Introduction
Cobra head deformity is encountered either due to faulty device design or erroneous deployment technique. For successful deployment of the device, the deformity needs either manual correction if it is transient or deployment of a new device in the case of permanent deformity. In this report, we describe the use of transient cobra head deformity as technical support for successful deployment of the device.
Case description
A 10-year-old boy was diagnosed to have a 21-mm ostium secundum atrial septal defect. He underwent transcatheter closure of the defect using a 24-mm atrial septal occluder (AGA Medical Corporation, Plymouth, Minnesota, United States of America). All initial attempts of device deployment failed including rapid deployment from the left and the right upper pulmonary vein. The left atrial disc was repeatedly prolapsing through periaortic area. After initial few attempts, the device assumed cobra head deformity (Fig 1a and b and Supplementary video S1). The deformation, however, was short lasting, and there was spontaneous resumption of normal shape. In yet another attempt, when the left atrial disc formed cobra head deformity, the right atrial disc of the device was quickly deployed in its position. By the time, the deformed left atrial disc regained its original shape, the right atrial disc was already in place and prevented the prolapse of the device resulting in successful placement of the device (Fig 1c). Follow-up echocardiogram showed a well-placed device with no residual flow.
Discussion
Cobra head deformity is a benign distortion of atrial septal occluder that occurs in approximately 3% device implantations. Reference Fischer, Stieh, Uebing, Hoffmann, Morf and Kramer1 Initially thought to result from faulty device, it is now apparent that this deformity stems from excessive device rotation. This excessive rotation and twisting of the nitinol wires occur within the delivery system or while deploying across the atrial septum. Reference Cooke, Gelman and Harper2,Reference Waight and Hijazi3 Various technical reasons, such as the opening of the device close to the left atrial wall, difficulty in loading, excessive twisting while advancing, kinking of the delivery sheath have been proposed for the formation of Cobra head deformity. A relatively slow deployment of the left atrial disc is yet another reason postulated for cobra head deformity. Reference Yip and Chan4 Larger devices, due to greater length of the device, and larger than recommended delivery sheath, due to its extra lumen, make cobra head more likely although there are reports wherein the deformity resolved using a larger sheath. Reference Trehan, Mukhopadhyay, Yusuf, Gupta, Suryavanshi and Mehta5–Reference Hoole, McNab, Rana, Davies and Shapiro7 An appropriate size sheath, ease of loading the device, and failed attempts even with rapid deployment technique exclude most of the aforementioned causes in our case. Instead, the most likely reason of the deformity was excessive but reversible twisting of the nitinol wire during multiple attempts of deployment that failed.
Once formed, depending upon the degree of rotation, the cobra head deformity may remain fixed or revert to normal shape spontaneously within the heart or once retrieved outside. While it is advisable to not use a device with fixed deformity, it is acceptable to implant a device with transient deformity that readily corrects itself. We hypothesise that in our case the cobra head deformity increased the inertia of the left atrial disc and resulted in slow movement of the left atrial disc. By the time the left atrium disc arrived at the periaortic region, the right atrial disc was already blocking the right atrial aspect of the defect and enabled successful deployment by preventing prolapse of the device.
Conclusion
Cobra head deformity is an uncommon deformity of the atrial septal occluder device. While it is advisable to not use a device with fixed deformity, it is acceptable to implant a device with transient deformity that readily corrects itself. Transient cobra head deformity and resultant delayed movement of the left atrial disc can be helpful in the successful deployment of the device.
Supplementary material
To view supplementary material for this article, please visit https://doi.org/10.1017/S1047951120004084
Acknowledgements
None.
Financial support
This research received no specific grant from any funding agency, commercial, or not-for-profit sectors.
Conflicts of interest
None.
Ethical standards
The authors assert that all procedures contributing to this work comply with the ethical standards as mentioned in the Helsinki Declaration of 1975, as revised in 2008.