The design, development, and evaluation of a prototypic, prosthetic venous valve
© Oberdier and Rittgers; licensee BioMed Central Ltd. 2008
Received: 06 June 2008
Accepted: 19 September 2008
Published: 19 September 2008
Chronic venous insufficiency is a serious disease for which there is no clearly successful surgical treatment. Availability of a proven prosthetic vein valve could provide such an option by reducing venous reflux while permitting normal antegrade flow.
A new prosthetic vein valve design has been developed which mimics the function of a natural valve by ensuring complete closure of the leaflets with minimal obstruction for antegrade flow. A 2:1 mock-up of the device was tested to evaluate its ability to prevent regurgitation and several key modifications were made. A subsequently re-designed 1:1 prototype was then built in 4 slightly different size configurations and then each tested under physiologic conditions of pulsatile flow in both supine and standing positions.
Each of the configurations showed acceptable amounts of antegrade resistance and effective orifice area and showed low values of regurgitation and % reflux with two of the prototype configurations (flange lengths of 2.5 mm and 3.75 mm) having corresponding values of <2.5 mmHg-min/L, >97%, 11 mL, and 36%, respectively. These values are particularly striking when compared to the corresponding regurgitation and % reflux values of 60 mL and 205%, respectively, when no device is present.
The results of this study show that this prototype vein valve design is capable of providing significant relief of reflux under realistic conditions without inducing any increase in antegrade flow resistance and warrants further testing with in vivo models.
In the United States, chronic venous insufficiency (CVI) afflicts ten to thirty-five percent of the adult population to some extent  and is the seventh most common chronic debilitating disease . Ulceration associated with CVI occurs at a rate of up to one and a half percent and in four percent of patients over sixty-five years of age in industrialized populations . CVI is distinguished from other chronic venous disorders by a variety of alterations of the skin due to prolonged venous hypertension . Incompetent venous valves directly result in reflux, which in turn produces hypertension and causes the most serious symptoms of CVI including ulcers . Increasing venous reflux and decreasing calf muscle pump ejection fraction have been shown via air plethysmography to be related to the incidence of ulceration .
Current CVI management strategies include external compression devices, intermittent pneumatic compression, other adjuvants (including dressings and skin substitutes), and drugs while surgical alternatives include but are not limited to ligation and stripping, thermal ablation, sclerotherapy, valvuloplasty, and venous segment transfer . However, non-operative therapies remain the primary treatment for CVI and ulceration . Unfortunately, non-operative techniques are only palliative in that they make the symptoms of CVI tolerable while not treating the underlying cause of the disease (i.e. venous reflux and hypertension).
It is believed that a prosthetic venous valve is capable of restoring normal hemodynamics as an alternative to surgery or for those patients without surgical options. Currently, there are no commercially available prosthetic venous valves as previous efforts have been hampered by late failure and biocompatibility issues . To date, only two independently designed bioprosthetic valves have undergone clinical trials [9–12] although several others have been evaluated in vitro and in animal models.
Wang et al.  were among the first to create and test bioprosthetic vein valves when they mounted bovine jugular valves in straight, tapered, and curved conduits. The devices were evaluated in an in vitro system where it was determined that different pulse pressure thresholds were necessary to "reestablish the CO [closure opening] operation mode" for each conduit geometry. Similarly, Delaria et al.  evaluated fresh and glutaraldehyde fixed bovine jugular vein conduits in an in vitro flow system and determined that the performance of the two valves is similar while fixation theoretically renders biocompatible and nonthrombogenic tissue. Therefore, it was suggested that when mounted and stented, a glutaraldehyde fixed valve has the potential to be the first clinical solution to CVI.
