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STATE-OF-THE-ART PAPER Table of Contents   
Year : 2009  |  Volume : 2  |  Issue : 1  |  Page : 3-23
The role of stents in the treatment of congenital heart disease: Current status and future perspectives


Department of Congenital Heart Disease/Pediatric Cardiology, Deutsches Herzzentrum Berlin, Germany

Click here for correspondence address and email

Date of Web Publication17-Jun-2009
 

   Abstract 

Intravascular or intracardiac stenoses occur in many forms of congenital heart disease (CHD). Therefore, the implantation of stents has become an accepted interventional procedure for stenotic lesions in pediatric cardiology. Furthermore, stents are know to be used to exclude vessel aneurysm or to ensure patency of existing or newly created intracardiac communications. With the further refinement of the first generation of devices, a variety of "modern" stents with different design characteristics have evolved. Despite the tremendous technical improvement over the last 20 years, the "ideal stent" has not yet been developed. Therefore, the pediatric interventionalist has to decide which stent is suitable for each lesion. On this basis, currently available stents are discussed in regard to their advantages and disadvantages for common application in CHD. New concepts and designs developed to overcome some of the existing problems, like the failure of adaptation to somatic growth, are presented. Thus, in the future, biodegradable or growth stents might replace the currently used generation of stents. This might truly lead to widening indications for the use of stents in the treatment of CHD.

Keywords: Stenting, aortic coarctation, pulmonary artery stenosis, patent ductus arteriosus, newer stent designs

How to cite this article:
Peters B, Ewert P, Berger F. The role of stents in the treatment of congenital heart disease: Current status and future perspectives. Ann Pediatr Card 2009;2:3-23

How to cite this URL:
Peters B, Ewert P, Berger F. The role of stents in the treatment of congenital heart disease: Current status and future perspectives. Ann Pediatr Card [serial online] 2009 [cited 2019 Aug 22];2:3-23. Available from: http://www.annalspc.com/text.asp?2009/2/1/3/52802



   Introduction Top


Since the first description of an interventional procedure in the field of congenital heart disease (CHD) by Rashkind in 1966, [1] the non-operative treatment of CHD has made enormous progress. While describing percutaneous transluminal angioplasty in 1964, Dotter and Judkins anticipated the need of an endovascular splint to keep the vessel lumen patent, [2] which later resulted in the first implantation of a spiral coil- spring prothesis in experimentally created vascular stenotic lesions. [3] Elastic recoil of vessel wall as well as intimal dissection may lead to acute closure. In these cases, increasing the balloon diameter may worsen the dissection or rupture the vessel. Stents provide more effective and predictable relief of obstruction by exerting a radial force that prevents elastic recoil. They also compress dissection flaps against the vessel wall and prevent acute closure. Stenting may also be helpful in the treatment of extensive vessel dissection after balloon dilatation thus avoiding or ameliorating the risk of aneurysm formation. Long-segment stenoses or hypoplastic vessel segments are not ideal for ballooning. In these cases, implantation of stents may be helpful in achieving long-lasting enlargement to the desired diameter.

Although intravascular stents still do not have the Food and Drug Authority (FDA) approval for use in congenital lesions and pediatric patients, since 1996, their use for congenital vascular lesions has been accepted as the standard of care by all centers and professional medical societies associated with the treatment of pediatric and CHD. This review will address some key questions in the common practice of the use of stents in the CHD population. Advantages and disadvantages of the different types of stents and stent designs currently used in CHD are presented. Furthermore, recent developments in stent technology intended to overcome some of the present problems in stent therapy that might expand the spectrum of indications for stenting are addressed. As this paper focuses on stent therapy within the heart and the central great vessels, the use of stents in peripheral arteries and veins is not discussed.


   Common Indications for Stenting Top


Common indications for stent deployment in CHD include treatment of obstructive lesions of the (1) branch and peripheral pulmonary arteries, (2) systemic and pulmonary veins, (3) aorta and branches, (4) right ventricular outflow tract (RVOT) conduits, (5) maintenance of patency of the arterial duct in duct-dependent circulation, (6) maintaining patency of stenosed aortopulmonary collateral vessels or surgically created but obstructed shunts and (7) maintaining patency of intracardiac communications.


   Most Commonly Used Stents in Congenital Heart Disease Top


Stents are classified on the basis of the material of which they are made, the target region, their configuration and their size. Additional features used in classifying them include coverage, special surface treatment and coatings and drug-eluting properties. But, the most common classification is based on their delivery mechanism: Balloon-expandable versus self-expandable stents.

Balloon-expandable stents

Balloon-expandable stents (BES) are mounted on balloons, positioned across the site of obstruction and are implanted by inflating the balloon. The size of the inflated balloon determines the expanded diameter of the stent. BES were introduced for the treatment of congenital heart lesions in 1987, [4],[5] with the development of the Palmaz stent. Since then, they have been the most commonly used stents in pediatric cardiology. The Palmaz stent consists of a 316 L stainless steel tube with laser-cut slots that form seven cells per row. The tremendous success of BES is due to its unique features that combine high radial force with accurate stent placement and oversizing properties (up to 10 mm). With its increasing use and the widening spectrum, some unfavorable characteristics have come into focus. They include marked foreshortening, rigidity, flaring of the sharp edges, vessel injury or balloon rupture and the unsatisfactory bending performance. These limitations have prompted development of new stent designs.

The "ideal" stent in congenital heart disease

Desirable features for an ideal stent design in pediatric cardiology are: (1) low stent profile combined with (2) high trackability and (3) flexibility to negotiate steep curves, (4) good radio-opacity and visibility for precise placement, (5) compatibility with magnetic resonance imaging (MRI) with no artifacts, (6) predictable expansion with minimal foreshortening, (7) sufficient radial strength, (8) low rigidity with no material fatigue over time, (9) full biocompatibility with resistance to thrombus formation and corrosion, (10) prevention of plaque protrusion, (11) avoidance of neointimal proliferation, (12) round and soft edges for avoidance of intimal damage, (13) possibility of redilation with patients' growth, (14) wide struts to maintain blood flow to jailed vessel branches and (15) retrievability and possibility of repositioning if needed. Obviously, there is no stent yet available that combines all of these requirements so that selecting the right stent for the appropriate condition is one of the most difficult challenges encountered by pediatric interventional cardiologist.

Design characteristics of balloon-expandable stents

Technically speaking, stent performance is related to the material characteristics, form, fabrication mode and geometry.

Materials of balloon-expandable stents

The most widely used material for BES is still stainless steel, typically 316 L. It is particularly corrosion resistant and in its fully annealed condition, easily deformable. Alternative materials for BES used in CHD are platinum alloys (Cheatham Platinum [CP] Stent; NuMED Inc., Hopkinton, New York, USA), tantalum (Strecker Stent; Boston Scientific, Natick, MA, USA) and cobalt alloys (the newly developed Andrastent XL and XXL; Andramed, Reutlingen, Germany). Cobalt chromium alloys are very interesting for use in pediatric cardiology as they allow lower crimping profiles with high radial strength. Recently, biodegradable stents have been introduced that are composed of polymeric substances, magnesium or biocorrodible iron. This new class of stents is discussed in the section "New developments in stent design and future perspectives" at the end of this article.

Slotted tube design

The vast majority of coronary and peripheral vascular stents are produced by laser cutting from tubing, the so-called slotted tube design. Intricate patterns can be produced using tube sizes from 0.5 mm diameter. BES are cut in crimped or near-crimped conditions, allowing a low profile. In slotted tube stents, those with the more conservative closed cell design need to be distinguished from those with the newer open cell design.

Closed cell design

The traditional closed cell design describes a sequential ring construction wherein bridging elements connect all internal infliction points of the structural members [Figure 1]. This is only possible with regular "peak-to-peak" connections, meaning that the bridging elements join adjacent structural members at the outer radii. Early slotted-tube type designs, such as the Palmaz stent, were strong but inflexible. Later designs such as the NIR™ stent (Boston Scientific, Natick, MA, USA), the Corinthian™ series (Johnson and Johnson Interventional Systems, Warren, NJ, USA) or the Genesis™ stent ("sigmoidal hinge connection"; Johnson and Johnson) improved upon this concept by adding a flex-connector (U-, V- S- or N-shaped elements)that plastically deforms during bending, allowing adjacent structural members to separate or nest together.

Thus, older Palmaz stents such as the Palmaz 8 series (P 108, P188, P308) and others have been replaced by the Genesis series. The Genesis stents represent the latest evolutionary step of the Palmaz "biliary" stent series. They are similar to the Corinthian stent (a further development of the original Palmaz stent), except for the new sigmoidal hinge. This element adds greater flexibility without compromising radial strength. They are available as unmounted and pre-mounted, the latter for only the smaller diameters - paradoxically named Genesis Medium. The Genesis Medium stents can easily be dilated to 5-8 mm, but overdilation up to 12 mm is possible. Genesis Large (PG295P, PG395P) are labeled as 5-10 mm, but may be dilatable to 12-15 mm. The Genesis XD (XD, extended diameter) can be dilated optimally to 10-12 mm but can easily be overexpanded to 18 mm. Some other commonly used stents with the closed cell design are listed in [Table 1].

The primary advantage of the closed cell design is optimal scaffolding and a uniform surface, regardless of the degree of bending. However, these advantages result in a structure that is typically less flexible than with a similar open cell design.

Open cell design

In open cell design, geometry does not connect consistently throughout the stent, forming incomplete and non-bridged cells. With expansion, the individual cells merge to form larger open areas; thus, there is no consistent shape of cells [Figure 1]. Examples for the open cell design are the Guidant Herculink™ and Omnilink™ (Guidant, Santa Clara, CA, USA), Jomed Wavemax™ (Jomed AB, Helsingborg, Sweden), the Medtronic AVE Bridge™ Stent (Medtronic/AVE, Santa Rosa, CA, USA) as well as the IntraStent™ DoubleStrut™, Mega™ LD and Maxi™LD series (EV3 Inc., Plymouth, MN, USA). Stents with open cell design have some characteristics that seem beneficial for their use in CHD: they foreshorten less, are conformable, are less likely to cause balloon rupture and can allow access to jailed branches. These characteristics have been documented for the IntraStent™ DoubleStrut™ (EV3 Inc.). [6],[7] This is laser cut out of a 316 L stainless steel tube. The parallel struts and the unique cell geometry allow flexibility around tight curves and minimize stent shortening (especially when serial dilation is performed). While it has similar radial strength to other stents up to diameters of 12 mm when dilated beyond 15 mm, it has less strength. [8] Therefore, in some lesions in which high radial strength is required, these stents may recoil. [6] Thus, if higher radial strength beyond 15 mm diameter is an issue, Intrastent™ Mega™ LD and Maxi™LD stents (EV3) have almost replaced the DoubleStrut stent. In these stents, the configuration of the cells is similar to that of the DoubleStrut stents, but the single struts are cut from a tubing of an initially thicker material, which makes each strut thicker and stronger than the double struts. They have very rounded edges to minimize trauma and their open cell design allows for access to the side branches as the individual cells can be dilated up to 12 mm in diameter. On the other hand, a higher incidence for protrusion of intimal tissue or plaque in between struts has been reported with the open cell design, which might impact long-term stent performance. [7] The Mega™ LD can be dilated up to 18 mm and the Maxi™LD up to 25mm with less than 25% foreshortening when expanded sequentially. Foreshortening can be much higher if these stents are expanded with a single large balloon directly to 15 or 18 mm. The reason for this is that the ends of the stent are compressed toward each other due to the typical "dumbbeling" of the balloon at the end of inflation while the center of the stent is expanding to its full diameter. This results in significant shrinkage of the overall length of the stent. Thus, if final length is critical, the delivery requires sequential balloon dilatation with increasing diameters or, even better, the use of a Balloon-in-Balloon (BIB™ catheter; NuMed Inc., Hopkinton, NY, USA). The recently introduced innovative Andrastent XL and XXL (Andramed, Reutlingen, Germany) are characterized by the so-called hybrid cell design, a combination of closed and open cells, intended to improve flexibility for better delivery performance compared with that of conventional large stents. According to the manufacturer, these stents show significant foreshortening of 48-47% at maximum diameter.

Welded tube design

In contrast to stents with the slotted tube design, the Cheatham platinum (CP) stent has been developed using a welded tube. It is manufactured from a wire, which is bent and welded to a cylindrical meshwork, forming the stent. This leads to more adjustable flexibility and a wide range of size and length, but radial strength is usually less than the ones with slotted tubes.

The most commonly used stent in pediatric cardiology is the CP stent, which is made from 90% platinum and 10% iridium. Each row of zigs is laser welded with the addition of gold soldering (since December 2002) at each welded spot to increase the total strength of the weld. The number of zigs affects the final diameter and the degree of shortening as well as the profile of the stent. While it is available in 6 and 8 rows, it is mostly used in the 8-zig configuration, as this shortens much less than the 6 zig at the equivalent diameters and can be dilated up to 28 mm (instead of 18 mm for 6 zig), with foreshortening of about 22-28%; however, dilatation to larger diameters is possible. [9],[10] These stents have excellent visibility on fluoroscopy and maintain excellent radial strength even at larger diameters. For introduction, sheaths 2 French larger than the recommended sheath size for balloon are required (as they have a slightly larger profile than other stents). They are available in different lengths (22, 29, 34, 39 and 45 mm) but can be customized in every desired length in increments of 6 mm by welding further segments together in longitudinal direction. They have rounded edges, are more malleable and are MR compatible. The rounded edges cause less trauma to the vessels and the balloons. This stent was the first to be developed for exclusive use in pediatric cardiology. [9],[10] It carries a CE mark and is now in routine use throughout most of the world except in the United States (the country where it was developed) due to restrictive FDA regulations. In the United States, the CP stent used to be available for compassionate or individual humanitarian emergency use, but even this availability has been suspended. Thus, the Palmaz XL stents are still in use but, due to their "old" stent design (as discussed earlier for the Palmaz 4 and 8 series), those stents have some potential disadvantages compared with the CP and the Maxi LD stents.

Covered stents

CP stents are available in a covered version, with an outer polytetrafluoroethylene (PTFE) membrane. The covering is initially approximately 7 mm in diameter and will stretch over the range of diameters of expansion (usually from 12 to 24 mm diameter) and will always be taut over the stent when expanded. To date, the covered CP stent is the most widely used covered stent in patients with CHD. [9],[11],[12],[13],[14],[15],[16],[17],[18],[19],[20],[21],[22],[23],[24],[25],[26]

Different sizes of balloon-expandable stents for congenital heart disease application

A very practice-orientated classification for the use of BES in CHD is based on the maximum expandable size of stents. It is important to note that, due to the lack of official recognition for use in pediatric and CHD patients, nearly all stent manufacturers test and label their stents with the maximum diameters for use in approved smaller diameter biliary system and peripheral vessels, rather than their true potential maximum diameter. Thus, stents can be categorized into four different sizes by their "true" maximal expandable size: Small (3-6 mm), medium (10-12 mm), large (up to 18 mm) and extralarge (up to 25 mm). [8] Small stents are almost exclusively used in coronary arteries and thus are not discussed here. Medium stents are appropriate for implantation in segmental and subsegmental branch pulmonary arteries, femoral and inominate veins, pulmonary veins and systemic-to-pulmonary shunt (Palmaz 4 series, Corinthian, Genesis medium and large, Guidant Omnilink, Guidant Herculink, Jostent Wavemax, Jostent peripheral, Bridge and NIR). Large stents may be adequate for branch pulmonary arteries, lobar branch pulmonary arteries, the caval vein, proximal iliac vein, aorta, Fontan baffles and (valved) homografts and conduits (Palmaz 8 series, Palmaz Genesis XD, Intrastent Double Strut LD, Mega LD stent and the CP 6 zig). The extralarge stents can be used for the aorta, large right ventricular baffles, Fontan conduits or homografts/conduits (Palmas XL, CP 8 zig, Maxi LD, Andrastent XL and XXL).

