TY - JOUR
T1 - Closure of Secundum Atrial Septal Defects by Using the Occlutech Occluder Devices in More Than 1300 Patients
T2 - The IRFACODE Project: A Retrospective Case Series
AU - Haas, Nikolaus A.
AU - Soetemann, Dagmar B.
AU - Ates, Ismail
AU - Baspinar, Osman
AU - Ditkivskyy, Igor
AU - Duke, Christopher
AU - Godart, Francois
AU - Lorber, Avraham
AU - Oliveira, Edmundo
AU - Onorato, Eustaquio
AU - Pac, Feyza
AU - Promphan, Worakan
AU - Riede, Frank Thomas
AU - Roymanee, Supaporn
AU - Sabiniewicz, Robert
AU - Shebani, Suhair Omar
AU - Sievert, Horst
AU - Tin, Do
AU - Happel, Christoph M.
N1 - Publisher Copyright:
© 2016 Wiley Periodicals, Inc.
PY - 2016/10/1
Y1 - 2016/10/1
N2 - Background: The Occlutech Figulla ASD device series (OFSO) shows an improved device design for interventional ASD closure, larger follow-up series are missing. Methods: We retrospectively reviewed the feasibility, safety, implantation properties, results, and follow-up of ASD closure using Occlutech devices over a 5 year period by establishing a multi-institutional collaborative result registry with 16 contributing centers from 11 countries (IRFACODE). Results: In 1315 patients of all age groups (female 66.9%), successful (98%) ASD closure was performed (mean age 28.9 years, weight 52 kg, height 148.6 cm). Of the defects, 47.9% showed no or only a deficient aortic rim; in 11.9%, there was more than one defect; a septum aneurysm was present in 21.5%; and the mean implanted device size was 20.5 mm. Immediate closure was achieved in 78.6%, at discharge in 83.1%, and 96.4% and 97.3% at 6 and 12 months follow-up, respectively. During a mean follow-up of 2.7 years (in total 3597 patient years), significant complications were minimal (total = 8, <1%) with secondary device embolizations in five and AV-blocks in three patients. No erosion or death was reported. Conclusion: ASD closure using OFSO is feasible in a large variety of patients, safe with only a minimal risk of severe side effects and especially without any aortic erosions despite a large percentage of large and complicated defects.
AB - Background: The Occlutech Figulla ASD device series (OFSO) shows an improved device design for interventional ASD closure, larger follow-up series are missing. Methods: We retrospectively reviewed the feasibility, safety, implantation properties, results, and follow-up of ASD closure using Occlutech devices over a 5 year period by establishing a multi-institutional collaborative result registry with 16 contributing centers from 11 countries (IRFACODE). Results: In 1315 patients of all age groups (female 66.9%), successful (98%) ASD closure was performed (mean age 28.9 years, weight 52 kg, height 148.6 cm). Of the defects, 47.9% showed no or only a deficient aortic rim; in 11.9%, there was more than one defect; a septum aneurysm was present in 21.5%; and the mean implanted device size was 20.5 mm. Immediate closure was achieved in 78.6%, at discharge in 83.1%, and 96.4% and 97.3% at 6 and 12 months follow-up, respectively. During a mean follow-up of 2.7 years (in total 3597 patient years), significant complications were minimal (total = 8, <1%) with secondary device embolizations in five and AV-blocks in three patients. No erosion or death was reported. Conclusion: ASD closure using OFSO is feasible in a large variety of patients, safe with only a minimal risk of severe side effects and especially without any aortic erosions despite a large percentage of large and complicated defects.
KW - ASD closure
KW - Flex
KW - Flex II
KW - IRFACODE project
KW - Occlutech device
UR - http://www.scopus.com/inward/record.url?scp=84963657364&partnerID=8YFLogxK
U2 - 10.1002/ccd.26497
DO - 10.1002/ccd.26497
M3 - Article
C2 - 27029396
AN - SCOPUS:84963657364
SN - 1522-1946
VL - 88
SP - 571
EP - 581
JO - Catheterization and Cardiovascular Interventions
JF - Catheterization and Cardiovascular Interventions
IS - 4
ER -