold blood cardioplegia. For the minithoracotomy cases, CPB was instituted with peripheral arterial and venous femoral cannulation, and cardioplegia was performed with a single dose of Custodiol solution®.
After gaining exposure of the mitral valve through a left atriotomy parallel to the interatrial groove, careful and systematic valve analysis was performed to identify all valve lesions producing valve dysfunction. Posterior leaflet prolapses were treated either by triangular or quadrangular resection of the prolapsing segments or by the insertion of neo-chords utilizing the "respect" concept. Whenever there was excess of posterior leaflet tissue, a sliding plasty was performed to reduce the height of the posterior leaflet in order to avoid systolic anterior motion (SAM). Anterior leaflet prolapse was preferentially corrected with the utilization of Gore-Tex neo-chords, but we also used the flipover technique or papillary muscle repositioning in some cases. In rheumatic cases, shaving and thinning of the leaflets as well as resection of scarred and fused primary and secondary chords were often necessary to increase leaflet mobility. Cusp extension of the anterior leaflet was utilized to increase surface coaptation in some cases. Mild or moderate areas of calcifications were fully debrided. In the presence of active bacterial endocarditis, all infected tissues were excised, and the resultant defects were corrected with patches of decellularized human pericardia.
Except for patients with acute endocarditis, a Carpentier-Edwards Physio II annuloplasty ring® (Edwards Lifesciences LLC, Irvine, CA, USA) or a posterior bovine pericardium band® (Cardioprótese Ltda, Curitiba, PR, Brazil) was employed to correct annular dilatation and to stabilize the repair. Valve competence was tested with saline solution or by pressurizing the left ventricle (LV) with blood through a cardioplegia line inserted in the apex of the LV. Tricuspid annulus dilatation with or without regurgitation (TR) was corrected with Carpentier-Edwards Tricuspid Physio ring® (Edwards Lifesciences, Irvine, CA, USA) and CABG was performed with standard techniques. To ascertain an adequate repair, intraoperative TEE was performed in all patients after weaning from CPB.
Patient Data and Clinical Follow-up
Preoperative clinical data were obtained by reviewing hospital charts and operative notes. Early mortality was defined as any death occurring before hospital discharge or during the first 30 postoperative days. Causes of early and late deaths were determined by hospital charts review, death certificates, information from the physician who was caring for the patient at that time or communication with the patient's family. Early and late postoperative complications were reported according to well-established guidelines[6].
Clinical follow-up was obtained at one, six, and 12 months after the operation and then annually thereafter in our outpatient clinic, with the referring cardiologist or by direct contact with the patient or his/her family. For this study, a database freeze was performed in March 2017. Clinical follow-up was obtained within two years of closure in 95% of the patients (five patients were lost to follow-up). Anticoagulation with sodium warfarin was indicated only to patients with AF, to those who had AF ablation or after an episode of cerebral embolism. Patients with RD were oriented to have lifelong oral penicillin as a secondary prophylaxis against rheumatic fever.
Echocardiographic Analysis
Mitral valve function was evaluated by transthoracic twodimensional Doppler echocardiography, performed by the referring cardiologist or at our outpatient clinic at yearly intervals. Whenever it was necessary, supplemental information was obtained with 2D or 3D TEE studies.
All patients were operated with intraoperative TEE control, including 3D real time images in the last two years.
MR was initially classified as none, trivial, mild, moderate, and severe, based on the length and area of the regurgitant jet and using American Society of Echocardiography's guidelines[7]. Valve failure was defined as recurrent significant regurgitation of more than 1+ MR (mild MR) or mitral valve reoperation.
Statistical Analysis
Statistical analysis was conducted with The R Project for Statistical Computing statistical software (www.cran.r-project.org/ version 3.3.1) and Graph Pad Prism Software (www.graphpad.com/guides/prism/7/). Data were presented as frequencies or means with standard deviations. The Kaplan-Meier method was used to estimate survival and freedom from morbid events, and results were considered meaningful up to 10 years. For outcomes other than death, patients were right censored in case of a late death. Age- and sex-matched Brazil general population survival estimates for the year 2013 (median year of surgery of the study cohort) were obtained from data published by the Instituto Brasileiro de Geografia e Estatística (http://www.ibge.gov.br), and statistical comparison with survival rates from the study cohort was done using a one-sample log-rank test.