In [Table 1], we list the BES currently used in pediatric cardiology. Their "true" expandable maximal diameter is in parentheses. Stents marked with an asterisk are currently used in our catheterization laboratory and are considered by us as "modern" stents.

Special balloons in stenting

The large majority of balloons currently used for stent deployment are still adapted from the adult vascular angioplasty and "biliary" applications. These large- diameter single-balloon catheters tend to expand first at their ends and thereby evert the stent ends such that they protrude radially from the stent center. Deploying a stent in this orientation can cause injury to the vessel wall and may be a risk factor for the development of aneurysm or dissection. One of the most important developments in equipment for the delivery of large-diameter stents has been the Balloon-in-Balloon (BIB™; NuMed Inc.) catheter, the first balloon specifically designed for stent delivery in the CHD population. These catheters have an inner balloon and a longer outer balloon that is double the diameter of the inner balloon. The BIB catheters are available in outer balloon sizes of 8-24 mm. The BIB catheters offer the important advantage of opening the stent more uniformly along its length but require a larger arterial sheath for introduction. With a stent hand crimped onto the balloon, it is necessary to upsize the long sheath by 1F, greater than is necessary for the BIB catheter alone. Therefore, with hand-mounted stents, BIB catheters with outer balloon diameters of 8-14 mm require a 9F sheath, 16 mm catheters a 10F sheath, 18-20 mm catheters an 11F sheath and 24 mm balloons a 12F sheath. Thus, while BIB catheters prevent stent flare and offer more precise control over stent placement, single-balloon catheters are still sometimes preferable in smaller patients to reduce risk of injury to the femoral artery at the access site.

The development of ultra high pressure (UHP) balloons like the Conquest (5-12 mm diameter) and the  Atlas More Details (12-26 mm diameter; Bard Peripheral Vascular Inc., Tempe, Ariz) may facilitate successful treatment of stent-associated stenoses that are resistant to conventional high-pressure dilation. These balloons, originally developed and approved for treatment of stenotic hemodialysis fistulas, [27] contain a cross-matrix woven layer of ultrahigh molecular weight polyethylene. They have rated burst pressures ranging from 18 to 27 atm, but can be inflated to substantially higher pressures without rupturing. [28] In a recently published paper, these balloons have been successfully used to treat resistant obstruction within or adjacent to previously implanted pulmonary artery (PA) stents, with successful dilation in 91% of the lesions proven to be resistant with other balloons, and no dilation-related complications. [28] It was even possible to enlarge completely expanded and foreshortened stents by breaking them longitudinally. In our own experience, they may also be helpful when significant residual stenosis remains, e.g. after percutaneous pulmonary valve implantation (PPVI) (Melody™; Medtronic Inc., Minneapolis, MN, USA) following pre-stenting with bare-metal stents (Max LD; EV3, Plymouth, MN, USA). As these balloons are relatively stiff and have a long nose, this may limit their applicability in some circumstances: if they are inflated across a curved or angled vessel, straightening of the balloon at high pressure may result in substantial excursion of the nose, potentially posing a risk of distal vascular injury. Given the very high stresses that can be generated, it is recommended to use a balloon/waist diameter ratio of around 1.2-1.3, which is smaller than that typically applied with standard or high-pressure PA angioplasty.

For lesions resistant to conventional high-pressure angioplasty, evidenced by a persistent waist, cutting balloons may be used before stenting. A Cutting Balloon™ (Boston Scientific, San Diego) has three or four longitudinal microtome blades bonded to a non-compliant balloon. Folded between the material of the balloon, the blades are exposed when the balloon is slowly inflated, achieving a profile of 0.127 mm from the surface. Their microblades are intended to incise only the intima and part of the media in a vessel, resulting in a more controlled dissection of the vascular intima. On deflation, the balloons refold very smoothly and the blades recess back to their original configuration in the surface of the balloon. As they are only available in sizes up to 8 mm, this limits their use in larger vessels. Currently, they have been shown to be very effective in pulmonary branch artery stenosis, [29],[30] major aortic-to- pulmonary collateral arteries [31] and enlargement of atrial septal defects (ASDs) [32],[33] before stenting.

Stent mounting

Only a minority of BES suitable for CHD are pre-mounted, like the Genesis medium stent (Cordis) that is available on a Slalom™, OptaPro™ and Aviator™ Balloon (Cordis). The pre-mounting represents a unique incorporation of the stent into the wall of the balloon. This fixes the stent very securely on the balloon and allows delivery of the stents to very circuitous locations without the need for a long sheath and with no displacement during delivery - although using a short sheath access may not always be advantageous, as monitoring of placement with contrast medium injection is more difficult. Currently, most stents for CHD come unmounted and have to be hand crimped over the desired balloon, which also has its own advantages. This offers more flexibility, as stocking is easier because multiple stent- balloon combinations are possible. We sometimes use a customized crimping device (Qualimed, Winsen/ Luhe, Germany) to obtain a very low profile and tight stent/ balloon assembly. Thus, it has been possible to deliver a Mega LD stent (EV3) on a 6 mm Powerflex P3™ (Cordis) balloon through a 6 Fr-long sheath (personal experience).

Self-expandable stents

Materials for self-expanding stents should exhibit large elastic strains. The most widely used material is nitinol, a nickel-titanium alloy that can be recovered from elastic deformations of up to 10%. This unusually large elastic range, commonly known as superelasticity, is the result of a thermoelastic martensitic transformation. The limited elastic range of more conventional materials, such as stainless steel (Cook "Z Stent") or certain cobalt-based alloys (BSC "WallStent"), offer limited design options. While the WallStent offers excellent wall coverage and flexibility, its shortcoming is its length change during deployment of up to 53.8%, making the newer design [Table 2] more superior.

Self-expandable stents, constrained within a covering delivery sheath, are delivered to the site of stenosis. Withdrawal of this sheath uncovers the stent, which then reassumes its original shape (the chosen diameter) to dilate the stenotic lesion. As these stents do not require a balloon for expansion, they can be delivered through a lower-profile delivery system. Compared with BES, they are more flexible and thus can be passed through very tortuous vessels and lesions, but have significantly lower radial strength. They are made from nitinol (nickel- titanium alloy) and are therefore fully MRI compatible. Because of the unique memory effect of nitinol, they show a delayed 10-20% additional expansion within the first month following implantation. This might partially compensate for the development of more neointimal hyperplasia [34] than with conventional BES. This unfavorable increased neointimal induction might be due to a cytotoxic effect of corrosion products of nitinol which have been shown to induce smooth muscle cell necrosis during the in vitro study. [35]

Traditionally, they have been used for peripheral vascular applications, where external compression can permanently deform a stainless steel stent, but not the nitinol thermoelastic stent. Their main disadvantage is that they cannot be further dilated to accommodate vessel growth. Therefore, use of this type of a stent in growing children is limited [34],[35],[36],[37] unless implanted in structures that are fully grown or do not show any growth potential, such as a surgical shunt, a baffle or a conduit.

Self-expandable stents currently used in CHD are listed in [Table 2].


   Stent Implantation for Specific Lesions Top


Stents in the pulmonary arteries

Overview

PA obstructions occur in both congenital and acquired disease and they are found as isolated or multiple lesions, discrete stenosis or diffuse hypoplasia. Genetic syndromes such as Williams or Allagille are associated with such obstructions. They may be part of simple or complex cardiac malformations, such as ventricular septal defect, pulmonary valve stenosis, tetralogy of Fallot (TOF), pulmonary atresia and others. The majority of the acquired lesions are remnants after surgical procedures in complex heart defects. Thus, stenoses may develop as a result of extensive scarring at a previous PA repair site or at the anastomosis between the PA and a conduit or along the aortopulmonary shunt. Sometimes stretching of vascular structures may contribute to formation of stenosis, as seen following the LeCompte maneuver for repair of d-TGA. Such examples indicate that the underlying etiology and thus the pathomechanism of the obstruction differ from case to case. Therefore, optimal therapeutic strategies, based on case characteristics, should be adapted. Universally accepted indications for intervention include symptoms, right ventricular systolic pressure of more than 50% of systemic systolic pressure, right ventricular dysfunction and significant differential pulmonary perfusion in unilateral stenosis. Non-invasive imaging, such as MRI or echocardiography, [38] are useful tools for monitoring patients with suspected problems and can be used to determine the optimal timing for interventions in the absence of symptoms. [38]

The disappointing results of surgical management of branch PA stenoses led to the introduction of balloon angioplasty in the early 1980s. [39],[40] With standard balloon angioplasty, an immediate success rate - most often defined as an increase in vessel diameter of more than 50% - of 32-72% has been reported. [41],[42] Reasons for acute failure of balloon dilation include resistance to vessel tears or disruption, as evidenced by persistent waist in the balloon, compliant lesions expanding with angioplasty but recoiling to the original diameter and narrowing caused by asymmetric compression from the adjacent structures. Stenoses in the lobar PA branches have been shown to be particularly resistant to conventional balloon angioplasty and are more likely to require the use of high-pressure balloons. [43] During long-term follow-up, restenosis occurs in up to one-third of all patients [44],[45] as a result of natural tissue recoil and subsequent scarring. Because of unpredictable and unsatisfactory long-term results following surgery and plain balloon angioplasty, PA stenting was introduced in 1991. [41],[46] Subsequent follow-up studies demonstrated that stents maintain long-term vessel patency [47],[48],[49] and can be further dilated at subsequent catheterizations. [48],[50],[51] In the meantime, intraoperative placement of stents under direct vision as a hybrid procedure has completed the spectrum of PA stenting. [52],[53],[54]

Indications and use of stents for dealing with PA stenosis have increased in recent times. Stents are mainly used to deal with origin stenosis occurring naturally or after previous surgery, kinking or tenting of the branch PA, external compression of the branch PA, elastic recoil, intimal tear after balloon angioplasty and recanalization of totally occluded vessels. In infants with prior implantation of an RV-PA conduit, stenting is used as a bridge to delay conduit replacement. Although stents are commonly placed after previous balloon angioplasty, there are indications where primary stenting should be considered. These include long-segment stenoses, where balloon angioplasty shows unsatisfactory results, [54] subatretic stenoses, severe forms of PA coarctation, and bifurcation stenting.

Central PA stenting

There are numerous published papers demonstrating excellent mid- and long-term results [55] after stenting of post-operative or congenital branch PA stenosis. [47],[48],[49],[ 50],[55] Therefore, PA stenting is now widely accepted as the first-line therapy of central PA stenoses. If there are additional lesions such as a (residual) VSD, which are not suitable for interventional therapy, a hybrid strategy with intraoperative stenting under direct vision or with fluoroscopic or endoscopic guidance may be beneficial. [52],[53],[ 54] This avoids difficult surgery on fragile pulmonary arteries, shortens time of cardiopulmonary bypass and makes the pulmonary arteries amenable to future percutaneous interventions. The kind of stent to be implanted depends on the anatomic situation, the age and size of the patient and the vascular access status. Usually large stents that may be redilated up to at least 18-20 mm to accommodate somatic growth in children are preferred. Our current choices for central branch stenoses are "modern" low-profile stents like the Palmaz Genesis XD™ stent or the Mega LD™ or the CP stent using a long-sheath access. If the transvenous approach fails due to unfavorable anatomy, a direct access to the branch pulmonary system using a left or right anterior small thoracotomy may be considered for successful stent deployment. [56] In very small children (below 10 kg), a palliative approach may be adequate to avoid early reoperation in complex defects. [57],[58] An example would be the implantation of a pre-mounted Genesis medium stent (Cordis) for treatment of early PA restenosis after corrective surgery for TOF. Advantages of these pre-mounted stents are their good deliverability without the need of a long sheath and the very low and flexible profile (5-6 F). Of course, these stents have to be removed later by the surgeon, but stenting can postpone surgery to a later point. [57],[58] The presence of a stent in the pulmonary arteries does not seem to interfere with suture lines during subsequent surgery. [52],[57] Incising across the stent and suturing through their interstices usually do not present a significant problem to the surgeon. Conduits have been connected to previously stented pulmonary arteries in Fontan completion without problems. [58]

The incidence of significant restenosis of single-vessel PA stents has been reported to be 1.5-7% in large pediatric series. [48],[50],[55] Two factors are involved: The first is intimal hyperplasia of more than 1-2 mm, particularly at the edges of the stents, at gaps between two stents with diameter mismatch and in lumina < 6 mm; the second is stenosis where no further growth is expected, depending on the initial age and size of the patients. It has been documented by various groups that redilation under these circumstances is a safe and efficient procedure even 10 years after initial stent application. [51],[59],[60] Considering these data, an intended staged serial dilatation is sometimes advisable to avoid vessel overdilatation that is considered to accelerate neointimal proliferation.

Interventional treatment of bifurcating stenoses in the PA involving either the proximal branch or lobar branch vessels can be technically challenging. Standard balloon angioplasty alone is often inadequate and placement of stents is frequently required to relieve obstruction. In such bifurcating pulmonary stenoses, a simultaneous approach (simultaneous stent placement in two or more adjacent pulmonary arteries) is in our view mandatory and has been described previously. [61],[62] The advantage of simultaneous placement is to prevent crushing of the proximal portion of a stent placed in the contralateral vessel, which could cause obstruction to that vessel and make access to the vessel for further intervention quite difficult or impossible. [62] Depending on the size of the vessels involved, "modern" large (Mega LD, Palmaz Genesis XD or CP stent) or extralarge stents are currently used. Our first choice would be the CP stent as it has enough flexibility for good vessel adaptation and has round edges at the "kissing point" of both stents. In very small children, a tightly crimped Mega LD stent (using a crimping device) might be an option as we have been able to deliver this through a 6 F long sheath (on a 6 mm Powerflex P3™ balloon, Cordis). In a recently published long-term study, the restenosis rate was higher in bifurcational stenting (31.8%) compared with singe-vessel PA stenting. [62] The reason for this is unclear but factors such as greater distortion of the vessel walls at the bifurcation after stent implantation, increased exposure of metallic surface of two stents at the bifurcation points or increased turbulence of flow at the bifurcation areas leading to significant intimal proliferation may play a role. [62] Repeat balloon angioplasty or additional stent implantation usually solves the problem.

