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Transcatheter transapical valve-in-valve implantation for degenerated mitral bioprosthesis

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345

Advances in Interventional Cardiology 2017; 13, 4 (50)

Image in intervention

Corresponding author:

Michał Lelek MD, PhD, 1st Department of Cardiology, Medical University of Silesia, Upper Silesian Medical Centre, 45/47 Ziołowa St, 40-635 Katowice, Poland, phone: +48 507 199 238, e-mail: michlel@wp.pl

Received: 4.10.2017, accepted: 28.10.2017.

Transcatheter transapical valve-in-valve implantation for degenerated mitral bioprosthesis

Michał Lelek1, Wojciech Wojakowski2, Damian Hudziak3, Anna Rybicka-Musialik1, Katarzyna Mizia-Stec1

11st Department of Cardiology, Medical University of Silesia, Upper Silesian Medical Centre, Katowice, Poland

23rd Department of Cardiology, Medical University of Silesia, Upper Silesian Medical Centre, Katowice, Poland

3Department of Cardiac Surgery, Medical University of Silesia, Upper Silesian Medical Centre, Katowice, Poland

Adv Interv Cardiol 2017; 13, 4 (50): 345–346 DOI: https://doi.org/10.5114/aic.2017.71621

A 76-year-old woman with a history of aortic and mi- tral valve (Mosaic 19 mm; Hancock II 25 mm bioprosthe- sis, Medtronic Inc., Minneapolis, Minnesota) replacement and former coronary artery bypass grafting in 2010 (left internal mammary artery-left anterior descending ar- tery (LIMA-LAD), aorta-obtuse marginal coronary artery (Ao-OM)) was admitted to our hospital with recurrent pulmonary edema. Her past medical history consisted of arterial hypertension, diabetes, renal insufficiency with an estimated glomerular filtration rate of 51 ml/min and previous stroke. Transthoracic (TTE) and transesopha- geal (TEE) echocardiography revealed a degenerated bi- oprosthesis in the mitral position with severe eccentric regurgitation (Figure 1 A); the aortic bioprosthesis was of normal function; moderate left ventricular systolic dys- function was observed (LVEF 45%). In coronary angiog- raphy patent LIMA-LAD and Ao-OM grafts were found.

Taking into account the high surgical risk, the Heart Team decided to perform a  mitral transcatheter valve- in-valve (TVIV) procedure. Mitral TVIV implantation was conducted under general anesthesia via the transapical approach. In the pre-procedural period the mitral bio- prosthesis was also evaluated and sized in multi-slice computed tomography (MSCT) (Figure 1 B). According to the manufacturer’s specifications with regard to the inner diameter of the Hancock II 25 mm bioprosthesis and the data obtained from MSCT, a 23 mm balloon-expandable SAPIEN XT valve (Edwards Lifesciences, Irvine, California) was slowly deployed extending 4 mm atrially relatively to the mitral radiopaque sewing ring during a short pe-

riod of rapid pacing (Figure 1 C). Peri-procedural TEE and TTE before discharge revealed good implant stability and no residual mitral regurgitation (Figure 1 D). The further in-hospital course was uneventful, and the patient was discharged on the seventh day after the procedure. Mi- tral TVIV implantation is an emerging clinically effective technique for eligible patients with a degenerated mitral bioprostheses [1]. The access to the mitral valve can be antegrade through the venous system with a transseptal approach or retrograde, through the left ventricle apex via a mini left thoracotomy. The first approach was found technically challenging, with difficulty in achieving co- axial alignment of the valve to the mitral prosthesis for optimal implantation [2]. The transapical approach pro- vides the shortest and co-axial access to the mitral valve.

A  potential complication of the mitral TVIV procedure is left ventricular outflow tract (LVOT) obstruction. The above risk should be determined by preoperative echo- cardiography and MSCT. In some cases a  high diastolic pressure gradient across the mitral orifice after TVIV pro- cedures was also reported [3]. Another important issue is selecting the proper implant size. The inner diameter of the previously implanted bioprosthesis provided by man- ufacturers as well as measurements obtained from MSCT are the most important. Generally, adequate oversizing should result in a “flared” or “conical” deployment, which will prevent atrial migration [4].

Conflict of interest

The authors declare no conflict of interest.

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Michał Lelek et al. ViV procedure for degenerated mitral bioprosthesis

346 Advances in Interventional Cardiology 2017; 13, 4 (50)

References

1. Dvir D, Webb J, Brecker S, et al. Transcatheter aortic valve re- placement for degenerative bioprosthetic surgical valves: re- sults from the global valve-in-valve registry. Circulation 2012;

126: 2335-44.

2. Webb JG, Wood DA, Ye J, et al. Transcatheter valve-in-valve implantation for failed bioprosthetic heart valves. Circulation 2010; 121: 1848-57.

3. Jagielak D, Kozaryn R, Jaguszewski M, et al. Patient-prosthesis mismatch   after mitral valve-in-valve procedure – at the cost of life or serious consequence? Postep Kardiol Interw 2015; 11:

154-5.

4. Bapat VV, Khaliel F, Ihleberg L.Delayed migration of Sapien valve following a  transcatheter mitral valve-in-valve implantation.

Catheter Cardiovasc Interv 2014; 83: 150-4.

Figure 1. A – Transesophageal echocardiography – severe mitral bioprosthesis regurgitation, B – computed tomography – inner diameter of Hancock II bioprosthesis, C – optimal position of implanted Sapien XT pros- thesis, D – three dimensional transesophageal echocardiography – visible good leaflet coaptation of Sapien XT prosthesis

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