Univariable analysis was carried out with chi-square tests and log-rank test to determine the risk factors for reoperation and valve failure, and they were considered significant when P<0.05. Predictors were expressed by their hazard ratios (HR) with 95% confidence intervals (CI). Variables tested included patient's age, gender, New York Heart Association (NYHA) functional class, etiology, AF, systemic arterial hypertension, chronic obstructive pulmonary disease (COPD), diabetes, smoking, renal failure, coronary artery disease (CAD), previous cardiac operations, concomitant procedures, cross-clamp, and extended extracorporeal circulation (ECC) times.
RESULTS
From January 2004 to March 2017, our surgical group has performed 538 MVR, of which 125 were done at INC-Cardio and are the subject of this study. During this period, 133 patients were operated with a diagnosis of organic MR, and only eight (acute endocarditis = 3, advanced mitral mixed lesions = 3, and failed previous MVR done elsewhere = 2) had a mitral valve replacement, yielding an overall 93.9% global repair rate. All patients (100%) with degenerative mitral valve disease undergoing a first operation had a MVR.
The demographics of the 125 MVR patients are summarized in Table 1. Mean patient age was 57±15 years (range: 9 - 87 years), 52 (42%) patients were males, and 23 (18%) were older than 70 years. The most common etiology was degenerative disease in 73 (58%) patients, followed by RD in 34 (27%). Preoperatively, 44 (35%) patients were in NYHA functional class III and IV, and the mean left ventricular ejection fraction (LVEF) was 67±8%. MR grade was considered severe in 115 patients (92%) and moderate in the remaining 10 (8%).
Variables | N (%) |
---|---|
Number of patients | 125 |
Age at surgery - mean±SD | 57±15 |
Range, years | 9 - 87 |
Sex, male | 52 (41.9%) |
Etiology | |
Degenerative | 73 (58.4%) |
Myxomatous degeneration | 57 (45.6%) |
Fibroelastic deficiency | 9 (7.2%) |
Barlow syndrome | 7 (5.6%) |
Rheumatic | 34 (27.2%) |
Congenital | 5 (4%) |
Pure annular dilatation | 3 (2.4%) |
Infective endocarditis | 9 (7.2%) |
Healed | 5 (4%) |
Active | 4 (3.2%) |
Endomyocardial fibrosis | 1 (0.8%) |
NYHA Class | |
I | 23 (18.4%) |
II | 58 (46.4%) |
III | 36 (28.8%) |
IV | 8 (6.4%) |
Previous cardiac operations | 13 (10.4%) |
Systemic arterial hypertension | 59 (47.2%) |
Chronic obstructive pulmonary disease | 3 (2.4%) |
Diabetes | 8 (6.4%) |
Smoking | 10 (8%) |
Renal failure | 8 (6.4%) |
Coronary artery disease | 9 (7.2%) |
Atrial fibrillation/Flutter | 36 (28.8%) |
LVEF (%) - mean±SD | 67±8.4 |
Range | 31-84 |
Below 50% | 5 (4%) |
DDLV (mm) - mean±SD | 55±7.2 |
Range | 41-76 |
SDLV (mm) - mean±SD | 34±6.1 |
Range | 25-56 |
Mitral regurgitation | |
Moderate | 10 (8%) |
Severe | 115 (92%) |
Tricuspid regurgitation | |
Moderate | 18 (14.4%) |
Severe | 2 (1.6%) |
Operative findings, repair techniques, and concomitant procedures are listed in Table 2.