Distal PA stenoses are usually multiple and represent complex lesions that are not accessible to the surgeon. [63] The smaller pre-mounted Genesis Medium stents (Cordis), although not suitable for more central or proximal branch pulmonary arteries, are very suitable for stenoses beyond the first branching of the right or left PA. With bi/multisegment hilar PA stenoses, a simultaneous approach comparable to the bifurcation stenting is often favored. [6] Therefore, if a side branch arising from a previously stented vessel is stenotic or its origin has been compromised, transcatheter dilation or even stent placement may be necessary. In these circumstances, the open cell design (e.g. IntraStent DoubleStrut LD™, Mega LD™) allows stent placement through the sides (cells) of a previously placed stent. [64] For the smaller pulmonary side branch vessel, pre-mounted stents (Plamaz Genesis medium or larger coronary stents) are usually adequate. If the peripheral PA stenosis is resistant to conventional high-pressure balloons (evidenced by persistent waist), the use of cutting balloons (Boston Scientific, IVT, San Diego, CA, USA) has been shown to be successful. Usually, the intimal dissection caused by the microblades is well tolerated. [29] Although the initial gain in the transluminal diameter is usually maintained during follow-up, [30] some patients still require stent placement.

Stenting of right ventricular outflow conduits

Failure of a bioprosthetic right ventricle-to-pulmonary artery conduit has been well documented and may require repeat surgical conduit replacement. Pathomechanisms involved are external compression (usually by the sternum), calcification, kinking, development of fibrotic intimal peel and aneurysm. In addition, conduit diameters are limited and young patients may outgrow the diameters. Balloon dilatation of stenotic valves has shown poor results, with minimal extension of the life span of the conduit. [65],[66] Thus, stent implantation has been shown to avoid or postpone surgical repair [47],[67],[68] by accepting high-degree pulmonary insufficiency. In contrast, recently introduced PPVI (Melody™; Medtronic, Minneapolis, MN, USA) treats both pulmonary stenosis and regurgitation with excellent immediate and long-term results [69] and has therefore has replaced the RVOT stent. PPVI is now considered the therapy of choice for stenotic RVOT conduits in selected patients.

Potential complications in PA stenting

Potential complications with PA stent deployment occur in 4-5% and include stent migration (2.4%), stent malposition, intimal flap obstruction, jailing of side branches, stent fracture, dissection, aneurysm, vessel rupture, hemoptysis (1.5%), thrombosis of stent, ipsilateral pulmonary edema (1.5%) and death (1.5%). [55] In a retrospective long-term survey over 12 years, no mortality or morbidity was observed for the last 4 years due to improvements in technology and material. [55]


   Stenting the Aorta Top


Stenting in coarctation of the aorta

Balloon dilation of aortic recoarctation (Re-CoA) was introduced in 1982 as treatment for post-operative restenosis after surgical repair with subsequent hypertension. [70],[71],[72] Intimal and medial vessel wall tears, aneurysm formation, residual CoA and Re-CoA are well known complications encountered at follow-up in patients with residual or native CoA treated with balloon dilation. [73],[74],[75] The incidence of early and late aneurysms after balloon angioplasty has been reported to be between 5 and 11.5%. [70],[74],[76],[77],[78],[79],[80] Increasing age has been found to be a risk factor for a suboptimal outcome. [81] This has been attributed to the presence of fibrotic changes in the aorta secondary to long-standing obstruction, [74],[77] and cystic medial necrosis observed after percutaneous balloon angioplasty of CoA as potential factors contributing to adverse consequences, such as Re-CoA and aneurysms. [82] Since the early 1990s, BES have been used in the treatment of CoA in children. [10],[83],[84],[85],[86],[87] The apposition of the torn vessel intima to the media and the ability to perform redilatation to accommodate the patient's somatic growth are the key features. Although they were initially used to reduce vessel wall disruption, aneurysm formation after stent implantation or aortic dissection after stent dilatation have been encountered in up to 5% of the patients. [74],[88],[89] These complications are inevitable consequences of the mechanism of dilation of the CoA site and so cannot be completely abolished. The perceived advantages of stenting compared with pure ballooning are the ability to expand a tubular long-segment coarctation or an hypoplastic isthmus and distal transverse aortic arch, to increase the diameter of the coarcted segment independent of the intimal tear, to decrease the prevalence of restenosis and to prevent aneurysm formation because of support to the weakened aortic wall segment by the stent. With growing experience in current studies, success rates approach 100%. [10],[26],[76],[81],[83],[85],[86],[87],[89],[90],[91] In the largest multicenter studies yet published with over 500 patients, acute complications have been reported in up to 14% of the patients. The patients above 40 years represent a high-risk group with 31% incidence of complication. Common complications include vessel disruption, [81],[86] displacement of the stent [81],[83],[86],[92] and aneurysm formation. [86],[92] Stent migration is the most frequently encountered technical problem, with an incidence of up to 5%. [81],[91] Balloon rupture with inadequate stent expansion [81],[83] may be prevented by avoiding kinking of the balloon/stent assembly by the use of newer stents with softer ends [81],[91] and by the use of BIB systems. [81],[91] Injury to access vessels with bleeding from the puncture site [81] (2.3%) is a consequence of the large sheath size required. Bleeding can be avoided in adults, using vascular closure devices like the 6 F Perclose ProGlide™ or A-T™ (Abbott Vascular Devices, CA, USA). With these techniques, safe and effective closure of the femoral access site can be performed up to 14 Fr and even higher. [93] Loss of pulse following femoral vessel closure is of course more likely to occur in patients under 6 years of age. [91] It is our practice, when there is loss of pulse after catheterization, to institute thrombolytic therapy with a bolus of recombinant tissue plasminogen activator (rtPA) that can be repeated after 6 hours Retroperitoneal hematoma due to high puncture point is rare. [81],[91] Cerebrovascular accidents have been observed in up to 1%. [81],[91] Stent migration is the most frequently encountered technical problem occurring in up to 5%. [81],[91] Balloon rupture with inadequate stent expansion [81],[83] may be prevented by avoiding kinking of the balloon/stent assembly by the use of newer stents with softer ends [81],[91] and by the use of BIB systems. [81],[91] Because of post-stenotic dilatation, the stent might not always completely adapt with its distal segments; usually, this is not critical, if good anchoring has been achieved in the proximal half to two-thirds of the stent. Some degree of apposition may be achieved with further flaring of the distal (and proximal) parts with larger balloons, but this carries the risk of stent migration. Sometimes with Re-CoA high-pressure balloons are necessary, but this condition is better dealt with by covered stents (this is addressed later). In severe native or even post-operative CoA, we often avoid full dilatation of the stent at the initial procedure in an attempt to minimize vascular damage, uncontrolled intimal tear and aneursym formation. [9],[23] Furthermore, a residual waist better secures the stent in its final position, thereby reducing the risk of stent migration. After complete endothelial healing (about 6 months later), full-stent dilatation to the desired size (usually the diameter of the pre-stenotic aortic arch or the descending aorta at diaphragm level) can be performed. [9],[23] Especially in native CoA, which might be relatively elastic, we usually avoid pre-dilatation with a balloon so that better anchoring of the primary implanted stent can be achieved. Aggressive pre-stent angioplasty could also increase the likelihood of later aneurysm formation. [81],[91] Large stents are needed for stenting CoA. Traditionally, the large Palmaz stents like the P8 and P10 series are the most commonly used stents in large multicenter studies. [81] Our first choice now is the CP stent [9] or the IntraStent Mega and Maxi LD (EV 3) as those stents are more flexible and can be easily dilated up to adult vessel diameters (20-25 mm) [Table 1]. The Genesis XD (Cordis) stent might also be suitable, but can only be dilated up to 18 mm. The innovate Andrastent - the first peripheral cobalt chromium stent - can be dilatated up to 25 mm in the XL and up to 32 mm in the XXL version. Thus, it may be very suitable for CoA treatment as has been described by De Giovanni (GUCH Unit, University Hospital, Birmingham, UK, personal communication). The chromium-cobalt technology allows very low profile designs and the hybrid closed/open cell design may be very helpful when placing the stent in a curved part of the aorta, but more experience is needed.

Redilatation in CoA

In general, CoA redilatation demonstrates good intermediate follow-up results. [91],[94] Aneurysm formation occurs in up to 9% of all patients, but often reintervention is not necessary. Recurrence of stenosis has been reported in around 11% of all patients. In general, there are two conditions leading to restenosis and late failure after primary successful stent implantation. One is "full-growth" stenosis, depending on the initial age and size of the patient. The other is hyperplasia of the endothelial intima of the vessel. Narrowing of the lumen by 1-2 mm is seen in all cases, but true intimal hyperplasia in less than 25% of patients. [86],[94] Risk factors promoting neointimal proliferation include younger age, lower weight and recurrent CoA [86],[94],[95] as well as stent overdilation, minimal stent overlap and sharp angle between the stent and the vessel wall. [60] Newer stent designs that are more flexible and thus show better adaptation to the vascular wall might induce less neointimal layer formation. In the largest reported series of stent procedures for CoA redilatation (28 patients), 93% success rate has been reported. [96] Four main factors could be identified contributing to the failure of CoA stent redilatation: Severe neointimal hyperplasia, a history of surgical CoA repair, the association of Williams syndrome and the rare occurrence of aortic wall dissection. [96] Drug-eluting stents (Koch, Ludwig et al. 2007; Riede, Schneider et al. 2007; Jhang, Chang et al. 2008; Wong, Yoo et al. 2008) or systemic administration of anti-proliferative drugs such as everolimus may theoretically overcome some of these problems, [97] but no sufficient data have yet been published. In conclusion, redilatation is unproblematic, safe and effective but limited by the maximal stent diameter. [96]

Covered stents and self-expandable stent grafts in CoA

In 1999, the first covered stent was used to treat coexistent CoA and aneurysm of the aorta in a young man. [98] Aneurysm formation, which has been described after both surgical [99] and endovascular treatment and dilatation, [100] is clearly associated with increased risk of aortic rupture. Covered stents [9],[11],[12],[17],[18],[22],[25],[98] or endoluminal stent grafts [101],[102],[103] have been successfully used in the management of aortic aneurysm in an effort to reduce the need for repeat surgery. The main disadvantage of stent grafts (e.g. the Valiant™ endoprosthesis; Medtronic, Minneapolis, MN, USA) is that they require large (22-25 F) vascular sheaths, [12] in contrast to the use of 12-16 F Mullins-type delivery sheaths with the most widely used covered CP stent.

Aneurysm formation may occur even after redilatation of a previously implanted uncovered stent; [96] the stent design and the aggressive protocol of redilatation might play a decisive role. However, the availability of covered stents can help to overcome this complication. Another potentially catastrophic complication of balloon angioplasty and stenting in CoA is aortic disruption [88],[104] and the risk is increased in elderly patients. [81] It may even occur after covered stent implantation. [11],[105] Aortic disruption may be managed in an emergency by the deployment of a (additional) readily available covered stent. [11],[105] Stent fracture is a well described but uncommon complication after CoA stenting, affecting even the CP stent with reinforced welded sites. [9],[18] It may be associated with recurrent CoA. In the case of a fractured stent disrupting the aortic wall at the level of the fracture margins, the use of covered stents could potentially seal any endothelial disruption.[11],[18] Besides emergency or rescue indications, covered stents for CoA are being preferentially deployed in the treatment of associated aneurysm, tight/subatretic native CoA, [13],[17],[18],[23] associated arterial duct or collateral vessel [17],[18],[21],[24] and in older patients, due to the potential for aortic disruption with advanced age. [11],[18],[22],[26],[90] They have been also recommended for patients with associated prominent dilatation of the aorta, suggestive of an aortopathic process like in bicuspid aortic valve. [12] Some operators have gone as far as to exclusively use covered stents in preference to bare stents in all cases of adolescent and adult CoA and Re-CoA, although this is not yet common practice. Theoretically, the ability to fully expand the covered stent while providing a degree of protection in the event of aortic wall disruption allows optimum dilatation of the stent thereby preventing migration and decreasing the risk of vessel recoil and recurrent CoA. To date, the covered CP stent is the most widely used covered stent in pediatric and CHD patients. [9],[11],[12],[13],[14],[15],[16],[17],[18],[19],[20],[21],[22],[23],[24],[25],[26] It may be used in children as redilatation is possible to accommodate somatic growth. [15],[16] Use in children is, however, limited due to the bigger sheath access, with increased risk of vascular injury. Thus, the sheath has to be chosen 3 F larger than required for the introduction of the balloon catheter, which is one reason why covered stents are currently used mostly in the adult size population. Our current benchmark with the CP stent in CoA is weight of around 15 kg.

One obvious limitation of covered stents is their potential to cover side branch vessels during deployment, usually the subclavian artery ostium. Jailing of subclavian artery is usually well tolerated without functional deficit but an intact vertebrobasilar system should be documented to avoid subclavian steal. [10],[92] To circumvent complications in the case of insufficient "aortic margin," uni- or even bilateral surgical reimplantation of the subclavian arteries end-to-side into the carotid arteries should be considered before stenting as this creates a stable "landing zone" for subsequent stent deployment. [12] Recanalization by perforating the covering of the CP stent followed by balloon angioplasty or side branch stenting might be another option to access trapped side branches. [106] Occlusion of side branches distal to the coarctation site may be more serious with spinal artery occlusion leading to paraplegia, as previously described using long stent grafts. [107] However, the spinal artery usually originates below the level of the ninth thoracic vertebra from the aorta below the diaphragm; [108] therefore, spinal artery occlusion is unlikely to occur. But, operators should keep in mind that stent migration with fixation of the dislocated stent by redilation in a smaller distal area of the aorta as a rescue procedure might potentially occlude critical side branches that it crosses.