The most extensive work was performed by Pavcnik et al. [15–21] who iterated on a bioprosthetic venous valve consisting of a small intestinal submucosa (SIS) leaflet material sutured to an expandable square stainless-steel wire stent. The device featured sinuses and barbs for vascular wall anchoring and was designed to be deployable via catheter. Wire thickness determined valve size and expansile force where ideal geometry was determined by constraining the diagonal axis of the square stent to a length of πr based on a vessel circumference of 2πr . When implanted in an ovine external jugular vein model, the valve restored antegrade circulation with little or no reflux and the SIS leaflet was shown to undergo endothelialization, neovascularization, and incorporation into the native vessel wall on the order of several months . However, in several animals, tilting of the valves lead to moderate reflux and thrombosis  prompting a second-generation design that consisted of either a stainless-steel stent attached to the apex of the original or a nonrestrained nitinol double-stent . The second-generation design effectively corrected for valve misalignment; nonetheless, sizing with the nitinol version and intimal hyperplasia with the stainless-steel device caused dysfunction . A later study indicated that spatial orientation is important and should correspond to that of the native valve . Although the previously described efforts by Pavcnik et al.  have shown favorable in vivo results in the short-term, a human feasibility study revealed that occlusion occurred in four of fifteen valves at 12-month follow-up. Additionally, three oversized valves opened too much resulting in leaflet-to-wall attachment and four devices exhibited undesirable leaflet pliability from adverse healing. Hence, the potential for clinical application of this bioprosthetic venous valve remains uncertain.
Work on synthetic valves has been more limited than those of bioprosthetic design. A synthetic bileaflet valve made of platinum or pyrolyte carbon covered titanium was reported by Taheri and Schultz . In nine canines, the device restored retrograde flow and remained patent in the short-term; however, within the initial three months, two of the valves migrated or were misoriented leading to failure. Within two years, all canines developed symptoms of CVI due to intimal hyperplasia. Sathe et al.  also created a synthetic venous valve, which is composed of a clinically approved polymer.
The objectives of the subsequently described prosthetic design were to preserve natural anatomic venous valve features while improving upon a conceptual first-generation device described in a prior patent  for which no quantitative testing was performed. The novel second-generation design features are also presented in a patent application currently under review .
Frame design began by rendering the valve flange in two-dimensions (in the transverse plane) followed by three-dimensional axial contouring. Then, the frame geometry was used to mathematically define a two-dimensional leaflet template. Next, the frame and leaflet were fabricated at a super-anatomic scale (2×) and a complete valve created by wrapping the leaflet template around the frame. The valve was then evaluated in a mock-up in vitro flow system (2:1 dynamic scaling) and, based on performance, the need for two additional frame features was defined: strut shoulders and a beveled leaflet attachment surface. Finally, a matrix of devices from the most advanced design were fabricated at anatomic scale (1×) and evaluated in a physiologically-based, in vitro flow system (1:1 dynamic scaling).
a. Two-dimensional frame design in the transverse plane
Inward directed flanges were introduced to occupy space in the transverse plane such that the frame base circumference exactly matches the leaflet closure path ensuring that pleating or gapping does not occur upon leaflet closure. One flange geometry fit this criterion while providing gradual curves and a simple mathematical relationship from which to design. In this configuration, each flange consists of two half-circles connected by two inverted quarter-circles of the same radius, which converge to a point directed towards the valve lumen. At the points where the flange intersects the frame base circumference, the half circles are connected with a straight line producing a flat flange "back". The point at which the flange back and half circle met was constrained as tangent to the circular base.
where R = the valve radius,
r = the flange radius, and
Q = a constant that compensates for the flat flange back and tangent point.