Variables | N (%) |
---|---|
Number of patients | 125 |
Etiology | |
Degenerative | 73 (58.4%) |
Anterior prolapse | 11 (15.0%) |
Posterior prolapse | 49 (67.1%) |
Bileaflet prolapse | 13 (17.8%) |
Rheumatic | 34 (27.2%) |
Congenital | 5 (4%) |
Pure annular dilatation | 3 (2.4%) |
Endomyocardial fibrosis | 1 (0.8%) |
Active infective endocarditis | 4 (3.2%) |
Healed infective endocarditis | 5 (4.0%) |
Incision | |
Median sternotomy | 115 (92.0%) |
Right minithoracotomy | 10 (8.0%) |
No annuloplasty ring | 11 (8.8%) |
Mitral annuloplasty ring | 114 (91.2%) |
Carpentier-Edwards Physio II Ring | 61 (48.8%) |
Bovine Pericardial band | 47 (37.6%) |
Gregori Ring 2 | 2 (1.6%) |
Carpentier Classic Ring | 3 (2.4%) |
Braile 1 | 1 (0.8%) |
Chordal replacement with Gore-Tex sutures | 76 (60.8%) |
Use of pericardial patches | 12 (9.6%) |
Triangular resection | 20 (16.0%) |
Quadrangular resection | 24 (19.2%) |
Tricuspid valve surgery | 20 (16.0%) |
Coronary artery bypass graft | 8 (6.4%) |
Atrial fibrillation ablation | 18 (14.4%) |
CPB time (min) - mean±SD | 93±35 |
Range | 35 - 240 |
Aortic clamping time (min) - mean±SD | 73±29 |
Range | 23 - 197 |
The mean clinical follow-up was 3.7±3.4 years (range: 0.1 - 12.4 years), with a total cumulative follow-up of 462.2 patientyears. In total, 697 echocardiograms were available for analysis. The latest echocardiogram was performed after a mean of 3.1±2.9 years (range: 0.1 - 12.3 years).
Early and Late Mortality
There were three early deaths with an overall early mortality of 2.4%. Among patients younger than 70 years, early mortality was 0.9% (1/102). Causes of early death were multi-organ failure in an 81-year-old patient with degenerative disease and healed bacterial endocarditis, respiratory failure in a 77-year-old patient with degenerative disease and low output syndrome in a rheumatic patient that was submitted to concomitant myocardial revascularization and AF ablation.
In addition, six patients died in the late postoperative period. Causes of late death were sudden death (n = 2), congestive heart failure, intracranial hemorrhage, hepatic cirrhosis, and unknown, in one case each. By Kaplan-Meier analysis, estimated five and 10 years survival were 89.5% (CI 95% = 78.8% - 94.9%) and 84.3% (CI95% = 67.1% - 92.9%), respectively, which were similar to an age- and gender-matched Brazilian population (Figure 1).
Risk factors for late mortality included age (HR = 3.30, CI95% = 0.85 - 12.7), associated CAD (HR = 2.48, CI95% = 0.42 - 14.2), diabetes (HR = 7.85, CI95% = 0.49 - 123.4), longer aortic crossclamp (HR = 4.07, CI95% = 1.09 - 15.1), and ECC times (HR=5.00, CI95% = 1.17-21.2) (Appendix 1).
Clinical Follow-up
Among the 111 survivors with known clinical status, 101 are in NYHA functional class I, nine in class II and only one in class III. This latter patient, despite a normally functioning mitral repair, developed moderate to severe tricuspid regurgitation and should undergo reoperation in the near future. During the observation period, five patients presented thromboembolic events, three were transient ischemic attacks and two were strokes. Freedom from thromboembolic events at five and 10 years was 93.1% (CI95% = 83.3% - 97.2%) (Figure 2). In addition, two patients presented with serious hemorrhagic complications, which were the cause of death in one. There were no documented cases of bacterial endocarditis.
By echocardiogram, late LVEF was 65.5±7.5% (range = 27 - 77), with only three being below 50%. Late diastolic dimension of the left ventricle (DDLV) was 48±6 mm (range = 37 - 74) and systolic dimension of the left ventricle (SDLV) was 31±6 mm (range = 22 - 68).
Reoperations and Mitral Valve Dysfunction
At discharge, only one patient had moderate MR with no further progression after six years.
During follow-up, two patients developed severe MR and were reoperated. Mitral valve could be re-repaired in both. Mechanisms of failure were dehiscence of the posterior leaflet suture line in one case (technical failure) and progression of the disease in another, with a new prolapse of the anterior leaflet. Freedom from severe MR and/or reoperation was 95.6% (CI95% = 82.5% - 98.9%) at 5 and 10 years (Figure 3).
