Premium
A new breakable stent for recoarctation in early infancy: Preliminary Clinical Experience
Author(s) -
Grohmann Jochen,
Sigler Matthias,
Siepe Matthias,
Stiller Brigitte
Publication year - 2016
Publication title -
catheterization and cardiovascular interventions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.988
H-Index - 116
eISSN - 1522-726X
pISSN - 1522-1946
DOI - 10.1002/ccd.26393
Subject(s) - medicine , fluoroscopy , stent , sedation , surgery , balloon , retrospective cohort study , single center
Objectives Transcatheter treatment of aortic coarctation (CoA) via stent implantation has become an established treatment option depending on the patient's age and CoA type. Background The Osypka BabyStent ® is a low‐profiled, balloon‐expandable cobalt‐chrome stent to treat aortic CoA in infants, which is breakable to permit unrestricted growth. We hereby evaluated our initial clinical experience to demonstrate the feasibility and efficacy of this new nonlicensed device, which we have occasionally implanted in critically ill patients or when redo‐surgery would entail an excessively high risk. Methods Retrospective single‐center analysis of all available data during and after treatment with a BabyStent implanted in infants with considerable re‐CoA or reobstruction of the aortic arch after former surgery. All interventions took place under fluoroscopy and conscious sedation with local anesthesia or general anesthesia. Results Five BabyStents were implanted in four infants with technical success in all of them—median age 10 weeks (range 5–21), median bodyweight 3.8 kg (range 2.7–4.5). Aortic diameters enlarged from median 2.25 mm (range 1.5–3.3) to median 5.3 mm (range 4.6–6.0). The follow‐up period lasting up to 26 months (median 8.5, range 2–26) was uneventful concerning stent‐related complications. Conclusions BabyStent ® implantation for recoarctation was effective. However, our initial experience with the device is limited to short‐ and midterm follow‐up only. None of the stents was subsequently overdilated with the intention to break due to our patients’ limited somatic growth so far. A multicenter survey has been initiated to justify device approval. © 2016 Wiley Periodicals, Inc.