Abstract

Injection laryngoplasty (IL), which has been practiced for more than a century, is a powerful, minimally invasive technique with the added potential of application in the outpatient setting. It has been advocated for the treatment of many laryngeal abnormalities that can result in symptomatic glottal incompetence. The recent increased attention to this procedure represents a resurgence of the laryngeal injection techniques that were widely touted in the 1960s and 1970s with the advent of polytef (Teflon) injection for paralytic dysphonia. Because several injectable dermal fillers, primarily designed for cosmetic uses, have since been developed, numerous new materials are currently available for vocal fold augmentation. Among them are micronized acellular human cadaveric dermis (Cymetra; LifeCell Corp, Branchburg, New Jersey), calcium hydroxylapatite, carboxymethylcellulose, and several products containing hyaluronic acid compounds. Newly described office-based, transnasal and percutaneous (thyrohyoid) routes for laryngeal injection have also been reported. 1,2 Despite all of these nuances of technique and injectable materials, the common technical pitfalls and complications of IL remain largely unchanged.

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