Although covered stents are primarily used for CoA treatment, they might be applied to other vessels. Thus, the use of a covered 8-zig CP stent for treatment of post-operative RVOT has been reported [109] Baffle leaks associated with baffle obstruction after atrial switch procedure may be successfully abolished. [14] One of the most innovative concepts is the "rebuilding" and "creation" of an internal venous tunnel with long and covered CP stents for completion of Fontan circulation in the catheterization laboratory. [20] Although the use of covered stents in the pediatric population is restricted by the need for larger sheaths, covered CP stents may be successfully applied in growing children. It has been demonstrated that those stents may be redilated up to 25 mm diameter as the ePTFE covering is quite abundant, very elastic and does not induce an inflammatory reaction. [15],[17],[18],[19]

Complex aortic arch lesions

With increasing experience in CoA stenting, the concept has been extended to the treatment of complex stenoses of the aortic arch and the descending aorta. [9],[17],[110] It has been shown that stenting of complex aortic arch lesions through the whole aortic arch can be performed safely and effectively with excellent, immediate and midterm results. Holzer et al. described an improvement to more than 90% of the "normal" adjacent aortic arch. [110] Patients with weight below 10 kg or after hybrid stage I palliation may be at increased risk of adverse events such as peripheral vascular complications or hemodynamic instability requiring administration of inotropes and/or chest compression. [110] Because of anatomical restrictions, overstenting of major arch vessels may be necessary, but is usually not problematic, as long-term follow-up demonstrated no compromise of distal perfusion in otherwise normal vasculature. [9] We primarily use the 8 zig CP stent, usually uncovered, as it has sufficient radial strength, flexibility and large cells to allow side branch flow. [9] The availability of the stent in many different lengths allows excellent adaptation to individual aortic anatomy and enables its use even in small children. [9] Alternatively, the Mega and Maxi LD (EV3) offer good options as they have even more radial strength with similar flexibility. The open cell design favors side branch access and, due to its low profile, sheath size 1-2 F less may be needed than for the CP stent. Stenting of trapped vessels through the stent cells is usually possible, if needed. [7],[64]

Stents in the systemic venous system

Several conditions may lead to stenosis of systemic veins, including superior and inferior caval vein obstruction occurring after atrial switch operation or cardiac transplantation, uni- or bidirectional Glenn anastomosis and total cavopulmonary connection, correction of anomalous pulmonary venous connections and the presence of transvenous pacing electrodes or central venous catheters. [111],[112],[113] As balloon dilatation may not be effective in these lesions, stent implantation represents an attractive treatment concept that was introduced nearly 20 years ago. [111] Usually, the presence of symptoms in association with a stenotic lesion makes an intervention necessary. Baffle obstruction following atrial switch operation (Mustard and Senning operation) is the most common indication for stent delivery in the venous system. Most studies show favorable results with relief of clinical signs of obstruction and improvement in pressure gradients and angiographic appearance. [14],[37],[112],[113],[114],[115],[116],[117],[118],[119],[120],[121],[122],[123],[124],[125],[126] We successfully recanalized an atretic superior caval vein with two covered 8 zig CP stents in a Mustard patient with transvenous pacing leads. Complete relief of superior caval vein congestion could be achieved. The use of covered (CP) stents should be considered in subatretretic or atretic lesions [117],[127] or if additional baffle leaks are present. [14] These stented vessels may accommodate newly placed pacing electrodes, but this carries a higher risk of recurrent stent occlusion. [128] Pulmonary venous baffle obstruction might also be addressed by stent therapy, but is technically more challenging. [119],[126] Rarely, patients who have undergone orthothopic heart transplantation may present with stenosis at the site of venous anastomosis that can be successfully treated by stent therapy. [129] Baffle fenestrations in total cavopulmonary connection may be closed using covered stents, [130] especially in the presence of a baffle stenosis. [123] The stenting of central pulmonary vessels after Glenn or Fontan procedure represents a very special situation as passive flow in the pulmonary arteries depends on optimal flow conditions. In those cases, any obstruction within the pulmonary circulation should be definitely abolished. [9] Although the use of self-expanding stents has been reported, [37] BES has become the treatment of choice for these systemic venous obstructions. We prefer 8 zig CP stents and those with modern open cell designs like the Mega or Maxi LD series (EV3) because they are less rigid, have smoother margins compared with older designs and are thus less traumatic to the thin venous vessel.

Stents for pulmonary vein stenosis

Pulmonary venous stenosis may be congenital or acquired after cardiac surgery. It is reported after repair of anomalous pulmonary venous return in about 10% of the patients. [131] Sutureless marsupialization that avoids any stitches in the cut edges of the pulmonary veins is now considered the best surgical approach, [132] but freedom from reoperation or death at 5 years is still only ≈50%. These stenoses are almost resistant to balloon angioplasty, [132],[133] although the use of cutting balloons (Boston Scientific, IVT, San Diego, CA, USA) may be beneficial. [134] Stenting initially seemed very appealing, but restenosis has been universal. [132],[135],[136] As the transcutaneous approach may be difficult, especially in small children, intraoperative placement of stent may be an alternative mode of delivery. [52],[137] Unless stent placement is considered to be a strictly temporary measure, only stents that allow future expansion to adult dimensions (> 12 mm) should be used. Therefore, stents like the pre-mounted Genesis medium stents (Cordis) may be a good choice. Compared with secondary stenosis, the so-called "congenital pulmonary venous stenosis" is an entity of its own, with an even more malignant course. Long-term results of surgery and stent treatment are very disappointing. Thus, stent therapy usually is of a palliative nature [52],[132],[138],[139] and may serve as a bridge to lung transplantation. [140]

Stents to ensure patency of intracardiac communications

For some complex congenital heart defects, an unrestrictive ASD is essential for adequate blood mixing at the atrial level or relief of right or left atrial hypertension to achieve an adequate cardiac output and/or systemic saturation. Transcatheter creation or enlargement of an ASD is usually achieved employing techniques including transeptal puncture or radiofrequency perforation (in the case of intact septum), balloon or blades septostomy and static balloon dilatation of the interatrial septum (IAS). However, due to the increased thickness of the IAS in infants beyond the neonatal period or in neonates with hypoplastic left heart syndrome, the use of those techniques may be ineffective to achieve and maintain an adequately sized communication. Therefore, atrial septal stent implantation has been successfully applied to promote a durable unrestrictive ASD. [32],[33],[141],[142],[143],[144],[145] The prior use of cutting balloons (Boston Scientific) may be helpful, [32],[33] as the microsurgical blades of the cutting balloon allow controlled tearing of the septal wall rather than stretching of the thickened ASD as seen with static balloon dilation. [33],[145] We and other authors in most cases use pre-mounted Palmaz-Genesis stents (Cordis; Johnson and Johnson, Miami, FL, USA) ranging from 7 to 8 mm in diameter and from 12 to 26 mm in length. Sometimes shaping the stent by redilating with a bigger-sized balloon to create a "diabolo" configuration secures the stent and avoids stent migration. Close follow-up is necessary as thrombus formation and progressive obstruction may occur. [32] Failing Fontan circulation is another modality where fenestration may be beneficial. Thus, the use of covered and non-covered stents has been described to maintain patency of the newly created communication. [146-149] Covered stents may have the potential to reduce the acute risk of bleeding. [148]

Stents in the arterial duct

In duct-dependent CHD, ensuring patency of the arterial duct may be a life-saving procedure. Stenting the arterial duct in defects such as pulmonary atresia, right ventricular hypoplasia, critical pulmonary stenosis, TOF and other complex lesions with reduced pulmonary blood flow may avoid (emergency) surgical shunt. The concept of stenting the ductus arteriosus to increase pulmonary blood flow in cyanotic neonates began with the arrival of stents designed for coronary arteries in the early 1990s. [150] Unfortunately, this strategy lost favor due to delivery systems being relatively stiff and articulated stent designs that resulted in early restenosis. [151] With the availability of new stent designs and catheter technology (low profile, flexible, pre- mounted stents with good scaffolding), better patient selection and preparation, optimal interventional access and covering of the complete length of the duct, results have significantly improved. [152],[153],[154],[155],[156] Transcatheter procedures have an advantage with respect to subsequent surgery since there is no scar tissue in the chest from previous thoracotomy or sternotomy. Usually the stent itself presents little surgical challenge. In our recent practice, we have opted for ductal stenting in the presence of special circumstances such as severe hypoxemia unresponsive to conservative treatment, unfavorable anatomy with ductal coarctation, children of Jehovah's Witnesses or others. In addition, implantation of stents represents an attractive alternative for reoperation in neonates and infants with acute complications after surgical creation of a systemic-to-pulmonary arterial shunt. [157] In most cases, balloon-expandable bare metal stents are utilized. For duct-dependent pulmonary circulation lesions, the stent should be expanded to 3.5-5 mm depending on the size of the patient. Any coronary stent (e.g. Libertι stent; Boston Scientific, Natick, MA, USA) or other pre-mounted low-profile stent can be used. The Palmaz Genesis medium stent is currently our first choice. Overlapping may be necessary to cover a long and tortuous duct. In the case of duct-dependent systemic circulation - usually in the hybrid approach for hypoplastic left heart syndrome - a stent size of 6-10 mm might be necessary. Therefore, self-expanding stents (e.g. PROTÉGÉ™ GPS™ Stent, EV3) are generally preferred. [158],[159]

RVOT stenting as a pallitative treatment

In severe forms of TOF with PA hypoplasia, critical RVOT obstruction and the presence of MAPCAs major aortopulmonary collateral arteries (MAPCA), primary repair may not be possible. For such a two-staged repair, early surgical options include a central aortopulmonary anastomosis, a modified Blalock-Taussig anastomosis, an RV outflow patch or ductal stenting as discussed in the previous section. In selected cases, RVOT stent implantation may be another alternative to surgical palliative treatment in order to achieve sufficient oxygen delivery and to induce PA development through pulsatile flow. [160],[161] RVOT stenting may also be considered after high frequency (HF) perforation in pulmonary atresia. [162] Because of the small size of these children, pre-mounted coronary or biliary stents like the Palmaz Genesis medium on Slalom balloon are preferred. [161] Although many of these stents cannot be dilated to adult size (coronary stents usually up to 4-6 mm, depending on the type, the Palmaz Genesis up to 12 mm), their efficacy in small infants (even premature [163] ) and children in whom further surgery will ultimately be required makes them desirable for this group of patients. [57],[161] Usually stents that are located in the RVOT are easily removed at the time of conduit replacement. [57] Those in the proximal PA can also be removed or cut open allowing for PA augmentation. [57] We successfully transferred the palliative concept of RVOT stenting in very small children to an adult patient (27 years) with pulmonary atresia, VSD and MAPCAs. After HF perforation of pulmonary atresia, several CP stents were implanted in the newly opened RVOT and a significant growth of the central pulmonary arteries could be achieved. The high forces from the hypertrophied muscular RVOT led to multiple stent fractures - a common feature with RVOT stent [164],[165] - resulting in loss of stent integrity, insufficient scaffolding of RVOT and subsequent restenosis so that serial stent-in-stent implantation was necessary. In total, we implanted four CP stents (two covered, two uncovered, maximum length 55 mm) over a period of 28 months. Thus, a communication of 20 mm diameter between the right ventricle and the PA was established, allowing the interventional closure of two MAPCAs with competitive flow. The development of the central pulmonary arteries with this concept was a tremendous success so that the patient is now awaiting corrective surgery. Although not observed in our patient, stent fragment embolization within 2 months of implantation has been described and vigilant follow-up is recommended for RVOT stents. [164]

Stenting aortopulmonary collateral arteries

Stenosis of aortopulmonary collateral arteries is common and frequently progressive in patients with unrepaired pulmonary atresia and ventricular septal defect, leading to severe hypoxemia and limitation of exercise capacity in up to 58-68% of the patients. [166] Surgical creation of a new aortopulmonary shunt may provide short-term palliation but may be associated with significant morbidity and mortality. Balloon dilation alone is usually not helpful as it produces minimal change in vessel caliber and no improvement of flow. [167] Therefore, stenting of stenosed aortopulmonary collaterals has become an attractive alternative resulting in significant clinical improvement. [167],[168],[169] As these stenoses tend to be extremely hard and thus resistant to high-pressure balloons, the use of a cutting-balloon catheter before stenting might be helpful. [31] Pre-mounted stents with high radial force (e.g. Genesis medium stents, Cordis) are necessary. We have observed radial stent fractures requiring repeat stent-in-stent implantation. The rate of complications is low but includes vessel rupture with pulmonary hemorrhage, dissection, aneurysm formation, vasospasm and occlusion of the arteries. [31],[167],[168],[169]

New developments in stent design and future perspectives

There are some recent developments in technology intended to overcome some of the disadvantages of currently used stents.


   Biodegradable Stents Top


Overview

As scaffolding is necessary to overcome late vessel remodeling only for a limited period - approximately the first 6 months following stent implantation - the concept of biodegradable stents has emerged. In addition to other advantages, this concept might solve one of the main problems in pediatric stenting - the adaption to growth. These systems should deliver a temporary longitudinal and radial straightening effect, offer better physiologic repair, allow reconstitution of local vascular compliance and should not restrict surgical or interventional revascularization thus allowing the possibility of growth and late positive remodeling. The ideal characteristics of a biodegradable stent have been defined as (1) sufficient radial strength to prevent vascular recoil, (2) minimal thrombotic and inflammatory response, (3) avoidance of intimal proliferation, (4) reabsorption of stent components within months, (5) no release of toxic products or embolic material during breakdown and (6) easy processing and sterilization. Based on these considerations, two different concepts have evolved: Absorbable polymer stents and absorbable metal stents.

Polymeric stents

There are several polymeric degradable stents in development but just a few merit mention at this stage on the basis of clinical data. The BVS stent (Abbott Laboratories, Abbott Park, IL, USA) is made from poly-L-lactic acid (PLLA) and results from clinical trials were recently published. [170],[171],[172] While the study demonstrated feasibility, it was a very small patient population (30 patients) and the degradation rate was slow (more than 1 year), which some consider to be one of the drawbacks of polymeric biodegradable stents. One of the earliest devices in this field was the Igaki-Tamai coronary stent (Kyoto Medical Planning Co., Kyoto, Japan), which is also manufactured from PLLA with a zigzag helical coil design. [173] A small trial (15 patients) with 6 months follow- up showed no pronounced intimal hyperplasia, unlike in stainless steel stents. Interestingly, there was evidence of vascular remodeling at the stented site, with an increase of the stent cross-sectional area associated with a decrease in the lumen cross-sectional area, although after the third month no further stent expansion was observed. [173] Although these promising findings demonstrated feasibility and safety, with acceptable efficacy in human coronary arteries, polymeric biodegradable stents have not yet been used in the pediatric population.

Magnesium alloy stents

The relative ease with which magnesium corrodes and its role as an essential element in the biological system makes it an excellent candidate for the biocorrosion concept. First data was published in 2003. [174] As an alternative to biocorrodible irons, magnesium alloys may offer several advantages. Their use has been tested in several trials in coronary arteries: Progress Trial [175] and BEST-BKT Trial. [176] The first report of implantation of absorbable metal stents in human use was in 2005, in a case of compassionate use to treat left PA stenosis as a hybrid approach, an absorbable magnesium stent (AMS, Biotronik™, Germany) was implanted by Zartner and coworkers in a premature newborn. It showed only mild intimal proliferation with no stent-related inflammatory reaction. [177],[178] Later, Schranz and coworkers demonstrated the use of the same stent for acute treatment of a newborn with severely impaired heart function due to a long-segment Re-CoA after complex surgical repair. [179] In this patient, early restenosis was due to accelerated degradation. Similarly, significant restenosis was observed 4 months after implanting a biodegradable magnesium stent within a stenotic aortopulmonary collateral in a 2-month-old girl with pulmonary atresia. [180] Another major disadvantage of AMS is the lack of radioopacity, which means that the stent is not visible during positioning, expansion and after balloon retrieval, which might cause difficulties in the detection of embolized stent part and in precise placement of overlapping stent segments. [177],[178],[179] Despite these drawbacks, AMS is an attractive and promising future concept.