Four additional patients developed moderate MR at late follow-up, but they are asymptomatic and under careful observation. Freedom from valve failure (more than mild MR or reoperation) was 88.2% (CI95% = 74.8% - 94.7%) at 5 years and 84.5% (CI95% = 68.8% - 92.6%) at 10 years. There was no difference in freedom from valve failure between degenerative and rheumatic valves at 10 years (Figure 4). Curiously, univariable analysis revealed renal failure as the only risk factor for late mitral valve dysfunction (HR = 9.31, CI95% = 0.22-397.66) (Appendix 1).
Tricuspid Valve Function
Four patients (moderate = 3, severe = 1) with preoperative TR underwent concomitant tricuspid annuloplasty during the operation. In addition, 16 patients with dilated tricuspid annulus, but with none or mild TR, also underwent "prophylactic"tricuspid repair with a Carpentier Edwards Tricuspid Physio ring®. None had more than mild TR at late follow-up. In contrast, new moderate (n = 6) or severe TR (n = 1) was detected in patients in whom the tricuspid valve was not addressed during the primary operation. Overall freedom from ≥ moderate TR was 66.1% (CI95% = 37.1 - 84.2%) at 10 years. Univariable analysis revealed RD as the only risk factor for development of late TR (HR = 6.69 [CI95% = 1.69 - 40.09] - P=0.044) (Figure 5, Appendix 1).
DISCUSSION
This study demonstrates that it is possible to obtain high rates of MVR for patients with organic MR, from different etiologies, in dedicated centers[8,9]. Our repair rate of 93.9% for all-comers includes not only patients with degenerative disease, but also those with more challenging rheumatic and acutely infected valves[10,11]. This aspect seems to be very relevant, at a time when the American College of Cardiology (ACC) and other cardiological societies are making efforts to create high volume regional reference centers that fulfill excellence criteria in the surgical management of patients with MR. It is our opinion that in Brazil, where global reparability rates are still very low, special programs such as specialized fellowships and dedicated symposiums should be promoted for adequate training of surgeons, clinicians, anesthesiologists and echocardiographists.
Several groups have documented excellent outcomes and a reparability rate ranging from 95-100% for patients with degenerative disease[12-16]. In the present series, 97.2% of degenerative valves were treated in this manner, with very acceptable early mortality and low incidence of residual regurgitation. The only two patients who had mitral valve replacement were cases with previous repairs done elsewhere and which were judged as suboptimal candidates for a second repair due to important scaring and distortion of the valve apparatus.
On the other hand, rheumatic and/or infected valves may impose special challenges, and reports about conservative surgical treatment in these situations have demonstrated a much lower reparability rate[10,11]. We believe, however, that with proper surgical expertise and an aggressive approach, it is possible to avoid valve replacement in a substantial number of cases in this subset of patients.
Our overall early mortality of 2.4% was acceptable in view of the wide range of pathologies treated and not limited to the more simple degenerative posterior mitral valve prolapse[8]. Our three deaths occurred only in older patients with extensive degenerative disease or in the presence of associated CAD. Mortality was 0% for patients with isolated primary mitral valve surgery, with or without concomitant tricuspid or AF, under the age of 70 years, which compares favorably with the STS database[5].
A relevant finding of this study was the excellent long-term survival, that was similar to the age- and sex-matched Brazilian population at least for the first decade after operation. This reinforces our tendency for recommending early surgery for patients with severe MR, even for asymptomatic patients, before they reach class I guideline triggers for surgery, such as AF and pulmonary artery hypertension[17]. Although some authors feel that a "watchful waiting" policy is safe and reasonable for asymptomatic patients[18], recent studies have demonstrated that long-term survival may be compromised with that approach[19,20].