When Q equals r, the distance along a line from the central valve lumen and perpendicular to the flat flange back (subsequently labeled the y-axis) is exclusively dependent on the flange geometry and independent of the valve radius, R. Hence, Q cannot equal r and solution requires a second design equation that is obtained by applying the Pythagorean Theorem to the variables already defining the frame. The second design equation is: R2 = r2 + (3r + Q)2
A minor limitation of the frame design is that the base circumference side of Equation 1 does not take the flat flange back into account. Nonetheless, this assumption results in an error of approximately 1E-5 mm for the quarter-plane closure path, which is not considered significant.
b. Three-dimensional frame design
With design in the transverse plane finalized, the flange geometry was then extended into a three-dimensional object with the goal of optimizing hemodynamics and biocompatibility. More specifically, zones of stasis and excessive local shear stress were intended to be diminished along the flange such that thrombus formation and blood damage would be minimized. Additionally, it was recognized that flange contouring has the potential to limit pressure drop and thus, minimize resistance. Therefore, the flanges were extruded with minimal slope discontinuities in the axial direction and tapered at their proximal and distal ends.
c. Leaflet design
Based on the second generation frame, leaflet design considerations were defined in anticipation of future in vivo application. For example, it was desirable to minimize material surface area to limit thrombogenicity. Further, it was important to decrease leaflet flexion angle because the proximal base edge is a high stress region and thus, would be the first area to fatigue from cyclic loading. Unfortunately, these criteria work opposite to one another in that decreasing the angle of leaflet closure (i.e. decreasing cyclic stress) requires axial lengthening of the flange and therefore, increasing surface area. Given the aforementioned considerations, it was useful to create a design constraint whereby all points of the proximal leaflet edge are required to coapt in a single transverse plane. Such a closure plane was defined to be at the midpoint of the flange and allowed the frame and leaflet surface areas to be minimized for a specific flange length.
Next, the frame was viewed in the xy-plane and points from the radial edge of the base were mapped to their corresponding points on the flange during full closure using a spreadsheet program (Microsoft Excel, Microsoft Corporation, Redmond, WA). In two-dimensions, the distance between these points is the minimum length the leaflet needs to have to guarantee full closure. For the mathematical details of the point mapping, see the Appendix.
where L = the minimum length of the leaflet for full closure
The valve base height was added to L and provided an overlap between frame and leaflet for the application of adhesive.
The completed valve prototype consists of a combination of the solid frame and flexible leaflet. The frame was accurately and precisely modeled using computer-aided design (CAD) software (ProE 2000 i2, Product Development Company, Needham, MA) and then fabricated with stereolithography (SLA) rapid prototyping technology that utilized a photo-activated polymer resin (RenShape® SL 5210, Huntsman Advanced Materials, Salt Lake City, UT) consisting of bis-(epoxycyclohexyl)-methylcarboxylate and 2,2-dimethoxy-2-phenylacetophenone. Upon polymerization, residual resin was removed by submersion in iso-propanol and further cured in a UV oven. The leaflets, on the other hand, were created using a hand fabrication technique. The data points composing the leaflet template were transferred to a different program (MATLAB 6.5, The MathWorks Incorporated, Natick, MA) for 2D plotting. The axes were scaled equally for proportionality and then printed on an 8.5 × 11.0 inch sheet of paper. A copy machine (Canon NP6545, Canon Incorporated, Japan) was then used to reduce the template to a size that corresponded to the valve frame. This size was determined via trial and error and the best fit selected based on circumference. For the mock-up valves (2×), the scaling factor was found to be 54% whereas the prototypes (1×) required a reduction of 50% followed by a subsequent scaling of 57%. Once the proper size template was acquired, the leaflet material was taped over the template and the geometry of the leaflet traced on the material using a black pen. For all created valves (both 2× mock-ups and 1× prototypes), 5 mil (0.1270 mm) thick sheets of BioSpan® (BioSpan®, Polymer Technology Group, Berkeley, CA) were used as the leaflet material upon which reference lines for the flange back and proximal base edge were also drawn. The leaflet was then cut out using a surgical scalpel and super-glue was applied to the portions of the leaflet that were to meet on the flange back and below the proximal base edge. Finally, the leaflet was attached to the frame by approximating the center of the leaflet to the flange back and then rolling the valve in either direction to evenly wrap the remainder of the leaflet around the frame base.
