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Ann Thorac Surg 1995;60:1652-1658
© 1995 The Society of Thoracic Surgeons


Original Articles: Cardiovascular

Exploring Better Methods to Preserve the Chordae Tendineae During Mitral Valve Replacement

Masashi Komeda, MD, PhD, Abe DeAnda, Jr, MD, Julie R. Glasson, MD, Ann F. Bolger, MD, Yasuko Tomizawa, MD, PhD, George T. Daughters, II, MS, Terrence L. Tye, MS, Neil B. Ingels, Jr, PhD, D. Craig Miller, MD

Department of Cardiovascular and Thoracic Surgery and Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, Palo Alto Veterans Affairs Medical Center, Palo Alto, and Department of Cardiovascular Physiology and Biophysics, Research Institute, Palo Alto Medical Foundation, Palo Alto, California


    Abstract
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
Background. It is not known how best to resuspend the mitral chordae tendineae during mitral valve replacement to optimize postoperative left ventricular (LV) systolic and diastolic function.

Methods. Six different techniques to preserve the chordae during mitral valve replacement were compared in 12 dogs using a nondistorting isovolumic technique: conventional, all chordae severed; anterior, all chordae preserved anteriorly; partial, anterior papillary muscle chordae preserved anteriorly; posterior, all chordae preserved posteriorly; oblique, anterior papillary muscle chordae directed anteriorly and posterior papillary muscle chordae posteriorly; and counter, opposite of oblique chordal direction. Control measurements (no chordal tension) were recorded between each experimental condition.

Results. The oblique method tended to have the best LV systolic function versus the conventional method (Emax = 4.0 ± 1.8 versus 3.3 ± 1.2 mm Hg/mL [mean ± standard deviation]; p = 0.08 by repeated-measures analysis of variance; physiologic intercept Ees100 = 20.3 ± 8.6 mL [p < 0.05 versus control]), with no major change in LV diastolic stiffness. The posterior method had a lower Emax (3.3 ± 1.2 mm Hg/mL) than the oblique method, but a similar Ees100 (20.8 ± 8.1 mL; p < 0.05 versus control) and the best diastolic LV performance (LV diastolic stiffness = 0.46 ± 0.23 mm Hg/mL). The counter method also had good systolic function (Emax = 3.8 ± 1.2 mm Hg/mL; Ees100 = 19.7 ± 7.5 mL; p < 0.05 versus control), but had less favorable diastolic properties (0.65 ± 0.37 mm Hg/mL; p < 0.05 by repeated-measures analysis of variance versus posterior).

Conclusions. In this isovolumic preparation in normal canine hearts, the oblique method of chordal resuspension was associated with the best LV systolic function, whereas the counter technique impaired LV diastolic function. These preliminary results warrant further study in ejecting and failing hearts to determine conclusively which chordal orientation best preserves LV performance after mitral valve replacement.


    Introduction
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
See also page 1658.

Preservation of chordae tendineae (CT) and papillary muscles (PM) during mitral valve replacement (MVR) [1] is known to enhance left ventricular (LV) systolic function [24], both early and late after MVR [5]. In an increasing number of institutions, MVR with chordal preservation is now performed in patients with diseased subvalvular apparati, such as those with mitral stenosis, which may involve using expanded polytetrafluoroethylene sutures to replace the native chordae [6]. In this case, the surgeon decides which direction to resuspend the CT. The optimal direction to resuspend the chordae, however, has not been clearly elucidated; studies to date have compared only the native CT in the anterior and posterior configurations [710] or anterior leaflet CT with posterior leaflet CT. Mitral valve replacement with placement of expanded polytetrafluoroethylene chordae does not seem to be as beneficial as native chordal preservation in terms of LV systolic performance [6], which may be related to the direction of CT reattachment. In this study, we compared six different directions of chordal preservation during MVR (including the conventional technique where no CT are preserved) in an attempt to identify which method resulted in the best LV systolic and diastolic function. We developed an isovolumic heart preparation (``double-balloon'') [11] that does not distort the preserved CT, and studied all 6 methods in each dog, allowing each animal to serve as its own control.