Iron stents

Limitations posed by biodegradable polymer and magnesium alloy stents, such as chronic inflammation and premature recoil, might be overcome by biocorrodible iron stents. The NOR-I Stent is a pure iron stent that has been implanted in an animal study, demonstrating low thrombogenicity, mild inflammatory response and no toxicity, no pronounced intimal hyperplasia and excellent patency, but a very slow degradation rate of several years. [181],[182] In addition, in vitro experiments showed that ions released from iron stents might reduce the proliferation rate of vascular smooth muscle cells by influencing growth-related gene expression and could therefore play a beneficial role in antagonizing restenosis. [183]

Limitations of biodegradable stents

All of the degradable technologies reviewed here have many specific challenges ahead of them, but, to date, common to all is the lack of clinical evidence demonstrating a clear advantage of this approach. Polymer systems face specific challenges in achieving adequate strength and resistance to recoil as well as a need to reduce degradation times. Magnesium systems appear to offer the most promise, with degradation times being closer to what may be required. Iron stents face big difficulties in terms of establishing that the degradation products would be acceptable.

Growth stent

Another interesting approach to overcome the "growth" problem is the development of the so-called Growth Stent. [184] It is made of two separate longitudinal halves of laser-cut and electropolished 0.16 mm stainless steel. The halves are connected with bioabsorbable sutures (Polydioxanon 7-0, PDS II, Ethicon, Norderstedt, Germany) to create a circular stent. The reabsorbable sutures will be completely absorbed after about 6 months. The stents are pre-mounted on dilatation balloons of 4-8 mm diameter (Tyshak II, Mini Ghost, or Tyshak Mini, NuMed Canada, Cornwall, Ontario) and they fit through a 5 F introducer sheath. [184],[185] After demonstrating feasibility of this "open-ring" stent concept within an initial animal study, [184] we successfully evaluated its clinical use in eight patients with aortic (Re-)CoA and four patients with stenosis of the aortic anastomosis after a Norwood I procedure. There was only one case of CoA in which early redilatation 3 months after implantation due to pronounced intimal hyperplasia was necessary. Six patients received a large stent after 19-34 months. In light of this promising data, a merely interventional concept for the treatment of native CoA in infants without the need of any surgery might evolve. Thus, the Growth Stent can be used as an effective bridge for infants to gain time until they have reached a body weight of 12-14 kg and can receive a larger conventional stent that will be able to be redilated in the future to adult sizes, i.e. larger than 20 mm in diameter (we recommend uncovered and covered CP stent or Mega LD™). Of course, long-term follow-up with more patients is needed and the results have to be compared with those of surgical therapy, still considered the gold standard in neonatal CoA. In the meantime, some of the observed problems, such as the absence of adaptive growth of the stented area, have to be addressed.

Surface processing and modification

Electropolishing is the state-of-the-art finishing process for nitinol implants, such as stents. Several studies have shown that electropolished nitinol surfaces exhibit better corrosion resistance, biocompatibility and overall surface quality than surfaces finished by other methods. [186],[187] Thus, the Growth Stent (Qualimed, Winsen/ Luhe, Germany) is finished through electropolishing. Such surface modifications might also lead to better biocompatibility of stents in CHD use, but currently no published studies exist. Another form of surface processing is the coating with drugs. The potential benefit of drug-eluting stents (DES) is attenuation of neointimal proliferation, which has been extensively described in adults with coronary arterial disease. [188] For use in CHD, implantation of DES has been reported in the arterial duct feeding an isolated left PA, [189] a conduit in the RVOT of an infant, [189],[190] the vertical vein of a supracardiac totally anomalous pulmonary venous connection, [191] an obstructed infracardiac totally anomalous pulmonary venous connection [192] and a pulmonary vein stenosis after orthotopic heart transplantation. [129] As most of the experience with DES comes from coronary stents in adults, the efficacy and safety of these devices in CHD and for pediatric use remain unknown. However, if the mechanism of restenosis is the same in coronary arteries and other vessels, these devices may hold future options for children with CHD.


   Conclusion Top


Over the last 20 years, the usefulness of stents in patients with CHD has become well established. Stent implantation is now considered to be a safe and effective method in relieving a wide variety of pre- and post-operative vascular stenoses not amenable to pure balloon dilatation. Thus, stent therapy is now considered to be the standard and first-line treatment for CoA in adults or post-operative PA branch stenoses. The majority of stent applications are intended to provide a long-lasting cure or reasonable palliation to avoid high-risk repeat operation. Thus, stents may now be used to ensure patency of naturally occurring (e.g. ASD or arterial duct) or artificially created intercirculatory communications. Because of a tremendous improvement in stent technology, the first-generation models like the original Palmaz stent have now been replaced by "modern" designs. But still the device that meets the requirements of an ideal stent for use in CHD patients remains to be developed. Thus, concepts for stent application in very small patients that allow adaptation for somatic growth until adulthood vessel size is reached are clearly needed. Another issue to be addressed is improvement of biocompatibility to avoid intimal hyperplasia and restenosis. Until these problems are solved, the crucial question in this interventional field still remains: Which stent(s) should we use for which lesion? To clarify these questions, anecdotal data are insufficient, underlying the clear need for large prospective trials to search for objective performance criteria. As the population with CHD is limited, independent objective multinational registries are needed. With these improvements, indications for stent treatment in CHD are likely to widen in the future.