Not only survival, but also long-term functional results were very gratifying, with most patients presenting normal functional recovery in NYHA class I and with low incidence of valve related complications. Thromboembolic events were uncommon, occurred more frequently during the first few years and had no relation with the presence of AF. However, it must be emphasized that all patients with documented AF were under anticoagulation therapy. Furthermore, 16 out of 18 patients who had AF treated by bipolar radiofrequency are in sinus rhythm as demonstrated by regular electrocardiograms and/or 24 hours Holter examination. It is also important that there were no cases of bacterial endocarditis during the observation period, even in patients that had acute or healed endocarditis as the primary reason for operation. Although this study did not intend to compare MVR with mitral valve replacement, one should expect a higher incidence of valve-related complications if these patients have had replacement as the surgical procedure[1,2,21].
One of the caveats of reconstructive mitral surgery is the possibility of recurrent MR and eventual need for reoperations. The main reasons for recurrent MR are technical failures, disease progression and scarring after the repair[22]. In this study, because the incidence of recurrent severe MR was infrequent and the number of patients was relatively small, statistical analysis had important limitations for establishing risk factors associated with this complication. One important finding, however, was that, at least up to ten years, results in rheumatic patients were similar to those with degenerative disease. We have been very aggressive in treating rheumatic pathologies, making extensive shaving of thickened and retracted tissues, debridement of calcified areas, cutting secondary chords and even performing partial and total primary chordal replacement to increase leaflet mobility and to obtain adequate coaptation surface areas. In the presence of retracted anterior leaflets, cusp extension with decellularized pericardium has been an important maneuver for a satisfactory result[23]. With that policy, the incidence of recurrent moderate or severe MR has been low, although we often must accept smaller final effective orifice areas (around 1.8 - 2.5 cm2) in patients with mixed lesions. In our country, Severino et al.[24] and Pomerantzeff et al.[25] have also shown the apparent feasibility and advantages of MVR in rheumatic patients. On the other hand, it must be emphasized that most rheumatic patients in this study had the so-called "burn-out" disease, that is less susceptible to newer acute inflammatory bursts of rheumatic fever, besides being carefully oriented and controlled with lifelong antibiotic prophylaxis against the disease[11].
Although still controversial, several recent reports have stressed the importance of avoiding late tricuspid regurgitation after a successful mitral operation[26-29]. It is becoming more apparent that the concept that any degree of functional tricuspid regurgitation would improve by correcting left-sided lesions only is misleading, and the occurrence of moderate to severe TR and eventual need for reintervention is not negligible[26]. This is corroborated in the present series in which approximately one third of the patients had more than mild TR late after the initial operation when the tricuspid valve was not addressed, especially in rheumatic patients. Furthemore, reoperations for isolated late TR after MVR carry a high operative risk and thus should be avoided[27]. In the initial phase of the present series, we have repaired the tricuspid valve whenever we found moderate or severe TR with symptoms of right side failure and visual right ventricular (RV) and right atrial (RA) enlargement during the operation. More recently, however, we moved towards a more aggressive approach on the tricuspid valve, and we performed tricuspid annuloplasty not only in patients with moderate or severe functional TR but also when dilatation of the tricuspid annulus was greater than 40 mm by echocardiography[30], as recommended by Chikwe et al.[26] and Dreyfus et al.[28]. Although follow-up is still short, we have not identified a single late TR after tricuspid annuloplasty with Carpentier-Edwards Tricuspid Physio ring.
This study has several limitations. All operations were performed by a single surgeon and selection biases and individual approaches to certain pathologies may influence outcomes, and the results may not be generalized. In the first years of this experience, tricuspid valve annulus size and degree of regurgitation were not evaluated in the same systematic manner as more recently, so underestimation of TR may have occurred. Furthermore, because TR is not a terminal event and longitudinal echocardiography data are not complete, any conclusion regarding the true incidence of more than mild TR should be done with caution. Some echocardiography data regarding late function of the mitral and tricuspid valves were obtained outside our clinic and may cause some inconsistencies.
CONCLUSION
In conclusion, we have demonstrated that MR due to organic mitral valve disease, from various etiologies, can be surgically treated with a high repair rate, low early mortality and long-term survival that are comparable to the matched general population. Concomitant treatment of AF and tricuspid valve may be important adjuncts to optimize long-term results. In our opinion, however, this can only be accomplished in reference centers with a dedicated heart valve team working in a focused and systematic way in order to obtain consistent results.
