Super telescopic catheter system parallel to a contralateral stiff guide wire to cross extremely complex pulmonary arteries

Access to complex stenotic pulmonary arteries can be challenging due to their anatomy or secondary to prior multiple surgeries and interventions. Two techniques have been previously described to address this issue: the telescopic catheter-in-long sheath parallel to a stiff guidewire technique and the use of a microcatheter in a telescopic scope. We integrated and modified these techniques creating a super telescopic system with a SuperCross (R) microcatheter-in-catheter-in-long sheath, parallel to a contralateral stiff guidewire to access a previously repaired and stented left pulmonary artery. The stiff wire support and the 90 degrees flexiblity of the Supercross (R) microcatheter assembled coaxial to the diagnostic catheter and the long sheath contributed to the successful ballooning and stenting-in-stent of the pulmonary artery

316 Percutaneous right outflow tract valve implantation: when should we pre-stent?

IntroductionPercutaneous pulmonary valve insertion has been recently introduced in clinical setting. Patient selection is widely accepted. Initial results demonstrated early and differed stent fractures that make consider pre-stenting as a previous step for the procedure. To date, differed or intra-procedure pre-stenting are both accepted techniques.Patients and methodsWe reviewed patients included over the last 6 months in the prospective study (REVALV) for patients undergoing RVOT intervention for severe stenosis and/or insufficiency. Only valved stent group is analyzed here. All patients undergoing valved stent implantation are previously pre-stented with a bare metal stent according to present recommendations. Thirty-seven patients were included, distributed in two gropus according moment of pre-stenting: differed pre-stenting (bare metal stent implantation several days before valved stent implantation -20 patients-) and same procedure pre-stenting (bare metal stent implantation at the same procedure of valved stent implantation-17 patients-). For analytical purposes, we considered RVOT anatomy (homograft, synthetic tube, patch-extended RVOT or native outflow tract).ResultsOverall, no differences were found regarding mean procedure times (77,35 vs 96,88, p=NS) and time of hospitalization (2,95 vs 3,63, p=NS). Mean delay time from pre-stenting to valvulation was 196,5 + −68 days. Rv to Ao ratio improvement from basal to valvulation was significantly better in intra-procedure pre-stenting group (0,172 vs 0,373, p=0,009). Concerning complications, bare metal stent mobilization happened just after implantation while trying to place valved stent delivery gain. Two pelvic hematomas were observed (one of each group).ConclusionsIntra-procedure pre-stenting influences final result when considering RV-to-Ao ratio improvement, probably related to increase radial strength. The risk, however, remains higher as freshly implanted bare metal stent can mobilize, especially in native RVOT. Stratification of patient should be considered while choosing candidates for valved stent implantation

286 – Percutaneous right outflow tract valve implantation: substrate matters

IntroductionPercutaneous pulmonary valve insertion has been recently introduced in clinical setting. Patient selection is widely accepted. These candidates are however heterogeneous, in regard of heart defects, and type of surgical right ventricular outflow tract (RVOT) reconstruction. It is presently unclear in the literature if type of surgical reconstruction matters for the success of the pulmonary valve insertion. Our goal was to compare the hemodynamic results of percutaneous pulmonary valve in patients with homografts, prosthetic conduit or RVOT reconstructed with patch.Patients and methodsWe reviewed patients included over the last 6 months in the prospective study (REVALV) for patients undergoing RVOT intervention for severe stenosis and/or insufficiency. Only valved stent group is analyzed here. All patients undergoing valved stent implantation are previously pre-stented with a bare metal stent according to present recommendations. Thirty-seven patients were included, distributed in three groups according to type of RVOT reconstruction (homograft REVALV is a multicentric prospective study for patients undergoing RVOT intervention for severe stenosis and/or insufficiency. Patients are distributed in three groups according to type of RVOT reconstruction (homograft, n = 10; prosthetic conduit, n = 20; RVOT enlargement by patch, n = 7).ResultsOverall, all groups were similar in RV to AP gradient improvement (after pre-stenting mean 30,79 vs 28 p = NS; final result mean 23,71 vs 28,17, p = NS), RV to aorta pressures ratio (after pre-stenting 0,187 vs 0,3117 p = NS; final result man 0,315 vs 0,317, p = NS). If considering non-extensible synthetic tubes we observe that RV-to-AP improvement is significantly worst to the rest of the group (mean 7,07 vs 0,17, p = 0,005). When focusing on outflow tract diameter, results did not differ in homograft group and patch group. In contrast, diameter did play a role in those patients having a synthetic tube, with a cut-off at 20mm diameter. Below 20mm, relieve of outflow tract gradient was significantly worse than for bigger conduits.DiscussionPulmonary valve insertion is efficient in all type of RVOT reconstruction at least in the short term. The diameter of the conduits did not play a role in RVOT obstruction relief as long as surgical substrates are homografts or patch enlargement. In patients with prosthetic conduits, size matters. In non-extensible synthetic tubes results are worst. Reduced distensibility and progressive diameter reduction may lead to not consider these patients as good candidates for this procedure

Transcatheter Closure of Patent Ductus Arteriosus in Infants With Weight Under 1,500 Grams.