    Material and Methods
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
Surgical Preparation
Twelve healthy adult mongrel dogs (27.7 ± 2.7 kg) were premedicated with acepromazine (0.01 to 0.05 mg/kg intramuscularly) and atropine (0.05 mg/kg intravenously). They were anesthetized with sodium pentobarbital (20 to 25 mg/kg intravenously), intubated, and placed on artificial ventilation (Ohio Anesthesia Ventilator, Madison, WI). General anesthesia was maintained with inhalational isoflurane at 1.5% to 2.2%. A catheter-tipped manometer (Millar Instruments Inc, Houston, TX) was zeroed in a 37°C water bath. Systemic arterial pressure was monitored using the manometer through the side port of the left femoral introducer. The left side of the chest was opened at the fifth intercostal space, and the fifth rib was resected. The heart was exposed and suspended in a pericardial cradle.

A latex balloon cut to the length of the LV long axis was tied onto a cannula that allowed passage of a catheter-tipped manometer into the balloon to measure the intraballoon pressure directly (Fig 1Go). Another latex balloon half as long as the first was made in the same fashion. These two balloons were connected to a Y-shaped circuit, which was connected to a 100-mL syringe mounted on a Harvard pump (model 55-1341; Harvard Apparatus). The circuit and the balloons were filled with water and completely deaired. In our preliminary study with porcine cadaver hearts, we confirmed that this double-balloon method provided accurate pressure-volume information with no or minimal distortion of the CT geometry; LV volume at pressures of 50 and 70 mm Hg with the double-balloon technique correlated well with LV volume by natural filling (r = 0.999). Left ventricular volume at the same pressures with use of a conventional balloon also correlated well (r = 0.923) but distorted the CT geometry [11].



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Fig 1. . Schematic illustration of the circuit and the double left ventricular (LV) balloons. Two balloons (A and B) are connected to an infusion syringe via a Y-circuit. A disk occluder was sewn to the mitral annulus to avoid balloon herniation; the cannulas to the balloons were placed through small slits in the edge of the mitral disc occluder. The LV volume data were derived from the volume sensor on the syringe, and the simultaneous LV pressure data from the Millar micromanometer catheters in the two LV balloons. (ECG = electrocardiogram; PM = papillary muscle.)

 
Each dog was fully heparinized. Four milligrams of UL-FS49 (Boehringer-Ingelheim, Ridgefield, CT; a highly specific negative chronotropic agent that does not change the Q-T interval, inotropic state, or systolic or diastolic blood pressure [12]) was given slowly intravenously to maintain a heart rate less than 130 beats/min. Another catheter-tipped manometer was inserted into the aortic root (1 cm above the aortic valve) via the brachiocephalic artery to monitor coronary perfusion pressure. A 14F or 16F arterial cannula was inserted into the right femoral artery, and a second 14F long arterial cannula was inserted into the aortic root via the left carotid artery. A two-stage venous cannula was inserted into the right atrium and the inferior vena cava through the right atrial appendage. The dog was placed on cardiopulmonary bypass using a roller pump (Pemco, Cleveland, OH) with a bubble oxygenator (Harvey H-1300; Bard Cardiopulmonary, Santa Ana, CA). The right ventricle was vented via the main pulmonary artery.

The left atrium was opened under electrically induced ventricular fibrillation to avoid ejecting air into the aortic root. As soon as both mitral leaflets were incised and detached from the mitral annulus, the heart was defibrillated with direct-current countershock at 10 to 20 J. Infusion via the second arterial cardiopulmonary bypass cannula was started at 100 mL/min. The ascending aorta was snared and the cardiopulmonary bypass flow in the aortic root cannula was increased to keep the mean aortic root pressure 80 to 140 mm Hg, to minimize LV subendocardial ischemia in the empty heart [13]. Six pledgeted 2-0 braided Dacron sutures were placed around the mitral annulus. Each mitral leaflet was then divided in the midline, and the bundles of CT from each papillary muscle were grouped together with 2-0 sutures, which were later used to pull the CT in the various directions.

