Introduction
Femoral arterial cannulation for arterial inflow is essential for cardiac surgical procedures, as well as for extra-corporal life support (ECLS) and extra-corporal membrane oxygenation (ECMO). The longer the femoral artery perfusion, the higher the risk of serious problems for distal perfusion. An eventual obstruction of the access vessel by traditional rectilinear cannulas design may cause irreversible hindrances such as amputation or even death. Several authors have stated an important risk of lower limb ischemic hitches after protracted cannulation of femoral artery, such as Hendrickson and Glower, who reported a rate of 11.5% after peripheral CPB [
1]. Also, Foley et al. [
2] and Huang et al. [
3] have demonstrated that ECMO support is correlated with lower limb ischemic problem at rates as high as 26%.
Collateral blood flow is responsible for the viability of the lower limb. Incidence of lower limb ischemia is often related to deprived flow rate, leading to an obligation for fasciotomy or even amputation. A number of techniques have been proposed to prevent this potentially devastating complication, including the use of a downstream femoral perfusion catheter [
1,
4‐
6] or an end-to-side femoral artery graft [
7,
8]. However, these techniques are often difficult to perform, and in addition to the complexity of the procedure, they are not always consistent. Besides, bleeding complications and high risk of infection are often related to these techniques [
9]. Thus, a new femoral cannulation system is necessary for clinical surgery and standard retrograde perfusion without reducing distal limb blood flow.
To overcome these difficulties, Smartcanula® LLC (Lausanne, Switzerland) developed a self-expandable bidirectional design for cannulation of femoral artery. This cannula has the enhanced performance of a nearly wall-less design as compared to the traditional rectilinear percutaneous cannulas. Besides, this cannula expands partially, i.e. at the insertion position only with regard to the vessel lumen, allowing thus parallel retrograde flow as the cannula body does not occupy the whole vascular lumen [
10]. This novel bidirectional design allowed for important high flow rates at lesser driving pressures. Here, we present an optimized configuration of this bidirectional arterial cannula. The optimization development consists in shortening the narrow covered section of the cannula, which we assume could enhance peripheral perfusion, and thus diminish the risk of lower limb ischemia and subsequent complications during ECLS with peripheral cannulation [
7]. Furthermore, we hypothesize that reducing size of the covered section may result in early cannulation and enhanced comfort without reducing the quality of peripheral perfusion.
Discussion
Overall, both self-expanding bidirectional showed better forward flow rate to each revolution per minute when compared to the standard control cannula. This superior forward flow rate with the virtually wall-less cannulas is probably due to their tinny wall thickness (0.36 mm) as compared to the wall leanness of percutaneous cannula (> 0.60 mm). This difference in wall thickness affects the effective cross-sectional area. The superiority of the bidirectional cannula was revealed with less positive pressure for each forward flow rate, compared with the regular control cannula (Fig.
4, upper panel) (
p < 0.001). In vivo perfusion with high positive pressure in rectilinear cannula design increases the risk of hemolysis and embolism formation.
Furthermore, the short bidirectional cannula design (60 mm of the 15 F covered access section), showed significantly higher forward flow rates at lower driving pressures as compared to the 90 mm covered. For a driving pressure of 100 mmHg, typical of a clinical situation, the corresponding flow rate is around 4.1 l/min for bidirectional 60 mm covered and versus 3.8 l/min for bidirectional cannula 90 mm covered, versus 3.2 l/min for control cannula corresponding to around 128% for 60 mm versus control and 108% for 60 mm versus 90 mm
. The advantages shown for the bidirectional 60 mm covered can be repeated at all pump speeds with minimal variations (CV between 1 and 4% for six repeated measures). Thus, shortening the 15 F free section length of the bidirectional cannula permits for higher flow rates at lower driving pressures. For a flow rate of 4.5 l/min the corresponding driving pressure is 180 mmHg for the regular design control of the same diameter versus 150 mmHg for bidirectional cannula 90 mm, versus 119 mmHg for bidirectional 60 mm covered, equal to around 150% for control versus 60 mm covered, and 126% for 90 mm covered versus 60 mm covered. (Fig.
4, upper panel). In addition, bidirectional 60 mm covered showed 160% more retrograde flow rate as compared to the 90 mm covered. With our experimental system, the rectilinear design Biomedicus control did not show retrograde flow rate.
In clinical practice, a considerable bigger size of a traditional rectilinear percutaneous cannula would be needed to reach the same flow rate at the same driving pressure, due to less or no space for retrograde flow to the limb. Our results indicate that a considerable smaller cannula diameter of bidirectional design with 15 F covered access section can be used to attain a given target flow rate and a physiologic driving pressure.
In the clinical setting, bidirectional cannula design is based on the “collapsed insertion and
in situ expansion principle”, which has been confirmed to be reliable [
8]. Thus, for the clinical application no concerns about the insertion and the removal of a bidirectional cannula with its fusiform segment larger than the cannula diameter at the site of insertion [
10] (Fig.
2). This function is achieved by extending the fusiform cannula section with a mandrel [
11]. Similarly, the bidirectional canula can be removed easily, because it collapses with simple traction. Digital compression for caudal bleeding.
The results of this study were performed with water as the testing medium, which might be considered as a limitation when compared to tests performed with blood, for describing results relevant to the clinical setting. Thus, we questioned whether the outperformance of the cannula would be identical using blood instead of water, and if the higher viscosity of the blood would change its performance. Our preceding studies demonstrated, that the viscosity of the blood decreased flow by about 10 and 6% less for rectilinear percutaneous cannulas and virtually wall-less cannulas respectively [
12], similar to the bidirectional design presented here. Also, Broman el. al [
13,
14] showed that when blood with hematocrit of 27% was used, the venous drainage pressure was steadily higher for a given flow than when water was used. Broman and co-authors demonstrated that blood flows with single-lumen return arterial cannulas for peripheral ECMO tested were lower than those provided by manufacturers using water. We think that water is a good testing medium for the cannula performance. The main advantage of water as test medium for cannula performance assessment is its reproducibility. This also explains why water is usually used as the industry standard medium for comparative to compare cannula performance validation. For the present set-up, the water transparency was necessary for assessment of the residual lumen resulting in retrograde flow.
Severe atheromatic disease access vessel or kinked access vessels may restrict the self-expanding mechanism of the bidirectional cannula and therefore the flow may also be delayed in one or both directions. The kinking assessment of self-expanding cannulas tests confirmed for all self-expanding cannula diameters (12F–36F), that the double helix design is extremely kink resistant (180
o and more) as shown in Fig.
6. However, a traditional rectilinear cannula with a fixed outer diameter may not even be inserted. The use of per-procedural ultrasound is a good tool in such complex situations as described above. The latter is helpful for target vessel identification and also guide-wire position clarification. For the bidirectional cannula, ultrasound allows in addition for identification of the flow direction by the means of the Duplex Color Doppler function [
8]. We conclude bidirectional flow for ECLS and ECMO can be achieved on the arterial side with cannulas having a 15 F section, that does not occupy completely the access vessel for a retrograde flow, and which performance can be optimized by shortening its covered section. We consider that this type of cannula can also be used and optimized for MICS [
15‐
17]. In vivo studies are planned as the next step for confirmation of these findings prior to clinical application.
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