Appendix 1.
Risk factors for mitral valve dysfunction | Hazard ratio (95%CI) | P-value |
---|---|---|
Age | 0.455 (0.085 to 2.423) | 0.453 |
Sex | 0.259 (0.056 to 1.182) | 0.177 |
NYHA functional class | 1.856 (0.413 to 8.337) | 0.409 |
Atrial fibrillation | 1.024 (0.197 to 5.329) | 0.976 |
Systemic arterial hypertension | 1.571 (0.355 to 6.950) | 0.549 |
Chronic obstructive pulmonary disease | 0 | 0.624 |
Diabetes | 3.121 (0.106 to 91.445) | 0.265 |
Smoking | 2.121 (0.122 to 36.685) | 0.475 |
Renal failure | 9.315 (0.223 to 387.661) | 0.001 |
Coronary artery disease | 0 | 0.645 |
Previous cardiac operations | 3.357 (0.303 to 37.079) | 0.123 |
Associated surgical procedures | 1.939 (0.371 to 10.118) | 0.375 |
Etiology | 2.033 (0.382 to 10.798) | 0.342 |
Cardiopulmonary bypass time | 0.959 (0.188 to 4.873) | 0.960 |
Aortic clamping time | 0.732 (0.155 to 3.451) | 0.705 |
Risk factors for mortality | Hazard ratio (95%CI) | P-value |
---|---|---|
Age | 3.301 (0.857 to 12.709) | 0.042 |
Sex | 1.979 (0.535 to 7.312) | 0.290 |
NYHA class | 1.552 (0.390 to 6.163) | 0.491 |
Atrial fibrillation | 0.871 (0.224 to 3.384) | 0.824 |
Systemic arterial hypertension | 1.753 (0.473 to 6.495) | 0.391 |
Chronic obstructive pulmonary disease | 0 | 0.682 |
Diabetes | 7.855 (0.499 to 123.422) | 0.000 |
Smoking | 0.563 (0.103 to 3.065) | 0.404 |
Renal failure | 2.546 (0.115 to 56.145) | 0.356 |
Coronary artery disease | 2.485 (0.432 to 14.295) | 0.029 |
Previous cardiac operations | 3.647 (0.294 to 45.196) | 0.079 |
Associated surgical procedures | 1.863 (0.491 to 7.065) | 0.292 |
Etiology | 0.430 (0.090 to 2.055) | 0.400 |
Cardiopulmonary bypass time | 5.002 (1.177 to 21.245) | 0.007 |
Aortic clamping time | 4.076 (1.099 to 15.115) | 0.034 |
Risk factors for tricuspid valve dysfunction | Hazard ratio (95%CI) | P-value |
---|---|---|
Age | 1.120 (0.115 to 10.844) | 0.918 |
Sex | 0 | 0 |
NYHA class | 2.422 (0.398 to 14.705) | 0.307 |
Atrial fibrillation | 1.749 (0.246 to 12.431) | 0.530 |
Systemic arterial hypertension | 4.339 (0.750 to 25.085) | 0.150 |
Chronic obstructive pulmonary disease | NaN | 1 |
Diabetes | 0 | 0.622 |
Smoking | 0 | 0.734 |
Renal failure | 0 | 0.773 |
Coronary artery disease | 0 | 0.872 |
Previous cardiac operations | 0 | 0.455 |
Associated surgical procedures | 0.730 (0.097 to 5.454) | 0.776 |
Etiology | 6.698 (1.094 to 40.998) | 0.044 |
Cardiopulmonary bypass time | 0 | 0.321 |
Aortic clamping time | 0 | 0.287 |
REFERENCES
1. Lazam S, Vanoverschelde JL, Tribouilloy C, Grigioni F, Suri RM,Avierinos JF, et al; MIDA (Mitral Regurgitation International Database)Investigators. Twenty-year outcome after mitral repair versus replacement forsevere degenerative mitral regurgitation: analysis of a large, prospective,multicenter, international registry. Circulation.2017;135(5):410-22. [MedLine]
2. Chikwe J, Goldstone AB, Passage J, Anyanwu AC, Seeburger J, CastilloJG, et al. A propensity score-adjusted retrospective comparison of early andmid-term results of mitral valve repair versus replacement in octogenarians. EurHeart J. 2011;32(5):618-26.