A specially designed transparent plastic disk occluder with the size of the canine mitral annulus at end-systole was selected, and the six annular sutures and four chordal sutures described above were passed through the occluder (Fig 2Go). As a result, each papillary muscle was connected to the disk in four different directions. Consequently, by pulling on a particular combination of sutures, any one of the six predetermined directions was created immediately without manipulating the occluder or the papillary muscles. The two balloons were then inserted into the LV through holes in the occluder: the larger balloon anteriorly down to the LV apex, and the smaller balloon posteriorly between the two papillary muscle bases. A Millar catheter in each balloon served as a guidewire to keep the balloons in the proper location, especially during empty beating. The disk was then snared down to the annulus.



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Fig 2. . Mitral disk occluder and the layout of the annular and chordal sutures (left), and the six directions of simulated chordal resuspension as seen from the left atrium (middle and right). Once the two balloons were inserted into the left ventricle and the disk occluder was secured, the chordal direction was changed by just pulling the two appropriate sutures (eg, sutures 1a and 2p were placed on tension for the anterior method). For the conventional method, all chordae were kept redundant. (APM = anterior papillary muscle; PPM = posterior papillary muscle.)

 
Experimental Protocol
We evaluated the following six methods of resuspending the chordae tendineae (as illustrated in Figure 2Go): (1) conventional, all chordae kept completely slack (to simulate total chordal severing); (2) anterior, all CT preserved anteriorly; (3) partial, anterior PM chordae preserved anteriorly and posterior PM chordae left loose; (4) posterior, all CT preserved posteriorly; (5) oblique, anterior PM chordae directed anteriorly and posterior PM chordae posteriorly (the direction that is theoretically aligned with the forces generated by LV systolic twist); and (6) counter, directions opposite oblique, ie, anterior PM chordae directed posteriorly and posterior PM chordae anteriorly (which would be expected to counteract LV twist systolic forces). Chordal tension was measured with a simple spring scale (sensitivity, 5 g; Oba Instrument Works Ltd, Tokyo, Japan) that was attached to the chest wall in a stable fashion. End-diastolic tension of the CT in the unloaded, beating state was maintained at 10 g by cross-clamping the choker on the CT suture on the surface of the disc occluder. In normal sinus rhythm, this technique was reproducible, as assessed by markers on the suture being the same length when identical degrees of tension were applied. Chordae tendineae tension was standardized in the above way during all experimental conditions except for the conventional method and control. Ten grams of tension, which was minimally palpable, was employed because our preliminary study showed better overall (ie, systolic and diastolic) LV function at 10 g CT tension compared with 0, 20, 30, and 40 g [14].

The LV pressure-volume relationship was measured by infusing fluid into both LV balloons at a constant rate of 72 mL/min until the balloon pressure reached 120 mm Hg; the balloons were then deflated by fluid withdrawal. During each measurement, heart rate was maintained in a normal range (110 to 130 beats/min). One to two milligrams of UL-FS49 was given as needed to avoid excessive tachycardia. A preliminary study showed that a stable preparation was achieved with three inflation/deflation cycles; in this study three to six inflation/deflation cycles were carried out, and data from the last infusion were analyzed. The pressure in both balloons was measured at the start of each infusion to assure equalization. The geometry of the preserved CT remained undisturbed by the ``sandwich'' effect of the double-balloon method as assessed by two-dimensional epicardial echocardiography.

To avoid possible time-dependent changes in the experimental preparation, the following two steps were taken: (1) randomization of the study order for the six methods in each dog and (2) control runs using the conventional method (ie, no CT preservation) immediately before and after each experimental technique to allow intragroup comparisons. The data obtained in the before and after control runs were averaged, and this mean value was defined as each individual group's control measurements at that point in time.

All animals received humane care in compliance with the ``Principles of Laboratory Animal Care'' formulated by the National Society for Medical Research and the ``Guide for the Care and Use of Laboratory Animals'' prepared by the National Academy of Sciences and published by the National Institutes of Health (DHEW [NIH] publication 85-23, revised 1985). The study was approved by the Stanford University Medical Center Laboratory Research Animal Review Committee and conducted according to Stanford University policy.

