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F20 Project: The Incisionizers

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Galo Arias, Leila Hollis, Dorian Lee, Victor Nguyen

 

Incisionizers

Retractor 360: A self-retaining surgical retractor to assist in exposure during small-incisional surgery

Multidimensional retraction with our NEW Retractor 360

Project Description: 

After an incision has been performed in a surgical procedure, retractors are used to hold the wound open while surgeons operate. There are several different retractors currently used during small-incision procedures. Each of these designs falls short of a complete solution for the surgeon’s needs for a variety of reasons. Hand-held retractors require assistance from a surgical assistant, which often overcrowds the surgical area and obstructs the surgeon’s field of view. Self-retaining devices retract only in one plane and are bulky. A self-retaining retractor for small incision surgeries (<5 cm) solves the problems of having only uni-axial retraction and overcrowding of the surgical field. A ball joint within a cart that holds the retractor facilitates customizable retraction of the tissue in the X, Y, and Z axes. The retractor carts hold retractors in place without human assistance and enable 360° access to the surgical site by traveling along the device’s ring that encircles the incision. Our device, Retractor 360, eliminates the need for hand-held retractors. The carts can hold retraction, illumination, and suction devices. Market research has shown that there is a $1.4 billion market for self-retaining retractors as of 2017 and growing at a rate of 3.2%, faster than the hand-held retractor market. Testing of Retractor 360 began with a virtual stress test using stainless steel 316L. After 20mmHg was applied to the model retractor, no load or tensile strength failure, nor plastic deformation was observed. A cadaveric leg was used as a model for small incision surgery. Device functionality was assessed qualitatively, along with the set-up time and stability through application of shear force to failure to hold set position. The results were within acceptable limits to move forward with the device.

Dr. Sarah Avila, MD

Oculoplastic Surgeon

Emory University Hospital

 

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