e. 2:1 mock-up, in vitro flow system and design modifications
f. Design matrix
The aforementioned methodology addresses the issues of conserving leaflet and flange material by defining a single closure plane; however, varying the angle of leaflet flexion and sinus volume was not addressed. Nonetheless, it was recognized that the generic design could be dimensionally modified to accommodate such considerations. A single feature of the flange was identified that influenced both leaflet flexion angle and sinus size and was referred to as the flange length (FL). Physically, the FL was described as the distance in the z-direction between the tapered tips of the fully developed flange. Four different flange lengths were chosen: 1.25, 2.50, 3.75, and 5.00 mm, which had the effect of varying the leaflet flexion angle in a linear range from 38.7 to 11.3°, respectively.
g. 1:1 physiologically-based, in vitro flow system
After the addition of the bevel and shoulder features, the prototypes were fabricated at 1× scale with threading at the distal end to allow reproducible insertion into the physiologic in vitro flow model as described by our group . A blood analog test fluid consisting of 3.45% dextran (Sigma-Aldrich Corporation, St. Louis, MO) in distilled water was utilized where the viscosity was 3.5 cP. The testing protocol and parameters of interest were preserved from the prior study although a less detailed review is concurrently presented.
The in vitro flow model was designed to simulate any combination of two body positions (supine and standing) and two dynamic conditions (breathing and ankle flexion). Therefore, a total of four simulations are possible: supine breathing (SUBR), standing breathing (STBR), supine ankle flexion (SUAF), and standing ankle flexion (STAF). Body position was controlled via hydraulic communication between hydrostatic pressure towers and the test section while dynamic condition was determined via the frequency of flow pulsatility provided by a roller pump. A "No Device" case was run in an attempt to simulate the dynamic conditions of CVI in which the valve system is compromised. As the nomenclature indicates, the "No Device" case consisted of executing the test protocol without a device in place where a completely open orifice existed and the system was sealed around the threaded adaptor. The "No Device" case was used to calculate the experimentally determined Effective Orifice Area (EOA) coefficient, Cd, appropriate for these conditions where the open orifice area was directly measured and Qrms and ΔP were obtained from sampled data . Cd values of 2.32 ± 0.030 and 6.38 ± 0.142 cm.mmHg1/2.s-1 were obtained for the SUBR and SUAF simulations, respectively.
h. Statistical methods
Since there currently exists no clinically approved 'de facto' standard device for comparison, it was hypothesized that the second-generation prototypes would significantly improve systemic level hemodynamics (as characterized by the Regurgitation, Percent Reflux, REL, AE, and Energy Retention parameters) when compared to the CVI simulated "No Device" case. Additionally, it was theorized that differing FLs lead to unique in vitro dynamic performance for each parameter. Statistical analysis of design matrix data consisted of a one-way analysis of variance (ANOVA) followed by post hoc SNK or Dunnet T3 procedures for equal and unequal variances, respectively. A comparison of duplicate prototypes of the same design utilized a series of independent-samples t-tests. Both statistical analyses were performed using a commercially available software package (SPSS 14, SPSS Incorporated, Chicago, IL) with a significance level of 0.05.
a. 2:1 mock-up, in vitro flow system
Although data was collected as part of mock-up testing, those results are not presented because the developmental value of the simulation was primarily qualitative. However, as previously described, mock-up testing resulted in the addition of the shoulder and bevel features, which provided leaflet support and created sinuses, respectively. It was found that sinuses are crucial for valve actuation upon venous diastole (a retrograde pressure gradient).
b. 1:1 physiologically-based, in vitro flow system
Data characterizing antegrade hemodynamic device performance is presented in Figure 8. For the supine position simulations, the devices with FLs of 1.25 and 2.50 mm statistically had the lowest Resistance with both achieving around 0.50 and 1.0 mmHg.min/L for the SUBR and SUAF simulations, respectively. With regard to EOA, devices with FLs of 1.25 and 2.50 mm exhibited statistically superior EOA performance with approximately 1.2 cm2 for both simulations. The "No Device" Resistance was defined as 0 mmHg.min/L whereas the "No Device" EOA was calculated as the cross-sectional area of the open tube. Hence, the "No Device" Resistance and EOA were not included in the ANOVA and the corresponding grouping nomenclature is different from that of the other parameters.
