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on July 19, 2004

Circulation. 2004
Published online before print July 19, 2004, doi: 10.1161/01.CIR.0000137116.12176.A6
A more recent version of this article appeared on August 3, 2004
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Submitted on July 1, 2003
Revised on April 1, 2004
Accepted on April 4, 2004

Transcatheter Device Closure of Congenital and Postoperative Residual Ventricular Septal Defects

Alison L. Knauth MD, PhD, James E. Lock MD, Stanton B. Perry MD, Doff B. McElhinney MD, Kimberlee Gauvreau ScD, Michael J. Landzberg MD, Jonathan J. Rome MD, William E. Hellenbrand MD, Carlos E. Ruiz MD, and Kathy J. Jenkins MD, MPH*

From the Department of Cardiology, Children’s Hospital, Boston, Mass (A.L.K., J.E.L., S.B.P., D.B.M., K.G., M.J.L., K.J.J.); Department of Pediatrics, Children’s Hospital of Philadelphia, Philadelphia, Pa (J.J.R.); Department of Pediatrics, Columbia University College of Physicians and Surgeons, New York, NY (W.E.H.); and Department of Pediatrics, University of Illinois, Chicago (C.E.R.). Dr Perry is now at Stanford University Medical Center, Stanford, Calif. Dr Ruiz is now at the University of Illinois, Chicago.

* To whom correspondence should be addressed. E-mail: kathy.jenkins{at}tch.harvard.edu.

Background--Our purpose was to describe a 13-year experience with patients undergoing transcatheter device closure of unrepaired congenital or postoperative residual ventricular septal defects (VSDs).

Methods and Results--Since 1989, 170 patients (median age, 3.9 years) have undergone catheterization for closure of 1 or more congenital (n=92) or postoperative (n=78) residual VSDs using successive generations of STARFlex-type devices. Outcomes included echocardiographic assessment of residual flow and device position, assessment of VSD shunt/severity, and adverse events. Among 168 patients in whom device implantation was performed, between 1 and 7 devices were placed per patient (median, 1), with multiple devices placed in 40%. There was a significant decrease in left-to-right shunting after device implantation (P<0.001) and significant improvement in VSD size/severity, and device position proved stable. Of 332 adverse events, 39 were related to the device and 261 were related to the catheterization; all but 5 occurred in the periprocedural period. At a median follow-up of 24 months (0 to 154 months), 14 patients had died and 18 had device(s) explanted.

Conclusions--Congenital and postoperative VSD closure using STARFlex-type devices resulted in stable improvement in clinical status and decreased interventricular shunting. Although periprocedural events occurred frequently, late events caused by the device were rare. Transcatheter device closure is an effective management option for patients with complex muscular VSDs that are difficult to approach surgically and for postoperative residual VSDs.


Key words: catheterization • heart septal defects • ventricles




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