3. Nishimura RA, Otto CM, Bonow RO, Carabello BA, Erwin JP 3rd, Guyton RA, et al; American College of Cardiology/AmericanHeart Association Task Force on Practice Guidelines. 2014 AHA/ACC guideline forthe management of patients with valvular heart disease: executive summary: areport of the American College of Cardiology/American Heart Association TaskForce on Practice Guidelines. J Am Coll Cardiol.2014;63(22):2438-88.
4. Joint Task Force on the Management of Valvular Heart Disease of theEuropean Society of Cardiology (ESC); European Association for Cardio-Thoracic(EACTS), Vahanian A, Alfieri O, Andreotti F, Antunes MJ, Barón-Esquivias G,Baumgartner H, et al. Guidelines on the management of valvular heart disease(version 2012). Eur Heart J. 2012;33(19):2451-96.
5. Gammie JS, Sheng S, Griffith BP, Peterson ED, Rankin JS, O'Brien SM,et al. Trends in mitral valve surgery in the United States: results from theSociety of Thoracic Surgeons Adult Cardiac Surgery Database. Ann Thorac Surg.2009;87(5):1431-7.
6. Edmunds LH Jr, Cohn LH, Weisel RD. Guidelines for reportingmorbidity and mortality after cardiac valvular operations. J Thorac CardiovascSurg. 1988;96(3):351-3.
7. Zoghbi WA, Enriquez-Sarano M, Foster E, Grayburn PA, Kraft CD,Levine RA, et al. Recommendations for evaluation of the severity of nativevalvular regurgitation with two-dimensional and Doppler echocardiography. J AmSoc Echocardiogr. 2003;16(7):777-802. [MedLine]
8. Castillo JG, Anyanwu AC, Fuster V, Adams DH. A near 100% repair ratefor mitral valve prolapse is achievable in a reference center: implications forfuture guidelines. J Thorac Cardiovasc Surg.2012;144(2):308-12.
9. David TE, Armstrong S, McCrindle BW, Manlhiot C. Late outcomes ofmitral valve repair for mitral regurgitation due to degenerative disease.Circulation. 2013;127(14):1485-92.
10. Kanemitsu H, Nakamura K, Fukunaga N, Koyama T. Long-term outcomes ofmitral valve repair for active endocarditis. Circ J.2016;80(5):1148-52.
11. Dillon J, Yakub MA, Kong PK, Ramli MF, Jaffar N, Gaffar IF.Comparative long-term results of mitral valve repair in adults with chronicrheumatic disease and degenerative disease: is repair for "burnt-out" rheumaticdisease still inferior to repair for degenerative disease in the current era? JThorac Cardiovasc Surg. 2015;149(3):771-7.
12. Bonow RO, Adams DH. The Time has come to define centers ofexcellence in mitral valve repair. J Am Coll Cardiol.2016;67(5):499-501. [MedLine]
13. Castillo JG, Anyanwu AC, El-Eshmawi A, Adams DH. All anterior andbileaflet mitral valve prolapses are repairable in the modern era ofreconstructive surgery. Eur J Cardiothorac Surg.2014;45(1):139-45.
14. David TE, Armstrong S, Ivanov J. Chordal replacement withpolytetrafluoroethylene sutures for mitral valve repair: a 25-year experience. JThorac Cardiovasc Surg. 2013;145(6):1563-9.
15. Koprivanac M, Kelava M, Alansari S, Javadikasgari H, Tappuni B, MickS, et al. Degenerative mitral valve disease-contemporary surgical approaches andrepair techniques. Ann Cardiothorac Surg. 2017;6(1):38-46. [MedLine]
16. Brandão CM, Guedes MA, Silva MF, Vieira ML, Pomerantzeff PM, StolfNA. Mitral valve repair with "Double Teflon" technique: 10-year results. RevBras Cir Cardiovasc. 2007;22(4):448-53.
