10-4-215 Introduction devices that are used postoperatively following endoscopic sinus surgery (ESS) to maintain patency of the sinus openings in the postoperative period to serve as a local drug delivery vehicle Indications Circumferentially exposed bone (after modified Lothrop for tumor resection or extensive mucosal denudation) Traumatic fracture of outflow tract Restenosis after surgery Frontal neo-ostium smaller than 5 mm Middle turbinate destabilization Recalcitrant inflammatory disease (purulence, granulation, osteitic bone, polypoid obstruction, granulomatous disease) Contraindications No absolute contraindications exist to placement of a frontal recess stent Manipulation and trauma of the frontal recess during frontal stent placement and any inflammatory reaction caused by the stent itself may lead to scarring and poor healing of the recess formation of biofilms limited indications for a well-defined period of time Type of Stents Middle meatal stent Frontal sinus stent Drug containing stents
Type of Stents (A)Sheet of 1/100-inch thick silastic fashioned into a T-shaped stent
(B) reinforced silastic sheet used for Draf 3 cavity
(F) Intersect ENT Propel sinus implant Complications T-tube may occlude due to poor position/incorrect size of T-Tube Granulation tissue may form at proximal or distal end of T-tube May be presence of cracking/splintering of the T-tube References Operative Techniques in Laryngology, Clark a. Rosen & C. Blake Simpson, Published by Springer Role of Stents in E.S.S, Dr. T. Balasubramanian Frontal Stenting Sinus Techniques, Devyani Lal, MD, American Academy of Otolaryngology-Head and Neck Surgery and American Rhinologic Society