 
   References Top

1.Rashkind WJ, Miller WW. Creation of an atrial septal defect without thoracotomy. A palliative approach to complete transposition of the great arteries. JAMA 1966;196:991-2.  Back to cited text no. 1    
2.Dotter CT, Judkins MP. Transluminal Treatment of Arteriosclerotic Obstruction. Description of a New Technic and a Preliminary Report of Its Application. Circulation 1964;30:654-70.  Back to cited text no. 2    
3.Dotter CT. Transluminally-placed coilspring endarterial tube grafts. Long-term patency in canine popliteal artery. Invest Radiol 1969;4:329-32.  Back to cited text no. 3    
4.Mullins CE, O'Laughlin MP, Vick GW 3rd, Mayer DC, Myers TJ, Kearney DL, et al. Implantation of balloon-expandable intravascular grafts by catheterization in pulmonary arteries and systemic veins. Circulation 1988;77:188-99.  Back to cited text no. 4    
5.O'Laughlin MP, Perry SB, Lock JE, Mullins CE. Use of endovascular stents in congenital heart disease. Circulation 1991:1923-39.  Back to cited text no. 5    
6.Rutledge JM, Mullins CE, Nihill MR, Grifka RG, Vincent JA. Initial experience with intratherapeutics Intrastent Doublestrut LD stents in patients with congenital heart defects. Catheter Cardiovasc Interv 2002;56:541-8.  Back to cited text no. 6    
7.Kreutzer J, Rome JJ. Open-cell design stents in congenital heart disease: A comparison of IntraStent vs. Palmaz stents. Catheter Cardiovasc Interv 2002;56:400-9.  Back to cited text no. 7    
8.Ing F. Stents: What's available to the pediatric interventional cardiologist? Catheter Cardiovasc Interv 2002;57:374-86.  Back to cited text no. 8    
9.Ewert P, Schubert S, Peters B, Abdul-Khaliq H, Nagdyman N, Lange PE. The CP stent--short, long, covered--for the treatment of aortic coarctation, stenosis of pulmonary arteries and caval veins, and Fontan anastomosis in children and adults: An evaluation of 60 stents in 53 patients. Heart 2005;91:948-53.  Back to cited text no. 9    
10.Cheatham JP. Stenting of coarctation of the aorta. Catheter Cardiovasc Interv 2001;54:112-25.  Back to cited text no. 10    
11.Tanous D, Collins N, Dehghani P, Benson LN, Horlick EM. Covered stents in the management of coarctation of the aorta in the adult: Initial results and 1-year angiographic and hemodynamic follow-up. Int J Cardiol 2008.  Back to cited text no. 11    
12.Kenny D, Margey R, Turner MS, Tometzki AJ, Walsh KP, Martin RP. Self-expanding and balloon expandable covered stents in the treatment of aortic coarctation with or without aneurysm formation. Catheter Cardiovasc Interv 2008;72:65-71.  Back to cited text no. 12    
13.Eicken A, Kaemmerer H, Ewert P. Treatment of aortic isthmus atresia with a covered stent. Catheter Cardiovasc Interv 2008;72:844-6.  Back to cited text no. 13    
14.Dragulescu A, Sidibe N, Aubert F, Fraisse A. Successful use of covered stent to treat superior systemic baffle obstruction and leak after atrial switch procedure. Pediatr Cardiol 2008;29:954-6.  Back to cited text no. 14    
15.Butera G, Gaio G, Carminati M. Redilation of e-PTFE covered CP stents. Catheter Cardiovasc Interv 2008;72:273-7.  Back to cited text no. 15    
16.Bruckheimer E, Dagan T, Amir G, Birk E. Covered Cheatham-Platinum stents for serial dilation of severe native aortic coarctation. Catheter Cardiovasc Interv 2008.  Back to cited text no. 16    
17.Butera G, Piazza L, Chessa M, Negura DG, Rosti L, Abella R, et al. Covered stents in patients with complex aortic coarctations. Am Heart J 2007;154:795-800.  Back to cited text no. 17    
18.Tzifa A, Ewert P, Brzezinska-Rajszys G, Peters B, Zubrzycka M, Rosenthal E, et al. Covered Cheatham-platinum stents for aortic coarctation: Early and intermediate-term results. J Am Coll Cardiol 2006;47:1457-63.  Back to cited text no. 18    
19.Butera G, Piazza L, Chessa M, Abella R, Bussadori C, Negura D, et al. Covered stents in patients with congenital heart defects. Catheter Cardiovasc Interv 2006;67:466-72.  Back to cited text no. 19    
20.Galantowicz M, Cheatham JP. Lessons learned from the development of a new hybrid strategy for the management of hypoplastic left heart syndrome. Pediatr Cardiol 2005;26:190-9.  Back to cited text no. 20    
21.Ewert P. Challenges encountered during closure of patent ductus arteriosus. Pediatr Cardiol 2005;26:224-9.  Back to cited text no. 21    
22.Qureshi SA, Zubrzycka M, Brzezinska-Rajszys G, Kosciesza A, Ksiazyk J. Use of covered Cheatham-Platinum stents in aortic coarctation and recoarctation. Cardiol Young 2004;14:50-4.  Back to cited text no. 22    
23.Ewert P, Abdul-Khaliq H, Peters B, Nagdyman N, Schubert S, Lange PE. Transcatheter therapy of long extreme subatretic aortic coarctations with covered stents. Catheter Cardiovasc Interv 2004;63:236-9.  Back to cited text no. 23    
24.Sadiq M, Malick NH, Qureshi SA. Simultaneous treatment of native coarctation of the aorta combined with patent ductus arteriosus using a covered stent. Catheter Cardiovasc Interv 2003;59:387-90.  Back to cited text no. 24    
25.Forbes T, Matisoff D, Dysart J, Aggarwal S. Treatment of coexistent coarctation and aneurysm of the aorta with covered stent in a pediatric patient. Pediatr Cardiol 2003;24:289-91.  Back to cited text no. 25    
26.de Giovanni JV. Covered stents in the treatment of aortic coarctation. J Interv Cardiol 2001;14:187-90.  Back to cited text no. 26    
27.Trerotola SO, Stavropoulos SW, Shlansky-Goldberg R, Tuite CM, Kobrin S, Rudnick MR. Hemodialysis-related Venous Stenosis: Treatment with Ultrahigh-Pressure Angioplasty Balloons. Radiology 2004;231:259-62.  Back to cited text no. 27    
28.Maglione J, Bergersen L, Lock JE, McElhinney DB. Ultra-High-Pressure Balloon Angioplasty for Treatment of Resistant Stenoses Within or Adjacent to Previously Implanted Pulmonary Arterial Stents. Circ Cardiovasc Intervent 2009;2:52-8.  Back to cited text no. 28    
29.Bergersen LJ, Perry SB, Lock JE. Effect of cutting balloon angioplasty on resistant pulmonary artery stenosis. Am J Cardiol 2003;91:185-9.  Back to cited text no. 29    
30.Bergersen L, Jenkins KJ, Gauvreau K, Lock JE. Follow-up results of Cutting Balloon angioplasty used to relieve stenoses in small pulmonary arteries. Cardiol Young 2005;15:605-10.  Back to cited text no. 30    
31.Mertens L, Dens J, Gewillig M. Use of a cutting balloon catheter to dilate resistant stenoses in major aortic-to- pulmonary collateral arteries. Cardiol Young 2001;11:574-7.  Back to cited text no. 31    
32.Pedra CA, Neves JR, Pedra SR, Ferreiro CR, Jatene I, Cortez TM, et al. New transcatheter techniques for creation or enlargement of atrial septal defects in infants with complex congenital heart disease. Catheter Cardiovasc Interv 2007;70:731-9.  Back to cited text no. 32    
33.Hill SL, Mizelle KM, Vellucci SM, Feltes TF, Cheatham JP. Radiofrequency perforation and cutting balloon septoplasty of intact atrial septum in a newborn with hypoplastic left heart syndrome using transesophageal ICE probe guidance. Catheter Cardiovasc Interv 2005;64:214-7.  Back to cited text no. 33    
34.Cheung YF, Sanatani S, Leung MP, Human DG, Chau AK, Culham JA. Early and intermediate-term complications of self-expanding stents limit its potential application in children with congenital heart disease. J Am Coll Cardiol 2000;35:1007-15.  Back to cited text no. 34    
35.Shih CC, Lin SJ, Chen YL, Su YY, Lai ST, Wu GJ, et al. The cytotoxicity of corrosion products of nitinol stent wire on cultured smooth muscle cells. J Biomed Mater Res 2000;52:395-403.  Back to cited text no. 35    
36.Redington AN, Weil J, Somerville J. Self expanding stents in congenital heart disease. Br Heart J 1994;72:378-83.  Back to cited text no. 36    
37.Brown SC, Eyskens B, Mertens L, Stockx L, Dumoulin M, Gewillig M. Self expandable stents for relief of venous baffle obstruction after the Mustard operation. Heart 1998;79:230-3.  Back to cited text no. 37    
38.Greenberg SB, Crisci KL, Koenig P, Robinson B, Anisman P, Russo P. Magnetic resonance imaging compared with echocardiography in the evaluation of pulmonary artery abnormalities in children with tetralogy of Fallot following palliative and corrective surgery. Pediatr Radiol 1997;27:932-5.  Back to cited text no. 38    
39.Lock JE, Castaneda-Zuniga WR, Fuhrman BP, Bass JL. Balloon dilation angioplasty of hypoplastic and stenotic pulmonary arteries. Circulation 1983;67:962-7.  Back to cited text no. 39    
40.Ring JC, Bass JL, Marvin W, Fuhrman BP, Kulik TJ, Foker JE, et al. Management of congenital stenosis of a branch pulmonary artery with balloon dilation angioplasty. Report of 52 procedures. J Thorac Cardiovasc Surg 1985;90:35-44.  Back to cited text no. 40    
41.Gentles TL, Lock JE, Perry SB. High pressure balloon angioplasty for branch pulmonary artery stenosis: Early experience. J Am Coll Cardiol 1993;22:867-72.  Back to cited text no. 41    
42.Rocchini AP, Kveselis D, Dick M, Crowley D, Snider AR, Rosenthal A. Use of balloon angioplasty to treat peripheral pulmonary stenosis. Am J Cardiol 1984;54:1069-73.  Back to cited text no. 42    
43.Zeevi B, Berant M, Blieden LC. Midterm clinical impact versus procedural success of balloon angioplasty for pulmonary artery stenosis. Pediatr Cardiol 1997;18:101-6.  Back to cited text no. 43    
44.Bergersen L, Lock JE. What is the current option of first choice for treatment of pulmonary arterial stenosis? Cardiol Young 2006;16:329-38.  Back to cited text no. 44    
45.Bush DM, Hoffman TM, Del Rosario J, Eiriksson H, Rome JJ Frequency of restenosis after balloon pulmonary arterioplasty and its causes. Am J Cardiol 2000;86:1205-9.  Back to cited text no. 45    
46.O'Laughlin MP, Perry SB, Lock JE, Mullins CE. Use of endovascular stents in congenital heart disease. Circulation 1991;83:1923-39.  Back to cited text no. 46    
47.O'Laughlin MP, Slack MC, Grifka RG, Perry SB, Lock JE, Mullins CE. Implantation and intermediate-term follow-up of stents in congenital heart disease. Circulation 1993;88:605-14.  Back to cited text no. 47    
48.Shaffer KM, Mullins CE, Grifka RG, O'Laughlin MP, McMahon W, Ing FF, et al. Intravascular stents in congenital heart disease: Short- and long-term results from a large single-center experience. J Am Coll Cardiol 1998;31:661-7.  Back to cited text no. 48    
49.Fogelman R, Nykanen D, Smallhorn JF, McCrindle BW, Freedom RM, Benson LN. Endovascular stents in the pulmonary circulation. Clinical impact on management and medium-term follow-up. Circulation 1995;92:881-5.  Back to cited text no. 49    
50.Ing FF, Grifka RG, Nihill MR, Mullins CE. Repeat dilation of intravascular stents in congenital heart defects. Circulation 1995;92:893-7.  Back to cited text no. 50    
51.McMahon CJ, El-Said HG, Grifka RG, Fraley JK, Nihill MR, Mullins CE. Redilation of endovascular stents in congenital heart disease: Factors implicated in the development of restenosis and neointimal proliferation. J Am Coll Cardiol 2001;38:521-6.  Back to cited text no. 51    
52.Ungerleider RM, Johnston TA, O'Laughlin MP, Jaggers JJ, Gaskin PR. Intraoperative stents to rehabilitate severely stenotic pulmonary vessels. Ann Thorac Surg 2001;71:476-81.  Back to cited text no. 52    
53.Bφkenkamp R, Blom NA, De Wolf D, Francois K, Ottenkamp J, Hazekamp MG. Intraoperative stenting of pulmonary arteries. Eur J Cardiothorac Surg 2005;27:544-7.  Back to cited text no. 53    
54.Hjortdal VE, Redington AN, de Leval MR, Tsang VT. Hybrid approaches to complex congenital cardiac surgery. Eur J Cardiothorac Surg 2002;22:885-90.  Back to cited text no. 54    
55.McMahon CJ, El Said HG, Vincent JA, Grifka RG, Nihill MR, Ing FF, et al. Refinements in the implantation of pulmonary arterial stents: Impact on morbidity and mortality of the procedure over the last two decades. Cardiol Young 2002;12:445-52.  Back to cited text no. 55    
56.Chiu KM, Chen JS, Yeh SJ, Lin TY, Ma JY, Li SJ, et al. Hybrid angioplasty for left pulmonary artery stenosis after total correction of tetralogy of Fallot: Report of one case. Acta Paediatr Taiwan 2005;46:174-7.  Back to cited text no. 56    
57.Ashwath R, Gruenstein D, Siwik E. Percutaneous stent placement in children weighing less than 10 kilograms. Pediatr Cardiol 2008;29:562-7.  Back to cited text no. 57    
58.Sreeram N, Emmel M, Ben Mime L, Brockmeier K, Bennink G. Perioperative placement of stents for relief of proximal pulmonary arterial stenoses in infants. Cardiol Young 2008;18:158-64.  Back to cited text no. 58    
59.Schneider MB, Zartner P, Duveneck K, Lange PE. Various reasons for repeat dilatation of stented pulmonary arteries in paediatric patients. Heart 2002;88:505-9.  Back to cited text no. 59    
60.Duke C, Rosenthal E, Qureshi SA. The efficacy and safety of stent redilatation in congenital heart disease. Heart 2003;89:905-12.  Back to cited text no. 60    
61.McMahon CJ, El-Said HG, Mullins CE. Three new applications of stent technology in a single patient. Tex Heart Inst J 2001;28:125-8.  Back to cited text no. 61    
62.Stapleton GE, Hamzeh R, Mullins CE, Zellers TM, Justino H, Nugent A, et al. Simultaneous stent implantation to treat bifurcation stenoses in the pulmonary arteries: Initial results and long-term follow up. Catheter Cardiovasc Interv 2009;73:557-63.  Back to cited text no. 62    
63.Rosales AM, Lock JE, Perry SB, Geggel RL. Interventional catheterization management of perioperative peripheral pulmonary stenosis: Balloon angioplasty or endovascular stenting. Catheter Cardiovasc Interv 2002;56:272-7.  Back to cited text no. 63    
64.Rutledge JM, Grifka RG, Bryant LL, Mullins CE, Vincent JA. Balloon dilation and stent implant through the side of a previously placed intravascular stent: A new option for the interventionalist. Catheter Cardiovasc Interv 2002;56:387-93.  Back to cited text no. 64    
65.Zeevi B, Keane JF, Perry SB, Lock JE. Balloon dilation of postoperative right ventricular outflow obstructions. J Am Coll Cardiol 1989;14:401-8. discussion 09-12.  Back to cited text no. 65    
66.Lloyd TR, Marvin WJ Jr, Mahoney LT, Lauer RM. Balloon dilation valvuloplasty of bioprosthetic valves in extracardiac conduits. Am Heart J 1987;114:268-74.  Back to cited text no. 66    
67.Hosking MC, Benson LN, Nakanishi T, Burrows PE, Williams WG, Freedom RM. Intravascular stent prosthesis for right ventricular outflow obstruction. J Am Coll Cardiol 1992;20:373-80.  Back to cited text no. 67    
68.Pedra CA, Justino H, Nykanen DG, VanArsdell G, Coles JG, Williams WG, et al. Percutaneous stent implantation to stenotic bioprosthetic valves in the pulmonary position. J Thorac Cardiovasc Surg 2002;124:82-7.  Back to cited text no. 68    
69.Lurz P, Coats L, Khambadkone S, Nordmeyer J, Boudjemline Y, Schievano S, et al. Percutaneous pulmonary valve implantation: Impact of evolving technology and learning curve on clinical outcome. Circulation 2008;117:1964-72.  Back to cited text no. 69    
70.Hijazi ZM, Fahey JT, Kleinman CS, Hellenbrand WE. Balloon angioplasty for recurrent coarctation of aorta. Immediate and long-term results. Circulation 1991;84:1150-6.  Back to cited text no. 70    
71.Singer MI, Rowen M, Dorsey TJ. Transluminal aortic balloon angioplasty for coarctation of the aorta in the newborn. Am Heart J 1982;103:131-2.  Back to cited text no. 71    
72.Maheshwari S, Bruckheimer E, Fahey JT, Hellenbrand WE. Balloon angioplasty of postsurgical recoarctation in infants: The risk of restenosis and long-term follow-up. J Am Coll Cardiol 2000;35:209-13.  Back to cited text no. 72    
73.Hellenbrand WE, Allen HD, Golinko RJ, Hagler DJ, Lutin W, Kan J. Balloon angioplasty for aortic recoarctation: Results of Valvuloplasty and Angioplasty of Congenital Anomalies Registry. Am J Cardiol 1990;65:793-7.  Back to cited text no. 73    
74.Ovaert C, Benson LN, Nykanen D, Freedom RM. Transcatheter treatment of coarctation of the aorta: A review. Pediatr Cardiol 1998;19:27-44; discussion 45-7.  Back to cited text no. 74    
75.Ino T, Ohkubo M. Dilation mechanism, causes of restenosis and stenting in balloon coarctation angioplasty. Acta Paediatr 1997;86:367-71.  Back to cited text no. 75    
76.Marshall AC, Perry SB, Keane JF, Lock JE. Early results and medium-term follow-up of stent implantation for mild residual or recurrent aortic coarctation. Am Heart J 2000;139:1054-60.  Back to cited text no. 76    
77.McCrindle BW, Jones TK, Morrow WR, Hagler DJ, Lloyd TR, Nouri S, et al. Acute results of balloon angioplasty of native coarctation versus recurrent aortic obstruction are equivalent. Valvuloplasty and Angioplasty of Congenital Anomalies (VACA) Registry Investigators. J Am Coll Cardiol 1996;28:1810-7.  Back to cited text no. 77    
78.Fletcher SE, Nihill MR, Grifka RG, O'Laughlin MP, Mullins CE. Balloon angioplasty of native coarctation of the aorta: Midterm follow-up and prognostic factors. J Am Coll Cardiol 1995;25:730-4.  Back to cited text no. 78    
79.Rao PS, Galal O, Smith PA, Wilson AD. Five- to nine-year follow-up results of balloon angioplasty of native aortic coarctation in infants and children. J Am Coll Cardiol 1996;27:462-70.  Back to cited text no. 79    
80.Mendelsohn AM, Lloyd TR, Crowley DC, Sandhu SK, Kocis KC, Beekman RH 3 rd . Late follow-up of balloon angioplasty in children with a native coarctation of the aorta. Am J Cardiol 1994;74:696-700.  Back to cited text no. 80    
81.Forbes TJ, Garekar S, Amin Z, Zahn EM, Nykanen D, Moore P, et al. Procedural results and acute complications in stenting native and recurrent coarctation of the aorta in patients over 4 years of age: A multi-institutional study. Catheter Cardiovasc Interv 2007;70:276-85.  Back to cited text no. 81    
82.Isner JM, Donaldson RF, Fulton D, Bhan I, Payne DD, Cleveland RJ. Cystic medial necrosis in coarctation of the aorta: A potential factor contributing to adverse consequences observed after percutaneous balloon angioplasty of coarctation sites. Circulation 1987;75:689-95.  Back to cited text no. 82    
83.Hamdan MA, Maheshwari S, Fahey JT, Hellenbrand WE. Endovascular stents for coarctation of the aorta: Initial results and intermediate-term follow-up. J Am Coll Cardiol 2001;38:1518-23.  Back to cited text no. 83    
84.Ebeid MR, Prieto LR, Latson LA. Use of balloon-expandable stents for coarctation of the aorta: Initial results and intermediate-term follow-up. J Am Coll Cardiol 1997;30:1847-52.  Back to cited text no. 84    
85.Thanopoulos BD, Hadjinikolaou L, Konstadopoulou GN, Tsaousis GS, Triposkiadis F, Spirou P. Stent treatment for coarctation of the aorta: Intermediate term follow up and technical considerations. Heart 2000;84:65-70.  Back to cited text no. 85    
86.Suαrez de Lezo J, Pan M, Romero M, Medina A, Segura J, Lafuente M, et al. Immediate and follow-up findings after stent treatment for severe coarctation of aorta. Am J Cardiol 1999;83:400-6.  Back to cited text no. 86    
87.Shah L, Hijazi Z, Sandhu S, Joseph A, Cao QL. Use of endovascular stents for the treatment of coarctation of the aorta in children and adults: Immediate and midterm results. J Invasive Cardiol 2005;17:614-8.  Back to cited text no. 87    
88.Varma C, Benson LN, Butany J, McLaughlin PR. Aortic dissection after stent dilatation for coarctation of the aorta: A case report and literature review. Catheter Cardiovasc Interv 2003;59:528-35.  Back to cited text no. 88    
89.Taylor PR, Gaines PA, McGuinness CL, Cleveland TJ, Beard JD, Cooper G, et al. Thoracic aortic stent grafts-early experience from two centres using commercially available devices. Eur J Vasc Endovasc Surg 2001;22:70-6.  Back to cited text no. 89    
90.Pedra CA, Fontes VF, Esteves CA, Arrieta SR, Braga SL, Justino H, et al. Use of covered stents in the management of coarctation of the aorta. Pediatr Cardiol 2005;26:431-9.  Back to cited text no. 90    
91.Golden AB, Hellenbrand WE. Coarctation of the aorta: Stenting in children and adults. Catheter Cardiovasc Interv 2007;69:289-99.  Back to cited text no. 91    
92.Magee AG, Brzezinska-Rajszys G, Qureshi SA, Rosenthal E, Zubrzycka M, Ksiazyk J, et al. Stent implantation for aortic coarctation and recoarctation. Heart 1999;82:600-6.  Back to cited text no. 92    
93.Mahadevan VS, Jimeno S, Benson LN, McLaughlin PR, Horlick EM. Pre-closure of femoral venous access sites used for large-sized sheath insertion with the Perclose device in adults undergoing cardiac intervention. Heart 2008;94:571- 2.  Back to cited text no. 93    
94.Forbes TJ, Moore P, Pedra CA, Zahn EM, Nykanen D, Amin Z, et al. Intermediate follow-up following intravascular stenting for treatment of coarctation of the aorta. Catheter Cardiovasc Interv 2007;70:569-77.  Back to cited text no. 94    
95.De Lezo JS, Sancho M, Pan M, Romero M, Olivera C, Luque M. Angiographic follow-up after balloon angioplasty for coarctation of the aorta. J Am Coll Cardiol 1989;13:689-95.  Back to cited text no. 95    
96.Zanjani KS, Sabi T, Moysich A, Ovroutski S, Peters B, Miera O, et al. Feasibility and efficacy of stent redilatation in aortic coarctation. Catheter Cardiovasc Interv 2008;72:552-6.  Back to cited text no. 96    
97.Kuehne T, Pietzner K, Lehmkuhl HB, Gelernter D, Peters B, Krueger JJ, et al. Oral everolimus inhibits neointimal proliferation in prosthetic pulmonary valved stents in pigs. J Heart Valve Dis 2008;17:465-72.  Back to cited text no. 97    
98.Gunn J, Cleveland T, Gaines P. Covered stent to treat co- existent coarctation and aneurysm of the aorta in a young man. Heart 1999;82:351.  Back to cited text no. 98    
99.Parks WJ, Ngo TD, Plauth WH Jr, Bank ER, Sheppard SK, Pettigrew RI, et al. Incidence of aneurysm formation after Dacron patch aortoplasty repair for coarctation of the aorta: Long-term results and assessment utilizing magnetic resonance angiography with three-dimensional surface rendering. J Am Coll Cardiol 1995;26:266-71.  Back to cited text no. 99    