17. Enriquez-Sarano M, Suri RM, Clavel MA, Mantovani F, Michelena HI,Pislaru S, et al. Is there an outcome penalty linked to guideline-basedindications for valvular surgery? Early and long-term analysis of patients withorganic mitral regurgitation. J Thorac Cardiovasc Surg.2015;150(1):50-8.
18. Rosenhek R. Watchful waiting for severe mitral regurgitation. SeminThorac Cardiovasc Surg. 2011;23(3):203-8.
19. Yazdchi F, Koch CG, Mihaljevic T, Hachamovitch R, Lowry AM, He J, etal. Increasing disadvantage of "watchful waiting" for repairing degenerativemitral valve disease. Ann Thorac Surg. 2015;99(6):1992-2000. [MedLine]
20. Suri RM, Enriquez-Sarano M. Better to avoid disaster than rescuedefeat: ventricular dysfunction after delayed mitral valve repair. J ThoracCardiovasc Surg. 2015;149(3):941-2.
21. Javadikasgari H, Gillinov AM, Idrees JJ, Mihaljevic T, Suri RM, RazaS, et al. Valve repair is superior to replacement in most patients withcoexisting degenerative mitral valve and coronary artery diseases. Ann ThoracSurg. 2017;103(6):1833-41. [MedLine]
22. Suri RM, Clavel MA, Schaff HV, Michelena HI, Huebner M, NishimuraRA, et al. Effect of recurrent mitral regurgitation following degenerativemitral valve repair: long-term analysis of competing outcomes. J Am CollCardiol. 2016;67(5):488-98.
23. Dillon J, Yakub MA, Pau KK, Taib ME. Leaflet extension for repairingrheumatic mitral valve regurgitation. Ann Cardiothorac Surg.2015;4(3):301-3.
24. Severino ES, Petrucci O, Vilarinho KA, Lavagnoli CF, Silveira FilhoLM, Oliveira PP, et al. Late outcomes of mitral repair in rheumatic patients.Rev Bras Cir Cardiovasc. 2011;26(4):559-64.
25. Pomerantzeff PM, Brandão CM, Leite Filho OA, Guedes MA, Silva MF,Grinberg M, et al. Mitral valve repair in rheumatic patients with mitralinsuficiency: twenty years of techniques and results. Rev Bras Cir Cardiovasc.2009;24(4):485-9.
26. Chikwe J, Itagaki S, Anyanwu A, Adams DH. Impact of concomitanttricuspid annuloplasty on tricuspid regurgitation, right ventricular function,and pulmonary artery hypertension after repair of mitral valve prolapse. J AmColl Cardiol. 2015;65(18):1931-8.
27. Filsoufi F, Chikwe J, Carpentier A. Rationale for remodellingannuloplasty to address functional tricuspid regurgitation during left-sidedvalve surgery. Eur J Cardiothorac Surg. 2015;47(1):1-3. [MedLine]
28. Dreyfus GD, Martin RP, Chan KM, Dulguerov F, Alexandrescu C.Functional tricuspid regurgitation: a need to revise our understanding. J AmColl Cardiol. 2015;65(21):2331-6.
29. Dion RA. Is the air in Toronto, Rochester, and Cleveland different from that in London, Monaco, Leiden, Genk, Milan, and New York? J Thorac Cardiovasc Surg. 2015;150(5):1040-3. [MedLine]
30. Raja SG, Dreyfus GD. Surgery for functional tricuspid regurgitation: current techniques, outcomes and emerging concepts. Expert Rev Cardiovasc Ther. 2009;7(1):73-84. [MedLine]
No financial support.
No conflict of interest.
Authors' roles & responsibilities
FDAC Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; final approval of the version to be published
DFFC Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; final approval of the version to be published
GLSM Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; final approval of the version to be published
KCSP Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; final approval of the version to be published
MCB Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; final approval of the version to be published
EMBF Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; final approval of the version to be published
MV Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; final approval of the version to be published
GM Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; final approval of the version to be published
ADAF Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; final approval of the version to be published
CC Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; final approval of the version to be published
Article receive on Saturday, June 24, 2017