A Antegrade intra-design variability as indicated by evluation of duplicate prototypes from the FL 2.50 mm design.
0.508 ± 0.041
1.18 ± 0.020
74.6 ± 5.12
0.878 ± 0.065
1.14 ± 0.018
78.3 ± 5.67
0.389 ± 0.046*
1.23 ± 0.024*
64.6 ± 5.00*
1.14 ± 0.208*
1.14 ± 0.045
92.1 ± 4.14*
* p < 0.05 versus FL 2.50A
B Retrograde intra-design variability as indicated by evaluation of duplicate prototypes from the FL 2.50 mm design.
11.0 ± 0.258
35.8 ± 1.63
9.55 ± 0.078
87.1 ± 1.18
7.82 ± 1.17*
27.6 ± 5.10*
4.95 ± 1.44*
92.2 ± 2.77*
2.19 ± 0.536
6.98 ± 1.71
0.400 ± 0.177
99.5 ± 0.227
6.06 ± 1.30*
17.8 ± 3.58*
3.02 ± 1.21*
96.7 ± 1.20*
* p < 0.05 versus FL 2.50A
a. Comparison with other studies
Several other published reports utilize similar hemodynamic conditions and parameters for evaluating prosthetic vein valves. More specifically, Delaria et al.  presented EOA data for fresh and fixed bioprosthetic valves with values around 1.1 and 0.70 cm2, respectively, at flow rates of 0.5 and 1 L/min. The fixed valves (that were suggested as most appropriate for native replacement) have smaller EOAs than the second-generation prototypes for which values of approximately 1.1 cm2 were obtained for the SUAF simulation where the steady component flow rate was 0.75 L/min. However, for these bioprosthetic devices, EOA data was obtained by a visual method while it was calculated as a function of pressure and flow for our second generation valves. Delaria et al. also presented several cycles of a waveform that show reversing flow.
Pavcnik et al. [18–21] qualitatively described hemodynamic performance of their bioprosthetic valve. More specifically, "minimal or no leak" was noted after immediate venogram in twenty-four of twenty-five devices implanted in porcine inferior vena cavas. Of twenty-six valves implanted in ovines, twenty-five had "no reflux" on immediate venography and twenty-two upon sacrifice . Two of the failed valves had "moderate reflux" at three months. In another ovine trial, four valves from a design array of forty-eight total valves had "significant leak" at six-week follow up on venogram . Further, one of six orthogonally oriented valves "showed reflux" on venography compared to none of the six in anatomic orientation . In patients, four of fifteen valves demonstrated "moderate leak" on venograms and ultrasound at twelve months .
With regard to prosthetic devices, Taheri et al.  reported regurgitant flow of 145 mL/min for a valve subjected to 300 mL/min of forward flow and back pressures of 100 mmHg. Further, in vitro test results of the prosthetic valve by Sathe et al.  showed that after more than 290,000 cycles the device had an opening pressure gradient of approximately 3 mmHg and a reflux rate of less than 3 mL/min at a pressure of over 150 mmHg. The valve was evaluated in an in vitro water system with a frequency of 40 cycles/min and an average proximal hydrostatic pressure of 65 mmHg. Unfortunately, the studies by Taheri et al. and Sathe et al. cannot be directly compared to each other or those of the second-generation prototypes. Hence, standardization of testing conditions and characterizing parameters are necessary as intended by our prior publication  and extended in the current manuscript.