100.Cowley CG, Orsmond GS, Feola P, McQuillan L, Shaddy RE. Long-Term, Randomized Comparison of Balloon Angioplasty and Surgery for Native Coarctation of the Aorta in Childhood. Circulation 2005;111:3453-6.  Back to cited text no. 100    
101.Ince H, Petzsch M, Rehders T, Kische S, Kφrber T, Weber F, et al. Percutaneous endovascular repair of aneurysm after previous coarctation surgery. Circulation 2003;108:2967-70.  Back to cited text no. 101    
102.Gawenda M, Aleksic M, Heckenkamp J, Krüger K, Brunkwall J. Endovascular repair of aneurysm after previous surgical coarctation repair. J Thorac Cardiovasc Surg 2005;130:1039-43.  Back to cited text no. 102    
103.Bell RE, Taylor PR, Aukett M, Young CP, Anderson DR, Reidy JF. Endoluminal repair of aneurysms associated with coarctation. Ann Thorac Surg 2003;75:530-3.  Back to cited text no. 103    
104.Fejzic Z, van Oort A. Fatal dissection of the descending aorta after implantation of a stent in a 19-year-old female with Turner's syndrome. Cardiol Young 2005;15:529-31.  Back to cited text no. 104    
105.Collins N, Mahadevan V, Horlick E. Aortic rupture following a covered stent for coarctation: Delayed recognition. Catheter Cardiovasc Interv 2006;68:653-5.  Back to cited text no. 105    
106.Tsai SF, Hill SL, Cheatham JP. Treatment of aortic arch aneurysm with a NuMED-covered stent and restoration of flow to excluded left subclavian artery: Perforation and dilation of e-PTFE can be done! Catheter Cardiovasc Interv 2009;73:385-9.  Back to cited text no. 106    
107.Gravereaux EC, Faries PL, Burks JA, Latessa V, Spielvogel D, Hollier LH, et al. Risk of spinal cord ischemia after endograft repair of thoracic aortic aneurysms. J Vasc Surg 2001;34:997-1003.  Back to cited text no. 107    
108.Wada T, Yao H, Miyamoto T, Mukai S, Yamamura M. Prevention and detection of spinal cord injury during thoracic and thoracoabdominal aortic repairs. Ann Thorac Surg 2001;72:80-4; discussion 85.  Back to cited text no. 108    
109.Rigatelli G, Cardaioli P, Dell'Avvocata F, Giordan M, Roncon L. Transcatheter-covered stent implantation in an unusual post-surgical right ventricle outflow tract stenosis. Eur Heart J 2008;29:1078.  Back to cited text no. 109    
110.Holzer RJ, Chisolm JL, Hill SL, Cheatham JP. Stenting complex aortic arch obstructions. Catheter Cardiovasc Interv 2008;71:375-82.  Back to cited text no. 110    
111.Elson JD, Becker GJ, Wholey MH, Ehrman KO. Vena caval and central venous stenoses: Management with Palmaz balloon-expandable intraluminal stents. J Vasc Interv Radiol 1991;2:215-23.  Back to cited text no. 111    
112.Rao PS, Wilson AD. Chylothorax, an unusual complication of baffle obstruction following Mustard operation: Successful treatment with balloon angioplasty. Am Heart J 1992;123:244-8.  Back to cited text no. 112    
113.Ward CJ, Mullins CE, Nihill MR, Grifka RG, Vick GW 3 rd . Use of intravascular stents in systemic venous and systemic venous baffle obstructions. Short-term follow-up results. Circulation 1995;91:2948-54.  Back to cited text no. 113    
114.Michel-Behnke I, Hagel KJ, Bauer J, Schranz D. Superior caval venous syndrome after atrial switch procedure: Relief of complete venous obstruction by gradual angioplasty and placement of stents. Cardiol Young 1998;8:443-8.  Back to cited text no. 114    
115.Cook SC, McCarthy M, Daniels CJ, Cheatham JP, Raman SV. Usefulness of multislice computed tomography angiography to evaluate intravascular stents and transcatheter occlusion devices in patients with d-transposition of the great arteries after mustard repair. Am J Cardiol 2004;94:967-9.  Back to cited text no. 115    
116.Ebeid MR, Gaymes CH, McMullan MR, Shores JC, Smith JC, Joransen JA. Catheter management of occluded superior baffle after atrial switch procedures for transposition of great vessels. Am J Cardiol 2005;95:782-6.  Back to cited text no. 116    
117.Asgar AW, Mirò J, Ibrahim R. Recanalization of systemic venous baffles by radiofrequency perforation and stent implantation. Catheter Cardiovasc Interv 2007;70:591-4.  Back to cited text no. 117    
118.Abdulhamed JM, al Yousef S, Khan MA, Mullins C. Balloon dilatation of complete obstruction of the superior vena cava after Mustard operation for transposition of great arteries. Br Heart J 1994;72:482-5.  Back to cited text no. 118    
119.Abdulhamed JM, Alyousef SA, Mullins C. Endovascular stent placement for pulmonary venous obstruction after Mustard operation for transposition of the great arteries. Heart 1996;75:210-2.  Back to cited text no. 119    
120.MacLellan-Tobert SG, Cetta F, Hagler DJ. Use of intravascular stents for superior vena caval obstruction after the Mustard operation. Mayo Clin Proc 1996;71:1071-6.  Back to cited text no. 120    
121.Benito F, Sαnchez C, Oliver J. [Stent implantation in systemic venous baffle obstruction after Mustard-type operation repair in an adult]. Rev Esp Cardiol 1997;50:904-5.  Back to cited text no. 121    
122.Bu'Lock FA, Tometzki AJ, Kitchiner DJ, Arnold R, Peart I, Walsh KP. Balloon expandable stents for systemic venous pathway stenosis late after Mustard's operation. Heart 1998;79:225-9.  Back to cited text no. 122    
123.Hijazi ZM, Ruiz CE, Patel H, Cao QL, Dorros G. Catheter therapy for fontan baffle obstruction and leak, using an endovascular covered stent. Cathet Cardiovasc Diagn 1998;45:158-61.  Back to cited text no. 123    
124.Miura T, Sano T, Matsuda H. Intravascular stenting of systemic venous baffle stenosis after corrective surgery for double outlet right ventricle with left isomerism. Heart 1999;81:218-20.  Back to cited text no. 124    
125.Schneider DJ, Moore JW. Transcatheter treatment of IVC channel obstruction and baffle leak after Mustard procedure for d-transposition of the great arteries using Amplatzer ASD device and multiple stents. J Invasive Cardiol 2001;13:306-9.  Back to cited text no. 125    
126.Daehnert I, Hennig B, Wiener M, Rotzsch C. Interventions in leaks and obstructions of the interatrial baffle late after Mustard and Senning correction for transposition of the great arteries. Catheter Cardiovasc Interv 2005;66:400-7.  Back to cited text no. 126    
127.Butera G, Aim E E, Carminati M. Use of radiofrequency energy and covered stents in patients with an occluded superior vena cava and requiring endocardial pacemaker implantation. J Invasive Cardiol 2008;20:E56-8.  Back to cited text no. 127    
128.Chintala K, Forbes TJ, Karpawich PP. Effectiveness of transvenous pacemaker leads placed through intravascular stents in patients with congenital heart disease. Am J Cardiol 2005;95:424-7.  Back to cited text no. 128    
129.Morchi GS, Pietra B, Boucek MM, Chan KC. Interventional cardiac catheterization procedures in pediatric cardiac transplant patients: Transplant surgery is not the end of the road. Catheter Cardiovasc Interv 2008;72:831-6.  Back to cited text no. 129    
130.Marini D, Boudjemline Y, Agnoletti G. Closure of extracardiac Fontan fenestration by using the covered Cheatham Platinum stent. Catheter Cardiovasc Interv 2007;69:1002-6.  Back to cited text no. 130    
131.Hancock Friesen CL, Zurakowski D, Thiagarajan RR, Forbess JM, del Nido PJ, Mayer JE, et al. Total anomalous pulmonary venous connection: An analysis of current management strategies in a single institution. Ann Thorac Surg 2005;79:596-606; discussion 596-606.  Back to cited text no. 131    
132.Devaney EJ, Chang AC, Ohye RG, Bove EL. Management of congenital and acquired pulmonary vein stenosis. Ann Thorac Surg 2006;81:992-5; discussion 95-6.  Back to cited text no. 132    
133.Lock JE, Bass JL, Castaneda-Zuniga W, Fuhrman BP, Rashkind WJ, Lucas RV Jr. Dilation angioplasty of congenital or operative narrowings of venous channels. Circulation 1984;70:457-64.  Back to cited text no. 133    
134.Seale AN, Daubeney PE, Magee AG, Rigby ML. Pulmonary vein stenosis: Initial experience with cutting balloon angioplasty. Heart 2006;92:815-20.  Back to cited text no. 134    
135.Michel-Behnke I, Luedemann M, Hagel KJ, Schranz D. Serial stent implantation to relieve in-stent stenosis in obstructed total anomalous pulmonary venous return. Pediatr Cardiol 2002;23:221-3.  Back to cited text no. 135    
136.Hyde JA, Stümper O, Barth MJ, Wright JG, Silove ED, de Giovanni JV, et al. Total anomalous pulmonary venous connection: Outcome of surgical correction and management of recurrent venous obstruction. Eur J Cardiothorac Surg 1999;15:735-40; discussion 40-1.  Back to cited text no. 136    
137.Michielon G, Di Donato RM, Pasquini L, Giannico S, Brancaccio G, Mazzera E, et al. Total anomalous pulmonary venous connection: Long-term appraisal with evolving technical solutions. Eur J Cardiothorac Surg 2002;22:184-91.  Back to cited text no. 137    
138.Mendeloff EN, Spray TL, Huddleston CB, Bridges ND, Canter CB, Mallory GB Jr. Lung transplantation for congenital pulmonary vein stenosis. Ann Thorac Surg 1995;60:903-6; discussion 07.  Back to cited text no. 138    
139.Mendelsohn AM, Bove EL, Lupinetti FM, Crowley DC, Lloyd TR, Fedderly RT, et al. Intraoperative and percutaneous stenting of congenital pulmonary artery and vein stenosis. Circulation 1993;88(5 Pt 2):II210-7.  Back to cited text no. 139    
140.Coulson JD, Bullaboy CA. Concentric placement of stents to relieve an obstructed anomalous pulmonary venous connection. Cathet Cardiovasc Diagn 1997;42:201-4.  Back to cited text no. 140    
141.Leonard GT Jr, Justino H, Carlson KM, Rossano JW, Neish SR, Mullins CE, et al. Atrial septal stent implant: Atrial septal defect creation in the management of complex congenital heart defects in infants. Congenit Heart Dis 2006;1:129-35.  Back to cited text no. 141    
142.Javois AJ, Van Bergen AH, Cuneo BF, Husayni TS. Novel approach to the newborn with hypoplastic left heart syndrome and intact atrial septum. Catheter Cardiovasc Interv 2005;66:268-72.  Back to cited text no. 142    
143.Holzer RJ, Wood A, Chisolm JL, Hill SL, Phillips A, Galantowicz M, et al. Atrial septal interventions in patients with hypoplastic left heart syndrome. Catheter Cardiovasc Interv 2008;72:696-704.  Back to cited text no. 143    
144.Cheatham JP. Intervention in the critically ill neonate and infant with hypoplastic left heart syndrome and intact atrial septum. J Interv Cardiol 2001;14:357-66.  Back to cited text no. 144    
145.Galantowicz M, Cheatham JP. Lessons learned from the development of a new hybrid strategy for the management of hypoplastic left heart syndrome. Pediatr Cardiol 2005;26:190-9.  Back to cited text no. 145    
146.Wilson J, Russell J, Williams W, Benson L. Fenestration of the Fontan circuit as treatment for plastic bronchitis. Pediatr Cardiol 2005;26:717-9.  Back to cited text no. 146    
147.Miga DE, Clark JM, Cowart KS, Radtke WA. Transcatheter fenestration of hemi-Fontan baffles after completion of Fontan physiology using balloon dilatation and stent placement. Cathet Cardiovasc Diagn 1998;43:429-32.  Back to cited text no. 147    
148.Michel-Behnke I, Luedemann M, Bauer J, Hagel KJ, Akintuerk H, Schranz D. Fenestration in extracardiac conduits in children after modified Fontan operation by implantation of stent grafts. Pediatr Cardiol 2005;26:93-6.  Back to cited text no. 148    
149.Bar-Cohen Y, Perry SB, Keane JF, Lock JE. Use of stents to maintain atrial defects and fontan fenestrations in congenital heart disease. J Interv Cardiol 2005;18:111-8.  Back to cited text no. 149    
150.Coe JY, Olley PM. A novel method to maintain ductus arteriosus patency. Journal J Am Coll Cardiol 1991;18:837-41.  Back to cited text no. 150    
151.Gibbs JL, Uzun O, Blackburn ME, Wren C, Hamilton JR, Watterson KG. Fate of the stented arterial duct. Circulation 1999;99:2621-5.  Back to cited text no. 151    
152.Alwi M, Choo KK, Latiff HA, Kandavello G, Samion H, Mulyadi MD. Initial results and medium-term follow- up of stent implantation of patent ductus arteriosus in duct- dependent pulmonary circulation. J Am Coll Cardiol 2004;44:438-45.  Back to cited text no. 152    
153.Michel-Behnke I, Akintuerk H, Thul J, Bauer J, Hagel KJ, Schranz D. Stent implantation in the ductus arteriosus for pulmonary blood supply in congenital heart disease. Catheter Cardiovasc Interv 2004;61:242-52.  Back to cited text no. 153    
154.Boshoff DE, Michel-Behnke I, Schranz D, Gewillig M. Stenting the neonatal arterial duct. Expert Rev Cardiovasc Ther 2007;5:893-901.  Back to cited text no. 154    
155.Gewillig M, Boshoff DE, Dens J, Mertens L, Benson LN. Stenting the neonatal arterial duct in duct-dependent pulmonary circulation: New techniques, better results. J Am Coll Cardiol 2004;43:107-12.  Back to cited text no. 155    
156.Schneider M, Zartner P, Sidiropoulos A, Konertz W, Hausdorf G. Stent implantation of the arterial duct in newborns with duct-dependent circulation. Eur Heart J 1998;19:1401-9.  Back to cited text no. 156    
157.Kaestner M, Handke RP, Photiadis J, Sigler M, Schneider MB. Implantation of stents as an alternative to reoperation in neonates and infants with acute complications after surgical creation of a systemic-to-pulmonary arterial shunt. Cardiol Young 2008;18:177-84.  Back to cited text no. 157    
158.Galantowicz M, Cheatham JP, Phillips A, Cua CL, Hoffman TM, Hill SL, et al. Hybrid approach for hypoplastic left heart syndrome: Intermediate results after the learning curve. Ann Thorac Surg 2008;85:2063-70; discussion 70-1.  Back to cited text no. 158    
159.Holzer RJ, Chisolm JL, Hill SL, Olshove V, Phillips A, Cheatham JP, et al. "Hybrid" stent delivery in the pulmonary circulation. J Invasive Cardiol 2008;20:592-8.  Back to cited text no. 159    
160.Dohlen G, Chaturvedi RR, Benson LN, Ozawa A, Van Arsdell GS, Fruitman DS, et al. Stenting of the right ventricular outflow tract in the symptomatic infant with tetralogy of Fallot. Heart 2009;95:142-7.  Back to cited text no. 160    
161.Zeidenweber CM, Kim DW, Vincent RN. Right ventricular outflow tract and pulmonary artery stents in children under 18 months of age. Catheter Cardiovasc Interv 2007;69:23-7.  Back to cited text no. 161    
162.Walsh MA, Lee KJ, Chaturvedi R, Van Arsdell GS, Benson LN. Radiofrequency perforation of the right ventricular outflow tract as a palliative strategy for pulmonary atresia with ventricular septal defect. Catheter Cardiovasc Interv 2007;69:1015-20.  Back to cited text no. 162    
163.Laudito A, Bandisode VM, Lucas JF, Radtke WA, Adamson WT, Bradley SM. Right ventricular outflow tract stent as a bridge to surgery in a premature infant with tetralogy of Fallot. Ann Thorac Surg 2006;81:744-6.  Back to cited text no. 163    
164.Breinholt JP, Nugent AW, Law MA, Justino H, Mullins CE, Ing FF. Stent fractures in congenital heart disease. Catheter Cardiovasc Interv 2008;72:977-82.  Back to cited text no. 164    
165.Peng LF, McElhinney DB, Nugent AW, Powell AJ, Marshall AC, Bacha EA, et al. Endovascular stenting of obstructed right ventricle-to-pulmonary artery conduits: A 15-year experience. Circulation 2006;113:2598-605.  Back to cited text no. 165    
166.Haworth SG. Collateral arteries in pulmonary atresia with ventricular septal defect. A precarious blood supply. Br Heart J 1980;44:5-13.  Back to cited text no. 166    
167.Brown SC, Eyskens B, Mertens L, Dumoulin M, Gewillig M. Percutaneous treatment of stenosed major aortopulmonary collaterals with balloon dilatation and stenting: What can be achieved? Heart 1998;79:24-8.  Back to cited text no. 167    
168.McLeod KA, Blackburn ME, Gibbs JL. Stenting of stenosed aortopulmonary collaterals: A new approach to palliation in pulmonary atresia with multifocal aortopulmonary blood supply. Br Heart J 1994;71:487-9.  Back to cited text no. 168    
169.Vimala J, Kulkarni S. Stenting stenosed aortopulmonary collateral arteries in pulmonary atresia with ventricular septal defect. Indian Heart J 2004;56:242-4.  Back to cited text no. 169    
170.Ormiston JA, Serruys PW, Regar E, Dudek D, Thuesen L, Webster MW, et al. A bioabsorbable everolimus- eluting coronary stent system for patients with single de- novo coronary artery lesions (ABSORB): A prospective open- label trial. Lancet 2008;371:899-907.  Back to cited text no. 170    
171.Serruys PW, Ormiston JA, Onuma Y, Regar E, Gonzalo N, Garcia-Garcia HM, et al. A bioabsorbable everolimus- eluting coronary stent system (ABSORB): 2-year outcomes and results from multiple imaging methods. Lancet 2009;373:897-910.  Back to cited text no. 171    
172.Tanimoto S, Bruining N, van Domburg RT, Rotger D, Radeva P, Ligthart JM, et al. Late stent recoil of the bioabsorbable everolimus-eluting coronary stent and its relationship with plaque morphology. J Am Coll Cardiol 2008;52:1616-20.  Back to cited text no. 172    
173.Tamai H, Igaki K, Kyo E, Kosuga K, Kawashima A, Matsui S, et al. Initial and 6-month results of biodegradable poly-l-lactic acid coronary stents in humans. Circulation 2000;102:399-404.  Back to cited text no. 173    
174.Li Z, Gu X, Lou S, Zheng Y. The development of binary Mg-Ca alloys for use as biodegradable materials within bone. Biomaterials 2008;29:1329-44.  Back to cited text no. 174    
175.Erbel R, Di Mario C, Bartunek J, Bonnier J, de Bruyne B, Eberli FR, et al. Temporary scaffolding of coronary arteries with bioabsorbable magnesium stents: A prospective, non-randomised multicentre trial. Lancet 2007;369:1869-75.  Back to cited text no. 175    
176.Peeters P, Bosiers M, Verbist J, Deloose K, Heublein B. Preliminary results after application of absorbable metal stents in patients with critical limb ischemia. J Endovasc Ther 2005;12:1-5.  Back to cited text no. 176    
177.Zartner P, Buettner M, Singer H, Sigler M. First biodegradable metal stent in a child with congenital heart disease: Evaluation of macro and histopathology. Catheter Cardiovasc Interv 2007;69:443-6.  Back to cited text no. 177    
178.Zartner P, Cesnjevar R, Singer H, Weyand M. First successful implantation of a biodegradable metal stent into the left pulmonary artery of a preterm baby. Catheter Cardiovasc Interv 2005;66:590-4.  Back to cited text no. 178    
179.Schranz D, Zartner P, Michel-Behnke I, Akinturk H. Bioabsorbable metal stents for percutaneous treatment of critical recoarctation of the aorta in a newborn. Catheter Cardiovasc Interv 2006;67:671-3.  Back to cited text no. 179    
180.McMahon CJ, Oslizlok P, Walsh KP. Early restenosis following biodegradable stent implantation in an aortopulmonary collateral of a patient with pulmonary atresia and hypoplastic pulmonary arteries. Catheter Cardiovasc Interv 2007;69:735-8.  Back to cited text no. 180    
181.Peuster M, Hesse C, Schloo T, Fink C, Beerbaum P, von Schnakenburg C. Long-term biocompatibility of a corrodible peripheral iron stent in the porcine descending aorta. Biomaterials 2006;27:4955-62.  Back to cited text no. 181    
182.Peuster M, Wohlsein P, Brugmann M, Ehlerding M, Seidler K, Fink C, et al. A novel approach to temporary stenting: Degradable cardiovascular stents produced from corrodible metal-results 6-18 months after implantation into New Zealand white rabbits. Heart 2001;86:563-9.  Back to cited text no. 182    
183.Mueller PP, May T, Perz A, Hauser H, Peuster M. Control of smooth muscle cell proliferation by ferrous iron. Biomaterials 2006;27:2193-200.  Back to cited text no. 183    
184.Ewert P, Riesenkampff E, Neuss M, Kretschmar O, Nagdyman N, Lange PE. Novel growth stent for the permanent treatment of vessel stenosis in growing children: An experimental study. Catheter Cardiovasc Interv 2004;62:506-10.  Back to cited text no. 184    
185.Ewert P, Peters B, Nagdyman N, Miera O, Kuhne T, Berger F. Early and mid-term results with the Growth Stent--a possible concept for transcatheter treatment of aortic coarctation from infancy to adulthood by stent implantation? Catheter Cardiovasc Interv 2008;71:120-6.  Back to cited text no. 185    
186.Tepe G, Wendel HP, Khorchidi S, Schmehl J, Wiskirchen J, Pusich B, et al. Thrombogenicity of various endovascular stent types: An in vitro evaluation. J Vasc Interv Radiol 2002;13:1029-35.  Back to cited text no. 186    
187.Tepe G, Schmehl J, Wendel HP, Schaffner S, Heller S, Gianotti M, et al. Reduced thrombogenicity of nitinol stents--in vitro evaluation of different surface modifications and coatings. Biomaterials 2006;27:643-50.  Back to cited text no. 187    
188.Serruys PW, Sianos G, Abizaid A, Aoki J, den Heijer P, Bonnier H, et al. The effect of variable dose and release kinetics on neointimal hyperplasia using a novel paclitaxel-eluting stent platform: The Paclitaxel In-Stent Controlled Elution Study (PISCES). J Am Coll Cardiol 2005;46:253-60.  Back to cited text no. 188    
189.Koch A, Ludwig J, Zink S, Singer H. Isolated left pulmonary artery: Interventional stenting of a persistent fifth aortic arch. Catheter Cardiovasc Interv 2007;70:105-9.  Back to cited text no. 189    
190.Riede FT, Schneider P, Dahnert I. Transient sirolimus serum levels after implantation of a sirolimus eluting stent in an infant. Clin Res Cardiol 2007;96:508-10.  Back to cited text no. 190    
191.Jhang WK, Chang YJ, Park CS, Oh YM, Kim YH, Yun TJ. Hybrid palliation for right atrial isomerism associated with obstructive total anomalous pulmonary venous drainage. Interact Cardiovasc Thorac Surg 2008;7:282-4.  Back to cited text no. 191    
192.Wong DT, Yoo SJ, Lee KJ. Implantation of drug-eluting stents for relief of obstructed infra-cardiac totally anomalous pulmonary venous connection in isomerism of the right atrial appendages. Cardiol Young 2008;18:628-30.  Back to cited text no. 192    