Data Acquisition
The volume of the syringe was measured using a linear differential transform sensor, which detected the relative location of the inner barrel of the syringe. All analog data, such as electrocardiogram, instantaneous syringe volume, and pressure in the two LV balloons, were acquired and digitized simultaneously at 240 Hz using a 486-based microcomputer (486-50 MHz; JDR Microdevices Inc, San Jose, CA) with a high-speed data acquisition card (DT3831-G; Data Translation Inc, Marlboro, MA) controlled by commercially available software (Labtech Control 3.2.0; Laboratory Technology Corp, Wilmington, MA).

Data Analysis
SYSTOLIC FUNCTION.
The digitized data files were imported into a commercial data analysis program (Origin, version 3.0; MicroCal Inc, Northampton, MA). The data from beats that generated systolic LV pressures between 80 mm Hg and 120 mm Hg were analyzed; data from premature contractions and the subsequent two beats were excluded. Linear regression analysis (least-squares) was performed on the peak LV systolic pressure and volume data. The slope of the peak systolic pressure-volume relationship was calculated as Emax (mm Hg/mL) (Fig 3Go).



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Fig 3. . Representative raw data as well as computed Emax, physiologic intercept (Ees100), and diastolic stiffness (Sd) of the left ventricle (LV). Both the top and the bottom pressure-volume points were calculated using least-square linear regression. (DPVR = LV diastolic pressure-volume relationship; ESPVR = LV end-systolic pressure volume relationship.)

 
From the same regression used to calculate Emax, the LV volume at a pressure of 100 mm Hg was computed (Ees100; mL); it should be noted that a smaller Ees100 value indicates better LV systolic function [15] (see Fig 3Go). Changes in this ``physiologic elastance intercept'' reflect both the slope and volume axis intercept of the systolic pressure-volume relation, but do not rely on linear extrapolation beyond the range of pressures measured or estimates of unstressed LV volume.

DIASTOLIC FUNCTION.
Diastolic LV dynamic function was assessed as end-diastolic stiffness. In a similar fashion, the minimum LV pressure-volume data points were identified, and linear regression analysis was performed. The slope of this line (Sd; mm Hg/mL), calculated within the same LV pressure range as used to derive Emax, indicated relative changes in LV diastolic function (see Fig 3Go).

Statistical Analysis
All data are reported as mean ± one standard deviation. Data obtained for all six methods were compared using repeated measures analysis of variance (rm-ANOVA). Post hoc intergroup comparisons were performed using Bonferroni's method. Intragroup comparison with each group's own control was done using paired t-tests. Statistical significance was inferred if the p value was less than 0.05; p values between 0.05 and 0.1 were judged to be nearly significant. Ordinal data were analyzed by Wilcoxon's test. For all statistical analyses, SYSTAT (version 5.02; SYSTAT Inc, Cary, NC) was employed.


    Results
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
Left Ventricular Systolic Function: Emax
The oblique group had the highest Emax, whereas the conventional and the posterior methods had the lowest Emax values, but these differences were only nearly significant (p = 0.08 by rm-ANOVA); post hoc testing revealed the major difference to be between the oblique and conventional methods. In general, most of the chordal preservation methods tended to have higher Emax values than the conventional group (Table 1Go); however, only the oblique and counter-oblique groups had higher Emax values compared with their own control values (p < 0.06 by paired t test). There was no significant difference among the control values between methods or over time by rm-ANOVA.


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Table 1. . Left Ventricular Systolic Function as Determined by Maximum Systolic Elastance (Emax)a
 
Left Ventricular Systolic Function: Ees100
There was no significant (intergroup) difference in Ees100 among the six groups. Intragroup comparisons, however, revealed significant improvement in LV systolic function in the oblique, posterior, and counter methods (p < 0.05 versus each method's own control) (Table 2Go). There was no significant difference among the control values among the six methods by rm-ANOVA.


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Table 2. . Systolic Left Ventricular Function as Evaluated by the Physiologic End-Systolic Elastance Intercept (Ees100)a
 
Left Ventricular Diastolic Function: Sd
The posterior method had the lowest Sd (implying the least [or best] LV diastolic stiffness), whereas the counter-oblique technique had the highest Sd (or worst diastolic stiffness) among the six groups (p < 0.05 by rm-ANOVA); post hoc comparison showed that the significant intergroup difference was between the posterior and the counter methods. All preservation methods except posterior showed a tendency toward higher Sd values (ie, more LV stiffness) compared with the conventional technique (Table 3Go). There was no significant difference in Sd among the various CT preservation methods, however, compared with their own (moving) controls. There was no significant difference among the control data between each method by rm-ANOVA.