Persistent patent ductus arteriosus (PDA) is very common in preterm infants, especially in extremely preterm infants. Despite significant advances in management of these vulnerable infants, there has been no consensus on management of PDA-when should we treat, who should we treat, how should we treat and in fact there is no agreement on how we should define a hemodynamically significant PDA. Medical management with non-steroidal anti-inflammatory drugs (NSAIDs) remains the first line of therapy with moderate success rate in closing the PDA. Paracetamol has been reported to be a safe and equally effective medical therapy for closure of PDA. However, additional studies on its long-term safety and efficacy in extremely low birth weight infants are needed before paracetamol can be recommended as standard treatment for a PDA in preterm infants. Surgical ligation of PDA is not without an increased risk of mortality and co-morbidities. Recently, there has been a significant interest in percutaneous transcatheter closure of PDA in preterm infants, including extremely low birth weight infants. Transcatheter PDA closure in preterm ELBW infants is technically feasible with high PDA occlusion success rates and acceptable complication rates as compared to surgical ligation. Many centers have reported promising early- and mid-term follow-up results. However, they need to be further tested in the prospective well-designed studies and randomized controlled trials comparing the results and outcomes of this technique with current treatment strategies including medical treatment before they can be used as the new standard of care for PDA closure in extremely low birth weight infants

Transcatheter Closure of a Secundum Atrial Septal Defect with Deficient Aortic Rim Through the Left Internal Jugular Vein in a Child with Situs Inversus and Interrupted Inferior Vena Cava: Device's Choice Matters

Percutaneous closure of secundum atrial septal defect (sASD) in children with interrupted inferior vena cava is challenging, especially in case of deficient aortic rim. Trans-jugular access is generally preferred in this scenario. Patients with situs inversus and sASD also carry technical difficulties for transcatheter closure because of the orientation of the atrial septum. We report a successful case of percutaneous closure of a sASD with deficient aortic rim using an occlutech figulla flex II ASD device through the left internal jugular vein in a child with situs inversus, dextrocardia, and interrupted IVC. This case was facilitated by the absence of left-sided hub of the Occlutech device to provide stable opening of the device into the left atrium, whereas the ball-connection of the delivery system allowed an angle of almost 180 degrees between the device and the atrial septum

Echocardiographic Diagnosis and Hemodynamic Evaluation of Patent Ductus Arteriosus in Extremely Low Gestational Age Newborn (ELGAN) Infants.

Persistent Patent ductus arteriosus (PDA) is a common finding in extremely low gestational age newborn infants and its prevalence is inversely proportional to the gestational age. The presence of a persistent PDA is associated with increased mortality and several significant morbidities including intraventricular hemorrhage, pulmonary hemorrhage, necrotizing enterocolitis, and chronic lung disease or bronchopulmonary dysplasia. However, treating PDA has not been demonstrated to have beneficial impact on the long term outcomes. Currently there is no consensus on whether to treat the PDA or not, and if treat, when to treat and how to treat. The echocardiography is the investigation of choice to diagnose PDA, estimating the magnitude of shunt volume and assessing its hemodynamic significance, and to exclude/diagnose any associated congenital heart defect before any intervention. Various echocardiographic parameters and staging/scoring systems have been described to help the clincians making the clinical decisions and some of theses scoring systems are quite complex to apply in a busy day to day clinical practice. This concised review paper is focused to help the clinicians in making a clinical decision based upon clincial and echocardiography parameters. Hence, only the parameters which are commonly used and helpful in making the clinical decisions in day to day clincial practice have been described in this paper

Transcatheter tricuspid valve implantation: A multicentre French study

SummaryBackgroundTranscatheter valve-in-valve (VIV) implantation in failing bioprosthesis is an emerging field in cardiology.AimTo report on a French multicentre experience and a literature review of tricuspid VIV implantation.MethodsWe approached different institutions and collected 10 unpublished cases; a literature review identified 71 patients, including our 10 cases. Clinical aspects and haemodynamic data are discussed.ResultsAmong our 10 unpublished cases, the reason for implantation was significant tricuspid stenosis (n=4), significant tricuspid regurgitation (n=1) or mixed lesion (n=5). Implantation was performed under general anaesthesia at mean age 28±17 years. The 22mm Melody valve was implanted in seven patients; the Edwards SAPIEN valve was implanted in three patients. The procedure succeeded in all cases, despite two embolizations in the right cardiac chambers; in both cases, the valve was stabilized close to the tricuspid annulus using a self-expandable stent, before implantation of a second Edwards SAPIEN valve. Functional class improved in all but one case. Mean diastolic gradient decreased from 9±2.45mmHg to 3.65±0.7mmHg (p=0.007); no more than trivial regurgitation was noticed. Among the published cases, the Melody valve was implanted in 41 patients, the Edwards SAPIEN valve in 29 patients and the Braile valve in one patient. Short-term results were similar for our 10 cases, but mid-term results are not yet available.ConclusionsTricuspid VIV implantation using the Melody or Edwards SAPIEN valves is a feasible and effective procedure for selected patients with failing bioprosthesis