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Correspondence Address:
Bjoern Peters
Abteilung für Angeborene Herzfehler, Deutsches Herzzentrum Berlin, Augustenburger Platz 1, 13353 Berlin
Germany
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DOI: 10.4103/0974-2069.52802

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14 Intravascular stent implantation for the management of pulmonary artery stenosis
Charles Krisnanda,Samuel Menahem,Geoffrey K. Lane
Heart, Lung and Circulation. 2013; 22(1): 56
[Pubmed] | [DOI]
15 Stenting a Pulmonary Artery Stenosis Through the Pulmonary Native Outflow Tract in a Congenitally Corrected Transposition of the Great Arteries
Joana Miranda,Maria João Baptista,Jorge Moreira
Pediatric Cardiology. 2013; 34(4): 1048
[Pubmed] | [DOI]
16 Stent angioplasty to relieve left pulmonary artery obstruction caused by patent ductus arteriosus device occlusion
Peter N. Dean,Michael C. Slack
Catheterization and Cardiovascular Interventions. 2013; 82(3): 480
[Pubmed] | [DOI]
17 Percutaneous Angioplasty of Upstream Right Pulmonary artery stenosis post Tetralogy of Fallot (TOF) repair with use of 3D Multi slice-CT imaging
Pankaj Jariwala,Saratchandra Koduganti
Journal of Indian College of Cardiology. 2013;
[Pubmed] | [DOI]
18 A pressing matter-mediastinal fibrosis with near obliteration of the pulmonary arteries
John Conleth Murphy,Nicola Johnston,Mark S. Spence
Catheterization and Cardiovascular Interventions. 2013; 81(6): 1079
[Pubmed] | [DOI]
19 Surgery following primary right ventricular outflow tract stenting for Fallotæs Tetralogy and variants: rehabilitation of small pulmonary arteries
D. J. Barron,B. Ramchandani,J. Murala,O. Stumper,J. V. De Giovanni,T. J. Jones,J. Stickley,W. J. Brawn
European Journal of Cardio-Thoracic Surgery. 2013; 44(4): 656
[Pubmed] | [DOI]
20 Reduction of the postoperative thrombogenic risk in reconstruction on the obstructed superior caval vein with autovenous in situ flap
Topalov, I. and Marinov, G. and Topalova, M.
Comptes Rendus de LæAcademie Bulgare des Sciences. 2013; 66(6): 897-904
[Pubmed]
21 Novel Bioresorbable Stent Design and Fabrication: Congenital Heart Disease Applications
Welch, T.R. and Eberhart, R.C. and Reddy, S.V. and Wang, J. and Nugent, A. and Forbess, J.
Cardiovascular Engineering and Technology. 2013; 4(2): 171-182
[Pubmed]
22 Stenting a pulmonary artery stenosis through the pulmonary native outflow tract in a congenitally corrected transposition of the great arteries
Miranda, J. and Baptista, M.J. and Moreira, J.
Pediatric Cardiology. 2013; 34(4): 1048-1049
[Pubmed]
23 First experience with andraStent XL implantation in children and adolescents with congenital heart diseases
Venczelova, Z. and Tittel, P. and Masura, J.
Catheterization and Cardiovascular Interventions. 2013; 81(1): 103-110
[Pubmed]
24 Intravascular stent implantation for the management of pulmonary artery stenosis
Krisnanda, C. and Menahem, S. and Lane, G.K.
Heart Lung and Circulation. 2013; 22(1): 56-70
[Pubmed]
25 Stenting Options for Coarctation of the Aorta
Bruckheimer, E. and Pedra, C.A.C.
Interventional Cardiology Clinics. 2013; 2(1): 115-129
[Pubmed]
26 The FDA review process for cardiac medical devices in children: A review for the clinician
Almond, C.S.
Progress in Pediatric Cardiology. 2012; 33(2): 105-109
[Pubmed]
27 The FDA review process for cardiac medical devices in children: A review for the clinician
Christopher S. Almond
Progress in Pediatric Cardiology. 2012; 33(2): 105
[Pubmed] | [DOI]
28 Per-operative stent placement in the right pulmonary artery; a hybrid technique for the management of pulmonary artery branch stenosis at the time of pulmonary valve replacement in adult Fallot patients
F. Windhausen, S. M. Boekholdt, B. J. Bouma, M. Groenink, A. P. C. M. Backx, R. J. Winter, B. J. M. Mulder, M. G. Hazekamp, D. R. Koolbergen
Netherlands Heart Journal. 2011;
[VIEW] | [DOI]
29 Complications of aortic stenting in patients below 20 years old: Immediate and intermediate follow-up
Molaei, A., Merajie, M., Mortezaeian, H., Rad, E.M., Shemirani, R.H.H.
# # Journal of Tehran University Heart Center. 2011; 6(4): 202-205
[Pubmed]
30 Atrial septal stenting to increase interatrial shunting in cyanotic congenital heart diseases: A report of two cases
Yalçin, Y., Zeybek, C., Önsel, I.Ö., Bilal, M.S.
Turk Kardiyoloji Dernegi Arsivi. 2011; 39(5): 422-426
[Pubmed]
31 Shape-memory polymers in biomedical applications | [polimery z pamie{ogonek}cia{ogonek} kształtu w zastosowaniach biomedycznych]
Kłosek, R., Komacki, J., Orchel, A., Dzierzewicz, Z.
Farmaceutyczny Przeglad Naukowy. 2010; 7(11): 39-44
[Pubmed]
32 Shape-memory polymers in biomedical applications [polimery z pamie{ogonek
KÅ‚osek, R. and Komacki, J. and Orchel, A. and Dzierzewicz, Z.
Farmaceutyczny Przeglad Naukowy. 2010; 7(11): 39-44
[Pubmed]
33 Poly(α-hydroxyacids) in biomedical applications: Synthesis and properties of lactic acid polymers
Lipsa, R. and Tudorachi, N. and Vasile, C.
E-Polymers. 2010; (087)
[Pubmed]
34 Stent graft exclusion of a pseudoaneurysm in a Blalock-Taussig shunt
Angel Sanchez-Recalde, Gonzalo Garzón, José M. Oliver
Catheterization and Cardiovascular Interventions. 2010; 76(2): 251
[VIEW] | [DOI]
35 Emergency balloon dilation or stenting of critical coarctation of aorta in newborns and infants: An effective interim palliation
Francis, E., Gayathri, S., Vaidyanathan, B., Kannan, B.R.J., Kumar, R.K.
Annals of Pediatric Cardiology. 2009; 2(2): 111-115
[Pubmed]



 

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