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Table 3. . Diastolic Left Ventricular Function as Assessed by Diastolic Stiffness (Sd)a
 

    Comment
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
In the natural condition, the chordal bundle has a shape of a fan [16]. It originates from the papillary muscle heads, and the chordal bundles spread in many directions to reach the mitral leaflets; these multiple chordal directions (including anterior, posterior, and oblique) make a rigorous study of the natural direction of chordal tension a difficult one.

Older studies reported the following directions for chordal-sparing MVR: posterior direction of posterior leaflet CT by Lillehei and associates [1], Lillehei's method and anterolateral direction of the anterior leaflet CT by David [17], lateral by Miki and colleagues [4], circumferential (anterior and posterior, or quasianatomic) by Khonsari and Sintek [18], and a simplified form of the Khonsari II technique by Rose and Oz [19]. Few comparative studies have been performed pertaining to the best direction to resuspend the CT, let alone comparison between anterior versus posterior leaflet CT [710]. These experiments did not focus on the specific directions of synthetic CT resuspension; they only investigated natural chordae tendineae, where altering specific reattachment sites was not controllable.

In this experimental protocol we compared six different methods of chordal preservation: conventional, anterior, partial, posterior, oblique, and counter-oblique. The conventional, anterior, and posterior methods were studied because they are all widely employed clinically. We designed the oblique method because a preliminary anatomic study from our laboratory in a canine model revealed mechanical linkage of the anterior leaflet and associated CT from the anterior papillary muscle to the central fibrous body; this suggests the possible presence of physiologic structural integrity in this direction. In fact, van Rijk-Zwikker and associates [16], in an endoscopic study in a beating porcine heart model, described that the central CT, which connects the anterior papillary tip and central fibrous body, were under tension throughout the cardiac cycle, and suggested that these chordae may play an important role in LV function. In the current experiment, the CT were suspended from the anterior papillary muscle to the annulus close to the right trigone, as shown in Figure 2Go, for possible clinical application in the future (ie, to avoid possible LV outflow tract obstruction by CT underneath the aortic valve). Moreover, on the basis of studying LV mechanics [20], we hypothesized that due to the oblique orientation of the LV subepicardial myocardial fibers, a similar (oblique) CT preservation method might allow papillary muscle contraction to augment systolic LV twist. For contrast, we also studied the counter-oblique method, which theoretically would act in the opposite direction to the forces generated by the LV subepicardial fibers during ejection. The partial method was studied because previous experiments suggested that the anterior PM may have a dominant role in terms of preserving postoperative LV systolic pump function compared with the posterior PM. Another implication of the partial method is simulation of chordal-sparing MVR in the setting of an injured, infarcted, or ruptured posterior PM.

In this study, the overall difference in Emax between the six groups did not reach significance (p = 0.08 by rm-ANOVA). We assumed two possible reasons were responsible for these findings: (1) this experimental preparation contained a large number of techniques (six), which made it less statistically powerful, and (2) we used normal canine hearts. Indeed, when only five groups were compared (excluding the partial method, which is anatomically in-between the anterior and conventional methods), the overall difference in Emax was significant (p < 0.05 by rm-ANOVA), favoring the oblique method. Although LV systolic twist and early diastolic recoil were not measured in this experiment, we speculate that the better LV systolic function in the oblique group may have been related to enhanced LV systolic twist. Theoretically, improved LV systolic twist will minimize transmural oxygen metabolic demands by virtue of equalizing sarcomere stresses and increase potential energy storage in the myocardium and LV interstitium at end-systole; release of this stored energy during diastole will then augment diastolic recoil, which should enhance early LV diastolic filling. The oblique method, however, was not associated with improved diastolic LV function in this experiment, perhaps in part due to fixation of the CT by clamping of the chordae at their end-diastolic length. In the normal heart, the mitral leaflets move toward the LV chamber during diastole, and the CT thereby become redundant; fixing the chordae at their end-diastolic length could potentially suppress LV recoil. This design is, however, relevant in the clinical setting, where CT are usually tacked to the mitral annulus. Alternatively, the isovolumic experimental preparation and the relatively crude assessment of LV diastolic properties we employed could have obscured such effects.