b. Device performance in 1:1 physiologically-based, in vitro flow system
The data of Figures 8 and 9 demonstrate that the in vitro flow system and corresponding parameters are capable of quantifying hemodynamic improvement from the CVI simulated "No Device" case relative to the second-generation prototypes. Also, the system is able to evaluate relative performance for device-specific selection as previously indicated by repeat measurements of the FL 1.25 mm prototype . However, intra-design variability confounds design-specific selection, which is evident by the current study and also by comparing the data of the FL 1.25 mm prototype from our previous study  and another device of the same design that is subsequently presented. Therefore, the following selection process is device-, but not design-specific with regard to the second-generation prototypes.
c. Relative importance of simulation position/condition and parameters
Devices were evaluated utilizing four physiologically relevant simulations by seven hemodynamic parameters without a single device being superior on all measures. Hence, selection must weigh the relative value of all parameters and simulations.
For the supine position simulations, Resistance and EOA were found to be significantly different from the "No Device" case for the four designs. However, all values are considered acceptable since they easily satisfied the acceptable performance criteria established a priori – namely, ΔP < 5 mmHg (≡ Resistance < 8.3 mmHg·min/L) and EOA > 80% of 'No Device' case (= 0.984 cm2), verifying that the devices did not notably impede antegrade flow.
With regard to the standing position simulations, STBR is the most demanding simulation for characterizing retrograde performance. This is because, in the STAF simulation, the higher frequency of the pumping cycle acts as an effective valve due to the reduced time available for the flow momentum to reverse. Hence, parameters of the STBR simulation are exclusively used in design selection. When considering specific parameters, most include reflux volume as an independent variable (with the exception of Antegrade Energy). As a result, there is inherent redundancy in the characterization of retrograde performance, which diminishes the multi-dimensional utility of the parameters in selection. Percent Reflux normalizes for periodic variations in antegrade volume and therefore, is reasoned as the only quantity necessary for selection of the second-generation prototypes.
While only one simulation and one parameter are necessary for device selection of the second-generation prototypes, a different combination of simulations and parameters may prove useful in distinguishing valves of more dissimilar designs. Of anticipated future importance are the Percent Reflux and Energy Retention parameters because they provide meaningful performance boundaries, which have physical significance. More specifically, Percent Reflux can be considered a valve ejection fraction where values greater than 100% are not possible and those less than 0% indicate a positive fluid accumulation in the distal venous space and CVI perpetuation. When the valve is operating in a range from 0 to 100% reflux, fluid accumulation in the distal venous space is negative and the conditions of CVI are being alleviated. Similarly, for the Energy Retention term, values less than 0% indicate the valve is allowing the hydrostatic fluid column to perform work on the calf muscle pump. Further, values greater than 0% indicate that the valve is permitting the energy exerted on the fluid from the calf muscle pump to be retained in the form of hydrostatic potential energy; hence, the term, Energy Retention. There is also an upper limit of 100% for the Energy Retention parameter. All second-generation prototypic, prosthetic valves perform in the optimal ranges of Percent Reflux and Energy Retention whereby the hemodynamics are favorable for CVI treatment.
Based on their statistically superior performance as quantified by the Percent Reflux parameter in the STBR simulation, the most advanced second-generation valves featuring FLs of 2.50 and 3.75 mm are superior to those of 1.25 and 5.00 mm. However, as previously described, this selection is device- and not design-specific.
e. Frame design
f. Future directions
Prospective development objectives include: 1) the selection of an appropriate biomaterial for the frame, and, 2) casting BioSpan® in a mold for more precise proximal edge contouring while scaling thickness for the 1× prototype (2.5 mil/0.0635 mm). It is also desirable to improve the reproducibility of leaflet-to-frame attachment to minimize intra-design variability. Finally, our group intends to report a CFD study of local hemodynamics including wall shear stress and residence time from the most advanced second-generation design prior to assessing biocompatibility in vivo utilizing an ovine external jugular vein model.