The counter method unexpectedly showed good systolic LV function. A possible explanation for this result is that this theoretically unnatural method may contribute to preload redistribution in the direction of the circumferentially aligned LV midwall fibers [3]. Another possible explanation may be that the counter technique increased transmural LV myocardial shear between the epicardium and the endocardium in the circumferential direction, which might have thereby increased LV wall thickening. The relatively poor diastolic LV function seen in the counter group, however, indicates that this method probably has no overall merit. The anterior and the partial methods seemed to provide some advantage in terms of LV systolic function, but the differences were not marked between the six different groups.

This experiment had several potential limitations, which should be mentioned. First, the protocol was performed under general anesthesia in an acute isovolumic preparation on cardiopulmonary bypass with the chest and the pericardium open. Second, although two-dimensional echocardiography confirmed that the preserved chordae were not markedly disturbed by the two LV balloons, this experimental preparation is certainly a nonphysiologic one compared with closed-chest, ejecting conditions. Third, LV remodeling over time cannot be studied in an acute model, and such postoperative remodeling may likely have important effects on cardiac function. Fourth, our experimental techniques and analytic methods were simplified; in clinical situations, native mitral leaflet tissue (with multiple chordal insertions) are usually preserved. We only examined one principal direction for each PM at each time. Fifth, this study used normal hearts; patients with mitral valve disease (especially chronic mitral regurgitation) and LV dysfunction may respond differently to these various methods of chordal preservation.

In spite of these limitations, these initial results suggest that possible benefits may be associated with the oblique CT preservation method, and this approach warrants further consideration. Future investigations in more physiologic, as well as pathophysiologic, ejecting heart models, including computation of LV systolic twist and early diastolic LV recoil employing myocardial markers or magnetic resonance imaging using transient radiofrequency myocardial tags, are clearly necessary to answer fully these questions.


    Acknowledgments
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
We gratefully acknowledge Geraldine C. Derby, RN, BSN, Cynthia E. Handen, BA, Erin M. Schultz, BS, and Mary K. Zasio, BA in the performance of this work and Ms. Phoebe E. Taboada for her assistance in the preparation of the manuscript.

Supported by grants HL-29589 and HL-48837 from the National Heart, Lung, and Blood Institute and the Veterans Affairs Medical Research Service.

Doctors Komeda, DeAnda, and Glasson are Carl and Leah McConnell Cardiovascular Surgical Research Fellows. Doctor DeAnda was also supported by Individual National Research Service Award HL-08928 from the National Heart, Lung, and Blood Institute, and Dr Glasson by The Thoracic Surgery Foundation Research Fellowship Award.


    Footnotes
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 
Presented at the Thirty-first Annual Meetings of The Society of Thoracic Surgeons, Palm Springs, CA, Jan 30–Feb 1, 1995.

Address reprint requests to Dr Miller, Department of Cardiovascular and Thoracic Surgery, Falk Cardiovascular Research Center, Stanford University School of Medicine, Stanford, CA 94305-5247.


    References
 Top
 Footnotes
 Abstract
 Introduction
 Material and Methods
 Results
 Comment
 Acknowledgments
 References
 