Results indicate that the STBR simulation provided the best means of discriminating among second-generation valves of varying FLs. Further, only one parameter, Percent Reflux, was appropriate for device selection. Statistical analysis, revealed the 2.50 and 3.75 mm FL devices are superior to those of 1.25 and 5.00 mm with a Percent Reflux of 36%. However, intra-device and intra-design variability confound design selection. Nonetheless, all prototypic, prosthetic valves provided a dramatic and statistically significant improvement when compared to the "No Device" case (Percent Reflux of 205%), which was a simulated reference to the dynamic conditions of CVI. This leads to the general conclusion that the most advanced prototypic, prosthetic venous valve has the potential to reestablish normal antegrade circulation.
Mathematically, the leaflet-closure plane point mapping was accomplished by first defining a variable, Θoffset, which is the angle formed by the x-axis, the origin, and the tangent point where the flange back meets the half circle. For the aforementioned optimized frame, Θoffset was found to be 12.7°. Then, the xy-coordinates of discreet points on the radial base edge were determined by incrementing the angle from the x-axis by 0.25 radians and applying the following equations:
X = R cosΘ
Y = R sinΘ
where X = the Cartesian coordinate of the radial base edge from the x-axis,
Y = the Cartesian coordinate of the radial base edge from the y-axis,
R = the valve radius, and
Θ = the angle from Θoffset in radians = angle – Θoffset.
Then, points on the radial base edge were mapped to their corresponding position on the flange using the following relationship: S = R Θ = rθ
where s = arc length,
R = the valve radius,
Θ = the angle from a point on the valve edge to Θoffset in radians,
r = the flange radius, and
θ = a reference angle corresponding to the mapped point on the flange.
In Equation 5, R was set at 6.25 mm and the solution of Equations 1 and 2 provided that r is 1.37 mm. Therefore, because Θ was incremented, θ is the dependent variable. Physically, θ is the angle formed by the θoffset reference point, the origin, and a specific point on the flange. Analogous to the radial base edge, two-dimensional Cartesian coordinates are found from the following equations:
x = r cos θ + x'
y = r sin θ + y'
where x = the Cartesian coordinate of the flange from the x-axis,
y = the Cartesian coordinate of the flange from the y-axis,
r = the flange radius,
θ = a reference angle corresponding to the mapped point on the flange,
x' = the x displacement of one flange circle, and
y' = the y displacement of the same flange circle.
The displacements are necessary because the points composing the flange are based on circles that have different centers. Thus, for the portion of the flange composed of the half-circle, x' equals (2r + Q) and for this specific design is 4.71 mm. Similarly, y' is r or 1.37 mm. For the quarter-circle portion, x' is Q or 1.97 mm and y' is r or 1.37 mm. The line connecting the tip of the flange and the origin is linear and therefore, requires a separate mathematical definition for mapping the remaining arc length of the radial base edge. These points were evenly distributed along the remainder of the closure path, which completed the two-dimensional considerations. Figure 4 depicts the Cartesian definitions for leaflet design in the transverse plane.
To resolve the coordinates in the third dimension, the frame was viewed in the yz-plane and the displacement in the z-direction was determined. For the radial base edge, the z-coordinate is zero by definition of the origin. Similarly, by design constraint, the z-coordinates of the closure plane all have a constant value. Staying consistent with nomenclature in the xy-plane, these relationships were expressed mathematically as:
Z = 0
z = H
where Z = the Cartesian coordinate of the radial base edge from the z-axis,
z = the Cartesian coordinate of the flange from the z-axis, and
H = the predetermined leaflet closure height.
This project was supported by a grant from the NIH STTR Program (1 R41 HL077984-01). The authors would like to thank Michelle Evancho-Chapman, Division of Surgical Research, Summa Health System, for her technical assistance and Dr. Steven P. Schmidt, also of the Division of Surgical Research, Summa Health System, for his overall support of the project. We'd also like to recognize the Polymer Technology Group of Berkley, California for donating samples of their BioSpan® product for use as a leaflet material.
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