  1. Lillehei CW, Levey MJ, Bonnabeau RC. Mitral valve replacement with preservation of the papillary muscles and the chordae tendineae. J Thorac Cardiovasc Surg 1964;47:532–43.[Medline]
  2. David TE, Burns RJ, Bacchus CM, Druck MN. Mitral valve replacement for mitral regurgitation with and without preservation of chordae tendineae. J Thorac Cardiovasc Surg 1984;88:718–25.[Abstract]
  3. Hansen DE, Cahill PD, DeCampli WM, et al. Valvular-ventricular interaction: importance of the mitral apparatus in canine left ventricular systolic performance. Circulation 1986;73:1310–20.[Abstract/Free Full Text]
  4. Miki S, Kusuhara K, Ueda Y, Komeda M, Ohkita Y, Tahata T. Mitral valve replacement with preservation of chordae tendineae and papillary muscles. Ann Thorac Surg 1988;45: 28–34.[Abstract]
  5. Komeda M, David TE, Rao V, Sun Z, Weisel RD, Burns RJ. Late hemodynamic effect of the preserved chordal attachment. Circulation 1994;90(Suppl 2):190–4.
  6. Okita Y, Miki S, Ueda Y, Tahata T, Sakai T, Matsuyama K. Mitral valve replacement with maintenance of mitral annulopapillary muscle continuity in patients with mitral stenosis. J Thorac Cardiovasc Surg 1994;108:42–51.[Abstract/Free Full Text]
  7. Hansen DE, Cahill PD, Derby GC, Miller DC. Relative contributions of the anterior and posterior mitral chordae tendineae to canine global left ventricular systolic function. J Thorac Cardiovasc Surg 1987;93:45–55.[Abstract]
  8. Hennein HA, Swain JA, McIntosh CL, Bonow RO, Stone CD, Clark RE. Comparative assessment of chordal preservation versus chordal resection during mitral valve replacement. J Thorac Cardiovasc Surg 1990;99:828–37.[Abstract]
  9. Oe M, Asou T, Kawachi Y, et al. Effects of preserving mitral apparatus on ventricular systolic function in mitral valve operations in dogs. J Thorac Cardiovasc Surg 1993;106: 1138–46.[Abstract]
  10. Moon MR, DeAnda A, Daughters GT II, Ingels NB Jr, Miller DC. Randomized, experimental evaluation of chordal preservation techniques in mitral valve replacement. Ann Thorac Surg 1994;58:931–44.[Abstract]
  11. Komeda M, DeAnda A, Bolger AF, et al. Improved methods to preserve the chordae tendineae during MVR. Proceedings of the 3rd Annual Meeting of the Asian Society of Cardiovascular Surgery 1995:70.
  12. Schipke JD, Harasawa Y, Sugiura S, Alexander J, Burkhoff D. Effect of a bradycardiac agent on the isolated blood-perfused canine heart. Cardiovasc Drug Therapy 1991;5:481–8.
  13. Archie JP Jr. Determinants of regional intramyocardial pressure. J Surg Res 1973;14:338–46.[Medline]
  14. Komeda M, DeAnda A, Glasson JR, et al. Optimal tension for chordal preservation during MVR. Proceedings of the 21st Annual Meeting of the Western Thoracic Surgical Association 1995:28.
  15. Yun KL, Niczyporuk MA, Sarris GA, Fann JI, Miller DC. Importance of mitral subvalvular apparatus in terms of cardiac energetics and systolic mechanics in the ejecting canine heart. J Clin Invest 1991;87:247–54.[Medline]
  16. Van Rijk-Zwikker GL, Delemarre BJ, Huysmans HA. Mitral valve anatomy and morphology: relevance to mitral valve replacement and valve reconstruction. J Card Surg 1994;9(Suppl):255–61.[Medline]
  17. David TE. Mitral valve replacement with preservation of chordae tendineae: rationale and technical considerations. Ann Thorac Surg 1986;41:680–2.[Abstract]
  18. Khonsari S, Sintek C. Mitral valve replacement with chordal preservation: clinical significance. In: Rivera R, Duran E, eds. Actualizatiòn cardiovascular 5. Madrid: Aran Ediciones, 1992:195–204.
  19. Rose EA, Oz MC. Preservation of anterior leaflet chordae tendineae during mitral valve replacement. Ann Thorac Surg 1994;57:768–9.[Abstract]
  20. Ingels NB Jr, Hansen DE, Daughters GT II, Stinson EB, Alderman EL, Miller DC. Relation between longitudinal, circumferential, and oblique shortening and torsional deformation in the left ventricle of the transplanted human heart. Circ Res 1989;64:915–27.[Abstract/Free Full Text]

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M. Komeda, A. DeAnda Jr, J. R. Glasson, A. F. Bolger, G. T. Daughters II, N. B. Ingels Jr, and D. C. Miller
Complete Unloading Alone May Not Adequately Protect the Left Ventricle
Ann. Thorac. Surg., November 1, 1997; 64(5): 1250 - 1255.
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